From the post "Wrong, Wrong, Wrong" dated 25 May 2015,
F=∫Fρdx
where Fρ=i√2mc2G.tanh(G√2mc2(x−xz))
F=2mc2.ln(cosh(G√2mc2(x−xz))
within the boundary of ψ where 0≤x≤aψ. For, x≥aψ, we use Gaussian flux,
F=FG14πr2
at r=aψ
FG14πa2ψ=q4πεoa2ψ=2mc2.ln(cosh(π))
for a point mass xz=0 (in retrospect xz was not necessary, xz was to prevent the function Fρ from blowing up at x=0).
FG=8mc2πa2ψ.ln(cosh(π))
where ln(cosh(π))=2.4503.
Also,
qεo=4πa2ψm.2c2ln(cosh(π))
where m is a point mass/inertia in the respective field. Which suggests,
εo=12c2ln(cosh(π))=12∗2997924582∗ln(cosh(π))
εo=2.2704e−18
when
q=4πa2ψm
That q is the distribution of m on the surface of a sphere of radius aψ. Which seems to solve the problem of extending a point mass of mass density m to a mass of finite extent aψ.
But, the quoted value of εo is 8.8542e−12 from the definition,
εo=1μoc2
where μo=4π×10−7
we have 4π≈12.5664 vs 2ln(cosh(π))≈4.9006 and a scaling factor of 10−7.
The derived εo and defined value do not match.
Monday, May 30, 2016
A Big Temperature Particle
From the post "A Ψ Gun" dated 31 May 2016,
fres=0.061caψ
If the Sun is one big temperature particle,
aψ=695700000
fres=0.061∗299792458/695700000=0.026286
which is a period of 1/0.026286=38.043s
What happen to the Sun every 38.0 seconds?
Given,
G=π√2mc2aψ
msun=1.989e30
G=π√2∗1.989e30∗2997924582695700000
G=2.7001e15
None of the G values matches up. If m is to be mass density,
Gv=√3G√4πa3ψ
Gv=7.1895e1
and we apply a similar CORRECTION to the previous values;
for the case of an electron,
Gv=4.511e8∗√3√4π∗(2.8179403267e−15)3
Gv=1.474e30
and Earth,
Gv=5.109e14∗√3√4π∗(6371e3)3
Gv=1.552e4
The values still do not match up. m is the mass of a point particle.
m=ΔMΔV=dMdV as ΔV→0
the condition ΔV→0 applies for the fact that m is a point.
When the mass is not a point mass, m is the total mass of the particle because the force involved acts on the total mass of the particle.
fres=0.061caψ
If the Sun is one big temperature particle,
aψ=695700000
fres=0.061∗299792458/695700000=0.026286
which is a period of 1/0.026286=38.043s
What happen to the Sun every 38.0 seconds?
Given,
G=π√2mc2aψ
msun=1.989e30
G=π√2∗1.989e30∗2997924582695700000
G=2.7001e15
None of the G values matches up. If m is to be mass density,
Gv=√3G√4πa3ψ
Gv=7.1895e1
and we apply a similar CORRECTION to the previous values;
for the case of an electron,
Gv=4.511e8∗√3√4π∗(2.8179403267e−15)3
Gv=1.474e30
and Earth,
Gv=5.109e14∗√3√4π∗(6371e3)3
Gv=1.552e4
The values still do not match up. m is the mass of a point particle.
m=ΔMΔV=dMdV as ΔV→0
the condition ΔV→0 applies for the fact that m is a point.
When the mass is not a point mass, m is the total mass of the particle because the force involved acts on the total mass of the particle.
Saturday, May 28, 2016
X Ray, Inner Electron Cloud And Just As Shocking
From the post "A Shield" and "A Ψ Gun" both dated 27 May 2016,
fres=0.061caψ
aψ is driven to oscillate about x=π√2mc2G. The work done in moving ψ forward is given by,
∫π+Apπ−Awtanh(x)dx
On the return, at position x, ψ radiates this energy gained. The energy radiated is,
X=∫π+Apπ−Awtanh(x)dx−∫xπ−Awtanh(x)dx
X=[ln(cosh(x))]π+Apπ−Aw−[ln(cosh(x))]xπ−Aw
X=Xo−ln(cosh(x))
with, Xo=ln(cosh(π+Ap))
A plot of log(cosh(pi+2))-log(cosh(x)) shows an almost linear decrease in energy radiated given the position x=aψ,
U1/2 marks the value of aψ where work done travelling on the left and right side are equal.
We would also expect an almost linear increase in X as the amplitude Ap is increased at any given position, for example x=π. ie
Xπ=ln(cosh(x1/2+x))−ln(cosh(x1/2))
is almost increasing linearly. In addition, when aψ drops below
n.2πfnaψ=c --- (*)
where the particle(s) is in resonance along 2πaψ with n wavelengths along the perimeter of a circle of radius aψ, a radiation peak occurs as aψ move to a lower energy state n−1.
aψ is driven to a higher value above x=π√2mc2G by an external field, on its return, it travels below it normal energy state. It loses energy continuously, when it passes a resonance point given by (*), it emits an resonance peak. This is not the energy states given by the Schrodinger wave equation of orbiting electrons, they are energy states when two or more particles interacting as waves exist in a cloud of energy density, ψ, from the post "Two Quantum Wells, Quantum Tunneling, vmin" dated 19 Jul 2015. In particular, the driving field is affecting the inner electron clouds that surrounds the nucleus below the orbiting T+ particles as described in the post "The Rest Are In The Clouds" dated 16 Apr 2016.
The following table is the X ray emission data using high energy electron bombardment,
aψ1 and aψ2 are calculated data.
The split into Eα1 and Eα2 is consistent with the split in the solution for aψ in the post "Two Quantum Wells, Quantum Tunneling, vmin" dated 19 Jul 2015. Eβ is due to the energy state available at the next lower level, n−1.
We estimate the value of n and the next lower energy state n−1 by taking the ratio of,
ave.EαEβ=nn−1
since,
n.2πaψ=cfn=λn
λnλn−1=nn−1
Using the average value of Eα1 and Eα2 and Eβ to find aψ1 and aψ2 respectively.
aψ=λnn.2π
For Cu, the inner electron cloud has a radius of aψ=0.02447∗10−10
which is one fifth the size of the atomic radius at 1.45 A. This lead us to the resonance frequency,
fres=0.0612997924580.02447∗10−10=7.473∗1018Hz=7.473EHz
needed to drive aψ to resonance. Given an elementary electron charge of 1.602176565*10^{-19} C, a bombardment at fres is
Ires=qe.fres=1.602176565∗10−19∗7.473∗1018=1.1974A
This radiation due to the excitation of the inner electron clouds is in the X ray region. If this is true, with fres, X ray production is safer and cheaper... Hurrah! Just before you electrocute yourself, that's 1.1974 A per electron cloud. Hurrah!
The good news is any integer division of fres will still set the system into resonance but slowly. For example,
f=fres1000
will still resonate but has a slow buildup.
Note: As the atomic size increases the inner electron cloud is compressed to a smaller radius.
fres=0.061caψ
aψ is driven to oscillate about x=π√2mc2G. The work done in moving ψ forward is given by,
∫π+Apπ−Awtanh(x)dx
On the return, at position x, ψ radiates this energy gained. The energy radiated is,
X=∫π+Apπ−Awtanh(x)dx−∫xπ−Awtanh(x)dx
X=[ln(cosh(x))]π+Apπ−Aw−[ln(cosh(x))]xπ−Aw
X=Xo−ln(cosh(x))
with, Xo=ln(cosh(π+Ap))
A plot of log(cosh(pi+2))-log(cosh(x)) shows an almost linear decrease in energy radiated given the position x=aψ,
U1/2 marks the value of aψ where work done travelling on the left and right side are equal.
We would also expect an almost linear increase in X as the amplitude Ap is increased at any given position, for example x=π. ie
Xπ=ln(cosh(x1/2+x))−ln(cosh(x1/2))
is almost increasing linearly. In addition, when aψ drops below
n.2πfnaψ=c --- (*)
where the particle(s) is in resonance along 2πaψ with n wavelengths along the perimeter of a circle of radius aψ, a radiation peak occurs as aψ move to a lower energy state n−1.
The following table is the X ray emission data using high energy electron bombardment,
Element | ave Eα | Eα1 | Eα2 | Eβ | n | aψ1 | aψ2 |
Cr2,8,13,1 | 2.29100 | 2.28970 | 2.29361 | 2.08487 | 11 | 0.0331517775 | 0.0331858844 |
Fe2,8,14,2 | 1.93736 | 1.93604 | 1.93998 | 1.75661 | 10 | 0.0308378963 | 0.0310675679 |
Co2,8,15,2 | 1.79026 | 1.78897 | 1.79285 | 1.62079 | 10 | 0.0284964345 | 0.0286654428 |
Cu2.8.18.1 | 1.54184 | 1.54056 | 1.54439 | 1.39222 | 9 | 0.0272691257 | 0.0277007991 |
Mo2,8,18,13,1 | 0.71073 | 0.70930 | 0.71359 | 0.63229 | 8 | 0.0141412915 | 0.0143778083 |
aψ1 and aψ2 are calculated data.
The split into Eα1 and Eα2 is consistent with the split in the solution for aψ in the post "Two Quantum Wells, Quantum Tunneling, vmin" dated 19 Jul 2015. Eβ is due to the energy state available at the next lower level, n−1.
We estimate the value of n and the next lower energy state n−1 by taking the ratio of,
ave.EαEβ=nn−1
since,
n.2πaψ=cfn=λn
λnλn−1=nn−1
Using the average value of Eα1 and Eα2 and Eβ to find aψ1 and aψ2 respectively.
aψ=λnn.2π
For Cu, the inner electron cloud has a radius of aψ=0.02447∗10−10
which is one fifth the size of the atomic radius at 1.45 A. This lead us to the resonance frequency,
fres=0.0612997924580.02447∗10−10=7.473∗1018Hz=7.473EHz
needed to drive aψ to resonance. Given an elementary electron charge of 1.602176565*10^{-19} C, a bombardment at fres is
Ires=qe.fres=1.602176565∗10−19∗7.473∗1018=1.1974A
This radiation due to the excitation of the inner electron clouds is in the X ray region. If this is true, with fres, X ray production is safer and cheaper... Hurrah! Just before you electrocute yourself, that's 1.1974 A per electron cloud. Hurrah!
The good news is any integer division of fres will still set the system into resonance but slowly. For example,
f=fres1000
will still resonate but has a slow buildup.
Note: As the atomic size increases the inner electron cloud is compressed to a smaller radius.
Friday, May 27, 2016
A Ψ Gun
If we express fres in terms of aψ, the extend of ψ,
aψ=π√2mc2G
fres=sech(π)2πG√m=sech(π)2√2c2aψ
fres=√22sech(π)caψ
fres=0.061caψ
Does the system work in reverse? Once ψ is set into resonance, and fres is reduced does aψ increases.
Can a shield be projected forward by suddenly decreasing fres and turning off. In effect, an energy density ψ projectile.
And I continue to dream anime... 看ψ!
aψ=π√2mc2G
fres=sech(π)2πG√m=sech(π)2√2c2aψ
fres=√22sech(π)caψ
fres=0.061caψ
Does the system work in reverse? Once ψ is set into resonance, and fres is reduced does aψ increases.
Can a shield be projected forward by suddenly decreasing fres and turning off. In effect, an energy density ψ projectile.
And I continue to dream anime... 看ψ!
A Shield
The three plots of Fρ, F′ρ and F″ρ are provided below,
in the case of a simple spring-particle system, the force from the retaining spring changes direction and reverses the travel direction of the attached particle. The particle's motion is periodic and oscillatory. In the case of a particle held by a field, the nature of the particle's interaction with the field as a particle or as a wave changes the direction of the force. The field is negative and attracts the particle beyond π, as the particle returns below π it is repelled by the field as a wave and is eventually pushed out towards π again.
When the particle is oscillating, energy is conserved,
∫ππ−Awtanh(x)dx=∫π+Apπtanh(x)dx
Solving,
∫ππ−Awtanh(x)dx=∫π+Apπtanh(x)dx
[ln(cosh(x))]ππ−Aw=[ln(cosh(x))]π+Apπ
ln(cosh(π))−ln(cosh(π−A))=ln(cosh(π+A))−ln(cosh(π))
2ln(cosh(π))−ln(cosh(π−Aw))=ln(cosh(π+Ap))
2ln(cosh(π))=ln(cosh(π+Ap)cosh(π−Aw))
cosh2(π)=cosh(π+Ap)cosh(π−Aw)
cosh(π−Aw)=cosh2(π)cosh(π+Ap)
A plot of cosh(pi)*cosh(pi)/cosh(pi+x) and cosh(pi-x) gives,
where valid solutions to Aw and Ap share a common value on the y-axis.
It is interesting that a valid solution swings the particle within the boundary of −π and π across the center of ψ.
And the thickness of this shield is Aw+Ap.
The actual expression for Fρ the post "Not Exponential, But Hyperbolic And Positive Gravity!" dated 22 Nov 2014 is,
Fρ=i√2mc2G.tanh(G√2mc2(x−xz))
∂Fρ∂x=G2sech2(G√2mc2x)
where we let xz=0, ie a point particle, and ignore i,
at G√2mc2x=π or,
x=π√2mc2G
we approximate fres=12π√gradient|πm=12π√G2sech2(π)m
fres=sech(π)2πG√m=0.01373G√m
where m is the mass of the particle.
From the same post "Not Exponential, But Hyperbolic And Positive Gravity!" dated 22 Nov 2014, G has the same dimension (units) as √2mc2 per meter, the expression for fres has a consistent unit of per second. But without an estimate for G it is useless.
If the radius of an electron is
ae=2.8179403267e−15m
and its mass
m=9.10938291e−31kg
and that the ψ of an electron extend up to ae then,
ae=π√2mc2G
G=π√2mc2ae
G=4.511e8
So, in the case of an electron,
fres=0.01373G√m=0.013734.511e8√9.10938291e−31
fres=6.489e21Hz
We can still achieve resonance at integer division of this number although slow, but this shield is just the size of an electron.
In the case of Earth as one big gravity particle,
aE=6371e3m
and mass
mE=5.972e24kg
G=pi*sqrt(2*5.972*(299792458)^2*10^(24))/(6371e3)
G=5.109e14 and
fres=0.01373*5.109e14/sqrt(5.972e24)
fres=2.870Hz
on the surface of earth.
This frequency can be reproduced.
Good luck! And I dream of anime...ZZZ...
Note: Newton Gravitational Constant G=6.67408∗10−11,
GME=6.67408∗10−11∗5.972∗1024
GME=3.9858∗1014
in the case of a simple spring-particle system, the force from the retaining spring changes direction and reverses the travel direction of the attached particle. The particle's motion is periodic and oscillatory. In the case of a particle held by a field, the nature of the particle's interaction with the field as a particle or as a wave changes the direction of the force. The field is negative and attracts the particle beyond π, as the particle returns below π it is repelled by the field as a wave and is eventually pushed out towards π again.
When the particle is oscillating, energy is conserved,
∫ππ−Awtanh(x)dx=∫π+Apπtanh(x)dx
Solving,
∫ππ−Awtanh(x)dx=∫π+Apπtanh(x)dx
[ln(cosh(x))]ππ−Aw=[ln(cosh(x))]π+Apπ
ln(cosh(π))−ln(cosh(π−A))=ln(cosh(π+A))−ln(cosh(π))
2ln(cosh(π))−ln(cosh(π−Aw))=ln(cosh(π+Ap))
2ln(cosh(π))=ln(cosh(π+Ap)cosh(π−Aw))
cosh2(π)=cosh(π+Ap)cosh(π−Aw)
cosh(π−Aw)=cosh2(π)cosh(π+Ap)
A plot of cosh(pi)*cosh(pi)/cosh(pi+x) and cosh(pi-x) gives,
where valid solutions to Aw and Ap share a common value on the y-axis.
It is interesting that a valid solution swings the particle within the boundary of −π and π across the center of ψ.
And the thickness of this shield is Aw+Ap.
The actual expression for Fρ the post "Not Exponential, But Hyperbolic And Positive Gravity!" dated 22 Nov 2014 is,
Fρ=i√2mc2G.tanh(G√2mc2(x−xz))
∂Fρ∂x=G2sech2(G√2mc2x)
where we let xz=0, ie a point particle, and ignore i,
at G√2mc2x=π or,
x=π√2mc2G
we approximate fres=12π√gradient|πm=12π√G2sech2(π)m
fres=sech(π)2πG√m=0.01373G√m
where m is the mass of the particle.
From the same post "Not Exponential, But Hyperbolic And Positive Gravity!" dated 22 Nov 2014, G has the same dimension (units) as √2mc2 per meter, the expression for fres has a consistent unit of per second. But without an estimate for G it is useless.
If the radius of an electron is
ae=2.8179403267e−15m
and its mass
m=9.10938291e−31kg
and that the ψ of an electron extend up to ae then,
ae=π√2mc2G
G=π√2mc2ae
G=4.511e8
So, in the case of an electron,
fres=0.01373G√m=0.013734.511e8√9.10938291e−31
fres=6.489e21Hz
We can still achieve resonance at integer division of this number although slow, but this shield is just the size of an electron.
In the case of Earth as one big gravity particle,
aE=6371e3m
and mass
mE=5.972e24kg
G=pi*sqrt(2*5.972*(299792458)^2*10^(24))/(6371e3)
G=5.109e14 and
fres=0.01373*5.109e14/sqrt(5.972e24)
fres=2.870Hz
on the surface of earth.
This frequency can be reproduced.
Good luck! And I dream of anime...ZZZ...
Note: Newton Gravitational Constant G=6.67408∗10−11,
GME=6.67408∗10−11∗5.972∗1024
GME=3.9858∗1014
Thursday, May 26, 2016
A Shield Forming...Heat Dispersion
If the temperature particles are interacting as waves, what is the difference between a B field and a T field? Moving electron generates a B field. The field around a temperature particle is a T field. Which points us the the magic value π.
Temperature particles interact within 2π range of the force density, Fρ. This is the T field. B field is interaction beyond the 2π range centered about zero. B and T fields are the same Fρ but are at different ranges.
Within the respective ranges, force density Fρ is such that,
Fρ≥0, ∂Fρ∂x=+ve and ∂2Fρ∂x2=−ve
make like particle attract each other. And
Fρ>0, ∂Fρ∂x=0 and ∂2Fρ∂x2=0
make like particle repel each other. (To interpret the graphs, place yourself on the resultant curves at the center of each particle and move towards zero force density. If the distance between the particles increases, they repel each other. When the distance between them decreases as they move towards Fρ=0 they attract each other.)
Notice that when two similar particles coalesce, the point along Fρ where ∂2Fρ∂x2=0 starts is pushed further along x, the distance from the center of the particles, by the separation between the centers of the coalesced particles.
A big particle has a wider range over which it interacts as a wave.
Temperature particles exist naturally as coalesces of many particles that behave over long distances as a wave, in a T field.
A B field will not drive a temperature particle as expected because the B field is within the range in which the particle behaves as wave. A B field will attract a T+ particle (moving opposite to the field direction) and repel a T− particle (moving along its pointed direction). When a negative particle and the positive B field is far enough apart and the T− particle is beyond its 2π range, it then will experience a force in the opposite direction. The particle is retarded and will return to the positive B field. This setup the particle to oscillate about the wave particle boundary. A similar situation arise with a positive particle and a negative field. In both cases, the particle is held oscillating at a distance from the field source. Many such particles will form a shield.
A big particle has to be broken up first to interact with a field. A field at the correct frequency may do just that... After which, the individual particles are sent oscillating at a distance to form a shield. If the field is switch off the particles will disperse at a distance.
Temperature particles interact within 2π range of the force density, Fρ. This is the T field. B field is interaction beyond the 2π range centered about zero. B and T fields are the same Fρ but are at different ranges.
Within the respective ranges, force density Fρ is such that,
Fρ≥0, ∂Fρ∂x=+ve and ∂2Fρ∂x2=−ve
make like particle attract each other. And
Fρ>0, ∂Fρ∂x=0 and ∂2Fρ∂x2=0
make like particle repel each other. (To interpret the graphs, place yourself on the resultant curves at the center of each particle and move towards zero force density. If the distance between the particles increases, they repel each other. When the distance between them decreases as they move towards Fρ=0 they attract each other.)
Notice that when two similar particles coalesce, the point along Fρ where ∂2Fρ∂x2=0 starts is pushed further along x, the distance from the center of the particles, by the separation between the centers of the coalesced particles.
A big particle has a wider range over which it interacts as a wave.
Temperature particles exist naturally as coalesces of many particles that behave over long distances as a wave, in a T field.
A B field will not drive a temperature particle as expected because the B field is within the range in which the particle behaves as wave. A B field will attract a T+ particle (moving opposite to the field direction) and repel a T− particle (moving along its pointed direction). When a negative particle and the positive B field is far enough apart and the T− particle is beyond its 2π range, it then will experience a force in the opposite direction. The particle is retarded and will return to the positive B field. This setup the particle to oscillate about the wave particle boundary. A similar situation arise with a positive particle and a negative field. In both cases, the particle is held oscillating at a distance from the field source. Many such particles will form a shield.
A big particle has to be broken up first to interact with a field. A field at the correct frequency may do just that... After which, the individual particles are sent oscillating at a distance to form a shield. If the field is switch off the particles will disperse at a distance.
Escape From A Solar Cell
What to do with all the p+ particles,
This is not electron-hole pairs generation and charge separation in the depletion region. But electrons that escape from the tapered end of the channel having higher velocities than those at the wide end. It is as if the escaped electrons have passed through an electric potential; an escape electric potential, Vec.
This virtual electric potential drives an external load.
Because of the p+ particles, another current flows through the PN junction. This PN current prevents the depletion region from closing the escape end. The electron that flows into the depletion region pairs up with a p+ and the repair are removed from the device. This PN current adds to the current drawn from the ground but does not provide useful work at the external load. Electrons that are removed through this current does not return to the circuit. For this reason, the +V end of the device is grounded to provide a source of electrons to replenish the device.
To remove the (p+e−) pair, a temperature gradient is used to move the spinning e− particles that generates a B field away from the P junction.
The P junction best be porous. The B field impart a spin on the electrons and prevents some of them from crashing into the depletion region. A circular path of electron perpendicular to the escape channel prevents the channel from closing. The velocity component of the electron along B is not affected. In this way, Vec increases as more electrons escape.
What is this (p+e−) pair? Why is temperature particles not detected? Because they behave more like waves than particles.
Note: Simply run water over the cells can remove p+ particles. The water is recycled and contained.
This is not electron-hole pairs generation and charge separation in the depletion region. But electrons that escape from the tapered end of the channel having higher velocities than those at the wide end. It is as if the escaped electrons have passed through an electric potential; an escape electric potential, Vec.
This virtual electric potential drives an external load.
Because of the p+ particles, another current flows through the PN junction. This PN current prevents the depletion region from closing the escape end. The electron that flows into the depletion region pairs up with a p+ and the repair are removed from the device. This PN current adds to the current drawn from the ground but does not provide useful work at the external load. Electrons that are removed through this current does not return to the circuit. For this reason, the +V end of the device is grounded to provide a source of electrons to replenish the device.
To remove the (p+e−) pair, a temperature gradient is used to move the spinning e− particles that generates a B field away from the P junction.
The P junction best be porous. The B field impart a spin on the electrons and prevents some of them from crashing into the depletion region. A circular path of electron perpendicular to the escape channel prevents the channel from closing. The velocity component of the electron along B is not affected. In this way, Vec increases as more electrons escape.
What is this (p+e−) pair? Why is temperature particles not detected? Because they behave more like waves than particles.
Note: Simply run water over the cells can remove p+ particles. The water is recycled and contained.
Temperature Redefined Old
From previously, the perpendicular temperature field due to temperature particles distributed over a surface is,
pd=TE=ρTτo
where ρT is the temperature charge density per unit area, τo is the analogue to εo.
The force on a temperature charge, T− due to two temperature charge distributions, between a hot and cold surface is,
T−.(pdh−pdc)=mTdvdt
where mT is the mass of the temperature charge. Over a contact surface, Ac,
T−∫Acpdh−pdcdA=T−∫Acρhτh−ρcτcdA=∫AcmT(A)dvdtdA
where mT(A) is the area mass distribution of the temperature charge in area Ac. When we consider an area the size of one temperature charge, AT,
T−mT∫ATρhτh−ρcτcdA=∫ATdvdtdA
ATT−mT(ρhτh−ρcτc)=dvdtAT
When we replace, ρh with T−ρn,
ρ=T−.ρn
where ρn is the number density of temperature particle per unit area, the velocity of one temperature charge crossing from the hot body to the cold body is,
dvdt=(T−)2mT(ρnhτh−ρncτc)
At thermal equilibrium,
dvdt=0⟹ρnhτh=ρncτc --- (*)
Only if both the hot and cold bodies are of the same material, in particular,
τh=τc then,
ρnh=ρnc
If everything attain the same temperature on thermal contact at equilibrium, then there cannot be any sort of thermal insulation. Expression (*) allows for materials of different τ to attain different ρn.
This points to ρn, the surface area number density of temperature particles as the temperature we measure with a contact thermometer.
pd=TE=ρTτo
where ρT is the temperature charge density per unit area, τo is the analogue to εo.
The force on a temperature charge, T− due to two temperature charge distributions, between a hot and cold surface is,
T−.(pdh−pdc)=mTdvdt
where mT is the mass of the temperature charge. Over a contact surface, Ac,
T−∫Acpdh−pdcdA=T−∫Acρhτh−ρcτcdA=∫AcmT(A)dvdtdA
where mT(A) is the area mass distribution of the temperature charge in area Ac. When we consider an area the size of one temperature charge, AT,
T−mT∫ATρhτh−ρcτcdA=∫ATdvdtdA
ATT−mT(ρhτh−ρcτc)=dvdtAT
When we replace, ρh with T−ρn,
ρ=T−.ρn
where ρn is the number density of temperature particle per unit area, the velocity of one temperature charge crossing from the hot body to the cold body is,
dvdt=(T−)2mT(ρnhτh−ρncτc)
At thermal equilibrium,
dvdt=0⟹ρnhτh=ρncτc --- (*)
Only if both the hot and cold bodies are of the same material, in particular,
τh=τc then,
ρnh=ρnc
If everything attain the same temperature on thermal contact at equilibrium, then there cannot be any sort of thermal insulation. Expression (*) allows for materials of different τ to attain different ρn.
This points to ρn, the surface area number density of temperature particles as the temperature we measure with a contact thermometer.
Wednesday, May 25, 2016
No Free Meal With Plasma
From the post "" dated
pVTn=−pVT=ln(T−An)+C
C=(pV)n=1
with T+,
pVTp=pVT=ln(T+An)+C=−ln(T−An)+C --- (*)
and
pVTn=−pVT=−T+τo.VAo
which is a constant.
with T+,
pVTp=pVT=T+τo.VAo
Both positive and negative temperature have the same equations, but does T+ does negative work? No, a spinning T+ particles does not produce a g field that act against gravity, it does produce an E field. Unless in the presence of an existing E field, T+ does not perform positive work. T− was removed from the system to decrease work done. Adding T− to the system will increase work done, and reduces temperature. T− itself does positive work against gravity. So, equation
ΔpV=−AΔTp
is not valid! And so equation (*) for T+ is not valid.
We plot pVT vs T, where T=Tn+Tp,
Work done per temperature is a constant over temperature. The increase in pVT after T=1+Tp is due to the removal of T−τo.VAo which is expected to act against T+τo.VAo.
This graph suggests that on cooling a hot gas by adding T− particles, pVT increases, but cooling by removing T+ particles, pVT remains constant.
There is no free gain. And removing negative temperature particles requires work.
pVTn=−pVT=ln(T−An)+C
C=(pV)n=1
with T+,
pVTp=pVT=ln(T+An)+C=−ln(T−An)+C --- (*)
pVTn=−pVT=−T+τo.VAo
which is a constant.
with T+,
pVTp=pVT=T+τo.VAo
Both positive and negative temperature have the same equations, but does T+ does negative work? No, a spinning T+ particles does not produce a g field that act against gravity, it does produce an E field. Unless in the presence of an existing E field, T+ does not perform positive work. T− was removed from the system to decrease work done. Adding T− to the system will increase work done, and reduces temperature. T− itself does positive work against gravity. So, equation
ΔpV=−AΔTp
is not valid! And so equation (*) for T+ is not valid.
We plot pVT vs T, where T=Tn+Tp,
Work done per temperature is a constant over temperature. The increase in pVT after T=1+Tp is due to the removal of T−τo.VAo which is expected to act against T+τo.VAo.
This graph suggests that on cooling a hot gas by adding T− particles, pVT increases, but cooling by removing T+ particles, pVT remains constant.
There is no free gain. And removing negative temperature particles requires work.
Tuesday, May 24, 2016
Temperature... Feels Hot
From the post "Add By Subtracting..." dated 23 May 2016,
pVT=−T+τo.VAo=−T+τo.12rhr+h
the problem with this expression is that the variation of pVT is dependent on the geometry of the experimental setup from which VAo is derived. In this case, a volume confined in a cylinder of base 2πr and variable height h.
This aside, from the same post above,
pd=TE=ρTτo=Tn.TEp
TEp=T−Aoτo
due to the distribution of Tn on the inner surface of the containment, could be the temperature that we commonly measure. This distribution of Tn particles on the side the containment or any body in thermal contact with another body of unequal temperature potential is the result of a flow of temperature particles. Flow stops when,
pd1=pd2
Tn1.TEp1=Tn2.TEp2
where it is possible that Tn1≠Tn2 and TEp1≠TEp2
This is different from electric potential difference that drive the electric current across similar conductor.
This explanation allows for two bodies of different materials in thermal contact to have different temperatures, but no temperature particles flow between them. One body is insulating the other hot body.
TEp is specific to a material and depended on the material lattice, τ a material constant and the availability of T−, Tn inside the material.
This at last is temperature.
Note: If pd1=pd2 is the case, then it is possible to push temperature particles from an insulator to a body and have the latter attain a higher temperature.
pVT=−T+τo.VAo=−T+τo.12rhr+h
the problem with this expression is that the variation of pVT is dependent on the geometry of the experimental setup from which VAo is derived. In this case, a volume confined in a cylinder of base 2πr and variable height h.
This aside, from the same post above,
pd=TE=ρTτo=Tn.TEp
TEp=T−Aoτo
due to the distribution of Tn on the inner surface of the containment, could be the temperature that we commonly measure. This distribution of Tn particles on the side the containment or any body in thermal contact with another body of unequal temperature potential is the result of a flow of temperature particles. Flow stops when,
pd1=pd2
Tn1.TEp1=Tn2.TEp2
where it is possible that Tn1≠Tn2 and TEp1≠TEp2
This is different from electric potential difference that drive the electric current across similar conductor.
This explanation allows for two bodies of different materials in thermal contact to have different temperatures, but no temperature particles flow between them. One body is insulating the other hot body.
TEp is specific to a material and depended on the material lattice, τ a material constant and the availability of T−, Tn inside the material.
This at last is temperature.
Note: If pd1=pd2 is the case, then it is possible to push temperature particles from an insulator to a body and have the latter attain a higher temperature.
Why Meet? Things to Share...
From the measured pVT vs p curves of a single type of gas at different temperature, there is a common intersection,
To examine this further, we look at the gaseous Tn expression for pressure,
pg−={ln(T−An)+C}TnV={ln(T−An)+C}ηT−
and the corresponding expression of T−,
pg+={ln(T+Ap)+C}TpV={ln(T+Ap)+C}ηT+
Both expression applies. But the change in work done is first via the removal of T− particles.
The change in work done is observed by adjusting pressure or temperature that remove the T− particles.
The transition from pg− to pg+ passes through Tn=1 as pressure changes. After Tn=1, only pg+ applies. At all temperature T, the system starts with a number of T− particles Tn≠0. This is possible when the experimental setup is first heated over the desired temperature T and then allowed to cool to T before the experiment starts. T− enters into the system as it cools. If this is the case, there will be one common point,
pg−={ln(T−An)+C}TnV=CV
when Tn=1.
And the pressure due to the distributed T− particles on the interior surface of the containment is,
pd−=TE=Tn.TEp=TEp
which is the same across curves of all temperature T. And the pressure p is,
p=pg−+pd−
Which is an assumption, because we can have,
p=pg−=pd−
where the pressure of the gas is the pressure on the containment wall. The pressure of the gas distributes T particles ON the surface of the containment which exert a force per unit temperature charge (like electron on the surface of a conductor) normal to the surface, outwards from the gas. This induced force acts against the containment (T^{-} particles IN the containment wall) and is equal to the pressure of the gas felt by the containment.
In both cases we have the same point p on the x-axis.
Then, in general,
pVTn=pηT
where ηT=TnV.
pVTn=pV1=C
This marks the same point on the y axis.
If p=pg−+pd− which is consistent with the way the practical plots are obtained theoretically,
pV=pg−V+pd−V=C+pd−V
All the curves with different T coincide except for the an offset of pd−V. Since pd− is due to one particle, the offset is small.
If p=pg−=pd− then, all the curves with different T coincide exactly.
This confusion arises because work done in the gas (ΔW), and work done on the surface of the gas pV is assumed to be synonymous.
ΔW=pV
whereas T− removed from inside the gas and those removed from the surface of the gas just before the surface of the containment are two processes that effect pV through different dependence on Tn and T− by equations
p=TE=Tn.TEp
and
p={ln(T−An)+C}ηT
from the post "Add By Subtracting..." dated 23 May 2016.
It is likely that p=pg−=pd−, where the pressure of the gas inside and that exerted by the gas on the containment at its surface is the same at an equilibrium, steady state. But the work done (pV) via the two processes (inside the gas and against the containment wall/movable piston) must be added for a total work done on the system.
And the rumble of a mad man goes on...
To examine this further, we look at the gaseous Tn expression for pressure,
pg−={ln(T−An)+C}TnV={ln(T−An)+C}ηT−
and the corresponding expression of T−,
pg+={ln(T+Ap)+C}TpV={ln(T+Ap)+C}ηT+
Both expression applies. But the change in work done is first via the removal of T− particles.
The change in work done is observed by adjusting pressure or temperature that remove the T− particles.
The transition from pg− to pg+ passes through Tn=1 as pressure changes. After Tn=1, only pg+ applies. At all temperature T, the system starts with a number of T− particles Tn≠0. This is possible when the experimental setup is first heated over the desired temperature T and then allowed to cool to T before the experiment starts. T− enters into the system as it cools. If this is the case, there will be one common point,
pg−={ln(T−An)+C}TnV=CV
when Tn=1.
And the pressure due to the distributed T− particles on the interior surface of the containment is,
pd−=TE=Tn.TEp=TEp
which is the same across curves of all temperature T. And the pressure p is,
p=pg−+pd−
Which is an assumption, because we can have,
p=pg−=pd−
where the pressure of the gas is the pressure on the containment wall. The pressure of the gas distributes T particles ON the surface of the containment which exert a force per unit temperature charge (like electron on the surface of a conductor) normal to the surface, outwards from the gas. This induced force acts against the containment (T^{-} particles IN the containment wall) and is equal to the pressure of the gas felt by the containment.
In both cases we have the same point p on the x-axis.
Then, in general,
pVTn=pηT
where ηT=TnV.
pVTn=pV1=C
This marks the same point on the y axis.
If p=pg−+pd− which is consistent with the way the practical plots are obtained theoretically,
pV=pg−V+pd−V=C+pd−V
All the curves with different T coincide except for the an offset of pd−V. Since pd− is due to one particle, the offset is small.
If p=pg−=pd− then, all the curves with different T coincide exactly.
This confusion arises because work done in the gas (ΔW), and work done on the surface of the gas pV is assumed to be synonymous.
ΔW=pV
whereas T− removed from inside the gas and those removed from the surface of the gas just before the surface of the containment are two processes that effect pV through different dependence on Tn and T− by equations
p=TE=Tn.TEp
and
p={ln(T−An)+C}ηT
from the post "Add By Subtracting..." dated 23 May 2016.
It is likely that p=pg−=pd−, where the pressure of the gas inside and that exerted by the gas on the containment at its surface is the same at an equilibrium, steady state. But the work done (pV) via the two processes (inside the gas and against the containment wall/movable piston) must be added for a total work done on the system.
And the rumble of a mad man goes on...
Monday, May 23, 2016
Gas Democracy
A plot of the two the two pVTn variations, keeping in mind that the increase in Tn reduces temperature, ie
pVTn=−pVT=ln(T−An)+C
and
pVTn=−pVT=−T+τo.VAo
where the sign of T− is accounted for.
VAo=12rhr+h
pVT=12T+τo.rhr+h
More importantly for the x variable axis,
p=TE=TE=Tn.T−Ao1τo=Tn.TEp
p∝Tn and p∝T−, p∝T+
We plot, 50*x/(x+50)*1/2 for r=50. h is a variable. In the same plot graph of -log(x) and 50*x/(x+50)*1/2-log(x).
And we have the practical Gas Law! What about adding T+ particles?
If T+ is added to a system, we start with,
pTVT=pV+ΔW
that results in,
pVTp=pVT=+Aln(Tn)+C=−ln(T−An)+C
and
pVTp=pVT=T+τo.VAo
in both cases they are the same graphs as when temperature is increased by removing T−. By comparing the sum of the two plots for adding T+ and subtracting T− with practical gas law plots
We have a visual match. This means the two variations are not equivalent at any level. The expression,
p=TE=Tn.TEp={ln(T−An)+C}ηT
is WRONG.
Both processes apply at the same time. How is it possible that Tn changes with T held constant? T is not related to Tn, as yet. It could be that, as the volume AND pressure changes the number of T− particles in the system changes to maintain T, because,
pVTn=pηT
where ηT is the volume density of Tn particles. Changing volume changes the interior surface area and redistributes T−. As area changes pressure changes. The total number of Tn particles changes because pressure changes via,
p=TE=Tn.TEp
The setup that maintains the temperature of the system adds or removes temperature particles.
It is possible that temperature T is related to, the pressure component
pd=TE=Tn.TEp
due to the distribution of Tn on the inner surface of the containment. And not the free (gaseous) component,
pg={ln(T−An)+C}TnV={ln(T−An)+C}ηT
from which negative work was derived.
Have a nice day.
pVTn=−pVT=ln(T−An)+C
and
pVTn=−pVT=−T+τo.VAo
where the sign of T− is accounted for.
pVT=12T+τo.rhr+h
More importantly for the x variable axis,
p=TE=TE=Tn.T−Ao1τo=Tn.TEp
p∝Tn and p∝T−, p∝T+
We plot, 50*x/(x+50)*1/2 for r=50. h is a variable. In the same plot graph of -log(x) and 50*x/(x+50)*1/2-log(x).
And we have the practical Gas Law! What about adding T+ particles?
If T+ is added to a system, we start with,
pTVT=pV+ΔW
that results in,
pVTp=pVT=+Aln(Tn)+C=−ln(T−An)+C
and
pVTp=pVT=T+τo.VAo
in both cases they are the same graphs as when temperature is increased by removing T−. By comparing the sum of the two plots for adding T+ and subtracting T− with practical gas law plots
We have a visual match. This means the two variations are not equivalent at any level. The expression,
p=TE=Tn.TEp={ln(T−An)+C}ηT
is WRONG.
Both processes apply at the same time. How is it possible that Tn changes with T held constant? T is not related to Tn, as yet. It could be that, as the volume AND pressure changes the number of T− particles in the system changes to maintain T, because,
pVTn=pηT
where ηT is the volume density of Tn particles. Changing volume changes the interior surface area and redistributes T−. As area changes pressure changes. The total number of Tn particles changes because pressure changes via,
p=TE=Tn.TEp
The setup that maintains the temperature of the system adds or removes temperature particles.
It is possible that temperature T is related to, the pressure component
pd=TE=Tn.TEp
due to the distribution of Tn on the inner surface of the containment. And not the free (gaseous) component,
pg={ln(T−An)+C}TnV={ln(T−An)+C}ηT
from which negative work was derived.
Have a nice day.
Add By Subtracting...
From the post "Temperature Particle And The Dip" dated 13 May 2016, the work removed from the system due to a drop in the number of negative temperature particles (ie temperature increases) is,
ΔW=AΔTn
where A is a constant.
The amount of energy remaining at a final temperature T,
pTVT=pV−ΔW
pTVTTn=pV−AΔTnTn=pVTn−AΔTnTn
ΔpVTn=−AΔTnTn
pVTn=−Aln(Tn)=ln(T−An)+C ---(1)
where C is the integration constant.
p={ln(T−An)+C}TnV={ln(T−An)+C}ηT --- (2)
where ηT=TnV is the number of negative temperature per unit volume. Substituting into (1),
pVTn=pηT --- (3)
In another view...
We postulate here that pressure is due to the T field of the T particles, behaving like charges on the surface of a conductor,
E=ρεo
in an analogous way,
TE=Tn.T−Ao1τo=Tn.TEp
acting normal to the surface of the containment, of area Ao, against other T− particles, outwards. Tn is the total number of negative temperature particles in the volume V. The T− spread themselves over the surface of the containment like charges on the surface of a conductor. This is the pressure on the containment.
p=TE=Tn.TEp
If this is true, then pressure depends on the change in surface area of the containment and not on its volume. Furthermore,
pV=Tn.TEpV
pVTn=TEpV=T−τo.VAo
and VAo gives a linear dimension of the containment. For example, in the case where a piston move to change the volume of a cylinder, VAo is
VAo=πr2.h2.πr2+2πr.h=12rhr+h
More importantly, if these two view are the equivalent at some level,
This is wrong, both views apply and act simultaneously.
But at an steady state, where the pressure in the gas is the same as the pressure on the containment wall, the rest still applies but for a different reason,
p=TE=Tn.TEp={ln(T−An)+C}ηT
TEp.V={ln(T−An)+C}
Tn.TEp=−Aln(B.Tn).ηT=−Aln(B.Tn)TnV
where B=ln(C)
TEp=−AVln(B.Tn)
−TEpAv=ln(B.Tn)
where Av=AV per unit volume
Tn=1Be−TEpAv
Tn=Ke−TEpAv
where K=1B is in units of Tn and Av = energy per change in Tn per unit volume.
K=TneTEpAv
K represents the effect of Tn number of T− particles in the system.
This discussion is strictly in the presence of T−, as such Tn>0. When Tn=1,
\require{cancel}
p_{n1}=\left\{\cancelto{0}{ln(T^{ -A }_n)}+C\right\}\eta _{ T }
p_{n1}=\cfrac{C}{V}
using \eta _{ T }=\cfrac{T_n}{V}=\cfrac{1}{V}
C is then the pressure due to one T^{-} particle per given volume. And
p_{n1}V=C
is a constant. Energy capacity per unit volume, A_v
A_v=-\cfrac{T_{ Ep }}{ln(B.T_{ n })}=\cfrac{T_{ Ep }}{ln(K.T^{-1}_{ n })}
\because p=T_{E}=T_n.T_{Ep}
p=T_{Ep}, for T_n=1
A_v is the change in pressure per ln(K.T^{-1}_{ n }) per unit volume.
If there is no T^{-} particle on the containment, there will be no positive pressure outward from the T^{-} particle being contained. If T^{-} particles on the containment are driven away, negative pressure develops on the containment as the T^{-} particles pulls the remaining T^{+} particles on the containment in.
The big assumption \Delta W=A\Delta T_{n} need to be examined closely.
And this is removing T^{-} to raise the temperature in a volume of particles.
ΔW=AΔTn
where A is a constant.
The amount of energy remaining at a final temperature T,
pTVT=pV−ΔW
pTVTTn=pV−AΔTnTn=pVTn−AΔTnTn
ΔpVTn=−AΔTnTn
pVTn=−Aln(Tn)=ln(T−An)+C ---(1)
where C is the integration constant.
p={ln(T−An)+C}TnV={ln(T−An)+C}ηT --- (2)
where ηT=TnV is the number of negative temperature per unit volume. Substituting into (1),
pVTn=pηT --- (3)
In another view...
We postulate here that pressure is due to the T field of the T particles, behaving like charges on the surface of a conductor,
E=ρεo
in an analogous way,
TE=Tn.T−Ao1τo=Tn.TEp
acting normal to the surface of the containment, of area Ao, against other T− particles, outwards. Tn is the total number of negative temperature particles in the volume V. The T− spread themselves over the surface of the containment like charges on the surface of a conductor. This is the pressure on the containment.
p=TE=Tn.TEp
If this is true, then pressure depends on the change in surface area of the containment and not on its volume. Furthermore,
pV=Tn.TEpV
pVTn=TEpV=T−τo.VAo
and VAo gives a linear dimension of the containment. For example, in the case where a piston move to change the volume of a cylinder, VAo is
VAo=πr2.h2.πr2+2πr.h=12rhr+h
More importantly, if these two view are the equivalent at some level,
This is wrong, both views apply and act simultaneously.
But at an steady state, where the pressure in the gas is the same as the pressure on the containment wall, the rest still applies but for a different reason,
p=TE=Tn.TEp={ln(T−An)+C}ηT
TEp.V={ln(T−An)+C}
Tn.TEp=−Aln(B.Tn).ηT=−Aln(B.Tn)TnV
where B=ln(C)
TEp=−AVln(B.Tn)
−TEpAv=ln(B.Tn)
where Av=AV per unit volume
Tn=1Be−TEpAv
Tn=Ke−TEpAv
where K=1B is in units of Tn and Av = energy per change in Tn per unit volume.
K=TneTEpAv
K represents the effect of Tn number of T− particles in the system.
This discussion is strictly in the presence of T−, as such Tn>0. When Tn=1,
\require{cancel}
p_{n1}=\left\{\cancelto{0}{ln(T^{ -A }_n)}+C\right\}\eta _{ T }
p_{n1}=\cfrac{C}{V}
using \eta _{ T }=\cfrac{T_n}{V}=\cfrac{1}{V}
C is then the pressure due to one T^{-} particle per given volume. And
p_{n1}V=C
is a constant. Energy capacity per unit volume, A_v
A_v=-\cfrac{T_{ Ep }}{ln(B.T_{ n })}=\cfrac{T_{ Ep }}{ln(K.T^{-1}_{ n })}
\because p=T_{E}=T_n.T_{Ep}
p=T_{Ep}, for T_n=1
A_v is the change in pressure per ln(K.T^{-1}_{ n }) per unit volume.
If there is no T^{-} particle on the containment, there will be no positive pressure outward from the T^{-} particle being contained. If T^{-} particles on the containment are driven away, negative pressure develops on the containment as the T^{-} particles pulls the remaining T^{+} particles on the containment in.
The big assumption \Delta W=A\Delta T_{n} need to be examined closely.
And this is removing T^{-} to raise the temperature in a volume of particles.
Thursday, May 19, 2016
The Other Term...
From the post "Not To Be taken Too Seriously, Please" and "Time For The Missing Term..." both dated 15 May 2016,
Z= \left\{ \int _{ 1 }^{sec(\theta_0) }{ e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }+ \int _{ 1 }^{ cos(\theta_0) }{ e^{ -\cfrac { x }{ a_{ e }y } }\left\{ \cfrac { 1 }{ y^{ 4 } } \right\} } { d\,y }\right\}
but \theta_0 is not small, in fact \cfrac{\pi}{2}\ge\theta_0\ge 0, so the simplification y=sec(\theta_0)\approx1 is not valid.
Consider,
II_2= \int _{ 1 }^{sec(\theta_0) }{ e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }= -\cfrac{a_e} {x}\int _{ 1 }^{sec(\theta_0) }{-\cfrac{x}{a_e}e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }
II_2=- \cfrac{a_e}{x}\int _{ 1 }^{sec(\theta_0) }{\left(e^{ -\cfrac { x.y }{ a_{ e } } }\right)^{'}\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }
Since,
y=sec(\theta ) and
\cfrac { r_{ e } }{ x } =tan(\theta )
\sqrt { y^{ 2 }-1 } =\sqrt { sec^{ 2 }(\theta )-1 } =tan(\theta )=\cfrac { r_{ e } }{ x }
II_{ 2 }=- \cfrac{a_e}{x}\int _{ 1 }^{sec(\theta_0) }{\left(e^{ -\cfrac { x.y }{ a_{ e } } }\right)^{'}\cfrac { r_{ e } }{ x } } { d\, y }
II_{2}=-\cfrac { a_{ e }r_{ e } }{ x^{ 2 } } \left[ e^{ -\cfrac { x.y }{ a_{ e } } } \right] _{ 1 }^{ sec(\theta _{ 0 }) }
Since,
B_{ o }=\cfrac {\mu_o q v }{4\pi r^2 }.\cfrac{ r^{ 3 }_{ e }}{a^3_e}.sin^{ 2 }(\phi ).Z
x^2=r^2_e+r^2_e-2r^2_ecos(\phi)=2r^2_e(1-cos(\phi))
x=r_e\sqrt{2(1-cos(\phi))}=2r_{ e }sin(\phi /2)
II_{2} =-\cfrac { a_{ e } }{ 4r_{ e }sin^2(\phi /2) } \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
So,
B_o=\cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } .sin^{ 2 }(\phi )\left\{ -\cfrac { a_{ e } }{ 4r_{ e }sin^{ 2 }(\phi /2) }\right\} \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
B_o=-\cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } .cos^{ 2 }(\phi /2) \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
At \phi=\cfrac{\pi}{2},
B_{ o }=-\cfrac { \mu _{ o }qv }{ 8\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \left\{ e^{ -\cfrac { \sqrt { 2 }r_{ e } sec(\theta _{ 0 }) }{ a_{ e } } }-e^{ -\cfrac { \sqrt { 2 }r_{ e } }{ a_{ e } } } \right\}
when \theta is small, at \phi=\cfrac{\pi}{2},
B_o\approx0
Which is all well...And time is fixed, no more time correction!
Note: For every given position x, \theta is evaluated up to \theta_0. x is not dependent on \theta nor on y=sec(\theta).
Z= \left\{ \int _{ 1 }^{sec(\theta_0) }{ e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }+ \int _{ 1 }^{ cos(\theta_0) }{ e^{ -\cfrac { x }{ a_{ e }y } }\left\{ \cfrac { 1 }{ y^{ 4 } } \right\} } { d\,y }\right\}
but \theta_0 is not small, in fact \cfrac{\pi}{2}\ge\theta_0\ge 0, so the simplification y=sec(\theta_0)\approx1 is not valid.
Consider,
II_2= \int _{ 1 }^{sec(\theta_0) }{ e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }= -\cfrac{a_e} {x}\int _{ 1 }^{sec(\theta_0) }{-\cfrac{x}{a_e}e^{ -\cfrac { x.y }{ a_{ e } } }\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }
II_2=- \cfrac{a_e}{x}\int _{ 1 }^{sec(\theta_0) }{\left(e^{ -\cfrac { x.y }{ a_{ e } } }\right)^{'}\left\{ \sqrt { y^{ 2 }-1 } \right\} } { d\, y }
Since,
y=sec(\theta ) and
\cfrac { r_{ e } }{ x } =tan(\theta )
\sqrt { y^{ 2 }-1 } =\sqrt { sec^{ 2 }(\theta )-1 } =tan(\theta )=\cfrac { r_{ e } }{ x }
II_{ 2 }=- \cfrac{a_e}{x}\int _{ 1 }^{sec(\theta_0) }{\left(e^{ -\cfrac { x.y }{ a_{ e } } }\right)^{'}\cfrac { r_{ e } }{ x } } { d\, y }
II_{2}=-\cfrac { a_{ e }r_{ e } }{ x^{ 2 } } \left[ e^{ -\cfrac { x.y }{ a_{ e } } } \right] _{ 1 }^{ sec(\theta _{ 0 }) }
Since,
B_{ o }=\cfrac {\mu_o q v }{4\pi r^2 }.\cfrac{ r^{ 3 }_{ e }}{a^3_e}.sin^{ 2 }(\phi ).Z
x^2=r^2_e+r^2_e-2r^2_ecos(\phi)=2r^2_e(1-cos(\phi))
x=r_e\sqrt{2(1-cos(\phi))}=2r_{ e }sin(\phi /2)
II_{2} =-\cfrac { a_{ e } }{ 4r_{ e }sin^2(\phi /2) } \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
So,
B_o=\cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } .sin^{ 2 }(\phi )\left\{ -\cfrac { a_{ e } }{ 4r_{ e }sin^{ 2 }(\phi /2) }\right\} \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
B_o=-\cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } .cos^{ 2 }(\phi /2) \left[ e^{ -\cfrac { 2r_{ e }sin(\phi /2)y }{ a_{ e } } }\right]_{ 1 }^{ sec(\theta _{ 0 }) }
At \phi=\cfrac{\pi}{2},
B_{ o }=-\cfrac { \mu _{ o }qv }{ 8\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \left\{ e^{ -\cfrac { \sqrt { 2 }r_{ e } sec(\theta _{ 0 }) }{ a_{ e } } }-e^{ -\cfrac { \sqrt { 2 }r_{ e } }{ a_{ e } } } \right\}
when \theta is small, at \phi=\cfrac{\pi}{2},
B_o\approx0
Which is all well...And time is fixed, no more time correction!
Note: For every given position x, \theta is evaluated up to \theta_0. x is not dependent on \theta nor on y=sec(\theta).
Wednesday, May 18, 2016
Emission Intensity Absorbed
From the post "Capturing T^{+} Particles." dated 15 May 2016,
x^{ 2 }=r^{ 2 }_{ e }+r^{ 2 }_{ e }-2r^{ 2 }_{ e }cos(\phi )=2r^{ 2 }_{ e }(1-cos(\phi ))
x=r_{ e }\sqrt { 2(1-cos(\phi )) } =2r_{ e }sin(\phi /2)
and
\cfrac { r_{ { T^{ + } } } }{ x } =tan(\theta _{ 0 })
\cfrac{ r_{ { T^{ + } } }}{tan(\theta _{ 0 })}=2r_{ e }sin(\phi /2)
\phi=2.sin^{-1}\left(\cfrac{ r_{ { T^{ + } } }}{2r_{ e }tan(\theta _{ 0 })}\right)
This is the relationship between \theta_0 and \phi, as x, the distance between the electron and the center of the T^{+} particle's orbit changes.
Low values of \theta_0 corresponds to T^{+} particles that are far away, (along x), from the electron. When r_e is finite,
\theta_{0\,\,min}=\theta_c=tan^{-1}(\cfrac{r_{\small{T^{+}}}}{\sqrt{2}.r_e})
Each orbiting T^{+} particle generates a E field perpendicular to it orbital plane, at an angle \pi/2-\phi_s to the reference \phi=0.
As different particles in different orbits oscillates with different amplitude,
all these oscillations overlap at the lower values of \theta_0, beside \theta_c.
But the traveling T^{+} particles has high velocities at these values of \theta_0 near \theta_c, the center of the oscillation; the equilibrium position. The particles pass through \theta_c quickly but dwell at the two ends of their oscillations.
If there is an uniform spread in oscillations from \theta_c to \theta_0=\pi/2, there will be a greater concentration of E fields from higher values of \theta_0, due to the T^{+} particle longer dwell time. (A math expression is needed here.)
This could explain why higher values of \theta_0 has higher energy and is associated with higher frequencies and so lower wavelength.
In this case however, T^{+} is oscillating along the electron orbit with frequency f_s, and is also revolving in its orbit perpendicular to the electron orbit at frequency f_o. The concentration of E field is due to both f_s and f_o. The spread of energy (sum of all overlapping E fields) however is due to f_s only.
If the traveling T^{+} particles has lower velocities (ie. lower energy oscillations), and their dwell time at higher values of \theta_0 is insignificant compared to the overlap, then values of lower \theta_0 will have higher energy and be associated with lower wavelength. The spectrum is reversed for low energy oscillations. This could explain why the emission spectrum is reversed at lower temperature.
Previously, the half angle of a light cone which give the strongest E field when at \pi/2, (c/f post "It's All Fluorescence Outside, Inside" dated 29 Jul 2015.), the angle also defined as \theta was polarization, not wavelength (color).
Good Night...
x^{ 2 }=r^{ 2 }_{ e }+r^{ 2 }_{ e }-2r^{ 2 }_{ e }cos(\phi )=2r^{ 2 }_{ e }(1-cos(\phi ))
x=r_{ e }\sqrt { 2(1-cos(\phi )) } =2r_{ e }sin(\phi /2)
and
\cfrac { r_{ { T^{ + } } } }{ x } =tan(\theta _{ 0 })
\cfrac{ r_{ { T^{ + } } }}{tan(\theta _{ 0 })}=2r_{ e }sin(\phi /2)
\phi=2.sin^{-1}\left(\cfrac{ r_{ { T^{ + } } }}{2r_{ e }tan(\theta _{ 0 })}\right)
This is the relationship between \theta_0 and \phi, as x, the distance between the electron and the center of the T^{+} particle's orbit changes.
Low values of \theta_0 corresponds to T^{+} particles that are far away, (along x), from the electron. When r_e is finite,
\theta_{0\,\,min}=\theta_c=tan^{-1}(\cfrac{r_{\small{T^{+}}}}{\sqrt{2}.r_e})
Each orbiting T^{+} particle generates a E field perpendicular to it orbital plane, at an angle \pi/2-\phi_s to the reference \phi=0.
all these oscillations overlap at the lower values of \theta_0, beside \theta_c.
But the traveling T^{+} particles has high velocities at these values of \theta_0 near \theta_c, the center of the oscillation; the equilibrium position. The particles pass through \theta_c quickly but dwell at the two ends of their oscillations.
If there is an uniform spread in oscillations from \theta_c to \theta_0=\pi/2, there will be a greater concentration of E fields from higher values of \theta_0, due to the T^{+} particle longer dwell time. (A math expression is needed here.)
This could explain why higher values of \theta_0 has higher energy and is associated with higher frequencies and so lower wavelength.
In this case however, T^{+} is oscillating along the electron orbit with frequency f_s, and is also revolving in its orbit perpendicular to the electron orbit at frequency f_o. The concentration of E field is due to both f_s and f_o. The spread of energy (sum of all overlapping E fields) however is due to f_s only.
If the traveling T^{+} particles has lower velocities (ie. lower energy oscillations), and their dwell time at higher values of \theta_0 is insignificant compared to the overlap, then values of lower \theta_0 will have higher energy and be associated with lower wavelength. The spectrum is reversed for low energy oscillations. This could explain why the emission spectrum is reversed at lower temperature.
Previously, the half angle of a light cone which give the strongest E field when at \pi/2, (c/f post "It's All Fluorescence Outside, Inside" dated 29 Jul 2015.), the angle also defined as \theta was polarization, not wavelength (color).
Good Night...
Lemmings Over The Cliff...
This is the variation of U_B with \theta_0 with various ratios of the size of the electron and its orbit, a=\cfrac{a_e}{r_e}, at \phi=\cfrac{\pi}{2} is plotted as,
(((2)^(1/2)/(2*cos(x)*cos(x))+(2)^(1/2)*a/(cos(x))-a^2)*e^(-(2^(1/2))/(a*cos(x)))+(-(2^(1/2)/2)-2^(1/2)*a+a^2)*e^(-(2^(1/2)/a)))^2
from,
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\\ \left\{ \left( { \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e } } } \right\} ^{ 2 }
For the case of a=1, we zoomed into the values of \theta_0 closer to zero,
There is two unique regions of oscillation along \theta_0 when,
\theta=0
and when,
\theta_0=\theta_d=double\,\,\, root
around the double root of U_B. Together they give the absorption profile of the body. When a is low, as shown in the next plot, there is only one region of oscillation, and the absorption profile of the body is flat.
This is a plot of U_B with varies value of a,
Low ratios of the size of the electron and its orbit, has low values of T^{+}, the T^{+} particles are not strongly held in orbit but leaves readily. If a material has high a at high temperature, then it will retain T^{+} strongly and not feel hot to the touch. It is an heat insulator. If a material has low a at high temperature, then it will not retain T^{+} as strongly and will feel hot to the touch as it loses T^{+} particle readily.
Which leads us to, the T field around T^{+} and the E field generated by it.
Is the T field responsible for heat flow between a hot and cold object or is the E field responsible? But we know for sure that an E field directed at the orbiting T^{+} particle will push or pull it (the particle is spinning) into oscillations or caused it to be ejected from orbit.
Next stop, ohmic heating...
Note: For double roots,
\left( \cfrac { \sqrt { 2 } }{ 2 } (2+x)+\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } \right) xe^{ x }=(1-e^{ x })\left( \cfrac { \sqrt { 2 } }{ 2 } +\sqrt { 2 } \cfrac { a_{ e } }{ r } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right)
where \frac { 1 }{ cos(\theta _{ 0 }) } =1+x...Obviously x=0 is a solution.
Anyway,
y=x\left( Ax+B \right) \frac { e^{ x } }{ (1-e^{ x }) } -C
where x=\frac { 1 }{ cos(\theta _{ 0 }) }-1 .
A=\cfrac { \sqrt { 2 } }{ 2 }
B=\sqrt { 2 } (1+\cfrac { a_{ e } }{ r_{ e } } )
C=\cfrac { \sqrt { 2 } }{ 2 } +\sqrt { 2 } \cfrac { a_{ e } }{ r } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } }
is a good fit for the equation. The only physical constraint is \cfrac{a_e}{r_e}, the ratio of electron radius to electron orbital radius.
(((2)^(1/2)/(2*cos(x)*cos(x))+(2)^(1/2)*a/(cos(x))-a^2)*e^(-(2^(1/2))/(a*cos(x)))+(-(2^(1/2)/2)-2^(1/2)*a+a^2)*e^(-(2^(1/2)/a)))^2
from,
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\\ \left\{ \left( { \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e } } } \right\} ^{ 2 }
There is two unique regions of oscillation along \theta_0 when,
\theta=0
and when,
\theta_0=\theta_d=double\,\,\, root
around the double root of U_B. Together they give the absorption profile of the body. When a is low, as shown in the next plot, there is only one region of oscillation, and the absorption profile of the body is flat.
This is a plot of U_B with varies value of a,
Low ratios of the size of the electron and its orbit, has low values of T^{+}, the T^{+} particles are not strongly held in orbit but leaves readily. If a material has high a at high temperature, then it will retain T^{+} strongly and not feel hot to the touch. It is an heat insulator. If a material has low a at high temperature, then it will not retain T^{+} as strongly and will feel hot to the touch as it loses T^{+} particle readily.
Which leads us to, the T field around T^{+} and the E field generated by it.
Is the T field responsible for heat flow between a hot and cold object or is the E field responsible? But we know for sure that an E field directed at the orbiting T^{+} particle will push or pull it (the particle is spinning) into oscillations or caused it to be ejected from orbit.
Next stop, ohmic heating...
Note: For double roots,
\left( \cfrac { \sqrt { 2 } }{ 2 } (2+x)+\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } \right) xe^{ x }=(1-e^{ x })\left( \cfrac { \sqrt { 2 } }{ 2 } +\sqrt { 2 } \cfrac { a_{ e } }{ r } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right)
where \frac { 1 }{ cos(\theta _{ 0 }) } =1+x...Obviously x=0 is a solution.
Anyway,
y=x\left( Ax+B \right) \frac { e^{ x } }{ (1-e^{ x }) } -C
where x=\frac { 1 }{ cos(\theta _{ 0 }) }-1 .
A=\cfrac { \sqrt { 2 } }{ 2 }
B=\sqrt { 2 } (1+\cfrac { a_{ e } }{ r_{ e } } )
C=\cfrac { \sqrt { 2 } }{ 2 } +\sqrt { 2 } \cfrac { a_{ e } }{ r } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } }
is a good fit for the equation. The only physical constraint is \cfrac{a_e}{r_e}, the ratio of electron radius to electron orbital radius.
Tuesday, May 17, 2016
T^{+} Oscillations, Brownian Motion
From the plot of U_B due to the presences of two electrons in orbit, T^{+} can oscillate about \phi=\cfrac{\pi}{2}, between the two electrons.
As T^{+} oscillates, \theta_0 changes in the expression for U_B,
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\\ \left( { \left| \cfrac { 1 }{ cos^{ 2 }(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }2cos^{ 2 }(\phi /2)sin(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ +\left| \cfrac { 2a_{ e } }{ r_{ e }cos(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }cos(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ -\left| \cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } cot(\phi /2)e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 } } \right) ^{ 2 }
and
x=2r_esin(\phi/2)
\cfrac{r_{\small{T^{+}}}}{x}=tan(\theta_0)
where r_{\small{T^{+}}} is the T^{+} particle orbit.
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\left\{ \left( { \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e } } } \right\} ^{ 2 }
at \phi=\cfrac{\pi}{2}.
The change of U_B at \phi=\cfrac{\pi}{2} with \theta_0 due to the electrons is obtained illustratively from a plot of
(((2)^(1/2)/(2*cos(x)*cos(x))+(2)^(1/2)*a/(cos(x))-a^2)*e^(-(2^(1/2))/(a*cos(x)))+(-(2^(1/2)/2)-2^(1/2)*a+a^2)*e^(-(2^(1/2)/a)))^2,
where 1.5\ge a\ge 0.7
At \theta_0=\cfrac{\pi}{2}, the T^{+} particle is in an orbit just over the electron. At \theta_0=0, the T^{+} particle is far from the electron. theta_0 can attain zero only if r_e is sufficiently large. Otherwise, \theta_0 is limited by,
tan(\theta_{0\,min})=\cfrac{r_{\small{T^{+}}}}{\sqrt{2}.r_e}
as r_e\rightarrow \infty, \theta_{0\,min}\rightarrow 0
It is possible that a\gt 1, the electron is then spinning about an axis passing through it. In this case, the orbit that captures T^{+} particles has only one electron.
Since cos(\cfrac{\pi}{2})=cos(-\cfrac{\pi}{2}, to account for U_B in the presence of another electron, we simply add two graphs and obtain 2U_B. The same plot scaled by two along U_B is obtained.
As T^{+} oscillates about \phi=0, \theta varies from \theta_{0\,max} to \theta_{0\,min}. As the amplitude of the oscillation increases \theta_{0\,max} increases. The energy states available for the T^{+} particles in oscillation are between \theta_{0\,max} and \theta_{0\,min}.
Energy at specific \theta_0 within this range can be absorbed by the T^{+} particles and free itself from the orbit.
If U_B is directly proportional to the number of T^{+} particles captured in orbit,
U_B\propto n_{\small{T^{+}}},
n_{\small{T^{+}}} being the number of T^{+}
If intensity is the number of T^{+} emitting through an unit area per unit time and the distribution of \theta_0 among that T^{+} particles is uniform, then the zoomed graph above also presents the emission spectrum of T^{+} over the range of permissible \theta_0.
When broad spectrum illumination is passed through a material with T^{+} particles, this is the emission spectrum recorded after parts of the illumination has been absorbed by the material.
As r_e increases with increasing temperature, so a increases with increasing temperature. At a specific value of U_B across the graphs of varying a,
\theta_0 can decrease as temperature increases. This means for that range of temperature, the amplitude of oscillation decreases with increasing temperature.
This type of oscillation is characteristic of Brownian motion where the amplitude of oscillation can decrease with higher temperature. Oscillating T^{+} particles can be the reason for Brownian motion.
As T^{+} oscillates, \theta_0 changes in the expression for U_B,
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\\ \left( { \left| \cfrac { 1 }{ cos^{ 2 }(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }2cos^{ 2 }(\phi /2)sin(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ +\left| \cfrac { 2a_{ e } }{ r_{ e }cos(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }cos(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ -\left| \cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } cot(\phi /2)e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 } } \right) ^{ 2 }
and
x=2r_esin(\phi/2)
\cfrac{r_{\small{T^{+}}}}{x}=tan(\theta_0)
where r_{\small{T^{+}}} is the T^{+} particle orbit.
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} ^{ 2 }\left\{ \left( { \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { r_{ e }\sqrt { 2 } }{ a_{ e } } } \right\} ^{ 2 }
at \phi=\cfrac{\pi}{2}.
The change of U_B at \phi=\cfrac{\pi}{2} with \theta_0 due to the electrons is obtained illustratively from a plot of
(((2)^(1/2)/(2*cos(x)*cos(x))+(2)^(1/2)*a/(cos(x))-a^2)*e^(-(2^(1/2))/(a*cos(x)))+(-(2^(1/2)/2)-2^(1/2)*a+a^2)*e^(-(2^(1/2)/a)))^2,
where 1.5\ge a\ge 0.7
At \theta_0=\cfrac{\pi}{2}, the T^{+} particle is in an orbit just over the electron. At \theta_0=0, the T^{+} particle is far from the electron. theta_0 can attain zero only if r_e is sufficiently large. Otherwise, \theta_0 is limited by,
tan(\theta_{0\,min})=\cfrac{r_{\small{T^{+}}}}{\sqrt{2}.r_e}
as r_e\rightarrow \infty, \theta_{0\,min}\rightarrow 0
It is possible that a\gt 1, the electron is then spinning about an axis passing through it. In this case, the orbit that captures T^{+} particles has only one electron.
Since cos(\cfrac{\pi}{2})=cos(-\cfrac{\pi}{2}, to account for U_B in the presence of another electron, we simply add two graphs and obtain 2U_B. The same plot scaled by two along U_B is obtained.
As T^{+} oscillates about \phi=0, \theta varies from \theta_{0\,max} to \theta_{0\,min}. As the amplitude of the oscillation increases \theta_{0\,max} increases. The energy states available for the T^{+} particles in oscillation are between \theta_{0\,max} and \theta_{0\,min}.
Energy at specific \theta_0 within this range can be absorbed by the T^{+} particles and free itself from the orbit.
If U_B is directly proportional to the number of T^{+} particles captured in orbit,
U_B\propto n_{\small{T^{+}}},
n_{\small{T^{+}}} being the number of T^{+}
If intensity is the number of T^{+} emitting through an unit area per unit time and the distribution of \theta_0 among that T^{+} particles is uniform, then the zoomed graph above also presents the emission spectrum of T^{+} over the range of permissible \theta_0.
When broad spectrum illumination is passed through a material with T^{+} particles, this is the emission spectrum recorded after parts of the illumination has been absorbed by the material.
As r_e increases with increasing temperature, so a increases with increasing temperature. At a specific value of U_B across the graphs of varying a,
\theta_0 can decrease as temperature increases. This means for that range of temperature, the amplitude of oscillation decreases with increasing temperature.
This type of oscillation is characteristic of Brownian motion where the amplitude of oscillation can decrease with higher temperature. Oscillating T^{+} particles can be the reason for Brownian motion.
Magnetic Energy of T^{+} Particles
A plot of U_B with changing a=\cfrac{a_e}{r_e} ratio is shown below,
r_e decreases with temperature, so a=\cfrac{a_e}{r_e} increases with temperature.
The minimum point of U_{B\,L}+U_{B\,R} increases along \phi=\cfrac{\pi}{2} as the ratio \cfrac{a}{r_e} increases with increasing temperature, up to a\le\approx0.6. Above a\approx0.6, the value of U_B, first increases then decreases, the value of U_B at a=0.1 is below the values of U_B at a=0.9.
U_B is indicative of the paired electrons ability to hold T^{+} particles in its B orbits. At high temperature, the paired electrons is comparatively weak at holding on to the T^{+}, the material in which the paired orbit electrons are part of, releases some of its T^{+} particles and appears hotter than its ambient temperature.
Have a nice day.
r_e decreases with temperature, so a=\cfrac{a_e}{r_e} increases with temperature.
The minimum point of U_{B\,L}+U_{B\,R} increases along \phi=\cfrac{\pi}{2} as the ratio \cfrac{a}{r_e} increases with increasing temperature, up to a\le\approx0.6. Above a\approx0.6, the value of U_B, first increases then decreases, the value of U_B at a=0.1 is below the values of U_B at a=0.9.
U_B is indicative of the paired electrons ability to hold T^{+} particles in its B orbits. At high temperature, the paired electrons is comparatively weak at holding on to the T^{+}, the material in which the paired orbit electrons are part of, releases some of its T^{+} particles and appears hotter than its ambient temperature.
Have a nice day.
B Field And Then U Energy
A plot of ((3*(2)^(1/2)/4-(3)^(1/2)/(2*x)-1/(2*x^2))*e^(-(3)^(1/2)*x)+(-2^(1/2)/2+2^(1/2)/(2*x)+1/(2*x^2))*e^(-2^(1/2)*x)), assuming ae=1 from
B=\left\{ \cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\}
of post "Too Hot! Keep Your Distance." date 16 May 2016 which graph the B field, is shown below,
We see that the T^{+} particle rest in a non-zero minimum resultant B field, at \phi=pi/2 between the two particles for high values of a=1 down to a=0.7. Below a=0.7 the minimum lifted and is now a maximum.
Below is a plot of (((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a))))^2 which graph the energy curve U_B with varying r_e.
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } . \right\} ^{ 2 }\cfrac { r^{ 4 }_{ e } }{ a^{ 4 }_{ e } } \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
When to zoom near the U_B=0 line,
U_B near zero, due to one electron, first increases then decreases monotonously. A peak values occurs before the descends to zero again.
The resultant U_B between two orbiting electron is (illustratively), from the plot
(((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a)))+((3*(2)^(1/2)/4+(3)^(1/2)*a/(pi-x)-a^2/(pi-x)^2)*e^(-(3^(1/2)*(pi-x)/a))+(-(2^(1/2)/2)-(2^(1/2))*a/(pi-x)+a^2/(pi-x)^2)*e^(-(2^(1/2)*(pi-x)/a))))^2
where 0.1\le a\le1 in steps of 0.1.
always pushes the T^{+} particle back to the minimum.
a\le\approx 0.6 set up an oscillatory system, where the T^{+} particle can swing closer to one electron then return to approach the other electron, in Simple Harmonic Motion.
For large values of a, a\ge\approx 0.6, U_B due to two electrons presents a maximum, the system is not oscillatory, because a displacement from the maximum creates a force that pushes T^{+} further away from the maximum.
a\approx0.6 marks the transition of elements able to absorb and retain heat (T^{+} particles) and elements that do not absorb heat. Elements that do not have T^{+} particles oscillating along the electron orbits do not have an emission spectrum. Emission spectrum will be discussed next...
B=\left\{ \cfrac { \mu _{ o }qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 2 }_{ e } }{ a^{ 2 }_{ e } } \right\} \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\}
of post "Too Hot! Keep Your Distance." date 16 May 2016 which graph the B field, is shown below,
B does not decreases monotonously. For increasing values of r_e, B dip below zero (the direction of spin is reversed of that from the right hand screw rule) and is negative.
When the other B field due to the other electron is drawn in and we zoom in to the resultant sum from the plot,
((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a)))+((3*(2)^(1/2)/4+(3)^(1/2)*a/(pi-x)-a^2/(pi-x)^2)*e^(-(3^(1/2)*(pi-x)/a))+(-(2^(1/2)/2)-(2^(1/2))*a/(pi-x)+a^2/(pi-x)^2)*e^(-(2^(1/2)*(pi-x)/a)))
When the other B field due to the other electron is drawn in and we zoom in to the resultant sum from the plot,
((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a)))+((3*(2)^(1/2)/4+(3)^(1/2)*a/(pi-x)-a^2/(pi-x)^2)*e^(-(3^(1/2)*(pi-x)/a))+(-(2^(1/2)/2)-(2^(1/2))*a/(pi-x)+a^2/(pi-x)^2)*e^(-(2^(1/2)*(pi-x)/a)))
We see that the T^{+} particle rest in a non-zero minimum resultant B field, at \phi=pi/2 between the two particles for high values of a=1 down to a=0.7. Below a=0.7 the minimum lifted and is now a maximum.
Below is a plot of (((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a))))^2 which graph the energy curve U_B with varying r_e.
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } . \right\} ^{ 2 }\cfrac { r^{ 4 }_{ e } }{ a^{ 4 }_{ e } } \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
U_B near zero, due to one electron, first increases then decreases monotonously. A peak values occurs before the descends to zero again.
The resultant U_B between two orbiting electron is (illustratively), from the plot
(((3*(2)^(1/2)/4+(3)^(1/2)*a/x-a^2/x^2)*e^(-(3^(1/2)*x/a))+(-(2^(1/2)/2)-(2^(1/2))*a/x+a^2/x^2)*e^(-(2^(1/2)*x/a)))+((3*(2)^(1/2)/4+(3)^(1/2)*a/(pi-x)-a^2/(pi-x)^2)*e^(-(3^(1/2)*(pi-x)/a))+(-(2^(1/2)/2)-(2^(1/2))*a/(pi-x)+a^2/(pi-x)^2)*e^(-(2^(1/2)*(pi-x)/a))))^2
where 0.1\le a\le1 in steps of 0.1.
We have a minimum at the middle of the two electrons when a is small, a\le\approx 0.6. We see that given a displace from this minimum, a force,
F=-\cfrac{\partial\,U_B}{\partial\,r_e}
F=-\cfrac{\partial\,U_B}{\partial\,r_e}
always pushes the T^{+} particle back to the minimum.
a\le\approx 0.6 set up an oscillatory system, where the T^{+} particle can swing closer to one electron then return to approach the other electron, in Simple Harmonic Motion.
For large values of a, a\ge\approx 0.6, U_B due to two electrons presents a maximum, the system is not oscillatory, because a displacement from the maximum creates a force that pushes T^{+} further away from the maximum.
a\approx0.6 marks the transition of elements able to absorb and retain heat (T^{+} particles) and elements that do not absorb heat. Elements that do not have T^{+} particles oscillating along the electron orbits do not have an emission spectrum. Emission spectrum will be discussed next...
This is provided that the expression for B and U_B is correct.
Monday, May 16, 2016
Forever \omega
This is our perpetual machine in the smallest scale,
Given the interaction of the forces involved, \omega is forever.
The fields generated by the spinning particles are,
looking just like an electron "d" orbital. The vertical loops are B fields and the torus loop is the E field. The E field marks the presence of two T^{+} particles being captured, in orbit with two electrons of the paired orbit.
Depending on the number of paired orbits and their orientations, their resultant fields manifest different scattering patterns of charged particles.
The torus E field, which is oddly both positive and negative is the result of a weak field generated by two spinning T^{+} in rotation around the perimeter of a circle.
The B field was expected of orbiting electron(s).
Until next time...
Given the interaction of the forces involved, \omega is forever.
The fields generated by the spinning particles are,
looking just like an electron "d" orbital. The vertical loops are B fields and the torus loop is the E field. The E field marks the presence of two T^{+} particles being captured, in orbit with two electrons of the paired orbit.
Depending on the number of paired orbits and their orientations, their resultant fields manifest different scattering patterns of charged particles.
The torus E field, which is oddly both positive and negative is the result of a weak field generated by two spinning T^{+} in rotation around the perimeter of a circle.
The B field was expected of orbiting electron(s).
Until next time...
Specific "Heat" Capacity
If two T^{+} are held by each paired orbit, then when the body starts to accumulate T^{+} particles,
C_p=N_A.2*T^{+}.n_p "heat" per mole
where N_A is Avogadro constant, n_p is the the number of outer paired orbits of the atom.
It is assume that a single orbit does not acquire a T^{+} particle and that the inner paired orbit does not acquire any T^{+}.
C_{p\small{T}}=2N_A.n_p "heat" per mole per T^{+}
Heat capacity is just twice the count of outer paired orbits, n_p multiplied by Avogadro constant, N_A.
This is after the negative T^{-} particles have been driven away. The negative particles in the T^{-} cloud are not associated with any specific orbits. But their numbers match the Atomic number of the element involved, when the nucleus follows the basic (g^{+},T^{+},p^{+}) particle sequence. One T^{+} for each p^{+} particle. T^{+} in the nucleus does not acquire a T^{-} particle because that would negate the weak field it generates that holds a p^{+},
C_n=N_A*|T^{-}|.N_a "heat" per mole
where N_a is the atomic number.
C_{n\small{T}}=N_A.N_a "heat" per mole per T^{-}
If a body holds negative temperature particles, C_n first applies then when all the negative particles have been removed, C_p applies. This body has two "heat" capacity values.
In these cases, "heat" is the change in the number of temperature particles. The rate of change of "heat" is the change in number of temperature particle per unit time (temperature particle flow). Temperature current are for real. As for temperature current transistors, tomorrow.
Even if this dream is a nightmare, I'll soon forget. "Only your enemy can give you the advantage." - Sun Tze
C_p=N_A.2*T^{+}.n_p "heat" per mole
where N_A is Avogadro constant, n_p is the the number of outer paired orbits of the atom.
It is assume that a single orbit does not acquire a T^{+} particle and that the inner paired orbit does not acquire any T^{+}.
C_{p\small{T}}=2N_A.n_p "heat" per mole per T^{+}
Heat capacity is just twice the count of outer paired orbits, n_p multiplied by Avogadro constant, N_A.
This is after the negative T^{-} particles have been driven away. The negative particles in the T^{-} cloud are not associated with any specific orbits. But their numbers match the Atomic number of the element involved, when the nucleus follows the basic (g^{+},T^{+},p^{+}) particle sequence. One T^{+} for each p^{+} particle. T^{+} in the nucleus does not acquire a T^{-} particle because that would negate the weak field it generates that holds a p^{+},
C_n=N_A*|T^{-}|.N_a "heat" per mole
where N_a is the atomic number.
C_{n\small{T}}=N_A.N_a "heat" per mole per T^{-}
If a body holds negative temperature particles, C_n first applies then when all the negative particles have been removed, C_p applies. This body has two "heat" capacity values.
In these cases, "heat" is the change in the number of temperature particles. The rate of change of "heat" is the change in number of temperature particle per unit time (temperature particle flow). Temperature current are for real. As for temperature current transistors, tomorrow.
Even if this dream is a nightmare, I'll soon forget. "Only your enemy can give you the advantage." - Sun Tze
Not A Free Ride...
How does the particles turn?
The top two pictures are the flip image of that directly below.
If the T^{+} particles are in opposing spin relative to each other, the paired electrons in orbit experience two forces, each from a T^{+} particle, the resultant of which is tangential to the orbit at their respective positions. These resultant forces drive the electrons to rotate in one consistent direction.
If the T^{+} particles are in the same spin relative to each other, the forces generated by them drive the electrons away from the orbit in a normal direction. This is likely to destroyed the orbit. Furthermore the direction of the electrons cannot generate opposing B field along its path. The two figures on the right are impossible.
The electrons will repel each other.
When protons are added to the mix...
The top two pictures are the flip image of that directly below.
If the T^{+} particles are in opposing spin relative to each other, the paired electrons in orbit experience two forces, each from a T^{+} particle, the resultant of which is tangential to the orbit at their respective positions. These resultant forces drive the electrons to rotate in one consistent direction.
If the T^{+} particles are in the same spin relative to each other, the forces generated by them drive the electrons away from the orbit in a normal direction. This is likely to destroyed the orbit. Furthermore the direction of the electrons cannot generate opposing B field along its path. The two figures on the right are impossible.
The electrons will repel each other.
When protons are added to the mix...
Too Hot! Keep Your Distance.
Consider the term,
c^{ 2 }=\left| \cfrac { a^{ 4 }_{ e } }{ r^{ 4 }_{ e } } \cfrac { cos^{ 2 }(\phi /2) }{ sin^{ 2 }(\phi /2) } e^{ -\cfrac { 4r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }
x=r_{ e }\sqrt { 2(1-cos(\phi )) } =2r_{ e }sin(\phi /2)
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } cos^{ 2 }(\phi /2).e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }
As \phi goes from 0 to \pi, x goes from 0 to 2r_e. The \cfrac{1}{x} term explodes at x=0.
It is too hot!
UNLESS, the electron and the T^{+} particle keep their distance. The T^{+} particle has a second spin, and spins with the same speed (possibly v=c) as the electron. In this way x\ne0.
Since the expression for energy is the expression c^2 integrated over \phi,
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } cos^{ 2 }(\phi /2).e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{\theta _{ 0 } }_{ 0 }=0
gives a turning point in \overline{U_B}. Which occurs when,
as,
1-sin^{ 2 }(\phi /2)=1-\cfrac { x^{ 2 } }{ 4r^{ 2 }_{ e } } =cos^{ 2 }(\phi /2)
we have,
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } \left( 1-\cfrac { x^{ 2 } }{ 4r^{ 2 }_{ e } } \right) e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }=0
x^2=4r^2_e, x=2r_e
When the T^{+} particle and the electron are at the opposite ends of a diameter along the orbit, U_B is at an extrememum.
How does the E field change and induce a B field when their relative positions are fixed? They are both spinning.
If this is true them the expression for U_B need only be evaluated only at \phi=\pi, without the average over time. When \phi=\pi,
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^2_{ e } }{ r^2_{ e } } \\ \left( { \left| \cfrac { 1 }{ cos^{ 2 }(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }2cos^{ 2 }(\phi /2)sin(\phi /2) \right| ^{\theta _{ 0 } }_{ 0 }\\+\left| \cfrac {2 a_{ e } }{ r_{ e }cos(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }cos(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ -\left| \cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } cot(\phi /2)e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 } } \right) ^{ 2 }
U_B=0, very funny!
A plot of 2*cos(x/2)^2*sin(x/2), cos(x/2) and cot(x/2) are given below,
U_B is indeed zero at \phi=\pi. But B_o=0 also as U_B=\frac{B^2_o}{2\mu_o}. The T^{+} particle will not be held in orbit.
But at \phi=\frac{\pi}{2}, there is a point of inflection. where,
x=\sqrt{2}r_e, cos(\theta)=\cfrac{x}{\sqrt{r^2_e+x^2}}=\cfrac{\sqrt{2}}{\sqrt{3}}
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \\ \left\{ { \left( \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
Another solution exists at \phi=-\frac{\pi}{2}. But this would cause an imbalance, a loss of symmetry. But in a paired orbit, two electrons sharing two T^{+} particles will be like,
All the particles have the same angular velocity around the major orbit, and they keep their relative distances from each other. The T^{+} particles have two spins, one around the major orbit on which two other electrons are spinning. The other spin is perpendicular to the plane of the orbit around a B orbit generated by the revolving e^{-} particles.
This is how a material gain positive temperature particles and increases temperature.
Note: In this model a p^{+} particle in circular motion generates a g field that does not interfere with a T field.
c^{ 2 }=\left| \cfrac { a^{ 4 }_{ e } }{ r^{ 4 }_{ e } } \cfrac { cos^{ 2 }(\phi /2) }{ sin^{ 2 }(\phi /2) } e^{ -\cfrac { 4r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }
x=r_{ e }\sqrt { 2(1-cos(\phi )) } =2r_{ e }sin(\phi /2)
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } cos^{ 2 }(\phi /2).e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }
As \phi goes from 0 to \pi, x goes from 0 to 2r_e. The \cfrac{1}{x} term explodes at x=0.
It is too hot!
UNLESS, the electron and the T^{+} particle keep their distance. The T^{+} particle has a second spin, and spins with the same speed (possibly v=c) as the electron. In this way x\ne0.
Since the expression for energy is the expression c^2 integrated over \phi,
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } cos^{ 2 }(\phi /2).e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{\theta _{ 0 } }_{ 0 }=0
gives a turning point in \overline{U_B}. Which occurs when,
as,
1-sin^{ 2 }(\phi /2)=1-\cfrac { x^{ 2 } }{ 4r^{ 2 }_{ e } } =cos^{ 2 }(\phi /2)
we have,
c^{ 2 }=\left| \cfrac { 4a^{ 4 }_{ e } }{ x^{ 2 } } \left( 1-\cfrac { x^{ 2 } }{ 4r^{ 2 }_{ e } } \right) e^{ -\cfrac { 2x }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 }=0
x^2=4r^2_e, x=2r_e
When the T^{+} particle and the electron are at the opposite ends of a diameter along the orbit, U_B is at an extrememum.
How does the E field change and induce a B field when their relative positions are fixed? They are both spinning.
If this is true them the expression for U_B need only be evaluated only at \phi=\pi, without the average over time. When \phi=\pi,
\require{cancel}
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^2_{ e } }{ r^2_{ e } } \\ \left( { \left| \cfrac { 1 }{ cos^{ 2 }(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }2cos^{ 2 }(\phi /2)sin(\phi /2) \right| ^{\theta _{ 0 } }_{ 0 }\\+\left| \cfrac {2 a_{ e } }{ r_{ e }cos(\theta ) } e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } }cos(\phi /2) \right| ^{ \theta _{ 0 } }_{ 0 }\\ -\left| \cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } cot(\phi /2)e^{ -\cfrac { 2r_{ e }sin(\phi /2) }{ a_{ e }cos(\theta ) } } \right| ^{ \theta _{ 0 } }_{ 0 } } \right) ^{ 2 }
U_B=0, very funny!
A plot of 2*cos(x/2)^2*sin(x/2), cos(x/2) and cot(x/2) are given below,
U_B is indeed zero at \phi=\pi. But B_o=0 also as U_B=\frac{B^2_o}{2\mu_o}. The T^{+} particle will not be held in orbit.
But at \phi=\frac{\pi}{2}, there is a point of inflection. where,
x=\sqrt{2}r_e, cos(\theta)=\cfrac{x}{\sqrt{r^2_e+x^2}}=\cfrac{\sqrt{2}}{\sqrt{3}}
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \\ \left\{ { \left( \cfrac { \sqrt { 2 } }{ 2cos^{ 2 }(\theta _{ 0 }) } +\cfrac { \sqrt { 2 } a_{ e } }{ r_{ e }cos(\theta _{ 0 }) } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e }cos(\theta _{ 0 }) } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
\overline { U_{ B } } =\cfrac { \mu _{ o } }{ 2 } \left\{ \cfrac { qv }{ 4\pi r^{ 2 } } .\cfrac { r^{ 3 }_{ e } }{ a^{ 3 }_{ e } } \right\} ^{ 2 }\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \\ \left\{ { \left( \cfrac { 3\sqrt { 2 } }{ 4 } +\cfrac { \sqrt { 3 } a_{ e } }{ r_{ e } } -\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 3 } r_{ e } }{ a_{ e } } }+\left( -\cfrac { \sqrt { 2 } }{ 2 } -\sqrt { 2 } \cfrac { a_{ e } }{ r_{ e } } +\cfrac { a^{ 2 }_{ e } }{ r^{ 2 }_{ e } } \right) e^{ -\cfrac { \sqrt { 2 } r_{ e } }{ a_{ e } } } } \right\} ^{ 2 }
Another solution exists at \phi=-\frac{\pi}{2}. But this would cause an imbalance, a loss of symmetry. But in a paired orbit, two electrons sharing two T^{+} particles will be like,
All the particles have the same angular velocity around the major orbit, and they keep their relative distances from each other. The T^{+} particles have two spins, one around the major orbit on which two other electrons are spinning. The other spin is perpendicular to the plane of the orbit around a B orbit generated by the revolving e^{-} particles.
This is how a material gain positive temperature particles and increases temperature.
Note: In this model a p^{+} particle in circular motion generates a g field that does not interfere with a T field.
Sunday, May 15, 2016
Temperature Not Energy But Particles
May be it is best to start over...
And the diagram that causes strabismus is back.
Have a nice day.
We are getting warmer!
Consider a charge on approach to a disc of radius r,
E_A=\int_{0}^{r} {2\pi xtan(\theta). Ecos(\theta) }d\,r
where the electric field from the charge is
E=E_oe^{-\cfrac{x}{a_{e}}}
the exponential form of an electric field analogous to the exponential form of the expression for gravity field.
E_A=\int_{0}^{r} {2\pi xtan(\theta). E_oe^{-\cfrac{x}{a_{e}cos(\theta)} }cos(\theta) }d\,r
the distance of the elemental ring from the charge is \cfrac{x}{cos(\theta)}
E_{ A }=2\pi E_{ o }\int _{ 0 }^{ r }{ xtan(\theta )e^{-\cfrac{x}{a_{e}cos(\theta)} }cos(\theta) } d\, r
and the change of E_A with time t,
\cfrac { \partial \, E_{ A } }{ \partial t } =2\pi E_{ o }\cfrac { \partial \, }{ \partial t }\int _{ 0 }^{ r }{ xtan(\theta )e^{-\cfrac{x}{a_{e}cos(\theta)} } cos(\theta)} d\, r
this was in the post "Electron Orbit B Field II" dated 17 Oct 2014, corrected for the term cos(\theta) to consider normal component of E through the disc.
The reason why the normal component through the disc was not taken is because later the electron travels in a circle away from the axis through the center of the disc. If the normal component is taken again by multiplying cos(\phi), some E field lines will be lost. As those taken out previously by multiplying cos(\theta), are now rotated and are normal to the disc.
I must be tired!
So, we are back to, the time varying E field through a disc is
The reason why the normal component through the disc was not taken is because later the electron travels in a circle away from the axis through the center of the disc. If the normal component is taken again by multiplying cos(\phi), some E field lines will be lost. As those taken out previously by multiplying cos(\theta), are now rotated and are normal to the disc.
I must be tired!
So, we are back to, the time varying E field through a disc is
\cfrac { \partial \, E_{ A } }{ \partial t } =2\pi E_{ o }\cfrac { \partial \, }{ \partial t }\int _{ 0 }^{ r }{ xtan(\theta )e^{-\cfrac{x}{a_{e}cos(\theta)} } } d\, r
And the diagram that causes strabismus is back.
Have a nice day.