This work was initiated due to the discovery that a direct relationship appears to exist between the density of matter and its gas-transition temperature, as can be seen in Fig 1.
Its purpose is to answer the following question:
Can the Newton-Coulomb atomic model be used to predict the properties of elemental matter using mathematics?
In this context, 'matter' is the term used to describe a collection of pure elements in their natural state at any temperature and/or pressure. Same-element matter refers to that in which all the atoms have the same atomic number. All these calculations refer to same-element matter.⁽¹⁾
The state of matter refers to its condition; viscous or gaseous; the only two conditions that exist for all matter.
The state of matter is entirely dependent upon its inter-atomic forces, from which we can predict all of its properties accurately using mathematics. In other words, we should no longer need to rely on documented data, which usually varies (sometimes significantly); most sources simply copy data from other sources - that may or may not be reliable - without verification.
The term 'viscosity' describes all and/or any matter when adjacent atoms are attracted to each other in solid or liquid form, and refers to the resistance in adjacent atoms to slip - plastically, as in plastic stress - relative to each other; Fₘ>Fₑ.
Liquid matter is no different to solid but the inter-atomic electrical separation force (Fₑ), which varies with temperature, is sufficient to reduce the effect of the attractive magnetic force (Fₘ) whereby slip between adjacent atoms occurs with little resistance (low viscosity). What we understand as 'solid' matter is simply that with a very high viscosity, you can still cause its atoms to slip by applying greater (than for liquid matter) force.
Liquidity refers to a body's ability to maintain its shape under the prevalent ambient conditions; gravitational acceleration, atmospheric pressure, etc. It will differ in all matter, for example, here on Earth and on our moon.
The density of viscous matter is [predominantly] constant because magnetism, which is the dominant force (Fₘ), remains constant at any temperature (Fig 2).
Gaseous is the term we use to describe matter when its atoms repel each other; i.e. when the electrical [charge] force of repulsion (Fₑ) is dominant.
This electrical force (Fₑ) is due to the positive electrical charge held in the nucleic protons, which varies with temperature (Fig 2).
As a gas, the force between adjacent atoms (F = Fₘ-Fₑ) is negative because Fₑ is greater than Fₘ, therefore, viscosity should not exist. However, at temperatures just above gas transition, magnetic attraction (Fₘ) is still evident and responsible for the resistance in bodies travelling through an atmosphere.
1) It has become clear that very little we see, hear and read concerning the state of matter is either accurate or true.
2) The term 'fluid' is a misnomer as it unites two disparate conditions; viscous and gaseous. All liquids are in a viscous state, gases are not.
3) There is no such property as the 'melting point' of matter. All matter will flow when it can no longer hold its shape under the influence of gravity. In other words, the 'melting point' of any matter will differ throughout the universe.
4) Hydrogen, either as a single proton or as a proton-electron pair, cannot exist in viscous form due to their positive [proton] electrical charges, which can only repel. Only as deuterium or tritium (containing one or two neutrons respectively) can this occur⁽³⁾.
5) Refer to our elemental data web-page for comparison values of elemental densities and temperatures.
6) Refer to our experiences on this matter.
The highest energy (e.g. temperature {Ṯ} or electro-magnetic {EME}) in any atom occurs in the proton-electron pairs whose electrons are orbiting in shell-1. It is these atomic proton-electron pairs that define the interaction between elemental atoms. All the following calculations are therefore based upon the performance of these proton-electron pairs, whose electrons are orbiting in shell-1, and designated in the calculations with the sub-script '1'; e.g. PE₁, KE₁, etc.
The temperature (Ṯ) we measure in matter is the EME generated by the proton-electron pairs (2-off#) whose electrons are orbiting in shell-1; the atom's innermost shell (Ṯ₁).
# All hydrogen atoms have only one orbiting electron in shell-1; all other atoms have two.
Density (ρ) is the sum of atomic masses contained in a unit volume, which, as explained above, does not vary in viscous matter due to the dominant constant magnetic [field] forces.
However, this is not strictly true; density does vary with temperature - but only slightly - due to changes in its lattice structure, together with the reduction in relative inter-atomic forces (δF = Fₘ - Fₑ) as a result of changes in electrical [charge] repulsion between adjacent neucleic protons, which varies linearly with temperature.
The properties of same-element matter at room temperature used in the following calculations and plots are listed in Table 1:
Ṯg refers to documented boiling temperature (K) of the elements.
ρ refers to documented viscous density (kg/m³) of the elements,
p refers to the inter-atomic pressure between adjacent atoms in elemental matter {N/m²) at a temperature of 300K,
Fₑ refers to the inter-atomic electrical charge force {N) of repulsion between adjacent atoms in elemental matter at a temperature of 300K,
Fₘ refers to the inter-atomic magnetic field force {N) of attraction between adjacent atoms in elemental matter at a temperature of 300K,
It is important to understand that 'boiling point' is the temperature at which matter vapourises. It remains in a viscous state; globules suspended in atmospheric gases. Vapourisation requires the presence of an atmosphere.
Gas transition temperature is that at which atoms repel each other; every atom (or molecule) exists as an individual entity.
These conditions do not always occur at the same temperature and pressure.
The force (Fₘ) holding adjacent atoms together is the magnetic field generated by their proton-electron pairs. This force is constant because the magnetic charge (currently referred to as mass) responsible, is constant.
The force (Fₑ) repelling adjacent atoms is due to the positive electrical charge collected by their [nucleic] protons. This charge (e') varies linearly with the EME collected by the orbiting electrons from their surroundings and transferred to - and held by - their proton partners.
If the electrical force is less than the magnetic force, the matter will exist in a viscous state.
If the electrical force is greater than the magnetic force, the matter will exist in a gaseous state.
The gas transition temperature occurs when these two forces are equal (Fₘ = Fₑ).
This relationship is the fundamental cause of the 'State of Matter' (Fig 2).
Gas transition temperature occurs when the electrical and magnetic forces are equal (Fₑ=Fₘ) (Fig 2)
The temperature at which this condition occurs here on Earth, depends upon the partial pressure of same-elemental atoms in the atmosphere.
Fig 1 reveals an undeniable relationship between the magnetic and electrical inter-atomic forces and the gas transition temperature of the elements.
Whilst documented values for the boiling-point of elemental matter are at best 'analogous', they do reveal a definite pattern (Fig 3). Their inconsistency is due to poorly controlled experimentation procedures along with the long-standing custom of copying data from unreliable sources.
However, the calculated values (CalQ), which are mathematically consistent, also follow the same pattern.
The density and gas-transition temperature of elemental matter is explained in detail on our Density & Temperature web-page.
The pressure in all matter - in both viscous and gaseous states - is due to the electrical [charge] forces of repulsion between adjacent atoms, which varies linearly with temperature.
In pure elemental matter, this pressure is total.
In a mixture of elements, this pressure between each same-elemental matter is referred to as a partial pressure.
The total pressure in a mixture of numerous same-element matters is the sum of all the partial pressures.
At first sight, Dalton's law and partial pressure theory appear to conflict.
If as Dalton states; each gas in a mixture of gases should be treated independently, the pressure in a container of mixed gases should be the maximum individual pressure. But this is not the case; partial pressure theory tells us that the total pressure is the sum of the individual gases.
This anomaly may be explained as follows:
All the atoms in a mixture of atoms will repel all other atoms but differently, because their nucleic arrangements differ. Inter-atomic repulsion between atoms with different atomic numbers (Z) will therefore be extant but random. I.e. you must add all pressures together to find the total pressure.
All same-element atoms contained in a mixture of different atoms will repel all other atoms of the same atomic number uniquely, according to their nucleic arrangement, filling their container and maximising their separation distances. This is why you must treat each same-element matter - within a mixture - individually; i.e. just as if the same-element atoms occupied the container alone. The resulting pressure will be a partial pressure.
The lattice structure of every element originates in - and is defined by - its nucleic protons, and is replicated in the atomic arrangement in all elemental matter in both gaseous and viscous states.
I.e. same element atoms always attract and repulse in a similar pattern to that held by the protons in an atom's nucleus. This pattern is what we today refer to as a lattice structure that depends upon the atom's nucleic arrangement.
We designate these lattice structures as; face-centre cubic, body-centre cubic, tetrahedra, close-packed hexagonal, etc. but they are not quite so simple. Whilst a particular group of atoms may resemble a single structure, they will not be identical; every lattice structure differs from every other.
This pattern applies to all same-element matter in both viscous and gaseous form, and is therefore responsible for partial pressure theory.
The lattice factor is calculated as follows:
ζ = ³√[(ψ-1)/K]
where;
K = (PEₙ/Y . Ṯg/Ṯₙ / d - Fₐₜₘ) / (ρ.hₑ²/Y)
Ṯ₁ = measured (shell-1) temperature of the elemental matter
d = inter-atomic separation
ρ = density of the elemental matter
Fₐₜₘ = inter-atomic [electrical charge] force between atmospheric atoms (see Forces below).
Fig 4 shows the relationship between the density and gas-transition (ρ/Ṯg) of elemental matter, and its lattice factor ((ψ-1)/K).
In other words ...
... if you pour two or more molten elements together, say; copper and nickel, they would coalesce independently, as same-element matter, despite the fact they are both FCC and only one atomic number apart (29 and 28 respectively)#.
That this division occurs naturally, is evidence that elemental lattice structures are not as we suspect, but unique for each and every element, which is borne out by the unique lattice factors (Fig 4).
In fact, the separation of all elements as they transpose through their a viscous states is due to their unique nucleic arrangements, that differ according to their neutronic ratios (ψ), all of which are also unique.
This means that whilst we currently compartmentalise elemental structures; FCC, BCC, HCP, Tetra, etc. this is only an approximation. Whilst some elemental structures may look the same, they are actually similar; not identical. Every element has a different lattice structure.
# alloys are formed by forcing more than one same-element matter together when viscous and pliable.
An average value for atomic spacing (d), which is due to inter-atomic forces, may be found from its density and atomic mass; d = ³√[mₐ/ρ].
Whilst 'd' will vary with direction (orientation) in same-element matter, it tends to be similar in any direction in amorphous matter.
The density of elemental matter may be calculated like this:
ρ = mₐ/d³
where; mₐ is the atomic mass, and the mean separation distance between two adjacent atoms (d) in a perfect crystal of any same element matter may be calculated thus:
d = ³√[mₐ/ρ]
The viscous density of elemental matter may be considered reliable because it does not vary (significantly) with ambient conditions. It can therefore be measured with a good degree of confidence.
Gas density is less reliable because it depends upon the purity of the elemental gas. But in a pressurised container of pure elemental matter, it too can be measured with reasonable confidence.
The density of gaseous matter in an unchanging container will not vary with fluctuating pressure and/or temperature.
Refer to our comparison between various sources.
Temperature is a term that has been given to the EME radiated by a proton-electron pair. It can be calculated like this:
Ṯ = PE / Y.kB = X.v²
where;
Ṯ is the temperature of EME radiated by the proton-electron pair {Kelvin}.
PE is the potential energy in the proton-electron pair {Joules}.
v is the orbital velocity of the electron {m/s}.
There are two principal temperatures for all matter …
… 'boiling point'; is the temperature at which matter vaporises,
… 'gas-transition'; is the temperature at which all adjacent atoms repel each other,
these temperatures are not always the same.
Because these temperatures are dependent upon ambient conditions, that may or may not be carefully monitored in experimental evaluation, you cannot rely on generally available documented data, which varies considerabley between sources.
Refer to our comparison between various sources.
The internal pressure between atoms can be calculated in elemental matter, in both viscous and gaseous states, if its density (ρ) and measured temperature (Ṯ₁) are both known, using a universally known and accepted formula:
p = Rᵢ.Ṯ₁.ρ / (RAM/1000) {kg.(m/s)² / K.mole . K . kg/m³ . mole/kg = kg.m/s² / m² = N/m²}
But the following formulas also generate exactly the same result, together with the correct units:
p = PE₁ / Y.d³
p = kB.Ṯ₁ / d³
p = ρ.kB.Ṯ₁/mₐ
all of which, ultimately break down to one equivalent formula;
p = mₑ.c² / Y.d³ . Ṯ₁/Ṯₙ
and then to;
p = PEₙ/Y . Ṯ₁/Ṯₙ / d³
The Newton-Coulomb atomic model is again verified here because;
Rᵢ.Ṯ₁.ρ / (RAM/1000) = PE₁ / Y.d³ = PEₙ/Y . Ṯ₁/Ṯₙ / d³
where 'PE₁' and 'PEₙ' refer to circular electron orbits and 'Ṯ₁' refers to shell-1 (measured) temperature.
The density of a gas depends entirely upon the mass of the atoms in its container and its temperature, i.e. its pressure.
Therefore, calculating the properties of a gas are entirely arbitrary unless you are provided with its temperature and its pressure or its density; if you have any two values, you can calculate the other using the above formulas.
The mean inter-atomic force of repulsion in elemental matter may therefore be defined using any of the following formulas, all of which give exactly the same result and the correct units:
Fₑ = p.d²
Fₑ = p . ⅔√[mₐ/ρ]
Fₑ = -PE₁ / Y.d
Fₑ = mₑ.c² / Y.d . Ṯ₁/Ṯₙ
Fₑ = PEₙ/Y . Ṯ₁/Ṯₙ / d {kg.m²/s² / m = kg.m/s² = N}
and which vary with temperature (Ṯ₁).
The mean inter-atomic distance in your block of elemental matter may be established thus:
d = ³√[mₐ/ρ]
from which you can calculate the inter-atomic magnetic field force of attraction thus:
Fₘ = μₒ.ξₘ/Y . (I₁.2π)² . (R₁/d)³ . RAM.mₙ/mₚ (Joseph Henry)
or;
Fₘ = ρ.hₑ²/Y (Isaac Newton)
both of which give excatly the same values and the correct units, but to which you need to apply a factor (K) to account for the lattice structure:
Fₘ = Fₘ.K
where: K = (ψ-1)/ζ³ = (PEₙ/Y . Ṯ₁/Ṯₙ / d - Fₐₜₘ) / (ρ.hₑ²/Y)
The above calculation is for a gas released into a vacuum. But in an atmosphere;
Fₘ = Fₘ + Fₐₜₘ
which does not vary with temperature.
When 'Fₑ' exceeds 'Fₘ', the elemental matter will exist as a gas, otherwise it will be viscous.
At gas transition temperature (Ṯg):
Fₑ = Fₘ + Fₐₜₘ
PEₙ/Y . Ṯ₁/Ṯₙ / d = K.ρ.hₑ²/Y + Fₐₜₘ
which may be rearranged to this:
Ṯg = Ṯ₁ = Ṯₙ.d.Y . (K.ρ.hₑ²/Y + Fₐₜₘ) / PEₙ
Where:
Ṯg = gas transition temperature of the elemental matter
Ṯ₁ = temperature of the elemental matter
I₁ = e.(Ṯ₁/Ṯₙ)¹˙⁵/tₙ
R₁ = Xᴿ/Ṯ₁ = Rₙ . Tₙ/Ṯ₁
PE₁ = mₑ.v₁² = mₑ.c² . Ṯ₁/Ṯₙ = kB'.Ṯ₁
v₁² = Ṯ₁/X
N = molecular quantity (1, 2 or 3)
Earth's atmosphere at sea level:
pₐₜₘ = 103591.0548 {N/m²}
mₐₜₘ = 2.32034373003935E-25 {kg}
ρₐₜₘ = 1.2769152769618 {kg/m³}
dₐₜₘ = ³√[mₐₜₘ/ρₐₜₘ] {m}
Fₐₜₘ = pₐₜₘ.dₐₜₘ² {N}
The specific heat capacity for all atoms, may be calculated thus; SHC = ΣKE / Ṯ.Y.mₐ
where ΣKE is the sum of the kinetic energies in all the proton-electron pairs in any atom, and mₐ is the atomic mass (Fig 6).
Fig 6 confirms the Newton-Coulomb atomic model with two electrons per orbital shell.
These forces (Fₘ & Fₑ) can now be used to predict various properties of matter, which when taken along with the relationship between neutronic ratio (ψ) and matter density (ρ) (Fig 3), it is evident that all the physical properties of matter can be predicted from an atom's neutronic ratio and its atomic mass. For example:
F = Fₘ-Fₑ
However, we now know that the properties of viscous elemental matter may also be calculated using the PVRT formulas.
The dynamic viscosity (μ) of all elements - at a specified temperature - can be calculated thus;
μ = p / Γ.ƒ (see Noble Gases below for a definition of 'Γ')
By way of comparison: the documented value for liquid mercury @ 293K is; μ = 0.001526 kg/m/s whereas the calculated value is; μ = 0.00165282 kg/m/s
Note: the kinematic viscosity (ν) may be derived thus; ν = μ/ρ
Surface tension is the linear force holding adjacent atoms together. It is measured in units of N/m and can be calculated thus;
γ = p.Y.d
By way of comparison: the documented value for liquid mercury @ 293K is; γ = 0.465 N/m whereas the calculated value is; γ = 0.4527 N/m

The yield stress of elemental viscous matter is simply a measurement of the internal pressure between atomic planes;
σᵧ = p
By way of comparison: the documented value for iron @ 293K is; 1.5E+08 < σy < 5.52E+08 N/m² whereas the calculated value is; σy = 3.40547E+08 N/m²
Young's modulus (E) for each element at a specified temperature may be determined thus (Fig 7);
E = p . (d/(h.sin(60°))³
where h = d.(1-sin(60°))
By way of comparison: the documented value for iron @ 293K is; E = 1.965E+11 N/m² whereas the calculated value is; E = 2.18031E+11 N/m²
Fig 8 reveals the noble gases based upon the neutronic ratio, which may be calculated thus;
Γ = 9.(ψ -1)
the noble gases occur when Γ is at or close to an integer; 1 to 5
The current method for calculating the resistance (force) generated in a body travelling through a gas was established by J. R. Morrison et. al.
However, because the magnetic [attraction] force (Fₘ) between adjacent atoms is responsible for the drag on bodies passing through an atmosphere, the Newton-Coulomb atomic model can now be used to determine this resistance based upon relative velocities and energies thus:
F = hₑ.ρ.ψ . N° . (vd/vₐ)² . (PEₙ/-PE₁)
where;
A = cross-sectional area
ρ = gas (e.g. air) density
N° = number of atoms in contact with the body (= A / π.Rₛ²)
vd = relative velocity between body and gas
v₁ = electron velocity in shell-1 (gas-atom)
PE₁ = potential energy proton-electron pair in shell-1 (gas-atom)
Whether or not inter-atomic magnetism is the cause of atmospheric drag, the above calculation makes this argument extremely compelling; yet again validating this atomic model.
The molecule (and atomic bonding) is the next step, which can also be solved mathematically using the same atomic forces.
Whilst Keith Dixon-Roche knows how to solve this problem,
due to the responses he has received as a result of his scientific discoveries and their possibilities, he has decided to leave this work up to you,
but he is willing to give you a hint:
'atomic and matter densities react differently with varying temperature;
e.g. the density of an iron atom @ 300K is 0.007533336 kg/m³ but the density of its matter is 7870 kg/m³.
That atomic density increases with rising temperature as matter density decreases, is a clue as to the functioning of chemical bonding; electron charge sharing.'.
Oh yes! and there is no such thing as co-valent bonding. Such bonding between atoms is due to quite a different function.
He wishes you luck.
You will find further reading on this subject in reference publications(69, 70, 71 & 73)