FPd50 from FPd5 crystal to Larger build 5th dimensional geometric chemistry to produce stable balanced larger scale power with a relatively low delta epsilon.

This is the “crystal” I designed using fluoride and palladium. It’s stable other than palladium’s beta decay but if we’re using it in teeth people must not care too much. talking millions of years here for a half life.
This is a larger build that is significantly heavier but much more powerful.

I compare things to Tesla 2020 roadsters battery pacts because it’s the only thing I’ve got to compare to. But here are my numbers after three minimizations:

Rerun on 2/24/2020

Energy: 6575298 kJ/Mole

Delta Epsilon: 282.72

Run again after jolting coordinates: Energy 6573762

Delta Epsilon: 310.07

Run once more: Energy 6571750 kJ/Mole

Delta Epsilon: 178.80

So let’s just say it’s 6570000 kJ/mol with a delta epsilon under 180 ish.

6570000kJ= 1825kWh
1 unit = 37.54953 kg

833/ 37.54953= 22.18403 units per weight replacement.

(22.18403×1825 kWh) / 200 kWh x 1000 km = 202,429.274 kilometers or 125,783.719 miles.

So if it’s feasible to build these, which I think I have a way of doing, wouldn’t they be better than lithium ion? I think them getting wet is an issue in that they would expand but shielding can be put into place.

Sorry for the blurry photo. Watch the videos for more information.

Much pleasure,

-J.

Monopoles and their descriptions/combination at certain eV’s By Jordan Townsend, February 18th, 2020.

+/- electrons from valence shells. This may be what makes them hard to make. Though it takes 297. kJ/mol to force the electron off of the atom maximum of hydrogen, so it’s a matter of finding the right electrical output to force these conditions. It may be a constant feed to get it to work too.

First iteration:

Made up of 15 atoms:

4^+4 Silicon Prism

Connected to a ruthenium core.
On either side are 3 Na atoms, One side being +1 each, the other Side being -1 each.

4^+4 carbon Prism.

At molecular orbital -1.39 eV 2e- you get this Positive Monopole: at the +4 carbon prism with Na assistance.

At -.99 eV 2e- you get this:

At the +4 silicon prism without Na assistance.

But if electrostatic potential is taken you get this:

The opposing negative force along it’s entirety. This is what is worrying me. That the system is malfunctioning and showing the wrong information.

If the carbons are 4^-4 you get the same build. Photos can be added to show you but they’re the same.

So let’s move on to the Negative build:


Now if you change the materials to Si prisms you get a different build.


At -1.17 eV 2e- you get with one -1 Na assistance.

At -.99 eV 2e- you get a pure Si prism.

with a weaker electrostatic potential. Still of the opposite type.

If you change one of the prisms to 4^-4 charge then the build remains the same for the same eV

If a combination of 4^-4, and 4^+4 prisms using just carbons at -1.39 eV 2e- are used you get Negative:

over the 4^+4 prism and at -1.12 eV 2e- you get this:

And with it’s electrostatic potential you get:

So that would be a dipole magnet and not of use to our builds. So my thoughts are there are combinations with the inert atom Ruthenium that works as a blocking agent of the magnetic pole to only allow one spin per one side while denying the spin of the other side depending on flow of electrons.

Knowing that they’re negative. It’ll likely flow towards the silicon since it can do both monopole types.

#but how does it over come the inert nature of the ruthenium. I would think quantum tunneling of a single atom given enough force would allow the receptive atoms to attain their electrons needed for the monopole to work.

Down below is a 10 atom version of a monopole: F5Pd5 100% Stable.

From all points forward it will be the upper bound of the eV that is used as highlighted here.

If you exchange for chlorine you get a nearly fully circular monopole.

Electrostatic potential is also positive. An improvement there.

Using Br.

Using I.

F and I between Pd gives a negative monopole, but if we add a Pd atom to the right side Pd atom we get the same shape of molecular orbital but it’s a reversed monopole.

The problem I have is that I don’t know for sure whether the Electrostatic Potential over rides the Molecular Orbital or if the Orbital can be of use if pressed in deeply enough or counteracted in some way as with the Iodine’s shape. But this is what I’ve come up with so far.

Much pleasure,
-J.

F5Pd5 to F30Pd30 Battery Design Using 5th Dimensional Chemistry (altered by bond order) by Jordan Townsend. Monday, February 17th, 2020.

After messing about with Ru and finding that it wasn’t what I wanted I tried this instead and got some interesting results. Warning shaky cam.
Palladium and Fluoride make an interesting battery setup. Stable. Long lasting. Extremely efficient and considerably light weight. Let’s compare it to the current Tesla Roadster Battery of 200 kWh = 1000 km. (I think they’re considered the standard at the moment, so why not.)

Sorry about the shaky cam. (Cerebral Palsy will do that to you).

Go to Lenntech for the Molecular Weight.

The weight in kgs.

Roadster is 833kgs battery/3.76255kg= 221.39240 units.

221 x (670933kJ/unit = 186.370278kWh/unit = 41187.83143 kWh

200 kWh = 1000 km.

41187.83143 kWh / 200 KwH x 1000 km = 205939.15715 km per charge or 127,964.66 miles

This beats the other designs as it’s a two atom build, and will last for ages and drive cars for 100,000’s of miles over multiple charges with a very low DeltaEpsilon.

This is currently my favourite battery build to use with stuff. Though if it gets wet I believe it swells up, so a waterproofing layer may need to be surrounding it, but that may be it for now.

985 JHA White Tesla from last night. Don’t be a dope. I’m trying to do more with less not to mention help, you sod. At least you’ve got server racks to compute and analyze your builds. All I have is a single CPU/GPU and they’re not that powerful for my needs. But this has been fun though. Great thought experiments.

Much Pleasure,
-J.

Been messing with 4th Dimensional Chemistry. It’s fun. Oh, and magnetic monopoles—with pictures!

So I mess about with simulated capacitors, whatever else I can think of, and their energy potentials and build things that may not be able to be made today, but if they were would be of use to people in the future or now if I could get a more powerful rig to show the possibilities of their derivatives. That includes magnetic monopoles. Yes. No, not in spin ice. Similar—but different enough that I could patent the suckers tomorrow and they’d be under my name. But we know that’s not my style.

So let’s play the game.

Let’s start with a little 4th Dimensional Chemistry. All you need (Currently: First Iteration [Did I mention first try].) is a Bismuth Core, Ruthenium Outer Sheath to connect the Geometry to the outer sides of what I would have to call icicles but in reality is Arsenic crystals if you want extra hydrogen joins or just optional join points. The other is a carbon crystal of the same build that offered a single Delta Epsilon of roughly 9.8 (I don’t know what that means. I’ve looked it up 4 times and it’s just not sticking. if I could ask someone I would.) for and output of 98919 kJ/mol or roughly 27 KwH. If you run electricity through them they expand violently and up the power of a single mole to roughly 150,000 kJ/mol and then return to their shape once the power is through. So perhaps useful in space where they can expand as a net to gather debris if carbide is used to bind them properly. Though the output requires a vastly larger Delta Epsilon. Hydrogen is a better carrier. They are interconnectable into a three tiered lattice. I doubt they would last too long due to the half life of arsenic being 10 Days and Ruthenium only 2 Years, but the cores can be reused if not garbage Bismuth as they have an unheavenly long half life that’s worth looking up. Go on. It’s so long and I’m so lazy. Here’s a picture of the design with no numbers because then I’d have to start up my Wacom and open the app and re run it and then snap the screen and I’m like—nah, you try it. It’s more fun that way.

Credit: -J Townsend. 4th Dimensional Chemistry 02/14/2020. 1:45 a.m. Totally Doable. But is it worth while for this particular build. I don’t think so.

So you say how do I build this? That’s easy enough, theoretically since I don’t have the tools at hand.
A Bi core can be made through 3D printing or layering of gels that hold the atoms in place, if you want to get insanely technical we can do it on the space station using lasers to slow the fall of the atoms into the right places at once so they bond as needed. Doing the same for the Ruthenium and then you have a solid inert core that can have the other crystal “icicles” bonded properly as needed. Then they can be repeated as needed until you have your weave/lattice/or 3D construction. But realize if you you reverse the directions of these builds and jolt them alternating the level of power you’ll get a self walking chemical nanobot. You just divide sections by inserted inert atoms and you have lines of travel that can be independently controlled. Fun times. I’ll have to get to the monopoles—With picutres! Tomorrow. Err later today. It’s almost 2 a.m. and I need to get some sleep. Have a good Night/Day. Yours, -J.

Episodes 91 and 92 are up! One for each of Animal Quest, and another for Divergent Mind.

Please go to anchor.fm/DivergentMind for the latest and greatest episodes until I can afford to upgrade my WordPress plan and get the plugin that allows something as simple as entering in a block. In the mean time here are links that all help me out to get to that goal faster.

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Much Pleasure.

-J

Making Coronavirus Inert for treatment and study. How to Beat Coronavirus (an attempt).

CoronaVirus’s

What we need to have to fight it.

Identification of damaging units of RNA
Protease reduction at site of entry. Something to absorb the hydrolysis., or at the very least move it away from the affected areas.

The 5’ methylated CH3 chain can be blocked by using Flash Photolysis to destroy the hydrogen that cuts into the amino acid/peptide. Breaking the chain so that the methylated cap binds to itself (shown how later) leaving only C Remainder bond open for set up.

Couldnt we intercept the Triple adenine base messenger RNA with Uracil or even Guanine if they can make it through and then flash them as well if its even needed as it could become inert at that point. At which the Damaging RNA is connectionless. Just within the cell.

So what we could build is a chain of Uracil since they’re hydrogen bonding, and excite them with an extra electron and add them to the end of the adenine seeing as you need 6 hydrogen to Uricils 4 meaning you would just excite three or add in addition hydrogen as needed (so that they are no longer strong enough for hydrolysis towards the host RNA). So it’s a matter of folding the carbon in on itself through propulsed flashing and then swinging it to bond to the other end of the virus making them inert. Shaped similarly like a pringle, I suppose.

So what happens if we insert these builds into the system through a breathing device after they’ve been flashed so that the farthest depth can be reached within the body making sure that the red blood cells carry the good stuff to the damaged area, so that they reach the cells that are affected, transfer into the systems of the cells, or at least bump into them, and cause the folding from interferons doing their duty once they realize that the virus is now inert and they can take it as waste to be disposed of while alerting other cells for the same infection.

But how to do this within a syringe. Flashing seems simple enough to, rapidly done over the body. Painful and dangerous perhaps due to the weakened state of the patient. Perhaps an IV that keeps the body cool and creates a greater heat difference between the virus RNA and the cell its infecting so that they can be found and flashed without bringing the overall temperature of the human body into unsafe measures.

Then it’s a matter of developing an interferon that can be made outside the body such as within inert viruses at differing temperatures and with the inert virus folded (showing that it can be done so first) so that it knows to attack it, which is should naturally know because its an unknown. Though it may present fever which may worsen people’s respiratory infections. Then those are injected through a shot and the body takes in the interferons and teaches it to immunize against the Coronavirus.

If I had more information at hand about the complexity of it’s structure I could build a better road map. So lets call this a trial run, since I have no laboratory.

Much Pleasure,
-J.