Pd300F290 Build. Can I ask for help with the output/ delta Epsilon in the video please.

Sorry for the long video but I didn’t want to alter it or speed it up so that you can see that it’s real.

Pd300F290 by Jordan Townsend. Minimization, and readouts for Energy and delta Epsilon. Done Twice.

So is this useful or something inherently dangerous outside of the basis of electricity being dangerous? Other than the -beta decay from the Pd, but we put it in teeth so I’m unsure if people care. It’s just that it lasts so long and can combine with the F while still obeying the rules. So it seems like a win as long as it shielded properly.

Edit: In response to the reddit posting asking for clarification:

Sorry for the lousy load time, I should have just put it on youtube.

Okay, let me see if I have the parts in order:

It’s minimizing the collection of atoms that I’ve put together into a chemical framework near ideal. By doing that it’s trying to get the proper bond length/atom position that gives an Energy readout within a boundary of if there’s an x-y graph, and delta is on the x axis and there are two points plus/minus delta (though I don’t know the unit—so assuming kJ/mol?) then it should assure that there is that Energy output within the y axis between two points plus/minus Epsilon (same unit). Uses a Universal Force Field (UFF). That’s my understanding for that.

If that’s true and that energy level is possible with those materials (can it be an electrical potential like lithium ion since you can use trace Pd or stable Pd depending on what’s available?), if possible to be built reasonable or for specialty uses, then is it useful as an energy source, or does that mean that it’s just explosive chemically and unsafe.

My software is limited as is my income as I’m on disability so I’ve only been able to find one software that I can afford, and these are the functions that it offers—within the reasonability of my hardware, which is years old at this point.

Did that help at all? I’m trying to research battery alternatives using long lasting element types that are stable if possible. Bill Gates is looking for a stage IV reactor, and so I’m just working towards that getting to the worlds needs one step at a time until I get the (or a range) of potential solutions. Thanks for your patience with the video by the way.

Sorry forgot to add in the numbers if they’re not visible from the video:
6592896 kJ/mole. = 1831.36 kWh
628.95 delta Epsilon.
Mole weight: 37435.54 g/mole. = 37.43554 kg.
This is just for comparison purposes:

Tesla Roadster has 833 kg Battery pack.
Assuming we can fit the same amount of this in the same space, and that they are equally packed. We can fit 833/37.43554= 22.25158 Units in the battery pack.
22.25158 x 1831.36 kWh = 40750.65355 kWh if rounded up.
Their car can go 200 kWh. So we divide 40750.65354/200kWh x 1000 km = range = 203,753.268 km or 126,606.411 miles per charge.

Been on an Art kick these past three days. Had to upgrade wordpress to get this working hopefully. Here goes.

Here’s todays Koala. Nettios wanted it, so she got it. Fur is hard…

Leatherman MUT a soldier gave me after Dad died. Had it ever since.
Dragon at the Beach I guess. Based off a chameleon.
First attempt at learning the new style.

Now on to making today’s podcast. I’ve got to get back into the groove of things, as I’ve been out for a few days. So let’s get shaking. 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.

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.

Just a few sketches. If you know who originally did the mouse please help me find them. Their style is gorgeous.

Martian water finder doing their job the old way.
My morning warmup. Nothing great here but it’s nice to practice.
This is not my character nor my background. It I loved them both so decided to draw and add them together.