4.24.2019

UltraWood 5: Petrified wood

Petrified wood is another ultrawood.  Petrified wood is easy to make and the patents on it expired in 2006.  Basically in my view here is the real process:

Soak wood in silicate solution

Let lignin degrade and the released carboxilic acids neutralizing the silicate (extra acid like citric or malic acid can be used to speed up the process if desired) transforming it into silica gel, preferably at an increased temperature with steam or warm water vapor present to prevent drying out and allow silica gel to crystalize into quartz.

Let dry out.  Repeat process as necessary.

Basically what is happening is you are creating quartz crystal within the wood.

This process can also use steps from other ultrawood posts or other steps entirely.  Some examples could be oxalic acid bath, hydroxide and/or urea baths, etc.

My current process would be:

Oxalic acid boil till wood sinks then boil in water wash

hydroxide/urea at room temp and/or freeze then no wash

oxalic acid boil then boil in water wash

silicate (with hydrogen peroxide if desired to help break lignin into acids) room temp soak

renove most of liquid and hold in moist environment for lignin to neutralize silicate to form silicagel.

oven dry at 300c or press at 300c till dry.

Uses for this could again be similar to other ultrawood types however this will be harder than those but more brittle.  Uses could include cutting and piercing items like knives arrowheards as well as grips like knife grips and gun grips.  Also would be great for floors and countertops.  Can add certain minerals to the sodium silicate to produce unique colors.

great article
https://answersingenesis.org/fossils/how-are-fossils-formed/instant-petrified-wood/

silica group
http://www.quartzpage.de/gen_mod.html

4.23.2019

Wind Repulsion (WR): How to minimize air resistance

As first described in my "A theory of friction" post, here this technology will be refered to as "Wind Repulsion" or "Wind Repulsion Technology" or "Wind Repulsive" or WR for short.

Wind repulsion (WR) is defined as using a surface charge, preferably negative, in order to repel specifically air.  It can also be used for other fluids as described in "a theory of friction" or even surfaces (like ski and snowboard bottoms, bearings, gears, bushings, etc.) however WR is specific to air so we can dig deeper into how exactly to achieve results in this specific medium, since air resistance is the most important form of resistance that we deal with in planes, trains, automobiles, ships, bikes, rockets, bullets,  etc

Any method to generate or maintain or set up a surface charge on something that will be exposed to relatively moving air is the claim of WR.

Teflon is an example of WR.  Teflon maintains electrons on its surface and this reduces friction of the teflon with air as well as many other types of friction besides just air.  I believe that the reason DuPont sponsored Jeff Gordon in Nascar is so they could work on a teflon based paint or surface coating for his car that would give the race team an invisible advantage.  Teflon is currently the most powerful passive WR in existance.

Nature also has active WR.  It is still "subconcious" but animals contain active WR.  On my bike I am always suprised with how little wind I feel on my exposed arms and legs.   Most of the resistance seems to come from my clothes.  Hair (and also skin to a lesser degree) generously donates electrons in triboelectric contact.  This is beneficial in my theory of friction to reduce friction or drag.   These donated electrons help repel air or wind resistance.  Since friction comes from the process of one material forcibly pulling electrons from another; if we rather give electrons freely, friction will be greatly reduced.  The way this happens in a hair/feather/skin/sweat gland system is the hair or feathers give electrons and sweat provides more electrons to the hair to replace what is lost.  Not only is water a resevoir and/or conductor for electrons, but also the process of water evaporating releases hydrogen bond energy, which likely is electrons or a negative polarity energy similar to electrons, which goes into the "pool" as water evaporates from the pool.  So basically in my theory of sweat; hydrogen bond energy generated by the evaporation of sweat is funneled into hair which then gives off the electrons to the air to minimize wind resistance.  So basically moving fast under your own power causes the body to heat and sweat and the wind causes the sweat to evaporate which in turn powers an active wind repulsion system through the hair or feathers.  Nature really is quite amazing.  The more we learn the more we realize our human technology is shit.

So like I said WR is creating a charge, actively or passively, on a surface which will tend to reduce air resistance.  One not so efficient embodiment of this is to simply charge the surface or skin of something, say clothing or metallic surfaces or skins or otherwise electrically conductive surfaces.  Say you have a wind repulsive wind breaker.  Or wind repulsive tents.  Or wind repellant skyscrapers or bridges, anything exposed to moving air is a candidate.  Preferably we would use a biomimetic method using evaporating water to power this, but actively creating a capacitive surface where the side exposed to the air is charged, preferably negatively, then you can have a very simple way to do this.  Simply connect a power supply or power storage device to the capacitive or conductive surface and you can achieve a wind repulsive surface.

Ultrawood 4: driftwood process

It turns out driftwood has some lignin removed wheras hemicellulose and cellulose remains unchanged.  We can use driftwood and then compress it or we can use driftwood as the starting material for any of the processes described in the ultrawood articles.

Using driftwood does not infringe on the Hu patents because the Hu patents describe lignin removal from natural wood, and driftwood is not a natural wood.  Also assuming extra lignin removal of driftwood will not be done, then no lignin removal step, chemical or otherwise, is needed at all.  Simply find driftwood, wash and soak in distilled water if desired, then press.


driftwood lignin removed
https://www.google.com/url?sa=t&source=web&rct=j&url=https://www.tandfonline.com/doi/pdf/10.1657/AAAR0014-082&ved=2ahUKEwik-PW5zObhAhXGwVQKHXisAIAQFjACegQIBRAB&usg=AOvVaw1Gn9GshK0P2Fn_QganL7a7

4.22.2019

UltraWood 3: A new 2 step method

Ultrawood 3 is a direct replacement protocol for the Hu patented "super wood" protocol.  In his patent first lignin needs to be removed from natural wood and then the wood is pressed under elevated temperature and pressure.  In this iteration presented here, lignin is not extracted from the wood.  The natural wood is simply (with or without first extractives [non-lignin] removal by the likes of water, ethanol, chloroform, acetone, oxalic acid, hydroxide, etc) to infuse the wood with alkaline hydrogen peroxide (or acidic or neutral but preferably alkaline), preferably ph 11.5, using any method.  Some example methods could be boiling, soaking, freezing, vacuum or pressure, etc.  Then when the wood is impregnated with alkaline hydrogen peroxide, the wood is pressed under elevated pressure and/or elevated temperature, preferably both.  Fenton reagents can be added at any point if desired but likely not effective.  Keeping the wood moist while pressing for some period of time is preferable to achieve full reaction.  Also preferably the chemical soaked wood is preheated to the proper reaction temperature before significant pressing.  What this does is degrade the lignin during pressing into smaller molecules thus allowing more densification of the wood than simple wet pressing.  This does not infringe on the hu patents because lignin is not removed from the natural wood prior to compression.

This process can also be done using the hydroxide/sulfite process like hu, hydroxide/urea process, cellulose acetate producing process, gaseous oxygen process, etc. or any other process that would modify one or more of the following; lignin, hemicellulose, or cellulose.

In addition to or alternatively another couple methods can be employed at any part in the process described in any article on ultrawood.  One is gaseous oxygen treatment of the wood.  This can include other gasses to improve the reaction like nitrous oxide or water vapor (ie:steam).  This would break some of the bonds of lignin but again will not infringe on the hu patent since lignin is not bieng removed from the natural wood.  Another option is enzymatic or biological breakdown of the lignin using bacteria and/or fungus and/or enzymes derived from such.  This can be apllied to any method including the Hu method yet will not infringe on the Hu patent because the removal of lignin via this is a biological or biochemical process, not simply a chemical process that the Hu patent necessitates.

Microwaves or any other radiation of any type like lasers or any other type can also assist or replace these methods for partial or full breakdown of lignin and/or hemicellulose and/or cellulose.

lignin breakdown by alkaline hydrogen peroxide
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443053/

fenton iron not effective higher temperature better
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350612/#!po=54.4444

Eucalyptus is a Hallucinogen: Eudesmic acid like mescaline

Ever since I started trying to work with non-extract herb powders I have been finding that common plants are hallucinogens! 3 so far, eucalyptus powder, basil powder, and thyme powder.  Here is my notes on eucalyptus, this was discovered right when I made sadc 7.0 a few months ago.

SADC 7.0 turned out to be psycadelic.  I believe this was from the eucalyptus leaf.  a total of 150mg of dried powdered eucalytptus leaf was taken in 4 capsules of SADC.  Here was the recipie used.  Psycadelic effects were mild and were countered by activated charcoal.  See my eucalyptus leaf powder trip report for more info on the effects.

7.0

30g cinnamon
20g garlic
20g gynostemma
10g tribulus
10g orange peel
30g ginger
30g wheatgrass
15g eucalyptus
10g cranberry

175g

150mg of eucalyptus per 4 capsules

It's alright to let go

The lesson of this trip is that it is ok to let go.

Dosage 150mg leaf powder taken with other leaf powders, some that contained steroidal and triterpenoid saponins that can enhance absorption.  Other herb powders were antibacterial so may have prevented active principle breakdown or conversion in the gut.  With DMT; breathing deeply mellows the trip, but with the eucalyptus compound, breathing shallowly mellows the trip and deep breathing enhances it.  To me this means the active principle is an oxidized version of a DMT precursor in eucalyptus, or a DMT or NMT analogue that has different oxidation metabolism effects. This would make sense based on the first step in the protocol for making mescaline from eucalyptus sawdust.

I have not tried mescaline to compare this, but it was quite comparable to an ayahuasca trip.  I can tell that indole acetic acid is not a breakdown product of this compound because with DMT I can smell the IAA in my nasal passages and that didn't happen with this.  Also this causes less "hangover" mental effects than DMT does for me, however the day after I do feel slowed down a bit, like a Koala.  I feel like this compound would actually be safer than DMT for long term use since it seems it doesn't feed brain bacteria like DMT seems to.  However it may have mental side effects of its own with large doses or prolonged use.

It does cause the charecteristic "Dread" that I get with the onset of an ayahuasca trip.  the onset was faster than acacia confusa powder, the eucalyptus came on in 2 hours wheras the acacia takes about 4 hours for me.

Since my dose was very low I basically had to be falling asleep to notice anything.  But it does tend to prevent you from falling asleep so you can be in that in-between state pretty easily.  I had to take activated charcoal to end the (very mild) trip before I could fall asleep.

Some of the things I saw was this table shelf thing that in my half-dream I wanted to fill with things.  Someone else was filling it with things.  I had the sense that "it is ok to let go, you have important goals and dreams but you are not alone to make them happen". That was a really good epiphany because I tend to shoulder a lot of the responsibility I feel to make the world a better place.

I also saw what seemed like a shadow creature, weird mabye glowy animals, "enchanted forest" type visuals.  Not 100% badass, lots of goofy things in these themes too.  I also saw talking heads (human) telling me something.  I kind of lost sense of my self for moments which frightened me but I feel this is why REM sleep is rejuvenating (because DMT released in rem).  Don't breathe deeply as this makes it worse.

I got up to eat at one point and I typically wolf down my food, and I tried to do that while in this state, and I felt like I may choke because I wasn't chewing fast enough to support my eating rate.  So I had to slow down eating.  I kind of felt like a koala or sloth, very mellowed out and mentally slowed.  Ayahuasca turns off my parasympathetic functions like salivating and defecating and sphincter tone, and this seemed similar to that except not those exact symptoms, more of just the mental side of it.  Bieng like a newborn.

I felt a sense of trancendence and importance of things I was looking at.  Things looked special when I saw them.  A sense of novelty like what terrence mckenna talks about (Although I do not condone the use of high doses of entheogens like he does).

The day after; my morning commute was much improved, instead of bieng boring and me getting mad that I see the same things every time, things felt fresh and new.  I felt much more rejuvenated mentally (mabye physically too) than normal from a weekend.

I like this better than acacia confusa.  Has the benefits but not the drawbacks in my estimation. My dose was quite small and is similar to what 150mg of acacia confusia would do.  If this relation holds true, 3g of eucalyptus powder would be a strong dose and I'm not sure that would be safe as I have read (but not seen any evidence presented) that eucalyptus is toxic.  However I noticed no toxic effects.  Perhaps the other powdered herbs I took with it prevented bacteria breaking down compounds into toxic byproducts.  This is the blend I made (I now call it PSYDC for psycadelic detox cleanse,) and took 4 x 00 capsules of this mixture:

Likely trimethoxybenzaldehyde
https://www.google.com/amp/s/www.vice.com/amp/en_us/article/qbeead/how-to-get-high-in-the-australian-bush

...oxidized to eudesmic acid
https://en.m.wikipedia.org/wiki/Eudesmic_acid

Thyme is a hallucinogen: Baicalein tyramine hallucinogen

I don't know what if any mechanism could be known but the hallucinogenic properties seem similar to dmt however with sort of a less emotional perspective.  I've never tried LSD but I assume it is similar.  This is also active seemingly without an MAOI.  One capsule of thyme powder along with echinacea and mustard and ginger, mabye they enhanced the absorption of the active principle of thyme.  These were all taken before bed and the thyme gave vivid exciting dreams in a way that I didn't want to wake up because I was more excited about the dreams than my own ideas and goals.  This is very important for me since I tend to not like sleeping and don't get enough.   I know it is the thyme becuase it has happened several times I've taken it and never with the other herbs which I also take a lot.  Mabye ut is related or even possibly the same but slightly different to the MDMA like molecule in basil.  Oh and this principle is not in the essential oil because I have taken large amounts of that with no effect.

actually its probably baicalin
https://www.ncbi.nlm.nih.gov/m/pubmed/26604025/

dopaminergic
https://drugs-forum.com/threads/did-thyme-just-make-me-high-or-is-it-placebo.287635/


UltraWood 2: Improving the method

First calcium, sugars, starches, and hemicellulose should be removed while keeping lignin mostly intact or even increasing it. This can be done with any method or series or combination of methods but I believe treating the wood with oxalic acid solution can accomplish all of these.

Next the cellulose should be partly dissolved to increase pore size in the wood and soften it, again preferably while keeping lignin intact as a structural component.  This can be done with brief and/or low temperature hydroxide/urea solution.  Keeping the temperature of this low will help prevent lignin removal or breakdown.  Also this solution works best at low temperature and also freezing.  This process should be carefully designed so as to not dissolve too much of the cellulose as to render the material fully dissolved or otherwise ruin the structure.  In addition to this or alternatively, lignin can be removed from the oxalic acid treated wood.  This would not infringe on the Hu patents because the wood is no longer "natural" after bieng treated with oxalic acid.  However I believe the lignin is an important structural component in the matrix and likely shouldn't be removed for the best final product and rather a little of the cellulose should be removed and/or modified instead.

Next preferably the surface (or bulk) of the cellulose fibers should be converted into cellulose acetate (and/or nitrate if combustibility is desired).  This will help water and humidity proof and adhere the cellulose fibers together in the compaction step.

Preferably next the matrix should be deacidified of any lingering acid with magnesium peroxide solution.  This is a step taken from the art of paper preservation.

Finally the matrix should be compressed at around 750psi or higher preferably at elevated temperature preferably 212-300f or higher.  The hope of this step is to get the cellulose acetate groups to bond the cellulose acetate (or plain celluose) fibers together

Each of these steps on their own are optional in this protocol but I believe the combination will give best results. For example natural wood can be treated to convert some of the cellulose to cellulose acetate and pressed.  Or oxalic acid boil could be done and pressed right away.  Or oxalic acid step, hydroxide step, then press, etc.  Any or all of these steps can be done in any order or combination but the full protocol I believe will be optimal for many applications.

See the previous ultrawood post for more references.

Also you can make thin sheets or plates or any other shape with this method and combine them in any way including with a binder like a glue or catalyst like acetic acid or cellulose acetate or anything else or just inherently melding the cellulose acetate to eachother since this behaves like a polymer.

oxalic acid hydrolyzes starch and hemicellulose
https://www.google.com/url?sa=t&source=web&rct=j&url=http://proceedings.itb.ac.id/download.php%3Ffile%3DA13488.pdf%26id%3D2256%26up%3D1&ved=2ahUKEwjP6bzhxOPhAhWP0VQKHV__CSwQFjAAegQIBRAB&usg=AOvVaw1u6LLoTVU8RLbiPJvWMpvi

4.21.2019

UltraWood: Polymerized super wood

So if you have heard of super wood or superwood, it is basically partially dissolved wood that is compressed to make it stronger than steel but much lighter.  Well of course I have an idea to improve it.

Enter ultrawood.  Besides adding preparation steps, the main added step is vacuum impregnation of a polymer somewhere between the initial hydroxide/urea (and/or other elements like oxalic acid pretreatment to remove calcium) step and the compression step.  After the wood is partially dissolved in the prep steps it has more porosity.  There may be a wash step after that or not, there may or may not be a de-lignan step of hydroxide/sulfite and then any polymer like epoxy or something else is vacuum impregnated into the voids.  Then it is compressed.  I think this method will not only fully prevent the 10% growth from humidity exposure that unpainted super wood is suseptible to, but also increase strength even higher.  Something like epoxy can increase strength whereas something like rubber latex might increase flexibility and toughness.  Also this impregnation might reduce the compression pressure and/or temperature needed to achieve a good product.  In super wood the bonds between cellulose have to be created by heat and compression, in vacuum impregnated version these bonds might become less important so the extreme pressure and elevated temperature may not be as important.


That bieng said of course other natural polymers (like cellulose acetate) can be used instead or addition to synthetic polymers for vacuum impregnation. Or a similar but slightly different thing can be done altogether.  Instead of vacuum impregnating with a premade polymer, what about a soak/boil step instead to make the cellulose itself more polymer like? Enter vinegar.  Yes the humble ingredient.  Simple acetic acid of any concentration preferably high concentration in water or another solvent or 100% glacial acetic acid (and/or not so simple acetic anhydride) or other more nasty things like trifluoriacetic acid can be used to turn the cellulose already present after the initial hydroxide/sulfite boil into a polymer itself or at least functionalize the surface of the cellulose fibers for better adherance after compression.  So basically you would have the same or slightly modified initial soak to increase wood porosity then you would boil or soak it in vinegar lets say for simplicity or anything else that achieves the same type of effect (namely neutralizing the OH groups to make it more unreactive to hydrogen bonding), then you would compress it.  So basically we are partially or fully converting the cellulose into cellulose acetate or cellulose nitrate or anything else) or just functionalizing the surface of the cellulose fibers to be more adherant and water repellant which is a sort of plastic polymer.  This will prevent expansion due to humidity and perhaps strengthen and/or toughen the material even more.

So the method I am going to pursue is soak in room temp 8%/8% hydroxide/urea then freeze 60 mins, boil/rinse/soak, then mabye remove lignan, boil/rinse/soak, soak in oxalic acid, boil in water rinse, boil in magnesium peroxide solution, short water boil rinse, boil in glacial acetic acid, boil in magnesium peroxide solution, boil in water rinse, heated press roughly 750psi and 212-300f.  This will in theory produce a long lasting water/humidity resistant, but still biodegradable product.

Simplified method I may use: (boil rinses probably between each step)
1. Soak in oxalic acid to remove calcium and hemicellulose and increase lignin.
2. Soak in room temp hydroxide/urea, freeze 60 mins.  Removes cellulose, enlarges pores.
3. soak in acetic acid optional sulfuric acid or other acetylating mix. Makes cellulose acetate.
4. Soak in magnesium bicarbonate to deacidify.
4. Press 750psi at 220-300f until proper thickness.

This does not infringe on the Liangbing Hu patents because his requires removing lignan from natural wood while keeping the cellulose structure substantially the same.  My method not only substantially changes the cellulose by a hydroxide/urea and/or oxalic acid pretreatment step, but this step also renders the wood no longer "natural wood", which also was a requisite to his claim.  So the chemically modified wood can be delignated if desired without infringing on the patent. However I feel keeping the structural component of the lignin would actually be a benefit to strength and toughness especially in light of the fact the cellulose will be significantly modified either in volumetric structure or at least surface structure to cellulose acetate.  Also lignin is removed at high temps so the hydroxide/urea step will not remove significant amounts of lignin.

Basically I am using cellulose acetate lamination process with deacidifying step of the magnesium bicarbonate.

super wood
https://www.scientificamerican.com/article/stronger-than-steel-able-to-stop-a-speeding-bullet-mdash-it-rsquo-s-super-wood/

trifluoroacetic acid to convert cellulose based matetials
https://cen.acs.org/articles/92/web/2014/07/Simple-Acid-Soak-Turns-Food.html

surface functionalization of cellulose by plain acetic acid
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pol.1954.120147805


acetate not good for adhesive, OH better
http://www.pvateplaamerica.com/materials/polymers-celluloseacetate.php

cellulose acetate lamination
https://rbm.acrl.org/index.php/rbm/article/view/16820/18410

deacidification of cellulose with magnesium bicarbonate
https://pubs.acs.org/doi/abs/10.1021/ba-1981-0193.ch008?src=recsys


phenol
https://www.sciencedirect.com/topics/engineering/densified-wood

cellulose acetate lamination with and without acetone  500psi 300f
https://www.google.com/url?sa=t&source=web&rct=j&url=http://americanarchivist.org/doi/pdf/10.17723/aarc.21.3.m4h7m16466048622&ved=2ahUKEwiKlYvkvuHhAhWOqp4KHWnHDhEQFjAAegQIBxAB&usg=AOvVaw3UMx25wlSps500OT9dHdPh

725psi 212f
https://www.motortrend.com/news/wood-be-weight-savior-technologue/

delignified wood patent
https://patents.google.com/patent/WO2019055789A1/en?inventor=liangbing+hu&oq=liangbing+hu&page=2

strong and tough wood materials
https://patents.google.com/patent/WO2018191181A1/en?inventor=liangbing+hu&oq=liangbing+hu&page=2

flexible wood
https://patents.google.com/patent/WO2018187238A1/en?inventor=liangbing+hu&oq=liangbing+hu&page=3

8g naoh 8g urea 84g dih2o lignin not degraded
https://bioresources.cnr.ncsu.edu/resources/enhanced-effect-of-naohthioureaurea-aqueous-solution-on-paper-strength-of-high-yield-pulp/

oxalic acid pretreatment
https://www.google.com/url?sa=t&source=web&rct=j&url=https://www.fpl.fs.fed.us/documnts/pdf2003/swane03a.pdf&ved=2ahUKEwiF9_6-nuLhAhWGv54KHdEjCvoQFjADegQIARAB&usg=AOvVaw3lz_JzaLLsJ1MG7ZcHSIAW

25% saturated magnesium bicarbonate sol
https://www.google.com/url?sa=t&source=web&rct=j&url=https://cool.conservation-us.org/coolaic/sg/bpg/annual/v22/bp22-07.pdf&ved=2ahUKEwi0j9r5uOLhAhXNl54KHU-bCcIQFjAGegQIAxAB&usg=AOvVaw3PUikl5H3XNVfqUH1r50ho

275ml dih20 100g oxalic acid 80c ish for 1hr (was 130c for 10 mins in paper) 9:07 to 10:07.  At end left with 75ml liquid.
Wood should have sunk to the bottom from bieng water logged. (using poplar wood).  Let soak in dih2o until next step.

magnesium bicarbonate:
http://aanationalarchivesworkshop.com/downloads/learning/seltzerdeacidification.pdf

oxalic acid precipitates not extracts lignin
http://www.globalsciencebooks.info/Online/GSBOnline/images/0906/AJPSB_3(1)/AJPSB_3(1)86-88o.pdf

Oxalic 1% pretreatment
http://www.woodresearch.sk/wr/201601/08.pdf

oxalic increases lignin?
https://www.ingentaconnect.com/content/tcsae/tcsae/2014/00000030/00000005/art00035#

Yes lignin increases, hemicellulose decreases.
https://www.fpl.fs.fed.us/documnts/pdf2010/fpl_2010_lee001.pdf

starch and sugar removal boiling 10min 80% ethanol and alpha amylase
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301340/

20% hcl extraction  of starch
https://bio-protocol.org/e1169

4.19.2019

Stiff neck caused by Haemophilis Influenzae cured with echinacea

The title says it all.  Stiff neck is caused by haemophilis bacteria likely non typable.  The best echinacea on the market is echinacea purpea root powder.  Put some of the powder on the tongue and if after a while it makes your tounge feel numb/cold/tingly then it is good quality.  Fill capsules with thebpowder and take around six OO capsules of the root powder spaced out over the course of several hours with plenty of water and the stiff nck should dissappear.

4.17.2019

The first sign of the Mark of the Beast is here

This is the first sign.  "People are not allowed to buy or sell unless they have the mark or the number of his name"

De-banking. Chase has now started closing accounts of people they don't like.

https://www.wnd.com/2019/04/major-u-s-bank-shuts-down-alt-right-accounts/

Suprisingly or unsuprisingly this actually happened to me.  I was approved for a chase account and deposited all of my money as everyone does when they switch banks.  Then out of the blue with no warning they shut down my account for no reason given and it took over a month for the check of my money to finally arrive at my mailbox.  I went into the branch and demanded a check but they refused and made me wait a month to get it by mail.  Needless to say this made me miss bill and rent payments.  Chase is total scum.

But mabye it had something to do with this site where I speak truth to power and question the official mainstream narrative.  If that is the case then they must be using some huge database compiled by southern poverty law center or Media Matters to drop clients.  This would make sense because I made the radar of these Nazi groups like media matters and SPLC when I questioned Justice Scalia's death and proved a connection between the owner of the ranch where scalia died and president Obama and how Obama mocked his death.

https://www.thedailybeast.com/meet-the-scalia-death-truthers-was-he-murdered-by-obama-or-aliens

Anyway this is what the mark of the beast looks like.  Those who refuse to swallow the blue pill will be rejected from society.  Get ready for it, in 2024 it explodes.

4.15.2019

Martin O'Malley is likely responsible for Pete Buttigieg's Presidential Run

In his announcement speech that he will be running for office, Pete said that he wasn't even thinking to run for president last year.

Then I see a video of martin omalley in feb 2017 (see link below) pushing for Pete to be DNC chair and basically saying that Pete went along with the plan to run for DNC chair ("hes wanting to throw himself into this task").  So basically what I am seeing is that Martin O'Malley and other high ups in the democratic party like Howard Dean are basically urging pete to do certain things.  Kind of like how Harry Edwards urged kaepernick to protest in the NFL.

https://m.facebook.com/story.php?story_fbid=10158530514155393&id=28684115392

Interestigly also in Martin O'Malleys speech he mentioned Pete going up against Trump ("take on trump").  I think this was a freudian slip.  His ultimate plan was to get Pete to run for president in 2020.  Why would he want this? Because Martin needs someone who will pave the way for Martin to run in 2024 - an election where democrats have a much higher chance to win the election (since most presidents win a second term, Martin knows Trump will get reelected).  Also Martin wants to get Pete out of the way in 2020 so Pete doesn't pose a threat to Martin's own run in 2024.

Pete Buttiegieg seems to me to be part of the archetype of the Antichrist.  He uses the guise of Christianity to condemn people based on his judgement of their character.  He would be the one to turn liberals on to this way of thinking which will pave the way for them to accept Martin O'Malley in 2024 and the fascism he plans to usher in.



4.14.2019

SADC Thoughts

So basically SADC has a few goals.  First and foremost is to clean out the gut of bacteria.  Secondly to support sleep.  Third to promote regularity.  And thats about it.

It is challenging because I want to makenit as accessible as possible which means I need to prefer using herb powders over extracts or essential oils.

Right now a good mix for me is natures fury (1:4 tribulus extract and gynostemma extract), ginger powder, food grade de, garlic powder, mint and cinnamon and eucalyptus essential oils, and agrimony

My thought is that:

natures fury kills strep and staph bacteria
ginger powder kills campylobacter
DE kills ecoli and pseudomonas
garlic powder kills mycoplasma
mint and cinnamon kills haemophilis
eucalyptus kills proteus
agrimony kills h pylori

However I wanted to substitute herb powders for:
natures fury- hard to get pure extracts
DE- contains aluminum
mint cinnamon and eucalyptus eo's- try to remove eo's
cold water extract willow bark- hurts liver
senna- causes electrolye imbalance and campylobacter overgrowth
wheatgrass- causes potato poisoning symptoms of numb arms during sleep.

So far I got trib and gyno powders to try in place of nqtures fury.  Doesn't work effectively.  In order to get the levels of saponins in natures fury I would probably have to take tablespoons of the herp powders which isn't practical.  So I need to use natures fury in sadc 7 which is in development.

I am trying to substitute mustard powder, thyme powder, and cinnamon powder for the DE.  This does seem promising.  Also tumeric with natures fury may also remove the insomnia that comes from the LPS from the bacteria.  So removing food grade de is looking promising.

Mint and cinnamon eo's for haemophilis I am trying to substitute with mint and cinnamon powder.  not quite sure how that is working currently.  Some potential in echinacea purpea root powder to kill haemo.

eucalyptus essential oil I am trying to replace with echinacea and cranberry and mabye uva ursi powder.  Not exactly sure how that is going yet but some slight promise with the cranberry. havent tried echinacea yet.

cold water willow extract I am trying to substitute with tumeric.  seems quite promising especially with natures fury as absorption enhancer.

senna I am trying ti substitute wuth slippery elm bark powder to promote regularity.

Wheatgrass I am tryubg to substitute with agrimony for h pylori.

Now i am encapsulating individual herbs instead of uing prototype blends so I can better pinpoint what is helping and what is needed:


The current powders I am working with:

echinacea-proteus and haemophilis
garlic-mycoplasma
tumeric- inflammation caused by a few types of bacteria including ecoli, kill hpylori
agrimony- hpylori
slippery elm- regularity
ginger- campylobacter
milk thistle- liver support
thyme- gram negative ecoli
mustard- gram negative ecoli
natures fury-absorption enhancer and strep and staph

notable missing ones that may need to be added:
cranberry- proteus and ecoli
cinnamon-pseudo and haemo
mint-haemo


4.13.2019

Mechanism of how inflammation causes insomnia

In my posts on this subject:

http://www.naturehacker.org/2018/08/symptoms-linked-to-bacteria-that.html?m=1

http://www.naturehacker.org/2017/08/4-chronic-bacterial-infections-that.html?m=1

http://www.naturehacker.org/2016/08/the-quintessential-guide-to-gut-microbes.html?m=1

http://www.naturehacker.org/2016/10/the-6-real-root-causes-of-insomnia.html?m=1

http://www.naturehacker.org/2016/10/one-of-most-common-causes-of-insomnia.html?m=1

I have learned a lot about what causes insomnia.  Most of it is empirical (experimental) but very litle is actually theoretical.  Well today we uncover some theory behind one of the causes insomnia I have duscovered.

Ecoli and other gram negative bacteria cause one of the most indetectible causes of insomnia.  A persistant low grade inflammation it turns out.  Of course, how did I not make the connection earlier between LPS (lipopolysaccharide which causes herxhiemer reaction) to sleep loss? Well I am now.

Turns out the LPS from these gram negative bacteria activate the COX-2 enzyme.  This enzyme causes the production of PGE2.  PGE2 is what causes fever and things like that.  Turns out this inflamatory molecule causes sleep loss.  However there is another inflammatory marker PGD2 which is sort of the opposite and it causes sleepiness.  So when COX-2 is suppressed, PGE2 stops bieng made and extra PGD2 is created.  This is exactly wht we want (besides the basics of killing the ecoli with mustard, thyme, activated charcoal, etc) Two herbs which can do this is a cold water extract of willow bark powder (Salicin and other polyphenols) and Tumeric (curcumin). These will literally lower PGE2 and elevate PGD2 inducing sleep.  Some say PGD2 is the most basic and powerful inducer of sleep in nature and is what causes narcolepsy when it is dysregulated.

Another way is to take mustard and thyme powder or actuvated charcoal and within 20-30 mins your Ecoli will be killed off as well.  If that diesn't help you see the above links for many other bactria that cause insomnia with mechanisms so far unknown, but whose cures are known.

References:
prostaglandin d2 inhibited by asprin

prostaglandin e2 opposite kf d2

pge2 reduced by asprin
https://www.ncbi.nlm.nih.gov/m/pubmed/27554763/

pge2 higher in insomnia and diabetes

imoortant feverfew k2
https://www.narcolepsysupport.org/forums/topic/inflammation-and-the-most-potent-sleep-promoting-substance/

cox2 mediates pge2 tumeric
http://www.naturehacker.org/2019/04/the-black-hole-picture-is-fake.html?m=1

willow bark beats asa
http://www.naturehacker.org/2019/04/the-black-hole-picture-is-fake.html?m=1

e2 vs d2
https://www.ncbi.nlm.nih.gov/m/pubmed/25532785/

d2 is sleep promoting
https://www.ncbi.nlm.nih.gov/m/pubmed/25307222/

turn off cox2->E2vD2^
https://www.sciencedirect.com/science/article/pii/S156757690400342X

willow only shuts off cox2 and boosts cox1
https://www.ncbi.nlm.nih.gov/m/pubmed/20648923/

curcumin tumeric also selective cox-2
https://www.ncbi.nlm.nih.gov/m/pubmed/11566484/

gyno is cox-2 mediated aromatase
https://www.ncbi.nlm.nih.gov/m/pubmed/16392624/

opposite low e2 high d2 causes balding
https://www.thehindu.com/sci-tech/health/medicine-and-research/cause-of-male-baldness-found/article3025234.ece

cox2 causes most asthma
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380345/


4.12.2019

Proof the Black Hole Picture is Fake

It makes you feel powerless when a false historical narrative is being woven before your very eyes and you feel powerless to correct it.  Folks, most of history is a lie.

So I archived this article that clearly shows the hoax of this supposed "historic" image.

https://web.archive.org/web/20190412110840/https://www.thelily.com/meet-the-29-year-old-scientist-behind-the-first-image-of-a-black-hole/

http://archive.is/y1Ev4-

Not only does the article report that the woman scientist faked the image, but it outright tells you they edited what she said in the interview.  Why would they do that??

Anyway before I go further here is an image that the archive failed to save.

So before I talk more remember that scientists have been saying recently that perhaps black holes are not at the center of galaxies but rather several supermassive stars are.  Well the above picture is an example of data that probably informed their theory of that.  Look closely at the picture above on her computer screen then read the article link below:

https://web.archive.org/web/20190412113202/http://www.cnn.com/TECH/space/9909/16/supermassive/index.html

The pictures that these scientists arrived at simply do not show a doughnut.  They show 4 massive bodies orbiting a common center of mass.  This is what objects look like that are orbiting eachother.  No mystical Black hole is needed to cause them to orbit eachother.  Bodies with a similar mass will orbit eachother in a ring shape.

Now this 4 body pattern is what this woman saw in her data.  Two other teams were also working on images and they presumably saw the same "4 body" pattern.  However one of those teams actually ran the data through a "disk" algorithm, a method designed for analyzing disks.  So that image probably was more ring like.  So what did they do?  Present all of their images and let people discuss the implications of the data?  Nope.  They "Blurred two of the images and then averaged them to the other image".  So what they did was fudge it so it looked like a doughnut.  I kid you not.  They took thier very hard earned data, and blurred it so it would look like a continuous ring.  Wow.  And that is admitted on the record.  So the one image that was created by running the data through the disk algorithm was probably the third one in her above quote.  Two of the teams presumably found the 4 body pattern so they blurred those to make them look less like bodies. Then the disk algorithm picture probably gave a faint ring/-disk, so it wasn't convincing enough to superimpose that faint disk on the blurred body images, they had to boost the brightness of the disk image which is what "averaged them to the other image" means.  So you basically have 2 images of the 4 body pattern and a disk image.  You blur the 4 body ones so they don't look as much like separate bodies, then you superimpose a faint disk image and boost its brightness so it fills in the gaps in the ring so it all combined looks like a doughnut.  Some real NASA style fakery there.

This is the most dishonest science I have ever personally witnessed in my life.  They are so hell bent on believing in black holes that they will literally smudge the pictures to make the data look like what they think it should.  Terrible day for the reputation of the scientific field.  And well earned, most scientists have been in the business of falsifying data ever since they started grad school.  It is the culture of these dogmatic and abusive scientific fields that create cheaters.  I know because I worked in them.

4.11.2019

Julian Assange is a true hero and martyr

Very few in the history of the world have done as much to free humanity as Julian Assange of Wikileaks.  Just like Jesus he condemned those in power and sought to empower the powerless people of the world.  Jesus used universal truths that could set mankind free.  Assange used exposing those in power and the evil deeds in high places.  Julian Assange was a counter-spy, he fought against the tyranical surviellance state worldwide that has been developed and weaponized to enslave humanity and it has been extremely effective.  Assange is one of the few people who have found the chink in the superstate's armor and has had the guts to seriously risk his own life to take the shot.

Julian Assange will go down in history as one of the greatest advocates for humanity that has ever existed and will join the ranks of the few and proud Humanitarians that have graced mankind with their presence.

Thank you Jullian Assange.  We are all in debt to you.

A Theory of Friction

This theory of friction is simple, the transfer of electrons from one surface to another surface is the primary cause of friction.  So triboelectric charging is the main cause of friction.  You may be wondering then why is teflon so low friction even though it is a highly negatively charging triboelectric material?  Well because it actually doesn't steal many electrons.  Since it is highly insulative and its fluorines (the reason it is so toxic) are highly electronegative and do not give up electrons easily.  So yes it does steal some electrons, but not very many and it is great at not giving them up, this is why it is so low on friction.

So if this is true how do we leverage this to make the next generation of low friction materials, particularly to air (or other fluids) resistance? Well air for example is typically positively charging.  This means air looses electrons to surfaces it is blowing over.  The more the surface steals electrons from the air, the more air resistance it has (basically any way the surface changes the energy of the air will create resistance but we already know about the mechanical aspect, streamlining, so this topic is beyond streamlining).  What we are talking about here is how to reduce drag when you already have a smooth and flat as possible surface.

The answer is that you charge the surface.  This can be harder to do than it seems.  You can't just hook the negative terminal of a battery up to something and expect it to have a negative charge, it doesn't work like that.  What my idea is is to create a preferably thin capacitive surface.  Similar to my tribogon/triborgone idea, but instead of those which are passive stealing/donating charge, we will actively generate a charge.  So take the triborgone idea, basically you have a skin that gives up electrons.  But this time you are charging the outside surface negatively and the inside surface positively say for example with a battery (or capacitor).  This is possible and easy to do, you just connect the negative terminal of the battery to the outer surface and the positive terminal to the inner surface.  This is how you charge a capacitor.

Which way to you hook it up?  I believe that you would hook it up so the negative charge is on the outside facing the friction source (like air).  The reason for this is if the positive charge was outside, it would be stealing electrons from the air and this process creates friction.  So if we charge the surface negatively, then it will give off electrons and the air will not be slowed down for the surface to strip electrons from the air, the air will simply slip over the electron laden surface.  So like triborgone, you may want a positive tribocharging material coated super thinly on a current collector.  The current collector would be the thing that is charged negatively, and the positive tribocharging materialcoated over that current collector would be the thing that interfaces with the air.  This positively tribocharging material would act as a diode, biasing the electrons to flow outwards from the surface into the air.

Now this is interesting because human skin or animal fur or feathers would act in this exact way.  The animal has electrons inside it and the positive tribocharging surface (skin/fur/feathers) would bias the electron flow out of the animal and into the air, doing exactly what we say in this theory.

Now there is one more wildcard, water evaporation.  Water evaporation is interesting because it acts like a battery.  Basically water needs to loose hydrogen bond energy to evaporate.  In a battery where the metal atoms are electrostatically bound together, loosing this bond energy in the form of electrons is what causes the metal to dissolve.  Loosing hydrogen bond energy from water allows it to "dissolve" into water vapor.  So water can be used as a source of negative energy if needed.  Not sure exactpy this couod help us other than provide a free source of electrons.  Water is just under air on the triboelectric series therefore charges negatively when air blows over it.  This is not really what we want so we wouod have to have something that charges positively in air connected to the water so that electrons are pulled out of the water and the water evaporates to compensate for the loss in its bond energy.  So water evaporating may just be a byproduct of negative energy flow from water into the air.  Mabye that is how hair works, hair donates negative energy to the air and in the process uses bond energy from water causing it to evaporate which also cools the animal.

So basically the gist is that however itnis accomplished, the air facing surface of a material must donate electrons to the air (or fluid) in some way to reduce drag.  This can be done passively or actively.  Even if done actively (like with a battery), which will cost energy, I still think the net effect will be more efficient travel if done right.

4.08.2019

Socialism: "Social Ownership" is a lie

Social ownership is the factor that underlies all socialism but it is not true.  Lets say that I am the socialist ruler and I split up all the marbles between the 100 citizens in my country.  Each person gets 10 marbles.  Now thier is "social ownership" of the marbles right? Wrong.  Billy trades his marbles for a hug.  But that isn't allowed because now the marbles are distributed unequally.  As the socialist dictator I say that you cannot trade or give away your marbles because then there is inequality.  Does Billy really have ownership of his marbles then?  No.  Ownership means you have sole authority over what you can do with what you own.  But in this case I am telling you what you can and cannot do with what you "own".  Therefore this is not ownership at all but rather posession.  The government owns everything in socialism since they control everything.  The government giving you the marbles is a bailment, you can posess things and perhaps use them how the government allows you to use it, but the government has control over what you can and cannot do with it.

Givism destroys socialism because what little you do own (that which you produce outside of your job) you can give away to meet peoples needs.  The more people that do this the more peoples needs will be met without the socialism controlled "day jobs". Once the government controlled jobs are no longer needed, then they will collapse.  People will then give freely and meet eachothers needs without a socialist overlord telling people what they need to do.

Capitalism isn't the answer either.  Capitalism is a competition over who gets to gain the monopoly.  There aren't winners and loosers in capitalism, there is one winner at which point capitalism ends and socialism begins.  Typically, instead of a competion deciding the winner, socialism is enacted by violence and the winner of the civil war aka "revolution" gets to be the socialist ruler.

4.05.2019

EA Needs to Kneecap Epic Games

When a fighter winds back and goes to throw a huge punch, they make themselves vulnerable to getting broadsided.  This is what Epic Store CEO Tim Sweeney is doing.  He is focusing on taking big shots at Valve's Steam.  However, EA has everything they need to come in and destroy the vulnerable Epic Games. 

All of Epic's money is coming from a single game Fortnight Battle Royale.  That is a precarious position and anything that reduces Fortnite's earnings could spell disaster for Epic.  EA has Apex Legends which is the biggest competitor to Fortnite.  EA needs to expand the team and bring on experts to drive Apex further up the charts versus Fortnite. 

Secondly EA has it's own launcher.  While Epic Store's biggest selling point, taking only a 12% cuts of games income, could easily be undercut by EA's Origin launcher.  EA could only take a 10% cut and make Epic look dumb.  Origin could also QA games that want to launch there and charge a flat $2,500 to make sure that all games that launch on Origin meet EA's standard of quality.  So titles would only have to pay $2,500 + 10% to launch on Origin. 

Thirdly Epic has Unreal Engine.  This engine is free to use and Epic charges developers 5% profits to use the engine in their games.  EA could easily beat this.  EA has Frostbite engine.  While this engine has some serious problems, it gives great graphics.  EA needs to open-source the Frostbite engine.  Immediately this engine would be the most used engine in the industry, a professional open source engine is unheard of.  All companies would be picking up this engine and using it in their games, and a huge development community would grow centered on this engine and making the engine better...for free.  EA has everything to gain and nothing to loose by open sourcing Frostbite.  As an added bonus to hype up developers into using the Frostbite engine, waive the $2,500 QA fee for launching on the Origin store if the company is using the Frostbite engine in their game.  This would help increase the prevalance of the Frostbite engine and have it compete with Unreal and also make it so the cheapest a game can launch on Epic store is 12% revenue, and the cheapest on Origen is a flat 10%.

In conclusion Epic racing after Steam with tunnel vision is like a Noob in a FPS game, crafty players will sneak up on the rusher and take them down from behind.  As I have said it is only a matter of time before Tim Sweeney gets picked off as a failed CEO for #EpicFail games.

4.02.2019

Tim Sweeney will be fired as Epic Games CEO within 3 years

I predict that the board of directors will oust Sweeney within 3 years as the head of the company.  He may "step down" which they will encourage him to do to save face.

Why will this happen?  Tim has made some very boneheaded moves in the recent past.  He somehow was able to turn the welcome competition against the Steam monopoly into a PR nightmare for his company by aggressivly pursuing games as exclusives for Epic game store.  No, it wasn't enough to have developers actually want to also list their games on Epic for a larger profit and mabye some kickbacks.  But Tim Sweeny wanted his cake and ate it too and wanted to make sure the games that promised to release on Steam CANNOT be on Steam and must ONLY be on Epic.  What a blowhard.  Not only did this hurt Epic but also hurt the game companies that did the deal with the devil as their fans can clearly see they sold them down the river for #FortniteMoney.

Also Epic responded to Apex Legends by screwing up Fortnite.  Tim Sweeny was like 'Respawning in a battle royale?  Ya well we will give health and materials for each kill to compete with apex's fast and contonuous gameplay'.  Well it backfired.  This led to a steep increase in the skill gap of fortnite and noobs got crushed.  However every good fortnite player got used to the change.  When Apex seemed like no longer a threat, Sweeney reverted the change, and fans and streamers of Fortnite are totally pissed.

Tim Sweeney is a vindictive, tone deaf, and trigger happy CEO who has already gotten Epic in a lot of hot water and will continue to do so into the future.  Having exclusive games on your platform isn't necessarily a bad thing but the way Sweeney went about it basically ensured that Epic will never be able to have exclusive games without invoking very bad memories in gamers.  He is ruining the Epic brand.

I used to have a lot of respect for Tim Sweeney in that he developed unreal engine 1 which I feel was a huge revolution in gaming and made its way into my favorite game, Everquest.  He also pioneered the "free to use" unreal engine model which was awesome, the free to play model of fortnite which is great, and even a fairer split for dev's on the Epic game store.  How any CEO is capable of spinning all of those great achievements in a way that makes everyone hate your company... is an #EpicFail.  This is the new brand Sweeney has created.