Hudson 1990 - David Hudson Lectures

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DavidHudsonLecturesThese are lectures David Hudson gave in the 1990'sDavid Hudson is the originator of the term “Orbitally RearrangedMonoatomic Elements”, and holds the patent. David Hudson patent can beseen: Hudson Patent for White Powder GoldMy name is David Hudson. I'm a third generation native Phoenician froman old family in the Phoenix area. We are an old family. We are veryconservative. I come from an ultra-conservative right wing background.For those of you who have heard of the John Birch Society, BarryGoldwater, these ultra right- wing Rush Limbaugh conservatives; that'sthe area that I come from. I'm not saying whether it is right or wrongbut that is my ( David Hudson) background.David Hudson had no idea he would be doing this type of work." In 1975-76 I was very unhappy with the bankingsystem here in the United States. I was farming about 70 thousand acresin the Phoenix area in the Yuma valley. I was a very large,materialistic person. I was farming this amount of ground. I had a fortyman payroll every week. I had a four million line of credit with thebank. I was driving Mercedes Benz's. I had a 15,000 square foot home."David Hudson referred to himself as "Mr. Material Man" during that period.David Hudson Discovery of Monoatomic ElementsIn 1975 David Hudson was doing an analysis of natural products in the areawhere he was farming. "You have to understand that in agriculture in thestate of Arizona we have a problem with sodium soil. This high sodiumsoil, which looks like chocolate ice cream on the ground, is justcrunchy black. It crunches when you walk on it. Water will not penetratethis soil. Water will not leach the sodium out of the ground. It's

called black alkali.What we were doing was going to the copper mines in the state of Arizonaand buying 93% sulfuric acid. For those of you who don't know, thebattery acid in your car is 40-60% acid. This was 93% sulfuric acid;very, very high concentration. We were bringing in truck and trailerloads of this sulfuric acid to my farm and I was injecting thirty tonsto the acre into the soil.We were putting six inch ribbons on the ground that would penetrateabout three or four inches into the ground. When you irrigate (nothingwill grow in Arizona unless you irrigate) the ground would actuallyfroth and foam due to the action of the sulfuric acid. What it did wasconvert the black alkali to white alkali, which was water soluble. Sowithin a year and a half to two years you would have a field that couldactually grow crops.In the work that I was doing with these soils, it is very important thatyou have a lot of calcium in the soil in the form of calcium carbonate.The calcium carbonate would act as a buffer for all the acid that wasbeing put on the soil. If you don't have enough calcium the acidity ofthe soil goes down, you get a pH of 4-4.5 and it ties up all of yourtrace nutrients. When you plant your cotton it will only get so tallthen it won't grow any more.It's very important when you are putting all of these amendments on yoursoil that you understand what is in your soil: how much iron is there,how much calcium is there and so on.In doing the analysis of these natural products we were coming acrossmaterials that no one seemed to be able to tell us what they were. Webegan to trace this material and we found that it seemed to come from aspecific geological feature. Whatever the problem with this material waswe felt that the area where it was in greatest abundance would be thebest place to study it.

David Hudson: The Chemistry of M-state ElementsWe took the material into chemistry and we dissolved it and got asolution that would be blood red. Yet when we precipitated this materialout chemically by using a reductant of powdered zinc the material wouldcome out as a black precipitant just like it was supposed to be if itwas a noble element. A noble element if you chemically bring it out ofthe acid it won't re-dissolve in the acid.So we precipitated this material out of the black and we took thematerial and dried it. In the drying process we took a large porcelainfunnel called a Butiner funnel about this big it had a filter paper onit. This material was about a quarter of an inch thick on top of thefilter paper. At that time I didn't have a drying furnace or a dryingoven so I just set it out in the Arizona sunshine which was about 115degrees at 5% humidity so it really dried fast.What happened was that after the material dried it exploded. It explodedlike no explosion I had ever seen in my life and I've worked with a lotof explosive materials. There was no explosion and there was noimplosion. It was as if somebody had detonated about fifty thousandflash bulbs all at one time just poof. All the material was gone, thefilter paper was gone and the funnel was cracked.So I took a brand new pencil that had never been sharpened and stood iton end next to the funnel and started drying another sample. When thematerial detonated it burned the pencil about 30% in two but did notknock the pencil over and all the sample was gone. So this was not anexplosion and was not an implosion. It was like a tremendous release oflight.It was like you set that pencil beside a fire place and after about 20minutes you saw it was smoking on one side and burning in two. That'swhat the pencil looked like immediately after the flash. Now this justhad me baffled. What ever this stuff is it's wild. We found that if we

dried it out of the sunlight it didn't explode but if we dried it in thesunlight it exploded.So then we took some of the powder that was dried out of the sunlightand we decided we were going to put it in what is called a cruciblereduction. A crucible reduction involves taking a crucible (which islike a big drinking glass made out of porcelain) and you mix your powderwith lead and all this flux and all and you heat it till the lead melts.What happens is the metals that are heavier than lead stay in the leadand all of those that are lighter float out. This is the basic premiseof your fire assays which have been done for hundreds of years.Now supposedly gold and silver will stay in the lead and all your othernon heavy elements will come out of the lead. This is the tried and trueway of doing metals analysis. Well this material settled to the bottomof the lead just like it was gold and silver. This material seemed to bedenser than lead. When we poured off the slag it would take everythingbut the noble elements, then we poured off the lead and this materialcame off as a constituency at the bottom of the molten lead. It wasseparated from it. Yet when you take this material and put it on a boneash cupel the lead soaks into the cupel and it leaves your bead of goldand silver. Well we did this and we got a bead that should have beengold and silver.We took this bead for analysis to all the commercial laboratories andthey said Dave there is nothing but gold and silver there. Except Icould take that bead and set it on a table and hit it with a hammer andit shattered like glass. Now there is no known alloy of gold and silverthat is not soft. Gold and silver dissolve in each other perfectly andthey form solid solutions and they are both very soft elements and soany alloy of gold and silver if that's all that's there is going to besoft and ductile. You can flatten it out and make a pancake out of it.Yet this material shattered like glass. I said something's going on herethat we are not understanding. Something unusual is happening.

So what we did is we took these beads of gold and silver and separatedthem chemically with the gold and silver out. What we had left is awhole bunch of black stuff. When I took this black stuff to thecommercial laboratories they told me that it was iron, silica andaluminum. I said this can't be iron, silica and aluminum. First of allyou can't dissolve it in any acids or any bases once it is totally dry.It doesn't dissolve in fuming sulfuric acid, it doesn't dissolve insulfuric nitric acid, it doesn't dissolve in hydrochloric nitric acid.Even this dissolves gold yet it won't dissolve this black stuff. Ithought this material is really strange. It just has to have anexplanation. No one could tell me what it was.Basically I went to Cornell University. I said we are just going to haveto throw some money at this problem. So I went and hired a Ph.D. atCornell who considered himself an expert on precious elements. Isuspected we were dealing with precious elements. I said I want to knowwhat this is. I paid him to come out to Arizona. He looked at theproblem. He said "we have a machine back at Cornell that can analyzedown to parts per billion". He said "you let me take this material backto Cornell and I'll tell you exactly what you have, exactly". Unless itis chlorine, bromine or one of the lighter elements, then we can'tanalyze it. But if it is anything above iron we will find it. When hegot back there he told me it was iron silica aluminum.I said "look doctor do you have a chemistry laboratory around here wecould borrow?" He said "yes." I said "let's go to the chemistrylaboratory." We worked in the chemistry laboratory all the rest of thatday and we were able to remove all the silica, all the iron and all thealuminum. We still had 98% of the sample and that was pure nothing. Isaid "look I can hold this in my hand, I can weigh it, I can performschemistries with it". "I said that is something". "I know that issomething." "It is not nothing."He said "the absorption or emissions spectrum does not agree with

anything we have programmed into our instrument." I said "well that issomething and I'm going to find out what." And he said "Mr. Hudson whydon't you give us a 35 0,000 dollar grant and we'll put graduatestudents to looking into it." Well I had already paid this man about 22,000 because he claimed he could analyze anything and he hadn't. Hedidn't offer to pay any of my money back. I said "sir, I don't know whatyou pay the people around here but we pay minimum wage on the farmwhereI work and I can get a lot more out of 350,000 than you can." "So I'mgoing to go back and do the work myself."I came back to Phoenix totally disillusioned with academia. I was notimpressed with the Ph.D's. I was not impressed with the people I hadpaid money to. I found out that it is just a big system where theyworked the graduate students to generate paper but they never sayanything but the government pays them for every paper they write so theyget their money based on the number of papers they turned out. They allsay the same thing they just re-word it and turn out another paper. Itreally is disillusioning when you find out what academia is doing rightnow.Fortunately I asked around the Phoenix area and I found out about a manwho was a spectroscopist. He had been trained in West Germany at theinstitute for spectroscopy. He had been the senior technician for LabTest company in Los Angeles which builds spectroscopic equipment. He'sthe man who blue printed them, designed them, constructed them then tookthem to the field and then made them work. I said here's a good man.This is not just a technician. Here is a man who knows how the machineworks.I went to him with a Soviet book that the fire assay man had given me.It was called The Analytical Chemistry of the Platinum Group Elements byGinsberg. It was published by the Soviet Academy of Sciences. In thisbook, according to the Soviets, you had to do a 300 second burn on theseelements to read them.

Now for those of you who have never done spectroscopy it involves takinga carbon electrode that is cupped at the top. You put the powder on thatelectrode and you bring the other electrode down above it and you strikean arc. In about fifteen seconds the carbon at this high temperatureburns away and the electrode's gone and your sample's gone. So all thelaboratories in this country are doing fifteen second burns and givingyou the results. According to the Soviet Academy of Sciences the boilingtemperature of water is to the boiling temperature of iron just like theboiling temperature of iron is to the boiling temperature of theseelements.As you know from driving a car as long as there is water in the motor ofyour car the temperature of that car engine will never hotter than theboiling temperature of water until all the water is gone. If you justheated the water on the stove in a pan you know that pan never getshotter than the boiling temperature of the water till all the water isgone. Once all the water is gone the temperature skyrockets really fast.As long as there is iron there the temperature of the sample can neverget hotter than the boiling temperature of the iron until all of theiron is gone so you can then heat this stuff. Now this is hard to fathomhow something with as high a boiling temperature as iron could be justlike water to these elements but it is. So literally we had to designand build an excitation chamber where argon gas could be put around thiselectrode so than no oxygen or air could get in to the carbon electrodeand we could burn it not for fifteen seconds but for three hundredseconds. According to the Soviet Academy of Sciences this is the lengthof time we have to burn the sample.We set up, we got the [PK blenders?], we got the standards, we modifiedthe machine, we did all the analysis for results, we did all thespectral lines on this three and a half meter instrument. That's thespec for how big the prism is which opens up the line spectrum. Forthose of you who don't know, most universities have a one point five

meter instrument. This is a three and a half meter instrument. A hugemachine. It took up the whole garage area. It was about thirty feet longand about eight or nine feet high.Anyway when we ran this material during the first fifteen seconds we gotiron, silica, aluminum, little traces of calcium, sodium maybe a littletitanium now and then and then it goes quiet and nothing reads. So atthe end of fifteen seconds you are getting nothing. Twenty seconds,twenty five seconds, thirty seconds, thirty five seconds, forty secondsstill got nothing. Forty five seconds, fifty seconds, fifty fiveseconds, sixty seconds, sixty five seconds but if you look in throughthe colored glass sitting there on the carbon electrode is this littleball of white material. There's still something in there.At seventy seconds, exactly when the Soviet Academy of Science said itwould read, palladium begins to read. And after the palladium platinumbegins to read. And after the platinum I think it was rhodium begins toread. After rhodium ruthenium begins to read. After ruthenium theniridium begins to read and after the iridium osmium begins to read.Now if you're like me I didn't know what these elements were. I hadheard of platinum, platinum jewelry, but what are these other elements.Well there are six platinum group elements in the periodic table notjust platinum. They didn't find out about them at the same time so theyhave been added one at a time. They are all elements just like iron,cobalt and nickel are three different elements ruthenium, rhodium andpalladium are light platinums and osmium, iridium and platinum are theheavy platinums.Well we came to find out that rhodium was selling for about threethousand dollars per ounce. Gold sells for about four hundred dollars anounce. Iridium sells for about eight hundred dollars an ounce andruthenium sells for one hundred and fifty dollars an ounce.Then you say gee these are important materials aren't they. They areimportant materials because in the world the best known deposit is now

being mined in South Africa. In this deposit you have to go a half mileinto the ground and mine an 18 inch seam of this stuff. When you bringit out it contains one third of one ounce per ton of all the preciouselements.Our analysis, which we ran for two and a half years and we checked overand over; we checked every spectral line, we checked every potential oninterference, we checked every aspect of this. We created apples andapples, oranges and oranges, bananas and bananas. We wanted exactmatches.When we were finished the man was able to do quantitative analysis andhe said "Dave, you have six to eight ounces per ton of palladium, twelveto thirteen ounces per ton of platinum, one hundred fifty ounces per tonof osmium, two hundred fifty ounces per ton of ruthenium, six hundredounces per ton of iridium, and eight hundred ounces per ton of rhodium.Or a total of about 2400 ounces per ton when the best known deposit inthe world is one third of one ounce per ton.As you can see this work wasn't an indicator that these elements werethere; these elements were there and they were there in boucoupsamounts. They were saying hey stupid man pay attention we are trying toshow you something.If they had been there in little amounts I probably would have contendedwith this. But they were there in such huge amounts I said golly, howcan they be there in these quantities and no one knew it. Now you keepin mind, it wasn't one spectral analysis it was two and a half years ofspectral analysis running this material every day. And the man actuallysent me away when they read because he couldn't believe it either. Andhe worked on it another two months before he called me up and apologizedto me and he said "Dave you are right." That is how skeptical he wasabout it. He couldn't apologize to me. He is a German researcher withGerman pride so he had his wife call and apologize to me.He was so impressed that he went back to Germany to the Institute of

Spectroscopy. He was actually written up in the spectroscopic journalsas having proven the existence of these elements in the SouthwesternUnited States in natural materials. It's not journals that you wouldever read but I actually saw the journals, he was written up.They had no idea where this stuff was coming from, how we were producingit, what concentrations we had gone through or anything, they just hadanalyzed this small amount of powder. The crazy thing about it is, allwe had done is remove the silica and sent the other stuff in. It waspretty unbelievable numbers. After we had come at this in every way weknow how, to disprove it, I decided all we have to do is throw money atthis problem because money solves everything, right?So at 69 seconds I stopped the burn. I let the machine cool down and Itook a pocket knife and dug that little bead out of the top of theelectrode. When you shut off the arc it sort of absorbs down into thecarbon and you have to dig down into the carbon to get it out; thislittle bead of metal.So I sent this little bead of metal over to Harlow Laboratories inLondon. They made a precious metals analysis on this bead. I get thereport back "no precious element detected". Now this was one secondbefore the palladium was supposed to start leaving. Yet according toneutron activation, which analyzes the nucleus itself, there were noprecious elements detected.This made absolutely no sense at all. There had to be an explanationhere. Either this material was converted to another element or it's in aform that we don't understand yet. So I decided that I just had to getmore information on it. I went to a Ph.D. analytical chemist, a man whowas trained at separating and purifying individual elements out ofunknown material. He was trained at Iowa State University and he had aPh.D. in metal separation systems. He's the man that Motorola and Sperryused in the state of Arizona to handle their waste water problems.He has worked with every element on the periodic table with the

exception of four. He has worked with all the rare earths, he has workedwith all the man made elements. He has physically separated everythingon the periodic table with the exception of four elements.Coincidentally I came to him to have him separate six elements. Four ofthose were the elements he had never worked on. He said "you know DavidHudson, I have heard this story before. All my life, and I'm a nativeArizonan too, I have heard this story about these precious elements. Iam very impressed with the way you have gone about this: with thesystematic way you have approached it. I cannot accept any money becauseif I accept money from you I have to write you a written report.All I have to sell is my reputation. All I have to sell is mycredibility. I'm a certified expert witness in the state of Arizona inmetallurgical separation systems. He said "David I will work for you atno charge until I can show you where you are wrong." "When I can tellyou where you are wrong I'll give you a written report." "Then you willpay me sixty dollars an hour for the time I spent." This would have cometo about twelve to fifteen thousand dollars. If this gets rid of thecurse; if this just gets the thing answered once and for all it's worthit. It was for me at the time. Do it, get on with it.Well, three years later he said "I can tell you it is not any of theother elements on the periodic table. We are educated; we are taught todo the chemical separation of the material and then send it forinstrumental confirmation."The example I use is rhodium because it has a very unique color to thechloride solution. It is a cranberry color almost like the color ofgrape juice. There is no other element that produces the same color inchloride solution. When my rhodium was separated from all the otherelements it produced that color of chloride. The last procedure you doto separate the material out is to neutralize the acid solution and itprecipitates out of solution as a red brown dioxide. That is heatedunder a controlled atmosphere to 800 degrees for an hour and that

creates the anhydrous dioxide. Then you hydro reduce that under acontrolled atmosphere to get the element and then you anneal away theexcess hydrogen.So when we did that, we neutralized the acid solution and precipitatedit out as a red-brown dioxide. Which is the color it is supposed toprecipitate. Then we filtered that out. We heated it under oxygen for anhour in a tube furnace then we hydro-reduced it to this gray-whitepowder: exactly the color rhodium should be as an element. Then weheated it up to 1400 degrees under argon to anneal away the material andit turned snow white.Now this wasn't expected. This just isn't what is supposed to happen. Sowhat John did was he said "Dave, I'm going to heat it to the anhydrousdioxide, I'm going to cool it down. I'm going to take one third of thesample and put it in a sealed vial. I'm going to put the rest of thesample back in the tube furnace and heat it up under oxygen, cool itback down, purge it with inert gas, heat it back up under hydrogen toreduce away the oxides and the hydrogen reacts with oxygen forming waterand cleans the metal. I'll cool that down to the gray-white powder. I'lltake half of that and put it in another sealed vial. I'll take the restof the powder and put it back in the furnace. I'm going to oxidize it,and hydro-reduce it and anneal it to the white powder. Then I will putit into a vial and send all three vials to Pacific Spectrochem over inLos Angeles, one of the best spectroscopic firms in the U.S.The first analysis comes back. The red-brown dioxide is iron oxide. Thenext material comes back; silica and aluminum. No iron present. Now justputting hydrogen on the iron oxide has made the iron quit being iron andnow it has become silica and aluminum. Now this was a big sample. Wejust made the iron turn into silica and aluminum. The snow whiteannealed sample was analyzed as calcium and silica. Where did thealuminum go? John said "Dave my life was so simple before I met you." Hesaid "this makes absolutely no sense at all." He said "what what you are

working with is going to cause them to re-write physics books tore-write chemistry books and come to a complete new understanding.John gave me his bill, it was a hundred and thirty thousand dollarswhich I paid. But he said "Dave, I have separated physically and I havechecked it chemically fifty different ways and you have four to sixounces per ton of palladium, twelve to fourteen ounces per ton ofplatinum, a hundred fifty ounces per ton of osmium, two hundred fiftyounces per ton of ruthenium, six hundred ounces per ton of iridium, andeight hundred ounces per ton of osmium. The exact same numbers that thespectroscopist had told me were there. It was such an incredible numberthat John said "Dave, I've got to go to the natural place where thisstuff comes from and I've got to take my own samples. So he went up andactually walked the property and took his own samples, put it in a bag,brought them back to the laboratory, pulverized the entire sample andthen started doing the analysis on what is called the master blendsample which represented the whole geology and he got the same numbers.David Hudson: Separating the M-state ElementsWe worked on this from 1983 until 1989. One Ph.D. chemist, three masterchemists, two technicians working full time. Using the Soviet Academy ofSciences, the U.S. Bureau of Standards-Weights and Measures informationas a starting point we literally learned how to do qualitative andquantitative separations of all of these elements. We learned how totake commercial standards and make them disappear. We learned how tobuyrhodium tri-chloride from Johnson, Mathew & Ingelhardt as the metal andwe learned how to break all the metal-metal bonding until it literallywas a red solution but no rhodium detectable. And it was nothing butpure rhodium from Johnson, Mathew & Ingelhardt.We learned how to do this with iridium, we learned how to do it withgold, we learned how to do it with osmium, we learned how to do it with

ruthenium. And what we found when we actually purchased a machine calledhigh pressure liquid chromatography.And for your information this person named John [Sycapose?] was the manwho actually wrote his Ph.D. thesis at Iowa State University on how tobuild this instrument. He conceptualized building this instrument backin 1963-64.After he graduated some of the graduate students there took thattechnology and developed it and eventually Dow Chemical came in andbought it. Dow went ahead and commercialized it and now it is the mostsophisticated chemical separation that the world has. It's computercontrolled, all high pressure and you can do very precise separationswith it. Because this is the man who conceptualized, designed it, toldthem what the limitations would be, eventually, on it he was the idealman to take the technology and perfect it.So we were able to use their basic technology and develop a separationsystem for taking the rhodium tri-chloride (we actually separated fivedifferent species in the commercial rhodium tri-chloride). What this isall about is the word "metal" is like the word "army". You can't have aone man army. The word metal refers to a conglomerate material. It hascertain properties, electrical conductivity, heat conduction and allthese other aspects of it.When you dissolve the metals in acid you get a solution that is clearwithout solids. You assume it's a free ion but when you are dealing withNobel elements it's still not a free ion, it's still what is calledcluster chemistry.Back since the 1950's there has been a whole area of research incolleges called cluster chemistry; catalytic materials. But what happensis the metal- metal bonds are still retained by the material. So if youbuy rhodium tri- chloride from Johnson, Matthew and Engelhardt you areactually getting Rh 12 Cl 36 or Rh 15 Cl 45. You really aren't gettingRhCl 3. There is a difference between the metal-metal bonding material

and the free ion. And so what you are buying when you buy it is clusterchemistry; you are not getting free ions.When you put it in for analytical instrumentation to analyze it, it isactually analyzing the metal-metal bonds of the cluster. It is notreally analyzing the free ions.I heard that General Electric was building fuel cells using rhodium andiridium. So I made contacts with their fuel cell people back inMassachusetts and traveled back there to meet with them. They had threeattorneys meet with us and the GE people were there. The attorneys werethere to protect the GE people because a lot of people say they havetechnologies and they meet with them then after the meeting they suethem claiming that GE stole their technology. Then to defend themselvesGE has to divulge what their technology really is. So GE is veryskeptical when you say that you have something new. They bring in theirhigh faluting attorneys to really screen you.After about an hour they said "these guys are for real. You attorneyscan leave". Because they had had the explosions also. They knew thatwhen they buy the commercial rhodium tri-chloride that it analyzes verywell. But to make it ready to go into their fuel cells they have to doeffusions on it using salt effusions where they melt the salt and putthe metal in with it to disperse it further. They know when they do thatthat the metal doesn't analyze as well any more.So when we told them that we had material that didn't analyze at allthey could conceive how this was possible. They had never seen it butthey said we are interested. Now these are the people who buildanalytical instrumentation, GE. They said "Dave, why don't you just makea bunch of rhodium for us and send it to us and we'll mount it in ourfuel cell technology. [What is the mechanism of conversion of monatomicrhodium to metallic rhodium in these fuel cells?] We'll see if it worksin a place where only rhodium works. No other metal has ever been foundwhich will perform the catalysis in the hydrogen evolving technology of

the fuel cell other than rhodium and platinum. And rhodium is uniquecompared to platinum because rhodium does not poison with carbonmonoxide and platinum does.They said "Dave we will just run it to see if it's a hydrogen evolvingcatalyst and if it is then we will see if it is carbon monoxide stableand if it is then it's rhodium or it's a rhodium alternative.

Monoatomic Elements”, and holds the patent. David Hudson patent can be seen: Hudson Patent for White Powder Gold My name is David Hudson. I'm a third generation native Phoenician from an old family in the Phoenix area. We are an old family. We are very conservative. I come from an ultra-conservative right wing background.

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