The Grail Vine is a newsletter which passes on materials to the Grail Ring.

Grail Zine is the electronic magazine of the Grail Ring. Grail News Now or GNN is its news service. Most Grail Vines and Zines are available when one has done the DI M!ND "!D# Training with nanda$%mman&el' which entitles one to a&tomatic s&bscription to these p&blications. (ome of the material within these p&blications come onto the web site' and &s&all) * months to a )ear later. +ere is one Grail Vine. s the earl) Zines and Vines point o&t' Tr&th Is ,l&ral' let )o&r own &ni-&e tr&th g&ide )o& b)... ll of the Grail Ring do not &se these elements witho&t Internal lchem) b) whole bod) ,hase./on0&gation' or Diamond "od) Vorte1i0ah b) compassionate ecstasis. s with the (omegenics with which the Gold is added .. Dail) practice comes first' there is no short c&t in alchem). "e a /oherent 2ni.,+Ier of 3Ma4ing the Inner li4e the o&ter' and the o&ter li4e the inner.3

GR I5 VIN% 66 (2,%R/!ND2/TING G!5D 7R!M (% T+% 5/+%MI/ 5 (T!N% 7R!M (% 8 T%R ( 5T

Dear %nGrailed brothers and sisters. fter hearing that some brothers and sisters have still been &sing the %theri&m and Isis 8hite Gold so&rces' which we have been repeatedl) rela)ing' for at least one )ear' contain radioactive ingredients' we send this posting' which tells one +!8 T! %9TR /T T+% M!N! T!MI/ (2,%R/!ND2/TING 5/+%MI/ 5 %5%M%NT( 7R!M (% 8 T%R. #es' 0&st as the n&na4i master lchemist %n4i$,tah' according to the most ancient (&merian :ings lists' e1tracted gold from sea water. ,lease investigate an) so&rce of monatomic elements' and consider that 6 )ear of radioactive elements and heav) metals will not brea4down' and ma) reach a dangero&s level after one )ear s&plementation. Treat this s&b0ect with wisdom' this is not 0&st a vitamine. The reason one ma) feel high with radioactives is that the life force is being released from the cells' the same mista4e made b) the Taoist alchemists according to their archaic literat&re. In other words' the) are slowl) d)ing' li4e chemotherap). The best wo&ld be to 1tract the stone )o&rself with /onscio&s Intent of the ;&ant&m observer in the heating process' so&nd' and heart coherence. #o& ma) want to &se the dead sea salts' or lpine mo&ntain waters' or other volcanic la4es' (alt 5a4e /it) salts can also be &sed. http<$$www.etheri&m.com =http<$$www.etheri&mgold.com> relate doc&mentation on their web site for monatomic elements in their form&la' b&t not monatomic gold which is necessar) for the pineal gland. 8ith all )o&r so&rces ma4e s&re to %9TR /T the monatomics' and &se wisel)' and sparingl). This is a ver) delicate field. !ne m&st 4now to find gold. !ne m&st see4 to find. !ne m&st open ones e)es. There is no short ro&te' onl) a Golden Middle 8a).

Instead of ?@&st sa) No'3 3@&st (a) :now.3 !ne lchemist colleag&e in Denmar4 has s&ccessf&ll) isolated the white powder gold from Dead (ea (alt' it tastes li4e (weet (perm' 0&st li4e the Green Valle) Tr&st Manna. fter A months it tastes li4e washing powder' 0&st li4e Green Valle) Tr&st Manna' and other lchemists e1tractions available non.commerciall) b) membership. +e said it was ver) simple indeed. ll Is God lchem) "e #o&' )e Merlin?s' and #e #eshe?s' /ompassionatel)...

5ight' 5ove' 5ife' . nanda' 7ebr&ar) 6Bth' CDDD

!RM2( = 5>./+%M.=Meia> ,R!D2/TI!N T%/+NI;2%(

This doc&ment ma) not be reprod&ced e1cept in its entiret)' and witho&t changes. "efore tr)ing an) of the proced&res described in this doc&ment' we advise )o& to thoro&ghl) read this doc&ment several times.

This doc&ment was created b) a gro&p of people who believe that this information is of inestimable val&e to h&manit) and sho&ld be made widel) available as soon as possible. The information here is declared to be in the p&blic domain and we wish that it not become the sole propert) of an) individ&al or gro&p.

+ere we describe some simple wa)s of ma4ing !RM2( so that readers can begin tr&e scientific and int&itive e1periments with these materials.

ll of these methods are e1perimental. The following information is presented to promote scientific research into the nat&re of these materials. ltho&gh these

methods are based on o&r best 4nowledge at this time' f&rther scientific research

ma) prove some of these processes or theories to be inacc&rate.

DI(/5 IM%R The processes described here have not all been tested e1tensivel). 8e do not g&arantee the proced&res in this doc&ment' nor the res&lts obtained b) &sing them. To the e1tent that )o& &se or implement these proced&res or the prod&cts thereof' )o& do so at )o&r own ris4. In no event will the a&thors of this doc&ment be liable to )o&' an)one else' or an) organization or government' for an) damages arising from )o&r &se' or )o&r inabilit) to &se these proced&res or the prod&ct thereof. ppl) these proced&res at )o&r own ris4.

V%RI7I/ TI!N

The material made b) some of these methods has been tested b) an independent lab &sing 9.ra) fl&orescence and photo spectrometr) to identif) the emission spectra of m.state materials. =The lab prefers to remain anon)mo&s>. The m.state spectral emissions signat&re was a broad' flat band rather than discrete lines. The test also showed a significant amo&nt of calci&m and magnesi&m' b&t no to1ins were evident in well.washed material made from &npoll&ted ocean water.

To f&rther prove that these materials are a different state of the precio&s elements mentioned above' it is possible to electroplate these elements o&t as precio&s metals.

,eople familiar with +&dson?s process claim that the materials prod&ced &sing these methods are similar to +&dson?s !RM% materials.

ING%(TI!N

8e do not recommend the ingestion of these materials since so little is 4nown abo&t them. This information is being provided so that scientific in-&ir) can commence into the nat&re of these materials. 8e realize that' despite recommendations to the contrar)' some people will ingest these materials. 8ith this in mind we offer the following information to minimize an) possible adverse effects from ingesting these materials. ,lease read the 8 RNING and / 2TI!N sections.

(ome people have ingested the m.state materials made b) these methods. The) s&ggest that benefits are most li4el) when dosage is 4ept small.

Three methods of ma4ing !RM2( are described in this doc&ment< the 8%T method' the DR# method' and the "!I5ING G!5D method. 7or the materials e1tracted b) the wet and dr) proced&res' one teaspoon of material' morning and evening' has been fo&nd b) them to be not harmf&l over several wee4s? time. m&ch smaller dose' on the order of a few drops a da)' wo&ld be more appropriate for the material prod&ced b) the boiling gold method. 8e believe that the m.state ma) be homeopathic' so a m&ch smaller dose ma) be the safest .. s&ch as 6$*E teaspoon dil&ted in one -&art of p&re water' ta4en two or three o&nces once or twice a da).

David +&dson gave some information on dosage in his Dallas speech at< http<$$monatomic.earth.com$david.h&dson$6BBF.DC.dallas.toc.html

8+IT%G!5D 8%" , G%

#o& can find a disc&ssion for&m on the 8hiteGold 8eb page. There )o& can post comments and -&estions on these proced&res' and on !RM2( in general. 8hiteGold 8eb page< http<$$www.zz.com$8hiteGold8eb$

6.!verview C.Necessar) (&pplies A.p+ ,aper or p+ Meter E.(afet) F.8et Method 6. (tarting Materials *.,roblems %nco&ntered G. voiding ,roblems

!V%RVI%8

This doc&ment describes three methods of prod&cing !RM2(< the 8%T method' the DR# method' and the "!I5ING G!5D method.

ll three methods &se a chemical lab techni-&e called 3meas&ring p+.3 The p+ of a sol&tion is a meas&re of its acid$base ratio. #o& ma) remember testing p+ with litm&s paper in high school. p+ val&es less than p+ G indicate an acid' li4e distilled white vinegar. p+ G is ne&tral' li4e p&re water. Greater than p+ G is al4aline' li4e l)e.

!RM2( precipitates between p+ H.F and 6D.GH.

The 8%T method prod&ces the least 3effective3 material b&t is relativel) simple to perform.

+ere is the basic 8%T method in brief. It will be disc&ssed later in detail<

6. (tart with drin4able water or clean sea water. C. (lowl) add a sol&tion of l)e mi1ed with water to raise the p+ above H.F b&t no higher than 6D.GH. A. white fl&ff) precipitate will form which )o& sho&ld allow to settle

overnight. E. Remove the li-&id above the precipitate. F. Thoro&ghl) wash the precipitate. It is calci&m h)dro1ide' magnesi&m h)dro1ide' and a small amo&nt of m.state material.

+ere is the DR# method in brief<

6. (tart with dr) mineral powder. C. "oil it in l)e water at p+ 6C. A. 7ilter and discard the precipitate. E. dd distilled white vinegar or h)drochloric acid =+/l> to the filtered

li-&id to lower the p+ to H.F. F. 5et the precipitate settle overnight. *. Remove the li-&id above the precipitate. G. 8ash the precipitate. That is calci&m h)dro1ide' magnesi&m h)dro1ide' and a small amo&nt of m.state material.

nd here is the "!I5ING G!5D method in brief<

6. "oil gold d&st in a l)e sol&tion.

C. 7ilter o&t an) solids. A. dd distilled white vinegar or +/l to the remaining li-&id to lower

the p+ to H.F. E. 5et the precipitate settle overnight. F. Remove the li-&id above the precipitate. *. 8ash the precipitate. It is almost p&re gold m.state material.

N%/%(( R# (2,,5I%( T! M :% M.(T T%

glass or stainless steel pot. If )o& &se stainless.steel pots' chec4 for steel particles in )o&r precipitate. ltho&gh &nli4el)' this problem ma) occ&r if )o&

&se large amo&nts of +/l to lower the p+. Never &se al&min&m containers or &tensils beca&se al&min&m will react with acids li4e +/l and al4alis li4e l)e' and will poison )o&.

Distilled water from a grocer) store.

stainless steel spat&la or 4nife for stirring' from a grocer) store. Never &se al&min&m containers or &tensils beca&se al&min&m will react with acids li4e +/l and al4alis li4e l)e' and will poison )o&.

few glass 0ars. Tall s4inn) ones wor4 best.

5)e =sodi&m h)dro1ide or Na!+>. 8e will &se the term 3l)e3 in this doc&ment rather than 3sodi&m h)dro1ide3 or 3Na!+3 since it is shorter and more familiar to most people. Grocer) store l)e' s&ch as 5ewis Red Devil 5)e' is not as p&re and &ncontaminated as laborator) or food.grade l)e. 8e strongl) recommend that laborator) or food grade sodi&m h)dro1ide be &sed if

the m.state is intended for ingestion since grocer) store l)e ma) contain dangero&s contaminants. Note< Virt&all) no l)e will be present in the final prod&ct so it will be safe to ingest. In an) case' l)e is not to1ic' and it is not ca&stic when s&fficientl) dil&ted =as in these methods>.

+/l =h)drochloric acid or m&riatic acid>. 8e will &se the term 3+/l3 in this doc&ment rather than 3h)drochloric acid3 or 3m&riatic acid3 since it is shorter. #o& can &se m&riatic acid =A6I +/l> from a hardware store' b&t laborator)' electronic or food.grade +/l is less li4el) to be contaminated. 8e strongl) recommend that laborator)' electronic or food grade h)drocholoric acid be &sed if the m.state is intended for ingestion since m&riatic acid from a hardware store ma) contain dangero&s contaminants. The presence of iron as a contaminant in the acid ma) interfere with the m.state materials in some applications.

Three e)edropper bottles from a pharmac).

n alternative to e)edroppers is

s-&irt bottles made of +D,%. 7ind them at a nat&ral foods store or other store which sells b&l4 li-&id prod&cts li4e vegetable oils or lotions.

large FD cc plastic s)ringe from a veterinar) s&ppl) shop or a lab.s&ppl) ho&se. (ome s&ppliers are listed near the end of this doc&ment &nder 5 " (2,,5I%(.

p+ paper or a p+ meter. #o& can get p+ paper =p+ 6 to 6C> from a lab.s&ppl) compan) or a mining s&ppl) store. 2se new paper beca&se old paper becomes inacc&rate. (ome s&ppliers are listed near the end of this doc&ment &nder 5 " (2,,5I%(.

p+ , ,%R !R p+ M%T%RJ

(ome e1perimenters sa) not to rel) on a p+ meter beca&se its readings var) with temperat&re and ionization. lso' a meter costs m&ch more than p+ paper.

Man) p+ meter probes can be damaged b) ver) strong acids or al4alis. "&t some sa) that a p+ meter is essential' for these reasons<

p+ paper cannot trac4 rapid changes in p+. p+ paper does not resolve p+ readings finel) eno&gh. It?s hard to tell the difference between p+ B.F' 6D.D' and 66.F. p+ meters are best &sed to get acc&rate readings between p+ H.F and 6D.GH' which is the main range of concern in these methods. p+ meters can spot chec4 an) reading with a standard b&ffer sol&tion. a p+ meter is more convenient.

2se onl) a meter that has an a&tomatic temperat&re.correcting f&nction &p to 6DD degrees /.

( 7%T# TI,(

/lean )o&r containers so that )o&?d feel safe drin4ing o&t of them. "oil containers' s)ringes' siphons and so on before &se to sterilize them.

/ 2TI!NKK

5)e can damage the e)es b) rendering the cornea opa-&e' a form of e)e damage that is irreparable. 5)e can b&rn s4in' clothes and e)es. 8or4 near a sin4' fa&cet' or other so&rce of wash water. #o& might 4eep a spra) bottle of distilled

white vinegar hand) to &se against spills.

If )o& spill l)e on )o&r clothes or bod)' immediatel) wash it off with lots of water. 8hen wor4ing with l)e' avoid to&ching )o&r face or r&bbing )o&r e)es. Do not handle l)e aro&nd food. 2se ade-&ate ventilation s&ch as a range hood. Do not d&mp waste water on the gro&nd. 5)e is generall) safe to p&t down the drain' b&t don?t mi1 it with an) acid that ma) be in the drain as it can react e1plosivel).

8hen wor4ing with l)e' please wear goggles or a f&ll.face visor =an ind&strial face protector>' neoprene gloves' and a ,V/ lab apron. (o&rces for this safet) clothing are in the ppendi1 near the end of this doc&ment.

:eep children and pets awa) from the wor4 area' and do not leave it &nattended if children or pets are aro&nd.

Glass can shatter with hot li-&ids. ,o&r boiling li-&id from )o&r heating container into a stainless steel mi1ing bowl to cool before po&ring the li-&id into a glass container.

T+% 8%T M%T+!D

(T RTING M T%RI 5( 7!R T+% 8%T M%T+!D

(ome starting materials prod&ce a lot of precipitate' while others do not. 5isted below are materials that have been shown to prod&ce some precipitate from the 8%T method<

(ome m&nicipal drin4ing water

(ome hot springs water witho&t s&lf&r Trace Minerals Inland (ea 8ater 2rine (ome la4e or river water whose bed or co&rse is limestone. (ome well water. Gro&nd water is probabl) more li4el) to contain m.state than s&rface water =e1cept for sea water>. (ea water and sea water reconstit&ted from certain brands of sea salt' especiall) from the Great (alt 5a4e. Dead (ea water. /ertain brands of &nrefined sea salt are as good as sea water< /eltic Gra) (ea (alt =from health food stores> and 5ima =from some health food stores>. method. 7ilter the sc&m first. tlantic (ea (alt

dd distilled water and &se the 8%T

The 8%T method performed on ocean or Dead (ea water prod&ces eleven different m.state elements.

The following materials are ran4ed in order from most to least m.state content<

6. Dead (ea water C. (alt 5a4e water A. !cean water E. 8ell water

5isted below are materials that have been fo&nd to prod&ce little or no precipitate from the 8%T method<

8ater from some al4ali la4es =p+ above H.F>. +ot springs with s&lf&r =beca&se s&lf&r red&ces m.state to metal>.

Mineral.free la4e or river water Dead (ea mineral salts that contain s&lf&r or s&lfates' s&ch as 3(ea Mineral "ath from the Dead (ea3 b) Dead (ea 8or4s 5td. for (ea Minerals /o.' and Trace Minerals Research 3/oncenTrace Trace Mineral Drops3 from the Great (alt 5a4e.

7or the following methods to wor4' some researchers claim that magnesi&m or magnesi&m h)dro1ide .. Mg=!+>C .. m&st be present in the starting material. =(ince the "oiling Gold method is effective witho&t an) magnesi&m' this claim will need to be tested.> (ea water alread) has Mg=!+>C' so )o& don?t need to add it to sea water. Tr) )o&r water first. If )o& don?t get an) precipitate' )o& might add a teaspoon per gallon of %psom salts to the starting material for its magnesi&m. If )o& do add %psom salts' the magnesi&m from them will be a large portion of the precipitate.

8 RNINGKK ,R!"5%M( %N/!2NT%R%D

The following problems have been enco&ntered b) some fol4s who have made m.state for cons&mption<

(ome people have gotten -&ite sic4 from cons&ming m.state made from sea water collected at a marina. This water contained high levels of lead and other contaminants. !ther people have gotten -&ite sic4 from cons&ming m.state materials which were made improperl). These materials were made witho&t the &se of p+ test paper or meters and the res&lting material contained to1ic metals. ,lease remember that old p+ paper can become

inacc&rate. ,eople have gotten sic4 from cons&ming m.state materials which contained bacteria beca&se the) were not sterilized or stored properl). It is possible to bring the p+ of )o&r so&rce material &p too -&ic4l)' especiall) if )o& &se l)e in too high a concentration. This co&ld res&lt in local areas of ver) high p+ within )o&r sol&tion. These high p+ areas co&ld allow to1ic metals to precipitate and mi1 with )o&r desired precipitate. M.state platin&m might be considered to1ic b) some since it ma4es )o& -&ite ill if )o& cons&me alcohol. No one has reported this effect from cons&ming m.state from sea water. (ome people have &sed Teflon coated al&min&m sa&ce pans for heating l)e or l)e water. The Teflon got scratched and the al&min&m started dissolving in the l)e water prod&cing h)drogen gas which co&ld have e1ploded. The li-&id was contaminated with al&min&m which is a poison.

V!IDING ,R!"5%M(

2se sea water' reconstit&ted sea water made from sea salt or Dead (ea salt' or salt la4e water. In general' start with a clean and deep so&rce of water. (ome people have gone o&t to sea in boats to collect sea water from 6DD feet deep. Generall) avoid water that has lead' arsenic or other to1ic elements in it. (tart with water that is drin4able e1cept for salt content. /ond&ct an elemental and to1ic anal)sis of -&estionable starting.material so&rces =s&ch as seawater collected close to the shore' or near so&rces of ind&strial waste r&noff>. "oiling in l)e water 4ills bacteria b&t it does not destro) to1ic metals or

chemicals in )o&r so&rce water. 7ollow these instr&ctions and slowl) change the p+ of )o&r sol&tion. void water with s&lf&r or s&lfates in it beca&se s&ch water prod&ces little or no m.state precipitate. Never &se al&min&m containers or &tensils beca&se al&min&m will react with acids li4e +/l and al4alis li4e l)e' and co&ld poison )o&.

!RM2( /+%MI/ 5 ,R!D2/TI!N T%/+NI;2%( /!NTIN2%D...

L"ac4 to first pageM L"ac4 to previo&s pageM

8et Method ,roced&re +ow to ,&rif) #o&r ,recipitate .. Removing Mg=!+>C 6. Method 6 C. Method C A. Method A E. Method E Dr) Method 6. %1tra (&pplies C. +older 7or 7ilters A. (tarting Materials E. ,roced&re "oiling Gold Method 6. %1tra (&pplies C. ,roced&re ppendi1 6. M.state (torage C. /hemical (&ppliers

A. 5ab (&pplies E. (tarting.Material (o&rces

8%T.M%T+!D ,R!/%D2R%

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

7irst )o& need to prepare a dil&te l)e sol&tion. 5abel an e)edropper bottle or s-&irt bottle 35)e.poison3 so the bottle will not conf&sed with something else. 8or4 in a sin4 so that an) spills will be contained. 5)e gives off e)e.stinging f&mes when mi1ed with water. To avoid inhaling f&mes' hold )o&r breath and wear goggles while doing the following proced&re.

8or4ing over a sin4' p&t H teaspoons of distilled water in a st&rd) glass then stir in 6 teaspoon of l)e. (tir &ntil the l)e is dissolved. +eat will be generated as the l)e dissolves and the glass ma) get fairl) hot. #o& ma) want to close )o&r e)es to avoid e)e.stinging f&mes' ta4ing a pee4 periodicall).

,o&r the l)e sol&tion into a labeled e)edropper bottle or s-&irt bottle.

If )o& are &sing p+ paper' tear off several 6$E3 pieces and p&t them on a piece of white paper on a plate.

7or the best acc&rac)' recalibrate the p+ paper thro&gho&t the da) with changes in temperat&re and h&midit)' as well as da).to.da). "&ffer sol&tions of p+ E' G and 6D will help with this. (o&rces of p+ b&ffer sol&tions are listed near the end of this doc&ment &nder 5 " (2,,5I%(.

If )o& are &sing dried sea minerals' mi1 6$C c&p of dr) material with C c&ps of distilled water. This ma4es sea water. Now proceed as described below<

6. 7irst' )o& might want to po&r the sea water thro&gh a coffee filter to remove an) sc&m.

C. If the starting material does not contain magnesi&m h)dro1ide =sea water does contain magnesi&m h)dro1ide>' add some' or add a teaspoon of %psom salts per gallon of water.

A. ,o&r the sea water into a stainless steel pot. (lowl)' drop.b).drop' add the l)e sol&tion 8+I5% (TIRRING. %ver) ten drops or so' test the p+. #o& might want to ta4e at least A to F samples from different regions of the li-&id. If )o& are &sing p+ paper' the goal is to bring the p+ &p to B.F' then stop to be on the safe side. If )o& are &sing a p+ meter' stop 0&st before )o& get to p+ 6D.GH.

white precipitate which incl&des m.state elements will form.

/ 2TI!N< #o& m&st proceed slowl) and patientl) so that )o& do not e1ceed p+ 6D.GH with a meter or p+ B.F with p+ paper. If )o& go higher than p+ 6D.GH' )o& might get a 3Gilcrest precipitate3 of to1ic heav) metals. It is alleged that the Dead (ea salt water does not prod&ce an) Gilcrest precipitate. This has not been proven and sho&ld not be ass&med.

E. !nce )o& are at the correct p+' stop.

F. ,o&r the sol&tion into a clean glass 0ar or test t&be.

*. The white precipitate =sl&rr)> slowl) settles on the bottom of the 0ar. 5et the sl&rr) settle overnight. If metals or other to1ins have been r&led o&t b) prior testing of )o&r starting material' the sl&rr) is probabl) mostl) calci&m h)dro1ide' Mg=!+>C' l)e' and a small amo&nt of m.state.

#o& can speed this settling process with a centrif&ge' which forces the precipitate to settle rapidl). Ine1pensive second.hand centrif&ges ma) be fo&nd at merican (cience and (&rpl&s' http<$$www.scipl&s.com.

G. 2sing a large s)ringe =or siphon>' remove the li-&id above the sl&rr).

H.

dd distilled water to the precipitate =filling the 0ar>' stir thoro&ghl)'

and let it settle again for at least E to F ho&rs' preferabl) overnight.

B. Repeat steps G and H at least three times to thoro&ghl) wash the precipitate. This sho&ld remove almost all of the l)e. The remaining l)e can be ne&tralized with +/l or distilled white vinegar as well. 8ashing three times is intended to red&ce the dissolved 3imp&rities3 =li4e salt' for e1ample> b) HG.FI. 7o&r washes wo&ld provide a BA.GFI red&ction' five washes a B*.HGFI red&ction' and so on.

t this point' the precipitate is li4el) to contain some m.state' mil4 of magnesia Mg=!+>C' calci&m' and perhaps some imp&rities.

,o&r the precipitate and water into a stainless steel pot on a stove b&rner. gas b&rner is preferred over electric beca&se an) magnetic

fields from the electric b&rner ma) drive off some of the m.state

material. /over the pot with a lid to contain the m.state' and boil the sol&tion for F min&tes to sterilize it. "e caref&l not to spill the hot sol&tionK 5et it cool bac4 to room temperat&re and rechec4 the p+ to ma4e s&re it hasn?t e1ceeded p+ B.

DI(/2((I!N< 8+%N T! "!I5 T+% (!52TI!N

In this doc&ment' we s&ggested that )o& not boil the sol&tion &ntil )o& have made the washed precipitate. +owever' boiling can be done earlier in the proced&re with certain advantages. +ere are fo&r times that boiling co&ld be done' with a disc&ssion of the pros and cons of each<

6. "oil before adding l)e sol&tion.

,R!(< 7aster reaction' faster precipitation. /!N(< #o& ma) spill the hot l)e sol&tion. #o& ma) inhale f&mes.

C. "oil while adding l)e sol&tion.

,R!(< 7aster reaction' faster precipitation. /!N(< #o& ma) spill the hot l)e sol&tion. #o& ma) inhale f&mes. Danger of l)e sp&rting o&t of pot. Not recommended.

A. "oil and cool after adding l)e sol&tion.

,R!(< No danger of inhaling f&mes. 5ittle danger of spilling hot l)e sol&tion. /!N(< (lower reaction' slower precipitation.

E. "oil the washed precipitate =recommended>.

,R!(< No danger of inhaling f&mes. No danger of spilling hot l)e sol&tion. p+ is &nli4el) to change after boiling beca&se the reaction has alread) ta4en place. /!N(< (lower reaction' slower precipitation. If safet) is the main iss&e' this seems to be the best method.

/a&tion< If )o& boil the sol&tion on an electric b&rner' the magnetic field in the b&rner ma) 3blow off3 some of the m.state materials' res&lting in a small )ield. This can be minimized b) adding a so&rce of sodi&m =s&ch as sodi&m h)dro1ide or salt> to the sol&tion before boiling.

(ince sea water contains sodi&m in salt' none of the boiling methods will be a problem with sea water. +owever' if )o& are starting with low.sodi&m fresh water' add a sodi&m so&rce =s&ch as table salt or l)e sol&tion> before boiling.

!nce the precipitate and water have been sterilized' the ne1t step is re-&ired to concentrate the m.state.

+!8 T! ,2RI7# #!2R ,R%/I,IT T%

The precipitate made from sea water contains mil4 of magnesia =Mg=!+>C>' which precipitates appro1imatel) aro&nd the same p+ range that m.state does.

+ere are fo&r methods to separate Mg=!+>C from m.state<

M%T+!D 6

6. (&ppose )o& 0&st made a precipitate b) adding l)e sol&tion to sea water. The precipitate is m.state mi1ed with Mg=!+>C.

C. 2se a s)ringe to remove the li-&id over the precipitate' and discard the li-&id. This leaves onl) the m.state$Mg=!+>C precipitate.

A. To the wet precipitate' add h)drochloric acid =+/l> &ntil )o& red&ce the p+ to 6.D . A.F. #o& can &se m&riatic acid =A6I +/l> from a hardware store' b&t lab.grade +/l is less li4el) to be contaminated. vinegar. safe alternative to +/l is distilled white

E. The white colloidal precipitate sho&ld dissolve' leaving a clear sol&tion.

F.

dd l)e sol&tion V%R# (5!85# drop.b).drop to bring

the p+ bac4 &p to H.F . H.G. The precipitate that forms sho&ld be m.state mostl) free of Mg=!+>C =beca&se m.state precipitates in this p+ range' and Mg=!+>C does not precipitate &ntil p+ B.>

Note that )o&r total )ield ma) be diminished beca&se )o& are not going past p+ H.G.

*. Remove the li-&id above the precipitate' and wash the precipitate. It sho&ld be mostl) m.state.

M%T+!D C

This proced&re removes the Mg=!+>C b) dissolving it below p+ B. 7irst get some +/l =or m&riatic acid> and coffee filters. safer alternative to +/l is distilled white vinegar.

6. Dr) the precipitate in a dar4 oven at abo&t CGF degrees 7 for one or two ho&rs. This forms a dr) powder.

C. Ta4e the dr) powder and p&lverize o&t an) cl&mps.

A. In a glass container' cover the powder with some distilled water. 7or e1ample' one liter of water for one c&p of powder.

E.

dd +/l or distilled white vinegar drop.b).drop to bring

the p+ to F or *.

F. (ha4e the bottle and let it sit overnight. The dried m.state sho&ld not dissolve at that p+' b&t the Mg=!+>C sho&ld dissolve.

*. The ne1t da)' after all the Mg=!+>C has dissolved' po&r ever)thing into filter paper.

G. 8ash the powder collected in the filter paper several times with distilled water to remove an) resid&al traces of +/l or vinegar.

H. The washed powder ma) be oven.dried again at abo&t CGF

degrees 7' and )o& sho&ld have m.state powder free of Mg=!+>C.

M%T+!D A

6. Dr) the original precipitate at abo&t CDD degrees 7.

C. Mi1 the res&lting powder with distilled white vinegar or ADI +/l. %ver)thing which does not dissolve in m.state. This will be -&ite a small amo&nt if )o& start with sea water. =If )o& mi1 p&re +/l with distilled water' remember< 8 T%R' N%V%R DD 8 T%R T! /ID>. DD /ID T!

A. Meas&re the amo&nt of +/l$m.state sol&tion =or vinegar$m.state sol&tion>.

E.

dd distilled water to the +/l$m.state sol&tion.

dd an

amo&nt of water that is at least ten times the amo&nt of +/l$m.state sol&tion. =#o& ma) s&bstit&te distilled white vinegar for +/l>.

F. 7ilter the sol&tion thro&gh F la)ers of coffee filters.

*. 8ash the powder at least three times in a large amo&nt of distilled water.

M%T+!D E

6. (tarting with clean wet precipitate' add l)e to bring the p+

&p to 6C. The m.state precipitate will dissolve' b&t magnesi&m h)dro1ide and the Gilcrest precipitate will not.

C. 7ilter o&t the precipitate.

A. To the remaining li-&id containing onl) m.state' add +/l or distilled white vinegar drop.b).drop &ntil the p+ reaches H.F.

E.

dd l)e sol&tion drop.b).drop to bring the p+ bac4 &p to

6D.GH. The res&lting precipitate sho&ld be onl) m.state.

F. 8ash the precipitate as described earlier.

*. To be safe' chec4 the p+ of the precipitate sl&rr). It sho&ld be B or less before ingesting.

DR# M%T+!D

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

This method ta4es longer than the 8%T method. In some cases' it involves boiling l)e for several ho&rs' which ma) spra) some ca&stic sol&tion aro&nd )o&r wor4 area. ,lease wear neoprene gloves' a ,V/ lab apron' and e)e goggles when )o& &se this method. (o&rces for this safet) clothing are listed near the end of this doc&ment &nder 5 " (2,,5I%(.

(ome people have reported adverse reactions to the 8%T method

precipitate or powder. This ma) be d&e to the Gilcrest precipitates which occ&r above p+ 66.F. The DR# method removes the dangero&s Gilcrest precipitates' so it res&lts in safer material.

%9TR

(2,,5I%( N%%D%D 7!R T+% DR# M%T+!D

6C.c&p coffee filters from a grocer) store.

+)drochloric acid. #o& can &se m&riatic acid =A6I +/l> from a hardware store' b&t lab.grade +/l is less li4el) to be contaminated. !ther acids can be &sed' b&t +/l will not harm the bod) if accidentall) ingested in wea4 sol&tions and in small amo&nts. #o& might prefer to &se distilled white vinegar instead of +/l. ltho&gh distilled white

vinegar =acetic acid> is wea4er than +/l' is it safer to wor4 with.

+eav) plastic +D,% cottage cheese containers' 6 pint and 6 -&art' to hold the coffee filters.

M :ING

+!5D%R 7!R T+% /!77%% 7I5T%R(

6. (tart with a pint and a -&art container for cottage cheese. Ma4e s&re the pint container will fit into the -&art container. The pint container sho&ld hang inside the lip of the -&art container.

C.

cross the bottom of the pint container' p&nch or drill

several holes' 6$H3 to 6$E3 diameter' abo&t 6$E3 apart.

A. If the small container fits too tightl) into the larger container'

)o& ma) need to drill some air.press&re e-&alization holes aro&nd the o&tside of the large container near the level of the bottom of the small container. !therwise the air press&re between the two containers will 4eep li-&id from draining from the coffee filters. 8hen )o& &se this filter' place the cottage cheese containers in a stainless steel or glass container to catch an) overflow. The l)e water that )o& will be filtering ma) damage co&nter tops or cabinets if it contacts them.

E. The coffee filters sho&ld fit nicel) into the smaller top cottage.cheese container.

DR# M%T+!D (T RTING M T%RI 5(

Generall) start with dr) material s&ch as sweepings from salt and al4ali flats' roc4 powders' limestone' mineral salts' Isis or %theri&m white gold powder' volcanic ash' plant cinders' etc.

These are some materials that prod&ce a lot of precipitate from the DR# method< /r&shed' &nheated limestone =/a&tion< agric&lt&ral grade powdered limestone from some so&rces contains s&fficient lead and$or arsenic to be a potential hazard> Golden Nectar trace mineral form&la %theri&m$Isis Gold powder ncient (ecrets Dead (ea Mineral (alts Masada salts =&nscented>

DR#.M%T+!D ,R!/%D2R%

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

7irst )o& need to prepare a dil&te l)e sol&tion. 5abel an e)edropper bottle or s-&irt bottle 35)e.poison3 so the bottle will not conf&sed with something else. 8or4 in a sin4 so that an) spills will be contained. 5)e gives off e)e.stinging f&mes when mi1ed with water. To avoid inhaling f&mes' hold )o&r breath and wear goggles while doing the following proced&re.

8or4ing over a sin4' p&t H teaspoons of distilled water in a st&rd) glass then stir in 6 teaspoon of l)e. (tir &ntil the l)e is dissolved. +eat will be generated as the l)e dissolves and the glass ma) get fairl) hot. #o& ma) want to close )o&r e)es to avoid e)e.stinging f&mes' ta4ing a pee4 periodicall).

,o&r the l)e sol&tion into a labeled e)edropper bottle or s-&irt bottle.

If )o& are &sing p+ paper' tear off several 6$E3 pieces and p&t them on a piece of white paper on a plate =as ill&strated above>. Now proceed as described below<

6. Grind the starting material to a fine powder.

C.

dd 6<E l)e sol&tion to cover the dr) material with a thin

la)er.

A. (tir in some distilled water to cover the powder and l)e b) C inches.

E. "ring to a boil =this is best done o&tdoors or in an e1ha&st hood>. The p+ sho&ld be at or slightl) above 6C. The l)e brings the m.state elements into sol&tion while leaving the Gilcrest precipitates as solids.

N!T%< If )o& start with sea salt' )o& can omit the boiling step with its no1io&s f&mes' and simpl) let the sol&tion sit for three da)s. Then go directl) to (tep G. =(ome other starting materials might also react witho&t boiling>.

F. If )o& are boiling the sol&tion' replace water as needed to maintain s&fficient reactant vol&me.

*. "oil for several ho&rs .. the longer the better .. in a closed container. The container ma) be open if )o& add li-&id as needed. 7o&r ho&rs sho&ld be s&fficient for %theri&m$Isis material.

G. (train the sl&rr) thro&gh A to F la)ers of coffee filters. #o& are removing the to1ic elements =Gilcrest precipitate> that precipitate above p+ 66.F.

(ave the li-&id that passes thro&gh the filters. Most m.state present will be in sol&tion in the li-&id.

H. 8hile stirring the li-&id' slowl) add +/l or distilled white vinegar to bring the p+ down to H.F. which is partl) m.state. white precipitate forms

If )o& go too far' the p+ will abr&ptl) shift' and )o& will have to start over. If this happens )o& m&st add l)e -&ic4l) and bring the p+ bac4 &p to 6C.

B. 5et the precipitate settle overnight.

6D. 2sing a large s)ringe =or a siphon>' remove the li-&id above the sl&rr).

66.

dd distilled water to the precipitate =filling the 0ar>' stir

thoro&ghl)' and let it settle again for at least E to F ho&rs' preferabl) overnight.

6C. Repeat steps 6D and 66 at least three times to thoro&ghl) wash the precipitate. This removes most traces of l)e and +/l =or vinegar>.

#o&?ll get a wet' white precipitate =sl&rr)> containing m.state elements. /hec4 that the p+ is B or less before ingesting. (ome of the precipitate ma) be mil4 of magnesia or calci&m. If )o& wish' )o& can remove them &sing the precipitate p&rification proced&res described above.

"!I5ING.G!5D M%T+!D

,lease read / 2TI!NKK and 8 RNINGKK before proceeding.

This method prod&ces p&re gold !RM2(. 8ith this method' )o& m&st boil some l)e sol&tion for one to two wee4s. This ma) spra) some ca&stic sol&tion aro&nd )o&r wor4ing area. ,lease wear neoprene gloves' a ,V/ lab apron' and e)e goggles when )o& &se this method. (o&rces for this safet) clothing are noted &nder 5 " (2,,5I%( near the end of this doc&ment.

%9TR M%T+!D

(2,,5I%( N%%D%D 7!R T+% "!I5ING.G!5D

/offee filters from a grocer) store.

+)drochloric acid =+/l>. #o& can &se m&riatic acid =A6I +/l> from a hardware store' b&t lab.grade +/l is less li4el) to be contaminated. Instead of +/l' )o& might prefer to &se distilled white vinegar =acetic acid>. Distilled white vinegar is wea4er than +/l b&t is safer to &se.

stainless steel pot or glass pot will wor4' b&t stainless steel and glass are attac4ed b) Na!+. Glass is preferred over stainless steel.

preferred container is a sealed Teflon or +D,% bottle in a water bath in a croc4 pot. ,lease note that a Teflon bottle is N!T the same as a Teflon coated al&min&m container. Never &se al&min&m or Teflon coated al&min&m containers and &tensils beca&se al&min&m will react with acids li4e +/l and al4alis li4e l)e' and will poison )o&.

If )o& &se a sealed Teflon or +D,% bottle in a water bath fill it onl) half f&ll with )o&r l)e and gold then s-&eeze the bottle to eliminate most of the air above the li-&id before )o& tighten the cap. This will

allow the bottle to e1pand as the li-&id is heated.

,R!/%D2R% 7!R T+% "!I5ING.G!5D M%T+!D

6.

dd BB.BBI p&re gold d&st to a l)e sol&tion of p+ 6C or

more.

C. "oil the sol&tion for two wee4s in a /5!(%D container. !ne wee4 ma) be s&fficient' b&t two wee4s will li4el) have a higher )ield. dd water as needed. / 2TI!N< Do not

inhale the vaporsK

A. (train the sol&tion &sing the coffee filter holder described above. (ave an) remaining gold for f&t&re &se.

E.

dd +/l or distilled white vinegar to bring the p+ down to n off.white precipitate will appear. 5et it settle

p+ H.F.

overnight.

F. 2sing a s)ringe' caref&ll) s&c4 o&t the li-&id above the precipitate.

*.

dd distilled water to the precipitate =filling the 0ar>' stir

thoro&ghl)' and let it settle again for at least E to F ho&rs' preferabl) overnight.

G. Repeat steps F and * at least three times to thoro&ghl) wash the precipitate.

,,%NDI9 M.(T T% (T!R G%

(tore m.state materials in

N Glass mason 0ars with wire.clamped glass lids and r&bber gas4ets N Glass 0ars with plastic lids' or N +D,% containers' which are stable in acid and al4ali

(tore m.state materials in the dar4 awa) from s&nlight or &ltraviolet light. 2ltraviolet light seems to move some m.state materials toward a metallic state.

"eca&se m.state materials are s&percond&ctors' the) sho&ld be stored in glass or +D,% containers inside of steel containers and awa) from moving magnetic fields. ,&t the glass or +D,% container =containing m.state> inside a steel tin s&ch as those &sed for /hristmas coo4ies' go&rmet popcorn or potato chips. If )o& intend to transport m.state materials' it is best to nest three or fo&r steel containers' one inside the other with ins&lating material between' and place the glass or +D,% container inside the inmost steel container.

#o& ma) notice that )o&r m.state materials have b&bbles rising from them for a period of time after the) are made. 8e believe that these b&bbles are m.state gas escaping. (ome people have reported that the m.state precipitate loses some of its effect as these b&bbles leave. This off.gassing seems to be red&ced if the m.state is stored between room temperat&re and bod) temperat&re in a magneticall) shielded container. It is advisable not to refrigerate m.state materials. t least one

researcher reports that refrigerated m.state materials are li4el) to move toward a warmer place.

(ince bacteria and mold can easil) grow in m.state precipitate' it is best to sterilize an) material which )o& wish to store for long periods of time and to store it &sing water bath canning methods.

/+%MI/ 5 (2,,5I%R(

Mowre 8.%. /o. 6ECF 2niversit) ve.

(t. ,a&l' MN FF6DE HDD.FEE.6FFD =*E*.6HBF>

This s&pplier sells gold b&llion' gold wire' gold shot' etc. The) sell to individ&als thro&gh the mail and will process small orders. Good prices. OOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOOO

(trem /hemicals' Inc. De1ter Ind&strial ,ar4 G M&lli4en 8a) Newb&r)port' M infoPstrem.com http<$$www.strem.com D6BFD.EDBH

No minim&m order.

=BGH> E*C.A6B6

=HDD> *EG.HGA*

(ome sample prod&cts<

BA.GB6F Gold powder =BB.BFI> FDD mg QFD. Cg Q6*D. BA.GB6A Gold shot =BB.BFI> FDD mg QED. Cg Q6CH.

5 " (2,,5I%(

/ole.,armer Instr&ment /o. HDD.ACA.EAED.

8eiss Research Inc. 66GEA 8est "ellfort' (&ite 6*H (tafford' T9 GGEGG http<$$www.hia.net$weissres$meters.htm The) have a Q6GF p+ meter =R ,+M.6FD> with a&to temperat&re compensation from D to 6DD degrees /' and a p+ meter with man&al temperat&re conversion for Q6CF.

McMaster./arr (&ppl) /o. ,.!. "o1 EAFF /hicago' I5 *D*HD.EAFF *AD.HAA.DADD fa1 GDH.HAE.BECG

McMaster./arr (&ppl) /o. ,.!. "o1 FEB*D 5os ngeles' / BDDFE.DB*D

A6D.*BC.FB66

fa1 A6D.*BF.CACA

,lastic s)ringe FD cc with tapered tip GF6D **F p4g. of 6D Q6H.FG Milled.neoprene gloves FADGTF QF.D6 8ide.range p+ test paper HGDGT66 QH.HB ,V/ apron FAEEFTGF QE.FF (afet) goggles with a face shield FECCT6C Q6H.BE.

lso available are a poc4et p+ meter for QFB' p+ sol&tions' water.test 4its' hot plates' plastic t&bing' and m&ch more.

No minim&m order. The) sell to an)one and ta4e VI( .

%dm&nd (cientific /ompan) 6D6 %ast Glo&cester ,i4e "arrington' N@ DHDDG.6AHD 2( /&stomer service< 6.*DB.FGA.*C*D B M to F ,M M.7

Disposable plastic s)ringes are available at man) veterinar) and agric&lt&ral s&ppl) stores. ,lastic inf&sion tips are available from the same so&rce.

More so&rces can be fo&nd at< http<$$monatomic.earth.com$database$lab.so&rces$

(T RTING.M T%RI 5 (!2R/%(

(ea water< (igma /hemical. Q6D$liter. 7rom the G&lf of Me1ico. (terile. http<$$www.sigma.sial.com$

(ea salt to reconstit&te sea water< +ealth.food store' oriental food store.

Target Glacial Roc4 D&st from Gaia Reso&rces in Grand 7or4s' "/' /anada.

Get gold from a coin dealer. Get gold d&st b) panning for it in a stream. Gold d&st might be available from :eene %ngineering in Northridge' / . (ee /+%MI/ 5 (2,,5I%R( earlier in this ppendi1.

lso chec4 o&t a gold mining s&ppl) store. In /alifornia tr) http<$$www.treas&renet.com$calgold$prospect.html The gold sho&ld be at least BB.BBI p&re gold.

Golden Nectar =trace minerals>. QED$gallon. http<$$b&l4sales.com$inde1.htm This ma) be at health food stores.

Trace Minerals Inland (ea 8ater =QG for H o&nces> at )o&r local health food store. Trace Minerals Research' ,.!. "o1 ECB' Ro)' 2T HEDG*. http<$$www.traceminerals.com http<$$b&l4sales.com

%theri&m white powder gold< http<$$www.etheri&mgold.com$ phone FDA.*CF.CHHD.

Isis white powder gold< http<$$onlinehealth.webCD6D.com$isis.html

lwa)s chec4 the s&pplier for radioactive materials and heav) metals. /onsider that these never brea4down overtime. /onsider what that co&ld mean after one )ear of s&pplementation. %1traction with /onscio&sness and 8isdom. ,5% (% :N!8. T+% 8 R !N DR2G(' 8% T+%R T+%# "% VIT MIN( ND MIN! /ID(' N%2R!TR N(MITT%R(' ,5 NT(' +!M%!, T+I/ M%DI/IN%' !R 5/+%MI/ 5 ,R!D2/T(' I( N(8%R%D "# @2(T ( # :N!8' IN(T% D !7 T+% M 7I (2,,!RTING 3@2(T ( # N!?. #!2 + V% "%%N 8 RN%D' 2(% #!2R +% RT IN #!2R MIND' ,R /TI/% D I5# INT%RN 5 5/+%M#' 8+!5% "!D# ,+ (%./!N@2G TI!N T+R!2G+ /!M, ((I!N T% %/(T (I( =see Vorte1i0ah>. T+%R% I( N!T (+!RT /2T 7!R T+% G!5D. N! " "# "!TT5% +%R%. ?(%%: #% (+ 55 7IND.?

ND

T+% /!M,5%T% T%9T 7!R T+I(

5/+%M# / N "% 7!2ND

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