Ormus – how to make it?

ORMUS CHEMICAL PRODUCTION TECHNIQUES

* It can be noted here that Manna Energy does not use any of these three production techniques for the products offered on this site.

After five years of study, research and chemistry we have developed an organic production technique that mixes minerals from a specific location off Tasmania, Australia with minerals from a specific pool at the Dead Sea to produce our Ormus elements.

We are sharing the three techniques to keep them open source and visible for people beginning their journey with alchemy and Ormus.

Where sodium hydroxide ( Lye) is mentioned we can confirm that pharmaceutical grade magnesium hydroxide (MgOH) and potassium hydroxide (KOH) can also be substituted.

This document may not be reproduced except in its entirety, and without changes. Before trying any of the procedures described in this document, we advise you to thoroughly read this document several times.

This document was created by a group of people who believe that this information is of inestimable value to humanity and should be made widely available as soon as possible. The information here is declared to be in the public domain and we wish that it not become the sole property of any individual or group.

Here we describe some simple ways of making ORMUS so that readers can begin true scientific and intuitive experiments with these materials.

All of these methods are experimental. The following information is presented to promote scientific research into the nature of these materials. Although these methods are based on our best knowledge at this time, further scientific research may prove some of these processes or theories to be inaccurate.

DISCLAIMER

The processes described here have not all been tested extensively. We do not guarantee the procedures in this document, nor the results obtained by using them. To the extent that you use or implement these procedures or the products thereof, you do so at your own risk. In no event will the authors of this document be liable to you, anyone else, or any organization or government, for any damages arising from your use, or your inability to use these procedures or the product thereof. Apply these procedures at your own risk.

VERIFICATION

The material made by some of these methods has been tested by an independent lab using X-ray fluorescence and photo spectrometry to identify the emission spectra of m-state materials. (The lab prefers to remain anonymous). The m-state spectral emissions signature was a broad, flat band rather than discrete lines. The test also showed a significant amount of calcium and magnesium, but no toxins were evident in well-washed material made from unpolluted ocean water.

To further prove that these materials are a different state of the precious elements mentioned above, it is possible to electroplate these elements out as precious metals.

People familiar with Hudson’s process claim that the materials produced using these methods are similar to Hudson’s ORME materials.

INGESTION

We do not recommend the ingestion of these materials since so little is known about them. This information is being provided so that scientific inquiry can commence into the nature of these materials. We realize that, despite recommendations to the contrary, some people will ingest these materials. With this in mind we offer the following information to minimize any possible adverse effects from ingesting these materials. Please read the WARNING and CAUTION sections.

Some people have ingested the m-state materials made by these methods. They suggest that benefits are most likely when dosage is kept small.

Three methods of making ORMUS are described in this document: the WET method, the DRY method, and the BOILING GOLD method. For the materials extracted by the wet and dry procedures, one teaspoon of material, morning and evening, has been found by them to be not harmful over several weeks’ time. A much smaller dose, on the order of a few drops a day, would be more appropriate for the material produced by the boiling gold method. We believe that the m-state may be homeopathic, so a much smaller dose may be the safest — such as 1/64 teaspoon diluted in one quart of pure water, taken two or three ounces once or twice a day.

David Hudson gave some information on dosage in his Dallas speech at: http://monatomic.earth.com/david-hudson/1995-02-dallas-toc.html

WHITEGOLD WEB PAGE

You can find a discussion forum on the WhiteGold Web page. There you can post comments and questions on these procedures, and on ORMUS in general.

WhiteGold Web page: http://www.zz.com/WhiteGoldWeb/

INDEX

OVERVIEW

This document describes three methods of producing ORMUS: the WET method, the DRY method, and the BOILING GOLD method.

All three methods use a chemical lab technique called “measuring pH.” The pH of a solution is a measure of its acid/base ratio. You may remember testing pH with litmus paper in high school. pH values less than pH 7 indicate an acid, like distilled white vinegar. pH 7 is neutral, like pure water. Greater than pH 7 is alkaline, like lye.

ORMUS precipitates between pH 8.5 and 10.78.

The WET method produces the least “effective” material but is relatively simple to perform.

Here is the basic WET method in brief. It will be discussed later in detail:

5. Thoroughly wash the precipitate. It is calcium hydroxide, magnesium hydroxide, and a small amount of m-state material.

Here is the DRY method in brief:

7. Wash the precipitate. That is calcium hydroxide, magnesium hydroxide, and a small amount of m-state material.

And here is the BOILING GOLD method in brief [the BOILING GOLD METHOD has never worked for those who have tried it and we don’t recommend its use]:

6. Wash the precipitate. It is almost pure gold m-state material.

NECESSARY SUPPLIES TO MAKE M-STATE

A glass or stainless steel pot. If you use stainless-steel pots, check for steel particles in your precipitate. Although unlikely, this problem may occur if you use large amounts of HCl to lower the pH. Never use aluminum containers or utensils because aluminum will react with acids like HCl and alkalis like lye, and will poison you.

Distilled water from a grocery store.

A stainless steel spatula or knife for stirring, from a grocery store. Never use aluminum containers or utensils because aluminum will react with acids like HCl and alkalis like lye, and will poison you.

A few glass jars. Tall skinny ones work best.

Lye (sodium hydroxide or NaOH). We will use the term “lye” in this document rather than “sodium hydroxide” or “NaOH” since it is shorter and more familiar to most people. Grocery store lye, such as Lewis Red Devil Lye, is not as pure and uncontaminated as laboratory or food-grade lye. We strongly recommend that laboratory or food grade sodium hydroxide be used if the m-state is intended for ingestion since grocery store lye may contain dangerous contaminants. Note: Virtually no lye will be present in the final product so it will be safe to ingest. In any case, lye is not toxic, and it is not caustic when sufficiently diluted (as in these methods).

HCl (hydrochloric acid or muriatic acid). We will use the term “HCl” in this document rather than “hydrochloric acid” or “muriatic acid” since it is shorter. You can use muriatic acid (31% HCl) from a hardware store, but laboratory, electronic or food-grade HCl is less likely to be contaminated. We strongly recommend that laboratory, electronic or food grade hydrocholoric acid be used if the m-state is intended for ingestion since muriatic acid from a hardware store may contain dangerous contaminants. The presence of iron as a contaminant in the acid may interfere with the m-state materials in some applications.

Three eyedropper bottles from a pharmacy. An alternative to eyedroppers is squirt bottles made of HDPE. Find them at a natural foods store or other store which sells bulk liquid products like vegetable oils or lotions.

A large 50 cc plastic syringe from a veterinary supply shop or a lab-supply house. Some suppliers are listed near the end of this document under LAB SUPPLIES.

pH paper or a pH meter. You can get pH paper (pH 1 to 12) from a lab-supply company or a mining supply store. Use new paper because old paper becomes inaccurate. Some suppliers are listed near the end of this document under LAB SUPPLIES.

pH PAPER OR pH METER?

Some experimenters say not to rely on a pH meter because its readings vary with temperature and ionization. Also, a meter costs much more than pH paper. Many pH meter probes can be damaged by very strong acids or alkalis. But some say that a pH meter is essential, for these reasons:

pH paper cannot track rapid changes in pH.
pH paper does not resolve pH readings finely enough. It’s hard to tell the difference between pH 9.5, 10.0, and 11.5.
pH meters are best used to get accurate readings between pH 8.5 and 10.78, which is the main range of concern in these methods.
pH meters can spot check any reading with a standard buffer solution.
a pH meter is more convenient.

Use only a meter that has an automatic temperature-correcting function up to 100 degrees C.

SAFETY TIPS

Clean your containers so that you’d feel safe drinking out of them. Boil containers, syringes, siphons and so on before use to sterilize them.

CAUTION!!
Lye can damage the eyes by rendering the cornea opaque, a form of eye damage that is irreparable. Lye can burn skin, clothes and eyes. Work near a sink, faucet, or other source of wash water. You might keep a spray bottle of distilled white vinegar handy to use against spills.

If you spill lye on your clothes or body, immediately wash it off with lots of water. When working with lye, avoid touching your face or rubbing your eyes. Do not handle lye around food. Use adequate ventilation such as a range hood. Do not dump waste water on the ground. Lye is generally safe to put down the drain, but don’t mix it with any acid that may be in the drain as it can react explosively.

When working with lye, please wear goggles or a full-face visor (an industrial face protector), neoprene gloves, and a PVC lab apron. Sources for this safety clothing are in the Appendix near the end of this document.

Keep children and pets away from the work area, and do not leave it unattended if children or pets are around.

Glass can shatter with hot liquids. Pour boiling liquid from your heating container into a stainless steel mixing bowl to cool before pouring the liquid into a glass container.

THE WET METHOD

STARTING MATERIALS FOR THE WET METHOD

Some starting materials produce a lot of precipitate, while others do not. Listed below are materials that have been shown to produce some precipitate from the WET method:

Some municipal drinking water
Some hot springs water without sulfur
Trace Minerals Inland Sea Water
Urine
Some lake or river water whose bed or course is limestone.
Some well water. Ground water is probably more likely to contain m-state than surface water (except for sea water).
Sea water and sea water reconstituted from certain brands of sea salt, especially from the Great Salt Lake.
Dead Sea water.
Certain brands of unrefined sea salt are as good as sea water: Celtic Gray Sea Salt (from health food stores) and Lima Atlantic Sea Salt (from some health food stores). Add distilled water and use the WET method. Filter the scum first.

The WET method performed on ocean or Dead Sea water produces eleven different m-state elements.

The following materials are ranked in order from most to least m-state content:

1. Dead Sea water
2. Salt Lake water
3. Ocean water
4. Well water

Listed below are materials that have been found to produce little or no precipitate from the WET method:

Water from some alkali lakes (pH above 8.5).
Hot springs with sulfur (because sulfur reduces m-state to metal).
Mineral-free lake or river water
Dead Sea mineral salts that contain sulfur or sulfates, such as “Sea Mineral Bath from the Dead Sea” by Dead Sea Works Ltd. for Sea Minerals Co., and Trace Minerals Research “ConcenTrace Trace Mineral Drops” from the Great Salt Lake.

For the following methods to work, some researchers claim that magnesium or magnesium hydroxide — Mg(OH)2 — must be present in the starting material. (Since the Boiling Gold method is effective without any magnesium, this claim will need to be tested.) Sea water already has Mg(OH)2, so you don’t need to add it to sea water. Try your water first. If you don’t get any precipitate, you might add a teaspoon per gallon of Epsom salts to the starting material for its magnesium. If you do add Epsom salts, the magnesium from them will be a large portion of the precipitate.

WARNING!!

PROBLEMS ENCOUNTERED
The following problems have been encountered by some folks who have made m-state for consumption:

Some people have gotten quite sick from consuming m-state made from sea water collected at a marina. This water contained high levels of lead and other contaminants.
Other people have gotten quite sick from consuming m-state materials which were made improperly. These materials were made without the use of pH test paper or meters and the resulting material contained toxic metals. Please remember that old pH paper can become inaccurate.
People have gotten sick from consuming m-state materials which contained bacteria because they were not sterilized or stored properly.
It is possible to bring the pH of your source material up too quickly, especially if you use lye in too high a concentration. This could result in local areas of very high pH within your solution. These high pH areas could allow toxic metals to precipitate and mix with your desired precipitate.
M-state platinum might be considered toxic by some since it makes you quite ill if you consume alcohol. No one has reported this effect from consuming m-state from sea water.
Some people have used Teflon® coated aluminum sauce pans for heating lye or lye water. The Teflon® got scratched and the aluminum started dissolving in the lye water producing hydrogen gas which could have exploded. The liquid was contaminated with aluminum which is a poison.

AVOIDING PROBLEMS

Use sea water, reconstituted sea water made from sea salt or Dead Sea salt, or salt lake water. In general, start with a clean and deep source of water. Some people have gone out to sea in boats to collect sea water from 100 feet deep.
Generally avoid water that has lead, arsenic or other toxic elements in it. Start with water that is drinkable except for salt content.
Conduct an elemental and toxic analysis of questionable starting-material sources (such as seawater collected close to the shore, or near sources of industrial waste runoff).
Boiling in lye water kills bacteria but it does not destroy toxic metals or chemicals in your source water.
Follow these instructions and slowly change the pH of your solution.
Avoid water with sulfur or sulfates in it because such water produces little or no m-state precipitate.
Never use aluminum containers or utensils because aluminum will react with acids like HCl and alkalis like lye, and could poison you.

WET-METHOD PROCEDURE

Please read CAUTION!! and WARNING!! before proceeding.

First you need to prepare a dilute lye solution. Label an eyedropper bottle or squirt bottle “Lye-poison” so the bottle will not confused with something else. Work in a sink so that any spills will be contained. Lye gives off eye-stinging fumes when mixed with water. To avoid inhaling fumes, hold your breath and wear goggles while doing the following procedure.

Working over a sink, put 8 teaspoons of distilled water in a sturdy glass then stir in 1 teaspoon of lye. Stir until the lye is dissolved. Heat will be generated as the lye dissolves and the glass may get fairly hot. You may want to close your eyes to avoid eye-stinging fumes, taking a peek periodically.

Pour the lye solution into a labeled eyedropper bottle or squirt bottle.

If you are using pH paper, tear off several 1/4″ pieces and put them on a piece of white paper on a plate.

For the best accuracy, recalibrate the pH paper throughout the day with changes in temperature and humidity, as well as day-to-day. Buffer solutions of pH 4, 7 and 10 will help with this. Sources of pH buffer solutions are listed near the end of this document under LAB SUPPLIES.

If you are using dried sea minerals, mix 1/2 cup of dry material with 2 cups of distilled water. This makes sea water. Now proceed as described below:

2. If the starting material does not contain magnesium hydroxide (sea water does contain magnesium hydroxide), add some, or add a teaspoon of Epsom salts per gallon of water.

3. Pour the sea water into a stainless steel pot. Slowly, drop-by-drop, add the lye solution WHILE STIRRING. Every ten drops or so, test the pH. You might want to take at least 3 to 5 samples from different regions of the liquid. If you are using pH paper, the goal is to bring the pH up to 9.5, then stop to be on the safe side. If you are using a pH meter, stop just before you get to pH 10.78.

A white precipitate which includes m-state elements will form.

CAUTION: You must proceed slowly and patiently so that you do not exceed pH 10.78 with a meter or pH 9.5 with pH paper. If you go higher than pH 10.78, you might get a “Gilcrest precipitate” of toxic heavy metals. It is alleged that the Dead Sea salt water does not produce any Gilcrest precipitate. This has not been proven and should not be assumed.

4. Once you are at the correct pH, stop.

5. Pour the solution into a clean glass jar or test tube.

6. The white precipitate (slurry) slowly settles on the bottom of the jar. Let the slurry settle overnight. If metals or other toxins have been ruled out by prior testing of your starting material, the slurry is probably mostly calcium hydroxide, Mg(OH)2, lye, and a small amount of m-state.

You can speed this settling process with a centrifuge, which forces the precipitate to settle rapidly. Inexpensive second-hand centrifuges may be found at American Science and Surplus, http://www.sciplus.com.

7. Using a large syringe (or siphon), remove the liquid above the slurry.

8. Add distilled water to the precipitate (filling the jar), stir thoroughly, and let it settle again for at least 4 to 5 hours, preferably overnight.

9. Repeat steps 7 and 8 at least three times to thoroughly wash the precipitate. This should remove almost all of the lye. The remaining lye can be neutralized with HCl or distilled white vinegar as well. Washing three times is intended to reduce the dissolved “impurities” (like salt, for example) by 87.5%. Four washes would provide a 93.75% reduction, five washes a 96.875% reduction, and so on.

At this point, the precipitate is likely to contain some m-state, milk of magnesia Mg(OH)2, calcium, and perhaps some impurities.

Pour the precipitate and water into a stainless steel pot on a stove burner. A gas burner is preferred over electric because any magnetic fields from the electric burner may drive off some of the m-state material. Cover the pot with a lid to contain the m-state, and boil the solution for 5 minutes to sterilize it. Be careful not to spill the hot solution! Let it cool back to room temperature and recheck the pH to make sure it hasn’t exceeded pH 9.

DISCUSSION: WHEN TO BOIL THE SOLUTION

1. Boil before adding lye solution.

PROS: Faster reaction, faster precipitation. CONS: You may spill the hot lye solution. You may inhale fumes.

2. Boil while adding lye solution.

PROS: Faster reaction, faster precipitation. CONS: You may spill the hot lye solution. You may inhale fumes. Danger of lye spurting out of pot. Not recommended.

3. Boil and cool after adding lye solution.

PROS: No danger of inhaling fumes. Little danger of spilling hot lye solution. CONS: Slower reaction, slower precipitation.

4. Boil the washed precipitate (recommended).

PROS: No danger of inhaling fumes. No danger of spilling hot lye solution. pH is unlikely to change after boiling because the reaction has already taken place. CONS: Slower reaction, slower precipitation. If safety is the main issue, this seems to be the best method.

Caution: If you boil the solution on an electric burner, the magnetic field in the burner may “blow off” some of the m-state materials, resulting in a small yield. This can be minimized by adding a source of sodium (such as sodium hydroxide or salt) to the solution before boiling.

Since sea water contains sodium in salt, none of the boiling methods will be a problem with sea water. However, if you are starting with low-sodium fresh water, add a sodium source (such as table salt or lye solution) before boiling.

Once the precipitate and water have been sterilized, the next step is required to concentrate the m-state.

HOW TO PURIFY YOUR PRECIPITATE

[Note – These methods were not well tested before being added to this document. More recent experimentation with these methods reveals that they do not work as suggested and may actually be detrimental to the final product. The “purification” step is not necessary to get good ORMUS precipitate for plant or animal use. Plant experiments suggest that if the precipitate is dried out it no longer has any measurable benefits for plants.

These methods are still included in this document because they might be useful as a basis for some future method of assaying the ORMUS content of the precipitate. The second method seems to work best.]

Here are four methods to separate Mg(OH)2 from m-state:

METHOD 1

2. Use a syringe to remove the liquid over the precipitate, and discard the liquid. This leaves only the m-state/Mg(OH)2 precipitate.

3. To the wet precipitate, add hydrochloric acid (HCl) until you reduce the pH to 1.0 – 3.5. You can use muriatic acid (31% HCl) from a hardware store, but lab-grade HCl is less likely to be contaminated. A safe alternative to HCl is distilled white vinegar.

4. The white colloidal precipitate should dissolve, leaving a clear solution.

5. Add lye solution VERY SLOWLY drop-by-drop to bring the pH back up to 8.5 – 8.7. The precipitate that forms should be m-state mostly free of Mg(OH)2 (because m-state precipitates in this pH range, and Mg(OH)2 does not precipitate until pH 9.)

Note that your total yield may be diminished because you are not going past pH 8.7.

6. Remove the liquid above the precipitate, and wash the precipitate. It should be mostly m-state.

METHOD 2

1. Dry the precipitate in a dark oven at about 275 degrees F for one or two hours. This forms a dry powder.

2. Take the dry powder and pulverize out any clumps.

3. In a glass container, cover the powder with some distilled water. For example, one liter of water for one cup of powder.

4. Add HCl or distilled white vinegar drop-by-drop to bring the pH to 5 or 6.

5. Shake the bottle and let it sit overnight. The dried m-state should not dissolve at that pH, but the Mg(OH)2 should dissolve.

6. The next day, after all the Mg(OH)2 has dissolved, pour everything into filter paper.

7. Wash the powder collected in the filter paper several times with distilled water to remove any residual traces of HCl or vinegar.

8. The washed powder may be oven-dried again at about 275 degrees F, and you should have m-state powder free of Mg(OH)2.

METHOD 3

2. Mix the resulting powder with distilled white vinegar or 30% HCl. Everything which does not dissolve in m-state. This will be quite a small amount if you start with sea water. (If you mix pure HCl with distilled water, remember: ADD ACID TO WATER, NEVER ADD WATER TO ACID).

3. Measure the amount of HCl/m-state solution (or vinegar/m-state solution).

4. Add distilled water to the HCl/m-state solution. Add an amount of water that is at least ten times the amount of HCl/m-state solution. (You may substitute distilled white vinegar for HCl).

5. Filter the solution through 5 layers of coffee filters.

6. Wash the powder at least three times in a large amount of distilled water.

METHOD 4

2. Filter out the precipitate.

3. To the remaining liquid containing only m-state, add HCl or distilled white vinegar drop-by-drop until the pH reaches 8.5.

4. Add lye solution drop-by-drop to bring the pH back up to 10.78. The resulting precipitate should be only m-state.

5. Wash the precipitate as described earlier.

6. To be safe, check the pH of the precipitate slurry. It should be 9 or less before ingesting.

DRY METHOD

CAUTION!!

WARNING!!

This method takes longer than the WET method. In some cases, it involves boiling lye for several hours, which may spray some caustic solution around your work area. Please wear neoprene gloves, a PVC lab apron, and eye goggles when you use this method. Sources for this safety clothing are listed near the end of this document under LAB SUPPLIES.

Some people have reported adverse reactions to the WET method precipitate or powder. This may be due to the Gilcrest precipitates which occur above pH 11.5. The DRY method removes the dangerous Gilcrest precipitates, so it results in safer material.

EXTRA SUPPLIES NEEDED FOR THE DRY METHOD

Hydrochloric acid. You can use muriatic acid (31% HCl) from a hardware store, but lab-grade HCl is less likely to be contaminated. Other acids can be used, but HCl will not harm the body if accidentally ingested in weak solutions and in small amounts. You might prefer to use distilled white vinegar instead of HCl. Although distilled white vinegar (acetic acid) is weaker than HCl, is it safer to work with.

Heavy plastic HDPE cottage cheese containers, 1 pint and 1 quart, to hold the coffee filters.

MAKING A HOLDER FOR THE COFFEE FILTERS

2. Across the bottom of the pint container, punch or drill several holes, 1/8″ to 1/4″ diameter, about 1/4″ apart.

3. If the small container fits too tightly into the larger container, you may need to drill some air-pressure equalization holes around the outside of the large container near the level of the bottom of the small container. Otherwise the air pressure between the two containers will keep liquid from draining from the coffee filters. When you use this filter, place the cottage cheese containers in a stainless steel or glass container to catch any overflow. The lye water that you will be filtering may damage counter tops or cabinets if it contacts them.

4. The coffee filters should fit nicely into the smaller top cottage-cheese container.

DRY METHOD STARTING MATERIALS

These are some materials that produce a lot of precipitate from the DRY method:

- - Crushed, unheated limestone (Caution: agricultural grade powdered limestone from some sources contains sufficient lead and/or arsenic to be a potential hazard)
  - Golden Nectar trace mineral formula
  - Etherium/Isis Gold powder
  - Ancient Secrets Dead Sea Mineral Salts
  - Masada salts (unscented)

DRY-METHOD PROCEDURE

CAUTION!!

WARNING!!

Pour the lye solution into a labeled eyedropper bottle or squirt bottle.

If you are using pH paper, tear off several 1/4″ pieces and put them on a piece of white paper on a plate (as illustrated above). Now proceed as described below:

2. Add 1:4 lye solution to cover the dry material with a thin layer.

3. Stir in some distilled water to cover the powder and lye by 2 inches.

4. Bring to a boil (this is best done outdoors or in an exhaust hood). The pH should be at or slightly above 12. The lye brings the m-state elements into solution while leaving the Gilcrest precipitates as solids.

NOTE: If you start with sea salt, you can omit the boiling step with its noxious fumes, and simply let the solution sit for three days. Then go directly to Step 7. (Some other starting materials might also react without boiling).

5. If you are boiling the solution, replace water as needed to maintain sufficient reactant volume.

6. Boil for several hours — the longer the better — in a closed container. The container may be open if you add liquid as needed. Four hours should be sufficient for Etherium/Isis material.

7. Strain the slurry through 3 to 5 layers of coffee filters. You are removing the toxic elements (Gilcrest precipitate) that precipitate above pH 11.5.

Save the liquid that passes through the filters. Most m-state present will be in solution in the liquid.

8. While stirring the liquid, slowly add HCl or distilled white vinegar to bring the pH down to 8.5. A white precipitate forms which is partly m-state.

If you go too far, the pH will abruptly shift, and you will have to start over. If this happens you must add lye quickly and bring the pH back up to 12.

9. Let the precipitate settle overnight.

10. Using a large syringe (or a siphon), remove the liquid above the slurry.

11. Add distilled water to the precipitate (filling the jar), stir thoroughly, and let it settle again for at least 4 to 5 hours, preferably overnight.

12. Repeat steps 10 and 11 at least three times to thoroughly wash the precipitate. This removes most traces of lye and HCl (or vinegar).

You’ll get a wet, white precipitate (slurry) containing m-state elements. Check that the pH is 9 or less before ingesting. Some of the precipitate may be milk of magnesia or calcium. If you wish, you can remove them using the precipitate purification procedures described above.

BOILING-GOLD METHOD [The BOILING GOLD METHOD has never worked for those who have tried it and we don’t recommend its use.]

CAUTION!!

WARNING!!

This method produces pure gold ORMUS. With this method, you must boil some lye solution for one to two weeks. This may spray some caustic solution around your working area. Please wear neoprene gloves, a PVC lab apron, and eye goggles when you use this method. Sources for this safety clothing are noted under LAB SUPPLIES near the end of this document.

EXTRA SUPPLIES NEEDED FOR THE BOILING-GOLD METHOD

Hydrochloric acid (HCl). You can use muriatic acid (31% HCl) from a hardware store, but lab-grade HCl is less likely to be contaminated. Instead of HCl, you might prefer to use distilled white vinegar (acetic acid). Distilled white vinegar is weaker than HCl but is safer to use.

A stainless steel pot or glass pot will work, but stainless steel and glass are attacked by NaOH. Glass is preferred over stainless steel.

A preferred container is a sealed Teflon® or HDPE bottle in a water bath in a crock pot. Please note that a Teflon® bottle is NOT the same as a Teflon® coated aluminum container. Never use aluminum or Teflon® coated aluminum containers and utensils because aluminum will react with acids like HCl and alkalis like lye, and will poison you.

If you use a sealed Teflon® or HDPE bottle in a water bath fill it only half full with your lye and gold then squeeze the bottle to eliminate most of the air above the liquid before you tighten the cap. This will allow the bottle to expand as the liquid is heated.

PROCEDURE FOR THE BOILING-GOLD METHOD

2. Boil the solution for two weeks in a CLOSED container. One week may be sufficient, but two weeks will likely have a higher yield. Add water as needed. CAUTION: Do not inhale the vapors!

3. Strain the solution using the coffee filter holder described above. Save any remaining gold for future use.

4. Add HCl or distilled white vinegar to bring the pH down to pH 8.5. An off-white precipitate will appear. Let it settle overnight.

5. Using a syringe, carefully suck out the liquid above the precipitate.

6. Add distilled water to the precipitate (filling the jar), stir thoroughly, and let it settle again for at least 4 to 5 hours, preferably overnight.

7. Repeat steps 5 and 6 at least three times to thoroughly wash the precipitate.

APPENDIX

M-STATE STORAGE

* Glass mason jars with wire-clamped glass lids and rubber gaskets
* Glass jars with plastic lids, or
* HDPE containers, which are stable in acid and alkali

Store m-state materials in the dark away from sunlight or ultraviolet light. Ultraviolet light seems to move some m-state materials toward a metallic state.

Because m-state materials are superconductors, they should be stored in glass or HDPE containers inside of steel containers and away from moving magnetic fields. Put the glass or HDPE container (containing m-state) inside a steel tin such as those used for Christmas cookies, gourmet popcorn or potato chips. If you intend to transport m-state materials, it is best to nest three or four steel containers, one inside the other with insulating material between, and place the glass or HDPE container inside the inmost steel container.

You may notice that your m-state materials have bubbles rising from them for a period of time after they are made. We believe that these bubbles are m-state gas escaping. Some people have reported that the m-state precipitate loses some of its effect as these bubbles leave. This off-gassing seems to be reduced if the m-state is stored between room temperature and body temperature in a magnetically shielded container. It is advisable not to refrigerate m-state materials. At least one researcher reports that refrigerated m-state materials are likely to move toward a warmer place.

Since bacteria and mold can easily grow in m-state precipitate, it is best to sterilize any material which you wish to store for long periods of time and to store it using water bath canning methods.

CHEMICAL SUPPLIERS

This supplier sells gold bullion, gold wire, gold shot, etc. They sell to individuals through the mail and will process small orders. Good prices. _________________________________________________

Strem Chemicals, Inc.
Dexter Industrial Park
7 Mulliken Way
Newburyport, MA 01950-4098
info@strem.com
http://www.strem.com

No minimum order.

(978) 462-3191
(800) 647-8736

Some sample products:

93-7915 Gold powder (99.95%) 500 mg $50. 2g $160.
93-7913 Gold shot (99.95%) 500 mg $40. 2g $128.

LAB SUPPLIES

Weiss Research Inc.
P.O. Box 720109
Houston, TX 77272
1-888-44-Weiss and fax: 281-879-9666 (24/7 fax)
http://www.weissresearch.com
They have a $175 pH meter (# PHM-150) with auto temperature compensation from 0 to 100 degrees C, and a pH meter with manual temperature conversion for $125.

McMaster-Carr Supply Co.
P.O. Box 4355
Chicago, IL 60680-4355
630-833-0300
fax 708-834-9427
http://www.mcmaster.com

McMaster-Carr Supply Co.
P.O. Box 54960
Los Angeles, CA 90054-0960
Sales & Customer Service: 562-692-5911
Fax: 562-695-2323 (24/7 fax)

Plastic syringe 50 cc with tapered tip 7510A665 pkg. of 10 $18.57
Neoprene gloves 5278T3 (S,M,L,XL,XXL)
Neoprene Rubber gloves 5283T6 (M,L,XL) size needs to be specified.
Wide-range pH test paper 8707T11 $8.89
PVC apron 53445T75 $4.55
Safety goggles with a face shield 5422T12 $18.94.

Also available are a pocket pH meter for $59, pH solutions,
water-test kits, hot plates, plastic tubing, and much more.

No minimum order. They sell to anyone and take VISA.

Edmund Scientific Company
101 East Gloucester Pike
Barrington, NJ 08007-1380 USA
Customer service: 1-609-573-6260 9 AM to 5 PM M-F

Disposable plastic syringes are available at many veterinary and agricultural supply stores. Plastic infusion tips are available from the same source.

More sources can be found at:
http://monatomic.earth.com/database/lab-sources/

STARTING-MATERIAL SOURCES

http://www.sigma.sial.com/

Sea salt to reconstitute sea water: Health-food store, oriental food store.

Target Glacial Rock Dust from Gaia Resources in Grand Forks, BC, Canada.

Get gold from a coin dealer.
Get gold dust by panning for it in a stream.
Gold dust might be available from Keene Engineering in Northridge, CA.
See CHEMICAL SUPPLIERS earlier in this Appendix.
Also check out a gold mining supply store.
In California try http://www.treasurenet.com/calgold/prospect.html
The gold should be at least 99.99% pure gold.

Golden Nectar (trace minerals). $40/gallon.
http://bulksales.com/index.htm

Ormus – how to make it?

* It can be noted here that Manna Energy does not use any of these three production techniques for the products offered on this site.

After five years of study, research and chemistry we have developed an organic production technique that mixes minerals from a specific location off Tasmania, Australia with minerals from a specific pool at the Dead Sea to produce our Ormus elements.

We are sharing the three techniques to keep them open source and visible for people beginning their journey with alchemy and Ormus.

Where sodium hydroxide ( Lye) is mentioned we can confirm that pharmaceutical grade magnesium hydroxide (MgOH) and potassium hydroxide (KOH) can also be substituted.

DISCLAIMER

VERIFICATION

INGESTION

WHITEGOLD WEB PAGE

INDEX

OVERVIEW

NECESSARY SUPPLIES TO MAKE M-STATE

pH PAPER OR pH METER?

SAFETY TIPS

THE WET METHOD

STARTING MATERIALS FOR THE WET METHOD

AVOIDING PROBLEMS

WET-METHOD PROCEDURE

DISCUSSION: WHEN TO BOIL THE SOLUTION

HOW TO PURIFY YOUR PRECIPITATE

METHOD 1

METHOD 2

METHOD 3

METHOD 4

DRY METHOD

EXTRA SUPPLIES NEEDED FOR THE DRY METHOD

MAKING A HOLDER FOR THE COFFEE FILTERS

DRY METHOD STARTING MATERIALS

DRY-METHOD PROCEDURE

BOILING-GOLD METHOD [The BOILING GOLD METHOD has never worked for those who have tried it and we don’t recommend its use.]

EXTRA SUPPLIES NEEDED FOR THE BOILING-GOLD METHOD

PROCEDURE FOR THE BOILING-GOLD METHOD

APPENDIX

M-STATE STORAGE

CHEMICAL SUPPLIERS

LAB SUPPLIES

STARTING-MATERIAL SOURCES

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