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Firefly Personal Plasma System |
Ovo Colloidal Gold Reactor Personal Colloidal Gold Systems Here is what you need to know before you get started making colloidal gold. |
Ovo Index 0. Ovo Index
Related Info 3. Optimal Colloidal Conditions
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The Video is a Basic Introduction to the System Components. The information on this page below relates the basic ingredients you will need.
1. Find a source of Seltzer Water. What you are looking for is a soda water that has a light mineral content. If you have a TDS Meter it would read 40-60ppm (45ppm being the perfect number if you wanted to know). A cheap TDS meter will do fine as expensive TDS meters are no better especially for our purpose. You can adjust soda waters that have low dissolved solids by adding small ammounts of a known mineral rich water such as Perrier or what might be available in your area. These mineral waters can range from 200-800ppm in dissolved mineral electrolytes so it shouldn't take more than 20-50ml of that mineral water to adjust an otherwise flat (contains zero dissolved solids) soda water. Obvious questions come to mind after reading this: Q. Should I be concerned that these electrolytes might react with the gold to make nitrates and other radical molecules that I have been warned about in making colloidal silver? A. Remember these important facts and it will get you through the rest of this process without being concerned about such unrelated factors. (unrelated? Yes, this is gold, not silver) I. Gold is not water soluble. II. Gold is not an electrolyte. (This follows with the idea that if gold is not soluble in water then it can not be an electrolyte since electrolytes are dissolved solids. That is how a TDS meter determines dissolved solids content, by the conductance of the water.) III. Gold is Hydrophobic. (water fearing) IV. Gold is 'The' Most noble element. (tends to remain gold in all cases and does not like to oxidize) It is for these reasons that making colloidal gold is somewhat difficult in the first place and why a typical colloidal silver setup will not make colloidal gold simply by using gold electrodes. (technically, it is possible but the results are poor and the time period to achive the best results all fall short of being something that you or I would want to do just for the small reward. 1-2ppm with a poor colloidal state after 2-4 days) To further simplify these statements understand that while there are many chemical means to make colloidal gold they most always begin with gold chloride as the starter of that process. In order to make gold chloride you would need Aqua Regia (acid made with Hydrochloric and Nitric acid mixture of 3/1 Hydrochloric acid to Nitric acid Ratio). The aggressive nitric acid, combined with hydrochloric acid (the hydrochloric providing the chlorine atom) allows for the gold chloride atomic bond. Gold is fairly un-responsive to pure Nitric acid, in fact nitric acid has long been used as a test for a pure gold in jewelry. If the nitric acid reacts with the 'gold' jewelry then it is not pure 24k gold. Under most circumstance gold treated with acid tends to chock the gold into it's base metal rather than a water soluble molecular state such as gold chloride. For this same reason only pure gold is found in nature, not Gold Hydroxide, Gold Chloride, Gold Oxide or any other variant molecular state of gold. (possibly gold ORME but that is a much larger conversation than I have space for on this page) One of the keys to the Ovo process is obvious if you read carefully...The Hydrochloric acid being a key in adding the chlorine atom in making gold chloride and the same Hydrogen component being used in the Ovo process. It is the Hydrogen, Oxygen pairs that seem to be critical in transforming gold which is interesting if you think about how gold is used for it's resistance to oxygen, hence it does not corrode. In the right combinations the most basic elementals (Oxygen, Hydrogen) can be used to break down gold into a finer state. In the Ovo process rather than create a molecule with gold the end result is a pure gold atomic cluster. Carbonic Acid (H2CO3) better known as Soda water, Bicarbonate of Soda water, Seltzer water is the key to the Ovo process having 3 Oxygen bound to H2 is one of the pre-cursors to the electro-kinetic processing of the gold. If you live in the USA: The best brands of Soda water are, Sams Choice No Sodium Seltzer water, Albertsons Soda water (and the flavored variety with natural fruit flavors actually work very well) and ACME (which is the same source as Albertsons). International Customers will have to do a bit of searching and I will have more information on this posted here shortly.
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2. Hydrogen Peroxide. A topical 3% Hydrogen Peroxide can be found in many pharmacies. What you need to know is that non-food grade H202 found in most pharmacies has tin based stabilizers. Food Grade Hydrogen Peroxide comes in concentrations of 35% and does not contain these stabilizers that are considered unhealthy for ingestion (yet at the same time the instructions say it's ok for a mouth rinse). My personal take on this is that it is ok to use Standard Topical 3% H202 for the following reasons. I. Superior end result for making colloidal gold. II. At 3% H202, the stabilizers are less than trace while we are only using 3.5ml of this solution for every 200-250ml of soda water. III. The process tends to break down or otherwise consume the H202 Solution. Both kinds work for the Ovo process however if you want some 35% H202 it is advise able to order 35% H202 from a supplier on the internet, or local store and dilute this by 1 part 35% H202, 10 parts distilled water to get your 3% Mixture. If you want to use 35% H202 diluted I still suggest you first begin with the inexpensive and widely available 3% H202 in order to get good results right off. After you have your first good results you can then experiment, at least you know the process works under your supervision before you start experimenting with the mixture.
When you have these two ingredients and an Ovo Unit, you are ready to make colloidal gold! (Additional)
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Copyright (C) Karl Reinhart 2005,2006,2007,2008 All Rights Resesrved |