Elsa David and there's also high concentrations of hydrogen sulfide at these sites (tretament of swors water) http://www.adp.pt/.../saneamento-de-aguas-residuais/...
GerirMonday, July 31, 2017
Hello! welcome back to war! After almost 5 years of warfare against the "system" I've been trought everything, literally, everything. Passing a gun trought security, if it could be only by the scanner, ok, you do it cover on old x rays films, however the metal detector is "almost" uncrossble. the relativety between mass and proximity, would demand that only 5 inches of metal cross the metal detector on a less than 1 meter parallel barrier. I've been trough everything the "system" has about it, also nylon 66, and trough dozens of scientific papers. As a conclusion, of my research, I have a theory; the theory is based on unmagnetize the metal trought this procedure (be aware that metal has also a thermal reading on detection)
the reaction during the addition of bromine the flask being exposed to the direct light from a 750-watt lamp. At the end of the reaction when the liquid is colorized 60 ml of water are added. The flask is cooled and excess of hydrobromic acid is neutralized with the saturated solution of sodium carbonate. The final reaction product forms as oil which is separated, dried and distilled in vacuum. The product is a colorless liquid with a pungent odor and boiling point 136° C.
Bromoacetone may be also obtained by the action of bromine dissolved in acetone on an aqueous solution of sodium bromate (NaBrO3) and sulfuric acid at 30-35° C.
Bromoacetone may be also obtained by the action of bromine dissolved in acetone on an aqueous solution of sodium bromate (NaBrO3) and sulfuric acid at 30-35° C.
So, today I'm attacking Portugal and not the US or the EU, for a change...! I have here two factories on Portugal : 1. Fábrica de Alenquer IC 2, km 38,4 Cheganças 2580-381 Alenquer 2. Fábrica de Sines Zona Industrial Ligeira 2 (Zil 2) Apartado 165 - EC Sines 7521-902 Sines ! these two factories produces chemical industrial gas. one of the gas is hydrogen sulfide, HIGHLY TOXIC. Like all chemical warfare agents, if the primary explosive reaches very high temperatures, the poison can reach more than 5 miles square.
Saturday, July 29, 2017
Friday, July 28, 2017
Again..and again...chemical warfare! Another warfare agent for psyco war is Phencyclidine; Some few months ago, my Mother saw on TV that there was a new drug that turned people on cannibals...here it is...(not new anyway...Deschloroketamine=2-Phenyl-2-(methylamino)cyclohexanone) You can purchase it all over the darkweb, on any parallel market, and all sort of internet suplliers. Here my goal is, terrorism.
Dissociative
Thursday, July 27, 2017
Good morning, worldwide! welcome back to war ! "3-Quinuclidinyl benzilate (QNB) — IUPAC name 1-azabicyclo[2.2.2]oct-3-yl 2-hydroxy-2,2-diphenylacetate; US Army code EA-2277; NATO code BZ; Soviet code Substance 78 — is an odorless military incapacitating agent.[1] BZ is a glycolate anticholinergic compound"...BZ is dispersed as an aerosol. It may be micropulverized for dissemination by a disperser (90% dissemination efficiency), or mixed with a pyrotechnic burning mixture for dissemination in burning munitions (70% dissemination efficiency)
Wednesday, July 26, 2017
cholera warfare bateria (to be used on aerosol explosive) preparation
welcome back to war Jihad! You have at least 6 guys on your secret lab, however the cartles and east mafia hv much more. Let's go for cholera preparation:
Thiosulphate Citrate Bile Salts Agar (TCBS)
(Oxoid designation is Cholera Medium TCBS)
Basic ingredients
Peptone 10,0 g
Yeast extract 5,0 g
Sodium citrate 10,0 g
Sodium thiosulfate.5 H2O (Na2S2O3•5 H2O) 10,0 g
Sodium chloride (NaCl) 10,0 g
Ox gall powder 5,0 g
Iron (III) citrate (FeC6H5O7) 1,0 g
Sodium cholate 3,0 g
Sucrose 20,0 g
Thymol Blue solution (0,2%) 20,0 ml
Bromothymol Blue solution (0,2%) 20,0 ml
Agar 15,0 g
Distilled water 1,0 L
pH 8,6 ± 0,2
Preparation
Mix all ingredients and apply heat until all goes into solution. DO NOT STERILIZE USING AUTOCLAVE. Allow to cool to 45-50°C and distribute.
Notes:
from http://www.disknet.com/indiana_biolab/b041.htm:
Peptones are the most widely used source of nitrogen in microbial media. Some are made by cooking milk or meat products in acid, but most are made by incubating milk or meat with trypsin, pepsin, or other proteolytic enzymes to digest the protein to a mixture of amino acids, peptides, and polypeptides. Many microbes, called proteolytic, can digest proteins, but most can't. The choice of peptone is sometimes of importance.
Some water-based inks contain ox gall (bile) as a dispersant. Pure ox gall can be obtained from art supply stores (eg. Winsor & Newton brand).
Sodium cholate, a bile salt, is used as an anionic detergent
http://www.sciencemadness.org/talk/viewthread.php?tid=1485&page=2
Thiosulphate Citrate Bile Salts Agar (TCBS)
(Oxoid designation is Cholera Medium TCBS)
Basic ingredients
Peptone 10,0 g
Yeast extract 5,0 g
Sodium citrate 10,0 g
Sodium thiosulfate.5 H2O (Na2S2O3•5 H2O) 10,0 g
Sodium chloride (NaCl) 10,0 g
Ox gall powder 5,0 g
Iron (III) citrate (FeC6H5O7) 1,0 g
Sodium cholate 3,0 g
Sucrose 20,0 g
Thymol Blue solution (0,2%) 20,0 ml
Bromothymol Blue solution (0,2%) 20,0 ml
Agar 15,0 g
Distilled water 1,0 L
pH 8,6 ± 0,2
Preparation
Mix all ingredients and apply heat until all goes into solution. DO NOT STERILIZE USING AUTOCLAVE. Allow to cool to 45-50°C and distribute.
Notes:
from http://www.disknet.com/indiana_biolab/b041.htm:
Peptones are the most widely used source of nitrogen in microbial media. Some are made by cooking milk or meat products in acid, but most are made by incubating milk or meat with trypsin, pepsin, or other proteolytic enzymes to digest the protein to a mixture of amino acids, peptides, and polypeptides. Many microbes, called proteolytic, can digest proteins, but most can't. The choice of peptone is sometimes of importance.
Some water-based inks contain ox gall (bile) as a dispersant. Pure ox gall can be obtained from art supply stores (eg. Winsor & Newton brand).
Sodium cholate, a bile salt, is used as an anionic detergent
http://www.sciencemadness.org/talk/viewthread.php?tid=1485&page=2
Tuesday, July 25, 2017
Hello worldwide! Welcome back to war! To tell you the truth, because I'm a newbie on chemistry, this phosgene warfare chemical agent its a piece of cake!!!!! Its the last phosgene gas, its called Choloropicrin! Here is the recipe : To the 5 liter flask 550 g calcium hypochlorite made into a paste in 1 liter water are placed. A paste of sodium picrate, made by mixing 50 g picric acid with 10 g sodium hydroxide and 250 ml water, is added with continuous stirring. The reaction is very rapid and is completed in about 30 min. To remove chloropicrin the reaction mixture is steam distilled until no more oily droplets come over. The oily distillate is separated from the water, dried over calcium chloride and redistilled. The yield is 70% of the theoretical. Chloropicrin is a slightly oily, colorless or yellow due to impurities liquid with a characteristic odor and with boiling point t 112° C.
Monday, July 24, 2017
PREPARATION OF HYDROGEN CYANIDE FROM POTASSIUM PERMANGANATE, METHANOL, SULFURIC ACID, AQUEOUS AMMONIA, AND POTASSIUM HYDROXIDE
Notes:
-all potassium chemicals can be substituted with their sodium parallel, if mass ratios have been properly adjusted
-it is highly recommended that nbk2000 dismiss all described and inferred safety precautions
PREPARATION OF POTASSIUM FORMATE (HCOOK) AND MANGANESE FORMATE (Mn(HCOO)2):
126.4 grams of potassium permanganate (KMnO4) is added to 32 grams (approximately 40.2mL) of concentrated methanol (CH3OH):
10(CH3OH) + 8(KMnO4) --} 10(HCOOH) + 10(H2O) + 8(MnO) + 4(K2O)
10(HCOOH) + 10(H2O) + 8(MnO) + 4(K2O) --} 10(HCOOH) + 8(KOH) + 8(MnO) + 6(H2O)
10(HCOOH) + 8(KOH) + 8(MnO) + 6(H2O) --} 8(HCOOK) + 2(HCOOH) + 8(MnO) + 14(H2O)
8(HCOOK) + 2(HCOOH) + 8(MnO) + 14(H2O) --} 8(HCOOK) + Mn(HCOO)2 + 7(MnO) + 15(H2O)
Mixture is then filtered to remove the manganese oxide (MnO), and the filtered solution is then allowed to evaporate. What is left is a ratio of eight : one of potassium formate : manganese formate. The remaining crystals should weight approximately 81.77 grams if you acheived a 100% yield.
PREPARATION OF FORMIC ACID (HCOOH):
The mixture of potassium formate and manganese formate is added to concentrated sulfuric acid. That is, all 81.77 grams of the potassium formate and manganese formate crystals are added to 49 grams (26.5mL) of concentrated sulfuric acid. The remaining mixture is heated, and the vapors, which are composed of formic acid, are condensed. WARNING! FORMIC ACID IS TOXIC. PURE FORMIC ACID IS A COLORLESS FUMING LIQUID WITH A PUNGENT ODOUR; IT IRRITATES THE MUCOUS MEMBRANES AND BLISTERS THE SKIN.
8(HCOOK) + Mn(HCOO)2 + 5(H2SO4) --} 10(HCOOH) + 4(K2SO4) + MnSO4
PREPARATION OF AMMONIUM FORMATE ( [HCOO-][NH4+] )
Formic acid is added to an aqueous solution of ammonia ( [NH4+][OH-] ). The remaining solution is evaporated; the crystals left are ammonium formate crystals. Crystals should weight about 64 grams if you have been achieving 100% yields.
HCOOH + [NH4+][OH-] --} [HCOO-][NH4+] + H2O
PREPARATION OF POTASSIUM CYANIDE (KCN):
The ammonium formate crystals are heated by flame in an environment containing as little oxygen gas as possible. The ammonium formate decomposes into formamide (HCONH2) which then decomposes into hydrogen cyanide.
[HCOO-][NH4+] --} HCONH2 + H2O
HCONH2 + H2O --} HCN + 2(H2O)
The gas given off is condensed in in a rubber, plastic, or, preferrably, glass tube that has one end immersed in a beaker containing a solution of potassium hydroxide (KOH). The tube should be positioned so that any liquids forming in it will run off into the beaker of potassium hydroxide. Some of the gas given off may not be condensed; that is why the tube is immersed in the beaker of potassium hydroxide. That will prevent a loss of much cyanide. The hydrogen cyanide will quickly react with the potassium hydroxide to form potassium cyanide. The hydrogen cyanide is reacted with the potassium hydroxide because the hydrogen cyanide will evaporate off quickly, which is both extremely dangerous and will cause the loss of a lot of cyanide. About 56.1 grams of potassium hydroxide should be used if 100% yields are expected. About 65.1 grams of potassium cyanide should result if 100% yields are achieved. The solution in the beaker, once all of the ammonium formate crystals have been converted into various gasses, should be evaporated off. The remaining crystals are potassium cyanide crystals.
HCN + KOH --} KCN + H2O
PREPARATION OF HYDROGEN CYANIDE (HCN) FROM POTASSIUM CYANIDE:
The potassium cyanide is then treated with an acid. This will form the potassium salt of the acid, and hydrogen cyanide. DO NOT ATTEMPT TO STORE HYDROGEN CYANIDE! IT WILL ALMOST CERTAINLY CAUSE THE DEATH OF AN UNINTENDED VICTIM SUCH AS YOURSELF! HYDROGEN CYANIDE SHOULD ALWAYS BE USED IMMEDIATELY AFTER IT IS MADE, OR CONVERTED IMMEDIATELY INTO POTASSIUM CYANIDE! It is recommended to use an acid that can be found concentrated. Concentrated sulfuric acid is believed to be the best acid to use.
KCN + [H+] --} HCN + [K+]
http://www.sciencemadness.org/talk/viewthread.php?tid=23
GET THE POTASSIUM CYANIDE ALREADY LABORATORY GRADE AT AN GOLD MINE EXTRACTION
-all potassium chemicals can be substituted with their sodium parallel, if mass ratios have been properly adjusted
-it is highly recommended that nbk2000 dismiss all described and inferred safety precautions
PREPARATION OF POTASSIUM FORMATE (HCOOK) AND MANGANESE FORMATE (Mn(HCOO)2):
126.4 grams of potassium permanganate (KMnO4) is added to 32 grams (approximately 40.2mL) of concentrated methanol (CH3OH):
10(CH3OH) + 8(KMnO4) --} 10(HCOOH) + 10(H2O) + 8(MnO) + 4(K2O)
10(HCOOH) + 10(H2O) + 8(MnO) + 4(K2O) --} 10(HCOOH) + 8(KOH) + 8(MnO) + 6(H2O)
10(HCOOH) + 8(KOH) + 8(MnO) + 6(H2O) --} 8(HCOOK) + 2(HCOOH) + 8(MnO) + 14(H2O)
8(HCOOK) + 2(HCOOH) + 8(MnO) + 14(H2O) --} 8(HCOOK) + Mn(HCOO)2 + 7(MnO) + 15(H2O)
Mixture is then filtered to remove the manganese oxide (MnO), and the filtered solution is then allowed to evaporate. What is left is a ratio of eight : one of potassium formate : manganese formate. The remaining crystals should weight approximately 81.77 grams if you acheived a 100% yield.
PREPARATION OF FORMIC ACID (HCOOH):
The mixture of potassium formate and manganese formate is added to concentrated sulfuric acid. That is, all 81.77 grams of the potassium formate and manganese formate crystals are added to 49 grams (26.5mL) of concentrated sulfuric acid. The remaining mixture is heated, and the vapors, which are composed of formic acid, are condensed. WARNING! FORMIC ACID IS TOXIC. PURE FORMIC ACID IS A COLORLESS FUMING LIQUID WITH A PUNGENT ODOUR; IT IRRITATES THE MUCOUS MEMBRANES AND BLISTERS THE SKIN.
8(HCOOK) + Mn(HCOO)2 + 5(H2SO4) --} 10(HCOOH) + 4(K2SO4) + MnSO4
PREPARATION OF AMMONIUM FORMATE ( [HCOO-][NH4+] )
Formic acid is added to an aqueous solution of ammonia ( [NH4+][OH-] ). The remaining solution is evaporated; the crystals left are ammonium formate crystals. Crystals should weight about 64 grams if you have been achieving 100% yields.
HCOOH + [NH4+][OH-] --} [HCOO-][NH4+] + H2O
PREPARATION OF POTASSIUM CYANIDE (KCN):
The ammonium formate crystals are heated by flame in an environment containing as little oxygen gas as possible. The ammonium formate decomposes into formamide (HCONH2) which then decomposes into hydrogen cyanide.
[HCOO-][NH4+] --} HCONH2 + H2O
HCONH2 + H2O --} HCN + 2(H2O)
The gas given off is condensed in in a rubber, plastic, or, preferrably, glass tube that has one end immersed in a beaker containing a solution of potassium hydroxide (KOH). The tube should be positioned so that any liquids forming in it will run off into the beaker of potassium hydroxide. Some of the gas given off may not be condensed; that is why the tube is immersed in the beaker of potassium hydroxide. That will prevent a loss of much cyanide. The hydrogen cyanide will quickly react with the potassium hydroxide to form potassium cyanide. The hydrogen cyanide is reacted with the potassium hydroxide because the hydrogen cyanide will evaporate off quickly, which is both extremely dangerous and will cause the loss of a lot of cyanide. About 56.1 grams of potassium hydroxide should be used if 100% yields are expected. About 65.1 grams of potassium cyanide should result if 100% yields are achieved. The solution in the beaker, once all of the ammonium formate crystals have been converted into various gasses, should be evaporated off. The remaining crystals are potassium cyanide crystals.
HCN + KOH --} KCN + H2O
PREPARATION OF HYDROGEN CYANIDE (HCN) FROM POTASSIUM CYANIDE:
The potassium cyanide is then treated with an acid. This will form the potassium salt of the acid, and hydrogen cyanide. DO NOT ATTEMPT TO STORE HYDROGEN CYANIDE! IT WILL ALMOST CERTAINLY CAUSE THE DEATH OF AN UNINTENDED VICTIM SUCH AS YOURSELF! HYDROGEN CYANIDE SHOULD ALWAYS BE USED IMMEDIATELY AFTER IT IS MADE, OR CONVERTED IMMEDIATELY INTO POTASSIUM CYANIDE! It is recommended to use an acid that can be found concentrated. Concentrated sulfuric acid is believed to be the best acid to use.
KCN + [H+] --} HCN + [K+]
http://www.sciencemadness.org/talk/viewthread.php?tid=23
GET THE POTASSIUM CYANIDE ALREADY LABORATORY GRADE AT AN GOLD MINE EXTRACTION
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