Acid bomb

PMMA Microwave acid Bomb Ashing Ashing... 

Nitric acid is the preferred medium for acid bomb digestion. Special care must be exercised when a mix with sulfuric acid is to be applied, to avoid violent reactions with the samples. Operating limits on most acid digestion bombs are usually set at around 250°C and 1800 psi. Perchloric... 

Dapalm The aluminium soap of naphthenic and palmitic acids used to gel gasoline. The thickened gasoline has been used for military flame throwers and incendiary bombs. See metallic soaps. 

It is prepared by the direct nitration of toluene with a mixture of nitric and sulphuric acids. TNT is a very stable, violent and powerful high explosive, but less sensitive to shock and friction than picric acid. It is widely used as a filling for shells, bombs, etc. often mixed with ammonium nitrate and other high explosives. The lower grades of TNT may contain isomers which under hot storage conditions may give rise to exudation. 

With most non-isothemial calorimeters, it is necessary to relate the temperature rise to the quantity of energy released in the process by determining the calorimeter constant, which is the amount of energy required to increase the temperature of the calorimeter by one degree. This value can be detemiined by electrical calibration using a resistance heater or by measurements on well-defined reference materials [1], For example, in bomb calorimetry, the calorimeter constant is often detemiined from the temperature rise that occurs when a known mass of a highly pure standard sample of, for example, benzoic acid is burnt in oxygen. 

METHOD 2 [89]--1M MDA or benzedrine and 1M benzaldehyde is dissolved in 95% ethanol (Everclear), stirred, the solvent removed by distillation then the oil vacuum distilled to give 95% yellow oil which is a Schiff base intermediate. 1M of this intermediate, plus 1M iodomethane, is sealed in a pipe bomb that s dumped in boiling water for 5 hours giving an orangy-red heavy oil. The oil is taken up in methanol, 1/8 its volume of dH20 is added and the solution refluxed for 30 minutes. Next, an equal volume of water is added and the whole solution boiled openly until no more odor of benzaldehyde is detected (smells like almond extract). The solution is acidified with acetic acid, washed with ether (discard ether), the MDMA or meth freebase liberated with NaOH and extracted with ether to afford a yield of 90% for meth and 65% for MDMA. That s not a bad conversion but what s with having to use benzaldehyde (a List chemical) Strike wonders if another aldehyde can substitute. 

Technically, the chemist could avoid the complex glassware apparatus of this procedure for a more crude approach [104]. This report shows some dudes de-methylating an amphetamine with concentrated HCI in a pressure cooker. A similar approach with good yields was also employed in ref. 83 and should work as well or better on guaiacol. Hydroiodic acid or hydrobromic acid will work better than hydrochloric acid but, you know, whatever floats the chemist s boat. To do this the chemist can just plain reflux HI or HBr with the guaiacol for a few hours and process as before or she can use HI, HBr or HCI and place the reactants in a pipe bomb for a few hours. 

Hydrides. Zirconium hydride [7704-99-6] in powder form was produced by the reduction of zirconium oxide with calcium hydride in a bomb reactor. However, the workup was hazardous and many fires and explosions occurred when the calcium oxide was dissolved with hydrochloric acid to recover the hydride powder. With the ready availabiHty of zirconium metal via the KroU process, zirconium hydride can be obtained by exothermic absorption of hydrogen by pure zirconium, usually highly porous sponge. The heat of formation is 167.4 J / mol (40 kcal/mol) hydrogen absorbed. 

A solution of sulfur trioxide [7446-11-9] dissolved in chlorosulfonic acid [7990-94-5] CISO H, has been used as a smoke (U.S. designation FS) but it is not a U.S. standard agent (see Chlorosulfuric acid Sulfuric acid and sulfur trioxide). When FS is atomized in air, the sulfur trioxide evaporates from the small droplets and reacts with atmospheric moisture to form sulfuric acid vapor. This vapor condenses into minute droplets that form a dense white cloud. FS produces its effect almost instantaneously upon mechanical atomization into the atmosphere, except at very low temperatures. At such temperatures, the small amount of moisture normally present in the atmosphere, requires that FS be thermally generated with the addition of steam to be effective. FS can be used as a fill for artillery and mortar shells and bombs and can be effectively dispersed from low performance aircraft spray tanks. FS is both corrosive and toxic in the presence of moisture, which imposes limitations on its storage, handling, and use. 

Phosphor-athcr, m. phosphoric ether (ester of phosphoric acid, specif, ethyl phosphate), -basis, phosphorus base, -bestimmung, /. determination of phosphorus, -blei, n. lead phosphide Min.) pyromorphite. -bombe, f. phosphorus bomb. -brandgranate, /. phosphorus incendiary shell, -brei, m. phosphorus paste, -bromid, n. phosphorus bromide, specif, phosphorus pentabromide, phos-phorus(V) bromide, -bromijr, n. phosphorus tribromide, phosphorus(III) bromide, -bronze, /. phosphor bronze, -calcium, n. calcium phosphide, -chlorid, n. phosphorus chloride, specif, phosphorus pcntachloride, phosphorus(V) chloride, -chloriir, n. phosphorous chloride (phosphorus trichloride, phosphorus(III) chloride), -dampf, tn. phosphorus vapor or fume, -eisen, n. ferrophos-phorus iron phosphide, -eisensinter, m. diadochite. 

Hydrolysis of D-(+)-1 (3-methoxyphenyl)-2-aminopropane 2.42 mols (40 g) of the compound are dissolved In 8N hydrochloric acid in a bomb tube consisting of stainless steel and having a capacity of 500 ml. Hydrogen chloride gas is passed into the ice-cooled solution until this is saturated. The solution is then heated to 130°C for 2 hours in an air bath. After cooling and driving off the hydrochloric acid at a slightly elevated temperature, the hydrochloride of the 3-hydroxyphenyl derivative is present in the form of a yellowish syrup. 

Salicylic acid, C7H603, is one of the starting materials in the manufacture of aspirin. When 1.00 g of salicylic acid burns in a bomb calorimeter, the temperature rises from 23.11°C to 28.91°C. The temperature in the bomb calorimeter increases by 2.48°C when the calorimeter absorbs 9.37 kj. How much heat is given off when one mole of salicylic acid is burned ... 

N 16.47%, OB to C02 —103.4%, triclinic needles (from ale). prisms (from acet), mp 238.2°, bp expl at 415°, d 1.48g/cc. Insol in w, si sol in hot ale eth, misc in hot acet benz. Can be prepd by treating mesitylene with a mixt of. nitric sulfuric acids in the cold (Refs 2 3). Blanksma (Ref 4) prepd it by dissolving mesitylene in sulfuric acid, partial sulfonation taking place, and then adding the soln to nitric acid, with the pptn of trinitio-mesitylene. Kholevo (Ref 6) nitrated mesitylene with nitric acid 27, sulfuric acid 69, water 4% to yield white crysts. The expl power of trinitro-mesitylene is less than PA (Ref 9), and it develops a bomb press 84% that of TNT (Ref 8), Its impact sensitivity is 52% that of TNT (Ref 7), and it expls at 415° (Ref 5)... 

Heat Test. Loss 1st 48 hrs 0,07% loss 2nd 48 hrs 0.00% explosion in 100 hrs none Hygroscopicity. % wt gain at 30°, 90% RH trace Vacuum Stability Test, cc/40 hrs at 90° none 100° none 120° 0.11 Sand Bomb Test (200g). 16.3 g sand Sensitivity to Initiation. Minimum detonating charge, g LA 0.20 Tetryl 0.25 Solubility. g/lOOcc solvent in water at 100° 0.10 NB at 150°, <15. Sol in acet ac, nitric acid, caustic potash v sol in dimethyl form-amide insol in ethyl ale, benz, butyl acetate, CC14 ethyl ether (Ref 6)... 

Human placenta (20 g) was completely dried at 105°C, crumbled, and a portion (5 g) was minerahzed by treating with nitric acid (12 M, 15 ml) at 110°C in a Teflon bomb. After mineralization, the contents were evaporated to dryness and the residue was dissolved in 1.0 ml of distilled water (termed sample A). An aliquot (10 pi) was chromatographed on RP-18 using MeOH -f HjO + CH3COOH (25 15 2) as the mobile phase. The separated spots of the metals were visualized by spraying the... 

Applications The determination and quantification of oligomers from PET has been carried out using various techniques Soxhlet extraction followed by gravimetric analysis with identification by HPLC-DAD, selective precipitation of the polymer (from a trifluoroacetic acid solution), and chloroform extraction under pressure in a sealed Parr bomb [112]. Heating of a 1 g sample in 20 mL chloroform at 100 °C for 2h allows a precision of 5 %. 

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