Fume formation

TRICHLOROPHON or TRICHLORO-PHON FN (52-68-6) C4HgCi304P Contact with alkaline materials (e.g., lime, lime sulfur) causes decomposition to dichlorvos. Incompatible with acids and bases (toxic fume formation) prolonged exposure to moisture or elevated temperatures + water. Conosive to many metals, including iron and steel. 

EXPLOSION and FIRE CONCERNS flammable liquid when exposed to heat, flame, or oxidants NFPA rating Health 2, Flammability 2, Reactivity 0 dangerous explosion hazard reacts vigorously with oleum and chlorosulfonic acid reaction with water or steam produces toxic and corrosive fumes formation of peroxides may occur in containers that have been opened and remain in storage incompatible with strong oxidizers decomposes in the presence of moisture to form hydrochloric acid use dry ehemical, foam, carbon dioxide, or water spray for firefighting purposes. 

Ester formation. Add carefully 1 ml. of the liquid to i ml. of ethanol and then warm gently for i minute. Pour into water, make alkaline with aqueous Na2C03 solution (to remove HCl and other acid fumes), and note the odour of ethyl acetate or ethyl benzoate. 

Formation of nitrosaminey RgN NO. (a) From monomethylaniline. Dissolve I ml. of monomethylaniline in about 3 ml. of dil. HCl and add sodium nitrite solution gradually with shaking until the yellow oil separates out at the bottom of the solution. Transfer completely to a smdl separating-funnel, add about 20 ml. of ether and sh e. Run off the lower layer and wash the ethereal extract first with water, then with dil. NaOH solution, and finally with w ter to free it completely from nitrous acid. Evaporate the ether in a basin over a previously warmed water-bath, in a fume cupboard with no flames near. Apply Liebermann s reaction to the residual oil (p. 340). 

Dibromide formation. Dissolve 0 2 ml. of styrene in 0 5 ml. of CCI4 in a test-tube. Add slowly, drop by drop, a 10% solution of bromine in CCI4. Note the decolorisation of the bromine and absence of HBr fumes (therefore reaction by addition and not by substitution). Continue to add the bromine solution until a faint brown colour persists. Scratch the sides of the tube and cool it in ice-water. Filter off the crystals that separate and recrystallise the styrene dibromide from methanol m.p. 72 . 

The top of the bench should always be kept clean and dry this can easily be done if a wet and a dry rag are kept at hand. Apparatus not immediately required (a) should be kept as far as possible in a cupboard beneath the bench if it must be placed on the bench, it should be arranged in a neat and orderly manner. All apparatus should be washed immediately after use and placed in a position to drain at the first opportunity, the apparatus should be dried. It must be emphasised that as a general rule a deposit of dirt or tar is more easily removed when it is freshly formed a suitable cleaning agent can usually be found while one still remembers the nature of the material or the circumstances attending its formation. It is hardly necessary to add that sohd waste and filter papers must not be thrown into the sink, and that all operations requiring the handhng of unpleasant and noxious materials sliould be carried out in the fume cupboard ( hood ). 

Difluorophosphoric Acid. Difluorophosphoric acid (2) is a mobile, colorless Hquid. It fumes on contact with air, probably owing to HE aerosol formation. The mp of anhydrous difluorophosphoric acid has been reported to be —96.5 1°C (63) and —91.3 1°C (64). The density at 25°C is 1.583 g/mL. It partially decomposes on heating above 80—100°C. An extrapolated normal boiling point is 116°C (63) although it boils at 107—111°C... 

Hexafluorophosphoric Acid. Hexafluorophosphoric acid (3) is present under ambient conditions only as an aqueous solution because the anhydrous acid dissociates rapidly to HF and PF at 25°C (56). The commercially available HPF is approximately 60% HPF based on PF analysis with HF, HPO2F2, HPO F, and H PO ia equiUbrium equivalent to about 11% additional HPF. The acid is a colorless Hquid which fumes considerably owiag to formation of an HF aerosol. Frequently, the commercially available acid has a dark honey color which is thought to be reduced phosphate species. This color can be removed by oxidation with a small amount of nitric acid. When the hexafluorophosphoric acid is diluted, it slowly hydrolyzes to the other fluorophosphoric acids and finally phosphoric acid. In concentrated solutions, the hexafluorophosphoric acid estabUshes equiUbrium with its hydrolysis products ia relatively low concentration. Hexafluorophosphoric acid hexahydrate [40209-76-5] 6 P 31.5°C, also forms (66). This... 

Scrap that is unsuitable for recycling into products by the primary aluminum producers is used in the secondary aluminum industry for castings that have modest property requirements. Oxide formation and dross buildup are encountered in the secondary aluminum industry, and fluxes are employed to assist in the collection of dross and removal of inclusions and gas. Such fluxes are usually mixtures of sodium and potassium chlorides. Fumes and residues from these fluxes and treatment of dross are problems of environmental and economic importance, and efforts are made to reclaim both flux and metal values in the dross. 

Reaction with cold nitric acid results primarily ia the formation of 5-nitrosahcyhc acid [96-97-9]. However, reaction with fuming nitric acid results ia decarboxylation as well as the formation of 2,4,6-trinitrophenol [88-89-1] (picric acid). Sulfonation with chlorosulfonic acid at 160°C yields 5-sulfosahcyhc acid [56507-30-3]. At higher temperatures (180°C) and with an excess of chlorosulfonic acid, 3,5-disulfosahcyhc acid forms. Sulfonation with hquid sulfur trioxide ia tetrachloroethylene leads to a nearly quantitative yield of 5-sulfosahcylc acid (1). 

During certain substitution reactions, the carboxyl group is often replaced by the entering group. An example is fuming nitric acid, which results in the formation of trinitrophenol. Another is the bromination of saUcyhc acid in aqueous solution to yield 2,4,6-tribromophenol [25376-38-9] (eq. 6). 

Airborne partieulate matter may eomprise liquid (aerosols, mists or fogs) or solids (dust, fumes). Refer to Figure 5.2. Some eauses of dust and aerosol formation are listed in Table 4.3. In either ease dispersion, by spraying or fragmentation, will result in a eonsiderable inerease in the surfaee area of the ehemieal. This inereases the reaetivity, e.g. to render some ehemieals pyrophorie, explosive or prone to spontaneous eombustion it also inereases the ease of entry into the body. The behaviour of an airborne partiele depends upon its size (e.g. equivalent diameter), shape and density. The effeet of partiele diameter on terminal settling veloeity is shown in Table 4.4. As a result ... 

Perchloric Acid Fume Cupboards Use of concentrated perchloric acid gives rise to special hazards and these special fume cupboards should be for perchloric acid use only. Contact of hot perchloric acid with organic materials and certain metals (especially copper) can lead to the formation of perchlorates which,... 

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