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Accelerators manufacturers

The electron accelerator employed has been an AS 2000 Van de Graaff accelerator manufactured by High Energy Corporation, Burlington, Mass. The electronic control circuit has been modified considerably, and at present, this accelerator is capable of delivering 30 ns to 5 ys electron pulses of 2 - 2.5 MeV energy and v 1.2 A current at a repetition rate of 60Hz or less. The accelerator can also be operated in the continuous beam mode. The focussed beam has a diameter of 0.3 cm at the output window. [Pg.173]

Electron beam irradiation has been carried out with an electrocurtain accelerator manufactured by Energy Sciences, lnc.(model CB/150/15/180). The samples were placed on steel plates in aluminum trays and passed through the conveyor system of the electron beam apparatus. The maximum available dose per pass was 20 Mrad, hence, for the highest dose used in this study(40 Mrad), two passes were utilized. In light of the depth-dose profile at 175 kilovolts electron energy level of the EB system, the radiation dose will be nearly unifiorm throughout the sample thickness(3 mil). [Pg.478]

Application of the component commonality principle caused some components used to be overrated for the duty, but cJlowed for a substcuiticJly accelerated manufacturing cycle, which was critical for such a fast tracked project as the Deeps. [Pg.610]

Antidegradant manufactured by Monsanto Chemical Company. Accelerator manufactured by Monsanto Chemical Company. [Pg.570]

Dimeihylamine, C2H7N, (CH3)2NH. Colourless, inflammable liquid with an ammoniacal odour, mp -96" C, b.p. 7°C. Occurs naturally in herring brine. Prepared in the laboratory by treating nitrosodimetbyl-aniline with a hot solution of sodium hydroxide. Dimethylamine is largely used in the manufacture of other chemicals. These include the solvents dimethylacetamide and dimethyl-formamide, the rocket propellant unsym-metrical dimethylhydrazine, surface-active agents, herbicides, fungicides and rubber accelerators. [Pg.260]

When the surface conditions are acidic or the ambient humidity is low enough to affect the cure significantly, a surface accelerator may be used to promote the reaction. Available from most manufacturers, these basic solutions may be dip, wipe, or spray appHed. Recentiy, new additive chemistry has been developed that accelerates the cure under adverse conditions without the need for a separate accelerator. [Pg.177]

Manufacture of Fatty Acids and Derivatives. Splitting of fats to produce fatty acids and glycerol (a valuable coproduct) has been practiced since before the 1890s. In early processes, concentrated alkaU reacted with fats to produce soaps followed by acidulation to produce the fatty acids. Acid-catalyzed hydrolysis, mostly with sulfuric and sulfonic acids, was also practiced. Pressurized equipment was introduced to accelerate the rate of the process, and finally continuous processes were developed to maximize completeness of the reaction (105). Lipolytic enzymes maybe utilized to spHt... [Pg.135]

In some cases, particularly with iaactive metals, electrolytic cells are the primary method of manufacture of the fluoroborate solution. The manufacture of Sn, Pb, Cu, and Ni fluoroborates by electrolytic dissolution (87,88) is patented. A typical cell for continous production consists of a polyethylene-lined tank with tin anodes at the bottom and a mercury pool (ia a porous basket) cathode near the top (88). Pluoroboric acid is added to the cell and electrolysis is begun. As tin fluoroborate is generated, differences ia specific gravity cause the product to layer at the bottom of the cell. When the desired concentration is reached ia this layer, the heavy solution is drawn from the bottom and fresh HBP is added to the top of the cell continuously. The direct reaction of tin with HBP is slow but can be accelerated by passiag air or oxygen through the solution (89). The stannic fluoroborate is reduced by reaction with mossy tin under an iaert atmosphere. In earlier procedures, HBP reacted with hydrated stannous oxide. [Pg.168]

The production of hexamethylenetetramine consumes about 6% of the U.S. formaldehyde supply (115). Its principal use is as a thermosetting catalyst for phenoHc resins. Other significant uses are for the manufacture of RDX (cyclonite) high explosives, in mol ding compounds, and for mbber vulcanisation accelerators. Some hexamethylenetetramine is made as an unisolated intermediate in the manufacture of nitfilotriacetic acid. [Pg.497]

The octane number requirement (ONR) of a car is the octane number which causes barely audible, ie, trace knock when driven by a trained rater. The Coordinating Research Council (CRC), a research organi2ation funded joindy by the American Petroleum Institute (API) and the American Automobile Manufacturers Association (AAMA), has defined test procedures for measuring ONR. Each car is driven under a set of light and heavy accelerations until the most sensitive driving mode is determined. Then a series of fuels is mn in the car until trace knock is determined. Each year, CRC members measure ONR of more than 100 cars and pubHsh the results. [Pg.181]

The above-mentioned codes contain requirements for accelerated durabiUty tests. In addition, interlayer manufacturers and laminators expose test samples for several years under extreme weather conditions, eg, the Florida coast and Arizona desert. The laminated products weather extremely well, with no change in the plastic interlayer. Occasionally, clouding is noted around the edges when exposed to high humidity for long periods, but this is reversible. Colored areas of PVB laminates may fade while subjected to extensive uv/solar irradiation, which could cause an appearance issue. This has not, however, been shown to alter the laminate s other performance properties. [Pg.526]

Lead sesquioxide is used as an oxidation catalyst for carbon monoxide ia exhaust gases (44,45) (see Exhaust control), as a catalyst for the preparation of lactams (46) (see Antibiotics, P-lactams), ia the manufacture of high purity diamonds (47) (see Carbon, diamond-natural), ia fireproofing compositions for poly(ethylene terephthalate) plastics (48), ia radiation detectors for x-rays and nuclear particles (49), and ia vulcanization accelerators for neoprene mbber (50). [Pg.69]

Silica and Alumina. The manufacture of Pordand cement is predicated on the reaction of lime with siUca and alumina to form tricalcium sihcate [12168-85-3] and aluminate. However, under certain ambient conditions of compaction with sustained optimum moisture content, lime reacts very slowly to form complex mono- and dicalcium siUcates, ie, cementitious compounds (9,10). If such a moist, compact mixture of lime and siUca is subjected to steam and pressure in an autoclave, the lime—silica reaction is greatiy accelerated, and when sand and aggregate is added, materials of concrete-like hardness are produced. Limestone does not react with siUca and alumina under any circumstances, unless it is first calcined to lime, as in the case of hydrauhc lime or cement manufacture. [Pg.168]

Although synthetic lubrication oil production amounts to only about 2% of the total market, volume has been increasing rapidly (67). Growth rates of the order of 20% per year for poly( a-olefin)s, 10% for polybutenes, and 8% for esters (28) reflect increasing automotive use and these increases would accelerate if synthetics were adopted for factory fill of engines by automotive manufacturers. The estimated production of poly( a-olefin)s for lubricants appears to be approximately 100,000 m /yr, esters 75,000, poly(alkylene glycol)s 42,000, polybutenes 38,000, phosphates 20,000, and dialkyl benzene 18,000 (28,67). The higher costs reflected in Table 18 (18,28) have restricted the volume of siUcones, chlorotrifluoroethylene, perfluoroalkylpolyethers, and polyphenyl ethers. [Pg.255]

Bulk Polymerization. This is the method of choice for the manufacture of poly(methyl methacrylate) sheets, rods, and tubes, and molding and extmsion compounds. In methyl methacrylate bulk polymerization, an auto acceleration is observed beginning at 20—50% conversion. At this point, there is also a corresponding increase in the molecular weight of the polymer formed. This acceleration, which continues up to high conversion, is known as the Trommsdorff effect, and is attributed to the increase in viscosity of the mixture to such an extent that the diffusion rate, and therefore the termination reaction of the growing radicals, is reduced. This reduced termination rate ultimately results in a polymerization rate that is limited only by the diffusion rate of the monomer. Detailed kinetic data on the bulk polymerization of methyl methacrylate can be found in Reference 42. [Pg.265]

The flow resistance of pipe fittings (elbows, tees, etc) and valves is expressed in terms of either an equivalent length of straight pipe or velocity head loss (head loss = Kv /2g ). Most handbooks and manufacturers pubHcations dealing with fluid flow incorporate either tables of equivalent lengths for fittings and valves or K values for velocity head loss. Inasmuch as the velocity in the equipment is generally much lower than in the pipe, a pressure loss equal to at least one velocity head occurs when the fluid is accelerated to the pipe velocity. [Pg.55]

Piperidines. A significant use of piperidine (18) has been ia the manufacture of vulcanization accelerators, eg, thiuram disulfide [120-54-7] (115) (see Rubber chemicals). Mepiquat dichloride [24307-26-4] the dimethyl quaternary salt of (18), is used as a plant growth regulator for cotton (qv). Piperidine is used to make vasodilators such as dipyridamole [58-32-2] (116) and minoxidil [38304-91-5] (117), and diuretics such as etozoline [73-09-6] (118). [Pg.341]


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See also in sourсe #XX -- [ Pg.154 , Pg.161 ]




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Rubber acceleration manufacture

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