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Pressure, high, equipment

The hquid-phase processes are more energy efficient than the vapor-phase processes, however, they iacur costiy high pressure equipment investment and also produce waste streams containing used catalyst (213). Both methods produce substantial quantities of by-products which cause refining difficulties. The by-products consist primarily of mesitylene [108-67-8] phorone [504-20-17, and the foUowiag xyUtone isomers (215) ... [Pg.495]

In designing faciUties for handling and processing nitromethane, it is recommended that nitromethane not be processed in high pressure equipment. AH vessels for nitromethane service should be protected to prevent adiabatic compression. Detonation traps should be installed at each end of transfer lines and in every 61 m (200 feet) of continuous line. Nitromethane lines should be located underground or in channels wherever possible. Pressure rehef devices (rated - 690 kPa = 100 psig) should be installed between closed valves (81). [Pg.103]

In this representation the FeCl2 which takes part in the first step of the reaction is not a tme catalyst, but is continuously formed from HQ. and iron. This is a highly exothermic process with a heat of reaction of 546 kj /mol (130 kcal/mol) for the combined charging and reaction steps (50). Despite the complexity of the Bnchamp process, yields of 90—98% are often obtained. One of the major advantages of the Bnchamp process over catalytic hydrogenation is that it can be mn at atmospheric pressure. This eliminates the need for expensive high pressure equipment and makes it practical for use in small batch operations. The Bnchamp process can also be used in the laboratory for the synthesis of amines when catalytic hydrogenation caimot be used (51). [Pg.262]

In 1955, a team of research workers at General Electric developed the necessary high pressure equipment and discovered solvent—catalytic processes by which ordinary forms of carbon could be changed into diamond. [Pg.561]

This equipment presents problems in estimating preliminary costs, since there is seldom enough information in-house to make good correlations. Vendors are by far the best source of costs. Guthrie (Reference 23) discusses the complexities of estimating high-pressure equipment and presents some cost data. [Pg.234]

Guthrie. K. M., Estimating the Cost of High-Pressure Equipment, Chemical Engineering, Dec. 2, 1968, pp. 144-148. [Pg.236]

Stress in crystalline solids produces small shifts, typically a few wavenumbers, in the Raman lines that sometimes are accompanied by a small amount of line broadening. Measurement of a series of Raman spectra in high-pressure equipment under static or uniaxial pressure allows the line shifts to be calibrated in terms of stress level. This information can be used to characterize built-in stress in thin films, along grain boundaries, and in thermally stressed materials. Microfocus spectra can be obtained from crack tips in ceramic material and by a careful spatial mapping along and across the crack estimates can be obtained of the stress fields around the crack. ... [Pg.439]

High-pressure equipment, the walls of gas eylinders, ete., are subjeeted to very high forees. Henee metallurgieal integrity is vital. [Pg.57]

The creep strength of steels is a factor limiting the maximum temperatures for such high-pressure equipment as shells and stirrers of high temperature reactors. Table 3.10 presents creep data for temperatures ranging from 400 to 600°C. The stress for 1% creep in 100,000 hours (which is a design criterion) is accepted to be not less than two-thirds of the creep stresses. [Pg.65]

For corrosion resistance, these steels (18% nickel, 9% cobalt, 3% molybdenum, 0.2% titanium and 0.02% carbon) are similar to the 13% chromium steels and, therefore, are suitable for mildly corrosive situations. Because of their very high strength after heat treatment (yield strength—1390 N/mm, elongation—15%, impact strength) maraging steels find some use in a very high-pressure equipment. [Pg.73]

In order to achieve high yields, the reaction usually is conducted by application of high pressure. For laboratory use, the need for high-pressure equipment, together with the toxicity of carbon monoxide, makes that reaction less practicable. The scope of that reaction is limited to benzene, alkyl substituted and certain other electron-rich aromatic compounds. With mono-substituted benzenes, thepara-for-mylated product is formed preferentially. Super-acidic catalysts have been developed, for example generated from trifluoromethanesulfonic acid, hydrogen fluoride and boron trifluoride the application of elevated pressure is then not necessary. [Pg.135]

With regard to pressure, another compromise is needed. It is expensive to build high pressure equipment. A pressure of about 350 atmospheres is actually used. Under these conditions, 350 atmospheres and 500°C, only about 30% of the reactants are converted to NH3. The NH3 is removed from the mixture by liquefying it under conditions at which N2 and H2 remain as gases. [Pg.151]

It is important that the tube surfaces be kept clean to avoid the initiation of corrosion. Regular waterside inspections and, if necessary, chemical cleaning of high-pressure equipment is recommended. The level of chloride that may be tolerated in such boilers during steady operation depends on the type of treatment employed. Where all-volatile alkaline treatments (AVT) are used, then the chloride levels should be lower than where nonvolatile alkalis (NVAT), such as sodium hydroxide and sodium phosphate, are used. The value may vary, depending on whether the boiler is coal-fired or oil-fired. [Pg.589]

DDT. With both the Eureka lemons and the Valencia oranges, trees were sprayed in a conventional manner with conventional high pressure equipment, and with the following mixtures ... [Pg.140]

A quick estimate of the cost for a process equipment module can be obtained by using Figure B-9. This cannot be used for high pressure equipment. It is not as accurate as the data used in example 9-6 or 9-7. [Pg.257]

High pressure equipment has been designed to measure foam mobilities in porous rocks. Simultaneous flow of dense C02 and surfactant solution was established in core samples. The experimental condition of dense CO2 was above critical pressure but below critical temperature. Steady-state CC -foam mobility measurements were carried out with three core samples. Rock Creek sandstone was initially used to measure CO2-foam mobility. Thereafter, extensive further studies have been made with Baker dolomite and Berea sandstone to study the effect of rock permeability. [Pg.502]

In addition, many other aspects must be considered when developing a catalytic reaction for industrial use these include catalyst separation, stability and poisoning, handling problems, space-time yield, process sensitivity and robustness, toxicity of metals and reagent, and safety aspects, as well as the need for high-pressure equipment. [Pg.1282]

As mentioned in a CCPS Safety Alert (CCPS 2001a), chemical reactivity is a highly desirable trait that permits numerous useful materials to be synthesized. It also allows products to be made under relatively moderate conditions of pressure and temperature, saving energy and reducing the physical risks of high-temperature or high-pressure equipment. However, the same properties that make chemical reactivity so useful also pose hazards... [Pg.13]

Liquefaction of wet biomass streams is done by hydrothermal processes at elevated pressures. The feed stocks for these high pressure liquefaction processes are slurries of biomass particles and water. Feeding these slurries into the high pressure equipment, at reasonable costs, is an important hurdle in the process development. For example, the reported operating conditions for high pressure liquefaction are in the range 280-360 °C and 90-250 bar [25, 26]. Under these conditions, biomass is converted, in a complex sequence of chemical reactions, into various compounds. Upon cooling, the reactor effluent consists of three... [Pg.135]

Souders, M. and Brown, G. G. Ind. Eng. Chem. 24 (1932) 519. Fundamental design of high pressure equipment involving paraffin hydrocarbons. IV. Fundamental design of absorbing and stripping columns for complex vapours. [Pg.716]

M. Kotowski and R. van Eldik, Coordn. Chem. Revs. 93, 19 (1989) for a succinct account of high pressure equipment used in various techniques. [Pg.120]

If using high pressure equipment, make your reaction box and door out of W steel plate. This can and should be welded air tight. [Pg.131]


See other pages where Pressure, high, equipment is mentioned: [Pg.2696]    [Pg.652]    [Pg.55]    [Pg.85]    [Pg.105]    [Pg.277]    [Pg.266]    [Pg.234]    [Pg.173]    [Pg.20]    [Pg.651]    [Pg.138]    [Pg.249]    [Pg.319]    [Pg.548]    [Pg.98]    [Pg.1282]    [Pg.121]    [Pg.203]    [Pg.142]    [Pg.143]    [Pg.94]    [Pg.107]    [Pg.222]    [Pg.112]    [Pg.48]    [Pg.88]   
See also in sourсe #XX -- [ Pg.262 ]

See also in sourсe #XX -- [ Pg.72 , Pg.163 ]




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