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Ethylene economics

This process thus enables gasoline production to be increased if the propylene can not be used for petrochemical manufacture. It recovers ethylene economically from fuel-gas. [Pg.376]

Methanol to Ethylene. Methanol to ethylene economics track the economics of methane to ethylene. Methanol to gasoline has been flilly developed and, during this development, specific catalysts to produce ethylene were discovered. The economics of this process have been discussed, and a catalyst (Ni/SAPO 34) with almost 95% selectivity to ethylene has been claimed (99). Methanol is converted to dimethyl ether, which decomposes to ethylene and water the method of preparation of the catalyst rather than the active ingredient of the catalyst has made the significant improvement in yield (100). By optimizing the catalyst and process conditions, it is claimed that yields of ethylene, propylene, or both are maximized. This is still in the bench-scale stage. [Pg.443]

Ethylene oxide production by direct oxhutiox of ethylene. Economic data (France conditions, mid-1986)... [Pg.9]

Example 2.2 Devise a process from the three reaction paths in Example 2.1 which uses ethylene and chlorine as raw materials and produces no byproducts other than water. Does the process look attractive economically ... [Pg.17]

At one time acetaldehyde was prepared on an industrial scale by this method Modern methods involve direct oxidation of ethylene and are more economical... [Pg.381]

Since 1960, the Hquid-phase oxidation of ethylene has been the process of choice for the manufacture of acetaldehyde. There is, however, stiU some commercial production by the partial oxidation of ethyl alcohol and hydration of acetylene. The economics of the various processes are strongly dependent on the prices of the feedstocks. Acetaldehyde is also formed as a coproduct in the high temperature oxidation of butane. A more recently developed rhodium catalyzed process produces acetaldehyde from synthesis gas as a coproduct with ethyl alcohol and acetic acid (83—94). [Pg.51]

Many catalytic systems have been described acidic solutions of mercuric salts are the most generally used. This process has long been superseded by more economical routes involving oxidation of ethylene or other hydrocarbons. [Pg.102]

In the 1980s cost and availabiUty of acetylene have made it an unattractive raw material for acrylate manufacture as compared to propylene, which has been readily available at attractive cost (see Acetylene-DERIVED chemicals). As a consequence, essentially all commercial units based on acetylene, with the exception of BASF s plant at Ludwigshafen, have been shut down. AH new capacity recendy brought on stream or announced for constmction uses the propylene route. Rohm and Haas Co. has developed an alternative method based on aLkoxycarbonylation of ethylene, but has not commercialized it because of the more favorable economics of the propylene route. [Pg.152]

Ethylene Cyanohydrin Process. This process, the fkst for the manufacture of acryhc acid and esters, has been replaced by more economical ones. During World War I, the need for ethylene as an important raw material for the synthesis of ahphatic chemicals led to development of this process (16) in both Germany, in 1927, and the United States, in 1931. [Pg.155]

Chlorine cannot be stored economically or moved long distances. International movements of bulk chlorine are more or less limited to movements between Canada and the United States. In 1987, chlorine moved in the form of derivatives was 3.3 million metric tons or approximately 10% of total consumption (3). Exports of ethylene dichloride, vinyl chloride monomer, poly(vinyl chloride), propylene oxide, and chlorinated solvents comprise the majority of world chlorine movement. Countries or areas with a chlorine surplus exported in the form of derivatives include Western Europe, Bra2il, USA, Saudi Arabia, and Canada. Countries with a chlorine deficit are Taiwan, Korea, Indonesia, Vene2uela, South Africa, Thailand and Japan (3). [Pg.478]

In 1991, the relatively old and small synthetic fuel production faciHties at Sasol One began a transformation to a higher value chemical production facihty (38). This move came as a result of declining economics for synthetic fuel production from synthesis gas at this location. The new faciHties installed in this conversion will expand production of high value Arge waxes and paraffins to 123,000 t/yr in 1993. Also, a new faciHty for production of 240,00 t/yr of ammonia will be added. The complex will continue to produce ethylene and process feedstock from other Sasol plants to produce alcohols and higher phenols. [Pg.167]

ElexibiHty allows the operator to pick and choose the most attractive feedstock available at a given point in time. The steam-cracking process produces not only ethylene, but other products as weU, such as propylene, butadiene, butylenes (a mixture of monounsaturated C-4 hydrocarbons), aromatics, etc. With ethane feedstock, only minimal quantities of other products ate produced. As the feedstocks become heavier (ie, as measured by higher molecular weights and boiling points), increasing quantities of other products are produced. The values of these other coproduced products affect the economic attractiveness and hence the choice of feedstock. [Pg.171]

The economics of the arc-coal process is sensitive to the electric power consumed to produce a kilogram of acetylene. Early plant economic assessments indicated that the arc power consumption (SER = kwh/kgC2H2) must be below 13.2. The coal feedcoal quench experiments yielded a 9.0 SER with data that indicated a further reduction to below 6.0 with certain process improvements. In the propane quench experiment, ethylene as well as acetylene is produced. The combined process SER was 6.2 with a C2H2/C2H4 production ratio of 3 to 2. Economic analysis was completed uti1i2ing the achieved acetylene yields, and an acetylene price approximately 35% lower than the price of ethylene was projected. [Pg.393]

Most by-product acetylene from ethylene production is hydrogenated to ethylene in the course of separation and purification of ethylene. In this process, however, acetylene can be recovered economically by solvent absorption instead of hydrogenation. Commercial recovery processes based on acetone, dimetbylform amide, or /V-metby1pyrro1idinone have a long history of successfiil operation. The difficulty in using this relatively low cost acetylene is that each 450, 000 t/yr world-scale ethylene plant only produces from 7000 9000 t/yr of acetylene. This is a small volume for an economically scaled derivatives unit. [Pg.394]

Ethylene Dichloride," Chemical Economics Handbook, SRI International, Menlo Park, Calif., June 1992. [Pg.451]

Until 1982, almost all methyl methacrylate produced woddwide was derived from the acetone cyanohydrin (C-3) process. In 1982, Nippon Shokubai Kagaku Kogyo Company introduced an isobutylene-based (C-4) process, which was quickly followed by Mitsubishi Rayon Company in 1983 (66). Japan Methacryhc Monomer Company, a joint venture of Nippon Shokubai and Sumitomo Chemical Company, introduced a C-4-based plant in 1984 (67). Isobutylene processes are less economically attractive in the United States where isobutylene finds use in the synthesis of methyl /i / butyl ether, a pollution-reducing gasoline additive. BASF began operation of an ethylene-based (C-2) plant in Ludwigshafen, Germany, in 1990, but favorable economics appear to be limited to conditions unique to that site. [Pg.250]

Solution Polymerization. Two types of solution polymerization technologies are used for LLDPE synthesis. One process utilizes heavy solvents the other is carried out in mixtures of supercritical ethylene and molten PE as a polymerization medium. Original solution processes were introduced for low pressure manufacture of PE resins in the late 1950s subsequent improvements of these processes gradually made them economically competitive with later, more advanced technologies. [Pg.399]

IFP Process for 1-Butene from Ethylene. 1-Butene is widely used as a comonomer in the production of polyethylene, accounting for over 107,000 t in 1992 and 40% of the total comonomer used. About 60% of the 1-butene produced comes from steam cracking and fluid catalytic cracker effluents (10). This 1-butene is typically produced from by-product raffinate from methyl tert-huty ether production. The recovery of 1-butene from these streams is typically expensive and requires the use of large plants to be economical. Institut Francais du Petrole (IFP) has developed and patented the Alphabutol process which produces 1-butene by selectively dimerizing ethylene. [Pg.440]

Organoaluminum Compounds. Apphcation of aluminum compounds in organic chemistry came of age in the 1950s when the direct synthesis of trialkylalurninum compounds, particularly triethylalurninum and triisobutylalurninum from metallic aluminum, hydrogen, and the olefins ethylene and isobutylene, made available economic organoalurninum raw materials for a wide variety of chemical reactions (see a-BONDED alkyls and aryls). [Pg.137]

A number of 2eohtic materials have been claimed to cataly2e this reaction and reaction temperatures are on the order of 200—350°C with pressures as high as 18000 kPa (2600 psi) reported. This is a low conversion process and recycle of the unconverted starting materials is necessary to provide an economical process. Amination of ethylene to produce ethylamines cataly2ed by ammonium iodide is reported, but not beheved to be practiced commercially (15,16). Alkyl Halide Amination (Method 7). The oldest technology for pioducing amines is the reaction of ammonia with an alkyl hahde. This... [Pg.200]

Heat Pumps. Because of added capital and complexity, heat pumps are rarely economical, although they were formerly commonly used in ethylene/ethane and propylene/propane spHtters. Generally, the former spHtters are integrated into the refrigeration system the latter are driven by low level waste heat, cascading to cooling water. [Pg.85]

Propanol economics are sensitive to the raw material costs of ethylene (qv) and the feedstock for synthesis gas, ie, natural gas or Hquid petroleum feedstocks (qv). Natural gas-based technology is slightly more economical. [Pg.119]

The ethylene feedstock used in most plants is of high purity and contains 200—2000 ppm of ethane as the only significant impurity. Ethane is inert in the reactor and is rejected from the plant in the vent gas for use as fuel. Dilute gas streams, such as treated fluid-catalytic cracking (FCC) off-gas from refineries with ethylene concentrations as low as 10%, have also been used as the ethylene feedstock. The refinery FCC off-gas, which is otherwise used as fuel, can be an attractive source of ethylene even with the added costs of the treatments needed to remove undesirable impurities such as acetylene and higher olefins. Its use for ethylbenzene production, however, is limited by the quantity available. Only large refineries are capable of deUvering sufficient FCC off-gas to support an ethylbenzene—styrene plant of an economical scale. [Pg.478]


See other pages where Ethylene economics is mentioned: [Pg.316]    [Pg.316]    [Pg.231]    [Pg.53]    [Pg.172]    [Pg.174]    [Pg.193]    [Pg.102]    [Pg.155]    [Pg.391]    [Pg.391]    [Pg.394]    [Pg.428]    [Pg.516]    [Pg.327]    [Pg.253]    [Pg.384]    [Pg.399]    [Pg.411]    [Pg.451]    [Pg.294]    [Pg.125]    [Pg.528]    [Pg.66]    [Pg.478]    [Pg.480]    [Pg.485]   
See also in sourсe #XX -- [ Pg.161 , Pg.171 ]




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