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Oligomeric produces

Ethyne is the starting point for the manufacture of a wide range of chemicals, amongst which the most important are acrylonitrile, vinyl chloride, vinyl acetate, ethanal, ethanoic acid, tri- and perchloro-ethylene, neoprene and polyvinyl alcohol. Processes such as vinylation, ethinylation, carbonylation, oligomerization and Reppe processes offer the possibility of producing various organic chemicals cheaply. Used in oxy-acetylene welding. [Pg.169]

In refining, the oligomerization process produces gasoline from C3 fractions containing approximately 75% propylene or fuel-gas containing ethylene and propylene. [Pg.376]

One of the mam uses of the linear a olefins prepared by oligomerization of ethylene is in the preparation of linear low density polyethylene Linear low density polyethylene is a copoly mer produced when ethylene is polymerized in the presence of a linear a olefin such as 1 decene [H2C=CH(CH2)7CH3] 1 Decene replaces ethylene at random points in the growing polymer chain Can you deduce how the structure of linear low density polyethylene differs from a linear chain of CH2 units ... [Pg.622]

Shell Higher Olefin Process) plant (16,17). C -C alcohols are also produced by this process. Ethylene is first oligomerized to linear, even carbon—number alpha olefins using a nickel complex catalyst. After separation of portions of the a-olefins for sale, others, particularly C g and higher, are catalyticaHy isomerized to internal olefins, which are then disproportionated over a catalyst to a broad mixture of linear internal olefins. The desired fraction is... [Pg.459]

Oligomeric 2-ChloroethylPhosphate. Akzo s Fyrol 99 [109640-81-5] is produced either by self-condensation of tris(2-chloroethyl) phosphate (82) or by insertion of phosphoms pentoxide into this phosphate (82) followed by ethoxylation. It is low in volatihty and useful in resin-impregnated air filters, in flexible urethane foam, rebonded foam, and stmctural foam. [Pg.477]

Oligomeric Vinylphosphonate. A water-soluble oligomer, Fyrol 76 [41222-33-7] is produced by reaction of bis(2-chloroethyl) vinylphosphonate and dimethyl methylphosphonate with elimination of all the chlorine as methyl chloride (127,128). This Hquid, containing 22.5% P, is curable by free-radical initiation, on cotton or other fabrics. Nitrogen components, such as A/-methylolacrylamide or methylolmelamines, are usually included in the finish, which can be durable to multiple launderings (129,130). [Pg.480]

The direct methane conversion technology, which has received the most research attention, involves the oxidative coupling of methane to produce higher hydrocarbons (qv) such as ethylene (qv). These olefinic products may be upgraded to Hquid fuels via catalytic oligomerization processes. [Pg.78]

The stoichiometric reaction of y -diisopropenylbenzene [3748-13-8] with two moles of j -butyUithium in the presence of triethylamine has been reported to produce a useful, hydrocarbon-soluble dilithium initiator because of the low ceiling temperature of the monomer (78,79) which is analogous in stmcture to a-methylstyrene however, other studies suggest that oligomerization occurs to form initiators with functionahties higher than two (80). [Pg.239]

Manufacture of Monomers. The monomers of the greatest interest are those produced by oligomerization of ethylene (qv) and propylene (qv). Some olefins are also available as by-products from refining of petroleum products or as the products of hydrocarbon (qv) thermal cracking. [Pg.425]

Other Higher Oleiins. Linear a-olefins, such as 1-hexene and 1-octene, are produced by catalytic oligomerization of ethylene with triethyl aluminum (6) or with nickel-based catalysts (7—9) (see Olefins, higher). Olefins with branched alkyl groups are usually produced by catalytic dehydration of corresponding alcohols. For example, 3-methyl-1-butene is produced from isoamyl alcohol using base-treated alumina (15). [Pg.425]

These detergent range (C C ) odd and even linear internal olefins are fed to oxo-alcohol plants to produce C22 C2 semilinear alcohols. Most of the alcohols are ethoxylated and sold into detergent markets (8). Shell balances carbon numbers by a combination of the ethylene oligomerization extent. [Pg.439]

It is very difficult to treat MDA as a single entity because the manufacturing processes of PMDA and MDA are essentially identical, with the exception of a separation step. This article focuses on the technology of 4,4 -MDA, and it also includes properties of isomers and oligomeric mixtures when they are of commercial importance. The 4,4 -MDA is a suspected human carcinogen, and therefore special handling of this material is required. AH of the MDA and PMDA produced is consumed in industries that are "destmctive" of MDA s chemical identity. Thus MDA loses its unique chemical identity and is not encountered by household consumers. [Pg.247]

The mechanistic steps are as follows paraffins dehydrogenate to olefins the olefins oligomerize and cyclize and the cycHcs aromatize. Because the first step is rate controlling, very Httie olefin is actually present. The BTX product is relatively free of nonaromatics and therefore is very desirable as a chemical feed. As in reforming, some C —C2 fuel gas is produced along with a valuable hydrogen stream. Prom a C —feed the BTX product is roughly 35 45 20, respectively. [Pg.310]

Oligomerization of Ethylene. 1-Butene is a small by-product in the production of linear alpha-olefins by oligomerisation of ethylene. Linear alpha-olefins have one double bond at the terminal position and comprise the homologous series of compounds with carbon atoms between 4 and 19. The primary use of alpha-olefins is in the detergent industry. About 245,000 t/yr of 1-butene was produced for chemical use in the Gulf Coast of the United States in 1988 (72). [Pg.368]

Diaminopropane Processes. 1,2-Propylenediamine can be produced by the reductive amination of propylene oxide (142), 1,2-propylene glycol [57-55-6] (143), or monoisopropanolamine [78-96-6] (144). 1,3-Propanediol [504-63-2] can be used to make 1,3-diaminopropane (143). Various propaneamines are produced by reducing the appropriate acrylonitrile—amine adducts (145—147). Polypropaneamines can be obtained by the oligomerization of 1,3-diaminopropane (148,149). [Pg.44]

The nature of the product strongly depends on the length of the hydroxy acid generally when the hydroxyl group is remote the yield of lactone drops significantly. For example, 10-hydroxydecanoic acid [1679-53-4] does not produce any decanoUde instead, the reaction proceeds by intermolecular oligomerization, and a complex mixture of di-, tri-, tetra-, and pentalactones results (90). However, when Pseudomonas sp. or Candida iylindracea]i 2Lses are incubated with 16-hydroxyhexadecanoic acid [506-13-8] hexadecanoUde is the predorninant product (91). [Pg.341]

Lipase-catalyzed intermolecular condensation of diacids with diols results in a mixture of macrocycUc lactones and liuear oligomers. Interestingly, the reaction temperature has a strong effect on the product distribution. The condensation of a,(D-diacids with a,(D-dialcohols catalyzed by Candida glindracea or Pseudomonas sp. Upases leads to macrocycUc lactones at temperatures between 55 and 75°C (91), but at lower temperatures (<45°C) the formation of oligomeric esters predorninates. Optically active trimers and pentamers can be produced at room temperature by PPL or Chromobacterium viscosum Upase-catalyzed condensation of bis (2,2,2-trichloroethyl) (+)-3-meth5ladipate and 1,6-hexanediol (92). [Pg.341]

Various techniques exist that make possible a normal mode analysis of all but the largest molecules. These techniques include methods that are based on perturbation methods, reduced basis representations, and the application of group theory for symmetrical oligomeric molecular assemblies. Approximate methods that can reduce the computational load by an order of magnitude also hold the promise of producing reasonable approximations to the methods using conventional force fields. [Pg.165]

While the chemistry of radiation curable hot melt adhesives is the same as that used in liquid (syrup) adhesives and coatings discussed elsewhere in this volume, there is a fundamental difference between the objectives of reaction in the two types of systems. Syrups consist largely or entirely of reactive monomeric and/or oligomeric materials. Radiation is used to initiate the polymerization of virtually the entire mass. In contrast, hot melts generally contain polymers initially, and these polymers are capable of reaction via radiation to produce chain extension and... [Pg.735]


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See also in sourсe #XX -- [ Pg.277 , Pg.732 ]




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