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Polyethylene groups

This growing chain could react with another polyethylene group such as -j CH2-tCH2 jj producing ... [Pg.1098]

Poly-Carb-Vn, Polycarbonate deflashing media. Composition Materials Co., Inc. Poly-Cure, Catalysts, OMG Americas, Inc. Poly-E, Low-density polyethylene, Chevron Chemical Co., U.S. Chemicals, Polyethylene Group... [Pg.927]

Although Pd is cheaper than Rh and Pt, it is still expensive. In Pd(0)- or Pd(ll)-catalyzed reactions, particularly in commercial processes, repeated use of Pd catalysts is required. When the products are low-boiling, they can be separated from the catalyst by distillation. The Wacker process for the production of acetaldehyde is an example. For less volatile products, there are several approaches to the economical uses of Pd catalysts. As one method, an alkyldi-phenylphosphine 9, in which the alkyl group is a polyethylene chain, is prepared as shown. The Pd complex of this phosphine has low solubility in some organic solvents such as toluene at room temperature, and is soluble at higher temperature[28]. Pd(0)-catalyzed reactions such as an allylation reaction of nucleophiles using this complex as a catalyst proceed smoothly at higher temperatures. After the reaction, the Pd complex precipitates and is recovered when the reaction mixture is cooled. [Pg.5]

In spite of the ene ending to its name polyethylene is much more closely related to alkanes than to alkenes It is simply a long chain of CH2 groups bearing at its ends an alkoxy group (from the initiator) or a carbon-carbon double bond... [Pg.268]

The properties that make polyethylene so useful come from its alkane like struc ture Except for the ends of the chain which make up only a tiny portion of the mole cule polyethylene has no functional groups so is almost completely inert to most sub stances with which it comes m contact... [Pg.268]

Polyethylene shrink film wrapping of cormgated ftberboard trays is in common use outside of the United States. Equipment erects the trays, fills the trays with primary packages such as cans or jars, wraps the grouping in shrink film, and heat shrinks the combination. Shrink film wrapping keeps primary and secondary packaging materials clean and dry. [Pg.450]

Lamination Inks. This class of ink is a specialized group. In addition to conforming to the constraints described for flexo and gravure inks, these inks must not interfere with the bond formed when two or more films, eg, polypropylene and polyethylene, are joined with the use of an adhesive in order to obtain a stmcture that provides resistance properties not found in a single film. Laminations are commonly used for food applications such as candy and food wrappers. Resins used to make this type of ink caimot, therefore, exhibit any tendency to retain solvent vapor after the print has dried. Residual solvent would contaminate the packaged product making the product unsalable. [Pg.252]

AH higher a-olefins, in the presence of Ziegler-Natta catalysts, can easily copolymerise both with other a-olefins and with ethylene (51,59). In these reactions, higher a-olefins are all less reactive than ethylene and propylene (41). Their reactivities in the copolymerisation reactions depend on the sise and the branching degree of their alkyl groups (51) (see Olefin polya rs, linear low density polyethylene). [Pg.430]

Carbon Cha.in Backbone Polymers. These polymers may be represented by (4) and considered derivatives of polyethylene, where n is the degree of polymeriza tion and R is (an alkyl group or) a functional group hydrogen (polyethylene), methyl (polypropylene), carboxyl (poly(acryhc acid)), chlorine (poly(vinyl chloride)), phenyl (polystyrene) hydroxyl (poly(vinyl alcohol)), ester (poly(vinyl acetate)), nitrile (polyacrylonitrile), vinyl (polybutadiene), etc. The functional groups and the molecular weight of the polymers, control thek properties which vary in hydrophobicity, solubiUty characteristics, glass-transition temperature, and crystallinity. [Pg.478]

Chlorosulfonated Polyethylene. This elastomer is made by the simultaneous chlorination and chlorosulfonation of polyethylene in an inert solvent. The resulting polymer is an odorless, colorless chip that is mixed and processed on conventional mbber equipment. The polymer typically contains 20-40% chlorine and 1% sulfur groups (see ElASTOL RS, SYNTHETIC-Cm OROSULFONATEDPOLYETHYLENE) (8). [Pg.233]

Meta.1 Oxides. Halogen-containing elastomers such as polychloropreae and chlorosulfonated polyethylene are cross-linked by their reaction with metal oxides, typically ziac oxide. The metal oxide reacts with halogen groups ia the polymer to produce an active iatermediate which then reacts further to produce carbon—carbon cross-links. Ziac chloride is Hberated as a by-product and it serves as an autocatalyst for this reaction. Magnesium oxide is typically used with ZnCl to control the cure rate and minimize premature cross-linking (scorch). [Pg.236]

Functional polyethylene waxes provide both the physical properties obtained by the high molecular weight polyethylene wax and the chemical properties of an oxidised product, or one derived from a fatty alcohol or acid. The functional groups improve adhesion to polar substrates, compatibHity with polar materials, and dispersibHity into water. Uses include additives for inks and coatings, pigment dispersions, plastics, cosmetics, toners, and adhesives. [Pg.317]

Chemically Modified Waxes. Hydrocarbon waxes of the microcrystaHine, polyethylene, and polymethylene classes are chemically modified to meet specific market needs. In the vast majority of cases, the first step is air oxidation of the wax with or without catalysts (11). The product has an acid number usuaHy no higher than 30 and a saponification number usuaHy no lower than 25. An alternative step is the reaction of the wax with a polycarboxyHc acid, eg, maleic, at high temperature (12). Through its carboxyl groups, the oxidised wax can be further modified in such reactions as saponification or esterification. Oxidised wax is easily emulsified in water through the use of surfactants or simple soaps, and is widely used in many coating and poHsh appHcations. [Pg.317]

To complete the assembly of a cell, the interleaved electrode groups are bolted to a cov er and the cover is sealed to a container. Originally, nickel-plated steel was the predominant material for cell containers but, more recently plastic containers have been used for a considerable proportion of pocket nickel-cadmium cells. Polyethylene, high impact polystyrene, and a copolymer of propylene and ethylene have been the most widely used plastics. [Pg.547]

Monoazo Pigments. In combination with other groups, the a2o linkage, —N=N—, imparts color to many dyes and pigments (see Azo Dyes). The simplest of these, ie, the Hansa yellows, toluidine reds, and naphthol reds, do not have the lightfastness and heat stabiUty required for plastics. Permanent YeUow FGL and Permanent Red 2B are stable enough for vinyls, polyethylene, polypropylene, and ceUulosics (11). Permanent Red 2B is available as the calcium, barium, or manganese salt. [Pg.460]

Fabric Softeners, Surfactants and Bleach Activators. Mono- and bisamidoamines and their imidazoline counterparts are formed by the condensation reaction of one or two moles of a monobasic fatty acid (typically stearic or oleic) or their methyl esters with one mole of a polyamine. Imidazoline formation requires that the ethyleneamine have at least one segment in which a secondary amine group Hes adjacent to a primary amine group. These amidoamines and imidazolines form the basis for a wide range of fabric softeners, surfactants, and emulsifiers. Commonly used amines are DETA, TETA, and DMAPA, although most of the polyethylene and polypropane polyamines can be used. [Pg.48]

Polybutenes enjoy extensive use as adhesives, caulks, sealants, and glaring compounds. They are used as plasticizers in mbber formulations with butyl mbber, SBR, and natural mbber. In linear low density polyethylene (LLDPE) blends they induce cling to stretch-wrap films. Polybutenes when modified at their unsaturated end groups with polar fiinctionahty are widely employed in lubricants as dispersants. Blends of polybutene with polyolefins produce semisoHd gels that can be used as potting and electrical cable filling materials. [Pg.487]


See other pages where Polyethylene groups is mentioned: [Pg.14]    [Pg.19]    [Pg.33]    [Pg.927]    [Pg.409]    [Pg.379]    [Pg.14]    [Pg.19]    [Pg.33]    [Pg.927]    [Pg.409]    [Pg.379]    [Pg.165]    [Pg.566]    [Pg.209]    [Pg.268]    [Pg.124]    [Pg.453]    [Pg.478]    [Pg.404]    [Pg.274]    [Pg.45]    [Pg.163]    [Pg.263]    [Pg.367]    [Pg.379]    [Pg.432]    [Pg.192]    [Pg.309]    [Pg.148]    [Pg.296]    [Pg.479]    [Pg.199]    [Pg.506]    [Pg.227]    [Pg.161]    [Pg.347]    [Pg.461]    [Pg.462]   
See also in sourсe #XX -- [ Pg.308 ]

See also in sourсe #XX -- [ Pg.610 ]




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Carbonyl groups polyethylene

Carboxyl end group for polyethylene terephthalate

Carboxylic groups polyethylene

Determination of Hydroxyl Groups in Polyethylene Glycol Silation - Spectrophotometry

Methyl groups polyethylene

Methylene groups polyethylene

Molecular weight (and carboxyl end group for polyethylene terephthalate)

Polyethylene hydroperoxide groups

Polyethylene terephthalate characteristic group

Polyethylene terephthalate groups

Trans-vinylene groups polyethylene

Vinyl groups polyethylene

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