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Poly , replacement

Fully modified yams had smooth, all-skin cross sections, a stmcture made up of numerous small crystaUites of cellulose, and filament strengths around 0.4 N/tex (4.5 gf/den). They were generally known as the Super tire yams. Improved Super yams (0.44—0.53 N/tex (5—6 gf/den)) were made by mixing modifiers, and one of the best combiaations was found to be dimethylamine with poly-(oxyethylene) glycol of about 1500 mol wt (25). Ethoxjlated fatty acid amines have now largely replaced dimethylamine because they are easier to handle and cost less. [Pg.349]

Structural Components. In most appHcations stmctural foam parts are used as direct replacements for wood, metals, or soHd plastics and find wide acceptance in appHances, automobUes, furniture, materials-handling equipment, and in constmction. Use in the huil ding and constmction industry account for more than one-half of the total volume of stmctural foam appHcations. High impact polystyrene is the most widely used stmctural foam, foUowed by polypropylene, high density polyethylene, and poly(vinyl chloride). The constmction industry offers the greatest growth potential for ceUular plastics. [Pg.416]

Letterpress. This is the oldest printing process stiU in use. It continues to be replaced by newer printing processes. Printing is conducted from a raised image area of the printing plate. Inks in the printing process are transferred directly from a raised area to a substrate. The printing plates contain a thick layer of photopolymer (often a mixture with polymer such as poly(vinyl alcohol) deposited over a plastic or aluminum base. [Pg.249]

In the second quarter of the twentieth century, with the development of poly(vinyl chloride), nylon, polyurethane, and other polymers, many new and improved leather-like materials, so-called coated fabrics (qv), were placed on the market. Shortages of leather after World War 11 led to the expansion of these leather-like materials ("man-made" leathers) to replace leather in shoes, clothing, bags, upholstery, and other items. DurabiUty and waterproof quahties superior to leather made coated fabrics advantageous, in spite of imperfection in breathabihty and flexibiUty. Demands for shoes, clothing, and other items are stiU increasing due to growing world population and urbanization. [Pg.88]

There are numerous further appHcations for which maleic anhydride serves as a raw material. These appHcations prove the versatiHty of this molecule. The popular artificial sweetener aspartame [22839-47-0] is a dipeptide with one amino acid (l-aspartic acid [56-84-8]) which is produced from maleic anhydride as the starting material. Processes have been reported for production of poly(aspartic acid) [26063-13-8] (184—186) with appHcations for this biodegradable polymer aimed at detergent builders, water treatment, and poly(acryHc acid) [9003-01-4] replacement (184,187,188) (see Detergency). [Pg.460]

The poly(vinyl acetal) prepared from acetaldehyde was developed in the early 1940s by Shawinigan Chemicals, Ltd., of Canada and sold under the trade name Alvar. Early uses included injection-molded articles, coatings for paper and textiles, and replacement for shellac. Production peaked in the early 1950s and then decreased as a result of competition from less expensive resins such as poly(vinyl chloride) (see Vinyl polymers, poly(vinyl chloride)). [Pg.449]

Poly(hydroxyethyl methacrylate)-dye copolymers —The color additives formed by reaction of one or more of the foUowiag reactive dyes with poly(hydroxyethyl methacrylate), so that the sulfate group (or groups) or chlorine substituent of the dye is replaced by an ether linkage to poly(hydroxyethyl methacrylate) (see Dyes, reactive). The dyes that may be used alone or ia combination are... [Pg.453]

The alcohol swells the poly (ethyl methacrylate) beads, rapidly promoting diffusion of the plasticizer into the polymer. As a result of the polymer-chain entanglement, a gel is formed. The conditioner is applied to the denture and provides a cushioning effect alcohol and plasticizer are slowly leached out, and the material becomes rigid. To ensure resiliency, the conditioner must be replaced after a few days. Some materials exhibit high flow over a short period compared with others with low initial flow the latter remain active longer. [Pg.490]

At one time butadiene-acrylonitrile copolymers (nitrile rubbers) were the most important impact modifiers. Today they have been largely replaced by acrylonitrile-butadiene-styrene (ABS) graft terpolymers, methacrylate-buta-diene-styrene (MBS) terpolymers, chlorinated polyethylene, EVA-PVC graft polymers and some poly acrylates. [Pg.341]

Substantial quantities of UPVC are also used for blow moulded containers for such diverse materials as consumable liquids such as fruit squashes, liquids for household use such as detergents and disinfectants, cosmetics and toiletries, and pharmaceuticals. For most of these applications UPVC is in competition with at least one other polymer, particularly poly(ethylene) terephthalate (Chapter 25), polyethylene (Chapter 10), polypropylene (Chapter 11) and, to a small extent, the nitrile resins (Chapter 15). The net result is that in recent years there has been some replacement of PPVC in these areas, in part because of problems of waste disposal. [Pg.357]

The use of ABS has in recent years met considerable competition on two fronts, particularly in automotive applications. For lower cost applications, where demands of finish and heat resistance are not too severe, blends of polypropylene and ethylene-propylene rubbers have found application (see Chapters 11 and 31). On the other hand, where enhanced heat resistance and surface hardness are required in conjunction with excellent impact properties, polycarbonate-ABS alloys (see Section 20.8) have found many applications. These materials have also replaced ABS in a number of electrical fittings and housings for business and domestic applications. Where improved heat distortion temperature and good electrical insulation properties (including tracking resistance) are important, then ABS may be replaced by poly(butylene terephthalate). [Pg.464]

As with poly(ethylene terephthalate) PBT-based copolymers have been introduced to overcome some of the deficiencies of the homopolymer. For example, the rather low notched impact strength of unreinforced grades has been overcome by partial replacement of the terephthalic acid with a longer chain aliphatic dicarboxylic acid. Improved toughness has also been obtained by grafting about 5% of ethylene and vinyl acetate onto the polyester backbone. [Pg.727]

Replacement of hydrogen with chlorine adjacent to the nitrogen in poly-fluoroalkylamines occurs in excellent yield [39 40 (equations 21 and 22)... [Pg.373]

As stated in Section I, columns should be selected so the low molar mass portions of the samples in question can be sufficiently separated from the elution interval of the system peaks. This task cannot always be accomplished, e.g., dimethylacetamide often replaces dimethylformamide as a GPC eluent the analyzed, mostly polar, samples require a neutral salt (e.g., FiBr) (7). The calibration is usually carried out with poly(methylmethacrylate) standards... [Pg.439]

Poly(vinyl chloride) (PVC) has replaced leather in many of its applications PVC tubes and pipes are often used in place of copper. [Pg.270]

Another possible modification of poly(sulfur nitride) that is expected to produce conducting polymers is the replacement of alternating sulfur in the thiazyl chain by an RC unit, i.e., [(R)CNSN]x. This type of polymer would have five r-electrons per four atoms in the repeating unit and, consequently, would have a partially occupied conducting band. The prospect of tuning the electronic properties of this polymer by... [Pg.280]


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See also in sourсe #XX -- [ Pg.49 , Pg.58 ]




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