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Polystyrene anhydride

Acetylation of aniline with polystyrene anhydride gives benzanilide in 90% yield. Similarly, ethyl benzoate is obtained in 90% yield by acylation of ethanol. [Pg.24]


Engineering resins can be combined with either other engineering resins or commodity resins. Some commercially successhil blends of engineering resins with other engineering resins include poly(butylene terephthalate)—poly(ethylene terephthalate), polycarbonate—poly(butylene terephthalate), polycarbonate—poly(ethylene terephthalate), polysulfone—poly (ethylene terephthalate), and poly(phenylene oxide)—nylon. Commercial blends of engineering resins with other resins include modified poly(butylene terephthalate), polycarbonate—ABS, polycarbonate—styrene maleic anhydride, poly(phenylene oxide)—polystyrene, and nylon—polyethylene. [Pg.277]

Formic anhydride is not stable. However, formate esters of alcohols and phenoHcs can be prepared using formic—acetic anhydride (69,70). Anhydrides can also be incorporated into polystyrene backbones which can then be treated with alcohols to afford the corresponding esters and carboxypolystyrene for recycle (71). [Pg.380]

Until the mid-1950s the main raw material source for the European plastics industry was coal. On destructive distillation coal yields four products coal tar, coke, coal gas and ammonia. Coal tar was an important source of aromatic chemicals such as benzene, toluene, phenol, naphthalene and related products. From these materials other chemicals such as adipic acid, hexamethylenedia-mine, caprolactam and phthalic anhydride could be produced, leading to such important plastics as the phenolic resins, polystyrene and the nylons. [Pg.9]

In the case of EVOH being used as an interlayer with polyethylene or polystyrene, it is necessary to use additional adhesive layers such as an ethylene-vinyl acetate-maleic anhydride terpolymer (e.g. Orevac— Atochem). [Pg.395]

The largest user of phenol in the form of thermosetting resins is the plastics industry. Phenol is also used as a solvent and in the manufacture of intermediates for pesticides, pharmaceuticals, and dyestuffs. Styrene is used in the manufacture of synthetic rubber and polystyrene resins. Phthalic anhydride is used in the manufacture of DMT, alkyd resins, and plasticizers such as phthalates. Maleic anhydride is used in the manufacture of polyesters and, to some extent, for alkyd resins. Minor uses include the manufacture of malathion and soil conditioners. Nitrobenzene is used in the manufacture of aniline, benzidine, and dyestuffs and as a solvent in polishes. Aniline is used in the manufacture of dyes, including azo dyes, and rubber chemicals such as vulcanization accelerators and antioxidants. [Pg.55]

D. Acylation Reaction of Polystyrene with Maleic Anhydride and Acetic Anhydride... [Pg.266]

PP-g-AA - acrylic acid grafted polypropylene PP-g-MAH - maleic anhydride grafted polypropylene PPacr - acrylic acid grafted polypropylene PPmal - maleic anhdride grafted polypropylene PPS - polyphenylene sulfide PS - polystyrene... [Pg.683]

Hydroxamic acids are an important class of compounds targeted as potential therapeutic agents. A-Fmoc-aminooxy-2-chlorotrityl polystyrene resin 61 allowed the synthesis and subsequent cleavage under mild conditions of both peptidyl and small molecule hydroxamic acids (Fig. 14) [70]. An alternative hydroxylamine linkage 62 was prepared from trityl chloride resin and tV-hydroxyphthalimide followed by treatment with hydrazine at room temperature (Scheme 30) [71]. A series of hydroxamic acids were prepared by the addition of substituted succinic anhydrides to the resin followed by coupling with a variety of amines, and cleavage with HCOOH-THF(l 3). [Pg.203]

Stabilizing agents are used to maintain drilling fluid rheological properties at highly elevated downhole temperatures. Chromium and chromium-free lignosulfonates, polyglycol ethers, sodium polystyrene sulfonate-co-maleic anhydride), and a melanin polymer have been used in this application. Additives such as sodium diethyldi-thiocarbamate have been used to stabilize aqueous polysaccharides such as xanthan gum (18). [Pg.12]

By using a combination of RAFT and ring opening polymerization (ROP), (polyethylene oxide) methyl ether)(polystyrene)(poly(L-lactide) 3-miktoarm star terpolymers have been successfully synthesized [182]. The synthetic approach involved the reaction of the cw-functionalized - OH group of the poly(ethylene oxide) methyl ether with maleic anhydride under conditions where only one hydroxyl group can be esterified (MPEO). The double bond... [Pg.109]

In order to compare efficacies, the scavenging was studied under conventional (room temperature) and microwave conditions (Fig. 7.11). At room temperature, the polystyrene-based diamine (3.0 equivalents of the amine functionality) required 1-2 h for complete sequestration of the excess anhydride. In contrast, under sealed-vessel microwave heating, this was accelerated to completion within 5-10 min. [Pg.384]

The earliest published example of microwave-assisted SPOS involved diisopropyl-carbodiimide (DlC)-mediated solid-phase peptide couplings [24], Numerous Fmoc-protected amino acids and peptide fragments were coupled with glycine-preloaded polystyrene Wang resin (PS-Wang) in DMF, using either the symmetric anhydride or preformed N-hydroxybenzotriazole active esters (HOBt) as precursors (Scheme 12.1). [Pg.407]

In a more recent study using dedicated multimode microwave reactors for chemical synthesis, which enable temperature and power control, it was demonstrated that microwave irradiation could be effectively employed to couple aromatic carboxylic acids to polystyrene Wang resin [25], if the symmetrical anhydride procedure was used, and not the three-component O-acylisourea activation method [19]. Almost quantitative loading was achieved in l-methyl-2-pyrrolidone (NMP) at 200 °C within 10 min under... [Pg.407]

Polymer Media Polymaleic Anhydride Poly Acrylic Acid Polyvinyl Phosphonic Acid Polyvinyl Sulfonic Acid Polystyrene Sulfonate Tripoly Phosphate... [Pg.28]

The mild conditions employed for the activation of sulfoxides, and the high reactivity of the glycosyl donor, suggested that the method might translate well to the solid phase. Moreover, the nonpolar nature of the sulfoxide, triflic anhydride, and DTBMP (solution-based reagents) should enable them to partition effectively into a non-polar, polystyrene-based resin. [Pg.50]

Polystyrene insulation on magnet wire 0.49 Encapsulated with phthalic anhydride cured bisphenol A-epichlorohydrin epoxide (epoxy hot melt cast). Impregnated. [Pg.158]

The heat distortion temperature of styrene polymers is insufficient for some applications, but can be improved by copolymerization with monomers such as -methylstyrene or maleic anhydride. Maleic anhydride copolymers are excellently suited to the manufacture of foamed articles. The advantages of glass-fiber reinforcement are greater in such copolymers than in polystyrene itself. [Pg.280]


See other pages where Polystyrene anhydride is mentioned: [Pg.24]    [Pg.24]    [Pg.231]    [Pg.135]    [Pg.19]    [Pg.896]    [Pg.675]    [Pg.682]    [Pg.31]    [Pg.32]    [Pg.88]    [Pg.75]    [Pg.21]    [Pg.27]    [Pg.333]    [Pg.365]    [Pg.381]    [Pg.743]    [Pg.180]    [Pg.85]    [Pg.115]    [Pg.132]    [Pg.1065]    [Pg.466]    [Pg.200]   
See also in sourсe #XX -- [ Pg.24 ]




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