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  2. Polyphenylene sulfide - Wikipedia

    en.wikipedia.org/wiki/Polyphenylene_sulfide

    The PPS (polyphenylene sulfide) polymer is formed by reaction of sodium sulfide with 1,4-dichlorobenzene: n ClC 6 H 4 Cl + n Na 2 S → [C 6 H 4 S] n + 2n NaCl Hill and Edmonds, developers of PPS. The process for commercially producing this material was initially developed by Dr. H. Wayne Hill Jr. and James T. Edmonds at Phillips Petroleum. [7]

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  5. Polysulfide - Wikipedia

    en.wikipedia.org/wiki/Polysulfide

    Fragment of the solid-state structure of Na 2 S 5. The S 2− 5 chain consists of the yellow-colored atoms. [3] The alkali metal polysulfides arise by treatment of a solution of the sulfide with elemental sulfur, e.g. sodium sulfide to sodium polysulfide: S 2− + n SS 2− n+1

  6. Polyphenylsulfone - Wikipedia

    en.wikipedia.org/wiki/Polyphenylsulfone

    PPSF is a moldable plastic often used in rapid prototyping and rapid manufacturing (direct digital manufacturing) applications.Polyphenylsulfone is heat and chemical-resistant suited for automotive, aerospace, and plumbing applications.

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  8. Polyphenyl ether - Wikipedia

    en.wikipedia.org/wiki/Polyphenyl_ether

    Polyphenyl ethers (PPEs) are obtained by repeated application of the Ullmann Ether Synthesis: reaction of an alkali-metal phenate with a halogenated benzene catalyzed by copper. [ 1 ] PPEs of up to 6 phenyl rings, both oxy and thio ethers, are commercially available.

  9. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    Sulfide is an angular functional group, the C–S–C angle approaching 90° The C–S bonds are about 180 pm. For the prototype, dimethylsulfide, the C-S-C angles is 99°, which is smaller than the C-O-C angle in ether (~110°). The C-S distance in dimethylsulfide is 1.81 Å. [3]

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