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  2. Acrylic acid - Wikipedia

    en.wikipedia.org/wiki/Acrylic_acid

    Acrylic acid and its esters readily combine with themselves (to form polyacrylic acid) or other monomers (e.g. acrylamides, acrylonitrile, vinyl compounds, styrene, and butadiene) by reacting at their double bond, forming homopolymers or copolymers, which are used in the manufacture of various plastics, coatings, adhesives, elastomers, as well ...

  3. Potassium polyacrylate - Wikipedia

    en.wikipedia.org/wiki/Potassium_polyacrylate

    The immense size and weight of its molecular structure allows each potassium polyacrylate granule to absorb purified water of over 500 times its dry weight. The polyacrylate structure does not bind water very tightly - a plant's root suction is sufficient to release just the requested amount - but tightly enough to prevent waterlogging or other ...

  4. Polyacrylic acid - Wikipedia

    en.wikipedia.org/wiki/Polyacrylic_acid

    Polyacrylic acid is a weak anionic polyelectrolyte, whose degree of ionisation is dependent on solution pH. In its non-ionised form at low pHs, PAA may associate with various non-ionic polymers (such as polyethylene oxide, poly-N-vinyl pyrrolidone, polyacrylamide, and some cellulose ethers) and form hydrogen-bonded interpolymer complexes. [17]

  5. Acrylate polymer - Wikipedia

    en.wikipedia.org/wiki/Acrylate_polymer

    Acrylic elastomer is a general term for a type of synthetic rubber whose primary component is acrylic acid alkyl ester (ethyl or butyl ester). [3] Acrylic elastomer possesses characteristics of heat and oil resistance, with the ability to withstand temperatures of 170–180 °C. It is used primarily for producing oil seals and packaging related ...

  6. Acrylate - Wikipedia

    en.wikipedia.org/wiki/Acrylate

    Acrylates (IUPAC: prop-2-enoates) are the salts, esters, and conjugate bases of acrylic acid. The acrylate ion is the anion CH 2 =CHCO − 2. Often, acrylate refers to esters of acrylic acid, the most common member being methyl acrylate. These acrylates contain vinyl groups.

  7. Butyl acrylate - Wikipedia

    en.wikipedia.org/wiki/Butyl_acrylate

    Butyl acrylate is of low acute toxicity with an LD 50 (rat) of 3143 mg/kg. [4]In rodent models, butyl acrylate is metabolized by carboxylesterase or reactions with glutathione; this detoxification produces acrylic acid, butanol, and mercapturic acid waste, which are excreted.

  8. 2-Acrylamido-2-methylpropane sulfonic acid - Wikipedia

    en.wikipedia.org/wiki/2-Acrylamido-2-methyl...

    2-Acrylamido-2-methylpropane sulfonic acid (AMPS [1]) was a Trademark name by The Lubrizol Corporation. It is a reactive, hydrophilic, sulfonic acid acrylic monomer used to alter the chemical properties of wide variety of anionic polymers. In the 1970s, the earliest patents using this monomer were filed for acrylic fiber manufacturing.

  9. Polycarboxylates - Wikipedia

    en.wikipedia.org/wiki/Polycarboxylates

    Polycarboxylates are organic compounds with several carboxylic acid groups. Butane-1,2,3,4-tetracarboxylate is one example. Often, polycarboxylate refers to linear polymers with a high molecular mass (M r ≤ 100 000) and with many carboxylate groups. They are polymers of acrylic acid or copolymers of acrylic acid and maleic acid.