Drying oils, polymerization

CH2=CHC = CCH = CH2. a colourless liquid which turns yellow on exposure to the air it has a distinct garlic-like odour b.p. 83-5°C. Manufactured by the controlled, low-temperature polymerization of acetylene in the presence of an aqueous solution of copper(I) and ammonium chlorides. It is very dangerous to handle, as it absorbs oxygen from the air to give an explosive peroxide. When heated in an inert atmosphere, it polymerizes to form first a drying oil and finally a hard, brittle insoluble resin. Reacts with chlorine to give a mixture of chlorinated products used as drying oils and plastics. 

Synthetic resins, such as phenoHc and cresyUc resins (see Phenolic resins), are the most commonly used friction material binders, and are usually modified with drying oils, elastomer, cardanol [37330-39-5] an epoxy, phosphoms- or boron-based compounds, or even combinations of two. They ate prepared by the addition of the appropriate phenol and formaldehyde [50-00-0] in the presence of an acidic or basic catalyst. Polymerization takes place at elevated temperatures. Other resin systems are based on elastomers (see Elastomers, synthetic), drying oils, or combinations of the above or other polymers. 

Maleic anhydride is important as a chemical hecause it polymerizes with other monomers while retaining the double bond, as in unsaturated polyester resins. These resins, which represent the largest end use of maleic anhydride, are employed primarily in fiber-reinforced plastics for the construction, marine, and transportation industries. Maleic anhydride can also modify drying oils such as linseed and sunflower. 

The product of cross-linking and oxidation processes in drying oils is described as a porous polymeric fraction with a wide range of molecular weight. The chemical structure that can be influenced by age, thickness and the presence of pigments, while nonbonded species are present in the interstices free mono- and dicarboxylic acids, mono-, di- and triglycerides, aldehydes, ketones, etc. 

Phenolic novolacs, 18 760-761 Phenolic resin adhesives, 18 783-784 Phenolic resin can coatings, 18 38 Phenolic resin composites, 18 792-794 Phenolic resin drying-oil varnishes, 18 783 Phenolic resin fibers, 18 797-798 mechanical properties of, 18 798 Phenolic resin foam, 18 795-796 Phenolic resin manufacturers, U.S., 18 774 Phenolic resin polymerization, 18 760-765 alkaline catalysts in, 18 762-765 neutral catalysts in, 18 761-762 strong-acid catalysts in, 18 760-761 Phenolic resin prepregs, 18 793 Phenolic resin production unit, 18 766 Phenolic resins, 10 409 18 754-755, 756-802 22 10 26 763 in abrasive materials, 18 786-787 in air and oil filters, 18 790 additional reactants in, 18 759 analytical methods for, 18 774-779 applications of, 18 781-798 batch processes for, 18 766 from biomass and biochemical processes, 18 769-770... 

Uses. Comonomer for preparation of cross-linked polymers in production of ion exchange beads and gel permeation chromatography polystyrene beads polymerization monomer for synthetic rubber, drying oils, and casting resins... 

Formation of peroxides by exposure to air and their involvement in polymerization processes is important for surface coating formulations containing polyunsaturated lipids called drying oils. Also nondrying oils, such as soybean oil, are under development as renewable sources for plastics and resins " . ... 

In chromatographic techniques, qualitative identitication of organic binders requires quantitication of species obtained from the original polymeric materials amino acids from proteins, fatty acids from drying oils, or monosaccharides in plant gums. 

For the structural analysis of cyclic fatty acid derivatives (polymerized drying oils, copolymerization products of fatty oils with various hydrocarbons), in principle the same graphical methods can be developed as have been described for the investigation of hydrocarbon mixtures. However, the construction of useful graphical representations is hampered by the fact that reliable data on physical constants are restricted to the normal saturated fatty acids and their methyl and ethyl esters the synthesis of pure unsaturated fatty acids is already extremely difficult, to say nothing of more complicated cyclic or branched compounds. 

Graphical representation of the activation and polymerization phenomena of drying oils is possible by means of the specific refraction and the iodine value74, as shown in Fig. 84. 

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