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Cycloaliphatic structures

Rosin is compatible with many materials because of its polar functionality, cycloaliphatic structure, and its low molecular weight. It has an acid number of ca 165 and a saponification number of ca 170. It is soluble in aliphatic, aromatic, and chlorinated hydrocarbons, as well as esters and ethers. Because of its solubility and compatibility characteristics, it is useful for modifying the properties of many polymers. [Pg.138]

Utilisation of sucrose as a starter polyol for rigid polyether polyols is extremely advantageous from the economic point of view. Sucrose is in fact a renewable raw material, commercialised on a large scale and available in a high purity form. The cycloaliphatic structure and the high functionality lead to high performance rigid polyether polyols. [Pg.362]

A very interesting natural diol with cycloaliphatic structure is betulinol, extracted from birch bark [16-18], which is a triterpene diol, having one primary and one secondary hydroxyl group (Figure 17.4). [Pg.440]

Thus, the dimerisation of unsaturated fatty acids takes place at higher temperatures in the presence of catalysts (for example acidic clays, montmorillonite type). One molecule of oleic acid (having one double bond) reacts with one mol of linoleic acid (having two double bonds) and this forms a dimeric acid with a cycloaliphatic structure. [Pg.466]

Table 9.5 presents families of random copolymers with cycloaliphatic structures in the main chain or in side groups that are appropriate for lithographic applications. Cycloaliphatic moieties, such as adamantyl groups, offer etch durability, while carboxylic acid groups, which become available through amplified deprotection processes, impart base solubility. [Pg.244]

The polyarylenesterketones have been obtained [399], which contain blocks of polyarylesterketones, block of triphenylphosphite oxide and those of binding agent into the cycloaliphatic structures. The film materials on their basis are used as pol5mier binder in thermal control coatings. [Pg.158]

Glycidyl esters of cycloaliphatic structures were initially investigated by Shell and Bayer in Europe. (14)... [Pg.305]

On the other hand. Pis containing cycloaliphatic structures are expected to have better transparency than aromatic ones, due to the prohibition of electron conjugation by the introduction of alicyclic moieties [45]. This property is a key factor in visualization of the cell culture morphology development on the patterned polymer substrate, but it is also required to obtain liquid crystal devices with good quality. Optical transparency of Epiclon-derived PI films was evaluated in the range of 290-1100 nm (Figure 4). The combination in the PI... [Pg.174]

Because of the compact structure of the cycloaliphatic resins the intensity of cross-linking occurring after cure is greater than with the standard diglycidyl ethers. The lack of flexibility of the molecules also leads to more rigid segments between the cross-links. [Pg.765]

The thermal properties of the resin are dependent on the degree of cross-linking, the flexibility of the resin molecule and the flexibility of the hardener molecule. Consequently the rigid structures obtained by using cycloaliphatic resins or hardeners such as pyromellitic dianhydride will raise the heat distortion temperatures. [Pg.772]

Cyclic Hydrocarbons. These are structures in which the carbon atoms form a ring instead of an open chain. They are also called carbocyclic or homocyclic compounds. They are divided into two classes alicyclic (or cycloaliphatic) and aromatic compounds. [Pg.308]

One of these products was a thermally stable insoluble chlorocarbon prepared from cyclooctadiene and hexachlorocyclopentadiene. The diadduct, dodecachlor-dodecahydrodi-methanodibenzo [a, e] cyclooctene, has the structure given in I and is commonly referred to as a cycloaliphatic chlorine compound (7). [Pg.90]

Telechelic polymers rank among the oldest designed precursors. The position of reactive groups at the ends of a sequence of repeating units makes it possible to incorporate various chemical structures into the network (polyether, polyester, polyamide, aliphatic, cycloaliphatic or aromatic hydrocarbon, etc.). The cross-linking density can be controlled by the length of precursor chain and functionality of the crosslinker, by molar ratio of functional groups, or by addition of a monofunctional component. Formation of elastically inactive loops is usually weak. Typical polyurethane systems composed of a macromolecular triol and a diisocyanate are statistically simple and when different theories listed above are... [Pg.131]

The acyclic terpenes are discussed separately in Section 2.2. Some of the cycloaliphatic fragrance and flavor materials are structurally related to the cyclic terpenes and are, therefore, discussed in Section 2.4 after the cyclic terpenes. [Pg.8]

In addition to cyclic terpenoids, several other cycloaliphatic compounds have above-average importance as fragrance materials some of them are structurally related to the terpenes. [Pg.75]

Specialty Epoxy Resins. In addition to bisphenol, other polyols such as aliphatic glycols and novolaks are used to produce specialty resins. Epoxy resins may also include compounds based on aliphatic, cycloaliphatic, aromatic, and heterocyclic backbones. Glycidylation of active hydrogen-containing structures with epichlorohydrin and epoxidation of olefins with peracetic acid remain the important commercial procedures for introducing the oxirane group into various precursors of epoxy resins. [Pg.363]

In this paper, we have evaluated three different protocols for the preparation of AQ-enzyme film using choline and glucose oxidases and mixture of AQ 29D and AQ 55D (1 1). This AQ mixture is recommended by Eastman Kodak to increase the adherency of the film to a surface such as a platinum electrode (17). The values 29 and 55 represent the glass transition temperature of each polymer. Also, the main structural difference between the two polymers is that, in the case of AQ 55D, an aliphatic glycol moiety replaces the cycloaliphatic glycol moiety found in the AQ29 (17,18). [Pg.29]

Cyclopolymerisation leading to polymers with monocyclic units in the main chain proceeds in two steps the first step involves a 1,2-insertion of the coordinated a, ffl-diolefin via one olefinic bond, and the second step, which is a ringclosing reaction, involves an intramolecular insertion of the other olefinic bond undergoing coordination scheme (89) presents both steps for 1,5-hexadiene cyclopolymerisation leading to a cycloaliphatic polymer with poly(methylene-1,3-cyclopentane) structural units [30,450,497] ... [Pg.194]

In the case of the formation of a cycloaliphatic polymer with bicyclic units in the main chain, such as the polymer with poly[methylene-l,3-(2,5-methanocy-clohexane)] structural units obtained in the cyclopolymerisation of 3-vinyl-1,5-hexadiene, the intramolecular insertion, analogous to that presented in scheme (89), is followed by another intramolecular insertion involving a vinyl substituting group ... [Pg.194]


See other pages where Cycloaliphatic structures is mentioned: [Pg.137]    [Pg.307]    [Pg.362]    [Pg.634]    [Pg.322]    [Pg.548]    [Pg.2657]    [Pg.206]    [Pg.201]    [Pg.476]    [Pg.79]    [Pg.137]    [Pg.307]    [Pg.362]    [Pg.634]    [Pg.322]    [Pg.548]    [Pg.2657]    [Pg.206]    [Pg.201]    [Pg.476]    [Pg.79]    [Pg.294]    [Pg.82]    [Pg.242]    [Pg.286]    [Pg.12]    [Pg.187]    [Pg.230]    [Pg.586]    [Pg.117]    [Pg.359]    [Pg.577]    [Pg.578]    [Pg.364]    [Pg.541]    [Pg.542]    [Pg.2337]    [Pg.87]    [Pg.4]   
See also in sourсe #XX -- [ Pg.158 ]

See also in sourсe #XX -- [ Pg.79 , Pg.80 , Pg.81 , Pg.82 , Pg.83 , Pg.84 , Pg.85 , Pg.86 ]




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Cross-linking cycloaliphatic structures

Cycloaliphatic

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