Hydrocarbon Backbone

AH corrosion inhibitors in use as of this writing are oil-soluble surfactants (qv) which consist of a hydrophobic hydrocarbon backbone and a hydrophilic functional group. Oil-soluble surfactant-type additives were first used in 1946 by the Sinclair Oil Co. (38). Most corrosion inhibitors are carboxyhc acids (qv), amines, or amine salts (39), depending on the types of water bottoms encountered in the whole distribution system. The wrong choice of inhibitors can lead to unwanted reactions. Eor instance, use of an acidic corrosion inhibitor when the water bottoms are caustic can result in the formation of insoluble salts that can plug filters in the distribution system or in customers vehicles. Because these additives form a strongly adsorbed impervious film at the metal Hquid interface, low Hquid concentrations are usually adequate. Concentrations typically range up to 5 ppm. In many situations, pipeline companies add their own corrosion inhibitors on top of that added by refiners. 

The specialty class of polyols includes poly(butadiene) and polycarbonate polyols. The poly(butadiene) polyols most commonly used in urethane adhesives have functionalities from 1.8 to 2.3 and contain the three isomers (x, y and z) shown in Table 2. Newer variants of poly(butadiene) polyols include a 90% 1,2 product, as well as hydrogenated versions, which produce a saturated hydrocarbon chain [28]. Poly(butadiene) polyols have an all-hydrocarbon backbone, producing a relatively low surface energy material, outstanding moisture resistance, and low vapor transmission values. Aromatic polycarbonate polyols are solids at room temperature. Aliphatic polycarbonate polyols are viscous liquids and are used to obtain adhesion to polar substrates, yet these polyols have better hydrolysis properties than do most polyesters. 

Just as the alkanes and alkenes had general formulas, the carbon derivatives all have general formulas. The hydrocarbon backbone provides a portion of the general formula, and the functional group provides the other part. In each case, the hydrocarbon derivative is represented by the formula R-, and the hydrocarbon backbone has its own specific formula. The term substituted hydrocarbon is another name for hydrocarbon derivative, because the functional group is substituted for one or more hydrogen atoms in the chemical reaction. 

Whenever a hydrocarbon backbone has two hydroxyl radicals attached to it, it becomes a special type of alcohol known as a glycol. The simplest of the glycols, and the most important, is ethylene glycol, whose molecular formula C2H4(OH)2. The molecular formula can also be written CHjOHCHjOH and may be printed as such on some labels. Ethylene glycol is a colorless, thick liquid with a sweet taste, is toxic by ingestion and by inhalation, and among its many uses is a permanent antifreeze and coolant for automobiles. It is a combustible liquid with a flash point of 240"F. 

The last group of substituted hydrocarbons produced by adding hydroxyl radicals to the hydrocarbon backbone are the compounds made when three hydroxyl radicals are substituted these are known as glycerols. The name of the simplest of this type of compound is just glycerol. Its molecular formula is 3115(011)3. Glycerol is a colorless, thick, syrupy liquid with a sweet taste, and has a flash point of 320°F, and is used to make such diverse products as candy and explosives, plus many more. Other glycerols are made, but most of them are not classified as hazardous materials. 

The ethers are a group of compounds with the general formula R-O-R . The R, of course, stands for any hydrocarbon backbone, and the R also stands for any hydrocarbon backbone, but the designation R is used to indicate that the second hydrocarbon backbone may be different from the first. In other words, both the hydrocarbon backbones in the formula may be the same, but the is used to indicate that it may also be different. R-O-R as the general formula for the ethers is also correct. The fact that there are two hydrocarbon backbones on either side of an oxygen atom means that there will be two hydrocarbon names used. 

The simplest of the ethers would be ether that has the simplest hydrocarbon backbones attached those backbones are the radicals of the simplest hydrocarbon, methane. Therefore, the simplest of the ethers is dimethyl ether, whose formula is CH3OCH3. Dimethyl is used because there are two methyl radicals, and di-" is the prefix for two. This compound could also be called methyl methyl ether, or just... 

The next simplest ether is the ether with the simplest alkane as one of the hydrocarbon backbones and the next alkane, which is methyl ethyl ether. Its molecular formula is CH3OC2H5. It is a colorless gas with the characteristic ether odor. It has a flash point of 31 °F, and an ignition temperature of only 374°F. This property, of course, makes it an extreme fire and explosion hazard. 

MMA onto cellulose was carried out by Hecker de Carvalho and Alfred using ammonium and potassium persulfates as radical initiators [30]. Radical initiators such as H2O2, BPO dicumylperoxide, TBHP, etc. have also been used successfully for grafting vinyl monomers onto hydrocarbon backbones, such as polypropylene and polyethylene. The general mechanism seems to be that when the polymer is exposed to vinyl monomers in the presence of peroxide under conditions that permit decomposition of the peroxide to free radicals, the monomer becomes attached to the backbone of the polymer and pendant chains of vinyl monomers are grown on the active sites. The basic mechanism involves abstraction of a hydrogen from the polymer to form a free radical to which monomer adds ... 

Epoxides are often encountered in nature, both as intermediates in key biosynthetic pathways and as secondary metabolites. The selective epoxidation of squa-lene, resulting in 2,3-squalene oxide, for example, is the prelude to the remarkable olefin oligomerization cascade that creates the steroid nucleus [7]. Tetrahydrodiols, the ultimate products of metabolism of polycyclic aromatic hydrocarbons, bind to the nucleic acids of mammalian cells and are implicated in carcinogenesis [8], In organic synthesis, epoxides are invaluable building blocks for introduction of diverse functionality into the hydrocarbon backbone in a 1,2-fashion. It is therefore not surprising that chemistry of epoxides has received much attention [9]. 

Ionic polymers are a special class of polymeric materials having a hydrocarbon backbone containing pendant acid groups. These are then neutralized partially or fully to form salts. lonomeric TPEs are a class of ionic polymers in which properties of vulcanized rubber are combined with the ease of processing of thermoplastics. These polymers contain up to 10 mol% of ionic group. These ionomeric TPEs are typically prepared by copolymerization of a functionalized monomer with an olefinic unsamrated monomer or direct functionalization of a preformed polymer [68-71]. The methods of preparation of various ionomeric TPEs are discussed below. 

Polymers used in medicine fall into two main categories those that are sufficiently inert to fulfill a long-term structural function as biomaterials or membranes, and those that are sufficiently hydrolytically unstable to function as bioeradible materials, either in the form of sutures or as absorbable matrices for the controlled release of drugs. For the synthetic organic polymers widely used in biomedicine this often translates to a distinction between polymers that have a completely hydrocarbon backbone and those that have sites in the backbone that are hydrolytically sensitive. Ester, anhydride, amide, or urethane linkages in the backbone usually serve this function. 

The double bond of maleic anhydride may undergo free radical polymerization with the proper initiator. Polymers of maleic anhydride (or copolymers made with another monomer) are commercially available (Polysciences). They consist of a linear hydrocarbon backbone (formed from the polymerization of the vinyl groups) with cyclic anhydrides repeating along the chain. Such polymers are highly reactive toward amine-containing molecules. 

Radicals are referred to as hydrocarbon "backbones". As an example, isobutane is more properly named methyl propane. Another isomer with a different proper name is isopentane, more properly called methyl butane. Neopentane is also named 2,2-dimethyl propane. 

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