Resin alcohol components

Quarpel is an important combination of fluorochemical finish and resin-based extender developed by the U.S. Army Natick Laboratories for military use. This finish typicaUy contains 4—6 wt % commercial fluorochemical emulsion, 4—6 wt % resin-based repeUent emulsion, 0.1 wt % acetic acid, and 5 wt % isopropyl alcohol. If necessary, the formulation includes a catalyst to cross-link the resin-based component. Quarpel specifications demand exceUent initial water and oU repeUency and exceUent durabUity to washing and dry cleaning. 

One other substantial development of the 1960s was the use of ureaformalde-hyde-furfuryl alcohol materials as foundry resins, particularly for hot-box operations. The furfuryl alcohol component of the resin is usually in the range 25-40%. 

A large variety of aliphatic compounds exist in the resin as shown in Table 5-4. The amounts of alkanes and alcohols are relatively small, arachinol (C20), behenol (C22), and lignocerol (C24) representing the major alcohol components. Compounds of this type are very lipophilic and stable. 

Triterpenoids occur in hardwood parenchyma resin, and closely related sterols are also present in softwoods (Fig. 5-6). Sterols typefied by the abundant /3-sitosterol, mostly have a hydroxyl group in the C-3 position. They also appear as the alcohol component in fatty acid esters (waxes). Triterpenoids and sterols are sparingly soluble substances contributing to pitch problems in pulping and paper making. Some trees contain polyterpenes and their derivatives known as polyprenols. Betulaprenols, present in birch wood, belong to this category of substances (Fig. 5-7). 

The lipophilic fraction, extractable with nonpolar solvents (ethyl ether, dichloromethane, etc.) consists mainly of fats, waxes, terpenes and terpenoids, and higher aliphatic alcohols (cf. Sections 5.3.1 and 5.3.2). Terpenes, resin acids, and sterols are located in the resin canals present in the bark and also occur in the cork cells and in the pathological exudate (oleore-sin) of wounded bark. Triterpenoids are abundant in bark /3-sitosterol occurs in waxes, as an alcohol component, and the cork cells in the outer bark (periderm) of birch contain large amounts of betulinol (cf. Fig. 5-6). 

Polymer-bound isonitrile (423), obtained from TentaGel-NH2 through treatment of the resin with formic acid and acetic anhydride, followed by dehydration of the resulting formamide with tosyl chloride and pyridine, has been employed in the preparation of N-substituted amino add ester [349]. Thus, Ugi MCR, performed in the presence of an alcohol instead of the carboxylic component, gave rise to an imino-ether spedes (426). Several Lewis acids were tested in searching for optimal reaction conditions. Boron trifluoride etherate displayed the better yields in term of desired product of the Ugi-type reaction. Amino acid methyl esters (427) were thus obtained when using methanol as the alcohol component, after deavage from the resin of the intermediate imino-ethers by an acetone/water mixture (Scheme 87). 

As an alternative to landfilling or high-temperature incineration, the acid-catalyzed decomposition in alcohol efficiently and safely converts the composite materials to alkyl levulinate at moderate temperatures. The product composition obtained by heating particle board chips in ethanol with sulforic acid catalyst for 30 min at 200°C was similar to that obtained from ordinary wood treatment. The charcoal product was removed by filtration the ethanol, water, and ethyl formate product flash-distilled and the ester levulinate separated from the resinous product by extraction into diethyl ether. In this case, the resinous products also contained the UF binding resins that were initially present in the waste board. The UF resin-derived components were intimately mixed with or chemically attached to the lignin resin there was no way to extract and separate the lignin from the UF component. 

Unsaturated poly(ester) resins may be made flame retardant by using bromine-containing or chlorineacid components or alcohol components, for example hexachloroendomethyl-enetetrahydrophthalic acid (HET acid), tetrabromophthahc acid or dibromoneopentyl glycol. Antimony trioxide is frequently used as synergist. 

Uses. Diacetone alcohol is a widely used solvent in the coatings industry where it finds appHcation in hot lacquers which require high boiling components, and in bmshing lacquers where its mild odor, blush resistance, and flow-out properties are desired. Diacetone alcohol is also a solvent for nitrocellulose, cellulose acetate, and epoxy resins. 

In the first step of the reaction, the acetoxylation of propylene is carried out in the gas phase, using soHd catalyst containing pahadium as the main catalyst at 160—180°C and 0.49—0.98 MPa (70—140 psi). Components from the reactor are separated into Hquid components and gas components. The Hquid components containing the product, ahyl acetate, are sent to the hydrolysis process. The gas components contain unreacted gases and CO2. After removal of CO2, the unreacted gases, are recycled to the reactor. In the second step, the hydrolysis, which is an equhibrium reaction of ahyl acetate, an acid catalyst is used. To simplify the process, a sohd acid catalyst such as ion-exchange resin is used, and the reaction is carried out at the fixed-bed Hquid phase. The reaction takes place under the mild condition of 60—80°C and ahyl alcohol is selectively produced in almost 100% yield. Acetic acid recovered from the... 

For aqueous inks, the resins are water- or alkali-soluble or dispersible and the solvent is mosdy water containing sufficient alcohol (as much as 25%) to help solubilize the resin. To keep the alkah-soluble resin in solution, pH must be maintained at the correct level. Advances include the development of uv inks. These are high viscosity inks that require no drying but are photocurable by uv radiation. In these formulations, the solvent is replaced by monomers and photoinitiators that can be cross-linked by exposure to uv radiation. The advantage of this system is the complete elimination of volatile organic compounds (VOC) as components of the system and better halftone print quaUty. Aqueous and uv inks are becoming more popular as environmental pressure to reduce VOC increases. 

The poly(vinyl alcohol) made for commercial acetalization processes is atactic and a mixture of cis- and /n j -l,3-dioxane stereoisomers is formed during acetalization. The precise cis/trans ratio depends strongly on process kinetics (16,17) and small quantities of other system components (23). During formylation of poly(vinyl alcohol), for example, i j -acetalization is more rapid than /ra/ j -acetalization (24). In addition, the rate of hydrolysis of the trans-2iQ. -A is faster than for the <7 -acetal (25). Because hydrolysis competes with acetalization during acetal synthesis, a high cis/trans ratio is favored. The stereochemistry of PVF and PVB resins has been studied by proton and carbon nmr spectroscopy (26—29). 

The major components of camauba wax are aHphatic and aromatic esters of long-chain alcohols and acids, with smaller amounts of free fatty acids and alcohols, and resins. Camauba wax is very hard, with a penetration of 2 dmm at 25°C and only 3 dmm at 43.3°C. Camauba also has one of the higher melting points for the natural waxes at 84°C, with a viscosity of 3960 rare]/s at 98.9°C, an acid number of 8, and a saponification number of 80. 

The major components of candelilla wax are hydrocarbons, esters of long-chain alcohols and acids, long-chain alcohols, sterols, and neutral resins, and long-chain acids. Typically, candelilla wax has a melting point of 70°C, a penetration of 3 drum at 25°C, an acid number of 14, and a saponification number of 55. Principal markets for candelilla include cosmetics, foods, and pharmaceuticals. The FDA affirmed Candelilla as GRAS for certain food apphcations in 21 CFR 184.1976. 

The composition of montan wax depends on the material from which it is extracted, but all contain varying amounts of wax, resin, and asphalt. Black montan wax may be further processed to remove the resins and asphalt, and is known as refined montan wax. White montan wax has been reacted with alcohols to form esters. The wax component of montan is a mixture of long-chain (C24—C q) esters (62—68 wt %), long-chain acids (22—26 wt %), and long-chain alcohols, ketones, and hydrocarbons (7—15 wt %). Cmde montan wax from Germany typically has a melting point of 80°C, an acid number of 32, and a saponification number of 92. 

Polyesters. Polyester is used in embedding resins for electronic components because of its low cost compared to siUcones and epoxides. Polyesters (qv) are condensation products of dicarboxyhc acids and dihydroxy alcohols the reaction provides a wide range of viscosities for polyesters. 

Chemistry of rosin. All three types of rosin consist primarily of C20 mono-carboxylic diterpene resin acids, the most common of which have the molecular formula C20H20O2. In addition, rosins contain small amounts of neutral and other acidic components (e.g. fatty acids in tall oil rosin). The neutral components of rosins are diterpene alcohols, hydrocarbons and aldehydes, and their contents generally vary between 5 and 15 wt%. 

Polymerized Alcohols. Polyhydric alcohols (qv) such as pentaerythritol, sorbitol and glycerin can be used as the polyol component of polyethers (qv) which are used as expl and propint binders. Polyoxypropylene derivs of sorbitol have been employed extensively as components of polyurethane resins (qv), also employed as a propint binder... 

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