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Fatty acids materials

Figure 1. Surface pressure versus area isotherm for a long-chain fatty acid material. Figure 1. Surface pressure versus area isotherm for a long-chain fatty acid material.
In other environments, other microalgae may contribute significantly to the 22 6co3 pool. In Trinity Bay, dinofiagellates were found to be a relatively more important source of fatty acid material before and after the spring bloom (Fig. 3 b). [Pg.200]

The collection of infrared curves of Barnes etal. 944) contains spectra of several fatty acid materials. Barcelo and Bellanato (1953) have reported the spectra of some vegetable oils and compared them with the spectra of long-chain fatty acids and glycerides. Bands displayed by the oils, but not the fatty acids, were found at 1095, 1115, 1140, and 1271 cm Shreve et al. (1950a) have studied long-chain fatty acids,... [Pg.147]

ACCUMULATION OF MVERSlON OF SACCHAROSE RESERVE FORMATION OF FATTY ACIDS MATERIALS... [Pg.136]

To avoid these problems, refiners commonly use additives called detergents" (Hall et al., 1976), (Bert et al., 1983). These are in reality surfactants made from molecules having hydrocarbon chains long enough to ensure their solubility in the fuel and a polar group that enables them to be absorbed on the walls and prevent deposits from sticking. The most effective chemical structures are succinimides, imides, and fatty acid amines. The required dosages are between 500 and 1000 ppm of active material. [Pg.243]

About this time Miss Pockelsf [3] showed how films could be confined by means of barriers thus she found little change in the surface tension of fatty-acid films until they were confined to an area corresponding to about 20 per molecule (the Pockels point). In 1899, Rayleigh [5] commented that a reasonable interpretation of the Pockels point was that at this area the molecules of the surface material were just touching each other. The picture of a surface film... [Pg.101]

Some fairly typical results, obtained by LaMer and co-workers [275] are shown in Fig. IV-24. At the higher film pressures, the reduction in evaporation rate may be 60-90%—a very substantial effect. Similar results have been reported for the various fatty acids and their esters [276,277]. Films of biological materials may offer little resistance, as is the case for cholesterol [278] and dimyristoylphosphatidylcholine (except if present as a bilayer) [279]. [Pg.147]

Prostaglandins arise from unsaturated C20 carboxylic acids such as arachidonic acid (see Table 26 1) Mammals cannot biosynthesize arachidonic acid directly They obtain Imoleic acid (Table 26 1) from vegetable oils m their diet and extend the car bon chain of Imoleic acid from 18 to 20 carbons while introducing two more double bonds Lmoleic acid is said to be an essential fatty acid, forming part of the dietary requirement of mammals Animals fed on diets that are deficient m Imoleic acid grow poorly and suffer a number of other disorders some of which are reversed on feed mg them vegetable oils rich m Imoleic acid and other polyunsaturated fatty acids One function of these substances is to provide the raw materials for prostaglandin biosynthesis... [Pg.1080]

Materials such as fatty acids are added to reduce the surface tension and improve the handling qualities of plastic films. [Pg.1010]

In the area of moleculady designed hot-melt adhesives, the most widely used resins are the polyamides (qv), formed upon reaction of a diamine and a dimer acid. Dimer acids (qv) are obtained from the Diels-Alder reaction of unsaturated fatty acids. Linoleic acid is an example. Judicious selection of diamine and diacid leads to a wide range of adhesive properties. Typical shear characteristics are in the range of thousands of kilopascals and are dependent upon temperature. Although hot-melt adhesives normally become quite brittle below the glass-transition temperature, these materials can often attain physical properties that approach those of a stmctural adhesive. These properties severely degrade as the material becomes Hquid above the melt temperature. [Pg.235]

Eats and oils from a number of animal and vegetable sources are the feedstocks for the manufacture of natural higher alcohols. These materials consist of triglycerides glycerol esterified with three moles of a fatty acid. The alcohol is manufactured by reduction of the fatty acid functional group. A small amount of natural alcohol is also obtained commercially by saponification of natural wax esters of the higher alcohols, such as wool grease. [Pg.446]

Fatty acids are susceptible to oxidative attack and cleavage of the fatty acid chain. As oxidation proceeds, the shorter-chain fatty acids break off and produce progressively higher levels of malodorous material. This condition is known as rancidity. Another source of rancidity in fatty foods is the enzymatic hydrolysis of the fatty acid from the glycerol. The effect of this reaction on nutritional aspects of foods is poorly understood andhttie research has been done in the area. [Pg.117]

One frozen dessert is made with Simplesse, a protein-based fat mimetic that contains no fat (37). Other dairy product developments include a fat flavor, produced by encapsulating milk fatty acids in maltodextrins (38) fat-free cottage cheeses and 2% fat milk, prepared by steam stripping cream with partial fat addback, with a cholesterol level about 60% lower than the starting material (39). [Pg.118]

Fats and oils are one of the oldest classes of chemical compounds used by humans. Animal fats were prized for edibiUty, candles, lamp oils, and conversion to soap. Fats and oils are composed primarily of triglycerides (1), esters of glycerol and fatty acids. However, some oils such as sperm whale (1), jojoba (2), and orange roughy (3) are largely composed of wax esters (2). Waxes (qv) are esters of fatty acids with long-chain aUphatic alcohols, sterols, tocopherols, or similar materials. [Pg.122]

Phospholipids. Glycerides esterified by fatty acids at the 1,2 positions and a phosphoric acid residue at the 3 position constitute the class called phosphoHpids (3). In older Hterature and in commercial practice, these materials are described as phosphatides. [Pg.123]

DeodoriZation. Removal of volatile odorous material and residual fatty acids is the final step ki ok processkig prior to packagkig or filling for bulk shipment (28). The ok is heated to 230—260°C under vacuum. Steam is passed through the ok to assist ki carrying over the volatile material. [Pg.127]

Detergents may be produced by the chemical reaction of fats and fatty acids with polar materials such as sulfuric or phosphoric acid or ethylene oxide. Detergents emulsify oil and grease because of their abiUty to reduce the surface tension and contact angle of water as well as the interfacial tension between water and oil. Recent trends in detergents have been to lower phosphate content to prevent eutrification of lakes when detergents are disposed of in municipal waste. [Pg.135]

The antagonisms that exist between unsaturated fatty acids, and carotene and vitamin E are compHcated and largely undefined. Linoleic acid acts as an antivitamin to i7/-a-tocopherol [59-02-9, 1406-18-9, 10191-41-0] (vitamin E) by reducing availabiHty through direct intestinal destmction. Various Hpoxidases destroy carotenes and vitamin A (73). Dicoumarol [66-76-2] (3,3 -methylenebis(4-hydroxycoumarin)) is a tme antimetaboHte of vitamin K [12001 -79-5] but seems to occur only in clover and related materials that are used primarily as animal feeds (74). [Pg.479]

Tetraethylene glycol may be used direcdy as a plasticizer or modified by esterification with fatty acids to produce plasticizers (qv). Tetraethylene glycol is used directly to plasticize separation membranes, such as siHcone mbber, poly(vinyl acetate), and ceUulose triacetate. Ceramic materials utilize tetraethylene glycol as plasticizing agents in resistant refractory plastics and molded ceramics. It is also employed to improve the physical properties of cyanoacrylate and polyacrylonitrile adhesives, and is chemically modified to form polyisocyanate, polymethacrylate, and to contain siHcone compounds used for adhesives. [Pg.363]

Off-Shoot-O. The methyl esters of the Cg—C 2 fatty acids (40) are collectively sold under the name Off-Shoot-O and are closely related to 1-decanol, the fatty alcohol sold to control axillary shoots in tobacco. The material is a contact-type chemical used to pinch ornamental plants such as a2aleas, cotoneaster, juniper Juniperus sp. privet, rhamnus, and taxus (Taxus sp. sp.). As a result of treatment the shmbs become bushier. The mode of action is by plasmolysis of the young, sensitive tissues. Therefore, appHcation timing may be critical. [Pg.426]

In certain brilliantine compositions, vegetable and animal oils are used as substitutes for mineral oil. In these systems, because of their potential for rancidity, antioxidants must be included. Other alternatives to mineral oils that have found utiHty in brilliantines are the polyethylene glycols which come in a variety of solubiHties and spreading properties. Use of these materials offers the advantage of chemical stabiHty to rancidity. Other additives found in brilliantines to improve their aesthetics include colorants, fragrance, medicated additives, lanolin, and fatty acid esters. [Pg.451]

Alkyd resins are produced by reaction of a polybasic acid, such as phthaUc or maleic anhydride, with a polyhydric alcohol, such as glycerol, pentaerythritol, or glycol, in the presence of an oil or fatty acid. The resulting polymeric material can be further modified with other polymers and chemicals such as acryhcs, siUcones, and natural oils. On account of the broad selection of various polybasic acids, polyhydric alcohols, oils and fatty acids, and other modifying ingredients, many different types of alkyd resins can be produced that have a wide range of coating properties (see Alkyd resins). [Pg.541]

Defoamers (qv) are available in several forms, composed of many different materials. Historically, paste and soHd defoamers were used extensively. Composed of fatty acids, fatty amides, fatty alcohols, emulsifiers (and mineral oil [8012-95-1] in the high soflds paste emulsions), these defoamers required emulsification (brick) or dilution (paste) before use. Liquid defoamers have become the preferred form, insofar as concern about handling and ovemse have been overcome. [Pg.16]

Emulsifiers are incorporated in oil and synthetic mud formulations to maintain a stable emulsion of the internal brine phase. These materials include calcium and magnesium soaps of fatty acids and polyamines and amides and their mixtures (123,127). The specific chemistry of these additives depends on the nature of the continuous phase of the mud, ie, whether diesel oil, mineral oil, or a synthetic Hquid. Lime is added along with the fatty acid to form the... [Pg.182]

Erodings of Slow-Releasing Core Tablets. The sustained-dose portion of a dmg is granulated with hydrophobic materials such as waxes, fatty acids, or fatty alcohols and compressed into a core. The initial dose is added to the core by a modified sugar coating process or by compression coating. Thus, a tablet within a tablet is created. The core erodes slowly to release the active ingredient. [Pg.231]

Reaction with Fatty Acids and Esters. Alkanolamines and long-chain fatty acids react at room temperature to give neutral alkanolamine soaps, which are waxy, noncrystaUine materials with widespread commercial appHcations as emulsifiers. At elevated temperatures, 140 —160°C, A/-aIkanolamides are the main products, at a 1 1 reaction ratio (7,8). [Pg.5]


See other pages where Fatty acids materials is mentioned: [Pg.126]    [Pg.3224]    [Pg.147]    [Pg.858]    [Pg.126]    [Pg.3224]    [Pg.147]    [Pg.858]    [Pg.184]    [Pg.381]    [Pg.384]    [Pg.485]    [Pg.1008]    [Pg.351]    [Pg.443]    [Pg.446]    [Pg.446]    [Pg.88]    [Pg.123]    [Pg.129]    [Pg.133]    [Pg.136]    [Pg.232]    [Pg.476]    [Pg.479]    [Pg.103]    [Pg.248]    [Pg.322]    [Pg.390]   
See also in sourсe #XX -- [ Pg.115 ]




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Acidic materials

Crystalline material, fatty acids

Fatty materials

Incorporation of monomeric cyclic fatty acids into biological material

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