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Oleics

HOOO(CH2)7COOH. Colourless plates, m.p. lOfi C. Made by the oxidation of oleic acid with ozones. [Pg.47]

The oleic acid series, C H2n-202 with one double bond, of which acrylic acid is the lowest member. [Pg.173]

Colourless liquid. B.p. 286 C/100 mm., insoluble in water. Oleic acid occurs naturally in larger quantities than any other fatty acid, being present as glycerides in most fats and oils. It forms one third of the total fatty acids of cow s milk. A crude grade from inedible tallow is used in the production of lubricants, detergents, resins and other products. [Pg.287]

HOOC-[CHa]8-COOH, CioH.aO. Colourless leaflets m.p. 134°C. Manufactured by heating castor oil with alkalis or by distillation of oleic acid. Forms an anhydride, m.p. 78 C. The esters of sebacic acid are used as plasticizers, especially for vinyl resins. [Pg.354]

SNG Substitute natural gas. soaps Sodium and potassium salts of fatty acids, particularly stearic, palmitic and oleic acids. Animal and vegetable oils and fats, from which soaps are prepared, consist essentially of the glyceryl esters of these acids. In soap manufacture the oil or fat is heated with dilute NaOH (less frequently KOH) solution in large vats. When hydrolysis is complete the soap is salted out , or precipitated from solution by addition of NaCl. The soap is then treated, as required, with perfumes, etc. and made into tablets. [Pg.362]

C8Hi7CH=CH(CH2)7COOH Oleic acid c/s-9-Octadecenoic acid... [Pg.103]

Spreading velocities v are on the order of 15-30 cm/sec on water [39], and v for a homologous series tends to vary linearly with the equilibrium film pressure, it", although in the case of alcohols a minimum seemed to be required for v to be appreciable. Also, as illustrated in Fig. IV-3, substrate water is entrained to some depth (0.5 mm in the case of oleic acid), a compensating counterflow being present at greater depths [40]. Related to this is the observation that v tends to vary inversely with substrate viscosity [41-43]. An analysis of the stress-strain situation led to the equation... [Pg.110]

Fig. IV-3. Velocity profiles for particles suspended in water with elapsed time, due to spreading of oleic acid. Time after onset of spreading O, 5 sec, , 5 sec. (From Ref. 31.)... Fig. IV-3. Velocity profiles for particles suspended in water with elapsed time, due to spreading of oleic acid. Time after onset of spreading O, 5 sec, , 5 sec. (From Ref. 31.)...
Absorption spectroscopy provides a means to study particular details about a monolayer. Transmission spectroscopy is difficult because the film, which is thin, absorbs little. Gaines [1] describes multiple-pass procedures for overcoming this problem. Reflection spectroscopy in the UV-visible range has been reported for lipid monolayers [150,151] and in the IR range for oleic acid [152]. [Pg.126]

Reactions in which a product remains in the him (as above) are complicated by the fact that the areas of reactant and product are not additive, that is, a nonideal mixed him is formed. Thus Gilby and Alexander [310], in some further studies of the oxidation of unsaturated acids on permanganate substrates, found that mixed hlms of unsaturated acid and dihydroxy acid (the immediate oxidation product) were indeed far from ideal. They were, however, able to ht their data for oleic and erucic acids fairly well by taking into account the separately determined departures from ideality in the mixed hlms. [Pg.155]

Rehbinder and co-workers were pioneers in the study of environmental effects on the strength of solids [144], As discussed by Frumkin and others [143-145], the measured hardness of a metal immersed in an electrolyte solution varies with applied potential in the manner of an electrocapillary curve (see Section V-7). A dramatic demonstration of this so-called Rehbinder effect is the easy deformation of single crystals of tin and of zinc if the surface is coated with an oleic acid monolayer [144]. [Pg.281]

It is quite clear, first of all, that since emulsions present a large interfacial area, any reduction in interfacial tension must reduce the driving force toward coalescence and should promote stability. We have here, then, a simple thermodynamic basis for the role of emulsifying agents. Harkins [17] mentions, as an example, the case of the system paraffin oil-water. With pure liquids, the inter-facial tension was 41 dyn/cm, and this was reduced to 31 dyn/cm on making the aqueous phase 0.00 IM in oleic acid, under which conditions a reasonably stable emulsion could be formed. On neutralization by 0.001 M sodium hydroxide, the interfacial tension fell to 7.2 dyn/cm, and if also made O.OOIM in sodium chloride, it became less than 0.01 dyn/cm. With olive oil in place of the paraffin oil, the final interfacial tension was 0.002 dyn/cm. These last systems emulsified spontaneously—that is, on combining the oil and water phases, no agitation was needed for emulsification to occur. [Pg.504]

Among the many applications of LB films, the creation or arrangement of colloidal particles in these films is a unique one. On one hand, colloidal particles such as 10-nm silver sols stabilized by oleic acid can be spread at the air-water interface and LB deposited to create unique optical and electrooptical properties for devices [185]. [Pg.561]

The term fat is applied to solid esters of fatty acids with glycerol (glycerides) if the fat is liquid at the ordinary temperature, it is conventionally called a fatty oil, vegetable oil or animal oil. The acids which occur most abundantly are palmitic ticid CH3(CHj),4COOH, stearic acid CH3(CH2)isCOOH and oleic acid CH3(CH2),CH=CH(CH2),C00H. Upon hydrolysis, fats yield glycerol and the alkali salts of these acids (soaps) ... [Pg.444]

Dissolve 7 g. of pure oleic acid in 30 ml. of dry ethyl chloride (chloroform may be used but is less satisfactory), and ozonise at about —30°. Remove the solvent under reduced pressure, dissolve the residue in 50 ml. of dry methyl alcohol and hydrogenate as for adipic dialdehyde in the presence of 0 5 g. of palladium - calcium carbonate. Warm the resulting solution for 30 minutes with a slight excess of semicarbazide acetate and pour into water. Collect the precipitated semicarbazones and dry the... [Pg.892]

When the groups on either end of a double bond are the same or aie shuctuially sum lar to each other it is a simple matter to describe the configuration of the double bond as CIS or trans Oleic acid for example a compound that can be obtained from olive oil has a CIS double bond Cmnamaldehyde responsible for the characteristic odor of cm namon has a trans double bond... [Pg.193]

Hgh nitrile polymers Hgh oleic canola Hgh oleic sunflower Hgh ortho novolaks... [Pg.479]


See other pages where Oleics is mentioned: [Pg.149]    [Pg.162]    [Pg.172]    [Pg.287]    [Pg.298]    [Pg.314]    [Pg.350]    [Pg.381]    [Pg.101]    [Pg.106]    [Pg.106]    [Pg.478]    [Pg.365]    [Pg.388]    [Pg.445]    [Pg.892]    [Pg.892]    [Pg.175]    [Pg.193]    [Pg.388]    [Pg.792]    [Pg.1073]    [Pg.30]    [Pg.460]    [Pg.483]    [Pg.504]    [Pg.989]    [Pg.1155]    [Pg.700]    [Pg.700]    [Pg.700]   
See also in sourсe #XX -- [ Pg.182 , Pg.203 ]

See also in sourсe #XX -- [ Pg.250 , Pg.251 ]

See also in sourсe #XX -- [ Pg.250 , Pg.251 ]




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Acid oleic, elaidizing

Aerobic Oxidation Step within a Three-Stage Conversion of Oleic Acid or Methyl Oleate

Antitumor and/or antimetastatic activit of oleic acid effects

Appendix Oleic Acid

Autoxidation oleic acid

Biosynthesis of oleic acid

Breast cancer oleic acid

Canola high-oleic

Carbon dioxide oleic acid

Cu NPs Capped by Cysteine, Oleic Acid and Other Small Molecules with Biological Relevance

D-10-Hydroxystearate from hydration of oleic

Dietary oleic acid

Dimerization of oleic acid

Edible Seed Oils Rich in Oleic Acid

Effect of oleic acid

Emersol 220 white oleic acid

Emersol 221 low titer white oleic acid

Emulsifying agents oleic acid

Engineering high oleic acid content

Epoxidation of oleic acid

Ester hydrolysis, oleic acid

Esterification oleic acid

Fatty acids oleic

Fatty oleic alcohol

High oleic acid canola oil

High oleic acid safflower oil

High oleic acid soybean oil

High oleic acid sunflower oil

High oleic low linolenic canola oil

High oleic oils

High oleic, low linolenic

High-oleic acid

High-oleic peanut oil

High-oleic rapeseed

Hydrogenation oleic acid

Hydrogenation oleic acid, selective

Hydroxy oleic acid

Interfacial tension oleic acid

Iso oleic acid

LLC cells DNA synthesis effect of oleic acid

Leukocytes effect of oleic acid

Lin oleic acid

Liver metastatic tumor colonies effect of oleic acid

Lung injury oleic acid-induced

Magnetic particles oleic acid

Major fatty acids oleic

Making oleic soaps

Matrigel-induced angiogenesis effect of oleic acid

Mid oleic sunflower

Mid oleic sunflower oil

Nonionic surfactant oleic acid

Nutrients Oleic acid

OLEIC ACID.336(Vol

Of oleic acid

Oils containing oleic, palmitoleic, y-linolenic and

Oilseeds Oleic acid

Oleic

Oleic

Oleic Acid from Olive Oil

Oleic Acid, Potassium Salt

Oleic Acid, Sodium Salt

Oleic acid

Oleic acid , health benefits

Oleic acid Constitution

Oleic acid Monounsaturated fatty acids

Oleic acid Omega

Oleic acid Subject

Oleic acid [CAS

Oleic acid absorption

Oleic acid advantage

Oleic acid amide

Oleic acid anhydride

Oleic acid anti-inflammatory effects

Oleic acid antitumor activity

Oleic acid biological activity

Oleic acid biosynthesis

Oleic acid blood

Oleic acid borage

Oleic acid canola oil

Oleic acid carbonyl compound

Oleic acid castor oil

Oleic acid catabolism

Oleic acid cells

Oleic acid chemical structure

Oleic acid cholesterol esters

Oleic acid colonies

Oleic acid content

Oleic acid coriander

Oleic acid coronary heart disease

Oleic acid cross-metathesis

Oleic acid derivatives

Oleic acid dietary sources

Oleic acid effect

Oleic acid emulsion

Oleic acid epoxidation

Oleic acid esterified

Oleic acid ethyl ester

Oleic acid fatty acids

Oleic acid film

Oleic acid formula

Oleic acid glycerol esters

Oleic acid hydroxy fatty acids produced

Oleic acid induction

Oleic acid inhibitory actions

Oleic acid into solid acids, Conversion

Oleic acid iodination

Oleic acid jojoba

Oleic acid lowers total cholesterol level

Oleic acid melting point

Oleic acid metabolism

Oleic acid methyl ester

Oleic acid methyl ester systems

Oleic acid oils

Oleic acid oleate

Oleic acid oleochemicals from

Oleic acid oxidation

Oleic acid oxidation rate

Oleic acid packaging

Oleic acid phase transition temperature

Oleic acid polymorphic forms

Oleic acid position

Oleic acid production

Oleic acid products

Oleic acid reactions

Oleic acid reactor

Oleic acid relative oxidation reaction rate

Oleic acid sources

Oleic acid structure

Oleic acid sunflower oil

Oleic acid surfactant

Oleic acid synthesis

Oleic acid transformations

Oleic acid triacylglycerol formation

Oleic acid unsaturation

Oleic acid vegetable oils

Oleic acid, 439 (Table

Oleic acid, addition

Oleic acid, corrosiveness

Oleic acid, dimer

Oleic acid, epoxidized

Oleic acid, esterification with

Oleic acid, infrared

Oleic acid, labelled

Oleic acid, magnesium salt

Oleic acid, oleate structure

Oleic acid, olein

Oleic acid, ozonization

Oleic acid, phase diagram

Oleic acid, solvent

Oleic acid, unsaturation test

Oleic acid-coated particles

Oleic add

Oleic alcohol

Oleic aldehyde

Oleic anhydride

Oleic configuration

Oleic double bond cleavage

Oleic hydrocarboxylation

Oleic iodine value

Oleic melting point

Oleic moieties

Oleic molecule geometry

Oleic oils

Oleic oxidation

Oleic ozonolysis

Oleic safflower

Oleic structure

Oleic uptake

Oxidation of oleic acid

Ozonolysis oleic acid

Penetration enhancement oleic acid

Penetration enhancer oleic acid

Phase oleic

Preparation of Oleic Acid Monoethanolamide

Safflower oil high-oleic

Sulphonated oleic acid esters

Sunflower high oleic mutant

Sunflower oil, high-oleic

Trans-Oleic acid

Triglycerides oleic acid

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