Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fatty acid alkyl esters properties

Knothe, G. Dependence of biodiesel fuel properties on the structure of fatty acid alkyl esters. Fuel Processing Technology, 2005, v. 86 (10), 1059-1070. [Pg.76]

Knothe, G. 2005. Dependence of Biodiesel Fuel Properties on the Structure of Fatty Acid Alkyl Esters. Fuel Processing Technology 86 (10) 1059-1070. [Pg.145]

TABLE 2.4 Properties of Fatty Acid Alkyl Esters Other Than Methyl... [Pg.26]

The ester is stable at neutral pH, but at < pH 4 can hydrolyze to the sulfonated fatty acid. The ester at pH > 9 can again hydrolyze and form the disodium salt of sulfonated fatty acid [2]. SMEs and the various versions of the sulfonated fatty acids aU have surfactant properties. These properties will be discussed later in this chapter. It is interesting to consider that, unlike amides and alkyl sulfates,... [Pg.117]

Many of the surfactants made from ethyleneamines contain the imidazoline stmcture or are prepared through an imidazoline intermediate. Various 2-alkyl-imidazolines and their salts prepared mainly from EDA or monoethoxylated EDA are reported to have good foaming properties (292—295). Ethyleneamine-based imida zolines are also important intermediates for surfactants used in shampoos by virtue of their mildness and good foaming characteristics. 2- Alkyl imidazolines made from DETA or monoethoxylated EDA and fatty acids or their methyl esters are the principal commercial intermediates (296—298). They are converted into shampoo surfactants commonly by reaction with one or two moles of sodium chloroacetate to yield amphoteric surfactants (299—301). The ease with which the imidazoline intermediates are hydrolyzed leads to arnidoamine-type stmctures when these derivatives are prepared under aqueous alkaline conditions. However, reaction of the imidazoline under anhydrous conditions with acryflc acid [79-10-7] to make salt-free, amphoteric products, leaves the imidazoline stmcture essentially intact. Certain polyamine derivatives also function as water-in-oil or od-in-water emulsifiers. These include the products of a reaction between DETA, TETA, or TEPA and fatty acids (302) or oxidized hydrocarbon wax (303). The amidoamine made from lauric acid [143-07-7] and DETA mono- and bis(2-ethylhexyl) phosphate is a very effective water-in-od emulsifier (304). [Pg.48]

Ether carboxylates are used not only in powdered detergents but in liquid laundry detergents for their hard water stability, lime soap dispersibility, and electrolyte stability they improve the suspension stability and rheology of the electrolyte builder [130,131]. Formulations based particularly on lauryl ether carboxylate + 4.5 EO combined with fatty acid salt and other anionic surfactants are described [132], sometimes in combination with quaternary compounds as softeners [133,163]. Ether carboxylates show improved cleaning properties as suds-controlling agents in formulations with ethoxylated alkylphenol or fatty alcohol, alkyl phosphate esters or alkoxylate phosphate esters, and water-soluble builders [134]. [Pg.339]

The development of monoalkyl phosphate as a low skin irritating anionic surfactant is accented in a review with 30 references on monoalkyl phosphate salts, including surface-active properties, cutaneous effects, and applications to paste and liquid-type skin cleansers, and also phosphorylation reactions from the viewpoint of industrial production [26]. Amine salts of acrylate ester polymers, which are physiologically acceptable and useful as surfactants, are prepared by transesterification of alkyl acrylate polymers with 4-morpholinethanol or the alkanolamines and fatty alcohols or alkoxylated alkylphenols, and neutralizing with carboxylic or phosphoric acid. The polymer salt was used as an emulsifying agent for oils and waxes [70]. Preparation of pharmaceutical liposomes with surfactants derived from phosphoric acid is described in [279]. Lipid bilayer vesicles comprise an anionic or zwitterionic surfactant which when dispersed in H20 at a temperature above the phase transition temperature is in a micellar phase and a second lipid which is a single-chain fatty acid, fatty acid ester, or fatty alcohol which is in an emulsion phase, and cholesterol or a derivative. [Pg.611]

Properties. Phenethyl alcohol is a colorless liquid with a mild rose odor. It can be dehydrogenated catalytically to phenylacetaldehyde and oxidized to phenylacetic acid (e.g., with chromic acid). Its lower molecular mass fatty acid esters as well as some alkyl ethers, are valuable fragrance and flavor substances. [Pg.98]


See other pages where Fatty acid alkyl esters properties is mentioned: [Pg.798]    [Pg.800]    [Pg.66]    [Pg.27]    [Pg.23]    [Pg.182]    [Pg.185]    [Pg.475]    [Pg.482]    [Pg.614]    [Pg.193]    [Pg.165]    [Pg.440]    [Pg.443]    [Pg.10]    [Pg.26]    [Pg.152]    [Pg.233]    [Pg.481]    [Pg.233]    [Pg.611]    [Pg.72]    [Pg.264]    [Pg.262]    [Pg.50]    [Pg.156]    [Pg.1044]    [Pg.2231]    [Pg.361]    [Pg.368]    [Pg.417]   
See also in sourсe #XX -- [ Pg.26 , Pg.28 ]




SEARCH



Alkyl esters

Esters alkylation

Esters properties

Fatty acid alkyl ester

Fatty acids esters

Fatty acids properties

© 2024 chempedia.info