Big Chemical Encyclopedia

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

Articles Figures Tables About

Fatty acids hydrogenated

The fatty acids obtained from the process can be used directly or further manipulated for improved or modified performance and stabiUty. Hardening is an operation in which some fraction of the unsaturated bonds present in the fatty acids are eliminated through hydrogenation or the addition of H2 across a carbon—carbon double bond. This process was initially intended to improve the odor and color stabiUty of fatty acids through elimination of the polyunsaturated species. However, with the growth in the use of specialty fatty acids, hydrogenation is a commercially important process to modify the physical properties of the fatty acids. [Pg.155]

Dry reduced nickel catalyst protected by fat is the most common catalyst for the hydrogenation of fatty acids. The composition of this type of catalyst is about 25% nickel, 25% inert carrier, and 50% soHd fat. Manufacturers of this catalyst include Calsicat (Mallinckrodt), Harshaw (Engelhard), United Catalysts (Sud Chemie), and Unichema. Other catalysts that stiH have some place in fatty acid hydrogenation are so-called wet reduced nickel catalysts (formate catalysts), Raney nickel catalysts, and precious metal catalysts, primarily palladium on carbon. The spent nickel catalysts are usually sent to a broker who seUs them for recovery of nickel value. Spent palladium catalysts are usually returned to the catalyst suppHer for credit of palladium value. [Pg.91]

Another barnacle species, Elminius modestus, was found to produce mono and trihydroxy fatty acids [146]. Analysis of the extract of whole animal homogenates by TLC provided two hatching factor active bands. The more polar band was tentatively identified as a trihydroxy fatty acid (THFA) band. The less polar band had an / r value similar to a 5-HETE standard. The compounds from this latter band were eluted from the TLC plate, methylated, and trimethylsilylated. GC-MS analysis detected several HEPE s and small amounts of monohydroxy derivatives of Ci8 1, C18 2, and C22 fatty acids. Hydrogenation and subsequent GC-MS analysis allowed identification of the major compound as 8-HEPE (ca. 70%). Five to ten percent of 9-, 11-, and 15-HEPE and minor amounts of 5-, 6-, 12-, and 13-HEPE were also detected. No stereochemical features of these oxylipins were determined. [Pg.163]

The concentrations of several specific odorants found in piggery slurry,in particular volatile fatty acids, hydrogen sulphide, ammonia and p-cresol, have been correlated with odour intensity (13, 14, 15 16). [Pg.334]

The deoitygenation reaction of ethyl stearate was carried out for 4-6 h at reaction temperatures between 270-360°C and under reactor pressure of 0-7 bar. The effect of the catalyst pretreatment and the catalyst mass as well as the influence of reaction temperature were studied. The observed products in the ethyl stearate reaction are the deoxygenation products (desired), intermediate product (fatty acid), hydrogenation products (unsaturated Et-SA) and by-products (Figure 3). [Pg.419]

Hydrogenation is utilized to reduce the unsaturation and poly-unsaturation of fatty acids. Hydrogenated fatty acids can also be... [Pg.1704]

The current process has some disadvantages discontinuous operation, strong hydrogen mass transfer control and low space-time-yields. The nickel on kiesel-guhr catalyst causes also some problems undesirable by-products, formation of nickel soaps in free fatty acid hydrogenation and disposal of nickel residues. [Pg.18]

Fats and fatty acids (Hydrogenated) vegetable oils, mono-/di-/tri-glycerides ... [Pg.349]

Percent by weight of fatty acids reported. Saturated fatty acids (Cl 4 0, Cl 6 0, Cl 8 0). Unsaturated fatty acids (Cl8 1, Cl8 2, Cl8 3). Calcium salt of palm oil fatty acids. Hydrogenated tallow. [Pg.2353]

Fatty acid Hydrogen CuCr Fatty alcohol Water... [Pg.3002]

Laurie acid is a fatty carboxylic acid isolated from vegetable and animal fats or oils. For example, coconut oil and palm kernel oil both contain high proportions of lauric acid. Isolation from natural fats and oils involves hydrolysis, separation of the fatty acids, hydrogenation to convert unsaturated fatty acids to saturated acids, and finally distillation of the specific fatty acid of interest. [Pg.406]

Gerson, T., John, A., and Sinclair, B.R. 1983. The effect of dietary N on in vitro lipolysis and fatty acid hydrogenation in rumen digesta from sheep fed diets high in starch. J. Agric. Sci. Camb. 101, 97-101. [Pg.211]

Derivation Purification of degras, a crude grease obtained by solvent-treatment of wool. Contains cholesterol esters of higher fatty acids. Hydrogenated, ethoxylated, and acetylated derivatives are available. [Pg.738]

The alkaline environment also precipitates calcium and phosphate ions from the GCF, causing dental calculus. Dental calculus interferes with self-administered oral hygiene (Sect. 13.1.2) and asaccharolytic metabolism intensifies. When sulfur-containing amino acids (cysteine and methionine) are metabohzed, they release hydrogen sulfide along with the ammonia and short chain fatty acids. Hydrogen sulfide is a major contributor of oral malodor that often accompanies moderate to severe periodontal disease. [Pg.12]

Soya bean oil fatty acids, hydrogenated 1969 Spezialfett 118 4016... [Pg.1091]

Fig. 5.15 Inhibitor experiment for the demonstration of substrates used by sulfate reducing bacteria in a coastal marine sediment. The concentrations of volatile fatty acids, hydrogen and methane are followed during a time-course experiment over 8 hours. At 3.5 hours (arrow) molybdate was added and the substrates accumulate at a rate corresponding to their rate of consumption before inhibition. The formation of methane shows the release of competition for the common substrates for methanogenesis and sulfate reduction (H and acetate). Data from Sorensen et al. (1981). Fig. 5.15 Inhibitor experiment for the demonstration of substrates used by sulfate reducing bacteria in a coastal marine sediment. The concentrations of volatile fatty acids, hydrogen and methane are followed during a time-course experiment over 8 hours. At 3.5 hours (arrow) molybdate was added and the substrates accumulate at a rate corresponding to their rate of consumption before inhibition. The formation of methane shows the release of competition for the common substrates for methanogenesis and sulfate reduction (H and acetate). Data from Sorensen et al. (1981).
The state-of-the-art technology in free fatty acid hydrogenation is characterized by discontinuous operation and the use of powdered nickel on silica catalysts. Known disadvantages of this process are discontinuous operation, low... [Pg.552]

Undigested amylose passes into the large intestine (colon) where it is fermented by bacteria that produce short-chain fatty acids, hydrogen and methane. These compounds cause intestinal discomfort and intestinal bloating and their production explains the well-known association between flatulence and the consumption of baked... [Pg.366]

The substances normally used as lubricants are higher alcohols, higher fatty acids, hydrogenated fats, and esters. They are added to processable mixtures in amounts of 0.2-2 %. [Pg.197]

Consider a cell membrane lipid derived from linoleic acid, which is an unsaturated fatty acid. Hydrogen atom abstraction of an allylic hydrogen by a hydroxyl radical leads to a resonance-stabilized free allylic radical in which the unpaired electron is delocalized over C-9, C-11, and C-13. [Pg.1005]

Coconut oil alkyl-1,3-propylenediamine diacetate. See Cocodiamine acetate (Coconut oil alkyl) trimethylammonium methyl sulfate. See Cocotrimonium methosulfate Coconut oil amides. See Cocamide Coconut oil amidopropyl betaine. See Cocamidopropyl betaine Coconut oil fatty acids. See Coconut acid Coconut oil fatty acids, hydrogenated. See Hydrogenated coconut acid Coconut oil fatty acids, sodium salt. See Sodium cocoate... [Pg.1021]

Uses Prep, of Ni catalysts for organic reactions, esp. fatty acid hydrogenation catalysts mfg. of Ni... [Pg.2804]

Huges PE, Tove SB (1982) Biohydrogenation of unsaturated fatty adds. Purification and properties of cis-9, trans-11-octadecanoate reductase. J Biol Chem 257 3643-3649 Hunter WJ, Baker FC, Rosenfeld IS, Keyser JB, Tove SB (1976) Biohydrogenation of unsaturated fatty acids. Hydrogenation by cell-free preparations of Butyrivibrio fibrisolvens. J Biol Chem... [Pg.280]


See other pages where Fatty acids hydrogenated is mentioned: [Pg.91]    [Pg.438]    [Pg.215]    [Pg.230]    [Pg.453]    [Pg.2982]    [Pg.3007]    [Pg.3010]    [Pg.799]    [Pg.596]    [Pg.28]    [Pg.327]    [Pg.551]    [Pg.193]    [Pg.2069]    [Pg.627]    [Pg.391]    [Pg.658]   
See also in sourсe #XX -- [ Pg.36 ]

See also in sourсe #XX -- [ Pg.79 ]




SEARCH



Abstraction, hydrogen from fatty acid

Dispersion Hydrogenation, fatty acids

Fatty acid carbon-hydrogen bond positions

Fatty acid esters hydrogenation

Fatty acid highly hydrogenated canola oil

Fatty acid in hydrogenated canola oil

Fatty acid lightly hydrogenated canola and soybean oils

Fatty acids direct hydrogenation

Fatty acids hydrogen peroxide formation

Fatty hydrogenation

Hydrogen fatty acids

Hydrogen fatty acids

Hydrogen in fatty acid synthesis

Hydrogen peroxide, fatty acid

Hydrogen peroxide, fatty acid oxidation

Hydrogen production volatile fatty acids

Hydrogenation free fatty acids

Hydrogenation of unsaturated fatty acids

Hydrogenation trans-fatty acid reduction

Hydrogenation, fatty acids

Hydrogenation, fatty acids

Trans fatty acid, from hydrogenation

Trans fatty acid, from hydrogenation mechanism

Unsaturated fatty acids, hydrogenation

Volatile fatty acids , hydrogen

© 2024 chempedia.info