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991.
M. Cartens E. Molina Grima A. Robles Medina A. Giménez Giménez J. Ibáñez González 《Journal of the American Oil Chemists' Society》1996,73(8):1025-1031
Eicosapentaenoic acid (EPA, 20∶5n-3) was obtained from the marine microalgaePhaeodactylum tricornutum by a three-step process: fatty acid extraction by direct saponification of biomass, polyunsaturated fatty acid (PUFA) concentration
by formation of urea inclusion compounds, and EPA isolation by semipreparative high-performance liquid chromatography (HPLC).
Alternatively, EPA was obtained by a similar two-step process without the PUFA concentration step by the urea method. Direct
saponification of biomass was carried out with two solvents that contained KOH for lipid saponification. An increase in yield
was obtained because the problems associated with emulsion formation were avoided by separating the biomass from the soap
solution before adding hexane for extraction of insaponifiables. The most efficient solvent, ethanol (96%) at 60°C for 1 h,
extracted 98.3% of EPA. PUFA were concentrated by the urea method with a urea/fatty acid ratio of 4∶1 at a crystallization
temperature of 28°C and by using methanol and ethanol as urea solvents. An EPA concentration ratio of 1.73 (55.2∶31.9) and
a recover yield of 78.6% were obtained with methanol as the urea solvent. This PUFA concentrate was used to obtain 93.4% pure
EPA by semipreparative HPLC with a reverse-phase, C18, 10 mm i.d.×25-cm column and methanol/water (1% acetic acid), 80∶20 w/w, as the mobile phase. Eighty-five percent of EPA
loaded was recovered, and 65.7% of EPA present inP. tricornutum biomass was recovered in highly pure form by this three-step downstream process. Alternatively, 93.6% pure EPA was isolated
from the fatty acid extract (without the PUFA concentration step) with 100% EPA recovery yield. This two-step process increases
the overall EPA yield to 98.3%, but it is only possible to obtain 20% as much EPA as that obtained by three-step downstream
processing. 相似文献
992.
Aranzazu García M Victoria Ruiz-Méndez Concepción Romero Manuel Brenes 《Journal of the American Oil Chemists' Society》2006,83(2):159-164
By definition, virgin olive oil is consumed unrefined, although a great proportion of the olive oil produced has to be refined
to render it edible. Phenolic compounds are among the substances eliminated during the refining process; in the present work
these were characterized by HPLC, and their evolution during the different refining steps was studied. The complete refining
process removed most polyphenols from oils, but the behavior of individual compounds at each step also was observed. o-Diphenols
(hydroxytyrosol, catechol, and hydroxytyrosol acetate) and flavonoids (luteolin and apigenin) were eliminated first during
the alkaline treatment. Tyrosol and 4-ethylphenol remained in the oil until the deodorization step. A large amount of phenolic
compounds was discovered in the refining by-products such as soapstocks and deodorization distillates. In the latter streams,
the concentrations of tyrosol and 4-ethylphenol reached up to 149 and 3720 mg/kg by-product, respectively. This high level
of 4-ethylphenol and its well-known strong off-odor can interfere during further processing of the deodorization distillates,
and this must be taken into account when deciding what is to become of them. Similarly, the results of this work open the
possibility of recovering phenolic compounds from the “second centrifugation olive oils” by adding a new washing step prior
to the refining process. By including this new step, the most polar polyphenols, hydroxytyrosol and tyrosol, will diffuse
from oil to water and a concentration of up to 1400 mg/L of hydroxytyrosol may be achieved. 相似文献
993.
Summary The ring-opening polymerization of 2-phenyl aziridine was studied with several catalyst systems: boron trifluoride etherate, chlorhydric acid, perchloric acid, dimethyl sulfate and methyl triflate. The corresponding polyamine was obtained as a pale yellow solid with a number average molecular weight around 2,000–3,000.A kinetic study is discussed in the case of perchloric acid and methyl triflate. 相似文献
994.
Poly(p-tert-butoxycarbonyloxystyrene): a convenient precursor to p-hydroxystyrene resins 总被引:1,自引:0,他引:1
An efficient synthetic route to pure, high molecular weight poly(p-hydroxystyrene) is reported. The route involves synthesis of a new monomer, p-tert-butoxycarbonyloxystyrene, polymerization by radical initiation or by cationic initiation in liquid SO2, followed by thermolysis or acidolysis of the tert-butoxycarbonyl protecting group. Porous, crosslinked resin beads containing the nucleophilic, phenol pendant group have been prepared in a similar fashion from the precursor terpolymer of p-tert-butoxycarbonyloxystyrene, styrene and divinylbenzene. The utility of this resin for solid-phase synthesis has been demonstrated. 相似文献
995.
996.
Edward Kostansek 《Journal of Coatings Technology and Research》2004,1(1):41-44
Coagulation of latex particles is most often carried out in the diffusion limited aggregation (DLA) regime where the time
for coagulation to take place is on the millisecond timescale. This process produces aggregates of low density, irregular
shape, and a broad particle size distributions. When the coagulation is carried out in the reaction limited aggregation (RLA)
regime, a coagulation time of about 1–120 sec, the system can be controlled by mixing to yield dense, spheroidal aggregates
with a very narrow particle size distribution. The important variables in the RLA process for butyl acrylate/methyl methacrylate
(BA/MMA) latexes were found to be mixing intensity, latex copolymer composition, and coagulation temperature. Dried aggregates
formed in the RLA process were found to have excellent powder flow properties and low dustiness. 相似文献
997.
中国加入WTO后,中国洗涤用品行业面临着新的机遇与挑战,中国洗涤用品市场将面临更加激烈的竞争。由于环保的呼声越来越高,中国已开始在部分地区禁磷。中国洗涤用品工业将如何发展,其前景如何,专家的看法又如何,就这些问题本刊专访了有关人士。 相似文献
998.
R. M. Tubaileh M. M. Graciani Constante M. Léon Camacho A. López López E. Graciani Constante 《Journal of the American Oil Chemists' Society》2002,79(10):971-976
Changes in the content of aliphatic waxes during industrial deodorization and/or physical refining of bleached olive oil were
studied in an experimental discontinuous pilot plant of 250 kg deodorizer using nitrogen as stripping gas in place of steam.
The kinetic constants for the decomposition of waxes during the deodorization process were determined. The reaction orders
studied are zero (or can be considered zero) within the working interval. The values of rate constants, activation energy,
frequency factor, increment of activation Gibbs free energy, activation enthalpy, and activation entropy are established. 相似文献
999.
Robert O. Dunn 《Journal of the American Oil Chemists' Society》2005,82(5):381-387
Biodiesel, an alternative diesel fuel derived from transesterification of vegetable oils or animal fats, is composed of saturated
and unsaturated long-chain FA alkyl esters. During long-term storage, oxidation caused by contact with air (autoxidation)
presents a legitimate concern with respect to monitoring and maintaining fuel quality. Extensive oxidative degradation may
compromise quality by adversely affecting kinematic viscosity, acid value, or PV. This work examines the oil stability index
(OSI) as a parameter for monitoring the oxidative stability of soybean oil FAME (SME). SME samples from five separate sources
and with varying storage and handling histories were analyzed for OSI at 60°C using an oxidative stability instrument. Results
showed that OSI may be used to measure relative oxidative stability of SME samples as well as to differentiate between samples
from different producers. Although addition of α-tocopherol or TBHQ increased OSI, responses to these antioxidants varied
with respect to SME sample. Variations in response to added antioxidant were attributed to aging and other effects that may
have caused oxidative degradation in samples prior to acquisition for this study. Results showed that OSI was more sensitive
than iodine value in detecting the effects of oxidative degradation in its early stages when monitoring SME during storage. 相似文献
1000.
The direct platinisation of a solid polymer electrolyte (Nafion® membrane) was realized by chemical reduction of a platinum salt. The Pt–PEM electrodes thus obtained were modified by tin to improve the electrocatalytic activity towards the electrooxidation of ethanol. The Pt–PEM and Pt–Sn–PEM electrodes were characterized by TEM, EDX and XRD analysis, cyclic voltammetry, and their polarisation curves for the electrooxidation of ethanol were determined under quasisteady state conditions. 相似文献