Quantitative estimation of sucrose esters of plamitic acid

Thin layer chromatography was adapted for direct quantitative estimation of sucrose esters of palmitic acid. Urea-phosphoric acid spray was used to detect the sucrose moiety of the various esters. The photometrically metermined density density of each spot on the thin layer plate was found to be proportional to its sucrose content. Ester content was then obtained by multiplying sucrose found by the factor, mol. wt. ester/mol. wt. sucrose. Ester mixtures were prepared by interesterifying sucrose with various proportions of methyl palmitate in dimethylformamide solution. Positional isomers were observed at each level of substitution but could not be adequately separated from each other for quantitative evaluation. Presented at the AOCS Meeting, Minneapolis, October 1969. So. Utiliz. Res. Dev. Div., ARS, USDA.     

Effects of experimental endogenous hyperlipemia on circulating leukocytes and erythrocytes

Effects of hyperlipemia on circulating leukocytes and erythrocytes were studied in dogs which were given repeated, intravenous injections of a nonionic detergent, Triton WR-1339. Erythrocyte lipid concentrations increased from 3.6±0.9 mg/10¹⁰ cells in control animals to 9.3±1.5 mg in the hyperlipemic group. This increase was accompanied by a shift in the distribution of total fatty acids toward a higher percentage of saturated and monounsaturated acids. In contrast to the changes observed in erythrocytes, the leukocyte lipid content remained unaltered in dogs with serum cholesterol levels ranging from 500 to more than 2,000 mg/100 ml. Leukocyte counts rose whereas hematocrit values, hemoglobin concentrations, and erythrocyte counts decreased. Oxygen utilization studies showed no significant metabolic differences between leukocytes which were isolated from hyperlipemic or control animals. Circulating leukocytes in dogs with an endogenously induced hyperlipemia were shown therefore to maintain normal lipid concentrations and did not participate in lipophage formation, as reported for certain diet-induced lipemias.     

Responses to prey chemicals by a lacertid lizard,Podarcis muralis: Prey chemical discrimination and poststrike elevation in tongue-flick rate

The ability to discriminate prey chemicals from control substances and the presence of a poststrike elevation in tongue-flicking (PETF) rate are experimentally demonstrated in the lacertid lizard,Podarcis muralis, The tongue-flick attack score, a composite index of response strength, was significantly higher in response to integumental chemicals from cricket than to cologne or distilled water. The cricket chemicals additionally elicited a significantly greater rate of tongue-flicking and higher proportion of attacks by the lizards than did control stimuli. PETF combined with apparent searching movements strongly suggest the presence of strike-induced chemosensory searching (SICS). Experimental evidence indicates that both PETF and SICS occur in insectivorous representatives of three families of actively foraging autarchoglossan lizards, suggesting their widespread occurrence in such lizards. The adaptive roles of chemosensory behavior in the foraging behavior of P.Muralis are discussed. It is proposed that these lizards may form chemical search images and that PETF and SICS may have been present in the lacertilian ancestors of snakes.     

A review of the unique features of HDL apoproteins

The human plasma high density lipoproteins (HDL) are a heterogeneous ensemble of five proteins associated with both neutral and polar lipids. The sequences of all five proteins are known. ApoA-I and apoA-II are the major protein components; apoC-I, apoC-II and apoC-III are the minor protein components. All these apoproteins spontaneously recombine with phospholipids to give stable lipid-protein complexes and freely exchange between the two major HDL subclasses, HDL₂ and HDL₃. In addition, ApoC-I, apoC-II, and apoC-III exchange between HDL and very low density lipoproteins. Furthermore, certain HDL apoproteins are activators for plasma enzymes that are important in lipid metabolism. ApoA-I and apoC-I activate lecithin/cholesterol acyltransferase; apoC-II is an activator of lipoprotein lipase. The regions of apoC-I and apoC-II that are involved in the activation of these enzymes have been localized with synthetic peptides. Studies of synthetic and native fragments of apoA-II, apoC-I, apoC-II, and apoC-III as well as model lipid-binding peptides have identified specific regions with structural features common to lipid-binding proteins. These special properties, which include helical potential, sequences with a critical amphipathic length, and high hydrophobicity of the nonpolar side of the amphipathic helix, are the determinants of HDL structure and metabolism.     

Effects of apitong (Dipterocarpus spp.) extractives on bond strength development and curing rate of adhesives

Emulsion polymer isocyanate ( ), polyvinyl acetate ( ) and resorcinol-formaldehyde ( ) adhesives were used to produce single lap shear specimens using resinous and non-resinous apitong (Dipterocarpus spp.) timbers. Tests showed that joints made with highly resinous apitong were about 40% weaker than similar joints made with non-resinous apitong. The resinous apitong was treated with different solvents to yield five different extractives which were characterized by infra-red analysis. Apitong extractives were then added to and adhesives and joints made with buna (Fagus crenata), a timber known to be low in extractives and easy to bond. Joints prepared using extractive-containing adhesives were generally weaker than those made with the unmodified adhesives. RF adhesives containing extractives cured more slowly than unmodified . It is thought that the acidic nature of the extractives changes the pH of the system sufficiently to affect the curing mechanism     

Separation and determination of mono-, Di-, and triglycerides in monoglyceride concentrates

Summary Monoglyceride concentrates are quantitatively separated into mono-, di-, and triglyceride components on silica gel columns by an adsorption chromatographic technique. The separated glycerides are determined gravimetrically. The adsorption on silica gel is dependent on the number of hydroxyl groups in the molecule, and the influence of unsaturation and chain length is minimized. Combinations of benzene and ethyl ether are used for elution, thus preventing isomerization, which frequently results when polar solvents such as alcohols are used. The procedure for the chromatographic separation is simple and straightforward. The equipment used is easily obtainable. The silica gel adsorbent requires only adjustment of its water content before use. Mixtures of both saturated and unsaturated glycerides and those having different fatty acid chain length have been separated. Known mixtures have also been analyzed. For a known mixture containing 15% tripalmitin, 45% distearin, and 38% monopalmitin the average deviations from the calculated values were 0.4%, 0.2%, and 0.6%, respectively     

Soap-based detergent formulations: VI. Alkylaryl sulfonamide derivatives as lime soap dispersing agents

Alkylbenzenes, such as industrial detergent alkylates, as well as pure 1-phenylalkanes whose side chain lengths varied C₈−C₁₂, were converted into the corresponding alkylbenzenensulfonyl chlorides with chlorosulfonic acid. Surface active sulfonamides were obtained from the reaction of the sulfonyl chlorides with various low mol wt aminosulfonic acids, such as N-methyltaurine, or with aminoalkyl esters of sulfuric acid, such as 2-aminoethyl hydrogen sulfate. The hydrolytic stability of the resulting surface active sulfonamide derivatives was investigated. As expected, the sulfonates were quite resistant to acid or alkaline hydrolysis, while the sulfates were more susceptible to hydrolysis. Hydrolytic stability of the sulfonamides was compared with that of the analogous fatty acid amide sulfactants. All of the compounds were excellent lime soap dispersing agents giving Borhetty-Bergman values of 4–10. The compounds were evaluated for detergency either alone or formulated either with tallow soap or with tallow soap and sodium silicate (Na₂O/SiO₂ ratio of 1∶1.6) The derivatives of the pure hydrocarbons which gave the best overall detergency were those of 1-phenyldecane and 1-phenyldodecane, whereas those of 1-phenyloctane exhibited poor detergency. This ranking was observed when the compounds were tested alone as well as when formulated. The sulfonamide derivatives of the detergent alkylate type of alkylbenzenes exhibited excellent detergency characteristics and showed substantial potentiation of detergency when mixed with soap or with a soap-sodium silicate blend. The detergency performance of some of these formulated detergents was equal to that of a commercial household detergent used as a control.     

Introductory remarks

Surface active agents are used in the textile industry during the processing of fibers into yarns and fabrics, the finishing of leather products and during the removal of soil from textile products by laundering or dry cleaning. In these introductory remarks to the symposium, attention is directed to the phenomena occurring at solid-liquid interfaces during these processes. The properties of the surface active agents and the solvents used, the surface free energy and structure of the polymeric textile products and other, often poorly defined, surface chemical and physical characteristics of the products influence the interactions of these agents. The interactions of surface active agents, often derived from fats and oils, dissolved or dispersed in liquids, with textile materials, including natural products such as cotton, wool and leather, as well as man-made fibers, are considered in this symposium. One of eight papers being published from the Symposium “Surface Active Agents in the Textile Industry,” presented at the AOCS meeting in New Orleans, April 1970. So. Utiliz. Res. Dev. Div., ARS, USDA.     

Characterizing the deformation of cold-rolled copper sheet

An advanced x-ray diffraction technique allows the development of texture components to be monitored and provides supplementary information about the cold work and residual stresses in cold-rolled copper sheet. The new technique confirms the results of an ultrasonic test, except for the ultrasonic test’s sensitivity to grain size. The new x-ray diffraction technique could be adapted to provide in-process, nondestructive evaluation of thin copper sheet, even for material moving at high speeds.