Environmental Control Symposium

MAN is but a part of the universe; his capabilities make him a significant link, in the cycle of life. To ensure this life, man must live in harmony with his environment. Recently, a disharmony has been discovered which could have grave effects upon the existence of man. It appears that man in his great thrust forward is destroying his own environment. The gravity of this threat to man's own existence carries some intrinsic problems of its own: man must allow his reason rather than his emotion to take command.     

A farm level approach to define successful mitigation strategies for GHG emissions from ruminant livestock systems

Ruminant livestock systems are a significant source of greenhouse gases (GHGs). Thus far, mitigation options for GHG emissions mainly focused on a single gas, and are treated as isolated activities. The present paper proposes a framework for a farm level approach for the full accounting of GHG emissions. The methodology accounts for the relevant direct and indirect emissions of methane, nitrous oxide and carbon dioxide, including carbon sequestration. Furthermore, the potential trade-off with ammonia volatilisation and nitrate leaching are taken into account. A ruminant livestock farm is represented with a conceptual model consisting of five pools: animal, manure, soil, crop and feed. The carbon and nitrogen inputs, throughputs and outputs are described, and the direct emissions are related to the carbon and nitrogen flows. The indirect emissions included in the methodology are mainly carbon dioxide emissions from energy use and nitrous oxide emissions related to imported resources and nitrogen losses. The whole farm approach is illustrated with a case of two dairy farms with contrasting livestock density and grassland management. It is shown that the inclusion of carbon sequestration and all indirect emissions have a major impact on the GHG budget of the farm. For one farm, the effect of four mitigation options on the GHG emissions was quantified. It was concluded that a whole farm approach of full accounting contributes to a better insight in the interactions between the carbon and nitrogen flows and the resulting emissions, within and outside the farm boundaries. Consequently, the methodology can be used to develop efficient and effective mitigation strategies.     

The Structure of the Irreversibly Bound Adhesion Promoter-Substrate Interfacial Layer of γ-Aminopropylsilanetriol on Crystalline Si, as Measured by XPS and FTIR

The irreversibly bound interfacial layer deposited by the γ-aminopropysilanetriol adhesion promoter onto a crystalline silicon substrate, which remains even after profuse washing, was found by XPS to have resulted from the fragmentation and rearrangement of the original γ-aminopropylsilanetriol molecule. A mechanism is proposed, involving the homolytic scission of the terminal N-C bond. One of the subsequent reactions is believed to involve hydrogen loss by abstraction and the formation of a terminal vinyl group, which bonds to the substrate. Support for this mechanism is found in IR spectroscopy of this layer.     

Fine Annealing of Optical Glass

Since the most important characteristic of optical glass is the uniformity of its refractive index, which is itself a function of fictive temperature, any fine annealing treatment must be such as to bring about substantial uniformity in fictive temperature. Methods of accomplishing this are reviewed. In terms of total required time in the annealing process, the most efficient method consists of soaking the glass for a short time at a temperature near the annealing point and cooling at a constant rate to a temperature below the annealing range and at an increased rate to room temperature. Formulas are given for specifying the parameters in the annealing schedule in terms of the final condition of the glass as to stress and index. The several outstanding advantages of this method of annealing are discussed.     

Potentiometric titration of long chain quaternary ammonium compounds using sodium tetraphenyl borate

Current methods for determining the activity of long chain quaternary ammonium compounds (QACS) are based either on dye partition, titration, or colorimetric analysis. The two major disadvantages of these methods are the disparity of partition coefficients among differently constituted QACS and the difficulty in detecting visual end points. Some potentiometric titration methods for QACS have been reported in the literature. However, back titration techniques, as well as complicated electrode systems, are generally involved. A new potentiometric titration system is presented which uses aqueous sodium tetraphenylborate (TPB) solution as a titrant and a platinum-platinum electrode system to detect the end point. Standard potentiometric titration instruments may be used for this method. This new potentiometric method is superior in precision and accuracy to visual (colorimetric) methods. Original version presented at the 1986 Annual AOCS Meeting in Honolulu, HI.     

Über die Darstellung und Sulfatierung von N-substituierten 12-Hydroxyoctadecen-(9)-säure-(1)-amiden

Preparation and Sulfation of N-Substituted 12-Hydroxy-octadecan-(9) Acid-(1) Amides Ricinoleic acid amides, substituted at the nitrogen atom, were converted to the sodium salts of the monosulfuric acid esters of the substituted ricinoleic acid amides (sodium salt of substituted 12-hydroxy sulfonyl-oxy-oleic acid amide) by sulfation with chlorosulfuric acid-diethyl ester-adduct followed by neutralisation. Washing capacity as well as surface tension, angle of contact and wetting capacity in relation to the concentration of the aqueous solutions of these anion active surfactants are measured.     

Determination of individual long-chain fatty acyl-CoA esters in heart and skeletal muscle

A method has been developed for determination of individual long-chain fatty acyl-CoA esters from heart and skeletal muscle using high performance liquid chromatography (HPLC). The esters were extracted from freezeclamped tissue of pig and rat hearts and rat skeletal muscle for analysis on a radially compressed C₁₈ 5μ reversephase column. Nine peaks in the extract with carbon chain lengths from C₁₂ to C₂₀ that subsequently disappeared on alkaline hydrolysis were identified. The major acyl-CoA peaks were 14∶1, 18∶2, 16∶0 and 18∶1 and additionally in rat heart 18∶0. Total long-chain acyl-CoA esters obtained by summation of the individual molecular species was 11.34±1.48 nmol/g wet wt. pig heart; 14.51±2.11 nmol/g wet wt. in rat heart, and 4.35±0.71 nmol/g wet wt. in rat skeletal muscle. These values were approximately 132% of those obtained using a separate procedure that measured total CoA by HPLC after alkaline hydrolysis of the esters. The described method demonstrates the quantitation of individual acyl-CoA species in muscle tissue. Therefore, it has a number of advantages in that it permits information to be obtained on the individual molecular species under various nutritional and metabolic conditions.     

Fatty acid composition of oils from 21 species of marine fish,freshwater fish and shellfish

The fatty acid composition of body lipids was determined by GLC for 14 species of saltwater fish, three species of freshwater fish and four species of shellfish. In addition, liver lipids of two species and egg lipids of one species were analyzed for comparison with the fish body lipids. The various species ranged from lean to fatty and contained from 0.7~15.5% oil in the tissues. Certain major fatty acids were found to vary widely among the species, as follows: 1.6~8.0% myristic, 9.5~33.4% palmitic, 2.0~11.2% palmitoleic, 5.2~29.1% oleic, 0.7~10.5% eicosenoic, 5.0~21.5% eicosapentaenoic, 0.2~11.6% docosenoic and 5.9~26.2% docosahexaenoic acids. Analyses of two separate mullet-oil samples illustrated the wide differences that are possible for a single species caught during different seasons. Significant differences in the amt of particular fatty acids were found in comparing freshwater-fish analyses with analyses for marine fish. Oysters and scallops showed large amt of pentaenoic and hexaenoic acids in their oils. Presented in part at the AOCS Meeting, New York, 1960.