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Use of immobilized lactase in processing cheese whey ultrafiltrateRoodpeyma, Shapoor. January 1980 (has links)
Thesis (M.S.)--University of Wisconsin--Madison. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 168-181).
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Whey fermentation by Saccharomyces fragilisStuiber, David Anthony, January 1956 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1966. / eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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Heat denaturation of the major whey proteins and the stability of the heat induced complex between [beta]-lactoglobulin and [kappa]-caseinHsu, Rosalind Mann-ching, January 1968 (has links)
Thesis (M.S.)--University of Wisconsin--Madison, 1968. / eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
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Cloning and expression of the Aspergillus niger Beta-Galactosidase gene in Saccharomyces cerevisiaeKumar, Vijay January 1988 (has links)
No description available.
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Anaerobic digestion of cheese whey in an upflow anaerobic sludge blanket reactorYan, Jing-Qing January 1991 (has links)
The anaerobic digestion of cheese whey was studied in an upfiow anaerobic sludge blanket reactor for its start-up characteristics, the effects of various process parameters, the effect of sulfate addition and the determination of optimal operating conditions.
Start-up of an UASB reactor treating cheese whey was extremely difficult due to its tendency to acidify. Various start-up strategies were tested to facilitate start-up and to ensure stable operation. Among the operating parameters, sludge loading rate was the most critical for proper start-up of the UASB reactor. The initial sludge loading rate during start-up period should not exceed 0.25 g COD/g VSS.
The response of whey digestion to several process parameters was investigated. Without
pH-control, over 97% COD removal was obtained for influent concentrations from 5 to 28.8 g COD/1 and HRT of 5 days. However, instability was observed when the influent concentration was increased to 38.1 g COD/1.
Gas production from whey is affected by organic loading rate (OLR). At an OLR less than 4 g COD/l-d, higher influent strength resulted in a higher methane production rate. When the OLR was greater than 6, higher strength feed or shorter hydraulic retention time (HRT) produced less methane.
From the profiles of substrate concentration measured at various levels above the bottom of the reactor, two reaction stages, acidogenesis and methanogenesis were distinguished.
It was experimentally illustrated that the rate of acidogenesis is much faster than the rate of methanogenesis in a whey anaerobic digestion system. The accumulation
of VFAs in the first stage being faster than its assimilation in the second stage creates a distinct acidogenic phase in the bottom of the reactor. The instability caused
by high influent concentration could be attributed to the accumulation of VFAs beyond the assimilative capacity of the methanogenic stage.
A set of empirical models for accumulation and degradation of VFAs was developed using linear regression analysis. The requirement for maintaining this system in a dynamic
balance was that the degradation capacity for VFA in the second stage be greater than the accumulation of VFA in the first stage. Based on this idea, the optimal influent concentration was given as between 25 to 30 g COD/1 for system stability.
A hypothesis was proposed in this study that a proper amount of sulfate may be applied to moderate the detrimental influence of excess hydrogen on a stressed anaerobic reactor. The effect of sulfate was tested to study the biochemical mechanism. The permissible influent COD concentration was increased from 30 g COD/1 to 50 g COD/1 by using sulfate addition. The pH in the reactor was on the average 0.8 units higher and the concentration of butyric acid in the acidogenic phase much lower with added sulfate than without sulfate addition. The significant improvement of process stability and treatment efficiency made by the addition of sulfate clearly illustrated that sulfate acted like a stimulator which helped to maintain conditions favorable to methanogenesis. The mechanism of this stimulation is explained according to thermodynamics and hydrogen regulation which suggested that sulfate is able to promote the β-oxidation of VFAs by consuming hydrogen.
A two-stage inhibition mechanism was proposed to explain the inhibition of high VFA concentrations and the stimulation of sulfate. Higher hydrogen pressure is the cause of preliminary inhibition, resulting in the accumulation of VFAs, which subsequently inhibit the activity and growth of methanogens in the second inhibition stage. The mechanism of inhibition of methanogens from VFAs was interpreted as being caused by the acidification of the internal cytoplasm and destruction of the pH gradient by non-ionized acids based on the theory of bacterial membrane transport. A new control strategy for stabilization
of an anaerobic system is recommended.
Under the optimal operating conditions based on the results in the first three steps, over 97% reduction of COD was achieved when the influent COD was 30 g /l using an HRT of 2 days, an OLR of 16.61 g COD/l-d and sulfate concentration of 0.2 g/1. / Applied Science, Faculty of / Chemical and Biological Engineering, Department of / Graduate
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Membrane processing of cheese whey and preparation of ferric whey protein by heatingAmantea, Gerald F. January 1973 (has links)
A concentrate containing up to 73% protein N was recovered from cheese whey by using cellulose acetate ultrafiltration
membrances designed to reject solutes larger than 30,000 molecular weight by a continuous washing procedure.
Conditions necessary for increasing the ultrafiltration
process for cheese whey are reported. Variables include pressure, membrane porosity, feed rate, clarification, temperature and pH. The objective was to prepare whey products with a minimum concentration of monovalent salts and maximum concentration of protein while still maintaining a high flux rate. As expected pH adjustment to 7.0 and clarification
at 2000 X g for 5 min were critical in increasing flux rate. However, membrane blockage occurred and gel electrophoresis indicated that (β-casein and αs-casein were the major components responsible yet salts and lactose may also be implicated to a lesser degree.
Flux rate increased with temperature but was not affected by pressure. Results indicate that concentrating 3-4X would be practical but higher levels would be uneconomical due to the accumulation of viscous materials on the membrane.
Gel filtration showed that whey proteins are retained almost quantitatively in the concentrate while low molecular weight nitrogen containing material pass the membrane into the permeate. / Land and Food Systems, Faculty of / Graduate
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Production of microbial polysaccharides from whey.Pye, Susan. January 1981 (has links)
No description available.
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Electrohydrodynamically-dried whey protein : electrophoretic and calorimetric analysisXue, Xin, 1972- January 1997 (has links)
No description available.
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Effect of processing on the composition, microstructure and functional properties of cheese whey protein concentrateMei, Fu-I January 1993 (has links)
No description available.
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Characterization of whey protein concentrates with regard to factors that affect their function at interfaces /Peltonen, Riitta Inkeri January 1982 (has links)
No description available.
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