Download Biotechnology in the Pulp and Paper Industry8 ICBPPI by L. Viikari and R. Lantto (Eds.) PDF

By L. Viikari and R. Lantto (Eds.)

This ebook covers either easy and technologies in a slightly targeted quarter of pulp and paper manufacture. the fundamental technology of lignocellulose enzymology and plant genetics is roofed additionally in lots of different contexts, while the applying of biotechnology in strategy and product improvement is carefully reviewed. all of the most modern advances in addition to new principles of the learn box are coated. This ebook will function an up-to-date and compact info package deal of biotechnical elements and the newest advances of the pulp and paper area.

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M. Sarkar, H. P. Didwania, E. Espinoza, and J. C. Benavides. "Paper Mill Evaluation of a Cellulolytic Enzyme and Polymers for Improving the Properties of Waste Paper Pulp" Presented at Papermakers Conference, 1996. J. Pere, S. Liukkonen, M. Siika-aho, J. Gullichsen, and L. Viikari. "Use of Purified Enzymes in Mechanical Pulping" presented at TAPPI Pulping Conference, Nashville, TN, 1996. D . J . Gregg, A. Boussaid, and J. N. Saddler. "Techno-economic Evaluations of a Generic Wood-to-Ethanol Process: Effect of Increased Cellulose Yields and Enzyme Recycle" Bioresource Technology, vol.

There is a growing interest in recovering and converting the polysaccharide fraction of plant materials to fermentable sugars to produce bioethanol as a sustainable form of energy. Unlike cellulose, which is a linear polymer of only glucose and has a relatively tight structure, hemicelluloses are made up of various pentoses and hexoses, have a branched structure, and are easily degraded under mild acidic conditions at higher temperatures. , corn stover, rice husk or wheat straw) are first pretreated.

5 ml of a series of enzyme solutions containing protein contents equivalent to those used with the woody substrates. The tubes were incubated at 4~ for 90 minutes, and were shaken vigorously every 15 minutes. The tubes were then centrifuged and the supernatant liquid was analyzed for protein content as described previously. 5. Enzymatic Hydrolysis All hydrolysis experiments were conducted in 125-ml Erlenmeyer flasks incubated in a gyratory water bath at 45~ shaking at 150 rpm. 8). The cellulase loading was varied as described below and supplemented with [3-glucosidase (CBU:FPU = 2:1) to prevent product inhibition by cellobiose.

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