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The Yaws Handbook of Vapor Pressure
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ISBN: 012803002X 0128029994 1336197897 9780128030028 9780128029992 Year: 2015 Publisher: Kidlington, Oxford Waltham, MA

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Increased to include over 25,000 organic and inorganic compounds, The Yaws Handbook of Vapor Pressure: Antoine Coefficients, 2nd Edition delivers the most comprehensive and practical database source for today's petrochemical. Understanding antoine coefficients for vapor pressure leads to numerous critical engineering applications such as pure components in storage vessels, pressure relief valve design, flammability limits at the refinery, as well as environmental emissions from exposed liquids, making data to efficiently calculate these daily challenges a fundamental need. Written by the worl


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Sublimation et distillation du magnésium et du calcium
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Year: 1936 Publisher: Paris : Ed. Blondel la Rougery ; Gauthier-Villars,

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Test No. 104: Vapour Pressure
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ISBN: 1280607521 9786610607525 9264069569 9789264069565 Year: 2006 Publisher: Paris : OECD Publishing,

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This Test Guideline describes eight methods to measure the vapour pressure. Each one can be applied in different vapour pressure ranges. The vapour pressure (in Pascal) of a substance is defined as the saturation pressure above a solid or liquid substance and is determined at various temperatures (in Kelvin). The methods used are: the dynamic method (Cottrell’s method), the static method, the isoteniscope Method, the effusion method: vapour pressure balance, the effusion method: Knudsen cell, the effusion method: isothermal thermogravimetry, the gas saturation method and the spinning rotor method. The vapour pressure from any of the preceding methods should be determined for at least two temperatures. Three or more are preferred in the range 0 to 50°C, in order to check the linearity of the vapour pressure curve. In case of Effusion methods and Gas saturation method, 120 to 150 °C is recommended for the measuring temperature range instead of 0 to 50°C.

Handbook of vapor pressure.
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ISBN: 1281077860 9786611077860 0080533833 9780080533834 0884153940 9780080533834 9780884153948 9781281077868 6611077863 0884151891 9780884151890 0884151905 9780884151906 0884151913 9780884151913 Year: 1995 Publisher: Houston Gulf Pub. Co.

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This series provides engineers with vapor pressure data for process design, production, and environmental applications.


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Freeze-drying of pharmaceutical and food products
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ISBN: 1845697472 1845697464 9781845697471 Year: 2010 Publisher: Cambridge Woodhead Publishing Ltd

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Freeze-drying is an important preservation technique for heat-sensitive pharmaceuticals and foods. Products are first frozen, then dried in a vacuum at low temperature by sublimation and desorption, rather than by the application of heat. The resulting items can be stored at room temperature for long periods. This informative text addresses both principles and practice in this area.The first chapter introduces freeze-drying. The authors then review the fundamentals of the technique, heat-mass transfer analyses, modelling of the drying process and the equipment employed. Further chapter


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Principes et applications de la lyophilisation des produits biologiques, pharmaceutiques et alimentaires : compte rendu de réunion de [la] Commission C1 : Tokyo (Japon), 20-22 mai 1985 = Fundamentals and applications of freeze-drying to biological materials, drugs and foodstuffs : proceedings of meeting of Commission C1, May 20-22, 1985, [Tokyo, Japan]
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ISBN: 2903633304 Year: 1985 Volume: 1985,1 Publisher: Paris : International Institute of Refrigeration (IIR) = Institut international du froid (IIF),

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International symposium on biological product freeze-drying and formulation : proceedings of a symposium [...], held at Bethesda, 24-26 October 1990
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ISBN: 3805554664 Year: 1992 Volume: vol 74 Publisher: Basel New York Sydney Karger


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Lyophilized Biologics and Vaccines : Modality-Based Approaches
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ISBN: 9781493923830 149392382X 9781493923823 1493923838 Year: 2015 Publisher: New York, NY : Springer New York : Imprint: Springer,

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This book provides a detailed account of the most recent developments, challenges and solutions to seamlessly advance and launch lyophilized biologics or vaccine products, based on diverse modalities, ranging from antibodies (e.g., monoclonal, fusion), complex biologics (e.g., antibody drug conjugates,  PEGylated proteins) and vaccines (e.g., recombinant protein based). The authors adeptly guide you through everything you need to know, from biophysical and chemical stability considerations of proteins, to critical assessment during process scale-up, technology transfer, packaging, alternate drying and device selection for a successful process validation, regulatory submission and launch of a stable, safe and effective product. Lyophilized Biologics and Vaccines: Modality-Based Approaches serves as a reference to all critical assessments and steps from early pre-formulation stages to product launch: Provides recent understanding of heterogeneity of protein environment in frozen systems, buffer stabilization, instrumental analysis and controlled ice nucleation technology Details product development strategies based on diverse modalities of biologics and vaccines, including plasmid DNA and lipid-based therapeutics Recent updates on quality-by-design and process analytical technology approaches, illustrated by case studies and FDA perspective Provides the latest account of alternate drying technologies including spray drying and bulk freeze-drying Chapters are written by one or more world-renowned leading authorities from academia, industry or regulatory agencies, whose expertise cover lyophilization of the diverse modalities of biopharmaceuticals.  Their contributions are based on the exhaustive review of literature coupled with excellent hands-on experiences in laboratory or GMP setup, making this an exceptional guide to all stages of lyophilized or dehydrated product development and commercial manufacturing.   Dushyant B. Varshney, Ph.D., has made significant contributions in manufacturing science and technology, due diligence, tech transfer, product and process development (including lyophilization), quality-by-design and process analytical technologies for biologics, vaccines and small molecules. He is currently a Director of Manufacturing Assessment, MS&T at Hospira Inc.   Manmohan Singh, Ph.D., is a well-known expert in the area of vaccine formulations and adjuvant research and has been working in vaccine R&D for the last 20 years. He is currently the Head of Global Drug Product Development at Novartis Vaccines and Diagnostics in Holly Springs, NC.

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