Analysis of Chemical Warfare Degradation Products - download pdf or read online

By Karolin K. Kroening

ISBN-10: 0470745878

ISBN-13: 9780470745878

This booklet describes nerve brokers and vesicants, their decomposition and their degradation items' chemistry in addition to their toxicity together with an inventory of detection concepts of nerve brokers and their degradation items. This ebook will current their heritage, toxicity, comparability among diversified pattern instruction tools, separation recommendations, and detection equipment all jointly in a quick, effortless to learn publication, tied jointly via a unmarried crew doing the writing and the enhancing to guarantee tender transition from bankruptcy to bankruptcy, with enough Tables and literature references for the reader who seems to additional detail.The textual content will illustrate the pluses and minuses of many of the recommendations with adequate references for the reader to acquire vast aspect.

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Appl. , 12, 360–371. H. (1984) Toxicologist, 4, 22. J. S. Army Medical Research and Development Command, Fort Detrick, MD. R. S. Army Armament Munitions Chemical Command, Chemical Research, Development and Engineering Center, Aberdeen Proving Ground, MD. [47] Thiokol/Ventron, (1980) Material Safety Sheet: Methylphosphonic Acid, Thiokol/Ventron Division, Danvers, MA. R. (1976) Mammalian Toxicological Evaluation of DIMP and DCPD. , Kensington, MD. , Polin, D. et al. (1979) Toxicology Study of Diisopropyl Methylphosphonate and Dicyclopentadiene in Mallard Ducks, Bobwhite Quail and Mink, Michigan State University, East Lansing, MI.

2), alkylation of RNA molecules, altered translation and altered protein synthesis leading to cell death. Binding to proteins mainly with the thiol group of cysteine produces structural changes, altering normal cell physicology, specifically enzyme activity. Relevant animal studies have shown the following results: LD50 , through skin contact, rat 9, dog 20 and rabbit 100 mg kg−1 ; LC50 , by inhalation (for 10 min), rat 100, rabbit 280 and monkey 80 mg m−3 [129]. Thiodiglycol is the main hydrolysis product of Sulfur Mustard and is a Schedule 2 compound.

H. (1984) Toxicologist, 4, 22. J. S. Army Medical Research and Development Command, Fort Detrick, MD. R. S. Army Armament Munitions Chemical Command, Chemical Research, Development and Engineering Center, Aberdeen Proving Ground, MD. [47] Thiokol/Ventron, (1980) Material Safety Sheet: Methylphosphonic Acid, Thiokol/Ventron Division, Danvers, MA. R. (1976) Mammalian Toxicological Evaluation of DIMP and DCPD. , Kensington, MD. , Polin, D. et al. (1979) Toxicology Study of Diisopropyl Methylphosphonate and Dicyclopentadiene in Mallard Ducks, Bobwhite Quail and Mink, Michigan State University, East Lansing, MI.

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Analysis of Chemical Warfare Degradation Products by Karolin K. Kroening


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