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dc.contributor.authorBuhaug, Janne Bjørntvedtnb_NO
dc.date.accessioned2014-12-19T13:10:45Z
dc.date.available2014-12-19T13:10:45Z
dc.date.created2002-06-28nb_NO
dc.date.issued2002nb_NO
dc.identifier124395nb_NO
dc.identifier.isbn82-471-5468-4nb_NO
dc.identifier.urihttp://hdl.handle.net/11250/244474
dc.description.abstract1,3,5-Tris(2-hydroxyethyl)-1,3,5-triazinane (1), in the industry often referred to as "Triazine", is a widely used liquid H2S scavenger. The goal of the work presented in this dissertation was to examine the chemistry of its reaction with H2S, and to determine the efficiency of 1 and other potential scavengers in H2S removal. It was found that two competing reactions take place when 1 is used as an H2S scavenger. One is the hydrolysis of the compound, in which ethanolamine (5) and formaldehyde is formed. The other reaction is the nucleophilic substitution of sulfur into the triazinane ring. By a combination of various NMR techniques, IR spectroscopy and elemental analysis, the latter reaction was found to proceed as follows:nb_NO
dc.languageengnb_NO
dc.publisherFakultet for naturvitenskap og teknologinb_NO
dc.relation.ispartofseriesDr.ingeniøravhandling, 0809-103X; 2002:70nb_NO
dc.titleInvestigation of the Chemistry of Liquid H2S Scavengersnb_NO
dc.typeDoctoral thesisnb_NO
dc.source.pagenumber122nb_NO
dc.contributor.departmentNorges teknisk-naturvitenskapelige universitet, Fakultet for naturvitenskap og teknologinb_NO
dc.description.degreedr.ing.nb_NO
dc.description.degreedr.ing.en_GB


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