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dc.contributor.authorSuchitraporn Sakullimcharoenen_US
dc.contributor.authorPanas Maniten_US
dc.contributor.authorTharathon Mongkhonsien_US
dc.date.accessioned2021-04-23T08:50:39Z-
dc.date.available2021-04-23T08:50:39Z-
dc.date.issued2008en_US
dc.identifier.citationChiang Mai Journal of Science 35, 1 (January 2008),163-170en_US
dc.identifier.issn2465-3845en_US
dc.identifier.urihttps://epg.science.cmu.ac.th/ejournal/dl.php?journal_id=357en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/72100-
dc.descriptionThe Chiang Mai Journal of Science is an international English language peer-reviewed journal which is published in open access electronic format 6 times a year in January, March, May, July, September and November by the Faculty of Science, Chiang Mai University. Manuscripts in most areas of science are welcomed except in areas such as agriculture, engineering and medical science which are outside the scope of the Journal. Currently, we focus on manuscripts in biology, chemistry, physics, materials science and environmental science. Papers in mathematics statistics and computer science are also included but should be of an applied nature rather than purely theoretical. Manuscripts describing experiments on humans or animals are required to provide proof that all experiments have been carried out according to the ethical regulations of the respective institutional and/or governmental authorities and this should be clearly stated in the manuscript itself. The Editor reserves the right to reject manuscripts that fail to do so.en_US
dc.description.abstractThe hydroxylation of benzene with hydrogen peroxide as an oxidant over TS-1 was carried out in a bubble reactor. The catalyst was prepared by hydrothermal synthesis. When the volume of benzene feeding in each period was increased while the feeding frequency constant, the conversion of benzene decreased. The amount of phenol increased when the reaction mixture was left for a period of time up to 4 hours, suggesting the reaction of benzene dissolved in the liquid phase. The extension of the experiment on the hydroxylation of toluene using the best condition obtained from the hydroxylation of benzene shows that o-cresol and p-cresol are two main hydroxylation products of toluene.en_US
dc.language.isoEngen_US
dc.publisherFaculty of Science, Chiang Mai Universityen_US
dc.subjectHydroxylationen_US
dc.subjectBenzeneen_US
dc.subjectTolueneen_US
dc.subjectTitanium silicalite-1en_US
dc.titleCatalytic Activity of TS-1 on the Hydroxylation of Benzene and Toluene with Hydrogen Peroxide in a Bubble Reactoren_US
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