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dc.contributor.authorNing Zhangen_US
dc.contributor.authorYongsheng Renen_US
dc.contributor.authorChengqi Liuen_US
dc.contributor.authorHaipeng Zhaoen_US
dc.date.accessioned2019-05-07T09:59:41Z-
dc.date.available2019-05-07T09:59:41Z-
dc.date.issued2017en_US
dc.identifier.issn0125-2526en_US
dc.identifier.urihttp://it.science.cmu.ac.th/ejournal/dl.php?journal_id=8489en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/63982-
dc.description.abstractMetastable zone widths (MSZW) of 2-cyanoguanidine in water, methanol, and ethanol are determined at different cooling rates ((6-30) K×h-1) using polythermal method, respectively. The metastable zone widths of solute in the three solvents increase linearly with the cooling rate increasing. Three nucleation theories are employed to estimate nucleation kinetic parameters based on measured MSZW data. The apparent nucleation order m is computed by Self-consistent Nývlt-like approach and Kubota’s model, which suggests that the nuclei are formed by instantaneous nucleation in methanol and ethanol, while the 2-cyanoguanidine nucleate in water shows the occurrence of progressive nucleation mechanism. The activation energy Esat for nucleation of crystals in solution also is estimated by Arrhenius-type equation.en_US
dc.languageEngen_US
dc.publisherScience Faculty of Chiang Mai Universityen_US
dc.titleInvestigation of Metastable Zone Width and Nucleation Kinetics of 2-cyanoguanidine by Cooling Crystallizationen_US
dc.typeบทความวารสารen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume44en_US
article.stream.affiliationsSchool of Chemistry & Chemical Engineering, Ningxia University, Yinchuan, P.R. China.en_US
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