Methanol amination over hydrothermally treated zeolites RHO and Modernite

dc.contributor.advisorO'Connor, Cyril Ten_ZA
dc.contributor.advisorVan Steen, Ericen_ZA
dc.contributor.authorVan Steen, Linda Heather Callananen_ZA
dc.date.accessioned2017-02-01T10:45:50Z
dc.date.available2017-02-01T10:45:50Z
dc.date.issued2000en_ZA
dc.date.updated2016-11-30T10:49:41Z
dc.description.abstractMethylamines are important chemicals in many industrial processes. They have use as intermediates for the production of many compounds containing amino groups as well as being used on their own. The acid catalysed amination of methanol generally yields a thermodynamically controlled product distribution. The equilibrium distribution for mono-, di-, and trimethylamine (MMA, DMA, and TMA), at 325°C and a molar methanol to ammonia ratio of 1, is 17, 21, and 62 mol % respectively. The market demand, on the other hand, is for about 33, 53, and 14 mol % MMA, DMA and TMA. Industrially, methylamines are formed by the reaction of methanol or dimethyl ether and ammonia over amorphous silica-alumina. This process involves large separation and recycle units which are both costly and energy intensive as the separation requires azeotropic distillation at 15 bar. Methylamines can be formed over other solid acid catalysts with definite crystal structures, namely zeolites. While being more active than amorphous silica-alumina, most zeolites do not show improved selectivity. Catalysts, which have, however, been reported to show improved selectivity to DMA, include zeolites Rho, ZK-5 and Chabazite. In addition, certain forms of hydrothermally treated Mordenite can produce nonequilibrium product distributions. The performance of Rho can also be improved with hydrothermal treatment. The objectives of this study were briefly as follows. Firstly, the question was asked as to which of the catalysts studied, viz. Rho and Mordenite, was the most suitable for the methanol amination reaction. The second objective was to find the optimal performance achievable from any catalyst using hydrothermal treatment. The third, and possibly most important, objective was to propose reasons for the changes caused to each catalyst by hydrothermal treatment.en_ZA
dc.identifier.apacitationVan Steen, L. H. C. (2000). <i>Methanol amination over hydrothermally treated zeolites RHO and Modernite</i>. (Thesis). University of Cape Town ,Faculty of Engineering & the Built Environment ,Department of Chemical Engineering. Retrieved from http://hdl.handle.net/11427/23806en_ZA
dc.identifier.chicagocitationVan Steen, Linda Heather Callanan. <i>"Methanol amination over hydrothermally treated zeolites RHO and Modernite."</i> Thesis., University of Cape Town ,Faculty of Engineering & the Built Environment ,Department of Chemical Engineering, 2000. http://hdl.handle.net/11427/23806en_ZA
dc.identifier.citationVan Steen, L. 2000. Methanol amination over hydrothermally treated zeolites RHO and Modernite. University of Cape Town.en_ZA
dc.identifier.ris TY - Thesis / Dissertation AU - Van Steen, Linda Heather Callanan AB - Methylamines are important chemicals in many industrial processes. They have use as intermediates for the production of many compounds containing amino groups as well as being used on their own. The acid catalysed amination of methanol generally yields a thermodynamically controlled product distribution. The equilibrium distribution for mono-, di-, and trimethylamine (MMA, DMA, and TMA), at 325°C and a molar methanol to ammonia ratio of 1, is 17, 21, and 62 mol % respectively. The market demand, on the other hand, is for about 33, 53, and 14 mol % MMA, DMA and TMA. Industrially, methylamines are formed by the reaction of methanol or dimethyl ether and ammonia over amorphous silica-alumina. This process involves large separation and recycle units which are both costly and energy intensive as the separation requires azeotropic distillation at 15 bar. Methylamines can be formed over other solid acid catalysts with definite crystal structures, namely zeolites. While being more active than amorphous silica-alumina, most zeolites do not show improved selectivity. Catalysts, which have, however, been reported to show improved selectivity to DMA, include zeolites Rho, ZK-5 and Chabazite. In addition, certain forms of hydrothermally treated Mordenite can produce nonequilibrium product distributions. The performance of Rho can also be improved with hydrothermal treatment. The objectives of this study were briefly as follows. Firstly, the question was asked as to which of the catalysts studied, viz. Rho and Mordenite, was the most suitable for the methanol amination reaction. The second objective was to find the optimal performance achievable from any catalyst using hydrothermal treatment. The third, and possibly most important, objective was to propose reasons for the changes caused to each catalyst by hydrothermal treatment. DA - 2000 DB - OpenUCT DP - University of Cape Town LK - https://open.uct.ac.za PB - University of Cape Town PY - 2000 T1 - Methanol amination over hydrothermally treated zeolites RHO and Modernite TI - Methanol amination over hydrothermally treated zeolites RHO and Modernite UR - http://hdl.handle.net/11427/23806 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/23806
dc.identifier.vancouvercitationVan Steen LHC. Methanol amination over hydrothermally treated zeolites RHO and Modernite. [Thesis]. University of Cape Town ,Faculty of Engineering & the Built Environment ,Department of Chemical Engineering, 2000 [cited yyyy month dd]. Available from: http://hdl.handle.net/11427/23806en_ZA
dc.language.isoengen_ZA
dc.publisher.departmentDepartment of Chemical Engineeringen_ZA
dc.publisher.facultyFaculty of Engineering and the Built Environment
dc.publisher.institutionUniversity of Cape Town
dc.subject.otherChemical Engineeringen_ZA
dc.titleMethanol amination over hydrothermally treated zeolites RHO and Moderniteen_ZA
dc.typeDoctoral Thesis
dc.type.qualificationlevelDoctoral
dc.type.qualificationnamePhDen_ZA
uct.type.filetype
uct.type.filetypeText
uct.type.filetypeImage
uct.type.publicationResearchen_ZA
uct.type.resourceThesisen_ZA
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