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Atmospheric hydrogenolysis of methyl formate to bio-methanol using Cu/MgO catalyst

Hendriyanaa, Susanto H.b, Subagjob

a Chemical Engineering Department, Faculty of Engineering, Universitas Jenderal Achmad Yani, Indonesia
b Chemical Engineering Department, Faculty of Industrial Technology, InstitutTeknologi Bandung, Indonesia

[vc_row][vc_column][vc_row_inner][vc_column_inner][vc_separator css=”.vc_custom_1624529070653{padding-top: 30px !important;padding-bottom: 30px !important;}”][/vc_column_inner][/vc_row_inner][vc_row_inner layout=”boxed”][vc_column_inner width=”3/4″ css=”.vc_custom_1624695412187{border-right-width: 1px !important;border-right-color: #dddddd !important;border-right-style: solid !important;border-radius: 1px !important;}”][vc_empty_space][megatron_heading title=”Abstract” size=”size-sm” text_align=”text-left”][vc_column_text]© 2017 Author(s).Activity at various operating condition on the hydrogenolysis of methyl formate to bio-metanol using Cu/MgO catalyst were tested in the range of 19.7 ± 75.5%-wt Cu, 120±180°C, 1±2 molar feed ratio (H2/HCOOCH3) and 1.4±4.3 kg.h/kmol. Methanol was produced under the studied conditions. Copper concentration have a significant effect on the activity of the catalyst. A maximum conversion of hydrogen was obtained at 51.7%-wt of Cu (C75M25). Higher temperatures and space time enhanced methanol productivity, while higher molar feed ratio decreased productivity. Kinetic experiments of hydrogenolysis of methyl formate were carried out using a C75M25 catalyst. Kinetic studies, interpreted by applying the basis of the Langmuir-Hinshelwood model, suggested that the rate-determining step involves the reaction of adsorbed methyl formate with adsorbed H atoms. The activation energy of this reaction was measured to be about 57 kJ.mol-1.[/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Author keywords” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Indexed keywords” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”Funding details” size=”size-sm” text_align=”text-left”][vc_column_text][/vc_column_text][vc_empty_space][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][vc_empty_space][megatron_heading title=”DOI” size=”size-sm” text_align=”text-left”][vc_column_text]https://doi.org/10.1063/1.5011862[/vc_column_text][/vc_column_inner][vc_column_inner width=”1/4″][vc_column_text]Widget Plumx[/vc_column_text][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row][vc_row][vc_column][vc_separator css=”.vc_custom_1624528584150{padding-top: 25px !important;padding-bottom: 25px !important;}”][/vc_column][/vc_row]