Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/458912
Title: Synthesis of higher carbon number Alcohols from ethanol
Researcher: Vinayagamoorthi, R
Guide(s): Shanthi, K
Keywords: Physical Sciences
Chemistry
Chemistry Applied
Ethanol condensation
Guerbet alcohols
Hydrogenation
University: Anna University
Completed Date: 2021
Abstract: Bio-fuels, based on renewable bio-mass resources, have emerged as newlinethe viable and sustainable alternatives to fossil-based fuels, with a potential to newlinereduce the global warming. Butanol is considered as the future bio-fuel with newlinemany advantages over ethanol. Besides their use as fuels and fuel additives, newlinehigher carbon number (C4-C8) alcohols find wide-spread applications as newlinefeedstocks, chemical intermediates, and in polymers, surfactants and detergent newlineindustries. The objective of the thesis is to develop supported metal catalysts newlinethat display high ethanol conversion with high selectivity for butanol and higher newlinealcohols, under moderate process conditions. newlineAlumina supported nickel catalysts is chosen as the base catalyst. newlineBoth active phase and the support have been subjected to two levels of newlinemodifications in order to improve the performance, as described below: newlinei) adding different metal oxide promoters to the alumina support newlineii) using three different bimetallic active phases -Ni-Co, Ni-Cu newlineand Ni-M with M=Pd, Ru and Au newlineAll the catalysts were prepared by wet impregnation and newlinecharacterized extensively by XRD, Electron microscopy, TPR, TPD of newlineammonia and CO2, XPS and DRS. newlineModification of alumina support by addition of promoter oxides like, newlineLa2O3, CeO2, ZrO2, MgO and TiO2 results in improvements in Ni metal newlinedispersion, reducibility, modulation of metal-support interactions and newlinevariations in total acidity - basicity, and their distribution newline
Pagination: xxii,197p.
URI: http://hdl.handle.net/10603/458912
Appears in Departments:Faculty of Science and Humanities

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01_title.pdfAttached File107.62 kBAdobe PDFView/Open
02_prelim pages.pdf2.91 MBAdobe PDFView/Open
03_content.pdf95.63 kBAdobe PDFView/Open
04_abstract.pdf91.23 kBAdobe PDFView/Open
05_chapter 1.pdf2.1 MBAdobe PDFView/Open
06_chapter 2.pdf687.62 kBAdobe PDFView/Open
07_chapter 3.pdf1.24 MBAdobe PDFView/Open
08_chapter 4.pdf1.01 MBAdobe PDFView/Open
09_chapter 5.pdf710.66 kBAdobe PDFView/Open
10_chapter 6.pdf312.03 kBAdobe PDFView/Open
11_annexures.pdf173.77 kBAdobe PDFView/Open
80_recommendation.pdf133.26 kBAdobe PDFView/Open
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