Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/2000
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dc.contributor.authorGRYGLEWICZ, Grazyna-
dc.contributor.authorStolarski, M-
dc.contributor.authorGryglewicz, S-
dc.contributor.authorKlijanienko, A-
dc.contributor.authorPiechocki, W-
dc.contributor.authorHoste, S-
dc.contributor.authorVANDRIESSCHE, Yves-
dc.contributor.authorCARLEER, Robert-
dc.contributor.authorYPERMAN, Jan-
dc.date.accessioned2007-11-09T22:37:26Z-
dc.date.available2007-11-09T22:37:26Z-
dc.date.issued2006-
dc.identifier.citationCHEMOSPHERE, 62(1). p. 135-141-
dc.identifier.issn0045-6535-
dc.identifier.urihttp://hdl.handle.net/1942/2000-
dc.description.abstractThe hydrodechlorination (HDCl) process of 2,3-, 2,4- and 2,5-dichlorobiphenyls was studied over a sulphided Ni-Mo/Al2O3 catalyst in a stirred autoclave at a hydrogen pressure of 3 MPa. The catalysts were prepared by spray-drying. They were characterized by N-2 adsorption, thermogravimetry and scanning electron microscopy with X-ray microanalysis. The reaction temperature of the catalytic HDCl process was varied in the range of 230-290 degrees C. Polychlorinated biphenyls (PCBs) free transformer oil was used as reaction medium. The HDCl degree of dichlorobiphenyl isomers was in the range of 82-93%. The efficiency in the chlorine removal was found to be related to the position of the substituted chlorine atom and decreased as follows 2,4-dichlorobiphenyl approximate to 2,5-dichlorobiphenyl > 2,3-dichlorobiphenyl. For comparison, the HDCl process of 2,3-dichlorobiphenyl (2,3-PCB) without catalyst was also studied. The chlorine removal was 85% for the catalytic HDCl of 2,3-PCB whereas non-catalytic process led only to 16% of dechlorination in the same operating conditions, i.e. at 290 degrees C after 120 min. Monodichlorobiphenyls were not detected in the reaction products. The data for both catalytic and non-catalytic conversion of 2,3-PCB fit to a first-order model. Kinetic constants and the activation energy of the overall HDCl reaction of 2,3-PCB to biphenyl were evaluated. Compared to non-catalytic process, a nearly threefold decrease in the activation energy was observed in the presence of Ni-Mo/Al2O3 catalyst prepared by spray-drying (48 kJ mol(-1) vs. 124 kJ mol(-1)). (c) 2005 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subject.otherhydrodechlorination; dichlorobiphenyls; Ni-Mo catalyst; kinetics-
dc.titleHydrodechlorination of dichlorobiphenyls over Ni-Mo/Al2O3 catalysts prepared by spray-drying method-
dc.typeJournal Contribution-
dc.identifier.epage141-
dc.identifier.issue1-
dc.identifier.spage135-
dc.identifier.volume62-
local.format.pages7-
local.bibliographicCitation.jcatA1-
dc.description.notesWroclaw Univ Technol, Dept Chem, Inst Chem & Technol Petr & Coal, PL-50344 Wroclaw, Poland. State Univ Ghent, Dept Inorgan & Phys Chem, Lab Solid State Chem & Ceram Superconductors, B-9000 Ghent, Belgium. Limburgs Univ Ctr, CMK, B-3590 Diepenbeek, Belgium.Gryglewicz, G, Wroclaw Univ Technol, Dept Chem, Inst Chem & Technol Petr & Coal, Ul Gdanska 7-9, PL-50344 Wroclaw, Poland.grazyna.gryglewicz@pwr.wroc.pl-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.bibliographicCitation.oldjcatA1-
dc.identifier.doi10.1016/j.chemosphere.2005.03.097-
dc.identifier.isi000234279300017-
item.contributorGRYGLEWICZ, Grazyna-
item.contributorStolarski, M-
item.contributorGryglewicz, S-
item.contributorKlijanienko, A-
item.contributorPiechocki, W-
item.contributorHoste, S-
item.contributorVANDRIESSCHE, Yves-
item.contributorCARLEER, Robert-
item.contributorYPERMAN, Jan-
item.validationecoom 2007-
item.accessRightsClosed Access-
item.fullcitationGRYGLEWICZ, Grazyna; Stolarski, M; Gryglewicz, S; Klijanienko, A; Piechocki, W; Hoste, S; VANDRIESSCHE, Yves; CARLEER, Robert & YPERMAN, Jan (2006) Hydrodechlorination of dichlorobiphenyls over Ni-Mo/Al2O3 catalysts prepared by spray-drying method. In: CHEMOSPHERE, 62(1). p. 135-141.-
item.fulltextNo Fulltext-
crisitem.journal.issn0045-6535-
crisitem.journal.eissn1879-1298-
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