Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method
Grażyna Gryglewicz
1
,
M. Stolarski
1
,
S. Gryglewicz
1
,
A Klijanienko
1
,
W. PIECHOCKI
1
,
S. Hoste
2
,
Isabel Van Driessche
2
,
R. Carleer
3
,
J. Yperman
3
3
Applied of Chemistry, Limburgs Universitair Centrum, CMK, B-3590 Diepenbeek, Belgium
|
Publication type: Journal Article
Publication date: 2006-01-01
scimago Q1
SJR: 1.896
CiteScore: 18.1
Impact factor: —
ISSN: 00456535, 18791298
PubMed ID:
15949837
General Chemistry
General Medicine
Environmental Chemistry
Environmental Engineering
Health, Toxicology and Mutagenesis
Public Health, Environmental and Occupational Health
Pollution
Abstract
The hydrodechlorination (HDCl) process of 2,3-, 2,4- and 2,5-dichlorobiphenyls was studied over a sulphided Ni-Mo/Al(2)O(3) 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 approximately 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/Al(2)O(3) catalyst prepared by spray-drying (48 kJ mol(-1) vs. 124 kJ mol(-1)).
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Gryglewicz G. et al. Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method // Chemosphere. 2006. Vol. 62. No. 1. pp. 135-141.
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Gryglewicz G., Stolarski M., Gryglewicz S., Klijanienko A., PIECHOCKI W., Hoste S., Van Driessche I., Carleer R., Yperman J. Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method // Chemosphere. 2006. Vol. 62. No. 1. pp. 135-141.
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RIS
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TY - JOUR
DO - 10.1016/j.chemosphere.2005.03.097
UR - https://doi.org/10.1016/j.chemosphere.2005.03.097
TI - Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method
T2 - Chemosphere
AU - Gryglewicz, Grażyna
AU - Stolarski, M.
AU - Gryglewicz, S.
AU - Klijanienko, A
AU - PIECHOCKI, W.
AU - Hoste, S.
AU - Van Driessche, Isabel
AU - Carleer, R.
AU - Yperman, J.
PY - 2006
DA - 2006/01/01
PB - Elsevier
SP - 135-141
IS - 1
VL - 62
PMID - 15949837
SN - 0045-6535
SN - 1879-1298
ER -
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BibTex (up to 50 authors)
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@article{2006_Gryglewicz,
author = {Grażyna Gryglewicz and M. Stolarski and S. Gryglewicz and A Klijanienko and W. PIECHOCKI and S. Hoste and Isabel Van Driessche and R. Carleer and J. Yperman},
title = {Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method},
journal = {Chemosphere},
year = {2006},
volume = {62},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/j.chemosphere.2005.03.097},
number = {1},
pages = {135--141},
doi = {10.1016/j.chemosphere.2005.03.097}
}
Cite this
MLA
Copy
Gryglewicz, Grażyna, et al. “Hydrodechlorination of dichlorobiphenyls over Ni–Mo/Al2O3 catalysts prepared by spray-drying method.” Chemosphere, vol. 62, no. 1, Jan. 2006, pp. 135-141. https://doi.org/10.1016/j.chemosphere.2005.03.097.