Gryglewicz G, Stolarski M, Gryglewicz S, Klijanienko A, Piechocki W, Hoste S, Van Driessche I, Carleer R, Yperman J
Institute of Chemistry and Technology of Petroleum and Coal, Department of Chemistry, Wrocław University of Technology, ul. Gdańska 7/9, 50-344 Wrocław, Poland.
Chemosphere. 2006 Jan;62(1):135-41. doi: 10.1016/j.chemosphere.2005.03.097. Epub 2005 Jun 9.
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)).
在搅拌高压釜中,于3 MPa氢气压力下,研究了硫化Ni-Mo/Al₂O₃催化剂上2,3-、2,4-和2,5-二氯联苯的加氢脱氯(HDCl)过程。催化剂通过喷雾干燥制备。通过N₂吸附、热重分析以及带有X射线微分析的扫描电子显微镜对其进行表征。催化HDCl过程的反应温度在230 - 290℃范围内变化。使用无多氯联苯(PCBs)的变压器油作为反应介质。二氯联苯异构体的HDCl程度在82 - 93%范围内。发现脱氯效率与取代氯原子的位置有关,且按以下顺序降低:2,4-二氯联苯≈2,5-二氯联苯>2,3-二氯联苯。为作比较,还研究了无催化剂时2,3-二氯联苯(2,3-PCB)的HDCl过程。2,3-PCB催化HDCl的脱氯率为85%,而在相同操作条件下(即290℃、120分钟后),非催化过程仅导致16%的脱氯。反应产物中未检测到单氯联苯。2,3-PCB催化和非催化转化的数据均符合一级模型。评估了2,3-PCB整体HDCl反应生成联苯的动力学常数和活化能。与非催化过程相比,发现通过喷雾干燥制备的Ni-Mo/Al₂O₃催化剂存在时,活化能降低了近三倍(48 kJ mol⁻¹对124 kJ mol⁻¹)。