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首页> 外文期刊>Catalysis Today >Hydrodechlorination of PCDDs, PCDFs and dl-PCBs in fly ashes from a Colombian incinerator over mono and multimetallic (Mo, Ni, Pd) alumina-supported catalysts
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Hydrodechlorination of PCDDs, PCDFs and dl-PCBs in fly ashes from a Colombian incinerator over mono and multimetallic (Mo, Ni, Pd) alumina-supported catalysts

机译:来自哥伦比亚焚烧炉的PCDD,PCDF和DL-PCB的PCDDS,PCDFS和DL-PCB的含水剂和多金属(MO,Ni,Pd)氧化铝支持的催化剂

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摘要

Mono, bi and trimetallic catalysts of Mo, Ni and Pd supported on gamma-Al2O3 were synhesized and tested for hydrodechlorination of PCDD/Fs and dl-PCBs of fly ashes from a Colombian solid waste incinerator. Catalysts were characterized by elemental analysis, BET, XRD, NH3-TPD, pyridine FTIR, H-2-TPR, UV-vis, CO chemisorption and TEM. BET surface area and total pore volume decreased slightly after metal incorporation. All the synthesized materials showed type IV isotherm with H1 hysteresis. No metal oxides were detected by XRD, suggesting a high dispersion of metals that was confirmed with CO analysis. UV-vis spectra showed a band associated with the charge transfer of O2- -> Mz+ and catalysts displayed media and strong acidity; only Lewis acid sites were identified by pyridine FTIR. The reduction of the metals in the catalysts was not complete under the used conditions; then no all the material was available for reaction. Bimetallic and trimetallic supported catalysts containing Pd showed a greater catalytic activity towards hydrodechlorination than the corresponding monometallic catalysts. The best activity was obtained over MoPdA catalyst that showed the highest medium acidity content (59%) with 0.32 and 0.64% wt of Pd and Mo, respectively. Conversion and reduction in toxicity was 99.9% for PCDD/Fs; and 97.1% conversion and 99.5% reduction in toxicity for dl-PCBs. Rate of disappearance of chlorinated compounds was favored by bimetallic catalysts that contained Pd.
机译:合成了以γ-Al2O3为载体的钼、镍和钯单金属、铋和三金属催化剂,并对哥伦比亚固体废物焚烧炉飞灰中的PCDD/Fs和dl-PCBs进行了加氢脱氯试验。通过元素分析、BET、XRD、NH3-TPD、吡啶FTIR、H-2-TPR、UV-vis、CO化学吸附和TEM对催化剂进行了表征。金属加入后,BET比表面积和总孔体积略有下降。所有合成材料均表现出具有H1滞后的IV型等温线。XRD未检测到金属氧化物,这表明金属的高度分散性已通过CO分析得到证实。紫外-可见光谱显示与O2的电荷转移有关的一条带--->Mz+,催化剂显示介质和强酸性;吡啶-FTIR仅鉴定出路易斯酸位点。在使用条件下,催化剂中的金属还原不完全;然后没有反应,所有的材料都可用于反应。与相应的单金属催化剂相比,含钯的双金属和三金属负载催化剂表现出更高的氢脱氯催化活性。MoPdA催化剂的活性最好,其中酸性含量最高(59%),Pd和Mo的重量分别为0.32%和0.64%。二恶英/二恶英的转化率和毒性降低率为99.9%;dl-PCBs的转化率为97.1%,毒性降低了99.5%。含钯的双金属催化剂有利于氯代化合物的消失速度。

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