Rapid, Photocatalytic, and Deep Debromination of Polybrominated Diphenyl Ethers on Pd-TiO<sub>2</sub>: Intermediates and Pathways
作者:Lina Li、Wei Chang、Ying Wang、Hongwei Ji、Chuncheng Chen、Wanhong Ma、Jincai Zhao
DOI:10.1002/chem.201402477
日期:2014.8.25
significant difference between the Pd–TiO2 and pristine TiO2 systems, and much less position selectivity for the debromination on Pd–TiO2 was observed than that on the pristine TiO2 surface. For another polybrominated diphenyl ether (BDE15), pristine TiO2 was incapable of its photocatalytic reduction, whereas the loading of Pd enabled its debromination to diphenyl ether within 20 min. In addition, an evident
带有表面负载钯的二氧化钛(Pd–TiO 2)在阳光或人工光源的照射下,在1 h内即可轻松地从十溴二苯醚(BDE209)中去除所有十个溴原子。相比之下,即使经过长时间照射(5小时),在原始TiO 2上也可以消除少于三个的溴原子。此外,在光催化脱溴过程中,所形成的BDE中间体在Pd-TiO 2和原始TiO 2体系之间显示出显着差异,并且观察到的脱溴在Pd-TiO 2上的位置选择性比在原始TiO 2表面上的位置选择性小得多。。对于另一种多溴二苯醚(BDE15),原始TiO2不能进行光催化还原,而Pd的负载使其能够在20分钟内脱溴成二苯醚。此外,在Pd-TiO 2上光催化脱溴BDE15出现了明显的诱导期。实验表明,Pd共催化作用会显着改变光催化还原性脱溴途径。