CAJ | 학술논문

将金属阳离子改性的磷钨酸盐(Co0.5PW，Cs2.5PW)负载到 MCM-41介孔分子筛上，制备了负载型磷钨酸(盐)催化剂(Co0.5PW/M，Cs2.5PW/M，PW/M)，考察其在苯甲醚与乙酸酐的 Friedel-Crafts 酰化反应中的催化活性；同时对催化剂样品进行XRD、N2吸-脱附测试、TG-DSC、IR、NH3-TPD等表征分析，对比研究杂多酸(盐)与载体之间的相互作用对催化剂活性影响。结果表明：磷钨酸盐(Co0.5PW和Cs2.5PW)用于苯甲醚的Friedel-Crafts酰化反应时，催化活性低于纯PW；其中，Cs2.5PW的活性高于Co0.5PW。将磷钨酸(盐)负载到MCM-41介孔分子筛后，PW/M的催化活性低于纯PW；Co0.5PW/M与Co0.5PW相比，催化活性显著提高，且高于PW/M；这是由于Co0.5PW较好地分散到载体上，且其与载体间的相互作用增加了酸中心数目，有效提高了催化活性。而Cs2.5PW/M几乎没有催化活性；这是由于Cs2.5PW与载体发生相互作用使Keggin结构发生畸变，酸强度显著减弱、酸中心数目显著减少所致。
장금속양리자개성적린오산염(Co0.5PW，Cs2.5PW)부재도 MCM-41개공분자사상，제비료부재형린오산(염)최화제(Co0.5PW/M，Cs2.5PW/M，PW/M)，고찰기재분갑미여을산항적 Friedel-Crafts 선화반응중적최화활성；동시대최화제양품진행XRD、N2흡-탈부측시、TG-DSC、IR、NH3-TPD등표정분석，대비연구잡다산(염)여재체지간적상호작용대최화제활성영향。결과표명：린오산염(Co0.5PW화Cs2.5PW)용우분갑미적Friedel-Crafts선화반응시，최화활성저우순PW；기중，Cs2.5PW적활성고우Co0.5PW。장린오산(염)부재도MCM-41개공분자사후，PW/M적최화활성저우순PW；Co0.5PW/M여Co0.5PW상비，최화활성현저제고，차고우PW/M；저시유우Co0.5PW교호지분산도재체상，차기여재체간적상호작용증가료산중심수목，유효제고료최화활성。이Cs2.5PW/M궤호몰유최화활성；저시유우Cs2.5PW여재체발생상호작용사Keggin결구발생기변，산강도현저감약、산중심수목현저감소소치。
Phosphotungstate acid or metal cation-modified phosphotungstate supported by siliceous MCM-41 molecular sieve (Co0.5PW/M,Cs2.5PW/M,PW/M) were prepared and their catalytic activities in the anisole Friedel-Crafts acylation reaction were investigated. The prepared samples were characterized by XRD, N2 adsorption-desorption, TG-DSC, IR and NH3-TPD in order to study the interaction between the active components and the supports and their effects on catalytic activities. The results show that, for Friedal-Crafts acylation, the catalytic activities of the cation-modified phosphotungstate are lower than that of bulk PW, while the catalytic activity of Cs2.5PW is higher than that of Co0.5PW. When supported on MCM-41,the catalytic activity of PW/M is lower than bulk PW, while the catalytic activity of Co0.5PW/M shows an obvious increase compared to that of Co0.5PW, which is attributed to the fine dispersion of Co0.5PW on the support, and also due to the increase of acidic sites on the surface of the catalyst by the interaction between Co0.5PW and the support. In the contrary, Cs2.5PW/M has little catalytic activity due to the decrease of acidic sites caused by the interaction between Cs2.5PW and the support.