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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Determination of Acid Site Location in Dealuminated MCM-68 by Al-27 MQMAS NMR and FT-IR Spectroscopy with Probe Molecules
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Determination of Acid Site Location in Dealuminated MCM-68 by Al-27 MQMAS NMR and FT-IR Spectroscopy with Probe Molecules

机译:Al-27MQMAS NMR和FT-IR光谱与探针分子的酸性MCM-68中酸性位点定位的测定

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A series of MCM-68 zeolites with different Si/Al ratios were prepared by treatment with nitric acid and compared with beta zeolites. Speciation of aluminum and location of acid sites changed depending on the Si/Al ratio. The location of Bronsted acid sites in MCM-68 samples was able to be classified by FT-IR measurements with pyridine and 2,6-di-tert-butylpyridine as probe molecules, and the number of Bronsted acid sites was quantified according to the locations. For high-aluminum MCM-68, Bronsted acid sites were broadly distributed in both the 12-ring channel and 10-ring windows as well as inside the supercage. The Bronsted acid sites in the 12-ring channel were easily removed by the acid treatment, and consequently, high-silica MCM-68 had Bronsted acid sites predominantly in the 10-ring windows and inside the supercage. Al-27 MQMAS NMR spectra of high-silica MCM-68 showed two specific peaks assignable to T6 and T7 sites, which did not face the 12-ring channel, forming the Bronsted acid sites highly tolerant to the acid treatment. MCM-68 catalysts showed better catalytic performance in dehydration of sorbitol than beta, mordenite, and ZSM-5. Large void spaces at the intersection of 12- and 10-ring channels and inside the supercage for MCM-68 made it easy to take bulky transition states in the dehydration of sorbitol, resulting in its high catalytic performance.
机译:通过用硝酸处理并与β沸石进行比较,制备一系列具有不同Si / Al比的MCM-68沸石。铝的形态和酸部位的位置根据Si / Al比而改变。 MCM-68样品中的正端酸位点的位置能够通过用吡啶和2,6-二叔丁基吡啶作为探针分子进行分类,并且根据位置定量棱镜酸位点的数量。对于高铝MCM-68,伪造酸部位在12环通道和10环窗口以及叠片内部分布。通过酸处理容易地除去12环通道中的刚性酸部位,因此高二氧化硅MCM-68主要在10环窗口和叠层内部具有正弦酸位点。高二氧化硅MCM-68的Al-27MMR Spectra显示出两种特异性峰,可分配到T6和T7位点,其不面对12环通道,形成高度耐受酸处理的伪造酸部位。 MCM-68催化剂在脱水山梨糖醇的脱水方面表现出比β,丝硝酸酯和ZSM-5更好的催化性能。在12-和10环通道和MCM-68的叠加器内部的大空隙空间使得在山梨糖醇的脱水中易于造成大笨重的过渡状态,导致其高催化性能。

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