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首页> 外文期刊>ChemCatChem >Facile in situ Encapsulation of Highly Dispersed Ni@MCM-41 for the Trans-Decalin Production from Hydrogenation of Naphthalene at Low Temperature
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Facile in situ Encapsulation of Highly Dispersed Ni@MCM-41 for the Trans-Decalin Production from Hydrogenation of Naphthalene at Low Temperature

机译:适用于高度分散的Ni @ MCM-41的封装,用于在低温下萘的氢化产生的反式癸酰蛋白产生

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Ni@MCM-41 catalyst that has uniformly distributed, highly dispersed Ni nanoparticles (about 2.3 nm) was designed and successfully synthesized by in situ encapsulation of Ni in the channels of MCM-41. This catalyst exhibits excellent thermal stability and hydrogenation activity. Water insoluble nickel acetylacetonate (Ni(acac)(2)) was first dissolved aqueous solution of cetyltrimethyl ammonium bromide (CTAB) and encapsulated in micelles of CTAB. Sodium silicate was used as a silicon source to rapidly hydrolyze and then wrap on the micelle surface to synthesize the MCM-41 zeolite. The MCM-41 zeolite encapsulating Ni(acac)(2) was synthesized within a short time (4 h) at 120 degrees C. Compared with conventional supported catalysts, thus 3 wt.% Ni@MCM-41 has ultra-small uniformly distributed Ni nanoparticles and exhibits improved activity for the hydrogenation of naphthalene to decalin at very low reaction temperatures. The TOF and the apparent activation energy of Ni@MCM-41 and the conventional catalysts (Ni/MCM-41 and Pt/MCM-41) were evaluated and compared. And the catalysis mechanism was analyzed. Furthermore, this Ni@MCM-41 catalyst offers an additional advantage of selectivity in decalin isomerization; 92 % trans-decalin selectivity was achieved at a wide temperature range.
机译:Ni @ MCM-41催化剂,其具有均匀分布的高度分散的Ni纳米颗粒(约2.3nm)设计并成功地通过在MCM-41的通道中封装Ni的封装而成功地合成。该催化剂表现出优异的热稳定性和氢化活性。水不溶性镍乙酰丙酮(Ni(ACAC)(2))首先溶解甲甲基三甲基溴化物(CTAB)的水溶液,并用CTAB的胶束包封。使用硅酸钠作为硅源以快速水解,然后在胶束表面上包装以合成MCM-41沸石。将MCM-41沸石包封Ni(ACAC)(2)在短时间内(4小时)在120℃下合成,与常规负载的催化剂相比,因此3重量%。%NI @ MCM-41具有超小均匀分布Ni纳米粒子并表现出在非常低的反应温度下萘氢化萘的活性。评估NI @ MCM-41和常规催化剂(Ni / MCM-41和Pt / MCM-41)的TOF和表观活化能量。分析了催化机制。此外,该NI @ MCM-41催化剂提供了癸蛋白异构化选择性的额外优点;在宽温度范围内实现了92%的反式癸蛋白选择性。

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