摘要:
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以无机盐为原料通过控制pH值,用水热法合成含Ni皂石,并以此皂石为前驱物、十六烷基三甲基溴化铵为模板剂,制备含Ni介孔分子筛。用X射线粉末衍射、Fourier变换红外光谱、程序升温还原、透射电子显微镜、比表面积和孔径测定等仪器和方法表征样品的物化性能。结果表明:制得了有序性好的含Ni介孔分子筛,其比表面积为811.2m2/g,平均孔径为3.64nm。所制备的含Ni介孔分子筛经850℃焙烧3h或100℃水热处理10d后仍然具有介孔结构,说明样品具有高的(水)热稳定性。cialis discount coupons go cialis 2015 coupon
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Saponites with Ni were synthesized by a hydrothermal method with inorganic salts as the raw material and with a con- trolled pH value. Then mesoporous molecular sieves with Ni were synthesized by the hydrothermal method with the above synthe- sized saponites as precursors and cetyl trimethyl ammonium bromide as template agent. The samples were characterized by X-ray diffraction, Fourier transform infrared spectra, temperature programmed reduction, transmission electron microscope, nitrogen ad- sorption surface area and porosity measurements. The results show that a highly ordered mesoporous molecular sieve with Ni is ob- tained with specific surface area of 811.2 m2/g and the average pore diameter of 3.64 nm. The prepared mesoporous molecular sieves with Ni still has a mesoporous structure after calcination at 850 ℃ for 3 h or hydrothermal treatment at 100 ℃ for 10 d. It is con- cluded that the obtained samples have high thermal and hydrothermal stability.
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基金项目:
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国家自然科学基金(50471051);;
江苏省高校自然科学基金(04KJD130040)资助项目
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作者简介:
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参考文献:
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[1]BECK J S,VARTULI J C,ROTH W J,et al.A new family of mesoporous molecular sieves prepared with liquid crystal templates[J].J Am Chem Soc,1992,114(27):10834–10843.
[2]HE N Y,GAO J M,BAO S L,et al.Room-temperature synthesis of an Fe-containing mesoporous molecular[J].Mater Lett,1997,31(1–2):133–136.
[3]ZHANG Q H,WANG Y,OSHIHIKO Y,et al.Vanadium-containing MCM–41for partial oxidation of lower alkenes[J].J Catal,2001,202(2):308–318.
[4]姜廷顺,赵谦,陆路德,等.纳米级含钴介孔分子筛的合成与表征[J].硅酸盐学报,2005,33(10):1197–1201.JIANG Tingshun,ZHAO Qian,LU Lude,et al.J Chin Ceram Soc(in Chinese),2005,33(10):1197–1201.
[5]RYOO R,KIM J M,KO C H,et al.Disordered molecular sieve with branched mesoporous channel network[J].J Phys Chem,1996,100(45):17718–17721.
[6]KIM J M,JUN S,RYOO R.Improvement of hydrothermal stability of mesoporous silica using salts:reinvetigation for time-dependent effects[J].J Phys Chem B,1999,103(30):6200–6205.
[7]ZHAO D Y,FENG J L,HUO Q S,et al.Triblock copolymer syntheses of mesoporous silica with periodic50to300angstrom pores[J].Sci-ence,1998,279(5350):548–552.
[8]TANAV P V,PINNAVAIA T J.A neutral templating route to mesopo-rous molecular sieves[J].Science,1995,267(5199):865–868.
[9]HUANG L M,GUO W P,DENG P,et al.Investigation of synthesizing MCM–41/ZSM–5composites[J].J Phys Chem B,2000,104(13):2817–2823.
[10]MATSUMOTO A,SASAKI T,NISHIMIYA N,et al.Thermal stability and hydrophobicity of mesoporous silica FSM–16[J].Colloids Surf A,2002,203(1–3):185–193.
[11]LIU Y,ZHANG W Z,PINNAVAIA T J.Steam-stable aluminosilicate mesostructures assembled from zeolite Y seeds[J].J Am Chem Soc,2000,122(36):8791–8792.
[12]ZHANG Z T,HUA Y,XIAO F S,et al.Mesoporous aluminosilicates with ordered hexagonal structure,strong acidity and extraordinary hydrothermal stability at high temperatures[J].J Am Chem Soc,2001,123(21):5014–5021.
[13]刘子阳.同晶取代2:1型层状硅酸盐及交联物的合成、改性、表征与催化作用[D].长春:吉林大学,1990.LIU Ziyang.Synthesis,modified,characterization,and catalytic per-formance of cross–linked substance and the layer silicate by isomorphous substitution.(in Chinese,dissertation).Changchun:Jilin University,1990.
[14]BARRETT E P,JOYNER L G,HALENDA P P.The determination of pore volume and area distributions in porous substances.I computation from nitrogen isotherms[J].J Am Chem Soc,1951,73(1):373–380.
[15]SELVARAJ M,PANDURANGAN A,SESHADRI K S,et al.Synthesis,characterization and catalytic application of MCM–41mesoporous molecular sieves containing Zn and Al[J].Appl Catal A:General,2003,242(2):347–364.
[16]WOJCIESZAK R,MONTEVERDI S,MERCY M,et al.Nickel containing MCM–41and AlMCM–41mesoporous molecular sieves characteristics and in the hydrogenation of benzene[J].Appl Catal A:General,2004,268(1–2):241–253.
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