翻译英语文章

由于写论文急用,麻烦大家帮我翻译以下两段英语文章,谢谢大家啦(帮忙调整好语序,谢谢各位仁兄了):1、Five samples with different Si/Ni molar ratios (8–100) were prepared by the conventional hydrothermal synthesis in an alkalifree medium. Nickel nitrate (Ni(NO3)2-6H2O), tetraethyl orthosilicate(TEOS,Si(OC2H5)4), cetyltrimethylammonium bromide (CTAB, C16H33(CH3)3NBr), and ammonia were used as precursors.The molar composition of the synthesis gel was 1TEOS:xNi:0.12CTAB:12.3NH4OH:84.4H2O. The resultant gels were crystallized in Teflon-lined autoclaves at 120 8C for 4 days under autogenous pressure. The solid products were recovered by filtration, washed with deionized water and dried at ambient temperature overnight. The template was removed by calcination at 540 8C for 6 h under flowing air. For comparison, siliceous MCM-41 and fumed-silica supported nickel catalysts with the same loading of nickel were prepared by wet impregnation with nickel nitrate solution.
2、The reducibility of catalysts was studied by hydrogen temperature-programmed reduction (TPR) on a Quantachrome Autosorb-1C apparatus. Prior to reduction, the sample (0.25 g) was pretreated with air at 500 8C for 60 min and then cooled to 90 8C.The TPR experiment was performed under 5 vol.% H2/Ar mixture at a heating rate of 8 8C/min from 90 to 950 8C. The consumption of hydrogen was monitored on-line with a build-in thermal conductivity detector (TCD).

1.用不同的Si/Ni槽牙比率(8-100)的五个样品由常规热液综合在alkalifree媒介准备。 镍硝酸盐(Ni (NO3) 2-6H2O),四乙orthosilicate (TEOS, Si (OC2H5) 4),十六烷基三甲基铵溴化物(CTAB, C16H33 (CH3) 3NBr)和氨使用了作为前体。综合胶凝体的槽牙构成是1TEOS :xNi :0.12CTAB :12.3NH4OH :84.4H2O. 总值胶凝体在聚四氟乙烯被排行的压热器被结晶了在120 8C 4天在自生的压力下。坚实产品由滤清恢复,用被去离子的水洗涤了并且隔夜被烘干了在周围温度。模板被锻烧去除在540 8C为6 h在流动的空气之下。 为比较、硅质的支持的MCM-41和fumed硅土镍催化剂以镍同样装货由湿注入准备用镍硝酸盐解答。
2.催化剂的还原性由氢温度被编程的减少(TPR)学习在Quantachrome Autosorb-1C用具。在减少之前,样品(0.25 g)预了处理与空气在500 8C 60分钟然后冷却了对90 8C。TPR实验执行了在5 vol.% H2/Ar混合物以下以8 8C/min的加热速率从90到950 8C。 氢的消耗量在网上监测了与a修造在导热性探测器(TCD)。
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第1个回答  2009-04-08
1 ,五款不同硅/镍摩尔比( 8-100 )编写了传统的水热合成在alkalifree媒介。硝酸镍(镍( NO3 ) 2的- 6H2O ) ,四乙基orthosilicate (正硅酸乙酯,硅( OC2H5 ) 4 ) ,十六烷基三甲基溴化铵( CTAB , C16H33 (甲基) 3NBr )和氨被用作precursors.The摩尔组成的合成凝胶是1TEOS : xNi : 0.12CTAB : 12.3NH4OH : 84.4H2O 。由此产生的凝胶体现在特氟龙内衬釜120 8C 4天的压力下自。固体产品收回的过滤,洗涤与去离子水,并在室温下干燥过夜。模板去除焙烧540 8C下为6小时的空气流动。相比之下,硅MCM - 41和气相二氧化硅支持镍催化剂具有相同载入中镍,制备了湿浸渍与硝酸镍的解决办法。
2 ,还原的催化剂,研究了氢程序升温还原(还原)的Quantachrome Autosorb - 1C号器具。之前减少,样本( 0.25克)预处理与空气在500 8C为60分钟,然后冷却至90 8C.The的TPR实验是在5卷。 % H2/Ar混合物加热速度在8 8C/min从90个增加到950 8C 。消费的氢气监测在线与建设中的热导检测器(中药) 。
第2个回答  2009-04-08
1、5个样品与不同的硅/镍摩尔配比(8 - 1)由传统的水热合成法的alkalifree介质。镍硝态氮(倪硝态氮2 - 6H2O),以orthosilicate正硅酸乙酯、Si(OC2H5(4),cetyltrimethylammonium)(溴化十六烷三甲基铵、C16H33(溴化3NBr)和CH3)被用作前兆氨…这个摩尔组成的合成1TEOS凝胶xNi:0.12CTAB:12.3NH4OH::84.4H2O。在阐明凝胶晶Teflon-lined 120小孔监视器4天的自体压力下。固体产品经过滤、洗涤和去离子水、乾室温过夜。这个模板被清除,监视器为540煅烧空气流动下6小时。与之相比,fumed-silica硅MCM-41支持镍催化剂,用同一加载的镍浸渍,并采用湿镍溶液。 二、还原性催化剂的研究temperature-programmed还原氢Quantachrome TPR)Autosorb-1C装置。前红色
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