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双语推荐:原位合成

原位合成技术日益引起科研人员的广泛关注,但是采用原位合成技术制备颗粒增强镍基复合材料的介绍相对较少。介绍了原位合成颗粒增强镍基材料的主要制备方法和工艺,从制造过程分析各方法的优缺点,指出当前研究中存在的主要问题,探讨未来镍基材料制备技术的发展方向。
In-situ synthesis technique is increasingly aroused abroad attention of scientific researchers, and becomes the hotspot of relative research in recent years.But the introduction of particulate reinforced Ni-based composite materials is relatively less.This article introduces the main fabrication methods and techniques of reinforced nickel-based composite materials with in-situ grown particles.By analysing these methods from manufacturing process, the advantages and disadvantages of current studies are discussed, and the future research is proposed .

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配位聚合物通常是指以金属离子或金属簇为中心,以有机配体为联结体,通过金属离子与有机配体之间的配位作用而形成的具有周期性网络结构的一类化合物.为了能得到结构新颖、功能独特的晶体材料,一些非常规的合成方法诸如原位合成法被发现和采用,本论文着重综述了配位聚合物的原位合成策略.
Coordination polymers are a class of compounds with periodical network structures,which usually constructed from metal ions or metal cluster as the center,and organic ligands as connectors? To get new crystal materials with intriguing structures and unique features,some unconventional synthesis methods,such as in?situ ligand synthesis was found and adopted? This paper focuses on review of in?situ synthesis strategy used in preparation of coordination polymers?

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本文报道了镁碱沸石和Beta分子筛在蜂窝状堇青石载体上的原位合成,并探讨了物料配比、晶化时间、载体预处理等因素对原位合成的影响,获得了适宜的合成条件.XRD和SEM的结果显示,使用水热法可使镁碱沸石和Beta分子筛均匀牢固地覆盖在蜂窝状堇青石载体的表面和孔道内壁.为今后使用这种新型复合材料作为汽车尾气净化催化剂打下了基础.
In-situ synthesis of ferrierite and Beta zeolites coated on the honeycomb-shaped cordierite was reported. The influences of composition of the synthesizing mixture, crystallizing time, pretreatment of cordierite and other related factors on the formation of zeolite layer were investigated. And the optimal synthesis conditions were obtained. The results of XRD and SEM show that under this hydrothermal synthesis condition, a continuous layer of ferrierite or Beta zeolite was coated on the both inner and outer surface of the honeycomb-shaped cordierite. It may be a novel monolithic catalyst material in the near future.

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采用共沉淀法合成镁铝硝酸根型层状双氢氧化物前驱体(MgAl-NO-3-LDHs),通过低温焙烧-重构、原位合成方法合成了镁铝尖晶石,研究了反应物中不同铝离子摩尔分数x值(Al3+/(Mg2++Al3+))、重构作用、原位合成温度等因素对合成产物相组成和结构特征的影响。结果表明:随着x值不断增大,镁铝尖晶石的结晶度和质量分数不断提高,晶体初始发育温度不断降低;重构作用使层状双氢氧化物在c轴上层状结构规整度降低,三价铝离子迁移,有助于镁铝尖晶石的合成;随着合成温度的升高,合成产物中镁铝尖晶石相含量和结晶度不断提高,在1 000℃时可以合成结晶良好的镁铝尖晶石。当x=0.60时,其含量达89.51%。
MgAl -NO3--LDHs was prepared by co-precipitation method.Mg-Al spinel was synthesized by LDHs as starting materials in low temperature roast-reconstruction and in-situ synthesis.The influence of recon-struction,mole fraction x value (Al3+/(Mg2++Al3+))and calcination temperature on the component and structure of resultant products was investigated.The results revealed that the relative amount and crystallinity of Mg-Al spinel increases gradually with x value,and the temperature Mg-Al spinel decreases with the increase of x value.The reconstruction of LDHs benefits synthesis of Mg-Al spinel.The relative amount and crystallinity of Mg-Al spinel increase with the increase of temperature,and the mass fraction of Mg-Al spinel reaches 89.5 1%when x equals to 0.60.

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以凹凸棒石黏土为原料,酸化后分别采用原位水热法和两步法制备P型沸石,考察了制备方法和碱液浓度对P型沸石合成的影响并研究其对Cu2+的吸附性能。结果表明,采用原位水热法,添加3~4 mol/L NaOH溶液可生成P型沸石;而采用两步法,NaOH溶液浓度为2~5 mol/L均可合成高结晶度的纯P型沸石,后者合成的P型沸石对水中Cu2+去除率更好。
Zeolite P was synthesized via in situ hydrothermal method and two-step method using acid-treated palygorskite as silica source, respectively. The effects of the method and NaOH concentration on the formation of zeolite P were investigated as well as the adsorption of Cu2+. The results indicated that zeolite P could be synthesized under the NaOH concentration range of 3~4 mol/L via an in situ hydrothermal method. Pure zeolite P with high crystallinity was obtained when the NaOH concentration was 2~5 mol/L via a two-step method and exhibited higher removal rate of Cu2+.

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综述高岭土合成Y型分子筛研究进展,分别从原位合成、纳米分子筛、高硅分子筛和其他合成方法进行评述,并分析各种合成方法的优缺点。原位合成Y型分子筛是合成性质优良Y型分子筛的重要方法,相关研究不断深化成熟,以此方法合成特殊性能的Y型分子筛成功应用于催化裂化催化剂。合成具有特殊形态和结构组成的分子筛如小晶粒Y型分子筛、高硅Y型分子筛是近年来的研究热点。分别从优化合成条件、加入分散剂和使用微波加热法介绍小晶粒Y型分子筛合成研究进展。高硅Y型分子筛的合成主要分为直接合成和二次改性方法,直接合成法反应条件苛刻,存在原料浪费等问题;二次改性方法工艺流程长,易导致合成成本增加。重点讨论具有特种性能的特种Y型分子筛合成研究进展,对离子液体合成Y型分子筛、干胶转化合成Y型分子筛和高岭土合成复合分子筛等新方法进行综述,并结合其他先进的分子筛合成方法,指出Y型分子筛合成的研究方向和前景。
The research advance in synthesis of Y zeolite from kaolin were reviewed. The synthesis of Y zeolite with different methods such as in-situ synthesis of Y zeolite by kaolin microsphere,the synthesis of nanosized molecular sieves,the synthesis of high silica Y zeolite,and other methods were introduced. The analysis and comparison of various raw materials and different synthetic methods were given. Y zeolite synthesized by in-situ crystallization technique from kaolin clay was the most important method for obtaining excellent FCC catalysts. Recent progress in in-situ crystallizing technique was also reviewed. The research on synthesis of special Y zeolite with excellent performance ,especially the synthesis of nanosized and high silica Y zeolite,was focused on. The methods for preparing nanosized Y zeolites,such as optimizing synthesis conditions,adding dispersant agents and microwave synthesis,were described. Y zeolites with high molar ratio of silica to alumina was synthesize

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发展了一种以金属无机盐为前躯体,蔗糖为碳源,介孔二氧化硅SBA-15为模板原位合成金属化合物@介孔碳硅复合材料(M@CS)的方法。采用SEM、TEM、EDS和XRD等手段对材料进行了表征。结果表明不同的原位合成过程对材料的组成和颗粒尺寸有比较重要的影响。本文结果对高稳定嵌入式介孔复合催化剂的制备具有较好的指导意义。
A situ-synthesis method for metal compounds@mesoporous carbon-silica composites (M@CS) was developed. The composites were synthesized using inorganic metal salt as metal precursor, sucrose as carbon precursor, and mesoporous silica SBA-15 as template. The samples were characterized by scanning electron microscopy (SEM), transmission electron microscope (TEM), energy-dispersive X-ray spectrum (EDS) and X-ray diffraction (XRD). The results showed that the synthetic procedures had great influence on the composition and particle size of the final products. This paper provided a good guidance on the synthesis of stabilized mesoporous embedded catalyst.

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介绍了二氧化碳直接还原成碳以及利用原位分解的碳进一步合成甲烷的研究成果,探讨了基本反应原理,并对今后此领域研究的发展趋势和前景作了展望.
The current research achievements on the direct decomposition of carbon dioxide to carbon and further methanation of the in-situ carbon deposited have been introduced, and the mechanism of the CO2 decomposition and further methanation has been discussed. In this paper, the trends of development and the prospect of the research in this field have been anticipated too.

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以改进的原位合成路线,于管状氧化铝载体上合成了高性能的LTA型分子筛膜.考察了常规加热和微波加热对合成的影响.对于95%的异丙醇原料液,常规加热合成和微波加热合成的分子筛膜表现出了相似的优良性能.但是,当原料液中的水含量低于2.0%时,常规加热合成的分子筛膜不再具有有效的脱水性能,这是由于其膜层中有相当数量的纳米级缺陷孔存在.采用微波加热在很大程度上消除了合成过程中非分子筛缺陷孔的生成.
High-performance LTA zeolite membranes were synthesized on tubular supports by a modified in situ synthesis strategy. The preparation by conventional heating (CH) and microwave heating (MH) was studied. Both CH- and MH-synthesized membranes showed high dehydration performance toward 95.0% isopropanol/water mixtures. However, when the water content in the feed was lower than 2.0%, the CH-synthesized membrane had no separation ability any more. This is due to the existence of nanosized non-zeolite pores in the zeolite membranes. These defects could be eliminated mostly using fast and homogenous MH.

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采用水热合成技术,在堇青石蜂窝陶瓷载体上原位合成了SSZ-13分子筛,并借助X射线衍射(XRD)和场发射扫描电子显微镜(FESEM)等手段对其进行表征.在此基础上,研究了合成时间对催化剂结构和机械性能的影响.另外,使用固定床反应器测试了离子交换度为50%的Cu-SSZ-13/堇青石催化剂和Cu-SSZ-13催化剂水热老化前后的氨气选择性催化还原(NH3-SCR) NO性能.结果表明,通过原位合成法制备的Cu-SSZ-13/堇青石催化剂在200-500° C的窗口温度内能达到80%以上的转化率,并在300° C时达到96.4%的转化率.在850°C水热老化12 h后, Cu-SSZ-13催化剂完全丧失了催化性能,而Cu-SSZ-13/堇青石催化剂在300°C时仍然保持91%的转化率.使用XRD和固体27Al核磁共振(27Al NMR)的方法,研究了水热老化前后两种催化剂结构的变化,结果表明,当水热老化12 h后, Cu-SSZ-13基本丧失了SSZ-13结构特征峰,而Cu-SSZ-13/堇青石仍然保持了一定的SSZ-13骨架结构.证明了通过原位合成法制备的Cu-SSZ-13/堇青石催化剂具有较好的抗水热老化性能.
SSZ-13 molecular sieves were synthesized in situ on the surface of a honeycomb-shaped cordierite support using a hydrothermal method, and the resulting material was characterized by X-ray diffraction (XRD) and field emission scanning electron microscope (FESEM). The process for preparing SSZ-13/cordierite was optimized in detail. Furthermore, the ion exchange levels of the 50%Cu-SSZ-13/cordierite and Cu-SSZ-13 catalysts were tested in the ammonia-selective catalytic reduction (NH3-SCR) of NO both before and after the hydrothermal treatment process using a fixed-bed reactor. The results of these experiments showed that the Cu-SSZ-13/cordierite prepared in situ by hydrothermal synthesis had good catalytic activity, and gave an NO conversion of more than 80%at temperatures in the range of 200-500 °C, with the highest NO conversion of 96.4%being reached at 300 °C. After being aged hydrothermal y at 850 °C for 12 h, the SCR activity of the Cu-SSZ-13 catalyst was significantly r

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