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化学强化剂在电动修复技术中的应用研究进展 被引量:8
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作者 马莉 张国庆 曾彩明 《化工进展》 EI CAS CSCD 北大核心 2008年第1期38-44,共7页
电动修复技术是一种环保、高效的原位修复技术。简述了电动修复技术的基本原理、特点以及待解决的问题。结合国内外现阶段的研究成果,介绍了各种化学强化剂的研究进展和实际应用,并提出了今后主要研究的方向。
关键词 化学强化剂 电动修复 电解液
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聚丙烯酰胺与强化剂联用对土-水界面磷素迁移的影响 被引量:4
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作者 江韬 邓丽莉 +3 位作者 魏世强 陈瑜鹏 卢松 刘双营 《土壤学报》 CAS CSCD 北大核心 2010年第3期473-482,共10页
采用静态吸附解吸试验结合模拟淹水试验,研究了聚丙烯酰胺(PAM)与四种化学强化剂(石灰石L,石膏G,沸石Z,腐殖质H)联用对土壤磷的吸持特性及土壤磷素向水体迁移释放的影响。吸附解吸试验结果表明:PAM和四种化学强化剂(添加量为5%)联用均... 采用静态吸附解吸试验结合模拟淹水试验,研究了聚丙烯酰胺(PAM)与四种化学强化剂(石灰石L,石膏G,沸石Z,腐殖质H)联用对土壤磷的吸持特性及土壤磷素向水体迁移释放的影响。吸附解吸试验结果表明:PAM和四种化学强化剂(添加量为5%)联用均能提高土壤固磷能力,磷平均解吸量和解吸率均小于对照(CK),其中以PAM+石灰石(P0.2+L)吸附能力最强,PAM+腐殖质(P0.2+H)次之;磷吸附动力学过程除PAM+石膏(P0.2+G)和P0.2+H符合抛物面扩散方程外,其余处理均符合Elovich方程和双常数方程。淹水试验结果表明:单施PAM时,0.1%PAM(P0.1)、0.2%PAM(P0.2)及0.4%PAM(P0.4)均可降低生物有效磷(BAP)的释放强度。当不同强化剂与PAM复合后,除P0.2+H外,其余均能有效抑制生物有效磷的释放,降低释放强度,其中以P0.2+L效果最好,上覆水体平均浓度和平均释放强度最低,分别为0.267 mgL-1和1.852 mgm-2d-1。干湿交替后,单施PAM抑制生物有效磷释放的效果明显降低,不同PAM施用量处理与对照无显著差异;而PAM与化学强化剂复合后,除P0.2+H外,其余处理均能持续抑制生物有效磷向水体的释放。 展开更多
关键词 聚丙烯酰胺 化学强化剂 淹水 干湿交替 生物有效磷
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Intensification of Deep Hydrodesulfurization Through a Two-stage Combination of Monolith and Trickle Bed Reactors 被引量:1
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作者 许闵 刘辉 +1 位作者 季生福 李成岳 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2014年第8期888-897,共10页
Deep hydrodesulfurization (HDS) is an important process to produce high quality liquid fuels with ultra-low sul- fur. Process intensification for deep HDS could be implemented by developing new active catalysts and/... Deep hydrodesulfurization (HDS) is an important process to produce high quality liquid fuels with ultra-low sul- fur. Process intensification for deep HDS could be implemented by developing new active catalysts and/or new types of reactors. In this work, the kinetics of dibenzothiophene (DBT) hydrodesulfurization over Ni-P/SBA-15/ cordierite catalyst was investigated at 340-380 ℃ and 3.0-5.0 MPa. The first-order reaction model with respect to both DBT and H2 was used to fit the kinetics data in a batch recycle operation system. It is found that both the activation energy and rate constant over the Ni-P monolithic catalyst under our operating conditions are close to those over conventionally used HDS catalysts. Comparative performance studies of two types of reactors, i.e., trickle bed reactor and monolithic reactor, were performed based on reactor modeling and simulation. The results indicate that the productivity of the monolithic reactor is 3 times higher than that of the trickle bed reactor on a catalyst weight basis since effective utilization of the catalyst is higher in the monolithic reactor, but the volumetric productivity of the monolithic reactor is lower for HDS of DBT. Based on simulation results, a two- reactor-in-series configuration for hydrodesulfurization is proposed, in which a monolithic reactor is followed by a tickled bed reactor so as to attain intensified performance of the system converting fuel oil of different sulfur-containing compounds. It is illustrated that the two reactor scheme outperforms the trickle bed reactor both on reactor volume and catalyst mass bases while the content of sulfur is reduced from 200 μg·g-1 to about 10 μ·g-1. 展开更多
关键词 Hydrodesulfurization (HDS) Kinetics Mass transfer Monolithic reactor Trickle bed reactor Reactor modeling
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Catalyst-Free Growth of Nanographene Films on Various Substrates 被引量:12
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作者 Lianchang Zhang Zhiwen Shi +3 位作者 Yi Wang Rong Yang Dongxia Shi Guangyu Zhang 《Nano Research》 SCIE EI CAS CSCD 2011年第3期315-321,共7页
We have developed a new method to grow uniform graphene films directly on various substrates, such as insulators, semiconductors, and even metals, without using any catalyst. The growth was carried out using a remote ... We have developed a new method to grow uniform graphene films directly on various substrates, such as insulators, semiconductors, and even metals, without using any catalyst. The growth was carried out using a remote plasma enhancement chemical vapor deposition (r-PECVD) system at relatively low temperatures, enabling the deposition of graphene films up to 4-inch wafer scale. Scanning tunneling microscopy (STM) confirmed that the films are made up of nanocrystalline graphene particles of tens of nanometers in lateral size. The growth mechanism for the nanographene is analogous to that for diamond grown by PECVD methods, in spite of sp2 carbon atoms being formed in the case of graphene rather than sp3 carbon atoms as in diamond. This growth approach is simple, low-cost, and scalable, and might have potential applications in fields such as thin film resistors, gas sensors, electrode materials, and transparent conductive films. 展开更多
关键词 NANOGRAPHENE CATALYST-FREE plasma enhancement chemical vapor deposition (PECVD) transparent and conductive film
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