积累知识产权优势实现市场竞争优势化

实现市场竞争的优势化实质就是在我国全面实施知识产权战略的前提下,通过科学规划,超前布局,集中力量,在涉及我国科技、文化、经济、贸易等领域,不断积累和掌握我们的后发优势——知识产权优势。     

刘载文 带动团队实现创新梦想

一个人要获得成功必须努力付出,正所谓不经风雨何以现彩虹。刘载文的成功正印证了这句话。刘载文,北京工商大学教授、博士生导师,北京工商大学计算机与信息工程学院院长,控制科学与工程学科建设负责人。     

《中国环境科学》获评“2012中国最具国际影响力学术期刊”

正2012年12月,《中国环境科学》被评为"2012中国最具国际影响力学术期刊"."中国最具国际影响力学术期刊"是中国科学文献计量研究中心、清华大学图书馆依据《CAJ国际引证报告》,按2011年度中国学术期刊被SCI期刊、SSCI期刊引用的总被引频次排序并经40多位期刊界专家审议,遴选出的TOP5%期刊.获评"中国最具国际影响力学术期刊"的科技类期刊共156种.统计分析结果表明,从定量分析的角度     

《中国环境科学》获评“RCCSE中国权威学术期刊(A+)”

正《中国环境科学》在武汉大学中国科学评价研究中心发布的第三届中国学术期刊评价中被评为"RCCSE中国权威学术期刊(A+)".中国学术期刊评价按照各期刊的各指标综合得分排名,将排序期刊分为A+、A、A-、B+、B、C 6个等级,评价的6448种中文学术期刊中有1939种学术期刊进入核心期刊区,其中权威期刊(A+)327种,核心期刊     

《中国环境科学》获评“百种中国杰出学术期刊”

正《中国环境科学》2012年被中国科学技术信息研究所评为"2011年度百种中国杰出学术期刊"."百种中国杰出学术期刊"是根据中国科技学术期刊综合评价指标体系进行评定的,包含总被引频次、影响因子、基金论文比、他引总引比等多个文献计量学指标.     

《中国环境科学》获评“2012中国最具国际影响力学术期刊”

正2012年12月,《中国环境科学》被评为"2012中国最具国际影响力学术期刊"."中国最具国际影响力学术期刊"是中国科学文献计量研究中心、清华大学图书馆依据《CAJ国际引证报告》,按2011年度中国学术期刊被SCI期刊、SSCI期刊引用的总被引频次排序并经40多位期刊界专家审议,遴选出的TOP5%期刊.获评"中国最具国际影响力学术期刊"的科技类期刊共156种.统计分析结果表明,从定量分析的角度     

催化还原法净化处理氮氧化物的工程实例

针对不锈钢产品酸洗处理过程中产生的氮氧化物浓度高、对大气污染的影响大、且难于净化治理等特性,在上海某不锈钢项目中设计了一套酸雾净化系统。该设计解决了酸洗中产生的氮氧化物难以净化的问题,提升了氮氧化物处理技术,它将成为不锈钢酸洗行业中氮氧化物净化处理技术的发展方向。     

Catalytic bubble-free hydrogenation reduction of azo dye by porous membranes loaded with palladium nanoparticles

Catalytic bubble-free hydrogenation reduction of azo dye by porous membranes loaded with palladium （Pd） nanoparticles was studied for the first time. The effects of Pd loading, dye concentration and reuse repetitions of membranes were investigated. In reduction, the dye concentration decreased whereas the pH rose gradually. An optimal Pd loading was found. The catalytic membranes were able to be reused more than 3 times.     

Reaction mechanism and metal ion transformation in photocatalytic ozonation of phenol and oxalic acid with Ag+/TiO2

Photocatalytic ozonation of phenol and oxalic acid （OA） was conducted with a Ag^＋/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag^＋ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger. It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag＋ was easily reduced and deposited on the surface of Tit2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag^＋ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants.     

Effects of metal and acidic sites on the reaction by-products of butyl acetate oxidation over palladium-based catalysts

Catalytic oxidation is widely used in pollution control technology to remove volatile organic compounds. In this study, Pd/ZSM-5 catalysts with different Pd contents and acidic sites were prepared via the impregnation method. All the catalysts were characterized by means of N2 adsorption- desorption, X-ray fluorescence （XRF）, HE temperature programmed reduction （H2-TPR）, and NH3 temperature programmed desorption （NH3-TPD）. Their catalytic performance was investigated in the oxidation of butyl acetate experiments. The by-products of the reaction were collected in thermal desorption tubes and identified by gas chromatography/mass spectrometry. It was found that the increase of Pd content slightly changed the catalytic activity of butyl acetate oxidation according to the yield of CO2 achieved at 90%, but decreased the cracking by-products, whereas the enhancement of strong acidity over Pd-based catalysts enriched the by-product species. The butyl acetate oxidation process involves a series of reaction steps including protolysis, dehydrogenation, dehydration, cracking, and isomerization. Generally, butyl acetate was cracked to acetic acid and 2- methylpropene and the latter was an intermediate of the other by-products, and the oxidation routes of typical by-products were proposed. Trace amounts of 3-methylpentane, hexane, 2-methylpentane, pentane, and 2-methylbutane originated from iso4merization and protolysis reactions.