CO2氧化丙烷脱氢制丙烯用Pd-Cu/V2O5-SiO2催化剂的研究

 采用等体积浸渍法制备了V2O5-SiO2负载的Pd-Cu双金属催化剂,以程序升温还原/程序升温氧化、红外光谱、程序升温脱附和微反技术表征了Pd-Cu/V2O5-SiO2对CO2和丙烷的化学吸附性能及对CO2部分氧化丙烷脱氢反应的催化性能. 结果表明,在催化剂表面金属活性位(Pd,Cu)和邻近的Vn+协同下形成的CO2卧式吸附态可在172和284 ℃断裂形成CO和晶格氧,以甲基氢和亚甲基氢双位吸附在V=O上的丙烷分子吸附态可在238 ℃脱氢生成丙烯. 在600 ℃,CO2/C3H8体积比为1和空速为1?286 h-1的条件下,丙烷转化率为35.22%,丙烯选择性为85.44%. 催化剂V=O中的晶格氧参与了丙烷氧化脱氢过程.     

非线性拉曼激光雷达系统检测CO2气体的受激拉曼过程

 利用气体的受激拉曼散射增益效应的非线性雷达技术是探测大气中的CO₂气体的重要方法，用Nd:YAG固体激光器（1 064 nm）的三倍频光（354.7 nm）注入装有CO₂和N₂高压气体的拉曼管中，气体的受激拉曼散射（SRS）过程产生两种气体的一阶斯托克斯光，用来作为拉曼雷达的发射种子光源。介绍了产生光源的实验装置，论述了SRS中气体气压变化与一阶斯托克斯光能量输出变化的定量关系，得到最佳能量输出的优化条件，并对SRS中一阶斯托克斯光产生过程的物理机制进行了讨论。并根据光源的试验结果，设计了非线性受激拉曼雷达系统，对前期的普通拉曼雷达进行了实验，得到了初步的实验结果。     

Influence of scanning velocity on bovine shank bone ablation with pulsed CO2 laser

The influence of scanning speed on hard bone tissue ablation is studied with a 10.6-μm laser. The groove morphology and the thermal damage created in bovine shank bone by pulsed CO2 laser are examined as a function of incident fluence by optical microscope following standard histological processing. The results show that ablation groove width, depth and ablation volume, as well as the zone of thermal injury, increase gradually with incident fluence. As compared to the result for high scanning speed, the lower scanning speed always produces larger ablation volume but thicker zone of thermal injury. It is evident that scanning speed plays an important role in the ablation process. In clinical applications, it is important to select appropriate scanning speed to obtain both high ablation rates and minimal thermal injury.     

助剂Li对CO2气氛下Fe-Li/AC催化剂上乙苯脱氢反应性能的影响

对 CO2 气氛下 Fe-Li/AC 催化剂上的乙苯脱氢反应性能进行了详细研究. N2 吸附-脱附、CO2 程序升温脱附和 X 射线衍射表征结果表明, 助剂 Li 不仅增加了催化剂比表面积和活性组分分散性, 而且增强了催化剂碱性和 CO2 吸附能力, 从而提高了 Fe/AC 对乙苯脱氢的催化性能. 助剂 Li 能显著提高 Fe/AC 催化剂的乙苯脱氢活性和 CO2 的促进作用, 抑制催化剂的失活. 在 Fe(3.0)-Li(0.6)/AC 催化剂(Fe 和 Li 的负载量分别为 3.0 和 0.6 mmol/g)上, 550 ℃、接触时间为 3.57 (g·h)/mol 和 CO2/乙苯摩尔比为 20 的条件下, 苯乙烯收率可达 62.9%, 选择性为 96.2%. CO2 气氛下的苯乙烯收率显著高于 N2 气氛下的, 归因于 CO2 能保持催化剂表面铁物种的高价态, 并通过逆水煤气变换反应在线除去脱氢反应生成的氢.     

Photolysis studies on HCOOH and HCOO− in presence of TiO2 photocatalyst as suspension in aqueous medium

Photolysis studies on formic acid (HCOOH) and formate ion (HCOO−) in presence of TiO2, a photocatalyst, as suspension in water were carried out separately using 350 nm ultraviolet light. The products, such as H2, CO, CO2 and CH4, generated during the experiments were monitored with varying the ambient, light exposure time, and the concentration of HCOOH/HCOO−. The yields of CO in all these systems increased with light exposure time. In aerated systems, CO yields were higher in contrast to the deoxygenated (Ar-purged) systems under identical conditions. It is proposed apparently that the formation of CO is taking place during the chemical reduction of in-situ generated CO2, a photo-mineralized product of HCOOH/HCOO−, but not through the direct photodecomposition or photodehydration (CO+H2O) of solute molecules. The rates of CO formation during 1.3 M HCOOH photolysis in presence of TiO2 photocatalyst were evaluated to be 0.21 and 0.13 μl/min in aerated and Ar-purged systems, respectively. As compared with HCOOH systems, the CO yields are lower when 0.2 M HCOONa was exposed to light under identical conditions. The CO growth rates were evaluated to be 0.07 and 0.046 μl·min−1 for aerated and deoxygenated HCOONa systems, respectively; moreover, the trend is quite similar to that of the HCOOH system. Under these conditions, the emission of H2 was also observed, and its yield was significantly higher in Ar-purged system as compared with the CO yields. However, in aerated system, the yields of these products were just opposite. The formation of low yield of methane was observed during photolysis of HCOOH/HCOO− ions. In CO2 ambient, the yields of CO and H2 varied drastically with time.     

Nanosized cobalt-based catalyst prepared by supercritical phase condition for Fischer-Tropsch synthesis

A series of nanosized Co/Zn/Mn/K composite catalysts for Fischer-Tropsch synthesis (FTS) were prepared by supercritical fluid drying (SCFD) method and common drying (CD) method. The nanosized cobalt-based catalysts were characterized by XRD, TEM and BET techniques. Their catalytic performances were tested in a slurry-bed reactor under FTS reaction conditions. The drying and crystallization were carried out simultaneously during SCFD, therefore, the catalysts prepared by SCFD method have ideal structure and show the FTS performance superior to the others prepared by CD method. The FTS activity and selectivity were improved via adding Zn, Mn and K promoters, and less CH₄ and CO₂ as well as higher yield of C₅₊ products were achieved. The optimal performance of a 92% CO conversion and a 65% C₅₊ product yield was obtained over a catalyst with the component of Co/Zn/Mn/K = 100/50/10/7. Furthermore, the catalytic performance was studied under the conditions of liquid-phase and supercritical phase slurry-bed, and C₅₊ product yield were 57.4% and 65.4%, respectively. In summary, better catalytic performance was obtained using the nanosized catalyst prepared by SCFD method under supercritical reaction conditions, resulting in higher conversion of CO, less CO₂ byproduct, and higher yield of C₅₊ products.     

Natural gas and biofuel as feedstock for hydrogen production on Ni catalysts

In this article,the aptitude of natural gas as feedstock in steam reforming process for hydrogen production is compared with that of different liquid fuels (pure compounds and commercial fuels),with the aim to investigate the potentialities of biofuels to overcome the CO2 emission problems deriving from fossil fuel processing.The performances of a nickel based catalyst (commercially used in steam reforming of natural gas) were evaluated in terms of feed conversion and yield to the different products as function of temperature,space velocity and water/fuel ratio.Furthermore,a preliminary evaluation of catalyst durability was effected by monitoring yield to H2 versus time on stream and measuring coke formation at the end of experimental tests.High yields to hydrogen were obtained with ail fuels investigated,whereas the deactivation phenomena,which are correlated to carbon deposition on the catalyst,were observed with all tested fuels,except for methane and biofuel.     

基于便捷理念的二氧化碳的制取及性质实验一体化设计

CO2的制取与性质是初中化学的重要内容,教材中的实验较适合教师演示,不便于学生动手操作。本实验设计使用塑料杯、塑料点滴板和塑料注射器进行实验,实现了CO2的制取与性质（密度比空气大且不支持燃烧,以1：1溶于水,水溶液显酸性,能使澄清石灰水变浑浊）一体化,该设计实现了小型化,便于操作,更容易实现学生分组实验、动手参与的目的。同时,对实验设计的思维方法和策略进行提炼,以供其他实验改进参考。     

H型电解池中CO2电化学还原的阳极电解液问题

采用自制的H型电解池开展了KHCO₃溶液中电化学还原CO₂制甲酸的研究. 研究发现,在电解池中长时间电解时阴阳两极间的电压（槽电压）会持续升高,导致电解过程不可持续. 经过恒电位电解、恒电流电解、pH测试以及电解前后阳极室KHCO₃浓度分析等实验研究,作者发现,这是由以下过程引起的：阳极上的析氧反应产生的H⁺与电解液中的HCO₃^-反应生成水和CO₂,导致阳极室的HCO₃^-的消耗,之后阳极室的K⁺被迫扩散进入阴极室而导致阳极室电解质浓度下降. 因此,阳极室电解液导电性下降,进而引起阳极电位的升高. 研究发现,阳极电解液具有碱性时,都可能发生此种现象,因此,为了保证电解过程可持续且保持高的能量转换效率,阳极液的电解质不能是任何具有碱性的物质.     

超临界二氧化碳制备聚合物微孔膜的研究进展

超临界二氧化碳做非溶剂制备聚合物微孔膜是一个新的研究热点,具有传质系数高、聚合物膜干燥速度快且不破坏结构、溶剂容易回收、CO2可循环使用、CO2的低毒性与环境友好性等特点.本文介绍采用超临界CO2制备聚合物微孔膜的热力学及动力学原理,重点介绍近年来采用此技术制备微孔膜的研究成果,如以聚苯乙烯（PS）、聚丙烯腈（PAN）、聚醚砜（PES）等为基体的微孔聚合物膜.