气相色谱法测定空气和废气中氯乙烯的改进

因填充柱装柱繁琐,柱效低,最低检出浓度高,不能判别无组织废气中氯乙烯的浓度是否达到《大气污染物综合排放标准》（GB16297—1996）排放限值的要求;用毛细管柱能满足分析的要求。     

Metal chlorides loaded on activated carbon to capture elemental mercury

Activated carbon (AC) was considered to be an effective sorbent to control mercury in combustion systems. However, its capture capacity was low and it required a high carbon-to-mercury mass ratio. AC loaded with catalyst showed a high elemental mercury (Hg0) capture capacity due to large surface area of AC and high oxidization ability of catalyst. In this study, several metal chlorides and metal oxides were used to promote the sorption capacity of AC. As a result, metal chlorides were better than metal oxides loaded on AC to remove gaseous mercury. X-ray diffractometer (XRD), thermogravimetric analyzer (TGA) and specific surface area by Brunauer- Emmett-Teller method (BET) analysis showed the main mechanisms: first, AC had an enormous surface area for loading enough MClx; second, Cl and MxOy were generated during pyrogenation of MClx; finally, there were lots of active elements such as Cl and MxOy which could react with elemental mercury and convert it to mercury oxide and mercury chloride. The HgO and HgCl2 might be released from AC’s porous structure by thermo regeneration. A catalytic chemisorption mechanism predominates the sorption process of elemental mercury. As Co and Mn were valence variable metal elements, their catalytic effect on Hg0 oxidization may accelerate both oxidation and halogenation of Hg0. The sorbents loaded with metal chlorides possessed a synergistic function of catalytic effect of valence variable metal and chlorine oxidation.     

加氢站用45 MPa高压储氢瓶式容器火烧试验模拟*

为研究加氢站用高压储氢容器在火灾下的安全性能,采用计算流体力学（CFD）方法对45 MPa高压储氢瓶式容器火烧试验过程进行模拟研究,结合气瓶火烧试验,分析高压储氢容器火灾下的热响应过程,研究不同因素对储氢容器压力泄放装置动作时间的影响。结果表明:613 s以内试验压力与模拟数据的最大相对误差为3.9%,模型误差在可接受范围;不同充装介质对安全泄放装置动作时间影响不大;不同充装压力对容器内介质压升速率影响较大,充装水平较高时压力泄放装置更快动作,较低的充装压力下容器内介质温升较快;不同环境温度对介质温升影响较小。     

Development of a PEMFC-based heat and power cogeneration system

Hydrogen-fed proton exchange membrane fuel cell (PEMFC) has to overcome high installation and operation cost before being adopted as a distributed power candidate. Cogeneration of power and heat is a good approach to increase hydrogen energy utilization rate. A PEMFC-based power and heat cogeneration system is proposed and established in the current study to investigate system’s technological and economical feasibility. This cogeneration of heat and power (CHP) system composes of a 2.5-kW fuel cell stack, hydrogen supply system, air supply system, water and heat management system, and heat recovery system. The control strategies to automate the system operation are realized by a programmable automation controller (PAC) system. Detailed measurement of the system is also constructed along with a web-based human–machine interface (HMI) platform to facilitate experiments and demonstration. Preliminary testing of the CHP system shows good performance of heat and power outputs. System’s electrical power conversion efficiency and thermal efficiency of the CHP system are measured at 38% and 35%, respectively. System combined efficiency therefore reached about 73%.     

Pd/Al2O3粒子电极电催化还原BrO3-的研究

针对常规方法难以去除水中Br_3~-的问题,采用浸渍煅烧法制备了负载型纳米Pd/Al_2O_3粒子电极,研究了该电极电催化还原Br O-3的效果.催化剂的结构表征表明该反应实现了Pd纳米晶的均匀负载,纳米Pd/Al_2O_3具有较高的电催化活性和较低的能耗,其最佳反应条件为3%Pd负载量,0.9 m A·cm-2电流密度和1 g·L催化剂投量,酸性条件可促进Br O-3的直接或间接还原.ESR检测证实了Pd的负载增强了反应体系活性物种[H]的生成,进而促进了Br O-3的间接电催化还原.     

纳米Fe_3O_4强化混凝-Fenton氧化预处理垃圾渗滤液

采用纳米Fe_3O_4与Fe Cl3制备复合混凝剂,利用混凝沉淀-Fenton氧化工艺预处理垃圾渗滤液原水,研究其处理效果。结果表明:在纳米Fe_3O_4投加量为2 g/L,Fe Cl3投加量为1.4 g/L时制备的复合混凝剂,在p H值为6.5,转速为300 r/min下快速搅拌1 min,转速为100 r/min下慢速搅拌30 min,沉淀时间为30 min的条件下,COD去除率为56.8%,ρ(COD)可由5 240 mg/L降低到2 264 mg/L;利用Fenton氧化处理混凝处理出水,在H_2O_2的投加量为5.5 g/L,n(H_2O_2)∶n(Fe2+)=4,p H值为6,反应时间为80 min,反应温度为25℃的最佳条件下,COD和氨氮的去除率分别为55.7%和40.1%,最终出水ρ(COD)和ρ(氨氮)分别为1 003 mg/L和670 mg/L;该组合工艺对垃圾渗滤液有较好的处理效果,COD、色度和氨氮的去除率分别为80.8%、59.5%和76.2%。     

翻堆频率对厨余垃圾堆肥过程中H_2S和NH_3排放的影响

为研究厨余垃圾堆肥过程中翻堆频率对H2S和NH3排放的影响,以大类粗分后的厨余垃圾为研究对象,玉米秸秆为调理剂,设置4组翻堆频率不同的处理(每周2次,2周1次,2周1次和不翻堆)进行对比研究。结果表明:翻堆频率的变化对H2S的排放影响不大,对NH3的排放有显著的影响,翻堆频率过高会增加NH3的累积排放量,翻堆频率过低虽然能降低NH3的累积排放量,但会影响到堆肥产物的腐熟。综合厨余垃圾堆肥的无害化指标、H2S和NH3的排放以及最终堆肥产品的毒性检验,在实验条件下,翻堆频率设为每周1次在堆料腐熟的基础上对H2S和NH3减排效果最好。     

板式生物滴滤塔高效净化硫化氢废气的研究

采用营养液分层喷淋、pH分别在线控制(pH 2.5、 4.5、 6.5)的板式生物滴滤塔(plate type-biotrickling filter, PTBTF)净化H₂S废气,考察PTBTF于挂膜启动及稳定运行阶段对H₂S的降解性能.结果表明,PTBTF系统在14 d内即完成挂膜,对浓度为188.6mg·m^-3的H₂S去除率达到100%;在进口浓度100～1000mg·m^-3、空床停留时间(EBRT)28～4 s的条件下,H₂S的去除率可达到99%以上;当H₂S去除率≥90%时, PTBTF系统的最大去除负荷随EBRT(3.3～6 s)的增加而增大,EBRT 6 s的最大去除负荷达到1019.0g·(m³·h)^-1;上、中、下3层填料对H₂S的去除负荷随进口H₂S负荷的波动呈显著变化;通过荧光染色观察填料上的细胞数,发现在挂膜阶段微生物数量增长明显,第125 d上层、中层和下层填料上的菌落数(以干填料计)分别达到了1.29×10⁷、 5.47×10⁸和1.07×10⁹个·g^-1;采用扫描电镜观察填料表面的生物膜,可见上填料层和下填料层的优势菌分别为杆菌和丝状菌;利用变性梯度凝胶电泳初步揭示了系统运行过程中生物群落的演替规律;通过对产物的分析,确定该PTBTF系统降解H₂S后主要产生SO^2-₄和单质硫.     

造纸废水中有机氯化物的酶处理技术研究进展

目前用于造纸废水有机氯化物处理的酶包括：过氧化物酶、酪氨酸酶、酚氧化酶和木质素过氧化酶等,反应机理是,先通过酶反应形成游离基,然后游离基发生化学聚合反应生成高分子化合物沉淀,影响酶处理效率的主要因素包括污染物种类和浓度,酶的种类和浓度、ｐＨ、絮凝剂和吸附剂以及污染物之间的协同效应等。     

SW型脱硫剂脱硫性能的研究

以硫酸烧渣为主要原料制备ＳＷ型脱硫剂,并对其脱硫性能进行了研究,对半水煤气、葡萄酒厂污水处理产生的沼气和焦炉煤气、水煤气中的Ｈ２Ｓ进行了工业脱硫试验,经半年以上运行证明,可使其Ｈ２Ｓ含量从３０００－５０００ｍｇ／ｍ＾３降为２０ｍｇ／ｍ＾３以下（符合国家标准）,当脱硫剂工作硫容达３０％时可返回硫酸生产中,再生周期一般为３个月,其主要性能达到国内外同类产品水平。