Carbonyl emissions from vehicular exhausts sources in Hong Kong

Vehicular emission (VE) is one of the important anthropogenic sources for airborne carbonyls in urban area. Six types of VE-dominated samples were collected at representative locations in Hong Kong where polluted by a particular fueled type of vehicles, including (i) a gas refilling taxis station (liquefied petroleum gas [LPG] emission); (ii) a light-duty passenger car park (gasoline emission); (iii) a minibus station (diesel emission); (iv) a single-deck-bus depot (diesel emission); (v) a double-deck-bus depot (diesel emission); and (vi) a whole-food market entrance for light- and heavy-duty vehicles (diesel emission). A total of 15 carbonyls in the samples were quantified. Formaldehyde was the most abundant carbonyl among the VE-dominated samples, and its contribution to the total quantified amount on a molar basis ranged from 54.8% to 60.8%. Acetaldehyde and acetone were the next two abundant carbonyls. The carbonyls were quantified at three roadside locations in Hong Kong. The highest concentrations of formaldehyde and acetaldehyde, 22.7 +/- 8.4 and 6.0 +/- 2.8 microg/m3, respectively, were determined in the samples collected at a main transportation gate for goods between Hong Kong and Mainland China. The total quantified carbonyl concentration, 37.9 +/- 9.3 microg/m3, was the highest at an entrance of a cross-harbor tunnel in downtown area. The theoretical carbonyls compositions of the three roadside locations were estimated according to the VE-dominated sample profiles and the statistics on vehicle numbers and types during the sampling period. The measured compositions of formaldehyde were much higher than the theoretical compositions in summer, demonstrating that photochemical reactions significantly contributed to the formaldehyde production in the roadsides.     

The effects of manganese precursors on Mn-based/TiO2 catalysts for catalytic reduction of NO with NH3

Manganese acetate (MnAc) and manganese nitrate (MnN) were employed as precursors for the preparation of MnAc)/TiO2, Mn (N)/TiO2, Mn(Ac)-Ce/TiO2, and Mn(N)-Ce/TiO2 by impregnation. These complexes were used as catalysts in the low-temperature selective catalytic reduction of NO with NH3. The influence of manganese precursors on catalyst characteristics, the reduction activity, and the stability of the catalysts to poisoning by H2O and SO2 were studied. Experiments showed that Mn(N) produced MnO2 with large grain sizes in Mn(N)/TiO2 catalyst. On the contrary, Mn(Ac) led to highly dispersed and amorphous Mn2O3 in Mn (Ac)/TiO2 catalyst, which had better catalytic activity and stability to SO2 at low temperatures. The doping of cerium reduced the differences in catalytic performance between the catalysts derived from different Mn precursors.     

改性粉煤灰对糖蜜废水的吸附效果及机理

采用改性粉煤灰(MCFA)吸附糖蜜废水中的有机污染物,对吸附行为和机理进行了考察和分析。结果表明,MCFA投加量为30 g/L及pH为5.0的优化条件下,COD去除率为88.6%,饱和吸附量为89.7 mg COD/g MCFA。准二级方程能更好地描述糖蜜废水在MCFA上的吸附动力学。颗粒内扩散方程结果表明孔扩散并非唯一的速度控制步骤。吸附平衡表明,Freundlich等温线最符合吸附模式,为优惠吸附。D-R模式中的吸附自由能Ea值推断更可能是物理吸附而不是化学吸附。吸附热力学参数ΔG0(<0)、ΔH0(5.130 kJ/mol)和ΔS0(19.936 J/(mol.K))表明MCFA对糖蜜废水的吸附过程为可行的,自发性的吸热反应。     

玉米深加工废水的混凝实验

在室温条件下,分别选用聚合氯化铝(PAC)、聚合氯化铝铁(PAFC)及三氯化铁(FeCl3)对玉米深加工废水进行混凝实验。综合考虑各种混凝剂对磷、COD以及SS的去除效果,最终选取PAC作为混凝剂。采用PAC和聚丙烯酰胺(PAM)作为复合混凝剂,对其去除效果做进一步研究,并确定了最佳投加量及pH值。实验结果表明,在PAC投加量25mg/L,PAM投加量0.5 mg/L,pH为8条件下,混凝效果最佳。磷、COD、SS去除率可分别达到90.1%、53.3%和88.2%,对应的出水质量浓度分别为0.41、26.8和2 mg/L。     

一株产絮酵母菌废菌体对Cd2+的吸附特性

将一株产絮酵母菌(编号B-02号)发酵后的废菌体制成生物吸附剂,研究该生物吸附剂对废水中Cd2+的生物吸附特性。结果表明:(1)pH值对Cd2+会产生较大的影响,偏酸性(pH=4～6)条件利于吸附;该吸附剂对Cd2+吸附速率较快,8～10 min就可达到吸附平衡;(2)吸附剂的吸附动力学符合二级动力学模型,吸附Cd2+的实验数据对Langmuir等温式的拟合情况良好,吸附剂吸附Cd2+的最大吸附量为70.752 mg/g。用0.5 mol/L HNO3对吸附Cd2+的酵母菌进行解吸,解吸率可达89.7%。     

Mo-N-TiO2光催化剂的制备、表征及其活性提高机制

以钼酸铵和氨水分别为钼源和氮源,采用溶胶-凝胶法制备了Mo-N-TiO2光催化剂,并对其进行了XRD、XPS和UV-visDRS表征。XRD结果表明,Mo、N共掺杂有效抑制了TiO2晶粒的生长,提高了TiO2由锐钛矿向金红石相的转变温度。UV-vis表明,Mo-N-TiO2光催化剂可见光吸收能力增强,吸收带边明显"红移",且钼酸铵添加量(相对TiO2)为0.5%的样品"红移"程度最大,最大吸收带边为550 nm。XPS分析结果表明,Mo取代了TiO2晶格中的部分Ti4+,以Mo6+形式存在的,而N以Ti—N及N—Ti—O形式存在。以罗丹明B为模型污染物,重点考察了钼酸铵添加量与焙烧温度对Mo-N-TiO2光催剂性能的影响。结果表明,400℃焙烧下、钼酸铵添加量为0.5%的样品催化活性最好。模拟太阳光下光照120min对罗丹明B的降解率达到96.8%,是纯TiO2的2.42倍。     

改进型波形潜流人工湿地处理猪场废水

提出了一种改进型波形潜流人工湿地(improved wavy subsurface flow constructed wetland,IW-SFCW)并研究了该湿地系统在5个水力停留时间(hydraulic retention time,HRT)(2、3、4、6和8 d)下对猪场废水的处理效果。结果表明,该湿地系统对猪场废水中各污染物有较好的去除效果。在水力停留时间为4 d,进水COD、TN、NH4+-N和TP浓度分别为511、120、110和10 mg/L左右时,该湿地系统对COD、TN、NH4+-N和TP的去除率分别为86.0%、54.4%、70.1%和91.6%。此外,该湿地系统对废水中COD、TP的去除效率随水力停留时间的延长逐渐提高,在HRT=8 d时去除效果最好,去除率分别达到92.7%和96.8%;但对TN、NH4+-N的去除率却随水力停留时间的延长出现先上升后下降的趋势,在HRT=4 d时去除率最高,分别为54.4%和70.1%。     

基于PROMETHEEⅡ法的污染场地土壤修复技术筛选及应用

依据当前污染场地土壤修复技术特点以及场地特征,构建4层12指标21方案的污染土壤修复技术决策分析结构,运用多属性决策分析方法——PROMETHEEⅡ偏好排序法,对当前场地修复技术以及典型场地条件进行了客观分析和综合评价,实现基于具体修复目标的污染场地土壤修复技术择优筛选,并采用该方法对虚拟特定污染场地的土壤修复技术筛选进行了实例应用。这为污染场地的治理和修复提供了方法依据和理论参考。     

电催化氧化技术处理制革综合废水

选择DSA电极中的钛基掺硼金钢石膜电极(Ti/BDD),用于制革综合废水的电催化氧化处理研究,考察了在不同的电流密度、电压、电解质、pH值和电解时间等因素对COD去除率和电流效率的影响。结果表明,控制电流密度为30mA/cm2,电压为8.0 V,电解质(NaCl)浓度为2.0 g/L,pH为4.0,电催化氧化处理2 h后,废水的COD和NH4+-N的去除率分别达到了83.6%和90.3%,BOD/COD为0.45,比能耗为35.34 kWh/kg COD,电流效率为37%。     

中国西北寒旱区农牧民生活碳排放评估

围绕碳排放权开展的气候谈判愈来愈关注贫困人口与弱势群体的生存权与发展权,一方面由于受制于其薄弱的社会经济水平,贫困人口与弱势群体在气候变化实践中表现出更高的脆弱性,另一方面则因气候变化减缓与适应行动而造成的贫困人口生活成本的增加以及生活水平的下降。然而,对这些地区和人口的排放权判断主要基于国家层面和地区层面宏观数据的分析,其结果掩盖了国家和地区内部不同社会经济水平下的人口排放差异,不能准确揭示贫困人口和脆弱群体的低碳排放事实。本文基于国际碳排放评估对人口生活排放的需求,结合IPCC参考方法,利用投入产出分析模型构建了人口生活碳排放评价指标体系,并用于对甘肃、青海和宁夏干旱-高寒地区农牧民生活碳排放的样本调查和分析。评估表明,中国西北干旱—高寒区人口生活碳排放仅为1.85tCO2/人,其中用于满足基本生活需要的碳排放量达到87.25%。研究发现,生活在更冷(海拔更高)区域内的人口生活排放量更高;随着家庭收入的增长,人口生活排放量也随之上升;家庭成员数量越多,家庭的人均碳排放量就会越低。