《环境化学》一九九五年总目录

第14卷吩氨向时脱除＊（）和N（）过刊的化”F动力学模拟—……,…,,…·,…………,··、·袁逮汁冯彼l门\Cu（）-Zn（）催比剂的XRf）阳EXAPS研究—……………··,………,触金海未明阳孙太十等！（3S:！A族和回A族金属的消烟助燃玫应及其理论—……·,,·,·、·,…··,·李上华刘治。卜许出二柠等且（了厂1乃卜人上＊0R化动力学—……………………………………………·张瑞芹前止3仑岔韵2（93）负载型稀上复合氧化物燃烧催化剂的大活研究—………………·沈岳年胡瑞生宋瑞畸等2（10超细高活性水合氧化钙的制备G表征…………………     

钛基燃烧催化剂的抗硫性能

本文研究了钛基非贵金属燃烧催化剂的硫中毒过程及载体吸硫特性。结果表明,催化剂的抗硫能力与载体吸硫量有关,不同催化剂的抗硫性能为:Cat.3>Cat.4>Cat.5>Cat.1>Cat.2,本文还讨论了硫中毒机理。     

超声搅拌萃取法富集水中痕量多环芳烃的研究

以一定的搅拌速度使有机萃取剂形成珠状均匀地分散在水样中,同时进行超声振荡,以加速萃取物同萃取剂分子间的接触几率,从而提高萃取物在萃取剂中的溶解速率。但是,超声搅拌后的萃取液易于乳化。给分离带来困难,为此,本文对乳化问题进行了研究。并以八种多环芳烃为例,取得了满意的回收率及实际样品分析数据。     

植物叶片相对吸硫量的研究及在绿化中的应用

为探索北京市本土植物对污染物硫的降解能力，从重度污染区(首钢邻山)、轻度污染区(北京植物园内山上)和对照区(北京周边数个森林公园)分别采集21种植物叶片，采用比浊法消解和定容、IRIS advantage型等离子体发射光谱仪测定其含硫量。分析不同程度污染区植物叶片的相对吸硫量。不同污染区绿化降硫时，考虑选用相应地带叶片净吸硫量大的植物类型。     

聚砜—磺化聚砜共混超滤膜的研究

本文以聚砜和磺化聚砜为原料，制备了低截留分子量的共混超滤膜，此种膜具有适中透水量，对分子量３０００的ＰＥＧ截留率在９０％以上，对膜的制备参数，如聚合物浓度，不同溶剂，不同添加剂和凝胶介质对膜性能的影响进行了较详细的的研究。     

伯胺N1923萃淋树脂吸萃汞（Ⅱ）的性能萃合物组成的研究

本文研究了Ｎ１９２３萃淋树脂对汞（Ⅱ）吸萃的性能，溶液的酸效应，吸附曙线，吸附速率及体系温度地吸萃分配比的影响。用饱和容量法，等摩尔系列法，斜率法等对吸萃物组成进行探讨，并用红外光谱法，核磁共振谱法对吸萃机理进行了分析。     

基于水泥窑协同处理石灰干化污泥工艺研究磷、硫对碳酸钙分解的影响

针对水泥窑协同处理石灰干化污泥工艺,利用热差分析仪、X射线衍射和扫描电子显微镜分别从碳酸钙分解热力学和碳酸钙微观演变的角度研究了不同量的磷和硫掺比对碳酸钙分解的影响规律.实验结果表明,在碳酸钙烧制中,掺加0.5%的磷(以磷酸钙计)和硫(以硫酸钙计),使碳酸钙表观分解能分别降低了7.35%和8.04%,峰值温度分别降低了70.82℃和59.32℃,有效促进碳酸钙的分解;对其促进机理研究发现,硫酸钙、磷酸钙及其分解产物焦磷酸钙自身并不与碳酸钙及其分解产物氧化钙发生反应,他们仅破坏了碳酸钙的表面结构,促进了二氧化碳的释放,从而利于的碳酸钙分解.本研究结果表明,掺加一定量的石灰干化污泥引入磷和硫,利于水泥熟料的烧成.     

厦门14种主要树种吸收硫及固碳能力

对厦门市14种主要树种吸硫强度以及不同环境(清洁环境和污染环境)对其固碳能力的影响进行研究。结果表明:不同树种叶片的吸硫强度在0.04~1.73 mg/g。单位绿地面积不同树种净化SO2量为8.84~1 513.05kg/(hm2·a),其中天竺桂最大,其次为黄槿、芒果和刺桐,洋紫荆最小。多数树种在污染环境下单位绿地面积年固碳量受到明显抑制,如大叶榕、高山榕、小叶榕和印度紫檀等树种。然而还有些树种其固碳能力在污染环境下受到促进,如鸡冠刺桐、夹竹桃和小叶榄仁,表明这些树种对污染环境有较强的适应能力。综上所述,夹竹桃、小叶榄仁和天竺桂等树种既能吸收相当数量的硫,同时其固碳能力未受到削弱,表明这些树种是适宜在污染环境下种植的树种。     

二硫代氨基甲酸盐型除油剂的性能研究

分别用二乙胺、乙二胺、三乙烯四胺与CS2 反应 ,合成了三种二硫代氨基甲酸盐 ,试验了其除油性能 .结果表明 ,三 ( 1 ,2 亚乙基 )四氨基四 (二硫代甲酸钠 )对含有一定量Fe2 + 的油田污水有较好的除油效果 .每升污水中加入 1 0mg除油剂 ,就能在1 5min内将污水中的油含量降至 1 0mg·l- 1.通过改变二硫代氨基甲酸盐的浓度、污水中Fe2 + 的浓度、搅拌速度、氨基的结构 ,发现多官能团的二硫代氨基甲酸盐 ,在较低的搅拌速度下 ,除油效果较好 .     

造孔剂对低温锰基多孔陶瓷NH3-SCR催化剂性能的影响

本文采用造孔剂法制备了以埃洛石(HAL)为添加剂的硅藻土(DE)基多孔陶瓷，并以该多孔陶瓷为载体，通过原位生长法制备了锰基硅藻土多孔陶瓷催化剂.探究了造孔剂的种类和含量对多孔陶瓷结构与形貌以及对催化剂脱硝性能的影响.采用XRD、SEM、XPS等方法对多孔陶瓷以及催化剂的理化性质进行了表征，结果表明，造孔剂的种类与含量影响多孔陶瓷的结构与形貌，更粗糙的表面和更高的孔隙率为MnO_x提供了更多的附着位点.此外，选取适当的造孔剂可以促进所制备样品表面原子价态分布，提升表面酸性位点含量，并增强其氧化还原能力，增强催化剂的脱硝性能.     

以膨润土为载体的碳酸盐吸收剂对二氧化碳的吸收

采用膨润土为载体,KHCO3为前驱物通过喷雾-干燥法制成固体碳酸钾吸收剂,制成的固体吸收剂粒径大小为0.5—2.0 mm,密度为1.73 g.mL-1.通过K2CO3负载量、吸收温度、吸收时间、床层纵横比等因素考察固体吸收剂对CO2气体的吸收效率及循环反应特性.分析碳酸钾吸收剂对CO2的吸收机理,并与以碳酸氢钠为前驱物制备的吸收剂进行对比,比较两种吸收剂对CO2吸收效果的差异性.通过XRD测试吸收剂吸收反应前后组成的变化,BET多点法测试吸收剂比表面积,扫描电镜观察吸收剂表面形态特征.结果表明,碳酸钾吸收剂和碳酸钠吸收剂对CO2气体均具有较高的吸收量,相比而言碳酸钾吸收剂的碳酸化反应速率较快,而且经过多次循环反应后吸收效果未发生衰减,在60℃—80℃范围内,碳酸钾吸收剂对CO2的吸收能力最佳.     

Preparation of a permanent magnetic hypercrosslinked resin and assessment of its ability to remove organic micropollutants from drinking water

A rapid and effective method based on a novel permanent magnetic hypercrosslinked resin W150 was proposed for the removal of organic micropollutants in drinking water. W150 was prepared by suspension and post-crosslinking reaction and found to possess a high specific surface area of 1149.7 m²·g^-1, a small particle size of 50 μm to 100 μm, and a saturation magnetization as high as 8 emu·g^-1. W150 was used to eliminate nitrofurazone (NFZ) and oxytetracycline (OTC) from drinking water compared with commercial adsorbents XAD-4 and F400D. The adsorption kinetics of NFZ and OTC onto the three adsorbents well fitted the pseudo-second-order equation (r>0.972), and the adsorption isotherms were all well described by the Freundlich equation (r>0.851). Results showed that the reduction in adsorbent size and the enlargement in sorbent pores both accelerated adsorption. Moreover, the effect of particle size on adsorption was more significant than that of pore width. Given that the smallest particle size and the highest specific surface area were possessed by W150, it had the fastest adsorption kinetics and largest adsorption capacity for NFZ (180 mg·g^-1) and OTC (200 mg·g^-1). For the adsorbents with dominant micropores, the sorption of large-sized adsorbates decreased because of the inaccessible micropores. The solution pH and ionic strength also influenced adsorption.     

几种金属氧化物TPS性能比较

通过程度升温硫化研究了ＣｕＯ,Ｆｅ２Ｏ３,ＳｎＯ２,ＭｎＯ２,ＣａＯ及ＺｎＯ等金属氧化物的脱硫性能,对各种金属氧化物的ＴＰＳ曲线进行比较发现,其硫化温度及速度都不相同,氧化锰的硫化温度最低,从３４５Ｋ开始有较强的硫化氢吸收峰出现;氧化铜的硫化在３７３Ｋ左右进行;对氧化铁和氧化锌,硫化从４７３Ｋ开始,而氧化锡的硫化在６５０Ｋ左右发生;氧化钙的硫化发生在７３５Ｋ。粒度对ＴＰＳ曲线有较明显的影响,粒度减     

Reaction mechanism of arsenic capture by a calcium-based sorbent during the combustion of arsenic-contaminated biomass: A pilot-scale experience

Pilot-scale combustion is required to treat arsenic-enriched biomass in China. CaO addition to arsenic-enriched biomass reduces arsenic emission. CaO captures arsenic via chemical adsorption to form Ca₃(AsO₄)₂. Large quantities of contaminated biomass due to phytoremediation were disposed through combustion in low-income rural regions of China. This process provided a solution to reduce waste volume and disposal cost. Pilot-scale combustion trials were conducted for in site disposal at phytoremediation sites. The reaction mechanism of arsenic capture during pilot-scale combustion should be determined to control the arsenic emission in flue gas. This study investigated three Pteris vittata L. biomass with a disposal capacity of 600 kg/d and different arsenic concentrations from three sites in China. The arsenic concentration in flue gas was greater than that of the national standard in the trial with no emission control, and the arsenic concentration in biomass was 486 mg/kg. CaO addition notably reduced arsenic emission in flue gas, and absorption was efficient when CaO was mixed with biomass at 10% of the total weight. For the trial with 10% CaO addition, arsenic recovery from ash reached 76%, which is an ~8-fold increase compared with the control. Synchrotron radiation analysis confirmed that calcium arsenate is the dominant reaction product.     

不同来源太湖沉积物粒径分布及其对Cu的吸附特征

以不同来源的太湖沉积物为研究对象,利用Mastersizer 2000型激光粒度分析仪测定沉积物的粒度组成,利用筛析法和吸管法对不同来源沉积物进行分级,测定不同粒径沉积物中Cu含量及不同粒径沉积物对Cu2＋的饱和吸附量,研究沉积物对水溶液中Cu（Ⅱ）的吸附特性,从粒径分级和动力学角度探讨了太湖沉积物对Cu的吸附机理。结果表明：太湖沉积物粒径范围在0.002-0.1 mm,其颗粒组成以粉砂级与粘粒级为主,养殖区沉积物小粒径比例较高,小于0.05 mm粒径沉积物的比例为82.45%;吸附实验研究表明,粒径小于0.005 mm和0.005-0.01 mm沉积物中Cu含量较高,且此粒径沉积物对Cu（Ⅱ）的吸附量最大;吸附动力学研究表明,沉积物的吸附过程分为快反应和慢反应两个阶段,且吸附过程以表面吸附为主,伪二级动力学方程对动力学曲线拟合较好,其R2值达0.999以上。吸附热力学的研究结果表明：Freundlich方程比较适合描述沉积物对Cu2＋的吸附等温线,其R2大于0.99,对照区、养殖区和生活污水区沉积物对Cu（Ⅱ）的最大吸附量分别为229.20,249.98,261.20 mg.kg-1,方程式中的强度因子1/n不适合描述沉积物与重金属离子的结合能力。     

99 % yield biodiesel production from rapeseed oil using benzyl bromide–CaO catalyst

Biofuels are sustainable fuels produced from modern biomass such as plants and algae. Biodiesel has high lubricity and ultra-low sulfur content. Biodiesel is produced from vegetable oil by transesterification. Actually, practical biodiesel production is limited by the low reaction rate of transesterification of vegetable oil with methanol catalyzed by CaO. Here we designed an efficient catalyst: benzyl bromide-modified CaO. Using benzyl bromide-modified CaO, we obtained a 99.2 % yield of fatty acid methyl esters in 3 h, compared with 35.3 % yield using commercial CaO under the same reaction conditions. The improved catalytic activity is explained by better fat diffusion to the surface of the benzyl bromide-modified CaO. The novelty of our findings is the much higher yield of our method compared to literature data on heterogeneous catalysis. In addition, the lifetime of our catalyst is excellent.     

Trichoderma harzianum: a green sorbent for Pb(II) uptake from aqueous solutions

This investigation describes the use of specially cultivated, nonliving biomass of Trichoderma harzianum as a biosorbent for the batch removal of Pb(II) from a stirred system under different experimental conditions. The metal removal depended upon pH, sorbent particle size, initial Pb(II) concentration, shaking speed, and sorption time. The optimal experimental conditions for the removal of Pb(II) by T. harzianum with an initial metal concentration of 100 mg L^?1 were obtained at a particle size of 53 μm, a pH of 4.5, a shaking speed of 200 rpm, and a contact time of 720 min. The results were analyzed in terms of adsorption isotherms and kinetic models. The Freundlich isotherm model and pseudo second-order model fitted well in the data. T. harzianum proved to be a good biomaterial for accumulating Pb(II) from aqueous solutions (q = 460 mg g^?1).     

Seasonal grazing of Pseudocalanus minutus on particles

Grazing by Pseudocalanus minutus on naturally occurring partieles has been investigated over a 2 year period at 5 m depth, in a small coastal embayment in Nova Scotia, Canada. Large variations in the standing stock of particulate matter in the water from 5 m depth were associated with seasonal changes in phytoplankton, and at times with runoff from rivers. Each size group displayed seasonal changes, with high amplitudes occurring in the large-particle size ranges. P. minutus consumption was associated with seasonal changes in total particle concentration as well as with the concentration in each size group. The food uptake was correlated (P>0.01) with the particle concentration in all particle categories, except in the size range below 3.57 . Frequency of positive electivity indices increased with particle sizes up to 57 and then decreased. Observations on particle spectra revealed considerable seasonal variability in both particle sizes and copepod feeding patterns. P. minutus adapted to seasonal variations within the particle spectrum by shifting its grazing pressure from one size range to another. By taking advantage of every particle peak concentration, P. minutus revealed a strong opportunistic feeding behaviour, and a very efficient utilization of the standing stock. Maximum consumption was recorded in early spring, when P. minutus fed on large-size particles. Feeding took place in the medium and small-size ranges during the summer and part of fall. Food uptake was rarely less than 2.26% of body weight during the winter, and reached up to 55% and sometimes more in spring. The unselective feeding patterus demonstrated by P. minutus suggest certain ecological implications of feeding pressure on standing stock.     

人居生活废弃物生物黑炭对水溶液中Cd^2＋的吸附研究

以人居生活废弃物生物黑炭为材料,探讨生物黑炭对Cd^2＋的吸附动力学及热力学特性,通过平衡吸附法研究吸附时间、Cd^2＋初始质量浓度、吸附剂投加量、溶液pH值以及黑炭粒径对Cd^2＋吸附率的影响。结果表明,吸附时间为2h时基本达到吸附平衡,准二级动力学方程能很好地描述生物黑炭对Cd^2＋的吸附过程。Langmuir模型能较好地描述生物黑炭对Cd^2＋的等温吸附过程,根据该模型模拟得到25℃条件下Cd^2＋最大吸附量为6．22 mg·g^-1 Cd^2＋去除率随生物黑炭投加量的增加而增大;生物黑炭对Cd^2＋吸附量随其粒径减小而增大;溶液初始pH值为4．0-7．5时,pH值变化对Cd2’吸附量的影响不显著。采用人居生活废弃物生物黑炭去除水溶液中Cd^2＋时,控制溶液Cd^2＋初始质量浓度30mg·L^-1,粒径小于0．25mm,投加水平8g·L^-1,反应温度25℃,反应时间1-2h,Cd^2＋去除率可达80％。人居生活废弃物生物黑炭可以作为去除污染水体中Cd^2＋的吸附剂。     

人居生活废弃物生物黑炭对水溶液中Cd2+的吸附研究

以人居生活废弃物生物黑炭为材料,探讨生物黑炭对Cd2+的吸附动力学及热力学特性,通过平衡吸附法研究吸附时间、Cd2+初始质量浓度、吸附剂投加量、溶液pH值以及黑炭粒径对Cd2+吸附率的影响.结果表明,吸附时间为2h时基本达到吸附平衡,准二级动力学方程能很好地描述生物黑炭对Cd2+的吸附过程.Langmuir模型能较好地描述生物黑炭对Cd2+的等温吸附过程,根据该模型模拟得到25℃条件下Cd2+最大吸附量为6.22mg·g-1.Cd2+去除率随生物黑炭投加量的增加而增大;生物黑炭对Cd2+吸附量随其粒径减小而增大;溶液初始pH值为4.0～7.5时,pH值变化对Cd2+吸附量的影响不显著.采用人居生活废弃物生物黑炭去除水溶液中Cd2+时,控制溶液Cd2+初始质量浓度30mg·L-1,粒径小于0.25 mm,投加水平8g·L-1,反应温度25℃,反应时间1～2h,Cd2+去除率可达80％.人居生活废弃物生物黑炭可以作为去除污染水体中Cd2+的吸附剂.