活性炭纤维对定型机油烟废气吸附性能研究

采用动态吸附实验装置研究了粘胶基活性碳纤维的耐温性能以及预处理、采样流速、进气浓度对粘胶基活性碳纤维吸附定型机油烟废气平衡吸附量的影响,实验结果表明粘胶基活性碳纤维耐温性能良好,同时经去离子水煮沸2小时的粘胶基活性碳纤维平衡吸附量最大,采样流速增大平衡吸附量减少,但吸附速率变大,采用一级动力学模型较好地反映了吸附过程,Langmuir、Freundlich方程适合拟合低浓度下的吸附等温线,DR方程则较吻合高浓度下的吸附。     

黄河包头段不同粒径沉积物分形校正下重金属的吸附研究

推导了分粒级的表面分形维数计算公式,根据推导公式计算了分粒级沉积物的分维值.应用已有的表面分形分维计算公式分别计算了黄河包头段沉积物整体的表面分形分维(1.91)及＜63 μm粒级的分维值(1.36),揭示出黄河水环境的磨蚀和分选2个原因引起黄河包头段沉积物低的分维值.用分形校正吸附模型、Freundlich和Langmuir吸附模型对黄河包头段重金属分粒级沉积物吸附进行了拟合,表明分形校正吸附模型具有较好的适用性,同时揭示分形校正吸附模型与MEA理论结合能更好的对热力学吸附结果进行描述;由吸附结果分析得出4种重金属因粒径引起的吸附量变化程度序列为Cu＞Pb＞Zn≈Cd,初始浓度高的吸附量曲线变化较初始浓度低的曲线变化明显,同时指出Cu、Pb的吸附主要与矿物组成有关,而Zn、Cd的吸附则与吸附剂沉积物空间几何性质(或沉积物表面物理特征)有关.     

Fenton工艺处理有机废水污染物影响因素研究

Fenton氧化技术能有效地处理有机废水难降解污染物。对电导率不同的废水,Fenton处理污染物效率不同。实验结果显示,在有机废水浓缩液中加入活性炭,活性炭的吸附改变了溶液的电导率,也影响了Fenton工艺降解污染物的效率,对COD和NH_3-N的降解率均有显著提升。对于难降解有机废水浓缩液,要提高Fenton工艺降解效率,可采用适当方式改变反应体系的电导率。     

盐水层中注水促进超临界CO2溶解的数值模拟

采用数值模拟的方法,通过考察不同注水模式、注水速率、注水位置、盐度和孔隙度下CO_2的分布特性和溶解行为,系统地分析了注水对CO_2溶解的影响。结果表明,超临界态CO_2呈倒锥形分布于注入井附近的盐水层顶部,并随时间延长缓慢向外扩展。注水虽不明显改变CO_2的分布,但能促进CO_2的溶解,降低超临界态CO_2的量。增大注水速率、靠近盐水层顶部注水、在注CO_2的过程中同时注水均可有效提高CO_2的溶解率。在一定范围内,CO_2的溶解量随盐水盐度降低而提高,但几乎不随岩石孔隙度变化。研究表明,通过优化注水条件可以显著促进CO_2的溶解封存。     

Role of hydrogen bond capacity of solvents in reactions of amines with CO2: A computational study

Various computational methods were employed to investigate the zwitterion formation,a critical step for the reaction of monoethanolamine with CO_2,in five solvents(water,monoethanolamine,propylamine,methanol and chloroform) to probe the effect of hydrogen bond capacity of solvents on the reaction of amine with CO_2 occurring in the amine-based CO_2 capture process.The results indicate that the zwitterion can be formed in all considered solvents except chloroform.For two pairs of solvents(methanol and monoethanolamine,propylamine and chloroform) with similar dielectric constant but different hydrogen bond capacity,the solvents with higher hydrogen bond capacity(monoethanolamine and propylamine) facilitate the zwitterion formation.More importantly,kinetics parameters such as activation free energy for the zwitterion formation are more relevant to the hydrogen bond capacity than to dielectric constant of the considered solvents,clarifying the hydrogen bond capacity could be more important than dielectric constant in determining the kinetics of monoethanolamine with CO_2.     

Characteristics of atmospheric volatile organic compounds in urban area of Beijing: Variations, photochemical reactivity and source apportionment

Atmospheric volatile organic compounds (VOCs) were observed by an on-line gas chromatography-flame ionization detector monitoring system from November 2016 to August 2017 in Beijing. The average concentrations were winter (40.27 ± 25.25 μg/m³) > autumn (34.25 ± 19.90 µg/m³) > summer (32.53 ± 17.39 µg/m³) > spring (24.72 ± 17.22 µg/m³). Although benzene (15.70%), propane (11.02%), ethane (9.32%) and n-butane (6.77%) were the most abundant species, ethylene (14.07%) and propene (11.20%) were the key reactive species to ozone formation potential (OFP), and benzene, toluene, ethylbenzene, m-xylene + p-xylene and o-xylene (54.13%) were the most reactive species to secondary organic aerosol formation potential (SOAFP). The diurnal and seasonal variations indicated that diesel vehicle emission during early morning, gasoline vehicle emission at the traffic rush hours and coal burning during the heating period might be important sources. Five major sources were further identified by positive matrix factorization (PMF). The vehicle exhaust (gasoline exhaust and diesel exhaust) was found to be contributed most to atmospheric VOCs, with 43.59%, 41.91%, 50.45% and 43.91%, respectively in spring, summer, autumn and winter; while solvent usage contributed least, with 11.10%, 7.13%, 14.00% and 19.87%, respectively. Biogenic emission sources (13.11%) were only identified in summer. However, both vehicle exhaust and solvent usage were identified to be the key sources considering contributions to the OFP and SOAFP. Besides, the contributions of combustion during heating period and gasoline evaporation source during warm seasons to OFP and SOAFP should not be overlooked.     

高温烟气静电除尘中试试验研究

为了研究在宽间距静电除尘器内部流动的大流量高温烟气中颗粒物的静电捕集特性,基于CFB锅炉中试试验平台设计并搭建了高温静电除尘中试装置.试验了板间距300mm、最高温度达到1020K的实际烟气中颗粒物的静电捕集特性,获得了放电电压、温度和烟气流速等关键因素对颗粒物的静电捕集的影响规律.实验结果表明,高温静电除尘器中烟气流速为0.3m/s,温度为1020K下达到了82.2%的除尘效率,证实了针对实际高温烟气,静电除尘器有较好的颗粒捕集效果.通过对比563K到1020K下的热态试验以及常温下的冷态试验,发现颗粒捕集效率随温度的上升迅速降低,这与高温下流速的上升、放电电压的降低以及气体黏性的增加有关.     

Effects of 1-octyl-3-methylimidazolium nitrate on the microbes in brown soil

The toxicity of ionic liquids(ILs) on soil organisms has aroused wide attention due to their high-solubility. The present investigation focused on the toxicity of 1-octyl-3-methylimidazolium nitrate([C_8mim]NO_3) on the microbial populations(bacteria, fungi, and actinomycetes), soil enzyme(urease, dehydrogenase, acid phosphatase, and β-glucosidase)activities, microbial community diversity using terminal restriction fragment length polymorphism(T-RFLP), and abundance of the ammonia monooxygenase(amoA) genes of ammonia-oxidizing archaea(AOA) and ammonia-oxidizing bacteria(AOB) using quantitative real-time polymerase chain reaction(q-PCR) in brown soil at each trial with doses of 0, 1.0, 5.0,and 10.0 mg/kg on days 10, 20, 30, and 40. The contents of [C_8mim]NO_3 in soil were measured using high performance liquid chromatography with recoveries of 84.3% to 85.2%, and changed less than 10% during the experimental period. A significant decrease was observed from the bacteria, fungi and actinomycetes populations at 10.0 mg/kg, at which the urease activity was inhibited and the β-glucosidase activity was stimulated on days 20, 30, and 40. In addition, [C_8mim]NO_3 inhibited the dehydrogenase activity at 10 mg/kg on days 30 and 40 and the acid phosphatase activity on day 20. The diversity of the soil microbial community and the gene abundance of AOA-and AOB-amo A were also inhibited. Furthermore, the present investigation provided more scientific information for the toxicity evaluation of ILs in soil.     

Atmospheric isoprene and monoterpenes in a typical urban area of Beijing: Pollution characterization, chemical reactivity and source identification

Continuous observation of isoprene, α-pinene and β-pinene was carried out in a typical urban area of Beijing from March 2014 to February 2015, using an AirmoV OC online analyzer. Based on the analysis of the ambient level and variation characteristics of isoprene, α-pinene and β-pinene, the chemical reactivity was studied, and their sources were identified. Results showed that the concentrations of isoprene, α-pinene and β-pinene in the urban area of Beijing were lower than those in richly vegetated areas; the concentrations of isoprene were at a moderate level compared with those of previous studies of Beijing. Concentrations of isoprene, α-pinene and β-pinene showed different seasonal, monthly, daily and diurnal variations, and all of the three species showed higher level at night than those in the daytime as a whole, the variations of isoprene, α-pinene and β-pinene mainly influenced by emission of sources, photochemical reaction, and meteorological parameters. Isoprene was the largest contributor to the total OFP values than α-pinene and β-pinene. α-Pinene was the largest contributor to the total SOAFP values than isoprene and β-pinene in autumn, while isoprene was the largest one in other seasons. Isoprene, α-pinene and β-pinene were derived mainly from biological sources; and α-pinene level were also affected by industrial sources. To reduce the concentrations of isoprene, α-pinene and β-pinene, it is necessary to scientifically select urban green plant species, and more strict control measures should be taken to reduce the emission of α-pinene from industrial sources, such as artificial flavors and resins synthesis processes.     

焦炭填料生物滤床净化VOC研究

采用焦炭为填料的生物滤床降解苯乙烯废气，试验过程中对焦炭进行循环挂膜，发现焦炭对苯乙烯这样的挥发性有机物（VOC）初期以吸附作用为主，随着生物膜的长成生物降解作用逐渐占有优势，表现为对苯乙烯的去除效率稳定在35％－55％左右。