基于MAX-DOAS的乌鲁木齐市NO2时空变化

为研究乌鲁木齐市NO2污染状况,了解其时空分布特征及其影响因素,基于多轴差分吸收光谱技术（MAX-DOAS）,利用2014年4月—2015年12月3个监测点和多次车载移动观测的数据,反演了乌鲁木齐对流层NO2垂直柱浓度（VCD）,并且结合气象和地形等因素进行了分析。结果表明：NO2 VCD由高到低的季节依次是冬季、春季、秋季和夏季,均值为10.84、7.78、5.98和3.56×1015 molec·cm-2;由高到低的监测站依次是城区站、工业区站和郊区站,年均值为9.52、8.44和5.58×1015 molec·cm-2;日变化上春冬两季呈U型,夏秋两季呈双峰型;NO2空间分布由南到北呈明显的"两头低中间高",高值通常出现在市区高架桥附近;乌鲁木齐NO2 VCD与气象因子温度、风速、相对湿度、日照时数都有较好的相关性;乌鲁木齐夏季盛行西北风,顺势于地形利于市区污染物传输出去,冬季盛行东北风,而东面有博格达山阻挡致使风速较低,污染物滞留堆积浓度高。     

用作固定SRB碳源的玉米芯的最佳改性条件

针对现阶段玉米芯作为SRB污泥颗粒内聚碳源所带来碳源释放不佳的问题,选用碱性H2O2对玉米芯进行改性,制备成SRB污泥颗粒处理AMD,经过单因素实验和正交实验分析,对玉米芯的最佳改性条件进行研究。结果表明,当玉米芯改性时间24 h,NaOH浓度为6%,H2O2浓度为1.5%,可制得最佳改性玉米芯。制备成SRB污泥颗粒处理AMD后,SO42-、Mn2+和Fe2+去除率分别为93%、78%和95%,较未改性提高了29%、3%和23%;COD释放量为215 mg·L-1,较未改性减少了545 mg·L-1;Fe2+剩余量为1.5 mg·L-1,较未改性减少了1.1 mg·L-1;溶液pH为7.8。同时经SEM和XRD分析,发现改性玉米芯颗粒较未改性玉米芯颗粒相比,内部结构变得的疏松多孔,且大分子物质被分解为小分子物质,可以更好被SRB所利用。说明了该改性法可以改善玉米芯的碳释性能,为微生物处理AMD的工程应用提供技术参考。     

Ti-Si-Ox脱硝催化剂载体的组分优化及其性能研究

采用挤出成型法制备系列Ti-Si-Ox复合氧化物催化剂载体,研究了Ti-Si-Ox催化剂载体组分配比、酸量、比表面积与脱硝性能和抗压强度的关系。采用XRD、Raman spectra、N2-BET、Py-IR以及XPS等表征技术对催化剂载体进行表征。结果表明：Ti/Si元素摩尔比为9∶1时Ti0.9Si0.1Ox催化剂载体的轴向抗压强度适中且脱硝催化活性最高;在5 000 h-1空速条件下,催化剂载体最高脱硝活性在400 ℃时达到99.0%且起燃温度降至260 ℃;另外,Ti0.9Si0.1Ox催化剂载体的比表面积为75.4 m2·g-1,介孔最可几分布为8.1 nm,轴向抗压强度为1.4 MPa,符合工业应用条件,即Ti-Si-Ox载体具有较好的工业应用前景。     

K2S2O8氧化吸收NO的热力学与传质分析

一氧化氮（NO）是燃煤锅炉烟气中的主要污染物,因其是酸雨和光化学烟雾的前体物而受到广泛关注。采用K2S2O8作为氧化剂开展了其对模拟烟气中NO的氧化去除研究,并分析了K2S2O8氧化脱硝反应的热力学过程以及NO从气相主体到液相主体的传质过程。结果显示：以K2S2O8为氧化剂氧化NO的总反应吉布斯自由能为-659.69 kJ·mol-1,小于零,说明该反应是自发过程;气液传质分析表明NO气体的吸收传质速率主要由液膜控制。实验采用添加Fe （Ⅱ） EDTA的方法增大化学反应对液相传质速率的放大系数,致使液膜传质阻力减小,从而使NO的去除率从30%提高至91.6%。该结果为K2S2O8湿法氧化脱硝工艺的后续研究和应用提供了理论参考和技术支持。     

TiO2、BiVO4、Cu2O光催化降解低浓度甲醛

比较研究了3种（TiO2,BiVO4,Cu2O）光催化剂对低浓度甲醛的降解过程,拟通过结构分析（晶粒尺寸、比表面积、禁带宽度）和实验评价其性能优劣,优选出光催化性能较好的材料。通过结构分析和降解甲醛实验发现,甲醛初始浓度较低时,BiVO4降解率优于其他,随甲醛浓度增加,催化剂降解率均呈上升趋势,TiO2-1（T-1）、TiO2-2（T-2）降解率增加显著。随环境湿度增大,降解率先上升后下降,BiVO4-1（B-1）、BiVO4-2（B-2）降解率下降的较为缓慢。同一物质当晶粒尺寸越小比表面积越大,其降解率越好。T-2比B-1有更好的稳定性。分析认为在较低甲醛浓度时,决定光催化降解率的主要因素是催化剂的表面反应速率。随着甲醛初始浓度的增加,吸附脱附成为主要限制步骤。随环境湿度增加,甲醛降解率先上升后下降,具有较小比表面积的BiVO4降解甲醛效率下降不显著。连续的工作产生甲醛分解副产物,不易堵塞具有大比表面积的T-2的活性位点,所以T-2有更好的稳定性。     

Euglena gracilis as a model for the study of Cu and Zn toxicity and accumulation in eukaryotic cells

We have observed the effect of copper and zinc on the biology of Euglena gracilis. The cells displayed different sensitivities to these metals, as the apparent LC₅₀ for Cu²⁺ was 0.22 mM, and for Zn²⁺ it was 0.88 mM. While Zn²⁺ was able to increase cell proliferation even at 0.1 mM, the minimal CuCl₂ concentration tested (0.02 mM) was sufficient to impair cell division. Higher concentrations of these metals not only inhibited cell division in a concentration-dependent manner, but also interfered with the metabolism of E. gracilis. A higher accumulation of proteins and lipids per cell was observed at the DI₅₀ concentration for metal-treated cells. These results suggest that the test concentration of both metals leads to a failure in completing cell division. Ultrastructural analysis indicated a chloroplast disorganization in copper-treated cells, as well as the presence of electron dense granules with different shapes and sizes inside vacuoles. Microanalysis of these granules indicated an accumulation of copper, thus suggesting a detoxification role played by the vacuoles. These results indicate that E. gracilis is an efficient biological model for the study of metal poisoning in eukaryotic cells. They also indicate that copper and zinc (copper being more poisonous) had an overall toxic effect on E. gracilis and that part of the effect can be ascribed to defects in the structure of chloroplast membranes.     

喷消石灰脱除垃圾焚烧炉尾气中HCl和SO2的试验研究

在日处理200t进口流化床垃圾焚烧炉上,进行烟气喷水降温加上喷消石灰粉末脱除尾气中的酸性气体HCl和SO2的试验研究,HCl和SO2浓度由布袋除尘器出口的在线气体分析仪测得,结果表明HCl和SO2的去除率在Ca/Cl摩尔比等于9时分别为80%和20%,说明该法消石灰利用率较低,宜改为半干法脱除HCl和SO2酸性气体,以便降低吸收剂用量,提高运行的经济性.     

催化湿式氧化法处理糖蜜酒精废液的研究

以非贵金属Cu、Fe、Mn和Ce为主要活性成分和TiO2、-γA l2O3为载体,制备了10种用于催化湿式氧化法处理糖蜜酒精废液的催化剂。考察了载体、焙烧温度、成分配比对催化剂催化活性与稳定性的影响,研究了氧气分压、催化剂投加量、反应温度和反应时间对催化湿式氧化过程的影响规律。结果表明:(1)Fe-Mn/-γA l2O3(3∶1∶1)催化剂是催化湿式氧化法处理糖蜜酒精废液的可选催化剂;(2)适宜的氧气供应量为理论需氧量的3.4~4.6倍,催化剂的投加量以10 g/L为佳;在300℃下反应30 m in或在280℃下反应60 m in,处理水可达到污水综合排放标准GB9878-1996的三级标准。     

Anaerobic degradation of diethyl phthalate, di-n-butyl phthalate, and di-(2-ethylhexyl) phthalate from river sediment in Taiwan

We investigated anaerobic degradation rates for three phthalate esters (PAEs), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), and di-(2-ethylhexyl) phthalate (DEHP), from river sediment in Taiwan. The respective anaerobic degradation rate constants for DEP, DBP, and DEHP were observed as 0.045, 0.074, and 0.027 1/day, with respective half-lives of 15.4, 9.4, and 25.7 days under optimal conditions of 30 °C and pH 7.0. Anaerobic degradation rates were enhanced by the addition of the surfactants brij 35 and triton N101 at a concentration of 1 critical micelle concentration (CMC), and by the addition of yeast extract. Degradation rates were inhibited by the addition of acetate, pyruvate, lactate, FeCl₃, MnO₂, NaCl, heavy metals, and nonylphenol. Our results indicate that methanogen, sulfate-reducing bacteria, and eubacteria are involved in the degradation of PAEs.     

Characteristics of roadside air pollution in Korean metropolitan city (Daegu) over last 5 to 6 years: temporal variations, standard exceedances, and dependence on meteorological conditions

The present study performed a roadside data analysis to provide baseline data for exploring associations between environmental exposure to four gaseous pollutants and health effects on residents living near roadways. The yearly roadside concentrations of CO and SO₂ showed a well-defined decreasing trend, whereas those of NO₂ and O₃ exhibited the reverse trend. In most cases, the diurnal trends of the roadside concentrations were well-defined for all seasons, plus the daytime concentrations were higher than the nighttime concentrations. In contrast to the other target pollutants, the daytime O₃ concentrations observed at the roadside sites were lower than those observed at the residential site, likely due to high-levels of fresh NO from traffic emissions that rapidly react with O₃, thereby reducing the O₃ roadside level. The Sunday roadside concentrations of CO, NO₂, and SO₂ were similar to or somewhat lower than the weekday concentrations. Conversely, for O_3, the Sunday roadside concentrations were similar to or somewhat higher than the weekday concentrations. The higher O₃ concentrations on Sunday may be due to the reduced titration from a decrease in NO_x emissions under VOC-limited conditions (low VOC/NO_x conditions). The monthly averages of O₃ concentrations exhibited the reverse seasonal variation to the other target compounds, with peak O₃ concentrations between April and June, and the second peak between August and October. It is also suggested that for O₃, the 8-h standard is more stringent than the 1-h standard, while for NO₂ and SO₂, the 1-h standard is more stringent than the 24-h standard. The multiple regression equations obtained from the relationship between the concentrations and five meteorological parameters indicated that the number and type of meteorological variables in the equations varied according to the pollutant, monitoring station, or season.