水稻与棉花秸秆不同预处理厌氧发酵产沼气

以猪粪为接种物,以棉花秸秆和水稻秸秆为发酵原料,分别对秸秆进行稀碱法预处理和稀碱法与超声波联合预处理,在发酵温度为(37±1)℃的条件下进行厌氧发酵产沼气的研究。结果表明,以联合预处理的秸秆为发酵原料,厌氧发酵的各项指标均比以稀碱预处理秸秆发酵的效果好,其中累积产气量和沼气中甲烷含量分别提高35.23%和2.4%,发酵后TS、VS含量相对减少2.6%～10.94%,发酵液代谢产物中的有机酸丙酮酸、乙酸和柠檬酸含量相对减少23.9%～25.9%、20.24%～24.53%和41.08%～45.91%。     

Effects of prenatal exposure to bisphenols on newborn leucocyte telomere length: a prospective birth cohort study in China

Environmental Science and Pollution Research - Telomere length (TL) at birth is related to diseases that may arise in the future and long-term health. Bisphenols exhibit toxic effects and can cross...     

灵芝漆酶对直接蓝86的催化脱色性能

利用灵芝菌Ganoderma lucidum U-281漆酶对直接蓝86进行酶促氧化脱色,并对其降解机理进行了探讨。结果表明,染料-漆酶共反应体系在20～50℃及pH小于5.0范围内,直接蓝86均可脱色50%以上;漆酶对直接蓝86具有宽泛的浓度适应性,对300 mg/L的该染料仍具有耐受性。最优脱色工艺参数为温度40℃、pH 5.0、染料初始浓度200 mg/L、漆酶用量1 U/mL。在优化条件下,直接蓝863 h的脱色率达到54.54%,48 h脱色率达到91.54%。紫外-可见吸收光谱分析表明,漆酶的酶促氧化导致染料的分子结构产生了变化,是造成直接蓝86脱色的主要发生机制。     

厌氧活性污泥处理废水中的U(Ⅵ)

用人工驯养的厌氧污泥进行除铀实验,探讨了微生物投加量(VSS)、pH值、U(Ⅵ)初始浓度、外加电子供体和污泥重复利用等对污泥处理U(Ⅵ)的影响,并进行了相关机理分析。实验结果表明,在适当的pH范围内(5.2～6.6),厌氧污泥对铀保持较长时间的高效去除率;当以还原铁粉和无水乙醇作电子供体时,U(Ⅵ)去除率保持在95%以上的时间为未加电子供体时的2倍。U(Ⅵ)去除速度与VSS投加量成正比关系,U(Ⅵ)初始浓度对去除效果的影响不大,厌氧污泥可以长期使用。pH值的影响最关键,其次是外加电子供体。厌氧污泥除U(Ⅵ)机理为氧化还原和吸附的共同作用。     

青萍(Lemna minor L.)对氮磷的吸收特征

以西部地区优势浮萍品种青萍为实验对象,研究了青萍对不同浓度硝态氮和磷酸盐的吸收特征。结果表明,硝态氮浓度在1～10 mg/L范围内,青萍对硝态氮有较好的吸收效果,M-M方程可以较好地描述硝态氮浓度与青萍对硝态氮的吸收速率之间的关系,通过M-M方程拟合得到青萍对硝态氮的最大吸收速率为0.1167 mg/(g FW.h),亲和力常数为6.9274。磷酸盐浓度在0.1～1.0 mg/L范围内,青萍对磷酸盐也有较好的吸收效果,二次多项式回归可以较好地描述青萍吸收速率与磷酸盐浓度的关系,回归方程得到青萍对磷酸盐的最大吸收速率为0.0193 mg/(g FW.h),对应磷酸盐浓度为0.6 mg/L。     

废轮胎与煤共热解失重特性研究

采用热解重量分析法研究了废轮胎粉、炼焦煤粉(简称煤粉)及混合样的热解特性。实验结果表明,废轮胎粉的热解出现三个显著的失重峰,煤粉热解仅出现一个显著失重峰。与煤粉热解相比,废轮胎粉热解开始失重温度和失重基本结束的温度相对较低,失重速率较大,且失重量较大。煤粉与废轮胎粉的显著失重存在重叠的温度区间(360～450℃),说明废轮胎粉与煤粉可以进行共热解。随废轮胎粉质量分数增加,共热解物料总失重率增加。废轮胎粉与煤粉共热解存在协同效应,在280～540℃时协同效应抑制共热解挥发分的逸出,导致失重量降低,最大失重速率峰温升高;高于540℃后,协同效应促进共热解反应,使共热解总失重率增大。     

秦皇岛海岸侵蚀动态研究

利用不同时期的地形图、遥感图片对比,并选取典型海岸岸滩监测剖面实测数据,对海岸侵蚀现状进行了分析和定量计算。分析结果显示,秦皇岛海岸全线处于侵蚀状态,平均蚀退率1.5～4 m/a,根据蚀退率可将秦皇岛海岸划分为严重侵蚀、强侵蚀、侵蚀、微侵蚀、稳定5种岸线侵蚀类型。     

Polybrominated diphenyl ethers in surface sediments from principal watersheds of Shanghai, China: levels, distribution, influencing factors, and risk assessment

Fourteen and 17 sediment samples were collected from three main rivers of Shanghai in July and November, respectively. Eight polybrominated diphenyl ether (PBDE) congeners (BDE-28, BDE-47, BDE-99, BDE-100, BDE-153, BDE-154, BDE-183, and BDE-209) were detected in these samples to clarify the pollution status in the metropolis. Instrumental analyses showed that the concentrations of ∑₈PBDEs ranged from 10.97 to 64.05 ng/g dry weight (dw), with an average value of 29.71 ng/g dw. BDE-209 was the predominant congener accounting for more than 97 % of total PBDEs, followed by BDE-47 and BDE-99. Remarkable spatial and seasonal distributions of PBDE concentrations were observed, suggesting that local sources, seasonal climates, and hydrologic conditions might be the influencing factors. Moderate correlations (r ²?=?0.28–0.51, p?<?0.05) were found between total organic carbon and PBDEs, which indicated that organic carbon content influenced the distributions of PBDEs in sediment of Shanghai at some extent. Hazard quotients revealed PBDEs posed no potential risk to benthic organisms in the study area at present.     

Ti（Ⅳ）催化臭氧／过氧化氢预处理酸性难降解废水

在Ti（Ⅳ）和过氧化氢存在条件下，考察了臭氧化酸性苯乙酮溶液、硝基苯溶液和垃圾渗滤液（浙江衢州某垃圾填埋场）的预处理效能。结果表明，在pH2．86条件下，单独臭氧化处理对苯乙酮、硝基苯和垃圾渗滤液的COD去除率分别为10．1％、44％和28．6％。BOD，／COD值分别从原来的0．039、0．060和0．085提高到了0．130、0．158和0．174，仍属生化难降解废水。当体系加入Ti（Ⅳ）后，臭氧化苯乙酮和硝基苯的COD去除率分别达到了75．5％和65％，BOD；／COD则提高到了0．679和0．314，可生化性提升明显。对于垃圾渗滤液，只有当体系加入Ti（Ⅳ）和H22后，臭氧化COD的去除率达到66．6％，BOD、／COD提高至0．425。上述结果对酸性难降解废水的处理实际意义非常突出。     

Perfluorosulfonates and perfluorocarboxylates in snow and rain in Dalian,China

Samples of precipitation events (snow and rain) in Dalian, a typical coastal town in China, were analyzed for perfluorosulfonates (PFSAs) and perfluorocarboxylates (PFCAs) to investigate atmospheric contamination by these compounds. In the snow event on December 16, 2006, samples were collected from 21 different sites and in another 6 precipitation events, samples were collected from a single location. Four PFSAs (C4, C6, C8, C10) and seven PFCAs (C6–12) were analyzed. Among the homologues, perfluorooctane sulfonate (PFOS) concentrations were the highest with a geometric mean (GM) of 145 ng/L (n = 21) during the snow event on December 16, 2006, followed by perfluorooctanoate (PFOA) with a GM of 24.7 ng/L (n = 21). Concentrations of perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS) and perfluoroheptanoate (PFHpA) were more than two orders of magnitude lower than that of PFOS. Other PFSAs and PFCAs were found to be below the limit of detection in all the samples. In other 6 precipitation events, PFSAs and PFCAs were detected approximately in the same order of magnitude in both snow and rain. The results indicate that wet deposition may be a potential transport mechanism of perfluorinated chemicals in the environment.