黑龙江及周边中强震前不同参数模型矩加速释放(AMR)现象特征分析

应用时间破裂分析方程中表征地震距释放程度的m值,选取不同空间尺度进行时空扫描研究,得到震前1年以每2个月为时间间隔的空间m值随时间变化的分布图像,运用不同参数设置计算了地震前Benioff累积应变释放特征。通过对比这些变化找出研究区内m值空间分布搜索主震破裂点扫描效果较好的参数模型,尝试性地给出了"矩释放程度空间扫描"方法应用于地震预测的经验指标。并结合与矩加速释放具有相同物理机制的加卸载响应比(Load/Unload Response Ratio)方法进行综合分析,利用这两种方法对地震进行中短期预测,达到两种方法互相检验、相互辅助的目的。考虑到本文仅对6个震例进行研究,无法给出具有统计显著性的结论,所以仍需结合其他方法进行点、线、面的综合分析。     

三种观测标准的霾日与空气污染日对比分析

目前气象观测业务和空气污染分析中存在对霾日统计的分歧,甚至出现空气污染日无霾的现象,对霾观测标准的科学划分,显得非常重要和紧迫。利用2013—2015年廊坊市气象观测站能见度、相对湿度、霾人工观测资料和廊坊市环保局AQI、PM25浓度等气象环保资料,对目前观测业务和空气污染分析中常用的三种霾观测、统计方法进行了对比分析。分析发现:目前廊坊气象观测站所依据的记录霾天气现象的标准,与实际大气污染相趋甚远,不能反映实际的空气污染状况,建议国家及省级相关部门及早根据实际情况,更新霾观测标准,更好地为当前大气污染的防治工作提供客观依据。     

固定化果胶酶抑制铜绿微囊藻生长研究

为证实固定化果胶酶抑制蓝藻生长的作用,在实验室条件下,以铜绿微囊藻（Microcystis aeruginosa）为受试藻种,用共培养法观察了固定化果胶酶对藻细胞群体的作用、用电镜观察了共培养后藻细胞的损伤状况,测定了对其生理生化特征的影响.结果表明固定化果胶酶与藻共培养液第3 d明显黄化,且黄化程度与固定化果胶酶的用量和培养时间呈正相关系;电镜照片显示固定化果胶酶对藻细胞有损伤作用,轻微损伤的藻细胞出现质壁分离,表面粗糙、凸凹不平,形状不规则,严重损伤的藻细胞表面发生深度皱缩或细胞结构完全解体;随着固定化果胶酶与铜绿微囊藻共培养时间的延长,藻细胞生长量、叶绿素a含量显著降低,表明藻细胞受到胁迫和伤害,藻细胞正常的光合作用受到严重影响.丙二醛（MDA）值显示藻细胞抗氧化防御体系被破坏,细胞内发生严重膜脂过氧化.固定化果胶酶能有效抑制铜绿微囊藻细胞的生长,铜绿微囊藻生长抑制率可高达96%.     

聚合氯化铁-聚(环氧氯丙烷-二甲胺)复合絮凝剂在模拟水处理中的混凝特性研究

制备出一系列具有不同聚合氯化铁(PFC)的碱化度(B)、不同聚(环氧氯丙烷-二甲胺)[P(EPI-DMA)]质量分数[ω(E)]和黏度(η)的PFC-P(EPI-DMA)复合混凝剂,并将其用于模拟染料废水和模拟天然地表水的絮凝脱色处理,对比探讨了ω(E)、η和B对PFC-P(EPI-DMA)中铁的形态分布及其混凝效果的影响,以及混凝作用机制.结果表明,复合絮凝剂中铁的有效形态含量随ω(E)的增大而不断降低;η=850 mPa.s时,复合混凝剂中铁的有效形态含量最高;随B值的增大,Feb含量先增大后减少,而Fec含量逐渐增大.一定程度上使用预水解程度较低、有机成分黏度较大的PFC-P(EPI-DMA)有利于混凝效果的提高,复合混凝剂中有机成分质量分数对混凝效果的影响则与处理对象有关.在模拟水处理中,复合混凝剂依靠电性中和及架桥吸附能力发挥混凝特性.     

改良型固定化Pseudomonas oleovorans DT4降解四氢呋喃的研究

成功构建出了新型的海藻酸钠-活性炭纤维复合固定化Pseudomonas oleovorans DT4来去除四氢呋喃,并优化了该复合固定化载体组分的含量,发现在海藻酸钠含量为3%,活性炭纤维含量为1.5%条件下,制备成细胞浓度为6×109g-1的协同固定化细胞在初始THF浓度为360 mg·L-1时的降解速率达到最大为24.0 mg·(L.h)-1,同时其机械强度也得到了显著的提升.此外与游离菌体相比,该固定化细胞在不同温度和pH条件下的降解速率表现得更加稳定,且去除效果均能稳定在80%以上.在改进的反应体系中,协同固定化小球高效降解THF的重复利用次数达到80批以上,显示出该载体良好的可行性.     

太湖流域典型河流沉积物重金属污染特征及生态风险评价

武宜运河位于太湖西部贯穿大部分太湖入湖河流,其重金属污染的研究,对太湖重金属污染来源,流域管理具有重要的意义。因此,2012年8月对武宜运河全程底质调查,分析了沉积物中Cu、Zn、Pb、Ni、Cr等元素,通过地累积指数评价、相关分析、潜在生态风险评价以及相关研究对比分析,得出以下结论:1)Cu、Zn、Pb、Ni、Cr污染浓度均值为129.38,207.74,52.13,28.26,77.06 mg/kg,其中Cu、Zn、Pb、Ni、Cr均超过毒性参考值(TRV),Cu超标达800%。Zn、Pb、Cr在世界湖泊沉积物中微量金属的范围(WCTMEL)内,Cu超出144%,Ni略低于WCTMEL;2)Ni-Cr、Zn-Pb具有较好的同源性。且Cu、Zn污染较高,达到"中—强"和"强"污染级别,Pb污染级别其次,Ni、Cr污染级别较低或无污染。可以排除武宜运河携带Ni、Cr污染物进入入湖河网的可能;3)Cu为武宜运河生态风险主要贡献因子。需加强工业园区地段重金属污染控制,减少污染来源,加大武宜运河对连同入湖水系的清水补充。     

复合膜生物反应器处理环氧氯丙烷废水

实验利用复合膜生物反应器处理以甘油为原料制备环氧氯丙烷产生的废水,考察了不同进水COD、水力停留时间以及盐度对处理能力的影响,并进行盐度冲击实验。生物处理后出水进行了深度处理的研究。结果表明:进水COD对处理能力影响较小;适当延长水力停留时间能优化出水水质;废水盐度高于22g/L时会对微生物产生抑制作用;深度处理能进一步降低出水COD;微生物通过一定时间的驯化期能适应并处理高盐度废水。     

Determination of 4-tert-octylphenol in surface water samples of Jinan in China by solid phase extraction coupled with GC-MS

Octylphenols, considered as xenoestrogens, mainly exist as 4-tert-octylphenol (OP) in aquatic environments. The high stability and accumulation of OP in aquatic systems have caused endocrine disruption. The OP in surface water in Jinan, China was analyzed by gas chromatography-mass spectrometry (GC-MS) coupled with solid phase extraction (SPE). Water samples were extracted by SPE on a cartridge system containing C-18 as sorbent. To increase sensitivity and selectivity, OP was derivatized to 4-tert-octyl-phenoxy silane. With the use of phenanthrene-d10 as internal standard, the detection limit based on signal-to-noise ratio (S/N = 3) was 0.06 ng/mL. The average recovery was from 84.67% to 109.7%. The precision of the method given as the relative standard deviations (RSD) was within the range 6.24%-12.96%. In the target water samples, the concentrations of OP were as follows: 15.88-71.24 ng/L for Jinxiuchuan Reservoir, 3.850-26.68 ng/L for the city moat, 6.930-41.56 ng/L for Daming Lake, 66.03-474.2 ng/L for Xiaoqing River, 14.66-17.72 ng/L for the Yellow River, and 10.60-26.43 ng/L for Queshan Reservoir. The Xiaoqing River was seriously polluted due to the discharge of wastewater from Jinan. Jinxiuchuan Reservoir had a higher concentration of OP compared with the Yellow River and Queshan Reservoir, which is ascribed to the surrounding human activities. These data are reported for the first time, providing strong support for the control of OP pollution in Jinan.     

Electrochemical and spectroscopic characteristics of dissolved organic matter in a forest soil profile

Dissolved organic matter （DOM） represents one of the most mobile and reactive organic compounds in ecosystem and plays an important role in the fate and transport of soil organic pollutants, nutrient cycling and more importantly global climate change. Electrochemical methods were first employed to evaluate DOM redox properties, and spectroscopic approaches were utilized to obtain information concerning its composition and structure. DOM was extracted from a forest soil profile with five horizons. Differential pulse voltammetry indicated that there were more redox-active moieties in the DOM from upper horizons than in that from lower horizons. Cyclic voltammetry further showed that these moieties were reversible in electron transfer. Chronoamperometry was employed to quantify the electron transfer capacity of DOM, including electron acceptor capacity and electron donor capacity, both of which decreased sharply with increasing depth. FT-IR, UV-Vis and fluorescence spectra results suggested that DOM from the upper horizons was enriched with aromatic and humic structures while that from the lower horizons was rich in aliphatic carbon, which supported the findings obtained by electrochemical approaches. Electrochemical approaches combined with spectroscopic methods were applied to evaluate the characteristics of DOM extracted along a forest soil profile. The electrochemical properties of DOM, which can be rapidly and simply obtained, provide insight into the migration and transformation of DOM along a soil profile and will aid in better understanding of the biogeochemical role of DOM in natural environments.