Carrousel氧化沟的流动特性研究

采用颗粒动态分析仪(PDA)对倒伞形表面曝气机曝气的Carrousel小试氧化沟进行测试,得出了氧化沟内较系统的流动特性参数.比较了固液两相在氧化沟内流动的差别,发现固液两相流动速度差别较小,由于惯性的影响,固相的沉降速度略大于液相.考察了表曝机的转速、表曝机相对于液面的位置、氧化沟的深度等因素对氧化沟内流动的影响,随着表曝机转速的增大和表曝机浸入液面深度的增加,流动速度和沉降速度均会增大,而氧化沟深度增加时,距离液面同一深度处的速度则会减小.实验结果与污水处理厂的实际情形进行比较发现,二者变化趋势一致,说明本实验结果可用于指导工程实际,为氧化沟的优化设计提供依据.     

粉尘点污染扩散模型的可视化研究

在分析和总结了瞬时点尘源在静止流体、均匀紊流和湍流条件下扩散模型的数学表达式和浓度分布方程的基础上,运用Matlab软件进行可视化处理,生成一系列的三维图形,可从不同的角度进行观察和分析,使之能够直观、形象的了解粉尘扩散过程,并从中了解到粉尘扩散的一些特点,该项研究对粉尘防治工作与危害预测都有重要的理论与实践意义。     

松花江:有待继续关注

最近,黑龙江省环保局向社会各界通报了今春解冻期松花江大面积水质不会超标、各江段用及沿岸鱼塘的鱼类可放心食用、今年春季用松花江水进行灌溉不会影响作物生长等人民群众普遍关注的问题.     

硝化悬浮填料塔中氨氧化细菌群落稳定性特征分析

利用PCR-DGGE分析技术,对于化学生物絮凝处理工艺中悬浮填料塔的氨氧化细菌(AOB)群落进行了研究。主要考察了曝气强度和水力停留时间2个运行参数调整的情况下,系统AOB群落结构的变化。生物膜样品直接取自硝化填料塔,多维尺度(MDS)方法用于DGGE电泳图谱的分析,分析结果以二维图形向量的方式显示,结果表明,曝气强度和水力停留时间均对AOB群落有一定的影响,主要的AOB种类在运行过程中基本不变,系统对于运行条件具有良好的稳定性。     

手性污染物与环境安全

本文就手性污染物在生命过程中对映体的差异作了简要评述,分析了手性污染物对映体的毒性差异及机理.同时指出了手性污染物今后研究的发展趋势.     

顺序氯化对微生物、副产物和生物稳定性的综合控制

在中试规模试验中,研究了“短时游离氯后转氯胺的顺序氯化消毒工艺”对微生物、消毒副产物和生物稳定性指标的控制效果.该顺序氯化消毒工艺综合利用了游离氯消毒灭活微生物迅速彻底,氯胺消毒副产物生产量低的特点,通过氯化消毒技术的组合,安全经济地实现了消毒卫生学和消毒副产物指标的双重控制.该消毒工艺对细菌总数、异养菌平板计数、总大肠菌群指标的控制效果略好于传统游离氯消毒,对脊髓灰质炎病毒和大肠杆菌f2噬菌体的灭活效果与游离氯相同.相同原水条件下,顺序氯化消毒工艺比游离氯消毒工艺产生的三卤甲烷浓度减少35.8%～77.0%;卤乙酸减少36.6%～54.8%.消毒进水水质越差,顺序氯化消毒工艺在消毒副产物控制方面就越有优势.该工艺对生物稳定性指标的控制效果明显高于游离氯消毒.     

流化催化裂化烟气脱硫助剂的制备及其脱硫活性

采用溶胶-凝胶法制备锌铝助剂,该助剂于700℃焙烧后与流化催化裂化（FCC）催化剂进行机械混合,制得混合催化剂;在FCC烟气工业模拟装置上考察混合催化剂的脱硫活性,用混合催化剂的脱硫活性来反映锌铝助剂的脱硫性能。实验结果表明,氧化锌质量分数为10％的锌铝助剂的脱硫活性最佳,脱硫率达62．5％。采用红外光谱和X射线衍射（XRD）对锌铝助剂的脱硫机理进行了研究,红外分析结果表明,弱的L酸中心有利于锌铝助剂脱硫,XRD分析结果表明,锌铝助剂在锌铝尖晶石结构尚未完全形成时,存在较多的晶格缺陷,能够有效地吸附烟气中的SOx,将其转化为H2S。     

丹江湿地国家级自然保护区及其内外区域2000—2015年土地覆被变化分析

为研究2000—2015年丹江湿地国家级自然保护区及其内外生态状况变化和保护成效,基于高分1号数据生产的2m高分辨率遥感影像数据对丹江湿地国家级自然保护区2015年人类活动状况进行分析,基于30 m分辨率的4期TM遥感影像生产的土地覆被数据和基于Modis遥感影像生产的植被覆盖度数据,对淅川县、丹江湿地国家级自然保护区及其核心区的土地覆被状况、土地覆被转类指数及其土地覆被转类途径的主导程度和3个相关区域范围内的生态系统质量以及不同区域土地覆被变化的主要变化原因进行分析。结果表明,保护区核心区的格局和质量在该区域处于最优,且土地覆被变化状况也以核心区转类指数最高;丹江湿地国家级自然保护区内的主要人类活动影响为耕地,其次包括居民点、采石场、养殖场; 15年间,保护区内外土地覆被均呈现转好趋势,但是保护区内变化优于保护区外,保护区核心区优于整个保护区,且转好的主导因素均是耕地变为湿地; 15年间植被覆盖度变化较小。     

Combination with catalyzed Fe(0)-carbon microelectrolysis and activated carbon adsorption for advanced reclaimed water treatment: simultaneous nitrate and biorefractory organics removal

A process combining catalyzed Fe(0)-carbon microelectrolysis (IC-ME) with activated carbon (AC) adsorption was developed for advanced reclaimed water treatment. Simultaneous nitrate reduction and chemical oxygen demand (COD) removal were achieved, and the effects of composite catalyst (CC) addition, AC addition, and initial pH were investigated. The reaction kinetics and reaction mechanisms were calculated and analyzed. The results showed that CC addition could enhance the reduction rate of nitrate and effectively inhibit the production of ammonia. Moreover, AC addition increased the adsorption capacity of biorefractory organic compounds (BROs) and enhanced the degradation of BRO. The reduction of NO₃^?–N at different pH values was consistently greater than 96.9%, and NH₄⁺–N was suppressed by high pH. The presence of CC ensured the reaction rate of IC-ME at high pH. The reaction kinetics orders and constants were calculated. Catalyzed iron scrap (IS)-AC showed much better nitrate reduction and BRO degradation performances than IS-AC and AC. The IC-ME showed great potential for application to nitrate and BRO reduction in reclaimed water.

     

Evaluation of photolysis and hydrolysis of pyraclostrobin in aqueous solutions and its degradation products in paddy water

This study evaluated the hydrolysis and photolysis kinetics of pyraclostrobin in an aqueous solution using ultra-high-performance liquid chromatography–photodiode array detection and identified the resulting metabolites of pyraclostrobin by hydrolysis and photolysis in paddy water using high-resolution mass spectrometry coupled with liquid chromatography. The effect of solution pH, metal ions and surfactants on the hydrolysis of pyraclostrobin was explored. The hydrolysis half-lives of pyraclostrobin were 23.1–115.5?days and were stable in buffer solution at pH 5.0. The degradation rate of pyraclostrobin in an aqueous solution under sunlight was slower than that under UV photolysis reaction. The half-lives of pyraclostrobin in a buffer solution at pH 5.0, 7.0, 9.0 and in paddy water were less than 12?h under the two light irradiation types. The metabolites of the two processes were identified and compared to further understand the mechanisms underlying hydrolysis and photolysis of pyraclostrobin in natural water. The extracted ions obtained from paddy water were automatically annotated by Compound Discoverer software with manual confirmation of their fragments. Two metabolites were detected and identified in the pyraclostrobin hydrolysis, whereas three metabolites were detected and identified in the photolysis in paddy water.