SBR快速实现短程硝化及影响因素

基于建立的序批式反应器(SBR),探索实现城市生活污水短程硝化的主要控制因素。研究结果表明,废水温度维持在(30±1)℃、p H值为7.8~8.2的条件下,采用间歇曝气的运行方式,仅驯化培养29 d,成功实现短程硝化,亚硝氮积累率为95%左右。通过对比发现,间歇曝气方式优于连续曝气方式,间歇曝气能有效地将溶解氧(DO)浓度控制在1.0mg/L以下,从而有利于进行短程硝化反应。此外,温度和p H可以影响亚硝氮的积累效果;当温度在25~35℃、进水p H为7.8~8.2时,亚硝氮的积累情况较好,积累率在91%以上。     

共存物及其投加方式对Tween 80 在中砂上吸附损失的影响

通过静态吸附实验,研究了25℃条件下,表面活性剂冲洗液Tween 80在中砂上的吸附,以及CaCl2、SDS和木质素磺酸盐(木质素磺酸钠和木质素磺酸铵)对其吸附量的影响.结果表明,向Tween 80溶液中加入CaCl2和SDS都可以显著增加其吸附量.投加量越多,吸附量越大,当投加量达到一定程度后,吸附达到饱和,不会继续增大.SDS以预吸附的方式注入同样会导致Tween 80吸附量升高.而木质素磺酸盐与Tween 80共混则可大大降低Tween 80的吸附量.随着投加量的增加,Tween 80吸附量明显下降.在低投加比例(1:10)时,木质索磺酸铵效果较好,可以减少20%-75%的吸附量.而木质素磺酸钠只能减少10%-60%.当投加较高比例(1:2)时,两者都口1以明显降低Tween 80的吸附量,可达70%-90%.而采用木质素磺酸盐预吸附的方式注入的效果较混合注入要好,相同投加最的情况下,所降低Tween 80的吸附量是混合注入时的1.2-1.8倍.因此.在表面活性剂原位冲洗过程中用木质素磺酸盐进行预冲洗,能够减少表面活性剂吸附量,降低冲洗成本,可以作为原位冲洗过程中降低吸附损失的一种手段.     

Degradation of bisphenol-A using ultrasonic irradiation assisted by low-concentration hydrogen peroxide

This study investigated the degradation of bisphenol-A (BPA) by ultrasonic irradiation in the presence of different additives (H2O2,air bubbles and humic acid) under various operating conditions,i.e.,ultrasonic frequency,power intensity and power density.The results demonstrated that the BPA degradation followed pseudo first-order kinetics under different experimental conditions.The optimum power intensities were 0.9,1.8,and 3.0W/cm 2 at the frequencies of 400,670,and 800 kHz,respectively.At the fixed frequ...     

电增强环氧树脂基聚合物膜萃取水样中的硝基苯

以环氧树脂基聚合物膜为萃取相,在电场作用下富集目标物,与高效液相色谱(HPLC)联用,应用于环境水样中硝基苯污染物的测定.考察了电压大小、萃取时间、洗脱时间、离子强度和溶液pH值对电增强萃取效率的影响.实验结果表明,环氧树脂基聚合物膜的萃取量与膜上所施加的控制电位相关,阴极极化时,膜对硝基苯的萃取量增大;在阳极极化时,膜萃取量减小.在电压为-0.3kV,硝基苯溶液pH=4的条件下,萃取20min,得到该方法的检出限为0.015μg·mL-1,在0.05～3.0μg·mL-1范围内具有良好的线性关系,可决系数为0.9929,变异系数小于5%.用上述方法分析鱼塘水,硝基苯3种不同加标水平的回收率为79.8%～108.2%.结果表明,该方法既可用于环境水样品中的硝基苯去除又可用于检测.     

抚顺地区土壤肥力分析与评价

通过对抚顺地区65个点位土壤pH、有机质、全氮、全磷、全钾五个指标的实地监测,得出抚顺地区土壤肥力基本状况为：土壤酸碱度处于中等,有机质含量和全磷含量丰富,全氮含量较丰富,全钾含量较缺,并针对该现状。提出了如何合理施用钾肥。     

Degradation of carbon tetrachloride in thermally activated persulfate system in the presence of formic acid

The thermally activated persulfate (PS) degradation of carbon tetrachloride (CT) in the presence of formic acid (FA) was investigated. The results indicated that CT degradation followed a zero order kinetic model, and CO ₂ ^– · was responsible for the degradation of CT confirmed by radical scavenger tests. CT degradation rate increased with increasing PS or FA dosage, and the initial CT had no effect on CT degradation rate. However, the initial solution pH had effect on the degradation of CT, and the best CT degradation occurred at initial pH 6. Cl^– had a negative effect on CT degradation, and high concentration of Cl^– displayed much strong inhibition. Ten mmol·L^–1HCO ₃ ^– promoted CT degradation, while 100 mmol·L^–1NO ₃ ^– inhibited the degradation of CT, but SO ₄ ^2– promoted CT degradation in the presence of FA. The measured Cl–concentration released into solution along with CT degradation was 75.8% of the total theoretical dechlorination yield, but no chlorinated intermediates were detected. The split of C-Cl was proposed as the possible reaction pathways in CT degradation. In conclusion, this study strongly demonstrated that the thermally activated PS system in the presence of FA is a promising technique in in situ chemical oxidation (ISCO) remediation for CT contaminated site.     

Enhanced degradation of trichloroethene by calcium peroxide activated with Fe(III) in the presence of citric acid

Trichloroethene (TCE) degradation by Fe(III)-activated calcium peroxide (CP) in the presence of citric acid (CA) in aqueous solution was investigated. The results demonstrated that the presence of CA enhanced TCE degradation significantly by increasing the concentration of soluble Fe(III) and promoting H₂O₂ generation. The generation of HO? and O₂^-? in both the CP/Fe(III) and CP/Fe(III)/CA systems was confirmed with chemical probes. The results of radical scavenging tests showed that TCE degradation was due predominantly to direct oxidation by HO?, while O₂^-? strengthened the generation of HO? by promoting Fe(III) transformation in the CP/Fe(III)/CA system. Acidic pH conditions were favorable for TCE degradation, and the TCE degradation rate decreased with increasing pH. The presence of Cl^-, HCO₃^-, and humic acid (HA) inhibited TCE degradation to different extents for the CP/Fe(III)/CA system. Analysis of Cl^- production suggested that TCE degradation in the CP/Fe(III)/CA system occurred through a dechlorination process. In summary, this study provided detailed information for the application of CA-enhanced Fe(III)-activated calcium peroxide for treating TCE contaminated groundwater.     

Recent advances in pharmaceuticals and personal care products in the surface water and sediments in China

Pharmaceuticals and personal care products (PPCPs) have been regarded as an emerging problem in the surface water environment in the past few decades. In China, although related studies were initiated several years ago, an increasing number of studies on this topic have been conducted in recent years. These studies have expanded knowledge of their occurrence, behavior and associated risk in the surface water environment in China. This review compiles the most recent literature related to the studies of PPCPs in the surface water environment in China. It includes PPCP occurrence in surface water and sediments, their geographical distribution, and outcomes of the associated risk assessment. It shows that antibiotics have received much more attention in both surface water and sediments than other PPCPs. Compared to other countries; most antibiotics in the collected sediments in China showed higher contamination levels. Many more study areas have been covered in recent years; however, attention has been given to only specific areas. Environmental risk assessment based on risk quotients indicated that sulfamethoxazole presents the most significant environmental risk to relevant aquatic organisms; followed by ofloxacin, ciprofloxacin, enrofloxacin, 17α-ethynylestradiol, ibuprofen and diclofenac. Despite limited research on the environmental risk assessment of PPCPs in sediments, higher risks posed by PPCPs in the sediments rather than surface water were identified highlighting the need for further risk assessment of PPCPs in sediment samples.

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红谷霉素对细菌耐药性质粒转移的抑制作用

以Shigella flexneri D15 R-plasmid CmR和Escherichia coil 1485 RifR为试验菌株,研究红谷霉素对细菌耐药性质粒在细菌之间转移的抑制作用及对两种细菌R质粒的消除作用.将红谷霉素(30μg/mL)与S.flexneri D15 R-plasmid CmR和E.coli 1485 RifR按实验设计混合并分别培养24 h和48 h,涂布在麦康凯琼脂平板上,计算相应菌落数.结果表明,当红谷霉素抑菌浓度为30μg/mL时,对细菌耐氯霉素的R质粒的转移抑制率分别达到92.82%(24 h培养)和96.04%(48 h培养),但对R质粒的消除作用不显著.说明红谷霉素对R质粒转移抑制作用强烈但不具有R质粒的消除作用.     

臭氧胁迫下外源喷施亚精胺和EDU对小麦生理指标的影响

采用开顶式气室模拟研究外源喷施亚精胺(Spd)和EDU对O3胁迫下小麦生理指标变化的影响,测定的生理指标包括丙二醛含量(MDA)、超氧化物歧化酶活性(SOD)、过氧化物酶活性(POD)、过氧化氢酶活性(CAT)、可溶性蛋白质含量、还原型谷胱甘肽含量(GSH)、谷胱甘肽还原酶活性(GR)、抗坏血酸含量(ASA)和抗坏血酸过氧化物酶活性(APX)。结果表明,外源喷施Spd和EDU可不同程度地提高小麦叶片的SOD、POD、CAT、APX和GR活性,降低MDA和ASA含量,提高GSH和可溶性蛋白含量。当Spd的浓度为0.25、0.50和0.75mmol·L-1时,小麦叶片POD活性比对照处理提高90.0%～226.7%,CAT活性提高21.4%～40.6%,APX活性提高164.2%～191.0%,MDA含量降低9.7%～42.5%。喷施300mg·L-1EDU可导致小麦叶片POD、CAT和APX活性分别比对照处理提高76.8%、27.4%和128.1%,MDA和ASA含量降低,GSH含量提高25.6%。以上结果说明Spd和EDU是2种比较有效的缓解小麦O3胁迫的抗氧化剂,可用来防护O3对小麦的毒害。