MBR在橡胶废水处理中的应用

橡胶废水具有含盐量高、色度高、有机污染成分含量高且难于生化降解等特点。膜生物反应器(MBR)技术的核心是生化处理加微滤膜过滤,通过将MBR技术应用于橡胶废水处理的实践表明,该技术对COD、氨氮、磷酸盐的平均去除率都达到了85%以上,再辅之以药剂处理后,降低了色度和难降解有机物含量,出水水质完全符合排放标准的要求,是一种解决橡胶污水处理难题的有效途径。     

粒状羟基氧化铁对废水中硝酸盐的吸附

本实验研究了粒状羟基氧化铁(GFH)对人工配制含氮废水中NO3--N吸附的影响因素、吸附等温线和吸附动力学。结果表明,GFH的吸附平衡时间为80 min,增加NO3--N溶液的初始浓度,去除率下降;pH值为5时GFH对NO3--N的吸附能力最强,pH值升高和降低,吸附能力均下降;GFH对NO3--N的吸附能力随着温度的升高略有降低;在25℃下,以Langmuir方程和Freundlich方程分别对GFH吸附NO3--N的等温线进行拟合,拟合效果以Langmuir方程较好,相关性达到0.9930。GFH吸附NO3--N的过程符合拟二级动力学方程,初始时刻的吸附速率h在35℃时最大,为1.653 mg/(g.mg),吸附速率常数随温度的升高而增大;吸附反应的活化能Ea为54.72 kJ/mol。本研究结果表明,GFH在饮用水脱氮和含氮浓度较低的污水再生回用领域有实际应用的潜力。     

多孔性Mn3O4的制备及其对水中镉的吸附

采用硫酸锰水解-氧化两步法制备了多孔性四氧化三锰,以X射线衍射、扫描电镜和氮吸附比表面仪对其进行了表征,研究了该多孔性Mn3O4在不同的溶液pH值、吸附时间、投加量和温度下对水中Cd(Ⅱ)的吸附行为,并测定了吸附过程的动力学和热力学参数。实验结果表明,该法合成的四氧化三锰属四方体心结构,一次晶粒尺寸为45.8 nm,颗粒间存在大量的孔洞,BET法比表面积为40.27 m2/g。在293 K,pH 5.5,吸附12 h时达到平衡,饱和吸附量为12.8 mg/g。该吸附过程符合准二级反应动力学模型,其反应的吸附活化能为2.743 kJ/mol,吸附等温线较好地符合Langmuir等温方程,吸附焓变和熵变均为正值,自由能变为负值,说明该吸附过程为自发的吸热过程。     

序批式生物膜反应器挂膜启动实现短程硝化

常温条件下(20～25℃),以模拟的人工配水为研究对象,采用序批式生物膜反应器(SBBR),在初期挂膜的基础上,笔者运用两种不同的挂膜方式即重新加入新泥和不加新泥而加大进水COD浓度来实现生物膜的快速启动。实验表明,2种挂膜启动通过14 d的培养与富集,NH4+-N与COD的处理效果都能分别达到85%和75%以上。将剩余污泥排尽后,采用第1种挂膜方式的反应器通过连续间歇曝气,达到了比较好的短程硝化效果。调整溶解氧,并且通过先下降后上升曝气量的方式,能进一步提高亚氮的出水。最终在DO为3.6 mg/L时,亚氮的积累率能达到平均74%左右,达到了比较好的亚硝化效果。而第2种挂膜方式培养的生物膜则以好氧反硝化菌为主,去除的氨氮由同化作用和培养的好氧反硝化菌去除,以后者为主。通过比较可以看出,为了实现短程硝化,第1种挂膜方式比第2种更具有优越性,有利于硝化菌种的生长和亚氮的积累,而第2种方式则有利于培养好氧反硝化菌。     

不同因素对人工湿地基质脱氮除磷效果的影响

在人工配制的污水中投入一定量的基质,不同条件下振荡培养,评价沸石、炉渣和陶瓷滤料3种基质在不同因素影响下对氨氮(NH4+-N)和总磷(TP)的吸附能力。结果表明,不同吸附时间时,沸石对NH4+-N的吸附效果最好,陶瓷滤料对TP的吸附效果最好;进水浓度对沸石吸附NH4+-N的影响较大,其吸附量随进水浓度的增大而增大,进水浓度对炉渣和陶瓷滤料吸附NH4+-N及炉渣吸附TP影响不大;3种基质对NH4+-N和TP的吸附量均是随吸附剂量的增加而降低,要达到较好的去污效果,应根据实验结果考虑基质投入量;pH值对沸石吸附NH4+-N影响显著,pH值6～7范围内吸附效果最好,pH值8～12的碱性条件有利于基质对TP的吸附。     

青海省海东地区工业污染现状及防治对策

"十一五"以来,海东地区环境工作迈上了新的台阶,但因经济基础薄弱发展滞后,全区环保工作的发展与可持续发展战略的要求仍有很大差距。根据工业污染调查资料和数据表明,该区的环境污染与工业发展模式和产业结构有直接的关系。改善环境质量,就必须严格环境执法,强化环境监管,同时推行和推广企业清洁生产,采取点上治理、产业结构优化辅以末端治理,实现环境效益和经济效益的统一。     

Critical Review of Norms and Standards for Biodegradable Agricultural Plastics Part II: Composting

The critical review of norms and standards and corresponding tests to determine the compostability of biodegradable plastics, possibly applicable also to biodegradable agricultural plastics, shows that many norms concerning testing and labelling of compostable plastics have been established at the international level. Some of them are about plastic materials, some others are about products like packaging. The media and conditions of testing cover mainly the conditions designed for industrial composting facilities, and only a few concern home composting conditions. Considering that the end of life management of biodegradable agricultural plastic products will be done at the farm to reduce the management of the waste and also its cost, only a few of these norms are considered to be suitable for adaptation to cover also biodegradable agricultural plastic products. The biodegradability validation criteria under composting conditions, such as the threshold percentage of biodegradation and disintegration, the time and temperature, and the ecotoxicity, are presented for the main norms and standard testing methods. Based on these different norms and their content, a list of specs and technical requirements that could be adapted to meet farm composting conditions for agricultural compostable plastics is proposed. These requirements may be used as criteria for the establishment of a new integrative norm for agricultural compostable plastics.     

表面铜螯合磁性二氧化硅固定化漆酶及其催化降解水中2，4-二氯酚

利用磁性二氧化硅表面接枝的聚丙烯酰胺络合Cu2＋离子，制备了表面铜螯合磁性SiO：材料，采用傅立叶红外光谱（FT．IR），X射线衍射（XRD）对该磁性材料进行了表征，并通过配位作用固定化漆酶，考察了其对水中2，4-二氯酚（2，4-DCP）的催化降解效能及主要影响因素。结果表明，表面铜螯合磁性SiO：固定化漆酶对2，4-DCP具有较好的催化降解效能，利用8g／L固定化漆酶催化降解50mL初始浓度为24．25mg／L的2，4-DCP，反应12h2，4-DCP去除率达91％；当pH值在3．0～6．0范围内时，2，4-DCP的去除率随反应pH值的增加而升高；2，4-DCP初始浓度在14．39～257．6mg／L范围内时，反应12h，2，4-DCP的去除率均达85％以上；给酶量增加促进2，4-DCP的去除，但过多的给酶量导致单位质量固定化漆酶催化降解2，4-DCP的速率下降；水中硫酸根离子对固定化漆酶催化降解2，4-DCP具有明显的促进作用，而碳酸氢根离子明显抑制反应的进行。     

苯胺-邻氨基酚共聚物对水中Hg(Ⅱ)吸附性能的研究

利用化学氧化法合成了苯胺-邻氨基苯酚的共聚物,并通过静态实验研究了材料对水中汞离子的吸附性能。研究结果表明,该共聚物对废水中汞离子有优异的去除效果,其吸附容量可达212.13 mg/g;吸附等温线符合Langmu ir单层吸附模型,动力学过程符合准二级动力学模型;溶液pH值对吸附影响不是很大,pH 5~10范围都有较好的吸附效果;氯离子易与汞离子形成水溶性更强的络合物,对共聚物的吸附有很大的抑制作用。     

Carbonyl emissions from vehicular exhausts sources in Hong Kong

Vehicular emission (VE) is one of the important anthropogenic sources for airborne carbonyls in urban area. Six types of VE-dominated samples were collected at representative locations in Hong Kong where polluted by a particular fueled type of vehicles, including (i) a gas refilling taxis station (liquefied petroleum gas [LPG] emission); (ii) a light-duty passenger car park (gasoline emission); (iii) a minibus station (diesel emission); (iv) a single-deck-bus depot (diesel emission); (v) a double-deck-bus depot (diesel emission); and (vi) a whole-food market entrance for light- and heavy-duty vehicles (diesel emission). A total of 15 carbonyls in the samples were quantified. Formaldehyde was the most abundant carbonyl among the VE-dominated samples, and its contribution to the total quantified amount on a molar basis ranged from 54.8% to 60.8%. Acetaldehyde and acetone were the next two abundant carbonyls. The carbonyls were quantified at three roadside locations in Hong Kong. The highest concentrations of formaldehyde and acetaldehyde, 22.7 +/- 8.4 and 6.0 +/- 2.8 microg/m3, respectively, were determined in the samples collected at a main transportation gate for goods between Hong Kong and Mainland China. The total quantified carbonyl concentration, 37.9 +/- 9.3 microg/m3, was the highest at an entrance of a cross-harbor tunnel in downtown area. The theoretical carbonyls compositions of the three roadside locations were estimated according to the VE-dominated sample profiles and the statistics on vehicle numbers and types during the sampling period. The measured compositions of formaldehyde were much higher than the theoretical compositions in summer, demonstrating that photochemical reactions significantly contributed to the formaldehyde production in the roadsides.