纳米级铁粉脱氯降解四氯化碳

四氯化碳的生产和使用,给人类带来了较大危害.为此,采用纳米铁粉这一新方法对其进行脱氯处理.试验以纳米级铁粉对四氯化碳的脱氯率为考察指标,选用L25(56)正交试验方案,考察了降解介质的初始pH值、纳米铁粉的质量、降解温度、摇床转速和脱氯时间5个影响因素.结果表明,pH值这一因素有极显著影响;在得出的纳米铁粉对四氯化碳脱氯的最佳工艺条件下,获得了99.5%的脱氯率,为有机氯化物脱氯开辟了一条新途径.     

活性碳纤维在环境保护中的应用

由于活性碳纤维的吸附面积大,可以作为固相微萃取的纤维用于对环境污染物质的分析检测,包括含硫和含氯的一些有机化合物.同时,活性碳纤维具有良好的导电性能,可以作为电极,能有效地去除环境中城市污水、燃料废水和腐植酸的污染.     

Fish mercury increase in Lago Manso, a new hydroelectric reservoir in tropical Brazil

It has been frequently demonstrated that mercury (Hg) concentrations in fish rise in newly constructed hydroelectric reservoirs in the Northern Hemisphere. In the present work, we studied whether similar effects take place also in a tropical upland reservoir during impoundment and discuss possible causes and implications. Total Hg concentrations in fish and several soil and water parameters were determined before and after flooding at Rio Manso hydroelectric power plant in western Brazil. The Hg concentrations in soil and sediment were within the background levels in the region (22-35 ng g(-1) dry weight). There was a strong positive correlation between Hg and carbon and sulphur in sediment. Predatory fish had total Hg concentrations ranging between 70 and 210 ng g(-1) f.w. 7 years before flooding and between 72 and 755 ng g(-1) f.w. during flooding, but increased to between 216 and 938 ng g(-1) f.w. in the piscivorous and carnivorous species Pseudoplatystoma fasciatum, cachara, and Salminus brasiliensis, dourado, 3 years after flooding. At the same time, concentrations of organic carbon in the water increased and oxygen concentrations decreased, indicating increased decomposition and anoxia as contributing to the increased Hg concentrations in fish. The present fish Hg concentrations in commonly consumed piscivorous species are a threat to the health of the population dependent on fishing in the dam and downstream river for sustenance. Mercury exposure can be reduced by following fish consumption recommendations until fish Hg concentrations decrease to a safe level.     

BAC生物活性炭法及其在水处理中的应用

介绍了生物活性炭(BAC)法去除有机物的方式,不同进水水质条件下的特征穿透曲线。总结了BAC法的优缺点以及国、内外对BAC生物再生的研究与观点,以及BAC技术的研究与应用进展。     

TiO2/活性炭催化剂对4-CP的吸附和光催化活性

采用常压金属有机物化学气相沉积技术在活性炭表面沉积构成纳米TiO2催化剂,XRD分析表明,沉积在活性炭表面的TiO2为锐钛矿晶型.TEM分析表明负载量为8%(wt)时,TiO2颗粒的粒径为10-20nm;载体负载前后BET面积仅改变了6%,表明负载TiO2后对活性炭的结构影响不大.利用Langmuir-Hinshelwood动力学模型探讨了TiO2/活性炭催化剂对4-CP的吸附行为和光催化活性之间的关系,求出4-CP降解反应速率常数Kr,在紫外光照条件下催化剂对4-CP的吸附明显增强.     

pH值与乙酸对易腐有机垃圾水解过程的抑制

通过外部添加水解酶比较和区分pH值和乙酸对水解的影响,结果表明:以固相挥发性固体和元素碳的减少以及液相有机碳的增加表征水解率,在pH=7时最大,144h的水解率可达66.9%;与pH=7相比,pH=8-9时,水解率降低8%-24%;pH=5-6,水解率降低40%-60%.20g·l-1乙酸的加入抑制了水解,在不同pH值条件下与不添加乙酸的水解相比,抑制程度为2%-35%,pH=7时乙酸的抑制最显著,可达35%.颗粒态物料的水解过程动力学符合Chen-Hashimoto公式.     

Field reconnaissance and estimation of petroleum hydrocarbon and heavy metal contents of soils affected by the Ebocha-8 oil spillage in Niger Delta, Nigeria

Field reconnaissance of the Ebocha-8 oil spill-affected site at Obiobi/Obrikom in the Niger Delta region of Nigeria was carried out to assess the extent of damage to the terrestrial ecosystem and delimit the epicenter of oil spillage. Following three successive reconnaissance surveys, the area to be sampled was delimited (200 x 200 m2), and soil samples were collected using the grid method from three replicate quadrats at two depths, surface (0-15 cm) and subsurface (15-30 cm). A geographically similar area located 50 m adjacent to the oil-polluted area was used as a reference (control) site. Total hydrocarbon content (THC) and heavy metal concentrations were later determined in the laboratory by extraction and spetrophotemetric techniques. Generally, the THC of soils at surface and subsurface depths of the oil-polluted plots was 2.06 x 10(4) +/- 4.97 x 10(3) mg/kg and 1.67 x 10(3) +/- 3.61 x 10(2) mg/kg soil, respectively, (no overlap in standard errors at 95% confidence limit) while concentrations of heavy metals(Pb, Cd, V, Cu and Ni) were enhanced, especially at the surface. The high levels of THC and heavy metals may predispose the site, which hitherto served as arable agricultural land, to impaired fertility and possible conflagration. When concentrations of heavy metals reach the levels obtained in this study, they may become toxic to plants or possibly bio-accumulate, thus leading to toxic reactions along the food chain. While the spilled-oil may have contributed to the enhanced levels of the metals in the affected soils, physico-chemical properties of the soils, mobility of metals, and the intense rainfall and flooding that preceded the period of study may have also contributed in part to their enhanced concentrations. The presence of high hydrocarbon content may cause oxygen deprivation, which may result in the death of soil fauna by asphyxiation. There is, therefore, an urgent need to clear the affected site of these excess hydrocarbon deposits so as to enhance the rehabilitation process of the affected mat layer of soils. Other appropriate mitigating measures, such as subsequent monitoring of hydrocarbon levels at suitable intervals after the clean up activities, are also recommended, with reference to the findings of this study, for effective management of the affected area.     

水溶性有机物对草萘胺在土壤中吸附与迁移的影响

采用批次吸附试验和土柱淋洗试验,研究了绿肥和污泥中水溶性有机物(DOM)对除草剂草萘胺在黄棕壤和石灰性潮土上吸附和迁移影响.结果表明,供试DOM均能明显降低草萘胺在2种土壤上的吸附,促进草萘胺的迁移,在黄棕壤上效果更明显.在所研究的草萘胺和DOM浓度范围内,绿肥DOM(GM)都比污泥DOM(SS)作用显著.草萘胺的吸附等温线可用Freundlich方程定量描述.绿肥DOM和污泥DOM可分别使黄棕壤中草萘胺吸附量比对照处理(不加DOM)减少22.9%和11.3%,使迁移出土体的草萘胺总量提高了73.42%和26.87%,而使潮土中草萘胺的吸附量减少了9.5%和6.5%,迁移出土体的草萘胺总量增加了43.54%和28.29%.因此,农业土壤中溶解性有机物对农药环境行为有一定影响.     

臭氧对有机物混凝的影响

采用PDA(Photometric Disperse Analysis)和有机物表观分子量分级、有机物化学极性分级技术从絮体形成过程、絮体表现、有机物分子水平变化等方面研究了臭氧预氧化对混凝过程的影响;并对比了不同混凝剂在预臭氧条件下的混凝过程和效率.结果表明:臭氧预氧化对混凝过程有复杂的影响,其剂量和水体有机物特征决定了其对混凝的整体影响效果.有机物分级显示,臭氧化对有机物结构有重要影响,导致有机物极性、亲水性组分含量大幅提高(36.7%),小分子量组分(<10×10³)大幅增高(100%左右);但总的DOC去除率不高(3.28%).对PACl而言,在中、低剂量(O₃/TOC<0.7)下,臭氧对絮体形成过程影响较小,但对絮体沉降性和浊度去除已经有阻碍作用.在中、高剂量下(O₃/TOC>0.7),对絮体形成有显著滞后,浊度、有机物去除效率下降.AlCl₃对臭氧化作用反应敏感,臭氧化在试验剂量条件下,对絮体形成和浊度、有机物去除都有明显的阻碍作用.     

电增强活性炭纤维吸附有机污染物的动力学研究

研究了在电极化条件下,几种具有代表性污染物质在活性炭纤维上的电吸附动力学特性.结果表明,各种污染物的电吸附动力学比较好地符合Lagergren一级吸附动力学,其平衡吸附量在电极化下的增加量各不相同.在400mV的极化电位下,苯酚钠的吸附量从开路时的0.008 3mmol·g^-1增加到0.18 mmol·g^-1,增加了17倍;而对硝基苯酚的吸附量从开路时的2.93mmol·g^-1降到2.65 mmol·g^-1.在-400mV的极化电位下,苯胺的吸附量从开路时的3.60 mmol·g^-1增加到3.88 mmol·g^-1;而十二烷基苯磺酸钠的吸附量从开路时的2.20 mmol·g^-1降到1.59 mmol·g^-1.说明不同取代基的苯衍生物,电吸附改变量不相同,供电子基团的单取代苯,正极化都能明显增强其吸附量;但是吸电子基团的单取代,正负极化对吸附量的影响都很小;供体-共轭桥键-受体型结构的苯衍生物,正负极化都使其吸附减弱但吸附速率加快.静电作用在离子型污染物的电吸附中表现明显.