Photocatalytic mineralization of glyphosate in a small-scale plug flow simulation reactor by UV/TiO2

The present work involves the photocatalytic mineralization of glyphosate on a plug flow reactor by UV/TiO₂. The effect of catalyst loading shows an optimal value (0.4 g L^?1) which is necessary to mineralize glyphosate. The kinetic rate of glyphosate mineralization decreases with the increasing initial concentration of glyphosate, and the data can be described using the first-order model. An alkaline environment is conducive to glyphosate mineralization. The mineralization efficiency increases with elevated flow rate to 114 mL min^?1, which is followed by a decrease with a further increase in flow rate due to the reduction of the residence time. The presence of external oxidants (K₂S₂O₈, H₂O₂ and KBrO₃) and photosencitizer (humic acid) can significantly enhance glyphosate mineralization. Photocatalysis oxidation ability of the three studied oxidants decrease in the order of: S₂O₈ ^2? > BrO₃ ^? > H₂O₂. Finally, the Langmuir–Hinshelwood (L-H) model was used to rationalize the mechanisms of reactions occurring on TiO₂ surfaces and L-H model constants were also determined.     

Degradation of fipronil under laboratory conditions in a tropical soil from sirinhaém pernambuco,Brazil

The objective of this research was to assess the degradation of fipronil [5-amino-1-(2,6-dichloro-α,α,α -trifluoro-p-tolyl)-4-trifluoromethylsulfinylpyrazole-3-carbonitrile] in soils from sugar cane fields in Northeastern Brazil. Degradation experiments were carried out under laboratory conditions (controlled temperature and in the dark), where sterile and non-sterile soils (Ustoxs) were incubated [under moisture content of 55% of the water holding capacity (WHC)] and analyzed for fipronil disappearance and metabolite formation. Microbial communities present in the soil degrade fipronil. However, biodegradation seems to be dependent on the bioavailability of the fipronil and the half-life according to the zero-order model. Fipronil degradation rate appeared to be biphasic. Degradation fipronil ranged from 83 days (initial concentration = 978 ng g^{? 1}; short-term experiment) to 200 days (initial concentration = 689 ng g^{? 1}; long-term experiment). This an initial slower rate followed by a faster rate after 90 days of incubation may lead to shorter half-life than that calculated with the zero-order model. The sulfone derivative (an oxidation product) was the predominant metabolite, but the sulfide (a reduction product) and amide (a hydrolysis product) derivatives were also formed under non-sterile conditions after 120 days of incubation. The metabolites underwent further biodegradation, particularly the sulfone derivative. Bioavailability appears to affect fipronil degradation in soils with an effective capacity to adsorb fipronil (such as Ustoxs), while redox potential was important for the formation of metabolites. Despite the fine texture, more aerobic sites were present, thus favoring the formation of the sulfone metabolite over that of the sulfide metabolite. Therefore, microaggregation of Ustoxs, with high clay content, played a very important role in determining the types of metabolites formed.     

Experimental Variability in Characterization of Cyfluthrin Sorption to Soil

To assess the risk of a pesticide to leach to groundwater or to run off to surface water after application, it is necessary to characterize the sorption of the pesticide to soil. For pyrethroids, their hydrophobicity, strong sorption to various materials, and low solubility make it difficult to accurately characterize sorption processes. The objective of this research was to evaluate the variability in cyfluthrin ((RS)-α -cyano-4-fluoro-3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate) sorption to soil as affected by experiment conditions. To minimize cyfluthrin sorption on the walls of glass, silanized-glass, stainless steel, and PTFE centrifuge tubes, cyfluthrin solution was added to aqueous soil slurries or directly to soil, after which it was equilibrated with aqueous solution. Depending on the soil, variation in sorption coefficients, K _oc, obtained using different experimental methodologies with one soil can be comparable to the variation in K _oc values obtained for soils with different physical and chemical properties using one method. K _oc values for cyfluthrin ranged from 56,000 to 300,000 L kg^?1. Sorption methodology needs to be evaluated before sorption coefficients are used in predictive transport models.     

光催化氧化深度处理电镀有机废水的工程化实验

采用光催化氧化联用技术对电镀有机废水进行深度处理工程化实验。探讨了uV、uV＋H2O3、uV＋H2O2＋TiO2、uV＋H2O2＋FeSO4、uV＋H2O2＋FeSO4＋TiO2、uV＋O3＋TiO2和uV＋03＋TiO2＋H2O2等体系对废水有机污染物去除率的影响。结果表明,相较于其他反应体系,uV＋O3＋TiO2＋H2O2体系具有更好的氧化效果,经碳滤处理后去除率达到90％以上,最终出水水质满足GB18918-20O2-级标准（A标准）的要求。实际运行项目偿还期5．33年,NPV〉0,内部收益率大于基准值10％。研究表明,uV＋O3＋TiO2＋H2O,体系能降低加药量,工作量及运行成本。可为电镀企业实际废水处理提供现实依据,为优化电镀废水的处理工艺提供参考。     

光催化电化学联合降解水中苯酚的研究

采用电化学、光催化联合工艺降解水中苯酚,在对其降解机理、反应动力学进行分析的基础上,考察了电解质浓度、电流密度及溶液pH等控制因素对降解速率的影响。实验结果表明：电化学和光催化同时作用时,产生了协同作用;以氯化钠为电解质可增强协同作用;光电联合工艺降解苯酚符合准一级反应动力学;弱酸性环境有利于降解反应的进行。在电流密度...     

The spectroscopic studies of humic acid extracted from sediment collected at different seasons

Gocza?kowice Reservoir is the biggest water reservoir in the south of Poland. For our studies bottom sediments were collected from eight different places of the reservoir at various seasons of the year.EPR spectroscopy was applied to analyse both quantitatively and qualitatively the humic acids (HA) present in the samples. EPR spectra of the extracted HA exhibited broad lines from the paramagnetic metal ions and narrow lines from free radicals. The values of the free radical concentration obtained for HA amounted to 1.14-13.6 × 1016 spin g⁻¹ depending on the season and the place of sample collection. The values of the g factor obtained for HA were of the range 2.0027-2.0035.The EPR studies show that HA extracted from bottom sediment collected at various points of the Gocza?kowice Reservoir exhibit similar physical-chemical properties. It was also observed that the depth of the reservoir affects the content of the oxygen functional groups as well as the free radical concentration in HA.The identification of the functional groups was done by means of IR. UV/VIS spectroscopy was used to estimate the maturity of the HA.     

Cell size dependence of additive versus synergetic effects of UV radiation and PAHs on oceanic phytoplankton

Polycyclic Aromatic Hydrocarbons’ (PAHs) toxicity is enhanced by the presence of ultraviolet radiation (UVR), which levels have arisen due to the thinning of the ozone layer. In this study, PAHs’ phototoxicity for natural marine phytoplankton was tested. Different concentrations of a mixture of 16 PAHs were added to natural phytoplankton communities from the Mediterranean Sea, Atlantic, Arctic and Southern Oceans and exposed to natural sunlight received in situ, including treatments where the UVR bands were removed. PAHs’ toxicity was observed for all the phytoplankton groups studied in all the waters and treatments tested, but only for the pico-sized group a synergetic effect of the mixture and UVR was observed (p = 0.009). When comparing phototoxicity in phytoplankton from oligotrophic and eutrophic waters, synergy was only observed at the oligotrophic communities (p = 0.02) where pico-sized phytoplankton dominated. The degree of sensitivity was related to the trophic degree, decreasing as Chlorophyll a concentration increased.     

Occurrence and profiles of organic sun-blocking agents in surface waters and sediments in Japanese rivers and lakes

Sun-blocking agents including eight UV filters (UVF) and 10 UV light stabilizers (UVLS) were measured in water and sediment collected from 22 rivers, four sewage treatment plant effluents (STPE) and three lakes in Japan. Total sun blocking agents levels ranged from N.D. to 4928 ng/L and from 2.0 to 3422 μg/kg dry wt in surface water and in sediment, respectively. Benzyl salicylate, benzophenone-3, 2-ethyl hexyl-4-methoxycinnamte (EHMC) and octyl salicylate were dominant in surface water receiving wastewater effluents and STPE, although UV-328, benzophenone and EHMC were dominant in other surface water except background sites. Three UVF and nine UVLS were observed from all sediment and their compositions showed similar patterns with UV-328 and UV-234 as the most prevalent compounds. Homosalate, octocrylene, UV-326, UV-327, UV-328 and UV-234 were significantly correlated with Galaxolide^® in sediments. Concentrations of UV-327 and UV-328 also had strong correlation between those of UV-326 in sediment.     

太阳紫外线(UV)辐射对植物的影响

本文就同温层臭氧出现部分空洞引发的太阳紫外线(UV)辐射变化及其对植物生长、植物次生化学特性和植物生殖生长影响方面最近研究的进展情况以及取得的一些结果加以综合评述。     

厌氧发酵系统温度的选择和热量平衡

本文分析了厌氧发酵温度的选择和厌氧系统中热量平衡的关系。并运用此关系对薯干酒糟过滤液在冬季最低温度为0℃,夏季最高温度为35℃的地区进行中温和高温厌氧发酵处理中的热量平衡关系分别进行了讨论,证明了对温度为50℃,COD浓度为23g/L的废液进行中温发酵能得到更大的经济效益,但也必须使用所产生的沼气作为能源加热或冷却废液。所需的热量和气温的关系为:Q_t=4.73×105to-3.73×106 (KJ/d)。