Fenton氧化/混凝沉淀协同处理腈纶聚合废水

采用Fenton法处理湿法腈纶聚合废水,考察了H2O2投加量、Fe2+投加量、p H和反应时间等因素对氧化和混凝作用去除废水污染物的影响,并分析了废水可生化性和特征污染物的变化。结果表明,Fenton法可以有效去除废水中有机污染物,在初始p H为3.0,Fe2+投加量为15.0 mmol/L,H2O2投加量为90.0 mmol/L的条件下,反应120 min后废水COD去除率可以达到56.8%,其中氧化和混凝作用对应的去除率分别为43.3%和13.5%;处理后废水的BOD5/COD由0.24升高至0.43;处理后废水中丙烯腈以及其他多数有机污染物能被有效去除。     

纳米腐植酸基复合树脂的制备及其对Ni~(2+)和Cd~(2+)的吸附

采用水溶液聚合法,以丙烯酸、丙烯酰胺及改性蒙脱土为原料,纳米腐植酸为基体,N,N’-亚甲基双丙烯酰胺为交联剂,过二硫酸钾为引发剂,制备了丙烯酸-蒙脱土-丙烯酰胺/纳米腐植酸复合树脂(简称复合树脂)。考察了溶液pH、吸附时间、吸附温度、初始离子浓度等因素对复合树脂分别吸附Ni~(2+)和Cd~(2+)的影响。实验结果表明:在吸附温度35℃、吸附时间90 min、溶液pH为7、初始Ni~(2+)和Cd~(2+)的浓度分别为0.02 mol/L、复合树脂加入量16.7 g/L的条件下,Ni~(2+)和Cd~(2+)的吸附量分别为383.02 mg/g和359.27 mg/g;复合树脂吸附Ni~(2+)和Cd~(2+)的吸附等温线均满足Langmuir等温吸附方程;吸附过程均符合准二级动力学方程;复合树脂重复使用6次,其对Ni~(2+)和Cd~(2+)的吸附量分别降低了17.1%和9.3%。     

Reaction mode between Si and Fe and evaluation of optimal species in poly-silicic-ferric coagulant

A kind of Fe-polysilicate polymer, poly-silicic-ferric （PSF） coagulant was prepared by co-polymerization （hydroxylation of mixture of Fe^3＋ and fresh polysilicic acid （PS））, in which PSF0.5, PSF1 or PSF3 denotes Si/Fe molar ratio of 0.5, 1 or 3, respectively. The effects of Si/Fe ratio and reaction time （co-polymerization time or aging time） on the reaction mode between Si and Fe were studies, and the optimal species of PSF was evaluated by pH change during the preparation of PSF and coagulation tests. The results showed that the characteristics of PSF are largely affected by both reaction time and Si/Fe ratio. PSF is found to be a essential complex of Si, Fe, and many other ions. The reaction mode between Si and Fe differs with various Si/Fe ratios. The pH of PSF0.5, PSF1 or PSF3 tended to be stable when reaction time is 10, 25 or 55 rain, respectively, which is almost consistent with the time reaching the relative stable morphology that is just the optimal species of higher coagulation efficiency. The optimal reaction time reaching optimal species can be evaluated by measuring the pH change during the polymerization process.     

Implications of denitrification in the ecological status of an urban river using enzymatic activities in sediments as an indicator

A better understanding of the effects of a number of environmental factors on denitrification is vital for analyzing its role as nitrogen sink and providing deeper knowledge about the ecological status of a nitrate-rich ecosystem. Since few studies have addressed the occurrence and implications of denitrification in river sediments, and complexity of interactions among all these environmental factors makes comprehension of the process difficult, the potential of sediments from the Deba River to attenuate nitrate excess through denitrification was investigated. For this purpose, we adapted an in vitro method to measure activities of two enzymes contributing to the entire multiple-step nitrate reduction: Nitrate Reductase and Nitrite Reductase. The environmental features that influence both or single enzymatic activities were identified as oxygen availability, regulated directly by the moisture content or indirectly through the aerobic respiration, organic matter and nitrate content of sediments, and electrical conductivity and exchangeable sodium percentage of water. Additionally, our results showed that Nitrate Reductase catalyzes the principal limiting step of denitrification in sediments. Therefore, taking this enzymatic activity as an indicator, the southern part of the Deba River catchment presented low potential to denitrify but nitrate-limited sediments, whereas the middle and northern parts were characterized by high denitrification potential but nitrate-rich sediments. In general, this study on denitrifying enzymatic activities in sediments evaluates the suitability of the management of the effluents from wastewater treatment plants and municipal sewages to ensure a good ecological status of the Deba River.     

Fast and Living Ring-Opening Polymerization of l-Lactide Initiated with In-situ–Generated Calcium Alkoxides

The ring-opening polymerization of l-lactide with calcium alkoxides generated in-situ from bis(tetrahydrofuran)calcium bis[bis(trimethylsilyl)amide] and 2-propanol are presented. The polymerization in THF at room temperature proceeds rapidly and in a living manner, giving poly(l-lactide)s of controlled molecular weight, low polydispersity, and tailored end-functionalities. Kinetic studies show the absence of an induction period and a pseudo-first order rate constant of 6.41 L mol^–1 min^–1, which is significantly higher than for related Y₅(-O)(O ⁱ Pr)_13– or aluminum alkoxide-initiated polymerizations. The initiation involves a two-step process: (1) alcoholysis of bis(tetrahydrofuran)calcium bis[bis(trimethylsilyl)amide] to give the corresponding calcium alkoxide and (2) ring-opening of l-lactide via acyl-oxygen cleavage and insertion into the calcium-alkoxide bond. In the presence of excess alcohol, fast and reversible exchange between free alcohol molecules and coordinated alkoxide ligands takes place. This allows tuning of the poly(l-lactide) molecular weight over a wide range.     

APM对小麦根尖分生组织细胞异常有丝分裂的诱导

探讨了不同浓度（c／μmol．L－1）和不同处理时间（t／h）下APM对小麦根尖分生组织细胞有丝分裂的影响．实验结果表明，在c（APM）＝1～4μmol／L、处理t＜5h可明显提高有丝分裂指数，对前期和中期细胞分裂的促进作用更为明显；但c（APM）的增加与有丝分裂指数的提高无明显线型关系；APM可促使间期细胞微核形成、中期细胞染色体聚合现象和扰乱纺锤丝的功能．纺锤丝功能上的扰乱可引起细胞的“不均等分裂”和“多极化分裂”形成上述两种细胞异常有丝分裂的临界浓度和处理时间分别为c＝5μmol／L和t＞5h．     

不饱和聚酯树脂生产废水治理技术

不饱和聚酯树脂生产废水CODCr高达 10 0 0 0 0mg/L ,pH为 1— 2 ,且排放无规律 ,处理难度大。采用先对缩聚废水进行蒸馏浓缩 ,再真空泵废水混合调质、降温、缺氧水解后 ,经高效的好氧生物处理工艺 (HCR)处理后与低浓度的冲洗水、生活废水混合 ,进行低负荷的生物接触氧化处理 ,出水CODCr稳定在 10 0mg/L以下。     

Species analysis methods for hydrolysis polymerization of aluminum

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生物法净化有机污染物的酶反应动力学修正

以生化法处理有机污染物的系统为讨论对象 ,从底物负荷影响微生物生长的角度出发 ,通过对有机污染物负荷与生化反应速度之间的关系的分析 ,得出进口底物浓度的大小会影响生物反应器内微生物的量的多少 ,从而影响器内的生化反应速率的结论 ,并按照“稳定平衡”假说的设想 ,建立了修正的Michaelis -Menten公式     

Rhizobacteria helps to explain the enhanced efficiency of phytoextraction strengthened by Streptomyces pactum

The ultimate purpose of phytoextraction is not only to remove heavy metals from soil but also to improve soil quality. Here, we evaluated how the joint effect of Streptomyces pactum (strain Act12) and inorganic (Hoagland's solution) and organic (humic acid and peat) nutrients affected the phytoextraction practice of cadmium (Cd) and zinc (Zn) by potherb mustard, and the microbial community composition within rhizosphere was also investigated. The results indicated that the nutrients exerted synergistically with Act12, all increasing the plant biomass and Cd/Zn uptakes. The inoculation of Act12 alone significantly increased dehydrogenase activity of rhizosphere soil (P < 0.05), while urease and alkaline phosphatase activities varied in different dosage of Act12. Combined application of microbial strain with nutrients increased enzymatic activities with the elevated dosage of Act12. 16S ribosomal RNA high-throughput sequencing analysis revealed that Act12 inoculation reduced the diversity of rhizosphere bacteria. The Act12 and nutrients did not change dominant phyla i.e., Proteobacteria, Bacteroidetes, Gemmatimonadetes, Actinobacteria and Acidobacteria, but their relative abundance differed among the treatments with: Peat > Act12 > Humic acid > Hoagland's solution. Comparatively, Sphingomonas replaced Thiobacillus as dominant genus after Act12 application. The increase in the Sphingomonas and Flavisolibacter abundances under Act12 and nutrients treatments gave rise to growth-promoting effect on plant. Our results revealed the important role for rhizosphere microbiota in mediating soil biochemical traits and plant growth, and our approach charted a path toward the development of Act12 combined with soil nutrients to enhance soil quality and phytoextraction efficiency in Cd/Zn-contaminated soils.