电絮凝处理油田生化出水

为了减轻对后续处理中超滤膜的污染，采用电絮凝法处理油田生化出水，降低油田生化出水中的有机物含量。研究了电流强度、曝气时间和pH值对水中总有机碳（TOC）和浊度除去效果的影响以及pH值随曝气时间的变化趋势，通过红外光谱对絮凝处理前后水中总溶解固体进行了分析，优化了电絮凝的工艺条件。研究表明，当水流速度控制在50 mL/s，电流强度为2 A，500 mL絮凝出水的曝气时间为30 min时，整套絮凝工艺对TOC的去除率为48%，浊度去除率为42.9%，COD去除率为44%。     

Shaping effects of rice,wheat, maize,and soybean seedlings on their rhizosphere microbial community

The rhizosphere microbiome plays critical roles in plant growth and is an important interface for resource exchange between plants and the soil environment. Crops at various growing stages, especially the seedling stage, have strong shaping effects on the rhizosphere microbial community, and such community reconstruction will positively feed back to the plant growth. In the present study, we analyzed the variations of bacterial and fungal communities in the rhizosphere of four crop species: rice, soybean, maize, and wheat during successive cultivations (three repeats for the seedling stages) using 16S rRNA gene and internal transcribed spacer (ITS) high-throughput sequencing. We found that the relative abundances of specific microorganisms decreased after different cultivation times, e.g., Sphingomonas, Pseudomonas, Rhodanobacter, and Caulobacter, which have been reported as plant-growth beneficial bacteria. The relative abundances of potential plant pathogenic fungi Myrothecium and Ascochyta increased with the successive cultivation times. The co-occurrence network analysis showed that the bacterial and fungal communities under maize were much more stable than those under rice, soybean, and wheat. The present study explored the characteristics of bacteria and fungi in crop seedling rhizosphere and indicated that the characteristics of indigenous soil flora might determine the plant growth status. Further study will focus on the use of the critical microorganisms to control the growth and yield of specific crops.

     

三级生物接触氧化除油生化池的生物膜特性

将生物接触氧化技术用于油田稠油污水的处理,在三级串联运行的生物接触氧化池中,生物膜特性主要由生物膜上原油成分决定。在沿水流方向上,生物膜上易降解原油组分含量降低,难降解组分含量上升,第一级生化池中的生物膜厚度和优势菌种数量明显超过第二级和第三级,藻类主要生长在一级生化池的后部和二、三级生化池中的生物膜上,原生动物出现在二级和三级生化池生物膜上,而后生动物只出现在三级生化池生物膜上。     

Spatial and seasonal distribution of nitrogen in marsh soils of a typical floodplain wetland in Northeast China

Horizontal and profile distributions of nitrogen in marsh soils in different seasons were studied in a typical site within the Erbaifangzi wetland in Northeast China. Results showed that there was higher spatial heterogeneity for nitrate nitrogen (NO₃^--_{3}^{-}-N) and ammonium nitrogen (NH₄⁺_{4}^{+}–N), as well as available nitrogen (AN), in surface soils in July compared to that in September. Relative to July, the mean nitrogen contents in surface soils were slightly higher in September; however, in November, soils contained significantly lower NO₃^--_{3}^{-}-N and NH₄⁺_{4}^{+}–N, higher AN, organic nitrogen (Org-N), and total nitrogen (TN). Except for mineral nitrogen, no significant differences were observed between Org-N and TN contents in September and November. Nitrogen contents generally declined exponentially with depth along soil profiles in three sampling dates (July, September, and November), except for a significant accumulation peak of NO₃^--_{3}^{-}-N at the 20–30 cm depth in September. However, NH₄⁺_{4}^{+}–N contents showed a vertical alternation of “increasing and decreasing” in both July and September, while nearly kept constant with depth in November. The depth ranking of nitrogen showed the shallowest distribution for AN, followed by Org-N and TN, while deeper distributions for NO₃^--_{3}^{-}-N and NH₄⁺_{4}^{+}–N. TN, Org-N, and AN were significantly correlated with soil organic matter and total phosphorus. Soil pH values were significantly correlated with TN and AN contents in surface soils. Clay contents showed significant correlations with nitrogen contents except for NO₃^--_{3}^{-}-N in surface soils and NH₄⁺_{4}^{+}–N in profile soils. However, soil moisture was not significantly correlated with nitrogen contents among all soil samples.     

Development of a multi-criteria index ranking system for urban runoff best management practices (BMPs) selection

Low impact development best management practices (LID-BMPs) are considered to be cost-effective measures for mitigating the water quantity and quality impact of urban runoff. Currently, there are many types of LID-BMPs, and each type has its own intrinsic technical and/or economical characteristics and limitations for implementation. The selection of the most appropriate BMP type(s) for a specific installation site is therefore a very important planning step. In the present study, a multi-criteria selection index system (MCIS) for LID-BMP planning was developed. The selection indexes include 12 first-level indices and 26 second-level indices which reflect the specific installation site characteristics pertaining to site suitability, runoff control performance, and economics of implementation. A mechanism for ranking the BMPs was devised. First, each individual second-level index was assigned a numeric value that was based on site characteristics and information on LID-BMPs. The quantified indices were normalized and then integrated to obtain the score for each of the first-level index. The final evaluation scores of each LID-BMP were then calculated based on the scores for the first-level indices. Finally, the appropriate BMP types for a specific installation site were determined according to the rank of the final evaluation scores. In order to facilitate the application of the MCIS BMP ranking system, the computational process has been coded into a software program, BMPSELEC. A case study demonstrating the MCIS methodology, using an LID-BMP implementation planning at a college campus in Foshan, Guangdong Province, is presented.     

基于模糊颜色Petri网的表决DVP安全软件模型初探

把模糊计算理论和有色Petri网有机地结合起来 ,提出了一种模糊颜色Petri网诊断表决算法 ,把该算法应用于DVP的软件模型 ,使之具有故障容忍和表决的能力。笔者对以模糊颜色Petri网为核心的DVP软件模型表决算法进行了较为深入的探讨 ,该模型对提高软件系统的安全性和可靠性具有实际意义。     

聚苯乙烯基硫代磺酸钾树脂的合成及其与卤代烃的反应

由聚苯乙烯基磺酰氯树脂与硫化氢钾反应制备聚苯乙烯基硫代磺酸钾树脂（Ｉ），树脂Ｉ与亲电的卤代烃反应，生成聚苯乙烯基硫代磺酸酯树脂（Ⅱ），树脂Ⅱ经过乙硫醇处理，使卤代烃结构部分以不对称二硫醚的形式游离下来，用ＧＣ／ＭＳ对其结构进行鉴定。从不对称二硫醚的结构可推导出原卤代烃的结构，所制备的聚苯乙烯基硫代磺酸钾树脂的转化效率为１．１１ｍｍｏｌ·ｇ＾－１。     

Cu–Mn–Ce ternary mixed-oxide catalysts for catalytic combustion of toluene

Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H₂-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the CeO₂ fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species.     

Promoting effect of vanadium on catalytic activity of Pt/Ce–Zr–O diesel oxidation catalysts

A series of Pt–V/Ce–Zr–O diesel oxidation catalysts was prepared using the impregnation method. The catalytic activity and sulfur resistance of Pt–V/Ce–Zr–O were investigated in the presence of simulated diesel exhaust. The effect of vanadium on the structure and redox properties of the catalysts was also investigated using the Brunauer–Emmett–Teller method,X-ray diffraction, H2temperature-programmed reduction, CO temperature-programmed desorption, X-ray photoelectron spectroscopy, and Energy Dispersive Spectroscopy. Results showed that the Pt particles were well dispersed on the Ce–Zr–O carrier through the vanadium isolation effect, which significantly improved the oxidation activity toward CO and hydrocarbons. An electron-withdrawing phenomenon occurred from V to Pt, resulting in an increase in the metallic nature of platinum, which was beneficial to hydrocarbon molecular activation.