水解-好氧系统处理生活污水的特性研究

采用新型 Yakult填料和中心导流式曝气方式 ,设计制作了新型生活污水净化装置 ,试验表明 ,停留时间 16 h左右 ,CODCr去除率 >80 % ,BOD5去除率 >90 % ,SS去除率 >85 % ,NH3 - N去除率 >87% ,出水水质达到国家一级排放标准     

水解酸化—厌氧工艺处理高浓度抗生素废水研究

研究了水解酸化与厌氧消化组合工艺处理高浓度抗生素废水,结果表明,水解酸化反应器最大CODcr容积负荷达到 16.84kg/m3·d,复合厌氧反应器CODcr容积负荷达到8.57kg/m3·d;系统进水SO42-浓度为1325mg/L,CODcr/SO42-值最低达到 3;CODCr与SO42-总去除率分别为75.5％和95.2％,对各种抑制物质和冲击负荷表现出很好的适应性。     

水解-接触氧化工艺处理高浓度米果废水

采用水解—接触氧化—沉淀工艺处理高浓度米果废水，设计规模为100m^3／d。处理后的CODcr，BOD5，SS和色度的去除率分别达到96．8％，97．7％，94.4％，94．7％，总排放口水质为：pH=7．61，CODcr=70．7mg／L，BOD5mg／L，SS=29．2mg／L；色度的稀释倍数为8。     

三甲基氯硅烷及六甲基二硅氮烷水解产物分析方法研究

研究采用吹扫捕集-气相色谱-质谱法测定三甲基氯硅烷及六甲基二硅氮烷水解产物的分析方法。结果表明,两种物质遇水迅速水解,水解产物均为三甲基硅醇与六甲基二硅氧烷。以该方法测定六甲基二硅氧烷的检出限为0.02ng/ml,精密度为1.3%～10.6%,线性范围为0.05～60ng/ml。水解动力学研究结果表明,三甲基氯硅烷及六甲基二硅氮烷水解产物含量随时间减少而降低,强酸、强碱条件下测试未发现生成其他的水解产物。该方法可为同类污染物的应急测试提供参考。     

高浓度制药废水处理技术的研发及应用

制药废水组成复杂,污染物浓度高,污水CODcr浓度达10000mg/l,含有大量有毒、有害物质。本中采用催化氧化预处理+水解酸化+UASB+接触氧化+炭滤吸附的工艺流程,通过改善细部参数及改良配套设备设计,提高了各单元去除效率,降低了能耗及处理成本,出水CODcr浓度达到污水综合排放标准.     

Acid generation upon thermal concentration of natural water: The critical water content and the effects of ionic composition

Thermal evaporation of a variety of simulated pore waters from the region of Yucca Mountain, Nevada, produced acidic liquids and gases during the final stages of evaporation. Several simulated pore waters were prepared and then thermally distilled in order to collect and analyze fractions of the evolved vapor. In some cases, distillates collected towards the end of the distillation were highly acidic; in other cases the pH of the distillate remained comparatively unchanged during the course of the distillation. The results suggest that the pH values of the later fractions are determined by the initial composition of the water. Acid production stems from the hydrolysis of magnesium ions, especially at near dryness. Near the end of the distillation, magnesium nitrate and magnesium chloride begin to lose water of hydration, greatly accelerating their thermal decomposition to form acid. Acid formation is promoted further when precipitated calcium carbonate is removed. Specifically, calcium chloride-rich pore waters containing moderate (10–20 ppm) levels of magnesium and nitrate and low levels of bicarbonate produced mixtures of nitric and hydrochloric acid, resulting in a precipitous drop in pH to values of 1 or lower after about 95% of the original volume was distilled. Waters with either low or moderate magnesium content coupled with high levels of bicarbonate produced slightly basic fractions (pH 7–9). If calcium was present in excess of bicarbonate, waters containing moderate levels of magnesium produced acid even in the presence of bicarbonate, due to the precipitation of calcium carbonate. Other salts such as halite and anhydrite promote the segregation of acidic vapors from residual basic solids. The concomitant release of wet acid gas has implications for the integrity of the alloys under consideration for containers at the Yucca Mountain nuclear waste repository. Condensed acid gases at very low pH, especially mixtures of nitric and hydrochloric acid, are capable of corroding even alloys, such as nickel-based Alloy 22, which are considered to be corrosion-resistant under milder conditions.     

Dichlorvos degradation studied by 31P-NMR

We studied the hydrolysis and TiO₂ photocatalysis of the pesticide dichlorvos at pH 2.6–9 using phosphorus-31 nuclear magnetic resonance (³¹P NMR). We found that the hydrolysis of dichlorvos led to the formation of dimethyl phosphate at pH 5.6–9. On the other hand, TiO₂ photocatalysis decomposed dichlorvos into dimethyl phosphate, which further reacted to form monomethyl phosphate at pH 2.6 and 9. Monomethylphosphate was hydrolysed into phosphate at pH 2.6. ³¹P NMR is therefore a promising tool to study the degradation of organophosphorus pesticides.     

Contribution of Pendant Ester Group Hydrolysis to the Erosion of Acrylic Polymers in Binders Aimed at Organotin-Free Antifouling Paints

Specific polymeric material applications as bioactive molecules delivery systems involve a strictly controlled degradation of polymer matrixes. One possibility to obtain a zero-order kinetic for small molecules release consists in a simple hydrolysis of ester groups contained in the macromolecular structure. The chemical degradation can lead to the continuous surface erosion of the formulated resins without loss of their mechanical properties and to a permanent activity of the delivery systems. Hydrolysis is a very well-known reaction in the case of organic molecules containing ester groups. The mechanism seems to be more complicated when ester groups are located in macromolecular structures. With the aim of antifouling applications, acrylic acid polymers bearing lateral ester groups of different chemical structures (hydrophilic, hydrophobic, hydrolyzable) have been prepared, characterized, and immersed in water, at pH 8, and their hydrolysis has been studied. Experimental data display two parameters, at least, which must be taken into account: the reactivity of the ester groups toward hydrolysis and the hydrophilic/hydrophobic balance of the polymer. The susceptibility of the acrylic polymers to hydrolysis has been compared to the erosion characteristics of the corresponding films. The results confirm that hydrolysis is necessary to obtain a regular degradation of the films without loss of mechanical properties. A relationship has been observed between the characteristics of hydrolysis and erosion for each studied polymer.     

“水解酸化—预曝气—人工湿地”处理生活污水的试验研究

试验研究了"水解酸化-预曝气-人工湿地"组合工艺对农村生活污水的处理效果,结果表明系统对COD、BOD5、TN、NH3-N、TP去除率分别为75%~85%8、8%~91%、54%~67%、75%~87%8、8%~94%。该工艺操作简易,处理效果好,符合村镇生活污水处理的需求。     

Improving biodegradation potential of domestic wastewater by manipulating the size distribution of organic matter

Carbon source is a critical constraint on nutrient removal in domestic wastewater treatment. However, the functions of particulate organic matter (POM) and some organics with high molecular weight (HMW) are overlooked in the conventional process, as they cannot be directly assimilated into cells during microbial metabolism. This further aggravates the problem of carbon source shortage and thus affects the effluent quality. Therefore, to better characterize organic matter (OM) based MW distribution, microfiltration/ultrafiltration/nanofiltration (MF/UF/NF) membranes were used in parallel to fractionate OM, which obtained seven fractions. Hydrolysis acidification (HA) was adopted to manipulate the MW distribution of dissolved organic matter (DOM) and further explore the correlation between molecular size and biodegradability. Results showed that HA pretreatment of wastewater not only promoted transformation from POM to DOM, but also boosted biodegradability. After 8 hr of HA, the concentration of dissolved organic carbon (DOC) increased by 65%, from the initial value of 20.25 to 33.48 mg/L, and the biodegradability index (BOD5 (biochemical oxygen demand)/SCOD (soluble chemical oxygen demand)) increased from 0.52 to 0.74. Using MW distribution analysis and composition optimization, a new understanding on the characteristics of organics in wastewater was obtained, which is of importance to solving low C/N wastewater treatment in engineering practice.