无机高分子絮凝剂聚合硅酸铝铁的研究

以ALCL3，FeCl3，Na2SiO3和盐酸为原料，采用NaOH作为碱化聚合剂，合成了具有不同碱化度（B），不同Al/Fe/Si摩尔比的铝铁硅共聚物（简称PAFSC），通过PH滴定法测定分析了铝、铁在其水解共聚合过程中PH值的变化，然后通过透射电镜和混凝实验对共聚物的晶形貌像和絮凝作用进行了研究，通过对模拟具有色悬浊水样的絮凝实验，并与现有的其它无机絮凝剂作比较后可以看出：在同样投加量情况下，PAFSC处理的水具有更低的剩余浊度和色度。     

水解酸化-SBR法在化工废水处理中的应用

针对高浓度、毒性大、难生物降解的工业有机废水,探索了水解酸化-SBR工艺的最佳运行参数和配套工艺措施,为工程设计提供依据.其中水解酸化采用ABR反应器,研究了温度、停留时间、毒性物质等因素对处理效果的影响,结果表明,该工艺处理三吉利香兰素化工废水取得了较好的处理效果.     

水解-混凝法处理糖蜜酒精废水试验

采用投加优势菌群的水解 -混凝法对糖蜜酒精废水进行试验 ,研究投加优势菌的水解阶段的处理效果 ,同时 ,以 10 %碱式AlCl3为混凝剂 ,对水解段的出水进行混凝处理 ,并对处理条件进行研究。结果表明 ,采用投加优势菌群的水解 -混凝法工艺处理该废水 ,可以取得 5 8%的CODCr去除率 ,且可去除一定的色度     

前处理-水解-生物接触氧化工艺处理染料废水

介绍了前处理-水解-生物接触氧化工艺处理染料废水的工程实例.当进水COD≤8000 mg/L时,出水可达到国家<污水综合排放标准>(GB8978-1996)二级标准.     

酶制剂废水处理的试验研究

采用直接混凝、直接水解 -接触氧化的生化处理以及混凝 -水解 -接触氧化 3种不同工艺对某酶制剂废水进行处理。结果表明 ,针对浓度为 6 2 0 0mg/L的原水 ,用本单位的混凝剂 4号进行直接的混凝处理 ,在加入量为 10 0mg/L时可以得到 6 6 %的CODCr处理率 ;同样浓度的原水直接进行水解 -接触氧化生化处理 ,在 34h的停留时间后可以达到国家二类二级排放标准 ;经过混凝处理后的出水进行的生化实验则表明 ,达到国家排放标准的生化停留时间可缩短至 2 2h。     

Distributions, cycling and recovery of amino acids in estuarine waters and sediments

Acid hydrolysis of estuarine water samples for the determination of amino acids (AAs) was tested and found to be effective at high (250 μM) nitrate concentrations when the anti-oxidant, ascorbic acid, was added to the samples. Hydrolysable AA concentrations were then determined in surface sediments collected from low and high salinity regions of the Tamar Estuary (UK) during winter 2003 and 2004, and in overlying water when simulated resuspension of sediment particles was performed. Concentrations of AAs in sediment samples comprised <50% of particulate nitrogen, fitting the paradigm that most sedimentary nitrogen is preserved within an organic matrix. When sediment samples were resuspended in overlying water (salinity 17.5), the rapid, measured increase in dissolved AA concentrations almost equalled the reported nitrate concentration in the lower estuary, with the subsequent decrease in the total dissolved AA levels suggested that bacterial uptake was occurring. Our data concur with previous studies on nitrogen desorption from sediments and suggest that an understanding of organic nitrogen cycling will be an important aspect of future effective estuarine management.     

浅论铝盐的水解和吸附电中和过程中被凝聚物浓度的影响

通过对凝聚机理和铝盐在水中水解过程的分析，提出了铝盐水解物吸附起胶本电和中和数学模式，论述了被凝聚物浓度对铝盐水解过程的影响，在实际的凝集过程中，铝盐的水解和向胶体表面的吸附是同时进行的，部分铝盐在完成水解之前就以中间产物的形态吸附于胶体表面，胶体溶液的浓度愈高，这种倾向就愈强，由于较低水解度的物种具有较高的单位电位浓度，它们能显示较强的电中和能力，因此，随着胶体溶液浓度增高，达到最佳凝聚ζ电位所     

混凝、水解酸化、活性污泥工艺处理啤酒生产废水工程实例

以化学混凝沉淀、水解酸化、传统活性污泥法处理啤酒生产污水,COD从2400mg/l降至100mg/l,BOD5从1599mg/l降至30mg/l,达到一级排放标准,采用集散式计算机控制系统,操作简单,管理方便.     

pH调节方法对厨余垃圾两相厌氧消化中水解和酸化过程的影响

通过间歇实验探讨了pH调节方法对厨余垃圾两相厌氧消化中水解酸化过程和水解酸化液中Na 浓度的影响实验比较了厨余垃圾在3种pH调节方法(利用NaOH溶液调节初始进料pH到7,利用NaOH和Ca(OH)2混合碱液每12h调节pH到7和利用调节C/N比调节pH到7)下水解酸化液中的Na 浓度、一级水解速率常数、挥发酸(VFA)浓度、乳酸浓度和VFA组分分配.结果表明,与利用NaOH溶液每12 h调节pH相比较,3种pH调节方法都能够有效降低水解酸化出料液中的Na 浓度,但利用调节C/N比来调节pH能够取得更高的水解酸化效率,一级水解速率常数可以达到0.199 d-1,VFA浓度在实验第3天即可达到35 g·L-1.发酵产物乳酸在实验第2天即达到高峰浓度24 g·L-1,后逐渐下降到6 g·L-1,VFA组分中丙酸不是优势组分.     

Surface characterization of metal oxides-supported activated carbon fiber catalysts for simultaneous catalytic hydrolysis of carbonyl sulfide and carbon disulfide

The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS) and carbon disulfide (CS₂) at relatively low temperatures of 60°C was tested. The effects of preparation conditions on the catalyst properties were investigated, including the kinds and amount of metal oxides and calcination temperatures. The activity tests indicated that catalysts with 5 wt.% Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS₂. The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), carbon dioxide-temperature programmed desorption (CO₂-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR). And the metal cation defects were researched by electron paramagnetic resonance (EPR) method. The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores, then improved catalytic hydrolysis activity. The DRFTIR results revealed that -OH species could facilitate the hydrolysis of COS and CS₂; -COO and -C–O species could facilitate the oxidation of catalytic hydrolysate H₂S. And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS₂ adsorption.