再生造纸废水絮凝除浊试验研究

本研究采用絮凝法对再生造纸废水中含细小纤维、无机填料的悬浮物进行处理试验，比较了硫酸亚铁与聚丙烯酰胺复合絮凝剂和聚硅酸氯化铁盐两种絮凝剂的絮凝效果，研究了制备聚硅酸氯化铁盐的铁硅比、pH值、碱化度以及投加量与废水除浊率之间的相互关系。实验结果表明：在最佳条件下，絮凝效果优异，除浊率达到98％，上清液无色透明。     

絮凝法处理麦草浆中段废水

采用无机絮凝剂硫酸铝和三种不同分子量的聚丙烯酰胺对麦草浆中段废水进行絮凝沉降处理。通过对各种影响絮凝作用的因素进行系统研究，比较得出，分子量为800万的聚丙烯酰胺与硫酸铝配合的絮凝效果最好。     

复合絮凝剂Al2(SO4)3+PAM处理生活污水中CODCr和浊度的实验研究

研究絮凝剂硫酸铝Al2(SO4)3与助凝剂聚丙烯酰胺(PAM)联合处理生活污水的效果。研究表明:Al2(SO4)3与PAM联用比单独用Al2(SO4)3处理生活污水效果更好;Al2(SO4)3 PAM对生活污水CODCr和浊度具有良好的去除能力;当投加1:1的50mg/L的Al2(SO4)3 0.5mg/L的PAM,调节水体pH=7时,处理效果最理想,CODCr去除率可达95.8%,浊度去除率可达97.5%。为复合絮凝剂Al2(SO4)3 PAM处理生活污水的应用提供了有价值的参考依据。     

一株微生物絮凝剂产生菌的絮凝特性及处理气田废水研究

从土壤中分离、筛选得到一株稳定高效的微生物絮凝剂产生菌,命名为B—27。考察了碳源、氮源、pH、温度、培养时间等多种因素对絮凝剂(命名MBF—27)絮凝效果的影响。实验结果表明,当碳源为葡萄糖、氮源为酵母膏、pH为7.0、温度为35℃、培养时间为72h时,絮凝剂MBF—27对高岭土悬浊液的絮凝率可达93.8%。红外光谱扫描分析表明,该絮凝剂的主要成分为多糖类物质。同时,生物絮凝剂MBF—27对气田废水的COD和色度去除率分别达到60.77%和86.1%,优于传统的絮凝剂聚乙烯丙胺(PAM)和三氯化铁(FeCl3)。     

聚硅酸硫酸铝絮凝剂的研制和性能研究

聚硅酸硫酸铝是一种新型无机阳离子型高效絮凝剂，本文就其研制及应用进行了探索。实验成功地研制了不同Al／Si的产品，并进行了絮凝比较实验。结果表明，Al／Si值是影响其作用效果的关键，其他影响因素还有：pH值、絮凝刺投加量、絮凝温度以及原水性质等，并在经济核算的基础上确定了最佳絮凝条件。该产品可应用于任何可以利用高聚物析出氢氧化铝凝胶系统的场合。     

PAC和PAM复合絮凝剂在洗涤剂废水处理中的应用研究

絮凝性能的实验研究表明,PAC和PAM复合絮凝剂是处理洗涤剂废水的理想絮凝剂,采用该复合絮凝剂处理洗涤剂废水时的最佳操作条件如下：PAC用量为1．5g／L,PAM用量为10mg／L,pH值约为7．0,絮凝搅拌速度60r／min,絮凝搅拌时间30min,沉淀池沉淀时间为30min。该实验结果在中试规模的应用中得到了较好地验证,中试试验研究表明采用PAC和PAM复合絮凝剂处理洗涤剂废水,CODCr和LAS(直链烷基苯璜酸钠)去除率分别可达85％和72％以上,有效地解决了LAS难以生物降解等问题。     

采油污水中聚丙烯酰胺的去除方法

采用实验室合成的絮凝剂和助凝剂,对聚合物驱采油污水进行了聚丙烯酰胺絮凝实验。通过絮凝效果的比较,筛选出两种絮凝效果较好的絮凝剂XN-Ⅲ和XN-Ⅳ。实验确定了絮凝剂的最佳加入量、沉降时间、pH值和温度条件。在此基础上,对采油污水中聚丙烯酰胺的不同去除方法进行了比较,得到最优去除方法,为现场采油污水中聚丙烯酰胺的脱除提供了依据。     

吉林油田稠油热采污水处理絮凝剂实验研究＊

在含油污水水质分析的基础上,采用烧杯实验和分光光度法研究絮凝剂的絮凝效果。筛选出以无机絮凝剂硫酸铝与两性高分子聚合物CE-3090的复配体系,同时研究了影响絮凝效果的因素并探究了其影响机理。结果表明:在温度为40℃,pH为7.72,170 r/min时高速搅拌1 min,然后50 r/min低速搅拌5 min,硫酸铝的加量为90 mg/L、CE-3090的加量为0.5 mg/L,絮凝沉降30 min后其絮凝效果较好。实验证明:该复配处理剂处理含油污水后,含油量和杂质含量都达到了SY/T 5329-94《碎屑岩油藏注水水质推荐指标及分析方法》油田污水回注的要求。     

聚合氯化铝与水解聚丙稀酰胺复合絮凝剂JX-3的制备及室内评价试验

在无机高分子絮凝剂聚合氯化铝(PAC)中引入有机高分子水解聚丙稀酰胺(PHP),制备出一种复合絮凝剂JX-3。PAC和PHP在其中可起到电性中和及絮凝桥架的的双重作用,使絮团紧密结合,提高絮凝效果,室内评价试验表明JX-3处理含轻油污水效果优于PAC和聚丙稀酰胺(PAM)。     

无机-有机高分子复合絮凝剂处理含油废水的试验研究

研究了用聚合氯化铝（PAC）、聚合硫酸铁（PFS）、聚丙烯酰胺（PAM）及改性蒙托石等不同无机—有机高分子絮凝剂复配使用处理炼钢厂连铸含油废水的除油效果,考察了不同絮凝剂的复配以及絮凝剂的不同复配比例对处理效果的影响。试验结果表明,用聚合氯化铝（PAC）＋聚合硫酸铁（PFS）＋聚丙烯酰胺（PAM）3种絮凝剂复配使用除油效果最佳,当3种絮凝剂的复配比为2∶2∶3时除油效果最好,除油率达到88.2%,达到国家排放标准。     

The leaching characteristics of selenium from coal fly ashes

The leaching characteristics of selenium from several bituminous and subbituminous coal fly ashes under different pH conditions were investigated using batch methods. Results indicated that pH had a significant effect on selenium leaching from bituminous coal ash. The minimum selenium leaching occurred in the pH range between 3 and 4, while the maximum selenium leaching occurred at pH 12. The release of selenium from subbituminous coal ashes was very low for the entire experimental pH range, possibly due to the high content of calcium which can form hydration or precipitation products as a sink for selenium. The adsorption results for different selenium species indicated that Se(VI) was hardly adsorbable on either bituminous coal ashes or subbituminous coal ashes at any pH. However, Se(IV) was highly adsorbed by bituminous coal ashes under acidic pH conditions and was mostly removed by subbituminous coal ashes across the entire pH range. This result suggests that the majority of selenium released from the tested fly ashes was Se(IV). A speciation-based model was developed to simulate the adsorption of Se(IV) on bituminous coal fly ash, and the pH-independent adsorption constants of HSeO3* and SeO3 2* were determined. The modeling approach is useful for understanding and predicting the release process of selenium from fly ash.     

Sorption of iron-cyanide complexes on goethite in the presence of sulfate and desorption with phosphate and chloride

Soils are contaminated with potentially toxic iron-cyanide complexes by some industrial activities. The influence of sulfate on the sorption of the iron-cyanide complexes ferricyanide, [Fe(CN)6]3-, and ferrocyanide, [Fe(CN)6]4-, on goethite was investigated in batch experiments. The experiments were conducted as influenced by pH and varying sulfate/iron-cyanide complex concentration ratios. Furthermore, the desorption of iron-cyanide complexes sorbed on goethite was studied using phosphate and chloride solutions as influenced by pH and anion concentration. Over the whole pH range (pH 3.5 to 8), ferricyanide and sulfate showed similar affinities for the goethite surface. The extent of ferricyanide sorption strongly depended on sulfate concentrations and vice versa. In contrast, ferrocyanide sorption was only decreased (approximately 12%) by sulfate additions at pH 3.5. Ferricyanide was completely desorbed by 1 M chloride, ferrocyanide not at all. Unbuffered phosphate solutions (pH 8.3) desorbed both iron-cyanide complexes completely. Even in 70-fold excess, pH-adjusted phosphate solutions could not desorb ferrocyanide completely at pH 3.5. For ferricyanide we propose a sorption mechanism that is similar to the sulfate sorption mechanism, including outer-sphere and weak inner-sphere surface complexes on goethite. Ferrocyanide appears to form inner-sphere surface complexes. Additionally, we assume that ferrocyanide precipitates probably as a Berlin Blue-like phase at pH 3.5. Hence, ferrocyanide should be less mobile in the soil environment than ferricyanide or sulfate.     

模拟酸雨对油菜生长影响的试验研究

酸雨对陆生生态环境及农作物的影响已引起人们的关注。国外有关这方面的研究已有不少报道,国内有过模拟酸雨对蔬菜、水稻、小麦生长影响的研究报道,但对油菜影响的研究报道尚未见到。为了正确估价酸雨对成都平原油菜生长可能产生的影响,本试验设计了采用盆栽与田间试验相结合的方法,进行模拟酸雨对油菜生长影响的试验研究,现将模拟酸雨对油菜的伤害症状、产量及品质的影响报道于下。     

Rhamnolipid morphology and phenanthrene solubility at different pH values

The effect of pH and rhamnolipids on the solubility of phenanthrene was investigated in a sand-water system. Batch phenanthrene solubilization experiments in this system showed that the highest phenanthrene solubility occurred at pH 5 in the presence of 240 and 150 mg L(-1) rhamnolipids. As the pH was increased from 5 to 7, the apparent solubility of phenanthrene decreased and then stabilized from pH 7 to 8. At pH 4, a dramatic decrease in phenanthrene solubility was observed. This result is in contrast to previous findings obtained in an aqueous system without soil particles. To investigate the reason for this decrease, the critical micelle concentrations (CMCs) were measured in the presence or absence of sand particles, and the maximum amount of sorbed biosurfactant at each pH was calculated based on the differences of the two CMC values. More rhamnolipid molecules were lost by the sorption into sand particles at pH 4 than at other pH values; this explains the dramatic decrease of solubility at pH 4 in the sand-water system. To confirm the explanation for the different solubilizing capacity that results from the structural change of biosurfactant aggregate, cryo-transmission electron microscopy was used. Micrographs showed that the rhamnolipid morphology changed from large lamellar sheets, to vesicle, and then to micelle as the pH increased. The large and multilamellar vesicles at pH 5 were considered to be the most effective structure for the solubilization of phenanthrene.     

氯消毒新工艺对大肠杆菌灭活作用的研究

研究了短时游离氯后转氯胺的联合消毒方法对大肠杆菌的灭活作用,并对其协同作用以及pH值和温度对协同作用的影响进行了探讨。结果表明：pH值在6．5～8范围内,温度不超过30℃时,短时游离氯后转氯胺的消毒方法对大肠杆菌的灭活具有协同作用,且随pH值的降低而加强,在低温下该方法的协同效果更加明显。     

The effect of pH on metal accumulation in two Alyssum species

Nickel phytoextraction using hyperaccumulator plants offers a potential for profit while decontaminating soils. Although soil pH is considered a key factor in metal uptake by crops, little is known about soil pH effects on metal uptake by hyperaccumulator plants. Two Ni and Co hyperaccumulators, Alyssum murale and A. corsicum, were grown in Quarry muck (Terric Haplohemist) and Welland (Typic Epiaquoll) soils contaminated by a Ni refinery in Port Colborne, Ontario, Canada, and in the serpentine Brockman soil (Typic Xerochrepts) from Oregon, USA. Soils were acidified and limed to cover pH from strongly acidic to mildly alkaline. Alyssum grown in both industrially contaminated soils exhibited increased Ni concentration in shoots as soil pH increased despite a decrease in water-soluble soil Ni, opposite to that seen with agricultural crop plants. A small decrease in Alyssum shoot Ni concentration as soil pH increased was observed in the serpentine soil. The highest fraction of total soil Ni was phytoextracted from Quarry muck (6.3%), followed by Welland (4.7%), and Brockman (0.84%). Maximum Ni phytoextraction was achieved at pH 7.3, 7.7, and 6.4 in the Quarry, Welland, and Brockman soils, respectively. Cobalt concentrations in shoots increased with soil pH increase in the Quarry muck, but decreased in the Welland soil. Plants extracted 1.71, 0.83, and 0.05% of the total soil Co from Welland, Quarry, and Brockman, respectively. The differences in uptake pattern of Ni and Co by Alyssum from different soils and pH were probably related to the differences in organic matter and iron contents of the soils.     

PERIVITELLINE pH OF SALMONIDE EGGS IN RELATION TO AMBIENT pH1

ABSTRACT: Eggs from salmon and brown trout were reared at 6 pH levels in the pH range 4.1–7.5. By micropuncture, the pH of the perivitelline fluid (PVF) was measured at different stages of development with an antimony microelectrode system. The pH of the PVF falls with decreased pH of the ambient media, although no point of equilibrium was found at the lower pH levels. When eggs were reared at pH levels 4.1–4.7, the pH of the PVF in salmon eggs was 0.4 units above the ambient media, while that in trout eggs was 1.0 pH units above. Decreased pH of the PVF during the later, actively ion accumulation, embryonic stages will subject the embryos to ion regulating stresses similar to those registered for adult fishes.     

Sorption of trace metals by standard and micro suction cups in the absence and presence of dissolved organic carbon

Both the bioavailability of a trace metal (TM) in a soil and the risk of leaching to the ground water are linked to the metals concentration in the soil solution. Sampling soil solution by tension lysimetry with suction cups is a simple and established technique that is increasingly used for monitoring dissolved TM in soils. Of major concern, however, is the sorption of TM by the walls of the samplers. Metal sorption by different materials used in suction cups can vary widely, depending also on the chemistry of the soil solution. We compared the sorption of Cu, Zn, Cd, and Pb by different standard-size and micro suction cups in the laboratory at two pH values (4.5 and 7.5 or 8.0) in absence and presence of dissolved organic carbon (DOC). In addition, we investigated the sorption of DOC from different origins by the cup materials. At both pH values, the weakest sorption of all four TMs was exhibited by standard-size suction cups based on nylon membranes and by hollow fibers made from polyvinyl alcohol (PVA). At alkaline pH, borosilicate glass, ceramic materials, and polytetrafluorethylene (PTFE) mixed with silicate were characterized by generally strong sorption of all investigated TMs. In addition, Cu and Pb were strongly sorbed at low pH by PTFE-silicate and a ceramic material used for the construction of standard-size suction cups. On the other hand, sorption of Cu, Zn, and Cd by ceramic capillaries produced from pure aluminum oxide was negligible at low pH. Micro suction cups made of an unknown polymerous tube sorbed Cu strongly, but were well suited to monitor Zn, Cd, and Pb at low pH, and, in the presence of DOC, also at high pH. Major cations (Na+, Mg2+, K+, Ca2+) and anions (Cl-, NO3-, SO4(2-)) were not or very weakly sorbed by all cup materials, except for Mg2+, K+, and Ca2+ by borosilicate glass at pH 7.5. Trace metal sorption by suction cups was generally greatly reduced in the presence of DOC, especially at alkaline pH. The sorption of DOC itself depended on its source. Dissolved organic carbon from leaf litter extracts with a probably large hydrophobic fraction was sorbed more strongly than mainly hydrophilic DOC from a mineral soil solution.     

Transport of cadmium and assessment of phytotoxicity after electrokinetic remediation

The use of ethylene diamine tetraacetic acid (EDTA) on the electrokinetic removal of cadmium-contaminated soil was evaluated. A total of four different tests were conducted using EDTA as a washing solution as well as a purging solution at the electrode compartments. The efficiency of electrokinetic extraction was significantly influenced by the pH of the soil medium. The results show that EDTA was effective in desorbing cadmium at a high pH, with Cd-EDTA(-) anion complexes migrating toward the anode. At low pH values near the anode area, cadmium existed as Cd(2+), migrating toward the cathode. Such contradicting directions of cadmium have resulted in its detrimental removal from the soil cell. However, accumulation of cadmium near the cathode was observed at the end of the tests due to the dominating low pH in the soil cell. The phytotoxicity after the electrokinetic process was investigated using Sorghum saccharatum, Lepidium sativum and Sinapis alba plants. The germination index was a major endpoint estimated by measuring seed germination and shoot elongation. The results obtained show that the phytotoxicity was increased after electrokinetic extraction. Despite, the extensive cadmium removal from two-thirds of the cell, the low pH of the soil was the principal parameter exhibiting the phytotoxicity.     

Effects of pH and manure on transport of sulfonamide antibiotics in soil

Sulfonamide antibiotics are a commonly used group of compounds in animal husbandry. They are excreted with manure, which is collected in a storage lagoon in certain types of confined animal feeding operations. Flood irrigation of forage fields with this liquid manure creates the potential risk of groundwater contamination in areas with shallow groundwater levels. We tested the hypothesis that-in addition to the soil characteristics-manure as cosolute and manure pH are two major parameters influencing sulfonamide transport in soils. Solute displacement experiments in repacked, saturated soil columns were performed with soil (loamy sand) and manure from a dairy farm in California. Breakthrough of nonreactive tracer and sulfadimethoxine, sulfamethazine, and sulfamethoxazole at different solution pH (5, 6.5, 8.5) with and without manure was modeled using Hydrus-1D to infer transport and reaction parameters. Tracer and sulfonamide breakthrough curves were well explained by a model concept based on physical nonequilibrium transport, equilibrium sorption, and first-order dissipation kinetics. Sorption of the antibiotics was low ( K? ≤ 0.7 L kg) and only weakly influenced by pH and manure. However, sulfonamide attenuation was significantly affected by both pH and manure. The mass recovery of sulfonamides decreased with decreasing pH, e.g., for sulfamethoxazole from 77 (pH 8.5) to 56% (pH 5). The sulfonamides were highly mobile under the studied conditions, but manure application increased their attenuation substantially. The observed attenuation was most likely caused by a combination of microbial transformation and irreversible sorption to the soil matrix.