操作条件对超滤膜运行经济稳定性能的影响

采用正交实验的方法对棕榈油生产废水二级处理出水的超滤工艺条件进行考察和优化,并用膜通量衰减系数、平均跨膜压差及产水量各自加权相加所得综合指标来表征不同超滤操作条件下膜运行的经济稳定性能。正交试验结果表明,减小膜表面流速和产水率,提高处理废水温度均有利于系统经济稳定地运行;各运行参数对综合指标影响的大小顺序为:膜表面平均流速>产水率>温度;在保证出水质量的前提下,最佳组合操作条件为膜表面平均流速0.7m/s,产水率80%,废水温度30℃。     

铝件表面处理废水治理所得化学污泥的再生利用研究

对混凝法处理铝件表面处理废水治理所得化学污泥再生利用进行了研究,得到了适宜的操作条件.结果表明,用浓硫酸溶解污泥的最佳用量为0.14～0.16 mL/g湿污泥,湿污泥的溶解率可达90%,铝的溶出率也可达95%以上.把污泥的溶解液作混凝剂回用于印染废水的混凝处理也取得了良好的效果,其COD去除率≥80%,脱色率≥90%.实现了资源的二次利用,改善了作业环境,获得了较好的经济效益和社会效益.     

焦化污染场地土壤多环芳烃的生物强化协同降解工艺研究

以某废弃焦化厂的多环芳烃（PAHs）污染土壤为研究对象,通过耦合表活淋洗、生物降解、化学氧化等技术设计了4种修复工艺,并进行了试验验证。结果表明：针对该实际焦化污染土壤,单一的生物泥浆降解工艺21 d后PAHs可实现58.64%的降解率;采用表活增溶+化学氧化+生物泥浆的降解工艺,26 d降解率可达到65.68%,但前置的化学氧化会抑制生物降解效果;采用干筛分+表活分批淋洗+化学氧化的降解工艺降解率可达到85.36%,有效缩短降解时间到13 d内,但土壤中残留的PAHs与土壤颗粒结合紧密,化学氧化降解率仍难以满足大于90%的要求;采用湿筛分+表活分批淋洗+生物泥浆+化学氧化的生物强化协同降解工艺,29 d降解率可达到95.32%,实现了土壤的修复目标。生物强化协同降解工艺路线,综合了多种修复技术的优点,实现了修复技术组合优化,为焦化污染土壤中多环芳烃降解修复提供了可行的工艺路径。     

四环素对不同品种蔬菜毒性阈值及其敏感性分布

研究抗生素污染对蔬菜毒性阈值及其敏感性分布,对于科学评价土壤抗生素污染的生态风险具有重要意义。采用室内培养方法,选取四环素(TC)作为代表抗生素,调查其对珠三角地区多种蔬菜品种种子萌发的影响。以影响程度最大的指标为测试终点,采用Log-logistic分布模型,对TC的毒性剂量-效应关系进行拟合,并计算其IC₅₀和IC₁₀。以IC₅₀为评价参数,采用物种敏感性分布法(Species sensitivity distributions,SSD),构建TC污染对不同蔬菜品种的SSD曲线,并获得TC毒性阈值(HC₅)和无效应浓度(PNEC)。结果表明,TC污染对实验所选品种蔬菜种子萌发指标的影响程度为：根长>芽长>发芽率,当TC质量浓度为10 mg·L^-1时,9种品种蔬菜种子相对根长、相对芽长和发芽率分别为16.9%-72.5%,42.3%-129.4%,83%-100%。TC污染对种子萌发的影响程度不仅与测试指标相关,还与蔬菜品种密切相关。当TC质量浓度为10mg·L<...     

Effect of humic substances on the precipitation of calcium phosphate

For phosphorus （P） recovery from wastewater, the effect of humic substances （HS） on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate （as P） and 20 mg/L HS （as dissolved organic carbon, DOC） at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium （Ca） and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction （XRD） and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0, the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite （HAP） by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate.     

Observation of atmospheric nitrous acid with DOAS in Beijing, China

Measurements of nitrous acid （HONO） and nitrogen dioxide （NO2） in Beijing City have been performed by means of a developed differential optical absorption spectroscopy （DOAS） system based on photodiode array （PDA）, during the autumn of 2004. HONO and NO2 were simultaneously identified by their characteristic absorption bands in the spectral region between 337 nm and 372 nm with high sensibility and time resolution. The concentrations of HONO exhibit obviously diurnal variation with a nocturnal maximum and a daytime minimum. The highest HONO value up to 11.8 μg/m^3 was observed during the night of 2/3 September. Possible sources of the observed HONO were discussed. Good correlation to NO2 indicates that NO2 is a main source component. The measurement also shows direct emission of HONO is an imnortant source in strongly polluted urban area.     

Degradation of 2,4-dichlorophenoxyacetic acid in water by ozone-hydrogen peroxide process

IntroductionAt present, several types of organic pollutantsreferred to as environmental endocrine disruptors(ED) have been suggested to be associated withabnormal sexual development (Hu, 2000). It wasreported that the ED led to the decline of reproductive…     

Selection of appropriate organic additives for enhancing Zn and Cd phytoextraction by hyperaccumulators

Chelant-enhanced phytoextraction is one of the most promising technologies to remove heavy metals from soil. The key of the technology is to choose suitable additives in combination with a suitable plant. In the present study, laboratory batch experiment of metal solubilization, cress seeds germination were undertaken to investigate the metal-mobilizing capability and the phytotoxicity of organic additives, including ethylene diamine triacetic acid （EDTA）, citric acid, acetic acid, oxalic acid, glutamine and monosodium glutamate waste liquid （MGWL） from food industry. Experiments in pots were carried out to study the effects of the additives on Zn and Cd phytoextraction. Furthermore, a leaching experiment with lysimeter was performed to evaluate the environmental risks of additive-induced leaching to underground water. The results showed that EDTA had a strong mobilizing ability for Zn and Cd, followed by mixed reagent （MR） and MGWL. MGWL and acetic acid at 5 mmol equivalent per liter resulted in seed germination index less than 2%. Experiments in pots verified the phytotoxicity of acetic acid and MGWL. Addition of the mixed reagent at 6--10 mmol/kg significantly increased Zn phytoextraction by Thlaspi caerulescens. The same for EDTA and the mixed reagent at 10 mmol/kg by Sedum dfredii. But only mixed reagents could significantly increase Cd phytoextraction by the studied hyperaccumulators. This suggested that the strong chelant was not always the good agent to enhance phytoextraction. S. alfredii combined with 2--10 mmol/kg soil MR was preferred for phytoremediation of Cd/Zn contaminated soils in southern China, this could result in high phytoextraction of Cd/Zn and reduce the leaching risk to underground water than EDTA assisted phytoextration.     

Selective extraction and separation of Fe, Mn oxides and organic materials in river surficial sediments

In order to investigate the adsorption mechanism of trace metals to surficial sediments （SSs）, a selective extraction procedure was improved in the present work. The selective extraction procedure has been proved to selectively remove and separate Fe, Mn oxides and organic materials （OMs） in the non-residual fraction from the SSs collected in Songhua River, China. After screening different kinds of conventional extractants of Fe and Mn oxides and OMs used for separation of heavy metals in the soils and sediments, NH2OH .HCl （0.1 mol/L） ＋ HNO3 （0.1 mol/L）, （NH4）2C2O4 （0.2 mol/L） ＋ H2C2O4 （pH 3.0）, and 30% of H2O2 were respectively applied to selectively extract Mn oxides, Fe/Mn oxides and OMs. After the extraction treatments, the target components were removed with extraction efficiencies between 86.09%--3.36% for the hydroxylamine hydrochloride treatment, 80.63%- 101.09% for the oxalate solution extraction, and 94.76%-102.83% for the hydrogen peroxide digestion, respectively. The results indicate that this selective extraction technology was effective for the extraction and separation ofFe, Mn oxides and OMs in the SSs, and important for further mechanism study of trace metal adsorption onto SSs.     

AAO+MBR+化学沉淀除磷工艺在高磷生活污水中的工程应用

针对湖北省某磷化工厂高磷浓度且含量复杂的生活污水及当地严格的排放限值要求,该工程采用了AAO+MBR+化学沉淀法工艺,主体处理规模120 m3/d,MBR膜工艺处理规模80 m3/d。工程运行情况显示,该工艺处理效果良好,出水水质优于GB 18918—2002《城镇污水处理厂污染物排放标准》一级A标准,总磷及氟化物等均满足环保达标要求,能有效削减排入汉江的污染物负荷。工程运营成本为1.339 9元/m3,对于沿江磷化工厂同类型生活污水的处理具有较高的推广应用价值。