改性沸石用于饮用水除氟的试验研究

试验针对存在的氟污染饮用水问题,将天然沸石用NaOH和Al2（SO4）3溶液改性制成除氟材料.静态试验研究表明：改性沸石除氟吸附反应快,其最佳pH值范围为5～9,而且对氟离子具有较好的离子选择性能.通过动态试验研究发现,降低进水流量和原水浓度可以增大滤层的吸附容量.两种再生方式对比试验表明：用Al2（SO4）3溶液再生效果优于用NaOH和Al2（SO4）3溶液联合再生.     

高活性絮凝剂产生菌芽孢杆菌TS-1培养条件研究

从土壤中分离、筛选得到一株高絮凝活性絮凝剂产生菌,TS-1,初步鉴定为芽孢杆菌.通过六因素五水平正交设计实验,探讨了该菌产絮凝剂的最优条件.在最优条件为乳糖2%、蛋白胨1%、KH2PO4 0.2%、K2HPO4 0.2%、NaCl 0.05%、(NH4)2SO4 0.05%、MgSO4·7H2O 0.05%、pH 6.0、34℃、180r/min、摇床培养40h下,所产絮凝剂对4‰的高岭土悬浊液的絮凝效率为91.3%.     

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。     

成都市春节期间PM_(2.5)中水溶性离子的污染特征分析

采用在线监测仪器对成都市春节期间大气中的PM_(2.5)及PM_(2.5)中的水溶性无机离子浓度进行了连续观测。结果表明:春节期间NO-3、SO2-4、NH+4是PM_(2.5)中水溶性离子的主要组成部分;烟花爆竹的集中燃放使PM_(2.5)的浓度短时间内迅速升高,同时PM_(2.5)中的SO2-4、K~+、Mg2+、Cl-的浓度亦显著升高,最大值分别为28.74μg/m3、33.40μg/m3、3.01μg/m3、23.53μg/m3,是基本无烟花爆竹燃放时段的2.90倍、303.6倍、376.2倍和13.8倍;相关性分析表明,春节期间PM_(2.5)中的K~+、Mg2+、Cl-可能有相同的来源,即烟花爆竹的燃放,部分SO2-4还可能以硫酸钾、硫酸镁的形式存在。     

南充市近十年酸雨变化特征及降水化学组成研究

依据南充市2003~2012年城区降水环境监测统计资料,分析了酸雨变化特征及降水离子化学组成。研究表明:这十年,酸雨频率平均为50.4%,2007年降雨量为最高,呈波动递减趋势变化,降水年平均pH值为4.88,呈现"低—高—低"的变化特征,城区酸雨频率和降水pH值月均值变化呈现高低交替的波动趋势。城区降水中主要阳离子成分是Ca2+,主要阴离子成分是SO2-4和NO-3。(SO2-4/NO-3)比值逐年下降,平均比值为7.82,酸雨污染类型仍以硫酸型为主;降水(NH+4+Ca2+)/(SO2-4+NO-3)和Ca2+/NH+4比值呈波动性变化,2007年分别达到最高值为6.71和50.27,除2010年比值均较低小于1外,近年来均有增加趋势,表明碱性离子缓冲能力增强了,降水酸度降低,pH值增加,但2007年pH值较低,主要与降雨量有关。综合分析,降水酸度不仅是酸性离子和碱性离子中和作用,也受其他离子浓度和降雨量、风向等气候条件、距离传输以及地形等影响。     

硫酸盐及其组合除藻的比较分析

研究了CuSO4·5n2O、Al2（SO4）3、KAl（SO4）2·12H2O单一除藻和与硅藻土、石英砂、泥沙组合除藻的规律,以及对COD、NH3-N、P、浊度4项指标的影响规律。试验结果表明,这3类硫酸盐对除藻都有很好的效果。在相同的初始条件下（即相同的水质条件、投药量、温度和搅拌强度）,Al2（SO4）3的除藻效果优于CuSO4·5H2O和KAl（SO4）2·12H2O,对浊度也有较高的去除率,而对COD、NH3-N、P等指标则无较大改善。     

雅安市夏季颗粒物水溶性离子组成特征

2010年夏季采集雅安市2个地点(四教和白马泉)的TSP、PM_(2.5)样品,并利用离子色谱和原子吸收等方法测定了颗粒物中主要水溶性离子的浓度。结果显示,四教TSP与PM_(2.5)的日均浓度分别为108.04±43.80μg/m3和85.84±29.65μg/m3,PM_(2.5)和TSP的百分比为0.79;白马泉TSP与PM_(2.5)的日均浓度分别为92.17±41.56μg/m3和72.30±28.55μg/m3,二者百分比为0.78。PM_(2.5)是TSP的主要组分。PM_(2.5)质量浓度昼夜变化明显,白天高于夜晚。阳离子与阴离子电荷总和之比值接近1。四教总离子浓度占TSP和PM_(2.5)的质量分数分别是26.10%和31.04%,而白马泉的分别为21.34%和24.07%。SO2-4、NO-3、NH+4为颗粒物中无机离子的主要组分,其昼夜浓度变化明显。相关性分析显示,两地的离子来源和组成形式均有所差异。NO-3/SO2-4在0.7以下,说明雅安市以固定污染源为主。PM_(2.5)中硫和氮的转化率均值均大于0.1,说明发生了二次转化,并且SO2的转化率远大于NO2。     

多花黄精总蛋白质提取工艺优化

对多花黄精主根与须根总蛋白质的提取工艺进行了研究.在对料液比、离心转速、NaCl溶液的浓度等进行单因素试验的基础上,通过正交试验确定了多花黄精主根与须根总蛋白质提取的最佳工艺条件,即对多花黄精主根蛋白质的提取最佳条件为料液比1:15、NaCl浓度0.10mol/L、转速为2500r/min;须根蛋白的提取最佳条件为料液比1:15、NaCl浓度0.20 mol/L、转速为4500r/min.在相同的提取条件下,多花黄精主根与须根的蛋白质得率差异显著.须根中蛋白质的含量与主根的差异性不显著,须根的利用价值也很高,有待于进一步开发利用.     

高氯低COD废水中COD的测定

以某污水厂的高氯低COD生化出水为研究对象,探讨了硫酸汞加入量、K2Cr2O7溶液浓度、反应酸度、取水样量等参数对COD测定的影响,探讨消除该厂Cl-干扰最简单有效方法,结果表明:控制硫酸汞与氯离子比为15∶1(质量比)、K2Cr2O7浓度为0.18 mol/L、水样稀释0.75倍、Ag2SO4-H2SO4加入量为28mL,皆可有效减少氯离子的干扰。该方法相对氯气校正法,操作简单、准确可靠。     

海南马尾藻海藻酸钠的提取工艺及表征

采用正交试验方案首次研究了海南马尾藻海藻酸钠的提取工艺,得出最佳的提取工艺条件:Na2CO3浓度为2%、消化温度为55℃、消化时间为3h,海藻酸钠提取率最高达40.4%.用FTIR表征发现,提取的马尾藻海藻酸钠与市场售的海带海藻酸钠在结构上差别不大,同时测得提取海藻酸钠的分子量为36万、粘度为185mPa.S,高于GB1976-80要求的150mPa.S.     

A study of the extraction of vanadium and nickel in oil-fired fly ash

Annual production of oil-fired fly ash in Taiwan is approximately 43 000 tons, of this approximately 13 000 tons is electrostatically precipitated, the rest is cyclonically collected. Structurewise, both consist of porous unburned carbon, vanadium and nickel oxide, and water-soluble sulfate. Electrostatically precipitated fly ash contains large amounts of ammonium sulfate. If these ashes are not properly disposed of, they become environmental problems, such as dusting, leakage of acid liquids, and pollution with heavy metals. This paper discusses the experimental extraction of vanadium and nickel from oil-fired fly ash. The results indicated that leaching of oil-fired fly ash in 0.5 N of sulfuric acid led to an extraction of 65% vanadium, 60% nickel, and 42% iron, along with an increase in the concentration of sulfuric acid. When leached in 2 N sodium hydroxide solution, the extraction of vanadium was 80%, and the extraction of nickel was negligible. If leached in an ammonia water, the extraction of nickel increased, along with an increase in the concentration of ammonia in water. When leached with 4 N ammonia water, the extraction of nickel was 60%, the extraction of vanadium was less than that obtainable from leaching in sulfuric acid solution or in sodium hydroxide solution. If electrostatically precipitated fly ash was leached in a solution of 0.25 N ammonia water and 2 N ammonium sulfate, it would yield an extraction of 60% nickel and 8% vanadium—leading to a selective extraction of nickel. This study has established an extraction flowsheet in which fly ash was first leached in an ammoniacal solution containing ammonium sulfate to recover nickel. The leached residues were then leached in an alkaline solution to recover vanadium.     

Use of alkaline extraction to quantify sulfate concentration in oxidized mine tailings

An alkaline extraction method has been developed for the determination of total sulfate in mine tailings containing secondary sulfate minerals formed by the oxidation of primary sulfides. Oxidized tailings were extracted with a 0.3 M NaOH solution at a liquid/solid ratio of 30 at room temperature for 16 h. The sulfate concentration in the extracts was determined by ion chromatography (IC). The coefficient of variation for sulfate determinations ranged from 1.9 to 3.2% for five tailings samples collected at two tailings impoundments. Mineralogical analysis of the tailings by scanning electron microscopy/X-ray energy dispersive spectrometry (SEM/EDS) demonstrated that the extraction of sulfate was complete, with the exception of extremely insoluble barite. The proposed method is simple, yields an accurate yet rapid measurement of sulfate, and involves a safer laboratory operation than conventional methods that make use of strong HCl acid solutions. Moreover, this method allows the specific measurement of sulfate in the extract, whereas conventional methods are generally limited to the measurement of total S by inductively coupled plasma atomic emission spectrometry (ICP-AES) due to the interference of chloride with sulfate in IC.     

Chemical extraction methods to assess bioavailable arsenic in soil and solid media

Soil ingestion by children is an important pathway in assessing public health risks associated with exposure to arsenic-contaminated soils. Soil chemical methods are available to extract various pools of soil arsenic, but their ability to measure bioavailable arsenic from soil ingestion is unknown. Arsenic extracted by five commonly used soil extractants was compared with bioavailable arsenic measured in vivo by immature swine (Sus scrofa) dosing trials. Fifteen contaminated soils that contained 233 to 17 500 mg kg(-1) arsenic were studied. Soil extractants were selected to dissolve surficially adsorbed and/or readily soluble arsenic (water, 1 M sodium acetate, 0.1 M Na2HPO4/0.1 M NaH2PO4) and arsenic in Fe and Mn oxide minerals (hydroxylamine hydrochloride, ammonium oxalate). The mean percent of total arsenic extracted was: ammonium oxalate (53.6%) > or = hydroxylamine hydrochloride (51.7%) > phosphate (10.5%), acetate (7.16%) > water (0.15%). The strongest relationship between arsenic determined by soil chemical extraction and in vivo bioavailable arsenic was found for hydroxylamine hydrochloride extractant (r = 0.88, significant at the 0.01 probability level). Comparison of the amount of arsenic extracted by soil methods with bioavailable arsenic showed the following trend: ammonium oxalate, hydroxylamine hydrochloride > in vivo > phosphate, acetate > water. The amount of arsenic dissolved in the stomach (potentially bioavailable) is between surficially adsorbed (extracted by phosphate or acetate) and surficially adsorbed + nonsurficial forms in Fe and Mn oxides (extracted by hydroxylamine hydrochloride or ammonium oxalate). Soil extraction methods that dissolve some of the amorphous Fe, such as hydroxylamine hydrochloride, can be designed to provide closer estimates of bioavailable arsenic.     

焦炉烟道气吸氨新工艺研究及其对大气C02减排分析

对利用焦炉烟道气吸氨生产碳酸氢铵的新工艺进行了可行性、减排效果以及经济效益分析。研究表明：用该工艺吸收焦化厂烟道气中CO2生产碳酸氢铵肥料,技术可行,该工艺的工业化将有利于解决焦化厂传统硫铵工艺存在的问题,如需购买原料硫酸、生产运营费用高、污染腐蚀等。年产100万t的冶金焦炭厂可减排CO2温室气体1．34万t,副产碳酸氢铵肥料每年可获利187万元,可实现经济效益和社会效益的双赢,符合可持续发展战略。     

Aerosol chemical and optical properties during the Mt. Zirkel Visibility Study

Aerosol chemical and optical properties were measured near the Mt. Zirkel Wilderness Area in northwestern Colorado. Six-hour PM2.5 (particles with aerodynamic diameters less than 2.5 microm) mass concentrations and PM2.5 dry particle light scattering at 550 nm averaged 4.6 microg m(-3) and 8.6 Mm(-1), respectively. Sulfates, organic carbon, and geological material were the principle components of particle mass and light scattering. Hygroscopic growth was consistent with that expected for ammonium sulfate aerosols. Size distributions derived from three-wavelength (i.e., 450, 550, and 700 nm) nephelometer data were similar to those measured in other remote areas of the western USA. Quasi-dry chemical light scattering efficiencies derived using Mie theory were 3.6 m2 g(-1) for organic carbon, 2.5 m2 g(-1) for sulfates (ammonium sulfate and ammonium bisulfate), 2.6 m2 g(-1) for ammonium nitrate, and 1.76 m2 g(-1) for geological material. These values are lower than but consistent with previously reported results. Realistic efficiencies could not be derived using the multiple linear regression (MLR) approach.     

从抽提叶绿素后的蚕沙中提取叶蛋白

本文分析了从抽提叶绿素后的蚕沙中提取叶蛋白的工艺条件。结果表明：以０７％ＮａＯＨ作提取剂,料比１∶７,于６０℃搅拌提取６ｈ,叶蛋白的提取率为８４１２％;再用（１＋１）ＨＣｌ调ｐＨ值为３５,即得叶蛋白沉淀。按上述工艺条件,叶蛋白得率（以蚕沙干物计）为１００９％,蛋白质含量为７６６８％,提高了蚕沙的综合利用价值     

Chromosomal genes conferring tolerance to heavy metal (Ag) toxicity

Bacterial strains were isolated from sediment samples from the Thames River. Successive transfer growth of the various strains on nutrient agar containing increasing concentrations of AgNO₃ revealed that three of the bacterial isolates were found to be capable of tolerating high concentrations of AgNO₃ ranging from 20 to 80 mM on a solid medium and up to 10 mM AgNO₃ in liquid medium. Molecular characterization and identification based on 16S rDNA gene sequencing of three strains of bacteria that are tolerant to silver nitrate showed that the major tolerant strains include the superbug, Shewanella oneidensis, Pseudomonas sp. and Bacillus sp. Protein extraction and two-dimensional (2D) sodium dodecyl sulfate SDS-polyacrylamide gel electrophoresis (PAGE) of the protein extracts in bacteria exposed to very high concentrations of AgNO₃ revealed a general reduction in the number of expressed proteins, although two protein spots were conspicuously over expressed in the exposed bacteria compared to control. The N-terminal amino acid sequence analysis of the protein spots identified the major up-regulated proteins as the outer membrane protein To1C (45.2 kDa) and the structural protein of the flagellar filament, flagellin (28.34 kDa), encoded for by the to1C and fliC genes, respectively. The roles of these genes in a number of multi-drug resistant pathogen and potentials for biotechnological applications in toxic metal control for treatment of contaminated ecosystems and biomining were discussed.     

氨/硫铵法烟气脱硫技术特点及市场前景分析

通过对我国二氧化硫污染现状及控制要求的分析,提出了氨/硫铵法作为一种资源回收型脱硫方法,具有反应速度快、工艺流程简单、吸收剂利用率高、适用范围广及可实现资源回收利用的特点;以工程案例的形式分析了氨/硫铵法的技术经济指标,并对氨/硫铵法的应用前景和市场需求进行了预测。     

Short- and longer-term effects of the willow root system on metal extractability in contaminated dredged sediment

Willow (Salix spp.) stands are often proposed as vegetation covers for the restoration and stabilization of contaminated and derelict land. Planting willows on dredged sediment disposal sites for biomass production can be an alternative to traditional capping techniques. However, with the introduction of willow stands on dredged sediment disposal sites, the possibility of increased contaminant availability in the root zone must be acknowledged as it can increase the risk of leaching. Two trials investigated the availability of Cd, Zn, Cu, and Pb in the root zones of willows grown on contaminated sediment. To assess the effects of willow root growth on metal extractability and mobility, bulk and rhizosphere sediment samples were extracted with deionized water, ammonium acetate at pH 7, and ammonium acetate-EDTA at pH 4.65. A rhizobox experiment was used to investigate the short-term effect of willow roots on metal availability in oxic and anoxic sediment. Longer-term effects were assessed in a field trial. The rhizobox trial showed that Cd, Zn, and Cu extractability in the rhizosphere increased while the opposite was observed for Pb. This was attributed to the increased willow-induced oxidation rate in the root zone as a result of aeration and evapotranspiration, which masked the direct chemical and biological influences of the willow roots. The field trial showed that Cu and Pb, but not Cd, were more available in the root zone after water and ammonium acetate (pH 7) extraction compared with the bulk sediment. Sediment in the root zone was better structured and aggregated and thus more permeable for downward water flows, causing leaching of a fraction of the metals and significantly lower total contents of Cd, Cu, and Pb. These findings indicate that a vegetation cover strategy to stabilize sediments can increase metal availability in the root zone and that potential metal losses to the environment should be considered.     

Chemical fractionation of phosphorus in stabilized biosolids

Three chemicals-ferrous sulfate (FeSul), calcium oxide (CaO), and aluminum sulfate (alum)-were applied at different rates to stabilize P in fresh, anaerobically digested biosolids (FBS) obtained from an activated sewage treatment plant. A modified Hedley fractionation procedure was used to assess P forms in these sludge-borne materials and in a biosolids compost (BSC) prepared from the same FBS. Each biosolids material exhibited a unique pattern of P distribution among fractions. The most available P forms, namely: (i) water-soluble P (WSP); (ii) membrane-P; and (iii) NaHCO(3)-P, were stabilized by small rates of each of the chemicals; but the P transformation into more stable forms depended on the type of chemical added. The stabilized P forms were enhanced by high rates of CaO and FeSul, but were reduced by high rates of alum. The organic P (P(o)) in the first three fractions of the FeSul- and alum-stabilized biosolids was enhanced by the chemical addition, and P(o) transformation from NaOH-P(o) into NaHCO(3)-P(o) was found in calcium-stabilized biosolids. A positive relationship was found between NaHCO(3)-P(o) and the NaHCO(3)-extracted organic C in all chemically stabilized biosolids. One-step extraction by NaHCO(3) or NaOH underestimated P extraction compared to the stepwise extraction. The reported results are consistent with solid-state P speciation reported earlier and contribute important information for optimizing biosolids stabilization to reduce P loss after incorporation in soils and for maximizing soil capacity to safely store pre-stabilized biosolids.