球磨零价镁/石墨(ZVMg/C)降解水中三氯乙烯

利用机械球磨法制备了零价镁/石墨(ZVMg/C)材料,并将其用于水溶液中三氯乙烯(TCE)的降解.研究通过SEM、BET和XRD等分析手段解析了ZVMg/C的表面形态结构和成分组成;采用正交实验方法优化了ZVMg/C的制备参数,比较了石墨含量对材料性能的影响;并考察了ZVMg/C投加量、溶液初始pH和地下水中常见阴(C...     

几种萃取剂对土壤中重金属生物有效部分的萃取效果

采用6种萃取剂:pH=7的0.01mol/L CaCl_2、pH=7.3的0.005mol/L DTPA+0.1mol/L TEA(三乙醇胺)+0.01mol/L CaCl_2O.1mol/L NaNO_3、0.43mol/L HOAc、pH=7的0.05mol/L EDTA和pH=4.65的0.5mol/L NH_4OAc+0.02mol/L EDTA浸取液.对污染土壤中的重金属Cu、Zn、Cd、Pb、的进行了萃取,并比较了萃取剂的萃取能力。实验结果表明,HOAc、EDTA以及NH_4OAc-EDTA萃取各种重金属的能力远远大于其它几种萃取剂的萃取能力,是比较理想的萃取剂。     

Screening zur Mobilisierbarkeit von Kupfer aus Böden und Schlämmen

In the presented paper, the pHstat-procedure is compared with four simple extraction procedures. These procedures make use of the following extraction solutions: distilled water (based on DIN 38414 part 4, DIN-S4), 1 mol/L ammonium nitrate, 1 mol/L ammonium acetate at pH 7.0 and 1 mol/L sodium acetate at pH 5.0, respectively. The extraction procedures were applied to 10 different soil samples and 2 sludges. The DIN-S4-procedure shows the lowest amounts of mobilized copper. The highest parts are extracted by sodium acetate solution. For the procedures investigated, the mobilized amounts extracted by ammonium acetate solution are most comparable with those of the pHstat-procedure. The simple sodium acetate procedure is useful for screening to select significant samples from a large number of soils. Thus, the high effort caused by the pHstat-procedure can be reduced to a minimum through the application of this screening procedure. The application of this screening, however, is difficult for samples containing large parts of organic compounds, e.g. sewage sludge. These samples show a different extracting behaviour.     

Efficiency of mercapto flavor compounds in removing acrylamide under high temperature and low humidity conditions

Acrylamide (AA) is a potential human carcinogen, genotoxicant, and neurotoxicant. Thus, the aim of this study was to examine the ability of mercapto flavor compounds to remove AA released from consumer packaging into food products. Four mercapto flavor compounds including 1,2-ethanedithiol, 1-butanethiol, 2-methyl-3-furanthiol, and 2-furanmethanethiol were employed to extract AA in model system using high temperature and low humidity. Our study showed that mercaptans were effective in eliminating AA in our model system. In order to remove 0.2 μmol AA, the optimal conditions in the reaction system were mercaptan flavor chemicals at 5 μmol, temperature 180 °C, and reaction time 25 min. In the presence of a higher pH, the greater was the amount of AA eliminated. Evidence indicates that employment of mercapto flavor chemicals under certain temperature and pH conditions is a reliable method to remove any unwanted AA from food products.     

Vc二步发酵离体实验系统的建立

以氧化葡萄糖酸杆菌和巨大芽孢杆菌混合培养物的无细胞抽提液为基本反应液，在试管中建立了Vc二步发酵离体实验系统，将底物山梨糖加入反应体系后在pH7．0，35℃下保温24h，2－酮基－L－古龙酸生成，加入巨大芽孢杆菌胞外活性物质对离体系统的产酸没有影响，一定量的L－山梨糖脱氢酶可促进产酸，试验了pH、θ／℃、金属离子、电子受体、去污剂等对该系统产酸的影响，并就其作用机理进行了探讨，结果表明离体系统产酸的最适pH和θ／℃分别是8和．40℃，Fe^3 促进产酸，Co^2 抑制产酸2，6－二氯酚定酚作为电子受体促进细胞膜组分产酸，但对细胞质组分没有影响，Triton X-100和Tween80抑制产酸。     

Lethal effects of elevated pH and ammonia on juveniles of neotropical fish Colosoma macropomum (Pisces, Caracidae)

Ammonia is the main nitrogenous waste material excreted by gills, then is oxided first to nitrite and then to nitrate. The proportion of ionized-un-ionized ammonia depends on pH and temperature, when this variables increase in a solution containing ammonia the equation goes to left, so the proportion of NH3 increases and the solution becomes more toxic. The purpose of this study was to investigate the acute lethal effects of elevated pH and ammonia on tambaqui juveniles. With a constant ammonia concentration of 5.0 mg/l NH3, there was no mortality a pH of 6.0 (control) and 7.0; but was of 10-20% a pH of 8.0 and 100% at 9.0. The lethal effects of elevated pH and un-ionized ammonia should be recognized as a potential factor contributing to the variable success of tambaqui production ponds, but this species is highly resistant in comparison with other freshwater fish.     

纳米TiO_2光催化降解水溶性染料溶液的研究

研究了纳米ＴｉＯ２光催化剂对活性黄Ｘ６Ｇ、活性红Ｘ３Ｂ、活性蓝ＸＢＲ、碱性绿、碱性紫５ＢＮ、碱性品红等６种染料溶液的光解脱色效果。结果表明，在ｐＨ２的酸性溶液中，对浓度为６０ｍｇ／Ｌ的６种染料溶液的脱色率均超过９３．３％；即使对浓度达２００ｍｇ／Ｌ的活性蓝溶液，其脱色率仍可达７８．８％。染料溶液的ｐＨ值对纳米ＴｉＯ２光催化脱色效果影响较大     

Rapid start-up of mesophilic dry anaerobic digestion of kitchen waste in a continuous stirred tank reactor (CSTR)

Under mesophilic conditions (37 °C), a bench-scale experiment of dry fermentation start-up using kitchen waste was conducted in a fed-batch single phase reactor over a period of 40 days. The results showed that (1) comparing biogas production, efficiencies, and methane concentrations, three apparent different stages emerged: adaption, growth, and stability; (2) in adaption and growth stages, daily biogas production was 0–0.2 L/day and 0.2–0.4 L/day, respectively, and the concentration of methane in the biogas was 22.91% and 48.79%, respectively, with a biodegradation rate of approximately 34.72% in the adaption phase and 27.60% during the growth phase; (3) in the stability stage, the biogas production efficiency attained the maximal level and stabilized at approximately 0.6–0.4 L/day and the concentration of methane was 54.32%. Furthermore, the pH fell to 4.15, and the concentration of chemical oxygen demand increased from 51.139 to 119.295 mg/ml.     

Variations in sperm motility of the Atlantic herring Clupea harengus

Sperm characteristics and fertilization success were measured in two groups of Manx autumn-spawning herring, Clupea harengus L., captured 1 wk apart. Samples contained motile sperm for up to 45 min after activation (average 7 min). Individual spermatozoa were motile for up to 5 min. The activation of individual spermatozoa is probably phased, although the mechanism for the delay is not clear. This can account for the overall low levels of active sperm at any one time, the periodic fluctuations observed in the proportion of motile sperm, and for successful fertilization rates achieved using samples of apparently immotile sperm. The proportion of motile sperm was not affected by the presence of eggs, but the duration of motility was longer when sperm was activated in the presence of eggs rather than in seawater alone. Individual males differed significantly in the duration of motility in their sperm samples and in the fertilization rates achieved, but not in the proportion of motile sperm in each sample. There were no consistent changes in the characteristics of the spawners or the sperm between the two sample dates. Sperm motility and duration of motility were significantly correlated, but none of the sperm characteristics measured was significantly related to fertilization success. Received: 13 March 1999 / Accepted: 20 May 1999     

Biosorption of Cu2+ from aqueous solutions by pretreated Cladosporium sp

In this paper, adsorption properties of a pretreated of Cladosporium sp. for Cu2 were studied. The fungi pretreated with some chemical reagents exhibited higher Cu2+ removal capacities than native biomass. The optimum chemical reagent was 0.2M NaOH. After 0.2M NaOH pretreatment, optimum conditions of biosorption were found to be pH 5.0, temperature 35 degrees C, and stirring speed of 100rpm. Equilibrium isotherms were obtained from adsorption experiments and the biosorption maximun capacity obtained was at 28.31mg/g. The biosorbed metal ions were effectively eluted by 0.05M HNO3 solution. After eluting, the biosorbed metal ions biomass was regenerated by washing with deionized water and then contacted with a solution containing 0. 1M of Ca2+, Mg2+ ions before further adsorption tests. The pretreated fungi biomass could be used for three cycles: biosorption, elution of biosorbed ion, regeneration of biomass.     

TAR柱前络合、毛细管电泳分析痕量金属离子

1　IntroductionTransitionmetalswereamongthemostconcernelementsinenvironmentalanalysisduetotheirpotentialrolestoplantandanimals[1 ].Theserolesoftransitionmetalsinenvironmentdependedontheirconcentrationinthesoil,waterandlivingthings.Currently ,themostutiliz…     

钢铁工业遗留场地土壤重金属洗脱剂筛选研究

土壤重金属污染限制了工业遗留场地再利用,通过振荡试验考察了HCl、HNO3和EDTA对工业遗留场地土壤中超标重金属Pb、Zn、Cd和As的洗脱效果。结果表明：土壤Pb、Zn、Cd、As的脱除效果均随洗脱剂浓度增加而增加;HCl、HNO3和EDTA等3种洗脱剂浓度分别为0.5、0.5和0.1 mol.L-1时,土壤Pb、Cd质量分数可降低至场地安全再利用的控制标准以内（分别为140 mg.kg-1、1mg.kg-1）;洗脱剂浓度分别增至2、2和0.2 mol.L-1时,土壤Pb、Cd质量分数继续降低,Zn、As质量分数有大幅降低但没有达到其相应的场地安全控制标准（分别为200、20 mg.kg-1）;与EDTA相比,HCl在低浓度时的重金属脱除效果较差,但HCl浓度增加对重金属脱除率的提高效果更为明显;洗脱液pH值（7.88~0.15）与重金属脱除率均呈显著负相关且与As的负相关系数最小,说明洗脱液pH值变化对As去除的影响相对较小;与HCl和HNO3相比,EDTA洗脱液pH值与Pb脱除率之间的负相关系数较大,与Zn、Cd、As脱除率之间的负相关系数较较小,说明EDTA洗脱液pH值变化更易对Pb的去除产生影响。     

土壤中植物有效锰的形态分级

用4种方法测定土壤有效态锰含量，并加以比较和评价，从而确定出最优的土壤有效锰测定方法。研究结果表明，采用一种顺序浸提的方法能比较准确地反映土壤的供锰状况，锰组分及其相应浸提剂为易溶态锰(O.05mol／LCa(NO     

Determination of the dissociation constants of polyepoxysuccinic acid

The dissociation constants of polyepoxysuccinic acid (PESA) were investigated in this study. Based on the potentiometric titration and the BEST program, the dissociation constants of PESA were determined. Considering the complexity of the dissociation of PESA in aqueous solution, several models were constructed to simulate the dissociation process of PESA. By comparison, the dissociation constants of PESA were obtained with model 4. The species distribution of PESA in aqueous solution as a function of pH was also presented according to the experimental and calculation results. It showed that the H₂L model with five basic structure units to describe the dissociation of PESA was reasonable, and the relevant constants had less error and better matching between the experimental and calculation data. The corresponding values of pK _ai were 4.68 and 4.92, respectively, for H₂L at 35°C with ionic strength of 0.1 mol/L.     

Hemolysins from the mucus of Spirographis spallanzani (Polychaeta: Sabellidae)

Specimens of Spirographis spallanzani (Polychaeta: Sabellidae) were collected in the Gulf of Taranto, Italy, in 1991, and their mucous secretion was examined. The mucus possesses thermolabile biologically active proteins which produce hemolysis in vertebrate erythrocytes. The molecules are ineffective against both unfertilized and fertilized echinoid eggs and spermatozoa. The lytic reaction against rabbit erythrocytes varies as a function of cations, pH and temperature, and displays a fast time-course. No immunological cross-reaction could be demonstrated between hemolysins of S. spallanzani and Eisenia foetida andrei. SDS-PAGE analysis of mucus proteins reacting with sheep erythrocytes revealed that at least three major (16, 22 and 40 kDa) and two minor (29 and 34 kDa) components interact with membrane targets.     

Characteristics and mechanisms of 4A zeolite supported nanoparticulate zero-valent iron as Fenton-like catalyst to degrade methylene blue

4A zeolite supported nanoparticulate zero-valent iron (nZVI/4A zeolite), synthesized through borohydride reduction method, was used as a catalyst with H₂O₂ to build Fenton-like reaction system to degrade methylene blue (MB) in model wastewater. The characteristics and primary mechanisms of the catalyst were investigated. The results show that nZVI/4A zeolite has the potential as a Fenton-like catalyst, and (about 30 mg/L) MB was degraded completely in 3 h with 10 mM H₂O₂, 0.2 g/L catalyst, and initial pH of 3.0. The MB degradation rates were obtained at least 70% in the tests with initial pH ranged from 2.0 to 9.0 and the catalyst dose rose from 0.2 to 5.0 g/L. Importantly, the catalyst also has a distinctive ability to increase the solution pH value from its initial acidic pH and then maintain the value at close to neutrality. This ability was controlled by both the initial pH and the catalyst dose. MB degradation clarified that hydroxyl radical was the dominated active oxidative specie in the tests with initial acidic pH and low catalyst dose (less 2.5 g/L); otherwise, Fe(VI) oxidation was the main mechanism for MB degradation; and the two processes shared synergistic effect in MB degradation in the present test. The catalyst has high operational stability in both of the composites with low iron leaching (less 2%) and catalyzing ability. Therefore, nZVI/4A zeolite has great potential as a Fenton-like catalyst and is used with H₂O₂ to build Fenton-like system which could be used to degrade MB efficiently.     

Modified pretreatment method for total microbial DNA extraction from contaminated river sediment

Extraction of high-quality microbial DNA from contaminated environmental samples is an essential step in microbial ecological study. Based on previously published methods for soil and sediment samples, a modified pretreatment method was developed for extracting microbial DNA from heavily contaminated river sediment samples via selection of optimal pretreatment parameters (i.e., reagent solution, reaction duration, and temperature). The pretreatment procedure involves washing the river sediment sample for three times with a solution containing 0.1 mol·L^-1 ethylene diamine tetraacetic acid (EDTA), 0.1 mol·L^-1 Tris (pH 8.0), 1.5 mol·L^-1 NaCl, 0.1 mol·L^-1 NaH₂PO₄, and Na₂HPO₄ at 65°C with 180 r·min^-1 for 15 min to remove humic materials and heavy metals prior to the employment of standard DNA extraction procedures. We compared the results of standard procedure DNA extraction following pretreatment, without pretreatment, and with using a commercial PowerSoil^TM DNA Isolation Kit. The results indicated that the pretreatment significantly improved the DNA quality based on DNA yield, DNA fragment length, and determination of prokaryotic diversity. Prokaryotic diversity exhibited in the DNA with the pretreatment was also considerably higher than that extracted with the PowerSoil^TM DNA Isolation Kit only. The pretreatment method worked well even with a small amount of sediment sample (0.25 g or even lower). The method provides a novel, simple, cost-effective tool for DNA extraction for microbial community analysis in environmental monitoring and remediation processes.     

Thermodynamics of tetracycline adsorption on silica

The adsorption of antibiotic tetracycline onto silica particles was investigated. The effects of pH, electrolyte concentration and temperature on the adsorption equilibrium were examined and the data correlated with a dual site adsorption model. Adsorption of tetracycline onto approximately 9% of the adsorption sites was found to be irreversible, whereas the rest exhibited Langmuir behaviour. Increasing pH of the solution had a strong negative effect on the adsorbed amounts. Adsorption decreased also with increasing ionic strength and temperature. The enthalpy and entropy of adsorption were found to be approximately −16 and −25 J/mol, respectively.     

Fe-Mn-sepiolite as an effective heterogeneous Fenton-like catalyst for the decolorization of reactive brilliant blue

A study of the decolorization of reactive brilliant blue in an aqueous solution using Fe-Mn-sepiolite as a heterogeneous Fenton-like catalyst has been performed. The Fourier transform infrared (FTIR) spectra of the catalyst showed bending vibrations of the Fe-O. The X-ray diffraction (XRD) patterns of the catalyst showed characteristic diffraction peaks of α-Fe₂O₃, γ-Fe₂O₃ and MnO. A four factor central composite design (CCD) coupled with response surface methodology (RSM) was applied to evaluate and optimize the important variables (catalyst addition, hydrogen peroxide dosage, initial pH value and initial dye concentration). When the reaction conditions were catalyst dosage= 0.4 g, [H₂O₂]= 0.3 mL, pH= 2.5, [reactive brilliant blue]_o = 50 mg·L⁻¹, and volume of solution= 500 mL at room temperature, the decolorization efficiency of reactive brilliant blue was 91.98% within 60 min. Moreover, the Fe-Mn-sepiolite catalyst had good stability for the degradation of reactive brilliant blue even after six cycles. Leaching of iron ions (<0.4 mg·L⁻¹) was observed. The decoloring process was reactive brilliant blue specific via a redox reaction. The benzene ring and naphthalene ring were first oxidized to open ring; these were then oxidized to the alcohol and carboxylic acid. The reactive brilliant blue was decomposed mainly by the attack of ·OH radicals including surface-bound ·OH radicals generated on the catalyst surface.     

Biosorption of copper, zinc, cadmium and nickel by Chlorella vulgaris

The sorption capacity of the microalga, Chlorella vulgaris, was investigated using different metals (Cu, Zn, Cd and Ni), in both monometallic and bimetallic solutions. The final metal concentrations were significantly low. In the case of copper, an acid pretreatment (at pH 3) of the biomass was required to avoid an excessive increase in pH and the subsequent precipitation of metal during tests. This pretreatment was not necessary for the rest of the metals. The study of the influence of pH led to a greater metal uptake at a higher pH, suggesting a clear competition between metal cations and protons during the biosorption process. The biomass concentration was also a relevant variable, and the best sorption capacities were achieved at the lowest biomass concentration. pH also had a great influence on the elution of the metal retained by the biomass. The best recovery yields were obtained for the lower pH of the eluent solution. Sorption isotherms were well fitted to the Langmuir model, for both single-metal and two-metal systems. In both cases, the biomass showed a greater affinity for Cd.