测定氨标样的两种方法比较

采用测定水中氨的方法与采用测定空气中氨的方法进行比较,分别用两种测定氨的方法对标样进行测定,得出用水中测定氨的方法测定"空气中的氨"标样比用空气中氨的方法更加简单、方便,结果较好.用两种方法分别对环境样品进行测定,测定结果基本一致,进一步验证了测定水中氨的方法可以用于"空气中的氨"测定.     

电极法测定植物低浓度氟影响因素浅析

测定含低浓度氟的植物样品时,常常受分析样品重量,溶液pH,样品浸取率,温度等因素影响使测定结果有偏差。经用先浸泡样品后测定与直接搅拌后测定两种方法进行比较,认为浸泡后测定,是减少误差提高测定质量的重要方法。     

紫外分光光度法测定污水COD值的误差分析研究

针对紫外分光光度法测定污水COD值的误差分析问题,给出了实验的仪器和试剂的配制方法,如测试主要仪器设备和主要试剂的配制,介绍了测定水样的采集地点,介绍了重铬酸钾法的测定原理及步骤,重铬酸钾法的测定原理和重铬酸钾法的测定步骤,紫外分光光度法的测定原理及步骤,如紫外分光光度法的测定原理和紫外分光光度法的测定步骤,并对结果进行了讨论,紫外分光光度法,标准曲线的确定,测定的结果比较和方法的准确度和精密度比较.     

土壤CEC测定的相关问题及解决对策

在参照《森林土壤阳离子交换量的测定》(LY/T 1243-1999)方法对大量土样的土壤阳离子交换量的分析测定中,总结出分析测定过程中遇到的若干问题,提出对此方法的改进对策,并归纳测定过程中的注意事项,以便分析人员在测定此项目时作参考,提高土壤阳离子交换量测定的结果的准确性和稳定性。     

用化学荧光溶氧仪测定生化需氧量(BOD5)研究

文章介绍了化学荧光溶氧仪法测定生化需氧量的测定方法,用该方法测定生化需氧量标准样品,得到的精密度和准确度均较好.通过与传统碘量法进行实际样品比对,用数理统计的方法对两种方法测定结果进行了比较,对于地表水和污水的测定,两种方法的测定结果无显著差异.建立的化学荧光溶氧仪测定BOD5方法精密度和准确度可以满足实际样品的测定.     

分光光度法与离子色谱法测定降水中铵离子的对比

采用分光光度法和离子色谱法测定降水中铵离子,比对研究两种方法的测定原理、标准曲线和检出限。结果表明,两种方法对标准样品和实际样品分析测定均能达到质控要求,测定结果基本一致。离子色谱法方便快捷,污染少,结果准确可靠,可以同时测定多种阳离子。     

砷、硒元素原子荧光法联合测定优化研究

为了进一步提高水体质量的检测精度,本文引入原子荧光法对水体中的砷、硒元素含量进行优化测定,通过分析元素组合与测定顺序、预处理试剂和还原剂的用量对联合测定结果的影响,进而提出了基于原子荧光法的砷、硒元素联合测定优化的过程,以期为后续水体中毒理指标的测定提供有价值的参考意见。     

底泥耗氧速率的测定方法比较

在对实验室法和现场法测定底泥耗氧速度（SOD）的步骤和操作参数综述中，对于实验室测定法。从底泥采样，测定容器，实验底泥厚度，上覆水，测定培养条件，溶解氧测定方法，溶解氧测定时间和测定间隔，空白样的测定以及SOD的计算等方面作了介绍；对于现场测定法，从测定容器，测定水力条件，溶解氧测定方法，空白水样的测定，溶解氧测定时间和测定间隔，SOD的计算方法等方面作了介绍，最后在原理，技术和费用上对以上2种方法加以比较。     

钼锑抗分光光度法测定总磷的精密度偏性试验分析

通过钼锑抗分光光度法测定总磷的精密度偏性试验及其结果分析,提出本标准方法用光程10mm比色皿比色测定时,由于测定的灵敏度较低,使总磷低浓度测定的精密度和准确度难于达到标准方法要求;建议钼锑抗分光光度法测定总磷时,最好选用30mm比色皿比色测定.     

原子荧光光度法同时测定土壤中砷、硒含量研究

土壤中砷和硒的测定有多种方法,一般对两种元素含量进行单独测定,过程比价繁琐,不利于批量分析。本文提出了一种可同时测定土壤中砷、硒含量的方法,该方法采用盐酸和高氯酸一次消解土样,用原子荧光光度法同时测定土壤中的砷、硒,具有操作简便、测定结果准确等特点。     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.     

Preparations of TiO2 film coated on foam nickel substrate by sol-gel processes and its photocatalytic activity for degradation of acetaldehyde

Anatase TiO2 films were successfully prepared on foam nickel substrates by sol-gel technique using tetrabutyl titanate as precursor. The characteristics of the TiO2 films were investigated by XPS, XRD, FE-SEM, TEM and UV-Vis absorption spectra. The photocatalytic activities of TiO2 films were investigated by photocatalytic degradation reactions of gaseous acetaldehyde, an indoor pollutant, under ultraviolet light irradiation. It was found that Ni^2＋ doping into TiO2 films due to the foam nickel substrates resulted in the extension of absorption edges of TiO2 films from UV region to visible light region. The pre-heating for foam nickel substrates resulted in the formation of NiO layer, which prevented effectively the injection of photogenerated electrons from TiO2 films to metal nickel. The TiO2 films displayed high photocatalytic activity for the degradation of acetaldehyde, and were enhanced by calcining the substrates and coating TiO2 films repeatedly. The high activity was mainly attributed to the improvement of the characteristics of substrate surface and the increase of active sites on photocatalyst.     

Reaction mode between Si and Fe and evaluation of optimal species in poly-silicic-ferric coagulant

A kind of Fe-polysilicate polymer, poly-silicic-ferric （PSF） coagulant was prepared by co-polymerization （hydroxylation of mixture of Fe^3＋ and fresh polysilicic acid （PS））, in which PSF0.5, PSF1 or PSF3 denotes Si/Fe molar ratio of 0.5, 1 or 3, respectively. The effects of Si/Fe ratio and reaction time （co-polymerization time or aging time） on the reaction mode between Si and Fe were studies, and the optimal species of PSF was evaluated by pH change during the preparation of PSF and coagulation tests. The results showed that the characteristics of PSF are largely affected by both reaction time and Si/Fe ratio. PSF is found to be a essential complex of Si, Fe, and many other ions. The reaction mode between Si and Fe differs with various Si/Fe ratios. The pH of PSF0.5, PSF1 or PSF3 tended to be stable when reaction time is 10, 25 or 55 rain, respectively, which is almost consistent with the time reaching the relative stable morphology that is just the optimal species of higher coagulation efficiency. The optimal reaction time reaching optimal species can be evaluated by measuring the pH change during the polymerization process.     

汽车排气尾流中微粒分布及其变化特性的研究

根据微粒核化、凝并及凝结模型对汽车排气尾流中微粒分布的变化特性进行了分析.结果表明,微粒的核化增加了排气尾流中超细微粒的数量;微粒的凝并和凝结将改变排气尾流中的微粒分布.在核化、凝并及凝结过程同时存在时,核化对微粒分布的影响相对较小,微粒分布的变化主要受凝并和凝结的作用.在排气管出口处,微粒的核化、凝并及凝结过程比较剧烈,微粒分布变化较大;随着距排气管出口距离的增加,微粒演变逐渐减弱.研究工作可以为汽车排放控制策略的确定以及汽车微粒对人体健康影响的研究提供依据.     

Activated carbons derived from oil palm empty-fruit bunches： Application to environmental problems

Activated carbons derived from oil palm empty fruit bunches （EFB） were investigated to find the suitability of its application for removal of phenol in aqueous solution through adsorption process, Two types of activation namely; thermal activation at 300, 500 and 800℃and physical activation at 150℃ （boiling treatment） were used for the production of the activated carbons. A control （untreated EFB） was used to compare the adsorption capacity of the activated carbons produced from these processes. The results indicated that the activated carbon derived at the temperature of 800℃ showed maximum absorption capacity in the aqueous solution of phenol. Batch adsorption studies showed an equilibrium time of 6 h for the activated carbon at 800℃. It was observed that the adsorption capacity was higher at lower values of pH （2-3） and higher value of initial concentration of phenol （200-300 mg/L）. The equilibrium data fitted better with the Freundlich adsorption isotherm compared to the Langmuir. Kinetic studies of phenol adsorption onto activated carbons were also studied to evaluate the adsorption rate. The estimated cost for production of activated carbon from EFB was shown in lower price （USD 0.50/kg of activated carbon） compared the activated carbon from other sources and processes.     

Impact of fertilization on chestnut growth, N and P concentrations in runo water on degraded slope land in South China

Growing fruit trees on the slopes of rolling hills in South China was causing serious environmental problems because of heavy application of chemical fertilizers and soil erosion. Suitable sources of fertilizers and proper rates of applications were of key importance to both crop yields and environmental protection. In this article, the impact of four fertilizers, i.e., inorganic compound fertilizer, organic compound fertilizer, pig manure compost, and peanut cake （peanut oil pressing residue）, on chestnut （Castanea mollissima Blume） growth on a slope in South China, and on the total N and total P concentrations in runoff waters have been investigated during two years of study, with an orthogonal experimental design. Results show that the organic compound fertilizer and peanut cake promote the heights of young chestnut trees compared to the control. In addition, peanut cake increases single-fruit weights and organic compound fertilizer raises single-seed weights. All the fertilizers increased the concentrations of total N and total P in runoff waters, except for organic compound fertilizer, in the first year experiment. The observed mean concentrations of total N varied from 1.6 mg/L to 3.2 mg/L and P from 0.12 mg/L to 0.22 mg/L, which were increased with the amount of fertilizer applications, with no pattern of direct proportion. On the basis of these experiment results, organic compound fertilizer at 2 kg/tree and peanut cake at 1 kg/tree are recommended to maximize chestnut growth and minimize water pollution.     

Effects of humic acid coatings on phenanthrene sorption to black carbon

Black carbon (BC) can strongly adsorb hydrophobic organic compounds (HOCs).The HOC sorption to coated BC could be attenuated in soil and sediment compared with that of the parent BC.To study the potential causes of the sorption attenuation,humic acid (HA) and BC were isolated.Phenanthrene (PHE) was selected as the representative of HOCs.BC was coated with the precipitated HA.The PHE sorption to the HA-coated BC was determined.The HA coatings on BC could result in the significant sorption attenuation of PHE to BC.The attenuation varied in different HA origin and was positively correlated to the aromaticity of HA.The attenuation could be explained by the direct competition between HA and PHE for the available sorption sites on BC and the reduction of the available sorption sites as a result of the pore blockage of BC caused by the HA coatings.Therefore,the HA coatings on BC was one potential cause of the attenuation of HOC sorption to BC in soil and sediment.     

基质对人工湿地污水蒸发量及净化能力的影响

选择5种常见的人工湿地基质(土、沙、沙+土、有机质+沙和有机质+沙+土),研究了不同基质对污水蒸发量及净化能力的影响.结果表明,不同基质对污水的蒸发量存在差异,其大小顺序为:(有机质+沙+土)>(有机质+沙)>沙>土>(沙+土);有机质+沙+土和有机质+沙2种基质的污水蒸发量显著高于其他基质(P<0.05)并与其温度比较高有关.5种基质的温度存在差异,有机质+沙+土的温度显著高于土和沙两种基质的温度(P<0.05),有机质+沙+土的温度比土的温度高2.2℃;相关分析显示,基质的污水蒸发量与高锰酸钾指数去除率和氨氮去除率呈正相关,其中与氨氮去除率呈显著正相关(P<0.05).基质加入有机质可增加基质的温度,提高基质的污水蒸发量,有利于提高基质对有机物和氮的去除效率.