微电解/Fenton法预处理炼油碱渣的实验

采用铁碳微电解/Fenton试剂组合工艺对炼油碱渣废水混凝沉淀处理后出水,进行降解研究。实验结果表明:pH值为3,废水与铁碳填料的体积比为2∶1,微电解反应时间2 h,曝气的条件下,废水的处理效果最好,COD的去除率超过42.5%。Fenton试剂处理微电解反应出水的最佳操作条件是:pH值在2～3之间、反应时间2.5 h、Fe2+浓度为800 mg/L左右、H2O2浓度为0.25 mol/L,在此条件下,Fenton试剂处理微电解处理后的炼油碱渣废水COD平均去除率为63.8%以上,微电解/Fenton工艺对COD的总去除率在79.2%左右,可生化性由0.16提高到0.56。     

改性粉煤灰在处理锑矿选矿废水中的应用

针对锑矿选矿废水中锑和丁基黄原酸钠严重超标的问题,用酸改性粉煤灰对其进行吸附处理.试验结果表明,当改性粉煤灰处理选矿废水的最佳质量体积比(g.mL-1)为1:100,pH值为3,静置时间为4h时,可以将选矿废水中的锑浓度从28.611mg.L-1降到0.05mg.L-1以下,去除率达99.8%以上;废水中的丁基黄原酸钠浓度可从0.373mg.L-1降到0.02mg.L-1以下,去除率达95.0%以上.处理废水后的改性粉煤灰用硫酸-硝酸浸提,浸出液中重金属离子浓度均低于国家浸出毒性标准,表明改性粉煤灰是一种很好的锑矿选矿废水处理剂.     

实验室有机废水处理方法探讨

对高校实验室废水的来源、种类及特性进行了阐述,同时对实验室废水的处理及污染防治措施进行了综合论述.以实验室废水为研究对象,通过普通蒸馏回收水样中的有机溶剂,采用Fenton试剂法氧化处理废水.实验结果表明:回收废水中的有机溶剂可使废水的COD值降低30%以上;通过正交试验确定了Fenton氧化反应的最佳操作条件,在此条件下,废水的COD去除率达到74.5%.     

Fenton试剂催化氧化--混凝法处理焦化废水的实验研究

用Fenton试剂结合自制聚硅硫酸铝对焦化废水进行了催化氧化—混凝试验研究 ,选择了最佳的工作条件。结果表明 ,经氧化—混凝处理后废水的COD从 1 1 73mg/L降至 38.2mg/L ,去除率达 96 .7%。研究中还发现 ,Fenton试剂具有将废水的 pH值调节为 2 .5～ 3的特性 ,为该工艺实际处理焦化废水提供了科学依据     

粉煤灰对印染废水的吸附处理研究

研究了粉煤灰对印染废水吸附脱色处理效果,确定了最佳脱色条件和穿透曲线的特征,并探讨了其对印染废水CODcr的去除率。结果表明：对色度都为700倍、CODcr分别为664.2 mg/L、947.1 mg/L的红、蓝色印染废水,粉煤灰处理的最佳用量分别为18 g和16 g,最佳吸附接触时间分别为2.0 h和2.5 h,最佳pH5－7,穿透体积分别为115 mL和120 mL,脱色率均可达到95（以上;CODcr的去除率分别为81.5%和41.1%。     

印染行业退煮漂废水处理工艺的实验研究

研究"混凝沉淀-Fenton试剂氧化"工艺处理印染行业退煮漂废水,结果表明,在选用的四种混凝剂中,最佳混凝药剂是聚硅酸硫酸铝(PASS),最佳投药量为3 g/L,适宜反应pH值为4~5;用Fenton试剂处理混凝沉淀后的上清液,最佳氧化工艺条件:反应时间为1.5 h、pH为3~5、H2O2投加量为0.2 mol/L、n(H2O2)∶n(Fe2+)值为1.5;经过"混凝沉淀-Fenton试剂氧化"全流程处理后,废水COD cr、BOD5、色度、SS均有较高的处理效果,COD cr去除率达93.55%、BOD5去除率达89.77%、色度去除率达85.71%、SS去除率达95.9%。     

芬顿试剂处理苯酚废水的实验研究

本文针对含苯酚废水来源广、危害大、成分复杂的特点,采用Fenton技术对苯酚废水的处理效果进行了研究,考察了催化剂的用量、氧化剂的用量、粉煤灰的用量和pH值对芬顿试剂氧化苯酚的影响。研究表明,当pH值为3,H2O2的加入量为0.3mol,Fe(II)的加入量为0.5mmo1的条件下,反应在10min内基本完成,苯酚的去除率达到97%;当Fenton试剂的组分不变,粉煤灰投加量为0.6g/L时,苯酚降解率在99%以上,去除效果稳定。     

微电解＋Fenton试剂预处理染料废水工程实例研究

采用微电解＋Fenton试剂预处理是有效地解决染料废水不可生化性和色度的一种简单方便技术。通过工程实践证明,采用微电解＋Fenton预处理染料废水能够提高其可生化性,降低色度,联用传统的生化处理技术,处理后的染料废水能够实现达标排放,污染物COD的平均去除率达97%以上。该工艺处理系统运行2年,效果明显、稳定可靠。     

Fenton法处理染发剂废水的试验分析

Fenton法是处理难降解有机污染物的一种有效方法。采用Fenton法处理染发废水,试验研究了影响CODcr去除率的各种因素,确定最佳工艺条件:pH为4.0、FeSO_4·7H_2O用量为2.05g/L、30%H_2O_2用量为12.2ml/L,在此条件下废水的CODcr去除率可达87.5%。     

粉煤灰改性处理啤酒废水的研究

以Na2CO3、CaO、HCI、H2SO4等多种试剂作改性剂对粉煤灰进行改性处理,得到改性粉煤灰,并以改性粉煤灰处理啤酒废水,研究了粉煤灰改性的最佳条件及改性粉煤灰处理啤酒废水的机理。结果表明:改性后粉煤灰的吸附混凝性能有显著的提高,啤酒废水中COD的去除率从50%增加到89%。实验确定Na2CO3为最佳改性剂,最佳改性条件为改性剂与粉煤灰的用量比为10mL:5g,室温下搅拌5min,静置30min。     

硝化抑制剂双氰胺对菜地土壤N_2O排放的影响

采用原状土柱试验研究了施用硝化抑制剂双氰胺（DCD）对菜地（小白菜和辣椒）土壤N2O排放的影响.结果表明,施用DCD能显著降低菜地土壤N2O排放通量和排放总量,小白菜未施用DCD时施氮处理土壤N2 O排放总量为0.22 kg.hm-2,施用DCD后则显著减少至0.11 kg.hm-2,相当于减少了49.33%的土壤N2...     

Effect of fertilizer and water content on N2O emission from three plantation soils in South China

Introduction Nitrousoxide(N2O)isoneofthemostimportantgreen housegases,whichcontributestoglobalwarmingand consumptionofO3inthestratosphere(Breuer,2000,Solomon,1999).N2Oconcentrationincreasesatarateof0.25%peryear,57%ofwhichisderivedfromthesoildue tonitrific…     

土壤净化槽对农村污水中内分泌干扰物的去除效果

以土壤净化槽污水处理系统为研究对象,采用固相萃取-色谱质谱检测方法,分析了云南洱海流域农村污水中3种天然雌激素类内分泌干扰物〔E1(雌酮)、E2(雌二醇)和E3(雌三醇)〕和2种人工合成内分泌干扰物〔EE2(炔雌醇)和BPA(双酚A)〕的质量浓度与去除效果. 结果表明,洱海流域农村污水中天然雌激素的质量浓度远高于人工合成内分泌干扰物,E1与E2为污水中天然雌激素内分泌干扰物的主要成分,占87.1%~99.2%. 土壤净化槽对天然雌激素类内分泌干扰物、EE2和BPA的净化能力分别为1.42~168.21、0.64和3.48mg/(m2·a). E1、E2和E3在土壤中的平均残留率分别为4.3%、6.3%和3.8%,其中90%以上的雌激素物质在土壤净化槽系统中被降解或转化. 土壤净化槽对天然雌激素、EE2和BPA的平均去除率分别为70.3%、63.6%和77.8%,对常规污染物COD_Cr(69.8%)、TP(88.7%)、TN(57.2%)和NH₃-N(88.7%)的去除效果也较好. 土壤净化槽可以有效去除村落污水中的内分泌干扰物、有机物以及氮磷污染物,对削减村镇面源污染、减少入湖污染负荷以及改善流域内的水环境质量具有重要作用.      

Elevated CO2 changes the moderate shade tolerance of yellow birch seedlings

To demonstrate the existence of light thresholds in plant growth and to examine the effects of elevated CO2 on the shade tolerance of a tree species, an experiment consisting of a completely randomized design for a total of 96 yellow birch (Betula alleghaniensis Britton) seedlings was conducted with 3 light levels (2.9%, 7.7%, 26.1% of full sunlight)×2 CO2 levels (350 and 700±10 ppm) with 4 replications in a phytotron. The study proved that thresholds exist and they vary in different plant organs. In ambient CO2, the thresholds were 13.3%, 18.7%, 15.0%, 15.2%, and 15.6% of full sunlight for stem, leaf, root, total plant biomass, and the averaged value, respectively. In 700 ppm CO2, the corresponding thresholds were 16.7%, 21.3%, 18.1%, 21.7% and 19.5% for stem, leaf, root, total plant biomass, and the averaged value, respectively. The lowest threshold in the stem is an indicator of the minimal light intensity for regular growth for seedlings of this species. Below this threshold, light-stressful growth occurs. The result of a paired t-test indicated that the thresholds in elevated CO2 were significantly higher than in ambient CO2. This suggests that yellow birch will lose its moderate shade tolerance, evolutionally becoming a shade-intolerant species, and that it may become more difficult to naturally regenerate in the future.     

Effects of free iron oxyhydrates and soil organic matter on copper sorption-desorption behavior by size fractions of aggregates from two paddy soils

Effects of free iron oxyhydrates (Fed) and soil organic matter (SOM) on copper (Cu2+) sorption-desorption behavior by size fractions of aggregates from two typical paddy soils (Ferric-Accumulic Stagnic Anthrosol (Soil H) and Gleyic Stagnic Anthrosol (Soil W)) were investigated with and without treatment of dithionite-citrate-bicarbonate and of H2O2. The size fractions of aggregates were obtained from the undisturbed bulk topsoil using a low energy ultrasonic dispersion procedure. Experiments of equilibrium sorption and subsequent desorption were conducted at soil water ratio of 1:20, 25℃. For Soil H, Cu2+ sorption capacity of the DCB-treated size fractions was decreased by 5.9% for fine sand fraction, by 40.4% for coarse sand fraction, in comparison to 2.9% for the bulk sample. However, Cu2+ sorption capacities of the H2O2-treated fractions were decreased by over 80% for the coarse sand fraction and by 15% for the clay-sized fraction in comparison to 88% for bulk soil. For Soil W, Cu2+ sorption capacity of the DCB-treated size fraction was decreased by 30% for the coarse sand fraction and by over 75% for silt sand fraction in comparison to 44.5% for the bulk sample. Cu2+ sorption capacities of the H2O2-treated fractions were decreased by only 2.0% for the coarse sand fraction and by 15% for the fine sand fraction in comparison to by 3.4% for bulk soil. However, Cu2+ desorption rates were increased much in H2O2-treated samples by over 80% except the clay-sized fraction (only 9.5%) for Soil H. While removal of SOM with H2O2 tendend to increase desorption rate, DCB- and H2O2-treatments caused decrease in Cu2+ retention capacity of size fractions. Particularly, there hardly remained Cu2+ retention capacity by size fractions from Soil H after H2O2 treatment except for clay-sized fraction. These findings supported again the dominance of the coarse sand fraction in sorption of metals and the preference of absorbed metals bound to SOM in differently stabilized status among the size fractions. Thus, enrichment and turnover of SOM in paddy soils may have great effects on metal retention and chemical mobility in paddy soils.     

N2:O emissions from a cultivated Andisol after application of nitrogen fertilizers with or without nitrification inhibitor under soil moisture regime

IntroductionNitrousoxide (N2 O)isoneoftheenvironmentallyimportanttracegases ,currentlyaccountingfor 2 %—4 %oftotalGreenhouseWarmingPotential (GWP ) .Itisalsoinvolvedinthedepletionofstratosphericozone .SoilhasbeenknownasthemajorsourceofN2 O ,accountingfor 6 5 %oftotalglobalemissions(Prather,1995 ) .Thus,reducingN2 Oemissionsfromsoilsisamaintaskfortheprotectionoftheglobalatmosphere .N2 Oisproducedastheresultofsoilmicrobialprocesses ,primarillybynitrification ,whentheoxidationhappensofNH+…     

Improved method for analyzing the degradation of estrogens in water by solid-phase extraction coupled with ultra performance liquid chromatography-ultraviolet detection

We established an improved method for the determination of four estrogens including estriol (E3), 17 -estradiol (E2), 17 -ethynylestrodiol (EE2) and estrone (E1) in water. The method consisted of solid-phase extraction (0.5 L water) and subsequent analysis of analytes by ultra-performance liquid chromatography (UPLC) with an ultraviolet detector (UVD). Base-line separation was achieved for all studied estrogens using a column (50 mm 2.1 mm) packed with 1.7 m particle size stationary phase. Recovery was higher than 88% and detection limits ranged between 12.5–23.7 ng/L for the four estrogens, with the RSD ranging from 7% to 11%. The method was successfully applied to determine E2 and EE2 in simulated natural water, which found that about 70% of E2 was degraded (with a half-life of about 30 hr) within 48 hr and about 55% of EE2 was degraded (with a half-life of about 36 hr). Low levels of E1 were found, however E3 was undetectable during the process.     

Size distribution, directional source contributions and pollution status of PM from Chengdu, China during a long-term sampling campaign

Long-term and synchronous monitoring of PM₁₀ and PM_2.5 was conducted in Chengdu in China from 2007 to 2013. The levels, variations, compositions and size distributions were investigated. The sources were quantified by two-way and three-way receptor models (PMF2, ME2-2way and ME2-3way). Consistent results were found: the primary source categories contributed 63.4% (PMF2), 64.8% (ME2-2way) and 66.8% (ME2-3way) to PM₁₀, and contributed 60.9% (PMF2), 65.5% (ME2-2way) and 61.0% (ME2-3way) to PM_2.5. Secondary sources contributed 31.8% (PMF2), 32.9% (ME2-2way) and 31.7% (ME2-3way) to PM₁₀, and 35.0% (PMF2), 33.8% (ME2-2way) and 36.0% (ME2-3way) to PM_2.5. The size distribution of source categories was estimated better by the ME2-3way method. The three-way model can simultaneously consider chemical species, temporal variability and PM sizes, while a two-way model independently computes datasets of different sizes. A method called source directional apportionment (SDA) was employed to quantify the contributions from various directions for each source category. Crustal dust from east-north-east (ENE) contributed the highest to both PM₁₀ (12.7%) and PM_2.5 (9.7%) in Chengdu, followed by the crustal dust from south-east (SE) for PM₁₀ (9.8%) and secondary nitrate & secondary organic carbon from ENE for PM_2.5 (9.6%). Source contributions from different directions are associated with meteorological conditions, source locations and emission patterns during the sampling period. These findings and methods provide useful tools to better understand PM pollution status and to develop effective pollution control strategies.     

Chemodynamics of heavy metals in long-term contaminated soils：Metal speciation in soil solution

The concentration and speciation of heavy metals in soil solution isolated from long-term contaminated soils were investigated. The soil solution was extracted at 70% maximum water holding capacity (MWHC) after equilibration for 24 h. The free metal concentrations (Cd2+, Cu2+, Pb2+, and Zn2+) in soil solution were determined using the Donnan membrane technique (DMT). Initially the DMT was validated using artificial solutions where the percentage of free metal ions were significantly correlated with the percentages predicted using MINTEQA2. However, there was a significant difference between the absolute free ion concentrations predicted by MINTEQA2 and the values determined by the DMT. This was due to the significant metal adsorption onto the cation exchange membrane used in the DMT with 20%, 28%, 44%, and 8% mass loss of the initial total concentration of Cd, Cu, Pb, and Zn in solution, respectively. This could result in a significant error in the determination of free metal ions when using DMT if no allowance for membrane cation adsorption was made. Relative to the total soluble metal concentrations the amounts of free Cd2+ (3%–52%) and Zn2+ (11%–72%) in soil solutions were generally higher than those of Cu2+ (0.2%–30%) and Pb2+ (0.6%–10%). Among the key soil solution properties, dissolved heavy metal concentrations were the most significant factor governing free metal ion concentrations. Soil solution pH showed only a weak relationship with free metal ion partitioning coefficients (Kp) and dissolved organic carbon did not show any significant influence on Kp.     

Tuning the fill percentage in the hydrothermal synthesis process to increase catalyst performance for ozone decomposition

The performance of Ce-OMS-2 catalysts was improved by tuning the fill percentage in the hydrothermal synthesis process to increase the oxygen vacancy density. The Ce-OMS-2 samples were prepared with different fill percentages by means of a hydrothermal approach (i.e. 80%, 70%, 50% and 30%). Ce-OMS-2 with 80% fill percentage (Ce-OMS-2-80%) showed ozone conversion of 97%, and a lifetime experiment carried out for more than 20?days showed that the activity of the catalyst still remained satisfactorily high (91%). For Ce-OMS-2-80%, Mn ions in the framework as well as K ions in the tunnel sites were replaced by Ce⁴⁺, while for the others only Mn ions were replaced. O₂-TPD and H₂-TPR measurements proved that the Ce-OMS-2-80% catalyst possessed the greatest number of mobile surface oxygen species. XPS and XAFS showed that increasing the fill percentage can reduce the AOS of Mn and augment the amount of oxygen vacancies. The active sites, which accelerate the elimination of O₃, can be enriched by increasing the oxygen vacancies. These findings indicate that increasing ozone removal can be achieved by tuning the fill percentage in the hydrothermal synthesis process.