改性丝瓜络纤维对水体日落黄的吸附特性

采用化学改性的方法将丝瓜络制备为阴离子吸附剂,并将其用于水体日落黄(SY)染料的吸附,分别考察了吸附剂的用量、日落黄染料的初始浓度(C0)、p H值、温度(K)、时间(T)5个因素对吸附效果的影响。通过模拟吸附等温曲线、吸附动力学以及热力学方程并通过比表面积(BET)和红外光谱(FTIR)分析改性丝瓜络吸附染料前后和丝瓜络改性前后的变化情况以此探究其吸附机理。结果表明,p H对吸附效果影响不明显;最大吸附量随温度升高而增大,在298 K温度时最大吸附量达到137 mg/g,是未改性丝瓜络的9.78倍。Langmuir方程拟合吸附过程描述最好,吸附类别为化学吸附。吸附过程符合伪二级动力学,是一个自发和吸热的过程。改性丝瓜络可以有效去除水体中的日落黄染料。     

基于GIS的太湖流域主要生态风险源危险度综合评价研究

以太湖流域主要生态风险源为评价对象,充分考虑多类型多等级风险源作用强度的差异性,构建了风险源危险度评价模型,并在此基础上依据风险源发生机率、强度及作用范围等建立了太湖流域洪涝、干旱、极端气象、土壤侵蚀及污染排放等主要生态风险源的危险度评价指标体系。在ArcGIS技术支持下,创建了太湖流域1 606个网格和24个县市的风险源危险度统计数据库,采用AHP权重法确定指标权重,运用叠加分析、空间分析等技术方法最终实现太湖流域单要素及综合生态风险源危险度的定量评价。结果表明流域内生态风险源的分布存在明显的空间分异规律。其中,高生态风险源危险区集中分布在环太湖北部一带,面积约占流域面积的1172%;较高危险区主要呈“西北 北 东北 东”半环状分布格局,所占面积约2452%,危险度较低的区域集中在流域西南部的苕溪流域一带,面积占1566%。此外,不同区域主导生态风险源组成亦不同,约599%的区域是以污染排放为主导生态风险源,主要分布在镇江 宜兴 长兴 安吉一线以东的地区;2545%的区域主导生态风险源为干旱,主要集中在镇江 宜兴 长兴 安吉一线以西;1244%的区域是以洪涝灾害为主导风险源,集中分布在湖州、宜兴等地;而以水土流失、极端气象灾害作为主导风险源地区相对较为分散,所占比例较小     

磷石膏水热法合成硫酸钙晶须

以磷石膏为原料,二水合硫酸钙、硫酸镁、甘油为添加剂,采用水热法合成硫酸钙晶须,考察了料浆含量、反应温度、反应时间、体系pH等因素对晶须的直径和长径比的影响;并采用SEM技术观察硫酸钙晶须的形貌。实验结果表明,当磷石膏含量2.5%（w）、反应温度130 ℃、反应时间4 h、体系pH 4时,制备得到的硫酸钙晶须长径比为56.24,平均直径为0.17 μm。SEM表征结果显示,硫酸钙晶须形貌规整、分散均匀、直径较小,达百纳米级。     

Heavy metal pollution in vegetables grown in the vicinity of a multi-metal mining area in Gejiu,China: total concentrations,speciation analysis,and health risk

A field survey was conducted to investigate the present situation and health risk of arsenic (As), lead (Pb), cadmium (Cd), copper (Cu), and zinc (Zn) in soils and vegetables in a multi-metal mining area, Gejiu, China. Furthermore, three vegetables (water spinach, potato, and summer squash) containing high metal concentrations were selected to further analyze metal speciation. The results showed that the average concentrations of five metals in soil exceeded the limiting values, and their bioavailable concentrations were significantly positively correlated to the total ones. Heavy metals in the edible parts of vegetables also exceeded the corresponding standards. The leaves of pakchoi, peppermint, and coriander had a strong metal-accumulative ability and they were not suitable for planting. Except the residue forms, the main forms of metals in the edible parts of three selected vegetables were ethanol-, NaCl-, and HAc-extractable fractions for As, Pb, and Cd, respectively; however, Cu was mainly presented as NaCl-extractable and Zn as HAc-extractable fractions. A high proportion of ethanol-extractable As showed that As bioactivity and toxic effects were the highest. Although the total and bioavailable Cd were high in soil, its speciation in vegetables was mainly presented as HAc-extractable fraction, which has a relatively low bioactivity. Lead and arsenic were imposing a serious threat on the local residents via vegetable consumption.     

Potential toxicity of amphenicol antibiotic: binding of chloramphenicol to human serum albumin

Antibiotics are widely used in daily life but their abuse has posed a potential threat to human health. To evaluate the toxicity of chloramphenicol (CAP) at the protein level, the interaction between CAP and human serum albumin (HSA) was investigated by fluorescence, Ultraviolet–visible (UV–Vis) absorption, Fourier transform infrared (FT-IR) spectroscopy and molecular docking methods. Fluorescence data revealed that the fluorescence quenching of HSA by CAP was the result of the formation of CAP–HSA complex, and the binding constant was determined to be 3.196?×?10⁴ L mol^?1 at 310 K. The thermodynamic determination indicated that the interaction was driven by enthalpy change and entropy change together, where the multiple hydrogen bonds (CAP and the residues Arg 222 and His 242 of HSA) and van der Waals forces were the dominant binding force. The site marker competition revealed that CAP bound into sub-domain IIA of HSA. The binding of CAP induced the drastic reduction in α-helix conformation and the significant enhancement in β-sheet conformation of HSA. Molecular docking study further confirmed the binding mode obtained by experimental study. This work provides a new quantitative evaluation method for antibiotics to cause the protein damage.     

抗铬菌株的筛选鉴定及其生物学特性和吸附特性

利用微生物分离纯化技术,在培养基中加入不同浓度的Cr3+、Cr6+,经过长时间驯化,从污染土壤中筛选出2株对Cr具有较高抗性的菌株(A和B),对其进行了形态、生理生化特性及分子生物学鉴定,并研究了其最佳生长条件及对Cr3+的生物吸附规律。结果表明,菌株A和B分别为蜡状芽孢杆菌(Bacillus cereus)和米根霉菌(Rhizopus oryzae)。菌株A和B的最适生长pH值均为7,最适生长温度均为30℃,最佳装液量为80~100 mL(250 mL摇瓶)。在培养时间一定时,随着Cr3+浓度的增加,菌株对Cr3+的吸附率减少,而生物吸附量则逐渐增大;在Cr3+浓度一定时,随着培养时间的延长,菌体对Cr3+的吸附率呈现出先增加后减少的趋势,这与生物吸附量的变化趋势基本一致。在Cr3+浓度为100 mg/L时,菌株A和B对Cr3+的吸附率达到最大,分别为51.47%和46.36%。     

鼠李糖脂洗脱氯丹和灭蚁灵污染场地土壤的工艺参数

优化了鼠李糖脂洗脱氯丹、灭蚁灵污染土壤的工艺条件,为开展有机氯农药污染场地土壤洗脱修复工程实践提供科学依据和技术参数。实验结果表明,随着洗脱剂———鼠李糖脂浓度的增加,氯丹和灭蚁灵的洗脱量呈现先增加后降低的趋势;洗脱时间和液固比对洗脱效果的影响趋势与浓度相同;在0~120 r/min范围内,氯丹和灭蚁灵洗脱量随着搅拌速度的增加而增大,80、120和200 r/min的洗脱量间差异不显著;单次洗脱量随洗脱次数的增加而降低,累计洗脱量则逐渐增大。综上所述,氯丹、灭蚁灵污染场地土壤鼠李糖脂洗脱的适宜工艺参数为鼠李糖浓度10 mmol/L,搅拌速度80 r/min,固液比1∶10,洗脱时间20 min,洗脱3次。     

Stability of 6:2 fluorotelomer sulfonate in advanced oxidation processes: degradation kinetics and pathway

Perfluorooctane sulfonate (PFOS), a widely used mist suppressant in hard chrome electroplating industry, has been listed in the Stockholm Convention for global ban. 6:2 Fluorotelomer sulfonate (6:2 FTS) acid and salts have been adopted as alternative products in the market, but no data about their abiotic degradation has been reported. In the present study, the degradability of 6:2 FTS potassium salt (6:2 FTS-K) was evaluated under various advanced oxidation processes, including ultraviolet (UV) irradiation, UV with hydrogen peroxide (H₂O₂), alkaline ozonation (O₃, pH = 11), peroxone (O₃/H₂O₂), and Fenton reagent oxidation (Fe²⁺/H₂O₂). UV/H₂O₂ was found to be the most effective approach, where the degradation of 6:2 FTS-K followed the pseudo-first-order kinetics. The intermediates were mainly shorter chain perfluoroalkyl carboxylic acid (C₇ to C₂), while sulfate (SO₄ ^2?) and fluoride (F^?) were found to be the final products. The high yields of SO₄ ^2? and F^? indicate that 6:2 FTS-K can be nearly completely desulfonated and defluorinated under UV/H₂O₂ condition. The degradation should firstly begin with the substitution of hydrogen atom by hydroxyl radicals, followed by desulfonation, carboxylation, and sequential “flake off” of CF₂ unit. Compared with PFOS which is inert in most advanced oxidation processes, 6:2 FTS-K is more degradable as the alternative.     

纳米TiO2-石墨烯光催化剂的水热合成及其光催化性能

以钛酸四正丁酯和石墨为原料,通过水热法制备了锐钛矿型为主的纳米TiO2复合光催化剂（纳米TiO2-石墨烯）,并采用XRD,FTIR,FESEM,TEM技术对其进行了表征。通过紫外光照射降解溶液中的罗丹明B（RhB）研究了TiO2-石墨烯的光催化活性,分析了初始罗丹明B质量浓度、催化剂加入量、溶液pH和催化剂使用次数等影响降解效果的因素。实验结果表明：在初始RhB质量浓度为20 mg/L、溶液pH为7.10、催化剂加入量为1.000 g/L的条件下,紫外光照射30 min时,纳米TiO2-石墨烯对RhB的降解率高达98.69%,明显高于纳米TiO2的44.69%;纳米TiO2-石墨烯稳定性较强,可多次重复使用。     

高效脱硫菌的筛选及其性能研究

从高硫污染的活性污泥中富集培养,分离纯化得到一株可以降解噻吩的菌株s_4,并对该菌株的形态特征进行观察。应用Design—Expert8．0．5b软件进行响应面优化实验,研究了反应时间、噻吩浓度、微生物浓度3个因素的组合对菌株s_4脱硫效果的影响,并拟合得到多元二次回归方程,得出最佳实验条件。拟合结果表明,当反应时间27．46h,噻吩浓度为1．04％,微生物浓度4．04％时,预测噻吩降解率为14．8％,通过验证得最佳条件下的降解率为14．3％,与预测值相符。