纳米材料在痕量重金属离子测定中的应用

介绍了纳米材料的吸附性能,评述了影响其分离富集重金属离子效果的主要因素,综述了纳米金属氧化物、碳纳米管及其他纳米材料在痕量重金属离子测定中的应用进展,提出提高纳米吸附材料的选择性和稳定性,开发便携式商品化的纳米材料萃取小柱是今后的发展方向.     

不同亲疏水性质纳米氧化铝存在下铜对斜生栅藻毒性效应的研究

纳米氧化铝是应用非常广泛的一类人工纳米材料。当它被释放到水环境中后,会与环境中原有的重金属发生相互作用并对其毒性产生影响。文章研究了不同亲疏水性质的纳米氧化铝存在下铜对斜生栅藻的毒性效应,测定了藻细胞的生长抑制、金属积累及超氧化物歧化酶、谷胱甘肽、丙二醛等生化指标的变化。结果表明,纳米氧化铝显著降低了铜离子对藻细胞的生长抑制,藻细胞内铜的积累量及氧化损伤降低。但不同亲疏水性质的纳米氧化铝之间并不存在显著差别。这可能是由于纳米氧化铝对水中的铜离子发生了吸附,间接降低了藻液中的不稳态铜的浓度,从而减轻了铜对藻细胞的毒害。而纳米氧化铝的不同亲疏水性质对吸附水中铜离子的能力没有显著的影响。     

氨基化有机-无机杂化整体柱分离富集环境水中五价砷

将四乙氧基硅烷(TEOS)和N-(β-氨乙基)-γ-氨丙基三乙氧基硅烷(AEAPTES)作为共聚前体,采用在毛细管内原位聚合的方式制备得到氨基功能化的有机-无机杂化整体柱,将其作为针式固相微萃取(SPME)介质,建立了现场分离富集环境水中As(V)的SPME方法,优化了有机-无机杂化整体柱富集As(V)的实验条件,并研究了整体柱对As(V)的吸附/洗脱性能和富集能力,实现了环境水样中As(V)的高效、快速、高选择性检测。     

放射性核素污染及监测(续一)

3　放射性核素从大气向陆地和水环境迁移3.1　湿沉降和干沉降自然界中的放射性核素分为天然放射性核素和人工放射性核素2种,核试验和核电站泄漏事故向大气中排放的放射性核素主要是后者。放射性沉降对海域、陆地和地表水产生污染,并经历化学反应、形态变化、生物浓缩、沉降吸收或吸附等反应过程后,一部分污染物蓄积在土壤、水系或生物体内[14,15]。天然放射性核素包括地球形成以来原始的放射性核素以及宇宙射线生成的放射性核素,一般存在于海洋、地壳内和地表面,而且会迁移至水环境,与人工放射性核素具有同样复杂的迁移转化行为。核试验和核…     

复合型聚合氯化铁絮凝剂的研究进展

介绍了聚合氯化铁（PFC）的几种制备方法，重点介绍了利用氯酸钠作氧化剂直接氧化钢铁盐酸酸洗废液的方法制备PFC．针对目前PFC得不到广泛应用的实际，提出了针对PFC的多种改性方法．如在聚合铁的制备过程中引入聚硅酸该絮凝剂同时具有电中和及吸附架桥作用；又如加入无机絮凝剂聚合氯化铝制成的聚合氯化铝铁，加入有机絮凝剂制成的有机铁盐复合絮凝剂．并且提出了聚合氯化铁今后的发展趋势．     

牛骨炭对水溶液中Hg（Ⅱ）吸附性的研究

以牛骨为原料，氯化锌为活化剂制备牛骨基炭，通过静态吸附试验研究了牛骨炭对水中Hg（Ⅱ）的吸附效果并确定了影响吸附性能的因素。研究结果表明：牛骨炭对Hg（Ⅱ）的最佳吸附时间约为2h、吸附温度为25℃、pH值为1、投加量为0．1g、吸附溶液的最大初始浓度为600mg／L，其最大吸附容量Q^0为43．1mg／g，吸附行为符合Freundl—ich吸附等温模型；通过BET分析和扫描电镜（SEM）等手段表征了牛骨炭的孔结构参数及形貌特征，经分析，所制备牛骨炭的孔径分布为中孔。     

BDE-47在土壤矿物质与有机质上的吸附解吸特征

以多溴联苯醚典型单体2，2′，4，4′?四溴联苯醚（BDE?47）为研究对象，阐明了其在土壤矿物质与有机质上的吸附解吸行为及特征。结果表明：土壤中无机矿物质对BDE?47的吸附贡献不大，而有机质是调控BDE?47在土壤中吸附行为的关键组分；有机质对BDE?47的吸附能力与其有机碳含量和物理化学特性相关；BDE?47在腐殖酸上的解吸存在显著的滞后现象。     

甲烷气体标准样品的研制

对称量制备甲烷气体标准样品的制备方法进行了详细研究 ,对可能引起甲烷量值不确定度的各种误差来源进行了分析。文中提出的甲烷气体标准样品制备方法具有很好的重现性 ,所制备的甲烷气体标准样品具有良好的压力稳定性并已能在三种气瓶中稳定保存 1 8个月 ,其量值准确、可比 ,并已在全国环境监测网试用。     

壳聚糖对Sb(III)的吸附动力学和热力学研究

论文通过研究壳聚糖对Sb(III)的吸附行为,分析了其吸附热力学和动力学特性,初步探讨了吸附机理。结果表明,在研究的浓度范围内,壳聚糖对Sb(III)的吸附行为符合Freundlich和Langmuir等温方程;不同温度下,壳聚糖吸附Sb(III)的吸附焓变ΔH、自由能变ΔG和吸附熵变ΔS均为负值,表明吸附是一个自发、放热的过程,降低温度有利于吸附的进行;壳聚糖对Sb(III)的吸附行为可用Langmuir单分子层吸附机理解释,且求得吸附表观活化能38.36kJ/mol和Lagergren一级速率常数0.80h-     

葫芦脲聚合膜的制备及其在水体被动采样技术中的应用

基于葫芦脲的超分子特性,以醋酸纤维素为载体,制备了葫芦脲膜,采用傅里叶红外光谱、扫描电镜、热重分析对膜的性能进行了表征,研究了葫芦脲膜对三氯生(TCS)和三氯卡班(TCC)的吸附性能,验证了以葫芦脲膜为结合相的被动采样技术测定2种物质的可行性。结果表明:葫芦脲分子确实被引入到醋酸纤维素中,相比于醋酸纤维素膜,葫芦脲膜具有更强的热稳定性和吸附性能;以葫芦脲膜为结合相的被动采样装置在不同环境因素(pH值、离子强度、可溶性有机质)下都具有良好的工作稳定性;将该装置布设到南京市秦淮河中的2个采样点,野外实验验证了该采样装置应用于监测实际水体中的TCS和TCC的可行性。     

核电厂放射性流出物监测工作探讨

简述了放射性流出物监测的重要性,分析了我国核电厂放射性流出物监测中存在问题,探讨了借鉴国际原子能机构安全及相关标准开展我国核电厂放射性流出物监测的管理机制、监测方案、监测报告和质量保证等具体要求与方法,并提出提升技术基础能力、完善法规标准、加强监管力度的建议.     

Estimation of Model VII humic binding constants for Pd2+, Sn2+, U4+, NpO2(2+), Pu4+ and PuO2(2+)

Using previously established procedures that utilise linear free energy relationships, we estimated binding constants for the Windermere Humic Aqueous Model VII (WHAM/Model VII) for several radionuclide cations (Pd(2+), Sn(2+), U(4+), NpO(2)(2+), Pu(4+) and PuO(2)(2+)). This extends the number of cations that can be calculated with the model above the 40 included in the original Model VII work. When combined with equilibrium constants for inorganic species this allows the calculation of equilibrium distributions of chemical species under a wide range of conditions.     

Analytical approaches to the determination of phosphorus partitioning patterns in sediments

Three methods for phosphorus fractionation in sediments based on chemical extractions have been applied to fourteen aquatic sediment samples of different origin and characteristics. Two of the methods used different approaches to obtain the inorganic fractions. The Hieltjes and Lijklema procedure (HL) uses strong acids or bases, whereas the Golterman procedure (G) uses chelating reagents. The third one, the Standards, Measurements and Testing (SMT) protocol, was proposed in the frame of the SMT Programme (European Commission) which aimed to provide harmonisation and the validation of such methodologies. This harmonised procedure was also used for the certification of the extractable phosphorus contents in a sediment certified reference material (CRM BCR 684). Principal component analysis (PCA) was used to group sediments according to their composition and the three extraction methods were applied to the samples including CRM BCR 684. The data obtained show that there is some correlation between the results from the three methods when considering the organic and the residual fractions together. The SMT and the HL methods are the most comparable, whereas the G method, using a different type of reagent, yields different distribution patterns depending on sample composition. In relation to the inorganic phosphorus, the three methods give similar information, although the distribution between non-apatite and apatite fractions can be different.     

A review on applicability of naturally available adsorbents for the removal of hazardous dyes from aqueous waste

The effluent water of many industries, such as textiles, leather, paper, printing, cosmetics, etc., contains large amount of hazardous dyes. There is huge number of treatment processes as well as adsorbent which are available for the processing of this effluent water-containing dye content. The applicability of naturally available low cast and eco-friendly adsorbents, for the removal of hazardous dyes from aqueous waste by adsorption treatment, has been reviewed. In this review paper, we have provided a compiled list of low-cost, easily available, safe to handle, and easy-to-dispose-off adsorbents. These adsorbents have been classified into five different categories on the basis of their state of availability: (1) waste materials from agriculture and industry, (2) fruit waste, (3) plant waste, (4) natural inorganic materials, and (5) bioadsorbents. Some of the treated adsorbents have shown good adsorption capacities for methylene blue, congo red, crystal violet, rhodamine B, basic red, etc., but this adsorption process is highly pH dependent, and the pH of the medium plays an important role in the treatment process. Thus, in this review paper, we have made some efforts to discuss the role of pH in the treatment of wastewater.     

Penetration of polar brominated DBPs through the activated carbon columns during total organic bromine analysis

Total organic bromine (TOBr) is a collective parameter representing all the brominated organic disinfection byproducts (DBPs) in water samples. TOBr can be measured using the adsorption-pyrolysis method according to Standard Method 5320B. This method involves that brominated organic DBPs are separated from inorganic halides and concentrated from aqueous solution by adsorption onto the activated carbon (AC). Previous studies have reported that some commonly known brominated DBPs can partially penetrate through the AC during this adsorption step. In this work, the penetration of polar brominated DBPs through AC and ozone-modified AC was explored with two simulated drinking water samples and one chlorinated wastewater effluent sample. Polar brominated DBPs were selectively detected with a novel precursor ion scan method using electrospray ionization-triple quadrupole mass spectrometry. The results show that 3.4% and 10.4% of polar brominated DBPs (in terms of total ion intensity) in the chlorinated Suwannee River fulvic acid and humic acid samples, respectively, penetrated through the AC, and 19.6% of polar brominated DBPs in the chlorinated secondary wastewater effluent sample penetrated through the AC. The ozone-modification of AC minimized the penetration of polar brominated DBPs during the TOBr analysis.     

Analysis of the key intermediates of RDX (hexahydro-1,3,5-trinitro-1,3,5-triazine) in groundwater: occurrence, stability and preservation

Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) is a widely used explosive that is present in soils at a number of military sites, including training and testing ranges. Because of its relatively weak adsorption to soil, RDX frequently migrates through the unsaturated zone and causes groundwater contamination. In the environment, RDX can transform to produce mono-, di-, and tri-nitroso derivatives (MNX, DNX, and TNX) and the ring cleavage products methylenedinitramine (MEDINA) and 4-nitro-2,4-diazabutanal (NDAB). The present study was undertaken to analyze RDX and its products in groundwater samples taken from various US military sites. The stability of some of the common transformation intermediates of RDX, including the nitroso derivatives, NDAB and MEDINA, under typical conditions in a groundwater aquifer is not well understood, and appropriate preservation methods for these compounds have not been established. Therefore, we studied the inherent stability of these compounds in deionized water and in groundwater, and evaluated various preservation techniques, including adjustment of pH, temperature, and salinity. NDAB and nitroso derivatives were stable under typical ambient environmental conditions, but MEDINA was highly unstable. The addition of sea salts (10% w/v) was found to stabilize MEDINA when the samples were stored at 4 °C. Using appropriate preservation techniques, we detected nitroso derivatives and NDAB, but no MEDINA, at some of the sites investigated. Stabilizing RDX intermediate products in field samples to allow detection is important because the presence of any of these chemicals can indicate past contamination by RDX and provide insight into the occurrence of in situ natural attenuation.     

Fish Bone as a Low-Cost Adsorbent for Dye Removal from Wastewater: Response Surface Methodology and Classical Method

This research studied the application of fish bone as a low-cost adsorbent for the removal of two basic dyes (C.I. Basic Blue 41 and C.I. Basic Yellow 28) from textile wastewaters. The surface morphology and functional groups of the fish bone was studied by scanning electron microscopy and Fourier transform infrared, respectively. The experiments were designed in two methods: classical method and response surface methodology (RSM). The effect of operating parameters including pH, initial dye concentration, adsorbent dosage, and inorganic salts was investigated by both methods. The optimum conditions to satisfy 75 % of dye removal for both dyes were predicted by RSM method and the results were very close to the experimental values. So, it was concluded that the fish bone can be used as a low-cost adsorbent for dye removal from effluents.     

ICP-MS在环境分析中的质谱干扰及其消除

针对环境领域20个无机元素的ICP-MS分析,总结了同量异位素、氧化物和双电荷、多原子离子等质谱干扰,探讨了影响质谱干扰的因素,提出了消除或降低每个元素质谱干扰的方法:选取合适的同位素、编辑校正方程、选择合适的模式、设置合理的等离子条件等,为建立ICP-MS相关环境标准方法提供参考。     

Preparation of 2-mercaptobenzothiazole-derivatized mesoporous silica and removal of Hg(ii) from aqueous solution

Mesoporous silicas (SBA-15 and MCM-41) have been functionalized by two different methods. Using the heterogeneous route the silylating agent, 3-chloropropyltriethoxysilane, was initially immobilized onto the mesoporous silica surface to give the chlorinated mesoporous silica Cl-SBA-15 or Cl-MCM-41. In a second reaction a multifunctionalized N,S donor compound (2-mercaptobenzothiazol) was incorporated to obtain the functionalized silicas denoted as MBT-SBA-15-Het and MBT-MCM-41-Het. Using the homogeneous route, the functionalization was achieved via the one step reaction of the mesoporous silica with an organic ligand containing the chelating functions, to give the modified mesoporous silicas denoted as MBT-SBA-15-Hom or MBT-MCM-41-Hom. The functionalized mesoporous silicas were employed as adsorbents for the regeneration of aqueous solutions at pH 6 contaminated with Hg(ii) at room temperature. Results obtained indicate that mercury adsorption was higher in the mesoporus silicas prepared by the homogeneous method, and the maximum adsorption value (0.24 +/- 0.02 mmol Hg(ii) g(-1)) was obtained for MBT-SBA-15-Hom. The chemically stability in acid medium of the functionalized silicas, possibility its regeneration washing with concentrate HCl, resulting in the reuse of the adsorbent material for several cycles.     

牡蛎中多环芳烃(PAHs)标准物质的研制

介绍了牡蛎中多环芳烃标准物质的研究、制备方法 ,进行了均匀性检验、稳定性检验 ,统计计算了检验结果 ,基本确定主要参数。检验结果表明 ,研制的牡蛎中难降解有机物标准物质均匀 ,在一年保存期间内稳定 ,可用于海洋环境监测中