Oxidized multiwalled carbon nanotubes modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole for solid phase extraction and preconcentration of some metal ions

In this work, a new procedure for the enrichment of the trace amount of Cu²⁺, Ni²⁺, Co²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions based on the utilization of multiwalled carbon nanotubes (MWCNT) modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole as chelating agent prior to their determination by flame atomic absorption spectrometry has been described. The influence of effective parameters including pH, amount of ligand and MWCNT, composition of eluent, and coexisting ions on recoveries of understudy metal ions was examined. At the optimum pH of 5.0, all metal ions were quantitatively sorbed onto the proposed solid phase and completely desorbed with 8?mL of 5.0?mol?L^?1 HNO₃. The detection limit of Cu²⁺, Co²⁺, Ni²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions was 1.7, 2.4, 2.3, 2.9, 2.8, and 1.4?µg?L^?1, while the preconcentration factor was 63 for Cu²⁺ and 94 for the other metal ions and relative standard deviations between 1.8 less than 3.0%. The proposed procedure was applied for the analysis of various samples.     

Determination of cadmium in water and herbal medicine by Penicillium chrysogenum immobilized on silica gel for flame atomic absorption spectroscopy

Penicillium chrysogenum was immobilized on silica to develop a simple and cost effective method for solid phase extraction of Cd(II) and determination using flame atomic absorption spectrometry (FAAS). The sorbent was characterized by Fourier transform infrared spectroscopy and packed into a column. The conditions for quantitative sorption and desorption of Cd(II) were optimized. The preconcentration factor was 100 while detection limit was 0.61 µg L^?1 with a relative standard deviation of 1.0%. The method was applied for determination of Cd in herbal medicine and tap water.     

Pah characteristics in ambient air within a steel industrial complex

Ambient air samples at ten sites in an iron and steel industrial complex were collected from June to December for analyzing polycyclic aromatic hydrocarbons (PAHs). Sixteen species of PAH components in air samples were identified. The results indicate that both gaseous phase and particle‐bound PAHs at the top of the cokemaking plants are unusually high. The profiles of particle‐bound PAHs indicate that the predominant species at the top of, the coke oven batteries are those of high molecular weight components. The major components of particle‐bound PAHs at sampling sites near the fenceline, however, include the medium molecular weight components. The PAH profiles of air samples within the industrial complex show a strong similarity to those of cokemaking plant samples. The concentrations and the specific content of benzo(a)pyrene in the iron and steel industrial complex are higher than those values measured in urban area, petrochemical industry park, and open‐air burning area.     

Cleanup by solid‐phase extraction and HPLC of organochlorine insecticides and PCBS in various nonfatty and fatty samples

An accurate, simple and cheap extraction and cleanup procedure for capillary GC analysis of organo‐chlorine insecticides (OCs) in vegetables (cabbage and carrots) at the ng/g level, and for soil at the μg/g level is presented. The cleanup is carried out on solid‐phase extraction (SPE) cartridges, filled with 500 mg silica, 1 g of deactivated Florisil (10% w/w water), and 100 mg of anhydrous sodium sulphate. Recoveries >90% are obtained. The cleanup of OCs in fatty samples on an HPLC LiChrosorb Si 100 column is evaluated for subsequent capillary GC analysis. Fractionation of OCs and Aroclor 1254 and 1260 on an HPLC Nucleosil 100 column appears to be satisfactory.     

Evaluation of linear alkylbenzenesulfonate (LAS) biodegradability in sediment by solid‐phase extraction and HPLC analysis

The linear alkylbenzenesulfonate (LAS) sorption on environmental sediments has been known long ago. Their high concentrations reflect the massive input of these chemicals from household and industrial uses. However few attempts were made to identify biodegradation metabolites of LAS in sediment. In this report, a method for the determination of these compounds in sediment samples by high‐performance liquid chromatography (HPLC) is described. The first step of our work was performed by solid‐phase extraction with octadecyl‐bonded silica (C18) mini‐columns and provided a suitable recovery of LAS (90 ± 5%) and most metabolites. Furthermore, laboratory investigations led to study the behaviour of LAS in sediment. The environmental samples used for this purpose were collected from a pond (named étang de Bolmon) located in the French Mediterranean coast. Our results were in agreement with an aerobic biodegradation process of LAS that occurred only with high values of sediment redox potential and needed the samples to be vigorously shaken to ensure adequate mixing and suspension of particulate material. In a stagnant sediment or under anaerobic conditions, LAS is not degraded. p‐Sulfophenylacetic acid and p‐sulfocinnamic acid were evidenced as predominant metabolites and were found not to be persistent.     

茶叶挥发物对白斑猎蛛觅食行为的影响

为了探明茶树叶片挥发物在白斑猎蛛(Evarcha albaria)选择觅食斑块过程中的作用,采用固相微萃取-气相色谱-质谱联用技术研究了其猎物假眼小绿叶蝉(Empoasca vitis)取食对茶树叶片挥发物释放的影响,同时利用蜘蛛行为观测平台研究了白斑猎蛛在不同味源侧(觅食斑块)的活动行为。结果表明,未损伤叶片(对照)仅释放出微量挥发物,而假眼小绿叶蝉成虫取食后的茶树叶片释放出14种挥发物;雌、雄蛛在进入处理味源(假眼小绿叶蝉取食后的茶树叶片)侧和对照侧的初次选择及进入频次上均无显著差异,但与对照相比,雌、雄蛛在虫害处理叶片中的停留时间显著增加。研究表明,假眼小绿叶蝉取食诱导了茶树叶片挥发物的释放,而挥发物种类和含量的变化造成了白斑猎蛛在不同味源侧停留时间的差异。     

煤矿瓦斯涌出时序预测的自组织数据挖掘方法

为分析煤矿瓦斯涌出复杂系统时间序列预测方法,提出自组织数据挖掘(SODM)与相空间重构(PSR)相结合的预测建模方法。首先应用C-C方法计算时间序列的最佳嵌入维数和延迟时间后进行PSR;然后以二元二次方程为传递函数,以嵌入维数变量为自变量,以延迟时间后的时间序列为因变量,通过内准则确定传递函数系数和外准则选择最优传递函数,并以最优传递函数的输出为下层迭代传递函数的输入,最后获得最优复杂度预测模型。算例结果表明:该方法对煤矿瓦斯涌出量预测的相对误差为-5.751 7% ~6.049 3%,平均相对误差2.145 7%,预测结果能满足煤矿安全生产实际工程应用要求。     

猪粪中典型类固醇雌激素的固相萃取/GC-MS检测

以猪粪中常见且具有较大潜在危害的E1(雌酮),17α-E2(17α-雌二醇),17β-E2(17β-雌二醇)和E3(雌三醇)为研究对象,建立了猪粪中这4种典型类固醇雌激素的GC-MS(气相色谱-质谱)分析检测方法.着重优化了样品的前处理方法,包括对超声提取剂、超声提取时间、固相萃取淋洗剂、衍生化温度和时间的优化选择.结果表明:在优化的试验条件下,猪粪中的典型雌激素E1,17α-E2,17β-E2和E3检出限分别为8.0,2.5,5.1和3.3 μg/kg,平均加标回收率在92.3%～137.4%之间.      

南宁城市内河水体和表层沉积物中有机氯农药分布特征

采用改进的固相萃取、加速溶剂萃取和气相色谱-电子捕获检测器,对广西壮族自治区南宁5条城市内河的水体和表层沉积物样品中7种痕量有机氯农药(OCPs)的残留状况进行了分析测定. 结果表明,南宁城市内河水体有机氯农药以HCHs为主,ρ(OCPs)为nd～0.141 μg/L. 5个点位沉积物中w(总OCPs)为2.13～2.80 μg/kg,均检出4,4′-DDE和4,4′-DDD,w(DDD)/w(DDE)<1,且DDTs在沉积物中的含量普遍高于HCHs. 各点位沉积物中有机氯农药各组分含量均低于美国环境保护署采用的无毒害风险浓度.      

EMC用V型人工电源网络的解析

本文分别对理想和实用的V型人工电源网络的阻抗(模和相位角)、隔离度进行计算和分析,并将其与某公司生产的ENV216型人工电源网络的测试参数进行比较,验证了ENV216型人工电源网络是完全符合标准要求的,加深了对电源端传导发射测试的理解。