CaH_2对Cu-Ce-La-ZSM-5催化分解NO性能的影响

实验采用一步离子交换法制备Cu-Ce-La-ZSM-5催化剂,然后采用共混法制得Cu-Ce-La-ZSM-5/CaH2催化剂。采用扫描电镜(SEM),电感耦合等离子体发射光谱(ICP-AES),X射线衍射(XRD),红外(FTIR)以及NO吸脱附(NO-TPD)对催化剂进行表征。结果显示CaH2的加入使得催化剂中铜离子存在形式发生变化,催化剂表面变光滑洁净,并且吸附NO能力增强。NO催化分解实验的结果表明CaH2提高了催化剂活性和抗氧性。CaH2助催性是由于其受热分解过程中产生的H2能将Cu2+还原为具有催化活性的Cu+,同时使催化剂表面洁净光滑更容易吸附NO。     

Persistent organic pollutants and heavy metals in adipose tissues of patients with uterine leiomyomas and the association of these pollutants with seafood diet, BMI, and age

Background, aim, and scope  

Persistent organic pollutants and heavy metals can cause diseases in women, however, the relationships of these pollutants and uterine leiomyomas (UL), which are non-cancerous tumors of the uterus, are unclear. This study focused on the quantification of organochlorine pesticides (OCPs), polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), polybrominated diphenyl ethers (PBDEs), and heavy metals in subcutaneous and visceral fat obtained from patients with UL and in subcutaneous fat of a control group of women without UL to determine if there were any correlations between concentrations of persistent organic pollutants (POPs) and heavy metals and the incidence of UL.     

沸石载体催化剂研制及其催化臭氧氧化染料废水的研究

以沸石为载体负载不同金属氧化物来制备催化剂,通过试验分析该催化剂催化臭氧氧化染料废水的效果及其影响因素。结果表明:(1)沸石对染料废水的吸附作用很小,总有机碳(TOC)去除率基本维持在3.2%左右,对于后期的试验可以忽略其影响。(2)以沸石作为载体制得的MnO2、Fe2O3、ZnO、CuO负载型催化剂(分别简写为MnO2/沸石、Fe2O3/沸石、ZnO/沸石、CuO/沸石),对臭氧氧化反应均有催化作用,其催化效果依次为MnO2/沸石Fe2O3/沸石ZnO/沸石CuO/沸石。同时,MnO2/沸石的重复使用率高。(3)MnO2/沸石催化臭氧氧化效率及重复使用率均优于以活性炭为载体的MnO2负载型催化剂。(4)臭氧氧化和MnO2/沸石催化臭氧氧化对染料的脱色率基本一致。MnO2/沸石催化臭氧氧化的TOC去除率比臭氧氧化提高较多,对染料废水有很好的处理效果。(5)以沸石为载体制得的负载型催化剂催化臭氧氧化实际染料废水的处理效果较好,具有较高的实用价值。     

有机磷农药对蛋白核小球藻的毒性相互作用研究

水体中农药复合污染产生的毒性效应具有潜在风险。为系统考察有机磷农药(OPs)混合物对淡水生态系统中绿藻的联合毒性效应,以马拉硫磷(MIT)、敌敌畏(DDVP)、敌百虫(TRC)、乐果(DIT)和氧乐果(OMT)等5种OPs作为混合物组分,运用直接均分射线法设计9组二元混合物体系共45条混合物射线。利用96孔微板测定5种OPs及其二元混合物对蛋白核小球藻(C. pyrenoidosa)的生长抑制毒性,通过基于置信区间的组合指数法分析混合物的联合毒性及毒性相互作用。结果表明,以p EC50为毒性指标,5种OPs对C. pyrenoidosa的毒性大小顺序为:TRCMITDDVPOMTDIT,OPs对C. pyrenoidosa的毒性大小受其中心磷原子的电正性影响;因混合组分的不同,部分OPs混合物对C. pyrenoidosa的联合毒性依赖于组分浓度比; OPs混合物对C. pyrenoidosa的毒性相互作用以加和为主,部分发生拮抗作用,发生拮抗作用的混合体系具有低效应区域呈加和作用,高效应区域呈拮抗作用的规律;与MIT混合的体系均有发生拮抗作用,且依赖于MIT浓度,MIT浓度比例越高,拮抗作用越强,OPs混合物的毒性相互作用与组分浓度比相关; OPs混合物的毒性相互作用组分浓度比依赖性与其联合毒性的组分浓度比依赖性规律不相关。     

Effective sorption of perfluorooctane sulfonate (PFOS) on hexadecyltrimethylammonium bromide immobilized mesoporous SiO2 hollow sphere

The hexadecyltrimethylammonium bromide (HDTMAB) immobilized hollow mesoporous silica spheres were prepared for the efficient removal of perfluorooctane sulfonate (PFOS) from aqueous solution. Besides the traditional sorption behavior including sorption kinetics as well as effect of solution pH and temperature, the effect of increasing volume which simulated the natural river where the rate of solute and solvent was relatively constant and solution volume was always changing was investigated. The result indicated that the residual PFOS concentrations in aqueous phase decreased with increasing solution pH and ionic strength, whereas they increased with increasing temperature. The HDTMAB immobilized material still maintained high efficiency after increasing volume, that is, the removal kept more than 99% after the treatment when the initial PFOS concentration was 1 mg L^?1. The uptake behavior and morphology of spheres which was characterized by transmission electron microscopy (TEM) revealed that the additional HDTMAB and mesoporous shell were responsible for the enhanced sorption of PFOS. It was concluded that electrostatic interaction and Ca-bridge role played an important role in the sorption of PFOS on the mesoporous SiO₂ hollow spheres, whereas, hydrophobic interaction contributed to the nice sorption performance of PFOS on the HDTMAB immobilized sorbent.     

VB程序实现微量元素相关比值的计算

微量元素的相关比值在许多领域都有不同的作用,随着研究工作的日益精细,数据越来越多,使得不少学者要把大量时间花在数据的整理和计算上,既不利于准确的统计,又浪费了时间.在探讨、实现了地壳中微量元素的相关比值的VB程序,使得在运用这些比值时方便、准确、省时,为研究工作减少许多不必要的麻烦.     

炼油废水污泥脱水工艺条件的优化

采用化学除油降黏—污泥调理—离心脱水工艺处理某炼油厂废水处理系统的混合污泥,并对工艺条件进行优化。实验结果表明,最佳的工艺条件为：化学除油降黏阶段处理体系的pH=4,反应温度35 ℃,H₂O₂加入量 2 g/L,m（H₂O₂）∶ m（Fe²⁺）=4,反应时间 60 min;污泥调理反应阶段的CaO加入量7.0 g/L;离心脱水阶段在分离因数为1 558时脱水5 min。在此条件下,得到的泥饼的含水率为70.0%~75.0%（w）,含油率小于2%（w）,污泥比阻约为3.0×10⁷ s²/g。     

酸雨损害农作物的对策研究——喷水消除酸雨对农作物的损害

经模拟酸雨处理植物的试验表明,酸雨对植物叶片的直接损害是由于酸雨水滴滞留在叶面引起的。若在雨后2h内喷水(pH7.0±0.2)以驱除滞留在叶面的水滴,叶片则无受害症状,叶绿素含量、生物产量和经济产量所受的影响也将减轻甚至完全不受影响。     

The residues, distribution, and partition of organochlorine pesticides in the water, suspended solids, and sediments from a large Chinese lake (Lake Chaohu) during the high water level period

The levels of organochlorine pesticides (OCPs) in the water, suspended solids, and sediments from Lake Chaohu during the high water level period were measured by a solid-phase extraction gas chromatograph–electron capture detector. The spatial distributions of the three phases and the water/suspended solids and sediment/water partition coefficients were analyzed. The results showed the following: (1) The mean contents of OCPs in the water, suspended solids, and sediments were 132.4?±?432.1 ng/L, 188.1?±?286.7 ng/g dry weight (dw), and 13.7?±?9.8 ng/g dw, respectively. The dominant OCP components were isodrin (85.1 %) for the water, DDTs (64.4 %) for the suspended solids, and both isodrin (48.5 %) and DDTs (31.8 %) for the sediments. (2) β-HCH was the primary isomer of HCHs in the water and sediments, and the proportions were 61.7 and 41.3 %; γ-HCH was the primary isomer in the suspended solids, accounting for 49.3 %; p,p′-DDT was the dominant content of DDTs in the water and suspended solids, whereas p,p′-DDD was the main metabolite of DDTs in the sediments. (3) The concentrations of contaminants in the water from the western lake were greater than those from the eastern lake, but the concentrations in the suspended solids from the western lake were less than those from the eastern lake. (4) There was no significant correlation between the water–suspended solids partition coefficient K _d and the n-octanol–water partition coefficient K _ow, and between the sediment–water organic-C weighted sorption coefficients K _oc and K _ow.     

光催化氧化降解垃圾渗滤液中溶解性有机物

研究了UV-TiO2光催化氧化降解垃圾渗滤液过程中溶解性有机物(DOM)的变化特征。结果表明:在适宜条件下,UV-TiO2光催化氧化降解垃圾渗滤液的色度、COD和DOC的去除率分别可达97%、72%和60%;紫外光谱分析说明渗滤液DOM中包括多种含有共轭双键、羰基的大分子有机物及多环芳香类化合物,不同光催化处理液中DOM具有基本一致的结构单元和官能团;红外光谱分析说明渗滤液DOM中含有大量包括羟基、羧基、氨基和苯环的芳香族化合物,在光催化处理液中这几种官能团都能被有效降解;GC/MS分析结果表明,渗滤液DOM中含有72种有机污染物,醇类、羧酸和酮类分别为25、14和12种;在光催化72 h处理液中,有机物减少为44种;酯类和醇类较多,分别为12种和16种;酮类8种,羧酸没有检出。