浅析机动车尾气污染成因及对人体健康的影响

机动车工作时,由于燃烧不完全等原因,会生成和排出CO、HC、No_x和颗粒物等污染物,对人体的呼吸系统和心血管系统造成危害。应从政策法规、监测监督和舆论宣传3个方面着手加以整治。     

压电复合阻尼减振材料和压电复合吸声降噪材料中压电陶瓷应用形态研究

我们曾经将压电陶瓷粉体复合到传统的吸声降噪材料与阻尼减振材料中 ,制作出了性能更好的新型吸声降噪材料和新型阻尼减振材料 ;而且还发现废品压电陶瓷的粉体与正品压电陶瓷的粉体具有相同的功效[1～4 ] ,分析了它们同样发挥压电效应的原因。     

SBR工艺处理维生素C废水试验研究

采用颗粒污泥和普通絮体污泥SBR反应器对维生素C生产废水进行可生化性对比试验研究，结果表明，在进水CODcr为400—1800mg／L，运行周期为8h，其中曝气时间为5．5h，换水比为80％的条件下，颗粒污泥反应器CODer去除率为75-90％，污泥浓度介于6．11～8．32g／L，污泥指数为20～40mL／g.     

污水处理厂污泥脱水滤液循环利用的研究

对污水处理厂污泥机械脱水滤液进行了循环利用研究。将滤液与剩余污泥（mlsss≤13000mg／l）按1比4的比例均匀混合。然后加入到沉淀器中进行重力浓缩试验，结果表明：它能够改善污泥的浓缩脱水性能，加快污泥的沉淀速度，增大浓缩污泥的浓度；生产运行数据分析显示：污泥脱水滤液与剩余污泥混合液进入浓缩池后，上清液更加清澈，污泥的固体负荷率显著提高，这既可降低污泥的处理成本，亦可减少污泥处理系统的基建投资，为污泥处理系统的工艺优化开辟了新途径。     

1952-2016年长江经济带天然与人为氮输入时空演变

过量氮输入是水体氮污染的关键驱动因子，解析氮输入的结构和时空变化模式成为氮素环境管理的重要基础和难点.基于1952—2016年长江经济带各地区氮活动数据，分别构建了天然氮输入和人为氮输入模型，评估了氮输入负荷的时空变化特征.结果表明：①长江经济带氮输入负荷总体越过EKC曲线拐点进入由增长向下降的发展阶段，拐点出现在人均GDP为35777~36299元·人^-1时，发生时间为"十二五"时期，主要原因是化肥和食物输入下降；②氮输入负荷存在显著的时空差异，东部地区表现为倒U型，中部为S型，西部为J型，表明氮负荷存在从东向西的空间转移，西部地区成为氮输入负荷增长的热点地区，这与东部地区化肥施用量下降有关；③人为输入是长江经济带氮输入的主要来源，输入量及其占总输入的比例均呈现显著的增长趋势，空间上表现为从西到东部逐步递增的变化规律，与氮驱动力分布一致；④植被的多年平均固氮量为1771 kg·km^-2·a^-1，其中，非农作物的固氮速率为763 kg·km^-2·a^-1，植被固氮量的年际波动较小，天然输入对长江经济带总体氮输入影响较小.     

Enhanced removal of high-As(Ⅲ) from Cl(-Ⅰ)-diluted SO4(-Ⅱ)-rich wastewater at pH 2.3 via mixed tooeleite and(Cl(-Ⅰ)-free) ferric arsenite hydroxychloride formation

An advanced cost-saving method of removal of high-As(Ⅲ) from SO₄(-Ⅱ)-rich metallurgi cal wastewater has been developed by diluting the SO₄(-Ⅱ) content with As(Ⅲ)-Cl(-Ⅰ)-rich metallurgical wastewater and then by the direct precipitation of As(Ⅲ) with Fe(Ⅲ) at pH2.3.As(Ⅲ) removal at various SO₄(-Ⅱ)/Cl(-Ⅰ) molar ratios and temperatures was investigated The results showed that 65.2–98.2%of As(III) immobilization into solids occurred at the SO₄(Ⅱ)/Cl(-Ⅰ) mo...     

Decomplexation of Cu-1-hydroxyethylidene-1,1-diphosphonic acid by a three-dimensional electrolysis system with activated biochar as particle electrodes

The feasibility of decomplexation removal of typical contaminants in electroplating wastewater, complexed Cu(II) with 1-hydroxyethylidene-1,1-diphosphonic acid (Cu-HEDP), was first performed by a three-dimensional electric reactor with activated biochar as particle electrodes. For the case of 50 mg/L Cu-HEDP, Cu(II) removal (90.7%) and PO initial pH 7, acid-treated almond shell biochar (AASB) addition 20 g/L, and reaction time 180 min, with second-order rate constants of 1.10 × 10⁻³ and 1.94 × 10⁻⁵ min⁻¹respectively. The growing chelating effect between Cu(II) and HEDP and the comprehensive actions of adsorptive accumulation, direct and indirect oxidation given by particle electrodes accounted for the enhanced removal of Cu-HEDP, even though the mineralization of HEDP was mainly dependent on anode oxidation. The performance attenuation of AASB particle electrodes was ascribed to the excessive consumption of oxygen-containing functionalities during the reaction, especially acidic carboxylic groups and quinones on particle electrodes, which decreased from 446.74 to 291.48 µmol/g, and 377.55 to 247.71 µmol/g, respectively. Based on the determination of adsorption behavior and indirect electrochemical oxidation mediated by in situ electrogenerated H₂O₂ and reactive oxygen species (e.g., •OH), a possible removal mechanism of Cu-HEDP by three-dimensional electrolysis was further proposed.     

汽油清净剂的研究应用及进展

随着环保要求的日趋严格及汽车工业的发展创新，开展汽油清净剂的研究和应用工作已势在必行。本文介绍了国内外汽油清净剂的发展过程、应用现状，同时还介绍了将清净分散剂、抗氧防腐剂、减磨剂、防锈剂等添加剂复合而成的汽油清净剂的研制情况。实验结果表明：该剂具有抑制和清除发动机燃燃油系统沉积物的性能，达到国外第三代同类产品的水平。     

高锰酸盐指数测定中校正系数K值的变化验证

运用数理统计方法,验证了高锰酸盐指数测定的校正系数K值在4～5h内不会随时间和水样的变化而变化,K值不必每个样品都测定。     

Adsorptive removal of phosphate by the bimetallic hydroxide nanocomposites embedded in pomegranate peel

This study aimed to fabricate new and effective material for the efficiency of phosphate adsorption. Two types of adsorbent materials, the zirconium hydroxides embedded in pomegranate peel (Zr/Peel) and zirconium-lanthanum hydroxides embedded in pomegranate peel (Zr–La/Peel) were developed. Scanning electronic microscopy (SEM), x-ray photoelectron spectroscopy (XPS) and x-ray diffraction (XRD) were evaluated to give insight into the physicochemical properties of these adsorbents. Zr–La/Peel exceeded the adsorption efficiency of Zr/Peel adsorbents in batch adsorption experiments at the same pH level. The peel as a host can strive to have a strong “shielding effect” to increase the steadiness of the entrenched Zr and La elements. La and Zr are hydroxide metals that emit many hydrogen ions during the hydrolysis reaction, which contribute to protonation and electrostatic attraction. The highest adsorption capacity of La–Zr/Peel for phosphate was calculated to be 40.21 mg/g, and pseudo second-order equation is very well fitted for kinetic adsorption. Phosphate adsorption efficiency was reduced by an increase of pH. With the background of coexisting Cl^?, little effect on adsorption efficiency was observed, while adsorption capacities were reduced by almost 20–30% with the coexistence of ${{\text{SO}}_4}^{2?}$, ${{\text{NO}}_3}^{?}$ and humic acid (HA).