新生态型聚硅酸铁锰处理染料废水的优化

为了提高混凝剂对染料废水的净化效率,本文利用硅酸钠、硫酸亚铁和高锰酸钾为原料合成了新型复配混凝剂聚硅酸铁锰(PSFM),分别以直接大红、分散蓝和活性黄染料废水为处理对象进行混凝模拟实验,研究了碱度和浊度等因素对PSFM混凝去除染料性能影响.结果表明,PSFM对直接大红和分散蓝染料废水具有较好的混凝净化效能,其色度和TOC去除率分别可达99.2%、95.4%和98.5%、93.8%,效果优于聚硅酸铁(PSF)、Al2(SO4)3和Fe Cl3等常规混凝剂,PSFM对活性黄染料废水色度和TOC去除率分别为56.3%和51.3%.浊度对PSFM混凝效能无明显影响.在碱度分别为50、0和75 mg·L~(-1)时,PSFM对直接大红、分散蓝和活性黄去除率分别达到最高.此外,利用扫描电子显微镜(SEM)、傅里叶红外(FTIR)和X射线衍射仪(XRD)等高级表征手段对PSFM进行了表征,对混凝过程中的混合液和絮体分别进行Zeta电位和絮体粒径在线监测,探索得PSFM混凝主要机制为Fe+与Mn+水解产生的带正电的多核配合物和聚硅的桥联聚合,同时还包括新生态水合二氧化锰和羟基氧化铁的吸附助凝作用.     

Study on the role of copper converter slag in simultaneously removing SO2 and NOx using KMnO4/copper converter slag slurry

To achieve “waste controlled by waste”, a novel wet process using KMnO4/copper converter slag slurry for simultaneously removing SO2 and NOx from acid-making tail gas was proposed. Through the solid-liquid separation for copper slag slurry, the liquid-phase part has a critical influence on removing NOx and SO2. Also, the leached metal ions played a crucial role in the absorption of SO2 and NOx. Subsequently, the effects of single/multi-metal ions on NOx removal was investigated. The results showed that the leached metal from copper converter slag (Al3+, Cu2+, and Mg2+) and KMnO4 had a synergistic effect on NOx removal, thereby improving the NOx removal efficiency. Whereas Fe2+ had an inhibitory effect on the NOx removal owing to the reaction between Fe2+ and KMnO4, thereby consuming the KMnO4. Besides, SO2 was converted to SO42? completely partly due to the liquid catalytic oxidation by metal ions. The XRD and XPS results indicated that the Fe (II) species (Fe2SiO4, Fe3O4) in copper slag can react with H+ ions with the generation of Fe2+, and further consumed the KMnO4, thereby resulting in a decrease in the NOx removal. The characterization of the slags and solutions before and after reaction led us to propose the possible mechanisms. The role of copper slag is as follows: (1) the alkaline substances in copper slag can absorb SO2 and NO2 by KMnO4 oxidation. (2) copper slag may function as a catalyst to accelerate SO2 conversion and improve NOx removal by synergistic effect between leached metal ions and KMnO4.     

Partitioning of polybrominated diphenyl ether (PBDE) congeners in human blood and milk

Polybrominated diphenyl ethers (PBDEs) are brominated flame retardants (BFRs) which have recently been detected in human blood and milk in the USA, and presently these PBDE levels are found to be the highest globally. On a population basis, individual blood and individual milk analyses show similar congener patterns and levels. Until now, there has not been a study comparing PBDE levels in milk and blood of the same individuals. This study is the first to report these levels for PBDEs, though partitioning between blood and milk has been done previously for dioxins and polychlorinated biphenyls (PCBs). Twelve congeners in 11 nursing mothers’ blood and milk were found and the data describe partitioning ratios between blood and milk. The data suggest it may be easier for smaller, less brominated congeners to move from blood to milk.     

Positive group affective tone and team creativity: Negative group affective tone and team trust as boundary conditions

Drawing on multiple group‐level theories, we explored boundary conditions of the relationship between positive group affective tone (PGAT) and team creativity. We collected data from members and leaders of 68 research and development teams and performed hierarchical linear modeling analyses to test our hypotheses. Consistent with the “group‐centrism” perspective, we found that PGAT was beneficial for team creativity only when team trust was low; when trust was high, PGAT had a negative relationship with team creativity. In accord with the “dual‐tuning” perspective, the positive effect of PGAT on creativity was present only when team trust was low but negative group affective tone was high. We discussed the theoretical and practical implications. Copyright © 2011 John Wiley & Sons, Ltd.     

基于环境影响的绿化物流成本初探

作为物流服务价值的重要组成部分,物流成本受到相关企业的普遍重视,物流成本核算对于制定科学合理的微观物流策略、提高企业经济运行质量和效率具有重要意义。然而作为物流成本核算的基础,当前的微观物流成本构成中并未考虑企业物流活动的环境影响,不能真正反映物流活动的全部成本,从而影响了企业的可持续健康发展。基于资源环境的价值理论,提出应以绿化物流成本来衡量企业物流活动的全部消耗,即在微观物流成本构成中考虑环境成本,并给出了微观绿化物流成本的基本公式。     

概率火灾安全分析方法研究

为分析和评估火灾对设备、建筑物等敏感目标结构安全的影响,结合化工定量风险评估方法和气体爆炸概率安全分析方法,提出概率火灾安全分析策略和实施流程。该方法包括火灾危害辨识、泄漏速率计算、火灾后果模拟、频率分析、绘制频率超越热载荷曲线、结构响应分析等关键步骤。以某柴油罐区为例,通过频率分析和火灾模拟,绘制出频率超越热载荷曲线,假定火灾风险可接受准则为10-4/a,求得对应的可信热载荷为21 kW/m2,并以此值作为结构热响应分析的输入参数。火灾概率安全分析方法侧重于描述火灾热辐射强度及其对应的发生可能性,判定敏感目标遭遇的可信火灾热载荷强度和结构热响应行为,评估消防减灾措施效果,确保结构完整性和可用性,不评价工艺系统潜在火灾风险的高低。     

丙烷催化还原脱硝中硫中毒Cu-Ir/H-ZSM-5催化剂的再生

考察了5%H₂/Ar还原再生丙烷催化还原NO_x中硫中毒Cu-Ir/H-ZSM-5催化剂的工艺参数影响,采用N₂吸附、X射线衍射、X射线光电子能谱和氢气程序升温还原等手段研究了催化剂再生行为的构效关系.结果表明,硫中毒Cu-Ir/H-ZSM-5催化剂由于CuSO₄的生成导致催化剂活性位损失,比表面积、微孔面积和孔体积的减小.H₂还原再生的最佳工艺参数为再生温度500℃和再生气体用量42.8L/g_催化剂,再生催化剂的活性可恢复到新鲜催化剂的95%.在最佳再生条件(500℃和42.857L/g_催化剂)下,再生催化剂表面CuSO₄含量最低(0.4%),且再生催化剂的比表面积、微孔面积和孔体积较失活催化剂有较大提高.     

华北地区夏季大气亚微米颗粒物的半挥发性特征

利用热扩散管TD(Thermal Denuder)与高分辨飞行时间气溶胶质谱仪(HR-ToF-AMS)联用法,于2013年6—7月对华北地区国家环境空气质量评价区域点香河的大气PM₁(亚微米颗粒物)及其组分〔OM(有机质)、SO₄2-、NO₃-、NH₄+、Cl-〕进行连续在线观测,并实现了PM₁不同化学组分半挥发性特征的模拟分析. 结果表明:在观测期间,ρ(PM₁)平均值为 (47.9±47.3) μg/m3,其中OM贡献最大,达到38.2%〔ρ(OM)占ρ(PM₁)的比例,下同〕,之后依次为SO₄2-(33.7%)、NH₄+(13.8%)、NO₃-(12.3%)、Cl-(2.0%). 在PM₁的各化学组分中,NO₃-和Cl-的MFR(质量剩余分数)值最低(约0.40),表明二者的半挥发性最高,当温度为50 ℃时,约60%的NO₃-或Cl-进入气相中;SO₄2-的半挥发性最低,在50 ℃时仍有约90%的质量剩余;而OM和NH₄+的半挥发性居中. NO₃-的半挥发性受大气PM₁污染水平的影响,50 ℃时其半挥发性随着ρ(PM₁)的增加而升高. 当温度从50 ℃升至200 ℃时,残留有机气溶胶的O/C(原子数比)从0.47增至0.60,说明半挥发性组分多为氧化态较低的有机化合物. 此外,真空动力学粒径在60~2 000 nm的颗粒物在不同粒径段表现出相近的半挥发性. 大气PM₁半挥发性的定量分析结果可为全面认识大气颗粒物的物化性质及污染机理提供数据,也有助于空气质量模型的完善.      

Effects of source size,monitoring distance and aquifer heterogeneity on contaminant mass discharge and plume spread uncertainty

Estimating the movement of dissolved contaminants in heterogeneous aquifers is very important for the monitoring design, risk assessment, and remediation of contaminated aquifers. This work explored the influence of source size, monitoring distance, and aquifer heterogeneity on the accuracy of contaminant mass discharge (CMD) estimation using leaching surface approach as well as on the plume spread uncertainty in a 2-D heterogeneous aquifer. The interaction among source size, monitoring distance, and aquifer heterogeneity regarding the accuracy of CMD estimation and the plume spread uncertainty at downstream of the contaminated aquifer was extensively investigated. The transient leaking of a contaminated aquifer in a saturated heterogeneous aquifer under steady-state flow conditions was simulated. The effect of aquifer heterogeneity on the CMD uncertainty was evaluated through the expected values and variance. The results showed that the CMD estimation error varied from underestimation in the mildly heterogeneous aquifer, over accurate estimation in the medium heterogeneous aquifer to overestimation in the highly heterogeneous aquifer. Additionally, the results illustrated that the mean and variance of the transverse spatial extent of the peak concentrations for the plume at the control plane were very sensitive to the aquifer heterogeneity and detectable concentrations of contaminants.     

A Cu-modified active carbon fiber significantly promoted H2S and PH3 simultaneous removal at a low reaction temperature

• Cu_0.15-ACF performs the best for H₂S and PH₃ simultaneous removal. • 550°C and 90°C are separately calcination and reaction temperatures. • The reason why Cu_0.15/ACF shows better performance was found. • The accumulation of H₂PO₄⁻ and SO₄²⁻(H₂O)₆ is the deactivation cause of Cu_0.15/ACF. Poisonous gases, such as H₂S and PH₃, produced by industrial production harm humans and damage the environment. In this study, H₂S and PH₃ were simultaneously removed at low temperature by modified activated carbon fiber (ACF) catalysts. We have considered the active metal type, content, precursor, calcination, and reaction temperature. Experimental results exhibited that ACF could best perform by loading 15% Cu from nitrate. The optimized calcination temperature and reaction temperature separately were 550°C and 90°C. Under these conditions, the most removal capacity could reach 69.7 mg/g and 132.1 mg/g, respectively. Characterization results showed that moderate calcination temperature (550°C) is suitable for the formation of the copper element on the surface of ACF, lower or higher temperature will generate more cuprous oxide. Although both can exhibit catalytic activity, the role of the copper element is significantly greater. Due to the exceptional dispersibility of copper (oxide), the ACF can still maintain the advantages of larger specific surface area and pore volume after loading copper, which is the main reason for better performance of related catalysts. Finally, increasing the copper loading amount can significantly increase the crystallinity and particle size of copper (oxide) on the ACF, thereby improving its catalytic performance. In situ IR found that the reason for the deactivation of the catalyst should be the accumulation of generated H₂PO₄⁻ and SO₄²⁻(H₂O)₆ which could poison the catalyst.