基于全隧道方案的渤海海峡跨海通道工程环境影响研究

渤海海峡跨海通道是疏通中国干线交通网战略布局中的咽喉工程,因工程规模浩大,其环境影响广泛而深远.简要回顾了工程建设方案的筛选进程及“深埋式全隧道”方案的环境优势;建议工程环境影响评价采用“协作型”环境影响评价模式,以合作和协调克服各方之间的分歧和矛盾;初步探讨了工程前期调研的主要内容;识别分析了通道工程对近岸海域、出入口城市的主要环境影响.结果表明:与其他方案相比,深埋式全隧道方案对自然人文景观、海洋生态环境、海洋资源开发利用等的影响是最小的,并提出了消除或减缓不良环境影响的对策措施,为通道工程的立项决策提供科学依据.     

基于多因子指数集成的流域面源污染风险研究

为掌握流域面源污染风险的整体趋势,基于风险评价时,单个因子对系统某种风险的贡献率可能大于1且因子对系统风险贡献呈一定结构性的问题,定义了风险标准值的概念和算法,建立了系统风险多因子集成评价方法,并在地理信息系统支持下对泸沽湖流域进行了案例研究.结果表明,泸沽湖流域面源污染流失风险处于较高的水平;系统风险多因子集成评价法在对多个同类系统间进行比较时,具有较大的优势;该方法可以与其他多种方法相结合对系统属性进行全面综合评价.     

用褐铁矿制备聚硅氯化硫酸铁的研究

通过正交实验研究了用盐酸、硫酸、褐铁矿和硅酸钠制备聚硅氯化硫酸铁（PSFCS）絮凝剂的工艺条件。实验结果表明,浸取时间为2.5-3 h,浸取温度为110℃,硫酸浓度为6 mol/L,盐酸浓度为3 mol/L,质量液固比为4∶1,铁的浸出率可达95.7%-96.3%。溶液中加入少量聚乙烯醇作稳定剂,亚硝酸钠作氧化催化剂。PSFCS的合成条件：Fe/Si摩尔比为2,硅酸活化pH值为2,硅酸活化时间是30-40 min,陈化时间是2-2.5 h。与聚合硫酸铁（PFS）和聚合氯化铝（PAC）比较了处理印染废水的效果,表明PSFCS具有良好的絮凝性能,COD和浊度的去除率分别可达81.4%和96.1%。     

催化剂及其制备对催化湿式氧化反应的影响

催化湿式氧化法是一种有效的处理有毒、有害、高浓度有机废水的水处理技术,文章专门针对催化剂本身的制备对催化湿式氧化的影响,以及催化剂的失活、再生、重复利用等研究做出总结,以期对有关研究者提供一定的参考。     

Effect of oxide nanoparticles on the morphology and fluidity of phospholipid membranes and the role of hydrogen bonds

Engineered oxide nanoparticles (NPs) are widely applied in insulators, catalyzers, paints, cosmetic products, textiles and semiconductors. Their attachment on cell membrane may lead to cytotoxicity. The effects of Al₂O₃, Fe₂O₃, SiO₂, TiO₂ and ZnO NPs on membrane integrity and fluidity were studied using giant or small unilamellar vesicles in this study. Al₂O₃ and SiO₂ NPs disrupted the oppositely charged membrane, indicating the important role of electrostatic attraction. However, Fe₂O₃, TiO₂ and ZnO NPs did not cause serious membrane disruption as Al₂O₃ and SiO₂ NPs. Membrane fluidity was evaluated by the generalized polarity (GP) values of Laurdan fluorescent emission. SiO₂ NPs induce the membrane gelation of both positively and negatively charged membrane. Al₂O₃ and ZnO NPs induced the gelation of the oppositely charged membrane, but did not cause obvious membrane gelation to the like charged membrane. The phospholipid molecular structural changes after NP exposure were analyzed by Fourier transform infrared (FT-IR) spectroscopy. FT-IR spectra revealed the hydrogen bond formation between NPs and the carbonyl/phosphate groups of phospholipids. Al₂O₃ and SiO₂ NPs showed strongest evidence of hydrogen bonding on their FT-IR spectra. It was consistent with the microscopic observation and fluorescent data that Al₂O₃ and SiO₂ NPs caused more serious membrane disruption and gelation. This study on membrane damage provides further knowledge on the cytotoxicity of nanomaterials and the safety of NP application.     

富氧条件下等离子体协同改性NaY分子筛催化分解NO_x研究

用不同浓度的Cu、Ce和La离子交换Na Y分子筛,对比了不同改性条件下等离子体协同分解NO_x的性能.实验结果表明:Cu是NO_x催化分解的主要活性组分,对于8%Cu-Na Y催化剂,当放电电压为10 k V,放电功率为7.6 W时,NO_x转化率可达46.3%,反应产物中没有NO_2,只有11 ppm的N_2O.Ce的加入可以有效提高催化剂催化活性,对于5%Ce-8%Cu-NaY催化剂,当放电电压为7.8 kV,功率为3.6 W时,NO_x转化率可达67.3%.La的加入同样可以使催化剂活性上升,但不同La含量催化剂的NO_x转化率相差较小.     

进一步探讨内蒙古自治区环境突发性污染事件应急监测工作

随着内蒙古经济社会的快速发展,环境突发性事件应急监测存在一些新问题,根据内蒙古实际情况,探讨环境突发性污染事件应急监测工作思路,进一步保护环境和人类生命安全。     

进一步探讨内蒙古自治区环境突发性污染事件应急监测工作

随着内蒙古经济社会的快速发展,环境突发性事件应急监测存在一些新问题,根据内蒙古实际情况,探讨环境突发性污染事件应急监测工作思路,进一步保护环境和人类生命安全。     

Modeling assessment for ammonium nitrogen recovery from wastewater by chemical precipitation

Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium nitrogen (NH4 +-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4 +-N recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4 +-N recovery from coking wastewater was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4 + molar ratio (Mg/N) and the initial NH4 +-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4 + and CO3 2??/NH4 + molar ratios (Ca/N and CO3 2??/N), respectively. The trends for NH4 +-N removal at different pH and Mg/N levels were similar to the thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3 2??/N), (pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4 +-N recovery.     

NaOH溶液对有机相苯酚反萃取的研究

本文系统进行了ＮａＯＨ溶液对负载苯酚的ＴＢＰ＋煤油溶剂的反萃取平衡实验。考虑苯酚的支萃取平衡和解离平衡,建立了反萃取的计算模式,并证明了模型的可行性。本文还讨论了ＮａＯＨ溶液浓度,油水相比,萃取平衡分配系数,溶剂中的负载苯酚浓度和ＮａＯＨ溶液中初始酚含量对反萃取率的影响。