摩托车防护头盔发展现状和展望分析

当今保护人类健康安全日益受到社会普遍重视,头部安全是摩托车乘员的首要问题。摩托车头盔防护依然十分重要;国际上其标准修定较快并不断完善;通过对TBT通报,头盔安全类发明专利等数据分析,得出摩托车头盔的技术研发高峰近期爆发。     

A2/O+MBR工艺运行效果与碳排放特征研究

对北京市通州区H再生水厂采用的A²/O+MBR工艺运行效果与不同环节碳排放特征进行研究.结果表明：2018年该再生水厂对BOD₅,COD_cr,NH₄⁺-N,TN和TP的平均去除率分别为97.3%,94.1%,98.6%,77.0%,96.2%;全厂碳排放总量和吨水碳排放量呈春夏季节逐渐降低,秋冬季节缓慢升高的特征,全厂综合吨水碳排放量约为2.26kgCO₂e/t.碳排放总量中能耗碳排放量占主要地位,CH₄,N₂O和物耗碳排放量占比较小;统计分析显示CH₄,能耗和物耗吨水碳排放量与BOD₅,TN进水浓度及BOD₅去除率显著相关;N₂O吨水碳排放量与TN与BOD₅进水浓度显著相关;直接,间接吨水碳排放量与水量无显著相关性.     

钒基催化剂同步去除燃煤烟气中甲苯与NOx研究

采用不同工艺制备V₂O₅-WO₃-MoO_x/TiO₂堇青石整体式催化剂,以甲苯和NO为探针分子,考察了Mo的负载量、涂覆方法、粘结剂的种类等制备工艺对整体式催化剂性能的影响,用XRD、SEM-EDS、FT-IR、BET等技术对催化剂进行了表征分析.结果表明,采用涂敷法,以添加量为1%的甲基纤维素为粘结剂所制备的V1W6Mo3/TiO₂堇青石蜂窝陶瓷整体式催化剂具有最优活性和稳定性（T₉₀为307℃,负载率为28.26%,脱落率为6.81%）,在燃煤烟气中具有优异的同步去除VOCs与NO性能,甲苯去除率可达99%,NO去除率为100%,N₂选择性为99%.XRD、SEM-EDS表明V、W、Mo活性组分分布均匀且高度分散.FT-IR证明添加甲基纤维素的整体式催化剂具有优异的抗硫性能.     

EGSB-CANON工艺启动及动力学特性

采用EGSB（Expanded Granular Sludge Bed）反应器,在启动全程自养脱氮（CANON）工艺中通过改变曝气方式以及优化曝气/非曝气逐步实现CANON工艺的稳定运行.通过研究不同曝气/非曝气条件下CANON工艺的脱氮性能的变化,探究系统内不同污泥粒径中功能菌的活性,揭示EGSB反应器不同的运行条件以及系统内不同粒径的微生物聚集体在CANON工艺启动过程中的影响机制与菌群结构特性.结果表明,当恒定曝气量为0.5L/min,曝气/非曝气为2：1（60min：30min）时,实现了AerAOB（Aerobic Ammonia-Oxidizing Bacteria）与AnAOB（Anaerobic Ammonium-Oxidation Bacteria）协同脱氮的目的,并成功将NOB（Nitrite-Oxidizing Bacteria）的活性由3.41mgN/（h·gVSS）抑制到0.75mgN/（h·gVSS）.在对AnAOB的双底物（NO₂^--N和NH₄⁺-N）抑制动力学结果进行Haldane拟合时,得到NH₄⁺-N和NO₂^--N的半饱和常数（k_s）、抑制动力学常数（k_h）分别为106.8,331.9mg/L,272.4,66.61mg/L,相关性系数（R²）分别为0.98133和0.99142.在CANON污泥颗粒化形成过程中,污泥粒径在0.154~0.335mm范围内主要以AerAOB为主,污泥粒径在1mm以上主要以AnAOB为主.不同粒径下微生物聚集体的协同作用以及稳定的群落结构实现了CANON工艺的稳定运行.     

Efficient degradation of Rhodamine B by magnetically recoverable Fe3O4-modified ternary CoFeCu-layered double hydroxides via activating peroxymonosulfate

Environment-friendly nano-catalysts capable of activating peroxymonosulfate (PMS) have received increasing attention recently. Nevertheless, traditional nano-catalysts are generally well dispersed and difficult to be separated from reaction system, so it is particularly important to develop nano-catalysts with both good catalytic activity and excellent recycling efficiency. In this work, magnetically recoverable Fe₃O₄-modified ternary CoFeCu-layered double hydroxides (Fe₃O₄/CoFeCu-LDHs) was prepared by a simple co-precipitation method and initially applied to activate PMS for the degradation of Rhodamine B (RhB). X-ray diffraction (XRD), fourier transform infrared spectrometer (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), Brunauer-Emmett-Teller method (BET), and vibrating sample magnetometer (VSM) were applied to characterize morphology, structure, specific surface area and magnetism. In addition, the effects of several key parameters were evaluated. The Fe₃O₄/CoFeCu-LDHs exhibited high catalytic activity, and RhB degradation efficiency could reach 100% within 20 min by adding 0.2 g/L of catalyst and 1 mmol/L of PMS into 50 mg/L of RhB solution under a wide pH condition (3.0-7.0). Notably, the Fe₃O₄/CoFeCu-LDHs showed good super-paramagnetism and excellent stability, which could be effectively and quickly recovered under magnetic condition, and the degradation efficiency after ten cycles could still maintain 98.95%. Both radicals quenching tests and electron spin resonance (ESR) identified both HO? and SO₄^?? were involved and SO₄^?? played a dominant role on the RhB degradation. Finally, the chemical states of the sample's surface elements were measured by X-ray photoelectron spectroscopy (XPS), and the possible activation mechanism in Fe₃O₄/CoFeCu-LDHs/PMS system was proposed according to comprehensive analysis.     

Particle Surface Hydrophobicity and the Dechlorination of Chloro-Compounds by Iron Sulfides

Halogenated aliphatic compounds (HACs) can be reduced by iron sulfides in aqueous systems. Generally, the thermodynamics and kinetics of dehalogenation reactions are controlled by the mineralogical and particle surface characteristics of the iron sulfide, the composition of the HAC and reaction conditions such as component concentrations, pH and Eh. In this theoretical and experimental investigation of CCl₄ and C₂Cl₆ reduction by FeS and FeS₂, the roles of hydrophobic and hydrophilic sites on the iron sulfides were analyzed. Experimental data obtained through zeta potential measurements, were used along with the Gouy-Chapman model and the simple two-layer surface complexation model to relate iron sulfide surface hydroxyl densities to the degree of HAC dehalogenation. The surface hydroxyl site densities of FeS and FeS₂ were found to be 0.11 sites/nm² and 0.21 sites/nm², respectively. During the dehalogenation reaction process, CCl₄ was found to decrease to its first intermediate product CHCl₃ within the first 20 hours followed by a slower process of conversion to CH₂Cl₂. The results also show that FeS is less hydrated (more hydrophobic) than FeS₂. For CCl₄ and C₂Cl₆, FeS is a better dehalogenator than FeS₂. These results imply that particle surface hydrophobicity is a critical factor in surface-mediated dehalogenation of chlorinated compounds.     

Effects of Climate and Land Cover on Hydrology in the Southeastern U.S.: Potential Impacts on Watershed Planning

The hydrologic response to statistically downscaled general circulation model simulations of daily surface climate and land cover through 2099 was assessed for the Apalachicola‐Chattahoochee‐Flint River Basin located in the southeastern United States. Projections of climate, urbanization, vegetation, and surface‐depression storage capacity were used as inputs to the Precipitation‐Runoff Modeling System to simulate projected impacts on hydrologic response. Surface runoff substantially increased when land cover change was applied. However, once the surface depression storage was added to mitigate the land cover change and increases of surface runoff (due to urbanization), the groundwater flow component then increased. For hydrologic studies that include projections of land cover change (urbanization in particular), any analysis of runoff beyond the change in total runoff should include effects of stormwater management practices as these features affect flow timing and magnitude and may be useful in mitigating land cover change impacts on streamflow. Potential changes in water availability and how biota may respond to changes in flow regime in response to climate and land cover change may prove challenging for managers attempting to balance the needs of future development and the environment. However, these models are still useful for assessing the relative impacts of climate and land cover change and for evaluating tradeoffs when managing to mitigate different stressors.     

Numerical Simulation of Light/Dark Cycle Frequency of Microalgae Fluid in a Helical Tubular Photobioreactor for Carbon Dioxide Capture

In the present study, three-dimensional numerical simulations are conducted on hydrodynamics and light-intensity distribution of microalgae fluid flow in a helical tubular photobioreactor for CO₂ capture. The effect of incident direction of the light illumination is discussed and the light/dark cycle frequency experienced by the microalgae fluid in the cross-section of the photobioreactor is investigated. The simulation results reveal the steadily nonhorizontal and unsymmetrical Dean roll-cells of the microalgae fluid flow in the cross-section of the helical tube. The external light projecting onto the helical tubular photobioreactor from the center is a better way for microalgae cultivation. The light/dark cycle frequency of the microalgae fluid flow is calculated based on the light-intensity distribution inside the photobioreactor. The light/dark cycle frequency keeps constant for the same stream trace of the microalgae flow while varies with different flow regions. Meanwhile, the light/dark cycle frequency increases with the increase in microalgae fluid velocity. The suitable demarcation between the light and the dark zone depends on the shape and the location of the Dean roll-cells.     

MWNTs/TiO2对典型氯苯类化合物的光催化降解研究

研究复合光催化剂MWNTs/TiO2对典型氯苯类有机化合物光催化降解动力学及主要光降解路径.结果表明,同一初始浓度和相同光催化降解实验条件下,60min时典型氯苯类有机化合物的光降解率均达到90%以上.其中六氯苯和五氯苯的光催化降解速率常数分别为0.0664h-1和0.0670h-1,其大小明显高于其它氯苯类化合物.1,二氯苯的光催化降解反应速率常数仅为0.0430h4--1,在典型氯苯类化合物中最小.三氯苯的3种同分异构体——1,3-三氯苯、24-三氯苯和1,5-三氯苯的光催化降解速率常数分别为0.0547h2,1,,3,-1、0445h0.-1和0.0439h-1.六氯苯的主要光催化降解路径为:HCB→PeCB→1,2,3,5-TeCB→1,2,4-TCB→1,4-DCB.     

大鹏湾表层沉积物中碳、氮、磷的多年调查结果和有机质来源分析

依据1998—2006年18个航次13个站的调查资料,简要描述和分析了大鹏湾表层沉积物中包括碳、氮、磷的多项生物地球化学要素多年的平均空间分布和年际变化,并依据TOC/TN原子比探讨沉积物中有机质的来源.结果表明,大鹏湾的水动力条件对沉积物中各生物地球化学要素的分布变化影响不大,TOC、TN和TP含量分别为(17600±4600) mg·kg^-1、(1738±446) mg·kg^-1和(562±89) mg·kg^-1,比珠江口和大亚湾高.9年调查期间,TOC、TC、TN和TP含量的年际变化趋势都是上升的,表明随着周边地区经济的迅速发展和人口的不断增加,产生的大量有机质通过小河流和地表径流排放入海,使大鹏湾中沉积物的环境逐渐恶化.TOC/TN原子比为12.4±2.5,介于海洋浮游生物源和陆生高等植物源之间,反映了大鹏湾表层沉积物中有机质是陆源和水生2种来源的混合输入.TOC/TN原子比呈逐年上升趋势,表明大鹏湾接受陆源有机质与水生有机质的比例逐渐增加.