基于白碳黑的水化硅酸钙制备及其磷回收特性简

以白碳黑、硅灰、硅藻土和硅胶筛选硅质原料，并与钙质原料电石渣制备了水化硅酸钙。借助XRF、BET、FTIR等表征手段，通过多次重复除磷实验，研究了硅质原料特性对水化硅酸钙回收磷性能的影响。结果表明，白碳黑具有极高的反应活性，因此可作为制备具有磷回收特性的水化硅酸钙的硅质原料。结合XRD等表征发现，白碳黑的有效利用率是影响水化硅酸钙回收磷性能的关键，该利用率取决于白碳黑与电石渣的摩尔配比以及水热反应温度。当电石渣与白碳黑的摩尔比为1.6：1，反应温度为170℃时，白碳黑具有最佳的利用效率。该条件制备的水化硅酸钙可作为晶种，在其表面结晶形成羟基磷灰石，从而达到磷回收的目的，磷回收后固体物质中的磷含量为19.05%。     

CuO/γ-Al2O3类Fenton试剂降解丁基黄药

CuO/γ-Al2O3类Fenton试剂是降解丁基黄药的优良试剂。该试剂与传统的Fenton试剂相比,提高了反应的pH值,可在较高pH(4~5)条件下反应,而传统的Fenton试剂的适宜pH值一般在3以下。采用单因素实验和正交实验相结合的方法研究了pH、催化剂投加量、过氧化氢投加量以及反应时间对丁基黄药降解效果的影响,并对催化剂的使用寿命进行了探讨。研究结果表明,反应的最佳条件为:pH为4~5,催化剂投加量为6 g/L,过氧化氢用量为30 mg/L,反应30min。在此反应条件下,丁基黄药的降解率达98%以上;影响丁基黄药降解效果的因素大小顺序为:pH>反应时间>H2O2用量>催化剂投加量,其中pH对CuO/γ-Al2O3类Fenton试剂降解丁基黄药的影响最为显著。     

Simulation of dam/levee-break hydrodynamics with a three-dimensional implicit unstructured-mesh finite element model

Dam failures usually cause huge economic and life losses , especially in urban areas where there is a high concentration of inhabitants and economic actors. In order to understand the physical mechanisms of the formation and development of dam-break flooding, lots of efforts have been put into different types of modelling techniques. However, most of existing models are 1D (one-dimensional) or 2D models based on the shallow water equations. In this paper, we present a 3D numerical modelling investigation of dam-break flow hydrodynamics in an open L-shape channel. A newly developed 3D unstructured mesh finite element model is used here. An absorption-like term is introduced to the Navier–Stokes equations in order to control the conditioning of the matrix equation in the numerical solution process and thus improve the stability. A wetting and drying algorithm is used here to allow the free surface height to be treated with a high level of implicitness and stability. The 3D model has been validated by comparing the results with the published experimental data. Good agreement has been achieved at six selected locations. This study shows that the 3D unstructured mesh model is capable of capturing the 3D hydraulic aspects and complicated local flows around structures in simulation of dam-break flows.     

TiO2载体对Mn-Ce/TiO2催化剂脱硝活性的影响

以TiO₂为载体,选取过渡金属元素Mn为活性组分,稀土金属元素Ce为活性助剂,采用分步共混法制备了Mn-Ce/TiO₂催化剂（活性组分负载量16%）,系统研究了TiO₂载体的晶型和晶粒尺寸对催化剂脱硝活性的影响。实验结果表明：分别以锐钛矿型和金红石型TiO₂为载体制备的催化剂,其低温脱硝活性相差不大,活性组分均以无定型态高度分散于载体中,以金红石型TiO₂为载体制备的催化剂中部分TiO₂转变为锐钛矿型;以不同晶粒尺寸TiO₂载体制备的催化剂的低温脱硝活性相差较大,比表面积较大、晶粒尺寸较小的TiO₂载体制备的催化剂,其脱硝活性低于晶粒尺寸较大的TiO₂载体制备的催化剂。     

DO浓度对间歇曝气单级自养脱氮系统N2O排放的影响

以单级自养脱氮系统为研究对象,采用有效容积为15 L的SBBR反应器,系统进水NH+4-N浓度约为360 mg/L,控制温度为(30±2)℃,采用间歇曝气方式运行,曝气段DO浓度从2.4~2.6 mg/L逐渐下降到0.9~1.1 mg/L,研究了单级自养脱氮系统的脱氮性能与N2O排放情况。结果表明,反应器曝气段DO浓度从2.4~2.6 mg/L下降到0.9~1.1mg/L,系统TN去除率均达到80%,但在相同运行时间内的TN去除率依次降低,NH+4-N平均反应速率从0.19 mg/(L·min)降低至0.05 mg/(L·min),NO-3-N累计产生量稳定于14.9~16.5 mg/L,NO-2-N浓度在反应器内未产生明显的积累。随着曝气段DO浓度的下降,最大N2O释放速率逐渐降低,N2O累计释放量从73.8 mg下降到61.0 mg,N2O转化率介于2.4%~2.9%。     

黄河甘宁蒙段表层沉积物中总磷3种提取方法的比较

通过微波消解法、标准测试方法(SMT)和碱熔法分别测定了水系沉积物成分分析标准物质GBW07307a(GSD-7a)中的总磷(TP)含量,并分别采用3种方法对采集于黄河流域甘宁蒙段表层沉积物样品进行TP含量和样品加标回收率的测定。结果表明:测定标准物质的相对误差绝对值:微波消解法碱熔法SMT法;变异系数:微波消解法碱熔法SMT法。同时,微波消解法提取的表层沉积物TP含量的范围为634.3~909.2μg/g;SMT法TP含量的范围为627.1~889.5μg/g;碱熔法TP含量的范围为559.1~784.8μg/g。微波消解法的测定结果相对偏高,SMT法的测定结果相对偏低。样品加标回收率平均值:微波消解法SMT法碱熔法;变异系数:微波消解法碱熔法SMT法。综合测定标准物质中TP含量以及样品加标回收率实验结果的准确度和精密度,对于黄河甘宁蒙段表层沉积物,使用SMT法提取TP较优于微波消解法和碱熔法。     

工业烟气氨法-络合法同时脱硫脱硝

在脱硫脱硝喷淋装置上采用氨法-络合法处理工业烟气。考察了吸收液pH、Fe(Ⅱ)EDTA浓度、初始烟气浓度、液气比对烟气同时脱硫脱硝效果的影响。实验结果表明:吸收液的酸碱度通过影响Fe(Ⅱ)与EDTA的络合形式进而影响NO去除率;SO_2去除率主要受吸收液pH和初始SO_2质量浓度的影响;当吸收液pH大于8、吸收液Fe(Ⅱ)EDTA浓度大于0.100 mol/L、初始SO_2质量浓度小于1 500 mg/m3、初始NO质量浓度为1 200 mg/m3时,SO_2去除率均在95%以上,NO去除率为54%;当液气比由1 L/m3增大至4 L/m3时,有效脱硫时间和有效脱硝时间分别增长了7 min和4 min。     

我国旅游景区经营模式的构想

本文以旅游景区的经营模式为研究核心，从现有国内外旅游景区组织结构分析入手，构建了适合我国国情和旅游景区可持续发展要求的两种经营模式：一种是国有国营的次国家公园模式，另一种是完全企业化经营，并且提出了两种模式运作的保障条件。     

Atmospheric deposition of phthalate esters in a subtropical city

In Chinese cities, air pollution has become a serious and aggravating environmental problem undermining the sustainability of urban ecosystems and the quality of urban life. Bulk atmospheric deposition samples were collected two-weekly, from February 2007 to January 2008, at three representative areas, one suburban and two urbanized, in the subtropical city, Guangzhou, China, to assess the deposition fluxes and seasonal variations of phthalate esters (PAEs). Sixteen PAE congeners in bulk deposition samples were measured and the depositional fluxes of ∑₁₆PAEs ranged from 3.41 to 190 μg m^?2 day^?1, and were highly affected by local anthropogenic activities. The significant relationship between PAEs and particulate depositional fluxes (correlation coefficient R² = 0.72, P < 0.001) showed PAEs are associated primarily with particles. Temporal flux variations of PAEs were influenced by seasonal changes in meteorological parameters, and the deposition fluxes of PAEs were obviously higher in wet season than in dry season. Diisobutyl phthalate (DiBP), Di-n-butyl phthalate (DnBP), and Di(2-ethylhexyl) phthalate (DEHP) dominated the PAE pattern in bulk depositions, which is consistent with a high consumption of the plasticizer market in China. PAE profiles in bulk deposition showed similarities exhibited in both time and space, and a weak increase of high molecular weight PAE (HMW PAE) contribution in the wet season compared to those in the dry season. Average atmospheric deposition fluxes of PAEs in the present study were significantly higher than those from other studies, reflecting strong anthropogenic inputs as a consequence of rapid industrial and urban development in the region.     

Bio-immobilization of Cu and Zn in recirculated bioreactor landfill

Purpose  

To protect the environmental quality of soil, groundwater, and surface water near the landfill site, it is necessary to make an accurate assessment of the heavy metal mobility. This study aims to present the bio-immobilization behavior of heavy metals in landfill and provide some reference suggestion for the manipulation of heavy metal pollution control after closure.