碳酸根对磷酸钙沉淀反应回收磷的影响简

以模拟的厌氧消化液为处理对象,通过小试实验,考察不同初始磷浓度C_P、Ca/P物质的量比、pH和温度下,碳酸根（CO₃^2-）对磷酸钙沉淀反应回收磷的影响;利用扫描电镜（SEM）、X射线衍射仪（XRD）和傅里叶变换红外光谱（FTIR）对沉淀产物进行表征。结果表明,高浓度的CO₃^2-对以磷酸钙沉淀反应去除和回收磷的效率影响较大;C_P相同时,CO₃^2-浓度（C_CO3^2-）越大,P的去除率越低,低C_P（20 mg/L）时尤为显著;当C_CO3^2-相同时,随着C_P的增大,反应速率加快,P的去除率逐渐升高,但升高幅度越来越小;增大Ca/P比和pH能提高P的去除率,降低CO₃^2-对磷酸钙沉淀反应的抑制作用,综合考虑实际效果,应选择Ca/P比为3.33,pH为9.0作为适宜的反应条件;升高温度对降低CO₃^2-对磷酸钙沉淀反应的抑制作用贡献不大。在C_P为60 mg/L,Ca/P比为1.67,pH为9.0,温度为20℃的条件下,当C _CO3^2-为0时,得到的沉淀产物主要为羟基磷灰石HAP;当C _CO3^2-为30 mmol/L时,得到的沉淀产物为磷酸钙和碳酸合磷灰石的混合物。     

水平潜流人工湿地在不同水力负荷下的水力效率及可视化分析

构建水平潜流人工湿地装置,通过NaCl示踪脉冲实验,得到不同水力负荷条件下的水力停留时间分布密度曲线,根据不同停留时间的关系计算相对水力效率,并利用染料,进行不同水力负荷下的可视化示踪实验,通过MATLAB处理得到高对比度的流态图像。观察"死区"分布,计算"死区"相对面积用以表征其水力效率。结果表明,湿地装置进水水力负荷较高或较低时,水力效率均较低,且水力负荷较大时更明显;水力分布散度(σ2θ)的大小会对水平潜流人工湿地水力效率造成较大影响;在不同水力负荷下,采用水力学效能(λ)所得到的排序结果相比短路值(s)和有效体积比(e)更能代表实际水平潜流人工湿地的水力效率。     

络合萃取技术分离制药废水中的金刚烷胺

以P204为络合剂萃取水溶液中的金刚烷胺,研究了正辛醇和煤油2种稀释剂对萃取效果的影响,分析了萃取过程的络合机理和热力学过程,并考察了该萃取体系对实际制药废水中金刚烷胺的萃取效果。结果表明,采用P204/正辛醇=3∶2的复配萃取剂,在初始pH为8.0,在油/水相比为1∶1的条件下,金刚烷胺的萃取效率可以达到99.8%以上;以2.0mol/L的HCl溶液为反萃取剂,可以将51.1%的负载金刚烷胺反萃回收;红外光谱分析表明,P204对金刚烷胺的萃取遵循离子交换和离子缔合成盐机制;萃取过程为放热过程,低温条件下有利于萃取反应的进行;P204/正辛醇复配萃取剂对实际制药废水中的金刚烷胺也具有很高的萃取效率。     

Green and compatible industrial development in Western China

Western China has lagged a lot in terms of industrial structure and economic development,compared with the national average.And China announced its target of CO_2 emission reduction,i.e.by 2020,CO_2 emission per GDP will drop by40-45%compared with 2005.The target will be incorporated into China's long-term industrial planning.Against this background,this paper will make a comprehensive examination of the industrial development of Western China,aiming to discover a green and compatible way.First,we analyze the spatiotemporal evolution of regional industrial structure for the period 2000-2010.Second,we try to discover the industrial structure optimization path for Western China by employing the Vector Auto Regression model.Lastly,we try to provide some advice and suggestions for further industrial development in Western China.Our examination shows that further industrial development in Western China should pay full attention to resource conservation and recycling,and develop on a green and compatible path.     

Mn/γ-Al2O3催化剂的制备及头孢合成废水的催化臭氧氧化法深度处理

对Mn/γ-Al₂O₃催化剂的制备条件及头孢合成废水的催化臭氧氧化法深度处理工艺条件进行了优化。实验结果表明：以Mn（NO₃）₂溶液为浸渍液,Mn/γ-Al₂O₃催化剂的最优制备条件为浸渍液浓度0.10 mol/L、浸渍时间9 h、焙烧温度400 ℃、焙烧时间2 h;在反应时间为30 min、废水pH为9.0、臭氧通量为4.6 mg/min、催化剂加入量为5 g/L的条件下,当进水COD、BOD₅、ρ（氨氮）和色度分别为220~250 mg/L,8~10 mg/L,10~12 mg/L和60~70倍时,出水COD、BOD₅、ρ（氨氮）和色度的平均去除率分别为53%,30%,33%和93%,出水水质满足GB 21904—2008《化学合成类制药工业水污染物排放标准》的要求。     

利用白云石石灰去除与回收污泥厌氧消化液中氮和磷

以白云石石灰为实验材料去除与回收污泥厌氧消化液中的氮磷,通过小试实验研究不同投药固液比S/L、初始pH值、反应温度、搅拌速度及反应时间对去除与回收氮磷效果的影响。实验结果表明,在最佳投药固液比S/L为300mg/L,最佳初始pH值范围为8.5~9.5,反应温度为25.0℃,搅拌速度为150 r/min,反应时间为24 h条件下,氨氮(NH+4-N)和磷(PO3-4-P)的去除率分别为37.26%和89.60%。利用X射线衍射仪(XRD)、扫描电镜(SEM)对沉淀产物进行了表征,通过分析可知沉淀产物中含有磷酸铵镁(MAP),可实现废水中氮磷经济有效的回收。     

添加天然沸石和石灰对土壤镉形态转化的影响

采用土壤培养实验,研究镉污染土壤中添加沸石、石灰及两者配施对土壤pH值和土壤镉形态变化的影响。结果表明,土壤pH值随沸石用量的增加而增加,随培养时间呈现先增加后下降并逐渐趋于稳定的趋势,但均高于对照。高剂量石灰的处理对土壤pH的影响最大,与对照相比土壤pH提高了3.33个单位。在土壤5~50 d培养过程中,石灰处理的土壤交换态镉含量呈现先逐渐降低而后略有升高的趋势,其余处理均呈下降趋势。培养50 d后,高剂量的沸石、石灰及高剂量沸石与石灰配施处理的土壤交换态镉含量从5 d时的67.54、61.95和55.56 mg/kg降低至54.65、49.93和45.96mg/kg。相关分析表明,不同培养时期交换态镉含量与土壤pH值呈负相关关系。在10个处理中,L2Z3(石灰2 g/kg土和沸石60 g/kg土)组合处理效果最好,使土壤交换态镉含量下降了34.68%,碳酸盐结合态镉含量上升了4.30%,铁锰氧化结合态镉含量上升了16.97%,有机结合态镉含量上升了1.31%,残渣态镉含量上升了12.11%。     

Oxidation of ofloxacin by Oxone/Co2+: identification of reaction products and pathways

Oxidative degradation of ofloxacin (OFX) by sulfate free radicals (SO₄ ^??) in the UV/Oxone/Co²⁺oxidation process was investigated for the first time, with a special focus upon identifying the transformation products as well as understanding the reaction pathways. Thirteen main compounds were identified after the initial transformation of OFX; the detailed structural information of which were characterized by high-performance liquid chromatography–high resolution mass spectrometry and MS fragmentation analysis. The degradation pathways mainly encompassed ring openings at both the piperazinyl substituent and the quinolone moiety, indicating that the usage of SO₄ ^?? aided the oxidative degradation of OFX to undergo more facile routes compared to those in previous reports by using OH^?/h⁺ as the oxidant, where the initial transformation attacks were mainly confined to the piperazine moiety. Moreover, in this study, smart control over the pH conditions of the oxidation system via different modes of Oxone dosage resulted in the selective degradation of the functional sites of OFX molecule, where it was shown that the SO₄ ^??-driven destruction of the quinolone moiety of OFX molecule favored the neutral pH conditions. This would be beneficial for the reduction of bacterial resistance against quinolones in the aqueous environment.     

Characterization of the interactions between tetracycline antibiotics and microbial extracellular polymeric substances with spectroscopic approaches

The antibiotics have attracted global attentions for their impact on aquatic ecosystem. The knowledge about the fate of antibiotics encountering extracellular polymeric substances (EPS) is, however, limited. In this study, we investigated the interacting mechanisms of tetracycline (TC) to EPS extracted from aerobic activated sludge. The contributions of the main components of EPS, extracellular proteins, and polysaccharides were evaluated using bovine serum albumin and alginate sodium, respectively. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and nuclear magnetic resonance indicated that hydroxyl, carboxyl, and amino groups were the domain chemical groups involved in the interaction between TC and EPS, and the binding of TC onto EPS changed the structure of these chemical groups, thus causing shifts in their UV–visible absorption spectra. In addition, we found that extracellular proteins, rather than polysaccharides, were the major active contents involved in the interaction. Three-dimensional excitation–emission matrix fluorescence spectroscopy showed that the fluorophores in EPS were clearly quenched by TC and the static quenching process was observed, implying the complex formation of TC and EPS. Furthermore, thermodynamic analysis indicated that the binding of TC with EPS is spontaneous and dominated by electrostatic forces.     

Methods for Quantifying Variability and Uncertainty in AP-42 Emission Factors: Case Studies for Natural Gas-Fueled Engines

Abstract

Quantitative methods for characterizing variability and uncertainty were applied to case studies of oxides of nitrogen and total organic carbon emission factors for lean-burn natural gas-fueled internal combustion engines. Parametric probability distributions were fit to represent inter-engine variability in specific emission factors. Bootstrap simulation was used to quantify uncertainty in the fitted cumulative distribution function and in the mean emission factor. Some methodological challenges were encountered in analyzing the data. For example, in one instance, five data points were available, with each data point representing a different market share. Therefore, an approach was developed in which parametric distributions were fitted to population-weighted data. The uncertainty in mean emission factors ranges from as little as ~±10% to as much as -90 to 21+180%. The wide range of uncertainty in some emission factors emphasizes the importance of recognizing and accounting for uncertainty in emissions estimates. The skewness in some uncertainty estimates illustrates the importance of using numerical simulation approaches that do not impose restrictive symmetry assumptions on the confidence interval for the mean. In this paper, the quantitative method, the analysis results, and key findings are presented.