木醋调质石灰石直接硫化反应特性研究

针对O2/CO2燃烧技术适于采用炉内喷钙脱硫方式脱硫而钙利用率仍有较大提升空间的问题,采用木醋废液调质改性石灰石,并利用热分析方法对木醋调质石灰石在O2/CO2气氛下的直接硫化反应特性进行了试验研究。试验结果表明石灰石经木醋调质后直接硫化反应性能显著提高,反应温度、吸收剂粒径以及反应气氛中SO2和O2的浓度都对直接硫化反应存在影响,分析认为调质对石灰石热解固体产物微观结构的改善是脱硫性能得以显著提升的主因。     

适合严寒地区直流换流站外冷却系统的研究

针对目前严寒地区直流换流站外水冷系统多采用空气冷却方式,而空气冷却方式存在造价高、占地多、运行费用高等不利因素,设计了一种新型外水冷系统,冬季利用漏水孔板淋水带走内水冷系统的热量,并采取必要的防冻措施。该系统应用于北方严寒地区,可以大大降低初投资,减少占地面积,运行费用降低,噪声减小,同时也保证了直流输电系统的安全可靠运行,具有极大的经济效益和推广价值。     

烧结法赤泥的强度演化规律

筑坝堆存是现在处理赤泥的主要方式,为了堆场安全继续向上堆载,对烧结法赤泥强度的演变规律进行了研究。通过对比不同深度处赤泥的抗剪强度,表明赤泥强度的形成与堆载时间没有必然的联系;再通过对新进场的赤泥进行强度追踪,得到赤泥强度形成过程中抗剪强度与滤水固结时间的关系曲线,从时间因素上为赤泥的安全堆载提供一个理论依据。     

脉冲电源电凝聚处理厨房废水的研究

将脉冲电源和直流电源分别作为电凝聚处理废水的外加电源,拟试验探明电源对电凝聚处理废水的电能消耗的影响和相关参数的优化.试验结果表明,脉冲电源相对直流电源能更加有效降低阳极的超电位,减缓电极的极化,从而降低槽电压,进而有效地降低电能消耗.在试验条件下,脉冲频率对处理效果影响不显著,而脉冲占空比对处理效果有明显的影响,较合适的脉冲电源电凝聚处理废水的优化参数是:脉冲频率1 000 Hz、占空比60%.同时,对电解槽沉积絮凝物的处理进行了说明.     

环境样品中全氟辛酸分析方法的研究进展

全氟辛酸作为一类持久有毒化学污染物引起了人们的高度关注。本文总结了含全氟辛酸样品的前处理方法和检测方法。主要介绍了HPLC和GC等方法,并对今后的研究方向进行了展望。     

Effect of high-voltage direct current link on small signal stability of a power system with different penetration level of doubly fed induction generator and direct drive synchronous generator based wind farms

High penetration level of wind power has significant impact on the dynamic performance of power system. Power system with existing high-voltage direct current (HVDC) link may influence the stability of power system at high penetration level of wind power. This article investigates the stability issues of power system with existing HVDC link for different penetration level of doubly fed induction generator (DFIG) and direct drive synchronous generator (DDSG) based wind farms. The small signal stability analysis shows that power system with HVDC link has improved the stability of the power system for increased penetration of DFIG- and DDSG-based wind farms.     

Cloud point extraction coupled with HPLC-UV for the determination of phthalate esters in environmental water samples

A method based on cloud point extraction was developed to determine phthalate esters including di-ethyl-phthalate （DEP）, di- （2-ethylhexyl）-phthalate （DEHP） and di-cyclohexyl-phthalate （DCP） in environmental water samples using high-performance liquid chromatography separation and ultraviolet detection （HPLC-UV）. The non-ionic surfactant Triton X-114 was chosen as extraction solvent. The parameters affecting extraction efficiency, such as concentrations of Triton X-114 and Na2SO4, equilibration temperature, equilibration time and centrifugation time were evaluated and optimized. Under the optimum conditions, the method can achieve preconcentration factors of 35, 88, 111 and detection of limits of 2.0, 3.8, 1.0 ng/ml for DEP, DEHP and DCP in 10-ml water sample, respectively. The proposed method was successfully applied to the determination of trace amount of phathalate esters in effluent water of the wastewater treatment plant and the lixivium of plastic fragments.     

Formation of multiple trimethylsilyl derivatives in the derivatization of 17α-ethinylestradiol with BSTFA or MSTFA followed by gas chromatography-mass spectrometry determination

N,O-bis(trimethylsily)trifluoroacetamide (BSTFA) and N-methyl-N(trimethylsily) trifluoroacetamide (MSTFA) are common derivatization reagents used in the GC-MS analysis of estrogen steroids such as estrone (E1) and 17(-ethinylestradiol (EE2). In this study, three trimethylsilyl (TMS) steroid derivatives, mono-and di-trimethylsilyl EE2 and mono-trimethylsilyl E1, were observed during the derivatization of EE2 with BSTFA or MSTFA and/or GC separation. Factors influencing the production of multiple TMS derivatives and their relative abundance were examined. It was found that both methanol and bisphenol A competed with estrogenic esteroids when reacting with silylation reagents, and thus affected the formation of TMS derivatives and their relative abundance in the derivatization products. Methanol was found to be more reactive than bisphenol A with the BSTFA reagent. None of the three solvents tested in this study could prevent the generation of multiple TMS derivatives during the derivatization of EE2 with BSTFA, followed by GC analysis. A similar result was observed using MSTFA as the derivative reagent followed by GC analysis. Thus, the suitability of BSTFA or MSTFA as the derivatization reagent for the determination of E1 and EE2 by GC-MS, under the conditions reported here, is questionable. This problem can be solved by adding trimethylsilylimidaz (TMSI) in the BSTFA reagent as recommended, and the performance of the method has been proved in this study.     

Effects of humic acid coatings on phenanthrene sorption to black carbon

Black carbon (BC) can strongly adsorb hydrophobic organic compounds (HOCs).The HOC sorption to coated BC could be attenuated in soil and sediment compared with that of the parent BC.To study the potential causes of the sorption attenuation,humic acid (HA) and BC were isolated.Phenanthrene (PHE) was selected as the representative of HOCs.BC was coated with the precipitated HA.The PHE sorption to the HA-coated BC was determined.The HA coatings on BC could result in the significant sorption attenuation of PHE to BC.The attenuation varied in different HA origin and was positively correlated to the aromaticity of HA.The attenuation could be explained by the direct competition between HA and PHE for the available sorption sites on BC and the reduction of the available sorption sites as a result of the pore blockage of BC caused by the HA coatings.Therefore,the HA coatings on BC was one potential cause of the attenuation of HOC sorption to BC in soil and sediment.     

Anoxic biodegradation of dimethyl phthalate （DMP） by activated sludge cultures under nitrate-reducing conditions

Worldwide extensive use of plasticized plastics has resulted in phthalates pollution in different environment. Nitrates from industry and agriculture are also widely disseminated in the soils, natural waters and wastewaters. Dimethyl phthalate (DMP) biodegradation by activated sludge cultures under nitrate-reducing conditions was investigated. Under one optimized condition, DMP was biodegraded from 102.20 mg/L to undetectable level in 56 h under anoxic conditions and its reaction fitted well with the first-order kinetics. Using the high-performance liquid chromatography (HPLC) and liquid chromatography mass spectrometry (LC-MS) analysis, mono-methyl phthalate (MMP) and phthalic acid (PA) were detected as the major intermediates of DMP biodegradation. When combined with the determination of chemical oxygen demand (CODCr) removal capacity and pH, DMP was found to be mineralized completely under anoxic conditions. The biodegradation pathway was proposed as DMP → MMP → PA → … → CO2 H2O.The molar ratio of DMP to nitrate consumed was found to be 9.0:1, which agrees well with the theoretical stoichiometric values of DMP biodegradation by nitrate-reducing bacteria. The results of the non-linear simulation showed that the optimum pH and temperature for the degradation were 7.56 and 31.4℃, respectively.