土壤中二价铁离子的伏安法测定

利用二价铁离子的联吡啶络合物,示差脉冲伏安法测定土壤中的二价铁离子．结果表明:二价铁离子的浓度与铁联吡啶络合物的峰电流在１．６×１０－６－９．８×１０－６ｍｏｌ·ｌ－１和９．８×１０－６－６．６× １０－５ｍｏｌ·ｌ－１浓度范围内成正比,检测下限为４．１× １０－７ｍｏｌ·ｌ－１,相对标准偏差为０．８４%(ｎ＝６)．在该方法中,联吡啶的浓度对二价铁离子联吡啶络合物的峰电位、峰电流及半峰宽度有影响,而测定体系的ｐＨ值和支持电解质的浓度对二价铁离子联吡啶络合物的峰电位、峰电流及半峰宽度影响较小．     

脉冲电流对电化学除氯的影响

目的 探究不同电流密度下,直流和脉冲2种电流模式对钢筋混凝土电化学除氯的影响,降低钢筋渗氢量,减小通电后阴极产生的氢气使钢筋发生氢脆的风险,提高除氯效率,改善电化学除氯效率的均匀性。方法 通过在电流密度为2、3、4 A/m²的条件下,对混凝土进行直流和脉冲电流电化学修复,测定处理后的钢筋的释氢电流,计算释氢总电量,来表示钢筋渗氢量,对比处理后强电流区和弱电流区混凝土的氯离子含量,分析2种方式除氯效率的均匀性,同时用扫描电子显微镜观察电化学除氯前后混凝土的微观结构。结果 计算得到不同通电电流密度下钢筋的释氢总电量和除氯效率,脉冲电流的释氢总电量比直流电流低约20%,而除氯效率提高了约10%。结论 增加电流密度可以提高除氯效率,但是会增加钢筋发生氢脆的风险。相较于直流电流,脉冲电流电化学修复可以降低钢筋渗氢量,显著提高弱电流区的除氯效率,从而改善除氯效率的均匀性。     

脉冲通风法治理“U”型工作面上隅角瓦斯积聚的理论及技术探讨

针对生产现场出现的“U”型采煤工作面上隅角瓦斯积聚问题 ,科学地分析了其形成的原因及目前解决上隅角瓦斯积聚的常用方法 ,提出了旋转脉冲法解决此问题的新途径 ,并进行了详细的理论分析。通过现场实验 ,验证了用旋转脉冲法解决上隅角瓦斯积聚是有效的、可行的。     

大型脉冲袋式除尘器的自动控制

对大型脉冲袋式除尘器自动控制的有关问题作了研讨。研制成功了以中型可编程控制器为主机的“BMC-V型大型脉冲袋式除尘器电脑控制系统”,实际运行效果良好。     

水解-交替脉冲曝气工艺处理城市污水研究

采用淹没式膜法水解-交替脉冲曝气系统对城市污水的处理效能进行研究,讨论了装置进水COD浓度变化对生活污水处理效果的影响、处理工艺沿程COD、NH3-N浓度变化状况、NH3-N的去除、水解对COD去除效果的影响以及进水COD/N比与反硝化的关系。研究表明,该系统能有效地去除COD和NH3-N。进水COD在450mg/L以下时,出水COD基本维持在60mg/L以下;进水NH3-N<50mg/L时,出水NH3-N<10mg/L。     

超声脉冲压缩法检测混凝土损伤的研究

为提高混凝土超声检测的信号噪声比,提高测量精度,研究脉冲压缩调频超声发射的方法。该方法发射具有包络的线性调频超声脉冲,在不提高发射声压的情况下增加了发射能量,可提高超声检测的有效作用距离和测量精度,提高信噪比。笔者给出脉冲压缩和解压的基本原理,设计了脉冲解压缩电路;经实验检测结果表明,脉冲压缩超声检测能在没有降低测量距离的情况下,明显提高检测的精度,检测到常规检测中不能发现的缺陷。     

Evaluation of large-scale CO2 storage on fresh-water sections of aquifers: An example from the Texas Gulf Coast Basin

Large-scale injections of CO₂ into subsurface saline aquifers have been proposed to remediate climate change related to buildup of green house gases in the atmosphere. The pressure buildup caused by such injections may impact a volume of the basin significantly larger than the CO₂ plume itself. In areas with hydrological settings similar to the Gulf Coast Basin, the perturbation of the flow-field in deep parts of the basin could result in brines or brackish water being pushed up-dip into unconfined sections of the same formations or into the capture zone of fresh-water wells. The premise of the current study is that the details of multiple-phase flow processes necessary to model the near field evolution of the CO₂ plume are not necessary to describe the impact of the pressure anomaly on up-dip aquifers. This paper quantitatively explores conditions under which shallow groundwater would be impacted by up-dip displacement of brines, utilizing an existing carefully calibrated flow model. Modeling an injection of water, arguably equivalent to 50 million tons of CO₂/year for 50 years resulted in an average water-table rise of 1 m, with minor increase in stream baseflow and larger increase in ground water evapotranspiration, but no significant change in salinity.     

Ultrasensitive determination of carbendazim in water and orange juice using a carbon paste electrode

A carbon paste electrode was used for the electrochemical quantification of carbendazim in water and orange juice samples. Carbendazim oxidation on the electrode surface was found to be controlled by adsorption. The novel electrochemical procedure for carbendazim quantification employed differential pulse voltammetry using a carbon paste electrode under optimal conditions. Carbendazim oxidation currents were linear at concentrations of 2.84 to 45.44 µg L^?1, with a limit of detection of 0.96 µg L^?1. The proposed method was applied to carbendazim quantification in ultrapurified water, river water, and orange juice. Recovery rates in water and orange juice samples were in the 97%–101% range, indicating that the method can be employed to determine carbendazim in these matrices, with advantages including shorter analysis time and lower cost than routine methods such as chromatography or spectroscopy. The electrode showed good reproducibility, remarkable stability, and especially good surface renewability by simple mechanical polishing. The recovery rates observed were highly concordant with those obtained for high-performance liquid chromatography, having a relative standard deviation of less than 1.3%.     

废弃印刷电路板上电子元器件拆卸新工艺及其机理

为了明确利用热空气模拟工业余热作为热源和脉动喷吹动力源拆卸废弃印刷电路板上电子元器件的拆卸机制,分析了废弃印刷电路板脉动喷吹性质,设计并建立了废弃印刷电路板拆卸实验室小试系统,利用Fluent数值模拟软件对拆卸过程中废弃印刷电路板自动拆卸设备内部温度场进行了详细考察,在此基础上,对实验结果进行验证。结果表明,短重边最佳喷吹条件(0.14 MPa,10 mm)下,振动角度为75°;短轻边最佳喷吹条件(0.12 MPa,10 mm)下,振动角度为76°;下进气条件(温度场更均匀,焊料面平均受热温度为198.81℃)更利于废弃印刷电路板上电子元器件的拆卸;采用下进气方式、当预热温度120℃、通气温度为260℃、设备内部达195℃继续通气(拆卸时间)1 min、短重边脉动喷吹压力0.14 MPa、短重边喷吹距离10 mm、短轻边脉动喷吹压力0.12 MPa、短轻边喷吹距离10 mm时,元器件拆卸率为95.1%,且元器件外观完好。本研究明确了废弃印刷电路板拆卸过程中的受热与受力机制,实现了废弃印刷电路板上电子元器件的高效拆卸,为此工艺大规模、工业化生产的实现奠定了理论基础。     

Kinetic studies of endosulfan photochemical degradations by ultraviolet light irradiation in aqueous medium

Kinetic studies of endosulfan photochemical degradation in controlled aqueous systems were carried out by ultraviolet light irradiation at λ = 254 nm. The photolysis of (α + β: 2 + 1) endosulfan, α-endosulfan and β-endosulfan were first-order kinetics. The observed rate constants obtained from linear least-squares analysis of the data were 1 × 10^?4 s^?1; 1 × 10^?4 s^?1; and 2 × 10^?5 s^?1, respectively, and the calculated quantum yields (φ) were 1, 1 and 1.6, respectively. Preliminary differential pulse polarographic (DPP) analysis allowed to observe the possible endosulfan photochemical degradation pathway. This degradation route involves the formation of the endosulfan diol, its transformation to endosulfan ether and finally the ether's complete degradation by observing the potential shifts.