北京市危险化学品企业安全生产风险评估分级研究

为对北京市危化品企业基本情况的全面掌握,开展了危险化学品企业安全生产风险评估分级研究,借鉴国外经验和国内有关科研成果,提出了固有风险和动态风险相结合的危化品安全生产风险评估方法。固有风险为企业的基本风险水平,主要由危险化学品物质量、工艺水平、安全监控和周边环境决定,为共性指标;动态风险,反映企业安全生产管理绩效的水平,主要包括安全基础管理和现场管理,为个性指标,不同企业类型,评估动态风险指标有差异。从大量数据中抽取了最能反应企业安全生产状态的指标因素,通过专家组打分法和层次分析法确定评价因素的权重,该评估方法具有较强的实用性和可操作性,是本质安全和安全绩效的创新结合,为企业安全生产评估分级提供了新思路。通过分级,按照"风险优先"原则,政府部门实行差别监管,降低安全监管成本,促进危险化学品安全生产工作向规范化、科学化转变。同时,研制了危化品企业安全生产风险分级系统,为建立北京市危化品企业风险分级数据库奠定了基础。     

安全投入模型的研究

从安全投入产出分析的角度为安全投入决策提出一个新视角,相比于直接用生产函数等数学方法得到安全投入与安全产出的关系,通过软件分析得出各个要素与安全产出的关系,再进行拟合,最后得到安全产出回归方程,这样得到的分析结果更准确和可信。通过实例可以证明如果要确定安全投入要素之间的分配比例可以采用生产函数分析方法,如要预测安全产出可以采用根据散点图做出的回归方程。另外,在分析安全投入要素相对重要度时,因为各个投入要素的数量级和单位的不同,回归方程系数应选择标准化回归系数;要预测安全投入产生的安全产出则应采用非标准化回归系数。     

微电解—芬顿氧化工艺预处理高浓度松香改性酚醛树脂生产废水

为了降低松香改性酚醛树脂生产废水的COD并改善其可生化性,采用微电解—芬顿氧化工艺对该废水进行预处理。研究了pH、微电解反应时间、曝气、双氧水投加量等对微电解和芬顿氧化处理效果的影响,考察了COD去除率和BOD₅/COD值的变化趋势。实验结果表明：曝气条件下,调节废水pH为4、进行2次微电解、微电解反应时间各2.0 h时,废水的COD去除率为38%,BOD₅/COD值提高为0.18;再投加7.5%（w）的双氧水,废水的COD去除率为65.3%,BOD₅/COD值为0.37。采用微电解—芬顿氧化的预处理工艺,不仅有效去除了废水的COD,而且显著改善了废水的可生化性。     

Evaluation of the technoeconomic feasibility of electrochemical hydrogen peroxide production for decentralized water treatment

• Gas diffusion electrode (GDE) is a suitable setup for practical water treatment. • Electrochemical H₂O₂ production is an economically competitive technology. • High current efficiency of H₂O₂ production was obtained with GDE at 5–400 mA/cm². • GDE maintained high stability for H₂O₂ production for ~1000 h. • Electro-generation of H₂O₂ enhances ibuprofen removal in an E-peroxone process. This study evaluated the feasibility of electrochemical hydrogen peroxide (H₂O₂) production with gas diffusion electrode (GDE) for decentralized water treatment. Carbon black-polytetrafluoroethylene GDEs were prepared and tested in a continuous flow electrochemical cell for H₂O₂ production from oxygen reduction. Results showed that because of the effective oxygen transfer in GDEs, the electrode maintained high apparent current efficiencies (ACEs,>80%) for H₂O₂ production over a wide current density range of 5–400 mA/cm², and H₂O₂ production rates as high as ~202 mg/h/cm² could be obtained. Long-term stability test showed that the GDE maintained high ACEs (>85%) and low energy consumption (<10 kWh/kg H₂O₂) for H₂O₂ production for 42 d (~1000 h). However, the ACEs then decreased to ~70% in the following 4 days because water flooding of GDE pores considerably impeded oxygen transport at the late stage of the trial. Based on an electrode lifetime of 46 days, the overall cost for H₂O₂ production was estimated to be ~0.88 $/kg H₂O₂, including an electricity cost of 0.61 $/kg and an electrode capital cost of 0.27 $/kg. With a 9 cm² GDE and 40 mA/cm² current density, ~2–4 mg/L of H₂O₂ could be produced on site for the electro-peroxone treatment of a 1.2 m³/d groundwater flow, which considerably enhanced ibuprofen abatement compared with ozonation alone (~43%–59% vs. 7%). These findings suggest that electrochemical H₂O₂ production with GDEs holds great promise for the development of compact treatment technologies for decentralized water treatment at a household and community level.     

含固率和接种比对叶菜类蔬菜垃圾厌氧消化的影响

通过叶菜类蔬菜垃圾中温批式厌氧消化实验,比较了含固率(3%、5%、7%)和接种比(1.5、2.5、3.5)对产甲烷效果的联合影响.结果表明,在研究实验参数范围内,含固率越低、接种比越高,越有利于缩短产甲烷反应迟滞期,平均日产甲烷速率越快.经过52d的培养,在含固率为3%、接种比为3.5的工况中,平均日产甲烷速率最快,达到9.5mL/(gVS?d),日最大产甲烷速率最快,达到49.8mL/(gVS?d),最早进入快速产甲烷期.当接种比为3.5时,随着含固率的升高,产甲烷速率下降,迟滞期延长,但单位底物累计产甲烷量增大,含固率7%时单位底物累计净产甲烷量为481mL/gVS.而当接种比为1.5时,含固率为5%和7%的工况均无法启动甲烷化反应,含固率为3%的工况的产气迟滞期达15d.挥发性有机酸的累积抑制甲烷化反应的启动,迟滞期随着液相中有机酸浓度的增加而延长,当有机酸浓度低于1260mg/L,甲烷化反应没有明显的迟滞期.     

城镇污水处理厂清洁生产等级评价二元语义模型与方法

为解决城镇污水处理厂清洁生产等级评价问题,采用定性分析与定量计算相结合的方法,着重构建了城镇污水处理厂清洁生产等级评价指标体系及其权重确定方法;利用线性加权综合评价方法、模糊数学和二元语义概念,建立了城镇污水处理厂清洁生产等级评价模糊综合模型,并据此提出级别特征值概念,进而建立城镇污水处理厂清洁生产等级评价的二元语义模型与方法.实例计算分析说明,文中建立的清洁生产等级评价二元语义模型与方法可操作性强,等级评定结果比采用隶属度最大原则更直观、更便于解释,具有很好的应用与推广价值.     

污泥浓度对双重后置反硝化工艺脱氮除磷的影响

利用城市实际污水考察了ρ(MLSS)在2 400、3 350、4 300和5 250 mg/L 4种工况下SBR反应器(厌氧/好氧/缺氧/再好氧/沉淀/排水/预缺氧运行模式)的脱氮除磷效果,并分析了反应器单个周期内有机物、氮和磷的转化过程及污泥产量. 结果表明:ρ(MLSS)由2 400 mg/L升至5 250 mg/L时,系统TN去除率由52.5%升至66.6%;后续缺氧及预缺氧工序的脱氮比例(该工序TN去除量占系统TN总去除量的比例)由12.7%增至23.1%;ρ(MLSS)为4 300 mg/L时系统TP去除率(75.6%)达到最大. 后续缺氧及预缺氧工序中,ρ(MLSS)与内源反硝化速率呈正相关(R2=0.703 7);提高ρ(MLSS)可使PAOs(聚磷菌)在下一个周期内获得更多的碳源,使厌氧释磷量由1.62 mg/L升至9.10 mg/L,但PAOs吸磷动力会减弱,对除磷不利. 在后置反硝化、污泥衰减、能量解偶联等减量机制共同作用下,ρ(MLSS)为4 300 mg/L时系统污泥减量可提高24.4%. 从脱氮除磷及污泥减量效果综合考虑,ρ(MLSS)是双重后置反硝化工艺重要的控制参数,在该研究条件下控制在4 300 mg/L最优.      

提高普通丝瓜制种产量的关键技术

丝瓜不仅营养价值丰富,而且具有极高的药用价值,是夏秋之际的美味佳肴和保健佳品,随着种植面积的不断扩大,对种子的需求量也越来越大.本文详细介绍了普通丝瓜制种的催芽、育苗、施肥、浇水、整枝、搭架、授粉、病害防治等关键技术,旨在为进一步提高丝瓜种子繁殖水平提供参考.图13,参5.     

Limiting explosible concentration of hydrogen–oxygen–helium mixtures related to the practical operational case

This paper presents data on the limiting (minimum) concentrations of hydrogen in oxygen, in the presence of added helium, at elevated temperature and pressure related to the practical operational case. A 5 L explosion vessel, an ignition sub-system and a transient pressure measurement sub-system were used. Through a series of experiments carried out using this system, the limiting concentrations of hydrogen in oxygen and helium at different initial pressures and temperatures for the practical operational case were studied, and the influence of ignition energy and initial temperature on the limiting concentration of hydrogen in oxygen and helium was analyzed and discussed. The variation of ignition energy within the studied range is found to have a significant effect on the limiting concentration of hydrogen in oxygen and helium at lower initial temperature. However, when the ignition energy is higher than 32 mJ, the limiting hydrogen concentration remains almost changeless as the initial temperature increases from 21 °C to 90 °C. The limiting explosible concentration of hydrogen–oxygen–helium mixture decreases as the ignition energy increases when the initial temperature is lower. When the initial temperature is higher, the ignition energy has little effect on the limiting hydrogen concentration of hydrogen–oxygen–helium mixtures. When the initial temperature reaches 90 °C, the limiting hydrogen concentration remains almost changeless with an increase in ignition energy. The limiting explosible concentration of hydrogen in the mixtures, at the initial temperature of 21 °C and the ignition energy of 0.5 mJ, is 8.5% and that of oxygen is 11.25%.     

Validation of the UN test method N.5

Many substances react with water in such a way that flammable gases are formed. For transport issues this reaction may possess a considerable hazard especially if the cargo is wetted by rain or by water from other sources. In the UN Recommendations on the Transport of Dangerous Goods these kinds of problems are addressed. The UN test N.5 “Test method for substances which in contact with water emit flammable gases” corresponds to this hazard. Classification according to the test method is done by measurement of the gas evolution rate of the flammable gas by any suitable procedure. At BAM a gravimetric approach is used to measure the gas evolution rate. In this paper we present the evaluation of the apparatus by means of an absolute calibration routine utilizing a reaction where a known amount of gas is produced as well as the evaluation of important parameters influencing the gas evolution rate using different substances. It can be shown that the apparatus is capable of measuring absolute gas volumes as low as 6 mL with an acceptable error of about 17% as determined from the reaction of Mg with demineralized water.