湿法脱硫多因素引起的浆液恶化原因分析及处理措施

在石灰石—石膏湿法脱硫系统中,吸收塔浆液恶化是系统运行经常出现的问题,浆液恶化不仅易影响浆液pH值,降低系统的脱硫效率,还会造成脱硫副产物石膏脱水困难。为此,结合2×600 MW机组湿法脱硫系统浆液恶化问题,通过检测与分析探讨了引起浆液品质变差的原因,并提出了解决措施。     

FGD系统中吸收塔浆液起泡溢流的原因分析及解决办法

在石灰石-石膏湿法烟气脱硫（FGD）工艺系统中,吸收塔浆液溢流是较为常见的现象,它对FGD系统的稳定运行非常不利。通过分析产生吸收塔浆液溢流的各种原因,提出解决吸收塔浆液溢流的办法,保证脱硫系统的稳定运行。     

600MW机组湿法脱硫吸收塔溢流原因分析及对策

阐述了火电厂600MW机组石灰石—石膏湿法脱硫系统吸收塔浆液溢流的危害,分析了吸收塔浆液溢流的原因,主要是石膏浆液品质差、氧化风量不合理、浆液循环泵、浆液喷淋的影响,溢流管接口位置布置不合理等。通过适当降低运行液位、合理布置吸收塔溢流管道等措施解决了吸收塔浆液溢流问题,确保脱硫系统稳定运行。     

石灰石／石灰-石膏湿法脱硫浆液溢流问题研究

在火电厂石灰石／石灰一石膏湿法脱硫系统中,吸收塔浆液溢流是运行过程中常见的问题之一,它对FGD系统的稳定运行非常不利。分析了吸收塔浆液溢流的成因,介绍了浆液溢流对FGD系统运行的危害,提出了吸收塔浆液溢流的预防和处理措施。     

添加剂在630MW机组湿法脱硫系统上的应用

在湿法脱硫系统吸收塔浆液中加入少量添加剂,可以促进浆液中石灰石的溶解和SO2的吸收,提高系统的脱硫率1.5%～2.0%。同时也可在浆液较低的pH值下,防止脱硫设备结垢堵塞,增加系统运行的稳定性。加入添加剂后,系统在保证脱硫效率的前提下可少开1台浆液循环泵,降低了运行成本。     

石灰石-石膏法脱硫浆液起泡研究

在石灰石一石膏法脱硫中,吸收塔浆液溢流是较为常见的现象,它会对脱硫系统的正常运行造成较大危害,如果不采取适当的预防和处理措施,甚至会导致诸如增压风机叶片损坏等重大事故.通过分析石灰石一石膏工艺中吸收塔浆液产生溢流现象的各种原因,提出防止和解决吸收塔浆液溢流的方法,以保证脱硫系统的正常运行.     

脱硫吸收塔在线pH计的技术改造

介绍了脱硫系统在线pH计的测量原理和吸收塔浆液的特性,分析了湿法烟气脱硫系统浆液pH值测量不准的原因,具体讲解了改造过程中遇到的难点和实施方案的要点.     

石灰石—石膏湿法脱硫浆液氟化铝络合原因分析及对策

石灰石—石膏湿法脱硫装置运行过程中,浆液氟化铝络合会影响石灰石的溶解度。以某电厂125MW燃煤机组脱硫改造工程为例,分析脱硫装置吸收塔浆液出现氟化铝缝合物造成石灰石闭塞的原因。依据A l3＋、F-络合原理及组分变化规律,及时采取技术措施,消除了石灰石闭塞,恢复脱硫装置正常运行。     

湿法脱硫装置SO2吸收系统增容改造方案探讨

国内越来越多火电厂石灰石—石膏湿法脱硫装置因燃煤硫分变化及其他原因需要进行增容改造。介绍了湿法烟气脱硫装置核心SO2吸收系统4种可行的增容改造方案,即塔外浆液箱方案、串联塔方案、并联塔方案、吸收塔重建方案,并对各方案的优缺点和适应性进行比较和论述,为同类烟气脱硫装置增容改造工程提供参考。     

湿法脱硫系统运行中存在问题探讨

分析了石灰石—石膏湿法脱硫系统中烟气系统、吸收塔系统、石灰石系统、石膏脱水系统、废水处理系统等在运行中存在问题,并提出了相应的对策。     

Determination of the Thermal Efficiency of Pre-boilover Burning of a Slick of Oil on Water

The burning rate of a slick of oil on a water bed is calculated by a simple expression derived from a one-dimensional heat conduction equation. Heat feedback from the flame to the surface is assumed to be a constant fraction of the total energy released by the combustion reaction. The constant fraction (χ) is named the burning efficiency and represents an important tool in assessing the potential of in situ burning as a counter-measure to an oil-spill. The total heat release, as a function of the pool diameter, is obtained from an existing correlation. It is assumed that radiative heat is absorbed close to the fuel surface, that conduction is the dominant mode of heat transfer in the liquid phase and that the fuel boiling temperature remains constant. By matching the characteristic thermal penetration length scale for the fuel/water system and an equivalent single layer system, a combined thermal diffusivity can be calculated and used to obtain an analytical solution for the burning rate. Theoretical expressions were correlated with crude oil and heating oil, for a number of pool diameters and initial fuel layer thickness. Experiments were also conducted with emulsified and weathered crude oil. The simple analytical expression describes well the effects of pool diameter and initial fuel layer thickness permitting a better observation of the effects of weathering, emulsification and net heat feedback to the fuel surface. Experiments showed that only a small fraction of the heat released by the flame is retained by the fuel layer and water bed (of the order of 1%). The effect of weathering on the burning rate decreases with the weathering period and that emulsification results in a linear decrease of the burning rate with water content.     

Calculation of carbon balances for evaluation of the biodegradability of polymers

Establishing carbon balances has been proven to be an applicable and powerful tool in testing biodegradability of polymers. In controlled degradation tests at a 4-L scale with the model polymer poly(-hydroxybutyrate) (PHB), it was shown that the degree of degradation could not be determined with satisfactory accuracy from CO₂ release alone. Instead, the course of degradation was characterized by means of establishing carbon balances for the degradation of PHB withAcidovorax facilis and a mixed culture derived from compost. Different analytical methods for determining the different carbon fractions were adapted to the particular test conditions and compared. Quantitative determination of biomass and residual polymer were the main problems in establishing carbon balances. Amounts of biomass derived from protein measurements depend strongly on assumptions of the protein content of the biomass. Selective oxidation of biomass with hypochlorite was used as alternative, but here problems arose from insoluble metabolic products. Determination of soluble components with the method of chemical oxygen demand (COD) also includes empirical assumptions but seems acceptable if the dissolved carbon fraction is in the range of some 10% total carbon. Results confirm both analytical assays and theoretical approaches, in ending up at values very close to 100%, within an acceptable standard deviation range under test conditions comparable to standard test practice.Paper presented at the Bio/Environmentally Degradable Polymer Society—Third National Meeting, June 6–8, 1994, Boston, Massachusetts.     

富拉尔基发电总厂200MW机组除尘器改造

对富拉尔基发电总厂5号炉的设计条件进行了分析，针对燃用低硫煤，飞灰比电阻高，场地较小，除尘效率要求高的情况，在电除尘器的设计上采取有效措施，达到了排放要求。     

Review of the kinetics of alkaline degradation of cellulose in view of its relevance for safety assessment of radioactive waste repositories

The degradation of cellulose (a substantial component of low- and intermediate-level radioactive waste) under alkaline conditions occurs via two main processes: a peeling-off reaction and a basecatalyzed cleavage of glycosidic bonds (hydrolysis). Both processes show pseudo-first-order kinetics. At ambient temperature, the peeling-off process is the dominant degradation mechanism, resulting in the formation of mainly isosaccharinic acid. The degradation depends strongly on the degree of polymerization (DP) and on the number of reducing end groups present in cellulose. Beyond pH 12.5, the OH^- concentration has only a minor effect on the degradation rate. It was estimated that under repository conditions (alkaline environment, pH 13.3-12.5) about 10% of the cellulosic materials (average DP = 1000-2000) will degrade in the first stage (up to 10⁵ years) by the peeling-off reaction and will cause an ingrowth of isosaccharinic acid in the interstitial cement pore water. In the second stage (10⁵-10⁶ years), alkaline hydrolysis will control the further degradation of the cellulose. The potential role of microorganisms in the degradation of cellulose under alkaline conditions could not be evaluated. Proper assessment of the effect of cellulose degradation on the mobilization of radionuclides basically requires knowing the concentration of isosaccharinic acid in the pore water. This concentration, however, depends on several factors such as the stability of ISA under alkaline conditions, sorption of ISA on cement, formation of sparingly soluble ISA-salts, etc. A discussion of all the relevant processes involved, however, is far beyond the scope of the presented overview.     

Study of Aging Characteristics of Ternary Blends of Polyethylenes—II

Six film samples of low-density polypropylene (LDPE)/linear LDPE (LLDPE)/high-density polypropylene (HDPE) with varying ratios of LDPE (20–45 ... wt%) and LLDPE (25–50 wt%) having a fixed amount of HDPE at 30 wt% were prepared by blown film extrusion technique. The samples were aged at four different temperatures, 55°, 70°, 85°, and 100°C, for four different time periods in the interval of between 150 hours and up to 600 hours. The change in the structure of various constituents and the formation of various oxygenated (peroxy and hydroperoxy) and unsaturated groups during thermo-oxidative degradation was discussed by infrared spectroscopy. The visiosity-average molecular weight was found to have decreased slowly in the initial aging hours and temperatures, whereas it decreased by 10% with its previous value tensile strength that is, 100°C when aged for 600 hours. The tensile strength of the sample first increased by 67% at 55°C and 89% at 70°C up to 450 hours, whereas the values increased by 52.5% at 85°C and 33.9% at 100°C when aged for 150 hours and then decreased. The percentage elongation at break increased by 2.7% at 55°C and 10.7% at 70°C for 150 and 300 hours of aging, respectively, whereas the percentage decreased when aged at 85°C and 100°C for up to 600 hours of aging. The values of gel content (percent) increased and initial degradation temperature decreased with aging time and temperature.     

Selection of adsorbents for treatment of leachate: batch studies of simultaneous adsorption of heavy metals

The simultaneous adsorption of copper (Cu), cadmium (Cd), nickel (Ni), and lead (Pb) ions from spiked deionized water and spiked leachate onto natural materials (peat A and B), by-product or waste materials (carbon-containing ash, paper pellets, pine bark, and semi-coke), and synthetic materials (based on urea-formaldehyde resins, called blue and red adsorbents) or mixtures thereof was investigated. The adsorbents that gave the highest metal removal efficiencies were peat A, a mixture of peat B and carbon-containing ash, and a mixture of peat A and blue. At an initial concentration of 5 mg/l for each metal, the removal of each species of metal ion from spiked water and spiked leachate solutions was very good (>90%) and good (>75%), respectively. When the initial concentration of each metal in the solutions was twenty times higher (100 mg/l), there was a noticeable decrease in the removal efficiency of Cu²⁺, Cd²⁺, and Ni²⁺, but not of Pb²⁺. Langmuir monolayer adsorption capacities, q_m, on peat A were found to be 0.57, 0.37, and 0.36 mmol/g for Pb²⁺, Cd²⁺, and Ni²⁺, respectively. The order of metal adsorption capacity on peat A was the same in the case of competitive multimetal adsorption conditions as it was for single-element adsorption, namely Pb²⁺ > Cd²⁺ ≥ Ni²⁺. The results show that peat alone (an inexpensive adsorbent) is a good adsorbent for heavy metal ions.     

袋式除尘器气流分布数值计算研究

采用结构化/非结构化混合网格技术、多孔介质模型及k-ε两方程湍流模型,对某袋式除尘器及进出口管道内的气体流场进行了数值计算.计算结果表明,合理布置导流板后,袋式除尘器两箱体流量偏差为1.8％;除尘器下游滤袋单元处理气量偏大,中游滤袋单元处理气量较小,最大流量与最小流量偏差为22.3％;靠近除尘器进口处灰斗内存在气流回流特性,易造成粉尘的二次附着现象.     

Kinetics of Hydrolytic Degradation of PLA

The chemical recycling of poly(lactic acid) (PLA) to its monomer is crucial to reduce both the consumption of renewable resources for the monomer synthesis and the environmental impact related to its production and disposal. In particular, the production of lactic acid from PLA wastes, rather than from virgin raw materials, it is also possible to achieve considerable primary energy savings. The focus of this work is to analyse deeply the PLA hydrolytic decomposition by means of a kinetic model based on two reactions mechanism. To this end, new experimental data have been gathered in order to investigate a wider temperature range (from 140 to 180 °C) and to extend the water/PLA ratio up to 50 % of PLA by weight. The reported results clearly highlight that more than 95 % of PLA is hydrolyzed to water-soluble lactic acid within 120 min, when it is hydrolyzed within 160–180 °C. Furthermore, the kinetic constant is highly influenced by reaction temperature. The proposed “two reactions” kinetic mechanism complies satisfactorily with the experimental data under analysis.     

Determination of the Burning Characteristics of a Slick of Oil on Water

The burning rate of a slick of oil on a water bed is characterized by three distinct processes, ignition, flame spread and burning rate. Although all three processes are important, ignition and burning rate are critical. The former, because it defines the potential to burn and the latter because of the inherent possibility of boilover. Burning rate is calculated by a simple expression derived from a one-dimensional heat conduction equation. Heat feedback from the flame to the surface is assumed to be a constant fraction of the total energy released by the combustion reaction. The constant fraction (χ) is named the burning efficiency and represents an important tool in assessing the potential of in situ burning as a counter-measure to an oil spill. By matching the characteristic thermal penetration length scale for the fuel/water system and an equivalent single layer system, a combined thermal diffusivity can be calculated and used to obtain an analytical solution for the burning rate. Theoretical expressions were correlated with crude oil and heating oil, for a number of pool diameters and initial fuel layer thickness. Experiments were also conducted with emulsified and weathered crude oil. The simple analytical expression describes well the effects of pool diameter and initial fuel layer thickness permitting a better observation of the effects of weathering, emulsification and net heat feedback to the fuel surface. Experiments showed that only a small fraction of the heat released by the flame is retained by the fuel layer and water bed (of the order of 1%). Ignition has been studied to provide a tool that will serve to assess a fuels ease to ignite under conditions that are representative of oil spills. Two different techniques are used, piloted ignition when the fuel is exposed to a radiant heat flux and flash point as measured by the ASTM D56 Tag Closed Cup Test. Two different crude oils were used for these experiments, ANS and Cook Inlet. Crude oils were tested in their natural state and at different levels of weathering, showing that piloted ignition and flash point are strong functions of weathering level.     

废旧冰箱塑料回收再生利用技术研究

目前我国的废旧冰箱已进入了一个报废高峰期,且大量废旧冰箱塑料的处理问题已成为当今地球环境保护的热点问题,而我国又是一个人均资源占有量很低的国家,因此,对废旧冰箱塑料进行回收与再生利用则具有极其重要的意义.介绍了废旧冰箱塑料的物理再生利用、化学再生利用、生物降解、能源回收利用的技术和方法.