燃煤电厂汞排放监测和控制研究现状

介绍了燃煤电厂汞控制研究现状,分析了燃煤中汞的含量和赋存状态、燃烧中汞的化学行为特性,探讨了汞的监测和控制技术,为我国燃烧电厂汞排放控制提供参考.     

燃煤电厂汞排放控制技术研究

近年来,燃煤电厂烟气中的汞成为继SO2、NOx和烟尘之后又一公认的大气环境污染物,我国已正式立法控制燃煤电厂汞排放,这使得燃煤电厂汞排放技术的研究迫在眉睫。不同形态汞的理化性质不同,元素态汞（ Hg0）较之氧化态汞（Hg2＋）和颗粒态汞（Hgp）更难去除,因此,脱汞的前提是提高Hg0的氧化率。介绍并简单分析了目前国内外已有的汞排放控制技术：燃烧前控制（清洁燃煤发电技术）、燃烧中控制（煤基添加剂技术和炉膛喷射技术）,和燃烧后控制（利用现有的烟气控制设备协同控制）,并对我国脱汞技术发展方向提出了展望。     

燃煤电厂汞减排技术研究

介绍了燃煤电厂汞的3种排放形态,分析了燃煤电厂汞减排技术,如燃烧添加剂技术、吸收剂喷射技术、稳定剂固汞防溢技术、络合剂絮凝脱汞技术等。在此基础上提出了燃煤电厂汞减排技术选择影响因素,即燃煤煤质、运行工况、脱汞后副产物等,为我国电力行业汞污染控制及减排提供了参考。     

燃煤电厂汞排放及其控制技术研究

燃煤电厂汞排放是最大的人为汞污染源,《火电厂大气污染物排放标准》(GB 13223-2011)首次提出了我国燃煤发电锅炉汞及其化合物的控制指标,规定汞及其化合物排放限值为0.03 mg/m3.介绍了国内外汞污染发展情况,汞的形态以及汞污染控制技术.汞控制技术主要分为三种:燃烧前脱汞、燃烧中脱汞和燃烧后脱汞,其中燃烧后脱汞的研究最广泛.     

电厂燃煤过程中汞控制技术研究

燃煤电厂汞控制技术分燃烧前、燃烧中和燃烧后脱汞,燃烧后脱汞技术为主要汞控制排放工艺,其中吸附剂吸附方法的研究较为广泛。基于国内外近几年燃煤电厂烟气脱汞技术的研究,综述了汞控制技术的最新进展。     

燃煤电厂烟气中汞的排放与控制研究进展

对煤中微量元素的丰度和赋存状态进行了论述，综述了燃煤烟气中重金属汞的排放、形态转化及分布情况，并重点论述了燃煤烟气中汞的监测和控制方法的最新进展，分析了燃煤电厂在汞控制方面存在的主要问题，并结合我国国情提出了相关建议。     

欧盟国家燃煤电厂环保政策及技术路线分析

温室气体的排放控制作为全球性的环境问题受到了广泛关注。中国是火力发电的大国,其燃煤机组的温室气体排放总量巨大。《火电厂大气污染物排放标准》（GB 13223-2011）提高了我国燃煤电厂的烟气污染物排放的要求,对火电厂烟气处理的技术选择和投资都会产生重大影响。针对中国燃煤电厂环保面临的新形势,阐述了欧盟国家的环保政策重点,并对欧盟国家燃煤电厂污染物控制的相关标准进行了分析,同时简要介绍了欧盟国家燃煤电厂环保的主要技术路线,在一定程度上可作为中国燃煤电厂污染物控制的借鉴和参考。     

燃煤电厂应对新标准的氮氧化物控制策略研究

介绍了我国燃煤电厂NOx排放标准及其控制技术发展状况,分析了NOx的排放现状及我国燃煤电厂NOx控制技术的特点及存在问题。结合新标准,提出在环境约束条件下效益―成本最大化的NOx控制策略。     

燃煤电厂多污染物控制联合脱汞方法

针对燃煤电厂汞排放特征,结合SO2、NOx控制技术,分析了实现汞联合控制的基理,介绍了近年来国内外烟气多污染物处理技术方面最新的研究进展,主要包括SO2控制设备联合脱汞技术以及SO2、NOx、汞联合脱除技术,并对其技术性能进行了对比.     

国内燃煤电厂烟气脱硝发展现状及建议

介绍国内燃煤电厂NOx排放现状和我国NOx控制法规,以及国内燃煤电厂脱硝技术的研究和工程应用现状,并对我国烟气脱硝产业的发展提出了几点建议.     

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.     

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.     

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.     

Model of technological alternatives of production of sodium chromate (VI) with the use of chromic wastes

This article presents a mathematical model which describes the sodium chromate (VI) production process with the use of chromic waste as a substitution of natural raw materials. This model is a function of selected process parameters common for all of the examined alternatives and based on equations of material balance. Optimization of the elaborated technological alternatives of the production process with use of recycling of chromic waste has been evaluated by determining the extreme value of the quality indicator WJ. This indicator defines the quantity of waste created in the process. Optimization results enabled the selection of the optimal technological solution from all of the alternatives possible for use in industrial practice. Negative values of the indicator prove that there is the possibility of introducing to the process a larger quantity of waste than the one obtained in the process and transported to the storage heaps.     

鼓泡式反应器高径比对氨法烟气脱碳性能的影响

以N2和CO2混合气模拟燃烧烟气,研究了鼓泡反应器的高径比以及反应条件对氨法烟气脱碳性能的影响。实验结果表明:在相同高径比的条件下,CO2吸收率随氨水质量分数的增加、反应温度的升高而逐渐增大,随进气CO2体积分数和模拟烟气流量的增加而逐渐减小;CO2吸收率随高径比的增加而增大,在高径比为3.98、氨水质量分数为28%、进气CO2体积分数为10%、模拟烟气流量为1.0L/min、反应温度为40℃的条件下,CO2吸收率最高可达100%。     

化学品生物降解性的评价与预测

介绍了有机化学物质生物降解性的测定方法及其预测方法研究概况，并讨论了生物降解性评价的发展前景。     

Structure-biodegradation relationships of polymeric materials. 1. Effect of degree of oxidation on biodegradability of carbohydrate polymers

The biodegradability of oxidized starch and inulin has been studied in relation to the degree of periodate oxidation to dialdehyde derivatives, by measuring oxygen consumption and mineralization to carbon dioxide. A higher degree of oxidation of dialdehyde starch and dialdchyde inulin results in a lower rate at which the polymers are biodegraded. It is demonstrated that the biodegradation rate of dialdehyde inulin derivatives decreases more than that of equivalent starch derivatives. The differences in biodegradation behavior between dialdehyde starch and dialdehyde inulin, resulting from comparable modifications, are discussed in terms of conformational structure.     

Mechanism of Microbial Degradation of Slow-Release Fertilizers

Methyleneureas are condensation products of urea and formaldehyde of different molecular mass and solubility; they are used in large amounts both as resins, binders, and insulating materials for industrial applications, as well as a slow-release nitrogen fertilizer for greens, lawns, or in bioremediation processes. In the present study, the microbial breakdown of these products was investigated. The nitrogen was released as ammonia and urea, and the formaldehyde released immediately oxidized via formiate to carbon dioxide. The enzymatic mechanism of metabolization of methyleneureas was studied in microorganisms isolated from soil, which were able to use these compounds as the sole source of nitrogen for growth. A strain of the Gram-negative bacterium Ralstonia paucula (formerly Alcaligenes sp. CDC group IVc-2) completely degraded methylenediurea and dimethylenetriurea to urea, ammonia, formaldehyde, and carbon dioxide. The enzyme initiating this degradation (methylenediurease) was purified and turned out to be different from the previously described enzyme from Ochrobactrum anthropi with regard to its regulation of expression and physicobiochemical properties. Fungal degradation of methyleneureas may occur via the formation of organic acids, thus leading to a nonenzymatic degradation of methyleneureas, which are unstable under acidic conditions.     

Effect of Degree of Substitution of Octenyl Succinate Starch on Enzymatic Degradation

Octenyl succinate starch of degree of substitution (ds) 0.03, 0.07, and 0.11 was synthesized in an aqueous medium. These compounds were then tested for the susceptibility to enzymatic degradation. The multiple-enzyme regime of -amylase, amyloglucosidase, and pullulanase was chosen for the evaluation. This combination of enzymes had been proven to degrade 99.5% of unmodified starch to glucose and hence was chosen for this study. It was found that even small amounts of subsituent caused a considerable decrease in the extent of degradation. The net extent of degradation decreased with increasing ds. Surprisingly, the amount of glucose from all three substituted substrates was quite similar, suggesting the effect small amounts of subtituent had on the enzymatic activity.