美国治理燃煤电厂氮氧化物排放的技术措施

综述美国热电厂为达到１９９０年修订的“空气洁净法”规定的燃煤锅炉ＮＯＸ排放要取的技术措施,引用实例介绍低公害型燃烧器,两段燃烧,集中燃烧及三段燃烧系统的工业应用结果。     

“W”火焰超临界锅炉煤质变化时的燃烧调整研究

介绍了2×650 MW超临界机组“W”火焰锅炉燃烧系统组成及特性,指出影响煤粉炉燃烧的主要因素有炉膛温度、煤粉的浓度和细度、燃煤挥发分及燃煤发热量等.分析了燃用煤质偏离设计值时,“W”火焰超临界锅炉燃烧状况,并给出了调整方案.     

日开发龙卷式垃圾焚烧炉

日本正在研究开发一项新的垃圾焚烧炉技术，它采用气化反应燃烧方式，能够抑制二恶英等有害物质的排放量。 这种新型锅炉叫做“龙卷炉”，垃圾气化后，在炉子的中央部分燃烧，仿佛是由火焰形成的龙卷风，火焰不接触炉体内侧，因此不需要耐火材料，并且炉体分段建造，结构简单，便于搬运和安装。 目前长崎县境内的大学、企业及有关团体成立了“龙卷炉”研究会，并且已经制作出试验炉，这种试验炉每小时可焚烧湿度在50%以下的垃圾200公斤，点火时只需要少量的柴油，以水作为助燃剂，燃烧温度可达1200至1300报氏度。 (张石)     

燃煤锅炉脱砷现状研究

通过对国内外燃煤锅炉脱砷现状的研究,探讨各种脱砷方法的优、缺点,提出锅炉脱砷的可行方案。把砷污染的产生与锅炉运行实际结合起来考虑,脱砷过程可以分为燃烧前、燃烧中、燃烧后三段。燃烧前脱砷对于无机砷可以达到70％以上的效率,而对有机砷则会产生富集作用;燃烧中脱砷可利用现有的脱硫技术和设备,如炉内喷钙技术和循环流化床锅炉,其脱除效率分别达到40％、80％;燃烧后脱砷方法主要包括提高除尘器效率法、化学法、吸收剂法,这些方法基本都能使除砷效率理论值达到90％以上,具有极佳的工业应用前景。     

W火焰600MW超临界锅炉中SCR脱硝岛的设计要求

从分析W火焰炉燃烧机理入手,着重分析了选择性催化还原(SCR)脱硝原理、工艺流程、脱硝岛在W火焰炉上整体布置方案、催化剂及脱硝烟道优化设计对后续设备的影响.     

分级燃烧技术在电站锅炉低NOx排放中的应用

分级燃烧技术是较为成熟的电站锅炉降氮燃烧技术,通过将炉膛二次风重新分配,使燃料经历富燃料和富氧两个过程,有效抑制了NOx的形成.台山电厂2号锅炉是典型的亚临界汽包炉,应用分级燃烧原理的低氮燃烧系统,降低了主燃区的氧浓度和温度,将炉膛出口NOx浓度由400 mg/m3降低到150 mg/m3,减排效果显著.     

煤洁净燃烧新技术（三）

3第二代燃煤发电新技术3．1前置式联合循环系统如前所述，IGCC系统需要庞大的制氧装置（AEU）和煤气净化设备；PFBC－CC系统则因燃气轮机的初温受到限制（≤900℃），不能进一步提高热效率。美国FosterWheeler公司最早提出第二代PFBC方案的概念，先使煤在炭化炉（或部分气化炉）内干馏（或部分气化），生成低热值煤气，送入燃气轮机的顶置燃烧室中燃烧，提高燃气轮机的初温，使联合循环的热效率有可能高达45～47％，焦炭则进入PFBC炉燃烧。Keilog公司也作了类似的设计研究。Tidd电厂在进行PFBC－CC试运行的同时，拟定了研究和…     

某“W”型锅炉炉效低的综合治理

针对某锅炉经济性差的问题,从设备、运行及自动控制等方面分析,并进行了相应整改。影响炉效的主要因素有煤质恶化、灰渣含碳量高、排烟温度高和CO浓度高等,同时炉膛燃烧不稳定也是影响燃烧效率的重要因素。通过漏风整改、制粉系统优化、燃烧优化调整和控制系统优化等方法有效提高了锅炉经济性。研究表明：分析锅炉经济性降低的影响因素时应抓住主要因素,兼顾其他,科学的生产管理是保证锅炉运行经济性的重要基础;入炉煤质恶化是最主要的外在因素;良好的自动控制系统能有效稳定燃烧参数,提高燃烧效率;降低飞灰含碳量的主要工作应集中在制粉系统优化调整;完整而系统的燃烧调整试验能够保证锅炉运行控制参数的科学合理,并需要正确调整氮氧化物排放和锅炉效率之间的关系。     

用煤直接液化油渣作循环流化床锅炉燃料的方法

该专利公开了一种用煤直接液化油渣作循环流化床锅炉燃料的方法。其步骤如下：（1）将煤直接液化后冷却固化的油渣经破碎后直接与煤、炉内脱硫剂和／或生物质混合,且煤直接液化油渣占所得混合燃料的10％～80％;所述炉内脱硫剂以石灰或石灰石为原料,控制Ca与S摩尔比为0．5～3．2;（2）用冷风作为拨煤风,将得到的混合燃料送入循环流化床锅炉中进行燃烧。     

国内简讯

川化集团一段炉节能改造样板工程建成投运由日本国新能源和产业技术开发机构与中国国家计委联合发起的“绿色合作计划示范项目”——合成氨厂一段炉节能改造及废热回收样板工程，于１９９８年１月６日在川化集团第二化肥厂顺利建成，经过连续１８ｄ的投产运行，３月２日通...     

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.     

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.     

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。     

Effects of temperature on the release of nutrient elements of solid organic materials under conditions of oversaturation

The effects of temperature on the release of chemical components of six solid organic materials under conditions of oversaturation were investigated in this paper. The six materials were peat moss (PM), weathered coals (WC), charred rice husks (CRH), sawdust (Sd), turfgrass clippings (TC), and chicken manure (CM). Significant differences were observed in the available nitrogen and phosphorus content of the aqueous extracts of organic materials at different temperatures. The available nitrogen content in aqueous extracts of PM and WC at 25 °C was higher than that registered at 15 °C and 35 °C. Available nitrogen content in the aqueous extracts of CRH, Sd, TC, and WC at 35 °C was higher than at 15 °C and 25 °C. The available phosphorus content in the aqueous extracts of organic materials at 35 °C was higher than that available at 15 °C and 25 °C, with the exception of Sd. In addition, the release of available phosphorus in the aqueous solution of organic materials at different temperatures varied constantly for 108 h. The release of potassium (K⁺) and sodium (Na⁺) ions in the aqueous extracts of organic materials was basically steady over time, with the exception of CM. High temperature (35 °C) may significantly hasten the release of K⁺ from organic substrates (except for WC) with low temperatures significantly inhibiting release of K⁺ in Sd and CRH. High temperatures (35 °C) might significantly facilitate the release of Na⁺ in CM and TC. However, no significant differences were manifested in the release of Na⁺ from organic substrates at different temperatures, with the exception of CM and TC. Moreover, no significant differences were observed in the release of calcium, magnesium and iron ions with time, nor were there any significant differences in the contents of iron ions in the aqueous extracts of organic materials at different temperatures. The results indicate that multiple mediums should be pretreated in water for a week before being used for planting. They should be used when all mineral elements of organic materials are steady and ignoring the effect of organic mediums.     

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.     

Effect of depth of landfill on the characteristics of soil-like material of aged waste: a case study of Bhalswa dumpsite,India

Journal of Material Cycles and Waste Management - This study characterizes the municipal solid waste (MSW) accumulated for more than 25 years at Bhalswa dumpsite, Delhi, India. 50...     

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.