钙基吸收剂脱除SO2和HCl研究进展

分别介绍了钙基吸收剂脱硫和脱氯的机理和影响因素,分析了脱硫、脱氯的相互影响.探讨了钙基吸收剂协同脱硫脱氯的可行性,指出了未来研究方向,为今后实现燃烧中同时脱硫、脱氯提供理论依据和技术参考.     

脱硫细菌的筛选及其对硫化氢降解性能研究

经富集培养、分离纯化,从含硫土壤中筛选到一株脱硫活性较高的菌株--无机化能自养型的脱氮硫杆菌(Thiobacillus. Denitrificans).通过正交试验确定了不同温度、pH及H2S浓度对脱氮硫杆菌生长的影响;同时研究了该菌对H2S的降解能力及生物脱硫的最佳条件.结果表明,3种因素中以pH对脱氮硫杆菌生长的影响最大.脱氮硫杆菌的最佳生长条件为温度30℃,pH7.0,H2S质量浓度15 mg/L;脱氮硫杆菌进行脱硫时的最适pH为7.0,最适温度为30℃;其脱硫产物主要是硫酸根离子,脱硫速率为91.3 mg/L·d.     

湿式吸收法同时烟气脱硫脱氮技术进展

同时烟气脱硫脱氮技术是燃煤烟气SO2和NOx污染控制的发展趋势和研究热点。系统地介绍了氧化吸收法、络合吸收法等能实现同时脱硫脱氮的吸收法烟气净化技术，分析了其特点和存在的问题，并从技术集成、副产物利用、与现有脱硫装置的配套和理论研究等方面提出了其研究方向。     

催化剂在工业废气脱氮技术中的应用

查阅了国内外有关工业废气脱氮技术中催化剂应用方面的大量资料,对催化剂在锅炉烟气脱氮、烟气联合脱硫脱氮、汽车尾气脱氮等氮氧化物控制技术中的应用原理、现状、发展趋势和主要优缺点进行了详尽的论述.通过对各种催化剂的性能、最佳应用条件、价格等方面的分析、综合和比较,提出了未来催化剂研究工作的重点;基于我国的实际情况提出了工业废气脱氮的可行方案,从而为工业废气脱氮催化剂的进一步开发和研究工作提供参考.     

活性碳纤维电极-生物膜反应器对废水的强化脱氮性能

利用自制的活性碳纤维电极-生物膜反应器对低碳氮比(碳元素与氮元素的质量比)废水进行了脱氮实验.实验结果表明:当进水COD和碳氮比较低时,碳氮比和电流密度均对反应器的脱氮性能有很大影响;当碳氮比小于3.0时,出水的ρ(NO3--N)随进水碳氮比的增大而减小;当进水COD为70 mg/L,ρ( NO3--N)为35 mg/L、碳氮比为2.0、电流密度为0.025 mA/cm2、反应时间为8h时,出水的ρ(NO3--N)达到最低值11.2 mg/L,NO3--N去除率为68.0％.在适宜的碳氮比条件下,电极-生物膜反应器具有显著的强化脱氮作用,其对NO3--N的去除率与单纯生物膜反应器相比可提高6.0～15.0个百分点.保持碳氮比不变,提高进水COD会导致所需电流密度的提高和脱氮能力的下降.     

DS-I催化剂脱硫脱氮技术的实验研究

以纯SO2及燃煤电厂烟气作实验气,利用积分法固定床CFB方式进行了DS-I型催化剂与活性炭催化性能的对比试验,对不同还进行了不同烟气温度、SO2浓度、湿度、烟气流速等工艺参数对DS-I型催化剂催化性能的影响试验.对不同催化剂进行优化组合,可在除尘器后直接脱硫、脱氮,其脱硫率达86%、脱氮率达68%.催化剂经再生,可反复使用.     

BaO/γ-Al2O3同时吸附脱除一氧化氮和二氧化硫

利用固定床连续流动反应器研究了BaO／γ—Al2O，同时吸附模拟烟气中NO和SO2的工艺条件和再生循环使用性能，对BaO／γ—Al2O3进行了比表面积和程序升温表面反应（TPSR）等表征分析。结果表明，BaO／γ—Al2O3的适宜工艺条件是SO2与NO体积比为2．9～8．4、原料气中O2体积分数大于4．5％、吸附温度448～523K。BaO／γ—Al2O3在循环使用过程中吸附能力下降。与NOXSO吸附催化剂Na2CO3／γ—Al2O3相比，BaO／γ-Al2O3同时吸附SO2和NO的能力大、再生循环使用性能好、适宜的SO2与NO体积比范围宽、热稳定性好。将BaO／γ—Al2O3应用于NOXSO工艺可望提高该工艺的脱硫、脱氮效率。     

脱硫废水生化处理初探

火电厂烟气脱硫过程产生的废水中污染物主要包括悬浮物、过饱和的亚硫酸盐、硫酸盐以及重金属等,燃煤电厂烟气系统增设脱硝装置后,进入脱硫废水的氨氮、总氮含量急剧增加。通过对国内外多个电厂的脱硫废水处理系统运行情况的调研及分析,采用厌氧氨氧化工艺作为废水脱氮方式是可行的。     

再燃法烟气脱硝技术

综述了再燃法烟气脱硝技术及其主要影响因素。通过对几种脱硝技术的分析比较，认为再燃脱硝是一种很有前景的脱硝技术，其投资和运行费用界于低NO。燃烧器和选择性催化还原技术之间，有喷氨条件下的先进再燃脱硝效率接近于选择性催化还原技术。总结了国内外对先进再燃脱硝技术各种参数影响条件的研究结果，并论述了该技术的应用要点。     

液体吸收法脱除烟气中二氧化硫的研究

对烟气中SO2有机吸收剂进行了筛选，研究出一种新型烟气脱硫吸收剂－二甲基亚砜加Mn^2 。与纯二甲基亚砜相比，添加Mn^2 对烟气脱硫效率有较大的影响。同时还进行了工艺条件试验，并对新型烟气脱硫吸收剂的吸收机理进行了探讨。     

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.     

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.     

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.     

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。     

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.     

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.     

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%。