烟气中粉尘浓度的估算

为了确定粉尘收集器的大小,必须知道烟气中粉尘的浓度。粉尘浓度可以直接从烟气测试获得,也可以不很精确地估算得出。对于使用煤粉的燃烧锅炉,可以用根据下列方程所得的计算图表来估算粉尘浓度:     

燃煤手烧炉烟尘生成特征及其控制

使用烟气净化测试系统,对燃煤手烧炉燃烧过程烟尘浓度变化进行了在线测定,对水浴净化前后烟气中的颗粒分散度进行了测定分析,并对SW型烟气净化装置的除尘效率进行了测定计算。实验表明,燃煤手烧炉的烟尘生成过程,与其加煤方式直接相关,且受燃烧温度的一定影响。在正常工作条件下,SW型燃煤炉窑烟气净化装置的平均除尘效率可达96 4%。     

燃煤手烧炉烟尘生成特征及其控制

使用烟气净化测试系统，对燃煤手烧炉燃烧过程烟尘浓度变化进行了在线测定，对水浴净化前后烟气中的颗粒分散度进行了测定分析，并对SW型烟气净化装置的除尘效率进行了测定计算。实验表明，燃煤手烧炉的烟尘生成过程，与其加煤方式直接相关，且受燃烧温度的一定影响。在正常工作条件下，SW型燃煤炉窑烟气净化装置的平均除尘效率可达96．4％。     

水泥旋窑并行处理城市污水厂污泥的污染物排放研究

通过重庆某水泥厂的工业试验，测定了水泥旋窑并行处理城市污水厂污泥的烟气参数及污染物排放指标，分析了并行处理污泥对旋窑烟气的影响程度及各项指标之间的相关性。结果表明：①在污泥添加速率增大时，烟气流速、排气量、含氧量、空气过剩系数、HF和SO₂等排放浓度均随之增加，粉尘、NO_x排放浓度基本保持不变，HCl排放浓度下降，CO排放浓度先剧增后缓慢下降，而总烃排放浓度无明显规律；②污泥添加速率与SO₂排放浓度、烟气流速与排气量、含氧量与空气过剩系数、总烃浓度与SO₂排放浓度、烟气流速与总烃浓度呈显著正相关，污泥添加速率与HCl浓度、SO₂浓度与HCl浓度、NO_x与总烃浓度呈显著负相关；③烟气排放的污染物主要来自煤的燃烧，各指标之间的相关性主要表现为煤耗量增加而引起的连锁效应，但污泥本身在高温条件下燃烧产生的污染物较少，由污泥燃烧产生的污染物之间的相关性较小；④污泥添加速率达到2.4 t/h时，水泥旋窑并行处理城市污水处理厂污泥过程中所有指标均满足国家及相应的控制标准，但其参数优化及污染物控制极为复杂，该方法处理污泥需要进行深入研究才能在工业上应用。     

医疗废物回转窑焚烧线中二恶英的生成

通过采集医疗废物回转窑焚烧生产线不同部位的烟气的二恶英样品,研究了医废焚烧过程二恶英在焚烧线200～600℃区间不同烟道断面烟气中分布变化情况。研究结果表明,医疗废物焚烧后烟气中二恶英的发生浓度要高于一般的生活垃圾焚烧烟气的浓度,大致在5～23.3 ng TEQ/m3的范围,锅炉出口到脱酸塔入口段的管道和设备为烟气中二恶英重新合成的高发区域,医废焚烧烟气中二恶英(TEQ)主要是以气态污染物的形态存在。     

火电厂大气污染物排放预测模型

根据大气污染物排放浓度变化特点,将无偏GM(1,1)模型与神经网络模型组合,并以矩阵型输入方式替代传统的数列型数据输入方式,得到改进型灰色神经网络模型,称为UGMN模型。接着,采用烟囱入口烟气自动监控系统(CEMS)数据,将模型运用于贵州省某电厂白天及夜间两段时间段内大气污染物排放浓度的模拟与预测。研究结果表明UGMN模型预测精度较好,可以应用于火电厂大气污染物排放浓度预测。     

基于QAR数据的民航发动机尾气污染物排放量估算

对现有航空发动机尾气污染物排放估算模型进行总结与分析,重点对一阶逼近3.0尾气颗粒污染物(particulate matter,PM)估算方法和ICAO尾气气体污染物估算方法进行了详细的研究。借助QAR记录的发动机相关性能数据,利用ICAO公布的排放指数,用一阶逼近3.0方法来估算CFM56民航发动机一个LTO阶段尾气颗粒污染物的排放情况,用ICAO气体排放模型估算CFM56民航发动机一个LTO阶段NO_x、CO、HC气体的排放情况。最终得到CFM56发动机一个典型航班LTO阶段的尾气污染物排放总体情况。实例计算得到CFM56发动机一个典型航班LTO阶段的排放情况为:NO_x,5 683.61 g;CO,3 821.89 g;HC,208.946 g;PM,121.287 g。本文提出的单机尾气污染物排放量估算方法可推广应用到估算整个机队LTO阶段的污染物排放量,以及整个机队某个时间段的排放情况,对评估机场附近区域大气环境提供了重要参考数据。     

香烟、电子烟自由燃烧烟雾中挥发性有机物的排放特征

采用密闭实验箱开展香烟、电子烟的自由燃烧实验,利用Tenax吸附管采集箱内烟气中挥发性有机物(VOCs)样品,采用热解吸—气相色谱/质谱方法测定108种VOCs化合物,定量研究香烟、电子烟自由燃烧烟雾中VOCs的浓度、种类、特征物及排放率,结果表明:(1)香烟自由燃烧烟雾108种VOCs中臭氧前体物(PAMs)、空气毒...     

城市生活垃圾在机械炉排炉内焚烧过程研究及数值模拟

研究城市生活垃圾在机械炉排炉内焚烧过程，建立了垃圾在炉排炉移动床内燃烧过程中垃圾体积变化、水分蒸发、挥发分析出及燃烧、垃圾颗粒的移动、气-固两相热传递、焦炭燃烧等各个反应阶段的热化学模型，采用一维非稳态模型分别建立了床层内气固两相介质控制方程。通过对炉排上垃圾焚烧过程的数值模拟研究，获得料层中温度分布、料层高度、炉床机械负荷、气相中反应物组分和污染物浓度分布。利用建立的模型对某大型垃圾焚烧炉的燃烧过程进行数值仿真，对燃烧过程、烟气成分进行预测，为垃圾焚烧炉排炉的设计和燃烧控制提供理论依据。     

湿法烟气脱硫系统的脱汞性能现场实验

分析湿法烟气脱硫系统的脱汞性能,对控制燃煤电厂的汞污染具有重要意义。利用安大略水法和吸附管法分别对某600 MW电厂湿法脱硫系统的进出口的烟气进行了采样,测量了烟气中各形态汞浓度,并分析了该系统对烟气总汞、气态氧化态汞的脱除效果以及对气态单质汞的影响。研究结果表明,安大略水法和吸附管法均能较为准确地测定湿法脱硫系统进出口烟气中的汞含量,测得入口和出口的氧化汞与平均值的相对误差的绝对值分别为3.5%和1.3%;入口和出口的单质汞与平均值相对误差的绝对值分别为16.6%和3.3%。其中吸附管法操作相对简单。通过湿法烟气脱硫系统后,烟气中氧化态汞的浓度可下降87.5%,其中约67.5%的氧化态汞被湿法脱硫系统脱除,约20%的氧化态汞在脱硫浆液的还原作用下被还原为单质汞,导致脱硫系统出口的单质汞浓度高于入口。     

The use of a sequential leaching procedure for assessing the heavy metal leachability in lime waste from the lime kiln at a caustizicing process of a pulp mill

A five-stage sequential leaching procedure was used to fractionate 13 heavy metals (Cd, Cu, Pb, Cr, Zn, Fe, Mn, Al, Ni, Co, As, V, Ba) and sulphur (S) in lime waste from the lime kiln at the causticizing plant of Stora Enso Oyj Veitsiluoto Pulp Mills at Kemi, Northern Finland, into the following fractions: (1) water-soluble fraction (H₂O), (2) exchangeable fraction (CH₃COOH), (3) easily reduced fraction (HONH₃Cl), (4) oxidizable fraction (H₂O₂ + CH₃COONH₄), and (5) residual fraction (HF + HNO₃ + HCl). Although metals were leachable in all fractions, the highest concentrations for most of the metals were observed in the residual fraction (stage 5). It was also notable that the total heavy metal concentrations in lime waste did not exceed the maximal allowable heavy metal concentrations for soil conditioner agents set by the ministry of the Agricultural and Forestry in Finland. The heavy metals concentrations in lime waste were also lower than the maximal allowable heavy metals concentrations of the European Union Directive 86/278/EEC on the protection of environment, and in particular of the soil, when sewage sludge is used in agriculture. The Ca concentration (420 g kg⁻¹; d.w.) was about 262 times higher than the typical value of 1.6 g kg⁻¹ (d.w.) in arable land in Central Finland. However, the concentration Mg (0.2 g kg⁻¹; d.w.) in lime waste was equal to the Mg concentration in arable land in the Central Finland. The lime waste has strongly alkaline pH (12.8) and a neutralizing value (i.e. liming effect) of 47.9% expressed as Ca equivalents (d.w.). This indicates lime waste to be a potential soil conditioner and improvement as well as a pH buffer.     

Extractability of trace elements in precipitated calcium carbonate (PCC) waste from an integrated pulp and paper mill complex

From the utilization point of view, it is notable that the total element concentrations in the precipitated calcium carbonate (PCC) waste were significantly lower than the maximal allowable heavy metal concentrations for fertilizers used in agriculture and in forestry, set on the basis of the EU and Finnish legislation. The easily soluble Ca concentration of 168.5g kg(-1) (d.w.) in PCC waste was 105 times higher than the typical value of 1.6g kg(-1) (d.w.) in the coarse mineral soil in Finland indicates that the PCC waste is a potential agent for soil remediation and for improving soil fertility if it is used as fertilizer. According to a five-stage sequential extraction procedure, the highest concentrations of most of the elements occurred either in HF+HNO3+HCl or H2O2+CH3COONH4 fraction. This means that the major part of the elements retained in the PCC waste are not easy to extract (leach) under conditions normally found in nature. This is beneficial since, if inorganic materials and by-products are utilized in earth construction, the content of harmful compounds must be low and the harmful components must be tightly bound to the matrix.     

医疗废物高温蒸气杀菌工艺中质热传递模型

医疗废物高温蒸气灭菌工艺中，如何使蒸气充分渗透到医疗废物内部是决定杀菌效果的关键。结合实际的操作工艺，以单片物料作为研究对象，将其视为多孔介质，从多孔物料传质传热的基本理论出发，建立了医疗废物内部传质传热数学模型，给出了其解析解，并通过实验验证了所建模型的合理性。     

Activated carbon from industrial solid waste as an adsorbent for the removal of Rhodamine-B from aqueous solution: kinetic and equilibrium studies

The activated carbon was prepared using industrial solid waste called sago waste and physico-chemical properties of carbon were carried out to explore adsorption process. The effectiveness of carbon prepared from sago waste in adsorbing Rhodamine-B from aqueous solution has been studied as a function of agitation time, adsorbent dosage, initial dye concentration, pH and desorption. Adsorption equilibrium studies were carried out in order to optimize the experimental conditions. The adsorption of Rhodamine-B onto carbon followed second order kinetic model. Adsorption data were modeled using both Langmuir and Freundlich classical adsorption isotherms. The adsorption capacity Q0 was 16.12 mg g(-1) at initial pH 5.7 for the particle size 125-250 microm. The equilibrium time was found to be 150 min for 10, 20 mg l(-1) and 210 min for 30, 40 mg l(-1) dye concentrations, respectively. A maximum removal of 91% was obtained at natural pH 5.7 for an adsorbent dose of 100mg/50 ml of 10 mg l(-1) dye concentration and 100% removal was obtained when the pH was increased to 7 for an adsorbent dose of 275 mg/50 ml of 20 mg l(-1) dye concentration. Desorption studies were carried out in water medium by varying the pH from 2 to 10. Desorption studies were performed with dilute HCl and show that ion exchange is predominant dye adsorption mechanism. This adsorbent was found to be both effective and economically viable.     

烟草下脚料发酵制取乙醇

通过单因素实验考察了硫酸浓度、固液比和水解时间对硫酸水解的影响。结果显示最优条件为:硫酸浓度为50%(w/w),固液比为10%(w/v),时间为100 min。烟草下脚料在最佳硫酸水解条件下,经5倍稀释,中和pH值至5～6。取经过滤后的水解液(FH)用酿酒酵母(Sacchharomyces cerevisiae)发酵产生乙醇,最大的乙醇浓度和乙醇产量分别为1.09g/L和54.5 g/kg。未过滤水解液(UFH,包括水解残渣)加入纤维素酶(70 U/100 mL)和酿酒酵母(Sacchharomyces cerevisiae)进行发酵,最大的乙醇浓度和乙醇产量分别为1.23 g/L和61.5 g/kg。     

新型转式垃圾焚烧过程中脱氯脱硫机理的研究

为了探讨有机垃圾焚烧过程钙基添加剂对HCl，SO_x生成特性的影响，分别在自行设计的中空水冷转式垃圾焚烧炉和固定床加热炉中进行了一系列的实验，研究结果表明新型转式焚烧炉具有强化传热传质特性，能提高HCl、SO_x的脱除率，可抑制有害气体的生成；同时也研究了 HCl，SO₂气体同时存在时，钙基添加剂对脱氯脱硫效率的影响规律。     

Laboratory testing of a continuous emissions monitor for hydrochloric acid

Continuous monitoring of exhaust flue gas has become a common practice in power plants in response to Federal Mercury and Air Toxics Standards (MATS) standards. Under the current rules, hydrochloric acid (HCl) is not continuously measured at most plants; however, MATS standards have been proposed for HCl, and tunable diode laser (TDL) absorption spectroscopy is one method that can be used to measure HCl continuously. The focus of this work is on the evaluation and verification of the operation performance of an HCL TDL over a range of real-world operating environments. The testing was conducted at the University of California at Riverside (UCR) spectroscopy evaluation laboratory. Laboratory tests were conducted at three separate temperatures, 25ºC, 100ºC, and 200ºC, and two distinct moisture levels for the enhanced temperatures, 0%, (2 tests) and 4%, over a concentration range from 0 ppmv to 25 ppmv-m at each of the elevated temperatures. The results showed good instrument accuracy as a function of changing temperature and moisture. Data analysis showed that the average percentage difference between the ammonia concentration and the calibration source was 3.33% for varying moisture from 0% to 4% and 2.69% for varying temperature from 25 to 100/200ºC. An HCl absorption line of 1.742 μm was selected for by the manufacturer for this instrument. The Hi Tran database indicated that CO₂ is probably the only major interferent, although the CO₂ absorption is very weak at that wavelength. Interference tests for NO, CO, SO₂, NH₃, and CO₂ for a range of concentrations typical of flue gasses in coal-fired power plants did not show any interference with TDL HCl measurements at 1.742 μm. For these interference tests, CO₂ was tested at a concentration of 11.9% concentration in N₂ for these tests. Average precision over the entire range for all 10 tests is 3.12%.

Implications: The focus of this study was an evaluation of the operation performance of a tunable diode laser (TDL) for the measurement of hydrochloric acid (HCl) over a range of real-world operating environments. The results showed good instrument accuracy as a function of changing temperature from 25ºC to 200ºC and moisture from 0% to 4%. Such as an instrument could be used for continuous monitoring of exhaust flue gas in power plants once the Federal Mercury and Air Toxics Standards (MATS) standards have been fully implemented.     

Sorption and Biodegradation of Vapor-Phase Organic Compounds with Wastewater Sludge and Food Waste Compost

ABSTRACT

To test the possible use of composted food waste and wastewater sludge as biofilters to treat gas-phase volatile organic compounds (VOCs), batch experiments were conducted with an isolated strain that could degrade aromatic compounds under aerobic conditions. A benzene and trichloroethylene (TCE) mixture was used as the gas-phase pollutant in experiments with composted food waste, sludge, and soil. Under aerobic conditions, benzene was degraded as a primary substrate and TCE was degraded cometabolically, with water contents varying from 6 to 60% (volume of water added/volume of solid). Optimal water content for VOC removal was 12% for the soil, 36% for the composted food waste, and 48% for the sludge.

The extent of VOC sorption and biodegradation at the optimal water content was different for each material. With the same initial VOC concentration, more VOCs were removed by sorption onto the composted food waste and the sludge, while less VOCs were biodegraded in comparison with the results using soil. The reason the biodegradation in the soil was greater may be partly attributed to the fact that, due to less sorption, the aqueous-phase concentration of VOCs, which microorganisms could utilize as a carbon source or cometabolize, was higher. We also speculate that the distribution of microorganisms in each medium affects the rate of biodegradation. A large number of microorganisms were attached to the composted food waste and sludge. Mass transfer of VOCs and oxygen to these microorganisms, which appear to have been heterogeneously distributed in clusters, may have been limited, resulting in hindered biodegradation.     

烟草下脚料发酵制取乙醇

通过单因素实验考察了硫酸浓度、固液比和水解时间对硫酸水解的影响。结果显示最优条件为：硫酸浓度为50%（w/w）,固液比为10%（w/v）,时间为100 min。烟草下脚料在最佳硫酸水解条件下,经5倍稀释,中和pH值至5～6。取经过滤后的水解液（FH）用酿酒酵母（Sacchharomyces cerevisiae）发酵产生乙醇,最大的乙醇浓度和乙醇产量分别为1.09g/L和54.5 g/kg。未过滤水解液（UFH,包括水解残渣）加入纤维素酶（70 U/100 mL）和酿酒酵母（Sacchharomyces cerevisiae）进行发酵,最大的乙醇浓度和乙醇产量分别为1.23 g/L和61.5 g/kg。     

Laboratory investigation of three distinct emissions monitors for hydrochloric acid

The measurement of hydrochloric acid (HCl) on a continuous basis in coal-fired plants is expected to become more important if HCl standards become implemented as part of the Federal Mercury and Air Toxics Standards (MATS) standards that are under consideration. For this study, the operational performance of three methods/instruments, including tunable diode laser absorption spectroscopy (TDLAS), cavity ring down spectroscopy (CRDS), and Fourier transform infrared (FTIR) spectroscopy, were evaluated over a range of real-world operating environments. Evaluations were done over an HCl concentration range of 0–25 ppmv and temperatures of 25, 100, and 185 °C. The average differences with respect to temperature were 3.0% for the TDL for values over 2.0 ppmv and 6.9% of all concentrations, 3.3% for the CRDS, and 4.5% for the FTIR. Interference tests for H₂O, SO₂, and CO, CO₂, and NO for a range of concentrations typical of flue gases from coal-fired power plants did not show any strong interferences. The possible exception was an interference from H₂O with the FTIR. The instrument average precision over the entire range was 4.4% for the TDL with better precision seen for concentrations levels of 2.0 ppmv and above, 2.5% for the CRDS, and 3.5% for the FTIR. The minimum detection limits were all on the order of 0.25 ppmv, or less, utilizing the TDL values with a 5-m path. Zero drift was found to be 1.48% for the TDL, 0.88% for the CRDS, and 1.28% for the FTIR.

Implications: This study provides an evaluation of the operational performance of three methods/instruments, including TDL absorption spectroscopy (TDLAS), cavity ring down spectroscopy (CRDS), and FTIR spectroscopy, for the measurement of hydrochloric acid (HCl) over a range of real-world operating environments. The results showed good instrument accuracy as a function of temperature and no strong interferences for flue gases typical to coal-fired power plants. The results show that these instruments would be viable for the measurement of HCl in coal-fired plants if HCl standards become implemented as part of the Federal Mercury and Air Toxics Standards (MATS) standards that are under consideration.