The Effect of CTBN Concentrations on the Kinetic Parameters of Decomposition of Blends of Epoxy Resins Modified with Carboxyl-Terminated Liquid Copolymer

Diglycidyl ether of bisphenol—A (DGEBA)—based epoxy resin was blended in the ratio of 3:1 (weight basis) with cycloaliphatic epoxy (CAE) resin. The prepared blend sample was further blended with different weight percentages of carboxyl-terminated butadiene acrylonitrile copolymer (CTBN) ranging between 0 and 25 wt% with an interval of 5 wt% and cured with stiochiometric amounts of 4, 4’- diamino diphenyl sulphone (DDS) cure agent. Structural changes during blending were studied by Fourier-transform infra-red (FTIR) spectroscopic analysis. The kinetic parameters, viz., order of decomposition reaction (n), activation energy (E), pre-exponential factor (Z) and rate decomposition constant (k), for the decomposition of the samples were calculated by applying Coats-Redfern equation over thermogravimetric (TG) data. The degradation of each sample followed second-order degradation kinetics, which was calculated by Coats-Redfern equation using best-fit analysis. This was further confirmed by linear regression analysis. The validity of data was checked by t-test statistical analysis. Further, the blend sample had higher initial degradation temperature and activation energy than its respective pure epoxy resin indicating that the CTBN acted as thermal stabilizer for epoxy resin which improved the thermal stability.     

Effect of Additives on the Improvement of Mechanical and Degradable Properties of Photografted Jute Yarn with Acrylamide

The jute yarn was grafted with acrylamide monomer (AA) under ultraviolet (UV) radiation to modify its mechanical and degradable properties. A number of AA solutions of different concentrations in methanol (MeOH) along with photoinitiator Irgacure 907 [2-methyl-1-(4-methylthiophenyl)-2-morpholinopropanone-1] were prepared. The monomer concentration and irradiation time were optimized. Jute yarn grafted with 30% AA under UV radiation for 60 min showed of the highest polymer loading (PL) value of 22% with a enhanced tensile strength (TS) value of 195% and elongation at break (Eb) value of 256% compared to untreated jute yarn. To further improve the properties of jute yarn, a number of additives (1%) such as urea, polyvinylpyrrolidone, urethane acrylate, and urethane diacrylate were used in the AA (30%) solution. Among all the additives used, urea significantly influenced the PL (27%), TS (230%), and Eb (264%) values of the treated jute yarns. Water uptake and the degradation properties of treated and untreated jute yarn caused by simulated weathering and in soil (25% water) were also studied. The rate of degradation of grafted sample is lower then that of untreated sample. DSC studies showed the thermal stability of the AA plus urea grafted sample.     

赖氨酸废水的处理和氨回收

对赖氨酸浓废水调 p H沉淀处理后的澄清水进行预处理 :先加入石灰乳 ,搅拌、沉淀 ,SO42 -从 2 0 0 0 0 m g/ L 左右降至 130 0 mg/ L 左右 ,去除率为 94%左右 ,然后进行空气吹脱 ,NH3- N从 5 0 0 0 mg/ L左右降至 80 m g/ L左右 ,去除率 >98%。吹脱出水经厌氧生化处理后 ,再进行空气吹脱 ,NH3- N从 70 0 mg/ L 左右降至 85 mg/ L 左右 ,去除率 >86 %。再吹脱出水与稀废水混合后进行好氧生化和 A/ O、O系统处理 ,出水的 COD<10 0 m g/ L,BOD5<2 0 mg/ L,SS<70 mg/ L,NH3- N<2 5 m g/ L。对浓废水与石灰乳混合后搅拌过程中及两次空气吹脱过程中挥发的 NH3进行回收 ,将其与 H2 SO4反应 ,生成的 (NH4) 2 SO4回用于生产     

A Study of Dynamic Mechanical and Thermal Behavior of Starch/Poly(vinylalcohol) Based Films

Starch/Poly(vinylalcohol) blends in two different ratios (60:40 and 50:50) were prepared with glycerol as a plasticizer. Films were cast by a solution casting method. One set of films were filled with 10 wt% of bentonite clay and another set of films were crosslinked with epichlorohydrin in an alkaline medium. The prepared film samples were characterized with dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA). The presence of clay and crosslinking with epichlorohydrin was found to have considerable effect on the dynamic mechanical properties and thermal stability of the films. Intercomponent H-bonding between starch, Poly(vinylalcohol) and glycerol enhanced the thermal stability of the films. But incorporation of clay and crosslinking with epichlorohydrin enhanced the steric crowding and lowered the thermal stability of the films.     

Critical evaluation of the use of the hydroxyapatite as a stabilizing agent to reduce the mobility of Zn and Ni in sewage sludge amended soils

The leachability of zinc (Zn) and nickel (Ni) was investigated in various soil types amended with sewage sludge and sewage sludge treated with hydroxyapatite. Sandy, clay and peat soils were investigated. For leachability tests, plastic columns (diameter 9 cm, height 50 cm) were filled with moist samples up to a height of 25 cm. Sewage sludge (1 kg) was mixed with 4.6 kg of clay and sandy soils and with 6.7 kg of peat soil. For sewage sludge mixtures treated with hydroxyapatite, 0.5 kg of the hydroxyapatite was added to 1 kg of the sewage sludge. Neutral (pH 7) and acid precipitation (pH 3.5) were applied. Acid precipitation was prepared from concentrated HNO(3), H(2)SO(4) and fresh doubly distilled water. The amount of precipitation corresponded to the average annual precipitation for the city of Ljubljana, Slovenia. It was divided into eight equal portions and applied sequentially on the top of the columns. The results indicated that the leachabilities of Zn in sewage sludge amended peat and clay soils were low (below 0.3% of total Zn content) and of Ni in sewage sludge amended sandy, clay and peat soil below 1.9% of total Ni content. In sewage sludge amended sandy soil, the leachability of Zn was higher (11% of Zn content). The pH of precipitation had no influence on the leachability of either metal. Treatment of sewage sludge with hydroxyapatite efficiently reduced the leachability of Zn in sewage sludge amended sandy soil (from 11% to 0.2% of total Zn content). In clay and peat sewage sludge amended soils, soil characteristics rather than hydroxyapatite treatment dominate Zn mobility.     

Effects of Waste Paper Sludge on the Physico-Mechanical Properties of High Density Polyethylene/Wood Flour Composites

The objective of this work was to determine some physical and mechanical properties of the high density polyethylene (HDPE) composites reinforced with various mixtures of the paper sludge and the wood flour, and to evaluate the coupling agent performance. The waste sludge materials originating from two different sources including paper making waste water treatment sludge (PS) and ink-eliminated sludge (IES) were characterized in terms of physico-chemical properties. In the experiment, four levels of paper sludge (20, 30, 40 and 60 wt%), three levels of wood flour (20, 40 and 60 wt%), and two levels of coupling agent (MAPE) content (2 and 3 wt%) were used. The flexural properties of the composites were positively affected by the addition of the sludge. Especially, tensile modulus improved with the increase of paper sludge content. With the addition of MAPE, flexural properties improved considerably compared with control specimens (without any coupling agent). The results showed that the water absorption (WA) and thickness swelling (TS) values of the samples decreased considerably with increasing sludge content in the composite, while they increased with increasing wood flour content. It is to be noted that with incorporation of MAPE in the composite formulation, the compatibility between the wood flour and HDPE was enhanced through esterification, which reduced the WA and TS and improved the mechanical properties. Composites made with IES exhibited superior physico-mechanical properties compared with the PS filled composites. Overall results suggest that the waste paper sludge materials were capable of serving as feasible reinforcing fillers for thermoplastic polymer composites.     

新型铝硅复合絮凝剂的制备及其絮凝性能研究

以高稳定性的有机硅(TEOS)代替聚硅酸(HS)加入到聚合铝(PAC)中,初步制备了一种新型铝硅复合絮凝剂(TEOS—PAC)。研究了制备过程中的滴碱速度、Si与Al摩尔比和碱化度等因素对该复合絮凝剂絮凝性能的影响,对比了TEOS—PAC与HS—PAC的絮凝效果。研究结果表明,制备TEOS—PAC时滴碱速度要控制适当(流量刻度定位40);随着Si与A1摩尔比的提高,TEOS—PAC复合絮凝剂的絮凝性能明显增强,最佳Si与A1摩尔比为0．2,最佳碱化度为2．5;在相同条件下,TEOS—PAC的最佳投药量低于HS—PAC,且TEOS—PAC在絮凝过程中形成的絮体沉降性能优于HS—PAC形成的絮体。     

含砷废渣的固化处理

为了处理有色金属冶炼厂产生的含砷废渣（简称砷渣）,以水泥、粉煤灰、矿渣、黄砂等作为固化材料对砷渣进行了固化研究。确定了砷渣固化的最佳工艺条件：w（砷渣）：50％、w（水泥）=15％、w（粉煤灰）：20％、w（矿渣）=10％、w（黄砂）=5％;砷渣、粉煤灰预先混合球磨10min,加水搅拌后陈化4h,烘干后与水泥、矿渣一起球磨20min,再与水（水与混合物料的质量比为0．175）、添加剂（质量分数为0．05％的添加剂B）及黄砂一起在搅拌机中搅拌6min,然后加压成型,成型后的固化体先放入24℃水泥砼试体养护箱养护14d,然后取出在室温下自然养护14d,养护时间共28d。扫描电子显微镜分析结果显示,砷渣固化体的胶凝状态良好。测试结果表明,砷渣固化体7d抗压强度为8．13MPa,28d抗压强度为14．20 MPa;As的浸出浓度为0．07mg／L,Hg的浸出浓度为0．008mg／L。砷渣固化体的性能达到了国家建材行业标准（JC239-2001《粉煤灰砖》）和危险废物鉴别标准（GB5085．3～1996《危险废物答别标准——浸出毒性答别》）的要求。     

Effect of the Pretreatment with UV and Gamma Radiations on the Modification of Plywood Surface by Photocuring with Epoxy Acrylate

In order to further improve the physical properties of plywood surface that was pretreated with UV and Gamma radiation at different radiation intensities before photocuring. After pretreatment with radiation the plywood surface was coated with different prepared formulations containing epoxyacrylate (EA-1020) as an oligomer, difunctional monomers such as tripropylene glycol diacrylate (TPGDA), 2-hexadioldiacrylate (HDDA), Ethylene Glycol dimethacrylate (EGDMA) and trifunctional monomer trimethyl propen triacrylate (TMPTA) with photoinitiator Darocur 1664. Thin polymer films were prepared on glass plate with these formulated solutions and cured under UV radiation. Pendulum hardness (PH) and gel content of the film were studied for selecting the formulations as top coat and as base coat. The polished plywood surface was coated with selected formulation and cured under UV radiation. Various rheological properties of UV cured plywood surface such as pendulum hardness, scratch hardness, microgloss, adhesion strength, percentage chipped off area and abrasion resistance were studied.     

Experimental and kinetic modeling of oxygen-enriched air combustion of municipal solid waste

The characteristics of oxygen-enriched air combustion of raw municipal solid waste (MSW) were studied by thermogravimetric analysis. Experiments on oxidative pyrolysis of MSW were carried out under different atmospheres (N(2), N(2):O(2)=7:3, N(2):O(2)=5:5, N(2):O(2)=4:6, and N(2):O(2)=2:8) at 30 degrees C/min. Two distinct peaks of weight loss were obtained according to the derivative thermogravimetric curves; one of them is centered on 305 degrees C with about 40% weight loss, and the second is centered on 420 degrees C with about 20% weight loss. Effects of oxygen concentration on the decomposition process and char combustion were analyzed, and then the process of oxygen-enriched air combustion of MSW was divided into four steps. Kinetic parameters were observed by direct non-linear regressions. According to the obtained data, the apparent activation energy and reaction order decreases along with the combustion process, while that of char combustion increases as oxygen concentration increases.     

A side-by-side comparison of two systems of sequencing coupled reactors for anaerobic digestion of the organic fraction of municipal solid waste.

The objective of this work was to compare the performance of two laboratory-scale, mesophilic systems aiming at the anaerobic digestion of the organic fraction of municipal solid wastes (OFMSW). The first system consisted of two coupled reactors packed with OFMSW (PBR1.1-PBR1.2) and the second system consisted of an upflow anaerobic sludge bed reactor (UASB) coupled to a packed reactor (UASB2.1-PBR2.2). For the start-up phase, both reactors PBR 1.1 and the UASB 2.1 (also called leading reactors) were inoculated with a mixture of non-anaerobic inocula and worked with leachate and effluent full recirculation, respectively. Once a full methanogenic regime was achieved in the leading reactors, their effluents were fed to the fresh-packed reactors PBR1.2 and PBR2.2, respectively. The leading PBR 1.1 reached its full methanogenic regime after 118 days (Tm, time to achieve methanogenesis) whereas the other leading UASB 2.1 reactor reached its full methanogenesis regime after only 34 days. After coupling the leading reactors to the corresponding packed reactors, it was found that both coupled anaerobic systems showed similar performances regarding the degradation of the OFMSW. Removal efficiencies of volatile solids and cellulose and the methane pseudo-yield were 85.95%, 80.88% and 0.109 NL CH4 g(-1) VS(fed) in the PBR-PBR system; and 88.75%, 82.61% and 0.115 NL CH4 g(-1) VS(fed0 in the UASB-PBR system [NL, normalized litre (273 degrees K, 1 ata basis)]. Yet, the second system UASB-PBR system showed a faster overall start-up.     

Stability of Aqueous Suspensions of Medium-Chain-Length Poly-3-Hydroxyalkanoate Particles

Although poly-3-hydroxyalkanoates (PHAs) and particularily medium-chain-length (mcl)-PHAs are likely to find industrial applications in a latex form, very few studies have examined their behavior in aqueous suspension and none have examined the dense suspensions required commercially. For this reason, the stability of mcl-PHA latexes containing saturated aliphatic (65 mol% 3-hydroxynonanoate, PHN), and for the first time, with vinyl (PHNU) or carboxylated side chains was examined. At 4 g L^?1 with no stabilizing agent, PHNU nanoparticles (199.4 ± 3.6 nm) were significantly smaller than those of PHN (211.5 ± 6.4 nm) while carboxylated PHN nanoparticles (76.1 ± 6.4 nm) were substantially smaller than those of either PHN or PHNU with particles stable for more than 110 days. Increasing the PHN concentration to 10 g L^?1 also resulted in stable latexes but with larger particles (410.8 ± 5.2 nm). Adjusting the pH of the suspending medium (water) before addition of the polymer (dissolved in acetone) resulted in much smaller PHN particles at pH = 11.3 (134 ± 2 nm) than at pH = 4.3 (312 ± 8 nm) at a 4 g L^?1 final polymer concentration. Zeta potentials of PHN suspensions decreased with pH, likely due to the carboxyl end groups. Above a pH of 4.0, adjusting the pH after particle formation had little effect. NaCl addition could be used to agglomerate and ultimately precipitate the particles. Stabilizers such as surfactants will likely be required to produce denser mcl-PHA latexes with suitable particle size for certain applications such as coatings and toner production.     

Synergistic Effects of Multiple Metal Contaminants on Electrokinetic Remediation of Soils

This article presents a bench‐scale study performed to investigate the removal of heavy metals when they exist individually and in combination in soils. Electrokinetic experiments were conducted using two types of clayey soils, kaolin and glacial till. These soils were contaminated with Cr(VI) only, with Ni(II) only, and with Cr(VI), Ni(II), and Cd(II) combined. It was found that in kaolin, a significant pH variation occurred due to electric potential application, affecting the adsorption‐desorption and dissolution‐precipitation, as well as the extent of migration of the contaminants. In glacial till, however, pH changes were not affected significantly. In both kaolin and glacial till, the migration of Cr(VI) and Ni(II) was higher when they were present individually compared to when they existed together with Cd(II). Cr(VI) migration as single or combined contaminant was lower in kaolin as compared to that in glacial till. This result was due to the low pH conditions created near the anode region in kaolin that led to high Cr(VI) adsorption to the clay surfaces. In glacial till, however, nickel precipitated with or without the presence of co‐contaminants due to high pH conditions in the soil. Overall, this study demonstrates that adsorption, precipitation, and reduction are the significant hindering mechanisms for the removal of heavy metals using electrokinetic remediation. The direction of the contaminant migration and overall removal efficiency depend on the polarity of the contaminant, the presence of co‐contaminants, and the type of soil. © 2001 John Wiley & Sons.     

Mechanical Properties with the Functional Group of Additives for Starch/PVA Blend Film

This paper deals with the mechanical properties and degree of swelling (DS) of starch/PVA blend film with the functional groups i.e., hydroxyl and carboxyl group, of additives. Starch/PVA blend films were prepared by using the mixing process. Glycerol (GL) with 3 hydroxyl group, sorbitol (SO) with 6 hydroxyl group, succinic acid (SA) with 2 carboxyl group, malic acid (MA) with 1 hydroxyl and 2 carboxyl group, tartaric acid (TA) with 2 hydroxyl and 2 carboxyl group and citric acid (CA) with 1 hydroxyl and 3 carboxyl group were used as additives. The results of measured tensile strength (TS) and elongation (%E) verified that both hydroxyl and carboxyl group as a functional groups increased the flexibility and strength of the film. Values of DS for GL-added and SA-added films were low. However, DS values of the films added MA, TA or CA with both hydroxyl and carboxyl group were comparatively high. When the film was dried at low temperature, the properties of the films were evidently improved. The reason is probably because the hydrogen bonding was activated at low temperature.     

Effects of Preparation Parameters on Properties of Soy Protein-Based Fiberboard

The effects of manufacturing parameters on mechanical properties of medium density fibreboard (MDF) bonded with modified soy protein-based glue were studied to find an appropriate manufacture technology. Physical properties of MDF made with different amount of wax emulsion were measured. Results indicated that water repellent had no obvious influence on physical properties of soy protein-based MDF boards. The fiberboards bonded with soy protein-based glue showed stronger water resistance properties than those bonded with urea–formaldehyde (UF) resins. Furthermore, the soy protein-based MDF boards had good quality [25.2% 24 h soak thickness swell (TS), 29.9 MPa modulus of rupture (MOR), 3130 MPa modulus of elasticity (MOE)], which met requirements of Chinese national standard. Practical processing parameters were obtained by orthogonal experiment, i.e., glue content 8.0%, hot-press temperature 200 °C, and hot-press time 150 s.     

Biostabilization of municipal solid waste

A mechanical-biological process for municipal solid waste (MSW) treatment was monitored for one year. Mechanical pre-treatment provided two fractions. The oversize fraction (diameter > 50 mm) (yield of 600 g kg(-1) ww) (46 Mg day(-1)) was used for refuse derived fuel production, after undergoing a mechanical refining processes, because of low moisture content (200-250 g kg(-1)) and high calorific value (2500-2800 kcal kg ww(-1)). The undersize fraction (diameter < 50 mm) (yield 400 g kg(-1) ww) (30 Mg day(-1)) contained about 800 g kg(-1) of the MSW organic matter. This fraction was biologically treated using an aerobic process with an organic waste fraction from separate collection (77 Mg day(-1)) and recycled stabilized material (62 Mg day(-1)) obtained from end-product sieve (diameter < 20 mm) used as bulking agent. A retention time of three weeks was sufficient to obtain stabilized products in agreement with up-dated rules of the Lombardy Region (North Italy) regarding biostabilization and composting processes. Dynamic Respiration Index (DRI), such as required by both Lombardy Region rules and suggested by the European Community, was chosen in preference to other indices in order to assess the degree of biological stability of the end products. A mean DRI value of 1164 mg O2 kg SV(-1) h(-1) was obtained and is in agreement with the proposed limit of 1000+/-200 mg O2 kg SV(-1) h(-1). Self-heating test, potential biogas production and fermentable volatile solids were also used as parameters to describe the potential impact of treated waste, providing further useful information. Nevertheless, all of these methods revealed analytical or interpretative limits. A complete mass balance of the biological treatment section showed that, from a net input of 107 Mg day(-1), only 250 g kg(-1) (27 Mg day(-1)) of the waste needed to be landfilled, with 750 g kg(-1) (80 Mg day(-1)) being lost as CO2 and H2O.     

Determination of Mark-Houwink Parameters and Absolute Molecular Weight of Medium-Chain-Length Poly(3-Hydroxyalkanoates)

Absolute molecular weight distributions were determined for different medium-chain-length poly(3-hydroxyalkanoates) (MCL PHAs) with predominantly 3-hydroxyoctanoate (PHO), 3-hydroxynonanoate (PHN) or 3-hydroxydodecanoate content. This is the first study to estimate the Mark-Houwink constants of these polymers in the commonly employed GPC carrier solvent tetrahydrofuran (THF). The absolute molecular weight averages were determined via triple-detector size exclusion chromatography and combined with analyses using various detectors. Unlike with the short-chain-length poly(3-hydroxybutyrate), PHB, uncorrected polystyrene calibration in THF provided a good estimate (within 10 %) of absolute MW values for these MCL PHAs, irrespective of side chain length. Weight-average MW values ranged from 172,000 Da for PHO to 18,200 for PHN with 30 mol% 3-hydroxyheptanoate, and dispersities of all samples were close to two. Melt viscosity data suggested an entanglement molecular weight around 8 × 10⁴ Da, significantly higher than most polymers.     

Effect of environmental parameters on the degradability of polymer films in laboratory-scale composting reactors

Previous research in our laboratory reported a convenient laboratory-scale composting test method to study the weight loss of polymer films in aerobic thermophilic (53°C) reactors maintained at a 60% moisture content. The laboratory-scale compost reactors contained the following synthetic compost mixture (percentage on dry-weight basis): tree leaves (45.0), shredded paper (16.5), food (6.7), meat (5.8), cow manure (17.5), sawdust (1.9), aluminum and steel shavings (2.4), glass beads (1.3), urea (1.9), and a compost seed (1.0) which is designated Mix-1 in this work. To simplify the laboratory-scale compost weight loss test method and better understand how compost mixture compositions and environmental parameters affect the rate of plastic degradation, a systematic variation of the synthetic mixture composition as well as the moisture content was carried out. Cellulose acetate (CA) with a degree of substitution (DS) value of 1.7 and cellophane films were chosen as test polymer substrates for this work. The extent of CA DS-1.7 and cellophane weight loss as a function of the exposure time remained unchanged when the metal and glass components of the mixture were excluded in Mix-2. Further study showed that large variations in the mixture composition such as the replacement of tree leaves, food, meat, and sawdust with steam-exploded wood and alfalfa (forming Mix-C) could be made with little or no change in the time dependence of CA DS-1.7 film weight loss. In contrast, substituting tree leaves, food, meat, cow manure, and sawdust with steam-exploded wood in combination with either Rabbit Choice (Mix-D) or starch and urea (Mix-E) resulted in a significant time increase (from 7 to 12 days) for the complete disappearance of CA DS-1.7 films. Interestingly, in this work no direct correlation was observed between the C/N ratio (which ranged from 13.9 to 61.4) and the CA DS-1.7 film weight loss. Decreasing moisture contents of the compost Mix-2 from 60 and 50 and 40% resulted in dramatic changes in polymer degradation such that CA DS-1.7 showed an increase in the time period for a complete disappearance of polymer films from 6 to 16 and 30 days, respectively.Guest Editor: Dr. Graham Swift, Rohm & Haas.Paper presented at the Bio/Environmentally Degradable Polymer Society—Second National Meeting, August 19–21, 1993, Chicago, Illinois.     

Leachability of Cr(VI) and other metals from asphalt composites with addition of filter dust

The potential use of filter dust in asphalt composites for road construction was investigated. Filter dust contains high concentrations of metals, of which Cr(VI) and Pb are leached with water. Compact and ground asphalt composites with addition of 2% of filter dust by mass were studied. In order to evaluate their environmental impact, leachability tests were performed using water and salt water as leaching agents. The concentrations of Cr(VI) and Pb were determined in leachates over a time period of 182 days. The results indicated that Pb was not leached with leaching agents from asphalt composites. Cr(VI) was also not leached with leaching agents from compact asphalt composites. However, in ground asphalt composites, Cr(VI) was leached with water in concentrations up to 220 microg L(-1) and in salt water up to 150 microg L(-1). From the physico-mechanical and environmental aspects, filter dust can be used as a component in asphalt mixtures.     

Influence of flue gas cleaning system on the energetic efficiency and on the economic performance of a WTE plant

Gas cleaning systems of MSW (Municipal Solid Waste) incinerators are characterised by the process employed to remove acid gases. The commonly used technologies for acid gas removal are: (1) dry treatment with Ca(OH)₂ or (2) with NaHCO₃, (3) semi-dry process with Ca(OH)₂ and (4) wet scrubbing. In some recent plants beside a wet cleaning system, a dry neutralization with Ca(OH)₂ is used. The goal is to reduce the amount of acid to be removed in the wet treatment and the liquid effluents produced. The influence of these different technologies on the electrical efficiency was investigated by a detailed simulation of a WTE (Waste To Energy) plant with a capacity of about 100,000 t/y of MSW. The effects of the different gas cleaning systems on electrical efficiency were significant. The difference of efficiency between the most advantageous technology, which is dry treatment with NaHCO₃, and the least advantageous technology which is semi-dry treatment, is about 0.8%. A simple economic analysis showed that the few advantages of dry technologies can often be lost if the costs of chemicals and the disposal of products are considered.