己二胺有机废液在流化床中焚烧的实验研究

在实验室规模的热态流化床试验台上，进行了含5％己二胺有机废液的焚烧 实验研究，在700－900℃范围内，研究温度及空气过剩系数对NOx沿床高的变化规律，以及它们对NOx排放浓度的影响。实验结果表明，沿高度方向上NOx浓度 逐渐降低，并且存在NO2浓度大于NO浓度这一有趣现象，在900℃下氧量增加有利于密相区NO、NO2浓度的降低，说明在 有氧条件下NH2促进NOx的还原，在不同空气 过剩系数下和然相区出口NOx几乎为零 ，表明900℃是己二胺有机废液焚烧 的合适温度。     

间歇通风和渗滤液循环对城市固体废物稳定化的影响

通过研究间歇通风对固体废物的产酸和产甲烷阶段的分离及接种微生物加快固体废物稳定化速度的有效性,评价了污染物原位去除的可行性. 结果表明:间歇通风有利于固体废物的产酸和产甲烷阶段分离,对固体废物的稳定具有积极的影响;用活性污泥接种微生物,加速了废物的稳定,提高了渗滤液的水质,COD_Cr的去除率达88%,ρ(BOD₅)/ρ(COD_Cr)由0.35降到0.12,总氮和NH4+的去除率分别达70% 和80%以上,对重金属也有很好的去除.因此,在填埋场进行污染物原位去除是可行的.      

垃圾焚烧飞灰中Pb及特征药剂稳定化处理

筛选几种重金属药剂用于稳定垃圾焚烧飞灰,以重金属Pb为处理目标,通过单一或复配形式研究药剂的稳定效果并采用红外光谱(FT-IR)和X射线衍射(XRD)分析重金属稳定机理.结果表明,有机药剂稳定后Pb的螯合率高于无机药剂,投加质量分数为2％二乙基DTC能使Pb的浸出满足危险废物填埋污染控制标准(GB 18598-2019...     

接种物浓度和负荷对餐厨垃圾消化性能及产气动力学的影响

为探析接种物浓度(Biomass concentration,BC)和负荷(Organic loading rate,OLR)对餐厨垃圾厌氧消化性能及产气动力学的影响,在中温批次厌氧消化反应器中进行BC和OLR梯度试验,采用理化分析探析各反应器的性能参数,并采用一阶模型和modified Gompertze模型评价各反应器的产气动力学特征.试验结果表明,超负荷会降低反应器运行效率,影响过程稳定性,而提高BC可以减少单位细胞承受的有机负荷,有利于优化厌氧消化过程.产甲烷阶段是餐厨垃圾厌氧消化的限速步骤,各实验条件下水解速率常数(k)始终大于产甲烷速率常数(R_m').OLR和BC对k和R_m'的影响是波动的,从两个参数的数值上无法判断反应器的稳定性.相比之下,高效运行的反应器k/R_m'保持在(2.54±0.62),k/R_m'随OLR的增加及BC的下降单调递增,而随着k/R_m'增加,反应器运行效率下降.这从反应动力学上证实了增加OLR会加剧产酸和耗酸过程的不匹配,引起反应器失稳;而提高的BC浓度有利于缓解这种失衡,对保证反应器的过程稳定具有重要意义.     

城市垃圾焚烧发电项目烟气中重金属干沉降对土壤的影响

焚烧炉烟气中重金属沉降造成的土壤污染是城市垃圾焚烧发电项目环境影响评价及环境保护管理工作关注的重点。以某城市垃圾焚烧发电项目为例,在确定焚烧炉排放源强及气象数据等资料的基础上,采用AERMOD模型预测焚烧烟气中Pb、Hg、Cd的沉降特征和对项目所在区域土壤环境质量的影响。结果表明:土壤中污染物浓度随离源距离的增加均呈现出先上升后下降的趋势,其中Hg的占标率最大为27.2%,其次Cd为21.8%,Pb的占标率最小为4.7%,预测的重金属浓度均满足《土壤环境质量标准》(GB 15618—1995)二级标准限值要求;污染物分布与风密切相关,利用污染系数衡量风对污染物扩散传输的影响,可知污染扩散距离北向大于南向、东向大于西向,南北向大于东西向,污染系数与污染物沉降量分布一致。研究可为气体涉重金属污染物扩散沉降对土壤环境影响相关领域的科研、应用工作提供参考和借鉴。     

有机负荷和进料频率对高含固厨余垃圾厌氧消化系统性能的影响

以系统降解效能和产甲烷量最大化为目标,分别考察不同有机负荷（8.93、10.71、13.39 kg·m^-3·d^-1）及进料频率（1、2、3次·d^-1）下厨余垃圾中温厌氧消化系统运行过程中甲烷产量、SCOD、氨氮、pH和挥发性脂肪酸（VFAs）的变化,旨在明确系统负荷边界及进料频率对系统稳定性的影响.结果表明,系统的有机负荷存在最优值,系统累计产甲烷量随负荷的增加而升高,随后降低,有机负荷为10.71 kg·m^-3·d^-1时获得最大累计产甲烷量37.17 L,VS降解率72.58%.负荷增加系统稳定性下降甚至失稳,各物质出现积累,不利于反应的进行.增加进料频率可优化系统运行参数,显著提高系统产气和产甲烷量,进料频率较高时,运行周期内系统的甲烷产量及产率最高,分别达到45.03 L和0.738 L·g^-1,呈线性增长,增加进料频率可提高系统对氨氮的耐受能力,显著提高系统稳定性,明显改善VFA和丙酸积累问题.     

基于呼吸强度和总有机碳综合评价存量生活垃圾好氧稳定化程度的方法研究

设计固定床好氧稳定化实验装置，在恒温、通风、含水量适宜条件下运行，研究东莞、厦门等地开采后的存量生活垃圾以及食堂餐厨垃圾样品稳定化过程中总有机碳（TOC）和4日呼吸强度（AT₄）随时间的变化规律以及两者变化趋势的相关性.优化了TOC和AT₄的检测方法，证明仪器法测定TOC结果更加合理；研究表明采用四分法取样、从迟滞期结束后开始计算得到的AT₄更有参考价值；4种垃圾样品TOC和AT₄之间具有良好的相关性，两者导数之间也具有良好的相关性，且相关系数均大于0.99（R²>0.99），证明了TOC和AT₄变化趋势的同步响应规律，说明可以利用能快速测定的TOC指标的变化趋势反映不能快速测定的AT₄指标的变化趋势，从而提出一种通过TOC的变化趋势和AT₄的数值综合评价存量垃圾好氧稳定化程度的新方法，既缩短了检测周期，又提高了好氧稳定性评价的客观性，为存量垃圾稳定化评价提供了新思路.     

温度和含水率对村镇垃圾焚烧烟气中有机物排放的影响

使用管式炉模拟村镇生活垃圾焚烧过程,研究不同焚烧温度和不同垃圾含水率条件下,村镇垃圾焚烧烟气中多环芳烃（PAHs）、氯苯及苯系物的生成和分布特性.结果表明,焚烧温度为550℃时,烟气中多环芳烃和氯苯的释放量最大,当温度小于550℃时,多环芳烃和氯苯的释放量随温度升高而增加,温度大于550℃时,多环芳烃和氯苯的释放量随温度升高而降低.高温焚烧不仅可以抑制烟气中多环芳烃的浓度及减少大分子量PAHs的排放,还能降低氯苯的释放量和氯代数,从而减小村镇垃圾焚烧烟气中的毒性;苯系物随着温度升高,由热解转变为高温合成,释放量也随着增加.水分对多环芳烃和氯苯有较大影响,对苯系物的影响较小.在400℃条件焚烧时,水分含量对多环芳烃总体上是促进的,而在850℃焚烧条件下则表现出抑制作用;而水分对氯苯则均表现出抑制作用,并且可以降低氯苯化合物的氯代数.     

含氯有机废水在流化床中焚烧HCl生成与控制的实验研究

在内径32mm的鼓泡流化床焚烧炉中，以含三氯乙醛有机废水为研究对象，在700－900℃的温度范围内，进行了含氯有机废水的焚烧及脱氯试验。研究了有机氯转化为HCI的转化率随温度的变化规律，发现随温度的升高，CI－HCI的转化率增加，900℃时CI－HCI的转化率达到98．5％，进行了高温下加CaO脱除HCI的实验研究，结果表明，温度升高，HCI脱率下降；在相同温度下，随着Ca/CI比的增中，HCI脱除率增加。通过对生成产物进行X射线能谱分析（EDAX）及扫描电子显微镜（SEM）分析的结果，解释了高温下CaO脱除HCI的效果差的原因。     

废水生化处理中有机物的分析和转化

有机物的种类、含量、物化特性、分子量等性质直接影响废水处理工艺的处理效果。本文综述了近年来废水生化处理中有机物的分析方法及废水生化处理过程中有机物的转化规律。     

Baseline options and greenhouse gas emission reduction of clean development mechanism project in urban solid waste management

The Clean Development Mechanism (CDM) was adopted in the Kyoto Protocol as a flexibility mechanism to reduce greenhouse gases (GHGs) and has been started with such projects as improving efficiency of individual technology. Although applying various countermeasures to urban areas has significant potentials for reducing GHGs, these countermeasures have not been proposed as CDM projects in the practical stage. A CDM project needs to be validated that it will reduce GHGs additionally compared with a baseline, that is, a predictive value of GHG emissions in the absence of the project. This study examined the introduction of solid waste incineration with electricity generation into three different cities, A, B and C. The combination of main solid waste treatment and fuel source are landfill and coal, respectively, in City A, incineration and natural gas in City B, and landfill and hydro in City C. GHG emission reductions of each city under several baseline options assumed here were evaluated. Even if the same technology is introduced, the emission reduction greatly varies according to the current condition and the future plan of the city: 1043–1406 kg CO₂/t of waste in City A, 198–580 kg CO₂/t in City B, and wide range of zero to over 1000 kg CO₂/tin City C. Baseline options also cause significant difference in the emission reduction even in the same city (City C). Incinerating solid waste after removing plastics by source separation in City B increased GHG emission reduction potential up to 730–900 kg CO₂/t, which enhances the effectiveness as a CDM project. This revised version was published online in August 2006 with corrections to the Cover Date.     

温度、pH值对城市垃圾中有机碳溶解及其降解特性的影响

通过实验及数值模拟的方法,研究了不同温度和pH值条件下有机碳的溶解动力学特性.结果表明,提高溶液温度有利于加速易溶解有机碳的溶解速率,但不能提高固相有机碳总的溶解量.降低溶液pH值有利于固相有机碳的溶解.实验样品在所有测试环境条件下,有机碳溶解速率为0.05~0.22m3/(kg·h);易溶解有机碳占总可溶解性有机碳百分比为30%~50%;易溶解有机碳溶解速率为14~65h-1,比难溶解有机碳溶解速率高出大约3个数量级.水溶性有机碳生物可降解性实验表明,79%以上水溶性碳难以在厌氧条件下被原生菌降解.     

生物法净化废气中低浓度挥发性有机物的过程机理研究

 针对生物法净化低浓度挥发性有机废气的过程机理研究表明，生物膜填料塔净化低浓度甲苯气体是一个以气膜控制为主的传质过程，其中甲苯的生化降解属于瞬时快速化学反应，即甲苯的生化降解反应速率远远超过甲苯在液膜中的扩散速率，甲苯的生化降解在气液相界面处即可发生，其宏观表现即为甲苯气体直接吸附在润湿的生物膜上后迅速被微生物生化降解。因此，可以从气体吸附理论的新角度去解释生物法净化废气中低浓度挥发性有机物的动力学过程。对于低浓度挥发性有机废气的生物法净化装置的设计与操作而言，凡能改善传质条件、减少气膜阻力的措施均能强化这一生物吸收净化过程。     

Impact of municipal solid waste incineration on heavy metals in the surrounding soils by multivariate analysis and lead isotope analysis

Municipal solid waste(MSW) incineration has become an important anthropogenic source of heavy metals(HMs) to the environment. However, assessing the impact of MSW incineration on HMs in the environment, especially soils, can be a challenging task because of various HM sources. To investigate the effect of MSW incineration on HMs in soils, soil samples collected at different distances from four MSW incinerators in Shanghai, China were analyzed for their contents of eight HMs(antimony, cadmium, chromium, copper,lead, mercury, nickel, and zinc) and lead(Pb) isotope ratios. Source identification and apportionment of HMs were accomplished using principal component analysis and Pb isotope analysis. Results indicated that the relatively high contents of cadmium, lead,antimony, and zinc in the soils at 250 m and 750–1250 m away from the MSW incinerators were related to MSW incineration, while the elevated contents of the other four HMs were associated with other anthropogenic activities. Based on Pb isotope analysis, the contribution ratio of MSW incineration(which had been operated for more than 14 years)to the accumulation of Pb in soil was approximately 10% on average, which was lower than coal combustion only. Incinerator emissions of Pb could have a measurable effect on the soil contamination within a limited area(≤1500 m).     

城市固废好氧加速稳定及碳氮迁移试验研究

选取上海市老港填埋场3~4a垃圾做室内强制通风单元体试验,监测固、液、气三相成分变化,并对有机污染负荷的削减规律以及碳、氮元素的迁移规律进行分析与研究.结果表明,固相纤维素/木质素(C/L)值从初始0.8降至0.4以下,固相中BDM、TOC、TN也有降低,固相指标降解速率呈现前期大后期小的特点,且上层垃圾降解程度更大.液相pH值、EC维持在固定区间,有机污染负荷得到了极大地削减,在整个试验期间,TOC、COD、BOD降解率分别达97%、94%、94%,TN、NH₄-N的降解率分别达到95%、94%.试验期间,累积CO₂释放量6.7kg,累计N₂释放量0.75kg.C/L值、降解稳定化归一指标β可作为固相垃圾稳定化程度判定指标,BOD/COD、NH₄-N/TN值可作为液相中可降解物质稳定化程度判定指标.根据质量守恒原理,对试验过程中碳、氮元素的迁移进行了分析.固相累积损失C质量2.09kg,液相累积流失C质量0.14kg,CO₂累积释放C质量1.83kg.固相累积损失N质量0.62kg,液相累积流失N质量0.08kg,N₂累积释放N质量0.75kg.降解基本结束后,固相中仍然残存着大量的不可降解或者难降解的含碳及含氮化合物.     

北京市城市生活垃圾处理温室气体排放特征及减排策略

根据《IPCC国家温室气体清单指南》和《省级温室气体清单编制指南》方法,建立北京市3种生活垃圾处理方式温室气体排放清单,测算2010—2019年不同生活垃圾处理方式下温室气体CH₄、CO₂、N₂O排放量,分析CO₂排放量随时间变化特征,并基于此提出碳减排策略。结果表明：1）2010—2019年北京市生活垃圾处理温室气体的排放量总体呈先增后减的趋势,且变动幅度减缓,2019年达到最低水平,这主要与近年来北京市生活垃圾处理方式从以卫生填埋为主转变为以焚烧为主有关。2）2018年北京市生活垃圾焚烧量已超过填埋量,而垃圾焚烧处理CO₂排放量远低于填埋处理,表明焚烧处理方式CO₂排放强度低于填埋处理。3）生活垃圾处理温室气体排放量与垃圾处理方式及处理量密切相关,随着生活垃圾产生量的日益增加,建议在生活垃圾管理全过程加强垃圾精细化分类,推进源头减量;合理开展垃圾处理设施的建设,优化垃圾收运系统,防止垃圾处理二次污染,探索适合我国城市生活垃圾处理低碳优化模式。

     

Effects of 5-year application of municipal solid waste compost on the distribution and mobility of heavy metals in a Tunisian calcareous soil

It is obvious that the application of solid waste compost improves the soil fertility. These wastes, however, may also have some negative effects on the agricultural environment due to their metal content. This research aimed at evaluating the influence of Tunisian municipal solid waste compost and farmyard manure on some chemical properties and the distribution of heavy metals in a calcareous Tunisian soil (clayey–loamy soil). A field plot experiment, without vegetation, was installed since 1999 at the experimental farm of the Agronomic National Institute of Tunis (INAT) in the region of Mornag (20 km south of Tunis, Tunisia). During 5 years, the field received yearly the following treatments: 0, 40, 80 and 120 t/ha of municipal solid waste compost and 0, 40 and 120 t/ha of manure. The fractionation of heavy metals in the soil was evaluated after 5 years using a sequential extraction procedure. The application of the two amendments was found to increase the content of organic matter, the total nitrogen content and the electrical conductivity, whereas it slightly decreased the soil pH. The addition of manure did not have a significant effect on the accumulation of heavy metals in the soil, whereas compost application increased the total concentration of heavy metals in the soil. The distribution of heavy metals between the different fractions in untreated and treated soils showed the residual fraction to be dominant, followed by the fraction bound to Fe and Mn oxides. The amount of Cu bound to the organic fraction increased with the application rate, which is probably caused by the formation of organic complexes. For the other metals, the increase of the association with organic matter is very limited. The application of compost moreover increases the amount of Zn associated with Fe and Mn oxides. The “Mobility Factor (MF)” was quite low and did not change after the 5-year application of the two organic amendments. It always remained lower than 10%, although for Cd it amounted to 17%.     

溶解有机质对微生物异化还原铁过程中砷含量及其形态赋存规律的影响

基于典型的希瓦氏金属还原菌(Shewanella decolorationis S12)和石英砂负载铁砷(As-IOCS)的相互作用,探讨了不同来源及组分溶解有机质和生物/非生物条件下对上述作用过程的影响.结果表明,不同类型及组分溶解有机质(DOM)均能使石英砂上负载的铁砷微生物还原解离/解吸程度得到一定程度的加强.而非生物反应体系中,只有含氧化还原敏感官能团结构的蒽醌类物质(0.1 mmol·L-1AQS)对铁砷的解离/解吸作用产生明显影响.在0.1 mmol·L-AQS和有机络合物(2 mmol·L-1 EDTA)的影响下,使得石英砂上负载铁的微生物异化还原程度加强,导致As(Ⅴ)从石英砂负载铁上的解吸程度也随之得到加强;在未加菌体系中,AQS和EDTA和不同组分的DOM类似,对As(Ⅴ)从IOCS上解吸程度影响微弱.对于As(Ⅲ)来说,只有在AQS的影响下,其含量得到显著增加,这可能是作为氧化还原中介体的AQS,在厌氧的生物/非生物条件下,能促进电子在As不同形态之间的转移,使得高价态As(Ⅴ)向还原态As(Ⅲ)的还原转变更易进行.当S12菌液接种含量增加时,在污泥不同组分DOM的影响下,As(Ⅴ)的解吸程度在反应300h前得到明显加强,而As(Ⅲ)的含量在整个反应期间,均快速上升,表明菌液含量高的体系,微生物铁异化还原过程得以持续进行,同时也促进了As(Ⅴ)向As(Ⅲ)的还原转变.     

Influence of SO2 in incineration flue gas on the sequestration of CO2 by municipal solid waste incinerator fly ash

The influence of CO2 content and presence of SO2 on the sequestration of CO2 by municipal solid waste incinerator(MSWI) fly ash was studied by investigating the carbonation reaction of MSWI fly ash with different combinations of simulated flue gas.The reaction between fly ash and 100% CO2 was relatively fast;the uptake of CO2 reached 87g CO2/kg ash,and the sequestered CO2 could be entirely released at high temperatures.When CO2 content was reduced to 12%,the reaction rate decreased;the uptake fell to 41g CO2/kg ash,and 70.7% of the sequestered CO2 could be released.With 12% CO2 in the presence of SO2,the reaction rate significantly decreased;the uptake was just 17g CO2/kg ash,and only 52.9% of the sequestered CO2 could be released.SO2 in the simulated gas restricted the ability of fly ash to sequester CO2 because it blocked the pores of the ash.     

有机物料对石灰性土壤磷素形态转化及吸附特性的影响研究

利用石灰性土壤,对猪粪(DR)、夏玉米秸秆(MR)和冬小麦秸秆(WR)单施或者与磷肥混施(在等磷量条件下)对土壤磷的吸附特性及其形态转化进行了为期15周的室内模拟培养研究.结果表明,无论是DR、MR和WR单施,还是有机物料与磷肥混施,都可以减少土壤对磷的吸附量,增加土壤磷的活性,其中有机物料单施处理的用NaHCO3或者NaOH提取的活性无机磷(Pi)和有机磷(Po)提高较大,顺序为:猪粪>夏玉米秸秆>冬小麦秸秆.夏玉米秸秆处理与对照(CK)相比NaHCO3提取的Pi、Po增加的量分别为6 0mg·kg-1,5 6mg·kg-1,NaOH提取的Po增加的量为12 7mg·kg-1,而猪粪处理与CK相比NaHCO3提取的Pi、Po增加的量分别为7 1mg·kg-1,5 4mg·kg-1,NaOH提取的Po增加的量为14 1mg·kg-1.通过Langmuir方程求得磷的最大吸附量(b)、磷吸附结合能常数(k)、磷素最大缓冲量(MPBC)、标准需磷量(SPR)的值,进一步说明了3种有机物料均可使土壤对磷的吸附能力降低,增加土壤中磷的活性.