Environmental behaviour of a construction made of a mixture of hydraulic binders and air pollution control residues from municipal solid waste incineration Part 1. Physico-chemical characterisation and modelling of the source term

The reuse of waste materials requires the development of assessment methods for the long-term release of pollutants (source term) from wastes (or materials containing wastes) in contact with water. These methods depend on the scenario conditions: characteristics of the materials (especially physical structure and composition), contact with water. The scenario studied here is a water storage reservoir for fire fighting. The reservoir construction is made of a mixture of hydraulic binders and air pollution control (APC) residues from a municipal solid waste incinerator (MSWI). The modelling of the source term is performed in 5 steps ranging from the physico-chemical characterisation of the material to the validation of the proposed model by means of field simulation devices. This article presents the first steps of the methodology: physico-chemical characterisation of the source term, identification of the main transfer mechanisms and laboratory scale modelling of the source term. During the physico-chemical characterisation, it has been shown that the solidified waste shows a high basic capacity and that a relative decrease in pH during leaching favours retention of the main pollutants. During the first leaching sequences, the dynamic leaching tests show that the release of pollutants such as cadmium, arsenic, zinc and lead is extremely low but that the release of alkaline species (sodium and potassium) and chloride is very high from the beginning, whereas the release of calcium remains very high even after 3600 h of leaching. Identification of the main transfer mechanisms concludes that the release of soluble pollutants is the combined result of diffusional transfer of pollutants in the solution and the physico-chemical specificity of the species. The modelling based on these features enables a good simulation of the release but reveals a deviation from the experimental results after 500 h for alkaline species and 1000 h for Ca and Cl leaching. However, this deviation only appears after release of the major part of these elements.     

Evaluation of recycling policies for PET bottles based on multiattribute utility indices

This study focused on waste plastic, especially the polyethylene telephthalate (PET) bottle as representative waste, which has been assigned as goods to be recycled by the Packaging Waste Recycling Law in Japan. We developed a plastic transport model which explained the entire flow of plastic from the production stage to the disposal stage within an the evaluation model of plastic recycle policy based on multiattribute utility theory. This model is designed to be used by local municipal governments in supporting the evaluation of the PET bottle recycling policy. In evaluating the plastics recycling policy, we selected indices relating to economy, ecology, and rate of resource recycling. The results indicate that when the evaluation of the material recycling policy and thermal recycling policy in the model city were characterized in terms of their economic and environmental aspects the thermal recycling policy had the highest utility within our scenario. Received: July 31, 1998 / Accepted: January 26, 1999     

废弃物焚烧中二恶英类的发生与对策

重点探讨和论述了废弃物焚烧过程中极毒物质二恶英类的毒理,生成机构及生成途径,并从工程应用中提出了相应的对策.     

除草剂莠去津(atrazine)在土壤-水环境中的吸附及其机理

为指导农药的使用 ,避免对后茬作物的影响 ,优化农药的施用量、减少环境污染 ,研究了土壤、腐殖酸、粘土矿对莠去津的吸附及其机理 .结果表明 :吸附强弱与土壤理化特性密切相关 ,Feundlich常数 K_af与 OM%有较好的相关性 ( r=0 .975) .腐殖酸对其的吸附起决定作用而粘土矿对其吸附作用并不强 .莠去津在土壤中的吸附可能有氢键、范德华力等作用 .     

内蒙高腐殖酸地下水中碘的分布特征与IDD病的关系

为探讨碘在高腐植酸地下水中的分布特征 ,研究内蒙古河套平原地区 51份水样 .分析结果显示 ,水质偏碱 (平均值 pH=7.91 ) ,水中腐植酸和 COD含量均高 ,地下水类型属于 HCO₃-Na和 HCO₃-Cl- Na型 .在这种高还原型盐水环境中水碘平均浓度达到 430 μg/L,超过了水碘安全浓度范围的上限 ( 5～ 200μg/L) .相关分析结果显示 ,水碘浓度与其它因素的相关顺序是 :COD>荧光强度 >电导率 >HCO^-₃>Cl^->Na⁺>pH>As>井深 .当地地下水中碘的分布呈现出碘浓度随腐植酸含量和盐渍化程度增加而增加的趋势 .由于这些因素的综合作用 ,当地没有发生高碘型碘缺乏病 ( IDD)的大面积流行 .     

Desulfurization of coke oven gas from the coking of coking coal blended with a sorbent and waste plastic

A new way to implement the simultaneous reutilization of solid waste, the desulfurization of coke oven gas (COG), and even the desulfurization of coke by the co-coking of coking coal (CC) and waste plastic (WP) blended with a sorbent is proposed; the evolution of H₂S and the removal efficiency of H₂S from COG during the co-coking process were investigated in a lab-scale cylindrical reactor. The experimental results indicated that for the coking of CC blended with ZnO, Fe₂O₃, or blast furnace dust (BFD) as a sorbent, the instantaneous concentration of H₂S in COG was lower than 500 mg/m³ (which meets the technical specification requirement of the Chinese Cleaner Production Standard–Coking Industry, HJ/T 126-2003) when the molar ratio between the key component of the sorbent and the volatile S in CC or the CC/WP blend, n _Zn+Fe/n _S, was about 1.2 for ZnO and Fe₂O₃, but not for BFD under the same conditions, suggesting that ZnO and Fe₂O₃ are promising sorbents, but that BFD must be treated chemical or thermally before being used as a sorbent because of the size and complicated nature of the influence of its phase/chemical composition on its desulfurization ability. However, for the co-coking of CC and WP blended with ZnO as a sorbent, n _Zn+Fe/n _S must increase to 1.4 and 1.7 for 100/2 and 100/5 blends of CC/WP, respectively, to ensure a satisfactory efficiency for H₂S removal from COG. Part of this paper was presented at the International Symposium on EcoTopia Science 2005 (ISET05), Aug 8–9, 2005, Chikusa-ku, Nagoya, Japan     

胡敏酸在土壤中的迁移

研究了不同条件下胡敏酸在土壤中的迁移过程.结果表明,其迁移过程表现出较大的差异,在溶液pH值、胡敏酸浓度和溶液流速均较高时,胡敏酸迁移的阻滞因子和在土壤中的吸附系数均较低,有利于胡敏酸在土壤中的迁移;在溶液pH值、胡敏酸浓度和溶液流速均较低时,土壤对胡敏酸迁移的阻滞作用较大.胡敏酸的迁移还与土壤性质有关,土壤黏粒含量和阳离子交换量越高,胡敏酸在土壤中吸附的越多,越不利于迁移.在土壤中的吸附是胡敏酸迁移的主要控制因素,在预测胡敏酸在水土环境中迁移时,应该充分考虑不同条件下胡敏酸在不同性质土壤中的吸附.     

Differential responses in American (<Emphasis Type="Italic">Castanea dentata</Emphasis> Marshall) and Chinese (<Emphasis Type="Italic">C. mollissima</Emphasis> Blume) chestnut (Falales: Fagaceae) to foliar application of jasmonic acid

Summary.  Tannins are plant defense compounds that exhibit antibiotic (e.g. toxic) and antixenotic (e.g. repellent) effects against an array of plant pests. They are broadly divided into two major groups, hydrolysable tannins (gallotannins and ellagitannins) and proanthocyanidins, each with an undetermined number of compounds. We investigated constitutive levels of hydrolysable tannins and proanthocyanidins in the leaves and stems of American (Castanea dentata Marshall) (Fagales: Fagaceae) and Chinese (C. mollissima Blume) chestnut. American chestnut contained more proanthocyanidins in leaves and stems than Chinese chestnut, but Chinese chestnut contained more foliar hydrolysable tannins. Regardless of these differences, gypsy moth (Lymantria dispar L, Lepidoptera: Lymantriidae) performance did not differ when fed American and Chinese chestnuts. We also investigated the effects of jasmonic acid (JA) treatment on differential tannin induction in American and Chinese chestnut leaves and stems. JA treatment increased proanthocyanidins in American chestnut stems and hydrolysable tannins in both tissue types of American chestnut, but did not influence tannin concentrations in Chinese chestnut leaves or stems. HPLC-ESI-MS analysis of pooled samples suggested that hydrolysable tannins in each tissue were qualitatively comprised primarily of ellagitannins, and JA generally increased the number of hydrolysable tannins that could be detected by ESI-MS. Third, we investigated the performance of gypsy moths on JA treated and untreated American and Chinese chestnut. Caterpillar relative growth was not influenced by JA treatment on Chinese chestnut, but decreased in response to JA application on American chestnut. Our results indicate that JA-dependent defenses differ between these chestnut species. This study improves our understanding of ecologically important differences in tannin induction and herbivore susceptibility in Castanea, and has important implications in efforts for American chestnut restoration and commercial chestnut production.     

水杨酸对梨叶感染轮纹菌后脂肪酸、叶绿素荧光参数和叶绿体超微结构的影响

用0.3 mmol L-1水杨酸预先处理梨叶片,3 d后接种轮纹病菌(Physalospora Piricola Nose),接种3 d后开始测定各种指标,随后每隔3 d测定1次,共5次.结果表明,经SA处理的梨叶片,感染轮纹病菌后不饱和脂肪酸含量(UFA)、不饱和脂肪酸指数(IUFA)、叶绿素含量、原初光能转换效率(Fv/Fm)、PSⅡ潜在活性(Fv/Fo)、光合电子传递量子效率(ΦPSⅡ)和光化学猝灭系数(qP)比未经SA处理的相应提高;非光化学猝灭系数(qN)比未经SA处理的相应下降.电镜观察表明,部分叶绿体膨大,变形;基粒片层弯曲、散开;淀粉粒数量减少;经SA处理后,症状减轻.图3表1参20     

Variations between rice cultivars in root secretion of organic acids and the relationship with plant cadmium uptake

To attempt to understand certain mechanisms causing the variations between rice cultivars with regard to Cd uptake and accumulation, pot soil experiments were conducted with two rice cultivars at different levels of Cd, i.e., 0 (the control), 10, 50 mg Cd kg⁻¹ soil. The two rice cultivars differ significantly with regard to Cd uptake and accumulation. Root secretions of low-molecular-weight organic acids (LMWOA) for each treatment were measured with ion chromatography. The results showed that LMWOA concentrations in the soil planted with Shan you 63 (a high soil Cd accumulator) were all higher than those in the soil planted with Wu yun jing 7 (low soil Cd accumulator) at different soil Cd levels, although the magnitudes of the differences varied for individual LMWOA and depend on soil Cd concentrations. For all six LMWOA, there were significant differences at P < 0.05 or < 0.01 levels for soils treated with 10 and 50 mg kg⁻¹ Cd. The magnitude of the differences was greater under soil Cd treatments, especially at relatively low levels (for example, 10 mg Cd kg⁻¹ soil), than in the control. Acetic acid and formic acid constituted more than 96% of the total concentration of the six LMWOA, while citric acid constituted only about 0.1%. The rice cultivar with higher concentrations of LMWOA in soil accumulated more Cd in the plants. The results indicate that LMWOA secretion by rice root, especially in Cd-contaminated soils, is likely to be one of the mechanisms determining the plant Cd uptake properties of rice cultivars.