共查询到20条相似文献,搜索用时 109 毫秒
1.
《再生资源与循环经济》2019,(5)
站在物流服务供应链中物流集成商的角度,在可持续发展、绿色循环理念下,对于功能型物流服务商的选择,在传统考虑的因素上着重考虑了生态环境的影响,在参考其他相关文献的基础上,对绿色物流服务商的评价指标进行探讨。 相似文献
2.
采用巨正则蒙特卡罗方法模拟了CO_2在FAU分子筛上的吸附情况,比较了不同CO_2逸度下,CO_2在分子筛模型上的吸附位、吸附量的变化,拟合了其吸附等温线。结果表明:在吸附饱和状态下,分子筛的孔结构越大,对CO_2的吸附量越大,对于比CO_2分子更小的微孔结构,吸附几乎不发生;在低逸度下,CO_2的吸附主要发生在小孔内,随着逸度的提高,CO_2的吸附量迅速上升;在高逸度下,吸附量的提高主要发生在大孔内;FAU分子筛吸附CO_2的过程符合Ⅰ型Langmuir吸附等温线,在高压下对CO_2的吸附能力远大于低压下的吸附能力。 相似文献
3.
4.
5.
6.
采用静态吸附法研究了聚丙烯酰胺(PAM)在大庆市盐碱土中的吸附行为,并通过室内土柱实验研究了PAM在盐碱土中的自然迁移和模拟降雨情况下的迁移行为。实验结果表明,随吸附时间延长、液固比增大,PAM在盐碱土中的吸附量逐渐增大。PAM在盐碱土中的饱和吸附条件为液固比25,平衡吸附时间8h,在此条件下得出的PAM在盐碱土中的吸附等温线符合Langmuir等温吸附模型,饱和吸附量为0.81mg/g.PAM在盐碱土中的迁移规律为:沿地表随盐碱土深度增加,PAM的含量减少。PAM溶液淋滤量越大,迁移深度越深,各层土壤中PAM的含量也相应增加。降雨迫使PAM沿地表向下多迁移1cm,迁移深度在5—6cm。盐碱土对PAM的截留能力较强,意外泄漏的PAM主要集中在地表下3cm以内处,占总淋滤量的86.1%~99.9%。PAM在大庆市盐碱土中的迁移深度不超过10cm。 相似文献
7.
8.
概述高梯度磁分离技术在燃煤脱硫除灰方面的应用与研究进展,超导磁分离技术在燃煤脱硫方面的研究,并展望了超导磁分离技术在环境保护中的应用前景。 相似文献
9.
10.
采用一维土柱装置模拟非水相液体(NAPLs)在我国两种典型土壤(北京潮土与湖南红壤)中的垂向迁移过程,以甲苯为例研究了其在两种土壤中的迁移性能;采用XRD技术测定土壤的矿物组成。实验结果表明,当潮土和红壤孔隙率均为45%时,甲苯在潮土中的迁移速率和最终迁移距离均显著高于在红壤中。甲苯在潮土中的阻滞系数(Rf=18.9)小于在红壤中(Rf=26.5),表明红壤对甲苯的吸附阻滞作用强于潮土。XRD表征结果显示,红壤中粒径小的黏粒含量较高,具有较多的黏土矿物,对甲苯具有更强的吸附阻滞能力,致使甲苯在红壤中垂向迁移速率小,最终迁移距离较短。 相似文献
11.
M. van der Zee J. H. Stoutjesdijk P. A. A. W. van der Heijden D. de Wit 《Journal of Polymers and the Environment》1995,3(4):235-242
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. 相似文献
12.
Eiji Ikada 《Journal of Polymers and the Environment》1999,7(4):197-201
Biodegradable polymers generally decompose in the various media in our environments. These environments contain soils, seawater, and activated sludge. If biodegradable materials waste is discarded, they decompose in these media. The biodegradation process of biodegradable polymers was investigated by scanning electron microscopy. Polycaprolactone, polybutylene succinate, and P(3HB-co-3HV) were tested. The shapes of holes on the decomposing surfaces are different according to the biodegradation media. Semispherical holes are observed on the surfaces of polybutylene succinate films degraded in activated sludge and cracks are observed on the surfaces of polycaprolactone films degraded in soil. 相似文献
13.
The oxidative degradation of polyolefins in the presence of transition metal catalysts is well known in the patent and technical literature. It has been suggested that a properly designed oxidatively degradable polymer could be used in limited lifetime articles and also on those whose primary method of disposal is composting, wherein the thermal activity is used to accelerate the oxidation process. The results of a detailed study of transition metal reactivity in the presence of numerous oxidation promoting species in polyolefins are presented. The oxidative degradation of these polyolefins was demonstrated at moderate temperatures under air and in a simulated compost environment. Approaches to determining the ultimate fate of these materials are discussed. 相似文献
14.
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. 相似文献
15.
16.
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. 相似文献
17.
对某石化企业含腈废水的处理工艺进行了评估,从污染物的来源、组成、处理效果等方面研究了污染物的转化规律,揭示了现有工艺在含腈废水处理过程中的问题。实验结果表明:该企业污水处理场的废水来源较多,丙烯腈生产废水经四效蒸发系统处理后的出水是其污染物的主要来源,含有相对较多的含氮共轭体系;与其他废水混合后,经氨化作用,有机腈转变为有机胺和铵盐;A/O工段矿化度较高,COD的去除率高达73.0%,但有机胺含量仍较高;在缺氧池—生物流化池—硝化池工段,COD进一步被去除,胺类物质浓度大幅降低,但总氮脱除效果并不理想。 相似文献
18.
Model oligo esters of terephthalic acid with 1,2-ethanediol, 1,3-propanediol, and 1,4-butanediol have been investigated with regard to their biodegradability in different biological environments. Well-characterized oligomers with weight-average molar masses of from 600 to 2600 g/mol exhibit biodegradation in aqueous systems, soil, and compost at 60°C. SEC investigations showed a fast biological degradation of the oligomer fraction consisting of 1 or 2 repeating units, independent of the diol component used for polycondensation, while polyester oligomers with degrees of polymerization higher than 2 were stable against microbial attack at room temperature in a time frame of 2 months. At 60°C in a compost environment chemical hydrolysis also degrades chains longer than two repeating units, resulting in enhanced degradability of the oligomers. Metabolization of the monomers and the dimers as well by the microorganisms could be confirmed by comparing SEC measurements and carbon balances in a Sturm test experiment. Based on these results degradation characteristics of potential oligomer intermediates resulting from a primary chain scission from copolyesters consisting of aromatic and aliphatic dicarbonic acids can be predicted depending on their composition. These results will have an evident influence on the evaluation of the biodegradability of commercially interesting copolyesters and lead to new ways of tailor-made designing of new biodegradable materials as well. 相似文献
19.
In the process of metal separation by ash-melting, Fe and Cu in the incineration residue remain in the melting furnace as molten metal, whereas Pb and Zn in the residue are volatilized. This study investigated the effects of the chemical composition of incineration fly ash on the metal-separation efficiency of the ash-melting process. Incineration fly ash with different chemical compositions was melted with bottom ash in a lab-scale reactor, and the efficiency with which Pb and Zn were volatilized preventing the volatilization of Fe and Cu was evaluated. In addition, the behavior of these metals was simulated by thermodynamic equilibrium calculations. Depending on the exhaust gas treatment system used in the incinerator, the relationships among Na, K, and Cl concentrations in the incineration fly ash differed, which affected the efficiency of the metal separation. The amounts of Fe and Cu volatilized decreased by the decrease in the molar ratio of Cl to Na and K in the ash, promoting metal separation. The thermodynamic simulation predicted that the chlorination volatilization of Fe and Cu was prevented by the decrease in the molar ratio, as mentioned before. By melting incineration fly ash with the low molar ratio in a non-oxidative atmosphere, most of the Pb and Zn in the ash were volatilized leaving behind Fe and Cu. 相似文献
20.
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. 相似文献