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81.
在Biot饱和多孔介质动力学理论的基础上,利用Fourier-Bessel级数展开法,通过对含有衬砌洞室的局部场地进行波场分析,得到饱和土半空间中圆柱形衬砌洞室对平面SV波的散射问题的解析解。经验证,本文得到的解可以退化为半空间单相介质的情况。通过与已有的单相弹性介质半空间中圆柱形衬砌洞室对平面SV波散射问题的解析解的对比,验证了此解的正确性。在解析解的基础上,数值计算给出洞口动应力集中放大系数,分析了入射频率和孔洞埋深对柱面上的应力集中因子的影响。 相似文献
82.
Dechlorination of polyvinyl chloride in NaOH/ethylene glycol solution by microwave heating 总被引:1,自引:1,他引:0
This study investigated the dehydrochlorination of flexible polyvinyl chloride (PVC) containing 59.2% PVC, 29.7% dioctyl phthalate
(DOP), and approximately 12% stabilizers. Flexible PVC was treated with NaOH/ethylene glycol (NaOH/EG) solutions at NaOH concentrations
in the range 0.5–4 mol/l and was heated in a microwave heater at a temperature between 100° and 160°C for 0–30 min. All chlorides
were completely eliminated by internal heating at 160°C using microwaves for 10 min in a 1 mol/l NaOH/EG solution, and the
residue was made up of hydrocarbons. The weight loss rate reached a maximum of 74.7% at a temperature of 160°C. It was discovered
that the use of microwaves significantly shortened the reaction time compared to using conventional electric heaters or other
external heating systems and also allowed the use of lower concentrations of NaOH.
Chemical Feedstock Recycling & Other Innovative Recycling Techniques 6 相似文献
83.
施用不同磷肥对植烟土壤中磷的淋失和有效磷的影响 总被引:1,自引:0,他引:1
采用土柱淋溶模拟试验和室内培养试验,研究不同磷肥施入土壤后磷的淋失和有效磷的变化.结果表明,在施磷量为35 mg/kg条件下,整个淋洗期间,钙镁磷肥、磷酸二氢钙、磷酸一氧铵、磷酸二氢铵、磷酸二氢钾5种肥料磷的淋失率很低;各处理从上而下各层土壤的Olsen-P质量比略有增加.施磷量为60 mg/kg、110 mg/kg、170mg/kg、230 mg/kg时.潮砂田肥料磷的淋失率分别为0.26%、0.74%、2.12%和3.17%;灰泥田肥料磷的淋失率分别为0.79%、1.31%、1.60%和1.94%.钙镁磷肥施人各种土壤后,随着培养时间的延长,土壤有效磷质量比逐渐增加,80 d后达到峰值并趋于稳定;磷酸二氢钾、磷酸二氧铵、磷酸一氢铵和磷酸二氢钙施人上壤后,土壤有效磷质量比逐渐降低,至培育60 d后.变化趋于平缓.不同土壤类型对磷的吸附固定率从大到小为潮砂田、灰泥田. 相似文献
84.
TOPSIS法在职业危害综合控制方案决策中的应用 总被引:1,自引:1,他引:0
职业危害控制方案决策属于多属性决策,应用Topsis法对职业危害控制方案进行决策,可以满足不同工艺、不同作业条件、不同经济、技术水平企业选择适宜的职业危害控制方案的需求,以达到有效控制职业危害的目的。Topsis法用于企业职业危害控制方案进行决策具有较好的准确性、实用性,是一种较易于操作、客观的综合决策方法。 相似文献
85.
Xuefei Tu Apichaya Aneksampant Shizusa Kobayashi Atsushi Tanaka Ryo Nishimoto 《Journal of environmental science and health. Part. B》2017,52(1):30-36
It had been reported that iron and manganese oxides in steel slag enhanced the production of humic acid (HA) from low-molecular-weight compounds, such as phenolic acids, amino acids, and saccharides. In the present study, this function of steel slag was applied to the composting of raw organic wastes (ROWs). The degree of humification of HAs is an important factor in evaluating compost quality. Thus, HAs were extracted from the prepared composts and the humification parameters were determined, in terms of elemental compositions, acidic functional group contents, molecular weights, spectroscopic parameters from UV–vis absorption and 13C NMR spectra. The timing for adding steel slag affected the degree of humification of HAs in the composts. The weight average molecular weight of a HA when slag was added initially (29 kDa) was significantly higher than when slag was added after elevating the temperature of the compost pile (17–18 kDa). These results show that ROWs are decomposed to low-molecular-weight compounds after the pile temperature is elevated and the presence of slag enhances the polycondensation of these compounds to produce HAs with a higher degree of humification. Because the slag used in the present study contained several-tens ng g?1 to several μg g?1 of toxic elements (B, Cu, Cr, and Zn), leaching tests for these elements from the prepared composts were carried out. Levels for leaching boron from composts prepared by adding slag (0.2–0.4 mg L?1) were obviously higher than the corresponding levels without slag (0.05 mg L?1). 相似文献
86.
Tanu Jindal Dileep K. Singh H. C. Agarwal 《Journal of environmental science and health. Part. B》2013,48(3):309-320
Abstract Dissipation, degradation and leaching of fresh 14C coumaphos, alkylated 14C coumaphos and aged residues of 14C coumaphos from vats were studied in alkaline sandy loam soil in soil columns in the field under subtropical conditions in Delhi for a year. Dissipation, degradation and bound residue formation was more in case of alkali treated coumaphos than fresh coumaphos. After 365 days total residues of fresh coumaphos accounted for 33.25% while that of alkali treated coumaphos was 19.12%. Bound residue formation was almost double in case of alkali treated coumaphos (18.95%) than fresh coumaphos (9.53%) after 150 days followed by release of bound residue in both the cases. The proportion of metabolites 4 ‐ methylumbelliferone, chlorferon and potasan collectively was 86.05% in fresh coumaphos extractable residues while the same was 91.74% in alkali treated coumaphos after 365 days. Aged residues from vats containing copper sulphate and buffer were found to be more persistent in soil as total residues remained were 95.58% in comparison with 83.09% total residues of aged residues from vats containing only buffer after 150 days of treatment. Copper sulphate seems to inhibit the degradatiion of coumaphos in soil by microorganisms. Chlorferon was the major metabolite in generally all the samples. Coumaphos did not leach below 10 cm in all the cases. 相似文献
87.
The effect of the addition of materials on the leaching pattern of As and metals (Cu, Zn, Ni, Pb, and Cd) in two contaminated soils was investigated. The examined materials included bentonites, silicates and industrial wastes, such as sugar foam, fly ashes and a material originated from the zeolitization of fly ash. Soil + material mixtures were prepared at 10% doses. Changes in the acid neutralization capacity, crystalline phases and contaminant leaching over a wide range of pHs were examined by using pHstat leaching tests. Sugar foam, the zeolitic material and MX-80 bentonite produced the greatest decrease in the leaching of pollutants due to an increase in the pH and/or the sorption capacity in the resulting mixture. This finding suggests that soil remediation may be a feasible option for the reuse of non-hazardous wastes. 相似文献
88.
Thioarsenates were previously determined as dominant species in geothermal and mineral waters with excess sulfide. Here, we used batch leaching experiments to determine their formation upon weathering or industrial leaching of the arsenic-sulfide minerals orpiment (As2S3) and arsenopyrite (FeAsS) under different pH and oxygen conditions. Under acidic conditions, as expected based on their known kinetic instability at low pH, no thioarsenates formed in either of the two mineral systems. Under neutral to alkaline conditions, orpiment dissolution yielded mono-, di- and trithioarsenate which accounted for up to 43-55% of total arsenic. Thioarsenate formation upon arsenopyrite dissolution was low at neutral (4%) but significant at alkaline pH, especially under suboxic to sulfidic conditions (20-43%, mainly as monothioarsenate). In contrast to orpiment, we postulate that recombination of arsenite and sulfide in solution is of minor importance for monothioarsenate formation during alkaline arsenopyrite dissolution. We propose instead that hydroxyl physisorption lead to formation of As-OH-S surface complexes by transposition of hydroxyl anions to arsenic or iron sites. Concurrently formed ironhydroxides could provide re-sorption sites for the freshly released monothioarsenate. However, sorption experiments with goethite showed slower sorption kinetics of monothioarsenate compared to arsenite, but comparable with arsenate. The discovery that thioarsenates are released by natural weathering and industrial leaching processes and that, once they are released, have a higher mobility than the commonly-investigated species arsenite and arsenate requires future studies to consider them when assessing arsenic release in sulfidic natural or mining-impacted environments. 相似文献
89.
90.
有机酸土柱淋洗法修复重金属污染土壤 总被引:10,自引:1,他引:9
通过室内模拟实验,采用土柱淋洗方法,研究草酸、柠檬酸、乙酸和酒石酸溶液对某电镀厂附近土壤中重金属的去除效果。探讨了淋洗剂浓度、淋洗次数和淋洗时间等对淋洗效果的影响,研究草酸淋洗前后土壤中重金属形态的变化。结果表明,淋洗过程中铬的去除效果明显滞后于铜、锌和镍3种重金属离子。1 mol/L的草酸在土水比为1∶1,淋洗5h,淋洗4次的条件下可以达到最佳淋洗效果,Cu、Zn、Ni和Cr的去除率分别是99.6%、66.98%、88.7%和18.23%。 相似文献