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1.
采用膜电解法对废丙烯腈-丁二烯-苯乙烯(ABS)电镀件进行退镀处理。以退镀废液作为阴极液和阳极液,在阳极室退镀ABS电镀件,在阴极室电解退镀废液,进行铜镍分离,回收铜粉和NiCl2。实验结果表明:在阴极电流密度为500 A/m2、初始铜离子质量浓度为24.00 g/L的条件下电解160 min,阴极铜回收率可达97.65%,电流效率达86.60%,得到的铜粉纯度为97%~99%,处理1 L退镀废液可回收铜粉20.0 g,2 mol/L盐酸0.87 L,NiCl2晶体43.8 g;在阳极电流密度为500 A/m2、液固比为6的条件下电解60 min, ABS电镀件的退镀率为77.22%。 相似文献
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采用NaBH4作为还原剂回收电镀废液中的铜。正交实验结果表明,各因素对剩余铜离子质量浓度的影响的显著性顺序为n(NaBH4)∶n(CuSO4)反应时间反应温度。最佳实验条件为:n(NaBH4)∶n(CuSO4)=1.50,反应温度30℃,反应时间25min。经该工艺可获得平均粒径为33nm的近球形立方晶系纳米铜粉,处理后废液中铜离子质量浓度低至0.2mg/L。在铜粉制备过程中加入非离子型表面活性剂可有效阻止晶粒长大,并提高其分散性能,使产物粒径均匀。采用苯骈三氮唑处理后的铜粉抗氧化能力明显提高。 相似文献
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沉淀-电解法回收COD分析废液中的银 总被引:3,自引:0,他引:3
采用沉淀-电解法从COD分析废液中回收银。首先将废液中银沉淀析出,制成高浓度含银电解液,然后以不锈钢作阴、阳极,在极距10mm、电流密度0.28A/dm ̄2条件下进行电解,回收废液中银。该方法操作简便,银回收率为95%以上,纯度达99.5%以上。 相似文献
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采用沉淀-电解法从COD分析废液中回收银。首先将废液中银沉淀析出,制成高浓度含银电解液,然后以不锈钢作阴、阳极,在极距10mm、电流密度0.28A/dm^2条件下进行电解,回收废液中银。该方法操作简便,银回收率为95%以上,纯度达99.5%以上。 相似文献
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利用含铜蚀刻废液生产碱式碳酸铜 总被引:14,自引:0,他引:14
介绍了利用含铜蚀刻废液生产碱式碳酸铜的生产工艺、技术特点、工艺流程和产品质量。以碳酸钠作蚀刻废液的除杂剂,对其进行除杂前处理,控制反应液的pH为3.5~4.0、反应液中碳酸钠的浓度为0.02~0.03mol/L。可除去其中大部分杂质。用碳酸钠与含铜溶液中的铜进行合成反应,控制反应温度为70~80℃、pH为8~9、碳酸钠和含铜溶液中铜的浓度均为1mol/L,反应生成碱式碳酸铜,此产品中铜的质量分数为56%,产品质量优于木材防腐用碱式碳酸铜国内外同类产品。 相似文献
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George Ice Liz Dent Josh Robben Pete Cafferata Jeff Light Brian Sugden Terry Cundy 《Water, Air, & Soil Pollution: Focus》2004,4(1):143-169
The major forest nonpoint source control programs in the West are largely regulatory, either under forest practices acts (California, Idaho, New Mexico, Nevada, Oregon, and Washington) or a streamside management act (Montana). These programs and the specific rules they enforce continue to undergo intensive scrutiny. Still, the questions are the same for these regulatory programs as for states that base nonpoint source control on voluntary BMPs (Arizona, Colorado, Utah, Wyoming). Are the rules or BMPs being applied, and are they effective in reducing nonpoint source pollution to levels that protect beneficial uses of water? The level of debate about forestry in the West has resulted in detailed monitoring and research to answer these questions. In the past, state agencies have assumed levels of BMP compliance based on the percent of operations without enforcement actions. These estimates are being replaced by statistically valid and reproducible monitoring of forest practices rules and BMP compliance levels. BMP effectiveness is being assessed using both qualitative and quantitative methods. This can involve field assessments, process-based research, and control watershed studies. Some trend monitoring is also beginning. With the regional implementation rate for forestry BMPs at about 94% and rising, it is likely that effectiveness testing will continue to be a priority and consume the majority of assessment resources for this region. 相似文献
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Elisângela Corradini Syed H. Imam José A. M. Agnelli Luiz H. C. Mattoso 《Journal of Polymers and the Environment》2009,17(1):1-9
Coconut, sisal and jute fibers were added as reinforcement materials in a biodegradable polymer matrix comprised of starch/gluten/glycerol.
The content of fibers used in the composites varied from 5% to 30% by weight of the total polymers (starch and gluten). Materials
were processed in a Haake torque rheometer (120 °C, 50 rpm) for 6 min. The mixtures obtained were molded by heat compression
and further characterized. Addition of lignocellulosic fibers in the matrix decreased the water absorption at equilibrium.
The diffusion coefficient decreased sharply around 5% fiber concentration, and further fiber additions caused only small variations.
The thermogravimetric (TG) analysis revealed improved thermal stability of matrix upon addition of fibers. The Young’s modulus
and ultimate tensile strength increased with fiber content in the matrix. The storage modulus increased with increasing fiber
content, whereas tanδ curves decreased, confirming the reinforcing effect of the fibers. Morphology of the composites analyzed
under the scanning electron microscope (SEM) exhibited good interfacial adhesion between the matrix and the added fibers.
Matrix degraded rapidly in compost, and addition of increased amounts of coconut fiber in the matrix caused a slowdown the
biodegradability of the matrix.
Names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard
of the product, and the use of the name by USDA implies no approval of the product to the exclusion of others that may be
suitable. 相似文献
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Roland Geyer Hans H. Richnow Dietmar Schlosser 《Water, Air, & Soil Pollution: Focus》2002,2(3):153-159
In experiments employing the lignocellulose-decaying basidiomycetes Trametes versicolor and Stropharia rugosoannulata degrading uniformly14C-labelled 2,4-dichlorophenol and pentachlorophenol, acombination of size exclusion chromatography (SEC),fractionation, and -scintillation counting wasapplied to quantify polymerisation products formed duringchlorophenol degradation. Time-dependent mass balances weregenerated by analysis of 14C in polymerisation products,CO2, as well as monomer non-polar and polar metabolites.Approximately 30% of the chlorophenols were found to bepolymerised. A major fraction of the polymerised productscorresponded to a molecular weight range from 0.24 – 40 kDa.Only a minor fraction could be attributed to a molecularweight >40 kDa. This method proved to be useful inquantification of polymerisation products and kinetics of thepolymerisation processes, whereas UV/Vis detection ofpolymerisation products separated by SEC led to false positiveresults. The SEC-14C method could also be applied forother complex processes where polymerisation ordepolymerisation occurs (humification, degradation oflignocellulose, formation of bound residues from xenobioticssuch as polycyclic aromatic hydrocarbons or 2,4,6-trinitrotoluene) and where spectrophotometric determinationsare difficult or impossible. 相似文献
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Tim Chatterton Stephen Dorling Andrew Lovett Michael Stephenson 《Water, Air, & Soil Pollution: Focus》2002,2(5-6):173-187
This study uses a combination of data from U.K. monitoringstations and from modelling undertaken with the U.K.Meteorological Office's NAME Model to investigate therelative influences of primary and secondary particulateson total PM10 levels at sites in the United Kingdom. Co-located PM10 and sulphate aerosol measurementsindicate that sulphate has a disproportionately largeinfluence on the variation of PM10 levels incomparison to its contribution to their total mass.Comparisons of measured PM10 at urban centre, roadsideand rural sites suggest that local primary sources havevery little influence on daily mean levels. NAME has beenused to model both primary particles and sulphate aerosolfrom sources across the whole of Europe. The discrepanciesbetween modelled and observed PM10 suggest that coarseparticles, such as windblown dust and resuspended roaddust,may comprise a very large, if not dominant, proportion ofobserved PM10 levels. The apparently minor role ofprimary particles (especially locally-sourced ones) raisesa number of issues regarding the suitability of current U.K.and European legislation to addressing the particle problem. 相似文献
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Hysteresis in Reversal of Central European Mountain Lakes from Atmospheric Acidification 总被引:2,自引:0,他引:2
Kopáček Jiří StuchlÍk Evžen Veselý Josef Schaumburg Jochen Anderson Iris C. Fott Jan Hejzlar Josef Vrba Jaroslav 《Water, Air, & Soil Pollution: Focus》2002,2(2):91-114
Extremely high emissions of S and N compounds in Central Europe (both 280 mmol m-2 yr-1) declined by 70and 35%, respectively, during the last decade. Decreaseddeposition rates of SO4
-2, NO3
-, and NH4
+ in the region paralleled emission declines. The reduction in atmospheric inputs of S and N to mountain ecosystemshas resulted in a pronounced reversal of acidification in the Tatra Mountains and Bohemian Forest lakes. Between the 1987–1990and 1997–1999 periods, concentrations of SO4
-2 and NO3
- decreased (average ± standard deviation) by 22±7 and 12±7 mol L-1, respectively, in theTatra Mountains, and by 19±7 and 15±10 mol L-1, respectively, in the Bohemian Forest. Their decrease was compensated in part (1) by a decrease in Ca2+ + Mg2+ (17±7 mol L-1) and H+ (4±6 mol L-1), and an increase in HCO3
-(10±10 mol L-1) in the Tatra Mountains lakes, and (2) by a decrease in Al (7±4 mol L-1), Ca2+ + Mg2+ (9±6 mol L-1), and H+ (6±5 mol L-1), in Bohemian Forest lakes. Despite the rapid decline in lake water concentrations of SO4
-2 and NO3
- in response to reduced S and N emissions, their present concentrations in some lakes are higher than predictionsbased on observed concentrations at comparable emission rates during development of acidification. This hysteresis in chemical reversal from acidification has delayed biological recovery of the lakes. The only unequivocal sign of biological recovery hasbeen observed in erné Lake (Bohemian Forest) where a cladoceran species Ceriodaphnia quadrangular has recentlyreached its pre-acidification abundance. 相似文献
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Stuchlík E. Appleby P. Bitušík P. Curtis C. Fott J. Kopáček J. Pražáková M. Rose N. Strunecký O. Wright R. F. 《Water, Air, & Soil Pollution: Focus》2002,2(2):127-138
Starolesnianske pleso is a small and shallow acid lake in the High Tatra Mountains, situated at 2000 m above sea level, on granitic bedrock, with sparse and thin soil cover. When detailed measurements began in the 1980s Starolesnianske pleso had pH below 5 and only one species of cladoceran zooplankton, the ubiquitous Chydorus sphaericusPalaeolimnological investigations show changes in cladoceran zooplankton and chironomid zoobenthic assemblages since about 1920 and a major change in 1970–1980. The dynamic acidification model MAGIC was used to reconstruct changes in water chemistry over the past 150 years. The results from MAGIC agree well with the sediment record; pH levels gradually decreased from 6.5 in the mid-1800s to about 5.6 in 1920 (first response in biota) to below 5.0 by 1970, and concentrations of inorganic aluminium rose dramatically beginning about 1960. In the 1990s the lake water chemistry showed clear signs of reversal in acidification brought about by a major decline in S deposition. 相似文献
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Armelle Braud Karine Jézéquel Emilie Vieille Adrien Tritter Thierry Lebeau 《Water, Air, & Soil Pollution: Focus》2006,6(3-4):261-279
Partly because of the low bioavailability of metals, the soil cleaning-up using phytoremediation is usually time-consuming.
In order to enhance the amount of metals at the plant's disposal, the soil bioaugmentation coupled together with phytoextraction
is an emerging technology. In this preliminary work, two agricultural soils which mainly differed in their Cr, Hg and Pb contents
(LC, low-contaminated soil; HC, high-contaminated soil) were bioaugmented in laboratory conditions by either bacterial (Bacillus subtilis, Pseudomonas aeruginosa, Pseudomonas fluorescens or Ralstonia metallidurans) or fungal inocula (Aspergillus niger or Penicillium simplicissimum) and incubated during three weeks. The LC soil pots bioaugmented with A. niger and P. aeruginosa contained higher concentrations of Cr (0.08 and 0.25 mg.kg−1 dw soil) and Pb (0.25 and 0.3 mg.kg−1 dw soil) in the exchangeable fraction F1 (extraction with MgCl2) by comparison with the non-bioaugmented soil where neither Cr nor Pb was detected. Conversely, immobilization of Cr and
Pb in the soil were observed with the other microorganisms. The soil bioaugmentation not only modified the metal speciation
for the most easily extractable fractions but also modified the distribution of metals in the other fractions, to a lesser
extent nevertheless. The difference in microbial concentrations between the bioaugmented or not HC soils reached up to 1.8
log units. Thus the microorganisms that we chose for the soil bioaugmentation were competitive towards the indigenous microflora.
The PCA analysis showed close positive relationships between the microorganisms which potentially produced siderophores in
the soil and the amount of Cr and Pb in the fraction F1. 相似文献
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The removal of a mixture of heavy (toxic) metal cations (copper, nickeland zinc) from liquid effluents was investigated in this study at pilotscale, using counter-current contact mode. The innovative processinvolved the abstraction of metal ions onto fungal biosorbents, followedby the application of flotation for the subsequent solid/liquid separationof biomass particles. The ability of microorganisms to remove metal ionsfrom aqueous solutions is a well-known phenomenon. Nevertheless,engineering considerations are very important in decisions, concerningthe commercial future of biosorption and practical solutions are neededfor certain problems, such as the efficient post-separation ofmetal-loaded biomass. The two processes (flotation and biosorption) caneffectively operate in combination, in what it was termed biosorptiveflotation process. The sorbents may be recycled, after appropriate elutionof metals, as well as the treated (clean) water. 相似文献
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采用二次酸浸出的方法回收镍钴湿法冶金工业污泥中的有价金属。先采用水和硫酸作为浸出剂浸出Mg和Na,最佳工艺条件为浸出液的pH 7.5、浸出时间5 min、浸出剂体积与干污泥质量的比(ω)为10 mL/g。再采用硫酸作为浸出剂、焦亚硫酸钠作为还原剂进行二次酸浸,在硫酸与污泥质量比为1.3、焦亚硫酸钠与污泥质量比为0.3、ω为5 mL/g、浸出温度85℃、浸出时间20 min的最佳工艺条件下,Co、Ni、Cu、Mn和Zn的浸出率分别达92.45%、93.48%、89.52%、97.78%和94.79%。经XRD表征,浸出后污泥中未见原污泥中的矿物相,说明原污泥中的矿物几乎全部被溶解。 相似文献
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以芦苇、小麦秸秆和竹子为原料,利用回流式炭化工艺制备3种生物炭。比较三者对NH_4~+-N、PO_4~(3-)-P的吸附性能,并对三者吸附性能差异的成因进行分析。实验结果表明:3种生物炭对PO_4~(3-)-P的吸附效果整体上优于NH_4~+-N,因为3种生物炭的阳离子交换容量CEC值和Zeta电位绝对值的水平均较低,不利于阳离子的吸附;竹炭Z-C对NH_4~+-N的吸附效果最佳,6 h去除率为3.59%,低的N含量、pH及Zeta电位绝对值对NH_4~+-N的吸附有利;芦苇炭LW-C中的O更多地与K、Mg等结合,形成能够与PO_4~(3-)反应生成磷酸盐沉淀或者晶体物质的金属氧化物,从而具有最好的PO_4~(3-)-P的吸附效果,6 h时去除率达16.91%。 相似文献