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991.
骨炭对水中不同形态Sb吸附和解吸的影响 总被引:1,自引:0,他引:1
采用骨炭作为吸附剂,研究其在不同骨炭用量、pH值和温度条件下对水中Sb(Ⅲ)和Sb(Ⅴ)吸附和解吸的影响。结果表明,骨炭对Sb(Ⅲ)的吸附效果远好于Sb(Ⅴ),在0.2~8.0 mmol/L的Sb(Ⅲ)和Sb(Ⅴ)浓度下,骨炭对这2种形态Sb的去除率分别为46.1%~78.6%和9.6%~31.7%。采用Langmuir方程和Freundlich方程均可以很好地拟合骨炭对Sb(Ⅲ)和Sb(Ⅴ)的吸附,Sb(Ⅲ)和Sb(Ⅴ)的最大吸附容量分别为110.1034 mg/g和17.4167 mg/g。骨炭对Sb(Ⅲ)的解吸也大于对Sb(Ⅴ)的解吸。骨炭对Sb(Ⅲ)和Sb(Ⅴ)的吸附受不同骨炭用量、pH值和温度影响。 相似文献
992.
为研究间歇运行式生物滴滤池对油漆生产厂废气净化能力,建立一座中试规模生物滴滤池(BTF),接种降解菌群,采用8 h/d运行方式净化某油漆厂包装车间废气,并用PCR-DGGE技术揭示BTF细菌群落结构与工艺运行条件间的联系。油漆厂包装车间废气中挥发性有机物(VOCs)主要为甲苯、乙苯、混合二甲苯(间、对和邻二甲苯),BTF对甲苯、乙苯、混合二甲苯最大去除率分别为88.8%、83.7%和86.3%。DGGE分析显示,BTF稳定运行时,主要优势菌相对丰度较为稳定(F,P>0.05),其细菌多样性显著低于启动期(F,P>0.05);同时,下层填料细菌多样性高于上层填料,其细菌结构变化也较上层明显;另外,提升培养液浓度至2倍和4倍对菌群结构亦无显著影响。 相似文献
993.
采用HZ-16型大孔树脂对含三(三溴苯氧基)三嗪(RDT-8)废水进行吸附及脱附处理。实验结果表明:在废水流量为4.0 BV/h的条件下,树脂最佳吸附工艺条件为出水体积88.0 BV,此条件下出水COD小于291 mg/L,挥发酚质量浓度小于0.08 mg/L;在脱附液流量为0.5 BV/h的条件下,树脂最佳脱附工艺条件为脱附液体积3.0 BV,此条件下脱附液中挥发酚质量浓度为30.6 mg/L,挥发酚脱附率高达76.4%。在最佳吸附-脱附工艺条件下,连续进行10次动态吸附-脱附实验,吸附出水中COD为137~294 mg/L,COD去除率为72.5%~89.1%,挥发酚质量浓度稳定在0.05 mg/L以下,挥发酚去除率为99.8%~100%,说明HZ-16型大孔树脂的吸附-脱附性能稳定。 相似文献
994.
995.
对比了酸析法和碱析法对碱法草浆造纸黑液中木质素的去除效果,并分析了聚合氯化铝(PAC)絮凝剂对酸析和碱析后木质素的絮凝效果。实验结果表明:酸析法和碱析法都能有效析出造纸黑液中的木质素,酸析法对色度的去除效果要优于碱析法;当造纸黑液pH为3时,COD去除率达到72.0%,色度去除率为97.7%;当造纸黑液pH为13时,COD去除率达到55.0%,色度去除率为22.3%;PAC对于酸析后木质素有较好的絮凝效果,当废水温度为55℃、PAC加入量为45mL/L时,COD去除率可以达到79.5%,色度去除率为98.5%;PAC絮凝剂对于碱析后的造纸黑液色度的去除效果较差。 相似文献
996.
Long-term (1860–2010) catchment mass balance calculations rely on models and assumptions which are sources of uncertainty
in acidification assessments. In this article, we report on an application of MAGIC to model acidification at the four Swedish
IM forested catchments that have been subject to differing degrees of acidification stress. Uncertainties in the modeled mass
balances were mainly associated with the deposition scenario and assumptions about sulfate adsorption and soil mass. Estimated
base cation (BC) release rates (weathering) varied in a relatively narrow range of 47–62 or 42–47 meq m−2 year−1, depending on assumptions made about soil cation exchange capacity and base saturation. By varying aluminum solubility or
introducing a dynamic weathering feedback that allowed BC release to increase at more acidic pHs, a systematic effect on predicted
changes in acid neutralizing capacity (ΔANC ca. 10–41 μeq l−1) and pH (ca. ΔpH = 0.1–0.6) at all sites was observed. More robust projections of future changes in pH and ANC are dependent
on reducing uncertainties in BC release rates, the timing, and extent of natural acidification through BC uptake by plants,
temporal changes in soil element pools, and fluxes of Al between compartments. 相似文献
997.
The influence of mariculture on mercury distribution in sediments and fish around Hong Kong and adjacent mainland China waters 总被引:1,自引:0,他引:1
To study the influence of mariculture on mercury (Hg) speciation and distribution in sediments and cultured fish around Hong Kong and adjacent mainland China waters, sediment samples were collected from six mariculture sites and the corresponding reference sites, 200-300 m away from the mariculture sites. Mariculture activities increased total mercury, organic matter, carbon, nitrogen and sulfur concentrations in the surface sediments underneath mariculture sites, possibly due to the accumulation of unconsumed fish feed and fish excretion. However, methylmercury (MeHg) concentrations and the ratio of MeHg to THg (% MeHg) in sediments underneath mariculture sites were lower than the corresponding reference sites. The % MeHg in sediments was negatively correlated (r = −0.579, p < 0.05) with organic matter (OM) content among all sites, indicating that OM may have inhibited Hg methylation in surface sediments. Three mariculture fish species were collected from each mariculture site, including red snapper (Lutjanus campechanus), orange-spotted grouper (Epinephelus coioides) and snubnose pompano (Trachinotus blochii). The average MeHg concentration in fish muscle was 75 μg kg−1 (wet weight), and the dietary intake of MeHg through fish consumption for Hong Kong residents was 0.37 μg kg−1 week−1, which was lower than the corresponding WHO limits (500 μg kg−1 and 1.6 μg kg−1 week−1). 相似文献
998.
Factors controlling the transport of geogenically-derived arsenic from a coastal acid sulfate soil into downstream sediments are identified in this study with both solid-phase associations and aqueous speciation clearly critical to the mobility and toxicity of arsenic. The data from both sequential extractions and X-ray adsorption spectroscopy indicate that arsenic in the unoxidised Holocene acid sulfate soils is essentially non-labile in the absence of prolonged oxidation, existing primarily as arsenopyrite or as an arsenopyrite-like species, likely arsenian pyrite. Anthropogenically-accelerated pedogenic processes, which have oxidised this material over time, have greatly enhanced the potential bioavailability of arsenic, with solid-phase arsenic almost solely present as As(V) associated with secondary Fe(III) minerals present. Analyses of downstream sediments reveal that a portion of the arsenic is retained as a mixed As(III)/As(V) solid-phase, though not at levels considered to be environmentally deleterious. Determination of arsenic speciation in pore waters using high performance liquid chromatography/Inductively Coupled Plasma-Mass Spectrometry shows a dominance of As(III) in upstream pore waters whilst an unidentified As species reaches comparative levels within the downstream, estuarine locations. Pore water As(V) was detected at trace concentrations only. The results demonstrate the importance of landscape processes to arsenic transport and availability within acid sulfate soil environments. 相似文献
999.
Dechlorination of PCBs in the simulative transformer oil by microwave-hydrothermal reaction with zero-valent iron involved 总被引:1,自引:0,他引:1
The conventional hydrothermal reaction with iron powder, NaOH and H2O as reactants was reported to occur at temperature above 423 K, and iron oxides (Fe3O4 and NaFeO2) and hydrogen were produced. In this study, microwave heating was adopted to take the place of conventional heating to induce the hydrothermal reaction. Under microwave irradiation, NaOH and H2O absorbed microwave energy by space charge polarization and dipolar polarization and instantly converted it into thermal energy, which initiated the hydrothermal reaction that involved with zero-valent iron. X-ray diffraction (XRD) analysis found Fe3O4/NaFeO2 and confirmed the occurrence of microwave-induced hydrothermal reaction. The developed microwave-hydrothermal reaction was employed for the dechlorination of PCBs. Hexadecane containing 100 mg L−1 of Aroclor1254 was used as simulative transformer oil, and the dechlorination of PCBs was evaluated by GC/ECD, GC/MS and ion chromatography. For PCBs in 10 mL simulative transformer oil, almost complete dechlorination was achieved by 750 W microwave irradiation for 10 min, with 0.3 g iron powder, 0.3 g NaOH and 0.6 mL H2O added. The effects of important factors including microwave power and the amounts of reactants added, on the dechlorination degree were investigated, moreover, the dechlorination mechanism was suggested. Microwave irradiation combined with the common and cheap materials, iron powder, NaOH and H2O, might provide a fast and cost-effective method for the treatment of PCBs-containing wastes. 相似文献
1000.
Combination of divergent active principles to achieve broad-spectrum control is gaining popularity to manage the weed menace in intensive agriculture. However, such application could have non-target impacts on the soil processes affecting soil ecology and environmental interactions. A field experiment was conducted to investigate the impact of separate and combined applications of herbicides bensulfuron methyl and pretilachlor on the emission of N2O and CH4, and related soil and microbial parameters in a flooded alluvial field planted to rice cv Lalat. Single application of the herbicide bensulfuron methyl or pretilachlor resulted in a significant reduction of N2O and CH4 emissions while the combination of these two herbicides distinctly increased N2O and CH4 emissions. Cumulative N2O emissions (kg N2O-N) followed the order of bensulfuron methyl (0.35 kg ha−1) < pretilachlor (0.36 kg ha−1) < control (0.45 kg ha−1) < bensulfuron methyl 0.6% + pretilachlor 6.0% single dose (0.49 kg ha−1) < bensulfuron methyl 0.6% + pretilachlor 6.0% double dose (0.54 kg ha−1). Cumulative CH4 emissions (kg CH4), on the other hand, followed the order of bensulfuron methyl (47.89 kg ha−1) < pretilachlor (73.17 kg ha−1) < bensulfuron methyl 0.6% + pretilachlor 6.0% single dose (93.50 kg ha−1) < control (106.54 kg ha−1) < bensulfuron methyl 0.6% + pretilachlor 6.0% double dose (124.67 kg ha−1). The inhibitory effect of separate application of herbicides bensulfuron methyl 0.6% and pretilachlor 6.0% on N2O emission was linked to lower mineral N, lower denitrifying and nitrifying activity and low denitrifier and nitrifier populations. Inhibitory effect on CH4 emission, on the contrary, was linked to prevention in the drop of redox potential, lower readily mineralizable carbon (RMC) and microbial biomass carbon (MBC) contents as well as lower methanogenic and higher methanotrophic bacterial population. Admittedly, stimulatory effect of combined application of herbicides bensulfuron methyl 0.6% and pretilachlor 6.0% at double dose on N2O and CH4 emission was related to reversal of the identified indicators of inhibition. Results indicate that while individual application of herbicides bensulfuron methyl 0.6% or pretilachlor 6.0% can reduce N2O and CH4 emission from flooded soil planted to rice, their combined application at normal dose can keep the emission at a comparatively lower level with significantly higher grain yield as compared to the herbicides applied alone. 相似文献