热解吸对土壤中POPs农药的去除及土壤理化性质的影响

为探索土壤热解吸修复技术对POPs污染土壤的修复效果及修复后土壤可耕作性,选择北京某农药厂旧址的POPs农药污染土壤,研究了不同温度下热解吸处理后土壤中滴滴涕(DDTs)和六六六(HCHs)各组分的去除率以及土壤理化性质的变化。结果表明,热解吸修复技术可有效去除土壤中POPs农药,其中,p,p’-DDE与α-HCH组分去除率受热解吸温度的影响比其他组分更为明显。∑HCH与∑DDT在310℃、340℃时分别达到97%、99%的去除率,且此时土壤中的污染物含量低于我国《展览会用地土壤环境质量评价标准》,此后去除率受温度的影响不明显。热解吸温度对修复后土壤的理化性质有一定的影响,不同温度影响的程度各不相同,其中,有机质含量与全氮含量分别由0.78%、0.0352%降至0.14%、0.0107%;pH波动幅度较小,由7.80变至8.25;阳离子交换量变化存在波动,但呈整体下降趋势,由7.87 mg/kg降至5.00mg/kg;土壤中速效磷显著增加,由7.59 mg/kg升至21.8 mg/kg。而在最优温度条件下,土壤理化性质受热解吸温度的影响较小。由此可以说明,热解吸技术可以用于POPs污染土壤的修复,选择适当的热解吸温度对土壤的可耕作性影响有限,因而是一种潜在的绿色修复技术。     

环丁砜-哌嗪溶液吸收烟道气中二氧化碳

采用搅拌实验装置,研究环丁砜溶液及不同配比的环丁砜-PZ复合溶液对烟道气中二氧化碳的吸收和解吸性能,揭示了吸收容量与酸碱度、时间之间的内在联系,并对CO2初始逸出温度、试液再生温度、试液再生率、再生pH下降率进行了细致记录分析。实验结果表明,环丁砜-PZ复合溶液配比为0.4∶0.6时:吸收效果最佳,吸收量约为0.126 mol;再生温度最高,为105℃;再生率最高,为90.34%。同时与相同配比的MEA、DEA相比具有较大再生优势。实验结果还表明,环丁砜-PZ复合体系之间存在负交互作用。     

旋转填料床/柠檬酸盐法吸收-解吸SO2

提出采用旋转填料床结合柠檬酸盐法脱除烟气中SO2的方法,考察了旋转填料床转子转速、液气比、初始柠檬酸根浓度和初始pH值等因素对脱硫效率的影响。结果表明,采用超重力法超重机转子转速为1 000 r/min、液气比为7L/m3、初始柠檬酸根浓度为1.5 mol/L、吸收液的初始pH值为5.0,脱硫效率稳定在99%左右。研究了水蒸气汽提法解吸SO2时初始柠檬酸根浓度、初始pH值、SO2浓度、富液流量和水蒸气流量对解吸效率的影响,得出了影响SO2解吸率的基本规律,并进行了分析。通过实验证明该方法在技术上是可行的,具有良好的应用前景。     

CPB改性沸石对磷酸盐的吸附-解吸性能研究

采用溴化十六烷基吡啶(CPB)对天然沸石进行改性,并考察了CPB改性沸石对磷酸盐的吸附-解吸性能。结果表明,CPB改性沸石对磷酸盐具备一定的吸附能力,且吸附行为满足Langmuir等温吸附模型;粒径、改性剂投加量、反应温度、pH值及共存阴离子等因素均会影响CPB改性沸石对磷酸盐的吸附能力;减小粒径和降低反应温度均有利于CPB改性沸石对磷酸盐的吸附去除;粒径≤0.18 mm CPB改性沸石吸附磷酸盐较优的改性剂投加量为250 mmol/kg;当溶液的初始pH值位于4~10之间时CPB改性沸石对磷酸盐的吸附能力随pH值的增加而增强;SO42-的存在会明显降低CPB改性沸石对磷酸盐的吸附效率,而提高溶液的pH值有助于消除SO42-存在对CPB改性沸石吸附磷酸盐的负面影响;HCO3-的存在会一定程度上抑制CPB改性沸石对磷酸盐的吸附去除,而提高溶液的pH值无法消除HCO3-存在对CPB改性沸石吸附磷酸盐的负面影响;CPB改性沸石吸附磷酸盐后一定条件下可以重新解吸出来,且随着解吸液SO42-浓度的增加解吸率明显增大。     

骨炭对水中不同形态Sb吸附和解吸的影响

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。     

HZ-16型大孔树脂吸附处理含RDT-8废水

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。     

Effect of lipids on sorption/desorption hysteresis in natural organic matter

The chemical composition and physical conformation of natural organic matter (NOM) play a major role in regulating its capacity to retain hydrophobic organic compounds. Naphthalene and phenanthrene were used to study the correlations between sorption/desorption isotherm nonlinearity and compositional data obtained from quantitative ¹³C solid-state DPMAS NMR spectroscopy for soil and peat organic matter with or without lipids. Sorption experiments were conducted using a batch equilibration method. Desorption experiments were carried out immediately following the sorption experiments by three successive decant-refill cycles. Hysteresis was observed in all samples. Nonlinear sorption behavior was increased by removal of lipids from the NOM. The hysteresis index, obtained from the ratio of the Freundlich exponents (N values) for the desorption and sorption isotherms, was lower in the lipid-extracted NOM samples than in the same samples without lipid extraction. The relationship between the extent of hysteresis and the characteristics of the ¹³C DPMAS NMR spectra indicates that altering NOM composition through lipid extraction not only increased the proportion of aromatic-C content, but also increased sorption/desorption hysteresis. Our data also suggest that the hysteresis index is negatively related to aromaticity.     

钠基蒙脱土对亚甲基蓝的吸附和解吸研究

采用正交实验方法,确定了钠基蒙脱土吸附亚甲基蓝染料的最佳吸附条件.采用试剂再生法、超声波法、高温焙烧法、氢氧化钠—高温焙烧结合法对钠基蒙脱土吸附亚甲基蓝进行解吸.用扫描电子显微镜照片和红外光谱对吸附前后的钠基蒙脱土的结构进行表征.实验结果表明:在亚甲基蓝溶液pH为10、吸附温度为60℃、亚甲基蓝质量浓度为1 300 m...     

Sorption and desorption kinetics of diuron,fluometuron, prometryn and pyrithiobac sodium in soils

Abstract

The sorption and desorption characteristics of four herbicides (diuron, fluometuron, prometryn and pyrithiobac‐sodium) in three different cotton growing soils of Australia was investigated. Kinetics and equilibrium sorption and desorption isotherms were determined using the batch equilibrium technique. Sorption was rapid (> 80% in 2 h) and sorption equilibrium was achieved within a short period of time (ca 4 h) for all herbicides. Sorption isotherms of the four herbicides were described by Freundlich equation with an r² value > 0.98. The herbicide sorption as measured by the distribution coefficient (K_d) values ranged from 3.24 to 5.71 L/kg for diuron, 0.44 to 1.13 L/kg for fluometuron, 1.78 to 6.04 L/kg for prometryn and 0.22 to 0.59 L/kg for pyrithiobac‐sodium. Sorption of herbicides was higher in the Moree soil than in Narrabri and Wee Waa soils. When the K_d values were normalised to organic carbon content of the soils (K_oC), it suggested that the affinity of the herbicides to the organic carbon increased in the order: pyrithiobac‐sodium < fluometuron < prometryn < diuron. The desorption isotherms were also adequately described by the Freundlich equation. For desorption, all herbicides exhibited hysteresis and the hysteresis was stronger for highly sorbed herbicides (diuron and prometryn) than the weakly sorbed herbicides (fluometuron and pyrithiobac‐sodium). Hysteresis was also quantified as the percentage of sorbed herbicides which is not released during the desorption step ω = [n_ad / n_de ‐1] x 100). Soil type and initial concentration had significant effect on ω. The effect of sorption and desorption properties of these four herbicides on the off‐site transport to contaminate surface and groundwater are also discussed in this paper.     

构造煤孔隙结构与瓦斯耦合特性研究

利用压汞法、低温氮吸附法、瓦斯等温吸附和解吸试验对平煤八矿构造煤和共生原生结构煤进行综合分析,探讨了构造煤孔隙结构与瓦斯耦合特性.结果表明,构造煤以微孔为主,中孔和大孔相对发育且含较多细颈瓶孔,孔隙连通性差.与共生原生结构煤相比,构造煤各孔径阶段的孔容和孔比表面积都有所增加.构造煤比表面积的增加具有阶段性,即孔径＜ 1.2 nm时为慢增加阶段,孔径=1.2 ～ 4.9nm时为快增加阶段,孔径＞4.9 nm时为稳定阶段.构造煤极限瓦斯吸附量a的增大与比表面积快增加阶段关系密切,但小于其BET比表面积的增幅.瓦斯解吸初期0～2 min内构造煤瓦斯解吸速度和解吸量明显大于共生原生结构煤,与中孔和大孔的变化一致,2 min以后瓦斯解吸迅速衰减.低煤体强度、高瓦斯含量的构造煤以气-煤共溶体形式储集更多弹性潜能,突然卸压时瓦斯膨胀能迅速释放,煤层中发育的构造煤增加了煤与瓦斯突出的危险性.