白酒糟稻壳吸附剂去除水面油污的研究

白酒糟稻壳活性炭吸附剂是一种产率高、悬浮率高、不存在二次污染、对水面油污吸附量大的良好吸附剂.该吸附剂对不同油脂吸附性能不同.本文对两种润滑油进行研究,发现吸附剂对二硫化钼润滑油的吸附容量比钙基润滑脂的大,对二硫化钼润滑油,仅10 min便达到其饱和吸油量6.26 g/g.白酒糟稻壳吸附剂吸收水蒸汽后,对二硫化钼润滑油的饱和吸油量仍为原吸油量的80%～90%.对特定油脂,白酒糟稻壳吸附剂是一种优良的亲油疏水吸附剂.研究结果为废弃物白酒糟稻壳资源化开辟了一条新途径,同时也为水面油污的去除提供了一种新方法.     

改性柚子皮吸附剂对模拟废水中pb2+的吸附性能

以废柚子皮为原料,经ZnCl2浸泡-加热的化学改性手段制备改性柚子皮生物吸附剂,并通过模拟试验研究该吸附剂对废水中pb2+的去除.考察了模拟废水的pH、吸附时间、吸附剂用量和pb2+初始浓度、温度等因素对柚子皮吸附剂去除pb2+的影响,并研究柚子皮吸附剂对pb2+的吸附动力学及吸附特征.结果表明,模拟废水的pH、吸附时间、吸附剂用量和pb2+初始浓度、温度等因素对柚子皮吸附剂吸附废水中pb2+均有显著影响.适宜的吸附条件为pH5.3～6.5,吸附时间1.5h,吸附剂用量10g· L-1,pb2初始质量浓度100 mg·L-1,温度30℃.在该条件下,废水中pb2+去除率在90％以上.柚子皮吸附剂对废水中pb2+的吸附符合动力学二级反应方程,等温吸附规律可用Langmuir、Freundlich和Temkin模型进行较好的描述.     

调控博物馆微环境的新型甲醛吸附剂的研制

近年来的研究表明,博物馆中馆藏的文物,包括金属、多孔的石器、陶瓷等都受到了甲酸的腐蚀,而这种腐蚀都是由室内污染气体之一的甲醛氧化而引起的。因此研制一种应用于常温无光照的博物馆微环境中的甲醛吸附剂是很有必要的。研制了三种壳聚糖负载MnO2-CeO2的复合型甲醛吸附剂,并对其进行了性能和XRD、BET表征。结果表明:三种吸附材料具有不同的甲醛吸附能力。在最佳配比下制得的壳聚糖甲醛吸附剂6 h后能将环境箱中甲醛浓度由1 340 mg/m3降为169 mg/m3,甲醛吸附量为3.018 mg/g,净化率达87.4%。     

Validation of polymer-based nano-iron oxide in further phosphorus removal from bioeffluent: laboratory and scaledup study

The efficient removal of phosphorous from water is an important but challenging task. In this study, we validated the applicability of a new commercially available nanocomposite adsorbent, i.e., a polymer-based hydrated ferric oxide nanocomposite (HFO-201), for the further removal of phosphorous from the bioeffluent discharged from a municipal wastewater treatment plant, and the operating parameters such as the flow rate, temperature and composition of the regenerants were optimized. Laboratory-scale results indicate that phosphorous in real bioeffluent can be effectively removed from 0.92 mg·L^-1 to<0.5 mg·L^-1 (or even<0.1 mg·L^-1 as desired) by the new adsorbent at a flow rate of 50 bed volume (BV) per hour and treatable volume of 3500–4000 BV per run. Phosphorous removal is independent of the ambient temperature in the range of 15°C–40°C. Moreover, the exhausted HFO-201 can be regenerated by a 2% NaOH+ 5% NaCl binary solution for repeated use without significant capacity loss. A scaled-up study further indicated that even though the initial total phosphorus (TP) was as high as 2 mg·L^-1, it could be reduced to<0.5 mg·L^-1, with a working capacity of 4.4–4.8 g·L^-1 HFO-201. In general, HFO-201 adsorption is a choice method for the efficient removal of phosphate from biotreated waste effluent.     

Removal of arsenic (V) from aqueous medium using manganese oxide coated lignocellulose/silica adsorbents

Arsenic (V) adsorption on manganese oxide coated rice wastes was investigated in this study. The modified adsorbents were characterized by Fourier-transform infrared spectroscopy, scanning electron microscopy, and pH measurements to determine the point of zero charge. Batch adsorption equilibrium experiments were conducted to study the effects of pH, contact time, and initial concentration on arsenic removal efficiency. The adsorption capacity of rice waste was significantly improved after modification with permanganate. The Langmuir isotherm model fitted the equilibrium data better than the Freundlich model which confirms surface homogeneity of the adsorbent. Maxima adsorption capacities are determined as 10 and 12 mg/g at pH 3 for manganese oxide coated rice husk and straw, respectively. The adsorption energy indicates that the adsorption process may be dominated by chemisorption. Pseudo-second-order rate equation described the kinetics sorption of arsenic with good correlation coefficients, better than a pseudo-first-order equation. Manganese oxide coated rice husk and straw appear to be promising low cost adsorbents for removing arsenic from water.     

Optimized porous clay heterostructure for removal of acetaldehyde and toluene from indoor air

Adsorption is the most widely used technology for the removal of indoor volatile organic compounds (VOCs). However, existing adsorbent-based technologies are inadequate to meet the regulatory requirement, due to their limited adsorption capacity and efficiency, especially under high relative humidity (RH) conditions. In this study, a series of new porous clay heterostructure (PCH) adsorbents with various ratios of micropores to mesopores were synthesized, characterized and tested for the adsorption of acetaldehyde and toluene. Two of them, PCH25 and PCH50, exhibited markedly improved adsorption capability, especially for hydrophilic acetaldehyde. The improved adsorption was attributed to their large micropore areas and high micropore-to-mesopore volume ratios. The amount of acetaldehyde adsorbed onto PCH25 at equilibrium reached 62.7 mg·g⁻¹, eight times as much as the amount adsorbed onto conventional activated carbon (AC). Even at a high RH of 80%, PCH25 removed seven and four times more of the acetaldehyde than AC and the unmodified raw PCHs did, respectively. This new PCH optimized for their high adsorption and resistance to humidity has promising applications as a cost-effective adsorbent for indoor air purification.     

Preparation,characterization of sludge adsorbent and investigations on its removal of hydrogen sulfide under room temperature

To recycle the sludge resource from sewage treatment plants and solve the problem of odor pollution, the sludge was converted into an adsorbent by carbonized pyrolysis and the process was optimized by orthogonal experiments. The capability for odor removal as well as the structure of the adsorbent was studied with H₂S as a target pollutant. The results indicate that the main factor affecting the deodorization performance of the adsorbent is the activating time. The sludge adsorbent sample SAC1 prepared under optimum conditions exhibits the best deodorization performance with a H₂S breakthrough time of 58 min and an iodine value nearly that of the coal activated carbon. The breakthrough time of H₂S is much longer than that on the coal activated carbon. On the other hand, characterization results from X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS) and scanning electron microscope (SEM) techniques show that SAC1 is composed of mainly graphite carbon with lower oxygen content on the surface. The bulk of SAC1 exhibits a honeycomb structure with well developed porosity and a high specific surface area of 120.47 m²·g^-1, with the average pore diameter being about 5 nm. Such a structure is in favor of H₂S adsorption. Moreover, SAC1 is detected to contain various metal elements such as Zn, Fe, Mg, etc., leading to a superior deodorization property to that of coal activated carbon.     

吸附法去除钨冶炼废水中的砷

采用一种自主研制的新型吸附剂KL-As01及其专用活化剂KL-AsH1深度去除某钨冶炼企业焙烧尾气碱洗废水和外排混合废水中的砷。在小试、中试研究的基础上,进一步设计了400 m~3/d外排混合废水的处理工艺路线。结果表明,废水经KL-As01吸附剂和KL-AsH1活化剂协同处理后,出水中砷质量浓度小于0.1 mg/L,满足GB 8978—1996《污水综合排放标准》中总砷的排放指标,估算运行成本为5.86元/t。该方法具有处理工艺简单、处理结果稳定、设备占地面积小、易操作、处理成本较低等优点,具有良好的发展和应用前景。     

Experimental study on the quenching process of methane/air deflagration flame with porous media

This article reports experimental investigation of deflagration flame quenching behavior by porous media. In this study, a semi-vented deflagration chamber with a porous media plate was constructed, taking account of effects of obstacles and porous media materials on the flame quenching process. A high speed video camera was used to image the process and behavior of flame propagation, meanwhile, the gas-phase temperatures and ion currents, upstream, within, and downstream of the porous media, were measured using micro-thermocouples and ion probes, respectively. Results show that methane/air deflagration flame can be quenched by the Al₂O₃ porous media with thickness of 20 mm and pore density of 10 ppi. However, the presence of obstacles along the flame path may lead to significant increase of flame speed, thereby both the decreases of gas-phase temperature and ion current when the flame passes through the porous medium in the case with continuous obstacles are less, eventually the unburnt gases downstream the porous media may be reignited. Compared to Al₂O₃, Al porous media shows superior flame quenching performance because this metallic material has higher thermal conductivity, which makes combusting flame release more heat to the pore walls and adjoining structures of the porous media.     

重金属离子天然吸附剂的解吸与再生

总结了重金属离子的天然吸附剂的解吸与再生的研究进展.着重论述了各类解吸剂的解吸原理、解吸特点和解吸性能.指出无机酸解吸剂是价廉高效的理想解吸剂,其中盐酸可在低浓度下达到较高的解吸率,且对吸附剂性能没有损害,而强碱溶液是以阴离子基团形式存在的Cr~(6+)的专有解吸剂.在解吸过程中采用超声波或微波有助于提高解吸率.多数天然吸附剂都具有良好的再生能力,经5次吸附-解吸循环操作仍能保持原有的吸附性能.