废白土榴莲壳粘土生物炭的制备及对Cr(VI)的吸附

以废白土与榴莲壳为原料制备了粘土生物炭吸附剂(spent bleaching earth biochar,SBEC)、以废白土为原料制备了粘土炭基吸附剂(spent bleaching earth,SBE)吸附废水中的Cr（VI）。用比表面积分析、SEM、XRD、FTIR对吸附剂进行了表征。考察了溶液初始pH、Cr(VI)溶液浓度、吸附剂投加量、吸附时间和吸附温度分别对吸附Cr(VI)的影响。25℃下pH为3时、SBEC 投加量为0.5g/L、Cr(VI)初始浓度为100mg/L、吸附时间120min,SBEC对Cr(VI)去除效率最高为86.1%,SBE则在pH为2去除效率最高为52.5%。SBEC、SBE对Cr(VI)的吸附过程符合准二级动力学模型，SBEC吸附过程符合Freundlich模型，SBE则与Langmuir吸附等温线模型较符合；吸附行为是自发吸热过程。经过5次吸附-脱附后,SBEC对Cr(VI)的去除率达58.8%。     

废白土榴莲壳粘土生物炭的制备及对Cr(VI)的吸附

以废白土与榴莲壳为原料制备了粘土生物炭吸附剂(spent bleaching earth biochar,SBEC)、以废白土为原料制备了粘土炭基吸附剂(spent bleaching earth,SBE)吸附废水中的Cr（VI）。用比表面积分析、SEM、XRD、FTIR对吸附剂进行了表征。考察了溶液初始pH、Cr(VI)溶液浓度、吸附剂投加量、吸附时间和吸附温度分别对吸附Cr(VI)的影响。25℃下pH为3时、SBEC 投加量为0.5g/L、Cr(VI)初始浓度为100mg/L、吸附时间120min,SBEC对Cr(VI)去除效率最高为86.1%,SBE则在pH为2去除效率最高为52.5%。SBEC、SBE对Cr(VI)的吸附过程符合准二级动力学模型,SBEC吸附过程符合Freundlich模型,SBE则与Langmuir吸附等温线模型较符合;吸附行为是自发吸热过程。经过5次吸附-脱附后,SBEC对Cr(VI)的去除率达58.8%。     

Comparing the efficacy of a novel waste-based adsorbent with PAC for the simultaneous removal of chromium (VI) and cyanide from electroplating wastewater

The potential of powdered pistachio hull (PHP) for the co-adsorption of Cr(VI) and cyanide from electroplating wastewater was compared to that of powdered activated carbon (PAC). The results of dynamic adsorption experiments indicated that the complete and simultaneous removal of Cr(VI) and cyanide from wastewater was achieved with 2 g/L of PHP after 60 min of contact. Alternatively, with PAC, 69.2 and 77.8% of Cr(VI) and cyanide, respectively, were removed under the same conditions. Adsorption of Cr(VI) and cyanide by PHP and PAC followed pseudo-second order kinetics, and the equilibrium adsorption data best fit the Langmuir isotherm. The maximum capacity of PHP for the co-adsorption of Cr(VI) and cyanide was 117.6 and 151.5 mg/g, respectively, and the maximum capacity of PAC for the adsorption of Cr(VI) and cyanide was 47.6 and 39.4 mg/g, respectively. It was found that which intraparticle diffusion controlled the adsorption of Cr(VI) and cyanide onto PHP and PAC under the selected conditions. Overall, PHP efficiently adsorbed Cr(VI) and cyanide from industrial effluents; thus, PHP is an affordable and cost-effective system for the treatment of wastewater.     

Adsorption of Cr(VI) onto a low-cost ceramsite: Preparation,kinetics, and thermodynamics

A novel composite ceramsite derived from bamboo powders and bentonite was developed as adsorbents for waste water treatment. The microstructure, morphology, and thermal properties of ceramsite were characterized by X-ray powder diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, energy dispersive X-ray fluorescence, and differential thermal analysis. The effect of compositions, sintering temperatures, sintering time, pH, and adsorption time on the adsorption performance of the ceramsites were studied. The results revealed that the maximum Cr(VI) removal rate of 99% can be obtained in the ceramsite with weight ratio bamboo to bentonite of 6:4, the annealing temperature of 1000°C, the solution pH 1 and contact time of 12 h. The adsorption kinetics and adsorption isotherm analysis revealed that the adsorption process best followed pseudo-second-order reaction kinetics and the Freundlich adsorption isotherm. The adsorption mechanism was discussed and both chemisorption and physiosorption were proposed as adsorption mechanism of Cr(VI). Moreover, the thermodynamic parameters, including changes in Gibbs free energy, entropy, and enthalpy, were studied in detail. The bamboo powder/bentonite composite ceramsite developed in this work is a promising candidate as an effective and economical adsorbent for Cr(VI) ions removal.     

Facile and Eco-Friendly Fabrication of Multifunctional Melamine Sponge for Labeled Cr(VI) Removal and Highly Efficient Oil/Water Separation

Fabrication of multifunctional adsorbent of single-phase material is quite challenging and meaningful for water treatment. In this work, a polyaminosiloxane functionalized melamine sponge is used to remove both heavy metal ions and oil from water. Benefiting from its porous structure, superhydrophobic surface, and abundant amino groups on the surface, the sponge shows excellent performance in Cr(VI) removal and oil/water separation. Notably, the sponge exhibits fluorescent detection function for Cr(VI) owing to the packing of Schiff-base bonds, facilitating the adsorption process to be monitored in real time. The maximum adsorption capacity of Cr(VI) is 252.82 mg g⁻¹ with good selectivity. In addition to the excellent Cr(VI) removal performance, its superhydrophobic nature allows it to adsorb 92.42 times the weight of oil and realize 99.97% oil/water separation efficiency. This trifunctional cost-effective adsorption material shows great potential for large-scale water purification application.     

垃圾焚烧飞灰水洗液纯化及无机盐分离

使用沉淀剂对垃圾焚烧飞灰水洗液中的重金属进行去除实验,并对去除重金属后水洗液中的无机盐进行分离回收。考察了无机、有机沉淀剂单独使用以及无机-有机沉淀剂联用对水洗液中重金属的去除效果,对纯化后的水洗液进行蒸发结晶分离,对不同沸点温度分离得到的无机盐的纯度进行分析。结果表明,无机沉淀剂碳酸钠与硫化钠相比硫化钠去除重金属的效果较好,在硫化钠与重金属物质的量比为1.5时重金属的总去除率可达89.02%;有机沉淀剂TMT-102、MT-103、RS-2568中去除重金属效果最好的是MT-103,在其添加量为400 mg/L时重金属的总去除率可达99.49%。将无机-有机沉淀剂联用,先以硫化钠与重金属物质的量比为1.5加入硫化钠,再加入40 mg/L的MT-103,飞灰水洗液中重金属的总去除率可高达99.60%。将纯化后的水洗液中的无机氯盐进行蒸发分离,蒸发沸点为114 ℃时一次蒸发结束,分离后的盐浆在不低于80 ℃条件下洗涤提纯,得到氯化钠的纯度在95%以上;将母液继续蒸发至沸点温度为126 ℃,然后降温结晶,粗钾按照液固质量比为1.5进行水洗,得到氯化钾的纯度在96%以上;最后的氯化钙母液蒸发至134 ℃,然后降温结晶,可得六水合氯化钙。     

Contribution of agro‐waste material main components (hemicelluloses,cellulose, and lignin) to the removal of chromium (III) from aqueous solution

BACKGROUND: Agro‐waste materials can be used as biosorbents of heavy metals in aqueous solution. However, it is necessary to further study the contribution of agro‐waste materials components (i.e. hemicelluloses, cellulose, and lignin) to the heavy metal ions removal from aqueous solution to better understand the biosorption mechanism, and also based on the biosorbents main components, to predict their potential to remove heavy metals. RESULTS: Cellulose is contained in major proportion (greater than 46%) in the agro‐waste materials reported herein compared with hemicelluloses (from 12% to 26%), lignin (varying from 3% to 10%), and other compounds (22% to 30%) that were removed after the neutral detergent fiber procedure. The identified functional groups in agro‐waste materials and their fractions included hydroxyl, carboxyl, and nitrogen‐containing compounds. Lignin contributed in higher proportion than hemicelluloses to Cr (III) adsorption capacity in both sorghum straw and oats straw. On the other hand lignin was the main fraction responsible for Cr (III) adsorption in agave bagasse. CONCLUSION: Hemicelluloses and lignin were the main contributors to Cr (III) removal from aqueous solution, and cellulose contained in the agro‐waste adsorbents studied did not seem to participate. Copyright © 2009 Society of Chemical Industry     

Iron(III) complex of an amino-functionalized poly(acrylamide)-grafted lignocellulosic residue as a potential adsorbent for the removal of chromium(VI) from water and industry effluents

A new adsorbent (AM-Fe-PGCP), iron(III) complex of an amino-functionalized poly(acrylamide)-grafted coconut coir pith(CP) was prepared through graft copolymerization of acrylamide onto CP (a lignocellulosic residue) in the presence of N, N′-methylenebisacrylamide as cross-linker using and potassium persulphate as an initiator, followed by loading with Fe(III) in the presence of HCl and was tested for its ability to recover chromium(VI) from water and industry effluents. The adsorbent was characterized using FTIR, SEM, XRD, TG/DTG, Surface area analyzer and potentiometric titrations. The potential of the AM-Fe-PGCP to adsorb Cr(VI) from aqueous solutions was investigated under different optimized conditions of pH, concentration of Cr(VI), contact time, and temperature. The effective pH for the removal of Cr(VI) was 4.0. Kinetic data followed a pseudo-second-order model. The equilibrium data were correlated with the Langmuir isotherm model. The equilibrium Cr(VI) sorption capacity was estimated to be 90.09 mg g^-1. Quantitative removal of 27.7 mg L^-1 Cr(VI) from 1.0 L of electroplating industry wastewater was achieved by 0.5 g adsorbent. The reusability of the adsorbent was demonstrated over four cycles using 0.1 M NaOH solution.     

Use of polyethylene films photografted with 2‐(dimethylamino)ethyl methacrylate as a potential adsorbent for removal of chromium (VI) from aqueous medium

A new polymeric adsorbent material based on polyethylene (PE) was prepared by photografting of 2‐(dimethylamino)ethyl methacrylate (DMAEMA) as a positively chargeable monomer to a PE film. The effects of the experimental parameters, such as the pH value, temperature, and grafted amount on adsorption of chromium(VI) (Cr(VI)) ions were investigated for the DMAEMA‐grafted PE (PE‐g‐PDAMEMA) films. The maximum adsorption capacity was obtained at the initial pH value of 3.0 for a PE‐g‐PDMAEMA film with 1.8 mmol/g and the maximum adsorption capacity obtained was higher than or compatible to those of many of the other polymeric adsorbents prepared for Cr(VI) ions. The adsorption kinetics obeyed the mechanism of the pseudo‐second order kinetic model and adsorption of Cr(VI) ions on PE‐g‐PDMAEMA films was well expressed by the Langmuir isotherm model. A high Langmuir adsorption constant suggests that the adsorption of Cr(VI) ions occurs between protonated dimethylamino groups and ions mainly through the electrostatic interaction. Cr(VI) ions adsorbed were successfully desorbed from a PE‐g‐PDMAEMA film in solutions of NaCl, NH₄Cl, NH₄Cl containing NaOH, and NaOH and a PE‐g‐PDMAEMA film was regenerated and repeatedly used for adsorption of Cr(VI) ions without appreciable loss in the adsorption capacity. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43360.     

Preparation and characterization of higher degree‐deacetylated chitosan‐coated magnetic adsorbent for the removal of chromium(VI) from its aqueous mixture

Chitosan (90% deacetylated) coated magnetic adsorbent prepared by coprecipitation method to remove Cr(VI) from its aqueous solution. The experimental studies depicts that the predominant option for removal of Chromium by adsorption from its aqueous phase using Magnetic‐Chitosan (MC). The subsequent physical, chemical, and magnetic properties of MC were characterized by X‐ray powder diffraction, scanning electron microscopy, Fourier transform infrared spectrometer, vibrating sample magnetometer. The influence of batch process parameters such as contact time, initial concentration, pH, and coexisting anions were investigated. The Box‐Behnken experimental design in response surface methodology was performed to design the experiment optimal operating conditions. The maximum percentage reduction of Cr(VI) is 96.3 that was obtained by magnetic chitosan with the optimal operating conditions of 149.53 mg/L at pH of 5.32 at the contact time of 80 min and at the temperature of 303 K. The average diameter of the magnetic chitosan was calculated from X‐ray diffractometer analysis as 24.5 nm. The equilibrium adsorption isotherm models such as Langmuir and Freundlich and the adsorption kinetics such as pseudo first order, pseudo second order and intra‐particle diffusion kinetic model were analyzed. The experimental data's suited for the best fit with the Langmuir isotherm model and pseudo first order kinetic model. It also revealed that Cr(VI) adsorption on MC is intrinsically exothermic and spontaneous. The magnetic chitosan was also used to investigate for the removal of Cr(VI) from the real water sources such as surface, underground, and tannery wastewater. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45878.     

A chelating cellulose adsorbent for the removal of Cu(II) from aqueous solutions

Regenerated cellulose wood pulp was grafted with the vinyl monomer glycidyl methacrylate (GMA) using ceric ammonium nitrate as initiator and was further fuctionalised with imidazole to produce a novel adsorbent material, cellulose‐g‐GMA‐imidazole. All cellulose, grafted cellulose and functionalized cellulose grafts were physically and chemically characterized using a number of analytical techniques, including elemental analysis, Fourier transform infrared spectroscopy, thermogravimetric analysis, differential thermal analysis, and scanning electron microscopy. The cellulose‐g‐GMA material was found to contain 1.75 mmol g^?1 epoxy groups. These epoxy groups permitted introduction of metal binding functionality to produce the cellulose‐g‐GMA‐imidazole final product. Following characterization, a series of adsorption studies were carried out on the cellulose‐g‐GMA‐imidazole to assess its capacity in the removal of Cu²⁺ ions from solution. Cellulose‐g‐GMA‐imidazole sorbent showed an uptake of ～70 mg g^?1 of copper from aqueous solution. The adsorption process is best described by the Langmuir model of adsorption, and the thermodynamics of the process suggest that the binding process is mildly exothermic. The kinetics of the adsorption process indicated that copper uptake occurred within 30 min and that pseudo‐second‐order kinetics best describe the overall process. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 2006     

Adsorption behavior and radiation effects of a silica-based (Calix(4)+Dodecanol)/SiO2-P adsorbent for selective separation of Cs(I) from high level liquid waste

A macroporous silica-based (Calix[4]+Dodecanol)/SiO₂-P absorbent for separation of Cs(I) from HNO₃ solution was prepared by impregnating the 1,3-[(2,4-Diethylheptylethoxy)oxy]-2,4-crown-6-calix[4]arene and its molecule modifier 1-dodecanol into a macroporous silica/polymer composite support. To establish its application into partitioning of Cs(I) from High Level Liquid Waste (HLLW), the adsorption properties and radiation effects on the adsorbent were investigated. The adsorbent showed a relatively large distribution coefficient of Cs(I) and fast equilibrium time in simulated HLLW. Additionally, the adsorbent under the gamma-ray field was found to be able to selectively adsorb Cs(I) with similar behavior to the adsorption without irradiation up to at least 170 kGy.     

Preparation of a novel poly(ether sulfone) adsorptive ultrafiltration membrane containing a crosslinked quaternary chitosan salt and chromate removal

To improve the removal performance of low‐concentration hexavalent chromium [Cr(VI)] in the ultrafiltration (UF) process, adsorptive UF membranes were prepared from suspensions consisting of poly(ether sulfone), N,N‐dimethylacetamide, poly(vinyl pyrrolidone), and crosslinked quaternary chitosan salt (CQS). The results show that the contact angle of the membrane increased from 67 to 83° when the content of CQS was changed from 0 to 10 wt %. Meanwhile, the initial rejection of bovine serum albumin decreased from 90 to 61%, and the pure water fluxes of the membranes showed no obvious change. The rejection of Cr(VI) increased from 20% to 87% when the content of CQS was changed from 0 to 10 wt % in the membrane. Adsorptive UF membranes could be generated by a 1 mol/L solution of NaCl. The adsorption data were more applicable for a pseudo‐second‐order kinetic model and the Langmuir isotherm model. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45198.     

A study of removal of Pb heavy metal ions from aqueous solution using lignite and a new cheap adsorbent (lignite washing plant tailings)

The present study determines the efficiency with which lignite and lignite washing plant tailings can adsorb Pb heavy metal ions. In the first experiment, the effect of size distribution on the absorbance capacity was investigated for the samples. Therefore, lignite sample was ground to five sizes (d₈₀ = 0.600, 0.355, 0.250, 0.106 and 0.063 mm) under nitrogen (N₂), and the tailings sample was classified into seven fractions, along with the original state (original state: d₆₀ = 0.063, −1 + 0.600, −0.600 + 0.355, −0.355 + 0.250, −0.250 + 0.106, −0.106 + 0.063 and −0.063 mm). The test results showed that the optimum size distributions for lignite and tailings were d₈₀ = 0.063 mm and the original state (d₆₀ = 0.063 mm), respectively. Simultaneously, the adsorption capacity results of the two optimum sizes were compared with each other, and the tailings sample (d₆₀ = 0.063 mm) gave the best results, with 9.30 mg/g Pb ions adsorbed value. Therefore, in the second study, a series of laboratory experiments using 2³ full factorial designs was conducted to determine the optimum pH, contact time and initial metal concentration using the original tailings sample. The experimental studies showed that pH 9, a 120 min contact time and 300 ppm initial metal concentration gave the best results, namely an adsorption of 29.92 mg Pb ions/g.     

Preparation and characterization of iron(III) complex of an amino‐functionalized polyacrylamide‐grafted lignocellulosics and its application as adsorbent for chromium(VI) removal from aqueous media

The growth and decay processes of optically induced birefringence in two novel azobenzene compounds [one was a hyperbranched poly(aryl ether) containing azobenzene groups, and the other was a hydrogen‐bonded complex] were studied. The temperature dependence of the birefringence signal was investigated. The curves for the buildup and decay of birefringence fit well to biexponential functions. The dependence of the fitting parameters on the temperature is also discussed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

A novel method for the management of sulfone-rich waste produced in the oxidative desulfurization (ODS) process

The oxidative desulfurization (ODS) process is one of the new desulfurization processes for the production of clean fuels. Despite the benefits of the ODS process, this process faces several important challenges. One of the most important challenges of this process is the management of a waste which is rich of sulfone compounds. In the present study, a new strategy which is the addition of waste to the bitumen with other solid waste such as high density polyethylene (HDPE) waste has been investigated. The experimental design method was applied to investigate the effect of addition of the sulfone and HDPE wastes to the properties of the bitumen blends including degree of penetration, softening point, and mass loss. It was found that the sulfone waste can be added to the bitumen as a softener. The results showed that several grades of bitumen including 50/60, 60/70, 85/100 can be produced through the addition of sulfone waste along with the HDPE waste to the base 60/70 bitumen. In general, the application of simple processes such as mixing the wastes with the bitumen can reduce the cost of waste management, considerably.     

Recent studies in adsorption of Pb(II), Zn(II) and Co(II) using conventional and modified materials:a review

ABSTRACT

Heavy metal contamination and its detrimental effects on human health and environment have been a worldwide concern. Over the years, various technologies have been adapted to tackle this problem. Adsorption is still considered to be one of the most feasible and cost-effective methods for treating wastewater contaminated with heavy metals. Adsorbents such as activated carbon, clay, zeolites and silica have been studied extensively in the past. Modification of these conventional adsorbents and the synthesis of nonconventional adsorbents such as nanocomposites and metal organic frameworks (MOF’s) have been the main focus of study in recent times. This review article attempts to present a detailed account of various adsorbents and their removal efficiencies for the treatment of wastewater contaminated with lead(II), zinc(II) and cobalt(II) in the current decade. Influence of various parameters, adsorption isotherms and kinetics best described for their removal have also been reviewed in detail. It is observed that most of the adsorbents followed pseudo second order kinetics suggestive of a chemisorption process. After conducting a thorough review of more than 120 recently published papers, it can be inferred that nanomaterials and nanocomposites have shown excellent adsorption capacity for removal of these heavy metals.     

A novel agricultural waste based adsorbent for the removal of Pb(II) from aqueous solution: Kinetics,equilibrium and thermodynamic studies

Fig sawdust was used as a precursor for the production of activated carbon by chemical activation with H₃PO₄. The developed Fig sawdust activated carbon (FSAC) was used as a biosorbent for the removal of Pb(II) from aqueous solution. Highest adsorption of Pb(II) (95.8%) was found at pH 4. Equilibrium data fitted very well with the Langmuir isotherm model. Maximum adsorption capacity was determined 80.645 mg g⁻¹ at pH 4. Kinetic studies demonstrated that the adsorption followed a pseudo second order kinetics model. The negative value of ΔG° confirmed the feasibility and spontaneity of FSAC for Pb(II) adsorption.     

Improved synthesis of a branched poly(ethylene imine)‐modified cellulose‐based adsorbent for removal and recovery of Cu(II) from aqueous solution

This study focuses on an improved synthesis of a branched poly (ethylene imine) (PEI)‐modified cellulose‐based adsorbent (Cell‐g‐PGMA‐PEI). We aim to improve the adsorbent capacity by reducing side reaction of epoxide ring opening during graft copolymerization of glycidyl methacrylate (GMA) onto cellulose which increases the content of epoxy groups, anchors to immobilize branched PEI moieties. FTIR spectra provided the evidence of successful graft copolymerization of GMA onto cellulose initiated by benzoyl peroxide (BPO) and modification with PEI. The amount of epoxy groups of Cell‐g‐PGMA was 4.35 mmol g^?1 by epoxy titration. Subsequently, the adsorption behavior of Cu(II) on cell‐g‐PGMA‐PEI in aqueous solution has been investigated. The data from the adsorption kinetic experiments agreed well with pseudo‐second‐order model. The adsorption isotherms can be interpreted by the Langmuir model with the maximum adsorption capacity of 102 mg g^?1 which was largely improved compared with the similar adsorbent reported. The dynamic adsorption capacity obtained from the column tests was 119 mg g^?1 and the adsorbent could be regenerated by HCl of 0.1 mol L^?1. Results indicate that the novel pathway for the synthesis of Cell‐g‐PGMA‐PEI exhibits significant potential to improve the performance of adsorbents in removal and recovery of Cu(II) from aqueous solution. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013