The use of toxic solid waste for the adsorption of dyes from waste streams

The use of chromium‐containing toxic solid wastes from the leather industry for the removal of dyes from waste‐waters has been studied. A batch adsorption model has been employed and the role of various experimental parameters on the efficiency of the process evaluated. The extent of dye removal was studied by varying parameters such as pH, contact time, initial concentration of the dye and amount of adsorbent. The experimental equilibrium data for this system has been analyzed using the linearized forms of Langmuir and Freundlich isotherms. The Langmuir isotherm was found to provide the best theoretical correlation of the experimental data and the adsorption was found to follow pseudo‐second‐order kinetics. The dye adsorbed solid wastes were used for the preparation of pigments. In essence, this study provides a greener solution for chromium‐containing solid wastes, dye containing waste‐waters and dye‐adsorbed chromium solid wastes. Copyright © 2007 Society of Chemical Industry     

A continuous process for dye removal from liquid effluents using carbonised wool waste

Industrial dyeworks are often conspicuous due to discoloration of rivers and streams into which they discharge waste materials. The adsorption process put forward for the treatment of such effluent makes use of wool-carbonising waste made up of carbonised keratinic fibres and a hydrolysed vegetable material rich in ionic groups. This agro-industrial by-product showed a remarkable capacity for fixing surfactants, metallic cations and dyes. The current pilot project studied the removal of Maxilon Red from aqueous solutions by adsorption of the dye into the vegetable part of waste from the carbonising process. The operation was carried out continuously in a series of mixers. An examination of the hydrodynamic behaviour of a particular type of extractor established operating conditions favouring efficient removal of dyes from the effluent. A maximum dye removal rate of around 98% was possible.     

Chitosan adsorbents for dye removal: a review

One of the most important decontamination techniques is considered to be adsorption. It is fast, simple, low cost with many opportunities to modify the initial materials after appropriate synthesis routes etc. Numerous adsorbent materials have been prepared in the last few years having as the ultimate scope to remove some pollutants especially from contaminated waters (effluents originating from industry). But the composition of each type of effluent varies. Dyes are some major components of industrial wastewaters. Chitosan (poly‐β‐(1 → 4)‐2‐amino‐2‐deoxy‐d ‐glucose) is a nitrogenous (amino‐based) polysaccharide which is produced in large quantities by N‐deacetylation of (its source compound) chitin. The major advantage of chitosan is the existence of modifiable positions in its chemical structure. Modification of the chitosan molecule by (i) grafting (inserting functional groups) or (ii) crosslinking reactions (uniting the macromolecular chains with each other) leads to the formation of chitosan derivatives with superior properties (enhancement of adsorption capacity and resistance in extreme medium conditions, respectively). This review summarizes the important contribution of chitosan derivatives to the dye removal process by adsorption. © 2017 Society of Chemical Industry     

Utilization of organically stabilized proteinous solid waste for the treatment of coloured waste‐water

BACKGROUND: Solid waste emanating from tanneries contains a high percentage of protein with raw trimmings from hides constituting a significant percentage of the solid waste. In this study, organically stabilized trimmings (OST) have been used as an adsorbent material for removal of colour from waste‐water. RESULTS: Various parameters such as adsorbent dosage, dye concentration and pH have been optimized. The effect of neutral salts on the dye adsorption capacity of OST has also been studied. The adsorption of dye by OST follows the Freundlich isotherm. More than 99% removal of colour has been achieved. Commercial trials prove the potential use of organically stabilized trimmings for the treatment of colored wastewater. CONCLUSIONS: Dye loaded OSTs have been employed in the manufacture of a tanning salt, which can be used in the leather industry. Thus, a holistic solution to the challenging solid waste disposal problem has been developed. Copyright © 2009 Society of Chemical Industry     

废水中除铜研究的最新进展

随着铜在工业生产中的广泛应用,铜污染废水的排放量逐渐增加,由于溶解性铜的生物毒性,铜污染废水的处理日益引起人们的重视。针对近五年来对废水中铜去除的研究,文章介绍了沉淀法、吸附法、离子交换法、电化学法,并对已有文献中的技术特点进行了简要总结与分析。对水体中除铜的未来发展方向进行了分析。分析表明,结合原始水质特点,多种方法的工艺组合是从水体中去除铜的未来重点研究方向之一。     

Recovery and reuse of chromium from tannery wastewaters using Turbinaria ornata seaweed

Brown seaweed (Turbinaria spp) was pre‐treated with sulfuric acid, calcium chloride and magnesium chloride and tested for its ability to remove chromium from tannery wastewater. Protonated seaweeds gave better uptake of chromium compared with calcium and magnesium treatments. Chromium uptake was optimal at pH 3.5. Turbinaria weed exhibited maximum uptake of about 31 mg of chromium for one gram of seaweed at an initial concentration of 1000 ppm of chromium. Freundlich and Langmuir adsorption isotherm models were used to describe the biosorption of chromium(III) by Turbinaria spp. The chromium‐loaded seaweed was reused as a reductant in the preparation of the tanning agent basic chromium sulfate (BCS). Leathers made from this tanning agent had properties comparable to conventionally processed chrome‐tanned leathers. Copyright © 2004 Society of Chemical Industry     

Cationized nylon as adsorbent for anionic residual dyes

For use as an ion exchanger, a cationized nylon (EPTMAC–nylon) was prepared by reacting nylon‐6,6 with epoxy propyl trimethyl ammonium chloride (EPTMAC), using anhydrous tin chloride (SnCl₂) as catalyst in a nonaqueous medium. Evidence of grafting was provided by atomic force microscopy and the exchange capacity of EPTMAC–nylon was evaluated by potentiometric titration. The adsorption of four dyes (Acid Blue 25, Acid Yellow 99, Reactive Yellow 23, and Acid Blue 74) from aqueous solutions using a batch process was studied according to the adsorption capacity of the cationized support. The effect of experimental parameters such as dye concentration and adsorption temperature were analyzed. The adsorption isotherms were determined at different temperatures and modeled using Langmuir, Freundlich, and Jossens equations. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2513–2522, 2004     

Tailoring of nanozeolite NaX for enhanced removal of a phytoestrogen from its aqueous solutions

This study represents the application of nanozeolite NaX (NZX) synthesized by hydrothermal treatment without addition of any expensive structure directing agent for the highly effectual adsorption of biochanin A from aqueous solution. The characteristics and surface morphology of NZX were determined using FT-IR, SEM, TEM, BET, and XRD. The adsorption performance of NZX was analyzed at different conditions such as temperature, pH, contact time, adsorbent dose, and initial adsorbate concentration. The adsorption mechanism was well verified by pseudo-second-order kinetic and Redlich–Peterson isotherm models. The thermodynamic parameters revealed that the removal process was exothermic and spontaneous.     

Fly ash as a sorbent for boron removal from aqueous solutions: Equilibrium and thermodynamic studies

ABSTRACT

This study presents the application of fly ash from brown coal and biomass burning power plant as a sorbent for the removal of boron ions from an aqueous solution. The adsorption process efficiency depended on the parameters, such as adsorbent dosage, pH, temperature, agitation time and initial boron concentration. The experimental data fitted well with the Freundlich isotherm model and the maximum capacity was found to be 16.14 mg g^?1. The adsorption kinetics followed the pseudo-second-order model. Also, the intra-particle diffusion model parameters were calculated. Thermodynamic parameters such as change in free energy (ΔG°), enthalpy (ΔH°), entropy (ΔS°) revealed on exothermic nature of boron adsorption onto the fly ash.     

Quaternized biomass as an anion exchanger for the removal of nitrate and other anions from water

Dried Chinese Reed (Miscanthus sinensis), a fast growing plant, was used as a model biomass for the development of anion exchangers using a quaternization agent, N‐(3‐chloro‐2‐hydroxypropyl)trimethylammonium chloride (CHMAC), and a cross‐linking agent, epichlorohydrin. Anions studied include nitrate, phosphate, perchlorate and sulfate. Batch mode adsorption studies were conducted using aqueous solutions of anions. Detailed kinetics were studied for nitrate removal. Parameters studied included anion concentration, agitation time, adsorbent dose, and pH. Adsorption equilibrium occurred in 10 min for all the anions studied. Equilibrium adsorption data followed both Langmuir and Freundlich isotherms. The presence of phosphate, perchlorate, fluoride and sulfate lowered the adsorption significantly. The effects of pH on adsorption and desorption show that ion exchange is involved in the adsorption process. The adsorption capacity of the cross‐linked and quaternized Chinese Reed for nitrate, sulfate, phosphate and perchlorate was found to be 7.55, 13.25, 16.61 and 10.07 mg of anion per g of the anion exchanger, respectively. Copyright © 2004 Society of Chemical Industry     

间二甲胺基苯甲酸生产中废水来源及污染防治

对间二甲胺基苯甲酸生产中废水来源及废水水质进行了分析，并提出了废水污染防治措施。     

城市固体废物焚烧二(口恶)英污染防治技术

二英的致命毒性及其对人类可能产生的长期影响已经引起国内外广泛关注。城市固体废物焚烧是二英的主要来源之一。简单地介绍了二英及其毒性、在焚烧过程中防止二英的生成和从焚烧烟气、飞灰中去除二英的技术。     

Feldspar/titanium dioxide/chitosan as a biophotocatalyst hybrid for the removal of organic dyes from aquatic phases

Feldspar/titanium dioxide/chitosan hybrid, a photoactive biocompatible adsorbent for anionic dyes, was synthesized, characterized, and successfully tested. The adsorbent characterization, pH role, adsorbent dose effect, equilibrium data, kinetic plats, and thermodynamic parameters are reported. The point of zero charge for the hybrid was measured to be 8.3, and the most favorable pH range for the adsorption process was found to be below this pH value. The adsorption equilibrium study demonstrated that the Freundlich model was best fitted to the experimental data. Without UV light exposure, the prepared adsorbent adsorbed 72 mg of Acid Black 1 (AB1)/g of sorbent (86% removal) from a 100‐mL solution with an initial dye concentration of 50 mg/L, whereas UV irradiation resulted in an increase in the elimination of AB1 dye (97% removal). The kinetic data was depicted well by the pseudo‐second‐order model. The thermodynamic parameters indicated that the reaction between the hybrid and the dye was exothermic and also spontaneous at lower temperatures. In the batch desorption process, several aqueous solutions adjusted to different pH values were tested, and the best desorption performance (90% desorption) was achieved at pH 11. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40247.     

Optimization of the process parameters for the removal of boron from drinking water by electrocoagulation—a clean technology

BACKGROUND: There are a number of articles related to removal of boron by electrocoagulation using aluminium electrodes, but there are fewer articles describing the use of magnesium as the anode material. The main disadvantage of aluminium electrodes is the residual aluminium present in the treated water due to cathodic dissolution, which can create health problems. In the case of magnesium electrodes, there is no such disadvantage. This paper presents the results of studies on the removal of boron using magnesium and stainless steel as anode and cathode, respectively. RESULTS: Results show that a maximum removal efficiency of 86.32% was achieved at a current density of 0.2 A dm^?2 and pH of 7 using magnesium as the anode and stainless steel as the cathode. The adsorption of boron fitted the Langmuir adsorption isotherm, suggesting monolayer coverage of adsorbed molecules. The adsorption process follows second‐order kinetics. Temperature studies showed that adsorption was endothermic and spontaneous in nature. CONCLUSIONS: The magnesium hydroxide generated in the cell remove the boron present in the water and reduced to a permissible level and making it drinkable. The process scale up results was consistent with the results obtained from the laboratory scale, showing the robustness of the process. Copyright © 2010 Society of Chemical Industry     

The usability of (sodium alginate/acrylamide) semi-interpenetrating polymer networks on removal of some textile dyes

In this study, (sodium alginate/acrylamide) interpenetrating polymer networks ((NaAlg/AAm)IPN) have been prepared at definite composition. The aqueous solution of 3% (w/v) sodium alginate and 50% (w/v) acrylamide was irradiated with ⁶⁰Co-γ rays at a dose rate of 0.07 kGy/h up to 5 kGy. The percent conversion was determined gravimetrically and 100% gelation was achieved at 5 kGy dose. To understand whether the semi-interpenetrating polymer network of sodium alginate is performed, Fourier Transform Infrared (FTIR) spectra of polyacrylamide (PAAm), sodium alginate, and the semi-interpenetrating polymer network were recorded. It is found that the FTIR spectra of PAAm, NaAlg, and the semi-interpenetrating polymer network are different. The thermograms of PAAm, sodium alginate, and the semi-interpenetrating polymer network were recorded for investigating their thermal character. (NaAlg/AAm)IPN hydrogels were immersed to swell in a solution of pH 7, at a temperature of 25°C. The swelling results at pH 7.0 indicated that (NaAlg/AAm)IPN hydrogel, containing 3% NaAlg showed maximum % swelling in water but swelling increased in the order of water > Magenta > Methylene Blue > Safranine-O > Methyl Violet. Diffusion of water and aqueous solution of dyes within (NaAlg/AAm)IPN hydrogels was found to be of Fickian character at the initial stage of swelling with regard to values calculated for diffusion coefficient of (NaAlg/AAm)IPN hydrogels in water and aqueous solution of dyes. Some diffusion parameters were calculated from swelling of (NaAlg/AAm)IPN in water and dyes and their adsorption isotherms were plotted. In the adsorption experiments, the efficiency of (NaAlg/AAm)IPN hydrogels to adsorb Magenta, Safranine-O, Methylene Blue, and Methyl Violet dyes from water was studied. (NaAlg/AAm)IPN hydrogels showed different adsorption for different aqueous solution of dyes at pH 7.0. Adsorption isotherms were constructed for (NaAlg/AAm)IPN-dye systems. S type adsorption in the Giles classification system was found. Thermal and spectroscopic characterization of semi-interpenetrating polymer network of sodium alginate and acrylamide and dye adsorbed semi-interpenetrating polymer network of sodium alginate and acrylamide was recorded. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Polymer‐derived ceramic adsorbent for pollutant removal from water

Polymer‐derived ceramic components (SiOC, sample W) were produced from preceramic polymer mixture and a catalyst. After curing and pyrolysis, some of the samples etched by hydrofluoric acid to obtain carbonaceous SiOC (C‐rich SiOC, sample W‐HF). W and W‐HF were tested as an adsorbent material to remove both heavy‐metal ions (Cr (III), Pb (III), and Cd (II)) and cationic dyes (Methylene Blue (MB), Rhodamine B (RB), and Crystal Violet (CV)) from aqueous solutions. HF‐treated high surface area SiOC samples had quite high adsorption affinity for cationic dyes. According the Langmuir isotherm model the maximum dye uptake values were found to be around to 50 mg/g for sample W, whereas those for sample W‐HF ranged from 104 to 186 mg/g. Regeneration studies were conducted both by heat treatment and leaching, high recovery yields (always above 97%) of MB adsorption were obtained.     

Utilization of polyampholyte hydrogels for simultaneous removal of textile dyes from aqueous solutions

The study aimed to create hydrogel structures with greater functionality, otherwise known as polyampholytes (PAHs), and to use these in simultaneous removal studies for remazol-type dyes found in environmental waste waters. Adsorption studies were accomplished at 20°C and 35°C, indicated that adsorption process was exothermic in nature. The Q_m values for the PAH-dye systems were in the interval 111–122 mg dye/g PAH with Ads% from 94% to 98%. The ability of PAH hydrogels to adsorb two different species of dye molecules at the same time is an advantage of PAH adsorbents compared to other hydrogel adsorbents prepared in this area.     

Chemically modified sunflower stalks as adsorbents for color removal from textile wastewater

Quaternary ammonium groups were chemically grafted onto sunflower stalks in order to improve their adsorption performance to anionic species in wastewater. The chemically modified sunflower stalks were evaluated as adsorbents for two basic dyes (Methylene Blue and Basic Red 9) and two direct dyes (Congo Red and Direct Blue 71) in aqueous solutions by using equilibrium isotherms and kinetic adsorption. Before the modification, sunflower stalks exhibited relatively low adsorption to the direct dyes but very high adsorption to the basic dyes. The modified sunflower stalks showed increased adsorption to the anionic dyes, but slightly reduced adsorption to the cationic dyes, due to the existence of quaternary ammonium ions on the surface of the residues. The maximum adsorption capacities of two direct dyes on the modified sunflower stalks are 191.0 and 216.0 mg g for Congo Red and Direct Blue 71 at 50°C, respectively, which were at least four times higher than that of the unmodified residues. The adsorption rates of two direct dyestuffs are much higher on the modified residues than on the unmodified ones. Within 30 min, about 80% of direct dyes were removed from the solutions by the residues. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1841–1850, 1999     

Macroporous polymeric ion exchangers as adsorbents for the removal of cationic dye basic blue 9 from aqueous solutions

Two macroporous cation‐exchange resins, Purolite C145, a strongly acidic cation macroporous resin, and Purolite C107E, a weakly acidic cation‐exchange resin, were used to remove the dye Basic Blue 9 (BB9) from an aqueous medium. Batch adsorption experiments were carried out to analyze the effect of various parameters, such as the phase contact time, initial dye concentration, initial solution pH, resin dose, and temperature. The experimental equilibrium data were evaluated by the Langmuir, Freundlich, and Dubinin–Radushkevich (DR) adsorption models. The Freundlich model better described the adsorption processes of the BB9 dye onto both cation exchangers, and the monolayer adsorption capacities were established as 31.9846 mg/g (C145) and 27.77 mg/g (C107E) at 20°C. The values of the mean free adsorption energy (E) obtained from the DR model suggested a porous structure of the adsorbents and proposed ion exchange at the main mechanism of the adsorption process. The values of the thermodynamic parameters showed that the retention of the cationic dye was a spontaneous and endothermic process. Environmental scanning electron microscopy and Fourier transform infrared spectroscopy were used to characterize the sorbent and also to validate the adsorption mechanism as ion‐exchange ones. The desorption experiments by a batch method were performed with different solutions: 0.1 and 1 mol/L HCl, 2.5 mol/L H₂SO₄, CH₃OH, and a mixture between 1 mol/L HCl and CH₃OH. Desorption performed with sulfuric acid was shown to be most effective because more than 85% of the adsorbed dye was removed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39620.