Copper Removal Capacity Research Articles

Characterization and Optimization of Polymeric Bispicolamine Chelating Resin: Performance Evaluation via RSM Using Copper in Acid Liquors as a Model Substrate through Ion Exchange Method.

Advanced technologies of electronics industries have led to environmental contamination concerns, especially waste print circuit boards containing a very high concentration of copper (II) ions, which can be discharged in wastewater containing many contaminated metals. A low pH is a necessity for treating industrial wastewater containing heavy metals to meet engineering process design. A novel polymeric bispicolamine chelating resin, Dowex-M4195, was applied as an alternative for investigating the behavior of copper (II) in acidic solution via an ion exchange method in a batch experiment system. Characterization of physical and chemical properties before and after ion exchange were also explored through BET, SEM-EDX, FTIR and XRD. Response surface methodology was also applied for optimization of copper (II) removal capacity using design of experiment for selective chelating resin at a low pH. The results indicate that H+ Dowex-M4195 chelating resin had a high-carbon content and specific surface area of >64% and 26.5060 m2/g, respectively. It was predominantly macropore porous in nature due to the N2 gas adsorption isotherm and exhibited type IV with insignificant desorption hysteresis loop of H1-type. It was spherical and cylindrical. After the ion exchange process of copper (II)-loaded H+ Dowex-M4195, the specific surface area and total pore volume decreased by about 17.82% and 5.39%, respectively, as compared to H+ Dowex-M4195. Hysteresis loop, isotherm and pore size distribution were also similar. Regarding the functional group, the surface morphology and crystalline structures of H+ Dowex-M4195 showed copper (II) compound based on the structure of chelating resin that confirmed effective ion exchange behavior. The design of optimization indicated that copper (II) removal capacity of about 31.33 mg/g was achieved, which could be obtained at 6.96 h, pH of 2 (a desirable low pH), dose of 124.13 mg and concentration of 525.15 mg/L. The study indicated that the H+ Dowex-M4195 (which is commercially available on the market) can successfully be applied as an alternative precursor through the ion exchange method for further reuse and regeneration of the copper (II) in the electronic waste industries and other wastewater applications needed to respond the policy of biocircular green economy in Thailand.

Characterization and storage study of chickpea flour films with UV-barrier and Cu-remove properties

An important challenge to food industries is the stability of oxidation-sensitive compounds in packaged foods. In this study, we developed an eco-friendly chickpea flour film (CFF) as an innovative active food packaging material. We investigated the functional properties of films, its copper removal activity and UV-barrier properties during 90 days of storage. The water vapor permeability (1.35 × 10−11 gm−1s−1Pa−1), water content (17.50%) and solubility (35.15%), optical and mechanical properties of chickpea flour films were comparable to that of other bio-based films. The properties of CFF did not change during storage. CFF had UV-light shielding behavior and copper-removal capacity. CFF blocked more than the 95% of the UV spectrum. Maximum Cu-removal capacity (∼ 99.5%) was no affected by the concentrations of copper ions studied. The adsorption data fitted the Langmuir adsorption model, suggesting monolayer coverage. These found properties and eco-friendliness endow the chickpea flour films with great application potential as active packaging film to protect foods against UV radiation and copper promoted oxidative degradation.

Synthesis of Zeolites from Greek Fly Ash and Assessment of Their Copper Removal Capacity

The objective of this study was to synthesize zeolites through fusion of lignite fly ash and NaOH or KOH pellets at 600 °C and assess their removal efficiency in terms of decontamination of solutions containing Cu(II) ions. The removal efficiency of the produced zeolites was tested in batch kinetic experiments using different zeolites and Cu(II) ion concentrations. Experimental data revealed that zeolites synthesized with the use of NaOH exhibited higher removal efficiency compared with those synthesized with the use of KOH. Kinetic data showed that the pseudo-second-order equations described well the removal process. Copper removal was mainly accomplished through the concerted action of chemisorption and intraparticle diffusion. Analytical techniques involving XRF, XRD, FTIR, SEM/EDS and XPS were used for the characterization and morphology analysis of the produced zeolites. SEM/EDS confirmed the presence of copper on the zeolite surface. XPS spectra of Cu2p at 934.3 eV proved the presence of Cu(II) oxidation state, confirming the possible formation of CuO and/or Cu-Cl.

Characterization and mechanism of copper biosorption by a highly copper-resistant fungal strain isolated from copper-polluted acidic orchard soil.

In this paper, a highly copper-resistant fungal strain NT-1 was characterized by morphological, physiological, biochemical, and molecular biological techniques. Physiological response to Cu(II) stress, effects of environmental factors on Cu(II) biosorption, as well as mechanisms of Cu(II) biosorption by strain NT-1 were also investigated in this study. The results showed that NT-1 belonged to the genus Gibberella, which exhibited high tolerance to both acidic conditions and Cu(II) contamination in the environment. High concentrations of copper stress inhibited the growth of NT-1 to various degrees, leading to the decreases in mycelial biomass and colony diameter, as well as changes in morphology. Under optimal conditions (initial copper concentration: 200mgL-1, temperature 28°C, pH 5.0, and inoculum dose 10%), the maximum copper removal percentage from solution through culture of strain NT-1 within 5days reached up to 45.5%. The biosorption of Cu(II) by NT-1 conformed to quasi-second-order kinetics and Langmuir isothermal adsorption model and was confirmed to be a monolayer adsorption process dominated by surface adsorption. The binding of NT-1 to Cu(II) was mainly achieved by forming polydentate complexes with carboxylate and amide group through covalent interactions and forming Cu-nitrogen-containing heterocyclic complexes via Cu(II)-π interaction. The results of this study provide a new fungal resource and key parameters influencing growth and copper removal capacity of the strain for developing an effective bioremediation strategy for copper-contaminated acidic orchard soils.

Rationally Designed CeNP@MnMoS4 Core‐Shell Nanoparticles for Modulating Multiple Facets of Alzheimer's Disease

Alzheimer's disease (AD) is a complicated multifactorial syndrome. Lessons have been learned through failed clinical trials that targeting multiple key pathways of the AD pathogenesis is necessary to halt the disease progression. Here, we construct core-shell nanoparticles (CeNP@MnMoS4 ) targeting multiple key pathways of the AD pathogenesis, including elimination of toxic metal ions, decrease of oxidative stress, and promotion of neurite outgrowth. The SOD activity and copper removal capacity of CeNP@MnMoS4 -n (n represents the number of layers of MnMoS4 , n=1-5) was investigated in vitro. We found that CeNP@MnMoS4 -3 made an excellent balance between SOD activity and copper removal capacity. The effect of CeNP@MnMoS4 -3 on Cu(2+) -induced Aβ aggregation was studied by gel electrophoresis, transmission electron microscope (TEM), and atomic force microscopy (AFM). Compared with MnMoS4 or CeNP alone, a synergistic effect was observed. Moreover, CeNP@MnMoS4 -3 promoted neurite outgrowth in a dose-dependent manner. Taken together, the results reported in this work show the potential of new multifunctional core-shell nanoparticles as AD therapeutics.

Cu2+ion reduction in wastewater over RDF-derived char

Refuse-derived fuel (RDF) produced using municipal solid waste was pyrolyzed to produce RDF char. For the first time, the RDF char was used to remove aqueous copper, a representative heavy metal water pollutant. Activation of the RDF char using steam and KOH treatments was performed to change the specific surface area, pore volume, and the metal cation quantity of the char. N2 sorption, Inductively Coupled Plasma-Atomic Emission Spectrometer (ICP-AES), and Fourier transform infrared spectroscopy were used to characterize the char. The optimum pH for copper removal was shown to be 5.5, and the steam-treated char displayed the best copper removal capability. Ion exchange between copper ions and alkali/alkaline metal cations was the most important mechanism of copper removal by RDF char, followed by adsorption on functional groups existing on the char surface. The copper adsorption behavior was represented well by a pseudo-second-order kinetics model and the Langmuir isotherm. The maximum copper removal capacity was determined to be 38.17 mg/g, which is larger than those of other low-cost char adsorbents reported previously.

Influence of feedstock on the copper removal capacity of waste-derived biochars

Biochar samples were generated by low temperature pyrolysis of different types of waste. The physicochemical characteristics of the different types of biochar affected the copper retention capacity, by determining the main mechanism involved. The capacity of the biochar to retain copper present in solution depended on the size of the inorganic fraction and varied in the following order: rice biochar>chicken manure biochar>olive mill waste biochar>acacia biochar>eucalyptus biochar>corn cob biochar. The distribution of copper between the forms bound to solid biochar, dissolved organic matter and free organic matter in solution also depended on the starting material. However, the effect of pH on the adsorption capacity was independent of the nature of the starting material, and the copper retention of all types of biochar increased with pH.

Copper removal using electrosterically stabilized nanocrystalline cellulose.

Removal of heavy metal ions such as copper using an efficient and low-cost method with low ecological footprint is a critical process in wastewater treatment, which can be achieved in a liquid phase using nanoadsorbents such as inorganic nanoparticles. Recently, attention has turned toward developing sustainable and environmentally friendly nanoadsorbents to remove heavy metal ions from aqueous media. Electrosterically stabilized nanocrystalline cellulose (ENCC), which can be prepared from wood fibers through periodate/chlorite oxidation, has been shown to have a high charge content and colloidal stability. Here, we show that ENCC scavenges copper ions by different mechanisms depending on the ion concentration. When the Cu(II) concentration is low (C0≲200 ppm), agglomerates of starlike ENCC particles appear, which are broken into individual starlike entities by shear and Brownian motion, as evidenced by photometric dispersion analysis, dynamic light scattering, and transmission electron microscopy. On the other hand, at higher copper concentrations, the aggregate morphology changes from starlike to raftlike, which is probably due to the collapse of protruding dicarboxylic cellulose (DCC) chains and ENCC charge neutralization by copper adsorption. Such raftlike structures result from head-to-head and lateral aggregation of neutralized ENCCs as confirmed by transmission electron microscopy. As opposed to starlike aggregates, the raftlike structures grow gradually and are prone to sedimentation at copper concentrations C0≳500 ppm, which eliminates a costly separation step in wastewater treatment processes. Moreover, a copper removal capacity of ∼185 mg g(-1) was achieved thanks to the highly charged DCC polyanions protruding from ENCC. These properties along with the biorenewability make ENCC a promising candidate for wastewater treatment, in which fast, facile, and low-cost removal of heavy metal ions is desired most.

Copper removal using a heavy-metal resistant microbial consortium in a fixed-bed reactor

A heavy-metal resistant bacterial consortium was obtained from a contaminated river in São Paulo, Brazil and utilized for the design of a fixed-bed column for the removal of copper. Prior to the design of the fixed-bed bioreactor, the copper removal capacity by the live consortium and the effects of copper in the consortium biofilm formation were investigated. The Langmuir model indicated that the sorption capacity of the consortium for copper was 450.0 mg/g dry cells. The biosorption of copper into the microbial biomass was attributed to carboxyl and hydroxyl groups present in the microbial biomass. The effect of copper in planktonic cells to form biofilm under copper rich conditions was investigated with confocal microscopy. The results revealed that biofilm formed after 72 h exposure to copper presented a reduced thickness by 57% when compared to the control; however 84% of the total cells were still alive. The fixed-bed bioreactor was set up by growing the consortium biofilm on granular activated carbon (GAC) and analyzed for copper removal. The biofilm-GAC (BGAC) column retained 45% of the copper mass present in the influent, as opposed to 17% in the control column that contained GAC only. These findings suggest that native microbial communities in sites contaminated with heavy metals can be immobilized in fixed-bed bioreactors and used to treat metal contaminated water.

Effects of supercritical carbon dioxide on waste banana peels for heavy metal removal

The effects of supercritical carbon dioxide (CO 2) on waste banana peels for copper adsorption were evaluated. Supercritical CO 2 was employed both in a solvent extraction for antioxidant compound recovery and in an emerging biomass treatment to increase the subsequent heavy metal-removal step; the latter is termed “explosion with supercritical CO 2”. This lignocellulosic biomass was analyzed before and after being subjected to both processes by scanning electron microscopy and X-ray patterning. Thermal gravimetric and differential scanning calorimetry analyses were performed to understand the different effects of supercritical carbon dioxide employed in these two processes on banana peels. The explosion with supercritical CO 2 process resulted in a more pronounced effect on the vegetable structure. Nevertheless, no increase in the copper-removal capacity was achieved. The adsorption studies showed similar behaviors for fresh and extracted samples, demonstrating that banana peels previously extracted with supercritical CO 2 retained their adsorption capacity for subsequent heavy metal removal.

Surface modification of pine cone powder and its application for removal of Cu(II) from wastewater

Pine cone powder is an agricultural waste material from the wood industry. In this investigation, chemical modification of pine cone powder using NaOH solution of different concentrations (0.01, 0.05, 0.10, and 0.15 mol dm−3) was carried out. The changes in surface properties produced by modification and the ability of the modified products to remove copper(II) from aqueous solution was examined. Chemical characterization of the adsorbent surface by FTIR and Bohem titration showed that an increase in NaOH concentration in the wash solution was found to reduce the amounts of carboxyl and phenolic groups and increase the iodine number. The pHPZC of the raw pine cone powder reduced with NaOH concentration in the wash solution from 7.49 to 2.55. Optimum NaOH concetration for pine cone powder surface modification was 0.15 mol dm−3, while the optimum solution pH, contact time and biosorbent dose for copper(II) removal were pH 5.0, 5 min and 4.0 g dm−3 for all samples. Copper(II) removal capacity was higher for samples washed with higher concentrations of NaOH solution (PCP 6.8 mg g−1, PCP 0.1 13.01 mg g−1, PCP 0.05 15.03 mg g−1, PCP 0.10 16.38 mg g−1 and PCP 0.15 17.22 mg g−1). The equilibrium solution pH at the end of the biosorption experiments were higher than the initial solution pH when modified samples were used for biosorption but lower than the initial pH when the raw pine cone powder was applied. This may suggest a different mechanism of copper(II) uptake by raw pine cone powder as compared with the modified samples. The paseudo-second order kinetics for copper(II) biosorption gave the best fit with the experimental data for both the raw and NaOH modified pine cone powder.

Removal of copper from industrial wastewaters by activated carbon prepared from periwinkle shells

The present study aims at the removal of copper from industrial wastewater by using a low-cost adsorbent. Activated periwinkle shell carbon (PSC) was prepared and characterized for various physiochemical properties. To determine copper removal capacity, the performance of PSC was compared with commercial activated carbon (CAC) and a mixture of activated periwinkle shell carbon and commercial activated carbon (PSC:CAC) in a ratio 1:1. The effect of adsorbent dose, contact time, pH, agitation speed and adsorbent particle size was studied for adsorption of copper from wastewater under batch conditions. The result obtained showed that PSC competes favourably with CAC. The maximum adsorption capacity was observed for PSC:CAC with 88.12% removal at an optimal pH of 8. The PSC and CAC had 84.19% removal and 85.15% removal, respectively. The equilibrium data obtained fitted both the Langmuir and the Freundlich models. Good correlation coefficients were obtained for the pseudo-second-order kinetic model.

Removal of copper on composite sewage sludge/industrial sludge-based adsorbents: The role of surface chemistry

Sewage sludge and industrial waste oil sludge were pyrolyzed in an inert atmosphere at 650 or 950 °C, either as single components or as 50:50 mixtures. Composite materials were used as adsorbents of copper ions from aqueous solution. The capacity for copper removal was comparable to that of commercial activated carbon. To relate the performance of materials to their properties, the surface features were characterized using adsorption of nitrogen, thermal analysis, XRF, potentiometric titration, and elemental analysis. The results indicated that a high copper removal capacity could be linked to basic surface pH and specific compounds present on the surface. The high removal ability of materials obtained at 650 °C is attributed to cation exchange reactions between calcium and magnesium in aluminosilicates, formed on their surface during heat treatment, and copper. On the other hand, the high degree of mineralization of the surface of the materials obtained at 950 °C promotes copper complexation and its surface precipitation as hydroxides or hydroxylcarbonate entities.

Role of various parameters in synthesis of insoluble agrobased xanthates for removal of copper from wastewater

The research identifies and studies the parameters involved in the synthesis of two types of insoluble agrobased xanthates, named insoluble baggase xanthate (IBX) and insoluble wood xanthate (IWX) and their ability to remove heavy metals from wastewater. Copper was selected as the model metal and the metal removal capacity of IBX and IWX were expressed by copper loading (mg of copper removed/g of IBX or IWX). It was observed that contact times of 3 h and alkali strengths of 4 mol/L were necessary during alkalization. The maximum base material to alkali ratio (w/w) was 1.125 without sacrificing proper mixing of the base material alkali mixture. Optimum contact time during xanthation was 4 h with a carbon-disulfide to base material ratio (w/w) of 1.25. Only strong bases like NaOH, KOH contributed high copper loadings and the starting liquor was reused twice without sacrificing the copper removal capacity of IBX and IWX. Maximum copper loadings achieved with IBX and IWX were 26.9 ± 0.15 and 27.8 ± 0.39 mg/g, respectively.

Removal of copper (II) by manganese-coated sand in a liquid fluidized-bed reactor

This study was performed in a fluidized-bed reactor (FBR) filled with manganese-coated sand (MCS) to treat copper-contaminated wastewater. The adsorption characteristics of MCS, the adsorption equilibrium of MCS, and the copper removal capacity by MCS in FBR were investigated. In terms of the adsorption characteristics of MCS, the surface of MCS was evaluated using a scanning electron microscope (SEM). Energy dispersive analysis (EDS) of X-rays indicated the composition of MCS, and the quantity of manganese on MCS was determined by means of acid digestion analysis. The experimental results indicated that copper was removed by both sorption (ion exchange and adsorption) and coprecipitation on the surface of MCS in FBR. Copper removal efficiency was highly dependent on the pH and increased with increasing pH from pH 2 to 8. After the copper adsorption by MCS, the pH in solution was decreased. When the MCS concentration was greater than 10 g/l, the copper adsorptivities obtained by FBR were almost the same as that from the shaker and when the MCS concentration reached 40 g/l, the copper adsorptivity in FBR was greater than that from the shaker. The adsorption sites of MCS could be used efficiently by the FBR. A Langmuir adsorption isotherm equation fit the measured adsorption data from the batch equilibrium adsorption test better than the Freundlich adsorption isotherm equation did. In addition, the adsorption rate increased when the influent wastewater was aerated.

Removal and recovery of heavy metals by bacteria isolated from activated sludge treating industrial effluents and municipal wastewater

A total of nineteen metal-resistant and non-resistant bacteria from activated sludge treating both metal-contaminated industrial effluents and municipal wastewater were isolated and identified. These included both Gram-positive (e.g. Micrococcus) and Gram-negative (e.g. Pseudomonas) bacteria. The biosorption capacity of these strains for five different heavy metals (copper, nickel, zinc, lead and chromium) was determined at pH 5 and initial metal concentration 100 mg/L. Pseudomonas pseudoalcaligenes and Micrococcus luteus were found to be capable of removing significant amounts of copper and lead. Hence, they were selected for further investigations. Langmuir adsorption isotherms adequately represented the distribution of copper and lead for both species. The study of pH effect on metal removal for both species indicated that the metal biosorption increased with increasing pH from 2 to 6. The effect of competing cations on biosorption of P. pseudoalcaligenes was studied. Sulphuric acid (0.05 M) was the most efficient desorption medium among the eleven reagents tested. Over 90% of copper sorbed on the cells of M. luteus could be recovered by washing with 0.05 M sulphuric acid within five minutes. The biosorbent was used for at least five biosorption and desorption cycles without loss of copper removal capacity. Immobilization of M. luteus in 2% calcium alginate and 10% polyacrylamide gel beads increased copper uptake by 61%.

Sorption of copper and silver from dilute aqueous solutions onto mercaptoacetimide of aminophenol resin duolite A-7

A new mercaptan-containing resin has been prepared by reacting mercaptoacetyl chloride with the aminophenol resin Duolite A-7 in free-base form, yielding a resin with high redox capacity—6.00 mequiv/g. The resin also has high copper removal capacity, 135 mg/g, and high silver removal capacity, 962 mg/g. Both Cu(II) and Ag(I) are reduced by the mercaptyl resin; the former to Cu(I) and the latter to Ag(0). There is a slight decrease in the copper sorption capacity of the resin in the presence of sodium chloride in solution. The sorbed Cu(I) is easily removed by stripping with dilute HCI. The resin is resistent to hydrolysis in dilute HCl media at ambient temperature, so permitting stripping with dilute HCl. The sorbed silver, which is in the metallic state, is removed with difficulty by dilute NH 4OH and HNO 3 but can be removed with hot nitric acid, which also decomposes the resin. With dilute HCI solution containing 5 % of thiourea, silver adsorbed on the resin can be removed to the extent of 32 %.