Synergistic enhancement of iodine capture from humid streams by microporosity and hydrophobicity of activated carbon fiber.

Activated carbon fibers (ACF) are widely used to remove gaseous radioiodine produced during spent fuel reprocessing owing to their excellent adsorption properties. However, ACF's strong affinity for moisture tends to dominate, significantly reducing its ability to capture iodine in humid environments. The study used a one-step facile modification method of spray-deposited poly(divinylbenzene) (PDVB) nanoparticles on ACF to prepare hydrophobic activated carbon fiber (ACF-PDVB1.5). Compared to the initial ACF, the ACF-PDVB1.5 enhances the specific surface area to 1571 m2/g while maintaining abundant active sites, overcoming the disadvantage of pore reduction caused by traditional modification methods. More importantly, they also have excellent acid and alkali resistance and hydrophobicity (water contact angle 131.1°), with a preference for I2 pores (97 % microporosity). The iodine capture capacity of ACF PDVB 1.5 showed a significant increase compared to the initial ACF, as indicated by both static and dynamic adsorption tests. Notably, the dynamic iodine adsorption capacity of ACF-PDVB1.5 in a mixed iodine-water vapor stream at actual temperature (75 °C) and humid (50 % RH) conditions was 1847.69 mg/g, an increase of 55.47 % over the capacity of initial ACF (1188.71 mg/g). This work improves the overall I2 adsorption performance through hydrophobicity and pore size coordination.

Activated carbon fiber as an efficient co-catalyst toward accelerating Fe2+/Fe3+ cycling for improved removal of antibiotic cefaclor via electro-Fenton process using a gas diffusion electrode.

The electro-Fenton (EF) based on gas-diffusion electrodes (GDEs) reveals promising application prospective towards recalcitrant organics degradation because such GDEs often yields superior H2O2 generation efficiency and selectivity. However, the low efficiency of Fe2+/Fe3+ cycle with GDEs is always considered to be the limiting step for the EF process. In this study, activated carbon fiber (ACF) was firstly employed as co-catalyst to facilitate the performance of antibiotic cefaclor (CEC) decomposition in EF process. It was found that the addition of ACF co-catalyst achieved a rapid Fe2+/Fe3+ cycling, which significantly enhanced Fenton's reaction and hydroxyl radicals (•OH) generation. X-ray photoelectron spectroscopy (XPS) results indicated that the functional groups on ACF surface are related to the conversion of Fe3+ into Fe2+. Moreover, DMSO probing experiment confirmed the enhanced •OH production in EF + ACF system compared to conventional EF system. When inactive BDD and Ti4O7/Ti anodes were paired to EF system, the addition of ACF could significantly improve mineralization degree. However, a large amount of toxic byproducts, including chlorate (ClO3-) and perchlorate (ClO4-), were generated in these EF processes, especially for BDD anode, due to their robust oxidation capacity. Higher mineralization efficiency and less toxic ClO4- generation were obtained in the EF + ACF process with Ti4O7/Ti anode. This presents a novel alternative for efficient chloride-containing organic removal during wastewater remediation.

Efficient Adsorption of Ammonia by Surface-Modified Activated Carbon Fiber Mesh.

In view of the characteristics and risks of ammonia, its removal is important for industrial production and environmental safety. In this study, viscose-based activated carbon fiber (ACF) was used as a substrate and chemically modified by nitric acid impregnation to enhance the adsorption capacity of the adsorbent for ammonia. A series of modified ACF-based adsorbents were prepared and characterized using BET, FTIR, XPS, and Boehm titration. Isotherm tests (293.15 K, 303.15 K, 313.15 K) and dynamic adsorption experiments were performed. The characterization results showed that impregnation with low concentrations of nitric acid not only increased the surface acidic functional group content but also increased the specific surface area, while impregnation with high concentrations of nitric acid could be able to decrease the specific surface area. ACF-N-6 significantly increased the surface functional group content without destroying the physical structure of the activated carbon fibers. The experimental results showed that the highest adsorption of ammonia by ACFs was 14.08 mmol-L-1 (ACF-N-6) at 293 K, and the adsorption capacity was increased by 165% compared with that of ACF-raw; by fitting the adsorption isotherm and calculating the equivalent heat of adsorption and thermodynamic parameters using the Langmuir-Freundlich model, the adsorption process could be found to exist simultaneously. Regarding physical adsorption and chemical adsorption, the results of the correlation analysis showed that the ammonia adsorption performance was strongly correlated with the carboxyl group content and positively correlated with the relative humidity (RH) of the inlet gas. This study contributes to the development of an efficient ammonia adsorption system with important applications in industrial production and environmental safety.

Preparation of Cellulose-Based Activated Carbon Fibers with Improved Yield and Their Methylene Chloride Adsorption Evaluation.

The recent rapid growth of the battery industry has led to a rapid increase in methylene chloride emissions. Methylene chloride causes health and social problems in humans. In this study, cellulose-based activated carbon fibers (CACFs) with improved yield were prepared for the removal of methylene chloride. The concentration of ammonium phosphate in the pretreatment controlled the crosslink density of cellulose fibers and improved the yield. From the results, the specific surface area and total pore volume of cellulose-based activated carbon fibers pretreated with ammonium phosphate (AP-CACFs) were determined to be 1920-2060 m2/g and 0.83-1.02 cm3/g, respectively, and the total yield improved by 6.78-11.59% compared to that of CACFs (4.97%). In particular, a correlation between the textural properties of CACFs and methylene chloride adsorption/desorption behavior was obtained. This correlation can be used to develop efficient adsorbents for methylene chloride removal.

Effects of Nickel Impregnation on the Catalytic Removal of Nitric Oxide by Polyimide-Based Activated Carbon Fibers.

Activated carbon fibers (ACFs) are beneficial for adsorbing harmful gases because of the well-developed micropores on their surface. Usually, the physical adsorption of harmful gases by ACFs is limited by their textural properties. In this study, the effect of nickel particle catalyst impregnation on the physicochemical removal of nitric oxide (NO) by polyimide (PI)-based ACFs (PI-ACFs) was investigated. Ni(NO3)2 was used as the precursor of nickel particle catalysts and impregnated on ACFs as a function of concentrations. The Ni(NO3)2/ACFs were then thermally reduced in an argon atmosphere containing 4% hydrogen (400 °C, 1 h). The gases generated during heat treatment were verified using Fourier transform infrared spectroscopy, and the impregnation amount of metallic nickel was also calculated based on the gas amount generated. The specific surface areas of the ACF and Ni-ACFs were determined to be 1010-1180 m2/g, while the nickel impregnation amount was 0.85-5.28 mg/g. The NO removal capacity of the Ni-ACF was found to be enhanced with the addition of Ni catalysts. In addition, metallic nickel particles on the ACFs maintained their chemical molecular structures before and after the NO removal tests.a.

Long-Term Fate and Efficacy of a Biomimetic (Sr)-Apatite-Coated Carbon Patch Used for Bone Reconstruction.

Critical bone defect repair remains a major medical challenge. Developing biocompatible materials with bone-healing ability is a key field of research, and calcium-deficient apatites (CDA) are appealing bioactive candidates. We previously described a method to cover activated carbon cloths (ACC) with CDA or strontium-doped CDA coatings to generate bone patches. Our previous study in rats revealed that apposition of ACC or ACC/CDA patches on cortical bone defects accelerated bone repair in the short term. This study aimed to analyze in the medium term the reconstruction of cortical bone in the presence of ACC/CDA or ACC/10Sr-CDA patches corresponding to 6 at.% of strontium substitution. It also aimed to examine the behavior of these cloths in the medium and long term, in situ and at distance. Our results at day 26 confirm the particular efficacy of strontium-doped patches on bone reconstruction, leading to new thick bone with high bone quality as quantified by Raman microspectroscopy. At 6 months the biocompatibility and complete osteointegration of these carbon cloths and the absence of micrometric carbon debris, either out of the implantation site or within peripheral organs, was confirmed. These results demonstrate that these composite carbon patches are promising biomaterials to accelerate bone reconstruction.

Particle and gas phase sampling of PCDD/Fs and dl-PCBs by activated carbon fiber and GC/MS analysis.

Polychlorodibenzo-p-dioxins (PCDDs), polychlorodibenzofurans (PCDFs), and polychlorobiphenyls (PCBs) are semi-volatile compounds and can be partitioned in the atmosphere between the gas and particulate phase, due to their physicochemical properties. For this reason, the reference standard methods for air sampling include a quartz fiber filter (QFF) for the particulate and a polyurethane foam (PUF) cartridge for the vapor phase, and it is the classical and most popular sampling method in the air. Despite the presence of the two adsorbing media, this method cannot be used for the study of the gas-particulate distribution, but only for a total quantification. This study presents the results and the performance aim to validate an activated carbon fiber (ACF) filter for the sampling of PCDD/Fs and dioxin-like PCBs (dl-PCBs) using laboratory and field tests. The specificity, precision, and accuracy of the ACF in relation to the QFF + PUF were evaluated through the isotopic dilution technique, the recovery rates, and the standard deviations. Then the ACF performance was assessed on real samples, in a naturally contaminated area, through parallel sampling with the reference method (QFF + PUF). The QA/QC was defined according to the standard methods ISO 16000-13 and -14 and EPA TO4A and 9A. Data confirmed that ACF meets the requirements for the quantification of native POPs compounds in atmospheric and indoor samples. In addition, ACF provided accuracy and precision comparable to those offered by standard reference methods using QFF + PUF, but with significant savings in terms of time and costs.

Synthesis and Characterization of Porous MgO Nanosheet-Modified Activated Carbon Fiber Felt for Fluoride Adsorption.

In the present work, the porous MgO nanosheet-modified activated carbon fiber felt (MgO@ACFF) was prepared for fluoride removal. The MgO@ACFF was characterized by XRD, SEM, TEM, EDS, TG, and BET. The fluoride adsorption performance of MgO@ACFF also has been investigated. The adsorption rate of the MgO@ACFF toward fluoride is fast; more than 90% of the fluoride ions can be adsorbed within 100 min, and the adsorption kinetics of MgO@ACFF can be fitted in a pseudo-second-order model. The adsorption isotherm of MgO@ACFF fitted well in the Freundlich model. Additionally, the fluoride adsorption capacity of MgO@ACFF is larger than 212.2 mg/g at neutral. In a wide pH range of 2-10, the MgO@ACFF can efficiently remove fluoride from water, which is meaningful for practical usage. The effect of co-existing anions on the fluoride removal efficiency of the MgO@ACFF also has been studied. Furthermore, the fluoride adsorption mechanism of the MgO@ACFF was studied by the FTIR and XPS, and the results reveal a hydroxyl and carbonate co-exchange mechanism. The column test of the MgO@ACFF also has been investigated; 505-bed volumes of 5 mg/L fluoride solution can be treated with effluent under 1.0 mg/L. It is believed that the MgO@ACFF is a potential candidate for a fluoride adsorbent.

Determination of Hydrophobic Dispersive Surface Free Energy of Activated Carbon Fibers Measured by Inverse Gas Chromatographic Technique.

Activated carbon fibers (ACFs) as one of the most important porous carbon materials are widely used in many applications that involve rapid adsorption and low-pressure loss, including air purification, water treatment, and electrochemical applications. For designing such fibers for the adsorption bed in gas and aqueous phases, in-depth comprehension of the surface components is crucial. However, achieving reliable values remains a major challenge due to the high adsorption affinity of ACFs. To overcome this problem, we propose a novel approach to determine London dispersive components (γSL) of the surface free energy of ACFs by inverse gas chromatography (IGC) technique at an infinite dilution. Our data reveal the γSL values at 298 K for bare carbon fibers (CFs) and the ACFs to be 97 and 260-285 mJ·m-2, respectively, which lie in the regime of secondary bonding of physical adsorption. Our analysis indicates that these are impacted by micropores and defects on the carbon surfaces. Comparing the γSL obtained by the traditional Gray's method, our method is concluded as the most accurate and reliable value for the hydrophobic dispersive surface component of porous carbonaceous materials. As such, it could serve as a valuable tool in designing interface engineering in adsorption-related applications.

Adsorption of ionic and neutral pharmaceuticals and endocrine-disrupting chemicals on activated carbon fiber: batch isotherm and modeling studies.

Activated carbon fiber (ACF) has received increasing attention as an adsorbent due to its excellent surface properties. However, the adsorption mechanism of ACF for micropollutants, especially those in ionic forms, has not been sufficiently characterized to date. Therefore, the adsorption property of ACF was characterized using isotherm experiments and linear free energy relationship (LFER). For the experiments, adsorption affinities of thirty-five chemicals, i.e., pharmaceuticals and endocrine-disrupting chemicals, on ACF were estimated. Afterward, the adsorption affinities were used as dependent variables to build the LFER modeling. Finally, three isolated models for each chemical species, i.e., cations, anions, and neutrals, and a comprehensive model for the whole dataset were developed. The LFER results revealed that the models for anionic and neutral compounds have high predictabilities in R2 of 0.97 and 0.96, respectively, while that for cations has a slightly lower R2 of 0.72. In the comprehensive model including cationic, anionic, and neutral compounds, the accuracy of it is 0.81. From the developed LFER model based on the whole dataset, the adsorption mechanisms of ACF for the selected substances could be interpreted, in which the terms of hydrophobic interaction, hydrogen bonding basicity, and anionic Coulombic force of the compounds were identified as the predominant interactions with ACF.

A novel magnetic adsorbent from activated carbon fiber and iron oxide nanoparticles for 2,4-D removal from aqueous medium.

Carbonaceous materials have been widely applied as adsorbents, but there are some factors that affect their efficiency. In this context, advances in nanotechnology provide new and more efficient methodologies for water treatment. This study evaluated the efficiency of a novel carbon-based adsorbent developed from Brazilian polyacrylonitrile textile fiber and functionalized with iron oxide magnetic nanoparticles for the removal of 2,4-dichlorophenoxyacetic acid (2,4-D) from the aqueous medium. The synthesized adsorbent (ACF-Fe3O4) was characterized by FTIR, XRD, VSM, Zeta potential, SEM, EDX, and TEM. The characterization techniques showed that the adsorbent has peaks characteristic of its precursors and superparamagnetic characteristics, confirming the efficiency of the synthesis method. The adsorption tests evaluated the influence of adsorbent dosage, pH of the contaminant solution, contact time and temperature on the removal of 2,4-D. The experimental data were better adjusted by the pseudo-second order kinetic model and by the Langmuir isothermal model. The thermodynamic parameters revealed that the process is exothermic, spontaneous and thermodynamically favorable. Under the best experimental conditions, the maximum adsorption capacity obtained was 51.10 mg g-1 with an adsorbent concentration of 0.33 g L-1, natural pH of the solution, temperature of 288 K at the equilibrium time of six hours. Adsorbent reusage was studied in four desorption cycles. The adsorption mechanism can be explained through π-π bonds, hydrogen bonds and electrostatic interactions. The prepared material presented high-efficiency adsorption capacity of 2,4-D compared to other carbonaceous materials present in the literature, demonstrating its viability for the removal of this contaminant from the aqueous medium.

Adsorption coupling photocatalytic removal of gaseous n-hexane by phosphorus-doped g-C3N4/TiO2/Zn(OAc)2-ACF composites.

VOCs emission reduction in the petroleum and petrochemical industry is a hot and difficult topic at present. The single method may not be able to meet the actual treatment status. Therefore, the adsorption coupled photocatalytic degradation technology was used to remove VOCs. Phosphorus-doped carbon nitride (PCN) and PCN/TiO2 were prepared by hydrothermal synthesis and sol-gel method, and then PCN/TiO2/Zn(OAc)2-ACF composites were prepared by ultrasonic impregnation on zinc acetate modified activated carbon fibers (Zn(OAc)2-ACF). The removal efficiency of n-hexane by composite materials was explored in a self-made reactor, and the factors affecting removal efficiency, removal mechanism, and possible ways of degradation were investigated. The results showed that under the optimum reaction conditions (initial concentration of n-hexane 200 mg/m3, space velocity 1000 h-1, light intensity 24 W, mass fraction of doped PCN 6%, loading twice, calcination temperature 450 °C), PCN/TiO2/Zn(OAc)2-ACF composite has the highest removal efficiency of n-hexane (90.2%). The adsorption capacity of the composites after doping the P element was 215.3 mg/g, which did not enhance the adsorption performance compared with that before doping, but the removal rate of n-hexane was higher. This showed that doping P element was helpful to enhance the photocatalytic activity of the composites.

Enhanced photoelectrocatalytic decomplexation of Ni-EDTA and simultaneous recovery of metallic nickel via TiO2/Ni-Sb-SnO2 bifunctional photoanode and activated carbon fiber cathode.

In order to enhance Ni-EDTA decomplexation and Ni recovery via photoelectrocatalytic (PEC) process, TiO2/Ni-Sb-SnO2 bifunctional electrode was fabricated as the photoanode and activated carbon fiber (ACF) was introduced as the cathode. At a cell voltage of 3.5 V and initial solution pH of 6.3, the TiO2/Ni-Sb-SnO2 bifunctional photoanode exhibited a synergetic effect on the decomplexation of Ni-EDTA with the pseudo-first-order rate constant of 0.01068 min-1 with 180 min by using stainless steel (SS) cathode, which was 1.5 and 2.4 times higher than that of TiO2 photoanode and Ni-Sb-SnO2 anode, respectively. Moreover, both the efficiencies of Ni-EDTA decomplexation and Ni recovery were improved to 98% from 86% and 73% from 41% after replacing SS cathode with ACF cathode, respectively. Influencing factors on Ni-EDTA decomplexation and Ni recovery were investigated and the efficiencies were favored at acidic condition, higher cell voltage and lower initial Ni-EDTA concentration. Ni-EDTA was mainly decomposed via ·OH radicals which generated via the interaction of O3, H2O2, and UV irradiation in the contrasted PEC system. Then, the liberated Ni2+ ions which liberated from Ni-EDTA decomplexation were eventually reduced to metallic Ni on the ACF cathode surface. Finally, the stability of the constructed PEC system on Ni-EDTA decomplexation and Ni recovery was exhibited.

Cu/ACF adsorbent modified by non-thermal plasma for simultaneous adsorption-oxidation of H2S and PH3.

Non-thermal plasma (NTP) surface modification technology is a new method to control the surface properties of materials, which has been widely used in the field of environmental protection because of its short action time, simple process and no pollution. In this study, Cu/ACF (activated carbon fiber loaded with copper) adsorbent was modified with NTP to remove H2S and PH3 simultaneously under low temperature and micro-oxygen condition. Meanwhile, the effects of different modified atmosphere (air, N2 and NH3), specific energy input (0-13 J/mL) and modification time (0-30 min) on the removal of H2S and PH3 were investigated. Performance test results indicated that under the same reaction conditions, the adsorbent modified by NH3 plasma with 5 J/mL for 10 min had the best removal effect on H2S and PH3. CO2 temperature-programmed desorption and X-ray photoelectron spectroscopy (XPS) analyzes showed that NH3 plasma modification could introduce amino functional groups on the surface of the adsorbent, and increase the types and number of alkaline sites on the surface. Brunauer-Emmett-Teller and scanning electron microscopy showed that NH3 plasma modification did not significantly change the pore size structure of the adsorbent, but more active components were evenly exposed to the surface, thus improving the adsorption performance. In addition, X-ray diffraction and XPS analysis indicated that the consumption of active components (Cu and Cu2O) and the accumulation of sulfate and phosphate on the surface and inner pores of the adsorbent are the main reasons for the deactivation of the adsorbent.

Comparison of Pore Structures of Cellulose-Based Activated Carbon Fibers and Their Applications for Electrode Materials.

This study presents the first investigation of cellulose-based activated carbon fibers (RACFs) prepared as electrode materials for the electric double-layer capacitor (EDLC) in lieu of activated carbon, to determine its efficacy as a low-cost, environmentally friendly enhancement alternative to nanocarbon materials. The RACFs were prepared by steam activation and their textural properties were studied by Brunauer-Emmett-Teller and non-localized density functional theory equations with N2/77K adsorption isotherms. The crystallite structure of the RACFs was observed by X-ray diffraction. The RACFs were applied as an electrode material for an EDLC and compared with commercial activated carbon (YP-50F). The electrochemical performance of the EDLC was analyzed using galvanostatic charge/discharge curves, cyclic voltammetry, and electrochemical impedance spectroscopy. The results show that the texture properties of the activated carbon fibers were influenced by the activation time. Crucially, the specific surface area, total pore volume, and mesopore volume ratio of the RACF with a 70-min activation time (RACF-70) were 2150 m2/g, 1.03 cm3/g and 31.1%, respectively. Further, electrochemical performance analysis found that the specific capacitance of RACF-70 increased from 82.6 to 103.6 F/g (at 2 mA/cm2). The overall high specific capacitance and low resistance of the RACFs were probably influenced by the pore structure that developed outstanding impedance properties. The results of this work demonstrate that RACFs have promising application value as performance enhancing EDLC electrode materials.

Photocatalytic oxidation of glyphosate and reduction of Cr(VI) in water over ACF-supported CoNiWO4-gCN composite under batch and flow conditions.

Photocatalytic treatment of wastewater using nanomaterials is an efficient energy saving technology. Yet the practical application of the technology is limited because of difficulty in developing the stable, supported photocatalytic nanoparticles that can be used under continuous flow conditions. Here, we report an efficient removal of glyphosate (GLP) and Cr(VI) from water under batch as well as continuous flow conditions using the activated carbon fiber (ACF)-supported nanocomposite of CoNiWO4 (CNW) and g-C3N4 (gCN), as a photocatalyst. CNW-gCN/ACF is synthesized using a one-step strategy, and spectroscopic characterization techniques are used to corroborate the formation of the Z-scheme-based CNW-gCN heterojunction in the ACF substrate. Efficacy of the photocatalyst is assessed in visible light irradiation. The batch activity data of the individual pollutant show the complete oxidation of GLP at 30 ppm and reduction of Cr(VI) at 200 ppm concentration levels in 60 and 150 min, respectively at 1 g/L dose of CNW-gCN/ACF. Photocatalytic efficiency of CNW-gCN/ACF in the simultaneous removal of both pollutants from co-contaminated feed is found to be greater than that in single-feed system under identical experimental conditions. Tested under flow conditions, CNW-gCN/ACF shows approximately the same rates of oxidation and reduction as prevalent under batch conditions, indicating the efficient immobilization of the nanocatalyst particles in ACF, which not only prevents elution of the catalyst but also improves its reusability. The toxicity data indicate the treated water samples to be non-toxic. The current study provides an efficient method for developing supported nanomaterial photocatalysts for treating flowing co-contaminated wastewater.

Calcium ion biorecovery from industrial wastewater by Bacillus amyloliquefaciens DMS6.

Calcium ions in industrial wastewater needs to be removed to prevent the production of limescale, which can have negative consequences. Biomineralization has become the focus due to its lower costs than traditional methods of remediation. In this study, calcium ions were bio-precipitated under the action of free and immobilized Bacillus amyloliquefaciens DMS6 bacteria, and the calcium ion removal efficiency was also compared. The results show that it only needed 3 days to decrease the calcium ion concentration to an ideal level of 76-116 mg/L under the action of DMS6 bacteria immobilized by activated carbon fiber, with calcium ion removal ratios reaching 99%-95% by the 7th day. DMS6 bacteria immobilized by activated carbon fiber were superior to free bacteria and bacteria immobilized by sodium alginate in calcium ion removal. Calcium ions are biomineralized into calcite, Mg-rich calcite, aragonite and monohydrocalcite with abundant organic functional groups, 4 types of secondary protein structures, amino acids, phospholipids, negative stable carbon isotope δ13CPDB values (-16.68‰ to-17.25‰) and negatively charged biomineral surface. Calcium ions were diffused into cells and took part in the intracellular biomineralization of monohydrocalcite, also facilitating calcium ion removal. The formation of intracellular monohydrocalcite has rarely been reported. This study demonstrates an economic and environmentally friendly method to remove calcium ions from industrial wastewater.

Synthesis of Microporosity Dominant Wood-Based Activated Carbon Fiber for Removal of Copper Ions.

Steam activation treatments were introduced in the preparation of activated carbon fiber from liquefied wood (LWACF), to enlarge its specific surface area and develop the pore size distribution. With increasing activation time, the average fiber diameter of LWACF decreased from 27.2 µm to 13.2 µm, while the specific surface area increased from 1025 to 2478 m2/g. Steam activation predominantly enhanced the development of microporosity, without significant pore widening. Prolonging the steam activation time exponentially increased the removal efficiency of Cu2+ at a constant adsorbent dose, as a result of an increase in the number of micropores and acidic-oxygenated groups. Moreover, for LWACF activated for 220 min at 800 °C, the removal efficiency of Cu2+ increased from 55.2% to 99.4%, when the porous carbon fiber dose went from 0.1 to 0.5 g/L. The synthesized LWACF was proven to be a highly efficient adsorbent for the treatment of Cu2+ ion-contaminated wastewater.

Cu(II) and Au(III) recovery with electrospun lignosulfonate CO2-activated carbon fiber.

The objectives of this study were twofold: developing lignosulfonate activated carbon fibers (LACFs) and determining the corresponding metal recovery mechanisms with batch experiments and non-linear modeling. LACFs were developed through electrospinning, followed by CO2-based physical activation. Physical and chemical characterizations revealed that the LACF sample that was activated for 60 min exhibited a higher specific surface area (376.54 m2/g), larger total pore volume (0.30 cm3/g), higher micropore ratio (32%), and more acidic and sulfur functional groups than did the other samples. Cu(II) and Au(III) adsorption behaviors on the LACF could be described with the Freundlich and Langmuir model, respectively. Both systems consist of physisorption and chemisorption, and the mechanisms include electrostatic forces, Van der Walls forces, cation exchange, surface complexation. In particular, Au(III) adsorption was faster, and LACF-Au bonds were stronger due to the additional microprecipitation. Furthermore, the LACF sample could regenerate after three adsorption-desorption cycles. Overall, this study provides the foundation for developing physically activated lignosulfonate carbon and its application in recovering valuable metal ions.

In vivo effectiveness of carbonated calcium-deficient hydroxyapatite-coated activated carbon fiber cloth on bone regeneration.

We have previously shown that activated carbon fiber cloth (ACC) either uncoated or coated with carbonated calcium-deficient hydroxyapatite (CDA), namely ACC and ACC/CDA, were biocompatible in vitro with human osteoblasts. Here we hypothesized that ACC and ACC/CDA could be used as tissue patches in vivo to accelerate wounded bone healing. In a model of rat femoral defect, we have compared spontaneous cortical bone regeneration with regeneration in the presence of ACC and ACC/CDA patches. At Day 7, 14, and 21, bone formation was evaluated using microcomputed tomography, magnetic resonance imaging, and histological analysis. Our results demonstrate first that these ACC tissues are highly biocompatible in vivo, and second that ACC/CDA patches apposition results in the acceleration of bone reconstruction due to a guiding action of the ACC fibers and an osteogenic effect of the CDA phase. We guess that this approach may represent a valuable strategy to accelerate bone regeneration in human.