Radiation Grafting Research Articles

Recent Advances in Superabsorbent Hydrogels Derived from Agro Waste Materials for Sustainable Agriculture: A Review.

Superabsorbent hydrogels made from agro waste materials have the potential to promote sustainable agriculture and environmental sustainability. These hydrogels not only help reduce water consumption and increase crop yields but also contribute to minimizing waste and lowering greenhouse gas emissions. Recent research on superabsorbent hydrogels derived from agro wastes has focused on the preparation of hydrogels based on natural polymers isolated from agro wastes, such as cellulose, hemicellulose, and lignin. This review provides an in-depth examination of hydrogels developed from raw agro waste materials and natural polymers extracted from agro wastes, highlighting that these studies start with raw wastes as the main materials. The utilization strategies for specific types of agro wastes are comprehensively described. This review outlines different methods utilized in the production of these hydrogels, including physical cross-linking techniques such as dissolution-regeneration and freeze-thawing, as well as chemical cross-linking methods involving various cross-linking agents and graft polymerization techniques such as free radical polymerization, microwave-assisted polymerization, and γ radiation graft polymerization. Specifically, this review explores the applications of agro waste-based superabsorbent hydrogels in enhancing soil properties such as water retention and slow-release of fertilizers for sustainable agriculture.

Synthesis of amidoxime adsorbent prepared by radiation grafting on upcycled low-density polyethylene sheet for removal of heavy metals from wastewater

The issue of discharging waste, especially heavy metals from industrial activities into the environment, not only adversely impacts environmental quality but also has impacts on communities and human health. Removal and reduction of heavy metal contamination in rivers and wastewater are, therefore, critical initiatives that require significant attention. This work studied the removal of heavy metals, including Zn(II), Cu(II), As(III), and Pb(II) by utilizing an upcycled amidoxime low-density polyethylene sheet (AO-sheet). The synthesized AO-sheet was analyzed for various physical properties, including scanning electron microscope, energy-dispersive x-ray spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. For the batch adsorption experiment, parameters affecting adsorption capacity were studied: initial concentration, submerging time, and pH. Adsorption isotherms were also studied. The results of the heavy metal adsorption study showed that the initial concentration was the most significant parameter; the higher the initial concentration, the greater the adsorption capacity. The adsorption capacity of Zn(II) and Pb(II) increased with submersion time, which achieved 21.07 and 0.855 mg/g-adsorbent, respectively, after four weeks of submersion under the highest initial concentration studied. The adsorption capacity of Cu(II) was 7.98 mg/g-adsorbent after two weeks of optimal adsorption duration under the highest initial concentration studied. The adsorption capacity of As(II) was 1.07 mg/g-adsorbent after one week of optimal submersion time under the highest initial concentration studied. Moreover, the appropriate pH range for effective adsorption of Zn(II), Cu(II), and Pb(II) was identified as 8–9, while for As(III), it was 6–8, with an adsorption duration of 0.43 weeks (3 days). From the Langmuir isotherm, it was found that the adsorption of this work was characterized by monolayer adsorption. The results demonstrate that the AO-sheet can be effectively used to remove heavy metals from wastewater. Its potential for reusability was up to 8 cycles, with the Zn(II) adsorption capacity being reduced to about 20.37%.

Anion exchange membrane with enhanced alkaline stability through radiation grafting of ETFE for solid polymer electrolytes

AbstractSolid polymer electrolyte membranes are considered as the nub of many electrochemical devices. Given the climate crisis and related concerns, the evolution of new membrane materials to support the sustainable systems is inevitable. Building on recent advances with the radiation technique and polymer chemistry, herein, anion exchange membranes (AEMs), ETFE‐g‐1VIm/4VP, were fabricated through graft copolymerization of vinyl heterocyclic monomer binary mixture, such as 1‐vinylimidazole (1‐VIm) and 4‐vinylpyridine (4‐VP) onto ethylene tetrafluoroethylene (ETFE), a main polymer backbone without aryl ether bonds. The grafting reaction was achieved at 60°C and then followed by quaternization as a subsequent step. The effects of various reaction grafting conditions were investigated. The ETFE‐g‐1VIm/4VP AEM were characterized w.r.t the morphological and structural features. The dense surface of the grafted membranes is proved by field emission‐scanning electron microscopy (FE‐SEM) images, which also show that the vinyl entities are clearly distributed in the prepolymer, which may lead to a continuous ion transport channel. AEMs processed from the highest graft yield showed good hydroxide conductivity at 90°C, reaching 16.9 mS/cm due to the presence of more transport sites. The same membrane has a relatively good alkaline stability, which is studied through weight percentage method and FT‐IR. Hence, we assume that the introduction of multi‐cationic moieties, pyridinium and imidazolium, contributes to the performance of anion exchange membranes and makes a perfect balance, especially the hydrophilicity and hydrophobicity. These data highlight the potential of the copolymer as an anion exchange membrane for wide spectra of electrochemical applications.Highlights AEMs based on ETFE‐g‐1VIm/4VP are developed via radiation grafting. The membrane exhibits remarkable alkaline stability. FT‐IR, SEM, and weight percentage methods were used to prove the alkaline stability. The membrane has the potential to be used for different electrochemical applications.

Application of Natural Antibacterial Plants in the Extraction of Uranium from Seawater.

Marine biofouling directly affects the performance and efficiency of uranium (U(VI)) extraction from seawater. Compared to traditional chemical methods, natural plant extracts are generally biodegradable and nontoxic, making them an environmentally friendly alternative to synthetic chemicals in solving the marine biofouling problem. The effectiveness of natural antibacterial plants (i.e., pine needle, peppermint, Acorus gramineus Soland, Cacumen platycladi, and wormwood) in solving the marine biofouling problem was evaluated in this work. Experimental results showed that natural antibacterial plants could kill Vibrio alginolyticus in solution and effectively solve the marine biofouling problem of U(VI) extraction. To improve the adsorption capacity of natural plants for U(VI) in seawater, poly(vinylphosphonic acid) (PVPA) was modified on natural antibacterial plant surfaces by irradiation grafting technology. PVPA and natural antibacterial plants work as active sites and base materials for the U(VI) extraction material, respectively. The recovery performance of PVPA/pine needle for U(VI) was preliminarily studied. Results show that the adsorption of U(VI) on PVPA/pine needle follows pseudo-second-order and Langmuir models, and the maximum adsorption capacity is 111 mg/g at 298 K and pH 8.2.

Radiation grafted polyacrylic acid–polyurethane foam copolymer for efficient toxic metal removal from aqueous waste: a sustainable approach to waste management

The acrylic acid-grafted functionalized base polyurethane foam (PAA-g-PUf) is synthesized through mutual radiation grafting technique using acrylic acid as functional monomers and polyurethane form (PUf) with macroporous structure as base polymer, for the extraction of lead from the aqoueous waste streams. The incorporation of functionality on PUf is identified and confirmed by FT-IR spectroscopy, degree of grafting and thermal stability by TGA–DSC technique while the surface morphology, and pores dimensions are evaluated by SEM techniques. The kinetics measurements indicate that the synthesized sorbent reaches its saturation sorption capacity within 10 min at ~ 25 °C under near-neutral pH condition. The monolayer sorption capacity of the synthesized PAA-g-PUf for lead ion (Pb2+) is calculated from Langmuir’s model and found to be ~ 257 mg g−1, which is quite good as compared to the other functionalized material available. These grafted foams are quite efficient over a wide range of concentrations and temperature of the experimental solutions. In this study, the adsorbed lead ions are eluted out in 0.5 M HCl strippent efficiently. These sorbents exhibit excellent reusability up to five cycles without losing appreciable capacity, suggesting better usability in real water samples for many cycles. The polyurethane foam used was obtained from municipal waste, and hence, they cannot generate any additional secondary waste to the environment and make the process more sustainable and economically viable.Graphical abstract

UV irradiation grafting of butyl acrylate on polyimide membrane for enhanced lubricant solvent recovery

UV irradiation grafting of butyl acrylate on polyimide membrane for enhanced lubricant solvent recovery

MOFs meet loofah: controlled preparation of pH-responsive biosorbent via radiation grafting in situ growth for efficient dyes removal

Herein, a novel pH-responsive adsorbent with selective adsorption effect on cationic and anionic dyes was further designed and prepared via radiation grafting in situ growth technique. The cheap, modifiable and benign natural renewable biomass loofah (LFs) was selected as the substrate, and then acrylic acid (AAc) was grafted onto the loofah substrate through electron beam (EB) radiation (grafting rate of 30.5 %). The introduction of –COOH effectively captured and fixed cobalt ions (Co2+), and zeolitic imidazolate framework-67 (ZIF-67) was grown in situ on the loofah surface with Co2+ as a metal center and 2-methylimidazole as the ligand, so a functional loofah-based adsorbent ZIF-67@LFs-AAc was obtained. The introduction of ZIF-67 significantly enhanced the adsorption efficiency and capability of biomass materials, and successfully combined the advantages of biomass and inorganic nanomaterials. The biosorbent is pH-responsive and can specifically adsorb anionic dyes in acidic setting. The equilibrium uptake capacity of Congo red (CR) is 433.9 mg/g at pH = 3. Cationic dyes can be selectively adsorbed under neutral and basic conditions, and the equilibrium uptake capacity of methylene blue (MB) is as high as 554.0 mg/g at pH = 7. When the addition of the ZIF-67@LFs-AAc was 1.0 g/L, the removed rates of MB and CR were 95.9 % and 91.8 %, respectively. With ZIF-67@LFs-AAc, the adsorption of dyes is promoted by electrostatic interaction, pore adsorption, π-π interaction and hydrogen bond. In summary, the integration of MOFs with loofah can lead to the development of a highly efficient biosorbent for treating dye-containing wastewater, thereby offering promising prospects for its application in water treatment.

GRAFTS COMPARISON BETWEEN QUADRICEPS TENDON AUTOGRAFT VS. ALLOGRAFT FOR ANTERIOR CRUCIATE LIGAMENT REVISIOON RECONSTRUCTION: A LITERATURE REVIEW

Introduction: Anterior cruciate ligament (ACL) reconstruction is one of the most common orthopaedic surgeries performed on active people in the world. One of the most important surgical decisions is graft type for use in the reconstruction. Recently, the quadriceps tendon has gained popularity for use as a graft source for ACL reconstruction. The graft choice is broadly between an autograft or allograft. This review aims to understand the current concepts in graft comparison between quadriceps tendon autograft vs. allograft for anterior cruciate ligament revision reconstruction. Methods: This literature review study was reported following the preferred reporting items for systematic reviews and adhered to a structured review protocol. The author searched the PubMed, ScienceDirect, and British Medical Journal databases. The authors comparing selected publications reporting patient outcomes with all types of reviews or descriptions of ACL revision reconstruction and its graft being used or other related subjects. Published in English is included. The author then formulates a synthesis to support the previously determined research objectives. Results: ACL reconstruction with partial thickness soft tissue quadriceps tendon graft is a reliable option. Where there are differences in the failure rates of ACL reconstructions between allografts and autografts, these can mostly be explained by irradiated grafts. Giving sufficient radiation to achieve sterility will likely weaken grafts and make them more likely to fail; therefore, irradiating grafts is not recommended. The evidence shows no significant differences in clinical effectiveness between autografts and non-irradiated allografts. Failure rates with both grafts are now low. Discussion: The primary goals of rehabilitation after ACL reconstruction do not vary considerably based on graft type and emphasize: (1) restoration of the full range of motion, (2) normalization of quadriceps strength, (3) improvement of overall lower extremity muscle strength, and (4) re-training of movement patterns to return to pre-injury sports participation while decreasing injury risk. Achieving full motion and quadriceps strength contributes to a rapid return to normal weight bearing, gait, and activities of daily living. In the setting of revision ACL reconstruction, there are various considerations regarding graft choice due to tunnel size or position, previous usage of other grafts, and reconstructions in the other leg, which may mean that allografts would be preferred to autografts. The other population not covered sufficiently in the literature is the elite sprinting athlete, where autograft choices may be influenced by the effect of graft harvesting on their sport. However, in most cases, allograft ACL reconstruction with non-irradiated grafts is as safe but more expensive than autograft ACL reconstruction, which is preferred as it is more cost-effective. Conclusion: There is little difference in the results of ACL reconstruction with autografts or non-irradiated allografts, with any advantage being with autografts. The cost is higher with allografts. So if autografts are available, allografts are not cost-effective.

Radiation-induced grafting of polyethyleneimine onto cellulose triacetate membrane for separation of cesium ions from aqueous solution

Radiation grafting of polyethyleneimine (PEI) onto the surface of cellulose triacetate (CTA) membrane was successfully performed. Pre-radiation and co-radiation were applied by gamma rays at the dose of 12 kGy. FT-IR, SEM, XPS, contact angle, zeta-potential, grafting ratio, etc. Were used to characterize the PEI-CTA membranes before and after grafting. The FT-IR spectrum showed that a notable discernible shoulder peak of N–H appeared for amide at co-radiation and pre-radiation, and XPS analysis indicated that co-radiation achieved the highest N percent of 9.75%, suggesting that PEI was introduced into the membrane surface. In a forward osmosis (FO) process, the PEI-CTA membrane obtained higher cesium, Cs(I), retention (95–97%) than the CTA membrane with Cs(I) retention of 92%. Cs(I) fluxes significantly decreased from 0.09 to 0.02–0.03 mmol m−2h−1 after PEI modification. Effective Cs(I) retention was attributed to increase of the positive charges on CTA membrane when PEI was added, which exerted a repulsive effect on Cs(I), preventing them from moving towards the membrane direction. In the FO process, the PEI-CTA membrane featured the water flux of 23 L m−2 h−1 a little lower than that of CTA membrane (24 L m−2 h−1). Although modified PEI increased the hydrophilicity, the increase of water flux did not occur with the co-irradiated membrane, which was related to the high graft, higher thickness and resistance of the membrane.

Preparation of Antioxidant and Antifouling Ultrafiltration Membrane by Co-blending Eugenol with Polyethylene Glycol-Modified Polyvinylidene Fluoride

Polyvinylidene fluoride-graft-polyethylene glycol methyl acrylate (PVDF-g-PEGMA) was prepared by grafting PEGMA onto PVDF using a homogeneous irradiation grafting method. After incorporating various concentrations of eugenol, a natural antioxidant component of clove oil, the membranes were fabricated through non-solvent induced phase separation. The results indicated that the addition of eugenol did not alter the inherent properties of the membrane but slightly reduced the pore size and water flux. The cyclic flux test showed that eugenol did not compromise the anti-fouling performance of the membrane, with the flux recovery ratio exceeding 93%. The antioxidant performance test revealed that eugenol enhanced the membrane’s capacity to remove free radicals and imparted oxidation resistance in NaClO solution, making the modified membrane suitable for use in oxidizing environments. This study successfully demonstrated a simple method to prepare a bifunctional membrane with anti-fouling and antioxidant properties, potentially extending its service life and applicability in oxidative contexts.

Antifouling and Antioxidant Properties of PVDF Membrane Modified with Polyethylene Glycol Methacrylate and Propyl Gallate.

In this study, molecules of propyl gallate (PG) and polyethylene glycol methacrylate (PEGMA) were covalently bonded via a transesterification reaction and subsequently grafted onto polyvinylidene fluoride substrates using a homogeneous radiation grafting technique. The enhancement of the membranes' hydrophilicity with the increment of the grafting rate was corroborated by scanning electron microscopy imaging and measurements of the water contact angle. At a grafting degree of 10.1% and after a duration of 4 min, the water contact angle could decrease to as low as 40.1°. Cyclic flux testing demonstrated that the membranes modified in this manner consistently achieved a flux recovery rate exceeding 90% across varying degrees of grafting, indicating robust anti-fouling capabilities. Furthermore, these modified membranes exhibited significant antioxidant ability while maintaining antifouling performance over 30 days. The ability of the modified membranes to scavenge 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS+) free radicals remained nearly unchanged after being stored in pure water for 30 days, and the flux recovery rate remained above 95% after immersion in sodium hypochlorite solution for 30 days. Among the tested membranes, the PVDF-g-PEGMAG modified membrane with a grafting degree of 7.2% showed the best antioxidant effect.

Efficient and selective removal of Pb(II) from landfill leachate using L-serine-modified polyethylene/polypropylene nonwoven fabric synthesized via radiation grafting technique

Efficient and selective removal of Pb(II) from landfill leachate using L-serine-modified polyethylene/polypropylene nonwoven fabric synthesized via radiation grafting technique

The Radiation Graft Copolymerization of Allylmethacrylate to Polyvinylidene Fluoride to Prepare of Membrane and Its Affordability for Domestic Wastewater Treatment

The Radiation Graft Copolymerization of Allylmethacrylate to Polyvinylidene Fluoride to Prepare of Membrane and Its Affordability for Domestic Wastewater Treatment

Efficient removal of radioactive iodide from contaminated seawater by radiation-resistant Ag+-doping polypropylene nonwoven adsorbents

For the efficient removal of radioactive iodide ions from medium and low radioactive contaminated water, an Ag-doped adsorbent was designed via radiation grafting method and chemical modification and applied based on the solid–liquid adsorption method. The silver loading content in the adsorbents could be flexibly decided by adjusting the sulfhydryl content. SEM/EDS, ATR, XPS, and XRD characterization methods were used to determine the features of the new adsorbents. With the silver content 67.9 mg/g and 125.6 mg/g in the adsorbents PGM25%-Ag+ and PGM220%-Ag+ respectively, the maximum I− adsorption capacities were varied at 29.92 mg/g and 100.82 mg/g. In wide pH conditions (pH7-11), PGM25%-Ag+ was sufficient to achieve 131I removal efficiency of over 92 %, and the removal efficiency was almost unaffected in the coexistence of high concentration (10 mmol/L) of anions and complex real contaminated seawater, highlighting the applicability and selectivity of the adsorbent. The adsorption behavior conformed to the Langmuir isothermal model and pseudo-second-order kinetics model. XPS analysis confirmed that excellent adsorption capacity and selectivity were attributed to the chemical adsorption mechanism of ion exchange and complexation occurs between I− and Ag on the solid–liquid interface, where AgI precipitation formed. In addition, the Ag+-doping adsorbent withstood the harsh conditions of 200 kGy irradiation by observing the ATR structure, thermal stability, and 131I removal property. This study provides a feasible solution for the treatment of low and medium-radioactive contaminated seawater.

Remediation of Cr(VI) using a radiation functionalized green adsorbent: Adsorption modelling, mechanistic insights and prototype water purifier demonstration

The work reports remediation of hexavalent Chromium (Cr(VI)) in water using a radiation functionalized cellulose based green adsorbent, fabricated via gamma radiation assisted Mutual Irradiation Grafting Process (MIGP), wherein poly(2-Trimethylammoniumethyl methacrylate chloride) (PTMAEMC) was grafted onto Woven Cotton Cellulose Fabric (WCCF). The grafted adsorbent “ChromClear” efficiently sequestered Cr(VI) from water and demonstrated a maximum adsorbent capacity of ∼55 mg.g−1, successfully curtailing Cr(VI) concentrations to <20 μg.L−1. Characterization of samples was performed using 13C NMR, XPS, SEM-EDS, FTIR, TGA, and BET analysis. The equilibrium adsorption, kinetic, and breakthrough curve data were analysed using various theoretical models to infer the adsorption mechanism and extract important process parameters. Artificial Neural Network (ANN) modelling was used to predict adsorption capacity and % Cr(VI) removal in continuous flow column mode under different operational conditions, with a high degree of agreement (R2 > 0.99) between experimental and modelled data. Density Functional Theory (DFT) calculations established the interaction between CrO42− and PTMAEMC groups of ChromClear to be occurring in a 1:2 ratio. ChromClear could be regenerated for over five recycled iterations with >88 % retention in adsorption capacity. Concept based prototype water purification systems were also developed for pump as well as gravity driven continuous flow operations, and successfully demonstrated for remediation of Cr(VI) contaminated ground water samples. The efficacy and simplicity of the process provides ample scope for further upscaling and deployment for community level water treatment applications, with a special emphasis on compliance with drinking water norms in affected areas.

Flame Retardancy of Short Flax Fibers Modified by Radiation-Induced Grafting of Phosphonated Monomers: Comparison between Pre- and Simultaneous Irradiation Grafting.

Short flax fibers have been modified by radiation-induced grafting using methacrylate monomers containing phosphorus to give them a flame-retardant character. Two methodologies, namely pre-irradiation and simultaneous irradiation grafting, were examined. Certain parameters, notably the dose and the irradiation source (e-Beam and γ rays), were evaluated. The grafting efficiency, in terms of phosphorus content (mass percentage), was measured by X-ray fluorescence spectrometry (XRF). Using simultaneous irradiation, 2.39 wt% phosphorus could be obtained from 10 kGy, compared to 100 kGy in pre-irradiation. Furthermore, for similar phosphorus levels, the location of the grafted polymer chains was different for the two methodologies. The effect of phosphorus content on thermal properties and fire behavior was evaluated on a microscopic scale using a pyrolytic flow combustion calorimeter (PCFC) and on a laboratory scale using a cone calorimeter. It was then pointed out that flammability was linked to the phosphorus content and likely its location, which is associated with the radiation-induced grafting methodology, showing that the grafting conditions influence the final fire properties. Simultaneous irradiation, thus, proved to be more interesting in terms of efficiency and final properties.

Radiation grafting mediated tailoring of a mercury (Hg(II)) selective adsorbent “RAdMer”: Mechanistic insights, uptake performance and reusability evaluation in artificially contaminated groundwater

The presence of mercury (Hg(II)) in water bodies poses a pressing threat not only to aquatic life forms but also human health. This work proposes the fabrication of a novel thiol (-SH), amine (–NH–) and carboxylic (-COOH) group containing trifunctional adsorbent based on a radiolytically surface engineered biodegradable platform for selective sequestration of Hg(II) from aqueous media. Polyacrylonitrile (PAN) was gamma radiolytically incorporated onto cotton fabric via Radiation Induced Graft Polymerization (RIGP) process, followed by chemical conversion of the nitrile groups using dl-Cysteine as the trifunctional agent. The developed adsorbent RAdMer was characterized by FTIR, TGA, SEM-EDX, EDXRF, XRD, CHNS, 13C NMR and XPS techniques, and tested for Hg(II) removal in batch and continuous flow adsorption modes. Adsorption kinetics and equilibrium characteristics were validated using various theoretical models as well column adsorption models. Density Functional Theory (DFT) calculations performed to determine the complexation mechanism revealed the binding to be occurring predominantly in a 1:2 metal to ligand ratio with calculated binding affinity of −19.63 kcal.mol−1. RAdMer demonstrated fast uptake kinetics with over 60 % of total Hg(II) adsorption occurring within the first 30 min, while peak adsorption capacity was calculated at 174.3 mg.g−1. Moreover, RAdMer could be reused for >5 iterative cycles using an optimized HCl-Thiourea eluent system. Acting upon the UNOs SDG6 principle of providing “clean water and sanitation for all”, RAdMer efficiency was demonstrated with Hg(II) spiked ground water samples to successfully achieve the WHO permissible limit of <1.0 μg.L−1, and can therefore be potentially upscaled as an efficient methodology for remediation of Hg(II) ions in contaminated water.

ETFE-grafting ionomers for anion exchange membrane water electrolyzers with a current density of 11.2 A cm−2

In the quest for efficient and sustainable hydrogen production, anion exchange membrane (AEM) water electrolyzers (AEMWEs) have gained significant attention. Development of AEMs has accelerated in the past few decades while the significance of the ionomer on AEMWE performance and durability is always unrecognized. In this study, we proposed a class of electrochemically durable ionomers by introducing the piperidinium group onto the ethylene tetrafluoroethylene (ETFE) backbone using a radiation grafting technology. To avoid disruption of the conformation of the piperidinium group during the functionalization process, we grafted the piperidinium group onto the polymer backbone at the gamma position of the N-piperidinium group using trifluoromethanesulfonic acid as a catalyst. The prepared ETFE-g-poly(styryl propyl piperidinium) ionomers exhibited outstanding electrochemical properties and enhanced alkaline stability. Most notably, the corresponding AEMWEs demonstrated an impressive current density of 11.2 A cm−2 at 2.0 V under 80 °C in 1 M KOH solution. Furthermore, they were continuously operated at a current density of 0.5 A cm−2 for over 300 h with a low voltage decay rate of 0.12 mV h−1. This study offers valuable insights into the development of robust solid-state ionomers through radiation grafting, paving the way for high-performance AEMWEs.

High adsorption capacity of Pb2+ by iminodiacetic acid functionalized ramie via radiation grafting

Wastewater containing heavy metal ions discharged from industries has caused serious pollution to water. As for how to use renewable resources as the substrate, green preparation of adsorbents through eco-friendly processes and effective disposal of metal ions has become urgent. In this work, the low-cost, environmentally-friendly and easily modified natural renewable biomass ramie was used as the substrate, and glycidyl methacrylate (GMA) containing epoxy functional group was grafted onto ramie via electron beam irradiation (grafting rate up to 332.3 %). A ramie-poly-GMA-IDA (RGD) adsorbent was prepared by ring-opening reaction and grafted with iminodiacetic acid (IDA). The adsorption process was affected by pH, the RGD could effectively uptake Pb2+ when the pH = 5.0, and the adsorption equilibrium can be quickly reached within 50 min. Moreover, RGD possessed excellent uptake properties, and the Pb2+ adsorption capacity maximized to 225.71 mg/g. The adsorption procedure obeys a pseudo-2nd-order kinetic and Langmuir equation. The possible mechanisms for Pb2+ adsorption are complexation, electrostatic interaction and ion exchange. This study presents that IDA-functionalized ramie can be used as an efficient biomass-based adsorbent for Pb2+ uptake. Thus, a green, closed-loop utilization of agricultural and forestry wastes is achieved, which helps reduce heavy metal ion pollution and resource consumption and protect the environment.

Adsorption of Zn(II) from aqueous solution and separation of zinc isotopes by displacement chromatography using chelating adsorbent

The removal of zinc ions (Zn(II)) in water and the separation of zinc isotopes were fully investigated in this study. Imidodiacetic acid (IDA) type adsorbent (named PSGI) based on polystyrene spheres (PS) was synthesized by simultaneous irradiation grafting. By adsorption method, the removal of Zn(II) from water by the chelating adsorbent was studied in batch experiments. Under optimized condition, PSGI showed the removal efficiency of more than 98 % for Zn(II) and the adsorption capacity of 70.1 mg/g. Langmuir isothermal and pseudo-second-order kinetic model fitted the experimental results better, indicating that the adsorption is dominated by chemical adsorption. The spent adsorbent (PSGI-Zn) was used for further zinc isotope separation by displacement chromatography using EDTA-NH4 solution as eluent. Due to the mass effect of isotopes, 70Zn was found to preferentially fractionated into the front-end effluents with the highest front enrichment values of 70Zn/64Zn. By extending the migration distance to 20 m, we obtained the best isotope enrichment with the front maximum enrichment values as 1.0949, 1.0739 and separation coefficient values as 1.977 × 10−3, 8.33 × 10−3 corresponding to the isotope pairs 66Zn/64Zn, 68Zn/64Zn.