Efficient Proton Transfer and Charge Separation within Covalent Organic Frameworks via Hydrogen-Bonding Network to Boost H2O2 Photosynthesis.

Photocatalytic synthesis based on the oxygen reduction reaction (ORR) has shown great promise for H2O2 production. However, the low activity and selectivity of 2e- ORR result in a fairly low efficiency of H2O2 production. Herein, we propose a strategy to enhance the proton-coupled electron transfer (PCET) process in covalent organic frameworks (COFs), thereby significantly boosting H2O2 photosynthesis. We demonstrated that the construction of a hydrogen-bonding network, achieved by anchoring the H3PO4 molecular network on COF nanochannels, can greatly improve both proton conductivity and photogenerated charge separation efficiency of COFs. Thus, COF@H3PO4 exhibited superior photocatalytic performance in generating H2O2 without sacrificial agents, with a solar-to-chemical conversion efficiency as high as 0.69%. Results indicated that a much more localized spatial distribution of energy band charge density on COF@H3PO4 led to efficient charge separation, and the small energy barrier of the rate-limiting step from *OOH to H2O2 endowed COF@H3PO4 with higher 2e- ORR selectivity.

Electronic Phosphide-Support Interactions in Carbon-Supported Molybdenum Phosphide Catalysts Derived from Metal-Organic Frameworks.

Interfacial interaction in carbon-supported catalysts can offer geometric, electronic, and compositional effects that can be utilized to regulate catalytically active sites, while this is far from being systematically investigated in carbon-supported phosphide catalysts. Here, we proposed a novel concept of electronic phosphide-support interaction (EPSI), which was confirmed by using molybdenum phosphide (MoP) supported on nitrogen-phosphorus codoped carbon (NPC) as a model catalyst (MoP@NPC). Such a strong EPSI could not only stabilize MoP in a low-oxidation state under environmental conditions but also regulate its electronic structure, leading to reduced dissociation energy of the oxygen-containing intermediates and enhancing the catalytic activity for oxidative desulfurization. The removal of dibenzothiophene over the MoP@NPC was as high as 100% with a turnover frequency (TOF) value of 0.0027 s-1, which was 33 times higher than that of MoP without EPSI. This work will open new avenues for the development of high-performance supported phosphide catalysts.

Simultaneous adsorption and biodegradation of oxytetracycline in wastewater by Mycolicibacterium sp. immobilized on magnetic biochar.

Due to the adverse effects of long-term oxytetracycline (OTC) residues in aquatic environments, an effective treatment is urgently needed. Immobilized microbial technology has been widely explored in the treatment of various organic pollutants in aquatic environments with its excellent environmental adaptability. Nevertheless, studies on its application in the removal of antibiotics are relatively scarce and not in sufficient depth. Only a few studies have further investigated the final fate of antibiotics in the immobilized bacteria system. In this study, a novel kind of OTC-degrading bacteria Mycolicibacterium sp. was immobilized on straw biochar and magnetic biochar, respectively. Magnetic biochar was proved to be a more satisfactory immobilization carrier due to its superior property and the advantage of easy recycling. Compared with free bacteria, immobilized bacteria had stronger environmental adaptability under different OTC concentrations, pH, and heavy metal ions. After 5 cycles, immobilized bacteria could still remove 71.8% of OTC, indicating that it had a stable recyclability. Besides, OTC in real swine wastewater was completely removed by immobilized bacteria within 2 days. The results of FTIR showed that bacteria were successfully immobilized on biochar and O-H, N-H, and C-N groups might be involved in the removal of OTC. The fate analysis indicated that OTC was removed by simultaneous adsorption and biodegradation, while biodegradation (92.8%) played a dominant role in the immobilized bacteria system. Meanwhile, the amount of adsorbed OTC (7.20%) was rather small, which could effectively decrease the secondary pollution of OTC. At last, new degradation pathways of OTC were proposed. This study provides an eco-friendly and effective approach to remedy OTC pollution in wastewater.

Combined effects of oxytetracycline concentration and organic loading rate on semi-continuous anaerobic digestion of swine wastewater.

High concentrations of antibiotics in swine wastewater raises concerns about the potential adverse effects of anaerobic digestion (AD). Current studies mainly focused on the effects of various antibiotic concentrations. However, these studies didn't take into account the fluctuation of swine wastewater quality and the change of reactor operating conditions in practical engineering applications. In this study, it was found that in the operating systems with COD of 3300 mg/L and hydraulic retention time (HRT) of 4.4 days, the continuous addition of oxytetracycline for 30 days had no effect on the AD performance. Nevertheless, when COD and HRT were changed to 4950 mg/L and 1.5 days respectively, oxytetracycline at 2 and 8 mg/L increased the cumulative methane yield by 27% and 38% at the cost of destroying cell membrane, respectively, while oxytetracycline at 0.3 mg/L improved the performance and stability of AD. These results could be referred for practical engineering applications.

Double-charged self-assembled rGO/g-C3N4 membrane prepared by "functional group substitution" for heavy metal ions rejection at low pressure.

Heavy metals are still the critical pollutants in industrial wastewater and there is an urgent need for efficient and environmentally friendly treatment technologies. Reduced graphene oxide (rGO) is widely used for preparations of nanofiltration (NF) membranes but suffers from poor hydrophilicity and electronegativity. In this work, a double-charged rGO/g-C3N4-P membrane was prepared for removal of heavy metals at low pressure. Graphitic carbon nitride (g-C3N4) assisted reduction of GO membranes under ultraviolet (UV) irradiation, and the modification of functional groups with high polarity improved the hydrophilicity of membrane surface. The filtration performance for heavy metals of rGO/g-C3N4-P membrane was evaluated under low pressure (1-2 bar). The rejection rates of Cu2+, Cr3+, Mn2+, Cd2+, and Pb2+ by membranes reduced by UV for 18 h (rGO/g-C3N4-18-P membrane) reached 94.72 %, 98.05 %, 82.32 %, 88.2 % and 77.15 %, respectively. In the experiment of mixed simulated wastewater, the rejection rates of NO3- and SO42- both reached >95 %. Outstanding rejection rates were attributed to the interaction and the synergy effect of double-charged layers as well as steric effects. Meanwhile, the water flux of rGO/g-C3N4-18-P membrane was as high as 37.14-50.16 L m-2h-1bar-1 (1-2 bar). The high flux was due to the reduced degree of oxidation so that water molecules transported between GO nanochannels more smoothly and the transport path was shortened through the nanopores of g-C3N4. Obviously, flux and heavy metal rejection of rGO/g-C3N4-18-P membrane were simultaneously improved, breaking "trade-off" effect. Furthermore, rGO/g-C3N4-18-P membrane showed excellent antifouling ability and the potential for heavy metal wastewater filtration in comparison with other NF membranes reported in literature.

Development of multifarious carrier materials and impact conditions of immobilised microbial technology for environmental remediation: A review.

Microbial technology is the most sustainable and eco-friendly method of environmental remediation. Immobilised microorganisms were introduced to further advance microbial technology. In immobilisation technology, carrier materials distribute a large number of microorganisms evenly on their surface or inside and protect them from external interference to better treat the targets, thus effectively improving their bioavailability. Although many carrier materials have been developed, there have been relatively few comprehensive reviews. Therefore, this paper summarises the types of carrier materials explored in the last ten years from the perspective of structure, microbial activity, and cost. Among these, carbon materials and biofilms, as environmentally friendly functional materials, have been widely applied for immobilisation because of their abundant sources and favorable growth conditions for microorganisms. The novel covalent organic framework (COF) could also be a new immobilisation material, due to its easy preparation and high performance. Different immobilisation methods were used to determine the relationship between carriers and microorganisms. Co-immobilisation is particularly important because it can compensate for the deficiencies of a single immobilisation method. This paper emphasises that impact conditions also affect the immobilisation effect and function. In addition to temperature and pH, the media conditions during the preparation and reaction of materials also play a role. Additionally, this study mainly reviews the applications and mechanisms of immobilised microorganisms in environmental remediation. Future development of immobilisation technology should focus on the discovery of novel and environmentally friendly carrier materials, as well as the establishment of optimal immobilisation conditions for microorganisms. This review intends to provide references for the development of immobilisation technology in environmental applications and to further the improve understanding of immobilisation technology.

Effects of activated carbon, biochar, and carbon nanotubes on the heterogeneous Fenton oxidation catalyzed by pyrite for ciprofloxacin degradation.

Pyrite and engineering carbon materials have received increasing attention for their catalytic potential in Fenton reactions due to their extensive sources and low cost. However, effects of carbon materials on the degradation of pollutants by pyrite-catalyzed heterogeneous Fenton oxidation have not been fully understood. In this study, the performance of pyrite-catalyzed heterogeneous Fenton system on the degradation of ciprofloxacin (CIP) was investigated in the presence of activated carbon (AC), biochar (BC), and carbon nanotubes (CNTs). Synchronous and asynchronous experiments (adsorption and catalysis) were conducted to elucidate the roles of the carbon materials in pyrite-catalyzed Fenton reactions. The results demonstrated that all the three carbon materials accelerated the pyrite-catalyzed Fenton oxidation of CIP. Under the experimental conditions, the reaction rates, which were obtained by fitting the synchronous experimental results with the pseudo-first-order kinetic model, of pyrite/AC, pyrite/BC and pyrite/CNTs with H2O2 for the removal of CIP were 8.28, 3.40 and 3.37 times faster than that of pyrite alone. Adsorption experiments and characterization analysis showed that AC had a higher adsorption capacity than BC and CNTs for CIP, which enabled it to distinguish itself in assisting the pyrite-catalyzed Fenton oxidation. In the presence of the carbon materials, the adsorption effect should not be neglected when studying the catalytic performance of pyrite. Free radical quenching experiments and electron spin-resonance spectroscopy (ESR) were used to detect and identify free radical species in the reactions. The results showed that hydroxyl radicals (•OH) contributed significantly to the degradation of CIP. The addition of carbon materials promoted the production of •OH, which favored the degradation of CIP. The results of this study suggested that the synergistic effect of oxidation and adsorption promoted the removal of CIP in pyrite/carbon materials/H2O2 systems, and coupling pyrite and carbon materials shows great potential in treating antibiotic wastewater.

Effects of heavy metals and antibiotics on performances and mechanisms of anaerobic digestion.

Anaerobic digestion (AD) is an efficacious technology to recover energy from organic wastes/wastewater, while the efficiency of AD could be limited by metals and antibiotics in substrates. It is of great significance to deeply understand the interaction mechanisms of metals and antibiotics with anaerobic microorganisms, as well as the combined effects of metals and antibiotics, which will help us break the inherent dysfunction of AD system and promote the efficient operation of AD. Therefore, this paper reviews the effects of metals, antibiotics and their combinations on AD performance, as well as the combined effects and interactional mechanisms of metals and antibiotics with anaerobic microorganisms. In addition, control strategies and future research needs are proposed. This review provides valuable information for the enhancement strategies and engineering applications of AD for organic wastes/wastewater containing metals and antibiotics.

Establishing a rabbit model of perianal fistulizing Crohn's disease.

BACKGROUND: Crohn's disease (CD) is a chronic nonspecific intestinal inflammatory disease. The aetiology and pathogenesis of CD are still unclear. Anal fistula is the main complication of CD and is a difficult problem to solve at present. The main limitation of developing new therapies is bound up with the short of preclinical security and effectiveness data. Therefore, an ideal animal model is needed to establish persistent anal fistula and an inflamed rectal mucosa. AIM: To improve the induction method of colitis and establish a reliable and reproducible perianal fistulizing Crohn's disease animal model to evaluate new treatment strategies. METHODS: Twenty male New Zealand rabbits underwent rectal enema with different doses of 2,4,6-trinitrobenzene sulfonic acid to induce proctitis. Group A was treated with an improved equal interval small dose increasing method. The dosage of group B was constant. Seven days later, the rabbits underwent surgical creation of a transsphincteric fistula. Then, three rabbits were randomly selected from each group every 7 d to remove the seton from the fistula. The rabbits were examined by endoscopy every 7 days, and biopsy forceps were used to obtain tissue samples from the obvious colon lesions for histological analysis. The disease activity index (DAI), colonoscopy and histological scores were recorded. Perianal endoscopic ultrasonography (EUS) was used to evaluate the healing of fistulas. RESULTS: Except for the DAI score, the colonoscopy and histological scores in group A were significantly higher than those in group B (P < 0.05). In the ideal model rabbit group, on the 7th day after the removal of the seton, all animals had persistent lumens on EUS imaging, showing continuous full-thickness high signals. Histological inspection of the fistula showed acute and chronic inflammation, fibrosis, epithelialization and peripheral proctitis of the adjoining rectum. CONCLUSION: The improved method of CD colitis induction successfully established a rabbit perianal fistula CD preclinical model, which was confirmed by endoscopy and pathology.

Modified Peroral Endoscopic Myotomy Technique for Type II Achalasia: A Multicenter Retrospective Study.

Aim: This retrospective study is aimed at evaluating the outcomes of a modified peroral endoscopic myotomy (POEM) technique in patients with type II achalasia. Methods: We performed a modified POEM procedure, which involved a shorter (total myotomy length = 4 cm), full-thickness myotomy, on 31 patients with type II achalasia. Clinical success rates, technical success rates, pre- and postoperative esophageal manometry results, complications, and reflux-related adverse events were evaluated. Results: The clinical success (Eckardt score ≤ 3) rates were 100% and 88.9% within 2 years and beyond 2 years postoperatively, respectively. The median lower esophageal sphincter pressures (LESP) decreased from 31.6 (26.7-49.7) mmHg preoperatively to 13.4 (10.5-21.6) and 11.8 (7.4-16.7) mmHg (P < 0.001) at 6 and 12 months postoperatively, respectively. The median integrated relaxation pressure (IRP) decreased from 27.8 (20.6-37.5) mmHg preoperatively to 12.9 (11.3-23.4) and 11.6 (9.6-16.8) mmHg (P < 0.001) at 6 and 12 months after POEM, respectively. Only one case (3.2%) of mucosal injury, four (12.9%) cases of reflux esophagitis, and two (6.5%) cases of gastroesophageal reflux symptoms were reported. Conclusions: The modified POEM technique showed excellent outcomes in patients with type II achalasia.

Gold nanoparticles-modified MnFe2O4 with synergistic catalysis for photo-Fenton degradation of tetracycline under neutral pH.

To decrease the adverse environmental and health-related effects of antibiotics, a series of MnFe2O4-Au (MFO-Au) composites were prepared by simple co-precipitation and photoreduction methods for efficient photo-Fenton degradation of tetracycline (TC). The synergistic effect of MFO and gold nanoparticles (AuNPs) with high absorption of visible light and strong photogenerated carrier separation efficiency endowed MFO-Au3 an outstanding photo-Fenton catalytic performance for TC degradation in neutral condition. The surface hydroxyl of MFO profited to generation of •OH, and negative charged or partially polarized AuNPs benefited to adsorption of H2O2, which had a synergistic effect on enhancing the photo-Fenton catalytic performance of MFO-Au. 88.3% of TC was efficiently removed and about 51.9% of TOC decreased within 90 min. The electron spin resonance and quenching tests suggested that h+ and e- were responsible for the high catalytic degradation and •OH and •O2- participated in the photo-Fenton reaction. The toxicity assessment by seed germination experiments showed efficient toxicity reduction of this system. Besides, MFO-Au exhibited high stability, good cycle, relatively economical and practical application performance, which is expected to provide potential guidance for the design and combination of noble nanoparticles with high stability and spinel bimetallic oxides with high catalytic activity in photo-Fenton reactions.

Microplastics and associated contaminants in the aquatic environment: A review on their ecotoxicological effects, trophic transfer, and potential impacts to human health.

The microplastic pollution and related ecological impacts in the aquatic environment have attracted global attention over the past decade. Microplastics can be ingested by aquatic organisms from different trophic levels either directly or indirectly, and transferred along aquatic food chains, causing different impacts on life activities of aquatic organisms. In addition, microplastics can adsorb various environmental chemical contaminants and release toxic plastic additives, thereby serving as a sink and source of these associated chemical contaminants and potentially changing their toxicity, bioavailability, and fate. However, knowledge regarding the potential risks of microplastics and associated chemical contaminants (e.g., hydrophobic organic contaminants, heavy metals, plastic additives) on diverse organisms, especially top predators, remains to be explored. Herein, this review describes the effects of microplastics on typical aquatic organisms from different trophic levels, and systematically summarizes the combined effects of microplastics and associated contaminants on aquatic biota. Furthermore, we highlight the research progress on trophic transfer of microplastics and associated contaminants along aquatic food chain. Finally, potential human health concerns about microplastics via the food chain and dietary exposure are discussed. This work is expected to provide a meaningful perspective for better understanding the potential impacts of microplastics and associated contaminants on aquatic ecology and human health.

Enhancement of Detoxification of Petroleum Hydrocarbons and Heavy Metals in Oil-Contaminated Soil by Using Glycine-ß-Cyclodextrin.

Soil contamination with petroleum hydrocarbons and heavy metals is a widespread environmental problem. In recent years, cyclodextrin has attracted research interest because of its special hole structure that can form inclusion complexes with certain small molecules. However, the solubility of ß-cyclodextrin (ß-CD) in water is low and it crystallizes easily, leading to its low utilization in practice. In this experiment, we connected ß-CD with glycine under alkaline conditions to prepare glycine-ß-cyclodextrin (G-ß-CD), which is water soluble, has stronger coordinating ability with heavy metals, and is more suitable for treating oil-contaminated soil. The results show that G-ß-CD provides better desorption of petroleum hydrocarbons and heavy metals in soils with low organic matter content (1%) and NaNO3 of 0.25 mol/L at 70 g/L G-ß-CD under mildly acidic (pH 5⁻6) conditions. The results indicate that petroleum hydrocarbons and heavy metals were removed simultaneously by means of pretreatment with G-ß-CD, and the results can provide a theoretical basis for remediation of petroleum-contaminated soil.

Influence of immobilization on phenanthrene degradation by Bacillus sp. P1 in the presence of Cd(II).

Suspended microbes gradually lost advantages in practical applications of PAHs and heavy metals bioremediation. Therefore this study investigated the effect of immobilization on phenanthrene degradation by Bacillus sp. P1 in the presence of different Cd(II) concentrations. Condensed Bacillus sp. P1 was immobilized with polyvinyl alcohol and sodium alginate and PVA-SA-cell cryogel beads were prepared. The results indicated that the use of gel beads increased the number of adsorption sites thus accelerating phenanthrene degradation. In addition, changes in detoxification indices, including superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH), were determined to elucidate the immobilization mechanisms related to cells protection from Cd(II) when degrading phenanthrene. By protecting the gel membrane, oxidative damage was minimized, while SOD activity increased from 55.72 to 81.33 U/mgprot as Cd(II) increased from 0 to 200 mg/L but later dropped to 44.29 U/mgprot as Cd(II) increased to 300 mg/L for the non-immobilized system. On the other hand, the SOD activity kept increasing from 52.23 to 473.35 U/mgprot for the immobilized system exposed to Cd(II) concentration between 0 and 300 mg/L. For CAT and GSH, immobilization only slowed down the depletion process without any change on the variation trends. The changes in surface properties and physiological responses of microbes caused the differences of immobilization effect on phenanthrene biodegradation in the presence of Cd(II), which is a novel finding.

Bioremediation mechanisms of combined pollution of PAHs and heavy metals by bacteria and fungi: A mini review.

In recent years, knowledge in regard to bioremediation of combined pollution of polycyclic aromatic hydrocarbons (PAHs) and heavy metals by bacteria and fungi has been widely developed. This paper reviews the species of bacteria and fungi which can tackle with various types of PAHs and heavy metals entering into environment simultaneously or successively. Microbial activity, pollutants bioavailability and environmental factors (e.g. pH, temperature, low molecular weight organic acids and humic acids) can all affect the bioremediation of PAHs and heavy metals. Moreover, this paper summarizes the remediation mechanisms of PAHs and heavy metals by microbes via elucidating the interaction mechanisms of heavy metals with heavy metals, PAHs/PAHs metabolites with PAHs and PAHs with heavy metals. Based on the above reviews, this paper also discusses the potential research needs for this field.

Polyvinyl alcohol-immobilized Phanerochaete chrysosporium and its application in the bioremediation of composite-polluted wastewater.

A novel biosorbent, polyvinyl alcohol (PVA)-immobilized Phanerochaete chrysosporium, was applied to the bioremediation of composite-polluted wastewater, containing both cadmium and 2,4-dichlorophenol (2,4-DCP). The optimum removal efficiency achieved was 78% for Cd(II) and 95.4% for 2,4-DCP at initial concentrations of 20 mg/L Cd(II) and 40 mg/L 2,4-DCP. PPBs had significantly enhanced the resistance of P. chrysosporium to 2,4-DCP, leading to the degradation rates of 2,4-DCP beyond 90% with varying initial 2,4-DCP concentrations. This research demonstrated that 2,4-DCP and secreted proteins might be used as carbon and nitrogen sources by PVA-immobilized P. chrysosporium beads (PPBs) for Cd(II) removal. Fourier transform infrared spectroscopy analysis showed that hydroxyl and carboxyl groups on the surface of PPBs were dominant in Cd(II) binding. The mechanism underlying the degradation of 2,4-DCP into fumaric acid and 1-hexanol was investigated. The adsorption-desorption studies indicated that PPBs kept up to 98.9% of desorption efficiency over three cycles.

Quantum dots and p-phenylenediamine based method for the sensitive determination of glucose.

By introducing p-phenylenediamine (PPD) to the hybrid system of Mn-doped CdS/ZnS quantum dots (QDs) and glucose oxidase (GOD), a sensitive label-free method was proposed for direct detection of glucose. With glucose and PPD as substrates, 2,5-diamino-N,N'-di-(4-aminophenyl)-2,5-cyclohexadiene-1,4-diimine (DDACD) that intensively quenches the fluorescence of QDs can be produced by the catalysis of GOD. A detection limit as low as 3.2 µM was obtained with the high-efficient fluorescence quencher. Two linear ranges, from 5.0 µM to 1000 µM and from 1.0 mM to 10.0 mM, were identified between time-gated fluorescence intensity and the concentration of glucose. It is shown that the newly proposed methods have high selectivity for glucose over other saccharides and coexisting biological species in serum. The method can be used directly to determine glucose in normal adult human serum without any complicated sample pretreatments. The recovery rate and repeatability of the method were also shown to be satisfactory.

Inactivation performance and mechanism of Escherichia coli in aqueous system exposed to iron oxide loaded graphene nanocomposites.

The challenge to achieve efficient disinfection and microbial control without harmful disinfection byproducts calls for developing new technologies. Magnetic-graphene oxide (M-GO) with magnetic iron oxide nanoparticles well dispersed on graphene oxide (GO) nanosheets exerted excellent antibacterial activity against Escherichia coli. The antibacterial performance of M-GO was dependent on the concentration and the component mass ratio of M/GO. The synergetic antibacterial effect of M-GO was observed with M/GO mass ratio of 9.09. TEM images illustrated the interaction between E. coli cells and M-GO nanocomposites. M-GO nanomaterials were possible to deposit on or penetrate into cells leading to leakage of intercellular contents and loss of cell integrity. The inactivation mechanism of E. coli by M-GO was supposed to result from both the membrane stress and oxidation stress during the incubation period. M-GO with excellent antibacterial efficiency against E. coli and separation-convenient property from water could be potent bactericidal nanomaterials for water disinfection.

Facile green extracellular biosynthesis of CdS quantum dots by white rot fungus Phanerochaete chrysosporium.

This study details a novel method for the extracellular microbial synthesis of cadmium sulfide (CdS) quantum dots (QDs) by the white rot fungus Phanerochaete chrysosporium. P. chrysosporium was incubated in a solution containing cadmium nitrate tetrahydrate, which became yellow from 12h onwards, indicating the formation of CdS nanocrystals. The purified solution showed a maximum absorbance peak between 296 and 298 nm due to CdS particles in the quantum size regime. The fluorescence emission at 458 nm showed the blue fluorescence of the nanoparticles. X-ray analysis of the nanoparticles confirmed the production of CdS with a face-centered cubic (fcc) crystal structure. The average grain size of the nanoparticles was approximately 2.56 nm, as determined from the full width at half-maximum (FWHM) measurement of the most intense peak using Scherer's equation. Transmission electron microscopic analysis showed the nanoparticles to be of a uniform size with good crystallinity. The changes to the functional groups on the biomass surface were investigated through Fourier transform infrared spectroscopy. Furthermore, the secretion of cysteine and proteins was found to play an important role in the formation and stabilization of CdS QDs. In conclusion, our study outlines a chemical process for the molecular synthesis of CdS nanoparticles.

Shellac-coated iron oxide nanoparticles for removal of cadmium(II) ions from aqueous solution.

This study describes a new effective adsorbent for cadmium removal from aqueous solution synthesized by coating a shellac layer, a natural biodegradable and renewable resin with abundant hydroxyl and carboxylic groups, on the surface of iron oxide magnetic nanoparticles. Transmission Electron Microscopy (TEM) imaging showed shellac-coated magnetic nanoparticle (SCMN) adsorbents had a core-shell structure with a core of 20 nm and shell of 5 nm. Fourier Transform Infrared Spectroscopic analysis suggested the occurrence of reaction between carboxyl groups on the SCMN adsorbent surface and cadmium ions in aqueous solution. Kinetic data were well described by pseudo second-order model and adsorption isotherms were fitted with both Langmuir and Freundlich models with maximum adsorption capacity of 18.80 mg/g. SCMN adsorbents provided a favorable adsorption capacity under high salinity conditions, and cadmium could easily be desorbed using mild organic acid solutions at low concentration.