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Efficient Activation of Peroxymonosulfate by Cobalt Supported Used Resin Based Carbon Ball Catalyst for the Degradation of Ibuprofen

ABSTRACT: The extensive use of ibuprofen (IBU) and other pharmaceuticals and personal care products (PPCPs) causes them widely to exist in nature and be frequently detected in water bodies. Advanced catalytic oxidation processes (AOPs) are often used as an efficient way to degrade them, and the research on heterogeneous catalysts has become a hot spot in the field of AOPs. Among transitional metal-based catalysts, metal cobalt has been proved to be an effective element in activating peroxymonosulfate (PMS) to produce strong oxidizing components. In this study, the used D001 resin served as the matrix material and through simple impregnation and calcination, cobalt was successfully fixed on the carbon ball in the form of cobalt sulfide. When the catalyst was used to activate persulfate to degrade IBU, it was found that under certain reaction conditions, the degradation rate in one hour could exceed 70%, which was far higher than that of PMS and resin carbon balls alone. Here, we discussed the effects of catalyst loading, PMS concentration, pH value and temperature on IBU degradation. Through quenching experiments, it was found that

SUBMITTER: Zhou G

PROVIDER: S-EPMC9321845 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Spiderweb-Like Fe-Co Prussian Blue Analogue Nanofibers as Efficient Catalyst for Bisphenol-A Degradation by Activating Peroxymonosulfate.

Project description:Prussian blue and its analogues (PBA) based nanomaterials have been widely applied to removing pollutants in the recent years. However, easy aggregation and poor recycling largely limit their practical applications. In this work, spiderweb-like Fe-Co Prussian blue analogue/polyacrylonitrile (FCPBA/PAN) nanofibers were prepared by electrospinning and applied to degrading bisphenol-A (BPA) by activating peroxymonosulfate (PMS). Detailed characterization demonstrated that a high loading of FCPBA (86% of FCPBA in FCPBA/PAN) was successfully fixed on the PAN nanofibers. 67% of BPA was removed within 240 min when 500 mg·L-1 PMS and 233 mg·L-1 FCPBA/PAN were introduced in 20 mg·L-1 BPA solution at initial pH of 2.8. Electron paramagnetic resonance (EPR) and radical inhibition experiments were performed to identify the possible degradation mechanism. For comparison, a low loading of FCPBA nanofibers (0.6FCPBA/PAN nanofibers, 43% of FCPBA in FCPBA/PAN) were also prepared and tested the catalytic performance. The results showed that the activity of FCPBA/PAN was much higher than 0.6FCPBA/PAN. Furthermore, a FCPBA/PAN packed column was made as a reactor to demonstrate the reusability and stability of FCPBA/PAN nanofibers, which also exhibited the bright future for the industrial application. This work makes it possible to fabricate efficient PBA nanocatalysts with excellent recyclability and promotes the application of PBA in industrial areas.

| S-EPMC6473942 | biostudies-literature

A cobalt-modified covalent organic framework enables highly efficient degradation of 2,4-dichlorophenol in high concentrations through peroxymonosulfate activation.

Project description:The development of covalent organic frameworks (COFs) which can rapidly degrade high concentrations of 2,4-dichlorophenol is of great significance for its practical application. In this work, we report a cobalt-doped two-dimensional (2D) COF (JLNU-307-Co) for the ultra-efficient degradation of high concentration 2,4-dichlorophenol (2,4-DCP) by activating peroxymonosulfate (PMS). The JLNU-307-Co/PMS system takes only 3 min to degrade 100% of 50 mg L-1 2,4-DCP and shows excellent catalytic stability in real water. The superoxide radical (O2˙-) and singlet oxygen (1O2) play a major role in the system through capture experiments and electron spin resonance (ESR) tests. Compared to most previously reported catalysts, JLNU-307-Co/PMS showed the highest efficiency to date in degrading 2,4-DCP. This work not only demonstrates the potential of COFs as a catalyst for water environmental treatment, but also provides unprecedented insights into the degradation of organic pollutants.

| S-EPMC11304524 | biostudies-literature

A Cobalt Tandem Catalyst Supported on a Compressible Microporous Polymer Monolith.

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| S-EPMC6644832 | biostudies-literature

Understanding the Iron-Cobalt Synergies in ZSM-5: Enhanced Peroxymonosulfate Activation and Organic Pollutant Degradation.

Project description:Iron- and cobalt-based heterogeneous catalysts are widely applied for activating peroxymonosulfate (PMS) to degrade organic pollutants. However, few studies have unveiled the clear synergistic mechanism of iron and cobalt in ZSM-5. In this paper, the synergistic mechanism of enhanced PMS activation was revealed by constructing iron and cobalt bimetal modified ZSM-5 zeolite catalysts (FeCo-ZSM-5). The tetracycline hydrochloride (TCH) degradation experiments showed that the catalytic activity of FeCo-ZSM-5-2:3 was much higher than those of Fe-ZSM-5 and Co-ZSM-5. In addition, the influences of catalyst dosage, PMS concentration, reaction temperature, initial pH, and coexisting ions on TCH removal were systematically investigated in this paper. Density functional theory calculations indicated that Co was the main active site for PMS adsorption, and Fe increased the area of Co's positive potential mapped to the electron cloud. The Fe-Co bimetallic doping increased the area of positive potential mapped to the electron cloud and benefited the adsorption of PMS on the catalyst surface, which revealed the synergistic mechanism of bimetals. Electron paramagnetic resonance spectra and quenching experiments showed that sulfate radicals, singlet oxygen, and hydroxyl radicals were involved in the degradation of TCH. Furthermore, liquid chromatography-mass spectrometry was conducted to propose possible degradation pathways. This work provides certain guiding significance in understanding the synergistic effect of heterogeneous catalysts for tetracycline wastewater treatment.

| S-EPMC9161407 | biostudies-literature

Efficient degradation of organic dyes using peroxymonosulfate activated by magnetic graphene oxide.

Project description:Magnetic graphene oxide (MGO) was prepared and used as a catalyst to activate peroxymonosulfate (PMS) for degradation of Coomassie brilliant blue G250 (CBB). The effects of operation conditions including MGO dosage, PMS dosage and initial concentration of CBB were studied. CBB removal could reach 99.5% under optimum conditions, and high removals of 98.4-99.9% were also achieved for other organic dyes with varied structures, verifying the high efficiency and wide applicability of the MGO/PMS catalytic system. The effects of environmental factors including solution pH, inorganic ions and water matrices were also investigated. Reusability test showed that CBB removals maintained above 90% in five consecutive runs, indicating the acceptable recyclability of MGO. Based on quenching experiments, solvent exchange (H2O to D2O) and in situ open circuit potential (OCP) test, it was found that ˙OH, SO4˙- and high-valent iron species were responsible for the efficient degradation of CBB in the MGO/PMS system, while the contributions of O2˙-, 1O2 and the non-radical electron-transfer pathway were limited. Furthermore, the plausible degradation pathway of CBB was proposed based on density functional theory (DFT) calculations and liquid chromatography-mass spectrometry (LC-MS) results, and toxicity variation in the degradation process was evaluated by computerized structure-activity relationships (SARs) using green algae, daphnia, and fish as indicator species.

| S-EPMC9301559 | biostudies-literature

Efficient degradation of organic pollutants by peroxymonosulfate activated with MgCuFe-layered double hydroxide.

Project description:In this study, MgCuFe-layered double hydroxide (MgCuFe-LDH) was for the first time used as a catalyst for peroxymonosulfate (PMS) activation towards the degradation of aqueous organic pollutants. Compared with both MgFe-LDH and MgCuAl-LDH materials, MgCuFe-LDH exhibited significantly higher catalytic activity to activate PMS for the degradation of acetaminophen. The effects of catalyst loading, PMS dosage, reaction temperature and initial solution pH on the degradation efficiency of acetaminophen were investigated. Acetaminophen (5 mg L-1) degradation at about 93.0% was achieved at 20 min by using 0.3 g L-1 MgCuFe-LDH and 0.5 mM PMS. Under the same conditions, rhodamine B (RhB, 5 mg L-1) can be almost completely decolorized (99.5%) within 45 min. Radical scavenger and electron paramagnetic resonance (EPR) experiments showed that sulfate radicals (SO4˙-) and hydroxyl radicals (·OH) existed in PMS/MgCuFe-LDH system. The generated radicals played vital roles in the catalytic degradation of organic pollutants. A possible activation mechanism of PMS on MgCuFe-LDH was put forward. This study indicates that MgCuFe-LDH is a promising catalyst to activate PMS for the efficient degradation of organic pollutants.

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Coordination tuning of cobalt phosphates towards efficient water oxidation catalyst.

Project description:The development of efficient and stable water oxidation catalysts is necessary for the realization of practically viable water-splitting systems. Although extensive studies have focused on the metal-oxide catalysts, the effect of metal coordination on the catalytic ability remains still elusive. Here we select four cobalt-based phosphate catalysts with various cobalt- and phosphate-group coordination as a platform to better understand the catalytic activity of cobalt-based materials. Although they exhibit various catalytic activities and stabilities during water oxidation, Na2CoP2O7 with distorted cobalt tetrahedral geometry shows high activity comparable to that of amorphous cobalt phosphate under neutral conditions, along with high structural stability. First-principles calculations suggest that the surface reorganization by the pyrophosphate ligand induces a highly distorted tetrahedral geometry, where water molecules can favourably bind, resulting in a low overpotential (∼0.42 eV). Our findings emphasize the importance of local cobalt coordination in the catalysis and suggest the possible effect of polyanions on the water oxidation chemistry.

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Bio-assisted synthesized Pd nanoparticles supported on ionic liquid decorated magnetic halloysite: an efficient catalyst for degradation of dyes.

Project description:Using natural materials, i.e. halloysite nanoclay that is a biocompatible naturally occurring clay and Heracleum persicum extract that can serve as a green reducing agent, a novel magnetic catalyst, Fe3O4/Hal-Mel-TEA(IL)-Pd, has been designed and fabricated. To prepare the catalyst, halloysite was first magnetized (magnetic particles with mean diameter of 13.06 ± 3.1 nm) and then surface functionalized with melamine, 1,4 dibromobutane and triethanolamine to provide ionic liquid on the halloysite surface (5 wt%). The latter was then used as a support to immobilize Pd nanoparticles that were reduced by Heracleum persicum extract. The characterization of the catalyst established that the loading of Pd in Fe3O4/Hal-Mel-TEA(IL)-Pd was very low (0.93 wt%) and its specific surface area was 63 m2g-1. Moreover, the catalyst showed magnetic property (Ms = 19.75 emu g-1) and could be magnetically separated from the reaction. The catalytic performance of the magnetic catalyst for reductive degradation of methyl orange and rhodamine B in the presence of NaBH4 in aqueous media was investigated. The activation energy, enthalpy, and entropy for the reduction of methyl orange were estimated as 42.02 kJ mol-1, 39.40 kJ mol-1, and -139.06 J mol-1 K-1, respectively. These values for rhodamine B were calculated as 39.97 kJ mol-1, 34.33 kJ mol-1, and -155.18 Jmol-1K-1, respectively. Notably, Fe3O4/Hal-Mel-TEA(IL)-Pd could be reused for eight reaction runs with negligible loss of the catalytic activity (~3%) and Pd leaching (0.01 wt% of the initial loading).

| S-EPMC7162915 | biostudies-literature

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Project description:We prepared novel flame retardants with concurrent excellent smoke-suppression properties based on lignin biomass modified by functional groups containing N and P. Each lignin-based flame retardant (Lig) was quantitatively added to a fixed amount of epoxy resin (EP), to make a Lig/EP composite. The best flame retardancy was achieved by a Lig-F/EP composite with elevated P content, achieving a V-0 rating of the UL-94 test and exhibiting excellent smoke suppression, with substantial reduction of total heat release and smoke production (by 46.6 and 53%, respectively). In this work, we characterized the flame retardants and the retardant/EP composites, evaluated their performances, and proposed the mechanisms of flame retardancy and smoke suppression. The charring layer of the combustion residual was analyzed using SEM and Raman spectroscopy to support the proposed mechanisms. Our work provides a feasible method for lignin modification and applications of new lignin-based flame retardants.

| S-EPMC7745397 | biostudies-literature

Printed Circuit Board-Derived Glass Fiber-Epoxy Resin-Supported Mo-Cu Bimetallic Catalyst for Glucose Synthesis.

Project description:A glass fiber-epoxy resin (GFER) framework derived from mixed waste printed circuit boards (MWPCBs) was utilized to prepare a cost-effective, reusable Mo-Cu bimetallic Bronsted-Lewis solid acid catalyst through wet-impregnation under near-infrared radiation (NIRR) activation. The efficacy of the novel Mo-Cu catalyst was assessed in the synthesis of glucose through hydrolysis of jute (Corchorus olitorius) fiber, and the process parameters were optimized (Mo precursor loading: 1.0 wt %, catalyst concentration: 5 wt %, hydrolysis temperature: 80 °C, and hydrolysis time: 10 min) through Taguchi orthogonal design. The GFER support and the prepared catalysts were characterized through thermogravimetric, X-ray diffraction (XRD), Fourier-transform infrared (FTIR), Brunauer-Emmett-Teller (BET)-density functional theory, and TPD analyses. The optimal Mo-Cu catalyst and the GFER support possessed 45.377 and 7.049 m2/g BET area, 0.04408 and 0.02317 cc/g pore volume, 1.9334 and 0.7482 nm modal pore size, and surface acidity of 0.48 and 0.40 mmol NH3/g catalyst, respectively. X-ray photoelectron spectroscopy bands confirmed the coexistence of Mo6+ and Cu2+ species; XRD and FTIR analyses indicated the presence of MoO3 and CuO crystalline phases in all prepared catalysts. The optimal catalyst prepared through NIRR (wavelength 0.75-1.4 μm)-activated hydrothermal treatment resulted in a significantly greater glucose yield (75.84 mol %) than that achieved (53.64 mol %) using a conventionally prepared catalyst. Thus, an energy-efficient application of NIRR (100 W) could significantly improve catalytic properties over conventional hydrothermal treatment (500 W). The present investigation provides an innovative application of MWPCB-derived GFER as a promising cost-effective support for the preparation of highly efficient inexpensive solid catalysts for sustainable synthesis of glucose from low-cost waste jute fiber.

| S-EPMC6643727 | biostudies-literature

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