A regional approach for health risk assessment of toxicants in plastic food containers.

Plastic food containers are being used popularly, generating a waste of about 115 million tons in Vietnam. Such waste is causing environmental and health issues. This study conducted a field survey with 250 local people and selected 59 samples out of 135 plastic food containers collected in Go Vap district, Vietnam. Collected plastic samples identified compositions were PET 13.6%, PP 28.8%, PS 16.9%, and 40.7% undefined plastics. Collected plastic samples were classified based on the plastic type using recycling code and quantitatively analyzed with X-ray fluorescence spectroscopy method to assess concentrations of Cd, Sb, Pb, Hg, Sn, Cr, Br, Cl, and S. Most of these collected plastic samples (91.5%) were found to contain 8/9 hazardous substances and most elements contained in these plastics were below their standard thresholds. These elements in plastic samples could be divided as the result into three hazard groups: (1) high hazard group (Sb, Cl, and S); (2) medium hazard group (Cr, Br and Hg); and (3) low hazard groups (Cd, Pb and Sn). Among substances in the high hazard group, element Sb was assessed for its migration because only Sb is regulated in Vietnam in QCVN 12-1: 2011/BYT. Substances of Cl, S, Cr, Br, and Hg (group 1, 2) do not have regulations related to the method of decontamination. Thus, additional health risks need to be assessed using the USEtox model. Finally, this study proposed a screening process to assess the risk of toxicity of elements contained in plastic food containers through ISO 31000:2018. Supplementary Information: The online version contains supplementary material available at 10.1007/s43188-023-00194-0.

Advanced Functional Carbon Nitride by Implanting Semi-Isolated VO2 Active Sites for Photocatalytic H2 Production and Organic Pollutant Degradation.

It is critical to facilitate surface interaction for liquid-solid two-phase photocatalytic reactions. This study demonstrates more advanced, efficient, and rich molecular-level active sites to extend the performance of carbon nitride (CN). To achieve this, semi-isolated vanadium dioxide is obtained by controlling the growth of non-crystalline VO2 anchored into sixfold cavities of the CN lattice. As a proof-of-concept, the experimental and computational results solidly corroborate that this atomic-level design has potentially taken full advantage of two worlds. The photocatalyst comprises the highest dispersion of catalytic sites with the lowest aggregation, like single-atom catalysts. It also demonstrates accelerated charge transfer with the boosted electron-hole pairs, mimicking heterojunction photocatalysts. Density functional theory calculations show that single-site VO2 anchored into the sixfold cavities significantly elevates the Fermi level, compared with the typical heterojunction. The unique features of semi-isolated sites result in a high visible-light photocatalytic H2 production of 645 µmol h-1 g-1 with only 1 wt% Pt. They also represent an excellent photocatalytic degradation for rhodamine B as well as tetracycline, surpassing the activities obtained from many conventional heterojunctions. This study presents exciting opportunities for the design of new heterogeneous metal oxide for a variety of reactions.

Coral-like potassium and phosphorous doped graphitic carbon nitride structures with enhanced charge and mass transfer dynamics toward photocatalytic hydrogen peroxide production and microbial disinfection.

This study provided insight on the design of co-doped graphitic carbon nitride (g-C3N4) structures by using potassium dihydrogen phosphate (KH2PO4) as a promising material for the supply of potassium (K) and phosphorus (P) elements. The addition of KH2PO4 to the cyanuric acid-melamine complex (CM) solution stabilized its structure by coordinating potassium ions (K+) in the hexagonal pores and dihydrogen phosphate ions (H2PO4-) in dangling bonds on the edge sites. The resultant supramolecular structure (KP-CM) with a unique skeleton governed the polycondensation process, resulting in K and P co-doped g-C3N4 structures with a distinct coral-like morphology (KP-CN). Employing the KP-CM complex as a precursor could modify the optoelectronic behaviour of the photocatalysts via the synergistic effect of the co-doping process. It could also be beneficial in terms of economic considerations by increasing the catalyst synthesis yield. The resulting g-C3N4 showed a remarkable hydrogen peroxide (H2O2) production rate of 216 µmol L-1h-1 compared to the rate of the pristine sample of 137 µmol L-1h-1. It also exhibited significant photocatalytic antibacterial activity in Escherichia coli (E. coli) disinfection.

Prospects of MXenes in energy storage applications.

The transition metal carbides/nitrides referred to as MXenes has emerged as a wonder material presenting newer opportunities owing to their unique properties such as high thermal and electrical conductivity, high negative zeta-potential and mechanical properties similar to the parent transition metal carbides/nitrides. These properties of MXenes can be utilized in various societal applications including for energy storage and energy conversion. In this focused review, we provide a ready glance into the evolutionary development of the MXene family and various efforts that are made globally towards property improvement and performance enhancement. Particular attention in this review is made to direct the attention of readers to the bright prospects of MXene in the energy storage and energy conversion process - which is extremely timely to tackle the current concern on climate change. The review concludes by offering fresh insights into the future research needs and challenges that need to be addressed to develop resilient energy solutions.

Superhydrophobic MS@CuO@SA sponge for oil/water separation with excellent durability and reusability.

We present a superhydrophobic material based on commercially melamine sponge (MS) with great durability, recyclability, and excellent sorption performance. The fabrication process of this sponge is facile without using toxic reagents or sophisticated equipment and therefore it is simple to scale up. The CuO layer utilized to give a rough surface of the substrate (MS) was successfully prepared in a commercial microwave to seed copper nucleuses in an alkaline medium. Stearic acid (SA) plays a role as the self-assembled monolayer on the surface of the sponge skeletons. Throughout this study, the properties of the modified sponge were fully characterized, and the changes in wettability were carefully examined. Water contact angle (WCA) measurements revealed the excellent superhydrophobicity of the material with high static WCA of 165.1° and low dynamic WCA of 8°. Furthermore, the as-prepared sponge demonstrated high efficiency in separation (over 99.0%) of different oils from water. Notably, several unique properties of as-modified material were found, consisting of ultrafast sorption capacities of up to 32-52 times of its own weight by using 80 mL of each oil, outstanding reusability with good sorption capacity even after 40 cycles. Even under various harsh environments, the novel materials proved its outstanding durability and ultrafast sorption capacity of oils. The durability, recyclability, and superhydrophobic properties of the novel superhydrophobic sponge provide it a solid basis for oil-water separation applications through an ultrafast sorption capacity of oils as well as quick recovery of the oil by easy squeezing process.

Simultaneous Enhancement of Charge Separation and Hole Transportation in a W:α-Fe2O3/MoS2 Photoanode: A Collaborative Approach of MoS2 as a Heterojunction and W as a Metal Dopant.

In this study, a facile approach has been successfully applied to synthesize a W-doped Fe2O3/MoS2 core-shell electrode with unique nanostructure modifications for photoelectrochemical performance. A two-dimensional (2D) structure of molybdenum disulfide (MoS2) and tungsten (W)-doped hematite (W:α-Fe2O3) overcomes the drawbacks of the α-Fe2O3 and MoS2 semiconductor through simple and facile processes to improve the photoelectrochemical (PEC) performance. The highest photocurrent density of the 0.5W:α-Fe2O3/MoS2 photoanode is 1.83 mA·cm-2 at 1.23 V vs reversible hydrogen electrode (RHE) under 100 mW·cm2 illumination, which is higher than those of 0.5W:α-Fe2O3 and pure α-Fe2O3 electrodes. The overall water splitting was evaluated by measuring the H2 and O2 evolution, which after 2 h of irradiation for 0.5W:α-Fe2O3/MoS2 was determined to be 49 and 23.8 µmol.cm-2, respectively. The optimized combination of the heterojunction and metal doping on pure α-Fe2O3 (0.5W:α-Fe2O3/MoS2 photoanode) showed an incident photon-to-electron conversion efficiency (IPCE) of 37% and an applied bias photon-to-current efficiency (ABPE) of 26%, which are around 5.2 and 13 times higher than those of 0.5W:α-Fe2O3, respectively. Moreover, the facile fabrication strategy can be easily extended to design other oxide/carbon-sulfide/oxide core-shell materials for extensive applications.

Unmasking the Role of an Amorphous/Amorphous Interface and a Crystalline/Amorphous Interface in the Transition of Charge Carriers on the CN/SiO2/WO3 Photocatalyst.

Making heterojunctions between semiamorphous carbon nitride (CN) and other well-matched semiconductors (or even insulators) can solve many photocatalytic problems such as the recombination of charge carriers. However, many researchers encounter intrinsic problems including the lack of detailed information on contact boundaries in their heterojunctions, particularly in the amorphous/amorphous interface. In addition, the roles of contact boundaries in the photocatalytic mechanisms of many heterojunctions are still obscure. This study synthesized a novel CN/SiO2/WO3 photocatalyst having two different contact features by constructing an amorphous/amorphous (CN/SiO2) interface and a crystalline/amorphous (WO3/CN) interface to provide deep insights into heterojunction interfaces. SiO2 plays an exceptional role as a major component in the separation and migration of charge carriers. It not only modifies the texture but also transfers electrons. Surprisingly, the amorphous/amorphous interface shows an unpredicted capability for decreasing the recombination of electron-hole pairs. Based on capturing experiments and photoluminescence investigations, the amorphous/amorphous interface is unprecedently present in the production of hydroxyl radicals, while the crystalline/amorphous interface gives more superoxide radicals. This work provides a platform that opens a new perspective on the selection of mutual photocatalysts. It extends boundaries of conventional heterojunctions.

Synthesis of hexagonal rosettes of g-C3N4 with boosted charge transfer for the enhanced visible-light photocatalytic hydrogen evolution and hydrogen peroxide production.

Photocatalytic sustainable fuel production attracted extensive attention because of the urgent need of the society to shift from fossil fuels to solar fuels. Herein, the synthesis of hexagonal rosettes of g-C3N4 with an efficient performance toward hydrogen evolution and hydrogen peroxide production as the two kinds of solar fuels were reported. The hexagonal rosettes of g-C3N4 were simply fabricated via controlled solid-state polymerization of three-dimensional hexagonal rosettes of cyanuric acid-melamine adduct at 500 °C. The hexagonal rosettes of g-C3N4 showed an amorphous nature with an extremely high surface area of 400 m2 g-1. Also, the as-obtained catalyst demonstrated remarkable photocatalytic activity in hydrogen production of 1285 µmol g-1 h-1 and hydrogen peroxide production of 150 µmol g-1 h-1. The mechanism for the polymerization process of the cyanuric acid-melamine (CM) complex to hexagonal rosettes of g-C3N4 was thoroughly described employing electron microscopy tools. This study identified that the CM complex condensation is accomplished via a dehydration process by producing a highly condensed and active structure of g-C3N4, which is different from the previously reported condensation mechanism of the melamine and its derivatives performed through a deamination process.

Ultrasonication-assisted liquid-phase exfoliation enhances photoelectrochemical performance in α-Fe2O3/MoS2 photoanode.

This study successfully manufactured a p-n heterojunction hematite (α-Fe2O3) structure with molybdenum disulfide (MoS2) to address the electron-hole transfer problems of conventional hematite to enhance photoelectrochemical (PEC) performance. The two-dimensional MoS2 nanosheets were prepared through ultrasonication-assisted liquid-phase exfoliation, after which the concentration, number of layers, and thickness parameters of the MoS2 nanosheets were respectively estimated by UV-vis, HRTEM and AFM analysis to be 0.37 mg/ml, 10-12 layers and around 6 nm. The effect of heterojunction α-Fe2O3/MoS2 and the role of the ultrasonication process were investigated by the optimized concentration of MoS2 in the forms of bulk and nanosheet on the surface of the α-Fe2O3 electrode while measuring the PEC performance. The best photocurrent density of the α-Fe2O3/MoS2 photoanode was obtained at 1.52 and 0.86 mA.cm-2 with good stability at 0.6 V vs. Ag/AgCl under 100 mW/cm2 (AM 1.5) illumination from the back- and front-sides of α-Fe2O3/MoS2; these values are 13.82 and 7.85-times higher than those of pure α-Fe2O3, respectively. The results of electrochemical impedance spectroscopy (EIS) and Mott-Schottky analysis showed increased donor concentration (2.6-fold) and decreased flat band potential (by 20%). Moreover, the results of IPCE, ABPE, and OCP analyses also supported the enhanced PEC performance of α-Fe2O3/MoS2 through the formation of a p-n heterojunction, leading to a facile electron-hole transfer.

Ultrasonically prepared photocatalyst of W/WO3 nanoplates with WS2 nanosheets as 2D material for improving photoelectrochemical water splitting.

A sonochemical treatment has been an emerged technique as an interesting method for fabricating different photocatalysts with unique photoelectrochemical (PEC) properties. This study investigated the PEC performance of WO3 with WS2 nanosheets as a 2D material before calcination (WO3/WS2-90) and after calcination (WO3/WS2-450) prepared with sonochemical treatment. The WS2 nanosheets were prepared from a liquid exfoliation phase with few-layer nanosheets, approximately 6.5 nm in thickness. The nanosheets were confirmed by UV-Vis spectroscopy and atomic force microscopy. Further, XPS, RAMAN, and SEM-EDAX analyses indicated that, following calcination of the WO3/WS2 electrode, the WS2 nanosheets initially transformed to 2D-WO3. After depositing the WS2 nanosheets on the WO3, the photocurrent density increased substantially. The WO3/WS2-450 films after calcination showed a photocurrent density of 5.6 mA.cm-2 at 1.23 V vs. Ag/AgCl, which was 3.1 and 7.2 times higher, respectively than those of the WO3/WS2-90 before calcination and pure WO3. Mott-Schottky and electrochemical impedance spectroscopy analyses confirmed the fabrication of the WO3/WS2 photoanode after calcination. The deposition of WS2 nanosheets onto pure WO3 increased the donor concentration (24-fold), reduced the space charge layer (4.6-fold), and decreased the flat band potential (1.6-fold), which could all help improve the photoelectrochemical efficiency. Moreover, the incorporation of WO3 with WS2 nanosheets as a 2D material (WO3/WS2-450) enhanced the incident photon current efficiency (IPCE) by 55%. In addition, the applied-bias photon-to-current conversion efficiency of the WO3/WS2-450 films was approximately 2.26% at 0.75 V (vs. Ag/AgCl), which is 5.6 and 9 times higher, respectively than those of WO3/WS2-90 and pure WO3.

Efficient Photodegradation of Rhodamine B and Tetracycline over Robust and Green g-C3N4 Nanostructures: Supramolecular Design.

Highly condensed g-C3N4 nanosheets with an exceptional surface area and porous structure were simply prepared by thermal condensation of stable preorganized supramolecular structures of cyanuric acid and melamine formed in water as the solvent. Different techniques were employed for the characterization of the structural, morphological, electrical, and optical features of the as-synthesized catalyst. All the characterizations confirmed the successful formation of nanosheets with magnificent properties compared to the pristine sample which was prepared by melamine polycondensation. Not only did these nanosheets exhibit a superb photocatalytic activity over the degradation of tetracycline (over 60%) and rhodamine B (100%) under visible light irradiation just for 15 min, but they also could maintain their stability during the reaction keeping over 98% of their original degradation even in 5 cycles. Superoxide anion radicals and holes were determined to be the main active species by trapping experiments. LC-Mass analysis was also performed to identify the intermediates and propose the possible pathway for photodegradation of tetracycline. The promising performance of this catalyst can be a notable step forward for prosperous industrial applications in the field of photodegradation of hazardous and not-easily degradable organic compounds in wastewater treatment plants.

Sono-oxidation treatment of hazardous ABS/PC surface for its selective separation from ESR styrene plastics.

This study reports the selective hydrophilization of the ABS/PC blend surface using the peroxide-sonochemical system and then its selective separation by froth flotation technique from other ABS-based plastics (ABS, ABS/PMMA) and PS/HIPS in electronic shredder residue (ESR). FT-IR and XPS measurements confirm that the hydrophilic moiety development on the ABS/PC surface led to increasing the wettability of ABS/PC and then decreased its floatability. The confocal scanning results also support the enhancement of microscale roughness of the treated ABS/PC surface. The enhanced surface roughness is attributed to the oxidative process which degrades hydrophobic moieties and promotes hydrophilic functional groups on the ABS/PC surface using commercial oxidant peroxide and ultrasound. This study also investigated removal of Br-containing compounds on the ABS/PC surface. The optimum conditions for selectively ABS/PC separation are peroxide concentration 2%, power cycle 70%, treatment time 5 min, temperature 50 °C, floating agent concentration 0.4 mg/L, flotation time 2 min, and airflow rate 0.5 L/min. ABS/PC was selectively separated from ESR styrene plastics with high recovery and purity of 98.9% and 99.8%, respectively. Hence, the developed novel surface treatments having removal of hazardous Br chemicals and none-formation of secondary pollutants should be applied for upgrading plastic recycling quality.

Ag-doped BiVO4/BiFeO3 photoanode for highly efficient and stable photocatalytic and photoelectrochemical water splitting.

In a conventional photoelectrochemical (PEC) water splitting system using BiVO4 (BVO), most of the charge carriers have very sluggish photocatalysis reaction kinetics because they are easily recombined from the defects developed from the bulk or the surface of the photoanodes before reaching the fluorine-doped tin dioxide (FTO). Herein, we present a facile design and fabrication technique for a Ag-BVO/BiFeO3 (BFO) heterostructure photoanode by Ag doping and surface passivation with BFO on the as-preparedBVO photoanode. Its photocatalytic properties for PEC water splitting and tetracycline (TC) degradation are compared to those of BVO/BFO, BVO, and Ag-BVO photocatalyst nanoparticle (NP) films. The effect of Ag-doping/BFO surface passivation on the morphological, structural, and optical properties and surface electronic structure of the as-obtainedBVO electrodes was investigated. The photocatalytic degradation of TC in aqueous solution by Ag-BVO/BFO was greatly increased (>1.5-fold) compared to that of BVO. The TC was completely photodegraded in 50 min of visible-light irradiation. The as-preparedAg-BVO/BFO heterojunction photoanode not only exhibited 4-fold higher PEC performance (0.72 mA cm-2 vs. RHE) and stability than those of the pure BVO components, but also the onset potential in the Ag-BVO/BFO photoanode was cathodically shifted by 600 mV compared to that of the bare BVO. The Ag-BVO/BFO photoelectrode with the highest donor density and the lowest charge transfer resistance exhibited a 4.46-fold higher carrier density than that of the pure BVO photoelectrode. More specifically, the Mott-Schottky (MS) and electrochemical impedance spectroscopy (EIS) results demonstrated that the Ag-doping not only effectively increased the carrier charge density of BVO, thus increasing the consumption rate of charge carriers, but also increased the charge transfer and transport efficiencies of the BVO photoanodes.

Environmentally Sustainable Synthesis of a CoFe2O4-TiO2/rGO Ternary Photocatalyst: A Highly Efficient and Stable Photocatalyst for High Production of Hydrogen (Solar Fuel).

Herein, a magnetically separable reduced graphene oxide (rGO)-supported CoFe2O4-TiO2 photocatalyst was developed by a simple ultrasound-assisted wet impregnation method for efficient photocatalytic H2 production. Integration of CoFe2O4 with TiO2 induced the formation of Ti3+ sites that remarkably reduced the optical band gap of TiO2 to 2.80 eV from 3.20 eV. Moreover, the addition of rGO improved the charge carrier separation by forming Ti-C bonds. Importantly, the CoFe2O4-TiO2/rGO photocatalyst demonstrated significantly enhanced photocatalytic H2 production compared to that from its individual counterparts such as TiO2 and CoFe2O4-TiO2, respectably. A maximum H2 production rate of 76 559 µmol g-1 h-1 was achieved with a 20 wt % CoFe2O4- and 1 wt % rGO-loaded TiO2 photocatalyst, which was approximately 14-fold enhancement when compared with the bare TiO2. An apparent quantum yield of 12.97% at 400 nm was observed for the CoFe2O4-TiO2/rGO photocatalyst under optimized reaction conditions. This remarkable enhancement can be attributed to synergistically improved charge carrier separation through Ti3+ sites and rGO support, viz., Ti-C bonds. The recyclability of the photocatalyst was ascertained over four consecutive cycles, indicating the stability of the photocatalyst. In addition, it is worth mentioning that the photocatalyst could be easily separated after the reaction using a simple magnet. Thus, we believe that this study may open a new way to prepare low-cost, noble-metal-free magnetic materials with TiO2 for sustainable photocatalytic H2 production.

Correction to "Environmentally Sustainable Synthesis of CoFe2O4-TiO2/rGO Ternary Photocatalyst: A Highly Efficient and Stable Photocatalyst for High Production of Hydrogen (Solar Fuel)".

[This corrects the article DOI: 10.1021/acsomega.8b03221.].

Sustainable hydrophilization to separate hazardous chlorine PVC from plastic wastes using H2O2/ultrasonic irrigation.

Polyvinyl chloride (PVC) products comprise a large portion of plastic wastes and cause severe environmental burdens in thermal recycling such as toxic release and disposal difficulties. Selective separation methods for PVC containing hazardous chlorine are required for the development of suitable disposal or material recycling processes. However, separating PVC selectively from municipal plastic waste mixtures is difficult due to their similar hydrophobic surface and appearance densities. This study presents a one-step, selective separation technique for PVC using H2O2 solution under ultrasonic irrigation to promote the selective development of hydrophilicity only on the PVC surface. The combined treatment helped to decrease air bubbles attached on the PVC surface because of increased wettability, which allowed the treated PVC to settle on the bottom of the flotation reactor. However, the remaining plastic wastes were easily floated off because they maintained their hydrophobicity. The combined treatment with a low concentration of 3% H2O2 and ultrasonic irrigation for 30 min afforded 100% purity and recovery of the PVC separated from the municipal plastic waste mixture. This proposed treatment is therefore a promising and inexpensive way to improve plastic recycling quality through selective PVC separation by the selective development of hydrophilicity on its surface.

Effect of pH on photocatalytic and photoelectrochemical (PEC) properties of monoclinic bismuth vanadate.

Monoclinic bismuth vanadate (c-BVO) was prepared via simple calcination of solvothermally processed tetrahedral BiVO4. The physicochemical and morphological properties of c-BVO demonstrated the successful synthesis of the photoactive monoclinic phase from the tetrahedral phase, which has low photoactivity properties. The photoactivities of c-BVO were investigated using the photodegradation of methylene blue (MB) and photoelectrochemical (PEC) measurements in acidic (pH = 2.5), neutral (pH = 6.5) and basic (pH = 9.5) media. The photocatalytic activity of c-BVO was increased with increasing pH, achieved 99% MB degradation in the basic condition, compared with 70 and 45% in the neutral and acidic media, respectively. Although the tetrahedral BiVO4 showed mainly adsorption with negligible photodegradation, c-BVO demonstrated both good adsorption and photodegradation activities. The PEC results indicated that the photocurrent density was affected by both pH and applied voltage. Impedance measurements showed faster charge transfer in the neutral condition than in the acidic and basic electrolytes. The incident photon conversion efficiency (IPCE) showed very low activity for tetrahedral BiVO4, but in comparison it was enhanced by 20- and 10-fold for c-BVO in the visible and simulated solar light, respectively.

Sonochemical-driven ultrafast facile synthesis of WO3 nanoplates with controllable morphology and oxygen vacancies for efficient photoelectrochemical water splitting.

Among the various synthetic techniques, the sonochemical method has emerged as an interesting method for fabricating different photocatalysis materials with unique photoelectrochemical (PEC) properties. In comparison with the classical method without sonication, this study examines the promoting effect of ultrasonic irradiation during the synthesis of tungsten oxide (WO3) nanoplates within short reaction times (15 and 30 min). The shorter ultrasonic reaction time (15 min) was sufficient for the uniform growth of thin and compact layers of WO3 nanoparticles (NPs) on the surface of a tungsten foil. In the classical method, however, partial cracks or patches formed when WO3 samples underwent acid treatment for either 15 min or 30 min at 90° C. The WO3 nanoplates fabricated with 15- or 30-min sonication followed by 15- or 30-min deposition (U-15/30-15/30) showed much higher photocurrent density than the WO3 samples fabricated with the classical method without sonication (C-15/30) at 90 °C. The as-prepared monoclinic WO3 with 30-min ultrasonication and 30-min deposition (U-30/30) showed a maximum photocurrent density of ∼6.51 mA/cm2 under simulated solar light at 1.8 V vs. Ag/AgCl, which was 2.12- to 2.93-fold higher than that of the two classical samples. The ultrasonic samples exhibited extraordinarily high stability for water oxidation by maintaining 98% of their initial photoactivity for 2200 sec, as compared to the low stability (66-61%) of both classical samples. The WO3 nanoplates prepared by sonication method had many advantages, such as facile synthetic route, compact, porous and uniform nanoplate morphology, decreased electron-hole pairs recombination rate and controlled oxygen vacancies for greatly enhanced PEC water splitting performance and stability over extended time.

Photolysis and photocatalysis of tetracycline by sonochemically heterojunctioned BiVO4/reduced graphene oxide under visible-light irradiation.

The widespread use of antibiotics in pharmaceutical therapies and agricultural practice has led to severe environmental pollution. In this study, the simultaneous photolysis and photocatalysis behaviors of tetracycline (TC), one of the most frequently prescribed groups of antibiotics, were investigated using BiVO4 (BVO) supported on reduced graphene oxide (rGO). The resulting BVO/rGO nanocomposite (NC) showed prominent adsorption performance and photocatalytic ability under wide initial pH conditions (from acidic to alkaline: pH 2.5, 6.7, 9.2 and 10.5). This study analyzed the kinetics and proposed a mechanism for the photolytic and photocatalytic degradation of TC under visible light irradiation with BVO and BVO/rGO. The photolysis and photocatalytic degradation efficiency of TC was largely influenced by the solution pH and increased with increasing initial pH. The TC was stable without significant photolysis at pH 2.5, while TC photolysis increased up to 17% at pH 9.2. With further increase in the solution pH from 9.2 to 10.5, the light absorption of TC at 356 nm showed a red shift to 372 nm and new absorption peaks at around 533 nm were formed due to the formation of new colored intermediates. The photocatalytic degradation activities of TC by BVO/rGO under visible light irradiation reached 55, 67, 92 and 99% at initial pH 2.5, 6.7, 9.2 and 10.5, respectively. However, when using BVO only, the photocatalytic degradation of TC was 42, 61, 73 and 85% at pH 2.5, 6.7, 9.2 and 10.5, respectively. The great improvement of photocatalytic activity of BVO/rGO is attributed to the reduced particle size, increased adsorption ability of rGO, extended photo responding range of BVO, and efficient separation of photogenerated charge carriers, which are derived from the ultimate coverage of the BVO by the rGO.

Ternary cross-coupled nanohybrid for high-efficiency 1H-benzo[d]imidazole chemisorption.

1H-Benzo[d]imidazole (BMA) has been considered as an emerging pharmaceutical organic contaminant, leading to the increasing BMA detection in wastewaters and need to be removed from ecosystem. This study investigated a highly synergistic BMA chemisorption using a novel ternary cross-coupled nanohybrid [γ-APTES]-Fe3O4@PAN@rGO. Magnetic nanoparticles (Fe3O4) were in situ core-shell co-precipitated with polyacrylonitrile polymer (PAN). Then, the prepared Fe3O4@PAN was decorated on hexagonal arrays of reduced graphene oxide (rGO) inside the framework of γ-aminopropyltriethoxysilane ([γ-APTES]). The final nanohybrid [γ-APTES]-Fe3O4@PAN@rGO produced adjacent inter-fringe distances of 0.2-0.4 nm corresponded well to (111), (220), and (311) parallel sub-lattices with two oblique intersections at 90° right angle and 60° triangle. The BMA adsorption was favorable in neutral pH 7, aroused temperature (50 °C), and controlled by endothermic process. The identified maximum adsorption capacity of 221.73 mg g-1 was 30% higher than the reported adsorbents. The adsorption mechanisms include ion exchange, hydrogen bond, dipole-dipole force, π-conjugation, electrostatic, and hydrophobic interaction. Graphical abstract The synthetic route of novel nanohybrid [γ-APTES]-Fe3O4@PAN@rGO was investigated. After BMA adsorption, the adsorbent surface was entirely changed, thus an efficiently facile magnetic separation within 8s. [γ-APTES]-Fe3O4@PAN@rGO formed different oblique intersections of 60° and 90° sub-lattices.