Higher Degradation Research Articles

Advancing wastewater treatment: The efficacy of carbon-based electrochemical platforms in removal of pharmaceuticals

The study addresses the efficiency of innovative biochar- and g-C3N4-coated electrochemical platforms in removing selected pharmaceuticals and their metabolites from wastewater, with a focus on cost-effective and scalable materials. Analysis of effluent from the wastewater treatment plant revealed significant concentrations of 25 pharmaceuticals, highlighting the plant’s limited treatment efficacy. Notably higher levels of Telmisartan, Tramadol, and Diclofenac were found. The novelty of this work lies in the use of biochar- and g-C3N4-coated Raschig rings and glass beads as efficient electrochemical anodes offering high degradation capabilities. Adsorption-only tests (without voltage load) confirmed that no significant pharmaceutical removal occurs without electrochemical activation, highlighting the importance of electrochemical degradation. For the first time, we observed the formation of hydroxyl radicals (•OH) and singlet oxygen (1O2) during the electrochemical degradation process using g-C3N4-coated anodes, significantly enhancing degradation efficiency. The biochar-coated Raschig rings achieved over 80 % removal efficiency for all tested pharmaceuticals, with a power consumption of 85.2 kWh/m3. In comparison, biochar-coated beads exhibited a removal efficiency ranging from 9 % to 99 %, consuming 75 kWh/m3, while g-C3N4-coated rings showed the lowest performance at an energy consumption of 45 kWh/m3. These findings demonstrate the potential of both, biochar- and g-C3N4-based electrochemical platforms as a viable, scalable solution for advanced wastewater treatment, particularly for pharmaceutical degradation.

Aromatic Poly(dithioacetal)s: Spanning Degradability, Thermostability, and High Refractive Index Towards Eco-friendly Optics.

In the quest for eco-friendly optics, high refractive index polymers (HRIPs) with degradability have been one of the desirable optical materials for realizing eco-friendly and efficient lighting technologies. However, it has been challenging for HRIPs to simultaneously realize thermostability, high refractive index (RI), visible transparency, and efficient degradability, all of which are essential for their practical use. In this context, we herein focus on aromatic poly(dithioacetal)s, composed of visible-transparent yet degradable dithioacetal moieties and rigid diphenyl disulfide spacers, exhibiting moderately high Tg (> 60 °C), high RI (> 1.7), and colorless film features. In addition, poly(dithioacetal)s can balance (1) high stability under the operating conditions even upon heating and (2) quantitative degradability that can selectively yield cyclic low-molecular-weight products that can be further repolymerized upon further addition of an acid catalyst. These results provide a key concept for high refractive index polymers that allow on-demand degradability and recyclability without compromising their high potential thermal and optical properties.

Design of ternary GO@AgNPs@g-C3N4 membranes for efficient dye removals in integrated photocatalysis-filtration reactors

Photocatalytic composite membranes (PCMs), which integrate the high degradation efficiency of photocatalysts and the physical separation properties of membranes, have emerged as a promising technology for wastewater treatment. Herein, the ternary GO@AgNPs@g-C3N4 PCM was fabricated through a facile vacuum-filtration assembly of graphene oxide (GO), graphitic phase carbon nitride (g-C3N4), and silver nanoparticles (AgNPs) onto commercial mixed cellulose ester (MCE) substrates. The effects of g-C3N4 synthesized from different precursors and various metal nanoparticles on the performance of PCM were systematically investigated. Interestingly, results show the addition of AgNPs not only significantly improves the photocatalytic performance of PCMs but also enhances the mechanical adhesion between the active layer and the MCE substrate. The resultant PCMs exhibit outstanding photocatalytic performance, maintaining dye removal above 89% even after 25 consecutive cycles. Moreover, dye degradation pathways over the PCMs were investigated through free radical scavenging experiments and electron spin resonance characterizations. This simple assembly method results in a 3–12 times increase in flux compared to the layer-by-layer assembly method. Accordingly, our designed PCMs exhibit significant potential for wastewater treatment and water purification applications.

How to get green with agricultural footprint: A global analysis of carbon emissions, environmental taxes, and agrochemical use

The agriculture sector, being highly vulnerable to climate change, plays a pivotal role in achieving green and sustainable economies. As the 2030 Agenda emphasizes the integrated development of environmental, social, and economic dimensions, it is crucial to understand how agricultural practices affect sustainability. This study investigates the environmental impact of the agricultural sector on the green economy by examining key environmental factors, such as agricultural energy emissions, environmental taxes, irrigated water use efficiency, fertilizer use, and pesticide application. The analysis is conducted using the Panel Quantile Autoregressive Distributed Lag (QARDL) model, with robustness checks performed through the comparison with the Panel ARDL model, using data from 2000 to 2020. To assess the green economy, an index is constructed based on 20 indicators related to environmental, social, and economic sustainability. The results show that agricultural energy emissions, despite their environmental cost, are positively associated with green economy development, highlighting the trade-off between high productivity and environmental degradation in a resource-efficient economy. Improved water use efficiency is found to enhance agricultural sustainability and production. Additionally, environmental taxes and regulations exert a significant positive effect on both environmental preservation and social welfare. Contrary to the belief that reducing agricultural production will lower carbon emissions, the study suggests that adopting environmentally friendly practices and imposing targeted taxes are more effective strategies. The findings also reveal a negative relationship between excessive fertilizer use and the green economy, indicating the need for minimal fertilizer application to promote sustainability. The study concludes with specific policy recommendations. Governments, particularly in countries that have not yet adopted sustainable agricultural practices, should implement environmental taxes and regulations to promote carbon neutrality and support the Sustainable Development Goals. These measures are essential to balancing economic growth, environmental sustainability, and social equity in the agricultural sector.

Silicon alleviates the toxicity of microplastics on kale by regulating hormones, phytochemicals, ascorbate-glutathione cycling, and photosynthesis

Kale is rich in various essential trace elements and phytochemicals, including glucosinolate and its hydrolyzed product isothiocyanate, which have significant anticancer properties. Nowadays, new types of pollutant microplastics (MP) pose a threat to global ecosystems due to their high bioaccumulation and persistent degradation. Silicon (Si) is commonly used to alleviate abiotic stresses, offering a promising approach to ensure safe food production. However, the mechanisms through which Si mitigates MP toxicity are unknown. In this study, a pot culture experiments was conducted to evaluate the morphogenetic, physiological, and biochemical responses of kale to Si supply under MP stress. The results showed that MP caused the production of reactive oxygen species, inhibited the growth and development of kale, and reduced the content of phytochemicals by interfering with the photosynthetic system, antioxidant defense system, and endogenous hormone regulation network. Si mitigated the adverse effects of MP by enhancing the photosynthetic capacity of kale, regulating the distribution of substances between primary and secondary metabolism, and strengthening the ascorbate-glutathione (AsA-GSH) cycling system. SummaryEffects of microplastic and silicon on key indicators of kale. Note: The red arrows and blue arrows indicate the MP treatment effect compared to the control and Si treatment effect compared to the MP treatment, respectively.

Photocatalytic NOx degradation and [formula omitted] adsorption by mortar modified with S-g-C3N4/MgAl-CLDH: Influence factors and stability

NOx is a harmful gas that causes respiratory diseases and acid rain. Commonly used photocatalysts for degrading NOx such as UV responsive TiO2 show weak photocatalytic degradation efficiency under visible light. Furthermore, the great concern is that the degradation product, nitrates (NO3-), from NOx could be washed away and increase the nitrogen deposition and eutrophication in the surrounding soil and aquatic environments, resulting in serious secondary pollution. To address these issues, this study proposes a novel solution by incorporating S-g-C3N4/MgAl-CLDH nanocomposites into a cementitious system which features high NOx degradation efficiency under visible light condition and the efficient capture and adsorption of NO3- in situ. The NOx degradation was comprehensively studied, encompassing the influencing factors and stability. The mechanism for NO3- adsorption process was expounded using the isothermal model. The results show that the amount of exposed S-g-C3N4/MgAl-CLDH and the contact area between S-g-C3N4/MgAl-CLDH and NOx are the essential reasons affecting the NOx degradation. The NOx degradation ability of photocatalytic mortar exhibits excellent stability with the NOx removal ratio decreasing by only 4.8 % and 14.5 % after ten consecutive tests and 120 min of ultrasonic washing, respectively. Furthermore, S-g-C3N4/MgAl-CLDH increases the NO3- adsorption capacity of photocatalytic mortar by about 1.5 times, and the adsorption process of NO3- follows the Freundlich isotherm. The study offers an alternate method for designing innovative nanocomposites in cement-based materials to control environmental pollution.

Sustainable and cost-effective metastable white cast iron powder for the degradation of textile dyes

The textile industry is one of the main consumers of dyes. The treatment of wastewater containing dyes is a major challenge worldwide for a sustainable and environmental friendly goods production. Therefore, it is necessary to develop an effective method for removing the dyes from wastewater. In this study, an economical and efficient white cast iron powder was reported to degrade reactive red 195A azo dye in an aqueous solution. The white cast iron powder was obtained by ball-milling a rapidly solidified cast iron ribbon, exhibiting unique metastable properties and a large surface area. These metastable phases are particularly effective in providing electrons for the dye degradation of NN double bonds, thereby improving the catalytic process, and enhancing the overall bond degradation efficiency. The influence of different parameters such as temperature, dye concentration, and reusability of metallic iron powder on the degradation efficiency was investigated. The experimental analysis revealed rapid and efficient dye degradation that was achieved within 15 min using 0.1 g of white cast iron powder. The study also demonstrated the effectiveness of the degradation rate improved significantly with an increase in temperature. Even after seven recycling experiments, the Fe82C15Si3 powders maintained high degradation efficiency toward the reactive red 195A solutions. This research will contribute to developing a new, highly efficient, and low-cost method for treating organic dye wastewater.

Thin film nanocomposite membrane ornamented with Z-scheme heterojunction carbon dot/NiFe–LDH for removal of organic contaminants from industrial wastewater

Removal of organics from wastewater is a tedious process and industries are looking for a facile, energy efficient strategy of wastewater treatment for producing clean water and recycling. Membrane technology is one of the efficient processes for wastewater treatment due to its energy efficient nature, simple operation and excellent performance. But, proneness of membrane fouling often limits its path to triumph. In this work, we have designed a ‘carbon dot/NiFe-layered double hydroxide (CD/NiFe–LDH)’ nanocomposite via in situ approach, which is coated on a poly(ethylene terephthalate) (PET) and cellulose based superhydrophillic membrane. The membrane is found to have excellent separation efficiency. The photocatalytic activity of CD/NiFe–LDH shows high oxidative degradation of the accumulated organics contaminants on the membrane surface providing self-cleaning ability and hence enhances the membrane’s lifetime. The membrane exhibits stable performance for 30 days continuous operation under UV-A light. The membrane flux is found to be ∼42 Lm−2 h−1 and 48 Lm−2 h−1 for crude oil–water emulsion and phenol respectively while rejection around ≥99 % is obtained for the both. The flux recovery ratio (FRR) of the post photo irradiated membrane is found to be 88.07 %. The membrane also shows organic solvent resistance property and prevents bacterial pathogens in wastewater.

Investigation of MO Adsorption Kinetics and Photocatalytic Degradation Utilizing Hollow Fibers of Cu-CuO/TiO2 Nanocomposite.

This comprehensive study explores the kinetics of adsorption and its photocatalytic degradation of methyl orange (MO) using an advanced copper-decorated photocatalyst in the form of hollow fibers (HFs). Designed to boost both adsorption capacity and photocatalytic activity, the photocatalyst was tested in batch experiments to efficiently remove MO from aqueous solutions. Various isotherm models, including Langmuir, Freundlich, Sips, Temkin, and Dubinin-Radushkevich, along with kinetic models like pseudo-first and pseudo-second order, Elovich, Bangham, and Weber-Morris, were utilized to assess adsorption capacity and kinetics at varying initial concentrations. The results indicated a favorable MO physisorption on the nanocomposite photocatalyst under specific conditions. Further analysis of photocatalytic degradation under UV exposure revealed that the material maintained high degradation efficiency and stability across different MO concentrations. Through the facilitation of reactive oxygen species generation, oxygen played a crucial role in enhancing photocatalytic performance, while the degradation process following the Langmuir-Hinshelwood model. The study also confirmed the robustness and sustained activity of the nanocomposite photocatalyst, which could be regenerated and reused over five successive cycles, maintaining 92% of their initial performance at concentrations up to 15 mg/L. Overall, this effective nanocomposite photocatalyst structured in the form of HF shows great promise for effectively removing organic pollutants through combined adsorption and photocatalysis, offering valuable potential in wastewater treatment and environmental remediation.

Elemental Zn modulation of interfacial structure and in situ construction of (FeCoNiCuZn)O high-entropy oxide/ZnO heterojunction for photocatalytic Rhodamine B dyes

In this study, inspired by the lattice distortion effect of HEOs, we adopt a non-equimolar strategy, fixing the molar ratios of Fe, Ni, Cu, and Co while varying the molar ratio x of Zn/(FeNiCuCo) (x=0.25, 0.5, 1.0, 1.5 and 2.0) to synthesize the HEO-x compounds. With an increase in the Zn content, lattice distortion occurred in the spinel phase of the (FeNiCuZnCo)O HEO, resulting in the gradual precipitation of ZnO nanocrystals. The (220) crystal plane of the spinel phase closely connects with the (100), (002), and (101) crystal planes of the ZnO phase, forming nano-heterojunctions. The HEO-1.5 prepared by controlling the Zn element proportion exhibits a high photocatalytic degradation rate of Rhodamine B (RhB) of up to 99.45 %. The kinetic degradation rate of HEO-1.5 is 17 times higher than that of HEO-0.25, attributed to the nano-heterojunctions formed by the spinel phase and ZnO phase, facilitating effective separation of photogenerated electron-hole pairs, promoting the generation of active free radicals, and rapidly degrading RhB.

Porous-suspended graphite carbon doped TiO2 improves the band structure of photocatalysts to enhance photocatalytic degradation of tetracycline in water

ABSTRACT In order to improve visible light utilization efficiency and enrich low-concentration antibiotics in water systems, a new type of floating TiO2 graphite carbon (FTDGC) photocatalyst was prepared by the one-pot method. These floating materials have good adsorption properties and sufficient mechanical strength, which makes them easy to recycle and reuse in processing. Its photocatalytic performance was evaluated by photocatalytic degradation of tetracycline (TC) in water. The results showed that FTDGC had a high adsorption degradation capacity for TC and the photocatalytic degradation process was accorded with a first-order kinetic equation. The Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy indicated the generation of Ti–C–Ti valence bonds and Ti–C–O bonds on the TiO2 surface with the modification of graphite carbon materials. Optimization of preparation conditions revealed that as the amount of activator phosphoric acid increased and the porosity of the solid surface increased, the external exposure of TiO2 made the effect of the composite catalyst more pronounced. The recycling experiment showed that FTDGC still had good degradation ability for TC after five times reuse. The catalysts developed in this research can provide a new idea and reference for the pretreatment of refractory organic wastewater, as well as for the reuse of medium water.

PTFE composite membrane with peroxymonosulfate activation self-cleaning for highly-efficient oil-water emulsion separation and dye degradation

Combining membrane separation with advanced oxidation technology can make the membrane self-cleaning, extending its service life. However, the preparation of composite membranes with excellent catalytic ability, self-cleaning performance, and stability remains a key research direction. In this study, a PTFE composite membrane with peroxymonosulfate activation self-cleaning ability was successfully prepared by in-situ growth of CoOOH and ZIF-67 on the surface of a l-DOPA/PEI modified PTFE membrane. The as-prepared membrane is superhydrophilic and has significant superoleophobic surfaces underwater, the separation efficiency of the as-prepared membrane for multiple oil-water emulsions exceeded 98.4 %. Meanwhile, the effective degradation of several organic dyes under visible light was simulated, with still high degradation efficiency (>99 %) after 10 cycles. Overall, this study puts forward a approach towards self-cleaning membranes based on PTFE material; the resulting composite membrane's high separation efficiency, stability under repeated use conditions as well as its self-cleaning ability position it as an attractive candidate for long-term wastewater purification applications.

A photocatalysis-self-Fenton system based on NCDs@ZnIn2S4 composites at neutral pH and low amount of Fe2+ for the effective degradation of antibiotics

Photocatalysis-self-Fenton combining photocatalytic production of H2O2 with Fenton reaction has been a hotspot, but the pH limitation and iron sludge production problems remain unsolved. Herein, we proposed a self-fenton system based on N-doped carbon dots modified ZnIn2S4 (NCDs@ZnIn2S4) composites that exhibits effective degradation of antibiotics under neutral pH using low amounts of Fe2+. The decoration of ZnIn2S4 with NCDs significantly increased the surface area, visible light absorption, charge transfer ability and oxygen adsorption ability. NCDs@ZnIn2S4 composites exhibited a high H2O2 production rate (1528 μM g−1•h−1) under visible light, which was 1.9 and 5.3 times higher than ZnIn2S4 and NCDs, respectively. Meanwhile, the Fe2+/NCDs@ZnIn2S4 system with a low concentration of Fe2+(1 mg/L) could remove over 95% levofloxacin and oxytetracycline within 30 min. Interestingly, the highest degradation efficiency occurred under neutral pH. Quenching experiments and analytical measurements indicated that the high catalytic performance under pH = 7 with low amounts of Fe2+ stemmed from the higher amount of inner-generate H2O2 under neutral pH and easy regeneration of Fe2+ by photoinduced electrons for high •OH yields. Additionally, the Fe2+/NCDs@ZnIn2S4 system exhibited high degradation performance under different water matrix and ultrahigh degradation efficiency towards levofloxacin under real sunlight irradiation. The work shows the prospects of photocatalysis-self-Fenton systems for overcoming the pH limitation and the difficulty of iron sludge separation in the purification of effluents.

Facile ultrasound-assisted synthesis of g-C3N4@Bi20TiO32/Bi2O2CO3 heterojunction with high photocatalytic performance for resistant-biodegradable dye

In this study, g-C3N4/Bi20TiO32/Bi2O2CO3 photocatalyst structured as a heterojunction was fabricated by an ultrasound-assisted methodology. It evaluated the activity in photocatalytic processes of g-C3N4/Bi20TiO32/Bi2O2CO3 composite material through simulated visible light-induced Rhodamine B photodegradation, demonstrating photodegradation efficiencies 5.6 and 13.84 times exceeding that of pure g-C3N4 and Bi20TiO32/Bi2O2CO3 in turn. Due to the formation of a ternary heterojunction, the g-C3N4/Bi20TiO32/Bi2O2CO3 composite material has a stronger visible light absorption capability compared to pure g-C3N4 and Bi20TiO32/Bi2O2CO3. The photocurrent density is also significantly increased (0.156 μA/cm2). The catalyst's efficiency remained a high degradation ratio (over 95 %) after five cycles, showing the composite's sustainable stability. In summary, based on its excellent performance, the ternary composite photocatalyst g-C3N4/Bi20TiO32/Bi2O2CO3 exhibits great potential for photodegradation of non-biodegradable dye.

Bi2MoO6/ZnIn2S4 S-scheme heterojunction containing oxygen vacancies for photocatalytic degradation of organic pollutant

Photocatalytic removal of organic pollutants is a promising strategy to alleviate environmental pollution. In this study, S-scheme heterojunctions Bi2MoO6/ZnIn2S4 (BMO/ZIS) containing oxygen vacancies were synthesized by the solvothermal method. Oxygen vacancies improved the utilization of sunlight and accelerated the separation of charge carriers. The S-scheme charge transfer mechanism provided a channel for the directed migration of photogenerated charges. 10Bi2MoO6/ZnIn2S4 (10BMO/ZIS) efficiently degraded various organic pollutants with a small amount of photocatalyst (15 mg) under visible light irradiation. 10BMO/ZIS presented the highest RhB removal efficiency of 96.52 %, which was 7.02 and 3.67 times greater than Bi2MoO6 containing oxygen vacancies (BMO-Vo) and ZnIn2S4 (ZIS), respectively. Meanwhile, in various inorganic salt ion solutions, 10BMO/ZIS still exhibited high degradation performance. In addition, the photocatalytic degradation pathway was inferred, and the threat of degradation intermediates to the ecological environment was evaluated. This work contributes to a deeper understanding of the photocatalytic mechanisms of oxygen vacancy-modified heterojunction photocatalysts and offers insights for designing efficient environmental remediation photocatalysts.

MoS2@MIL-53 (Ni) nanocomposite for water splitting and water remediation through real time effluent treatment

A novel molybdenum disulfide@ materials institute of Lavoisier (MoS2@MIL-53 (Ni)) hetero-structure material has been designed to act as a hydrogen/oxygen generator and as a water remediation agent. Two-dimensional layered MoS2@MIL-53 (Ni) nanocomposites were prepared through the hydrothermal method. Flower and layered morphology were observed for MoS2, and MIL-53 (Ni), respectively in the field emission scanning electron microscopy (FESEM) images. The MoS2@MIL-53 (Ni) nanocomposite demonstrated a high dye degradation efficiency of ∼98 % and ∼96 % for Rhodamine B (RhB) and bodactive blue (BAB) within 80 minutes of time duration, respectively. In the case of untreated textile industrial effluent (TIE), the nanocomposite achieved an efficiency of around 86 % over a period of 9 hours. The ultraviolet-visible absorption spectra of RhB, BAB, and TIE displayed peaks at ∼565 nm, 665 nm, and 530 nm, respectively. Additionally, the nanocomposite exhibited excellent stability over five cycles when tested against RhB. During hydrogen evolution reaction (HER), MoS2@MIL-53 (Ni) nanocomposite showed a Tafel slope of 105 mV/decade and overpotential of −0.073 V vs. RHE. Similarly, oxygen evolution reaction (OER) studies exhibited a reduced over potential at 0.49 V vs. RHE @ 10 mA/cm2 and the Tafel slope was calculated to be 42 mV/decade. Further, the chronoamperometry analysis of MoS2@MIL-53 (Ni) confirmed that the sample exhibited relatively good stability with respect to both HER and OER analysis for 24 hours. This is indicative of MoS2@MIL-53 (Ni)’s structural stability and its strong electrocatalytic activity.

Three-dimensional gel network structure of agarose interlayer dispersed Pd nanoparticles in copper foam electrode for electrocatalytic degradation of doxycycline hydrochloride

In this study, we successfully prepared palladium/agarose/copper foam (Pd/AG/CF) composite electrodes by utilizing the three-dimensional network structure agarose (AG), a green material derived from biomass, and homogeneously immobilizing palladium (Pd) atoms on a copper foam (CF) substrate through a facile route. The electrode showed excellent performance in the electrocatalytic degradation of doxycycline (DOX), with a high DOX degradation rate of 92.19 % in 60 min. In-depth studies revealed that palladium can form metal-metal interactions with the CF substrates, which enhances the electron transfer on the catalyst surface. In addition, the introduction of agarose effectively prevented the agglomeration of palladium nanoparticles. In addition, the hydroxyl functional groups in the molecular structure of agarose facilitate interactions between water molecules and the electrode interface through the formation of hydrogen bonds, thereby further enhancing the efficiency of the electrocatalytic reaction. In addition to good stability and reusability. Microbial toxicity test results show that the degraded wastewater has minimal impact on the environment. Also, possible degradation pathways of DOX were explored in this study. Finally, a novel continuous flow reactor was designed, featuring a unique design that ensures full contact between wastewater and the composite electrodes, thereby achieving continuous and efficient treatment of antibiotic wastewater.

Bio-inspired helicoidal hemp/basalt/polyurethane rubber bio-composites: Experimental, numerical and analytical ballistic impact study with residual velocity prediction using artificial neural network

Recent body armour trends emphasize mobility, flexibility, and cost reduction while maintaining ballistic effectiveness through the use of natural fiber composite. This study evaluates the ballistic impact performance of soft and hard armor using experimental, analytical, numerical, and machine learning methods. We developed a soft armor bio-composite using monolithic, hybrid, and helicoidal structured Hemp (H)/Basalt (B)/Polyurethane (PU) rubber and tested its V50 ballistic limit according to Millitary-Standred-662 F. For hard armour, a multi-layer armor system (MAS) consisting of Al2O3/SiC ceramic, intermediate soft armour bio-composites, and an Aluminum (Al)-5052 plate backing was tested with armour-piercing bullets as per National Institute of Justice (NIJ)-0101.06 standards (Level IV). Soft armor performance was evaluated using macro-homogeneous finite element (FE), the Ipson-Retch analytical, and an Artificial Neural Network (ANN) regression model. Results showed minimal discrepancies from experimental data, with differences of 13.33 %, 12.08 %, and 8.08 % in V50 ballistic limit. The mechanical and thermal behaviors of bio-composites were assessed using un-notched Charpy, FTIR, and TGA methods. Helicoidal laminates improved Charpy toughness by 9.44 %, 19.30 %, and 40.28 % compared to hybrid and monolithic ([H]15 and [H]10) laminates, and exhibited lower weight reduction at high degradation temperature of 395.76 ℃. Helicoidal laminates increased V50 ballistic performance by 155.80 %, 76.22 %, and 16.61 % compared to [H]10, [H]15, and hybrid laminates, respectively. Due to spiral load distribution reduces stress concentration and enhanced the damage resistance of the laminate. Stand-alone soft armor demonstrates crater formation and radial cracks (petaling) due to fiber wedging and the shearing effect of a bullet. In conclusion, MAS revels a maximum back face deformation (BFD) of 18.06 mm. Al2O3/Helicoidal/Al-plate MAS reduced weight and cost by 69.21 %, and 233.72 % compared to Kevlar™-based MAS, promoting sustainable, lightweight, economical designs. Due to its higher fracture toughness and lower density, SiC ceramic in MAS provides lower trauma and further reduced weight compared to Al2O3 ceramic.

Boosting Photogenerated Electrons Transfer from FeVO4 to Peroxymonosulfate via Cu Doping for Stable Degradation of Organic Contaminants

Comprehensive SummaryElectron transfer is an important way to activate persulfate. Currently, the electrons for persulfate activation mainly originate from organic contaminants or the catalyst itself, which can lead to selective activation of persulfate or oxidation of the catalyst, respectively, and thus become a bottleneck restricting its application. In this work, Cu−doped FeVO4 (Cu−FVO) was prepared, and the results showed that Cu doping can significantly improve the photocatalytic activity and stability of FVO for peroxymonosulfate (PMS) activation. The optimized Cu−FVO/PMS/light system exhibited a high BPA degradation rate that is 4.3 times higher than that of the FVO/PMS/light. This system manifested a broad applicability to various organic contaminants even with complex matrix. Photoelectrochemical analysis and DFT theoretical calculations revealed that Cu doping boosted the photogenerated charge separation and the adsorption of PMS on FVO. Furthermore, Cu doping led to the establishment of an electron transfer channel from Cu−FVO to PMS, through which photogenerated electrons achieved an efficient PMS activation. Meanwhile, holes were consumed by organic contaminants to avoid the oxidation of catalyst. These collectively enhanced the photocatalytic activity and stability of Cu−FVO, which also maintained high catalytic activity even after 20 cycling degradation reactions.

S-scheme 2D/2D B-doped N-deficient g-C3N4/ZnIn2S4 heterojunction for efficient H2 production intergrated with tertracycline degradation under visible-light illumination

A novel S-scheme 2D/2D boron-doped nitrogen-deficient g-C3N4/ZnIn2S4 (BDCNN/ZnIn2S4) heterojunction was successfully fabricated via the in-situ assembly of ZnIn2S4 onto BDCNN in an oil bath. To assess the quality and characteristics of the synthesized photocatalysts, a comprehensive range of characterizations were conducted. The innovative S-scheme 2D/2D BDCNN/ZnIn2S4 heterojunction, equipped with a deliberately established inter-built electric field, facilitates rapid electron transfer and enhanced separation efficiency of photo-induced carriers. Consequently, this heterojunction demonstrates remarkable enhancements in both H2 production and TC degradation under visible-light illumination (λ > 420 nm). The optimized BDCNN/ZnIn2S4 heterojunction exhibited impressive photocatalytic performance, achieving a promising H2 evolution rate of 2378.8 μmolg−1h−1 and a high degradation efficiency exceeding 90 % (k = 0.021 min−1) for TC. This noteworthy improvement in photocatalytic performance is primarily attributed to the synergistic effects of boron-doping and nitrogen-defects within BDCNN, coupled with the unique S-scheme photocatalytic mechanism inherent to the BDCNN/ZnIn2S4 heterojunction. Overall, this study introduces a groundbreaking approach for constructing 2D/2D g-C3N4-based heterojunctions that exhibit exceptional visible-light photocatalytic capabilities, thereby offering significant potential for various photocatalytic applications.