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A binary S-scheme heterojunction photocatalyst, ZIF-67/Ag 3 VO 4 (ZAV), was successfully synthesized using a hydrothermal technique. The optimal ZAV-30 (ZIF-67/30 wt%Ag 3 VO 4) demonstrated excellent performance by degrading 98.5% of Venlafaxine (VEN) within 60 min under visible light. Extensive investigations were carried out regarding the crystal structure, morphology, composition, specific surface area, optical characteristics and electrochemical impedance. The ZAV-30 heterojunction photocatalyst outperformed bare ZIF-67 and Ag 3 VO 4 photocatalysts, primarily due to enhanced photon absorption and improved charge carriers' separation via S-scheme transfer, redox capability and high charge transfer capacity supported by electrochemical experiments and photoluminescence. The S-scheme transfer was validated by in-situ XPS measurements after light exposure. Scavenger experiments indicated that both •OH and •O 2 − played crucial roles as active species in the photocatalytic process. Mass spectrometry (MS) analysis of intermediates facilitated the proposal of a probable photocatalytic degradation pathway for VEN. The photoactivity of the heterojunction was influenced by a range of factors including the pH of the VEN solution, initial VEN concentration, ZAV photocatalyst dosage, and ion effects. Interestingly the ZAV-30 heterojunction exhibited superior performance in lake water, tap water and river water too. Importantly, the ZAV-30 heterojunction exhibited excellent stability and reusability, making it a promising photocatalyst. [Display omitted] • ZIF-67/Ag 3 VO 4 S-scheme heterojunction synthesized by hydrothermal technique. • ZAV-30 demonstrated 98.5% degradation of Venlafaxine within 60 min under visible light. • The S-scheme transfer accelerates charge transfer, separation and strong redox capability. • •OH and •O 2 − as main active species for photocatalytic degradation • High mineralization, reusability and durability. [ABSTRACT FROM AUTHOR]

Pollution and the rising energy demand are two major society issues, requiring urgent solutions. Here, we review the simultaneous production of hydrogen and removal of pollutants, with a focus on mechanisms, synthesis of photocatalysts, and applications. Remarkably, this method utilizes organic pollutants as sacrificial agents for photocatalytic hydrogen production, thus both reducing pollution and producing energy. Metal-doped, cocatalyst-loaded, organic and inorganic composite, heterostructure and heterojunction photocatalysts are described. We present applications to the removal of antibiotics and organic dyes. Pollutant degradation rates range from 5.3 to 100%, with hydrogen evolution of 13.7–2724.89 μmol·g–1h–1. [ABSTRACT FROM AUTHOR]

In pursuit of advancing photocatalysts for superior performance in water treatment and clean energy generation, researchers are increasingly focusing on layered double hydroxides (LDHs) which have garnered significant attention due to their customizable properties, morphologies, distinctive 2D layered structure and flexible options for modifying anions and cations. No review has previously delved specifically into ZnCr and NiCr LDH-based photocatalysts and therefore, this review highlights the recent surge in ZnCr and NiCr-based LDHs as potential photocatalysts for their applications in water purification and renewable energy generation. The structural and fundamental characteristics of layered double hydroxides and especially ZnCr-LDHs and NiCr-LDHs are outlined. Further, the various synthesis techniques for the preparation of ZnCr-LDHs, NiCr-LDHs and their composite and heterostructure materials have been briefly discussed. The applicability of ZnCr-LDH and NiCr-LDH based photocatalysts in tackling significant issues in water treatment and sustainable energy generation is the main emphasis of this review. It focuses on photocatalytic degradation of organic pollutants in wastewater, elucidating the principles and advancements for enhancing the efficiency of these materials. It also explores their role in H 2 production through water splitting, conversion of CO 2 into valuable fuels and NH 3 synthesis from N 2 , shedding light on their potential for clean energy solutions. The insights presented herein offer valuable guidance for researchers working towards sustainable solutions for environmental remediation and renewable energy generation. [Display omitted] • Fundamentals and properties of Layered Double Hydroxides (LDHs). • ZnCr and NiCr LDHs as photocatalysts-Properties and Performance. • Water treatment and clean energy production-Mechanism and issues. • ZnCr and NiCr LDH based water treatment & clean energy production. • The challenges and future development direction for sustainable use are discussed. [ABSTRACT FROM AUTHOR]

Herein, we report the designing of a C3N4/BiOI heterostructure that is supported on gum acacia-crosslinked-poly(acrylamide) hydrogel to fabricate a novel nanocomposite hydrogel. The potential application of the obtained nanocomposite hydrogel to remediate crystal violet dye (CVD) in an aqueous solution was explored. The structural and functional analysis of the nanocomposite hydrogel was performed by FTIR (Fourier transform infrared spectroscopy), X-ray diffraction (XRD), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The different reaction parameters, such as CVD concentration, nanocomposite hydrogel dosage, and working pH, were optimized. The C3N4/BiOI heterostructure of the nanocomposite hydrogel depicts Z-scheme as the potential photocatalytic mechanism for the photodegradation of CVD. The degradation of CVD was also specified in terms of COD and HR-MS analysis was carried to demonstrate the major degradation pathways. [ABSTRACT FROM AUTHOR]

Providing sustainable energy and cleaning water pollution are actually major societal issues requiring new catalysts. In particular, transition metal phosphides are emerging as effective photocatalytic materials. Here we review synthetic strategies for metal phosphides by various methods. We discuss passivation strategies for engineering electronic and structural properties of metal phosphide nanocomposites. Electronic properties, stability and activity depend upon the type of metal phosphides, either phosphorus-rich or metal-rich. Typically, a high content of phosphorous in metal phosphides improves the catalysis. The crystalline structure of metal phosphides also varies and depends upon their chemical composition. We present the latest developments in H2 production and photodegradation of aqueous pollutants using metal phosphide-based heterojunctions, with focus on type-II-, Z-scheme- and S-scheme-based heterojunctions. [ABSTRACT FROM AUTHOR]

Microplastics (MPs), as emerging pollutants, have attracted the attention of environmentalists, statespersons, and the scientific community over the last few decades. To address the spread of MPs in the environment, it is imperative to develop various removal techniques and materials that are effective, scalable, and ecologically benign. However, to the best of our knowledge, no review has systematically examined the removal of MPs using adsorption or provided an in-depth discussion on various adsorbents. Adsorption is an inexpensive and effective technology for wastewater treatment. Recently, many researchers have conducted studies on MP remediation using diverse adsorbent materials, such as biochar, activated carbon, sponges, carbon nanotubes, metal-layered oxides, metal-organic frameworks (MOFs), and zeolites. Each adsorbent has advantages and disadvantages. To overcome their disadvantages, researchers have been designing and developing hybrid adsorbents for MP remediation. This review provides insights into these individual adsorbents and also discusses hybrid adsorbents for MP removal. Finally, the review elaborates on future possibilities and ways to enable more efficient, scalable, and environmentally friendly MP cleanup. Overall, this review bridges the gap between contemporary MP remediation using adsorption techniques and adsorbent development. [Display omitted] • Adsorption-based microplastic remediation was reviewed. • The factors affecting microplastic adsorption were thoroughly discussed. • A comprehensive analysis is presented on several microplastic adsorbents. • Microplastic adsorption challenges and future perspectives are examined. [ABSTRACT FROM AUTHOR]

[Display omitted] • Oxygen vacancies fundamentals and importance in photocatalysis. • Oxygen vacancies rich heterojunction-Synthetic strategies. • OVs rich Z-scheme and S-scheme heterojunctions- Photocatalytic mechanism. • Applications for Hydrogen production and water treatment. • The existing challenges and future perspectives. Photocatalytic removal of pollutants and energy production is a green, low cost and environment friendly technology for addressing the mounting pressure of energy crisis and environmental deterioration. Developing efficient photocatalysts is still a big challenge for accelerating the photocatalytic hydrogen production and pollutant degradation especially utilizing solar light. Therefore, constructing oxygen vacancies rich Z-scheme and S-scheme semiconductor heterojunctions emerged as a promising approach to enhance the light harvesting and increasing the redox capability of photocatalysts. This review comprehensively summarises the state of art focus on oxygen vacancy's role in photocatalysts especially in Z-scheme and S-scheme heterojunctions including synthesis process and modifications. In particular, the functions of oxygen vacancy in supporting the main processes in photocatalytic energy production and pollutant removal, such as light absorption, charge separation and conversion are highlighted in this review. The current issues and future prospective in oxygen vacancies rich heterojunctions for efficient photocatalytic removal of pollutant and energy production are also addressed. Finally, a brief discussion on challenges and future prospects is demonstrated. [ABSTRACT FROM AUTHOR]

Pectin-crosslinked gum ghatti hydrogel (PGH) has been synthesized utilizing pectin and gum ghatti through an uncomplicated and inexpensive copolymerization method. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM-elemental mapping), Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS) characterization techniques have been employed to determine various structural, chemical and compositional characteristics of fabricated PGH. Three different weight ratios (1:1, 2:1, or 1:2 for pectin and gum ghatti, respectively) were employed to synthesize three distinct types of PGH. Swelling studies has been done to determine the best ratios for PGH fabrication. PGH has been assessed as an adsorbent for the removal of malachite green dye from aqueous solutions. The effects of PGH dosage (100–400 mg/L), dye concentration (10–160 mg/L), pH (2–9 pH), adsorption time (0–480 min), and temperature (25–55 °C) has been examined through batch solutions. According to Langmuir isotherm analysis, the maximum adsorption capacity is 658.1 mg/g. By using pseudo-second-order kinetics and the Freundlich adsorption isotherm, the adsorption process could be well explained. After five consecutive cycles, PGH had an adsorption percentage of 86.917 % for the malachite green dye. It is safe for the environment and may be used to remove malachite green (MG) dye from aqueous solutions. [Display omitted] • Pectin-crosslinked gum ghatti hydrogel (PGH) synthesis using copolymerization • Study of physicochemical properties of PGH • PGH effectively adsorbed malachite green (MG) dye. • Showing a maximum capacity of 658.1 mg/g according to Langmuir isotherm analysis • Freundlich isotherm model fits well, indicating a heterogeneous adsorption process. [ABSTRACT FROM AUTHOR]

The population explosion and rapid economic development has led to tremendous increase in the per capita use of fossil fuel energy resulting in major environmental consequences. To tackle these significant energy and environmental concerns, semiconductor photocatalysis is viewed as a promising environmentally friendly and sustainable solution. The photocatalytic hydrogen evolution utilizes solar energy into clean hydrogen energy which makes it green, environmentally friendly and effective technique to meet energy demands. This process requires workable catalysts to reach a significant reaction rate because of their multiple electrons and multiple proton nature. Among various visible light active photocatalytic materials, metal molybdates have been reported as emerging class of materials owing to their outstanding features as stable crystal structure, photo-corrosion inhibition, high redox efficiency, low cost and toxicity and suitable band structure. The present research provides an extensive review of the most recent advances and new insights into the utilization of metal molybdates in photocatalytic clean energy production and environment challenges. This review article summarizes the recent progresses in advanced strategies applied in metal molybdate based photocatalysts to enhance the photocatalytic performance. The advanced strategies are categorized as control over morphology and surface modification, doping of heteroatom, co-catalyst loading, noble metal deposition and construction of heterojunction, which are devoted to photocatalytic H 2 production and CO 2 reduction and to overcome the fast recombination of charge carriers and increasing the light absorption capacity. The fabrication strategies of metal molybdates and based materials are discussed in detail, as well as their usage as catalysts for H 2 evolution and CO 2 reduction have been analysed. Metal molybdates are promising photocatalysts for addressing present environmental issues, and this work paves the way for future photocatalytic research and development, which may assist in the development of highly effective photocatalysts for sustainable energy needs. [Display omitted] • Metal molybdates as photocatalysts-Structure and properties. • Introduced the synthetic routes: Effect on properties and photocatalytic performance. • Discussed strategies to improve the photocatalytic potential of metal molybdates. • Application for superior hydrogen evolution and CO 2 conversion-Recent advances. • Fundamentals and bottlenecks along with future prospects are discussed. [ABSTRACT FROM AUTHOR]

Photocatalysis has established itself as a fascinating topic, giving promise for effective processing of greenhouse gases and contaminants into useful products, in the search for renewable energy sources and atmospheric rehabilitation. This review study provides a thorough examination of S-scheme heterojunction photocatalysts with an emphasis on their uses in the photocatalytic reduction of CO 2 , N 2 fixation and NO x degradation processes. The review explains various environment-related issues, the basic ideas of photocatalysis and heterojunctions, emphasizing the benefits of S-scheme topologies in increasing interfacial transmission of charges and lowering electron-hole recombination. The fundamentals and issues of photocatalytic CO 2 reduction, nitrogen fixation and NO x degradation, outlining the mechanics involved in employing S-scheme heterojunctions have been discussed. The recent advancements of S-scheme photocatalysts for a variety of applications are highlighted in this review. The future prospects of such assemblies are also critically evaluated, highlighting the importance of full use of solar spectrum, wide scale preparation of photocatalysts, maintaining the redox capability and mechanism elucidation to prepare superior S-scheme heterojunctions to resolve the important energy and environmental issues. [Display omitted] • S-scheme heterojunctions as efficient photocatalysts –Fundamentals and advantages. • Mechanisms of photocatalytic CO 2 reduction, N 2 fixation and NO x degradation. • Designing and synthesis of S-scheme heterojunction photocatalysts. • Applications for reducing CO 2 into fuels, fixation of N 2 into NH 3 and degrading NO x. [ABSTRACT FROM AUTHOR]

In this work, the physical properties of nanocrystalline samples of La0.7Sr0.3Mn1−xFexO3 (0.0 ≤ x ≤ 0.20) perovskite manganites synthesized by the reverse micelle (RM) technique were explored in detail. The phase purity, crystal structure, and crystallite size of the samples were determined using X‐ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. All the samples had rhombohedral crystal structure and crystallite size increased with increase in Fe content in La0.7Sr0.3MnO3. The scanning electron micrographs (SEMs) exhibited smooth surface morphology and nonuniform shape of the particles. The optical properties studied using UV‐visible absorption spectroscopy revealed a decrease in the absorbance and optical band gap with an increase in Fe content in La0.7Sr0.3MnO3 compound. The temperature‐dependent resistivity measurements revealed semiconducting nature of x = 0 and 0.1 samples up to the studied temperature range, while a metal‐to‐insulator transition was observed at higher Fe doping. Magnetic studies revealed weak ferromagnetism in all the samples and a reduction in the maximum magnetization with an increase in Fe content. A close correlation between electrical transport and magnetic properties was observed with the doping of Fe ion in La0.7Sr0.3MnO3 at Mn site. These results advocate strong interactions associated with the double exchange mechanism among Fe3+ and Mn3+ ions. [ABSTRACT FROM AUTHOR]

In the present work, we report the successful synthesis of Iron oxide nanoparticles by efficient, economic and fast solution combustion method. Solution combustion method has been modified for preparation of Fe2O3 nanoparticles and the influence of fuel to oxidizer ratio, and synthesis temperature has been analyzed for the phase purity. Optical properties of prepared samples have been determined using UV-Visible spectroscopy and optical band gap is obtained using Tauc's Plot. Vibrating sample magnetometer and Mössbauer spectroscopy of the prepared samples were recorded and analyzed for magnetic properties. Magnetic results support and explain the modified properties based on choice of synthesis route. [ABSTRACT FROM AUTHOR]

The dramatic rise in carbon dioxide levels in the atmosphere caused by the continuous use of carbon fuels continues to have a significant impact on environmental degradation and the disappearance of energy reserves. Past few years have seen a significant increase in the interest in photocatalytic carbon dioxide reduction because of its ability to lower CO 2 releases from the burning of fossil fuels while also producing fuels and important chemical products. Because of their excellent catalytic efficiency, great uniformity, lengthy charge diffusion layers and texture flexibility that enable accurate band gap and band line optimization, perovskite-based nanomaterials are perhaps the most advantageous among the numerous semiconductors proficient in accelerating CO 2 conversion under visible light. Firstly, a brief insight into photocatalytic CO 2 conversion mechanism and structural features of perovskites are discussed. Further the classification and selection of perovskites for Z and S-scheme heterojunctions and their role in photocatalytic CO 2 reduction analysed. The efficient modification and engineering of heterojunctions via co-catalyst loading, morphology control and vacancy introduction have been comprehensively reviewed. Third, the state-of-the-art achievements of perovskite-based Z-scheme and S-scheme heterojunctions are systematically summarized and discussed. Finally, the challenges, bottlenecks and future perspectives are discussed to provide a pathway for applying perovskite-based heterojunctions for solar-to-chemical energy conversion. [Display omitted] • Insight into the mechanism and research progress of photocatalytic CO 2 reduction. • Properties of perovskites as photocatalysts and their synthetic routes. • Boosting the CO 2 conversion through perovskite based Z and S-scheme heterojunctions • The charge transfer mechanism and designing of perovskite based heterojunctions • The future expectations, challenges and outlook are presented. [ABSTRACT FROM AUTHOR]

Environmental pollution and climate change are requiring new methods to clean pollutants and produce sustainable energy. Aerogels and metal organic frameworks are emerging as advanced porous materials with higher functionality, high surface area, high porosity and flexible chemistry. Aerogels are dried gels prepared using the sol-gel procedure, whereas metal organic frameworks are networks of organic ligands and metal ions connected by coordination bonds. Applications of aerogels include the removal of heavy metals, CO2 capture and reduction, photodegradation of pollutants, air cleanup and water splitting. This article reviews the synthesis and types of aerogels and metal organic frameworks, and the application to pollutant removal, energy production including hydrogen, methane reforming, CO2 conversion and NOx removal. [ABSTRACT FROM AUTHOR]

• g-C 3 N 4 and MOFs based heterojunctions –synthesis routes and advantages. • Types of g-C 3 N 4 and MOFs heterojunctions were discussed-modification strategies. • g-C 3 N 4 and MOFs based heterojunctions for photocatalytic environmental remediation and energy production. • Conclusion and future research prospects on g-C 3 N 4 and MOFs based on heterojunctions. Photocatalytic technology has emerged as a promising solution for environmental remediation and energy production, and the development of efficient and stable photocatalysts is of great importance. Recent advances in g-C 3 N 4 /Metal Organic Frameworks (MOFs) heterojunctions have shown excellent potential in achieving high-performance photocatalytic environmental remediation and energy production. In this review, we have summarized the recent advances in the design and synthesis of g-C 3 N 4 /MOFs heterojunctions and their application in photocatalytic environmental remediation and energy production. We have discussed the advantages and challenges of g-C 3 N 4 /MOFs heterojunctions, such as enhanced light absorption, increased surface area, and improved electron-hole separation, and their effects on photocatalytic performance. We also highlight the recent research progress in the utilization of g-C 3 N 4 /MOFs heterojunctions for various environmental remediation applications, including the degradation of organic pollutants and the removal of heavy metals, as well as for energy production applications such as hydrogen evolution and CO 2 reduction. Furthermore, we provide an overview of the latest theoretical and experimental investigations into the mechanisms of photocatalysis in g-C 3 N 4 /MOFs heterojunctions, which can help to guide the rational design of high-performance photocatalysts. Our analysis of the literature reveals that g-C 3 N 4 /MOF heterojunctions have demonstrated excellent photocatalytic activity for the degradation of various pollutants, such as methyl orange, rhodamine B, and bisphenol A. For instance, a g-C 3 N 4 /ZIF-8 heterojunction achieved a photocatalytic degradation rate of 99.9% for methyl orange under visible light irradiation within 60 min. Moreover, the g-C 3 N 4 /MOF heterojunctions have also been found to be efficient in water splitting for hydrogen production. For instance, a g-C 3 N 4 /UiO-66 heterojunction achieved a hydrogen production rate of 1260 μmol h−1g−1 under visible light irradiation. The recent data on the advances in g-C 3 N 4 /MOFs heterojunctions demonstrate their enormous potential for practical applications in photocatalytic environmental remediation and energy production. [ABSTRACT FROM AUTHOR]

Here in, we report a, wide spectrum active, Bi nanodots incorporated CuBi 2 O 4 /Bi/CuFe 2 O 4 (CBC) heterojunction for synchronous photodegradation of imidacloprid pesticide (ICP) and photo-reduction of Cr(VI) to Cr(III). The best performing heterojunction sample CBC-30 shows nearly 100% Cr(VI) photo reduction (in less than 45 min) along with 98.2% ICP removal in 60 min. 88.7% Cr (VI) reduction & 83.2% ICP degradation was achieved under sunlight with good activity in NIR region. Scavenging experiments reveal the synchronous role of photoreduction-oxidation with electrons as active species for chromium reduction and holes for organic pollutant degradation. This is ensured by effective Z-scheme transfer between CuBi 2 O 4 and CuFe 2 O 4 leading to protection of high potential conduction and valence bands with strong redox capabilities. The Bi nanodots played an important role via wide spectral response owing its surface plasmon resonance as well as photoinduced electron transfer mediation which promotes the electrons transfer efficiency and enhanced photocatalytic ability. [Display omitted] • Z-scheme CuBi 2 O 4 /Bi/CuFe 2 O 4 has excellent charges separation efficiency. • Bi nanodots-wide spectral activity-mediator- provide hot electrons. • Remarkable synchronous removal of imidacloprid and Cr (VI). • Degradation route for ICP and cooperative mechanism for reduction-degradation. • Efficient activity in solar light and river water too. [ABSTRACT FROM AUTHOR]

Iron nanoparticles (Fe NPs), monometallic Fe@carbon quantum dots (Fe@CQDs) and bimetallic Fe/Ag@carbon quantum dots (Fe/Ag@CQDs) nanocomposites were prepared by simple co-precipitation/reduction method. The nanoparticles (NPs), monometallic nanocomposite (MNCs) and bimetallic nanocomposite (BMNCs) were characterized using various techniques. The adsorptional/photocatalytic activity of NPs, MNCs, and BMNCs were investigated for the removal of fast green (FG) dye from aqueous medium. The degradation of FG dye under combined adsorptional/photocatalytic condition was efficient. The catalytic nature of synthesized NPs, MNCs and BMNCs was also explored for the oxidation of benzyl alcohol and esterification of acetic acid. For oxidation of benzyl alcohol with H 2 O 2 in the presence of acetonitrile (ratio of butyl alcohol: H 2 O 2 was 2:1) at temperature 80 °C, the Fe NPs gave maximum yield (87%). The esterification of acetic acid with ethyl, isopropyl and butyl alcohol showed that butyl alcohol gave maximum yield of 82%, 80%, and 84% for Fe NPs, Fe@CQDs MNCs and Fe/Ag@CQDs BMNCs, respectively. [ABSTRACT FROM AUTHOR]

The present work is focused on the replacement of Fe 3+ ions by rare-earth Nd 3+ ions and their influence on the cations distribution, structural, magnetic and Mössbauer properties of Mg-Mn nanoferrites. Nanosized Nd-doped Mg-Mn nanoferrites, Mg 0.9 Mn 0.1 Nd x Fe 2−x O 4 , where x = 0.1, 0.2 & 0.3, were successfully synthesized for the first time through solution combustion technique. X-ray diffraction studies confirmed the formation of single phase nature of the synthesized nanoferrites. Williamsons-Hall plots were used to obtain the particle size and strain while the lattice parameter was obtained from Nelson-Riley plots. The particle size was observed to decrease (19.2–13.5 nm) while lattice parameter was observed to increase (8.373–8.391 Å) with the incorporation of Nd 3+ ions. Cation distribution between the tetrahedral (A-site) and octahedral (B-site) was estimated by using the X-ray diffraction method & magnetization technique. The estimated cation distribution was used to investigate the detailed structural parameters. Room temperature M−H study revealed a decrease of saturation magnetization (10.15–1.83 emu/g) and an increase in coercivity (22.86–27.19 Oe) with the increasing substitution of Nd 3+ ions. Magnetic results obtained in the present study indicated that the synthesized nanoferrites can be a useful candidate for electromagnet applications. [ABSTRACT FROM AUTHOR]

In this research work we report synthesis of g-C 3 N 4 /FeVO 4 (CI) and g-C 3 N 4 /FeVO 4 /Fe@NH 2 -Biochar (CIB) nano-hetero assemblies for removal of methyl paraben (MeP) and 2-cholrophenol (2-CP) via adsorption, photocatalysis and photo-ozonation. CI and CIB have been characterized by FT-IR, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), UV–Vis spectroscopy, photoluminescence (PL), vibrating sample magnetometry (VSM), Brauner-Emmet Teller surface area analyzer (BET). CIB shows good photocatalytic activity owing to higher specific area, nanosheet porous structure, stability, broader solar spectrum response and reduced charge carriers recombination. Fe@NH 2 -biochar facilitates the degradation via high adsorption capability due to reduced recombination, better charge separation, adsorption and acting of biochar as sink of electrons. The CIB photocatalytic system was tested under three experimental conditions for photodegradation of MeP and 2-CP; adsorption followed by photo-degradation (AP); simultaneous adsorption and photocatalysis (SAP); SAP + O 3 . An apparent synergism between adsorption, photocatalysis and photo-ozonation brings out excellent and promising results. 98.4% of MeP and 90.7% of CP degradation was achieved under simultaneous adsorption and photocatalysis in presence of CIB. The results were analyzed in terms of reaction kinetics, adsorption isotherms, scavenger effect, liquid chromatography-mass spectrometry (LC-MS), Total Organic Carbon (TOC) analysis and cytotoxicity analysis of treated water. An efficient TOC removal 74.2 & 73.9% for MeP and 2-CP were respectively achieved under SAP + O 3 +CIB photocatalysis system. Degradation pathways have been proposed for degradation of MeP and CP thorough photo-degradation and photo-ozonation. The cyto-toxicity studies on Human peripheral blood lymphocytes provide a reference for removal of noxious pollutants in real systems. This experimental work paves a way to design tuneable simple junctions for photocatalytic applications by utilizing various experimental protocols. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fundamentals of S-scheme and dual S-scheme have been discussed. • Types of heterojunctions are elaborated with mechanism comparisons. • Recent developments in synthetic methods and different morphology of S-scheme and dual S- schemes. • S-scheme and dual S-scheme for photocatalytic environmental remediation and energy production. • Bottlenecks, conclusion and future prospects discussed. Discovering alternative materials and technologies that provide the meaningful potential to environmental and energy-related challenges in critical to the long-term viability of industrial activity and the evolution of society. Photocatalysts are undeniably important, and scientists are working hard to improve their photocatalytic performance. The high recombination rates of photogenerated electron-hole pairs as well as poor redox capability are addressed via heterojunction modification. In this direction, oxidation type and reduction type photocatalysts based S-scheme heterojunctions are highly promising owing to highly diminished recombination facilitated by internal electric field. This review has focused on the shift from Z-scheme to new revolutionary S-scheme based photocatalytic materials with high performance applications in the field of energy and environment. It can be concluded that controllable built-in electric field intensity and stable interfacial carrier transport process make S-scheme heterostrctures ideal. However their application is mainly limited to powder photocatalysts, don't apply to photo-chemistry and solar cells with external circuit, reaction thermodynamics and dynamics management in S-scheme photocatalysts is not adequate. To some extent, dual S-schemes address to these limitations and further research is to be carried out to fight the bottlenecks. Several perspectives on the future of S-scheme and dual S-scheme heterostructure were also provided based on rigorous review of the reported results. A discussion on the previously reported different types of heterojunctions and S-schemes is presented in this review along with plausible charge transfer mechanisms. The synthetic routes to S-scheme heterojunctions are also provided along with modifications and combinations. The current designing and perspective applications in numerous pollutant degradation, hydrogen production and CO 2 conversion is selectively highlighted. The transition of mechanism elucidation from Z-scheme to S-scheme has been discussed with suitable case studies. However, S-scheme heterojunctions designing and fabrication is still new commercially and so present readiness and bottlenecks have been discussed. Hence it is quite imperative for a future roadmap to be laid to design and develop economically viable high performance S-scheme heterojunctions. [ABSTRACT FROM AUTHOR]

Al doped Mn ferrite, MnAl x Fe 2-x O 4 (x = 0.1, 0.2, & 0.3), nanoparticles were synthsized by facile and simple solution combustion route. Effect of Al3+ ions substitution on the structural, optical, electrical and magnetic properties were explored. X-Ray diffraction (XRD) results confirm the formation of pure cubic phase for all the synthesized nanoparticles having spinel structure. Various structural parameters like crystallite size, lattice parameter, site radii and bond lengths were estimated from XRD data. For the strain analysis and consideration of contribution of every peak in XRD data, W-H and N-R plots were analysed. Scannining electron microscopy (SEM) revealed the compact surface morphology with grain size in nano meter range. FTIR spectra confirmed the presence of metal stretching vibrations at tetrahedral and octahedral sites for all MnAl x Fe 2-x O 4 nanoparticle compositions, which is typical of spinel ferrites with FCC structure. Raman spectroscopy helped in analysing metal stretching vibrations of the synthesized samples and obtained raman modes were found to be as predicted by group theory. Dielectric constant decreases with increase in frequency reflecting the normal behaviour of the ferrites. Dielectric loss also followed the same trend. Both the behaviours have been explained in view of Koop׳s theory and Maxwell–Wagner polarization-model. The synthesized ferrite samples exhibited the soft magnetic nature as confirmed by vibrating sample magnetometer. The room temperature hysteresis curves indicate the decrease in saturation magnetization as well as retentivity with the increase in Al3+ ions doping. The decrease in magnetic moment values have been explained on the basis of cation preference for the sites and also on weakening of exchange interaction upon aluminium doping. • Al3+ substituted MnFe 2 O 4 nanoferrites are synthesized for the first time by SC method. • Magnetic parameters suggest the utility for electromagnet application. • Low values of dielectric loss tangent are obtained. [ABSTRACT FROM AUTHOR]

Objectives: To evaluate the diagnostic role of cerebrospinal fluid (CSF) ferritin and albumin index (AI = CSF albumin/serum albumin × 1000) in differentiating acute bacterial meningitis (ABM) from acute viral meningitis (AVM) in children. Methods: The study included 42 cases each of ABM and AVM in pediatric age group. Receiver operating characteristic (ROC) analysis was carried out for CSF ferritin and AI. Binary logistic regression was also done. Results: CSF ferritin and AI were found significantly higher in ABM compared to AVM. Model obtained using AI and CSF ferritin along with conventional criteria is better than existing models. [ABSTRACT FROM PUBLISHER]

Objective: The quality and duration of sleep is impaired during pregnancy. Our study aimed to determine whether maternal sleep deprivation occurring during the second and third trimester of pregnancy could alter fetal well-being with respect to birth weight and APGAR score by altering the inflammatory status and oxidative stress in the mothers. Method: Sleep adequacy was assessed using the Pittsburgh Sleep Quality Index (PSQI). We investigated the inflammatory status and oxidative stress at term in the blood of pregnant subjects with and without sleep deprivation by measuring the levels of protein-bound sialic acid (PBSA), high-sensitivity C-reactive protein (hsCRP), malondialdehyde (MDA) and protein carbonyl (PCO). Homocysteine (Hcy) and its vitamin determinants were also measured. Fetal outcome with respect to birth weight and APGAR score were compared between study subjects. Results: A significant increase was observed in the levels of hsCRP, PBSA, Hcy, MDA, and PCO, in the sleep-deprived group when compared to the control group. Fetal outcome at birth showed a significant difference between the cases with high sleep deprivation and those with low sleep deprivation. Conclusion: Sleep deprivation in pregnancy leads to an increase in the inflammatory parameters, oxidative stress, and Hcy levels. Fetal outcome at birth was affected more in mothers with high sleep deprivation than those with low sleep deprivation. Follow-up in these babies are needed to reveal any differences in their growth and development. [ABSTRACT FROM AUTHOR]

Mg0.9Mn0.1Gd x Fe2-x O4 nanoferrites were processed for the first time by a solution combustion technique. X-ray diffraction studies revealed the spinel cubic structure of the synthesized ferrites. The particle size was observed to increase (13-16nm) with an increase in Gd3+ ion content. The cation distribution is inferred from the X-ray diffraction. It is observed from cation distribution that Gd3+ ions preferred octahedral (B) sites. The DC resistivity was found to be increasing with an increase in Gd3+ content. The dielectric constant ε' and loss tangent (tan &#948) was observed to decrease with the addition of Gd3+ content as well as with the increase in frequency. The variations in DC resistivity as well as dielectric constant with the increasing substitution of Gd3+ ions have been correlated to the cation distribution. The very high values of DC resistivity (~108 Ωcm) and low values of loss tangent (0.9-0.008) are the prime achievements of this work. [ABSTRACT FROM AUTHOR]

As there are no specific non-invasive markers for the diagnosis of tubal ectopic pregnancy, our objective in the present study was to explore the role of inflammatory cytokines IL-6 and IL-8 in the diagnosis of ruptured tubal ectopic pregnancy. Twenty-eight women with tubal ectopic pregnancy, 31 patients with intrauterine abortion and 29 gestational age matched women having normal intrauterine pregnancy were included in the study. Five millilitre of blood was collected at the time of admission, serum was separated and stored at −70 °C for subsequent analysis of β hCG, IL-6 and IL-8 levels. The level of IL-6 was a significant increase in the women with tubal ectopic pregnancy compared to intrauterine abortion and normal pregnancy. IL-8 levels decrease significantly in the tubal ectopic pregnancy and in intrauterine abortion patients when compared with the normal pregnancy group. At the cutoff of 26.48 pg/ml IL-6 level predicted the tubal ectopic pregnancy with moderate accuracy. Therefore, it can be concluded that measurement of IL-6 may have relevance in the diagnosis of ectopic pregnancy as a novel inflammatory serum biomarkers. [ABSTRACT FROM PUBLISHER]

Highlights: [•] A novel nanocomposite Fe0.01Ni0.01Zn0.98O/polyacrylamide was synthesized. [•] FNZP/PAM nanocomposite shows good degradation efficiency for MB and MG. [•] Rapid decolouration of dyes was observed under coupled adsorption and photocatalysis. [•] Dye degradation followed the pseudo first-order kinetics. [•] A higher recycle efficiency and antibacterial activity was achieved for nanocomposite. [Copyright &y& Elsevier]

[Display omitted] • porous Zn/Fe LDH exhibited appreciable adsorption capacity. • Successful decomposition of H 2 O 2 present between the LDH layers. • Introduction of pores in the layers enhanced the surface area and adsorption activity. • Successfully reusable for consecutive 6 cycles adsorption cycles. Present work include the designing of a novel porous Zn/Fe layered double hydroxide (LDH) based adsorbent using a combination of three methods, namely, co-precipitation, hydrothermal, and thermal treatment. The Zn/Fe LDH was synthesized by co-precipitation followed by hydrothermal method. The LDH was then intercalated with H 2 O 2 and its decomposition under the thermal treatment created oxygen bubbles that pierce holes in the layered structure of the LDH by local pressure build-up. Major techniques used for assessing the morphology and surface area characteristics of the LDH and porous LDH were Scanning electron microscope (SEM) and Brunauer-Emmet-Teller (BET). The intercalation of H 2 O 2 and its later decomposition triggered by thermal treatment lead to the introduction of pores in the LDH layers that increased the surface area from 108.863 m2/g to 168.923 m2/g. The synthesized adsorbent was utilized for the removal of an antibiotic; ciprofloxacin (CIP) from the aqueous solution. The porous Zn/Fe LDH adsorbent was featured with an admirable CIP adsorption capacity of 344.83 mg/g at pH 6.5 and temperature 298 K. The adsorption of CIP onto porous Zn/Fe LDH adsorbent followed the Freundlich isotherm model and pseudo-second-order kinetic model. The temperature increase negatively affected the adsorption rate. The adsorption mechanism of CIP onto porous Zn/Fe LDH was also projected and established, and Cπ- metal interactions, hydrogen bonding, and electrostatic interactions, were found to be the major interactive forces. The thermodynamic study revealed the exothermic and spontaneous nature of the adsorption experiments. Overall, the synthesized adsorbent is sustainable in terms of its usability and non-toxic nature. [ABSTRACT FROM AUTHOR]

[Display omitted] • Integrating calcium alginate and Ag@Bi 4 O 5 I 2 /SPION- Wide-spectral response. • Faster and selective photocatalytic reduction of NO 3 – into N 2. • Ag and Fe greatly enhance N 2 selectivity-under visible, NIR and solar light. • High performance degradation of azithromycin-●O 2 – active species-ESR probe. • In Built I 3 -/I- and Fe3+/Fe2+ redox and high CAlg adsorption potential. Wide spectral responsive photocatalysts with improved charge separation and transfer capacity have attracted researchers for various photo-oxidative and reductive applications. This work reports Vis-NIR active photocatalyst Ag@Bi 4 O 5 I 2 /SPION@calcium alginate (here in designated as ABSA) prepared by hydrothermal impregnation for high performance degradation of azithromycin (AZY) and selective reduction of NO 3 – into N 2. The composite catalyst ABSA shows 98.4% AZY degradation in 90 min with visible light. Surprisingly, the apparent rate constant for ABSA catalyst (0.08321 min−1) is ~ 8 times higher than bare Bi 4 O 5 I 2. The photocatalyst is capable of selectively reducing NO 3 – into N 2 with formic acid at a wide range of pH especially in acidic conditions with ~ 100% photo-reduction and 97.6% N 2 selectivity. The high performance is manifested in the excellent photoreduction and oxidative capabilities under UV, visible, NIR and sunlight. SPIONs and Ag improve the visible activity, I 3 -/I- redox mediates better charge flow and Ag provides "hot electrons" via SPR effect. ●O 2– radicals are the active species during AZY degradation as confirmed by ESR probe. ●CO 3 – plays immensely important role in selective NO 3 – reduction into N 2. This work reports a relatively simple photocatalytic system with more bio-benevolence utilizing Bi 4 O 5 I 2 and Calg and modifying with Fe 3 O 4 and Ag as dopants for a wide spectral photo-redox capability. The hybrid wide spectrum responsive material integrates environmental friendliness, robust structure, full recycling and stability with sturdy improvement in photocatalytic efficiency. [ABSTRACT FROM AUTHOR]

• Nanocomposite based photocatalyst is designed. • Nanocomposite demonstrated high degradation activity under visible light. • Photodegradation of dyes with degradation rate of 90–96%. • High reusability. Highly visible light efficient photocatalyst; ferric oxide/zinc oxide/silicon nitride (Fe 3 O 4 /ZnO/Si 3 N 4) nanocomposite has been designed. Its photocatalytic activity has been studied for the degradation of two dyes; sunset yellow and methyl orange from aqueous solution. Results showed high degradation rate of 90 and 96% for sunset yellow and methyl orange, respectively. Scavenging studies indicated the major involvement of OH radicals in the degradation process. Reusability study has been conducted for 6 consecutive cycles indicating its appreciable activity even after repetitive cycles. Antimicrobial activity studied against E. Coli and Pseudomonas strains showed an appreciable inhibition zone. [ABSTRACT FROM AUTHOR]

The voluminous anthropogenic activities and non-regulated discharge of emerging pharmaceutical pollutants have led to deterioration of water quality characteristics and shortage of potable water. One of most ubiquitous problems is that the pharmaceutical pollutants are slowly developing resistance in pathogens, which increases the risks manifold. Conventional water treatment methods and technologies have been known to be inadequate for elimination of recalcitrant and emerging pollutants. Advanced oxidation processes have been exploited to the most for mineralizing the pollutants with some limitations especially toxic metal based catalysts and secondary pollution. However Fenton-based systems are considered to be safer as they utilize non-toxic chemicals. Homogeneous Fenton processes suffer from limitations as limited pH operational range, generation of Fe containing sludge etc. have shifted focus to heterogeneous systems. This review focusses on removal of pharmaceutical pollutants by homogeneous and heterogeneous Fenton, electro-Fenton, sono-Fenton, photo-Fenton and photo-electro-Fenton processes using nano-catalysts. Various types of new pharmaceutical pollutants, their emergence, characteristics and toxicity have been discussed to have an insight into quantity and variety. New Fenton-like catalysts have been designed and used for degradation of pollutants and high mineralization is also achieved in a wide pH-range. In addition Fenton catalysts capable of showing high mineralization using solar light have been prepared by various methods with and without iron based materials. In addition in this review we have also focused on complexities related to removal of pharmaceutical effluents and how they are addressed by Fenton systems. The review aims to assist researchers and engineers to gain fundamental understandings and critical view of Fenton process and its optimization processes, and hopefully with the knowledge it could bring new opportunities for the optimization and future development of Fenton process. The key advances in Fenton catalysts are innovations in design of ligands, junction designing for effective radical generation, reaction engineering, hydro-dynamical effects and complete mineralization. The combinations and coupling of biological oxidation, semiconductor photocatalysis with Fenton process for high performance pharmaceutical pollutants removal in pilot-scale experiments have been discussed and evaluated. • Pharmaceutical pollutants as emerging class of toxic pollutants. • Fenton, electro-Fenton, photo-Fenton processes: Safe, Cheap and environmental benign. • Controllable parameters for effective degradation of pharmaceutical pollutants. • Heterogeneous photo-Fenton reaction better than homogenous. • Focus on coupled Fenton and biological oxidation systems. [ABSTRACT FROM AUTHOR]