Ecologically sustainable removal of pharmaceuticals: A mechanistic study of bismuth sulfide-graphene oxide/silver nanocomposite.

Bismuth sulfide nanoparticles (BiS NPs) were synthesized via the hydrothermal method, and reduced graphene oxide(rGO) and silver nanoparticles (Ag), which acted as substrates, have prepared using the chemical reduction method. The synthesized nanoparticles have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible spectroscopy, and photoluminescence spectroscopy. Commercially available paracetamol-500 mg (PAM) and aspirin-300 mg (ASP) were selected for photodegradation under visible light using the as-prepared composites in an aqueous solution. Photoluminescence spectroscopy was used to detect PAM and ASP using the photo-excited electron transfer (PET) process, and the limit of detection (LOD) has obtained for PAM(8.70 ppm) and ASP(4.43 ppm) with a sensitivity of 0.9954 and 0.8002, respectively. Fourier transform infrared spectroscopy (FTIR) was used to analyze the before and after degradation products and to confirm the disintegrated products such as -COOH and -CH- both before and after disintegration.. The experimental data were found to fit well with the Freundlich isotherm, suggesting that the as-prepared nanocomposites exhibited a heterogeneous nature for PAM (5119 mg/L), and the pseudo-first-order kinetic model suggests ASP (1030 mg/L) with R2 values of 0.9119 and 0.7075. The risk assessment analysis of PAM was 9.823 µg/L(RQ > 1) and that of ASP was 0.2106 µg/L(RQ < 1), indicating that PAM has a higher potential risk than ASP. The demographic data of the participants indicated that PAM was the most stockpiled medicine at home; this work also encompasses the action of a single PAM and ASP tablet toward the environment, if it is accidently disposed of improperly could create massive water/soil pollution; hence, the care/duty of each person should follow the proper disposal of medical waste because we cannot replace this environment.

Effect of Red Mud and Rice Husk Ash-Based Geopolymer Composites on the Adsorption of Methylene Blue Dye in Aqueous Solution for Wastewater Treatment.

In this study, geopolymer originating from locally industrial byproducts as red mud (RM) was successfully prepared in the presence of different loadings of rice husk ash (RHA) used for the adsorption of methylene blue (MB) in wastewater. During geopolymerization, various mixing amounts between RM and RHA were conducted when the weight ratio of binder solution/activated alkali-metal solution (Na2SiO3/ NaOH 7 M) was 2.5 and the curing temperature was set at 60 °C for 24 h. As a result, the surface area value of the prepared geopolymer composited with RHA at 0 and 60% was increased from 19.2 to 29.5 m2/g, while the BJH pore size of the prepared geopolymer was reduced to 6.68 and 5.76 nm, respectively. In the dye removal test, higher additions of RHA in the RM-geopolymer maintained better retention of the MB ion due to the increase in the adsorption binding site. The maximum uptake amount of dyes performed at pH 8 was changed from 6.59 to 10.74 mg/g, while RHA was from 0 to 60% after 180 min of immersion in MB solution. The adsorption isotherms well obeyed the Langmuir model, as the relative coefficient R2 was 0.999. Based on these, the initial agricultural waste as RHA and industrial byproducts as RM were valued as functional materials used for dye treatment in wastewater.

Loading of Silver (I) Ion in L-Cysteine-Functionalized Silica Gel Material for Aquatic Purification.

The L-cysteine-functionalized silica (SG-Cys-Na+) matrix was effectively loaded with silver (I) ions using the batch sorption technique. Optimal Ag(I) loading into SG-Cys-Na+ reached 98% at pHi = 6, 80 rpm, 1 mg L-1, and a temperature of 55 °C. The Langmuir isotherm was found to be suitable for Ag(I) binding onto SG-Cys-Na+ active sites, forming a homogeneous monolayer (R2 = 0.999), as confirmed by FTIR spectroscopy. XRD analysis indicated matrix stability and the absence of Ag2O and Ag(0) phases, observed from diffraction peaks. The pseudo-second-order model (R2 > 0.999) suggested chemisorption-controlled adsorption, involving chemical bonding between silver ions and SG-Cys-Na+ surface. Thermodynamic parameters were calculated, indicating higher initial concentrations leading to increased equilibrium constants, negative ΔG values, positive ΔS values, and negative ΔH. This study aimed to explore silver ion saturation on silica surfaces and the underlying association mechanisms. The capability to capture and load silver (I) ions onto functionalized silica gel materials holds promise for environmental and water purification applications.

Biomass derived green carbon dots for sensing applications of effective detection of metallic contaminants in the environment.

The rapid consumption of metals and unorganized disposal have led to unprecedented increases in heavy metal ion concentrations in the ecosystem, which disrupts environmental homeostasis and results in agricultural biodiversity loss. Mitigation and remediation plans for heavy metal pollution are largely dependent on the discovery of cost-effective, biocompatible, specific, and robust detectors because conventional methods involve sophisticated electronics and sample preparation procedures. Carbon dots (CDs) have gained significant importance in sensing applications related to environmental sustainability. Fluorescence sensor applications have been enhanced by their distinctive spectral properties and the potential for developing efficient photonic devices. With the recent development of biomass-functionalized carbon dots, a wide spectrum of multivalent and bivalent transition metal ions responsible for water quality degradation can be detected with high efficiency and minimal toxicity. This review explores the various methods of manufacturing carbon dots and the biochemical mechanisms involved in metal detection using green carbon dots for sensing applications involving Cu (II), Fe (III), Hg (II), and Cr (VI) ions in aqueous systems. A detailed discussion of practical challenges and future recommendations is presented to identify feasible design routes.

The development of ZnO nanoparticle-embedded graphitic-carbon nitride towards triple-negative breast cancer therapy.

The present study deals with the effects of curcumin-loaded ZnO nanoparticles (NPs) embedded in graphitic-carbon nitride (g-C3N4) sheets for breast cancer cells. The synthesis of these sheets was carried out by a simple co-precipitation method. The physicochemical and thermal properties of the composite sheets were studied using various characterization techniques. The powder X-ray diffraction and high-resolution transmission electron microscopy analyses confirmed the hexagonal wurtzite phase of the ZnO nanoparticles, which were randomly distributed on the g-C3N4 nanosheets, generating a finely bonded interface between the two components. The X-ray photoelectron spectroscopy analysis confirmed the successful formation of the g-C3N4@ZnO composite, while the thermal studies revealed the thermal stability of the composite. In addition, the drug release and kinetics studies proved that the release of curcumin was more significant under acidic conditions (pH 5) compared with neutral pH (7.4). Further, the biological assays verified the antibacterial activity (against two different cultures of E. coli and S. aureus) and anticancer activity (against MDA-MB-231 cancer cells) of the g-C3N4@ZnO/C nanocomposite. Finally, the lactate dehydrogenase activity assay presented the cytotoxic assessment of the nanocomposite based on its cytoplasmic activity and the extent of enzymes released from the damaged cells.

Enhancement of Catalytic Activity on Crude Palm Oil Hydrocracking over SiO2/Zr Assisted with Potassium Hydrogen Phthalate.

In this study, the catalytic activity of bifunctional SiO2/Zr catalysts prepared by template and chelate methods using potassium hydrogen phthalate (KHF) for crude palm oil (CPO) hydrocracking to biofuels was investigated. The parent catalyst was successfully prepared by the sol-gel method, followed by the impregnation of zirconium using ZrOCl2·8H2O as a precursor. The morphological, structural, and textural properties of the catalysts were examined using several techniques, including electron microscopy energy-dispersive X-ray with mapping, transmission electron microscopy, X-ray diffraction, particle size analyzer (PSA), N2 adsorption-desorption, Fourier transform infrared-pyridine, and total and surface acidity analysis using the gravimetric method. The results showed that the physicochemical properties of SiO2/Zr were affected by different preparation methods. The template method assisted by KHF (SiO2/Zr-KHF2 and SiO2-KHF catalysts) provides a porous structure and high catalyst acidity. The catalyst prepared by the chelate method assisted by KHF (SiO2/Zr-KHF1) exhibited excellent Zr dispersion toward the SiO2 surface. The modification remarkably enhanced the catalytic activity of the parent catalyst in the order SiO2/Zr-KHF2 > SiO2/Zr-KHF1 > SiO2/Zr > SiO2-KHF > SiO2, with sufficient CPO conversion. The modified catalysts also suppressed coke formation and resulted in a high liquid yield. The catalyst features of SiO2/Zr-KHF1 promoted high-selectivity biofuel toward biogasoline, whereas SiO2/Zr-KHF2 led to an increase in the selectivity toward biojet. Reusability studies showed that the prepared catalysts were adequately stable over three consecutive runs for CPO conversion. Overall, SiO2/Zr prepared by the template method assisted by KHF was chosen as the most prominent catalyst for CPO hydrocracking.

Z-scheme NiO/g-C3N4 nanocomposites prepared using phyto-mediated nickel nanoparticles for the efficient photocatalytic degradation.

Highly-effective photocatalyst of NiO/g-C3N4 with was successfully synthesized by using phyto-mediated-synthesized nickel nanoparticles. The preparation was initiated by synthesizing nickel nanoparticles by using Tinosphora cordifolia stem extract under ultrasound-assisted method followed by the dispersing onto g-C3N4 structure. The study focused on physicochemical characterization and photocatalytic activity as function of the percentage of Ni in the nanocomposite. The photocatalytic activity examinations were carried out to rhodamine B and tetracycline photocatalytic oxidation. The results demonstrated that graphitic carbon nitride is effectively improved the photocatalytic activity of NiO for both photocatalytic oxidation reactions. From the varied Ni content of 5; 10; and 20 %wt., it was also found that the highest photoactivity was achieved by the composite having 10 %wt. of nickel content. The high effectivity was showed by degradation efficiency of 95% toward Rhodamine B and 98% toward tetracycline. The examination on effect of scavengers suggests that Z-scheme involved in the photocatalytic mechanism which facilitated the efficient separation of the photogenerated electron-hole pairs under visible light illumination. In summary, the present findings provide a green approach for fabricating the effective photocatalysts for organic contaminant degradation.

Controlled Growth of Semiconducting ZnO Nanorods for Piezoelectric Energy Harvesting-Based Nanogenerators.

Zinc oxide (ZnO) nanorods have attracted considerable attention in recent years owing to their piezoelectric properties and potential applications in energy harvesting, sensing, and nanogenerators. Piezoelectric energy harvesting-based nanogenerators have emerged as promising new devices capable of converting mechanical energy into electric energy via nanoscale characterizations such as piezoresponse force microscopy (PFM). This technique was used to study the piezoresponse generated when an electric field was applied to the nanorods using a PFM probe. However, this work focuses on intensive studies that have been reported on the synthesis of ZnO nanostructures with controlled morphologies and their subsequent influence on piezoelectric nanogenerators. It is important to note that the diatomic nature of zinc oxide as a potential solid semiconductor and its electromechanical influence are the two main phenomena that drive the mechanism of any piezoelectric device. The results of our findings confirm that the performance of piezoelectric devices can be significantly improved by controlling the morphology and initial growth conditions of ZnO nanorods, particularly in terms of the magnitude of the piezoelectric coefficient factor (d33). Moreover, from this review, a proposed facile synthesis of ZnO nanorods, suitably produced to improve coupling and switchable polarization in piezoelectric devices, has been reported.

Sensor to Electronics Applications of Graphene Oxide through AZO Grafting.

Graphene is a two-dimensional (2D) material with a single atomic crystal structure of carbon that has the potential to create next-generation devices for photonic, optoelectronic, thermoelectric, sensing, wearable electronics, etc., owing to its excellent electron mobility, large surface-to-volume ratio, adjustable optics, and high mechanical strength. In contrast, owing to their light-induced conformations, fast response, photochemical stability, and surface-relief structures, azobenzene (AZO) polymers have been used as temperature sensors and photo-switchable molecules and are recognized as excellent candidates for a new generation of light-controllable molecular electronics. They can withstand trans-cis isomerization by conducting light irradiation or heating but have poor photon lifetime and energy density and are prone to agglomeration even at mild doping levels, reducing their optical sensitivity. Graphene derivatives, including graphene oxide (GO) and reduced graphene oxide (RGO), are an excellent platform that, combined with AZO-based polymers, could generate a new type of hybrid structure with interesting properties of ordered molecules. AZO derivatives may modify the energy density, optical responsiveness, and photon storage capacity, potentially preventing aggregation and strengthening the AZO complexes. They are potential candidates for sensors, photocatalysts, photodetectors, photocurrent switching, and other optical applications. This review aimed to provide an overview of the recent progress in graphene-related 2D materials (Gr2MS) and AZO polymer AZO-GO/RGO hybrid structures and their synthesis and applications. The review concludes with remarks based on the findings of this study.

Hydrothermally synthesized titanium/hydroxyapatite as photoactive and antibacterial biomaterial.

The present work investigated hydrothermal synthesis of titanium/hydroxyapatite (Ti/HA) nanocomposite at varied Ti content. The synthesis was performed by coprecipitation method using CaO, ammonium dihydrogen phosphate and titanium oxide chloride precursor with the additional cetyl trimethyl ammonium chloride as templating agent, followed by hydrothermal treatment at 150 °C. The derived materials were characterized by x-ray diffraction, x-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy analyses. The photocatalytic properties of materials were tested on methyl violet (MV) photocatalytic oxidation, meanwhile the antibacterial testing was performed against Escherichia coli, Staphylococcus aureus, Klebsiella pneumonia, and Streptococcus pyogenes. In addition, cytotoxicity evaluation of the materials as potential biomaterial was also conducted. The results showed that physicochemical character of Ti/HA exhibits exhibit the excellent properties to be photocatalyst along with antibacterial activity. From the detail study of effect of varied titanium content ranging from 5 to 10 %wt., the increasing crystallite size of anatase phase of about 25.81 nm and 38.22 nm for Ti content of 5 and 10 % wt., respectively. In other side, the band gap energy value increases as the increasing Ti content, i.e. the values are 3.08; 3.18; and 3.20 eV for Ti content of 5, 10, 20 % wt., respectively. The band gap energy is correlated with the photocatalytic activity which the highest MV degradation was 96.46% over Ti/HA with 20% wt. of Ti (Ti20/HA). The nanocomposites also express the antibacterial activity with comparable minimum inhibitory concentration (MIC) with other similar Ti/HA nanocomposites. The MIC values of Ti20/HA against E. coli, S. aureus, K. pneumonia, and S. pyogenes are 25; 25; 50 and 50 µg/mL, respectively. In addition, the cytotoxicity test revealed the potency to be a biomimetic material as shown by severe toxicity.

Recent Progress on Functionalized Graphene Quantum Dots and Their Nanocomposites for Enhanced Gas Sensing Applications.

Gas-sensing technology has witnessed significant advancements that have been driven by the emergence of graphene quantum dots (GQDs) and their tailored nanocomposites. This comprehensive review surveys the recent progress made in the construction methods and applications of functionalized GQDs and GQD-based nanocomposites for gas sensing. The gas-sensing mechanisms, based on the Fermi-level control and charge carrier depletion layer theory, are briefly explained through the formation of heterojunctions and the adsorption/desorption principle. Furthermore, this review explores the enhancements achieved through the incorporation of GQDs into nanocomposites with diverse matrices, including polymers, metal oxides, and 2D materials. We also provide an overview of the key progress in various hazardous gas sensing applications using functionalized GQDs and GQD-based nanocomposites, focusing on key detection parameters such as sensitivity, selectivity, stability, response and recovery time, repeatability, and limit of detection (LOD). According to the most recent data, the normally reported values for the LOD of various toxic gases using GQD-based sensors are in the range of 1-10 ppm. Remarkably, some GQD-based sensors exhibit extremely low detection limits, such as N-GQDs/SnO2 (0.01 ppb for formaldehyde) and GQD@SnO2 (0.10 ppb for NO2). This review provides an up-to-date perspective on the evolving landscape of functionalized GQDs and their nanocomposites as pivotal components in the development of advanced gas sensors.

Biosynthesised Silver Nanoparticles Loading onto Biphasic Calcium Phosphate for Antibacterial and Bone Tissue Engineering Applications.

Biphasic calcium phosphate (BCP) serves as one of the substitutes for bone as it consists of an intimate mixture of beta-tricalcium phosphate (ß-TCP) and hydroxyapatite (HAP) in different ratios. BCP, because of its inbuilt properties such as osteoconductivity, biocompatibility, and biostability in several clinical models serves as a bone substituent for orthopedic applications. Therefore, the present study aimed to assess the effectiveness of silver (Ag) nanoparticles (NPs) combined with BCP composites for the orthopedic sector of bone tissue regeneration and growth. In this regard, we first synthesized Ag-BCP microclusters by the double-emulsion method and then characterized the composite for various physicochemical properties, including the crystallinity and crystal structure, bonding and functionality, porosity, morphology, surface charges, topography, and thermal stability. In addition, the antibacterial activity of Ag-BCP was tested against gram-positive and gram-negative microorganisms such as Staphylococcus aureus, Candida albicans, and Escherichia coli. Finally, the cytocompatibility of Ag-BCP was confirmed against the fibroblast cells in vitro.

Nanocomposite of Nickel Nanoparticles-Impregnated Biochar from Palm Leaves as Highly Active and Magnetic Photocatalyst for Methyl Violet Photocatalytic Oxidation.

Photocatalysis has been recognized as a feasible method in water and wastewater treatment. Compared to other methods such as adsorption and chemical oxidation, the use of photocatalyst in the advanced oxidation processes gives benefits such as a longer lifetime of the catalyst and less consumable chemicals. Currently, explorations into low-cost, effective photocatalysts for organic contaminated water are being developed. Within this scheme, an easily separated photocatalyst with other functionality, such as high adsorption, is important. In this research, preparation of a magnetic nanocomposite photocatalyst based on agricultural waste, palm leaves biochar impregnated nickel nanoparticles (Ni/BC), was investigated. The nanocomposite was prepared by direct pyrolysis of palm leaves impregnated with nickel (II) chloride precursor. Furthermore, the physicochemical characterization of the material was performed by using an X-ray diffractometer (XRD), scanning electron microscopy-energy dispersive X-ray fluorescence (SEM-EDX), transmission electron microscopy (TEM), gas sorption analysis, X-ray photoelectron spectroscopy (XPS) and vibrating sample magnetometer (VSM). The photocatalytic activity of Ni/BC was evaluated for methyl violet (MV) photocatalytic oxidation. The results from XRD, XPS and TEM analyses identified single nickel nanoparticles dispersed on the biochar structure ranging from 30-50 nm in size. The dispersed nickel nanoparticles increased the BET specific surface area of biochar from 3.92 m2/g to 74.12 m2/g oxidation. High photocatalytic activity of the Ni/BC was exhibited by complete MV removal in 30 min for the concentration ranging from 10-80 mg/L. In addition, the Ni/BC showed stability in the pH range of 4-10 and reusability without any activity change until fifth usage. The separable photocatalyst is related to magnetism of about 13.7 emu/g. The results highlighted the role of biochar as effective support for Ni as photoactive material.

Pathological Features and Neuroinflammatory Mechanisms of SARS-CoV-2 in the Brain and Potential Therapeutic Approaches.

The number of deaths has been increased due to COVID-19 infections and uncertain neurological complications associated with the central nervous system. Post-infections and neurological manifestations in neuronal tissues caused by COVID-19 are still unknown and there is a need to explore how brainstorming promoted congenital impairment, dementia, and Alzheimer's disease. SARS-CoV-2 neuro-invasion studies in vivo are still rare, despite the fact that other beta-coronaviruses have shown similar properties. Neural (olfactory or vagal) and hematogenous (crossing the blood-brain barrier) pathways have been hypothesized in light of new evidence showing the existence of SARS-CoV-2 host cell entry receptors into the specific components of human nerve and vascular tissue. Spike proteins are the primary key and structural component of the COVID-19 that promotes the infection into brain cells. Neurological manifestations and serious neurodegeneration occur through the binding of spike proteins to ACE2 receptor. The emerging evidence reported that, due to the high rate in the immediate wake of viral infection, the olfactory bulb, thalamus, and brain stem are intensely infected through a trans-synaptic transfer of the virus. It also instructs the release of chemokines, cytokines, and inflammatory signals immensely to the blood-brain barrier and infects the astrocytes, which causes neuroinflammation and neuron death; and this induction of excessive inflammation and immune response developed in more neurodegeneration complications. The present review revealed the pathophysiological effects, molecular, and cellular mechanisms of possible entry routes into the brain, pathogenicity of autoantibodies and emerging immunotherapies against COVID-19.

Green Synthesis of Antibacterial Nanocomposite of Silver Nanoparticle-Doped Hydroxyapatite Utilizing Curcuma longa Leaf Extract and Land Snail (Achatina fulica) Shell Waste.

Preparation of green synthesized silver nanoparticle (AgNPs)-doped hydroxyapatite (Ag/HA) utilizing Curcuma longa leaf extract and land snail (Achatina fulica) shell waste was performed. Physicochemical characteristics and antibacterial activity of Ag/HA composite as a function of Ag content was studied. Instrumental analysis such as XRD, SEM-EDX, TEM, and XPS were employed to characterize the nanocomposites. The physicochemical study revealed the maintained porous structure of HA after Ag immobilization, and from TEM analyses, it was found that the distributed spherical particles are associated with the dispersed Ag and have a particle diameter of around 5-25 nm. Antibacterial activity of the nanocomposite was evaluated against Escherichia coli, Staphylococcus aureus, Kliebsiella, pneumonia, and Streptococcus pyogenes. The results showed that the varied Ag content (1.0; 1.6; and 2.4% wt) influenced the nanoparticle distribution in the nanocomposite and enhanced the antibacterial feature.

A Review on Recent Progress of Stingless Bee Honey and Its Hydrogel-Based Compound for Wound Care Management.

Stingless bee honey has a distinctive flavor and sour taste compared to Apis mellifera honey. Currently, interest in farming stingless bees is growing among rural residents to meet the high demand for raw honey and honey-based products. Several studies on stingless bee honey have revealed various therapeutic properties for wound healing applications. These include antioxidant, antibacterial, anti-inflammatory, and moisturizing properties related to wound healing. The development of stingless bee honey for wound healing applications, such as incorporation into hydrogels, has attracted researchers worldwide. As a result, the effectiveness of stingless bee honey against wound infections can be improved in the future to optimize healing rates. This paper reviewed the physicochemical and therapeutic properties of stingless bee honey and its efficacy in treating wound infection, as well as the incorporation of stingless bee honey into hydrogels for optimized wound dressing.

Enhanced Photocatalytic Activity of Zn-Al Layered Double Hydroxides for Methyl Violet and Peat Water Photooxidation.

Zn-Al Layered Double Hydroxides (Zn-Al LDHs) and its calcined form were successfully prepared and utilized for the removal of methyl violet (MV) and treatment of peat water by photocatalytic oxidation. The research was aimed to evaluate the effect of calcination to Zn-Al LDHs for the effect on the physicochemical character and the capability as a photocatalyst. The characterization of the samples was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer-Emmet-Teller specific surface area (BET), and X-ray photoelectron spectroscopy (XPS). The results showed that the increased BET specific surface area along with the enhanced porous structure was achieved by the calcination procedure, which is associated with the enhanced interlayer space of d003 identified by XRD analysis. Thermal conversion showed an influence to the increased band gap energy from 3.10 eV in the uncalcined Zn-Al LDHs into 3.16 eV for the calcined material. These character changes contributed to the enhanced photocatalytic activity of the Zn-AL LDHs by calcination, which was proposed and verified by experiments. It was observed that photocatalytic activity of the material for MV gave about a 45.57% removal of MV and a 68% removal for the natural organic material of the peat water.

Synthesis of Polyaniline Supported CdS/CdS-ZnS/CdS-TiO2 Nanocomposite for Efficient Photocatalytic Applications.

Photocatalytic degradation can be increased by improving photo-generated electrons and broadening the region of light absorption through conductive polymers. In that view, we have synthesized Polyaniline (PANI) with CdS, CdS-ZnS, and CdS-TiO2 nanocomposites using the chemical precipitation method, characterized and verified for the photo-degradation of Acid blue-29 dye. This paper provides a methodical conception about in what way conductive polymers "PANI" enhances the performance rate of composite photocatalysts (CdS, CdS-ZnS and CdS-TiO2). The nanocomposites charge transfer, molar ratio, surface morphology, particle size, diffraction pattern, thermal stability, optical and recombination of photo-generated charge carrier properties were determined. The production of nanocomposites and their efficient photocatalytic capabilities were observed. The mechanism of photocatalysis involved with PC, CZP and CTP nanocomposites are well presented by suitable diagrams representing the exchange of electrons and protons among themselves with supported equations. We discovered that increasing the number of nanocomposites in the membranes boosted both photocatalytic activity and degradation rate. CdS-Zinc-PANI (CZP) and CdS-TiO2-PANI(CTP) nanocomposites show entrapment at the surface defects of Zinc and TiO2 nanoparticles due to the demolition of unfavorable electron kinetics, and by reducing the charge recombination, greater photocatalytic activity than CdS-PANI (CP) with the same nanoparticle loading was achieved. With repeated use, the photocatalysts' efficiency dropped very little, hinting that they may be used to remove organic pollutants from water. The photocatalytic activity of CZP and CTP photocatalytic membranes was greater when compared to CdS-PANI, which may be due to the good compatibility between CdS and Zinc and TiO2, as well efficient charge carrier separation. PANI can also increase the split-up of photo-excited charge carriers and extend the absorption zone when combined with these nanoparticles. As a result, the development of outrageous performance photocatalysts and their potential uses in ecological purification and solar power conversion has been facilitated. The novelty of this article is to present the degradation of AB-29 Dye using nanocomposites with polymers and study the enhanced degradation rate. Few studies have been carried out on polymer nanocomposites and their application in the degradation of AB-29 dyes and remediation of water purposes. Nanoparticle CdS is a very effective photocatalyst, commonly used for water purification along with nanoparticle ZnS and TiO2; but cadmium ion-leaching makes it ineffective for practical and commercial use. In the present work, we have reduced the leaching of hazardous cadmium ions by trapping them in a polyaniline matrix, hence making it suitable for commercial use. We have embedded ZnS and TiO2 along with CdS in a polyaniline matrix and compared their photocatalytic activity, stability, and reusability, proving our nano-composites suitable for commercial purposes with enhanced activities and stabilities, which is a novelty. All synthesized nanocomposites are active within the near-ultraviolet to deep infrared (i.e., 340-850 nm). This gives us full efficiency of the photocatalysts in the sunlight and further proves the commercial utility of our nanocomposites.

Photocatalytic activity of CuO nanoparticles for organic and inorganic pollutants removal in wastewater remediation.

Heterogeneous photocatalysis is a promising technology for eradicating organic, inorganic, and microbial pollutants in water and wastewater remediation. It is a more preferable method to other conventional wastewater treatment approaches on account of its low cost, environmental benignity, ability to proceed at ambient temperature and pressure conditions, and capability to completely degrade pollutants under appropriate conditions into environmentally safe products. In heterogeneous photocatalysis, pollutant removal is mainly induced by in-situ generated reactive radicals and their subsequent attack when energetic radiation impinges on the semiconductor catalyst. As such, for the effective and economical removal of wastewater pollutants, the employed catalyst should have high photonic efficiency, less toxic, abundant, chemically and photochemically stableand visible light active. Copper (II) oxide (CuO) is one among such promising compounds and its photocatalytic performance has been hampered primarily by rapid recombination and slow mobility of photogenerated charge carriers. So, this review provides an overview of the strategies adopted to mitigate the aforementioned drawbacks and also other operational parameters to boost its catalytic activity towards the elimination of toxic organic and inorganic metal ion contaminants in an aqueous media.

Enhanced photocatalytic degradation of Acid Blue dye using CdS/TiO2 nanocomposite.

Photocatalytic degradation is essential for the successful removal of organic contaminants from wastewater, which is important for ecological and environmental safety. The advanced oxidation process of photocatalysis has become a hot topic in recent years for the remediation of water. Cadmium sulphide (CdS) nanostructures doped with Titanium oxide (CdS/TiO2) nanocomposites has manufactured under ambient conditions using a simple and modified Chemical Precipitation technique. The nanocomposites crystal structure, thermal stability, recombination of photo-generated charge carriers, bandgap, surface morphology, particle size, molar ratio, and charge transfer properties are determined. The production of nanocomposites (CdS-TiO2) and their efficient photocatalytic capabilities are observed. The goal of the experiment is to improve the photocatalytic efficiency of TiO2 in the visible region by doping CdS nanocomposites. The results showed that as-prepared CdS-TiO2 nanocomposites has exhibited the highest photocatalytic activity in the process of photocatalytic degradation of AB-29 dye, and its degradation efficiency is 84%. After 1 h 30 min of visible light irradiation, while CdS and TiO2 showed only 68% and 09%, respectively. The observed decolorization rate of AB-29 is also higher in the case of CdS-TiO2 photocatalyst ~ 5.8 × 10-4mol L-1 min-1) as compared to the reported decolorization rate of CdS ~ 4.5 × 10-4mol L-1 min-1 and TiO2 ~ 0.67 × 10-4mol L-1 min-1. This increased photocatalytic effectiveness of CdS-TiO2 has been accomplished by reduced charge carrier recombination as a result of improved charge separation and extension of TiO2 in response to visible light.