Photodegrading rhodamine B dye with cobalt ferrite-graphitic carbon nitride (CoFe2O4/g-C3N4) composite.

The present research utilizes a sol-gel approach to create a CoFe2O4/g-C3N4 nanocomposite (NC) and explored several analytical methods to evaluate physical, chemical and optical based characteristics via XRD, FTIR, UV-vis, SEM/EDS and XPS for the prepared pure CoFe2O4, g-C3N4, and CoFe2O4/g-C3N4 NC. The XRD results show that the prepared g-C3N4, CoFe2O4, exhibits hexagonal and cubic phases respectively, whereas the g-C3N4/CoFe2O4 NC exhibit mixing of two phases. The energy band gaps for pure g-C3N4, CoFe2O4 and g-C3N4/CoFe2O4 NC values are viz., 2.75, 1.3, and 2.4 eV. As photocatalysts, synthesized materials were utilized for the decomposition of Rhodamine-B (RhB) dye. Finally, the CoFe2O4/g-C3N4 NC showed good performance of photocatalysis for RhB dye disintegration under the stimulus of visible light. According to the induced visible light, the rate at which the photocatalytic degradation occurs for the CoFe2O4/g-C3N4 NC was found to be 57% in 120 min and this is greater when compared with pure catalysts like CoFe2O4 (28%) and g-C3N4 (10%). These outcomes suggest that the prepared NC have efficiently worked during the photocatalytic process compared with its pure materials.

Microplastics in marine ecosystems: A comprehensive review of biological and ecological implications and its mitigation approach using nanotechnology for the sustainable environment.

Microplastic contamination has rapidly become a serious environmental issue, threatening marine ecosystems and human health. This review aims to not only understand the distribution, impacts, and transfer mechanisms of microplastic contamination but also to explore potential solutions for mitigating its widespread impact. This review encompasses the categorisation, origins, and worldwide prevalence of microplastics and methodically navigates the complicated structure of microplastics. Understanding the sources of minute plastic particles infiltrating water bodies worldwide is critical for successful removal. The presence and accumulation of microplastics has far reaching negative impacts on various marine creatures, eventually extending its implications to human health. Microplastics are known to affect the metabolic activities and the survival of microbial communities, phytoplankton, zooplankton, and fauna present in marine environments. Moreover, these microplastics cause developmental abnormalities, endocrine disruption, and several metabolic disorders in humans. These microplastics accumulates in aquatic environments through trophic transfer mechanisms and biomagnification, thereby disrupting the delicate balance of these ecosystems. The review also addresses the tactics for minimising the widespread impact of microplastics by suggesting practical alternatives. These include increasing public awareness, fostering international cooperation, developing novel cleanup solutions, and encouraging the use of environment-friendly materials. In conclusion, this review examines the sources and prevalence of microplastic contamination in marine environment, its impacts on living organisms and ecosystems. It also proposes various sustainable strategies to mitigate the problem of microplastics pollution. Also, the current challenges associated with the mitigation of these pollutants have been discussed and addressing these challenges require immediate and collective action for restoring the balance in marine ecosystems.

Coastal aquatic pollutants degradation using ZnCo2O4 nanorods.

Water pollution has caused problems in coastal areas, rivers, lakes, and other important water sources around the world as a result of inappropriate waste management. Meanwhile, these pollutants are harmful to humans and aquatic life. Textile dye effluent methyl orange (MO) was used in this work for dye degradation studies employing nanocomposites. As a result, the importance of synthesizing pure ZnO and Co3O4 nanoparticles with composites of ZnCo2O4 (zinc cobaltite) nanorods in three various proportions (90:10, 75:25, and 50:50) is emphasized in this study. Many advanced approaches were used to assess the various features of these materials, including size and shape. Fourier transform infrared (FT-IR) spectroscopy was used to determine the vibrational modes of the materials. The absorption measurements were then carried out using UV-vis spectroscopic techniques, and the photocatalytic breakdown of MO was done under visible light irradiation. The findings revealed that pure materials were inadequate for visible light activity, resulting in decreased degradation efficiencies. Spinel cobaltite structures have potential degradation efficiency under visible light, while ZnCo2O4 (50:50) catalyst has superior degradation efficiency of 59.8% over MO. The crystallite size, morphology, functional group, absorption wavelength, and band gap all play important roles in enhancing the material's photocatalytic activity under visible light. Meanwhile, ZnCo2O4 spinel structures are crucial for increasing charge carriers and reducing electron-hole recombination. As a result, zinc cobaltite minerals are widely used in industrial dye degradation applications.

Support based metal incorporated layered nanomaterials for photocatalytic degradation of organic pollutants.

An effective approach to producing sophisticated miniaturized and nanoscale materials involves arranging nanomaterials into layered hierarchical frameworks. Nanostructured layered materials are constructed to possess isolated propagation assets, massive surface areas, and envisioned amenities, making them suitable for a variety of established and novel applications. The utilization of various techniques to create nanostructures adorned with metal nanoparticles provides a secure alternative or reinforcement for the existing physicochemical methods. Supported metal nanoparticles are preferred due to their ease of recovery and usage. Researchers have extensively studied the catalytic properties of noble metal nanoparticles using various selective oxidation and hydrogenation procedures. Despite the numerous advantages of metal-based nanoparticles (NPs), their catalytic potential remains incompletely explored. This article examines metal-based nanomaterials that are supported by layers, and provides an analysis of their manufacturing, procedures, and synthesis. This study incorporates both 2D and 3D layered nanomaterials because of their distinctive layered architectures. This review focuses on the most common metal-supported nanocomposites and methodologies used for photocatalytic degradation of organic dyes employing layered nanomaterials. The comprehensive examination of biological and ecological cleaning and treatment techniques discussed in this article has paved the way for the exploration of cutting-edge technologies that can contribute to the establishment of a sustainable future.

Progressive yield of nickel cobaltite nanocubes for visible light utilization and degrading activities of methyl orange dye pollutant.

In this study, pure cobalt oxide (Co3O4) as well as nickel cobaltite (NiCo2O4) were investigated with their capacity of degradation efficiency for textile dyes like methyl orange (MO) employing visible light irradiation. Two variable concentrations of nickel cobaltite (NiCo2O4) with 75:25 and 50:50 wt ratios along with the pure metal oxides were synthesized by thermal decomposition method and analyzed by various sophisticated instruments. Initially, the structural characteristics described the fine crystalline nature of NiCo2O4 and also exhibits reduced size than the pure component material (Co3O4). Besides, NiCo2O4 catalysts represented nano cubic shaped particles, and also their coordinating functional groups were evaluated. Further, the absorption wavelength confirms the two band positions of NiCo2O4 which leads to promote visible light absorption, and degrading efficiency of about 47.5% for NiCo2O4 (75:25) sample compared with NiCo2O4 (50:50) which produced only 26.3% degradation. This higher efficiency of the former was due to high crystallinity and interfacial charge transfer of combined Ni2+, Ni3+, Co2+ and Co3+ redox couples. This consecutively produces effective OH radicals that brought the degradation effectively under visible light. The recycling capacity up to 5 repeated cycles has been studied with the NiCo2O4 (75:25) and therefore the catalyst can further be used in other dye degradation.

Biochar supported nano core-shell (TiO2/CoFe2O4) for wastewater treatment.

The porous structure of biochar, its large surface area, and its anti-oxidant properties are extensively used for pollutant removal strategies. The literature to date has reported that the biochar assisted metal-oxide core-shells have a dominating degradation ability under solar irradiation. Therefore, this study is significantly focused on cinnamon biochar as an active anti-oxidant agent incorporated in titania-cobalt ferrite nanocore-shell (Biochar/TiO2/CoFe2O4) structures for the first time in wastewater treatment against chlorophenol pollutants. Pure materials, core-shells, and biochar aided composites were synthesized by chemical methods, and their characteristics were analyzed using various instrumentation techniques. The diffraction outcomes of Biochar/TiO2/CoFe2O4 showed the mixed phases containing biochar, TiO2, and CoFe2O4. The morphological characteristics revealed that the biochar creates porosity and a peripheral layer covering the core-shell. Meanwhile, absorption studies of TiO2/CoFe2O4 core-shell and Biochar/TiO2/CoFe2O4 samples achieved 65% and 92% degradation efficiencies when exposed to visible light against chlorophenol pollutants, respectively. All these results confirm the presence of distinct functional groups as well as the combined synergistic effects that activated the charge separation, resulting in the successful destruction of water pollutants. In addition, the highly efficient Biochar/TiO2/CoFe2O4 sample was recycled, and the efficiency was maintained stable for five repeated degradation processes. Thus, Biochar/TiO2/CoFe2O4 will be utilized to expand the possibilities for biofuel generation and energy storage devices.

Selective removal of copper (II) ions from aqueous solution using pyridyl-bridged mesoporous organosilica hybrid adsorbent.

The incorporation of active functional groups into the mesoporous organosilica hybrid materials is efficient for various applications. A newly designed mesoporous organosilica adsorbent was prepared using diaminopyridyl groups bridged-(bis-trimethoxy)organosilane (DAPy) precursor by using Pluronic P123 as structure directing template via sol-gel co-condensation method. The hydrolysis reaction of DAPy precursor and tetraethyl orthosilacate (TEOS) with a DAPy content of about 20 mol% to TEOS were incorporated into the mesopore walls of the mesoporous organosilica hybrid nanoparticles (DAPy@MSA NPs). Low-angle XRD and FT-IR, N2 adsorption-desorption analysis, SEM, TEM, and TG analysis were used to characterize the synthesized DAPy@MSA NPs. The DAPy@MSA NPs exhibit an order mesoporous structure with a high surface area, mesopore size and pore volume of approximately ∼465 m2/g, 4.4 nm and 0.48 cm3/g, respectively. The pyridyl groups integrated DAPy@MSA NPs showed the selective adsorption of Cu2+ ions from the aqueous medium by metal-ligand complex coordination of Cu2+ ions with the integrated pyridyl groups and the pendant hydroxyl (-OH) functional groups present into the mesopore walls of the DAPy@MSA NPs. In the presence of other competitive metal ions (Cr2+, Cd2+, Ni2+, Zn2+, and Fe2+), the DAPy@MSA NPs showed relatively high adsorption of Cu2+ ions (276 mg/g) from aqueous solution as compared to the other competitive metal ions at the same concentration (100 mg/L) of initial metal ion solution.

Smart and sensitive nanomaterial-based electrochemical sensor for the determination of a poly (ADP-ribose) polymerase (PARP) inhibitor anticancer agent.

In this research, we propose a novel approach for constructing a sensitive and selective electrochemical sensor utilizing high-quality multi-walled carbon nanotubes functionalized with amino groups (MWCNT-NH2) for the detection of Talazoparib (TLZ), a poly (ADP-ribose) polymerase (PARP) enzyme inhibitor, in real samples. The MWCNT-NH2-based sensor exhibited remarkable performance characteristics, including excellent repeatability, reproducibility, and high selectivity against various interferences. Under optimized conditions, the sensor demonstrated a wide linear concentration range of 1.0-5.0 µM, with a low limit of detection (LOD) of 0.201 µM. Substantiated by rigorous analysis of pharmaceutical and biological matrices, our methodology emerges as a paragon of reliability, boasting recovery rates within the satisfactory bracket of 96.38-105.25%. The successful application of the MWCNT-NH2-based sensor in practical sample analysis highlights its potential for implementation in clinical and pharmaceutical settings. This research not only advances the application of MWCNT-NH2 in electrochemical sensing but also opens new avenues for the development and monitoring of innovative anticancer treatments. The insights gained from our study have far-reaching implications, pointing toward a future where precision and innovation converge to improve patient care and treatment outcomes.

A mechanothermal approach for the synthesis of Fe3O4 nanoparticles as dopant on mesoporous TiO2 for electrochemical determination of catechol.

The subject of water contamination and how it gets defiled to the society and humans is confabulating from the past decades. Phenolic compounds widely exist in the water sources and it is emergent to determine the toxicity in natural and drinking water, because it is hazardous to the humans. Among these compounds, catechol has sought a strong concern because of its rapid occurrence in nature and its potential toxicity to humans. The present work aims to develop an effective electrochemical sensing of catechol using mesoporous structure of Fe3O4-TiO2 decorated on glassy carbon (GC) electrode. The creation of pure TiO2 using the sol-gel technique was the first step in the synthesis protocol for binary nanocomposite, which was then followed by the loading of Fe3O4 nanoparticles on the surface of TiO2 using the thermal decomposition method. The resultant Fe3O4-TiO2 based nanocomposite exhibited mesoporous structure and the cavities were occupied with highly active magnetite nanoparticles (Fe3O4) with high specific surface area (90.63 m2/g). When compared to pure TiO2, catechol showed a more prominent electrochemical response for Fe3O4-TiO2, with a significant increase in anodic peak current at a lower oxidation potential (0.387 V) with a detection limit of 45 µM. Therefore, the prepared magnetite binary nanocomposite can serve as an efficient electroactive material for sensing of catechol, which could also act as a promising electrocatalyst for various electrocatalytic applications.

Mesoporous NiO/Ni2O3 nanoflowers for favorable visible light photocatalytic degradation of 4-chlorophenol.

The present study highlights the treatment of industrial effluent, which is one of the most life-threatening factors. Herein, for the first time, two types of NiO (green and black) photocatalysts were prepared by facile chemical precipitation and thermal decomposition methods separately. The synthesized NiO materials were demonstrated with various instrumental techniques for finding their characteristics. The X-ray diffraction studies (XRD) and X-ray photoelectron spectroscopy (XPS) revealed the presence of Ni2O3 in black NiO material. The transmission electron microscopic (TEM) images engrained the nanospherical shaped green NiO and nanoflower shaped black NiO/Ni2O3 materials. Further, the band gap of black NiO nanoflower was 2.9 eV compared to green NiO having 3.8 eV obtained from UV-vis spectroscopy. Meanwhile, both NiO catalysts were employed for visible light degradation, which yields a 60.3% efficiency of black NiO comparable to a 4.3% efficiency of green NiO within 180 min of exposure. The higher degrading efficiency of black NiO was due to the presence of Ni2O3 and the development of pores, which was evident from the Barrett-Joyner-Halenda (BJH) method. Type IV hysteresis was observed in black NiO nanoflowers with high surface area and pore size measurements. This black NiO/Ni2O3 synthesized from the thermal decomposition method has promoted better photocatalytic degradation of 4-chlorophenol upon exposure to visible light and is applicable for other industrial pollutants.

Multifunctional natural derived carbon quantum dots from Withania somnifera (L.) - Antiviral activities against SARS-CoV-2 pseudoviron.

Natural carbon dots (NCQDs) are expediently significant in the photo-, nano- and biomedical spheres owing to their facile synthesis, optical and physicochemical attributes. In the present study, three NCQDs are prepared and optimized from Withania somnifera (ASH) by one-step hydrothermal (bottom-up) method: HASHP (without dopant), nitrogen doped HASHNH3 (surface passivation using ammonia) and HASHEDA (surface passivation with ethylenediamine). The HR-TEM images reveal that HASHP, HASNH3, HASHEDA are spherically shaped with 2.5 ± 0.5 nm, 4 ± 1 nm and 5 ± 2 nm particle size, respectively, whereas FTIR confirms the aqueous solubility and nitrogen doping. The XRD patterns ensure that the NCQDs are amorphous and graphitic in nature. Comparatively, HASHNH3 (32.5%) and HASHEDA (27.6%) portray better fluorescence quantum yield than HASHP (5.6%). The increase in quantum yield for the doped NCQDs can be attributed to the surface passivation using ammonia and ethylenediamine. Surface passivation plays a crucial role in enhancing the fluorescence properties of quantum dots. The introduction of nitrogen through ammonia and ethylenediamine provides additional electronic states, possibly reducing non-radiative recombination sites and hence boosting the QY. In addition, an antiviral study unveils the striking potential of surface passivated NCQDs to curb Covid-19 crises with around 85% inhibition of SARS-CoV pseudoviron cells, which is better in comparison to the non-doped NCQDs. Hence, to understand the paramount efficacy of these NCQDs, a hypothesis on their possible mechanism of action against Covid-19 is discussed.

Occurrences and removal of pharmaceutical and personal care products from aquatic systems using advanced treatment- A review.

Pharmaceuticals, personal care items, steroid hormones, and agrochemicals are among the synthetic and indigenous products that make up micropollutants, also known as emerging contaminants. Pharmaceutical and personal care products (PPPs) are a class of developing micropollutants that can harm living organisms even at low concentrations. Many are detected in surface water and wastewater from the treatment process, with quantities ranging from ng L-1 to gL-1; however, residual PPPs at dangerously high levels have indeed recently been recognized in the ecosystem. Residential sewage treatment plant (STP) dump the largest majority of these pollutants into the environment on a regular basis. As a result of its robust structure, it has a longer lifespan in the environment. This review article discusses how surface water pollutants such pesticides, petroleum hydrocarbons, and perfluorinated compounds affect water quality, as well as the most cost-effective adsorbents for removing these PPPs. The goal of this study is to provide information about the origins of PPP, as well as diagnostic procedures and treatment options. Research on developing contaminants is also aimed at evaluating the efficacy and affordability of adsorption.

Existence of Ti3+ and dislocation on nanoporous CdO-TiO2 heterostructure applicable for degrading chlorophenol pollutant.

This study addresses the significance of wastewater recuperation by a simple and facile treatment process known as photocatalyst technology using visible light. Titanium di-oxide (TiO2) is the most promising photocatalyst ever since longing decades, has good activity under UV light, owing to its small band gap. Hence, TiO2 has been modified with metal oxides for the positive response against visible light. Since this is an efficient process, the novelty has been made on nanometal oxide CdO (cadmium oxide) combined with TiO2 to acquire the best efficiency of degrading organic chlorophenol contaminant. Initially, the composites were synthesized by sol-gel and thermal decomposition methods and investigated for their various outstanding properties. The characterized outcomes have exhibited heterostructures with reduced crystallite size from the X-ray diffraction studies. Then, the determination of nanoporous feature was recognized through HR-TEM analysis which was also detected with some dislocations. The EDX spectrum was identified the perfect elemental composition. The nitrogen adsorption-desorption equilibrium was attained that offers many pores measured with high surface area. The XPS result convinced that Ti3+ was accessible along with TIO2/CdO composite. Further the absorption towards higher wavelength was obtained from UV-vis spectra. Finally, for the photocatalytic application of chlorophenol, the composite shows higher percentage of degrading efficiencies than the pristine TiO2. The photocatalytic mechanism was discussed in detail.

Photocatalytic degradation of 2,4-dichlorophenol using bio-green assisted TiO2-CeO2 nanocomposite system.

In recent times, cost effective synthesis of semiconductor materials has been a subject of concern for the day to today applications. In this work, novelty has been made on the facile synthesis of metal oxides (TiO2 and CeO2) and nanocomposites (TiO2-CeO2) through sol-gel and precipitation methods of imparting lemon extract. The synthesized materials behave as the functional catalysts which has been further carried out for the photocatalytic degradation against 2,4-Dichlorophenol (2,4-DCP). The materials are then valued for the structural and optical properties. The lemon extract used in synthesis has played a premier role in upgrading the charge carrier separation, bandgap, and size reduction of the composite system. Further, the CeO2 supported TiO2 sample acts as the better visible light catalyst, due to the prevention of aggregation and existence of line dislocation that supported to access the additional electron trap sites.

Nanocarrier optimization: Encapsulating Hydrastis canadensis in chitosan nanoparticles for enhanced antibacterial and dye degradation performance.

This study focuses on the optimization of Hydrastis canadensis-based nanocarriers in environmental and microbial applications like antibacterial and dye degradation. Hydrastis canadensis (H. canadensis) is loaded into the nanocarrier using a gelation method. Characterization involves pH analysis, UV-VIS spectrophotometry, scanning electron microscopy, Fourier-transform infrared spectroscopy, dynamic light scattering, high-performance liquid chromatography, encapsulation efficiency. Further antimicrobial activity against Staphylococcus aureus and Escherichia coli were tested. Dye degradation was evaluated at concentrations of 1 % of high molecular (HM) and 1.5 % of low molecular (LM) chitosan nanoparticles with both 3C and 1000C concentrations of the drug. The obtained results confirm the presence of chitosan nanocarrier alongside the pure drug in 1 % HM and 1.5 % LM chitosan particles with a notable encapsulation efficiency activity in both 3C and 1000C concentrations. Antimicrobial studies were carried out using the agar well diffusion method and revealed a significant zone of inhibition of 20 mm and 25 mm for E. coli and S. aureus, respectively in chitosan nanocarrier-loaded samples compared to pure drug and chitosan nanocarriers samples. The dye degradation studies of four dyes methylene blue, methylene orange, methylene red, and safranin using both pure drugs and chitosan nanocarrier-loaded drugs showed the highest percentage of degradation (76 %) against methylene blue in the chitosan nanocarrier-drug loaded formulation. These findings cumulatively underscore chitosan nanoparticles can be used as an effective carrier for Hydrastis Canadensis, with enhanced antimicrobial and dye degradation capabilities. Varied concentrations and molecular weights highlight the versatility of the ionotropic gelation method in optimizing drug delivery. Enhanced efficacy of the nanocarrier was evident in the observed zone of inhibition in antimicrobial testing. The substantial degradation percentage in methylene blue emphasizes the formulation's applicability in environmental dye removal processes, with potential avenues for improvement explored through interactions between the chitosan nanocarrier and H. canadensis characteristics. Future investigations may focus on scaling up the optimized formulation for large-scale applications and exploring release kinetics and comprehensive toxicity assessments for a holistic understanding of potential environmental and biomedical implications.

The degradation of bisphenol-A organic pollutant using the dispersal of TiO2 nanorods onto the partial reduction of graphene oxide nanosheets.

The notion of innovative combinations of semiconducting metal oxides for photocatalytic destruction is a key factor in the removal of environmental contaminants. However, for the first time, the combination was made possible for the aforementioned reason by embedding one-dimensional titanium dioxide (TiO2) semiconductor nanorods on two-dimensional rGO (reduced graphene oxide) nanosheets utilizing hydrothermal and a modified Hummers' method. By applying several sophisticated procedures, the properties of these catalysts were found, and then the degradation of BPA (bisphenol-A) was examined with UV and visible light sources. Further, all the analyses were performed on pure TiO2 material. As a result of the synergistic interaction between TiO2 and rGO, the rGO-TiO2 catalyst produced a favorable photocatalytic outcome. The structural investigation of rGO-TiO2 has confirmed that the TiO2 was in anatase phase along with GO and rGO peaks, and the morphological characterization showed that the TiO2 nanorods were integrated randomly into the rGO nanosheets along with defective sites. Also, adding rGO to TiO2 causes charge separation, and π-π interactions to improve the visible light absorption range. In this study, the main model organic component in the photocatalytic degradation is bisphenol-A (BPA). During visible light irradiation, the OH radicals were finally produced by the redox reactions. Furthermore, the rGO surface adsorbs the phenol molecules due to graphene π-π interactions, thus narrowing the band gap and increasing the efficiency of BPA degradation.

Nanosized core-shell (NiFe2O4/TiO2) heterostructure for enhanced photodegradation against polycyclic aromatic hydrocarbons.

The global level of attention has been raised for photocatalytic pollutant removal technologies for degrading organic pollutants because of rising concerns about their toxicity. In this study, NiFe2O4/TiO2 core shells and pure samples of NiFe2O4 and TiO2 were synthesized using the sol-gel process and used to degrade naphthalene which is one among the polycyclic aromatic hydrocarbons (PAHs) pollutant. The synthesized materials were evaluated using a variety of analytical techniques, and the typical NiFe2O4/TiO2 core-shell results showed good purity and a lack of other impurity structures. Through morphological characterization, the core-shell structure of NiFe2O4/TiO2 has been established. However, the activity of visible light degradation was boosted by the generation of hydroxyl radicals after the electron-hole pair was delayed. Additionally, a lower band gap in NiFe2O4/TiO2 than in pure materials promotes photocatalytic activity. Similarly, photocatalytic naphthalene elimination by the core-shell achieved 67% efficiency after 150 min of visible light exposure. Furthermore, the produced core-shell has a high magnetic property, making separation from the photo-irradiated solutions easier; as a result, recycling was likely successful up to three cycles. The photocatalytic mechanism of the NiFe2O4/TiO2 composite was proposed. This research could also be applied to the degradation of other polycyclic aromatic hydrocarbon contaminants.

Facile synthesis of CuO/g-C3N4 nanolayer composites with superior catalytic reductive degradation behavior.

The cupric oxide (CuO) loaded graphitic carbon nitride (g-C3N4) nanocomposites (CuO/g-C3N4) were prepared by a facile calcination method. The formation of monoclinic CuO nanocrystals along with g-C3N4 was confirmed by X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopic analysis. X-ray photoelectron spectral (XPS) analysis further confirms the formation of CuO/g-C3N4. Distribution of CuO stone-like crystalline nanoparticles on g-C3N4 nanosheets was observed by transmission electron microscopic images. The influence of CuO loading on the optical property of g-C3N4 was determined by ultraviolet (UV)-visible absorption and photoluminescence (PL) spectral analysis. Band gap was decreased from 2.7 to 2.3 eV by the addition of CuO nanoparticles. The catalytic performance of the synthesized samples in 4-nitrophenol (4-NP) and methyl orange (MO) reduction was evaluated. The 5 wt% CuO/g-C3N4 showed 99.5% (7 min) and 99.7% (4 min) reduction efficiency for 4-NP and MO respectively. The 5 wt% CuO/g-C3N4 could become a potential catalyst in the chemical treatment of organic pollutants.

Nanocubic copper cobaltite for methyl orange degradation through photocatalytic process.

In this study, cubic spinel structured CuCo2O4 (Copper cobaltite) nanospheres were fabricated by thermal decomposition method. The visible light degradation of organic contaminant methyl orange (MO) was focused in this study using the synthesized pure CuO, Co3O4 and CuCo2O4 with different weight ratios of raw materials (90:10, 75:25 and 50:50). It could be well realized that after the characterization techniques, the synthesized CuCo2O4 materials resembled cubic spinel structure as confirmed by X-ray diffraction (XRD) investigation. Meanwhile, all the synthesized materials through transmission electron microscopy (TEM) have showed cubic shaped particles and among the CuCo2O4 materials, CuCo2O4 (50:50) expressed not as much of crystallinity due to the agglomerated nanospheres. On the other hand, well crystalline CuCo2O4 (75:25) displayed higher surface area than the other materials when analysed through Brunauer-Emmett-Teller (BET) method. The Fourier transform infra-red (FTIR) spectrum has evinced the formation of CuCo2O4 nanostructures. In addition, the cubic spinel structured CuCo2O4 provided positive results over visible light irradiation. Finally, the CuCo2O4 (75:25) sample has scored high as much of 85% MO degradation compared with others. This sample was progressed with repetitive recycling tests and presented the best photocatalytic degradation efficiency. The upgraded results of CuCo2O4 sample have been linked with the developed synergistic effects during the formation of binary metal oxides. Also, the interfacial electron-hole formation leads to the migration and hindering of charge carriers for visible light activity.

Harvesting visible light for enhanced catalytic degradation of wastewater using TiO2@Fe3O4 embedded on two dimensional reduced graphene oxide nanosheets.

Carbon-integrated binary metal oxide semiconductors have gained prominence in the last decade as a better material for photocatalytic wastewater treatment technology. In this regard, this research describes the investigation of the binary metal oxide TiO2@Fe3O4 embedded on reduced graphene oxide (rGO) nanosheets synthesized through a combination of sol-gel, chemical precipitation, and Hummer's processes. Besides, the catalyst is applied for the photocatalytic degradation of organic chlorophenol pollutants. The characterized diffraction results showed the peak broadening of the rGO-TiO2@Fe3O4 composite formed with tetragonal and cubic structures having small crystallite sizes. The TEM observation shows an enormous miniature of TiO2@Fe3O4 nanospheres spread on the folded 2D-rGO nanosheets with a large BET surface area. The XPS result holds the mixed phases of Fe3O4 and Fe2O3. Finally, the catalyst demonstrated a low band gap with extended light absorption towards visible light irradiation. The synergistic interactions between Fe3+ and Fe2+ improved the visible light activity due to the incorporation of rGO, and also possessed good recycling capacity. The increased mobility of electrons at the interfaces of TiO2 and Fe3O4 due to the mixing of rGO results in the separation of charge carriers by elevating the photocatalytic degradation efficiency of chlorophenol.