Fabrication,characterization, and photocatalytic performance of TiO<Subscript>2</Subscript> hybridized with SiO<Subscript>2</Subscript>

Nanostructures TiO₂–SiO₂ photocatalysts were successfully synthesized using the sol-gel method, hydro-calcination, co-precipitation and room-temperature solid-phase synthesis technology. X-ray powder diffraction pattern (XRD), Fourier transform infrared spectrum (FTIR), photoluminescence (PL) spectra, thermal analyses (TG–DTA), scanning electron micrographs (SEM), X-ray photoelectron spectroscopy (XPS), and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) were used to characterize the as-synthesized catalysts. Photocatalytic performances of the catalysts were evaluated by the degradation of methyl orange (MO) under s imulated natural light and the degradation rate of MO is 97.2%. The composites showed a good stability: after five recycling runs there are no significant decreases in the photocatalytic activity. The photodegradation of methylene blue, rhodamine B, methyl violet, naphthol green B, basic fuchsin, malachite green, and methyl red were also tested, and the degradation rate of dyes could reach over 94.2 %. A possible mechanism for the photocatalysis with the TiO₂–SiO₂ was proposed.     

ZnO-based ternary nanocomposite for decolorization of methylene blue by photocatalytic dynamic membrane

In this article, novel Ag–ZnO/g-C₃N₄/GO ternary nanocomposites were prepared via co-precipitation method by 1%w Ag, 50% w g-C₃N₄, 10% w GO concentration and applied in dynamic membranes. The characteristics of Ag–ZnO/g-C₃N₄/GO nanocomposite were evaluated by various techniques such as X-ray diffraction, field emission scanning electron microscopy, energy dispersive X-ray map, transmission electron microscopy, X-ray photoelectron spectroscopy, photocatalyst. The photocatalytic degradation of methylene blue was investigated under visible light. The photocatalytic efficiency of 93.43% for methylene blue degradation was obtained for Ag–ZnO/g-C₃N₄/GO nanocomposite after 50 min of irradiation, which was remarkably higher than that of pure ZnO, bare g-C₃N₄, Ag–ZnO, and Ag–ZnO/g-C₃N₄ at the same irradiation time. Likewise, in self-forming and pre-coated membranes, ternary nanocomposites can play a vital role in the membrane surface properties, as well as their decolorization performance. The rejection of methylene blue was 30% in pure polyethersulfone membrane, while the photocatalytic degradation of methylene blue in Ag–ZnO/g-C₃N₄/GO nanocomposites was 88.46% and 98.86% after 10 and 15 min of irradiation in both self-forming and pre-coated dynamic membranes, respectively. Experimental results show that the dynamic membrane possesses a higher ability for degradation of MB in a shorter period of time than the static system.     

Biosynthesis of silver and gold nanoparticles using Sargassum horneri extract as catalyst for industrial dye degradation

This study focuses on the green synthesis of silver and gold nanoparticles using the marine algae extract, Sargassum horneri, as well as the degradation of organic dyes using biosynthesized nanoparticles as catalysts. The phytochemicals of the brown algae Sargassum horneri acted as reducing and capping agents for nanoparticle synthesis. Ultraviolet–visible absorption spectroscopy, dynamic light scattering, high-resolution transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray spectroscopy, X-ray powder diffraction, and Fourier transform infrared spectroscopy were used to characterize the biosynthesized nanoparticles. The green-synthesized SH-AgNPs and SH-AuNPs exhibited high catalytic activity for degradation of organic dyes, such as methylene blue, rhodamine B, and methyl orange. The reduction reactions of dyes are based on pseudo-first-order kinetics.     

Enhanced Photocatalytic Degradation of Synthetic Dyes and Industrial Dye Wastewater by Hydrothermally Synthesized G–CuO–Co<Subscript>3</Subscript>O<Subscript>4</Subscript> Hybrid Nanocomposites Under Visible Light Irradiation

To enhance the degradation of colour and chemical oxygen demand using photocatalytic activity, Graphene–CuO–Co₃O₄ hybrid nanocomposites were synthesized using an in situ surfactant free facile hydrothermal method. The photocatalytic degradation of synthetic anionic dyes, methyl orange (MO) and Congo red (CR), and industrial textile wastewater dyes under visible light irradiation was evaluated. The synthesized nanocomposite was characterized structurally and morphologically using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, high-resolution transmission electron microscope, and Fourier transform infrared spectroscopy. Evaluation of the colour indicated complete removal at 15 min of irradiation for the MO and CR dyes, with 99% degradation efficiency. The reaction time for the primary effluent wastewater dye was 60 min for 81% dye removal. In contrast, a longer reaction time was required to meet the national discharge regulation for the raw wastewater dye, 300 min for 60% dye removal. The mechanism for dye degradation using the Graphene–CuO–Co₃O₄ hybrid nanocomposite was elucidated using the Langmuir–Hinshelwood model, and the rate constant and half-life of the degradation process were calculated. The results demonstrate that photocatalytic degradation using a hybrid nanocomposite and visible light irradiation is a sustainable alternative technology for removing colour from wastewater dye.     

Synthesis and photocatalytic properties of sunlight-responsive BiOBr–CoWO4 heterostructured nanocomposites

Efficient sunlight-responsive BiOBr–CoWO₄ heterostructured nanocomposite photocatalysts were prepared via a chemical precipitation route at 100°C in 4 hours. The prepared BiOBr–CoWO₄ heterostructures were characterized for phase identification, chemical composition, surface morphology, optical properties and surface area using various techniques. The X-ray diffraction pattern of the BiOBr–CoWO₄ nanocomposite was composed of diffraction peaks equivalent to both the tetragonal phase of BiOBr and the monoclinic phase of CoWO₄ nanoparticles. X-ray photoelectron spectral study of the BiOBr–CoWO₄ nanocomposite revealed orbitals of both BiOBr and CoWO₄ compounds. Transmission electron microscopy images revealed that spherical particles of CoWO₄ (20–25 nm) were dispersed on the surface of BiOBr. UV–visible–near-infrared spectral study of the BiOBr–CoWO₄ nanocomposite showed good visible-light absorption. Among the manufactured materials, BiOBr–CoWO₄-2 nanocomposite showed better charge carrier separation efficiency, as demonstrated by photoluminescence and time-resolved fluorescence. To study the practical utility of the prepared materials, their photocatalytic capability was examined for the degradation of rhodamine B (RhB) aqueous solution under sunlight irradiation. The photodegradation results showed that BiOBr–CoWO₄-2 nanocomposite degraded 98.69% RhB solution and the degradation constant was 0.067 min⁻¹, which was 5.6 and 22.5 times larger than that of pure BiOBr and CoWO₄ nanoparticles, respectively, after 60 minutes of sunlight irradiation. The superior photoactivity was facilitated by electron–hole pair separation and transfer driven by the heterostructure interface between BiOBr particles and CoWO₄ nanoparticles. The removal of RhB was initiated by photogenerated h⁺, O₂^{• −} and ^•OH reactive species based on the scavenger effect.     

TiO2 nanoparticles in mesoporous TUD-1: synthesis, characterization and photocatalytic performance in propane oxidation

A series of TiO2-TUD-1 samples was synthesized with a variable Ti loading in the range Si/Ti = 100, 20, 2.5, and 1.6, by using a one-pot surfactant-free procedure. The materials obtained were characterized by elemental analysis; X-ray diffraction (XRD); N2 sorption measurements; high-resolution TEM (HR-TEM); 29Si NMR, UV-visible and Raman spectroscopy. As a function of increasing metal loading either isolated Ti atoms, or (above a Ti loading of approximately 2.5 wt- %) combinations of isolated Ti atoms and anatase (TiO2) nanoparticles were obtained; both were incorporated in the highly porous siliceous matrix. The photocatalytic performance of these materials was tested by studying the propane oxidation process following irradiation at lambda = 365 nm, selectively activating the anatase nanoparticles. In comparison to commercial anatase powder, TiO2 nanoparticles in TUD-1 showed high photochemical selectivity towards acetone, the sample with a Si/Ti ratio of 1.6 being the most selective. Size and confinement effects are consistent with the difference in performance of the TUD-1 materials and TiO2, limiting the number of electron transfers available for each propane molecule.     

Nickel ferrite/zinc oxide nanocomposite: Investigating the photocatalytic and antibacterial properties

A facile strategy was used for the synthesis of nickel ferrite/zinc oxide (NiFe₂O_4/ZnO) nanocomposite via an ultra-sonication method and observed its recyclability and photostability with enhanced visible light-driven photocatalytic performance. The photo degradation activities of as-synthesized photocatalysts were investigated using various dyes including methylene blue, crystal violet and methyl orange under solar light irradiation. Prepared material degrades 49.2% methyl orange, 44.4% methyl blue and 41.3% crystal violet in 40 min. Further, the synergistic effect of nickel ferrite and zinc oxide can reduce the probability of recombination of charge carrier and boost the charge separation which leads to remarkable photocatalytic performance. Magnetic properties of nickel ferrite reduces the agglomeration of material and increases the recyclability. The NiFe₂O_4/ZnO nanocomposites also exhibited better antibacterial activity for Pseudomonas aeruginosa and Staphylococcus aureus, which shows that they can be used for both environmental and biological applications.     

Alga-mediated facile green synthesis of silver nanoparticles: Photophysical,catalytic and antibacterial activity

A facile, convenient and green method has been employed for the synthesis of silver nanoparticles (AgNPs) using dried biomass of a green alga, Chlorella ellipsoidea. The phytochemicals from the alga, as a mild and non-toxic source, are believed to serve as both reducing and stabilizing agents. The formation of silver nanoparticles was confirmed from the appearance of a surface plasmon resonance band at 436 nm and energy dispersive X-ray spectroscopy. The transmission electron microscopy images showed the nanoparticles to be nearly spherical in shape with different sizes. A dynamic light scattering study revealed the average particle size to be 220.8 ± 31.3 nm. Fourier transform infrared spectroscopy revealed the occurrence of alga-derived phytochemicals attached to the outer surface of biogenically accessed silver nanoparticles. The powder X-ray diffraction study revealed the face-centred cubic crystalline structure of the nanoparticles. The as-synthesized biomatrix-loaded AgNPs exhibited a high photocatalytic activity for the degradation of the hazardous pollutant dyes methylene blue and methyl orange. The catalytic efficiency was sustained even after three reduction cycles. A kinetic study indicated the degradation rates to be pseudo-first order with the degradation rate being 4.72 × 10⁻² min⁻¹ for methylene blue and 3.24 × 10⁻² min⁻¹ for methyl orange. The AgNPs also exhibited significant antibacterial activity against four selected pathogenic bacterial strains.     

ZnO/graphene-oxide nanocomposite with remarkably enhanced visible-light-driven photocatalytic performance

In this work, a high-performance photocatalyst of ZnO/graphene-oxide (ZnO/GO) nanocomposite was synthesized via a facile chemical deposition route and used for the photodegradation of organic dye from water under visible light. The nanocomposite was characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, Brunauer-Emmett-Teller N(2) adsorption-desorption analysis, and UV-Vis diffusion reflectance spectroscopy. The ZnO/GO nanocomposite consisting of flower-like ZnO nanoparticles anchored on graphene-oxide sheets has a high surface area and hierarchical porosity, which is benefit to the adsorption and mass transfer of dye and oxygen species. For the photodegradation of organic dyes under visible light, ZnO/GO nanocomposite exhibited remarkably enhanced photocatalytic efficiency than graphene-oxide sheets and flower-like ZnO particles. Moreover, the photocatalytic efficiency of ZnO/GO nanocomposite could be further improved by annealing the product in N(2) atmosphere. The outstanding photocatalytic performance was ascribed to the efficient photosensitized electron injection and repressed charge carriers recombination in the composite with GO as electron collector and transporter, thus leading to continuous generation of reactive oxygen species for the degradation of methylene blue.     

Three-Dimensional Hierarchical Superstructures of CuO Nanoflowers: Facile Synthesis and Applications for Enhanced Photocatalytic Activity of Dyes

A new nano-flower shaped material of CuO (3D CuONFs) with three-dimensional (3D) hierarchical superstructures were synthesized using mild experimental conditions, which showed high-efficiency and conveniently recyclable for five degradation including methylene blue (MB), methyl orange (MO), methyl violet (MV), bromocresol green (BG) by visible light irradiation. The structure of 3D CuONFs was important to improve the photo-degrading efficiency, due to the large specific surface area. The 3D CuONFs was characterized by various techniques including Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption/desorption isotherms, and powder X-ray diffraction (XRD), which evidently support the mentioned mechanism.

     

Band structure tuning of ZnO/CuO composites for enhanced photocatalytic activity

The toxic dye pigments, even in small quantities, can damage ecosystems. Removing organic, inorganic, and microbiological contaminants from wastewater via heterogeneous photocatalysis is a promising method. Herein, we report the band structure tuning of ZnO/CuO nanocomposites to enhance photocatalytic activity. The nanocomposites were synthesized by a chemical approach using step-wise implantation of p-type semiconductor CuO to n-type semiconductor ZnO. Various characterization techniques such as X-ray diffraction analysis (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray analysis (EDX) and UV spectroscopy were used to investigate the crystal structure, surface morphology, elemental composition and optical properties of the synthesized samples. As the CuO content increased from 10% to 50% in ZnO/CuO nanocomposites, the optical bandgap decreased from 3.36 to 2.14 eV. The photocatalytic activity of the samples was evaluated against the degradation of methylene blue (MB) under visible irradiation. Our study demonstrates a novel p–n junction oxide photocatalyst based on wt. 10% CuO/ZnO with superior photocatalytic activity. Effectively 66.6% increase in degradation rate was achieved for wt. 10% CuO/ZnO nanocomposite compared to pure ZnO nanoparticles.     

Synthesis and analysis of ZnO-CoMoO4 incorporated organic compounds for efficient degradation of azo dye pollutants under dark ambient conditions

In recent years, the degradation of organic dyes under dark conditions, at room temperature and atmosphere pressure, without additional lights or chemical stimulants, has been widely investigated. Here, a nanocomposite of ZnO-CoMoO₄ was synthesized using an organic template and investigated as a catalyst to degrade methyl orange in aqueous environment under dark, ambient conditions. The organic compounds of Abies Pindrow Royle were reacted with a precursor solution following sol–gel synthesis methodology to modify the chemistry and morphology of ZnO-CoMoO_4, so formed. The structure of the nanocomposite was confirmed by X-ray diffraction, Raman spectroscopy and energy dispersive X-ray spectroscopy while nanostructures were examined by field emission scanning electron microscopy. Organic functional groups were determined by Fourier transform infrared spectroscopy and Gas chromatography–mass spectrometry. The organic compound incorporated nanocomposite was revealed to be an excellent catalyst with 95% degradation of methyl orange in aqueous environment under dark ambient conditions within 10 min. The catalyst also revealed 99% degradation of azo dye in the presence of solar light. Furthermore, the catalysts illustrated good stability with pseudo first order kinetics (R² < 1) in the light as well as in the dark conditions with outstanding reusability till four cycles of experiments. Therefore, nanostructure and organic species of Abies Pindrow Royle were found to enhance the catalytic behavior of ZnO-CoMoO₄ towards methyl orange degradation even in dark conditions.     

Chemical and biological treatment of waste water with a novel silver/ordered mesoporous alumina nanocomposite

One of the serious problems in the present century is chemical and biological pollution of the environment. Nanocomposites are multiphase solid materials that have been used as adsorbent of pollutants such as dyes, pesticides, anions and etc. in the last decades. In this study, a novel nanocomposite including silver nanoparticles and ordered mesoporous alumina (OMA) has been synthesized and used for the removal of dyes pollutants (methyl orange, bromothymol blue and reactive yellow) from aqueous solution. The characterization of synthesized nanocomposite has been performed by TEM, N₂ adsorption/desorption, XRD and energy dispersive X-ray spectroscopy analysis. The adsorption kinetic and equilibrium data have been obtained by UV–vis spectroscopy. The results show that the silver/OMA nanocomposite (Ag/OMA nanocomposite) is good adsorbent for the removal of anionic dyes from aqueous solution, and also this nanocomposite has a biocidal action against both Gram-negative and Gram-positive bacteria.     

纳米碳纤维固载TiO_2

采用聚乙烯吡咯烷酮(PVP)溶胶通过静电纺丝法制备了PVP纳米纤维。将PVP纳米纤维直接固载在碳棒上,在250℃预氧化,850℃炭化,得到碳纳米纤维。将碳纤维渍取钛酸丁酯,200℃下热处理后在550℃空气中焙烧,制得负载型纳米TiO2。利用扫描电子显微镜、红外吸收光谱、X射线衍射等测试技术对纳米纤维进行了表征。并把负载型TiO2分散在亚甲基蓝溶液中,分析了TiO2固载纳米碳纤维的光催化活性。结果表明,在100mL20mg/L亚甲基蓝溶液中加入1.0mgTiO2固载碳纳米纤维,光催化降解40min后,亚甲基蓝的分解率接近75%。     

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.     

Graphene Nanosheets Decorated with Copper Oxide Nanoparticles for the Photodegradation of Methylene Blue

Textile industries extensively use colorants, such as methylene blue, and if disposed off untreated, they contaminate the effluent streams, causing a severe impact on the environment and aquatic life. Photocatalytic degradation has been found as an inevitable approach to treat them. Herein, we decorated the copper oxide nanoparticles on graphene nanosheets during the reflux process. The resultant copper oxide/graphene nanocomposites were analyzed for structural and functional attributes. It was observed that on increasing the copper oxide contents, the z-average size of the resultant nanocomposites decreased. The X-ray diffraction analysis demonstrated the crystalline nature of the nanocomposite. The surface morphology of the copper oxide nanoparticles appeared to be spherical and that of the copper oxide/graphene composite somehow wrinkled. The infrared analysis indicated successful intercalation of precursors in the nanocomposite. The bandgap of copper oxide/graphene nanocomposites varied in the range of 1.03-1.30 eV, which indicated their effective photocatalytic activity. The results demonstrated that after 120 min of exposure, the methylene blue removal efficiency reached 94.0%, 92.2%, and 89.4%(mass fraction) on the copper oxide/graphene nanocomposite at copper oxide nanoparticles to graphene nanosheets ratios of 1:1, 1.5:1, and 2:1 (mass ratio), respectively. The photodegradation performance of the prepared nano-catalyst was found satisfactory even after five cycles.     

Facile large scale synthesis of CuCr2O4/CuO nanocomposite using MOF route for photocatalytic degradation of methylene blue and tetracycline under visible light

MIL-101(Cr) template method has been employed successfully to synthesize CuCr₂O₄/CuO composite. The synthesized sample was characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy, N₂ adsorption–desorption isotherm (BET) analysis, and UV vis- diffuse reflectance spectroscopy (UV-DRS). The photocatalytic efficiency of the nanocomposite was evaluated towards the degradation of methylene blue (MB) dye and antibiotic tetracycline (TC) solution. The morphological studies confirmed that the CuO was uniformly dispersed on the CuCr₂O₄ matrix. The CuCr₂O₄/CuO nanocomposite showed high degradation efficiency of about 90% in the presence of H₂O₂ where the MB degradation reaction got completed in a mere 35 min and ~95% TC got degraded within 120 min.     

Fe-doped and ZnO-pillared titanates as visible-light-driven photocatalysts

Fe-doped cesium titanate was obtained by a solid state reaction with a mixture of Cs(2)CO(3), TiO(2), and Fe(2)O(3). ZnO-pillared doped titanate nanocomposite was successfully fabricated by exfoliating doped titanate and restacking its nanosheets with ZnO nanoparticles. The resulting nanocomposite was characterized by powder X-ray diffraction, scanning electron microscope, X-ray photoelectron spectroscopy, N(2) adsorption-desorption measurement, thermogravimetric analysis and UV-vis spectroscopy. It was revealed that the present nanocomposite exhibits greatly increased specific surface area with mesoporous texture and that there exists an electronic coupling between the host sheets and the guest nanoparticles in the pillared system. The results of degradation of methylene blue under visible light radiation suggest that doping iron ions improves the material spectral response region and that hybridizing with ZnO nanopillars can suppress the recombination of photogenerated electron-hole pairs.     

Facile Biosynthesis of Calcium Hydroxide Nanoparticles Using <Emphasis Type="Italic">Andrographis echioides</Emphasis> Leaf Extract and Its Photocatalytic Activity Under Different Light Source

Effective removal of organic pollutants from wastewater becomes notable research because of its ecological and environmental importance. In the present study Andrographis echioides leaf extract was used for the synthesis of calcium hydroxide nanoparticles (Ca(OH)₂-NPs) from calcium oxide as the calcium source. The secondary metabolites present in the plant source act as a capping agent for the formation Ca(OH)₂-NPs. Further NPs were applied for photocatalytic degradation. The intention of the approach is to be low-cost preparation and easy degradation (degradation of dye without any effect) to the environment. The synthesized Ca(OH)₂-NPs was characterized by X-ray diffraction, Fourier transform infrared spectroscopy, ultra violet diffuse reflectance spectroscopy, energy dispersive X-ray spectroscopy, zeta potential and high-resolution transmission electron microscopy. The photocatalytic degradation of methylene blue (dye pollutant) studied under three different light sources such as UV, visible and sun light using Ca(OH)₂-NPs. Degradation efficiency of Methylene blue dye examined under UV–Vis spectroscopy. Degradation percentage of Ca(OH)₂-NPs under UV, visible and sunlight are (98.96, 97.52 and 96.38%) respectively. The overall study suggests that Ca(OH)₂-NPs exhibit excellent photocatalytic property against UV, visible and sunlight.     

Magnetic ZnO Crystal Nanoparticle Growth on Reduced Graphene Oxide for Enhanced Photocatalytic Performance under Visible Light Irradiation

Magnetite zinc oxide (MZ) (Fe₃O₄/ZnO) with different ratios of reduced graphene oxide (rGO) was synthesized using the solid-state method. The structural and optical properties of the nanocomposites were analyzed using transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, Fourier-transform infrared spectroscopy (FTIR), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis/DRS), and photoluminescence (PL) spectrophotometry. In particular, the analyses show higher photocatalytic movement for crystalline nanocomposite (MZG) than MZ and ZnO nanoparticles. The photocatalytic degradation of methylene blue (MB) with crystalline ZnO for 1.5 h under visible light was 12%. By contrast, the photocatalytic activity for MZG was more than 98.5%. The superior photocatalytic activity of the crystalline nanocomposite was detected to be due to the synergistic effect between magnetite and zinc oxide in the presence of reduced graphene oxide. Moreover, the fabricated nanocomposite had high electron–hole stability. The crystalline nanocomposite was stable when the material was used several times.