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Bioorganic & Organic Chemistry

Research Article Volume 2 Issue 5

Catalytic activity of graphene oxide hybridized ZnWO4 for dyes degradation and oxidation of functionalized benzyl alcohols

Sailaja BBV, Ajay Kumar Paliki, Sathish Mohan Botsa

Department of Inorganic & Analytical Chemistry, Andhra University, India

Correspondence: Sailaja BBV, Assistant Professor, Department of Inorganic & Analytical Chemistry, School of chemistry, Andhra University, Visakhapatnam , India, Tel +919441328956

Received: August 06, 2018 | Published: October 29, 2018

Citation: Paliki AK, Botsa SM, Sailaja BBV. Catalytic activity of graphene oxide hybridized ZnWO4 for dyes degradation and oxidation of functionalized benzyl alcohols. MOJ Biorg Org Chem. 2018;2(5):230-234 DOI: 10.15406/mojboc.2018.02.00087

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Abstract

A simple sol-gel method was used to prepare the GO hybridized ZnWO4 nanoparticles (NPs). The size and morphology of prepared GO/ZnWO4 NPs can be controlled by adjusting the reaction time and temperature. The NPs were characterized using XRD, FTIR and UV-DRS to study their optical properties. The resultant sample is a phase pure GO/ZnWO4 was confirmed by XRD. As-prepared GO/ZnWO4 shows band gap energy of 2.32eV, which shown a path to study the catalytic studies i.e. dyes degradation and oxidation of functionalized benzyl alcohols. The obtained results declared the prepared GO/ZnWO4 NPs have better catalytic efficiency in dyes degradation of Caramine Indigo (CI) and Crystal Violet (CV) under visible-light illumination.

Keywords: GO/ZnWO4, sol-gel, caramine indigo, crystal violet, 2-chloro benzyl alcohol, 4-hydroxy benzyl alcohol, 4-hydroxy 3-methoxy benzyl alcohol, 3-nitro benzyl alcohol and 3,4-dimethoxybenzyl alcohol

Introduction

Recently, nanomaterials have great attention due to their unique size, shape, and crystallinity dependent optical, electronic, magnetic and chemical properties.1 Metal tungstates such as. Bi2WO6, CdWO4, PbWO4, MnWO4 and FeWO4 are inorganic functional nanomaterials and widely used in scintillators materials, sensors, magnetic devices, photocatlaytic and magnetism field.2 Among them, ZnWO4 has a great potential in photocatalytic degradation of organic dye pollutants under UV light illumination.2−3 But, the efficiency is very low because of sunlight captures only 5% while visible light captures the 35%. Hence, this material activity brings to visible region by doping of ions, form hybrids or composites with graphene or CNT. Graphene is a sp2 hybridized carbon with zero band gap energy and has specific physicochemicoelectrical properties thus it shows excellent applications in photocatalysis and organic conversions.4 There have been persistent efforts to load photocatalysts on the structure of graphene oxide (GO) to enhance the photo catalytic activity, but few studies have focused on the surface coating by GO on the photcatalyst for enhancing the photo catalytic efficiency and producing visible photocatalytic activity.

In order to enhance the sensitivity of photocatalyst, ZnWO4 controlled by tuning morphologies, controlling crystallinity and ion doping, or to explore the photoelectrocatalytic activities. The dye pollutants such as 4-chlorophenol, Methylene blue, Rhodamine B, Phenol, Crystal violet, Caramine indigo, Salicylic acid, Methyl orange and Acetaldehyde under visible light irradiation were degraded by ZnWO4 have been reported earlier.2,5 For instance, synthesized ZnWO4 nanorods doped with cadmium ions successfully by a hydrothermal method for the photocatalytic degradation of rhodamine B in aqueous solution which showed that cadmium ions doping also greatly improved the photocatalytic efficiency of ZnWO4 nanorods.6 Recently, reported the several ZnWO4-based composites of high UV light photocatalytic activities via hydrothermal, microwave and co-precipitation methods.7 The sol-gel technique has been used to synthesize metal tungstate nanocomposites especially in the fabrication of self-cleaning film and glass coating due to require a low synthesis temperature, the physical properties of the doping component could be retained by controlling the mixture between the guest molecule and the host matrices.8

To the best of our knowledge, this is the first report on visible light photoactivity of graphene oxide hybridized ZnWO4. Herein, a simple and facile route to synthesize the visible-light responsive GO hybridized ZnWO4 NPs was developed. Furthermore, the catalytic activity was examined for dyes degradation and benzyl alcohol oxidation.

Experimental section

Materials and methods

Zinc Nitrate (Zn(NO3)2.4H2O), sodium tungstate (Na2WO4.2H2O), ethylene glycol, Graphite flakes, sodium nitrate (NaNO3), sulphuric acid (H2SO4), hydrogen peroxide (H2O2), hydrochloric acid (HCl) and potassium permanganate (KMnO4) were procured from Sigma Aldrich, India and used without further purification. Milli Q water was used in whole experiment.

Synthesis of Graphene Oxide (GO)

The preparation of graphene oxide (GO) was carried out by unique modified Hummer’s method.4 In a typical synthesis, 1g of graphite flakes was added into 2.5g of NaNO3 and 100mL of concentrated H2SO4 under stirring. Then, 3g of KMnO4 was added gradually to this mixture at 10°C under stirring for 2h. The resulting mixture was added to 100mL of distilled water and then heated to 98°C. The obtained mixture was continued to be stirred for 2h. After that, 10mL of H2O2 was added in the mixture with stirring for 2h. The colour of the mixture changed to bright yellow. Finally, the mixture was filtered and washed with a 5% HCl aqueous solution to remove metal ions, followed by distilled water for removal of the acid. The resulting solid with brown black colour was separated by ultrasonic treatment in water and dried at 60°C for 12h.

Synthesis of ZnWO4

In a typical experiment, Nanoparticles of ZnWO4 were prepared by dissolving 0.05mmol of Zn(NO3)2.4H2O and 0.05mmol of Na2WO4.2H2O was dissolved separately in ethylene glycol (EG) under continuous stirring. After complete dissolution, the two mixtures were stirred at constant temperature for 24h, and cooled to room temperature. Excess of sodium was removed by washing with distilled water and finally with absolute ethanol. The precipitate thus formed was dried at 70°C and calcinated at 300°C.2

Synthesis of GO hybridized ZnWO4

A certain amount of GO was dispersed in water, then exfoliation of GO was achieved by ultrasonicating the dispersion for 60min. The obtained brown dispersion was then subjected to centrifugation to remove the unexfoliated GO. The obtained exfoliated GO was then dispersed in 100mL ethylene glycol, and the as-prepared ZnWO4 was added into the dispersion and dispersed by ultrasonication for 30min and stirred for 48h. In a typical procedure, and ammonia solution (28wt% in water) were added to the above dispersion. After being vigorously stirred for a few minutes, the dispersion was put into a water bath (90°C) for 3h. An opaque powder was obtained after evaporation at 60°C for 12h. GO/ZnWO composites with different mass ratios ranging from 1% and 2% were prepared according to this method. Amongst the composites, 2% shows the phase and photocatalytic activity.

Characterization

The formation of pure phase was confirmed by XRD (Bruker-6000) with Cu KR radiation (λ) 0.154178nm). The functional groups were identified using FTIR (IR prestige 21) and band gap was calculated using UV-DRS (Shimadzu 2600R) spectra was taken from 200-800cm-1 with BaSO4 as reference. The photocatalytic test was carried out using UV-visible spectrophotometer (Shimadzu 2600) by taking spectra from 200 to 800cm-1.

Photocatalytic activity

The prepared NPs were tested for photocatalytic activity towards degradation of two model dyes under visible-light illumination. Initially, 0.1g of prepared catalyst was added to 20mg/L of dye solution and stirred for 30minutes to attain adsorption-desorption thermal equilibrium. After that, the dye solution was irradiated to visible light which is source from metal halide lamp. For every half an hour, collected the aliquots and centrifuged to separate the catalyst. Finally, the solution was studied the photocatalytic activity by UV-visible spectrophotometer. The degradation efficiency was calculated using the following equation.

Photo degradation % = C 0 C t C 0 ×100 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfa4aaSaaae aacaWGdbWaaSbaaeaacaaIWaaabeaacqGHsislcaWGdbWaaSbaaKqb GeaacaWG0baajuaGbeaaaeaacaWGdbWaaSbaaKqbGeaacaaIWaaaju aGbeaaaaGaey41aqRaaGymaiaaicdacaaIWaaaaa@4267@

Where C0 and Ct corresponds to the initial absorbance and absorbance at time‘t’ respectively.

Results and discussion

Characterization techniques

X-ray diffraction (XRD) analysis: The XRD patterns of GO/ZnWO4 are shown in Figure 1. The GO/ZnWO4 sample should present a two-phase composition of GO and ZnWO4 and compared with standard JCPDS file (No.88-0251). No impurity phase was observed, which is evident in the GO/ZnWO4 NPs. Notably, no typical diffraction peak belonging to the separate GO is observed in the GO/ZnWO4 nanocomposites. The reason is that the main characteristic peak of graphene at 24.5° might be shielded by the main peak of ZnWO4, which is at 24.5° and indexed to (110) crystal planes. Figure 2 (ESI) shows the XRD patterns of GO which exhibits a (001) plane reflection at 2θ=9.12o is contributed to a basal spacing of d001=0.961nm.4,9 Based on this, the interlayer spacing of GO was calculated to be 0.961nm. This value is higher than interlayer spacing of graphite flakes (d-spacing= 0.334nm, 2θ=26.4°), due to the presence of oxygenated functional groups and intercalated water molecules. The average crystalline size of prepared NPs was calculated using Debye-Scherrer equation.

D= 0.94λ βcosθ MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaOaamirai abg2da9maalaaabaGaaGimaiaac6cacaaI5aGaaGinaiabeU7aSbqa aiabek7aIjGacogacaGGVbGaai4CaiabeI7aXbaaaaa@432E@

Where λ is the wavelength at angle θ of inclined plane. The calculated crystalline size of GO/ZnWO4 is 18.3nm which is lower than ZnWO4 (29.6nm). This is due to that the incorporation of ZnWO4 onto GO sheets.

Figure 1 XRD spectrum of GO/ZnWO4.

Figure 2 FTIR spectrum of GO.

FTIR: FT-IR spectrum of the GO is shown in Figure 3 (ESI). The presence of different types of oxygen functionalities in GO were confirmed at broad and wide peak at 3447cm-1 which is attributed to O-H stretching vibrations of the C-OH groups and water.4,9 The absorption peaks at 1560cm-1 can be ascribed to benzene rings. The sharp intense peak at 1419cm-1 can be attributed to CO group.7

Figure 3 XRD spectrum of GO.

FTIR spectrum of GO/ZnWO4 is shown Figure 4. The vibrational peaks of GO are consistent with fingerprint groups such as carboxylic species, hydroxyl species, and epoxy species (C=O, 1734cm−1 OH deformation, 1400cm−1 the C−OH stretching, 1230cm−1 C−O−C stretching, 1061cm−1 skeletal ring stretch, 1624cm−1). The absorption peak at around 1580cm−1 clearly shows the skeletal vibration of the GO sheets, indicating the formation of a graphene structure.4 The two peaks at 3447 and 1629cm−1 observed for ZnWO4 implies the existence of basic hydroxyl groups in the ZnWO4 sample. These results clearly indicate that the surface of ZnWO4 is hydroxylated. Another peak was observed at 1385cm−1 results from the O-H absorption of hydrogen-related defects. The peak at 1385cm−1 decreased and the peak at 1230cm−1 (C−OH) is slightly observed for GO/ZnWO4, indicating that defect sites may be occupied by graphene. The broad peak is located at 907cm−1, corresponding to the stretching W−O mode. Thus, a supposition could be proposed that the GO and ZnWO4 are chemically bonded.

Figure 4 FTIR spectrum of GO/ZnWO4.

UV-Visible Diffuse reflectance spectra: UV-Vis DRS was performed between 200 to 800nm range and BaSO4 was used as a reference. Spectral grade BaSO4 was taken as reference for the reflectance spectra Photoabsorptive ability of the sample is assessed by UV-DRS shown in Figure 5. UV-DRS show an absorption edge in the region close to 550nm from which the estimated band gap of the synthesized GO/ZnWO4 powder is calculated to be 2.32eV, suggested that it is apt to captures the visible-light when compared to pure ZnWO4 (3.2eV) which is fall in UV region.2

Figure 5 UV DRS spectrum of GO/ZnWO4.

Catalytic activity applications

Photocatalytic degradation of dyes

The photocatalytic activity of GO/ZnWO4 NPs was tested via degradation of aqueous solutions of dyes, CI and CV under Visible light irradiation at similar conditions (catalyst dose is 0.1g, pH is 9.5 and concentration is 20mg/L of dye solutions). Figures (6 & 7) show the photocatalytic degradation of CI and CV at different time intervals with decreasing intensity of peaks. The complete degradation was taken in 150min for CI and 120min for CV under visible light irradiation by synthesized GO/ZnWO4. This result was strongly supported by the UV-DRS spectrum and indicated the band gap energy of GO/ZnWO4 was 2.3eV. There is no change observed in the degradation of CI and CV in the absence of catalyst after continuous irradiation of visible light for 3h. The rate constants of the degrading process also calculated as shown in Figure 8, which indicates that entire process follows the pseudo first order reaction. The linear relationship between ln (đ¶/đ¶0) and time demonstrates pseudo-first-order kinetics.

η= ln (C/ C 0 ) =kt MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacqaH3oaAcqGH9aqpcaqGGaGaamiBaiaad6gacaqGGaWdaiaa cIcapeGaam4qaiaac+cacaWGdbWdamaaBaaajuaibaWdbiaaicdaaK qba+aabeaacaGGPaWdbiaabccacqGH9aqpcaWGRbGaamiDaaaa@45A2@

Where đ¶/đ¶0 is normalized CI and CV concentrations, t is the reaction time, and k is the reaction rate constant (min−1).

Figure 6 Photocatalytic degradation of CI using GO/ZnWO4 under visible light irradiation.

Figure 7 Photocatalytic degradation of CV using GO/ZnWO4 under visible light irradiation.

Figure 8 Rate constants of (c) CI (d) CV using GO/ZnWO4 under visible light irradiation.

Mechanism

The basic principle of the photocatalysis can be described by water splitting technology.1,4,9 As the light is absorbed by the ZnWO4, the electrons are emitted from valence band (VB), leaving a hole behind and this electron enters into conduction band (CB) while the light has equal or higher photon energy than the band gap of the material. Reduction of the H+ ions to H2 occurs by the electrons in the CB, while the oxidation of H2O to O2 occurs by the holes in the VB. GO was irradiated with light, then it releases electrons into CB of ZnWO4 (Eqs 1-5). A possible mechanism was explained in Figure 9. Catalysts with smaller band gaps can absorb the light in higher wavelengths and thus active in a larger part of the solar spectrum. Therefore, finding the material which has a smaller band gap is one of the main concerns

 ZnW O 4 + hυ ZnW O 4 ( e +  h + ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaGGGcGaamOwaiaad6gacaWGxbGaam4ta8aadaWgaaqcfasa a8qacaaI0aaajuaGpaqabaWdbiabgUcaRiaabccacaWGObGaeqyXdu NaeyOKH4QaaiiOaiaadQfacaWGUbGaam4vaiaad+eapaWaaSbaaKqb GeaapeGaaGinaaqcfa4daeqaamaabmaabaWdbiaadwgapaWaaWbaae qajuaibaWdbiabgkHiTaaajuaGcqGHRaWkcaqGGaGaamiAa8aadaah aaqabKqbGeaapeGaey4kaScaaaqcfa4daiaawIcacaGLPaaaaaa@5285@ -----------Eq (1)

GO + hυ  e MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGhbGaam4taiaabccacqGHRaWkcaGGGcGaamiAaiabew8a 1jabgkziUkaacckacaWGLbWdamaaCaaabeqcfasaa8qacqGHsislaa aaaa@42F8@ ------------------ Eq(2)

e CB +  O 2   O 2 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGLbWdamaaCaaabeqcfasaa8qacqGHsislaaqcfa4damaa BaaabaWdbiaadoeacaWGcbaapaqabaWdbiabgUcaRiaabccacaWGpb WdamaaBaaajuaibaWdbiaaikdaaKqba+aabeaacqGHsgIRpeGaaiiO amaaCeaabeqcfasaaiabgkci3caajuaGcaWGpbWdamaaBaaajuaiba WdbiaaikdaaKqba+aabeaadaahaaqabKqbGeaapeGaeyOeI0caaaaa @48F3@ ----------------- Eq(3)

ZnW O 4 ( h + ) + OH O H     MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGAbGaamOBaiaadEfacaWGpbWdamaaBaaajuaibaWdbiaa isdaaKqba+aabeaadaqadaqaa8qacaWGObWdamaaCaaabeqcfasaa8 qacqGHRaWkaaaajuaGpaGaayjkaiaawMcaa8qacaqGGaGaey4kaSIa aeiiaiaad+eacaWGibGaeyOKH46aaWraaeqajuaibaGaeyOiGClaaK qbakaad+eacaWGibGaaiiOaiaacckacaGGGcGaaiiOaaaa@4EBE@ -------------Eq(4)

O H+ O 2 +NBC O 2 +  H 2 O MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qadaahbaqabKqbGeaacqGHIaYTaaqcfaOaam4taiaadIeacqGH RaWkdaahbaqabKqbGeaacqGHIaYTaaqcfaOaam4ta8aadaWgaaqcfa saa8qacaaIYaaajuaGpaqabaWdbiabgUcaRiaad6eacaWGcbGaeyOK H4Qaam4qaiaad+eapaWaaSbaaKqbGeaapeGaaGOmaaqcfa4daeqaa8 qacqGHRaWkcaqGGaGaamisa8aadaWgaaqcfasaa8qacaaIYaaajuaG paqabaWdbiaad+eaaaa@4D73@ ---------------Eq(5)

Figure 9 Possible mechanism of photocatalytic degradation of dyes.

Evaluation of oxidation capacity of GO/ZnWO4

GO/ZnWO4 NPs assemblies were used for benzyl alcohol oxidation as a catalyst. In the reaction mixture, 0.5mL of substituted benzyl alcohol was added with 25mL of acetonitrile (as solvent) in a round bottomed flask. Then, 100mg of GO/ZnWO4 powder and 3mL of 30% H2O2 solution were introduced into the mixture and heated at 70°C for about 12h as shown in Figure 10. The flask was fitted with aluminium foil to avoid the impinging of atmospheric oxygen. A usual almond smell represents the formation of benzaldehyde, which stipulates the completion of reaction. After completion of the reaction, the products were purified and recrystallized with methanol.2,10 The final products were further confirmed by 1H NMR, FT-IR, and 13C NMR studies

Spectral data of 4-hydroxy 3-methoxybenzaldehyde

IR (KBr pellet) : 3300 cm-1, 3100cm-1, 1660cm-1, 1600cm-1, 1100cm-1 1H NMR (400MHz/CDCl3) δppm : 7.17(1H,d), 7.32(1H,s), 6.72 (1H, d), 9.87 (1H, s), 3.62 (1H, s) 13C NMR (22.5 MHz/CDCl3) δppm : 189.2, 149.2, 148.3, 130.1, 117.2, 116.7, 55.5 Mass-ESI: 151 (M).

Figure 10 Benzyl alcohol oxidation using GO/ZnWO4.

Conclusion

The GO/ZnWO4 NPs were synthesized by sol-gel approach. The photocatalytic activity of GO/ZnWO4 NPs were evaluated by testing the photo degradation of model dyes like caramine indigo and crystal violet under visible light irradiation. This result indicated that the complete degradation of 100mL aqueous solutions of 20ppm CI and CV under visible light irradiation in 150 and 180min respectively. Also, synthesized GO/ZnWO4 NPs are apt to the synthesis of benzaldehydes under solvent-free conditions with good yield.

Acknowledgements

None.

Conflict of interest

Authors declare that there is no conflict of interest.

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