Assembly of functional carboxymethyl cellulose/polyethylene oxide/anatase TiO_(2) nanocomposites and tuning the dielectric relaxation, optical, and photoluminescence performances

Nanocomposite films consisting of carboxymethyl cellulose,polyethylene oxide(CMC/PEO),and anatase titanium diox-ide(TO)were produced by the use of sol-gel and solution casting techniques.TiO2 nanocrystals were effectively incorporated into CMC/PEO polymers,as shown by X-ray diffraction(XRD)and attenuated total reflectance fourier transform infrared(ATR-FTIR)analysis.The roughness growth is at high levels of TO nanocrystals(TO NCs),which means increasing active sites and defects in CMC/PEO.In differential scanning calorimetry(DSC)thermograms,the change in glass transition temperature(Tg)val-ues verifies that the polymer blend interacts with TO NCs.The increment proportions of TO NCs have a notable impact on the dielectric performances of the nanocomposites,as observed.The electrical properties of the CMC/PEO/TO nanocomposite undergo significant changes.The nanocomposite films exhibit a red alteration in the absorption edge as the concentration of TO NCs increases in the polymer blend.The decline in the energy gap is readily apparent as the weight percentage of TO NCs increases.The photoluminescence(PL)emission spectra indicate that the sites of the luminescence peak maximums show slight variation;peaks get wider,while their intensities decrease dramatically as the concentration of TO increases.These nanocomposite materials show potential for multifunctional applications including optoelectronics,antireflection coatings,pho-tocatalysis,light emitting diodes,and solid polymer electrolytes.

Photocatalytic ozonation-based degradation of phenol by ZnO—TiO_(2)nanocomposites in spinning disk reactor

Spinning disk reactor(SDR)has emerged as a novel process intensification photocatalytic reactor,and it has higher mass transfer efficiency and photon utilization for the degradation of toxic organic pollutants by advanced oxidation processes(AOPs).In this study,ZnO—TiO_(2)nanocomposites were prepared by solgel method,and coated on the disk of SDR by impregnation-pull-drying-calcination method.The performance of catalyst was characterized by X-ray diffraction,scanning electron microscope,X-ray photoelectron spectroscopy,photoluminescence and ultraviolet—visible diffuse reflectance spectroscopy.Photocatalytic ozonation in SDR was used to remove phenol,and various factors on degradation effect were studied in detail.The results showed that the rate of degradation and mineralization reached 100%and 83.4%under UV light irradiation after 50 min,compared with photocatalysis and ozonation,the removal rate increased by 69.3%and 34.7%,and mineralization rate increased by 56.7%and 62.9%,which indicated that the coupling of photocatalysis and ozonation had a synergistic effect.The radical capture experiments demonstrated that the active species such as photogenerated holes(h^(+)),hydroxyl radicals(·OH),superoxide radical(·O_(2)-)were responsible for phenol degradation,and·OH played a leading role in the degradation process,while h+and·O_(2)^(-)played a non-leading role.

Deflagration to detonation transition in weakly confined conditions for a type of potentially novel green primary explosive:Al/Fe_(2)O_(3)/RDX hybrid nanocomposites

The properties of the combustion and deflagration to detonation transition(DDT)of Al/Fe_(2)O_(3)/RDX hybrid nanocomposites,a type of potentially novel lead-free primary explosives,were tested in weakly confined conditions,and the interaction of Al/Fe_(2)O_(3)nanothermite and RDX in the DDT process was studied in detail.Results show that the amount of the Al/Fe_(2)O_(3)nanothermite has a great effect on the DDT properties of Al/Fe_(2)O_(3)/RDX nanocomposites.The addition of Al/Fe_(2)O_(3)nanothermite to RDX apparently improves the firing properties of RDX.A small amount of Al/Fe_(2)O_(3)nanothermite greatly increases the initial combustion velocity of Al/Fe_(2)O_(3)/RDX nanocomposites,accelerating their DDT process.When the contents of Al/Fe_(2)O_(3)nanothermite are less than 20 wt%,the DDT mechanisms of Al/Fe_(2)O_(3)/RDX nanocomposites follow the distinct abrupt mode,and are consistent with that of RDX,though their DDT processes are different.The RDX added into the Al/Fe_(2)O_(3)nanothermite increases the latter's peak combustion velocity and makes it generate the DDT when the RDX content is at least 10 wt%.RDX plays a key role in the shock compressive combustion,the formation and the properties of the DDT in the flame propagation of nanocomposites.Compared with RDX,the fast DDT of Al/Fe_(2)O_(3)/RDX nanocomposites could be obtained by adjusting the chemical constituents of nanocomposites.

Influence of tool rotational speed on mechanical and corrosion behaviour of friction stir processed AZ31/Al_(2)O_(3)nanocomposite

Nano-sized reinforcements improved the mechanical characteristics efficiently by promoting more implicit particle hardening mechanisms compared to micron-sized reinforcements.Nano-sized particles lessen the critical particle solidification velocity for swamp and thus offers better dispersal.In the present investigation,the friction stir processing(FSP)is utilized to produce AZ31/Al_(2)O_(3)nanocomposites at various tool rotation speeds(i.e.,900,1200,and 1500 rpm)with an optimized 1.5%volume alumina(Al_(2)O_(3))reinforcement ratio.The mechanical and corrosion behavior of AZ31/Al_(2)O_(3)-developed nanocomposites was investigated and compared with that of the AZ31 base alloy.The AZ31 alloy experienced a comprehensive dynamic recrystallization during FSP,causing substantial grain refinement.Grain-size strengthening is the primary factor contributed to the enhancement in the strength of the fabricated nanocomposite.Tensile strength and yield strength values were lower than those for the base metal matrix,although an upward trend in both values has been observed with an increase in tool rotation speed.An 19.72%increase in hardness along with superior corrosion resistance was achieved compared to the base alloy at a tool rotational speed of 1500 rpm.The corrosion currents(Jcorr)of all samples dropped with increase in the rotational speed,in contrast to the corrosion potentials(Ecorr),which increased.The values of Jcorr of AZ31/Al_(2)O_(3)were 42.3%,56.8%,and 65.5%lower than those of AZ31 alloy at the chosen rotating speeds of 900,1200,and 1500 rpm,respectively.The corrosion behavior of friction stir processed nanocomposites have been addressed in this manuscript which has not been given sufficient attention in the existing literature.Further,this work offers an effective choice for the quality assurance of the FSP process of AZ31/Al_(2)O_(3)nanocomposites.The obtained results are relevant to the development of lightweight automobile and aerospace structures and components.

Enhanced photocatalytic activity of methylene blue using heterojunction Ag@TiO_(2)nanocomposite:Mechanistic and optimization study

The objective in this study is to investigate the adsorption-degradation of the methylene blue(MB)dye using a fabricated heterojunction Ag@TiO_(2)nanocomposite.The batch factors used in photo catalytic reactions were pH,UV-irradiation time,temperature,catalytic dosage,and concentration of MB.The results showed that 0.2×10^(3) g·ml^(-1))of the catalytic dose caused the Ag@TiO_(2)adsorption to degrade by 96.67%with darks and UV exposure.Using the Langmuir-Hinshelwood model to determine the kinetic,the Ag@TiO_(2)displays a greater kinetic rate than TiO_(2)and silver nanoparticle(AgNPs).The photocatalytic degradation of MB,which is an endothermic reaction involving all catalysts,is shown by the thermodynamic parameter to have the positive value of enthalpy(ΔH°).The enthalpies observed were Ag@TiO_(2)(126.80 kJ·mol^(-1))<AgNPs(354.47 kJ·mol^(-1))<TiO_(2)(430.04 kJ·mol^(-1)).Ascorbic acid(·OH scavenger),2-propanol(·O_(2)scavenger),and ammonium oxalate(AO)(hole h+scavenger)were employed to conduct the scavenger effects.The Ag@TiO_(2)demonstrated a reduction in MB degradation when combined with 2-propanol,and this clearly demonstrated that,in contrast to hydroxyl radicals(·OH)and holeh scavengers,superoxide radical anion(O_(2)scavenger)plays a significant role in MB degradation.Utilizing density functional theory(DFT)to elucidate the mechanism and B3LYP/6-311+G(d,p)level optimization,the degradation-adsorption process was explained.When the N-N,C-N or C-C bonds were severed,the Fukui faction was demonstrated for nucleophilic,electrophilic,and radical attack.

Template synthesis of MnO_2/CNT nanocomposite and its application in rechargeable lithium batteries

Nanostructured MnO2/CNT composite was synthesized by a soft template approach in the presence of Pluronic P123 surfactant. The product was characterized by X-ray diffraction, thermogravimetric and differential thermal analyses, Fourier transformed infrared spectroscopy and high-resolution transmission electron microscopy. The results show that the sample consists of poor crystalline α-MnO2 nanorods with a diameter of about 10 nm and a length of 30-50 nm, which absorb on the carbon nanotubes. The electrochemical properties of the product as cathode material for Li-MnO2 cell are evaluated by galvanostatic charge-discharge and electrochemical impedance spectroscopy （EIS）. Compared with pure MnO2 electrode, the MnO2/CNT composite delivers a much larger initial capacity of 275.3 mA-h/g and better rate and cycling performance.

MoS_(2)/ZnO异质结纳米材料降解亚甲基蓝的光催化性能研究

为了提高ZnO的光转换效率,选用带隙较低的MoS_(2)形成异质结提高ZnO的光催化性能。通过水热法制备ZnO纳米棒,并进一步制备MoS_(2)/ZnO异质结构的纳米复合材料。通过扫描电镜(SEM)、X射线粉末衍射仪(XRD)、固体紫外可见漫反射测试仪(UV-Vis)和紫外可见分光光度计(UV-245)等分析方法对样品的形貌、结构及光学性能等进行表征。结果表明,MoS_(2)/ZnO异质结复合材料呈棒状结构,并由于内建电场存在可有效增强光生载流子的分离效率,进而提高了可见光区的吸收,提高了光催化性能。在模拟太阳光(包含紫外波段)下,60 min时MoS_(2)-15/ZnO纳米复合材料对亚甲基蓝的降解率可达99%,比纯ZnO的降解率提高了10%。

Preparation and shape memory properties of TiO_2/PLCL biodegradable polymer nanocomposites

The preparation of TiO2/poly（L-lactide-co-ε-caprolactone）（PLCL） nanocomposites and their properties were reported.TiO2nanoparticles were surface modified by ring-opening polymerization of ε-caprolactone（ε-CL）.The resulting poly（ε-caprolactone）-grafted TiO2（g-TiO2） was characterized by Fourier transform infrared spectroscopy（FTIR）,thermogravimetric analysis（TGA） and transmission electron microscopy（TEM）.The g-TiO2can be uniformly dispersed in chloroform and the g-TiO2/PLCL nanocomposites were successfully fabricated through solvent-casting method.The effects of the content of g-TiO2nanoparticles on tensile properties and shape memory properties were investigated.A significant improvement in the tensile properties of the 5% g-TiO2/PLCL mass fraction nanocomposite is obtained：an increase of 113% in the tensile strength and an increase of 11% in the elongation at break over pure PLCL polymer.The g-TiO2/PLCL nanocomposites with a certain amount of g-TiO2content have better shape memory properties than pure PLCL polymer.The g-TiO2nanoparticles play an additional physical crosslinks which are contributed to improvement of the shape memory properties.

Solution combustion synthesis of Ni-Y_2O_3 nanocomposite powder

Ni-Y2O3 nanocomposite powder with uniform distribution of fine oxide particles in the metal matrix was successfully fabricated via solution combustion process followed by hydrogen reduction. The combustion behavior was investigated by DTA-TG analysis. The influence of urea to nickel nitrate（U/Ni） ratio on the combustion behavior and morphology evolution of the combusted powder was investigated. The morphological characteristics and phase transformation of the combusted powder and the reduced powder were characterized by FESEM, TEM and XRD. The HRTEM image of Ni-Y2O3 nanocomposite powder indicated that Y2O3 particles with average particle size of about 10 nm dispersed uniformly in the nickel matrix.

BiOCl-Bi12O17Cl2 nanocomposite with high visible-light photocatalytic activity prepared by an ultrasonic hydrothermal method for removing dye and pharmaceutical

A BiOCl-Bi12O17Cl2 nanocomposite with a high visible-light response and a low photoinduced electron-hole pair recombination rate was successfully synthesized using an ultrasonic-hydrothermal method.The texture,structure,optical,and photocatalytic properties of the composite were characterized.The results showed that the composite had a sheet flower-like structure with a large specific surface area.Ultraviolet-visible diffuse reflection spectra and photoluminescence spectra showed that the composite had an excellent visible-light response and a low recombination rate of photoinduced electron hole pairs.The photocatalytic property of the composite was evaluated by the removal efficiency of rhodamine B and ciprofloxacin under visible-light illumination.The composite’s reaction rate constant of removing rhodamine B(/ciprofloxacin)was approximately 8.14(/4.94),42.63(/11.91)and 64.66(/36.07)times that of Bi12O17Cl2,P25,and BiOCl,respectively.Furthermore,the composite showed a wide applicable pH range and excellent reusability.Mechanism analysis showed that photogenerated holes played a dominant role and·O2–also contributed to photocatalytic degradation.In summary,this study presents a high-efficiency photocatalyst for wastewater treatment.

Surface functionalized N-C-TiO_(2)/C nanocomposites derived from metal-organic framework in water vapour for enhanced photocatalytic H generation

Surface-functionalized nitrogen/carbon co-doped polymorphic TiO_(2) phase junction nanoparticles uniformly distributed in porous carbon matrix were synthesized by a simple one-step pyrolysis of titanium based metal-organic framework(MOF),NH_(2)-MIL^(-1)25(Ti) at 700℃ under water vapour atmosphere.Introducing water vapour during the pyrolysis of NH_(2)-MIL^(-1)25(Ti) not only functionalizes the derived porous carbon matrix with carboxyl groups but also forms additional oxygen-rich N like interstitial/intraband states lying above the valence band of TiO2 along with the self-doped carbo n,which further narrows the energy band gaps of polymorphic TiO2 nanoparticles that enhance photocatalytic charge transfer efficiency.Without co-catalyst,sample N-C-TiO2/CArW demonstrates H_(2) evolution activity of 426 μmol gcat-1h^(-1),which remarkably outperforms commercial TiO_(2)(P-25) and N-C-TiO_(2)/CAr with a 5-fold and 3-fold H_(2) generation,respectively.This study clearly shows that water vapour atmosphere during the pyrolysis increases the hydrophilicity of the Ti-MOF derived composites by functionalizing porous carbon matrix with carboxylic groups,as well as enhancing the electrical conductivity and charge transfer efficiency due to the formation of additional localized oxygen-rich N like interstitial/intraband states.This work also demonstrates that by optimizing the anatase-rutile phase composition of the TiO2 polymorphs,tuning the energy band gaps by N/C co-doping and functionalizing the porous carbon matrix in the N-C-TiO2/C nanocomposites,the photocatalytic H_(2) generation activity can be further enhanced.

Ag/TiO_2/freeze-dried graphene nanocomposite as a high performance photocatalyst under visible light irradiation

Ag/TiO2/freeze-dried graphene nanocomposites have been prepared via a facile one-step solvothermal method for the photocatalytic degradation of Rh B under visible light irradiation. During the solvothermal process, reduction of graphene oxide and loading of Ag/TiO2nanoparticles on graphene sheets were achieved. Investigation of chemical state of products showed that covering of Ag/TiO2surface with higher weight ratio of graphene resulting in that Ag metals in Ag/TiO2were oxidized to Ag2 O in nanocomposite structure after solvothermal process. Degree of photocatalytic activity enhancement strongly depends on the coverage of Ag/TiO2surface by porous graphene. The sample of 1 wt% porous graphene hybridized Ag/TiO2showed the highest photocatalytic activity, which is related to high migration efficiency of photoinduced of electrons and reduction of electron–hole recombination rate due to high electrical conductivity of graphene. Expanding of absorption to visible light region was ascribed to surface plasmon resonance effect of Ag metals and presence of graphene. Investigation of photocatalytic performance of formic acid as a dye-less organic pollutant showed that dye sensitization effect of Rh B molecules during evaluation of photocatalytic performance was negligible.

Study on Preparation and Properties of La_2O_3/MC Nylon Nanocomposites

A series of La2O3/MC nylon nanocomposites were prepared via in situ polymerization. The effects of content of nano-La2O3 on the mechanical properties of nanocomposites were studied. Dispersion of nano-La2O3 in MC nylon matrix was observed with SEM. The crystal structure of nanocomposites was characterized by means of XRD. SEM analysis shows that La2O3 nanoparticles are uniformly dispersed in MC nylon matrix and little clustering exists when the content of nano- La2O3 is lower than 1%, however, when the content of nano-La2O3 is more than 1%, it begins to cluster. XRD analysis indicats that nano-La2O3 does not change the crystal structure of MC nylon. Mechanical properties tests show that the tensile strength, elongation at break, impact strength, flexural strength, and flexural modulus of nanocomposites first increase then decrease as the content of nano-La2O3 is increased. When the content of nano-La2O3 is 0.5%, the tensile strength and elongation at break of nanocomposites reach maximum, which are 17.9% and 52.1% higher respectively than those of MC nylon. When the content of nano-La2O3 is 1.0%, the impact strength, flexural strength and flexural modulus of nanocomposites reach maximum, which are 36.6 %, 12.7 % and 16.3 % higher respectively than those of MC nylon.

ZIF⁃67衍生Co@C/MoS_(2)纳米复合材料的制备及微波吸收性能

通过碳化技术和水热反应相结合成功制备了Co@C/MoS_(2)复合吸波材料。结果表明,ZIF⁃67的碳化温度和Co@C/MoS_(2)的微观结构对Co@C/MoS_(2)复合材料的吸波性能具有重要影响。Co@C/MoS_(2)的褶皱结构增强了入射波的反射与散射,进而优化了阻抗匹配,提高了材料的电磁波(EMW)吸收性能。当碳化温度为800℃,样品匹配厚度为1.7 mm时,Co@C/MoS_(2)复合材料展现出最佳的吸波性能,最小反射损耗(RL_(min))和有效吸收带宽(EAB)分别达到-101.84 dB和7.4 GHz。

Recent progress on gas sensors based on graphene-like 2D/2D nanocomposites

Two-dimensional(2D)nanomaterials have demonstrated great potential in the field of flexible gas sensing due to their inherent high specific surface areas,unique electronic properties and flexibility property.However,numerous challenges including sensitivity,selectivity,response time,recovery time,and stability have to be addressed before their practical application in gas detection field.Development of graphene-like 2D/2D nanocomposites as an efficient strategy to achieve high-performance 2D gas sensor has been reported recently.This review aims to discuss the latest advancements in the 2D/2D nanocomposites for gas sensors.We first elaborate the gas-sensing mechanisms and the collective benefits of 2D/2D hybridization as sensor materials.Then,we systematically present the current gas-sensing applications based on different categories of 2D/2D nanocomposites.Finally,we conclude the future prospect of 2D/2D nanocomposites in gas sensing applications.

BaF_(2)纳米复合闪烁体的闪烁特性研究

为研究基于BaF_(2)无机纳米颗粒复合闪烁体的闪烁特性,将粒径约为20 nm的BaF_(2)无机纳米颗粒与塑料闪烁体结合,制作了不同质量分数的BaF_(2)纳米复合闪烁体。通过闪烁光谱测量系统、时间关联单光子计数系统、基于钴源的γ射线辐照系统,实验测量了BaF_(2)纳米复合闪烁体在低能X射线和γ射线(1.25 MeV)辐射下的闪烁效率、闪烁光谱和发光衰减时间。实验结果表明,在低能X射线和γ射线激发下,基于BaF_(2)纳米颗粒的复合闪烁体可以将发光效率分别提升83.1倍和16.4倍;同时由于BaF_(2)无机纳米颗粒的尺寸效应有效地压制了其慢衰减时间的发光成分(来源于自陷态激子效应),从而使得该BaF_(2)纳米复合闪烁体具有与塑料闪烁体相近的闪烁光谱,快衰减时间约为2 ns。

Preparation and Photocatalytic Activity of BiOBr/TiO_2 Heterojunction Nanocomposites

An efficient visible-light-responsive BiOBr/TiO2 heterojunction nanocomposite was fabricated successfully using in-situ depositing technique at room temperature by introducing BiOBr onto the surface of TiO2 nano- belts pre-prepared by hydrothermal reaction and etched with H2SO4. The obtained particles were characterized by XRD, SEM, TEM, XPS, UV-Vis DRS and PL techniques. BiOBr/TiO2 heterojunction nanocomposites with different mass ratios of m （BiOBr）/m （TiO2） were discussed in order to get the best photocatalytie activity, and BiOBr/TiO2-1.0 was proved to be the optimal mass ratio. BiOBr/TiO2-1.0 exhibited excellent photocatalytic activity in the degradation of RhB compared with TiO2 nanobelts, pure BiOBr and the mechanical mixture of TiO2 nanobelts and BiOBr. At last, a possible mechanism ofphotocatalytic enhancement was proposed.

Synthesis of a PEBAX-1074/ZnO nanocomposite membrane with improved CO_2 separation performance

In this investigation, polymeric nanocomposite membranes（PNMs） were prepared via incorporating zinc oxide（ZnO） into poly（ether-block-amide）(PEBAX-1074) polymer matrix with different loadings. The neat membrane and nanocomposite membranes were prepared via solution casting and solution blending methods, respectively. The fabricated membranes were characterized by field emission scanning electron microscopy（FESEM） to survey cross-sectional morphologies and thermal gravimetric analysis（TGA）to study thermal stability. Fourier transform infrared（FT-IR） and X-ray diffraction（XRD） analyses were also employed to identify variations of the chemical bonds and crystal structure of the membranes, respectively. Permeation of pure gases, CO, CHand Nthrough the prepared neat and nanocomposite membranes was studied at pressures of 3–18 bar and temperature of 25 °C. The obtained results showed that the fabricated nanocomposite membranes exhibit better separation performance compared to the neat PEBAX membrane in terms of both permeability and selectivity. As an example, at temperature of 25 °C and pressure of 3 bar, COpermeability, ideal CO/CHand CO/Nselectivity values for the neat PEBAX membrane are 110.67 Barrer, 11.09 and 50.08, respectively, while those values are 152.27 Barrer,13.52 and 62.15 for PEBAX/ZnO nanocomposite membrane containing 8 wt% ZnO.

Photoluminescence behavior and visible light photocatalytic activity of ZnO,ZnO/ZnS and ZnO/ZnS/α-Fe_2O_3 nanocomposites

In order to achieve effective, economic, and easily achievable photocatalyst for the degradation of dye methyl orange（MeO）, ZnO, ZnO/ZnS and ZnO/ZnS/α-Fe2O3 nanocomposites were prepared by simple chemical synthetic route in the aqueous medium. Phase, crystallinity, surface structure and surface behavior of the synthesized materials were determined by X-ray diffraction（XRD） and Brunauer-Emmett-Teller analysis（BET） techniques. XRD study established formation of good crystalline ZnO, ZnO/ZnS and ZnO/ZnS/α-Fe2O3 nanomaterials. By using intensity of constituent peaks in the XRD pattern, the compositions of nanocomposites were determined. From the BET analysis, the prepared materials show mesoporous behavior, type Ⅳ curves along with H4 hysteresis. The ZnO/ZnS/α-Fe2O3 composite shows the largest surface area among three materials. From the UV-visible spectra, the band gap energy of the materials was determined. Photoluminescence spectra（PL） were used to determine the emission behavior and surface defects in the materials. In PL spectra, the intensity of UV peak of ZnO/ZnS is lowered than that of ZnO while in case of ZnO/ZnS/α-Fe2O3, the intensity further decreased. The visible emission spectra of ZnO/ZnS increased compared with ZnO while in ZnO/ZnS/α-Fe2O3 it is further increased compared with ZnO/ZnS. The as-synthesized materials were used as photocatalysts for the degradation of dye MeO. The photo-degradation data revealed that the ZnO/ZnS/α-Fe2O3 is the best photocatalyst among three specimens for the degradation of dye MeO. The decrease of intensity of UV emission peak and the increase of intensity of visible emission cause the decrease of recombination of electrons and holes which are ultimately responsible for the highest photocatalytic activity of ZnO/ZnS/α-Fe2O3.

Preparation of TiO_2/Kaolinite Nanocomposite and Its Photocatalytical Activity

Titanium dioxide/ kaolinite nanocomposite was prepared by the sol-gel method, with layered kaolinite as a substrate and Ti （ OC4H9 ）4 as a precursor. The effects of hydrolysis, drying and calcination on the production of nanometric titanium dioxide were discussed. The optimal conditions for preparation were＂ bbtained through experiments. The 1- 10 nrn thick monolayer anatase nano TiO2 crystal was produced under the conditions as follows： hydrolyzed at 37-42 ℃ for 4 h, dried at 70-80 ℃ for 1 h, and calcined at 550-650℃ for 3 h. The rate of degradation of 40 mg/ L azo dye and 20 mg/ L acid red dye can reuch 96% and 81.45%, respectively.