A Tremella-like Mesoporous Calcium Silicate Loaded by TiO_(2) with Robust Adsorption and Photocatalytic Degradation Capabilities

A titanium dioxide loaded tremella-like mesoporous calcium silicate hydrate(TiO_(2)@CSH)with both adsorption and photocatalytic degradation activity was successfully prepared by a hydrothermal method combined with sol-gel strategy in two steps in this work.Tremella-shaped CSH provides abundant active sites for accommodating of TiO_(2),thus the corresponding TiO_(2)@CSH achieved a high loading ratio of 36.73%.Such a special shaped TiO_(2)@CSH exhibits excellent pre-enrichment capacity and photocatalytic degradation capacity for organic pollutants.Bisphenol A(BPA)removal experiments show that TiO_(2)@CSH can remove 91.17%of BPA from aqueous solutions.Studies on removal mechanism suggest that BPA tends to bind on the interface between CSH and TiO_(2) and the pre-enrichment process conforms to the intraparticle diffusion model;and then,it is decomposed to harmless substances of CO_(2) and H_(2)O during the photocatalytic process.The experimental results show that loading functional nanoparticles such as TiO_(2) on the surface of inorganic porous materials can endow inert porous materials with new functions such as photocatalytic degradation,which effectively expands the application range of inorganic porous materials.

Fabrication of the TiO_(2)/Ti_(3)C_(2) loaded ceramic membrane targeting for photocatalytic degradation of PPCPs:ciprofloxacin,tetracycline,and ibuprofen

Photocatalytic membranes offer an effective strategy to overcome the difficulties of solid-liquid separation and secondary contamination of powdered photocatalysts.MXene is a 2D material of layered Ti_(3)C_(2),which is considered to limit electron-hole separation and contribute to photocatalysis.In this work,the etched Ti_(3)C_(2) MXene was loaded on the surface of ceramic membranes using polydopamine(PDA)as a binder,followed by one-step calcination to produce TiO_(2) nanoparticles(NPs)in situ.The characterizations supported that the TiO_(2)/Ti_(3)C_(2) ceramic membranes had high mechanical strength while retaining the layered structure of Ti_(3)C_(2),which was conducive to the inhibition of electron and hole complexation,improving the photocatalytic performance.Degradation experiments revealed that the material showed enhanced degradation of pharmaceuticals and personal care products(PPCPs)such as ciprofloxacin(CIP),tetracycline(TCN)and ibuprofen(IBP).The LC-MS and toxicity prediction models indicated that the developmental toxicity of CIP degradation products decreased with prolonged photocatalytic reaction,exhibiting no acute toxicity to fish.The MT650 exhibited significantly enhanced water flux properties(320 L/(m^(2)·h).The TiO_(2)/Ti_(3)C_(2) ceramic membranes explored in this work are expected to target the treatment of PPCPs with excellent engineering promise.

Photocatalytic degradation of organic dyes with H_3PW_(12)O_(40)/TiO_2-SiO_2

H3PW12O40/TiO2-SiO2 was synthesized by impregnation method which significantly improved the catalytic activity under simulated natural light. The prop- erties of the samples were characterized by Fourier trans- form infrared spectra （FTIR）, X-ray powder diffraction pattern （XRD）, Scanning electron micrographs （SEM）, and Zeta potential. Degradation of methyl violet was used as a probe reaction to explore the influencing factors on the photodegradation reaction. The results show that the opti- mal conditions are as follows： initial concentration of methyl violet of 10 mg·L^-1, pH of 3.0, catalyst dosage of 2.9 g·L^-1, and light irradiation time of 2.5 h. Under these conditions, the degradation rate of methyl violet is 95.4 %. The reaction on photodegradation for methyl violet can be expressed as the first-order kinetic model, and the possible mechanism for the photocatalysis under simulated natural light is suggested. After used continuously for five times, the catalyst keeps the inherent photocatalytic activity for degradation of dyes. The photodegradation of methyl orange, methyl red, naphthol green B, and methylene blue was also tested, and the degradation rate of dyes can reach 81%-100%.

Enhanced charge separation by incomplete calcination modified co-doped TiO_(2)nanoparticle for isothiazolinone photocatalytic degradation

Photocatalytic oxidation techniques are promising for degradation of the highly ecotoxic and refractory isothiazolinone bactericides in relevant industrial wastewaters.However,low charge separation and directional transport efficiency under solar light radiation restrain their practical application.Here,we report a nanostructured photocatalyst doped with Gd and B in TiO_(2)with carbon incorporation and defect formation through incomplete calcination.The specific surface area,grain size,and hydrophilicity of TiO_(2)are improved,which is beneficial for the interfacial reaction between the photocatalyst and pollutants.The reduction of the bandgap,the broadening of the photo-absorption range,and the retarded electron-hole recombination promote the photocatalytic performance due to the improved oxygen vacancies based on the electron distribution modification.The difference in partial density of states(ΔPDOS)between the current catalyst and raw TiO_(2)indicates that the co-doping of Gd and B with incomplete calcination changes the electronic hybridization of conduction band and valence band near the Fermi level,and affects the band gap energy.It improved charge separation and directional transport efficiency and benefited the formation of main active species,including•OH and O_(2)•−,for the pollutant decomposition.The rate of photocatalytic removal of benzisothiazolinone(BIT)by the current photocatalyst reaches 1.25 h^(−1),being 4.31 times that of TiO_(2).The current work offers a constructive approach to the design and synthesis of nanostructured photocatalysts for the photocatalytic degradation of refractory organic pollutants.

Ti_(3)C_(2) MXene co-catalyst assembled with mesoporous TiO_(2) for boosting photocatalytic activity of methyl orange degradation and hydrogen production

Photocatalytic degradation and hydrogen production using solar energy through semiconductor photocatalysts are deemed to be a powerful approach for solving environmental and energy crisis.However,the biggest challenge in photocatalysis is the efficient separation of photo-induced carriers.To this end,we report that the mesoporous TiO_(2)nanoparticles are anchored on highly conductive Ti_(3)C_(2)MXene co-catalyst by electrostatic self-assembly strategy.The constructed mesoporous TiO_(2)/Ti_(3)C_(2)composites display that the mesoporous TiO_(2)nanoparticles are uniformly distributed on the surface of layer structured Ti_(3)C_(2)nanosheets.More importantly,the as-obtained mesoporous TiO_(2)/Ti_(3)C_(2)composites reveal the significantly enhanced light absorption performance,photo-induced carriers separation and transfer ability,thus boosting the photocatalytic activity.The photocatalytic methyl orange degradation efficiency of mesoporous TiO_(2)/Ti_(3)C_(2)composite with an optimized Ti_(3)C_(2)content(3 wt%)can reach 99.6%within 40 min.The capture experiments of active species confirm that the·O_(2)-and·OH play major role in photocatalytic degradation process.Furthermore,the optimized mesoporous TiO_(2)/Ti_(3)C_(2)composite also shows an excellent photocatalytic H2 production rate of 218.85μmol g^(-1)h^(-1),resulting in a 5.6 times activity as compared with the pristine mesoporous TiO_(2)nanoparticles.This study demonstrates that the MXene family materials can be applied as highly efficient noble-metal-free co-catalysts in the field of photocatalysis.

Continuous near-complete photocatalytic degradation of toluene by V/N-doped TiO_(2)loade d on honeycomb ceramics under UV irradiation

Photocatalytic degradation of volatile organic compounds(VOCs)is a significant applying aspect of pho-tocatalysis.Both the modulation of photocatalysts and the rational dispersion of them on supports are key for solar-driven VOC degradation.Conventional batch-type photoreactors have low efficiency while continuous-flow photoreactors suffer from the problem of incomplete removal of VOCs.Herein,aiming for continuous and complete degradation of toluene gas as the target contaminant,continuous-flow pho-tocatalytic degradation reactors were made by adhering the vanadium and nitrogen codoped TiO_(2)on honeycomb ceramics(V/N-TiO_(2)@HC)by a simple sol-gel method.In such a reactor,the rich ordered pores in the HC accelerate mass transport of toluene,and the introduction of V/N dopants narrows the bandgap and widens the light absorption range of TiO_(2),together resulting in continuous and nearly-complete pho-tocatalytic degradation of toluene.The unique and stable structure of HC allows the photocatalysts to be reused.The degradation rate of toluene gas can reach 97.8%,and after 24 rounds of photocatalytic degra-dation,there is still a degradation rate of 96.7%.The impacts of loading times and gaseous flow rate on the photocatalytic performance of V/N-TiO_(2)@HC are studied in detail.Our study provides a practical so-lution for the continuous and complete photocatalytic degradation of VOCs and opens a new application field for HC.

Photocatalytic degradation of organochlorine compounds using TiO_2 supported on fiberglass cloth

The feasibility of photocatalytic degradation of organochlorine compounds using TiO 2 supported on fiberglass cloth as a photocatalyst was studied. The results showed that 2 0×10 -4 mol/dm 3 of dichloroethylene, trichloroethylene and tetrachloroethylene can be completely photocatalytically degraded within a short time under illumination with a 375W medium pressure mercury lamp. The effects of parameters such as illumination time, initial concentration of organochlorine compounds, amount of air flow and concentration of H 2O 2 on the photocatalytic degradation were investigated. The TiO 2 supported on the fiberglass was not easily detached and after 500h illumination there was no significant loss of photocatalytic activity of TiO 2. The passible mechanisms of photocatalytic degradation were discussed.

Tetracycline sensitizes TiO_(2) for visible light photocatalytic degradation via ligand-to-metal charge transfer

Treatment of antibiotics contaminated water remains a global environmental challenge.In this study,tetracycline(TC)was found to effectively sensitize pure TiO_(2) for visible light photocatalytic degradation via a ligand-to-metal charge transfer mechanism.The sensitization was attributed to the formation of TC-TiO_(2) complex and the overlap of the molecular orbitals of TC and the conduction band of TiO_(2).The intermediate degradation products of TC,however,did not sensitize TiO_(2),which was the reason for the low mineralization rate.Nevertheless,our results showed that the intermediate degradation products of TC had significantly reduced bactericidal effects and less induction of antibiotic-resistance genes(ARGs).This study showcases an effective treatment of antibiotics-containing wastewater using the most common photocatalyst TiO_(2) with reduced risk in the spread of ARGs.

Design of metal-organic frameworks(MOFs)-based photocatalyst for solar fuel production and photo-degradation of pollutants

Metal organic frameworks(MOFs)is a research hotspot in the solar fuel production and photo-degradation of pollutants field due to high surface area,rich metal/organic species,large pore volume,and adjustability of structures and compositions.Therefore,in this review,we first summarized the design factors of photocatalytic materials based on MOF from the perspective of"star"MOF.The modification strategies of MOFs-based photocatalysts were discussed to improve its photocatalytic activity and specific applications were summarized as well,including photocatalytic CO_(2)reduction,photocatalytic water splitting and photo-degradation of pollutants.Finally,the advantages and disadvantages of MOFs-based photocatalysts were discussed,the current challenges were highlighted,and suggestions for future research directions were proposed.

Constructing 0D/1D Ag3PO4/TiO_(2) S-scheme heterojunction for efficient photodegradation and oxygen evolution

An S-scheme heterojunction photocatalyst is capable of boosting photogenerated carrier separation and transfer,thus maintaining high photooxidation and photoredox ability.Herein,a 0D Ag_(3)PO_(4) nanoparticles(NPs)/1D TiO_(2) nanofibers(NFs)S-scheme heterojunction with intimate interfacial contact was designed via the the hydro-thermal method.Benefiting from the abundant hydroxyl groups and size confinement effect of TiO_(2) NFs,the average diameter of the Ag_(3)PO_(4) nanoparticles decreased from 100 to 22 nm,which favored the construction of a 0D/1D geometry heterojunction.The multifunctional Ag_(3)PO_(4)/TiO_(2) sample exhibited excellent photocatalytic activity and stability in photocatalytic oxygen production(726μmol/g/h)and photocatalytic degradation of various organic contaminants such as rhodamine B(100%),phenol(60%)and tetracycline hydrochloride(100%).The significant improvements in the photocatalytic performance and stability can be attributed to the intimate interfacial contacts and rich active sites of 0D/1D geometry,fast charge carrier migration,and outstanding photoredox properties induced by the S-scheme charge-transfer route.This work offers a promising strategy for constructing 0D/1D S-scheme heterojunction photocatalysts for improved photocatalytic performance.

Photocatalytic degradation of methyl orange using ZnO/TiO_(2) composites

ZnO/TiO_(2)composites were synthesized by using the solvothermal method and ultrasonic precipitation followed by heat treatment in order to investigate their photocatalytic degradation of methyl orange(MO)in aqueous suspension under UV irradiation.The composition and surface structure of the catalyst were characterized by X-ray diffraction(XRD),field emission scanning electron microscope(FE-SEM),and transmission electron microscopy(TEM).The degradation efficiencies of MO at various pH values were obtained.The highest degradation efficiencies were obtained before 30 min and after 60 min at pH 11.0 and pH 2.0,respectively.A sample analysis was conducted using liquid chromatography coupled with electrospray ionization ion-trap mass spectrometry.Six intermediates were found during the photocatalytic degradation process of quinonoid MO.The degradation pathway of quinonoid MO was also proposed.

Photocatalytic degradation of sulfadiazine in suspensions of TiO_(2)nanosheets with exposed(001)facets

Antibiotics such as sulfonamides are widely used in agriculture as growth promoters and medicine in treatment of infectious diseases.However,the release of these antibiotics has caused serious environmental problems.In this paper,photocatalytic oxidation technology was used to degrade sulfadiazine(SDZ),one of the typical sulfonamides antibiotics,in UV illuminated TiO_(2)suspensions.It was found that TiO_(2)nanosheets(TiO_(2)-NSs)with exposed(001)facets exhibit much higher photoreactivity towards SDZ degradation compared to TiO_(2)nanoparticles(TiO_(2)-NPs)with a rate constant increases from0.017 min^(-1)to 0.035 min^(-1),improving by a factor of 2.1.Under the attacking of reactive oxygen species(ROSs)such as superoxide radicals(*O_(2)^(-))and hydroxyl radicals(*OH),SDZ was steady degraded on the surface of TiO_(2)-NSs.Based on the identification of the produced intermediates by LC–MS/MS,possible degradation pathways of SDZ,which include desulfonation,oxidation and cleavage,were put forwards.After UV irradiation for 4 h,nearly 90%of the total organic carbon(TOC)can be removed in suspensions of TiO_(2)-NSs,indicating the mineralization of SDZ.TiO_(2)-NSs also exhibits excellent stability in photocatalytic degradation of SDZ in wide range of pH.Even after recycling used for 7 times,more than 91.3%of the SDZ can be efficiently removed,indicating that they are promising to be practically used in treatment of wastewater containing antibiotics.

Synergistic effect of CuO coupled with MoS_(2) for enhanced photodegradation of organic dyes under visible light

A series of MoS_(2)-modified CuO(CuO/MoS_(2))heterostructures were successfully fabricated.The photodegradation properties of organic dyes were explored in detail under visible light.The photocatalytic results demonstrate that the CuO/MoS_(2)-3 heterostructure delivers superior degradation rates towards methyl violet dye(MV)and rhodamine B(RhB),reaching 99.8%and 95.3%within 30 min,respectively.The decent photodegradation activity is due to improved visible light adsorption and faster transfer of electron-hole pairs.The radical trapping experiments show that superoxide radicals(O_(2)^(-))and holes(h+)are the main active species in the removal of MV.Furthermore,the CuO/MoS_(2)-3 composite possesses the prominent stability and recyclability.This work offers a highly sustainable technique for designing a high-efficiency photocatalyst to remove environmental pollutants.

活性炭负载TiO_2光催化降解1-萘胺

用活性炭载TiO2 (TiO2 /C)催化剂光催化降解1 萘胺。在用XRD、SEM、比表面积、亚甲蓝吸附值、二氧化钛的负载量对TiO2 /C催化剂进行表征的基础上,考察了催化剂用量、溶液的pH值、1-萘胺的初始浓度等因素对1 萘胺降解率的影响。结果表明,在溶液的pH=7 .10、TiO2 /C光催化剂用量为1 .0g、1 萘胺溶液浓度为1 .40×10-3 mol/L,光照时间为2. 5h时, 1 萘胺的降解率可达80%。

负载型TiO_2/蛇纹石光催化降解4BS染料的研究

以蛇纹石为载体,利用TiOSO4为前驱体,采用水解-沉积法将TiO2超细粒子包覆在蛇纹石表面制得TiO2/蛇纹石负载型光催化剂。探讨了pH值、焙烧温度及光催化剂中TiO2与蛇纹石比例对偶氮直接耐酸大红4BS水溶液的光催化脱色降解的影响。结果表明,在pH为2～4,500℃条件下有明显地脱色效果。

TiO_2光催化剂在污水处理中的应用

在污水处理方面TiO2 光催化剂以其独特的氧化活性、光学性能和无机化能力引起了人们极大的关注。对TiO2 光催化原理、农药、染料和环境荷尔蒙等有机污染物的分解 ,提高催化效率的方法以及其实用技术等方面 。

玻璃纤维支撑TiO_2对有机污染物的光催化降解

介绍了纳米TiO2 粉体的制备方法 ,通过对不同浓度、不同光照条件下的悬浮状和支撑状TiO2 光催化降解有机污染物 (以苯甲酰胺为例 )的试验结果分析 ,发现包覆在玻璃纤维上的TiO2

Photocatalytic parameters and kinetic study for degradation of dichlorophenol-indophenol (DCPIP) dye using highly active mesoporous TiO_2 nanoparticles

Highly active mesoporous TiO_2 of about 6 nm crystal size and 280.7 m^2/g specific surface areas has been successfully synthesized via controlled hydrolysis of titanium butoxide at acidic medium. It was characterized by means of XRD（X-ray diffraction）, SEM（scanning electron microscopy）, TEM（transmission electron microscopy）, FT-IR（Fourier transform infrared spectroscopy）, TGA（thermogravimetric analysis）, DSC（differential scanning calorimetry） and BET（Brunauer–Emmett–Teller） surface area. The degradation of dichlorophenol-indophenol（DCPIP） under ultraviolet（UV） light was studied to evaluate the photocatalytic activity of samples. The effects of different parameters and kinetics were investigated. Accordingly, a complete degradation of DCPIP dye was achieved by applying the optimal operational conditions of 1 g/L of catalyst, 10 mg/L of DCPIP, pH of 3 and the temperature at 25 ± 3°C after 3 min under UV irradiation. Meanwhile, the Langmuir–Hinshelwood kinetic model described the variations in pure photocatalytic branch in consistent with a first order power law model.The results proved that the prepared TiO_2 nanoparticle has a photocatalytic activity significantly better than Degussa P-25.

Degradation of Rhodamine B in the photocatalytic reactor containing TiO_(2)nanotube arrays coupled with nanobubbles

Although photocatalytic technology is applied in water treatment,the challenge still exists due to its low photocatalytic performance.Herein,a photocatalytic reactor coupled with nanobubbles(NBs)is developed to degrade organic pollutants in wastewater.The reactor contains Ti mesh coated with TiO_(2)nanotube arrays as a photocatalyst.The introduction of NBs in the reactor increases the dissolved oxygen content to enhance photocatalytic performance.The photocatalytic reactor exhibits outstanding photocatalytic performance,and the degradation ability of Rhodamine B is 95.39%after 2 h of irradiation treatment.The reactor also shows excellent photodegradation performance for other organic pollutants,such as methylene blue(74.23%),tetracycline(68.68%),and oxytetracycline hydrochloride(64.10%).Radical trapping experiments further prove that·O_(2)−,h^(+)and·OH are the active species for the degradation of RhB in the photocatalytic system.Therefore,this work provides a feasible strategy to design a photocatalytic reactor coupling with nanobubbles technology for the photodegradation of organic pollutants in wastewater.

TiO_(2)/MMT复合材料降解盐酸四环素的研究

为解决抗生素废水排放带来的环境污染问题,以蒙脱土(MMT)为原料,采用水解法制备TiO_(2)/MMT复合材料,利用扫描电镜(SEM)、X射线衍射(XRD)、傅里叶红外光谱(FT-IR)和X射线光电子能谱(XPS)对TiO_(2)/MMT进行物相表征。以盐酸四环素(TC)为目标降解分子,考察了所制备的复合材料对TC的降解性能,并采用紫外-可见分光光谱(UV-vis)跟踪检测TC降解过程。物相表征表明,TiO_(2)均匀分散在MMT的表面;TiO_(2)/MMT中TiO_(2)为锐钛矿相。TiO_(2)/MMT回收样检测到N元素存在。活性数据表明,30%TiO_(2)/MMT(400℃,2 h)复合材料具有最优光催化降解TC性能,在紫外光下对100 mg/L TC的降解率达87.64%,优于纯TiO_(2)(68.74%)和纯MMT(72.22%)。循环试验6次后,催化剂对TC降解率仍达到75%,表明TiO_(2)/MMT对TC具有较高的降解活性和化学稳定性。·O_(2)^(-)和h^(+)是TiO_(2)/MMT光催化降解盐酸四环素的主要活性物质。