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1.
A Ga2O3–TiO2 photocatalyst was synthesized by a mechanomixing method followed by a sonication technique using different amplitudes of sonication (0%, 25%, 50%, and 75% of 20 kHz). The prepared photocatalysts were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, Fourier-transform infrared, Brunauer–Emmett–Teller (BET) surface area (SBET), zeta potential, and optical techniques. Ga2O3–TiO2 exhibited an excellent photocatalytic activity for Rhodamine B (RhB) dye degradation under UV irradiation. The RhB degradation rate rose linearly with the increase of sonication amplitude. The photodegradation rate (k) of the synthesized samples was calculated according to the Langmuir–Hinshelwood kinetic expression. It reached a maximum of 5.25 × 10−2 min−1 with R2 of 0.99 for Ga2O3–TiO2 (75%) photocatalysts. The main reactive species were detected through radical scavenging experiments. The formation of hole reactive species is the rate-determining step in the case of Ga2O3–TiO2 (75%) photocatalysts.  相似文献   

2.
Photocatalytic degradation of methyl orange by TiO2–SiO2–NiFe2O4 suspensions was investigated. Adsorption studies revealed photocatalytic degradation occurred mainly on the surface of the TiO2–SiO2–NiFe2O4. The disappearance of the compound followed the zero-order kinetics according to the Langmuir–Hinshelwood model and the rate constant was 0.0035 mg L?1 min?1. The rate constant depended on the amount of photocatalyst, initial pH, and the presence of additional scavengers. ?OH radicals and h+ had important roles in the photocatalytic degradation of methyl orange by TiO2–SiO2–NiFe2O4.  相似文献   

3.
A high‐activity AgBr/Ag3PO4 heterojunction photocatalyst was synthesized based on hexadecyltrimethylammonium bromide. Its microspheres were characterized using X‐ray diffractometry, transmission electron microscopy and ultraviolet–visible diffuse reflectance spectroscopy. The new photocatalyst with high photocatalytic activity exceptionally outperforms pure Ag3PO4 and AgBr in methyl orange degradation. The enhancement of photocatalytic activity is attributed to the efficient separation of electron–hole pairs. In this photocatalytic reaction, h+ and ?O2? are the main reactive species that induce visible‐light‐driven degradation.  相似文献   

4.
The degradation of ofloxacin (OFX) at low concentration in aqueous solution by UVA-LED/TiO2 nanotube arrays photocatalytic fuel cells (UVA-LED/TiO2 NTs PFCs) was investigated. TiO2 nanotube arrays (TiO2 NTs) photoanode prepared by anodization-constituted anatase–rutile bicrystalline framework. The results indicated that the degradation efficiency of OFX by UVA-LED/TiO2 NTs PFC was significantly enhanced by 14.3% compared with UVA-LED/TiO2 NTs photocatalysis. The pH affected the degradation efficiency markedly; the highest degradation efficiency (95.0%) and the pseudo-first-order reaction rate constant k value (0.049 min?1) were achieved in neutral condition (pH 7.0). The degradation efficiency increased with the increasing concentration of dissolved oxygen (DO) in the UVA-LED/TiO2 NTs PFC. The main reactive species of OFX degradation are positive holes (h+) and superoxide ion radicals (O 2 ·? ) in a DO sufficient condition. Furthermore, the possible pathways of OFX degradation were proposed.  相似文献   

5.
A magnetized nano‐photocatalyst based on TiO2/magnetic graphene was developed for efficient photodegradation of crystal violet (CV). Scanning electron microscopy, X‐ray diffraction, energy‐dispersive X‐ray spectroscopy and elemental mapping were used to characterize the prepared magnetic nano‐photocatalyst. The photocatalytic activity of the synthesized magnetic nano‐photocatalyst was evaluated using the decomposition of CV as a model organic pollutant under UV light irradiation. The obtained results showed that TiO2/magnetic graphene exhibited much higher photocatalytic performance than bare TiO2. Incorporation of graphene enhanced the activity of the prepared magnetic nano‐photocatalyst. TiO2/magnetic graphene can be easily separated from an aqueous solution by applying an external magnetic field. Effects of pH, magnetized nano‐photocatalyst dosage, UV light irradiation time, H2O2 amount and initial concentration of dye on the photodegradation efficiency were evaluated and optimized. Efficient photodegradation (>98%) of the selected dye under optimized conditions using the synthesized nano‐photocatalyst under UV light irradiation was achieved in 25 min. The prepared magnetic nano‐photocatalyst can be used in a wide pH range (4–10) for degradation of CV. The effects of scavengers, namely methanol (OH? scavenger), p‐benzoquinone (O2?? scavenger) and disodium ethylenediaminetetraacetate (hole scavenger), on CV photodegradation were investigated.  相似文献   

6.
用酸催化溶胶-凝胶法制备了Fe3+掺杂TiO2/凹凸棒(Fe3+-TiO2/ATP)复合光催化剂,对其结构、微观形貌、光吸收性能和可见光下的光催化性能进行了表征。XRD和TEM测试结果表明,Fe3+-TiO2/ATP具有较好的热稳定性,经450 ℃热处理后的ATP晶体结构基本保持不变,锐钛矿TiO2均匀的分布在ATP表面,TiO2颗粒之间无团聚,且平均粒径小于纯TiO2。UV-Vis-DRS测试结果表明,Fe3+的掺杂可明显增强复合光催化剂对可见光的吸收,光响应范围拓展到了整个紫外-可见光区。在可见光下,Fe3+-TiO2/ATP复合光催化剂对亚甲基蓝具有很好的催化降解活性。Fe3+-TiO2/ATP的反应速率常数分别为TiO2/ATP、P25和纯TiO2的1.37、4.83和6.51倍。复合光催化剂的沉降性能优于纯TiO2和P25,易于分离。  相似文献   

7.
Oxygen Vacancy (OVs) and carbon doping of the photocatalyst body will significantly enhance the photocatalytic efficiency. However, synchronous regulation of these two aspects is challenging. In this paper, a novel C@TiO2-x photocatalyst was designed by coupling the surface defect and doping engineering of titania, which can effectively remove rhodamine B (RhB) and has a relatively high performance with wide pH range, high photocatalytic activity and good stability. Within 90 minutes, the photocatalytic degradation rate of RhB by C@TiO2-x (94.1 % at 20 mg/L) is 28 times higher than that of pure TiO2. Free radical trapping experiments and electron spin resonance techniques reveal that superoxide radicals (⋅O2−) and photogenerated holes (h+) play key roles in the photocatalytic degradation of RhB. This study demonstrates the possibility of regulating photocatalysts to degrade pollutants in wastewater based on an integrated strategy.  相似文献   

8.
The methods for preparing the H2O2 generating air (oxygen) electrode and the composite electrode of photocatalyst-TiO2/C loading on the surface of the air (oxygen) electrode were introduced.In the case of the composite electrode,the current efficiency of electro-generated H2O2 is higher than 80%(J≤15mA/cm^2).The degradation of aniline was used as an example to measure the influence of the composite electrode and compared with the system in which the air (oxygen) electrode and the photocatalyst-TiO2 were sqparated.The results confirmed that the composite electrode played an active role on accelerating the degradation rate of aniline.According to the measurement of the polarization curves of composite electrode and TiO2 photo anode,and of the adsorbing amount of aniline on the surface of the composite electrode,the principle of descending the recombination reta of photo-generated electron and hole and of enhancing the oxidation rate of organic molecule was described.The mechanism about the degradation of aniline was also discussed.  相似文献   

9.
We synthesized a novel recoverable and reusable photocatalyst system for tartrazine degradation by one‐step incorporation of Fe3O4 and TiO2 nanoparticles into a molecularly imprinted polymer through a facile precipitation polymerization method. The as‐prepared samples were systematically characterized using X‐ray diffraction, infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, energy‐dispersive spectroscopy, and vibrating sample magnetometry. Benefiting from the positive synergistic effect, tartrazine was almost completely degraded under UV‐C within 180 min by the multicomponent photocatalyst (Fe3O4 + TiO2 + MIP) in comparison with far fewer activities by the corresponding NIP system and the nonmagnetic and bare structures. On the other hand, the central composite design in response surface methodology was applied to optimize the tartrazine photocatalytic degradation process. Twenty experiments were conducted by adjusting three parameters (nanocomposite dosage, initial pH of the reaction solution, and initial dye concentration) in the multiple variable analysis method. A satisfactory correlation between the experimental and predicted values was obtained (R2 = 0.956). Additionally, ANOVA analysis with a p value of 1.15 × 10–5 indicated that the model terms are highly significant. Under the determined optimum conditions, a verification experiment was conducted and shown the adequately approximate value between the predicted (99%) and the experimental (97%) results, which confirmed the validity of the model.  相似文献   

10.
《中国化学快报》2022,33(12):5200-5207
The matched energy band structure and efficient carrier separation efficiency are the keys to heterogeneous photocatalytic reactions. A novel organic/inorganic step scheme (S-scheme) heterojunction PDI-Urea/BiOBr composite photocatalyst was constructed by simple solvothermal reaction combined with in-situ growth strategy. The composite photocatalyst not only has high chemical stability, but also can generate and accumulate a large number of active species (h+, ?O2?, ?OH, H2O2). PDI-Urea/BiOBr showed higher photocatalytic activity for the degradation of antibiotic such as ofloxacin (OFLO), tetracycline (TC) and the production of H2O2 in the spectral range of 400–800 nm. The apparent rate constant of 15% PDI-Urea/BiOBr for photocatalytic degradation of TC (or OFLO) was 2.7 (or 2.5) times that of pure BiOBr and 1.7 (or 1.8) times that of pure PDI-Urea. The H2O2 evolution rate of 15% PDI-Urea/BiOBr was 2.5 times that of PDI-Urea and 1.5 times that of BiOBr, respectively. This work has formed a mature S-scheme heterojunction design thought and method, which offers new visions for the development of heterogeneous photocatalysts.  相似文献   

11.
A visible light-driven Bi2O3–TiO2 composite photocatalyst was prepared by an ethylene glycol-assisted sol–gel method in which ethylene glycol acted as a polycondensation agent to capture metal ions by reacting with bismuth and titanium sources via a complex polycondensation pathway. The photocatalyst was characterized by X-ray photoelectron spectroscopy, X-ray diffraction, acquisition of N2 adsorption–desorption isotherms, transmission electron microscopy, and UV–visible diffuse reflectance spectroscopy. The results revealed that the Bi2O3–TiO2 composite was of smaller particle size, greater specific surface area, and had stronger absorbance in the visible light region than pure TiO2. The photocatalytic activity of the as-prepared catalyst was evaluated by degradation of rhodamine B under visible light irradiation (λ > 400 nm); the as-prepared Bi2O3–TiO2 composite was substantially more active than pure TiO2. This was ascribed to the high surface area and the heterojunction structure.  相似文献   

12.
TiO2 pillared montmorillonites were prepared by introducing Ti4+ into a layer of montmorillonite modified with or without cetyltrimethylammonium bromide. The components and texture of the prepared composites were characterized by thermogravimetric analysis, X-ray powder diffraction and scanning electron misroscopy. The adsorption and photocatalytic degradation performance of a model environmental endocrine disruptor, dimethyl phthalate ester, were investigated using this newly prepared hydrophobic TiO2 pillared montmorillonite photocatalyst. The adsorption of dimethyl phthalate ester from water varied from 9% to 28% on the prepared hydrophobic photocatalyst. Although the experimental results showed that the photocatalytic activity of the hydrophobic photocatalyst was slightly lower than that of hydrophilic one, electron spin resonance verified that hydroxyl radicals were also generated in hydrophobic TiO2 pillared montmorillonite photocatalyst under UV irradiation. To elucidate the decomposition mechanism of dimethyl phthalate ester, 12 main photocatalytic intermediates were identified during the photocatalytic degradation process, and a plausible degradation mechanism was also proposed.  相似文献   

13.
Kaolinite/TiO2 composites were prepared by using sol-gel method and raw kaolin, pretreated kaolinite and tetrabutyl titanate as the main raw materials. X-ray diffractometer, field-emission scanning electron microscope and infrared spectrometer analysis were carried out to characterize the phase composition and microstructure of the samples. The photocatalytic performance of the kaolinite/TiO2 composites were evaluated by degrading the methylene blue (MB) and phenol aqueous solution, respectively. The results show that intercalation and exfoliation reduced the size and thickness of kaolinite particles. Acid treatment improved the distribution and the loading quantity of TiO2 grains. When the kaolinite/TiO2 composites were calcined at 500?°C, the tetragonal structure of anatase particles of 30–100?nm in size were obtained, but the exfoliated kaolinite crystals were damaged. The degradation rate of MB increased gradually with the extension of photocatalytic reaction time and the enhancement of photocatalyst dosage. The adsorption performance of acid-treated kaolinite/TiO2 composite (AKT) was nearly the same as that of raw kaolin/TiO2 composite (RKT), but that of the exfoliated kaolinite/TiO2 composite (EKT) was the most excellent. The photocatalytic performance of AKT and EKT were better than that of RKT, and AKT exhibited the optimum property. Under a certain photocatalyst dosage and photocatalysis time, the absorption rate and the degradation rate decreased gradually with the enhancement of initial concentration of MB. Similar result was also acquired for the degradation of phenol. Both the acid treating and the exfoliating to kaolinite enhanced the photocatalytic performance of the kaolinite/TiO2 composite photocatalysts, but acid treatment may be more helpful to the preparation of high performance kaolinite/TiO2 composite photocatalyst.  相似文献   

14.
The unique heterojunction photocatalyst of graphite carbon nitride(g-C3N4) modified ultrafine TiO2(gC3N4/Ti O2) was successfully fabricated by electrochemical etching and co-annealing method. However,the effects of various environmental factors on the degradation of TC by g-C3N4/Ti O2and the internal reaction mechanism are still unclear. In this study, the effects of initial p H, anions, and cations on the ph...  相似文献   

15.
Sulfur doped ZnO/TiO2 nanocomposite photocatalysts were synthesized by a facile sol‐gel method. The structure and properties of catalysts were characterized by X‐ray diffraction (XRD), X‐ray photoelectron spectroscopy (XPS), UV‐vis diffusive reflectance spectroscopy (DRS) and N2 desorption‐adsorption isotherm. The XRD study showed that TiO2 was anatase phase and there was no obvious difference in crystal composition of various S‐ZnO/TiO2. The XPS study showed that the Zn element exists as ZnO and S atoms form SO2?4. The prepared samples had mesoporosity revealed by N2 desorption‐adsorption isotherm result. The degradation of Rhodamine B dye under visible light irradiation was chosen as probe reaction to evaluate the photocatalytic activity of the ZnO/TiO2 nanocomposite. The commercial TiO2 photocatalyst (Degussa P25) was taken as standard photocatalyst to contrast the prepared different photocatalyst in current work. The improvement of the photocatalytic activity of S‐ZnO/TiO2 composite photocatalyst can be attributed to the suitable energetic positions between ZnO and TiO2, the acidity site caused by sulfur doping and the enlargement of the specific area. S‐3.0ZnO/TiO2 exhibited the highest photocatalytic activity under visible light irradiation after Zn amount was optimized, which was 2.6 times higher than P25.  相似文献   

16.
A novel Pt–TiO2/Ag nanotube photocatalyst has been synthesized successfully via a facile method. TiO2 nanotubes are assembled with numerous ultrathin TiO2 nanosheets and show a highly open structure. The gaps between adjacent TiO2 nanosheets can serve as channels for the access of reactants, accelerating the mass transfer process. During the fabrication process of the Pt–TiO2/Ag nanotube photocatalyst, high‐quality Pt–SiO2 nanotubes are synthesized first with the structure‐directing effect of polyvinylpyrrolidone. Then a TiO2 layer is coated on the outside surface of the silica nanotubes. The introduced titanium species can be converted into TiO2 nanosheet structure during the subsequent hydrothermal treatment, gradually constructing nanosheet‐assembled nanotubes. Lastly, after the introduction of another electron sink function site of Ag through UV irradiation, the Pt–TiO2/Ag nanotube photocatalyst with dual electron sink functional sites is obtained. The specially doped Pt and Ag NPs can simultaneously inhibit the recombination process of photogenerated charge carriers and increase light utilization efficiency. Therefore, the as‐synthesized Pt–TiO2/Ag nanotube catalyst exhibits a high photocatalytic degradation performance for rhodamine B of 0.2 min?1, which is about 3.2 and 5.3 times as high as that of Pt–TiO2 and TiO2 nanotubes because of the enhanced charge carrier separation efficiency. Furthermore, in the unique nanoarchitecture, the nanotubes are assembled with numerous ultrathin TiO2 nanosheets, which can absorb abundant active species and dye molecules for photocatalytic reaction. On the basis of experimental results, a possible rhodamine B degradation mechanism is proposed to explain the excellent photocatalytic efficiency of the Pt–TiO2/Ag nanotube photocatalyst.  相似文献   

17.
Photocatalytic activity of titanium(IV) oxide (TiO2) can be enhanced through modification of its surface‐active sites. Here, iron(III) carboxylate [MIL‐53[Fe]]‐incorporated TiO2 (as MIL‐53(Fe)/TiO2) was prepared using a hydrothermal method. This material was then calcined at 500°C to obtain a MIL‐53(Fe)‐derived γ‐Fe2O3/TiO2 photocatalyst. A photocatalytic study of MIL‐53(Fe)/TiO2 and MIL‐53(Fe)‐derived γ‐Fe2O3/TiO2 toward cationic methylene blue (MB) and anionic methyl orange (MO) showed that MIL‐53(Fe)/TiO2 (0.25 wt%) and MIL‐53(Fe)‐derived γ‐Fe2O3/TiO2 (0.75 wt%) resulted the best degree of dye degradation. The MIL‐53(Fe)‐derived γ‐Fe2O3/TiO2 (0.75 wt%) composite for instance is capable of degrading almost 100% of 20‐ppm MB and MO, respectively, within 6 hr. Photocatalytic degradation of MB and MO was well fitted to the Langmuir‐Hinshelwood pseudo‐first order kinetics model, which indicates physisorption as the key partway that facilitates dye decomposition on the surface of a photocatalyst under UV‐A irradiation. This study provides new insights into the exploration of MILs/TiO2 materials for the environmental remediation and pollution control.  相似文献   

18.
Visible‐light‐driven Ag/AgBr/TiO2/activated carbon (AC) composite was prepared by solgel method coupled with photoreduction method. For comparison, TiO2, TiO2/AC, and Ag/AgBr/TiO2 were also synthesized. Their characteristics were analyzed by XRD, SEM‐EDS, TG‐DSC and UV–vis techniques. Photocatalytic activity and antibacterial performance under visible‐light irradiation were investigated by ICP‐AES, ATR‐FT‐IR and spectrophotometry methods using methylene blue and Escherichia coli as target systems, respectively. The results showed that Ag/AgBr was successfully deposited on anatase TiO2/AC surface, and exhibited a distinct light absorption in the visible region. Ag/AgBr/TiO2/AC displayed excellent antibacterial performance both in dark and under visible‐light illumination. The growth of E. coli cell was inhibited in the presence of Ag/AgBr/TiO2/AC in dark. Moreover, upon visible‐light illumination, a significant damage of cell membrane was noticed. Ag/AgBr/TiO2/AC was also shown higher photocatalytic efficiency for methylene blue degradation than those of TiO2, TiO2/AC, and Ag/AgBr/TiO2. This is attributed to the synergetic effect between AC and Ag/AgBr/TiO2, of which AC acts as the role of increasing reaction areas, continuous enriching, and transferring the adsorbed MB molecules to the surface of supported photocatalysts, and the Ag/AgBr/TiO2 acts as a highly active photocatalyst for degrading MB molecules under visible‐light irradiation.  相似文献   

19.
以钛粉、钽粉为原料,炭黑作为反应性模板,通过熔盐法在炭黑表面原位生长了TaTiC2纳米碳化物涂层,并以所得TaTiC2/C复合物为碳化物前驱体,再经可控氧化制备出中空Ta2O5/TiO2复合光催化剂。采用X射线粉末衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、紫外-可见(UV-Vis)漫反射(DRS)及N2物理吸附等手段对所制备的光催化剂进行形貌、显微结构及孔结构表征。以高压汞灯为紫外光源,以亚甲基蓝为目标降解物,通过光催化降解实验评价中空Ta2O5/TiO2复合光催化剂的光催化活性。结果表明,熔盐法生长碳化物涂层厚度均匀(20~30 nm),碳化物主要以TaTiC2晶相存在且具有纳米级的颗粒尺寸。中空Ta2O5/TiO2复合光催化剂同时具有200 nm左右的中空大孔结构及壳层10 nm左右的介孔结构。中空大孔和介孔的存在提高了所制备催化剂对亚甲基蓝的吸附能力。此外,TiO2与Ta2O5通过电子能带结构的耦合,有效提高了光生电子和空穴的分离效率,从而显著提高了光催化活性。nTinTa=2.5∶1.5时,相应的中空Ta2O5/TiO2复合光催化剂表现出最佳的光催化活性,对亚甲基蓝的紫外光催化降解率高达97%。  相似文献   

20.
Photocatalysis has recently been regarded as one of the most viable technologies for water treatment. Scholars all over the world are focusing on nanocomposites for water treatment for efficient and effective sanitization of bodies of water. Because of their high surface area, high chemical reactivity, excellent mechanical strength, low cost, and nanoscale composite materials have enormous potential to purify water in a various way. In this study, n-type TiO2 was synthesized and tailored to produce a TiO2/BiOI n–p nanocatalyst for enhanced photodegradation of 2,4-dinitrophenol (2,4-DNP) under UV-A and solar light respectively. Because of the formation of a heterojunction between BiOI and TiO2, the photocatalytic activity in TiO2/BiOI absorbs strongly in both the UV and visible regions and it has a lower recombination rate of the e-/h+ pairs. Furthermore, the generation of OH?, O2?– radicals during the oxidation process is attributed to the photodegradation of 2,4-DNP. The results revealed that the TiO2/BiOI manifest outperformed BiOI and TiO2 in terms of photocatalytic function. XRD, BET, HR-SEM-EDX with ECM, HR-TEM, FT-IR, PL, and UV-DRS techniques determined the photocatalyst composition. The HR-SEM images clearly showed that the particles are less than 27 ?nm in size. Thus, nanocomposite materials have played an important role in water purification.  相似文献   

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