Enhanced Photocatalytic Performance and Mechanism of Ag3PO4 Particles Synthesized via a Sonochemical Process

2018 ◽  
Vol 10 (3) ◽  
pp. 337-345 ◽  
Author(s):  
Chengxiang Zheng ◽  
Hua Yang ◽  
Yang Yang ◽  
Haimin Zhang

A facile sonochemical method was used to synthesize Ag3PO4 particles and the effect of pH value, reaction temperature and reaction time on the products was investigated. It is found that the samples prepared at neutral (pH = 7) and alkaline (pH = 11) environments exhibit a similar particle morphology and size. The particles are shaped like spheres with a size distribution majorly focusing on a range of 200–450 nm, and the average particle size is about 300 nm. The sample prepared at acidic environment (pH = 3) is composed of polyhedral microparticles with size of 5–8 μm. At relatively low temperatures of 20–50 °C, the spherical nanoparticles do not undergo obvious morphology/size changes; however, when the temperature is increased up to 80 °C, the nanoparticles are aggregated to form large-sized polyhedral microparticles in the size range of 4–7 μm. Compared to the pH value and reaction temperature, the reaction time has a minor effect on the morphology of Ag3PO4 particles. RhB was chosen as the target pollutant to evaluate the photocatalytic activity of the as-prepared Ag3PO4 samples under simulated-sunlight irradiation. It is shown that the samples consisting of spherical nanoparticles exhibit an extremely high photocatalytic activity, and the degradation percentage of RhB after reaction for 50 min reaches over 90%. The samples of polyhedral microparticles have a relatively low photocatalytic activity, which is possibly due to their large particle size. Hydroxyl (.OH) radical was detected by spectrofluorimetry using terephthalic acid as a .OH scavenger and was not found to be produced over the simulated-sunlight-irradiated Ag3PO4 catalyst. The effect of ethanol, benzoquinone and ammonium oxalate on dye degradation was also investigated. Based on experimental results, the direct oxidation by h+ is suggested to the dominant mechanism toward the dye degradation.

2013 ◽  
Vol 791-793 ◽  
pp. 303-306
Author(s):  
Yong Guang Bi ◽  
Xu Si Xu

In order to obtain hydroxyapatite nanoparticles smaller particle size distribution is relatively uniform, spherical shape and the particle sample, by exploring the reaction temperature, reaction time, concentration and pH on hydroxyapatite nanosize and distribution impact conditions, the results show that when the reaction temperature is 50°C; reaction time 2h; concentration 0.6mol/L; pH value of 10, the prepared nanohydroxyapatite regular shape, less agglomeration, uniform size high crystallinity. Description concentration and pH on nanoparticle size has a significant impact.


Nanomaterials ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 171
Author(s):  
Gui Bing Hong ◽  
Yi Hua Luo ◽  
Kai Jen Chuang ◽  
Hsiu Yueh Cheng ◽  
Kai Chau Chang ◽  
...  

In the scientific industry, sustainable nanotechnology has attracted great attention and has been successful in facilitating solutions to challenges presented in various fields. For the present work, silver nanoparticles (AgNPs) were prepared using a chemical reduction synthesis method. Then, a low-temperature sintering process was deployed to obtain an Ag-conductive ink preparation which could be applied to a flexible substrate. The size and shape of the AgNPs were characterized by ultraviolet–visible spectrophotometry (UV-Vis) and transmission electron microscopy (TEM). The experiments indicated that the size and agglomeration of the AgNPs could be well controlled by varying the reaction time, reaction temperature, and pH value. The rate of nanoparticle generation was the highest when the reaction temperature was 100 °C within the 40 min reaction time, achieving the most satisfactorily dispersed nanoparticles and nanoballs with an average size of 60.25 nm at a pH value of 8. Moreover, the electrical resistivity of the obtained Ag-conductive ink is controllable, under the optimal sintering temperature and time (85 °C for 5 min), leading to an optimal electrical resistivity of 9.9 × 10−6 Ω cm. The results obtained in this study, considering AgNPs and Ag-conductive ink, may also be extended to other metals in future research.


2020 ◽  
Vol 10 (2) ◽  
pp. 88-97
Author(s):  
Zafer Ekinci ◽  
Esref Kurdal ◽  
Meltem Kizilca Coruh

Background: Turkey is approximately 72% of the world’s boron sources. Colemanite, tincal, ulexite and pandermite are among the most significant in Turkey. Boron compounds and minerals are widely used in many industrial fields. Objective: The main purpose of this study was to investigate the control of impurities in the boric acid production process using colemanite by carrying out the reaction with a mixture of CO2 and SO2 - water, and determining the appropriate process conditions to develop a new process as an alternative to the use of sulfuric acid. Due to worrying environmental problems, intensive studies are being carried out globally to reduce the amount of CO2 and SO2 gases released to the atmosphere. Methods: The Taguchi method is an experimental design method that minimizes the product and process variability by selecting the most appropriate combination of the levels of controllable factors compared to uncontrollable factors. Results: It was evaluated the effects of parameters such as reaction temperature, solid-to liquid ratio, SO2/CO2 gas flow rate, particle size, stirring speed and reaction time. The optimum conditions determined to be reaction temperature of 45°C; a solid–liquid ratio of 0.083 g.mL−1; an SO2/CO2 ratio of 2/2 mL.s−1; a particle size of -0.354+0 .210 mm; a mixing speed of 750 rpm and a reaction time of 20 min. Conclusion: Under optimum operating conditions, 96.8% of colemanite was dissolved. It is thought that the industrial application of this study will have positive effects on the greenhouse effect by contributing to the reduction of CO2 and SO2 emissions that cause global warming.


2014 ◽  
Vol 609-610 ◽  
pp. 311-316
Author(s):  
Xiao Cai Yu ◽  
Dong Dong Hu ◽  
Jin Fang Chen ◽  
Xiao Jie Jin ◽  
Xu Zheng

ZnO and Ag-droped ZnO photocatalysts with different Ag loadings (0.5, 1.0, 1.5, 2.0at%) and different calcination temperature (300, 400, 500, 600, 700°C) were synthesized by a sonochemical method. The morphology and crystal pattern of some prepared catalysts were characterized by XRD and SEM techniques which demonstrated that the prepared catalysts were of hexagonal wurtzite structure. Ag loadings, calcination temperature and other factors, dosage of photocatalyst, reaction time and pH value of seawater, were also taken into consideration in the procedure of photocatalytic degradation reaction under UV light. An orthogonal experiment was carried out to investigate the best combination of factors which can reach the best diesel pollution removal rate and the influence order of factors. Reaction time and dosage of catalyst were the most influential factors in this experiment, and the factor of calcination temperature was the weakest influential factor. The removal rate of diesel can up to 78% when the experiment was undertaken under the very conditions: the dosage of catalyst 2.0g/L, reaction time 2.0h, Ag loading of catalyst 1.0 at%, calcinations temperature 400°C and pH value 8.5.


2013 ◽  
Vol 856 ◽  
pp. 22-24 ◽  
Author(s):  
Ramita Batra ◽  
Nidhi Sharotri ◽  
Dhiraj Sud

The present study is an attempt to synthesize N-doped TiO2 nanophotocatalyst using sonochemical method, having photocatalytic activity in the visible region. Non-metal doped nanocatalysts have been successfully synthesized and characterized structurally and physiochemically by using XRD, SEM, TEM, EDX, UV-VIS, FT-IR, Raman and PL. The photocatalytic activity of the synthesized photocatalyst was investigated for the degradation of 2-CP as model compound. The result confirms the successful synthesis of N-doped photocatalyst with particle size 34 nm having anatase phase and shows new peak in a visible region at 587 nm..


2013 ◽  
Vol 662 ◽  
pp. 437-440
Author(s):  
Lin Zhuan Ma ◽  
Jun Ming Guo ◽  
Qiong Fang Cui ◽  
Man Hong Liu ◽  
Ying Jie Zhang

The technology of the acidification is adopted to prepare arsenic trioxide (As2O3). With a concentration of 98% of concentrated sulfuric acid and Orpiment made into a certain ratio of the slurry suspension. Arsenic trioxide’s content is 99.94%, extraction yield can reach to 98.92%. The optimal conditions is reaction temperature at 120°Cand the reaction time in 2.5 h; the slurry ratio is less than 1/6 and particle size is less than 0.080 mm.


2011 ◽  
Vol 402 ◽  
pp. 253-260
Author(s):  
Lan Jie Li ◽  
Shi Li Zheng ◽  
Dong Hui Chen ◽  
Shao Na Wang ◽  
Hao Du ◽  
...  

Leaching of an extracted vanadium residue in sodium sub-molten salt medium was investigated. The significant effects of reaction temperature, particle size of residue, reaction time and NaOH-to-residue mass ratio on vanadium extraction were studied. By the orthogonal experiment study, it can be concluded that the impact order of factors is Tr> t>R according to the significance to the leaching process. Under conditions of reaction temperature 170°C, NaOH-to-residue 4:1, stirring speed 700 rpm, particle size -74 µm and reaction time around 180 min, leaching efficiency of vanadium obtained is higher than 90%. And, the leaching process of vanadium, with activation energy 27.69 kJ•mol-1, is controlled by the chemical reaction-controlled as the following rate equation. ln(1-x)=-kt


2013 ◽  
Vol 781-784 ◽  
pp. 2324-2327
Author(s):  
Xu Zheng ◽  
Xiao Cai Yu ◽  
Yun Qing Liu ◽  
Xiao Xv ◽  
Jin Fang Chen

Sea water joining diesel was selected to prepare simulated marine oil pollution. With the target of removing diesel from seawater, the influence of various factors on the laccase-catalyzed degradation process was discussed. The experimental results show that the laccase-catalyzed degradation process was significantly affected by laccase dosage, reaction temperature, reaction time, pH of the solution and initial concentration of diesel in the oily wastewater. A systematic optimization study was carried out through a orthogonal test on the basis of the results of the single-factor experiments,and the optimum reaction conditions of laccase catalytic degradation diesel pollutants in seawater was determined. The results indicate that under the conditions of diesel initial concentration of 0.1g/L, laccase dosage of 8mg/L, pH value of 6, the reaction temperature of 25°C and the reaction time of 4h, laccase catalytic degradation rate of diesel pollution can be up to 63.85%.


2016 ◽  
Vol 852 ◽  
pp. 618-625
Author(s):  
Qin Ku Zhang ◽  
Bing Hua Yao

Hydrogarnet Ba3In2(OH)12 was synthesized by hydrothermal method from raw materials Ba(NO3)2 and In(OH)3. The obtained sample was characterized by X-ray diffraction (XRD), scanning electron microscope(SEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS) and N2 adsorption-desorption isotherms (BET). Photocatalyitc activity was tested via rhodamine B(RhB) degradation as the modle pollutant. The influence of hydrothermal reaction temperature (T), hydrothermal reaction time (t), Ba/In molar ratio(Ba/In), and NaOH concentration(Cg) on the photocatalytic activity of Ba3In2(OH)12 were investigated. The results showed that the synthetic Ba3In2(OH)12 exhibited highest photocatalytic activity under the optimum hydrothermal reaction conditions of T=200°C, t=14 h, Ba/In=2:1 and Cg=7 mol/L. RhB can be completely mineralized by Ba3In2(OH)12 under 125 W mercury light irradiation for 3 hours. There are many scholars and experts engaged in the research of various types of photocatalytic materials and applied in the degradation of environmental pollutants in the last 40 years. Such as, the oxide of In2O3[1], ZnO, TiO2 et al. The ternary oxide of indium, molybdate, tungstate and vanadate et al. New type quaternary metal oxide. In the past 20 years, indium-based semiconductor material were got rapid development in the field of display, laser, microwave devices, light-emitting diodes and photocatalyst because of which had good gas sensitivity, heat sensitivity, photosensitivity and other characteristics. CaIn2O4 was synthesized using self-propagating high-temperature sysnthesis method[2]. RhB can be absolutely mineralized under solar irradiation for 2 hours. The g-C3N4/CaIn2O4 composite was synthesized using facile solvothermal method[3]. The g-C3N4/CaIn2O4 composite reached a high H2 evolution rate of 62.5 μmol/h from CH3OH/ H2O solution when the content of grapheme was 1wt%. Furthermore, the 1wt% g-C3N4/CaIn2O4 composite did not show deactivation for H2 evolution for longer than 32 h. The core-shell like composite In2O3@Ba2In2O5 was synthesized via chemical impregnation method with sample calcination[4]. It degraded 100% of the MB in 30 min compared with P-25, which degraded 100% of the MB in 120 min. C-CdIn2O4 nanoparticle was synthesized by sol-gel templating method[5]. Natural sunlight illumination experiments showed the H2 evolution rate of C-CdIn2O4 was 17 μmol/h as compared to 2.1 μmol/h for the Pt:TiO2. Hydrogarnet Ba3In2(OH)12 was first described by Kwestroo et al in 1977, who used the prolonged refluxing of BaCl2 and In2O3 in 12 mol/L NaOH at 110°C[6]. The pure Ba3In2(OH)12 was prepared by first preparing pure Ba3In2O6 by prolonged reaction of stoichiometric amounts of BaCO3 and In2O3 at 1300 °C. Then, the pure Ba3In2O6 was reacted with 12 mol/L NaOH at 85 °C for 12 hours under a pure nitrogen atmosphere[7]. Hydrogarnet Ba3In2(OH)12 was synthesized by hydrothermal method, using In(OH)3, Ba(NO3)2 and NaOH. With RhB as a model degradation pollutant, the influence of hydrothermal reaction temperature, hydrothermal reaction time, Ba/In molar ratio and NaOH concentration on the photocatalytic activity of Ba3In2(OH)12 were investigated and the photocatalytic degradation mechanism of RhB were investigated. The results can provide references for the research and application of this material system in the future.


2008 ◽  
Vol 58 ◽  
pp. 121-128 ◽  
Author(s):  
Ying Su ◽  
Xing Dong Lv ◽  
Guo Sheng Gai ◽  
Yu Fen Yang

An attempt was made to prepare the SiO2/cenosphere composite, for which a dense layer of SiO2 particles were successfully coated on the surface of cenospheres by chemical precipitation technique. Surface morphology was observed under SEM, and the exterior constitution was examined through EDX. The result indicated that the amount of SiO2 particles coating on cenospheres decreased with the increasing pH value and the declining reaction temperature, and the particle size reduced as reaction temperature fell down.


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