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1.
Halloysite nanotubes (HNTs) coatings were prepared by electrophoretic deposition (EPD) from different alcoholic suspensions using polyethyleneimine (PEI) as the dispersant. The results of conductivity, zeta potential, FTIR and thermal analysis showed that PEI is protonated in alcoholic suspensions and then adsorbed on the surface of HNTs enhancing their zeta potential and so colloidal stability. Optimum concentration of PEI decreased with molecular size of alcohol due to the more adsorption of PEI on HNTs. Kinetics of EPD was the fastest from the suspensions with the highest zeta potential. HNTs coatings exhibited high resistance against cracking during their drying due to the self-reinforcement provided by long HNTs and the presence of PEI in their composition which acts as the binder. The coating (6cm2) deposited from ethanolic suspension with 0.5?g/l of PEI (optimum suspension) removed 36% of MB from its aqueous solution (concentration: 5?mg/l and volume: 30?ml) within 2?h.  相似文献   

2.
Titania nanostructured coatings with different porous patterns were fabricated by electrophoretic deposition (EPD) in isopropanolic suspension including different concentrations of carbon active (CA) or carbon black (CB) particles as the porogen additives. Finer and negatively charged CA particles were electrostatically adsorbed on the coarser and positively charged titania particles and formed CA-titania particles. While, finer and positively charged titania particles were electrostatically adsorbed on the coarser and negatively charged CB particles to form titania-CB particles. Both CA-titania and titania-CB particles had the net positive surface charge and so cathodic EPD was applicable. EPD was carried out at optimized conditions of 60?V and 10?s. Thermogravimetry (TG) analysis showed that CA and CB burn out between 450?°C and 600?°C. The higher the carbon content in the suspension the higher was their content in the coating. The coatings were characterized by SEM, AFM, adhesion strength and bioactivity tests. Even coatings with interconnected fine pores and low roughnesses were obtained after the heat treatment of CA-titania coatings. While, rough coatings with coarse and isolated pores were obtained after the heat treatment of titania-CB coatings. The porosity of coating increased as the carbon content increased in the suspension. The hydroxyapatite layer grew on the coatings after their soaking in simulated body fluid for 1week at 37.5?±?1.5?°C.  相似文献   

3.
Hydroxyapatite/titania nanocomposite coatings were electrophoretically deposited from ethanolic suspensions of titania and fiber shaped hydroxyapatite (FHA) nanoparticles. Triethanolamine (TEA) was used to enhance the colloidal stability of particles in suspensions. Electrophoretic deposition (EPD) was performed using the suspensions with different concentrations (wt%) of titania/FHA particles. EPD rate decreased more rapidly with time for suspensions with higher wt% of FHA due to the higher voltage drop over the deposits shaped from them. Stacking of long FHA particles on the substrate during EPD resulted in the formation of coarse pores in the deposits. It was found that titania nanoparticles can more efficiently infiltrate through and fill the pores in TEA containing suspensions due to the stronger electrostatic repulsion force between pore walls (FHA) and titania nanoparticles in them. The coatings deposited from the suspensions with 50 wt% of FHA or more did not crack during drying due to the significant reinforcement action provided by high wt% of FHA in them. Nanocomposite coatings deposited from TEA containing (2 mL/L) suspensions with 50 and 75 wt% of FHA had the best corrosion resistance in simulated body fluid (SBF) solution due to their crack-free microstructure and efficiently filled pores.  相似文献   

4.
Hydroxyapatite (HA) coatings with controlled porosity were prepared by electrophoretic deposition (EPD) method. Carbon black (CB) particles were used as the sacrificial template (porogen agent). Two component suspensions containing different concentrations of HA and CB particles were prepared in isopropanol. It was found that the finer and positively charged HA nanoparticles are heterocoagulated on the coarser and negatively charged CB particles to form CB–HA composite particles with net positive charge. The deposition rate from the suspensions with WR (CCB/CHA ratio) of 0.25 was faster than that of those with WR: 0.5 at initial times of EPD. However the situation was reversed at longer EPD times. It was also found that the amount of porosity in the coatings increases as the CB concentration in the suspension increases (15%, 24%, 31%, 43% for the coatings deposited from the suspensions with 20 g/L HA nanoparticles and 0, 5, 10 and 20 g/L CB particles, respectively).  相似文献   

5.
《Ceramics International》2017,43(5):4663-4669
Three component suspensions of hydroxyapatite (HA), chitosan and CNTs were prepared in ethanol base solution (15 vol% water and 0.05 vol% acetic acid). The adsorption of HA nanoparticles on CNTs was investigated by FTIR and SEM analysis. It was found that HA nanoparticles are adsorbed on CNTs via chemical bonding between -NH2 groups of chitosan (adsorbed on their surface) and -COOH groups of CNTs. Current density as well as kinetics of EPD was studied at 60 V. It was found that current density increases or remains nearly constant during EPD due to the rise in water electrolysis as deposit grows on the substrate. Deposition weight against EPD time showed a linear trend due to the absence of any voltage drop over the deposit during EPD. The incorporation of chitosan and CNTs in the microstructure of coatings was confirmed by TG/DTA and SEM analysis. CNTs exhibited high efficiency in reinforcing the microstructure of coatings and preventing from their cracking. CNTs incorporation in the coatings improved their mechanical properties (adhesion strength, hardness and elastic modulus) and corrosion resistance.  相似文献   

6.
The suspensions of hydroxyapatite (HA) nanoparticles were prepared in different alcohols. The zeta potential of HA nanoparticles was the highest in butanolic suspension (65.65 mV) due to the higher adsorption of RCH2OH2+ species via hydrogen bonding with surface P3OH group of HA. Electrophoretic deposition was performed at 20 and 60 V/cm for different times. Deposition rate was faster in low molecular weight alcohols due to the higher electrophoretic mobility of HA nanoparticles in them. The coating deposited from butanolic suspension had the highest adhesion strength and corrosion resistance in SBF solution at 37.5 °C. The surface of this coating was covered by apatite after immersion in SBF solution for 1 week.  相似文献   

7.
The suspensions of titania nanoparticles in different alcohols (methanol, ethanol and butanol) were prepared using triethanolamine (TEA) as a dispersant. The optimum concentration of TEA was 16.67, 8 and 0.33 mL/L in methanol, ethanol and butanol, respectively. Two component suspensions of titania (20 g/L) and carbon nanotubes (CNTs) (0.1, 0.2, 0.5 and 1 g/L) were prepared in different alcohols without and with optimum concentration of TEA. The finer and positively charged titania nanoparticles were heterocoagulated on the surface of coarser and negatively charged CNTs and generated the titania–CNT composite particles with the net positive charge. In the presence of TEA, titania nanoparticles completely covered CNTs surface due to their higher positive surface charge. At same CNT concentration, the deposition rate was faster for suspensions with TEA additive due to the faster mobility of the composite particles. The photocatalysis efficiency of coatings for methylene blue degradation increased as CNTs were incorporated in their microstructure.  相似文献   

8.
Abstract

Two alginate (Alg) based composite coatings on stainless steel AISI 316L substrates, one containing titania nanoparticles (n-TiO2) and another one a mixture (50/50 wt-%) of n-TiO2 and bioactive glass (BG), intended for biomedical applications, were developed by electrophoretic deposition (EPD) from ethanol/water suspensions. Different n-TiO2 (2–10 g L?1) and BG (1–5 g L?1) contents were studied for a fixed alginate concentration (2 g L?1), and the properties of the electrophoretically obtained coatings were characterised. Coatings with high ceramic content (up to 67 vol.-%) were obtained. The presence of BG particles improves the mechanical properties of the coatings by increasing the adhesion to the substrate and also accelerates the formation of hydroxyapatite after immersion of the coatings in simulated body fluid. The electrochemical behaviour of the coated substrates, evaluated by polarisation curves in Dulbecco’s modified eagle medium at 37°C, confirmed the corrosion protection function of the novel EPD coatings. The present polymer–ceramic composite coatings belong to an emerging family of bioactive, compliant coatings that are promising for a range of biomedical applications.  相似文献   

9.
《Ceramics International》2020,46(8):12111-12119
The Na+ co-doped CaTiO3:Eu3+ powders were produced through the solution combustion method. The phase structure and optical properties of the synthesized samples were adequately characterized by X-ray diffraction (XRD), photoluminescence (PL) spectra, ultraviolet–visible (UV–vis) diffuse reflection spectroscopy and scanning electron microscopy (SEM). The XRD patterns revealed that a low level of Eu3+ doping could not cause lattice distortion of CaTiO3. Photoluminescence (PL) displayed the CaTiO3:0.5% Eu3+ sample synthesized at 900 °C has the weakest PL emission and the low electrons and holes recombination rate. The morphology of the sample was small nanoscale spherical particles. The UV–vis diffuse reflection spectra proved that doping Na+ and Eu3+ enlarged the absorption region and reduced band energy of pure CaTiO3. The photocatalytic properties of Na+ co-doped CaTiO3:Eu3+ samples were investigated via degrading methylene blue (MB) under ultraviolet light irradiation. The CaTiO3:0.5% Eu3+, 0.5% Na+ sample, by contrast, exhibited the greatest photocatalytic property and the degradation rate was as high as 96.62%, which makes it a promising multi-functional material (photocatalytic material and red phosphor) for decreasing organic pollution in water.  相似文献   

10.
《Ceramics International》2022,48(17):24943-24952
In order to effectively reduce the high recombination rate of photogenerated carriers when Bi12TiO20 (BTO) was excited by visible light, Ti3C2Tx/BTO/fluorine-doped tin oxide photoanodes were conveniently prepared with the aid of mechanical coating by gentle ultrasonic mixing. Systematic characterization and the degradation of methylene blue in a photoelectrochemical cell were performed. The results showed that the Ti3C2Tx/BTO composite exhibited a strong light absorption ability and the effective separation of photogenerated carriers. The optimal anode (6 wt% Ti3C2Tx/BTO) degraded 85.4% of methylene blue within 120 min at an applied electric field of 1 V, with a reaction rate that was 3.5 times that of BTO. It was proved that Ti3C2Tx, as a useful co-catalyst, creates an internal electric field at the contact interface with BTO and an external electric field, which are responsible for the enhanced photoelectrocatalytic degradation capacity of the composite anode materials.  相似文献   

11.
Electrophoretic deposition (EPD) method is employed to obtain mesoporous TiO2 film on a titanium (Ti) foil; the film is then mechanically compressed and sintered at 350 °C before being subjected to dyeing. A comprehensive study was made on the mechanistic aspects of the EPD process. The dye-sensitized solar cell (DSSC) using the thus formed TiO2 film rendered a power conversion efficiency (Eff.) of 6.5%. Effects of various compression pressures on the photovoltaic parameters and on other characteristic parameters of the pertinent DSSCs are studied. Electrochemical impedance spectroscopy (EIS) is applied for the first time, using a novel equivalent model, to study the impedance behavior of the DSSC with this type of TiO2 film. We also obtain characteristic parameters of the TiO2 photoanode by using EIS. The coordination number of the TiO2 film, and the ratio of charge transfer resistances of electron recombination and electron transport are also obtained and analyzed. Moreover, we employ a multilayer approach and increase the film thickness to prepare TiO2 films with the same coordination number and porosity; DSSCs using such TiO2 films obtained from P90 and P25 rendered efficiencies of 6.5% and 5.24%, respectively. Scanning electron microscopy (SEM) micrographs are obtained to characterize the TiO2 films formed by the EPD technique and laser-induced transient technique is used to estimate the electron lifetime in the TiO2 films.  相似文献   

12.
A procedure based on electrophoretic deposition (EPD) was developed to coat metal plates with powder catalysts. The method was tested on stainless-steel plates with three Ni-based catalysts for the steam reforming of ethanol. The catalysts (Ni/La2O3/γ-Al2O3) contained 15% Ni and 8% La, and were prepared using three types of γ-alumina with different textural properties. The powder catalysts were suspended in isopropanol, and EPD deposition was performed with a voltage of 100 V and a distance between electrodes of 2 cm. Deposition time was varied between 3 and 7 min, which gave a thickness of the catalyst layer from around 30 to 100 μm. The morphology of the catalyst layer was dependent on the textural characteristics of the γ-Al2O3 used to prepare the catalyst. The activity of the catalyst plates was tested at 773 K using a steam to carbon molar ratio of 4. Significant differences in the selectivity towards ethanol dehydrogenation, reforming, and dehydration to ethylene could be observed between the three catalysts. Carbon deposition on the surface of the plates could be easily determined by SEM/ESEM.  相似文献   

13.
Silver nanoparticles are synthesized by an eco-friendly protocol using Litchi chinensis fruit juice as a reducing and capping agent. UV-vis spectroscopy (SPR band around 447 nm), XRD (crystallinity), HRTEM (size and morphology), EDS (elemental composition) and FTIR (surface functionalities) were used to characterize silver nanoparticles. They are highly dispersed, mostly spherical with an average size of 10 nm. The prepared nanoparticles exhibited rapid reduction of 4-nitro phenol to 4-amino phenol (K = 0.09/min) and photodegradation of methylene blue (K = 0.0335/min) under visible light. The prepared nanoparticles could be an excellent candidate for the separation of hazardous materials.  相似文献   

14.
The extensive occurrence of textile and pharmaceutical contaminants and their metabolites in water systems has posed significant concerns regarding their possible threat to human health and the environmental system. As a result, herein ZnFe2O4 nanoparticles were synthesized through the use of Monsonia burkeana plant extract. The synthesized nanoparticles were characterized using XRD, FTIR, UV–vis, SEM, EDS, TGA, BET, PL, EPR and VSM. XRD showed that the crystalline structure of ZnFe2O4 nanoparticles with a calculated crystal size of 25.03 nm was formed. FT-IR confirmed the characteristic functional groups contained within the M. burkeana plant were deposited on the formed ferrite nanoparticles. BET analysis confirmed the mesoporous nature of ZnFe2O4 with an average pore diameter of 31.6 nm. Morphological studies demonstrated that the formed nanoparticles had spherical as well as rod-like shapes. ZnFe2O4 photocatalyst illustrated that it may be effortlessly detached by an external magnetic field. The optimum conditions for the 99.8% removal of Methylene Blue was obtained at pH12, within 45min and at the optimum dosage of 25 mg of the catalyst. The as-prepared ZnFe2O4 nanoparticles proved to be easily separated and recycled, and remained efficient even after 5 reuses, proving that the material is highly stable. The ROS studies also demonstrated that electrons are the main factors contributing to the degradation of MB. Upon testing the photocatalytic performance of the sulfonamide antibiotic, sulfisoxazole in water showed a degradation of 67%. This study has shown that these materials can be used in targeting textile and pharmaceutically polluted water.  相似文献   

15.
《Ceramics International》2022,48(6):7605-7612
In recent work, pure α-Fe2O3 (F-1) and series of 5% Cu doped Fe2O3 (CF-5) , 10% Cu doped Fe2O3 (CF-10) and 15% Cu doped Fe2O3 (CF-15) nanoparticles by facile chemical coprecipitation method were synthesized to study the effect of concentration of doping for photocatalytic activity. As prepared F-1, CF-5, CF-10, CF-15 nanoparticles were subjected to X-ray diffraction (XRD) and Fourier transform infra-red (FTIR) techniques to analyse the structural and functional groups features. These characterization techniques confirmed the successful doping of Cu 2+ ions in α-Fe2O3. The crystallite size of synthesized samples was calculated by Scherrer formula. Gradually decline in crystallite size from 18 to 15 nm was observed for undoped to doped samples. Scanning electron microscopic (SEM) analysis expressed that doping of Cu reduced the aggregation of particles and enhanced the surface area of nanoparticles. UV–Visible spectroscopic analysis of synthesized samples was used to calculate the bandgap energy of F-1, CF-5, CF-10, CF-15 nanoparticles i.e., 2.0, 1.7, 1.5, 1.4eV respectively. Narrowing bandgap energy of doped hematite supported to perform excellent photocatalytic activity. Maximum degradation of methylene blue was recorded via CF-10 within 140 min. Higher degradation rate of methylene blue by optimal concentration of CF-10 is due to effective electron trapping ability of photocatalyst.  相似文献   

16.
A new signal amplification strategy employing nanocomposites composed of gold nanoparticles (GNPs) with DNA and methylene blue (MB) as labels has been developed to construct a novel immunosensor for the highly sensitive bioanalysis of carcinoembryonic antigen (CEA). To fabricate the label, DNA was first linked to GNPs through the formation of an Au–S bond. Next, the resulting bioconjugates were sequentially bound with MB via the guanine (G) bases in DNA specifically and then with secondary CEA antibody (Ab2) via the crosslinking of glutaraldehyde (GA). The receptor–analyte complex is formed by the biorecognition of the as-obtained MB labeled Ab2 with the primary CEA antibody (Ab1) immobilized on the surface of a modified GNP/Chitosan (Chits) composite electrode. After the receptor–analyte complex has formed, square wave voltammetry (SWV) was employed to oxidize the labeled MB in order to detect the CEA. This immunosensor shows a linear response from 0.10 to 2.0 pg mL−1 CEA with an improved detection limit of 0.05 pg mL−1 as compared to the conventional immunoassay. In addition, this new protocol shows acceptable stability, reproducibility and good recovery (97.5–110.0%) for CEA in human serum with great potential for clinical applications.  相似文献   

17.
Ag-ZnO catalysts for UV-photodegradation of methylene blue   总被引:3,自引:0,他引:3  
High surface area Ag-ZnO catalysts have been made by flame spray pyrolysis (FSP) and characterized by X-ray diffraction (XRD), nitrogen adsorption, UV–vis spectroscopy and electron microscopy (SEM and transmission electron microscopy (TEM)) combined with energy dispersive X-ray spectroscopy (EDXS) for elemental mapping. Silver metal clusters deposited directly on ZnO nanocrystals were obtained from this process. The Ag loading (1–5 at.%) controlled the Ag cluster size from 5 to 25 nm but did not influence the ZnO crystal size. Photodegradation of 10 ppm methylene blue (MB) solution was used to evaluate the performance of these FSP-made Ag-ZnO and was compared to wet-made Ag-ZnO and reference titania photocatalysts. The rate of photodegradation was optimal for Ag loading around 3 at.%. The best photocatalytic performance was exhibited by flame-made Ag-ZnO produced at the longest high-temperature residence times having high crystallinity as determined by XRD and UV–vis.  相似文献   

18.
A comprehensive study pertaining to liquid emulsion membrane (LEM) extraction process of methylene blue from wastewater is presented. The liquid membrane is made of an emulsifying agent (Monumal 80) with various organic diluents. Surfactant (5 wt%) (Monumal 80) and kerosene gave good extraction. Important variables affecting LEM permeation process include stability of membrane, contact time of extraction, strip phase concentration, treat ratio (strip phase: organic phase), stirring speed, feed phase concentration were systematically studied for percentage of extraction by LEM. Kerosene as diluent gave 99.57% extraction with NaOH as strip phase. © 2012 Canadian Society for Chemical Engineering  相似文献   

19.
TiO2 and SnO2/TiO2 nanoparticles with different SnO2 contents (0–20 wt%) were synthesized via surfactant-assisted sol-gel method using a cationic surfactant (cetyltrimethylammonium bromide, CTAB). The effects of SnO2 content on the structural, optical, and catalytic activity of TiO2 have been studied by X-ray diffraction (XRD), Transmission electron microscope (TEM), Scanning electron microscope (SEM), Fourier transformer infrared (FTIR) and UV–vis diffuse reflection spectroscopy (DRS). The total surface acidity of the prepared samples was measured by nonaqueous titration of n-butylamine in acetonitrile and the types of Brönsted and Lewis acid sites were distinguish using FTIR spectra of chemisorbed pyridine. XRD patterns analysis indicates that the crystallite size reduced remarkably and the transformation of anatase-to-rutile phase accelerated greatly with increasing the SnO2 content. TEM images exhibit a spherical shape with an average particle size varying in the range 10–24 nm and high-resolution TEM images (HRTEM) show lattice fringes with interplanar spacing 0.35 nm and 0.32 nm which corresponding to anatase and rutile phases, respectively. SEM images show the amount of SnO2 on the TiO2 surface increases with increasing the SnO2 content and the particles of SnO2 were aggregated on TiO2 surface with increasing SnO2 content to 20% wt. The catalytic activity was tested by various applications: Photodegradation of Methylene Blue (MB) and Rhodamine B (RhB) under UV–vis irradiations and synthesis of xanthene (14-phenyl-14H-dibenzo [a,j] xanthene). Antibacterial and antioxidant activities were also studied. The antibacterial property test was carried out via agar disc diffusion method, and the results indicated that the prepared catalysts showed moderate antibacterial activity.  相似文献   

20.
《Ceramics International》2022,48(4):4563-4575
A liquid metal corrosion (LMC) resistant and metallophobic lanthanum phosphate (LaPO4) coating was prepared on SUS316 stainless steel using electrophoretic deposition (EPD) technique. A specific hierarchical surface structure was created on coating surface by adjusting EPD process parameters. LMC test was performed using three different metal melts, Al–Zn–Mg alloy, Mg–Al–Mn alloy, and pure Zinc. Results indicated that steel bare surface was severely attacked by all three melts. The mechanism of corrosion process was explained in each case. After coating, the LaPO4 covered steel showed an excellent resistance against all three liquid metals. Besides, wetting of steel surface by liquid metals was strongly decreased by application of LaPO4 surface coating. This can be attributed to the intrinsic metallophobic characteristic of LaPO4 as well as the hierarchical surface structure developed on coating surface.  相似文献   

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