scholarly journals Synthesis and Characterizations of (CoxMg(2−x))SiO4 Forsterite Ceramic Pigments from Mirror Waste

Materials ◽  
2018 ◽  
Vol 11 (7) ◽  
pp. 1210 ◽  
Author(s):  
Niti Yongvanich ◽  
Kullada Supanichwatin ◽  
Jitat Penglan ◽  
Narit Triamnak

Ceramic pigments have been widely used in a variety of industries because of their excellent properties, such as high thermal stability, low-cost productions, and simple manufacturing processes. Re-use of mirror waste, which consists of silicon dioxide greater than 70%, is a method that can reduce raw materials cost. In this work, ceramic pigment with forsterite structure, Mg2SiO4, was synthesized via conventional solid state reaction by using mirror waste as a precursor. Solid solutions of Co-doped forsterite pigment, CoxMg(2−x)SiO4 where x = 0.02–1.6, were calcined at 1000 °C for 2 h. The calcined powders were characterized by X-ray diffraction technique (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis spectrophotometer, and color measurement (CIEL*a*b*). XRD results confirmed that forsterite phase was found as a main phase in the ceramic powder. However, the forsterite phase decreased with increased concentration of Co to x = 0.8–1.6. This could be because of the solubility limit of Co in solid solution. In addition, the use of mirror waste as a raw material was able to reduce calcination temperature compared to the use of oxide reagents. Color measurements or CIEL*a*b* color space of forsterite pigments were located in red-blue quadrant for Co-doped pigment.

Cerâmica ◽  
2010 ◽  
Vol 56 (338) ◽  
pp. 156-161 ◽  
Author(s):  
M. H Aly ◽  
I. S Ismael ◽  
F Bondioli

The aim of this work is not only the synthesis of black ceramic pigment with spinel structure using local and inexpensive minerals (chromite and manganese ores) but also throw some light on the relations between the structure and the colour of obtained pigment. Ultimate utilization spinel solid solution in ceramic materials is mostly due to their structure characteristics, their thermal and chemical stability. In this study colour pigments were ned by calcinations at 1250 ºC starting from a mixture of chromite and manganese oxide. Different compositions were tested containing 30, 40 and 50 wt.% of manganese oxide (low and high content respectively). The phase composition and microstructure characterization of both raw material and obtained pigments were evaluated by X-ray diffraction, X-ray fluorescence, polarizing microscope and scanning electron microscope. Furthermore, the colour measurements of the obtained pigments and tiles were evaluated. Composition of all pigments reveal the spinel structure with Cr2FeO4; hematite was also recorded in the mixture of low manganese. The degree of lightness is relatively same in the pigments mixtures of both manganese types. However, tiles could be considered lightness compared with its pigments, especially of the high manganese type. The solid state calcinations reactions are indeed able to form intense brown pigments that can be used as a stain for industrial ceramic applications. The production of less expensive black ceramic pigments from low cost and less pure raw materials that can be utilized in Egypt to substitute for the imported pure oxides or salts is proved superior performance for producing painted pigments.


Energies ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4483
Author(s):  
Yuyingnan Liu ◽  
Xinrui Xu ◽  
Bin Qu ◽  
Xiaofeng Liu ◽  
Weiming Yi ◽  
...  

In this study, corn cob was used as raw material and modified methods employing KOH and KMnO4 were used to prepare activated carbon with high adsorption capacity for mercury ions. Experiments on the effects of different influencing factors on the adsorption of mercury ions were undertaken. The results showed that when modified with KOH, the optimal adsorption time was 120 min, the optimum pH was 4; when modified with KMnO4, the optimal adsorption time was 60 min, the optimal pH was 3, and the optimal amount of adsorbent and the initial concentration were both 0.40 g/L and 100 mg/L under both modified conditions. The adsorption process conforms to the pseudo-second-order kinetic model and Langmuir model. Scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and Zeta potential characterization results showed that the adsorption process is mainly physical adsorption, surface complexation and ion exchange.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Kangqiang Huang ◽  
Li Chen ◽  
Jianwen Xiong ◽  
Meixiang Liao

The Fe-N co-doped TiO2nanocomposites were synthesized by a sol-gel method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectroscopy (UV-vis) and X-ray photoelectron spectroscopy (XPS). Then the photocatalytic inactivation of Fe-N-doped TiO2on leukemia tumors was investigated by using Cell Counting Kit-8 (CCK-8) assay. Additionally, the ultrastructural morphology and apoptotic percentage of treated cells were also studied. The experimental results showed that the growth of leukemic HL60 cells was significantly inhibited in groups treated with TiO2nanoparticles and the photocatalytic activity of Fe-N-TiO2was significantly higher than that of Fe-TiO2and N-TiO2, indicating that the photocatalytic efficiency could be effectively enhanced by the modification of Fe-N. Furthermore, when 2 wt% Fe-N-TiO2nanocomposites at a final concentration of 200 μg/mL were used, the inactivation efficiency of 78.5% was achieved after 30-minute light therapy.


2011 ◽  
Vol 268-270 ◽  
pp. 356-359 ◽  
Author(s):  
Wen Song Lin ◽  
C. H. Wen ◽  
Liang He

Mn, Fe doped ZnO powders (Zn0.95-xMnxFe0.05O2, x≤0.05) were synthesized by an ameliorated sol-gel method, using Zn(CH3COO)2, Mn(CH3COO)2and FeCl2as the raw materials, with the addition of vitamin C as a kind of chemical reducer. The resulting powder was subsequently compacted under pressure of 10 MPa at the temperature of 873K in vacuum. The crystal structure and magnetic properties of Zn0.95-xMnxFe0.05O2powder and bulk samples have been investigated by X-ray diffraction (XRD) and vibrating sample magnetometer (VSM). X-ray photoelectron spectroscopy (XPS) was used to study chemical valence of manganese, iron and zinc in the samples. The x-ray diffraction (XRD) results showed that Zn0.95-xMnxFe0.05O (x≤0.05) samples were single phase with the ZnO-like wurtzite structure. No secondary phase was found in the XRD spectrum. X-ray photoelectron spectroscopy (XPS) showed that Fe and Mn existed in Zn0.95-xMnxFe0.05O2samples in Fe2+and Mn2+states. The results of VSM experiment proved the room temperature ferromagnetic properties (RTFP) of Mn, Fe co-doped ZnO samples.


2021 ◽  
Vol 13 (3) ◽  
pp. 371-380
Author(s):  
Yongjun Wu ◽  
Nina Xie ◽  
Lu Yu

A novel Ag–Si–TiO2 composite was prepared via sol–gel method for removing residual formaldehyde in shiitake mushroom. The structure of Ag–Si–TiO2 composite was characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses. Ultraviolet-visible absorption spectroscopy (UV-Vis) and N2 adsorption-desorption tests showed that Ag and Si co-doped decreased the band gap, the Brunauer-Emmett-Teller (BET) specific surface area of the samples increased and the recombination probability of electron-hole pairs (e--h+) reduced. Effect on removal rate of formaldehyde with different Ag-Si co-doped content, formaldehyde concentration and solution pH were investigated, and the results showed that 6.0 wt%Ag-3.0 wt%Si-TiO2 samples had an optimum catalytic performance, and the degradation efficiency reached 96.6% after 40 W 365 nm UV lamp irradiation for 360 min. The kinetics of formaldehyde degradation by Ag–Si–TiO2 composite photocatalyst could be described by Langmuir-Hinshelwood first-order kinetic model.


2011 ◽  
Vol 89 (7) ◽  
pp. 845-853 ◽  
Author(s):  
Sadok Letaief ◽  
Wendy Pell ◽  
Christian Detellier

The clay mineral kaolinite was used as support of gold nanoparticles for heterogeneous catalysis of oxidation reactions, particularly of carbon monoxide oxidation. The application of clay minerals in the preparation of new functional materials provides an alternative approach for the use of these abundant raw materials. To improve the physicochemical properties of kaolinite, as well as to ensure a strong immobilization of the adsorbed species, kaolinite was functionalized by grafting 2-amino-2-methyl-1,3-propanediol on the internal and external surfaces of the octahedral sheets by reaction with the aluminol groups. Gold nanoparticles were then deposited on the external surfaces of the fine particles of the functionalized kaolinite. The resulting gold kaolinite nanohybrid material was characterized by various physicochemical techniques. X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and energy-dispersive X-ray spectrometry confirmed that gold was effectively reduced to the metallic state during adsorption onto the external surfaces of the modified kaolinite. The gold nanoparticles have a narrow size distribution: more than 88% are less than 4 nm in diameter. Gold nanoparticles deposited on kaolinite catalyze the electro-oxidation of carbon monoxide in alkaline solution at room temperature.


2019 ◽  
Vol 12 (04) ◽  
pp. 1950045 ◽  
Author(s):  
Lin Zhao ◽  
Yanzhao Xie ◽  
Qiuyu Lin ◽  
Rongze Zheng ◽  
Yong Diao

A series of composite catalysts of C, N and P co-doped TiO2 were prepared by sol-gel method, using a biomass (soluble starch) dopant. The samples were characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS), fourier transform infrared (FTIR) spectroscopy. The results show that TiO2 is co-doped with C, N and P by one step. The resulting composite exhibited higher specific surface area, wider visible-light absorption band with respect to the pure TiO2. The sample calcined at 400∘C for 2[Formula: see text]h with a doping amount of 6[Formula: see text]g soluble starch showed the best electrochemical performance. The C, N and P co-doped TiO2 was also used for the degradation of methylene blue (MB) and degradation ratio was up to 98% in 80[Formula: see text]min under visible light irradiation.


2014 ◽  
Vol 936 ◽  
pp. 986-991
Author(s):  
Chuan Hui Gao ◽  
Li Ding ◽  
Yu Min Wu ◽  
Chuan Xing Wang ◽  
Jun Xu

A low-cost raw material, bittern obtained from the production process of sea salt, was used to prepare magnesium oxysulfate hydrate (MgSO4·5Mg (OH)2·2H2O, abbreviated as 152MOS) whiskers via hydrothermal synthesis with ammonia and magnesium sulfate as the other starting raw materials. The bittern was firstly filtered and then used directly without de-coloring. X-ray powder diffraction (XRD), transmission electron microscope (TEM), selected area electron diffraction (SAED), energy dispersive X-ray spectroscopy (EDX) and scanning electron microscope (SEM) were employed to investigate the composition and morphology of the products. It was found that the 152MOS whiskers synthesized from bittern at 190°C for 3 hours exhibited fanlike morphology. The formation of the fanlike whiskers was inhibited and most of the whiskers presented as single fibers when ethanol was used as crystal control agent in the hydrothermal process. From the two-dimensional steps observed at tips of the whiskers, a possible growth mechanism was speculated that it was the extension of dislocations that made the growth of the whiskers.


Clay Minerals ◽  
2018 ◽  
Vol 53 (4) ◽  
pp. 621-641 ◽  
Author(s):  
Ágnes Gál ◽  
Corina Ionescu ◽  
Mátyás Bajusz ◽  
Vlad A. Codrea ◽  
Volker Hoeck ◽  
...  

ABSTRACTSecond-century CE (common era) household pottery sherds found in the city ofNapoca(present day Cluj-Napoca, Romania) in Roman Dacia were investigated by polarized light optical microscopy, X-ray powder diffraction, Fourier-transform infrared spectroscopy and cold field emission scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy to obtain information on technology, raw materials and site of production. Compositionally, all samples are similar with comparable fine and semi-fine microstructures and oriented microtextures. Optically, there is a gradual transition from microcrystalline to an amorphous illitic-muscovitic matrix. The small aplastic inclusions are mostly quartz and feldspar. Fine-grained carbonate aggregates are distributed inhomogeneously in the ceramic body. Well-preserved Middle Miocene foraminifera tests are characteristic of the ceramics. The gradual thermal changes of the matrix and the newly formed phases upon firing, such as ‘ceramic melilite’, Fe-gehlenite, clinopyroxene, glass, hematite and some maghemite support inferences regarding the technological constraints in producing the pottery. The firing took place in a mostly oxidizing atmosphere and the temperature extended from at least 850°C to >900°C. The Middle Miocene marly clay from the area surrounding the site shows similar mineralogical and micropalaeontological contents to those of the ceramic specimens and is the best candidate for the raw material used for local production of the Roman pottery.


Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 631 ◽  
Author(s):  
Osmín Avilés-García ◽  
Jaime Espino-Valencia ◽  
Rubí Romero-Romero ◽  
José Rico-Cerda ◽  
Manuel Arroyo-Albiter ◽  
...  

Various W and Mo co-doped titanium dioxide (TiO2) materials were obtained through the EISA (Evaporation-Induced Self-Assembly) method and then tested as photocatalysts in the degradation of 4-chlorophenol. The synthesized materials were characterized by thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy (RS), N2 physisorption, UV-vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The results showed that the W-Mo-TiO2 catalysts have a high surface area of about 191 m2/g, and the presence of an anatase crystalline phase. The co-doped materials exhibited smaller crystallite sizes than those with one dopant, since the crystallinity is inhibited by the presence of both species. In addition, tungsten and molybdenum dopants are distributed and are incorporated into the anatase structure of TiO2, due to changes in red parameters and lattice expansion. Under our experimental conditions, the co-doped TiO2 catalyst presented 46% more 4-chlorophenol degradation than Degussa P25. The incorporation of two dopant cations in titania improved its photocatalytic performance, which was attributed to a cooperative effect by decreasing the recombination of photogenerated charges, high radiation absorption capacity, high surface areas, and low crystallinity. When TiO2 is co-doped with the same amount of both cations (1 wt.%), the highest degradation and mineralization (97% and 74%, respectively) is achieved. Quinones were the main intermediates in the 4-chlorophenol oxidation by W-Mo-TiO2 and 1,2,4-benzenetriol was incompletely degraded.


Sign in / Sign up

Export Citation Format

Share Document