Analysis of the Ash from One Shanghai Plant Using XRD (X-Ray Diffraction)

2013 ◽  
Vol 664 ◽  
pp. 232-235
Author(s):  
Guo Xian Ma ◽  
Hai Ying Zhang

This study aims to develop a methodology for thermal characterization of APC (air pollution control)fly ash using XRD (X-ray diffraction). It performed XRD analysis as a function of temperature between room temperature and 1200 °C. It is found that major mineralogical components of fly ash involve SiO2, CaCl2, Ca3Si2O7, Ca2SiO4–0.35H2O, Ca9Si6O21–H2O, K2Al2Si2O8–3.8H2O and AlCl3–4Al(OH)3–4H2O. Glass phases account for around 57%, which is conducive to reduction of energy in recycling of the ash. Salts decompose firstly with increase of temperature and then oxides derived from the decomposition process react with SiO2, forming silicates, calcium-silicates and aluminosilicates.

2013 ◽  
Vol 811 ◽  
pp. 240-243
Author(s):  
Guo Xian Ma ◽  
Hai Ying Zhang

APC (air pollution control) fly ash, generated in incineration process of municipal solid waste, is regarded as a hazardous waste because of enrichment of heavy metals. In this work, stabilization of the ash with cement was studied. In addition, XRD analysis of the cement stabilized body was performed as a function of conservation time period. It was It was found that the hydration products cement fly ash and other particles together, which rises with increase of the cement / ash ratio and duration of conservation. Major mineralogical compositions CaCO3, Ca (0H)2 and C-H-S hydration products. Content of Ca (0H)2 and C-H-S rises with increase of conservation period and cement / ash ratio.


2014 ◽  
Vol 893 ◽  
pp. 69-74
Author(s):  
Johar Banjuraizah ◽  
Mohd. Haziq Che Ani ◽  
A.R. Mohamed

Transition metal oxide-doped CCTO (CaCu3Ti4O12) ceramics were prepared by a conventional solgel synthesis method and the effects of pure CCTO and CCTO doped with Mn, Fe, Co, Ni to the crystal structure, microstructures and dielectrical properties of samples were investigated. The phase composition and microstructure were studied by means of X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD analysis reveals that all samples exhibited multiphases with the pseudo-perovskite cubic CCTO phase with space group Im-3 as the main phase in undoped and doped CCTO samples. Peaks of monoclinic CuO and peroveskite CaTiO3 could also be seen in all samples which indicate that solid solution of CuO in CaTiO3 lattice was incomplete.SEM results show that doping effectively enhanced densification. SEM micrographs also suggested that the morphologies of doped CCTO ceramics had showed a matrix consisting of large grains wherein the small grains were embedded between the larger grains. Dielectric properties of pure and doped CCTO were investigated in a broad frequency range of the dielectric constant reached a value as high as εr = 29.4 at room temperature for CCTO doped with Ni at frequency (1000 Hz). Besides the sintering conditions, the microstructure and the dielectric properties of the CCTO are strongly influenced by type of doping elements.


Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3502
Author(s):  
Fangzhou Song ◽  
Masayoshi Uematsu ◽  
Takeshi Yabutsuka ◽  
Takeshi Yao ◽  
Shigeomi Takai

LATP-based composite electrolytes were prepared by sintering the mixtures of LATP precursor and La2O3 nano-powder. Powder X-ray diffraction and scanning electron microscopy suggest that La2O3 can react with LATP during sintering to form fine LaPO4 particles that are dispersed in the LATP matrix. The room temperature conductivity initially increases with La2O3 nano-powder addition showing the maximum of 0.69 mS∙cm−1 at 6 wt.%, above which, conductivity decreases with the introduction of La2O3. The activation energy of conductivity is not largely varied with the La2O3 content, suggesting that the conduction mechanism is essentially preserved despite LaPO4 dispersion. In comparison with the previously reported LATP-LLTO system, although some unidentified impurity slightly reduces the conductivity maximum, the fine dispersion of LaPO4 particles can be achieved in the LATP–La2O3 system.


2017 ◽  
Vol 866 ◽  
pp. 199-203
Author(s):  
Chidchanok Chainej ◽  
Suparut Narksitipan ◽  
Nittaya Jaitanong

The aims of this research were study the microstructures and mechanical properties for partial replacement of cement with Fly ash (FA) and kaolin waste (KW). Ordinary Portland cement were partially replaced with FA and KW in the range of 25-35% and 10-25% by weight of cement powder. The kaolin waste was ground for 180 minutes before using. The specimen was packing into an iron mold which sample size of 5×5×5 cm3. Then, the specimens were kept at room temperature for 24 hours and were moist cured in the incubation lime water bath at age of 3 days. After that the specimens were dry cured with plastic wrap at age of 3, 7, 14 and 28 days. After that the compounds were examined by x-ray diffraction patterns (XRD) and the microstructures were examined by scanning electron microscopy (SEM). The compressive strength was then investigated.


2020 ◽  
Vol 849 ◽  
pp. 113-118
Author(s):  
Yayat Iman Supriyatna ◽  
Slamet Sumardi ◽  
Widi Astuti ◽  
Athessia N. Nainggolan ◽  
Ajeng W. Ismail ◽  
...  

The purpose of this study is to characterize Lampung iron sand and to conduct preliminary experiments on the TiO2 synthesis which can be used for the manufacturing of functional food packaging. The iron sand from South Lampung Regency, Lampung Province that will be utilized as raw material. The experiment was initiated by sieving the iron sand on 80, 100, 150, 200 and 325 mesh sieves. Analysis using X-Ray Fluorescence (XRF) to determine the element content and X-Ray Diffraction (XRD) to observe the mineralization of the iron sand was conducted. The experiment was carried out through the stages of leaching, precipitation, and calcination. Roasting was applied firstly by putting the iron sand into the muffle furnace for 5 hours at a temperature of 700°C. Followed by leaching using HCl for 48 hours and heated at 105°C with a stirring speed of 300 rpm. The leaching solution was filtered with filtrate and solid residue as products. The solid residue was then leached using 10% H2O2 solution. The leached filtrate was heated at 105°C for 40 minutes resulting TiO2 precipitates (powder). Further, the powder was calcined and characterized. Characterization of raw material using XRF shows the major elements of Fe, Ti, Mg, Si, Al and Ca. The highest Ti content is found in mesh 200 with 9.6%, while iron content is about 80.7%. While from the XRD analysis, it shows five mineral types namely magnetite (Fe3O4), Rhodonite (Mn, Fe, Mg, Ca) SiO3, Quart (SiO2), Ilmenite (FeOTiO2) and Rutile (TiO2). The preliminary experiment showed that the Ti content in the synthesized TiO2 powder is 21.2%. The purity of TiO2 is low due to the presence of Fe metal which is dissolved during leaching, so that prior to precipitation purification is needed to remove impurities such as iron and other metals.


2000 ◽  
Vol 5 (S1) ◽  
pp. 412-424
Author(s):  
Jung Han ◽  
Jeffrey J. Figiel ◽  
Gary A. Petersen ◽  
Samuel M. Myers ◽  
Mary H. Crawford ◽  
...  

We report the growth and characterization of quaternary AlGaInN. A combination of photoluminescence (PL), high-resolution x-ray diffraction (XRD), and Rutherford backscattering spectrometry (RBS) characterizations enables us to explore the contours of constant- PL peak energy and lattice parameter as functions of the quaternary compositions. The observation of room temperature PL emission at 351nm (with 20% Al and 5% In) renders initial evidence that the quaternary could be used to provide confinement for GaInN (and possibly GaN). AlGaInN/GaInN MQW heterostructures have been grown; both XRD and PL measurements suggest the possibility of incorporating this quaternary into optoelectronic devices.


Inorganics ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 28
Author(s):  
Kriti Pathak ◽  
Chandan Nandi ◽  
Jean-François Halet ◽  
Sundargopal Ghosh

Synthesis, isolation, and structural characterization of unique metal rich diamagnetic cobaltaborane clusters are reported. They were obtained from reactions of monoborane as well as modified borohydride reagents with cobalt sources. For example, the reaction of [Cp*CoCl]2 with [LiBH4·THF] and subsequent photolysis with excess [BH3·THF] (THF = tetrahydrofuran) at room temperature afforded the 11-vertex tricobaltaborane nido-[(Cp*Co)3B8H10] (1, Cp* = η5-C5Me5). The reaction of Li[BH2S3] with the dicobaltaoctaborane(12) [(Cp*Co)2B6H10] yielded the 10-vertex nido-2,4-[(Cp*Co)2B8H12] cluster (2), extending the library of dicobaltadecaborane(14) analogues. Although cluster 1 adopts a classical 11-vertex-nido-geometry with one cobalt center and four boron atoms forming the open pentagonal face, it disobeys the Polyhedral Skeletal Electron Pair Theory (PSEPT). Compound 2 adopts a perfectly symmetrical 10-vertex-nido framework with a plane of symmetry bisecting the basal boron plane resulting in two {CoB3} units bridged at the base by two boron atoms and possesses the expected electron count. Both compounds were characterized in solution by multinuclear NMR and IR spectroscopies and by mass spectrometry. Single-crystal X-ray diffraction analyses confirmed the structures of the compounds. Additionally, density functional theory (DFT) calculations were performed in order to study and interpret the nature of bonding and electronic structures of these complexes.


2014 ◽  
Vol 625 ◽  
pp. 661-664
Author(s):  
Chen Chuang Lok ◽  
Yin Fong Yeong

In the present work, ZIF-8/6FDA-durene mixed matrix membranes (MMMs) were synthesized and characterized. ZIF-8 nanocrystals, which were used as the inorganic filler, were synthesized using rapid room-temperature synthesis method whereas 6FDA-durene polyimide was synthesized by polycondensation method followed by chemical imidization. Pure and 6FDA-durene membranes loaded with 5 wt%, 10 wt% and 15 wt% of ZIF-8 were fabricated. The structural properties and morphology of the resultant membranes were characterized by using X-ray Diffraction (XRD) and Field emission scanning electron microscope (FESEM) . The EDX images showed that ZIF-8 particles agglomerated in the polymer matrix. However, no phase separation was observed for all resultant MMMs.


2009 ◽  
Vol 63 (6) ◽  
Author(s):  
Yan Li ◽  
Chuan-Sheng Liu ◽  
Yun-Ling Zou

AbstractZnO nano-tubes (ZNTs) have been successfully synthesized via a simple hydrothermal-etching method, and characterized by X-ray diffraction, field emission scanning electron microscopy and room temperature photoluminescence measurement. The as-synthesized ZNTs have a diameter of 500 nm, wall thickness of 20–30 nm, and length of 5 µm. Intensity of the plane (0002) diffraction peak, compared with that of plane (10$$ \bar 1 $$0) of ZNTs, is obviously lower than that of ZnO nano-rods. This phenomenon can be caused by the smaller cross section of plane (0002) of the nano-tubes compared with that of other morphologies. On basis of the morphological analysis, the formation process of nano-tubes can be proposed in two stages: hydrothermal growth and reaction etching process.


2015 ◽  
Vol 754-755 ◽  
pp. 225-229 ◽  
Author(s):  
Yusrina Mat Daud ◽  
Kamarudin Hussin ◽  
Che Mohd Ruzaidi ◽  
Azlin Fazlin Osman ◽  
Mohd Mustafa Al Bakri Abdullah ◽  
...  

Several epoxy nanocomposites incorporating layered silicates and fly ash based geopolymer were analysed by utilising the wide angle X-Ray diffraction (XRD) to characterise the nanoscale dispersion of the layered silicates. The morphological study of the nanocomposites using X-ray diffraction was an operative method to identify exfoliated and intercalated structures in the nanocomposite. It was discovered that the exfoliated structure was observed in the nanocomposites filled with montmorillonite (MMT) and fly ash-based geopolymers; while the intercalated structure was found in the nanocomposites with 3wt% of MMT. The results suggest that that the addition of fly ash-based geopolymers into epoxy/MMT mixture may contribute to superior compressive properties, in comparison to those nanocomposites without geopolymer filler addition.


Sign in / Sign up

Export Citation Format

Share Document