Application of vermiculite and limestone to desulphurization and to the removal of dust during briquette combustion

2003 ◽  
Vol 67 (6) ◽  
pp. 1243-1251 ◽  
Author(s):  
A. Lu ◽  
D. Zhao ◽  
J. Li ◽  
C. Wang ◽  
S. Qin

AbstractSmall domestic cooking furnaces are widely used in China. These cooking furnaces release SO2 gas and dust into the atmosphere and cause serious air pollution. Experiments were conducted to investigate the effects of vermiculite, limestone or CaCO3, and combustion temperature and time on desulphurization and dust removal during briquette combustion in small domestic cooking furnaces. Additives used in the coal are vermiculite, CaCO3 and bentonite. Vermiculite is used for its expansion property to improve the contact between CaCO3 and SO2 and to convey O2 into the interior of briquette; CaCO3 is used as a chemical reactant to react with SO2 to form CaSO4; and bentonite is used to develop briquette strength. Expansion of vermiculite develops loose interior structures, such as pores or cracks, inside the briquette, and thus brings enough oxygen for combustion and sulphation reaction. Effective combustion of the original carbon reduces amounts of dust in the fly ash. X-ray diffraction, optical microscopy, and scanning electron microscopy with energy dispersive X-ray analysis show that S exists in the ash only as anhydrite CaSO4, a product of SO2 reacting with CaCO3 and O2. The formation of CaSO4 effectively reduces or eliminates SO2 emission from coal combustion. The major factors controlling S retention are vermiculite, CaCO3 and combustion temperature. The S retention ratio increases with increasing vermiculite amount at 950°C. The S retention ratio also increases with increasing Ca/S molar ratio, and the best Ca/S ratio is 2-3 for most combustion. With 12 g of the original coal, 1 to 2 g of vermiculite, a molar Ca/S ratio of 2.55 by adding CaCO3, and some bentonite, a S retention ratio >65% can be readily achieved. The highest S retention ratio of 97.9% is achieved at 950°C with addition of 2 g of vermiculite, a Ca/S ratio of 2.55 and bentonite.

2019 ◽  
Vol 966 ◽  
pp. 200-203
Author(s):  
Zaenal Arifin ◽  
Triwikantoro ◽  
Bintoro Anang Subagyo ◽  
Mochamad Zainuri ◽  
Darminto

Abstract. In this study, the CaCO3 powder has been successfully synthesized by mixing CaCl2 from natural limestone and Na2CO3 in the same molar ratio. The mixing process of solutions was carried out by employing the molar contents of 0.125, 0.25, 0.375 and 0.5M at varying temperatures of 30, 40, 60 and 80ᴼC. The produced CaCO3 microparticles were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The highest content of aragonite phase with morphology rod-like of the samples is around 29 wt%, resulting from the process using solution of 0.125 M at 80 ᴼC. While at 30 ᴼC and 40 ᴼC produced 100 wt% calcite phase.


2008 ◽  
Vol 368-372 ◽  
pp. 995-997
Author(s):  
Cui Wei Li ◽  
Hong Xiang Zhai ◽  
Yang Zhou ◽  
Shi Bo Li ◽  
Zhi Li Zhang

In this study, free Ti/Si/Al/C powder mixtures with molar ratio of 3:0.4:0.8:1.8 were heated in Argon with various schedules, in order to reveal the possibility for the synthesis of Ti3Si0.4Al0.8C1.8 solid solution powder. X-ray diffraction (XRD) was used for the evaluation of phase identities of the powder after different treatments. Scanning electron microscopy (SEM) was used to observe the morphology of the Ti3Si0.4Al0.8C1.8 solid solution. XRD results showed that predominantly single phase samples of Ti3Si0.4Al0.8C1.8 was prepared after heating at 1400oC for 5 min in Argon and the lattice parameters of Ti3Si0.4Al0.8C1.8 lay between those of Ti3SiC2 and Ti3AlC2.


2006 ◽  
Vol 530-531 ◽  
pp. 593-598 ◽  
Author(s):  
D.S. Gouveia ◽  
Ana Helena A. Bressiani ◽  
José Carlos Bressiani

Calcium phosphates with different Ca/P molar ratio can be obtained depending the precipitation conditions such as pH and temperature. In this work the effect of the pH’s variation during the H3PO4 addition in the synthesis of hydroxyapatite-HA, (Ca/P molar ratio 1.67) by neutralization method, was studied. The H3PO4 addition’s rate was 1.0, 1.5, 8.0 mL.min-1 and in other experiment the H3PO4 was added at a time. After the addition was completed the pH ranged from 7-12. The suspensions were kept during 24 hours for ripening. The precipitate was separated from the suspension by vacuum filtration, washed with distilled water and dried at 70°C/24h. Afterwards the materials were analyzed by thermogravimetric analysis (TGA) with heating rate of 10°C/min in air. The calcination of the powders was accomplished at 800°C/3h with heating rate of 10°C.min-1. The powders were characterized by X-ray diffraction (XRD), infrared spectrometry (FTIR), specific surface area (BET), and scanning electron microscopy (SEM). The results indicated that the ratio of addition of the acid can influence both the morphology and the formation of the phases (HA and TCP) in the obtained powders.


2014 ◽  
Vol 32 (4) ◽  
pp. 696-701 ◽  
Author(s):  
Hong-Yan Sun ◽  
Xin Kong ◽  
Wei Sen ◽  
Zhong-Zhou Yi ◽  
Bao-Sen Wang ◽  
...  

AbstractEffect of different Sn contents on combustion synthesis of Ti2SnC was studied using elemental Ti, Sn, C and TiC powders as raw materials in the Ti-Sn-C and Ti-Sn-C-TiC system, in which the molar ratio of Ti/C was set as 2:1. The reaction mechanism for the formation of Ti2SnC was also investigated. The results showed that the amount of Ti2SnC in combustion products firstly increased with increasing of Sn content (0.6 to 0.8 mol), and then decreased with further increasing of Sn content (1.0 to 1.2 mol). Upon addition of 15 % TiC instead of Ti and C, the optimum addition of Sn decreased to 0.7 mol and a higher purity of Ti2SnC was obtained. The Ti2SnC powders were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD).


2012 ◽  
Vol 538-541 ◽  
pp. 2236-2239 ◽  
Author(s):  
Peng Deng ◽  
Yu Qin Liu ◽  
Da Jian Ma ◽  
Hong Wen Ma

The present paper focuses on the experimental investigation of the aluminothermic reduction of magnesia under vacuum condition with the fixed magnesia to aluminum molar ratio of 11:6. The influences of reaction temperature and time on the reduction ratio of magnesia were studied. The chemical composition, phase constitution and morphology of the condensed magnesium and the briquettes after thermal reduction were investigated by X-ray diffraction, scanning electron microscopy equipped with energy dispersive spectrometry. The reduction ratio of magnesia increases with the increase in the reaction temperature and time. The briquettes after thermal reduction at 1050°C-1150°C are mainly composed of the spinel, unreacted magnesia and aluminum. The briquette after 1 hrs thermal reduction at 1200°C contains corundum, magnesium aluminium oxide, trace amount of spinel, unreacted MgO and aluminium.


2018 ◽  
Vol 18 (4) ◽  
pp. 607
Author(s):  
Meyga Evi Ferama Sari ◽  
Suprapto Suprapto ◽  
Didik Prasetyoko

Alkalinity is one of the most important factors that influence the crystallization process of zeolite and the product properties. The influence of alkalinity on the synthesis of sodalite from kaolin without calcinations was reported in this research. The synthesis of sodalite using molar ratio of Na2O/Al2O3 = x, H2O/Na2O = 128/x and SiO2/Al2O3 = 2/x, where x was the variation of molar ratio of alkalinity: 10, 20, 30, and 40. The synthesis has done by stirring for 6 h, without aging, and the crystallization time was 24 h under hydrothermal method (100 °C). The products were characterized by X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), and Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX). The X-ray diffraction pattern and infrared spectroscopy shown that pure sodalite was formed by using molar ratio of alkalinity 10, 20, and 30. The crystallinity and particle size increase along with increasing of alkalinity. Quartz was formed by using molar ratio of alkalinity 40.


2011 ◽  
Vol 121-126 ◽  
pp. 65-69
Author(s):  
Li Peng Zhang ◽  
Xian Jin Yu ◽  
Zhi Wei Ge ◽  
Yun Hui Dong ◽  
Dang Gang Li

Al-Ni Alloys were obtained from NiCl2-AlCl3-1-ethyl-3-methylimidazolium bromide ([EMIM]Br) ionic liquid at room temperature. The analysis of Al-Ni alloys that co-deposited at different potentials for 2h were performed using Scanning Electron Microscopy (SEM) and X-ray diffraction analysis (XRD). It appears that Ni has been rapidly solidified in the alloys and homogeneous Al-Ni alloys can be obtained at room temperature. As increasing the overpotential, the amount of Ni in the alloys was decreased whereas the amount of Al was increased. The chloride pitting potentials of alloys with the molar ratio of NiCl2/AlCl3/[EMIM]Br 0.03:2:1 was approximately 0.3 V more than pure Al.


2016 ◽  
Vol 680 ◽  
pp. 301-305 ◽  
Author(s):  
Ai Qing Jia ◽  
Wei Jun Zhang ◽  
Xing Yu Cheng ◽  
Zhuo Feng Liu

The CaO-B2O3-SiO2 glass ceramics system with four different boron contents (14 wt. %, 16.4 wt. %, 18.6 wt. %, 21 wt. %) were prepared under 900oC. The properties and microstructures are characterized by Differential Scanning Calorimeter (DSC), X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The effects of boron contents on the composition of crystalline phases and the properties of CaO-B2O3-SiO2 glass ceramics system were studied. The results show that when the molar ratio of CaO/SiO2 is 1.06, as the content of B2O3 increases, the major crystalline phases experiences the transformation from CaSiO3 to CaB2O4 and the content of α-SiO2 crystalline phase decreases, and the dielectric constant increases firstly but it decreases after the content of B2O3 reaches to 18.6 wt. %, while the dielectric loss tgδ of decreases gradually with the addition of boron content. When the content of B2O3 is 16.4 wt. %, the CaO-B2O3-SiO2 glass ceramics with a bulk density of 2.47 g/cm3 exhibits good dielectric properties (1 MHz): εr=6.03, tgδ=3.49×10-3.


Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.


Author(s):  
Howard S. Kaufman ◽  
Keith D. Lillemoe ◽  
John T. Mastovich ◽  
Henry A. Pitt

Gallstones contain precipitated cholesterol, calcium salts, and proteins. Calcium (Ca) bilirubinate, palmitate, phosphate, and carbonate occurring in gallstones have variable morphologies but characteristic windowless energy dispersive x-ray (EDX) spectra. Previous studies of gallstone microstructure and composition using scanning electron microscopy (SEM) with EDX have been limited to dehydrated samples. In this state, Ca bilirubinates appear as either glassy masses, which predominate in black pigment stones, or as clusters, which are found mostly in cholesterol gallstones. The three polymorphs of Ca carbonate, calcite, vaterite, and aragonite, have been identified in gallstones by x-ray diffraction, however; the morphologies of these crystals vary in the literature. The purpose of this experiment was to study fresh gallstones by environmental SEM (ESEM) to determine if dehydration affects gallstone Ca salt morphology.Gallstones and bile were obtained fresh at cholecystectomy from 6 patients. To prevent dehydration, stones were stored in bile at 37°C. All samples were studied within 4 days of procurement.


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