Ash Fusion During Combustion of Single Corn Straw Pellets

2020 ◽  
Vol 143 (6) ◽  
Author(s):  
Ming Zhai ◽  
Xinyu Wang ◽  
Yichi Zhang ◽  
Aidin Panahi ◽  
Peng Dong ◽  
...  
Keyword(s):  
Elevated Temperatures ◽  
Air Flow ◽  
X Ray Diffraction ◽  
Corn Straw ◽  
Heating Rates ◽  
X Ray ◽  
Carbon Burnout ◽  
Ash Melting ◽  
Increasing Temperature ◽  
Straw Ash

Abstract This investigation identified conditions at which corn straw ash melts and examined how this phenomenon affects the combustion of char residues. Corn straw was pelletized in cylinders and was burned at elevated temperatures in the range of 1200–1400 °C, and at different air flow velocities. The pellets were inserted in a preheated furnace, where they were subjected to moderately high heating rates. Their combustion behavior was observed with cinematography, thermometry, and thermogravimetry. Upon insertion in the furnace, the pellets devolatilized and formed volatile envelope flames, upon extinction of which, the chars experienced concurrent heterogeneous combustion and ash fusion. Residues were assessed by X-ray diffraction (XRD) and scanning electron microscopy (SEM), coupled to energy dispersive spectroscopy (EDS). The burnout times of the volatiles and the chars decreased drastically with increasing temperature. At 1300 °C and 1400 °C, the remaining ash underwent complete melting and the final structures of the pellets collapsed to molten pools. At 1400 °C, all of the chlorine and most of the potassium were released into the gas phase. The straw ash was identified as a high-density silicate melt. Although surface ash melted completely, it flowed to the base of the pellet. Therefore, it did not significantly hinder the oxidation of the carbonaceous char. Hence, to increase the likelihood of complete corn straw carbon burnout and of ash melting and flowing to the bottom of the furnace, operating temperatures higher than 1300 °C, in conjunction with mild air flow rates, are recommended.

scholarly journals High-temperature Fe oxidation coupled with redistribution of framework cations in lobanovite, K2Na(Fe2+ 4Mg2Na)Ti2(Si4O12)2O2(OH)4 – the first titanosilicate case

2019 ◽  
Vol 75 (4) ◽  
pp. 578-590 ◽  
Author(s):  
Elena S. Zhitova ◽  
Andrey A. Zolotarev ◽  
Frank C. Hawthorne ◽  
Sergey V. Krivovichev ◽  
Viktor N. Yakovenchuk ◽  
...  
Keyword(s):  
High Temperature ◽  
Elevated Temperatures ◽  
Iron Oxidation ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Different Temperatures ◽  
Bond Strengths ◽  
Increasing Temperature

The high-temperature (HT) behaviour of lobanovite, K2Na(Fe2+ 4Mg2Na)Ti2(Si4O12)2O2(OH)4, was studied using in situ powder X-ray diffraction in the temperature range 25–1000°C and ex situ single-crystal X-ray diffraction of 17 crystals quenched from different temperatures. HT iron oxidation associated with dehydroxylation starts at 450°C, similar to other ferrous-hydroxy-rich heterophyllosilicates such as astrophyllite and bafertisite. A prominent feature of lobanovite HT crystal chemistry is the redistribution of Fe and Mg+Mn cations over the M(2), M(3), M(4) sites of the octahedral (O) layer that accompanies iron oxidation and dehydroxylation. This HT redistribution of cations has not been observed in titanosilicates until now, and seems to be triggered by the need to maintain bond strengths at the apical oxygen atom of the TiO5 pyramid in the heteropolyhedral (H) layer during oxidation–dehydroxylation. Comparison of the HT behaviour of lobanovite with five-coordinated Ti and astrophyllite with six-coordinated Ti shows that the geometry of the Ti polyhedron plays a key role in the HT behaviour of heterophyllosilicates. The thermal expansion, geometrical changes and redistribution of site occupancies which occur in lobanovite under increasing temperature are reported. A brief discussion is given of minerals in which the cation ordering (usually for Fe and Mg) occurs together with iron oxidation–dehydroxylation at elevated temperatures: micas, amphiboles and tourmalines. Now this list is expanded by the inclusion of titanosilicate minerals.

The Application of X-Ray Diffraction at Elevated Temperatures to Study the Mechanism of Formation of Sodium Tripolyphosphate

1961 ◽  
Vol 5 ◽  
pp. 276-284
Author(s):  
E. L. Moore ◽  
J. S. Metcalf
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Amorphous Phase ◽  
Elevated Temperatures ◽  
Sodium Tripolyphosphate ◽  
X Ray Diffraction ◽  
Mechanism Of Formation ◽  
X Ray ◽  
Temperature Form ◽  
High Temperature Form

AbstractHigh-temperature X-ray diffraction techniques were employed to study the condensation reactions which occur when sodium orthophosphates are heated to 380°C. Crystalline Na4P2O7 and an amorphous phase were formed first from an equimolar mixture of Na2HPO4·NaH2PO4 and Na2HPO4 at temperatures above 150°C. Further heating resulted in the formation of Na5P3O10-I (high-temperature form) at the expense of the crystalline Na4P4O7 and amorphous phase. Crystalline Na5P3O10-II (low-temperature form) appears after Na5P3O10-I.Conditions which affect the yield of crystalline Na4P2O7 and amorphous phase as intermediates and their effect on the yield of Na5P3O10 are also presented.

Polydomain Structure of Epitaxial PbTiO3 films on MgO

1997 ◽  
Vol 493 ◽  
Author(s):  
S. P. Alpay ◽  
A. S. Prakash ◽  
S. Aggarwal ◽  
R. Ramesh ◽  
A. L. Roytburd ◽  
...  
Keyword(s):  
Domain Structure ◽  
Pulsed Laser ◽  
Laser Deposition ◽  
X Ray Diffraction ◽  
X Ray ◽  
Theoretical Predictions ◽  
The Stability ◽  
Increasing Temperature ◽  
Stable Domains ◽  
Domain Stability

ABSTRACTA PbTiO3(001) film grown on MgO(001) by pulsed laser deposition is examined as an example to demonstrate the applications of the domain stability map for epitaxial perovskite films which shows regions of stable domains and fractions of domains in a polydomain structure. X-ray diffraction studies indicate that the film has a …c/a/c/a… domain structure in a temperature range of °C to 400°C with the fraction of c-domains decreasing with increasing temperature. These experimental results are in excellent agreement with theoretical predictions based on the stability map.

Oxidation of Alloy-X in Subcritical, Transition, and Supercritical Water

CORROSION ◽  
10.5006/3881 ◽  
2021 ◽  
Author(s):  
Zachary Karmiol ◽  
Dev Chidambaram
Keyword(s):  
Supercritical Water ◽  
Photoelectron Spectroscopy ◽  
Focused Ion Beam ◽  
Elevated Temperatures ◽  
Subcritical Water ◽  
Ion Beam ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Based Superalloy ◽  
Before And After

This work investigates the oxidation of a nickel based superalloy, namely Alloy X, in water at elevated temperatures: subcritical water at 261°C and 27 MPa, the transition between subcritical and supercritical water at 374°C and 27 MPa, and supercritical water at 380°C and 27 MPa for 100 hours. The morphology of the sample surfaces were studied using scanning electron microscopy coupled with focused ion beam milling, and the surface chemistry was investigated using X-ray diffraction, Raman spectroscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy before and after exposure studies. Surfaces of all samples were identified to comprise of a ferrite spinel containing aluminum.

X-ray diffraction investigations of structural changes in Co/Cu multilayers at elevated temperatures

2002 ◽  
Vol 411 (2) ◽  
pp. 234-239 ◽  
Author(s):  
M Hecker ◽  
W Pitschke ◽  
D Tietjen ◽  
C.M Schneider
Keyword(s):  
Structural Changes ◽  
Elevated Temperatures ◽  
X Ray Diffraction ◽  
X Ray

Fundamental and Technological Aspects of Actinide Oxide Pyrochlores: Relevance For Immobilization Matrices

1999 ◽  
Vol 556 ◽  
Author(s):  
P. E. Raison ◽  
R. G. Haire ◽  
T. Sato ◽  
T. Ogawa
Keyword(s):  
Elevated Temperatures ◽  
Materials Science ◽  
Oxidation Potential ◽  
Oxygen Stoichiometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxidation Reduction ◽  
Reduction Cycle ◽  
Fluorite Type ◽  
The Stability

AbstractPolycrystalline pyrochlore oxides consisting of selected f elements (lanthanides and actinides) and Zr and Hf have been prepared and characterized. Characterization to date has been primarily by X-ray diffraction, both at room and at elevated temperatures. Initial studies concentrated on selected lanthanides and the Np, Pu and Am analogs (reported here) but have been extended to the other actinide elements through Cf. Data from these studies have been used to establish a systematic correlation regarding the fundamental materials science of these particular pyrochlores and structurally related fluorite-type dioxides. In addition to pursuing their materials science, we have addressed some potential technological applications for these materials. Some of the latter concern: (1) immobilization matrices; (2) materials for transmutation concepts; and (3) special nuclear fuel forms that can minimize the generation of nuclear wastes. For f elements that display both a III and IV oxidation state in oxide matrices, the synthetic path required for producing the desired pyrochlore oxide is dictated by their pseudo-oxidation potential the stability of the compound towards oxygen uptake. For the f elements that display an oxidationreduction cycle for pyrochlore-dioxide solid solution, X-ray diffraction can be used to identify the composition in the oxidation-reduction cycle, the oxygen stoichiometry and/or the composition. This paper concentrates on the Np, Pu and Am systems, and addresses the above aspects, the role of the crystal matrix in controlling the ceramic products as well as discussingsome custom-tailored materials.

scholarly journals Effect of Locally Available Wheat Straw Ash in Developing High Strength Concrete

2021 ◽  
pp. 19-28
Author(s):  
Muhammad Armaghan Siffat ◽  
Muhammad Ishfaq ◽  
Afaq Ahmad ◽  
Khalil Ur Rehman ◽  
Fawad Ahmad
Keyword(s):  
Mechanical Properties ◽  
Compressive Strength ◽  
Wheat Straw ◽  
High Strength Concrete ◽  
High Strength ◽  
Optimum Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Strength Concrete ◽  
Straw Ash

This study is supervised to assess the characteristics of the locally available wheat straw ash (WSA) to consume as a substitute to the cement and support in enhancing the mechanical properties of concrete. Initially, after incineration at optimum temperature of 800°C for 0.5, the ash of wheat straw was made up to the desirable level of fineness by passing through it to the several grinding cycles. Subsequently, the X-ray fluorescence (XRF) along with X-ray diffraction (XRD) testing conducted on ash of wheat straw for the evaluation its pozzolanic potential. Finally, the specimens of concrete were made by consuming 10% and 20% percentages of wheat straw ash as a replacement in concrete to conclude its impact on the compressive strength of high strength concrete. The cylinders of steel of dimensions 10cm diameter x 20cm depth were acquired to evaluate the compressive strength of high strength concrete. The relative outcomes of cylinders made of wheat straw ash substitution presented the slight increase in strength values of the concrete. Ultimately, the C-100 blends and WSA aided cement blends were inspected for the rheology of WSA through FTIR spectroscopy along with Thermogravimetric technique. The conclusions authenticate the WSA potential to replace cement in the manufacturing of the high strength concrete.

scholarly journals Structural and thermoelectric properties of the Pr2Zr2O7 compound

2019 ◽  
pp. 4-9
Author(s):  
Adolfo Quiroz-Rodríguez ◽  
Cesia Guarneros-Aguilar ◽  
Ricardo Agustin-Serrano
Keyword(s):  
Electron Microscopy ◽  
Thermal Conductivity ◽  
Thermoelectric Properties ◽  
Crystal Size ◽  
Ambient Pressure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Increasing Temperature ◽  
Thermal Stability Of ◽  
Scanning Electron

In this research, it is presented a detailed study of the structural and thermoelectric properties of the pyrochlore zirconium Pr2Zr2O7 compound prepared by solid-state reaction (SSR) in air at ambient pressure. The synthesized sample was characterized using powder X-ray diffraction. The thermal stability of the thermoelectric compound (TE) Pr2Zr2O7 was tested by thermogravimetric analysis (TGA) and differential thermal analysis (DTA). Scanning electron microscopy shows that the crystal size varies between 0.69 and 2.81μm. Electrical conductivity (\sigma) of the sample calcined at 1400 °C presented values increase irregularly with the increasing temperature from 0.001 to 0.018 S cm-1 as expected in a semiconductor material. The thermal conductivity is lower than 0.44 - 775 W m-1 K-1 which is quite anomalous in comparison with the thermal conductivity of other oxides.

scholarly journals Formation of metal oxide-based hydroxysodalite by alkali-activation of kaolinite

Chemija ◽  
2020 ◽  
Vol 31 (3) ◽  
Author(s):  
Ehab AlShamaileh ◽  
Muayad Esaifan ◽  
Qusay Abu-Afifeh
Keyword(s):  
Activation Energy ◽  
Metal Oxide ◽  
Alkali Activation ◽  
Dsc Analysis ◽  
X Ray Diffraction ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrd Study ◽  
Dsc Curves

The formation of metal oxide-based hydroxysodalite by alkali-activation of kaolinite is studied using X-ray diffraction (XRD) study and differential scanning calorimetry (DSC) analysis. Different metal oxides (CoO, MgO, FeO and SiO2) were used to form the metal oxide-based hydroxysodalite. The transformation from kaolinite into hydroxysodalite is confirmed by XRD. In the thermodynamic study, the maximum peak temperatures for DSC curves at various heating rates were used to determine the activation energy (Ea) of the hydroxysodalite formation. With magnesium oxide and cobalt oxide, the formation process was found to be exothermic while it was endothermic with iron oxide.

Synthesis and Luminescence Properties of Chalcopyrite-Type CuAlS2

2006 ◽  
Vol 301 ◽  
pp. 177-180 ◽  
Author(s):  
Yuichiro Kuroki ◽  
Tomoichiro Okamoto ◽  
Masasuke Takata
Keyword(s):  
Diffraction Analysis ◽  
Room Temperature ◽  
Single Phase ◽  
Elevated Temperatures ◽  
Emission Peak ◽  
Maximum Intensity ◽  
X Ray Diffraction ◽  
Ultraviolet Emission ◽  
X Ray ◽  
Copper Aluminum

Copper aluminum disulfide (CuAlS2) powders were synthesized in an evacuated ampoule at elevated temperatures. X-ray diffraction analysis revealed that the powders heated at temperatures higher than 800oC were single-phase CuAlS2. In the cathodoluminescence (CL) spectra measured at room temperature, the powders heated at temperatures higher than 600oC exhibited a visible emission peak at approximately 1.8 eV and a distinct ultraviolet emission peak at 3.45 eV. The powder heated at 700oC showed the maximum intensity of ultraviolet emission which is considered to be associated with excitons.

Sign in / Sign up

Export Citation Format

Share Document