scholarly journals Effect of Cr on the Mineral Structure and Composition of Cement Clinker and Its Solidification Behavior

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1529
Author(s):  
Haihong Fan ◽  
Mengqi Lv ◽  
Xiaosha Wang ◽  
Jianmin Xiao ◽  
Xiaofan Mi ◽  
...  
Keyword(s):  
Relative Content ◽  
Cement Industry ◽  
Cement Clinker ◽  
Magic Angle ◽  
Solidification Behavior ◽  
Mineral Phase ◽  
Metal Solidification ◽  
X Ray ◽  
Oxygen Tetrahedron ◽  
Silicon Oxygen

In order to reveal the solidification behavior of Cr in the cement clinker mineral phase, 29Si magic-angle spinning nuclear magnetic resonance, X-ray diffraction, and scanning electron microscopy with energy-dispersive X-ray spectroscopy techniques were used to analyze the morphology and composition of the cement clinker mineral phase doped with Cr. The results showed that the addition of Cr did not change the chemical environment of 29Si in the clinker mineral phase, and it was still an isolated silicon–oxygen tetrahedron. Cr affected the orientation of the silicon–oxygen tetrahedron and the coordination number of calcium, leading to the formation of defects in the crystal structure of the clinker mineral phase, by replacing Ca2+ into the mineral phase lattice to form a new mineral phase Ca3Cr2(SiO4)3. Cr acted as a stabilizer for the formation of β-C2S in the clinker calcination. As the amount of Cr increased, the relative content of C3S decreased and the relative content of C2S increased. Further, Cr easily dissolved in C2S, while it was not found in C3S. This study is conducive to further research on the mechanism of heavy metal solidification in cement clinker. Furthermore, it is important to evaluate the environmental risk of heavy metals in the process of sludge disposal through cement kiln and promote the utilization of sludge resources and the sustainable development of the cement industry.

scholarly journals Metal magnesium industry waste for partial replacement of Portland cement

2020 ◽  
Vol 13 (6) ◽  
Author(s):  
Maysa Lorena Figueiredo Martins ◽  
Richard Rodrigues Barreto ◽  
Paulo Roberto Ribeiro Soares Junior ◽  
Ivete Peixoto Pinheiro ◽  
Augusto Cesar da Silva Bezerra
Keyword(s):  
Portland Cement ◽  
Mineralogical Composition ◽  
High Energy ◽  
Cement Industry ◽  
Cement Clinker ◽  
Partial Replacement ◽  
Supplementary Cementitious Material ◽  
X Ray ◽  
Industry Waste ◽  
Energy Demands

ABSTRACT: The high demand for concrete has triggered studies on the mitigation of Portland cement production impacts, such as greenhouse gas emissions and energy demands, in addition to enabling cost reduction. Partial replacement of cement with other materials has been employed as an alternative to minimize the damage caused by the cement industry. In this regard, it is necessary to use materials that efficiently replace cement clinker. This study uses waste generated from the production of metallic magnesium as a partial replacement for Portland cement. The substitution is aimed at reducing the amount of clinker used, as its production necessitates high energy consumption and results in emission of large quantities of CO2 into the atmosphere. The tailings were characterized via X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), and granulometric analysis. For evaluating the mechanical behavior and porosity, 25% of the cement (by mass) was replaced with tailings, and the resulting composite was molded into cylindrical specimens. After curing for 28 and 91 days, all specimens underwent compression testing. The results of the physical characterization showed that more than 65% of the tailing grain was lesser than 45 μm in size, which contributes to the packaging effect. In terms of the chemical and mineralogical composition, the tailing had high levels of calcium, and the predominant phases could be identified. The compressive strength of the mortar with substitution was higher than 40 MPa. The convergence observed between the results of the different characterization techniques demonstrates the efficiency of using the waste as a supplementary cementitious material.

scholarly journals Synthesis and Characterization of a Hybrid Cement Based on Fly Ash, Metakaolin and Portland Cement Clinker

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1084 ◽  
Author(s):  
Adriagni C. Barboza-Chavez ◽  
Lauren Y. Gómez-Zamorano ◽  
Jorge L. Acevedo-Dávila
Keyword(s):  
Fly Ash ◽  
Portland Cement ◽  
Ordinary Portland Cement ◽  
Cementitious Materials ◽  
Cement Industry ◽  
Supplementary Cementitious Materials ◽  
Cement Clinker ◽  
Dense Matrix ◽  
X Ray ◽  
Reduction Of Co2

Hybrid cement has become one of the most viable options in the reduction of CO2 emissions to the environment that are generated by the cement industry. This could be explained by the reduction of the content of clinker in the final mixture and substitution of the remaining percentage with supplementary cementitious materials with the help of an alkaline activation. Following that, properties that are provided by an Ordinary Portland Cement and of a geopolymer are mixed in this type of hybrid material and could be achieved at room temperature. Thereafter, the main objective of this research was to synthesize hybrid cements reducing the clinker content of Portland Cement up to 20% and use metakaolin and fly ash as supplementary cementitious materials in different proportions. The mixtures were alkaline activated with a mixture of sodium silicate and sodium hydroxide, calculating the amounts according to the percentage of Na2O that is present in each of the activators. The samples were then characterized using Compressive strength, X-ray diffraction, Fourier Transform Infrared Spectroscopy, and Scanning Electron Microscopy with energy-dispersive X-ray spectroscopy. The results indicated that the hybrid cements have similar mechanical properties than an Ordinary Portland Cement, and they resulted in a dense matrix of hydration products similar to those that are generated by cements and geopolymers.

scholarly journals Synthesis of Silica Particles Using Ultrasonic Spray Pyrolysis Method

Metals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 463
Author(s):  
Srecko Stopic ◽  
Felix Wenz ◽  
Tatjana-Volkov Husovic ◽  
Bernd Friedrich
Keyword(s):  
Spray Pyrolysis ◽  
Sol Gel ◽  
Ultrasonic Spray Pyrolysis ◽  
Silica Particles ◽  
Cement Industry ◽  
Submicron Particles ◽  
Spherical Particles ◽  
Spray Pyrolysis Method ◽  
X Ray ◽  
Ultrasonic Spray

Silica has sparked strong interest in hydrometallurgy, catalysis, the cement industry, and paper coating. The synthesis of silica particles was performed at 900 °C using the ultrasonic spray pyrolysis (USP) method. Ideally, spherical particles are obtained in one horizontal reactor from an aerosol. The controlled synthesis of submicron particles of silica was reached by changing the concentration of precursor solution. The experimentally obtained particles were compared with theoretically calculated values of silica particles. The characterization was performed using a scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDS). X-ray diffraction, frequently abbreviated as XRD, was used to analyze the structure of obtained materials. The obtained silica by ultrasonic spray pyrolysis had an amorphous structure. In comparison to other methods such as sol–gel, acidic treatment, thermal decomposition, stirred bead milling, and high-pressure carbonation, the advantage of the ultrasonic spray method for preparation of nanosized silica controlled morphology is the simplicity of setting up individual process segments and changing their configuration, one-step continuous synthesis, and the possibility of synthesizing nanoparticles from various precursors.

A 13C and 15N nuclear magnetic resonance study of solid ammonium thiocyanate

1987 ◽  
Vol 65 (5) ◽  
pp. 941-946 ◽  
Author(s):  
Ross M. Dickson ◽  
Michael S. McKinnon ◽  
James F. Britten ◽  
Roderick E. Wasylishen
Keyword(s):  
Ammonium Thiocyanate ◽  
Nuclear Magnetic Resonance Study ◽  
Magic Angle Spinning ◽  
Magic Angle ◽  
Chemical Shielding ◽  
X Ray ◽  
Shielding Constants ◽  
Angle Spinning ◽  
Good Agreement ◽  
C Nmr

The static 13C nmr powder pattern for solid ammonium thiocyanate is analyzed to obtain the 13C chemical shielding anisotropy, 321 ± 7 ppm, and the 13C–14N dipolar splitting, 1295 ± 25 Hz. Slow magic angle spinning 15N nmr experiments are analyzed to obtain a nitrogen chemical shielding anisotropy of 415 ± 15 ppm. The 13C–14N dipolar splitting leads to an effective C—N bond length of 1.19 ± 0.01 Å, in good agreement with the value of 1.176 Å reported from accurate X-ray and neutron crystallographic studies. In solid NH4NCS absolute values of the average shielding constants [Formula: see text] and ct[Formula: see text] are 52 and 34 ppm, respectively. Comparison of calculated and observed [Formula: see text] values indicates that intermolecular interactions decrease the 13C and 15N shielding constants by approximately 10 and 30 ppm, respectively.

Silicon oxycarbide glasses: Part II. Structure and properties

1991 ◽  
Vol 6 (12) ◽  
pp. 2723-2734 ◽  
Author(s):  
Gary M. Renlund ◽  
Svante Prochazka ◽  
Robert H. Doremus
Keyword(s):  
Silicon Carbide ◽  
Coefficient Of Thermal Expansion ◽  
Random Network ◽  
Silicon Oxycarbide ◽  
Index Of Refraction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Silicon Oxycarbide Glasses ◽  
Oxycarbide Glass ◽  
Silicon Oxygen

Silicon oxycarbide glass is formed by the pyrolysis of silicone resins and contains only silicon, oxygen, and carbon. The glass remains amorphous in x-ray diffraction to 1400 °C and shows no features in transmission electron micrographs (TEM) after heating to this temperature. After heating at higher temperature (1500–1650 °C) silicon carbide lines develop in x-ray diffraction, and fine crystalline regions of silicon carbide and graphite are found in TEM and electron diffraction. XPS shows that silicon-oxygen bonds in the glass are similar to those in amorphous and crystalline silicates; some silicons are bonded to both oxygen and carbon. Carbon is bonded to either silicon or carbon; there are no carbon-oxygen bonds in the glass. Infrared spectra are consistent with these conclusions and show silicon-oxygen and silicon-carbon vibrations, but none from carbon-oxygen bonds. 29Si-NMR shows evidence for four different bonding groups around silicon. The silicon oxycarbide structure deduced from these results is a random network of silicon-oxygen tetrahedra, with some silicons bonded to one or two carbons substituted for oxygen; these carbons are in turn tetrahedrally bonded to other silicon atoms. There are very small regions of carbon-carbon bonds only, which are not bonded in the network. This “free” carbon colors the glass black. When the glass is heated above 1400 °C this network composite rearranges in tiny regions to graphite and silicon carbide crystals. The density, coefficient of thermal expansion, hardness, elastic modulus, index of refraction, and viscosity of the silicon oxycarbide glasses are all somewhat higher than these properties in vitreous silica, probably because the silicon-carbide bonds in the network of the oxycarbide lead to a tighter, more closely packed structure. The oxycarbide glass is highly stable to temperatures up to 1600 °C and higher, because oxygen and water diffuse slowly in it.

A single crystal, linearly polarized Fe 2p X-ray absorption study of gillespite

1998 ◽  
Vol 62 (1) ◽  
pp. 65-75 ◽  
Author(s):  
P. F. Schofield ◽  
G. van der Laan ◽  
C. M. B. Henderson ◽  
G. Cressey
Keyword(s):  
Single Crystal ◽  
Ground State ◽  
Branching Ratio ◽  
Linear Dichroism ◽  
Electronic Charge ◽  
Magic Angle ◽  
X Rays ◽  
X Ray ◽  
Peak Structure ◽  
X Ray Absorption

AbstractThe Fe 2p X-ray absorption spectra of single crystal gillespite, BaFeSi4O10, show a strong linear dichroism, i.e. a large difference in the absorption when measured with the polarization of the X-rays either parallel or perpendicular to the plane of the FeO4 group. The isotropic spectrum, obtained from measurement at the ‘magic angle’, and the polarization dependent spectra have been compared to atomic multiplet calculations and show an excellent agreement with theory. Analysis of the branching ratio, the linear dichroism, and the detailed peak structure confirms that the 5A1 level is the ground state at room temperature and pressure. The 5B2 level is sufficiently low in energy that a distortion of the electronic charge density, induced by increased pressure, may result in a 5B2 ground state.

scholarly journals A crystallographic study of crystalline casts and pseudomorphs from the 3.5 Ga Dresser Formation, Pilbara Craton (Australia)

2018 ◽  
Vol 51 (4) ◽  
pp. 1050-1058 ◽  
Author(s):  
Fermin Otálora ◽  
A. Mazurier ◽  
J. M. Garcia-Ruiz ◽  
M. J. Van Kranendonk ◽  
E. Kotopoulou ◽  
...  
Keyword(s):  
High Temperature ◽  
Geological History ◽  
X Ray Diffraction ◽  
Mineral Phase ◽  
X Ray ◽  
Crystallographic Study ◽  
History Of ◽  
Degree Of Confidence ◽  
High Degree ◽  
Pilbara Craton

Crystallography has a long history of providing knowledge and methods for applications in other disciplines. The identification of minerals using X-ray diffraction is one of the most important contributions of crystallography to earth sciences. However, when the crystal itself has been dissolved, replaced or deeply modified during the geological history of the rocks, diffraction information is not available. Instead, the morphology of the crystal cast provides the only crystallographic information on the original mineral phase and the environment of crystal growth. This article reports an investigation of crystal pseudomorphs and crystal casts found in a carbonate-chert facies from the 3.48 Ga-old Dresser Formation (Pilbara Craton, Australia), considered to host some of the oldest remnants of life. A combination of X-ray microtomography, energy-dispersive X-ray spectroscopy and crystallographic methods has been used to reveal the original phases of these Archean pseudomorphs. It is found with a high degree of confidence that the original crystals forming in Archean times were hollow aragonite, the high-temperature polymorphs of calcium carbonate, rather than other possible alternatives such as gypsum (CaSO4·2H20) and nahcolite (NaHCO3). The methodology used is described in detail.

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