scholarly journals Kaolinite deposits in the upper Iguaçu river, Brazil: formation and mineralogical attributes

2021 ◽  
Author(s):  
Daniela N. Ferreira ◽  
Vander de Freitas Melo ◽  
Pablo Vidal-Torrado ◽  
Jairo Calderari Oliveira
Keyword(s):  
Clay Fraction ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Serra Do Mar ◽  
Silt Fraction ◽  
Weathering Processes ◽  
South Of Brazil ◽  
Planar Growth ◽  
Iguaçu River

Kaolinite (Kt) is the most studied mineral, being widely used in the ceramic, pharmaceutical and cellulose industries, in addition to being the main soil mineral in the world. Found in different parts of the planet, it differs in genesis and may be formed as a result of local weathering of the rocks, occurring in the silt fraction; and also due to the mineral's neogenesis with a predominance of clay-sized particles. The plain of upper Iguaçu river has the largest kaolinitic deposit in the south of Brazil and it’s formation raised doubts if this kaolin was transported or formed in situ due the high organic matter in the alluvial plain. To elucidate the origin of kaolin deposits, we sampled a possible font of the mineral, in the mountains of Serra do Mar and sampled two tubes that reach 4 m depth in the upper Iguaçu plain. We performed textural analysis, organic carbon, X-ray diffraction, Kt crystallography in silt and clay fractions, thermal analysis (TDA/TG) to quantify Kt and Gb in the clay fraction and scanning electron microscopy (SEM) with dispersive energy spectroscopy (EDS). The TDA/TG analysis demonstrated that saprolite has 66% of the kaolinite found in the plain. The XRD analysis shows a significant presence of mica (Mc) in all samples of the silt fraction, both in Serra do Mar and in the plain. In SEM/EDS, crystals with planar growth are observed, and the presence of pseudomorphic Mc-Kt in the silt fraction of all analyzed samples, with emphasis on the tubes sample with the crystal having almost twice the size of that observed in the saprolite sample from Serra do Mar, allowing to infer that the Kt of the silt fraction of the wetland soils were formed on site by the diagenesis of mica particles. The results obtained in this work indicate that the kaolinitic material found in the wetland of the upper Iguaçu plain is the result of weathering processes in the wetland itself, evidenced by the large pseudomorphs found, even greater than those observed in Serra do Mar.

Semiquantitative Analysis by X-Ray Powder Diffraction (SQXRD) of the < 2 mm to 0.002 mm and < 0.002 mm Fractions of Soil

1988 ◽  
Vol 3 (3) ◽  
pp. 144-152 ◽  
Author(s):  
G. A. Raab
Keyword(s):  
Particle Size ◽  
Clay Fraction ◽  
Internal Standard ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Freeze Dried ◽  
Strict Protocol ◽  
Attention To Detail

AbstractThe method described in this paper is a strict protocol for X-ray diffraction (XRD) analysis of mineral phases found in soils. Its application is not restricted to soils and is an attempt to standardize XRD sample preparation and analysis. The protocol requires the particle size of the < 2 mm - 0.002 mm fraction be reduced to 0.002 mm before analysis. In die qualitative section, the clay fraction ( < 0.002 mm particle size) is prepared as oriented slides. The suspended clay fraction is saturated with ethylene glycol, K +, and Mg+2; pipeted; air-dried; heat-treated at 110°C, 350°C, and 550°C; and X-rayed at each step in order to properly identify the clay minerals. In the quantitative section, the method employs a matrix-flushing agent, corundum (Al2O3). The corundum acts also as an internal standard, a calibration standard, and a reference standard. The suspended clay fraction is freeze-dried and corundum is added to each sample. Randomly oriented powder mounts are prepared from the < 2 mm - 0.002 mm fraction, and the < 0.002 mm fraction, and X-rayed. A series of reference standards are prepared based on the existing mineralogy, corundum is added, and each mixture is X-rayed. The software integrates the area under specific peaks (chosen for intensity and no overlap) in each sample, calculates the reference intensity ratios (RIRs) and calculates the percentage of each mineral based on the equation of Chung (1974). The attention to detail allows documentation and verification of the results yielding data of known quality.

MECHANICAL PROPERTIES OF A POLYURETHANE/MONTMORILLONITE NANOCOMPOSITE FEATURING ORGANOMODIFICATION SYNTHESIZED VIA IN SITU POLYMERIZATION

2015 ◽  
Vol 88 (1) ◽  
pp. 138-146 ◽  
Author(s):  
Rouhollah Bagheri ◽  
Reza Darvishi
Keyword(s):  
Mechanical Properties ◽  
In Situ Polymerization ◽  
Xrd Analysis ◽  
Silicate Layer ◽  
X Ray Diffraction ◽  
X Ray ◽  
End Groups ◽  
Layer Sample ◽  
Silicate Layers

ABSTRACT In this study, polyurethane (PU)/organomodified montmorillonite (cloisite®30B) is synthesized via in situ polymerization by reaction of an ether-based prepolymer with the isocyanate end groups and adiamine chain extender (4, 4-methylene-bis(2-chloroaniline)) in the presence of different amounts of nanoparticles dispersed in the prepolymer matrix by an ultrasonic mixer for 1 h. The synthesized polymers are cast on a pretreated carbon steel sheet and cured at 120 °C in an oven. The PU and its composites have been characterized by using Fourier transform infrared spectroscopy, X-ray diffraction (XRD), and mechanical testing. The XRD analysis of the cured samples containing 1 to 3 wt% cloisite30B showed intercalation segments in the silicate layers and exfoliation for 0.5 wt% nanoparticles. The highest mechanical properties were obtained using the cured exfoliated silicate layer sample. A twofold increase in the ultimate tensile strength and a 2.3 times increase in the adhesion strength were found for 0.5 wt% organoclay/PU as compared with that of pure PU. In addition, the exfoliated structure sample exhibited a 16% reduction in abrasion compared with that of pure PU.

Bi-Based Superconducting Multilayers Obtained by Molecular Beam Epitaxy

1999 ◽  
Vol 13 (09n10) ◽  
pp. 991-996
Author(s):  
M. Salvato ◽  
C. Attanasio ◽  
G. Carbone ◽  
T. Di Luccio ◽  
S. L. Prischepa ◽  
...  
Keyword(s):  
Molecular Beam Epitaxy ◽  
Molecular Beam ◽  
Xrd Analysis ◽  
High Energy ◽  
X Ray Diffraction ◽  
One Dimensional ◽  
X Ray ◽  
Diffraction Model ◽  
Different Thickness

High temperature superconducting multilayers have been obtained depositing Bi2Sr2CuO6+δ(2201) and ACuO2 layers, where A is Ca or Sr, by Molecular Beam Epitaxy (MBE) on MgO and SrTiO3 substrates. The samples, formed by a sequence of 2201/ACuO2 bilayers, have different thickness of ACuO2 layers while the thickness of the 2201 layers is kept constant. The surface structure of each layer has been monitored by in situ Reflection High Energy Electron Diffraction (RHEED) analysis which has confirmed a 2D nucleation growth. X-ray diffraction (XRD) analysis has been used to confirm that the layered structure has been obtained. Moreover, one-dimensional X-ray kinematic diffraction model has been developed to interpret the experimental data and to estimate the period of the multilayers. Resistive measurements have shown that the electrical properties of the samples strongly depend on the thickness of the ACuO2 layers.

Surface Energy and Crystallite Size Comparisons by Applying Direct Current and Pulse Direct Current on Substrate Bias in PVD Process

2013 ◽  
Vol 315 ◽  
pp. 98-102
Author(s):  
H. Hanizam ◽  
Md Nizam Abd Rahman ◽  
Noraiham Mohamad ◽  
A.R. Soufhwee
Keyword(s):  
Surface Energy ◽  
Crystallite Size ◽  
Direct Current ◽  
Substrate Surface ◽  
Film Coating ◽  
Xrd Analysis ◽  
Substrate Bias ◽  
X Ray Diffraction ◽  
Adhesion Failure

Surface morphology homogeneity and energy modifications for in situ PVD process are two critical factors to prevent unexpected adhesion failure during machining or service. Unlike during film depositing, there is still much gap to be explored on applying pulsed biasing concepts to the substrate during in situ, to ensure the substrate surface readiness prior to film coating. The purpose of this paper is to study the effects of conventional direct current (DC) and pulse direct current (PDC) applied at substrate bias to the surface energy and crystallite size. Tungsten carbide (WC) cutting tool insert and titanium nitride (TiN) were used as substrate and hard coating respectively. The runs were conducted to compare the bias at DC (-500V) and PDC (-200V, -500V, -800V). The surface energy and crystallite size were characterized through wettability test and X-ray diffraction (XRD) analysis. The applying of PDC on the substrate bias was found to further enhance the characteristics of the surface compared to the conventional DC substrate bias.

Synthesis of Calcium Carbonate-Polyethylene Oxide Hybrid Nanofibers Through In-Situ Electrospinning

2008 ◽  
Vol 8 (5) ◽  
pp. 2627-2631 ◽  
Author(s):  
Reza Faridi-Majidi ◽  
Naser Sharifi-Sanjani ◽  
Mohammad Madani
Keyword(s):  
Calcium Carbonate ◽  
Calcium Hydroxide ◽  
Polyethylene Oxide ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
Hybrid Nanofibers ◽  
Carbon Dioxide Atmosphere ◽  
Transmission Electron ◽  
Gaseous Carbon Dioxide

In this work, calcium carbonate nanoparticles-polyethylene oxide nanofibers as organic–inorganic hybrid were prepared via in-situ electrospinning. Thus, electrospinning of polyethylene oxide solution saturated with calcium hydroxide was carried out in gaseous carbon dioxide atmosphere. Transmission electron microscopy (TEM) showed that calcium carbonate (CaCO3) nanoparticles were formed on the produced nanofibers of 200–300 nm in diameter. The existence of the formed CaCO3 was also proved by thermogravimetric analysis (TGA) via loss of gaseous CO2 related to the decomposition of CaCO3 at about 500–840 °C. X-ray diffraction (XRD) analysis of the nanofibers showed that the formed CaCO3 nanoparticles have vaterite morphology. DSC analysis was used to determine melting point and to calculate the crystallinity of the produced hybrid nanofibers. The TEM, TGA, XRD and DSC analyses results of the obtained nanofibers were compared with those of the nanofibers produced in electrospinning of pure polyethylene oxide solution and polyethylene oxide solution having calcium hydroxide, both in air.

Investigation of Magnetic Properties and Nanostructure of Fe2.75Mn0.25O4@ PANI Materials and their Potential as the Magnetic Ink

2020 ◽  
Vol 855 ◽  
pp. 308-314
Author(s):  
Nadiya Miftachul Chusna ◽  
Sunaryono ◽  
Yunan Amza Muhammad ◽  
Rosabiela Irfa Andin ◽  
Ahmad Taufiq
Keyword(s):  
Magnetic Properties ◽  
Crystal Size ◽  
In Situ Polymerization ◽  
Xrd Analysis ◽  
Hysteresis Curve ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Polymerization Method

The Fe2.75Mn0.25O4 nanoparticles were successfully synthesized by using the coprecipitation method, while the Fe2.75Mn0.25O4@PANI materials were successfully fabricated by using the in situ polymerization method. This research aimed to investigate the magnetic properties and nanostructure of the Fe2.75Mn0.25O4 nanoparticles and Fe2.75Mn0.25O4@PANI materials. Some characterizations of the samples were successfully carried out by using X-Ray Diffraction (XRD) instruments, Fourier Transform Infrared (FTIR), and Vibrating Sample Magnetometer (VSM) each of which was conducted to characterize the crystal structure, functional groups, morphology, and the magnetic properties of the materials. The XRD analysis results showed that the Fe2.75Mn0.25O4@PANI materials had a crystal size of 8.09 nm. Meanwhile, the FTIR spectrum represented vibrations due to the atomic bonds that made up the Fe2.75Mn0.25O4@PANI materials. Furthermore, the hysteresis curve from the VSM characterization results showed that the Fe2.75Mn0.25O4@PANI material saturation magnetization value was around 2.85 emus/g. From those characterization results, the Fe2.75Mn0.25O4@PANI materials are very potential to be applied as magnetic ink

Quantitative in situ X-ray diffraction analysis of early hydration of Portland cement at defined temperatures

2009 ◽  
Vol 24 (2) ◽  
pp. 112-115 ◽  
Author(s):  
C. Hesse ◽  
F. Goetz-Neunhoeffer ◽  
J. Neubauer ◽  
M. Braeu ◽  
P. Gaeberlein
Keyword(s):  
Portland Cement ◽  
Free Water ◽  
Xrd Analysis ◽  
Quantitative Phase Analysis ◽  
X Ray Diffraction ◽  
Early Hydration ◽  
X Ray ◽  
Main Period ◽  
Diffraction Patterns

Investigation into the early hydration of Portland cement was performed by in situ X-ray diffraction (XRD). Technical white cement was used for the XRD analysis on a D5000 diffractometer (Siemens). All diffraction patterns of the in situ measurement which were recorded up to 22 h of hydration at defined temperatures were analyzed by Rietveld refinement. The resulting phase composition was transformed with respect to free water and C-S-H leading to the total composition of the cement paste. The hydration reactions can be observed by dissolution of clinker phases as well as by the formation of the hydrate phases ettringite and portlandite. With increasing temperatures the reactions proceed faster. The formation of ettringite is directly influenced by the rate of dissolution of anhydrite and tricalcium aluminate (C3A). The beginning of the main period of hydration is marked by the start of portlandite formation. The experiments point out that a quantitative phase analysis of the cement hydration is feasible with standard laboratory diffractometers.

scholarly journals Preparation and Physicochemical Characterization of a Diclofenac Sodium-Dual Layer Polyvinyl Alcohol Patch

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2459
Author(s):  
Shafizah Sa’adon ◽  
Mohamed Nainar Mohamed Ansari ◽  
Saiful Izwan Abd Razak ◽  
Joseph Sahaya Anand ◽  
Nadirul Hasraf Mat Nayan ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Diclofenac Sodium ◽  
Physicochemical Characterization ◽  
Xrd Analysis ◽  
Tensile Tests ◽  
Spectroscopic Techniques ◽  
X Ray Diffraction ◽  
Water Contact ◽  
Freeze Thaw

The aim of this study is to prepare a dual layer polyvinyl (PVA) patch using a combination of electrospinning techniques and cryogelation (freeze-thaw process) then subsequently to investigate the effect of freeze-thaw cycles, nanofiber thickness, and diclofenac sodium (DS) loading on the physicochemical and mechanical properties and formulation of dual layer PVA patches composed of electrospun PVA nanofibers and PVA cryogel. After the successful preparation of the dual layer PVA patch, the prepared patch was subjected to investigation to assess the effect of freeze-thaw cycles, nanofiber thickness and percentages of DS loading on the morphology, physiochemical and mechanical properties. Various spectroscopic techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR), water contact angle, and tensile tests were used to evaluate the physicochemical and mechanical properties of prepared dual layer PVA patches. The morphological structures of the dual layer PVA patch demonstrated the effectiveness of both techniques. The effect of freeze-thaw cycles, nanofiber thickness, and DS percentage loading on the crystallinity of a dual layer PVA patch was investigated using XRD analysis. The presence of a distinct DS peak in the FTIR spectrum indicates the compatibility of DS in a dual layer PVA patch through in-situ loading. All prepared patches were considered highly hydrophilic because the data obtained was less than 90°. The increasing saturation of DS within the PVA matrix increases the tensile strength of prepared patches, however decreased its elasticity. Evidently, the increasing of electrospun PVA nanofibers thickness, freeze-thaw cycles, and the DS saturation has improved the physicochemical and mechanical properties of the DS medicated dual layer PVA patches, making them a promising biomaterial for transdermal drug delivery applications.

scholarly journals Sustainable Functionalization of PAN to Improve Tinctorial Capacity

Polymers ◽  
2021 ◽  
Vol 13 (21) ◽  
pp. 3665
Author(s):  
Vasilica Popescu ◽  
Ingrid Ioana Buciscanu ◽  
Melinda Pruneanu ◽  
Stelian Sergiu Maier ◽  
Angela Danila ◽  
...  
Keyword(s):  
Chemical Structure ◽  
Xrd Analysis ◽  
Hypervalent Iodine ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yellow Orange ◽  
The Fourier Transform ◽  
Scanning Electron ◽  
Pan Fibers

This study may open a new way to obtain the coloration of a polymer during functionalization. Two polyacrylonitrile (PAN) polymers in the form of textile fibers (Melana and Dralon L) were subjected to functionalization treatments in order to improve the dyeing capacity. The functionalizations determined by an organo-hypervalent iodine reagent developed in situ led to fiber coloration without using dyes. KIO3 was formed in situ from the interaction of aqueous solutions of 3–9% KOH with 3–9% I2, at 120 °C. The yellow-orange coloration appeared as a result of the transformations in the chemical structure of each functionalized polymer, with the formation of iodinehydrin groups. The degree of functionalization directly influenced the obtained color. The results of the Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDX), Map and Temogravimetric Analysis (TG) plus Differential Thermal (DTA) analyses indicated the presence of new functional groups, such as iodine-oxime. The X-ray diffraction (XRD) analysis confirmed the change of the crystalline/amorphous ratio in favor of the former. The new groups introduced by functionalization make it possible to dye with classes of dyes specific to these groups, but not specific to PAN fibers, thus improving their dyeing capacity.

scholarly journals In-Situ MMC Production through VXBY Intermetallics Formation in an Al Matrix

2003 ◽  
Vol 12 (1) ◽  
pp. 096369350301200
Author(s):  
C. Polyzos ◽  
S. Skolianos ◽  
H. Lefakis ◽  
D.N. Tsipas
Keyword(s):  
Aluminum Matrix ◽  
Xrd Analysis ◽  
Synthesis Temperature ◽  
Second Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Second Phase Particles ◽  
Stirring Time ◽  
Al Matrix

The production of in-situ MMC's (Metal Matrix Composite) of an aluminum matrix with VxBy intermetallic compounds as the reinforcing phase has been investigated. The approach is modelled after that of Al-Ti-B alloys and salts added to an Al matrix to produce in-situ grain-refining TiB2. In the present work, V was used instead of Ti in an effort to investigate the possibility of an in-situ synthesis of a new, alternative, B-V reinforcing compound. Al, Al-V4.5wt% and Al-B5.5wt% alloys and a B-salt (KBF4) were used as starting materials. The synthesis temperature, the stirring time and the reaction holding time (RHT) were 1000°C, 5 min and 5 or 10 min respectively. The microstructure of the resulted MMC's consisted of second-phase particles, ranging in size between 1 and 10 μm, dispersed within an Al matrix. The second phase particles were identified by X-ray diffraction (XRD) analysis as VB2 and VB.

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