scholarly journals Effect of the Degree of Substitution on the Hydrophobicity, Crystallinity, and Thermal Properties of Lauroylated Amaranth Starch

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2548
Author(s):  
Vicente Espinosa-Solis ◽  
Yunia Verónica García-Tejeda ◽  
Everth Jimena Leal-Castañeda ◽  
Víctor Barrera-Figueroa
Keyword(s):  
Photoelectron Spectroscopy ◽  
Thermal Characterization ◽  
Fatty Acyl ◽  
Degree Of Substitution ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Amaranthus Hypochondriacus ◽  
Two Samples ◽  
Acyl Chains

In this paper, we consider amaranth starch extracted from the seeds of Amaranthus hypochondriacus L. An amphiphilic character is conferred to the starch by a chemical modification, which involves an esterification by lauroyl chloride at three modification levels. The degree of substitution (DS) after the modification ranged from 0.06 to 1.16. X-ray photoelectron spectroscopy analysis confirmed the presence of fatty acyl chains on the surface of the esterified starches. The hydrophobicity of starches was confirmed by their adsorption isotherms, which showed a decrease in the moisture adsorption of lauroylated as DS increased. X-ray diffraction analysis revealed a higher crystallinity, which was observed in the two samples subjected to the highest levels of modification. A higher crystallinity is related to a higher gelatinization enthalpy. These results are in agreement with the thermal characterization obtained by differential scanning calorimetry (DSC). An inhibition of the retrogradation properties of lauroylated amaranth starches was also observed.

scholarly journals Diethylstilbestrol Modifies the Structure of Model Membranes and Is Localized Close to the First Carbons of the Fatty Acyl Chains

Biomolecules ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 220
Author(s):  
Alessio Ausili ◽  
Inés Rodríguez-González ◽  
Alejandro Torrecillas ◽  
José A. Teruel ◽  
Juan C. Gómez-Fernández
Keyword(s):  
Membrane Surface ◽  
Water Layer ◽  
Fatty Acyl ◽  
31P Nmr Spectroscopy ◽  
Relaxation Rates ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Acyl Chains ◽  
Dynamics Simulations

The synthetic estrogen diethylstilbestrol (DES) is used to treat metastatic carcinomas and prostate cancer. We studied its interaction with membranes and its localization to understand its mechanism of action and side-effects. We used differential scanning calorimetry (DSC) showing that DES fluidized the membrane and has poor solubility in DMPC (1,2-dimyristoyl-sn-glycero-3-phosphocholine) in the fluid state. Using small-angle X-ray diffraction (SAXD), it was observed that DES increased the thickness of the water layer between phospholipid membranes, indicating effects on the membrane surface. DSC, X-ray diffraction, and 31P-NMR spectroscopy were used to study the effect of DES on the Lα-to-HII phase transition, and it was observed that negative curvature of the membrane is promoted by DES, and this effect may be significant to understand its action on membrane enzymes. Using the 1H-NOESY-NMR-MAS technique, cross-relaxation rates for different protons of DES with POPC (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine) protons were calculated, suggesting that the most likely location of DES in the membrane is with the main axis parallel to the surface and close to the first carbons of the fatty acyl chains of POPC. Molecular dynamics simulations were in close agreements with the experimental results regarding the location of DES in phospholipids bilayers.

The Synthesis and Characterization of Oxide Free Tin Nanoparticles

2014 ◽  
Vol 670-671 ◽  
pp. 26-29
Author(s):  
Zhi Long Pan ◽  
Shi Liang Ao ◽  
Jian Ping Jia
Keyword(s):  
Reduction Method ◽  
Chemical Reduction ◽  
Thermal Characterization ◽  
X Ray Diffraction ◽  
Chemical Reduction Method ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrd Study ◽  
Tin Nanoparticles

Oxide free Tin nanoparticles were synthesized from a chemical reduction method. Their morphological and thermal characterizations were studied in this paper. The X-ray diffraction (XRD) study showed that no oxides of Tin nanoparticles were formed. The thermal characterization by differential scanning calorimetry (DSC) exhibited the size dependency of the melting points. The melting point was as low as 202.16°C.

STUDIES ON SURFACE STRUCTURE, MORPHOLOGY AND COMPOSITION OF Co–W COATINGS ELECTRODEPOSITED WITH DIRECT AND PULSE CURRENT USING GLUCONATE BATH

2013 ◽  
Vol 20 (01) ◽  
pp. 1350006 ◽  
Author(s):  
PARTHASARATHI BERA ◽  
H. SEENIVASAN ◽  
K. S. RAJAM
Keyword(s):  
Photoelectron Spectroscopy ◽  
Pulse Current ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Force Microscopy ◽  
Dsc Studies ◽  
Atomic Force ◽  
Electrodeposited Coating

Co–W alloy coatings were deposited with direct current (DC) and pulse current (PC) electrodeposition methods using gluconate bath at pH5 and characterized by X-ray diffraction, field emission scanning electron microscopy, atomic force microscopy, differential scanning calorimetry (DSC) and X-ray photoelectron spectroscopy (XPS). DSC studies hint at the possibility of formation of metallic glasses. Detailed XPS studies of these alloy coatings have been carried out to compare elemental states and composition of Co and W in DC and PC electrodeposited alloys. DC-plated alloy has significant amount of Co and W metal along with their respective oxidized species. In contrast, mainly oxidized metals are present in the following layers of as-deposited coatings prepared with PC plating. Concentration of Co metal is observed to increase during sputtering, whereas there is no change in W6+ concentration. Microhardness measurement of all the Co–W coatings shows higher hardness compared to Co metal and 1:1 and 1:4 PC electrodeposited coatings show little higher hardness compared to 1:2 PC electrodeposited coating.

Atomic layer deposition of HfO2, Al2O3, and HfAlOx using O3 and metal(diethylamino) precursors

2007 ◽  
Vol 22 (12) ◽  
pp. 3455-3464 ◽  
Author(s):  
Rajesh Katamreddy ◽  
Ronald Inman ◽  
Gregory Jursich ◽  
Axel Soulet ◽  
Christos Takoudis
Keyword(s):  
Atomic Layer Deposition ◽  
Photoelectron Spectroscopy ◽  
Thermal Characteristics ◽  
Atomic Layer ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Metal Precursors ◽  
Layer Deposition ◽  
Xrd Techniques

Tetrakis-diethylamino hafnium (TDEAH), tris-diethylamino aluminum (TDEAA), and ozone were used for the atomic layer deposition (ALD) of HfO2, Al2O3, and HfAlOx films. The ALD rates were measured to be 1.1 Å/cycle for HfO2 and 1.3 Å/cycle for Al2O3. The ALD temperature windows were found to be between 200 and 325 °C for TDEAA, and between 200 and 275 °C for TDEAH. The overlap of these ALD windows between 200 and 275 °C is critical for ALD of the composite film, HfAlOx. In addition to the overlapping ALD temperature windows, the two metal precursors have similar thermal characteristics, as shown by TGA and differential scanning calorimetry. As-deposited films and films postannealed at 600 and 800 °C films were analyzed using Fourier transformed infrared (FTIR) spectroscopy, x-ray photoelectron spectroscopy, and x-ray diffraction (XRD) techniques. FTIR spectra revealed interfacial oxide growth during deposition of both HfO2 and Al2O3 whose thickness increased with annealing temperature. The FTIR data also indicated hydroxyl and nitrate groups in the films; these species were removed after annealing in Ar at a temperature of ⩾600 °C. Both FTIR and XRD results indicated the crystallization of pure HfO2 after annealing at temperatures as low as 600 °C. On the other hand, pure Al2O3 remained amorphous after annealing at temperatures up to 800 °C. XRD data of the composite HfAlOx film show that films deposited by alternating five cycles of HfO2 and one cycle of Al2O3 remained amorphous after annealing at 600 °C. Rutherford backscattering analysis of HfAlOx deposited with a varied number of alternating HfO2 and Al2O3 cycles demonstrated a strong correlation between the cyclic dosage of TDEAA and TDEAH and the film composition.

Thermal Characterization of the Interaction of Silanes with a Dihydroxy Vulcanized Fluoroelastomer

2006 ◽  
Vol 79 (5) ◽  
pp. 765-782
Author(s):  
Michael Benjamin Sands ◽  
Vijay Subramanian ◽  
Guangzhao Mao
Keyword(s):  
Photoelectron Spectroscopy ◽  
Vinylidene Fluoride ◽  
Thermal Characterization ◽  
Peak Shift ◽  
Amine Group ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Lower Temperature ◽  
Bisphenol Af

Abstract The reactivity of aminosilane and vinylsilane with a dihydroxy (Bisphenol AF) crosslinkable fluoroelastomer containing only vinylidene fluoride (VF2) and hexafluoropropylene (HFP) was monitored using Differential Scanning Calorimetry (DSC) and X-ray Photoelectron Spectroscopy (XPS). The DSC results showed that the introduction of an aminosilane, or a combination of aminosilane and vinylsilane solutions, to the cure system of the fluoroelastomer resulted in a peak shift. This shift indicates that crosslinking in fluoroelastomer-silane system occurs at a lower temperature when aminosilane is present. Results also confirm that the organofunctional group on the silane reacts with the elastomer. XPS analysis of the silane-coated fluoroelastomer heated at 120 °C, 160 °C and 200 °C reveals that dehydrofluorination of the polymer is one of the steps in the reaction. It is our hypothesis that the amine group on the aminosilane is a contributor to the dehydrofluorination of the fluoroelastomer.

Synthesis of Oriented BiFeO3 Thin Films by Chemical Solution Deposition: Phase, Texture, and Microstructural Development

2005 ◽  
Vol 20 (8) ◽  
pp. 2127-2139 ◽  
Author(s):  
F. Tyholdt ◽  
S. Jørgensen ◽  
H. Fjellvåg ◽  
A.E. Gunnæs
Keyword(s):  
Thin Films ◽  
Photoelectron Spectroscopy ◽  
Chemical Solution Deposition ◽  
Microstructural Development ◽  
Chemical Solution ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Solution Deposition ◽  
X Ray ◽  
Glass Substrates

Textured, thin films of BiFeO3 (∼120 nm thickness) were synthesized by chemical solution deposition from a mixture of iron- and bismuth- 2-methoxyethoxides on Si(100)/SiO2/TiO2/Pt substrates. The use of alkoxides ensured good homogeneity and a low degree of organics that further facilitated low crystallization temperatures. Crystalline films were according to x-ray diffraction already obtained at 480 °C. Precursor characteristics were investigated using thermogravimetry and differential scanning calorimetry, whereas phase purity, microstructure and film topography were examined by x-ray diffraction, transmission electron microscopy, atomic force microscopy, and x-ray photoelectron spectroscopy. A small (10%) Bi excess was found necessary to obtain dense, pore-free films. Such additions also prevented decomposition of BiFeO3 at high temperatures. The observed (012) texture is believed to originate from the growth mechanism as no relation to the substrate is found. This is also confirmed by observing (012) texture for films on glass substrates.

Chemical synthesis and characterization of polyaniline-molybdenum trisulfide composite

1999 ◽  
Vol 14 (5) ◽  
pp. 1805-1813 ◽  
Author(s):  
Florence Fusalba ◽  
Daniel Bélanger
Keyword(s):  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
Scanning Electron Micrographs ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Chemical Polymerization ◽  
X Ray ◽  
Scanning Electron

A novel polyaniline-molybdenum trisulfide composite has been prepared by chemical polymerization from an acidic (1 M HCl) aqueous solution containing aniline and ammonium tetrathiomolybdate. The presence of molybdenum trisulfide in the polyaniline matrix induces morphological change to the polymer as evidenced by scanning electron micrographs. X-ray diffraction and differential scanning calorimetry indicate that polyaniline-molybdenum trisulfide is slightly less crystalline than polyaniline-HCl. X-ray photoelectron spectroscopy (XPS) and elemental analysis have been used to confirm the presence of molybdenum trisulfide in the polymer matrix. The XPS data also confirm that molybdenum trisulfide and tetrathiomolybdate anions are present with polyaniline to form a new inorganic-organic composite.

scholarly journals Dehydrogenation/rehydrogenation mechanism in aluminum destabilized lithium borohydride

2009 ◽  
Vol 24 (8) ◽  
pp. 2720-2727 ◽  
Author(s):  
Xuebin Yu ◽  
Guanglin Xia ◽  
Zaiping Guo ◽  
Huakun Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Hydrogen Desorption ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Lithium Borohydride ◽  
Hydrogen Storage Properties ◽  
X Ray ◽  
Before And After ◽  
Storage Properties ◽  
Desorption Cycle

LiBH4/Al mixtures with various mol ratios were prepared by ball milling. The hydrogen storage properties of the mixtures were evaluated by differential scanning calorimetry/thermogravimetry analyses coupled with mass spectrometry measurements. The phase compositions and chemical state of elements for the LiBH4/Al mixtures before and after hydrogen desorption and absorption reactions were assessed via powder x-ray diffraction, infrared spectroscopy, and x-ray photoelectron spectroscopy. Dehydrogenation results revealed that LiBH4 could react with Al to form AlB2 and AlLi compounds with a two-step decomposition, resulting in improved dehydrogenation. The rehydrogenation experiments were investigated at 600 °C with various H2 pressure. It was found that intermediate hydride was formed firstly at a low H2 pressure of 30 atm, while LiBH4 could be reformed completely after increasing the pressure to 100 atm. Absorption/desorption cycle results showed that the dehydrogenation temperature increased and the hydrogen capacity degraded with the increase of cycle numbers.

Structure and thermal analysis of Ba0.5La0.5MnO3 polycrystalline powder

2019 ◽  
Vol 33 (22) ◽  
pp. 1950244 ◽  
Author(s):  
R. F. Hashimov ◽  
F. A. Mikailzade ◽  
S. V. Trukhanov ◽  
N. M. Lyadov ◽  
I. R. Vakhitov ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Structural Studies ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Cubic Symmetry ◽  
X Ray ◽  
Enthalpy Changes ◽  
Polycrystalline Powder ◽  
Scanning Electron

The structure and thermal properties of Ba[Formula: see text]La[Formula: see text]MnO3 polycrystalline powder have been investigated using X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) techniques. The structural studies have shown that Ba[Formula: see text]La[Formula: see text]MnO3 compound crystallizes in perovskite structure with Pm-3m cubic symmetry group. The lattice parameters were obtained to be a = b = c = 3.9073 Å. Mass changes have been observed from thermogravimetric (TG) and differential thermogravimetric (DTG) curves obtained in a wide temperature interval of 30–950[Formula: see text]C. Free energy and enthalpy changes for all observed transformations were determined. Observed endo and exo effects.

scholarly journals Structure and Properties of Silk Grafted with N, N-Dimethylaminoethyl Methacrylate via the ARGET ATRP Method

2012 ◽  
Vol 7 (2_suppl) ◽  
pp. 155892501200702
Author(s):  
Tieling Xing ◽  
Shiwei Li ◽  
Xia Xu ◽  
Guoqiang Chen
Keyword(s):  
Photoelectron Spectroscopy ◽  
Gas Permeability ◽  
Antibacterial Properties ◽  
Structure And Properties ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Dimethylaminoethyl Methacrylate ◽  
Dsc Measurements ◽  
Arget Atrp

Silk with antibacterial properties was grafted using dimethylaminoethyl methacrylate (DMAEMA) in water by the ATRP method. The structure and properties of silk-grafted-PDMAEMA (Silk-g-PDMAEMA) and quaternized grafted silk (Q-Silk-g-PDMAEMA) were investigated. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS) analysis confirmed the grafting of DMAEMA and the quarternization. Differential scanning calorimetry (DSC) measurements indicate that the thermal stability of Silk-g-PDMAEMA slightly increased compared with the control silk. X-ray diffraction (XRD) curves demonstrate that the crystalline structure of Silk-g-PDMAEMA remained unchanged regardless of the DMAEMA grafting. The Q-Silk-g-PDMAEMA had good antibacterial properties when exposed to both Staphylococcus aureu and Escherichia coli, and had good washing fastness. The breaking strength, whiteness and gas permeability of Silk-g-PDMAEMA slightly decreased, which had no effect on the intrinsic properties of silk fabric.

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