scholarly journals Microstructure evolution and properties of polyimide fibers containing trifluoromethyl units

2019 ◽  
Vol 32 (1) ◽  
pp. 39-46
Author(s):  
Hongqing Niu ◽  
Mengying Zhang ◽  
Ang Li ◽  
Ziqi Wang ◽  
Xiaodong Wang ◽  
...  
Keyword(s):  
Molecular Design ◽  
Nitrogen Atmosphere ◽  
Wet Spinning ◽  
Fiber Direction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Polyimide Fibers ◽  
Initial Modulus ◽  
Molecular Alignments ◽  
Biphenyltetracarboxylic Dianhydride

A series of copolyimide (co-PI) fibers containing trifluoromethyl units were successfully obtained on the molecular design of 3,3′,4,4′-biphenyltetracarboxylic dianhydride, p-phenylenediamine, and 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane (HFBAPP) via a widely utilized two-step wet-spinning method. Significant variations on the microstructures and properties of the resulting co-PI fibers were observed after the incorporation of HFBAPP moieties. The tensile strength and initial modulus of the fibers decreased from 0.70 GPa to 0.38 GPa and from 69.63 GPa to 9.60 GPa, respectively. However, the dielectric permittivity decreased from 3.62 to 2.85 in the frequency of 10 MHz as a result of the incorporation of trifluoromethyl units. Two-dimensional wide-angle X-ray diffraction showed that the fibers exhibited highly oriented molecular alignments along the fiber direction and low lateral packing degree in the transverse direction. In addition, the co-PI fibers possessed excellent thermal–oxidative stabilities with the 5% weight loss temperature ranging from 532°C to 552°C under nitrogen atmosphere and the glass transition temperature ranging from 312°C to 330°C.

Properties of Carbon Nanofibers Prepared from Polyacrylonitrile/Poly(methyl Methacrylate) Blend

2009 ◽  
Vol 79-82 ◽  
pp. 353-356
Author(s):  
Wei Pan ◽  
Yan Chen ◽  
Xiao Wei He
Keyword(s):  
Methyl Methacrylate ◽  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
Nitrogen Atmosphere ◽  
Wet Spinning ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate ◽  
Graphite Crystallite ◽  
Raman Microspectrometry

The polyacrylonitrile(PAN)/poly (methyl methacrylate)(PMMA) blend fibers were prepared by wet-spinning technique and carbonized over the temperature range of 400-1000°C in nitrogen atmosphere. After carbonization of the blend fibers, the PMMA component removed and the PAN component left in the form of carbon nanofibers. Morphology of the carbon nanofibers were investigated via scanning electron microscopy (SEM), and the carbonization behavior of the fibers were examined via x-ray diffraction (XRD), Raman microspectrometry. The optimal condition made carbon fibers with great L/D ratio and diameter less than 200 nm. XRD and Raman spectra shows that the PAN/PMMA blend fibers treated at 600°C produced some graphite crystallite.

scholarly journals Functional Bionanocomposite Fibers of Chitosan Filled with Cellulose Nanofibers Obtained by Gel Spinning

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1563
Author(s):  
Sofia Marquez-Bravo ◽  
Ingo Doench ◽  
Pamela Molina ◽  
Flor Estefany Bentley ◽  
Arnaud Kamdem Tamo ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Mechanical Performance ◽  
Cellulose Nanofibers ◽  
Microstructural Characterization ◽  
Fiber Formation ◽  
Fiber Direction ◽  
Composite Fibers ◽  
X Ray Diffraction ◽  
Gel Spinning ◽  
X Ray

Extremely high mechanical performance spun bionanocomposite fibers of chitosan (CHI), and cellulose nanofibers (CNFs) were successfully achieved by gel spinning of CHI aqueous viscous formulations filled with CNFs. The microstructural characterization of the fibers by X-ray diffraction revealed the crystallization of the CHI polymer chains into anhydrous chitosan allomorph. The spinning process combining acidic–basic–neutralization–stretching–drying steps allowed obtaining CHI/CNF composite fibers of high crystallinity, with enhanced effect at incorporating the CNFs. Chitosan crystallization seems to be promoted by the presence of cellulose nanofibers, serving as nucleation sites for the growing of CHI crystals. Moreover, the preferential orientation of both CNFs and CHI crystals along the spun fiber direction was revealed in the two-dimensional X-ray diffraction patterns. By increasing the CNF amount up to the optimum concentration of 0.4 wt % in the viscous CHI/CNF collodion, Young’s modulus of the spun fibers significantly increased up to 8 GPa. Similarly, the stress at break and the yield stress drastically increased from 115 to 163 MPa, and from 67 to 119 MPa, respectively, by adding only 0.4 wt % of CNFs into a collodion solution containing 4 wt % of chitosan. The toughness of the CHI-based fibers thereby increased from 5 to 9 MJ.m−3. For higher CNFs contents like 0.5 wt %, the high mechanical performance of the CHI/CNF composite fibers was still observed, but with a slight worsening of the mechanical parameters, which may be related to a minor disruption of the CHI matrix hydrogel network constituting the collodion and gel fiber, as precursor state for the dry fiber formation. Finally, the rheological behavior observed for the different CHI/CNF viscous collodions and the obtained structural, thermal and mechanical properties results revealed an optimum matrix/filler compatibility and interface when adding 0.4 wt % of nanofibrillated cellulose (CNF) into 4 wt % CHI formulations, yielding functional bionanocomposite fibers of outstanding mechanical properties.

High Functional PET Sericin Composite Fabric

2012 ◽  
Vol 430-432 ◽  
pp. 49-52
Author(s):  
Gang Xian Zhang ◽  
Xiao Hua Shi ◽  
Wei Hu ◽  
Feng Xiu Zhang ◽  
Da Yang Wu
Keyword(s):  
High Pressure ◽  
Glycidyl Ether ◽  
Air Permeability ◽  
Sucrose Ester ◽  
Random Coil ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pet Fabric ◽  
Initial Modulus ◽  
Ft Ir

Though poly(ethyleneteraphthalate)(PET) fabrics have high initial modulus, outstanding creasability and wash-well character, but its hydrophilicity and biocompatibility are very poor. In this paper, the PET fabric was encased sucrose ester at high pressure and high temperature to endue it enough hydroxyl to grafting protein. The sericin was grafted on PET fabric by sucrose eater glycidyl ether (SEGE). The FT-IR spectra showed that sericin was grafted on PET fabric, and the structure of sericin was random coil conformation. X-ray diffraction spectra showed the structure of PET fiber did not changed. DSC showed the thermostability increased a little. After the PET fabric grafted with sericin, the hydrophilicity of PET sericin composite fabric was improved greatly, the cockle elasticity kept well, and the broken strength in creased a little. Certainly, the whiteness and air permeability decreased a little. The PET sericin composite fabric was high functional.

scholarly journals Spin State Behavior of A Spin-Crossover Iron(II) Complex with N,N′-Disubstituted 2,6-bis(pyrazol-3-yl)pyridine: A Combined Study by X-ray Diffraction and NMR Spectroscopy

Crystals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 793
Author(s):  
Elizaveta K. Melnikova ◽  
Dmitry Yu. Aleshin ◽  
Igor A. Nikovskiy ◽  
Gleb L. Denisov ◽  
Yulia V. Nelyubina
Keyword(s):  
Nmr Spectroscopy ◽  
Spin State ◽  
Metal Ion ◽  
Spin Crossover ◽  
Molecular Design ◽  
Chemical Shifts ◽  
Variable Temperature ◽  
High Spin State ◽  
X Ray Diffraction ◽  
X Ray

A series of three different solvatomorphs of a new iron(II) complex with N,N′-disubstituted 2,6-bis(pyrazol-3-yl)pyridine, including those with the same lattice solvent, has been identified by X-ray diffraction under the same crystallization conditions with the metal ion trapped in the different spin states. A thermally induced switching between them, however, occurs in a solution, as unambiguously confirmed by the Evans technique and an analysis of paramagnetic chemical shifts, both based on variable-temperature NMR spectroscopy. The observed stabilization of the high-spin state by an electron-donating substituent contributes to the controversial results for the iron(II) complexes of 2,6-bis(pyrazol-3-yl)pyridines, preventing ‘molecular’ design of their spin-crossover activity; the synthesized complex being only the fourth of the spin-crossover (SCO)-active kind with an N,N′-disubstituted ligand.

scholarly journals Hydrogen desorption kinetics of MgH2 synthesized from modified waste magnesium

2014 ◽  
Vol 32 (3) ◽  
pp. 385-390
Author(s):  
Aysel Kantürk Figen ◽  
Bilge Coşkuner ◽  
Sabriye Pişkin
Keyword(s):  
Hydrogen Desorption ◽  
Nitrogen Atmosphere ◽  
Desorption Kinetics ◽  
X Ray Diffraction ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrf Scanning ◽  
Isothermal Kinetic ◽  
Kinetics Of

AbstractIn the present study, hydrogen desorption properties of magnesium hydride (MgH2) synthesized from modified waste magnesium chips (WMC) were investigated. MgH2 was synthesized by hydrogenation of modified waste magnesium at 320 °C for 90 min under a pressure of 6 × 106 Pa. The modified waste magnesium was prepared by mixing waste magnesium with tetrahydrofuran (THF) and NaCl additions, applying mechanical milling. Next, it was investigated by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) techniques in order to characterize its structural properties. Hydrogen desorption properties were determined by differential scanning calorimetry (DSC) under nitrogen atmosphere at different heating rates (5, 10, and 15 °C/min). Doyle and Kissenger non-isothermal kinetic models were applied to calculate energy (Ea) values, which were found equal to 254.68 kJ/mol and 255.88 kJ/mol, respectively.

scholarly journals Preparation, Characterization and Intermediate-Temperature Electrochemical Properties of Er3+-Doped Barium Cerate–Sulphate Composite Electrolyte

Materials ◽  
2019 ◽  
Vol 12 (17) ◽  
pp. 2752
Author(s):  
Fufang Wu ◽  
Ruifeng Du ◽  
Tianhui Hu ◽  
Hongbin Zhai ◽  
Hongtao Wang
Keyword(s):  
Maximum Output Power ◽  
Nitrogen Atmosphere ◽  
Maximum Output ◽  
Barium Cerate ◽  
X Ray Diffraction ◽  
Ac Impedance Spectroscopy ◽  
Raman Spectrometry ◽  
Composite Electrolyte ◽  
X Ray ◽  
Doped Barium Cerate

In this study, BaCe0.9Er0.1O3−α was synthesized by a microemulsion method. Then, a BaCe0.9Er0.1O3−α–K2SO4–BaSO4 composite electrolyte was obtained by compounding it with a K2SO4–Li2SO4 solid solution. BaCe0.9Er0.1O3−α and BaCe0.9Er0.1O3−α–K2SO4–BaSO4 were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectrometry. AC impedance spectroscopy was measured in a nitrogen atmosphere at 400–700 °C. The logσ~log (pO2) curves and fuel cell performances of BaCe0.9Er0.1O3−α and BaCe0.9Er0.1O3−α–K2SO4–BaSO4 were tested at 700 °C. The maximum output power density of BaCe0.9Er0.1O3−α–K2SO4–BaSO4 was 115.9 mW·cm−2 at 700 °C, which is ten times higher than that of BaCe0.9Er0.1O3−α.

Substrates Effect on the Phase Transition of GaN Thin Films by Sputter Deposition

2019 ◽  
Vol 971 ◽  
pp. 79-84
Author(s):  
Chun Guang Zhang
Keyword(s):  
Thin Films ◽  
Phase Transition ◽  
Nitrogen Atmosphere ◽  
Sputter Deposition ◽  
X Ray Diffraction ◽  
Pure Nitrogen ◽  
X Ray ◽  
Zinc Blende ◽  
Planar Magnetron ◽  
Pure Nitrogen Atmosphere

As a promising third generation semiconductor material, gallium nitride (GaN) has become a research hotspot in optoelectronic field nowadays. In this paper, GaN thin films were grown by radio frequency (RF) planar magnetron sputtering of a powder GaN target in a pure nitrogen atmosphere at (0.2 – 2.0) Pa, (10 - 100) W onto various substrates such as GaAs (100), Si (100), Si (111), Al2O3(0001) and glass without any buffer layer. A clear phase transition from the metastable cubic zinc-blende (c - ZB) to the stable hexagonal wurtzite (h - WZ) dependence on substrates has been found in the GaN thin films. And the phase transition of GaN films were studied by X-ray diffraction (XRD), photoluminescence (PL) and Raman spectroscopy.

X-ray powder diffraction analysis of the heteropoly-molybdate (MoO2)0.5PMo14O42

2003 ◽  
Vol 18 (3) ◽  
pp. 236-239 ◽  
Author(s):  
L. Marosi ◽  
J. Cifré ◽  
C. Otero Areán
Keyword(s):  
Catalytic Activity ◽  
Diffraction Analysis ◽  
Computer Modeling ◽  
Powder Diffraction ◽  
Rietveld Analysis ◽  
Nitrogen Atmosphere ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffraction Patterns

The new heteropoly blue compound (MoO2)0.5PMo14O42, which is relevant in the context of catalytic activity of heteropoly-molybdates, was prepared by controlled thermolysis of (NH4)3PMo12O40 at 730 K in a nitrogen atmosphere. Powder X-ray diffraction analysis showed that this compound has a cubic unit cell, space group Pn3m (No. 224), with ao=11.795(2) Å, Z=2 and DXR=4.2466 g cm−3. Computer modeling and Rietveld analysis of powder diffraction patterns led to a proposed structure of the corresponding Keggin-cage unit PMo14O42.

The Study of High Temperature Annealing of a-SiC:H Films

2006 ◽  
Vol 514-516 ◽  
pp. 18-22
Author(s):  
Shibin Zhang ◽  
Z. Hu ◽  
Leandro Raniero ◽  
X. Liao ◽  
Isabel Ferreira ◽  
...  
Keyword(s):  
High Temperature ◽  
Chemical Vapor ◽  
Nitrogen Atmosphere ◽  
High Temperature Annealing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Metal Induced Crystallization ◽  
Vapor Deposition Technique ◽  
Crystallization Effect ◽  
Induced Crystallization

A series of amorphous silicon carbide films were prepared by plasma enhanced chemical vapor deposition technique on (100) silicon wafers by using methane, silane, and hydrogen as reactive resources. A very thin (around 15 Å) gold film was evaporated on the half area of the a- SiC:H films to investigate the metal induced crystallization effect. Then the a-SiC:H films were annealed at 1100 0C for 1 hour in the nitrogen atmosphere. Fourier transform infrared spectroscopy (FTIR), X-Ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to analyze the microstructure, composition and surface morphology of the films. The influences of the high temperature annealing on the microstructure of a-SiC:H film and the metal induced metallization were investigated.

Reduced electrical resistivity of reaction-sintered SiC by nitrogen doping

2008 ◽  
Vol 23 (4) ◽  
pp. 1020-1025 ◽  
Author(s):  
Young-Sam Jeon ◽  
Hyunho Shin ◽  
Young-Hyun Lee ◽  
Sang-Won Kang
Keyword(s):  
Heat Treatment ◽  
Electrical Resistivity ◽  
Photoelectron Spectroscopy ◽  
Nitrogen Doping ◽  
Nitrogen Atmosphere ◽  
X Ray Diffraction ◽  
Post Heat Treatment ◽  
X Ray ◽  
Sic Particles ◽  
Transmission Electron

A post heat treatment of reaction-sintered SiC at 1700 °C in nitrogen atmosphere significantly reduced electrical resistivity. A trace of insulating Si3N4 phase was detected via nitrogen heat treatment in high-resolution transmission electron microscopy observation; however, based on x-ray photoelectron spectroscopy, the evidence of nitrogen doping into SiC lattice has been claimed as the mechanism to the decreased resistivity. The increase of the total volume of SiC was apparent in x-ray diffraction during the nitrogen heat treatment, which was interpreted to stem from the growth of the nitrogen-doped intergranular SiC particles and surface doping of the primary SiC to reduce the contact resistance between the primary SiC particles.

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