Structure and Thermo-Regulated Performance of Outlast Viscose Fiber

2011 ◽  
Vol 332-334 ◽  
pp. 812-815 ◽  
Author(s):  
Hai Xia Zhang ◽  
Xi Chang Zhang ◽  
Rui Chao Xu
Keyword(s):  
Phase Change ◽  
Decomposition Temperature ◽  
Viscose Fiber ◽  
Fiber Structure ◽  
X Ray Diffraction ◽  
Crystallization Peak ◽  
Double Peaks ◽  
Change Temperature ◽  
Cooling Velocity ◽  
Better Than

To analyze the structure and thermo-regulated performance of Outlast viscose fiber, the fiber structure was observed respectively by FTIR spectra, X-ray diffraction and scanning electron microscope, and the thermo-regulated performance was investigated by differential scanning calorimeter, thermal gravimeter analysis and step cooling test. The results indicate that the structure of Outlast viscose fiber is similar to that of normal viscose fiber. Both the melting peak and crystallization peak of Outlast viscose fiber are double peaks, and the phase change temperature range is applicable and the phase change enthalpy is high. The decomposition temperature of Outlast viscose fiber is about 280-320°C. The cooling velocity of Outlast viscose fiber decreases exponentially with the increase in time, and the thermo-regulated ability of Outlast viscose fiber is better than that of normal viscose fiber.

Study on Characteristics of Outlast Acrylic Fiber

2012 ◽  
Vol 627 ◽  
pp. 85-89 ◽  
Author(s):  
Hai Xia Zhang ◽  
Xi Chang Zhang
Keyword(s):  
Mechanical Properties ◽  
Phase Change ◽  
Physical And Mechanical Properties ◽  
Decomposition Temperature ◽  
X Ray Diffraction ◽  
Acrylic Fiber ◽  
Change Temperature ◽  
And Performance ◽  
Cooling Velocity ◽  
Better Than

To analyze the structure and performance of Outlast acrylic fiber, the fiber structure was observed respectively by FTIR spectra, X-ray diffraction and scanning electron microscope, the normal physical and mechanical properties were measured, and the thermo-regulated performance was investigated by differential scanning calorimeter, thermal gravimeter analysis and step cooling test. The results indicate that the structure and normal physical and mechanical properties of Outlast acrylic fiber are slightly different from that of normal acrylic fiber. Both the melting peak and crystallization peak of Outlast acrylic fiber are single peaks, and the phase change temperature range is applicable and the phase change enthalpy is high. The decomposition temperature of Outlast acrylic fiber is around 311.85°C. The cooling velocity of Outlast acrylic fiber decreases exponentially with the increase in time, and the thermo-regulated ability of Outlast acrylic fiber is better than that of normal acrylic fiber.

Electrochemical Performance of Li4Ti5O12/TiO2/Li0.4TiO2/C Composite Prepared by the Electrospinning Method Using as Lithium Battery Anode Material

2016 ◽  
Vol 852 ◽  
pp. 959-962 ◽  
Author(s):  
Chun Hua Chen ◽  
Jia Jia Feng ◽  
Wei Quan Shao ◽  
Sha Ou Chen ◽  
Li Zhu He ◽  
...  
Keyword(s):  
Electrochemical Impedance ◽  
Raw Materials ◽  
Electronic Conductivity ◽  
Specific Capacity ◽  
Impedance Spectra ◽  
Fiber Structure ◽  
X Ray Diffraction ◽  
Electrochemical Impedance Spectra ◽  
Electrospinning Method ◽  
Better Than

Li4Ti5O12(LTO) and Li4Ti5O12/TiO2/Li0.4TiO2/C (LTO/C) composite were prepared by the electrospinning method using acetic acid, ethanol, butyl titanate, lithium acetate and PVP (K90) as the raw materials. The phase structure and the morphology were characterized by the X-ray diffraction (XRD) and the scanning electron microscopy (SEM), respectively. It was found that the specific capacity was 356mAh/g at 0.5C for the composite, which was higher than the theoretical specific capacity of the pure Li4Ti5O12 due to the inclusion of other phase. Moreover, the C-rate performance for the composite was also better than that of the pure Li4Ti5O12 resulting from the formation of carbon-based fiber structure. Electrochemical impedance spectra (EIS) revealed that the composite exhibited the improved electronic conductivity than that of Li4Ti5O12.

scholarly journals High-temperature X-ray scattering studies of atomic layer deposited IrO2

2020 ◽  
Vol 53 (2) ◽  
pp. 369-380
Author(s):  
Mikko J. Heikkilä ◽  
Jani Hämäläinen ◽  
Esa Puukilainen ◽  
Markku Leskelä ◽  
Mikko Ritala
Keyword(s):  
High Temperature ◽  
Phase Change ◽  
High Sensitivity ◽  
Atomic Layer ◽  
Ex Situ ◽  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Atomic Force ◽  
Change Temperature

IrO2 is an important material in numerous applications ranging from catalysis to the microelectronics industry, but despite this its behaviour upon annealing under different conditions has not yet been thoroughly studied. This work provides a detailed investigation of the annealing of IrO2 thin films using in situ high-temperature X-ray diffraction and X-ray reflectivity (HTXRR) measurements from room temperature up to 1000°C in oxygen, nitrogen, forming gas and vacuum. Complementary ex situ scanning electron microscopy and atomic force microscopy measurements were conducted. The combined data show the dependencies of crystalline properties and surface morphology on the annealing temperature and atmosphere. The reduction of IrO2 to Ir takes place at a temperature as low as 150°C in forming gas, but in oxygen IrO2 is stable up to 800°C and evaporates as a volatile oxide at higher temperatures. The IrO2 crystallite size remains constant in oxygen up to 400°C and increases above that, while in the more reducing atmospheres the Ir crystallites grow continuously above the phase-change temperature. The role of HTXRR in the analysis is shown to be important since its high sensitivity allows one to observe changes taking place in the film at temperatures much below the phase change.

scholarly journals Synthesis and Characterization of N-Substituted Polyether-Block-Amide Copolymers

Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 773
Author(s):  
Jyun-Yan Ye ◽  
Kuo-Fu Peng ◽  
Yu-Ning Zhang ◽  
Szu-Yuan Huang ◽  
Mong Liang
Keyword(s):  
Titanium Isopropoxide ◽  
Decomposition Temperature ◽  
Phenyl Isocyanate ◽  
Cross Linking ◽  
Resonance Spectroscopy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Degradation Temperature ◽  
Melt Polycondensation ◽  
Structural Regularity

A series of N-substituted polyether-block-amide (PEBA-X%) copolymers were prepared by melt polycondensation of nylon-6 prepolymer and polytetramethylene ether glycol at an elevated temperature using titanium isopropoxide as a catalyst. The structure, thermal properties, and crystallinity of PEBA-X% were investigated using nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, differential scanning calorimetry, wide angle X-ray diffraction, and thermogravimetric analysis. In general, the crystallinity, melting point, and thermal degradation temperature of PEBA-X% decreased as the incorporation of N-methyl functionalized groups increased, owing to the disruption caused to the structural regularity of the copolymer. However, in N-acetyl functionalized analogues, the crystallinity first dropped and then increased because of a new γ form arrangement that developed in the microstructure. After the cross-linking reaction of the N-methyl-substituted derivative, which has electron-donating characteristics, with poly(4,4′-methylenebis(phenyl isocyanate), the decomposition temperature of the resulting polymer significantly increased, whereas no such improvements could be observed in the case of the electro-withdrawing N-acetyl-substituted derivative, because of the incompleteness of its cross-linking reaction.

On the nature of the phase transitions of aluminosilicate perrhenate sodalite

2020 ◽  
Vol 235 (6-7) ◽  
pp. 213-223
Author(s):  
Hilke Petersen ◽  
Lars Robben ◽  
Thorsten M. Gesing
Keyword(s):  
Raman Spectroscopy ◽  
Phase Transitions ◽  
Decomposition Temperature ◽  
Second Phase ◽  
Structure Property ◽  
X Ray Diffraction ◽  
Temperature Dependent ◽  
Two Phase ◽  
Structure Property Relationships ◽  
Heat Capacity Measurements

AbstractThe temperature-dependent structure-property relationships of the aluminosilicate perrhenate sodalite |Na8(ReO4)2|[AlSiO4]6 (ReO4-SOD) were analysed via powder X-ray diffraction (PXRD), Raman spectroscopy and heat capacity measurements. ReO4-SOD shows two phase transitions in the investigated temperature range (13 K < T < 1480 K). The first one at 218.6(1) K is correlated to the transition of dynamically ordered $P\overline{4}3n$ (> 218.6(1 K) to a statically disordered (<218.6(1) K) SOD template in $P\overline{4}3n$. The loss of the dynamics of the template anion during cooling causes an increase of disorder, indicated by an unusual intensity decrease of the 011-reflection and an increase of the Re-O2 bond length with decreasing temperature. Additionally, Raman spectroscopy shows a distortion of the ReO4 anion. Upon heating the thermal expansion of the sodalite cage originated in the tilt-mechanism causes the second phase transition at 442(1) K resulting in a symmetry-increase from $P\overline{4}3n$ to $Pm\overline{3}n$, the structure with the sodalites full framework expansion. Noteworthy is the high decomposition temperature of 1320(10) K.

Influence of High Current Pulsed Electron Beam Irradiation on Ni-P Electroless Plating

2011 ◽  
Vol 299-300 ◽  
pp. 77-81
Author(s):  
Yang Xu ◽  
Sheng Zhi Hao ◽  
Xiang Dong Zhang ◽  
Min Cai Li ◽  
Chuang Dong
Keyword(s):  
Electroless Plating ◽  
Electron Beam Irradiation ◽  
Xrd Analysis ◽  
High Current ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pulsed Electron Beam ◽  
6063 Aluminum Alloy ◽  
Pre Treatment ◽  
Better Than

The surface irradiation of 6063 aluminum alloy by high current pulsed electron was conducted with the aim of replacing the complicated pre-treatment in the processes of electroless plating. To explore the microstructure changes, optical metallography, SEM (scanning electron microscope), XRD (X-ray diffraction) analyses were carried out, and the sliding tests were used for the detection of wear resistance. It was concluded that the HCPEB irradiation could replace the pre-treatment of aluminum substrate as required in conventional electroless plating with a decreased surface roughness of Ni-P alloy plating layer. The plates exhibited an amorphous microstructure as demonstrated by XRD analysis. The plates, produced with the routine of HCPEB irradiation, activation and electroless plating possess, also exhibited good quality, even better than that of conventional electroless plating technique.

scholarly journals Purification, crystallization and preliminary X-ray diffraction analysis of a hydroxycinnamoyl-CoA shikimate/quinate hydroxycinnamoyltransferase (HCT) fromCoffea canephorainvolved in chlorogenic acid biosynthesis

2012 ◽  
Vol 68 (7) ◽  
pp. 824-828 ◽  
Author(s):  
Laura A. Lallemand ◽  
James G. McCarthy ◽  
Sean McSweeney ◽  
Andrew A. McCarthy
Keyword(s):  
Structural Data ◽  
Coffea Canephora ◽  
Molecular Replacement ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cell Parameters ◽  
Key Enzyme ◽  
Substrate Specifities ◽  
Drop Technique ◽  
Better Than

Chlorogenic acids (CGAs) are a group of soluble phenolic compounds that are produced by a variety of plants, includingCoffea canephora(robusta coffee). The last step in CGA biosynthesis is generally catalysed by a specific hydroxycinnamoyl-CoA quinate hydroxycinnamoyltransferase (HQT), but it can also be catalysed by the more widely distributed hydroxycinnamoyl-CoA shikimate/quinate hydroxycinnamoyltransferase (HCT). Here, the cloning and overexpression of HCT fromC. canephorainEscherichia colias well as its purification and crystallization are presented. Crystals were obtained by the sitting-drop technique at 293 K and X-ray diffraction data were collected on the microfocus beamline ID23-2 at the ESRF. The HCT crystals diffracted to better than 3.0 Å resolution, belonged to space groupP42212 with unit-cell parametersa=b= 116.1,c= 158.9 Å and contained two molecules in the asymmetric unit. The structure was solved by molecular replacement and is currently under refinement. Such structural data are needed to decipher the molecular basis of the substrate specifities of this key enzyme, which belongs to the large plant acyl-CoA-dependent BAHD acyltransferase superfamily.

Study on Modified Rapeseed Oil/Montmorillonite Nanocomposites

2010 ◽  
Vol 123-125 ◽  
pp. 1291-1294 ◽  
Author(s):  
Bin Lü ◽  
Jian Zhong Ma ◽  
Dang Ge Gao ◽  
Lei Hong
Keyword(s):  
Rapeseed Oil ◽  
Fourier Transforms ◽  
Raw Materials ◽  
Infrared Spectrometry ◽  
Emulsifying Properties ◽  
X Ray Diffraction ◽  
Layer Spacing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Better Than

Modified rapeseed oil(MRO) was prepared by using rapeseed oil, ethylene diamine and acrylic acid as the raw materials. Modified rapeseed oil/montmorillonite(MRO/MMT) nanocomposite was prepared by using modified rapeseed oil and montmorillonite. The emulsifying properties of MRO and MRO/MMT were determined respectively. Fourier transforms infrared spectrometry (FT-IR) and Transmission Electron microscope (TEM) results showed that MRO/MMT was prepared successfully. X-ray diffraction (XRD) results showed that modified rapeseed oil could smoothly enter the interlayer of montmorillonite, and modified the montmorillonite; with an increase in the amount of montmorillonite, the layer spacing of montmorillonite in the MRO/MMT lower after the first increase. The results of emulsifying properties indicated that emulsifying properties of MRO/MMT was better than MRO.

Preparation and characterization of solution spinning of protein/cellulose fiber: A new flame-retardant grade

2016 ◽  
Vol 47 (2) ◽  
pp. 233-251 ◽  
Author(s):  
Zhou Zhao ◽  
Weiren Bao ◽  
Youbo Di ◽  
Jinming Dai
Keyword(s):  
Flame Retardant ◽  
Cellulose Fiber ◽  
Decomposition Temperature ◽  
Major Product ◽  
Viscose Fiber ◽  
Compact Structure ◽  
Before And After ◽  
Solution Spinning ◽  
Warmth Retention

A new flame-retardant protein viscose fiber with safely wearing performance has been prepared through blending protein solution, flame retardant (hexaphenoxycyclotriphosphazene) and viscose spinning solution, in which wool protein was used and added to spinning solution on the basis of 16% flame retardant, and the properties of the fiber were investigated. The product has more compact structure inside the fiber and evenly scattered small pores on the surface. Flame-retardant protein viscose fiber can reach the flame-retardant standard both before and after 30 times wash test, and the mechanical strength of the fiber was also improved. The introduction of hexaphenoxycyclotriphosphazene lowered the primary decomposition temperature of viscose fiber, reduced its weight loss. The flame-retardancy of the fiber can be improved by the introduction of protein. In thermal processes, the major product of thermal decomposition was CO2, no hazardous and noxious gases were released. Due to the introduction of protein, moisture regain of the fiber is a little lower than that of viscose fiber, but higher than flame-retardant viscose fiber. Warmth retention property was also improved. Friction coefficient of the product is lower than that of flame-retardant viscose fiber. Bulking intensity was increased, which is better than that of viscose fiber.

Sign in / Sign up

Export Citation Format

Share Document