Conversion of Lignin-Nanofibers to CNFs

NANO ◽  
2015 ◽  
Vol 10 (06) ◽  
pp. 1550092 ◽  
Author(s):  
Aili Ma ◽  
Li Zhou ◽  
Jie Chang
Keyword(s):  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
Carbonization Temperature ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Compact Structure ◽  
Graphitization Degree ◽  
Novel Method ◽  
Thermal Stability Of

In this study, a novel method, electrospinning, was used to prepare lignin-based carbon nanofibers. The major material was lignin. The chemical and thermal properties of different lignins were characterized to determine their suitability for partial incorporation of polyacrylonitrile (PAN). Then the precursor fibers were carbonized at a temperature from 600°C to 1000°C, respectively to prepare biomass-based carbon nanofibers. The influences of carbonization temperature on prepared carbon nanofibers were investigated by X-ray diffraction (XRD), Raman, thermal gravimetric analysis (TGA), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). The results indicated that the diameter of prepared precursor fibers and carbon fibers were about 200nm and 100nm, respectively. The increase of temperature has little influence on the carbon fiber graphitization degree. The D band of the carbon fibers carbonized at 900°C is lowest. The thermal stability of the carbon fibers changes little with rising temperature when carbonized temperature exceeds 900°C, and carbon fibers carbonized under 900°C have most compact structure. Therefore, the above conclusions make clearly that 900°C is the optimal carbonization temperature for preparing lignin-based carbon nanofibers in this technique. Meanwhile, the study is a doubled-edged enterprise that aims to recycle the waste from pulping industry as well as to turn it into a valuable material.

scholarly journals Effect of Sr2TiMnO6 fillers on mechanical, dielectric and thermal behaviour of PMMA polymer

2015 ◽  
Vol 05 (03) ◽  
pp. 1550018 ◽  
Author(s):  
P. Thomas ◽  
B. S. Dakshayini ◽  
H. S. Kushwaha ◽  
Rahul Vaish
Keyword(s):  
Coefficient Of Thermal Expansion ◽  
Thermo Gravimetric Analysis ◽  
Mechanical Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Transition Formula ◽  
Thermal Stability Of ◽  
Pmma Polymer

Composites of poly(methyl methacrylate) (PMMA) and [Formula: see text] (STMO) were fabricated via melt mixing followed by hot pressing technique. These were characterized using X-ray diffraction (XRD), thermo gravimetric analysis (TGA), differential scanning calorimetry (DSC), thermo mechanical analysis (TMA) and impedance analyser for their structural, thermal and dielectric properties. The coefficient of thermal expansion (CTE) was measured between 40°C and 100°C for pure PMMA is 115.2 ppm/°C, which was decreased to 78.58 ppm/°C when the STMO content was increased to 50 wt.% in PMMA. There was no difference in the glass transition ([Formula: see text]) temperature of the PMMA polymer and their composites. However, the FTIR analysis indicated possible interaction between the PMMA and STMO. The density and the hardness were increased as the STMO content increased in the PMMA matrix. Permittivity was found to be as high as 30.9 at 100 Hz for the PMMA+STMO-50 wt.% composites, indicating the possibility of using these materials for capacitor applications. The thermal stability of polymer was enhanced by incorporation of STMO fillers.

scholarly journals Preparation, Stabilization and Carbonization of a Novel Polyacrylonitrile-Based Carbon Fiber Precursor

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1150 ◽  
Author(s):  
Huichao Liu ◽  
Shuo Zhang ◽  
Jinglong Yang ◽  
Muwei Ji ◽  
Jiali Yu ◽  
...  
Keyword(s):  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
High Performance ◽  
Great Influence ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Electrospinning Method ◽  
Lower Heat ◽  
Group 2

The quality of polyacrylonitrile (PAN) precursor has a great influence on the properties of the resultant carbon fibers. In this paper, a novel comonomer containing the sulfonic group, 2-acrtlamido-2-methylpropane acid (AMPS), was introduced to prepare P(AN-co-AMPS) copolymers using itaconic acid (IA) as the control. The nanofibers of PAN, P(AN-co-IA), and P(AN-co-AMPS) were prepared using the electrospinning method. The effect of AMPS comonomer on the carbon nanofibers was studied using scanning electron microscopy (SEM), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and Raman spectrum. The structural evolutions of PAN-based nanofibers were quantitatively tracked by FTIR and XRD during the thermal oxidative stabilization (TOS) process. The results suggested that P(AN-co-AMPS) nanofibers had the lower heat release rate (ΔH/ΔT = 26.9 J g−1 °C−1), the less activation energy of cyclization (Ea1 = 26.6 kcal/mol and Ea2 = 27.5 kcal/mol), and the higher extent of stabilization (Es and SI) during TOS process, which demonstrated that the AMPS comonomer improved the efficiency of the TOS process. The P(AN-co-AMPS) nanofibers had the better thermal stable structures. Moreover, the carbon nanofibers derived from P(AN-co-AMPS) precursor nanofibers had the better graphite-like structures (XG = 46.889). Therefore, the AMPS is a promising candidate comonomer to produce high performance carbon fibers.

scholarly journals Preparation and Characterization of Spherical Submicron CL-20 by Siphon Spray Refinement

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Jiangtao Xing ◽  
Weili Wang ◽  
Wenzheng Xu ◽  
Tianle Yao ◽  
Jun Dong ◽  
...  
Keyword(s):  
Impact Sensitivity ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Crystal Forms ◽  
Refined Method ◽  
Diffraction Angle ◽  
Ultrasonic Assisted ◽  
The Impact ◽  
Thermal Stability Of

In order to improve the safety of hexanitrohexaazaisowurtzitane (CL-20), submicron CL-20 particles were prepared by a siphon ultrasonic-assisted spray refining experimental device. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC), and the impact sensitivity of the samples was tested. The results show that the particle size of siphon-refined CL-20 is about 800 nm~1 μm, which is more smooth, mellow, and dense than that of CL-20 prepared by a traditional pressure-refined method. The peak diffraction angle of pressure- and siphon-refined CL-20 is basically the same as that of raw CL-20, and their crystal forms are ε type. The peak strength of pressure- and siphon-refined CL-20 decreased obviously. The apparent activation energy of pressure-refined CL-20 and siphon-refined CL-20 is 13.3 kJ/mol and 11.95 kJ/mol higher than that of raw CL-20, respectively. The thermal stability of CL-20 is improved. The activation enthalpy (ΔH#) is significantly higher than that of raw CL-20, and the characteristic drop is 70.4% and 82.7% higher than that of raw CL-20. The impact sensitivity of siphon-refined CL-20 is lower than that of pressure-refined CL-20, so the safety performance of an explosive is improved obviously.

scholarly journals A Facile Method to Construct MXene/CuO Nanocomposite with Enhanced Catalytic Activity of CuO on Thermal Decomposition of Ammonium Perchlorate

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2457 ◽  
Author(s):  
Haifeng Zhao ◽  
Jing Lv ◽  
Junshan Sang ◽  
Li Zhu ◽  
Peng Zheng ◽  
...  
Keyword(s):  
Thermal Decomposition ◽  
Catalytic Activity ◽  
Ammonium Perchlorate ◽  
Photoelectron Spectra ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Improved Performance ◽  
Calcination Method

In this work, a mixing-calcination method was developed to facilely construct MXene/CuO nanocomposite. CuO and MXene were first dispersed in ethanol with sufficient mixing. After solvent evaporation, the dried mixture was calcinated under argon to produce a MXene/CuO nanocomposite. As characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), and X-ray photoelectron spectra (XPS), CuO nanoparticles (60–100 nm) were uniformly distributed on the surface and edge of MXene nanosheets. Furthermore, as evaluated by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA), the high-temperature decomposition (HTD) temperature decrease of ammonium perchlorate (AP) upon addition of 1 wt% CuO (hybridized with 1 wt% MXene) was comparable with that of 2 wt% CuO alone, suggesting an enhanced catalytic activity of CuO on thermal decomposition of AP upon hybridization with MXene nanosheets. This strategy could be further applied to construct other MXene/transition metal oxide (MXene/TMO) composites with improved performance for various applications.

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 Characterization of the Interface Between the Bulk Glass Forming Alloy Zr41Ti14Cu12Ni10Be23 with Pure Metals and Ceramics

2000 ◽  
Vol 15 (7) ◽  
pp. 1617-1621 ◽  
Author(s):  
Jan Schroers ◽  
Konrad Samwer ◽  
Frigyes Szuecs ◽  
William L. Johnson
Keyword(s):  
Sessile Drop ◽  
Bulk Glass ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Glass Forming ◽  
Processing Times ◽  
Thermal Stability Of

The reaction of the bulk glass forming alloy Zr41Ti14Cu12Ni10Be23 (Vit 1) with W, Ta, Mo, AlN, Al2O3, Si, graphite, and amorphous carbon was investigated. Vit 1 samples were melted and subsequently solidified after different processing times on discs of the different materials. Sessile drop examinations of the macroscopic wetting of Vit 1 on the discs as a function of temperature were carried out in situ with a digital optical camera. The reactions at the interfaces between the Vit 1 sample and the different disc materials were investigated with an electron microprobe. The structure and thermal stability of the processed Vit 1 samples were examined by x-ray diffraction and differential scanning calorimetry. The results are discussed in terms of possible applications for composite materials.

scholarly journals The Development of Rapidly Solidified Magnesium – Copper Ribbons

2016 ◽  
Vol 61 (2) ◽  
pp. 1083-1088
Author(s):  
M. Pastuszak ◽  
G. Cieślak ◽  
A. Dobkowska ◽  
J. Mizera ◽  
K.J. Kurzydłowski
Keyword(s):  
Corrosion Resistance ◽  
Cooling Rate ◽  
Melt Spinning ◽  
Diffraction Method ◽  
Electrode System ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Copper Addition ◽  
Rapidly Solidified ◽  
Thermal Stability Of

Abstract The aim of the present work was to plan and carry out an experiment consisting of amorphization of industrial magnesium alloy WE 43 (Mg - 4 Y - 3 RE - 0.5 Zr) modified by the copper addition. Investigated alloy modified with 20% of copper was rapidly quenched with the use of melt spinning technique. The effects of cooling rate on the structure and properties of the obtained material were extensively analyzed. The structure and phase analysis of samples were examined using X-ray diffraction method (XRD) while the thermal stability of the samples was determined by differential scanning calorimetry (DSC). Microstructure observations were also conducted. The microhardness tests (HV0.02) and corrosion resistance tests were carried out to investigate the properties of the material. Corrosion resistance measurements were held using a typical three-electrode system. As the result of the research, the effect of cooling rate on microstructure and properties of investigated alloy was determined.

Thermotropic Copolyesters Based on Polyethylene Terephthalate and 4-Hydroxybenzoic Acid for High Modulus Fibers

2021 ◽  
Vol 887 ◽  
pp. 3-9
Author(s):  
T.R. Deberdeev ◽  
A.I. Akhmetshina ◽  
S.V. Grishin
Keyword(s):  
Dimethyl Ester ◽  
Hydroxybenzoic Acid ◽  
Gravimetric Analysis ◽  
Scanning Calorimetry ◽  
Polarizing Microscopy ◽  
Polymer Backbone ◽  
Molecular Compounds ◽  
Anisotropic Phase ◽  
Thermal Stability Of ◽  
Thermotropic Copolyesters

The copolyesters derived from dimethyl ester of terephthalic acid, ethylene glycol, and 4-hydroxybenzoic acid (HBA) have been synthesized via catalytically promoted polycondensation omitting the acetylation step. FTIR spectroscopy results have evidenced an insertion of HBA along a polymer backbone. Of note, thermal gravimetric analysis has shown that the HBA moieties substantially improved the thermal stability of polyesters. As found by differential scanning calorimetry and polarizing microscopy, the copolyesters are capable of forming an anisotropic phase in a temperature range of 150-170 °C. Additionally, the free surface energy of the samples was determined to evaluate the compatibility of thermotropic copolyesters with other high-molecular compounds.

scholarly journals Development and In-Vitro Evaluation of pH Responsive Polymeric Nano Hydrogel Carrier System for Gastro-Protective Delivery of Naproxen Sodium

2019 ◽  
Vol 2019 ◽  
pp. 1-13
Author(s):  
Rai Muhammad Sarfraz ◽  
Muhammad Rouf Akram ◽  
Muhammad Rizwan Ali ◽  
Asif Mahmood ◽  
Muhammad Usman Khan ◽  
...  
Keyword(s):  
Drug Release ◽  
Naproxen Sodium ◽  
Research Work ◽  
Entrapment Efficiency ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Swelling Behaviour ◽  
X Ray

Current research work was carried out for gastro-protective delivery of naproxen sodium. Polyethylene glycol-g-poly (methacrylic acid) nanogels was developed through free radical polymerization technique. Formulation was characterized for swelling behaviour, entrapment efficiency, Fourier transform infrared (FTIR) spectroscopy, Differential scanning calorimetry (DSC), and Thermal Gravimetric Analysis (TGA), Powder X-ray diffraction (PXRD), Zeta size distribution, and Zeta potential measurements, and in-vitro drug release. pH dependent swelling was observed with maximum drug release at higher pH. PXRD studies confirmed the conversion of loaded drug from crystalline to amorphous form while Zeta size measurement showed size reduction. On the basis of these results it was concluded that prepared nanogels proved an effective tool for gastro-protective delivery of naproxen sodium.

The Influence of Calcination Temperature on Quantitative Phase of Hematite from Iron Stone Tanah Laut

2015 ◽  
Vol 1112 ◽  
pp. 489-492
Author(s):  
Ali Mufid ◽  
M. Zainuri
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Thermo Gravimetric Analysis ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Particle Size Analyzer ◽  
Co Precipitation

This research aims to form particles of hematite (α-Fe2O3) with a basis of mineral iron ore Fe3O4 from Tanah Laut. Magnetite Fe3O4 was synthesized using co-precipitation method. Further characterization using X-ray fluorescence (XRF) to obtain the percentage of the elements, obtained an iron content of 98.51%. Then characterized using thermo-gravimetric analysis and differential scanning calorimetry (TGA-DSC) to determine the calcination temperature, that at a temperature of 445 °C mass decreased by 0.369% due to increase in temperature. Further Characterization of X-ray diffraction (XRD) to determine the phases formed at the calcination temperature variation of 400 °C, 445 °C, 500 °C and 600 °C with a holding time of 5 hours to form a single phase α-Fe2O3 hematite. Testing with a particle size analyzer (PSA) to determine the particle size distribution, where test results indicate that the α-Fe2O3 phase of each having a particle size of 269.7 nm, 332.2 nm, 357.9 nm, 412.2 nm. The best quantity is shown at a temperature of 500 °C to form the hematite phase. This result is used as the calcination procedure to obtain a source of Fe ions in the manufacture of Lithium Ferro Phosphate.

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