Preparation and characterisation of electrospun composite nanofibre polyvinyl alcohol/ nanofibrillated cellulose isolated from oil palm empty fruit bunches

BioResources ◽  
2020 ◽  
Vol 15 (4) ◽  
pp. 7906-7917
Author(s):  
Erni Misran ◽  
Basuki Wirdjosentono ◽  
Nasrudin M. Noor ◽  
Saharman Gea ◽  
Suhut Alexander Situmorang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Polyvinyl Alcohol ◽  
Oil Palm ◽  
Nanofibrillated Cellulose ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Electrospinning Technique ◽  
Empty Fruit Bunches ◽  
Transmission Electron ◽  
Explosion Method

Composite nanofibre polyvinyl alcohol (PVOH) was prepared in this work reinforced with nanofibrillated cellulose (NFC) using an electrospinning technique. NFC was isolated from oil palm empty fruit bunches (OPEFB) by steam explosion method followed by acid hydrolysis. A 12 wt% PVOH solution in distilled water was prepared under constant reflux at 80 ºC for 5 h. Several concentrations of NFC were added to the polymer solution of 2.5, 5.0, and 7.5 wt%. The nano-dimension of NFC was analysed using transmission electron microscopy (TEM). The morphology of electrospun nanofibre was characterised using scanning electron microscopy (SEM). The morphology of PVOH nanofibre was smooth and uniform without beads. The presence of NFC in the PVOH nanofibre decreased the diameter. The morphology of PVOH/NFC nanofibre at a concentration of NFC 2.5% was fairly uniform with good quality. However, the preparation of PVOH/NFC nanofibre at concentrations of NFC 5.0% and 7.5% resulted in elliptical beads. The crystallinity of NFC and electrospinning nanofibre was investigated using X-ray diffraction (XRD). In addition, the thermal properties of the samples were analysed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The results showed that NFC improved the thermal stability of electrospun PVOH nanofibre.

scholarly journals Isolation and Characterisation of Cellulose Nanofibre and Lignin from Oil Palm Empty Fruit Bunches

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2290 ◽  
Author(s):  
Saharman Gea ◽  
Amir Hamzah Siregar ◽  
Emma Zaidar ◽  
Mahyuni Harahap ◽  
Denny Pratama Indrawan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Oil Palm ◽  
Crystallinity Index ◽  
X Ray Diffraction ◽  
Simple Method ◽  
Empty Fruit Bunches ◽  
Chemical Structures ◽  
Transmission Electron ◽  
Nmr Spectrometry ◽  
Soda Pulping

A study on isolation and characterisation of cellulose nanofibre (CNF) and lignin was conducted to expand the application of CNF and lignin from oil palm biomass. CNF was extracted by steam explosion and the by-product was precipitated to obtain lignin by using the soda-pulping method. The concentrations of NaOH used for CNF by-product precipitation were 2%, 4%, and 6%. The morphology of CNF and lignin was characterised using scanning electron microscopy (SEM). The nanofibre of CNF with dimension between 50 nm and 100 nm was investigated using transmission electron microscopy (TEM). The functional group was observed using Fourier-transform infrared (FTIR) spectroscopy, showing that CNF had the structure of cellulose-I. In addition, the chemical structures of isolated and commercial lignin were analysed using 1H-NMR spectrometry. CNF had a 72% crystallinity index characterised by X-ray diffraction (XRD), while lignin showed an amorphous form. The characterisation of isolated lignin was compared with commercial lignin. The two lignins had similar particle size distribution from 1 to 100 μm. From UV-visible analysis, the lignin had aromatic rings/non-conjugated phenolic groups. The morphology of isolated lignin was rough and flaky. Commercial lignin was in powder form with near-spherical morphology. Thermogravimetric analysis (TGA) of CNF showed 30% of residue at 600 °C. The results showed a simple method to isolate CNF and lignin from oil palm empty fruit bunches.

scholarly journals A comparative study on the VOCs sensing behaviors of various ZnO nanostructures

2020 ◽  
Vol 9 (4) ◽  
pp. 117-122
Author(s):  
Vuong Nguyen Minh ◽  
Dung Dinh Tien ◽  
Hieu Hoang Nhat ◽  
Nghia Nguyen Van ◽  
Truong Nguyen Ngoc Khoa ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Hierarchical Structure ◽  
Hydrothermal Process ◽  
Zno Nanostructures ◽  
X Ray Diffraction ◽  
Wet Chemical Method ◽  
Electrospinning Technique ◽  
Transmission Electron ◽  
Volatile Organic ◽  
Wet Chemical

The volatile organic compounds (VOCs) sensing layers were studied using ZnO nanomaterials with different morphologies including hierarchical nanostructure (ZnO-H), nanorods (ZnO-NRs), commercial nanoparticles (ZnO-CNPs) and wet chemical synthesized nanoparticles (ZnO-HNPs). ZnO hierarchical structure was fabricated by an electrospinning technique followed by hydrothermal process. ZnO vertical nanorods structure was fabricated by hydrothermal method, while ZnO nanoparticles based sensors were prepared from commercial powder and wet chemical method. The morphology and properties of the fabricated samples were examined by scanning electron microscopy (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM). VOCs sensing responses toward acetone, ethanol and methanol with respect to altered ZnO nanostructureswas systematically compared at different working temperatures. The enhanced response at low working temperatures induced by theopen space hierarchical structure was observed. The VOCs sensing mechanisms of the ZnO nanostructures based sensing layer were also explained and discussed in detail. 

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

Preparation, characterization, and properties of polystyrene/Na-montmorillonite composites

2018 ◽  
Vol 32 (8) ◽  
pp. 1078-1091 ◽  
Author(s):  
Sibel Erol Dağ ◽  
Pınar Acar Bozkurt ◽  
Fatma Eroğlu ◽  
Meltem Çelik
Keyword(s):  
Electron Microscopy ◽  
Interlayer Spacing ◽  
Decomposition Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Sem Images ◽  
Specific Pore Volume ◽  
Transmission Electron ◽  
Thermal Stability Of

A series of polystyrene (PS)/unmodified Na-montmorillonite (Na-MMT) composites were prepared via in situ radical polymerization. The prepared composites were characterized using various techniques. The presence of various functional groups in the unmodified Na-MMT and PS/unmodified Na-MMT composite was confirmed by Fourier transform infrared spectroscopy. Morphology and particle size of prepared composites was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). According to the XRD and TEM results, the interlayer spacing of MMT layers was expanded. SEM images showed a spongy and porous-shaped morphology of composites. TEM revealed the Na-MMT intercalated in PS matrix. The thermal stability of PS/unmodified Na-MMT composites was significantly improved as compared to PS, which is confirmed using thermogravimetric analysis (TGA). The TGA curves indicated that the decomposition temperature of composites is higher at 24–51°C depending on the composition of the mixture than that of pure PS. The differential scanning calorimetry (DSC) results showed that the glass transition temperature of composites was higher as compared to PS. The moisture retention, water uptake, Brunauer–Emmett–Teller specific surface area, and specific pore volume of composites were also investigated. Water resistance of the composites can be greatly improved.

Nanofibres of Ceramic Compounds by Electrospinning

2006 ◽  
Vol 45 ◽  
pp. 735-740 ◽  
Author(s):  
W. Nuansing ◽  
S. Maensiri
Keyword(s):  
Electron Microscopy ◽  
X Ray Diffraction ◽  
Thermoelectric Oxide ◽  
Electrospinning Technique ◽  
Experimental Procedure ◽  
Transmission Electron ◽  
Set Up ◽  
Ceramic Compounds ◽  
Typical Process

This paper reports on the fabrication of nanofibres of ceramic compounds using electrospinning technique. In a typical process, ceramic nanofibres are fabricated by electrospinning a precursor mixture of appropriated metal sources, polymer and solvent, followed by calcination treatment of the electrospun composite nanofibres. In this work, the electrospinning set up as well as experimental procedure are described in detail. The fabrication of thermoelectric oxide NaCo2O4, ferroelectric Ba1-xSrxTiO3 and semiconductor TiO2 nanofibres with diameter of ~20-200 nm are demonstrated. The characterization of the fabricated nanofibres using TG-DTA, X-ray diffraction, Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy is also investigated.

Crystallization of Amorphous Si In Al/Si Multilayers

1991 ◽  
Vol 230 ◽  
Author(s):  
Toyohiko J. Konno ◽  
Robert Sinclair
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Layered Structure ◽  
Heat Of Reaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Amorphous Si

AbstractThe crystallization of amorphous Si in a Al/Si multilayer (with a modulation length of about 120Å) was investigated using transmission electron microscopy, differential scanning calorimetry and X-ray diffraction. Amorphous Si was found to crystallize at about 175 °C with the heat of reaction of 11±2(kJ/mol). Al grains grow prior to the nucleation of crystalline Si. The crystalline Si was found to nucleate within the grown Al layers. The incipient crystalline Si initially grows within the Al layer and then spreads through the amorphous Si and other Al layers. Because of extensive intermixing, the original layered structure is destroyed. The Al(111) texture is also enhanced.

Synthesis of (Y,Gd)2O3:Eu nanopowder by a novel co-precipitation processing

2004 ◽  
Vol 19 (12) ◽  
pp. 3586-3591 ◽  
Author(s):  
Jiyang Chen ◽  
Ying Shi ◽  
Jianlin Shi
Keyword(s):  
Electron Microscopy ◽  
Ammonium Hydroxide ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Hydrogen Carbonate ◽  
Ammonium Hydrogen ◽  
Intense Luminescence ◽  
Co Precipitation

Nano-sized (Y,Gd)2O3:Eu powders were synthesized by a novel co-precipitation processing in which a mixture of ammonium hydroxide and ammonium hydrogen carbonate was adopted as a complex precipitant. Evolution behaviors of precursors during calcinations were studied by means of thermogravimetry-differential scanning calorimetry-mass spectrum, Fourier transform infrared, x-ray diffraction, scanning electron microscopy, and transmission electron microscopy in detail. Nano-sized (Y,Gd)2O3:Eu powder as prepared possessed a primary grain size of about 30 nm and specific surface area of 38 m2/g after being calcined at 850 °C for 2 h, showing much finer grains and less agglomeration. The as prepared nanopowder shows intense luminescence at 611nm under x-ray or ultraviolet excitation. Transparent (Y,Gd)2O3:Eu ceramics can also be fabricated using this high sinterable nanopowder.

Low-temperature instability of Ti2SnC: A combined transmission electron microscopy, differential scanning calorimetry, and x-ray diffraction investigations

2009 ◽  
Vol 24 (1) ◽  
pp. 39-49 ◽  
Author(s):  
J. Zhang ◽  
B. Liu ◽  
J.Y. Wang ◽  
Y.C. Zhou
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Differential Scanning Calorimetry ◽  
Low Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Temperature Instability ◽  
X Ray ◽  
Transmission Electron ◽  
Ceramic Microstructure

Transmission electron microscopy (TEM), differential scanning calorimetry (DSC), and x-ray diffraction (XRD) investigations were conducted on the hot-pressed Ti2SnC bulk ceramic. Microstructure features of bulk Ti2SnC ceramic were characterized by using TEM, and a needle-shaped β-Sn precipitation was observed inside Ti2SnC grains with the orientation relationship: (0001) Ti2SnC // (200) Sn and Ti2SnC // [001] Sn. With the combination of DSC and XRD analyses, the precipitation of metallic Sn was demonstrated to be a thermal stress-induced process during the cooling procedure. The reheating temperature, even as low as 400 °C, could trigger the precipitation of Sn from Ti2SnC, which indicated the low-temperature instability of Ti2SnC. A substoichiometry Ti2SnxC formed after depletion of Sn from ternary Ti2SnC phase. Under electron beam irradiation, metallic Sn was observed diffusing back into Ti2SnxC. Furthermore, a new Ti7SnC6 phase with the lattice constants of a = 0.32 and c = 4.1 nm was identified and added in the Ti-Sn-C ternary system.

Room Temperature Synthesis of Cu2O Nanospheres: Optical Properties and Thermal Behavior

2014 ◽  
Vol 21 (1) ◽  
pp. 108-119 ◽  
Author(s):  
Daniela Nunes ◽  
Lídia Santos ◽  
Paulo Duarte ◽  
Ana Pimentel ◽  
Joana V. Pinto ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Thermal Behavior ◽  
Room Temperature ◽  
Diffuse Reflectance Spectroscopy ◽  
Ion Beam ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron

AbstractThe present work reports a simple and easy wet chemistry synthesis of cuprous oxide (Cu2O) nanospheres at room temperature without surfactants and using different precursors. Structural characterization was carried out by X-ray diffraction, transmission electron microscopy, and scanning electron microscopy coupled with focused ion beam and energy-dispersive X-ray spectroscopy. The optical band gaps were determined from diffuse reflectance spectroscopy. The photoluminescence behavior of the as-synthesized nanospheres showed significant differences depending on the precursors used. The Cu2O nanospheres were constituted by aggregates of nanocrystals, in which an on/off emission behavior of each individual nanocrystal was identified during transmission electron microscopy observations. The thermal behavior of the Cu2O nanospheres was investigated with in situ X-ray diffraction and differential scanning calorimetry experiments. Remarkable structural differences were observed for the nanospheres annealed in air, which turned into hollow spherical structures surrounded by outsized nanocrystals.

Solid State Amorphization of Ti60Si40 Alloy via Mechanical Alloying

2021 ◽  
Vol 876 ◽  
pp. 7-12
Author(s):  
Petr Urban ◽  
Fátima Ternero Fernández ◽  
Rosa M. Aranda Louvier ◽  
Raquel Astacio López ◽  
Jesus Cintas Físico
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Mechanical Alloying ◽  
Amorphous Phase ◽  
Milling Time ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Heating Up

The effect of milling time on the microstructure evolution and formation of amorphous phase of Ti60Si40 alloy produced by mechanical alloying (MA) has been investigated. Laser diffraction, Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), Transmission Electron Microscopy (TEM) and Differential Scanning Calorimetry (DSC) were employed to characterize the particle size, morphology and structure of mechanically alloyed Ti60Si40. When the milling time is increased to 20 h, the particle size decreases from 23.7 to 4.7 μm, the shape of the particles changes to spherical and the crystalline structure is transformed into an amorphous phase. The amorphous Ti60Si40 alloy is stable when heating up to 750oC. Above this temperature, the cold crystallization of the intermetallic compounds Ti5Si3 and/or Ti5Si4 begins.

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