scholarly journals Effect of Aminosilane Modification on Nanocrystalline Cellulose Properties

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Nurul Hanisah Mohd ◽  
Nur Farahein Hadina Ismail ◽  
Johan Iskandar Zahari ◽  
Wan Farahhanim bt Wan Fathilah ◽  
Hanieh Kargarzadeh ◽  
...  
Keyword(s):  
Ftir Spectroscopy ◽  
Elemental Analysis ◽  
Xrd Analysis ◽  
Nanocrystalline Cellulose ◽  
Hydroxyl Groups ◽  
X Ray Diffraction ◽  
X Ray ◽  
Empty Fruit Bunches ◽  
Transmission Electron ◽  
Thermal Stability Of

The application of renewable nanomaterials, like nanocrystalline cellulose (NCC), has recently been widely studied by many researchers. NCC has many benefits such as high aspect ratio, biodegradability, and high number of hydroxyl groups which offer great opportunities for modification. In this study, the NCC derived from empty fruit bunches (EFB) was modified with aminosilane, 3-(2-aminoethylamino)propyl-dimethoxymethylsilane (AEAPDMS), and the characterization was performed to investigate the potential as carbon dioxide (CO2) capture. Modification of NCC with AEAPDMS was carried out in water/ethanol solvent (80/20) (v/v) with a ratio of NCC to aminosilane of 1 : 1, 1 : 2, 1 : 3, and 1 : 4 w/w%. The effects of AEAPDMS on NCC were characterized using Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD) analysis, elemental analysis (CHNS), and transmission electron microscopy (TEM). The existence of AEAPDMS onto NCC was confirmed by ATR-FTIR spectroscopy as the new peaks of NH2were bending and wagging, and Si-CH3appeared. The thermal stability of NCC increased after modification due to the interaction with AEAPDMS. The elemental analysis result showed that the nitrogen content increased with an enhancement ratio of the modifiers. The XRD indicated that the crystallinity decreased while the rod-like geometry of NCC was maintained after amorphous AEAPDMS grafted on the NCC. Since AEAPDMS can be grafted on the NCC, the sample is applicable as CO2capture.

Formation and Thermal Stability of Nd0.32Y0.68Si1.7 Layers Formed by Channeled Ion Beam Synthesis

1998 ◽  
Vol 514 ◽  
Author(s):  
M. F. Wu ◽  
A. Vantomne ◽  
S. Hogg ◽  
H. Pattyn ◽  
G. Langouche ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Ion Beam ◽  
Hexagonal Structure ◽  
Orthorhombic Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Good Crystalline Quality ◽  
Ion Beam Synthesis ◽  
Thermal Stability Of

ABSTRACTThe Nd-disilicide, which exists only in a tetragonal or an orthorhombic structure, cannot be grown epitaxially on a Si(111) substrate. However, by adding Y and using channeled ion beam synthesis, hexagonal Nd0.32Y0.68Si1.7 epilayers with lattice constant of aepi = 0.3915 nm and cepi = 0.4152 nm and with good crystalline quality (χmin of Nd and Y is 3.5% and 4.3 % respectively) are formed in a Si(111) substrate. This shows that the addition of Y to the Nd-Si system forces the latter into a hexagonal structure. The epilayer is stable up to 950 °C; annealing at 1000 °C results in partial transformation into other phases. The formation, the structure and the thermal stability of this ternary silicide have been studied using Rutherford backscattering/channeling, x-ray diffraction and transmission electron microscopy.

Immobilization of hemoglobin on stable mesoporous multilamellar silica vesicles and their activity and stability

2005 ◽  
Vol 20 (10) ◽  
pp. 2682-2690 ◽  
Author(s):  
Yufang Zhu ◽  
Weihua Shen ◽  
Xiaoping Dong ◽  
Jianlin Shi
Keyword(s):  
Thermal Stability ◽  
Pore Size ◽  
X Ray Diffraction ◽  
X Ray ◽  
Practical Applications ◽  
Silica Material ◽  
Transmission Electron ◽  
Mesoporous Support ◽  
Adsorption Desorption ◽  
Thermal Stability Of

A stable mesoporous multilamellar silica vesicle (MSV) was developed with a gallery pore size of about 14.0 nm. A simulative enzyme, hemoglobin (Hb), was immobilized on this newly developed MSV and a conventional mesoporous silica material SBA-15. The structures and the immobilization of Hb on the mesoporous supports were characterized with x-ray diffraction, transmission electron microscopy, N2 adsorption-desorption isotherms, Fourier transform infrared, ultraviolet-visible spectroscopy, and so forth. MSV is a promising support for immobilizing Hb due to its large pore size and high Hb immobilization capacity (up to 522 mg/g) compared to SBA-15 (236 mg/g). Less than 5% Hb was leached from Hb/MSV at pH 6.0. The activity study indicated that the immobilized Hb retained most peroxidase activity compared to free Hb. Thermal stability of the immobilized Hb was improved by the proctetive environment of MSV and SBA-15. Such an Hb-mesoporous support with high Hb immobilization capacity, high activity, and enhanced thermal stability will be attractive for practical applications.

Surface Modification of 1-Butyl-3-Methylimidazolium Chloride -Treated Lignocellulosic Materials

2020 ◽  
Vol 1010 ◽  
pp. 526-531
Author(s):  
Asanah Radhi ◽  
Abdullah Othman ◽  
Muhammad Afif Aziz ◽  
Nik Raihan Nik Yusoff
Keyword(s):  
Electron Microscopy ◽  
Surface Modification ◽  
Functional Group ◽  
Hydroxyl Groups ◽  
Lignocellulosic Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hexadecyl Trimethylammonium Bromide ◽  
Thermal Stability Of ◽  
Scanning Electron

Lignocellulosic materials are generally considered hydrophilic due to the high density of hydroxyl groups. The use of lignocellulosic materials in hydrophobic systems thus require surface modification. Therefore, in this study, cellulose (MCC) and sawdust (SD) have been pretreated with ionic liquid, 1-butyl-3-methylimidazolium chloride (BMIMCl) prior to surface modification with cationic surfactant, hexadecyl trimethylammonium bromide (CTAB). The effect of BMIMCl pretreatment prior to surface modification has been investigated. Crystallinity, functional group changes, morphology and thermal stability of the sawdust and cellulose upon BMIMCl pretreatment and surface modification have been studied using x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and thermogravimetric Analysis (TGA). XRD results showed that the structure of lignocellulosic materials became more amorphous upon pretreatment with BMIMCl. FTIR results indicated that the modification of lignocellulosic is more efficient in BMIMCl-pretreated samples. Percentage of decomposition is higher for the BMIMCl-pretreated and CTAB modified samples.

Preparation and Characterization of CdSe Nanoparticles Synthesized Using the Ultrasonic Irradiation

2007 ◽  
Vol 124-126 ◽  
pp. 1229-1232 ◽  
Author(s):  
Myoung Seok Sung ◽  
Yoon Bok Lee ◽  
Yong Jin Kim ◽  
Yang Do Kim
Keyword(s):  
Ultrasonic Irradiation ◽  
Photoelectron Spectroscopy ◽  
Irradiation Time ◽  
Xrd Analysis ◽  
Cdse Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Emission ◽  
Transmission Electron ◽  
Average Size

Cadmium selenide(CdSe) nanoparticles were prepared in the aqueous solution containing isopropyl alcohol by the ultrasonic irradiation at room temperature. The cadmium chloride (CdCl2) and sodium selenosulfate (Na2SeSO3) were used as the cadmium and selenium source, respectively. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), UV-Vis absorption spectra and PL spectra were used to characterize the CdSe nanoparticles. XRD analysis revealed the formation of cubic structure CdSe. TEM images showed aggregated CdSe nanoparticles with the size of nanometer scale. Average size of CdSe nanoparticles were about 3.9, 5.0 and 5.1nm with sonication time of 6, 30 and 40 minutes, respectively. The surface emission became less intensive and shifted to red with increasing irradiation time. This paper presents the effects of ultrasonic on the formation of CdSe nanoparticles and its characteristics.

scholarly journals Selective Synthesis of Manganese/Silicon Complexes in Supercritical Water

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Jiancheng Wang ◽  
Zhaoliang Peng ◽  
Bing Wang ◽  
Lina Han ◽  
Liping Chang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Supercritical Water ◽  
Silica Sand ◽  
Hydroxyl Groups ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Silicon Materials ◽  
Manganese Salts ◽  
Silicon Sources

A series of manganese salts (Mn(NO3)2, MnCl2, MnSO4, and Mn(Ac)2) and silicon materials (silica sand, silica sol, and tetraethyl orthosilicate) were used to synthesize Mn/Si complexes in supercritical water using a tube reactor. X-ray diffraction (XRD), X-ray photoelectron spectrometer (XPS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) were employed to characterize the structure and morphology of the solid products. It was found that MnO2, Mn2O3, and Mn2SiO4could be obtained in supercritical water at 673 K in 5 minutes. The roles of both anions of manganese salts and silicon species in the formation of manganese silicon complexes were discussed. The inorganic manganese salt with the oxyacid radical could be easily decomposed to produce MnO2/SiO2and Mn2O3/SiO2. It is interesting to found that Mn(Ac)2can react with various types of silicon to produce Mn2SiO4. The hydroxyl groups of the SiO2surface from different silicon sources enhance the reactivity of SiO2.

The structure and chemical layering of Proterozoic stromatolites in the Mojave Desert

2015 ◽  
Vol 14 (3) ◽  
pp. 517-526 ◽  
Author(s):  
Susanne Douglas ◽  
Meredith E. Perry ◽  
William J. Abbey ◽  
Zuki Tanaka ◽  
Bin Chen ◽  
...  
Keyword(s):  
Elemental Analysis ◽  
Mojave Desert ◽  
Environmental Scanning Electron Microscopy ◽  
Xrd Analysis ◽  
Environmental Scanning ◽  
X Ray Diffraction ◽  
Mars Rover ◽  
X Ray ◽  
High K ◽  
Representative Samples

AbstractThe Proterozoic carbonate stromatolites of the Pahrump Group from the Crystal Spring formation exhibit interesting layering patterns. In continuous vertical formations, there are sections of chevron-shaped stromatolites alternating with sections of simple horizontal layering. This apparent cycle of stromatolite formation and lack of formation repeats several times over a vertical distance of at least 30 m at the locality investigated. Small representative samples from each layer were taken and analysed using X-ray diffraction (XRD), X-ray fluorescence (XRF), environmental scanning electron microscopy – energy dispersive X-ray spectrometry, and were optically analysed in thin section. Optical and spectroscopic analyses of stromatolite and of non-stromatolite samples were undertaken with the objective of determining the differences between them. Elemental analysis of samples from within each of the four stromatolite layers and the four intervening layers shows that the two types of layers are chemically and mineralogically distinct. In the layers that contain stromatolites the Ca/Si ratio is high; in layers without stromatolites the Ca/Si ratio is low. In the high Si layers, both K and Al are positively correlated with the presence and levels of Si. This, together with XRD analysis, suggested a high K-feldspar (microcline) content in the non-stromatolitic layers. This variation between these two types of rocks could be due to changes in biological growth rates in an otherwise uniform environment or variations in detrital influx and the resultant impact on biology. The current analysis does not allow us to choose between these two alternatives. A Mars rover would have adequate resolution to image these structures and instrumentation capable of conducting a similar elemental analysis.

Modification of clays with styrenic ionic liquid by Synthesis of in-situ Polystyrene Nanocomposite

e-Polymers ◽  
2013 ◽  
Vol 13 (1) ◽  
Author(s):  
Mohammad Galehassadi ◽  
Fatemeh Hosseinzadeh ◽  
Mehrdad Mahkam
Keyword(s):  
Electron Microscopy ◽  
Ionic Liquid ◽  
Clay Nanocomposites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Modified Montmorillonite ◽  
Transmission Electron ◽  
Insitu Polymerization ◽  
Thermal Stability Of

Abstract Nanocomposites of polystyrene (PS) was prepared with new styrenic ionic liquid, N-(4-vinyl benzyl)-(N,N-dimethylamino) pyridinium chloride[VBMAP], surfactants used as organic modifications for the clays. Sodium montmorillonite (Na-MMT) was successfully modified by [VBMAP] to become OMMT through cation exchange technique which is shown by the increase of basalspacing of clay by XRD. The composite material based on polystyrene and organo-modified montmorillonite (OMMT) was prepared by insitu polymerization and characterized. The morphology of the polymer/clay hybrids was evaluated by X-ray diffraction (XRD) ,transmission electron microscopy (TEM) and scanning electron microscopy (SEM), showing good overall dispersion of the clay. The thermal stability of the polymer/clay nanocomposites were enhanced, as evaluated by thermogravimetric analysis.

A new high-temperature inorganic–organic proton conductor: lanthanum sulfophenyl phosphate

2016 ◽  
Vol 70 (3) ◽  
Author(s):  
Ming-Feng Song ◽  
Zhong-Fang Li ◽  
Guo-Hong Liu ◽  
Su-Wen Wang ◽  
Xiao-Yan Yin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Layered Structure ◽  
Proton Conductor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Good Thermal Stability ◽  
Transmission Electron ◽  
Good Crystallinity ◽  
Different Temperatures ◽  
Thermal Stability Of

AbstractLanthanum sulfophenyl phosphate (LaSPP) was synthesized by m-sulfophenyl phosphonic acid and lanthanum nitrate. UV-Vis spectrophotometry and Fourier-transform infrared spectroscopy indicate that the desired product was obtained and its elementary composition and typical layered structure were determined by energy dispersive X-ray spectroscopy and scanning electron microscopy. Transmission electron microscopy (TEM) proved its typical layered structure and X-ray diffraction spectroscopy indicated its good crystallinity and the interlayer distance of about 15.67 Å , which matches the value obtained by TEM (2.0 nm). Thermogravimetry and differential thermal analysis revealed good thermal stability of LaSPP. Proton conductivity of LaSPP was measured at different temperatures and relative humidities (RH), reaching values of 0.123 S cm

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

The grain refinement mechanism of electrodeposited copper

2009 ◽  
Vol 24 (10) ◽  
pp. 3226-3236 ◽  
Author(s):  
Guoyong Wang ◽  
Zhonghao Jiang ◽  
Jianshe Lian ◽  
Qing Jiang
Keyword(s):  
Grain Refinement ◽  
Large Angle ◽  
Xrd Analysis ◽  
Dislocation Cell ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
Transmission Electron ◽  
Refinement Mechanism ◽  
Dislocation Cells

Microstructure features of five electrodeposited coppers with different grain sizes were systematically characterized by using transmission electron microscopy (TEM) observations and x-ray diffraction (XRD) analysis. Based on the experimental observations, two mechanisms for the grain refinement in electrodeposited copper were identified: (i) twin–twin intersection can directly create grains with large-angle boundaries as small as 10 nm and (ii) grains can also be refined via formation of dislocation cells, transformation of dislocation cell walls into sub-boundaries with small misorientations, and evolution of sub-boundaries into highly misoriented grain boundaries. Besides, dislocations are also effective to cut twin lamellas into pieces and make twin boundaries curved and round.

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