scholarly journals Covalent Functionalization of Graphene Oxide with Fructose, Starch, and Micro-Cellulose by Sonochemistry

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 490
Author(s):  
María Montserrat Cruz-Benítez ◽  
Pablo Gónzalez-Morones ◽  
Ernesto Hernández-Hernández ◽  
José Roberto Villagómez-Ibarra ◽  
Javier Castro-Rosas ◽  
...  

In this work, we report the synthesis of graphene oxide (GO) nanohybrids with starch, fructose, and micro-cellulose molecules by sonication in an aqueous medium at 90 °C and a short reaction time (30 min). The final product was washed with solvents to extract the nanohybrids and separate them from the organic molecules not grafted onto the GO surface. Nanohybrids were chemically characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy and analyzed by thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and X-ray diffraction (XRD). These results indicate that the ultrasound energy promoted a chemical reaction between GO and the organic molecules in a short time (30 min). The chemical characterization of these nanohybrids confirms their covalent bond, obtaining a grafting percentage above 40% the weight in these nanohybrids. This hybridization creates nanometric and millimetric nanohybrid particles. In addition, the grafted organic molecules can be crystallized on GO films. Interference in the ultrasound waves of starch hybrids is due to the increase in viscosity, leading to a partial hybridization of GO with starch.

Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 777 ◽  
Author(s):  
Yang Gong ◽  
Yingchun Yu ◽  
Huixuan Kang ◽  
Xiaohong Chen ◽  
Hao Liu ◽  
...  

Chitosan, a semi-crystalline biomolecule, has attracted wide attention due to its high synthesis flexibility. In this study, to improve the mechanical properties of chitosan aerogels (CSAs), graphene oxide (GO) was extracted and introduced into chitosan aerogels as fillers. The porous CSAs/GO composite aerogels were fabricated by an environmentally friendly freeze-drying process with different GO contents (0, 0.5, 1.0, 1.5, wt.%). The characteristics of the CSAs/GO were investigated by scanning electron microscopy (SEM), mechanical measurements and mercury porosimeter. The crystallinity of samples was characterized by X-ray diffraction (XRD). The mechanism of the effect of graphene oxide on chitosan was studied by Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The results show that the microstructure of the samples is developed in the network structure. The porosity of CSAs/GO aerogels is as high as 87.6%, and the tensile strength of the films increased from 6.60 MPa to 10.56 MPa with the recombination of graphene oxide. The crystallinity (CrI) of composite aerogels increased from 27% to 81%, which indicates that graphene oxide improves the mechanical properties of chitosan by chemical crosslinking.


Sensors ◽  
2020 ◽  
Vol 20 (11) ◽  
pp. 3175
Author(s):  
Sabina Drewniak ◽  
Marcin Procek ◽  
Roksana Muzyka ◽  
Tadeusz Pustelny

In this study, the sensitivity of reduced graphene oxide structures (rGO) to the action of selected gases (especially hydrogen, but also nitrogen dioxide and ammonia) was examined. Two sensing structures, based on rGO structures, obtained by different methods of oxidation (the modified Hummers, and the modified Tour’s method respectively), were investigated. We show here that the method used for the oxidation of rGO influences the sensitivity of the sensing structure during contact with various gaseous atmospheres. We performed our experiments in the atmosphere, containing hydrogen in a concentration range from 0 to 4% in nitrogen or synthetic air, both in dry and wet conditions. The temperature range was from 50 °C to 190 °C. Finally, we checked how the resistance of the samples changes when the other gases (NO2, NH3) appear in tested gas mixtures. The gas investigations were supplemented by the characterization of rGOs materials using scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and N2 sorption method.


MRS Advances ◽  
2019 ◽  
Vol 5 (11) ◽  
pp. 581-589 ◽  
Author(s):  
J. Rodríguez-López ◽  
R. Rangel ◽  
P. Bartolo-Pérez ◽  
J.J. Alvarado-Gil ◽  
J. L. Cervantes-López ◽  
...  

ABSTRACTThe present research was aimed to study the degradation of 2-Chlorophenol through the use of bismuth molybdate (γ-Bi2MoO6) structures supported on graphene oxide (GO) which is intended to control the recombination of charge carriers. γ-Bi2MoO6/GO systems were doped with nitrogen via chemical reaction, to reduce their energy gap, improving their photocatalytic activity. Structural and physicochemical characterization of the resulting catalysts were performed using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-Vis. The obtained compounds show good photo catalytic performance when using visible energy to degrade 2-Chlorophenol, obtaining 80% of degradation in 65 min.


Author(s):  
W. W. Barker ◽  
W. E. Rigsby ◽  
V. J. Hurst ◽  
W. J. Humphreys

Experimental clay mineral-organic molecule complexes long have been known and some of them have been extensively studied by X-ray diffraction methods. The organic molecules are adsorbed onto the surfaces of the clay minerals, or intercalated between the silicate layers. Natural organo-clays also are widely recognized but generally have not been well characterized. Widely used techniques for clay mineral identification involve treatment of the sample with H2 O2 or other oxidant to destroy any associated organics. This generally simplifies and intensifies the XRD pattern of the clay residue, but helps little with the characterization of the original organoclay. Adequate techniques for the direct observation of synthetic and naturally occurring organoclays are yet to be developed.


Materials ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2160
Author(s):  
Alexander Bogdanov ◽  
Ekaterina Kaneva ◽  
Roman Shendrik

Elpidite belongs to a special group of microporous zirconosilicates, which are of great interest due to their capability to uptake various molecules and ions, e.g., some radioactive species, in their structural voids. The results of a combined electron probe microanalysis and single-crystal X-ray diffraction study of the crystals of elpidite from Burpala (Russia) and Khan-Bogdo (Mongolia) deposits are reported. Some differences in the chemical compositions are observed and substitution at several structural positions within the structure of the compounds are noted. Based on the obtained results, a detailed crystal–chemical characterization of the elpidites under study was carried out. Three different structure models of elpidite were simulated: Na2ZrSi6O15·3H2O (related to the structure of Russian elpidite), partly Ca-replaced Na1.5Ca0.25ZrSi6O15·2.75H2O (close to elpidite from Mongolia), and a hypothetical CaZrSi6O15·2H2O. The vibration spectra of the models were obtained and compared with the experimental one, taken from the literature. The strong influence of water molecule vibrations on the shape of IR spectra of studied structural models of elpidite is discussed in the paper.


2014 ◽  
Vol 805 ◽  
pp. 343-349
Author(s):  
Carine F. Machado ◽  
Weber G. Moravia

This work evaluated the influence of additions of the ceramic shell residue (CSR), from the industries of Lost Wax Casting, in the modulus of elasticity and porosity of concrete. The CSR was ground and underwent a physical, chemical, and microstructural characterization. It was also analyzed, the environmental risk of the residue. In the physical characterization of the residue were analyzed, the surface area, and particle size distribution. In chemical characterization, the material powder was subjected to testing of X-ray fluorescence (XRF). Microstructural characterization was performed by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The residue was utilized like addition by substitution of cement in concrete in the percentages of 10% and 15% by weight of Portland cement. It was evaluated properties of concrete in the fresh and hardened state, such as compressive strength, modulus of elasticity, absorption of water by total immersion and by capillarity. The results showed that the residue can be used in cement matrix and improve some properties of concrete. Thus, the CSR may contribute to improved sustainability and benefit the construction industry.


2015 ◽  
Vol 2015 ◽  
pp. 1-6 ◽  
Author(s):  
YiChao Yan ◽  
Wei Shi ◽  
HongChuan Jiang ◽  
Jie Xiong ◽  
WanLi Zhang ◽  
...  

The redox reaction between Al and metallic oxide has its advantage compared with intermetallic reaction and Al/NiO nanomutlilayers are a promising candidate for enhancing the performance of energetic igniter. Al/NiO nanomutlilayers with different modulation periods are prepared on alumina substrate by direct current (DC) magnetron sputtering. The thicknesses of each period are 250 nm, 500 nm, 750 nm, 1000 nm, and 1500 nm, respectively, and the total thickness is 3 μm. The X-ray diffraction (XRD) and scanning electron microscope (SEM) results of the as-deposited Al/NiO nanomutlilayers show that the NiO films are amorphous and the layered structures are clearly distinguished. The X-ray photoelectron spectroscopy (XPS) demonstrates that the thickness of Al2O3increases on the side of Al monolayer after annealing at 450°C. The thermal diffusion time becomes greater significantly as the amount of thermal boundary conductance across the interfaces increases with relatively smaller modulation period. Differential scanning calorimeter (DSC) curve suggests that the energy release per unit mass is below the theoretical heat of the reaction due to the nonstoichiometric ratio between Al and NiO and the presence of impurities.


2013 ◽  
Vol 873 ◽  
pp. 152-157
Author(s):  
Long Long Chen ◽  
Jun Ming Li ◽  
Xiao Min Gong ◽  
Jian Li

Using a chemically induced transition in an FeCl2 solution, γ-Fe2O3 nanoparticles can be prepared from an amorphous precursor composed of FeOOH and Mg (OH)2. Surface modification by adding ZnCl2 during liquid-phase synthesis was attempted. The magnetization, morphology, crystal structure, and chemical species of as-prepared samples were characterized by vibrating sample magnetometer (VSM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray energy-dispersive spectroscopy (EDX), and X-ray photoelectron spectroscopy (XPS). The experimental results showed that the surface of the γ-Fe2O3 nanoparticles can be modified by adding ZnCl2 to form composite nanoparticles with a γ-Fe2O3/ZnFe2O4 ferrite core coated with Zn (OH)2 and absorbed FeCl36H2O; this modification can be enhanced by additional NaOH.


2013 ◽  
Vol 28 (2) ◽  
pp. 68-71 ◽  
Author(s):  
Thomas N. Blanton ◽  
Debasis Majumdar

In an effort to study an alternative approach to make graphene from graphene oxide (GO), exposure of GO to high-energy X-ray radiation has been performed. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM) have been used to characterize GO before and after irradiation. Results indicate that GO exposed to high-energy radiation is converted to an amorphous carbon phase that is conductive.


Sign in / Sign up

Export Citation Format

Share Document