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1.
Materials (Basel) ; 15(8)2022 Apr 09.
Artigo em Inglês | MEDLINE | ID: mdl-35454461

RESUMO

This study evaluated the effect of carbon nanofibers (CNFs) coated by aluminum oxide Al2O3 as a reinforcement on compressive strength, frost resistance, and drying shrinkage of cement mortars. Three weight ratios of 0.125%, 0.25%, and 0.5% of Al2O3/CNFs and bare CNF cement mortars were compared with reference cement mortar samples. The reactive porous and high surface area layer of alumina induced the hydration reaction and promoted the production of well-distributed hydration gel. Derivative thermal analysis-differential thermogravimetric (TGA-DTG) and X-ray powder diffraction (XRD) characterization showed that Al2O3/CNFs reinforcement led to greater hydration gel production than bare CNFs. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were performed to study the coating and microstructure of the cement mortars evaluated in this paper. The results show that the optimum enhancement of the cement mortar properties was obtained at ratios of 0.125% for Al2O3/CNFs and 0.25% for CNFs. This enhancement was greater with Al2O3/CNFs-reinforced specimens in terms of high compressive strength, less compressive strength degradation after 150 cycles, and less drying shrinkage. The low use of the CNFs in Al2O3/CNFs samples indicates the coating is an economical and promising approach for improving the performance of cement mortars.

2.
Chemosphere ; 286(Pt 2): 131769, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34365171

RESUMO

Porous alumina has been shown to be an excellent adsorbent for Congo Red (CR) dye. In this work, highly porous g-Al2O3 nanoshells were synthesized from alumina coated carbon black (CB) obtained from a new deposition technique and used for removal of CR dye from aqueous solutions. Adsorption experiments were conducted in a batch mode and a series of parameters were investigated, including contact time, initial dye concentrations, ionic strength and pH of the solutions. It was found that equilibrium for CR adsorption can be reached within 30 min, much faster than reported by other studies in the literature on similar adsorbents. It was also found that the adsorption capacity of Al2O3 nanoshells is 44.8 % higher than that of alumina/CB. The adsorption capacity of Al2O3 nanoshells was more favorable at lower pH, and the optimal adsorption ability was achieved at pH 4.0 with a removal efficiency at 98.6 %. The Al2O3 nanoshells have a maximum adsorption capacity of 370.4 mg g-1 (25 °C; pH 7; no salt added), better than or comparable to those reported in the literature. A pseudo-second-order kinetics model can best fit the kinetics of CR adsorption, which follows the Langmuir isotherm. The high adsorption capacity is attributed to the strong hydrogen-bonding interactions between the anionic dye and Al2O3 nanoshells surface as well as to the electrostatic interactions between CR dye and the Al2O3 nanoshells.


Assuntos
Nanoconchas , Poluentes Químicos da Água , Adsorção , Óxido de Alumínio , Corantes , Vermelho Congo , Concentração de Íons de Hidrogênio , Cinética , Porosidade , Soluções
3.
ACS Omega ; 6(13): 8986-9000, 2021 Apr 06.
Artigo em Inglês | MEDLINE | ID: mdl-33842769

RESUMO

Atomic layer deposition (ALD) provides uniform and conformal thin films that are of interest for a range of applications. To better understand the properties of amorphous ALD films, we need an improved understanding of their local atomic structure. Previous work demonstrated measurement of how the local atomic structure of ALD-grown aluminum oxide (AlO x ) evolves in operando during growth by employing synchrotron high-energy X-ray diffraction (HE-XRD). In this work, we report on efforts to employ electron diffraction pair distribution function (ePDF) measurements using more broadly available transmission electron microscope (TEM) instrumentation to study the atomic structure of amorphous ALD-AlO x . We observe electron beam damage in the ALD-coated samples during ePDF at ambient temperature and successfully mitigate this beam damage using ePDF at cryogenic temperatures (cryo-ePDF). We employ cryo-ePDF and reverse Monte Carlo (RMC) modeling to obtain structural models of ALD-AlO x coatings formed at a range of deposition temperatures from 150 to 332 °C. From these model structures, we derive structural metrics including stoichiometry, pair distances, and coordination environments in the ALD-AlO x films as a function of deposition temperature. The structural variations we observe with growth temperature are consistent with temperature-dependent changes in the surface hydroxyl density on the growth surface. The sample preparation and cryo-ePDF procedures we report here can be used for the routine measurement of ALD-grown amorphous thin films to improve our understanding of the atomic structure of these materials, establish structure-property relationships, and help accelerate the timescale for the application of ALD to address technological needs.

4.
Materials (Basel) ; 13(10)2020 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-32443661

RESUMO

Carbon nanotubes (CNTs) are synthesized by the flame fragment deposition (FFD) technique using Iraqi liquefied petroleum gas (LPG) as a source of carbon in a hand-made reactor at a low temperature (160 °C) without using a catalyst. Purification of the multi-walled carbon nanotubes (MWCNTs) is carried out using a two-step process consisting of sonication in 30 wt.% hydrogen peroxide (H2O2) solution at room temperature to remove amorphous impurities adhering to the walls of the CNTs and carbon nanoparticles (CNPs), followed by sonication in an acetone bath to remove the polyaromatic hydrocarbons (PAH) formed during the LPG gas burning. Comprehensive characterizations such as X-ray diffraction (XRD), atomic force microscopy (AFM), thermo-gravimetric analysis (TGA), and transmission electron microscopy (TEM) were conducted to verify the efficiency of the purification process. The results clearly demonstrated that this process is promising for the purification of the synthesized CNTs.

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