Dinh Quang Khieu

Multi-wall carbon nanotubes (MWCNTs)-doped polypyrrole DNA biosensor for label-free detection of genetically modified organisms by QCM and EIS

In this paper, we describe DNA electrochemical detection for genetically modified organism (GMO) based on multi-wall carbon nanotubes (MWCNTs)-doped polypyrrole (PPy). DNA hybridization is studied by quartz crystal microbalance (QCM) and electrochemical impedance spectroscopy (EIS). An increase in DNA complementary target concentration results in a decrease in the faradic charge transfer resistance (R(ct)) and signifying signal-on behavior of MWCNTs-PPy-DNA system. QCM and EIS data indicated that the electroanalytical MWCNTs-PPy films were highly sensitive (as low as 4pM of target can be detected with QCM technique). In principle, this system can be suitable not only for DNA but also for protein biosensor construction.

Fe3O4/Reduced Graphene Oxide Nanocomposite: Synthesis and Its Application for Toxic Metal Ion Removal

The synthesis of reduced graphene oxide modified by magnetic iron oxide (Fe3O4/rGO) and its application for heavy metals removal were demonstrated. The obtained samples were characterized by X-ray diffraction (XRD), nitrogen adsorption/desorption isotherms, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), and magnetic measurement. The results showed that the obtained graphene oxide (GO) contains a small part of initial graphite as well as reduced oxide graphene. GO exhibits very high surface area in comparison with initial graphite. The morphology of Fe3O4/rGO consists of very fine spherical iron nanooxide particles in nanoscale. The formal kinetics and adsorption isotherms of As(V), Ni(II), and Pb(II) over obtained Fe3O4/rGO have been investigated. Fe3O4/rGO exhibits excellent heavy metal ions adsorption indicating that it is a potential adsorbent for water sources contaminated by heavy metals.

3-Mercaptopropyltrimethoxysilane Modified Diatomite: Preparation and Application for Voltammetric Determination of Lead (II) and Cadmium (II)

In this study, functionalized diatomite was prepared by grafting of 3-mercaptopropyltrimethoxysilane (MPTMS) to diatomite (MPTMS-diatomite). The diatomite with thermal treatment from 100 to 700°C was functionalized by MPTMS under dry and humid conditions. The obtained MPTMS-diatomite was characterized by X-ray diffraction (XRD), thermal gravity-differential scanning calorimeter (TG-DSC), and Fourier transformation infrared (FT-IR). The results showed that an increase in treatment temperature seems to reduce the loading of MPTMS onto diatomite. The humidity of diatomite was favorable for the grafting of functional groups on the surface. The possible mechanisms of MPTMS loading to diatomite (MPTMS-diatomite) were also proposed. The performance of a carbon paste electrode (CPE) modified with MPTMS-diatomite in the simultaneous determination of Cd(II) and Pb(II) ions was addressed.

Synthesis of Iron Doped Zeolite Imidazolate Framework-8 and Its Remazol Deep Black RGB Dye Adsorption Ability

Zeolite imidazole framework-8 (ZIF-8) and the iron doped ZIF-8 (Fe-ZIF-8) were synthesized by the hydrothermal process. The obtained materials were characteristic of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), nitrogen adsorption/desorption isotherms, and atomic absorption spectroscopy (AAS). The results showed that the obtained Fe-ZIF-8 possessed the ZIF-8 structure with a large specific area. ZIF-8 and Fe-ZIF-8 were used for the removal of Remazol Deep Black (RDB) RGB dye from aqueous solutions. The various factors affecting adsorption such as pH, initial concentration, contact time, and temperature were investigated. The results showed that the introduction of iron into ZIF-8 provided a much larger adsorption capacity and faster adsorption kinetics than ZIF-8 without iron. The electrostatic interaction and π-π interaction between the aromatic rings of the RDB dye and the aromatic imidazolate rings of the adsorbent were responsible for the RDB adsorption. Moreover, the coordination of the nitrogen atoms and oxygen in carboxyl group in RDB molecules with the Fe2

Catalytic wet peroxide oxidation of phenol solution over Fe–Mn binary oxides diatomite composite

Abstract Mn–Fe binary oxides incorporated into diatomite (denoted as FM-diatomite) was prepared by the redox reaction of KMnO4 and FeSO4 with pH ranging from 3 to 9. The catalytic activities of FM-diatomite were studied for phenol oxidation and were compared with iron oxide modified diatomite (F-diatomite) and manganese oxide modified diatomite (M-diatomite). The obtained catalysts were characterized by scanning electron microscope, powder X-ray diffraction, energy dispersive spectroscopy, transmission electron microscope, X-ray photoelectron spectroscopy, and nitrogen adsorption/desorption isotherms. The results show that Fe–Mn binary oxides were highly dispersed on the diatomite surface in which manganese oxide and iron oxide displayed multiple oxidation states including Mn4+, Mn3+, Fe2+ and Fe3+. The phenol oxidation by H2O2 through the use of Mn–Fe-diatomite as a catalyst was conducted. FM-diatomite exhibited as an excellent catalyst for the total oxidation of phenol and main intermediates (catechol and hydroquinone). The conversion of phenol and main intermediates by means of FM-diatomite was 100xa0% under 50xa0min while that by F-diatomite also was 100xa0% after 110xa0min but other intermediates still remained. While phenol conversion by M-diatomite was close to zero due to speedy hydroperoxide decomposition over the manganese oxide catalyst. These results show that there was a synergized effect of iron and manganese oxide present in FM-diatomite.

Monodisperse Uniform CeO2 Nanoparticles

Ceria nanostructure-based catalysts have attracted much attention in recent years because of their unique physiochemical properties. Herein, we have presented a simple two-phase approach for the synthesis of ceria nanocrystals. Structural and morphological characterization by XRD and TEM showed that the as-synthesized monodisperse CeO2 nanoparticles NPs had cubic fluorite crystal structure with average particle size about 6.75u2009nm. The effects of hydrothermal temperature, annealing time, and concentration of cerium nitrate on the nanostructures of the products were also investigated and discussed. In addition, the CeO2 nanocrystals proved to be an effective catalyst for the photodegradation of blue methylene under UV illumination.Ceria nanostructure-based catalysts have attracted much attention in recent years because of their unique physiochemical properties. Herein, we have presented a simple two-phase approach for the synthesis of ceria nanocrystals. Structural and morphological characterization by XRD and TEM showed that the as-synthesized monodisperse CeO 2 nanoparticles (NPs) had cubic fluorite crystal structure with average particle size about 6.75 nm. The effects of hydrothermal temperature, annealing time, and concentration of cerium nitrate on the nanostructures of the products were also investigated and discussed. In addition, the CeO 2 nanocrystals proved to be an effective catalyst for the photodegradation of blue methylene under UV illumination.

A novel approach for synthesis of hierarchical mesoporous Nd 2 O 3 nanomaterials

Abstract A novel route to the fabrication of hierarchical mesoporous Nd 2 O 3 nanostructures including nanospheres and nanoporous network was described. Their structure and morphology evolution of the as-synthesized materials were determined by various techniques such as scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, Fourier transforminfrared spectra, nitrogen adsorption/desorption isotherm, and a formation mechanism was proposed. The results revealed that the Nd 2 O 3 nanospheres had the diameter of 300 nm, which were composed of small primary nanoparticles (NPs) with the size of 10 nm. The nanoporous structure also formed the NPs of ca . 10 nm which were connected with each other to form a three-dimensional (3D) texture. This simple and mild approach to fabricate hierarchical mesoporous Nd 2 O 3 nanostructures could be easily scaled up and potentially extended to synthesize other oxide hierarchical structures.

Microwave synthesis and voltammetric simultaneous determination of paracetamol and caffeine using an MOF-199-based electrode

AbstractIn the present paper, the microwave synthesis of MOF-199 and its application as an electrode modifier for the simultaneous voltammetric determination of paracetamol (PAR) and caffeine (CAF) were demonstrated. The obtained materials were characterised by X-ray diffraction, a scanning electron microscope (SEM), nitrogen adsorption/desorption isotherms and thermal gravity. The microwave (MW) synthesis of MOF-199 has been compared to its conventional hydrothermal synthesis. It is found that by using the MW synthesis, MOF-199 can be obtained in a much shorter synthesis time with improved yield and textural properties. The electrode modified by MOF-199 was used in order to develop an electroanalytical method that can be used to simultaneously quantify PAR and CAF.n The kinetic parameters of the electrode reaction process were also investigated.n This proposed method was successfully employed for the simultaneous detection of PAR and CAF in pharmaceutical formulations using the standard addition method and the obtained results compared with the results determined by means of HPLC were found to be statistically similar.n

A Study on Astrazon Black AFDL Dye Adsorption onto Vietnamese Diatomite

In the present paper, the adsorption of Astrazon Black AFDL dye onto Vietnamese diatomite has been demonstrated. The diatomite was characterized by XRD, SEM, TEM, EDS, and nitrogen adsorption/desorption isotherms. The results show that diatomite mainly constituted centric type frustules characterized by pores as discs or as cylindrical shapes. The adsorption kinetics and isotherms of dye onto Vietnam diatomite were investigated. The experimental data were fitted well to both Freundlich and Langmuir in the initial concentration range of 400–1400 mg L−1. The average value of maximum adsorption capacity, , calculated from Freundlich equation is statistically similar to the average value of maximum monolayer adsorption capacity calculated from Langmuir equation. The thermodynamic parameters evaluated from the temperature dependent on adsorption isotherms in the range of 303–343 K show that the adsorption process was spontaneous and endothermic. The Webber and pseudo-first/second-order kinetic models were used to analyze the mechanism of adsorption. The piecewise linear regression and Akaike’s Information Criterion were used to analyze experimental data. The results show that the dye adsorption onto diatomite was film diffusion controlled and the goodness of fit of experimental data for kinetics modes was dependent on the initial concentration.

Iron doped zeolitic imidazolate framework (Fe-ZIF-8): synthesis and photocatalytic degradation of RDB dye in Fe-ZIF-8

This paper presents a study on the synthesis of iron doped ZIF-8 with different molar ratio of Zn/Fe (Fe-ZIF-8) and sunlight driven photocatalytic activity of obtained materials. The materials were characteristic of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption/desorption isotherms, diffusive reflectance UV–Vis (DR-UV–Vis) and atomic absorption spectroscopy (AAS). The results showed that Fe(II) as iron source could be directly introduced into ZIF-8 to form Fe-ZIF-8. Depending on the amount of iron(II) introduced, the Fe(II) or both Fe(II) and Fe(III) may exist in ZIF-8. Fe-ZIF-8 was selected as photocatalyst to decompose Remazol deep black B (RDB), a model of dye contaminant, under sunlight illumination. Undoped ZIF-8 seems not to catalyze for degradation of RDB while Fe-ZIF-8 exhibited sunlight-driven photocatalytic degradation of RDB. The kinetics of photocatalytic reaction were also addressed. This study suggests iron doped zeolite-imidazole framework Fe-ZIF-8 to be promising catalyst for the heterogeneous photo-catalytic dye degradation technique in visible region.