Synthesis and characterization of functionalized ordered hexagonal nanoporous carbon nitride with melamine-based dendrimer amines

Mesoporous carbon nitride (MCN-1) and functionalized MCN-1 with melamine-based dendrimer amine (MDA-MCN-1) have been synthesized. These materials are characterized by means of nitrogen adsorption–desorption isotherms, thermogravimetric analysis (TGA), Fourier transform infrared (FT-IR) spectroscopy, small-angle X-ray scattering (SAXS), wide angle X-ray diffraction (XRD) pattern and Energy dispersive X-ray (EDX). Two bands at 1,434 and 1,550 cm^?1 in FT-IR spectrum of MDA-MCN-1 are clear evidence of an aromatic triazine ring and confirm that the melamine-based dendrimer is formed. The pore diameter is centered at 4.74 nm with a relatively high BET surface area of 102.2 m² g^?1 and a pore volume of 0.12 cm³ g^?1. TGA curves show that samples (MCN-1 and MDA-MCN-1) have high thermal stability compared to the earlier species. The carbon-to-nitrogen ratio calculated from the EDX analysis significantly decreases from 3.87–4.35 to 1.26 in MDA-MCN-1 than MCN-1 material. This indicates that MDA-MCN-1 has high nitrogen content and active adsorption sites in comparison to MCN-1 species.     

Removal of malachite green from dye wastewater using mesoporous carbon adsorbent

Mesoporous carbon was synthesized for the removal of a cationic dye malachite green (MG) from aqueous solution. The studies were carried out under various experimental conditions such as contact time, dye concentration, adsorption dose and pH to assess the potentiality of mesoporous carbon for the removal of malachite green dye from wastewater. The sorption equilibrium was reached within 30 min. In order to determine the adsorption capacity, the sorption data were analyzed using linear form of Langmuir and Freundlich equation. Langmuir equation showed higher conformity than Freundlich equation. More than 99% removal of MG was reached at the optimum pH value of 8.5. From kinetic experiments, it was concluded that the sorption process followed the pseudo-first-order kinetic model. This study showed that mesoporous carbon can be recommended as an excellent adsorbent at high pH values.     

Determination of 222Rn in Iranian mineral waters using liquid scintillation alpha-spectrometry

Liquid scintillation counting (LSC) method has been used for the measurement of ²²²Rn in mineral water samples under a pilot project for the first surveillance in Iran. Low level background LSC counter Quantulus and pulse-shape analysis method have been employed. The concentration of ²²²Rn found in mineral waters of the studied areas ranges from about 1 to 75 Bq/l. The best lower limit of detection obtained with the applied technique was 0.069 Bq/l for a counting time in the range of 236–296 minutes.     

纳米多级孔分子筛：简短的综述

分子筛是一种三维微孔结构的硅铝酸盐晶体,具有灵活多变的骨架和组成、较高的物理和水热稳定性、无毒、高比表面积、离子可交换性以及很低的成本等特点,因而在油品精制、石油化学、农业、水和污水处理等众多领域中用作离子交换剂、催化剂和吸附剂。尽管分子筛的应用是基于其本身的微孔结构,但微孔也导致体积较大的反应物和产物分子的传质阻力高。通过制备纳米尺度和多级孔结构的分子筛等多种手段可克服常规分子筛所具有的传质限制。人们已经开发了多种方法制备了新型的分子筛材料,并考察了它们在各种催化反应和吸附反应中的性能。在反应体系中采用这种多级孔的纳米分子筛,有可能提高催化剂的使用寿命和催化性能,抑制积碳和失活。本综述概述了多级孔分子筛和纳米分子筛的高性能及其合成方法的最新进展,讨论了每个合成方法的优缺点,简述了纳米分子筛和二级孔结构分子筛的催化应用,并与常规分子筛进行了比较。     

Synthesis and characterization of ordered mesoporous carbon as electrocatalyst for simultaneous determination of epinephrine and acetaminophen

In this research, we report an easy method for synthesis of ordered mesoporous carbon (OMC) with hexagonal arrays of tubes (CMK-5). The synthesized OMC was characterized using X-ray diffraction (XRD), scanning electronic microscopy (SEM) and nitrogen sorption isotherms techniques. Due to the large surface area and high conductivity of OMC, OMC-modified glassy carbon (OMCs/GC) electrode was prepared. The unique electrochemical activity of OMCs/GC electrode was illustrated using cyclic voltammetry (CV) and electron impedance spectroscopy (EIS) in which OMC showed a faster electron transfer rate, as compared with glassy carbon electrode. The electrochemical behavior of epinephrine (EN) and acetaminophen (AP) at OMC/GC electrode was also investigated using cyclic voltammetry. The OMC/GC electrode exhibited high electrocatalytic activities toward oxidation of EN and AP and displayed good voltammetric peak separation between them. In differential pulse voltammetry technique, both EN and AP give sensitive oxidation peaks at 120?mV and 320?mV, respectively. Therefore, investigated method was applied for simultaneous determination of EN and AP. AP and EN give linear response over the range of 0.2–15?μM and 4–100?μM, respectively. The lower detection limits were found to be 0.07?μM for AP and 0.94?μM for EN.     

Development of new sorbents: I. Ordered porous phase of titanium phosphate

A new phase of titanium phosphate with a highly organized porous framework has been synthesized by a non-thermal digestion method. FTIR, TGA-DTA, XRD and SEM have been employed to study the primary product, calcined and digested materials. Pore diameters in the range of 22–90 Å have been obtained for the digested material as determined by nitrogen absorption measurements. Quantitative removal of copper(II) phthalocyanine and its derivative from aqueous medium have been achieved.     

Ordered Nanoporous Carbon-Based SPME and Determination by GC

CMK-1 (carbon mesoporous from Korea) type ordered nanoporous carbon was investigated as a novel solid-phase microextraction fiber for the first time. The microextraction process was coupled with GC-FID and used to extract benzene, toluene, ethylbenzene and xylenes (BTEX) from the head space of the solution samples. Prepared fibers featured advantages like easy and fast preparation, high thermal and mechanical stability in which a fiber could be used for more than 60 tests. Employing Taguchi method and orthogonal array design; OA₁₆ (4⁵), the HS-SPME of BTEX was optimized. Under the optimized conditions for all BTEX components, the linearity was from 3 to 800 μg L^?1, the relative standard deviation (RSD%) of the method was between 4.2 and 9.4% and limit of detections was between 0.27 and 1.1 μg L^?1. The recovery values were from 87.1 to 106.2% in water samples. Finally, the applicability of the proposed method was evaluated by the extraction and determination of BTEX in the water and petrochemical samples.     

Synthesis of nanoporous TiO2 materials using a doubly surfactant system and applying them as useful adsorbents

Hydrothermal and non-hydrothermal nanoporous TiO₂ materials were synthesized via a doubly surfactant route by using cationic cetyltrimethylammonium bromide and anionic sodium dodecyl sulfate surfactants as the molecular template/structure directing agent. Hydrothermal treatment was performed for comparison. The bulk chemical and phase compositions, crystalline structures, particle morphologies, thermal stabilities and surface texturing were determined by means of X-ray powder analysis, SEM and N₂ sorptiometry. The nanoporous TiO₂ materials were found to have a spherical morphology with a diameter range of 50–200 nm and a high surface area (390 m² g^?1). Hydrothermal and non-hydrothermal nanoporous TiO₂ materials were applied for adsorption of heavy metal cations and the toxic organic compound, copper phthalocyanine, from water for evaluation of their adsorption properties. Both nanoporous TiO₂ materials were found to have similar adsorption capacities toward heavy metal cations and CuPc. Both hydrothermal and non-hydrothermal TiO₂ nanoporous materials were found to have very good potential for application as a new adsorbent especially for adsorbing heavy metal cations from wastewaters.     

Highly efficient CO2 capture with a metal–organic framework‐derived porous carbon impregnated with polyethyleneimine

Global warming is considered as one of the great challenges of the twenty‐first century. Application of CO₂ capture and storage technologies to flue gas is considered to be a useful method of lessening global warning. Highly porous carbon has played an important role in tackling energy and environmental problems. We attempted to synthesize a highly porous carbon adsorbent by carbonizing a highly crystalline metal–organic framework (MOF) without any carbon precursors and focused on the adsorption of CO₂ and CH₄ gases and CO₂/CH₄ selectivity at 298, 323 and 348 K using a volumetric apparatus. The MOF‐derived porous carbon (MDC) was prepared by direct carbonization of MOF‐199 as a template at 900 °C under nitrogen atmosphere. Amino‐impregnated MDC samples exhibited enhanced adsorption capacities by a combination of physical and chemical adsorption. Polyethyleneimine (PEI) was selected as the amine source, which was found to greatly enhance CO₂ capture when supported on the porous carbon. Novel PEI‐impregnated MDC nanocomposites were synthesized by wetness impregnation and then characterized using various methods.     

Preparation of titanium dioxide nanostructure from ilmenite through sulfate-leaching process and solvent extraction by D<Subscript>2</Subscript>EHPA

In this study, TiO₂ nanoparticles have been obtained from low-grade ilmenite ore via two consecutive acid digestion and solvent extraction processes. The as-extracted TiO₂ (Anatase phase) product was characterized using techniques such as XRD, XRF, FESEM, FTIR and BET surface area. Diluted sulfuric acid and D₂EHPA (bis-(2-ethyl-hexyl) phosphoric acid) were used as digester agent and an extraction solvent, respectively. The effects of main parameters such as recycling capacities and D₂EHPA concentration, as well as the extraction time and temperature on TiO₂ extraction were investigated. The results demonstrated that the best performance and efficiency for titanium and total iron uptake were 99 and 3.8%, respectively, at the lowest concentration of D₂EHPA.