qing Li

Effects of activated carbon surface properties on the adsorption of volatile organic compounds.

Physical and chemical properties of activated carbon (AC) were analyzed to investigate the effects of adsorbate properties on AC adsorption performance. Fixed-bed adsorption experiments were conducted with toluene, acetone, and xylene as adsorbates. From the results, the adsorption capacities of the three adsorbates had the following order: xylene > toluene > acetone. The correlation between experimental data and adsorbate properties was also analyzed. The results showed that different functional groups corresponding to the properties of adsorbates influenced the adsorptive properties of AC differently. The adsorption capacity of AC increased linearly as the molecular weight, dynamic diameter, boiling point, and density of the adsorbate increased. However, adsorption capacity decreased as the polarity index and vapor pressure of the adsorbate increased. For adsorption onto three types of AC, the adsorption energies of the three adsorbates had the following order: xylene > toluene > acetone. Implications: This paper focused on the research on adsorption behavior of activated carbon based on adsorbate properties. Adsorption experiments were conducted under the same condition while the adsorbates were toluene, acetone, and xylene, respectively. Correlation analysis between experimental data and adsorbate properties was conducted. The different groups have different influence on the adsorptive properties of ACs. The adsorption capacity of activated carbon increases with the increase of adsorbate molecular weight, dynamic diameter, boiling point, and density, and that this relationship is linear. The relationship between adsorption capacity and the polarity index and vapor pressure of adsorbate shows an opposite trend, and the adsorption capacities and adsorption energies of three kinds of activated carbon for these three adsorbates had the following order: xylene > toluene > acetone.

Preparation and Characterization of Activated Carbons from Tobacco Stem by Chemical Activation

ABSTRACT Activated carbons were prepared from tobacco stem by chemical activation using potassium hydroxide (KOH), potassium carbonate (K2CO3), and zinc chloride (ZnCl2). The effects of the impregnation ratio (activating agent/precursor) and activating agents on the physical and chemical properties of activated carbons were investigated. The textual structure and surface properties of activated carbons were characterized by nitrogen (N2) adsorption isotherm, scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), x-ray photoelectron spectroscopy (XPS), and thermogravimetry (TG). ZnCl2, acting as a superior activating agent compared to the others, produced much more porosity. The maximum specific surface area reached 1347 m2/g, obtained by ZnCl2 activation with an impregnation ratio of 4.0. Moreover, ZnCl2 activation yielded products with an excellent thermostability, attributed to different activation mechanisms. Various oxygen functions were detected on the activated carbon surface, and hydroxyl and ester groups were found to be in the majority. Implications: Tobacco stem, the residue from cigarette manufacturing, is usually discarded as waste, leading to serious resource waste and environmental problems. This study provides an effective utilization available for this solid residue by using it as the starting material in the preparation of activated carbon with chemical activation. Activated carbons with high specific area and various surface functions have been prepared, and the effects of the amount and type of activating agents on the physical and chemical properties of activated carbon were investigated as well.

Activated carbons modified by magnesium oxide as highly efficient sorbents for acetone

Porous activated carbon modified with MgO was synthesized by an evaporation-induced self-assembly (EISA) method for its application to acetone capture. The textural and chemical characteristics of five modified activated carbon composites (AC–MgO) were characterized using X-ray diffraction, scanning electron microscopy, transmission electron microscopy and nitrogen adsorption isotherm measurements. The adsorption behaviors of samples for acetone were investigated and correlated to their physical and chemical properties. Density functional theory was also employed to calculate the charge transfer, the equilibrium distance, and the adsorption energy of acetone adsorbed on a carbon surface functionalized with crystalline MgO. An AC–MgO-10% sample with balanced surface area, microporosity and MgO content exhibited the highest acetone adsorption capacity (432.7 mg g−1). The results indicate that an appropriate MgO content on AC can effectively improve the adsorption capacity of acetone ascribed to strong chemisorption between MgO nanoparticles and acetone molecules.

Highly Nitrogen-Doped Porous Carbon Derived from Zeolitic Imidazolate Framework-8 for CO2 Capture

Setting the trap: A nitrogen-doped porous carbon, with a nitrogen content of up to 25.52u2009% and specific surface area of 948u2005m2 u2009g-1 , exhibits a superior CO2 uptake of 3.7u2005mmolu2009g-1 at 25u2009°C and 1u2005bar. Experimental and theoretical results indicate that the nitrogen-containing functional groups enhance CO2 uptake through electrostatic, Lewis acid-base, and hydrogen-bonding interactions.

Recovery of elemental sulfur from zinc concentrate direct leaching residue using atmospheric distillation: a pilot-scale experimental study.

Recovery of elemental sulfur from zinc concentrate direct leaching residue (DLR) using atmospheric distillation was systematically investigated on a pilot-scale system for the first time. Batch operating mode was suggested for recovery of elemental sulfur from water-rich DLR using atmospheric distillation. Elemental sulfur with purity higher than 99% was obtained under certain conditions in batch operating mode. With an appropriate feed amount of 1,200 kg, batch experiment conducted at 460°C resulted in sulfur purity of 96.22% and a recovery rate higher than 85%. Only 0.59 and 1.24 kWh power was needed to handle 1.0 kg DLR and produce 1.0 kg elemental sulfur, respectively. The results suggest that recovery of elemental sulfur from zinc concentrate DLR using atmospheric distillation is technologically and economically feasible. Moreover, other metal elements such as zinc were enriched in the distillation concentrate, which could be used for metal refining. Technologies could effectively lower the moisture content of DLR, and lowering the distillation temperature would be of great value for recovery of elemental sulfur from DLR using a distillation method. Implications: Distillation is a promising solution for recovery of elemental sulfur from DLRs. This work revealed the possibility of separation of elemental sulfur from zinc concentrate DLR using atmospheric distillation. Such knowledge is of fundamental importance in developing field-scale separation and purification technologies and devices in which simultaneous sulfur recovery and precious metal enrichment are possible. Important tasks for follow-up research are also suggested.

Nitrogen-Containing Functional Groups-Facilitated Acetone Adsorption by ZIF-8-Derived Porous Carbon

Nitrogen-doped porous carbon (ZC) is prepared by modification with ammonia for increasing the specific surface area and surface polarity after carbonization of zeolite imidazole framework-8 (ZIF-8). The structure and properties of these ZCs were characterized by Transmission electron microscopy, X-ray diffraction, N2 sorption, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. Through static adsorption tests of these carbons, the sample obtained at 600 °C was selected as an excellent adsorbent, which exhibited an excellent acetone capacity of 417.2 mg g−1 (25 °C) with a very large surface area and high-level nitrogen doping (13.55%). The microporosity, surface area and N-containing groups of the materials, pyrrolic-N, pyridinic-N, and oxidized-N groups in particular, were found to be the determining factors for acetone adsorption by means of molecular simulation with density functional theory. These findings indicate that N-doped microporous carbon materials are potential promising adsorbents for acetone.

Estimates of parameters for formaldehyde emission model from plywood panel under various temperature and relative humidity conditions

Abstract The initial emittable concentration, Cm,0, the material phase diffusion coefficient, Dm, and the air/material partition coefficient, K, are the key parameters used to predict the formaldehyde emissions from indoor building materials. This work presents formaldehyde emission experiments of plywood panels in a climatic chamber under various environmental conditions, which provides information on how relative humidity, temperature, and loading degree affect the formaldehyde emission. The experimental results showed that formaldehyde concentration in the climatic chamber increased rapidly during the initial 3u2009h, and then reached equilibrium after 7u2009h. The equilibrium concentration of formaldehyde in the closed chamber was increased by 1.1–1.3 times with the relative humidity increased by 20%, and 1.3–2.5 times with the temperature increased by 5u2009°C, respectively. In agreement with the experimental treatment, a new method of estimating parameters was carried out in a theoretical model from formaldehyde emission, opening the way to a factorial analysis of the relevant parameters for relative humidity and temperature. The theoretical model with estimated parameters was further validated by experiments with different environmental conditions, which should help to quickly determine the parameters needed to predict formaldehyde emissions.