Strength,sorption and abrasion characteristics of concrete using ferrochrome ash (FCA) and lime as partial replacement of cement

This paper presents the results of experimental investigations and microstructure study carried out to evaluate the possibility of utilization of ferrochrome ash (FCA), a waste product from ferroalloys industries for partial replacement of cement in concrete preparation. FCA is used in four different substitution rates such as 10, 20, 30 and 40% along with 7% lime. Various strength and durability tests were conducted to understand the effects of FCA and lime on performance of concrete. Test results revealed that replacement of cement by FCA in various % with 7% lime enhanced the 28 days compressive strength 1.5–13.5%, flexural strength 4.5–9%, bond strength 15–29%, abrasion resistance 10–23% and reduced the sorptivity 25–43%. The concrete containing 40% FCA and 7% lime, replacing 47% of ordinary Portland cement (OPC) in total, exhibited strength of normal concrete or even more at all ages. XRD and petrography studies confirmed the results of mechanical and durability properties.     

Plasma grafting montmorillonite/iron oxide composite with β-cyclodextrin and its application for high-efficient decontamination of U(VI)

β-Cyclodextrin (CD) was grafted onto montmorillonite/iron oxides to prepare a novel magnetic CD/MMT/iron oxide composite by low-temperature plasma technology, and applied to remove U(VI) from aqueous solutions. The sorption irreversibility was attributed to inner-sphere binding of U(VI) on CD/MMT/iron oxide surface sites. The thermodynamic parameters indicated that the sorption of U(VI) on CD/MMT/iron oxide was an endothermic and spontaneous process. The maximum sorption capacity of U(VI) on CD/MMT/iron oxide was considerably higher than that of U(VI) on other reported materials. The CD/MMT/iron oxide can be potentially used as a cost-effective material for the purification of actual U(VI)-bearing effluents.     

从稀土矿石浸出液中分离稀土元素 1.用离子交换树脂从矿石浸出液中吸附稀土

用001×7阳离子交换树脂可以从矿石浸出液中吸附稀土元素。小型试验与扩大试验表明,采用流化床设备进行连续逆流离子交换是可行的。     

Evaluation of the Sorption Equilibrium and Effect of Drying Temperature on the Antioxidant Capacity of the Jaboticaba (Myrciaria cauliflora)

In recent years, interest toward berries has increased (e.g., Myrciaria cauliflora or jaboticaba) because of their high phenolic content (phenolic acids, flavonoids, and anthocyanins) that has been associated with positive effects on consumer health and which play an important role in the antioxidant properties of food. This study analyzed the sorption isotherms, thermodynamic properties of sorption (isosteric heat and Gibbs free energy), and the evolution of the antioxidant capacity during the drying process. The effects of drying temperatures of 40°, 50°C, and 60°C on the antioxidant capacity and thermodynamic properties of sorption were evaluated. The gravimetric static method for sorption isotherm determination over a range of relative humidity levels from 0.10 to 0.90 was used. The sorption isotherms exhibited a Type II behavior, typical for many foods. The Guggenheim, Anderson, and Boer (GAB); Oswin; Peleg; and Lewicki models were used to fit the experimental data, and it was determined that the GAB and Peleg models were most appropriate for describing the sorption curves. The isosteric heat and Gibbs free energy were obtained from the experimental sorption equilibrium. The isosteric heat of adsorption decreased when the moisture content increased, while the Gibbs free energy increased. In addition, the phenolic content and antioxidant capacity increased while drying at 50°C and 60°C, whereas these factors decreased at 40°C. Our results provide the food industry with information concerning the best drying conditions to preserve antioxidant properties.     

Degradation of soil-sorbed trichloroethylene by stabilized zero valent iron nanoparticles: effects of sorption, surfactants, and natural organic matter

Zero valent iron (ZVI) nanoparticles have been studied extensively for degradation of chlorinated solvents in the aqueous phase, and have been tested for in-situ remediation of contaminated soil and groundwater. However, little is known about its effectiveness for degrading soil-sorbed contaminants. This work studied reductive dechlorination of trichloroethylene (TCE) sorbed in two model soils (a potting soil and Smith Farm soil) using carboxymethyl cellulose (CMC) stabilized Fe-Pd bimetallic nanoparticles. Effects of sorption, surfactants and dissolved organic matter (DOC) were determined through batch kinetic experiments. While the nanoparticles can effectively degrade soil-sorbed TCE, the TCE degradation rate was strongly limited by desorption kinetics, especially for the potting soil which has a higher organic matter content of 8.2%. Under otherwise identical conditions, ∼44% of TCE sorbed in the potting soil was degraded in 30 h, compared to ∼82% for Smith Farm soil (organic matter content = 0.7%). DOC from the potting soil was found to inhibit TCE degradation. The presence of the extracted SOM at 40 ppm and 350 ppm as TOC reduced the degradation rate by 34% and 67%, respectively. Four prototype surfactants were tested for their effects on TCE desorption and degradation rates, including two anionic surfactants known as SDS (sodium dodecyl sulfate) and SDBS (sodium dodecyl benzene sulfonate), a cationic surfactant hexadecyltrimethylammonium (HDTMA) bromide, and a non-ionic surfactant Tween 80. All four surfactants were observed to enhance TCE desorption at concentrations below or above the critical micelle concentration (cmc), with the anionic surfactant SDS being most effective. Based on the pseudo-first-order reaction rate law, the presence of 1×cmc SDS increased the reaction rate by a factor of 2.5 when the nanoparticles were used for degrading TCE in a water solution. SDS was effective for enhancing degradation of TCE sorbed in Smith Farm soil, the presence of SDS at sub-cmc increased TCE degraded by ∼10%. However, effect of SDS on degradation of TCE in the potting soil was more complex. The presence of SDS at sub-cmc decreased TCE degradation by 5%, but increased degradation by 5% when SDS dosage was raised to 5×cmc. The opposing effects were attributed to combined effects of SDS on TCE desorption and degradation, release of soil organic matter and nanoparticle aggregation. The findings strongly suggest that effect of soil sorption on the effectiveness of Fe-Pd nanoparticles must be taken into account in process design, and soil organic content plays an important role in the overall degradation rate and in the effectiveness of surfactant uses.     

Separation and determination of cadmium in water by foam column prior to inductively coupled plasma optical emission spectrometry

The sorption profile of cadmium (II) ions from aqueous iodide media onto procaine hydrochloride (PQ⁺·Cl⁻) treated polyurethane foams (PUFs) solid sorbent was studied. PQ⁺·Cl⁻ treated PUFs solid sorbent was found suitable and fast for Cd²⁺ uptake as [CdI4]_aq²⁻. Thus, removal of Cd²⁺ at trace levels by the sorbent packed columns was achieved. The sorbed Cd²⁺ species onto packed column were recovered with HNO₃ (10.0 mL, 1.0 mol L⁻¹) prior determination by inductively coupled plasma-optical emission spectrometry (ICP-OES). Plot of Cd²⁺ ions concentration was linear in the range 0.05–15 μg L⁻¹. The limits of detection and quantification of Cd²⁺ were found 0.01 μg L⁻¹ and 0.033 μg L⁻¹, respectively. Such limits could be improved to lower values by retention of Cd²⁺ species from large sample volumes of the aqueous phase at the optimized conditions. The relative standard deviation of the packed column for the extraction and recovery of standard aqueous solutions (0.1 L) containing 1.0 and 5.0 μg L⁻¹ (n = 3) of Cd²⁺ ions at flow rate of 5.0 mL min⁻¹ were 1.98 and 2.9%, respectively. The method was validated by analysis of Cd in certified reference materials (CRMs) IAEA-Soil-7 and TMDW water and wastewater samples.     

Vapor barrier properties of polycaprolactone montmorillonite nanocomposites: effect of clay dispersion

Different compositions of poly(ε-caprolactone) (PCL) and (organo-modified) montmorillonite were prepared by melt blending or catalyzed ring opening polymerization of ε-caprolactone. Microphase composites were obtained by direct melt blending of PCL and sodium montmorillonite (MMT-Na⁺). Exfoliated nanocomposites were obtained by in situ ring opening polymerization of ε-caprolactone with an organo-modified montmorillonite (MMT-(OH)₂) by using dibutyltin dimethoxide as an initiator/catalyst. Intercalated nanocomposites were formed either by melt blending with organo-modified montmorillonite or in situ polymerization within sodium montmorillonite. The barrier properties were studied for water vapor and dichloromethane as an organic solvent. The sorption (S) and the zero concentration diffusion coefficient (D₀) were evaluated for both vapors. The water sorption increases with increasing the MMT content, particularly for the microcomposites containing the unmodified MMT-Na⁺. The thermodynamic diffusion parameters, D₀, were compared to the value of the parent PCL: both microcomposites and intercalated nanocomposites show diffusion parameters very near to PCL. At variance exfoliated nanocomposites show much lower values, even for small montmorillonite content. In the case of the organic vapor, the value of sorption at low relative pressure is mainly dominated by the amorphous fraction present in the samples, not showing any preferential adsorption on the inorganic component. At high relative pressure the isotherms showed an exponential increase of sorption, due to plasticization of the polyester matrix. The D₀ parameters were also compared to those of the unfilled PCL; in this case, both the exfoliated and the intercalated samples showed lower values, due to a more tortuous path for the penetrant molecules.     

A Study of Surface Wetting When Coating Paper

Abstract

The objective of this work will be to look at basic micro-level simulations of liquid state and movement. Defining liquid movement at fiber-coating boundaries is essential when modeling surface wetting of paper fibers. Drying studies have shown that chemical additives in base paper or coating color may reduce or increase quality, productivity, and energy efficiency considerably. The latest question is, Which are the factors that are significantly influencing liquid movement at fiber-coating boundaries? A phenomenon of less liquid drainage at lower paper moisture content is studied in this work together with the fiber hornification process. Fiber hornification is a complex change in the physicochemical properties of the fiber surface and the state of boundary molecules. Another important objective is to show how hornification may be accounted for in basic calculations. This while, printing properties of paper (mottling, etc.), may then be connected to the formation of the base paper and its drying history, explaining in more detail the importance of microlevel physicochemical property changes at fiber surfaces.     

憎水有机物在水/土壤、沉积物体系中吸附与解吸

憎水有机物在水/沉积物体系中吸附与解吸的问题一直是环境化学与工程领域研究的热点问题,在过去30多年的研究中提出各种理论、模型和经验公式,通过总结过去的研究成果,指出存在的问题,提出今后需要解决的关键问题。