A total of 258 particulate matter (PM 10 ) filter samples and 69 source samples applicable to receptor model source apportionment were collected and chemically analyzed from February to August 2007 in Panzhihua, China. Contributive sources were identified and the chemical profiles were reported for resuspended dust, paved and unpaved road dust, coalfired power plant exhaust, emissions from coking plants and other industrial sources in Panzhihua. All samples were analyzed for 19 elements (Na-Pb), two ions (NO 3 -and SO 4 2-) and organic and total carbon. Elevated abundances of geological components (Al, Si, Ca and Fe) from fugitive dust materials and elements (Ti, Cr, Mn, Cu and Zn) from special industry plants were found in the profiles. The contributions to the ambient PM 10 levels at six sites in three seasons (spring, summer and winter) were estimated using a chemical mass balance receptor model. The concentration of PM 10 was high (150 μg/m 3 ) on winter days and low in summer and spring (133 and 129 μg/m 3 , respectively). Apportionment results indicate that coal combustion ash, iron and steel industry dust, vehicle exhaust and secondary SO 4 2-were major contributors, accounting for about 70% of PM 10 . More attention should be paid to particulate matter emitted by iron and steel manufacturing facilities in view of high contribution and potentially toxic metals.

The increasing petroleum price and the foreseeable depletion of fossil fuels has prompted research on bioenergy, particularly bioethanol and biobutanol from renewable lignocellulosic biomass, the primary component of which is cellulose. One key requirement of lignocellulose degradation is to improve the efficiency of a group of enzymes with general name cellulase, the collaboration of which degrades cellulose to glucose. Significant progress has been made in the last decade on understanding the structural and chemical properties of the substrate cellulose, the structural and biochemical properties of cellulases, their enzymatic mechanisms and the mechanism of synergistic catalysis by cellulases. This manuscript reviews the progress in the aforementioned fields, particularly the structural basis and enzymatic mechanisms of reactions leading to the degradation of cellulose. Based on these discoveries, popular models of enzymatic cellulose degradation are discussed, in the hope of benefiting further in‐depth investigations of this complex, multi‐component enzymatic reaction.© 2012 Society of Chemical Industry

The deterioration of early-age concrete performance caused by SO42− internal diffusion in concrete is a critical factor of concrete durability. In this study, the mechanical properties, heat of hydration, and pore structure of early-age cast-in-situ concrete with different sodium sulfate (Na2SO4) concentrations were studied. The mechanism of SO42− internal corrosion was evaluated by measuring the dynamic elastic modulus, compressive strength, and heat of hydration rate. Scanning electron microscopy, energy dispersive spectroscopy, X-ray computed tomography, X-ray diffraction, thermogravimetry-derivative thermogravimetry, and differential scanning calorimetry were applied to analyze microstructural variations and complex mineral assemblages of concrete samples. The results indicated that during the hardening process of cast-in-situ concrete, Na2SO4 first promoted and then hindered the hydration rate of cement, and also hindered the early strength development of the cement. As the concentration of Na2SO4 solution increases, the corrosion products of ettringite (AFt) and gypsum (Gyp) gradually increase, causing cross cracks in the concrete. The proportion of small and medium pores first increases and then decreases, and the large pores first decrease and then increase. The mechanical properties of concrete gradually decrease and diminish the mechanical properties of the concrete (thereby accelerating the damage to the concrete).

The diffusion of sulfate (SO42−) and chloride (Cl−) ions from rivers, salt lakes and saline soil into reinforced concrete is one of the main factors that contributes to the corrosion of steel reinforcing bars, thus reducing their mechanical properties. This work experimentally investigated the corrosion process involving various concentrations of NaCl-Na2SO4 leading to the coupled erosion of concrete. The appearance, weight, and mechanical properties of the concrete were measured throughout the erosion process, and the Cl− and SO42− contents in concrete were determined using Cl− rapid testing and spectrophotometry, respectively. Scanning electron microscopy, energy spectrometry, X-ray diffractometry, and mercury porosimetry were also employed to analyze microstructural changes and complex mineral combinations in these samples. The results showed that with higher Na2SO4 concentration and longer exposure time, the mass, compressive strength, and relative dynamic elastic modulus gradually increased and large pores gradually transitioned to medium and small pores. When the Na2SO4 mass fraction in the salt solution was ≥10 wt%, there was a downward trend in the mechanical properties after exposure for a certain period of time. The Cl− diffusion rate was thus related to Na2SO4 concentration. When the Na2SO4 mass fraction in solution was ≤5 wt% and exposure time short, SO42− and cement hydration/corrosion products hindered Cl− migration. In a concentrated Na2SO4 environment (≥10 wt%), the Cl− diffusion rate was accelerated in the later stages of exposure. These experiments further revealed that the Cl− migration rate was higher than that of SO42−.

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