Photocrosslinking of functionalized rubbers. X. Butadiene–acrylonitrile copolymers

The photocrosslinking of polyacrylonitrile‐block‐polybutadiene‐block‐polyacrylonitrile (ABA) was shown to proceed within seconds at ambient temperature upon UV exposure in the presence of an acylphosphine oxide photoinitiator. The curing process was followed by infrared spectroscopy, insolubilization, and hardness measurements. Complete insolubilization could not be achieved with the neat ABA rubber because of the poor reactivity of the 2‐butene double bond and the low vinyl content of the polybutadiene chain. The addition of multifunctional acrylate monomers (20 wt %) causes a substantial increase of both the reaction rate and the crosslink density of the polymer, which becomes completely insoluble in toluene in less than 1 s upon UV irradiation. An even greater effect was observed by using small amounts (1 wt %) of a trifunctional thiol crosslinker. Both the thiol and the photoinitiator concentrations were shown to affect the kinetics of the thiol–ene polymerization and the polymer network crosslink density. A direct relationship was found to exist between the swelling degree of the UV‐cured rubber and the interchain molecular weight of the network. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 2204–2216, 2001     

Positivity and stability of mixed fractional‐order systems with unbounded delays: Necessary and sufficient conditions

This article provides a comprehensive study on quantitative properties of linear mixed fractional‐order systems with multiple time‐varying delays. The delays can be bounded or unbounded. We first obtain a result on existence and uniqueness of solutions to these systems. Then, we prove a necessary and sufficient condition for their positivity. Finally, we provide a necessary and sufficient criterion to characterize asymptotic stability of positive linear mixed fractional‐order systems with multiple time‐varying delays.     

Modeling of chloride diffusivity coupled with non-linear binding capacity in sound and cracked concrete

The objective of this research is to establish a model that can predict chloride transport phenomena in sound and cracked concrete. The chloride diffusivity is formulated based on computed micro-pore structure, which considers tortuosity and constrictivity of porous network as reduction factors in terms of complex micro-pore structure and electric interaction of chloride ions and pore wall. In the real environment, concrete structures are not always crack-free, therefore chloride transport in cracked concrete is also simulated by section large void spaces in a control volume to represent the crack and by proposing a model of chloride diffusivity through the cracked region The proposed models are implemented into a finite-element computational program DuCOM, which simulates the early-age development process of cementitious materials. The calculated concentration profiles of total chloride ions are verified through a comparison with experiments results.     

Synergistic activation of CTP:phosphocholine cytidylyltransferase by phosphatidylethanolamine and oleic acid

CTP:phosphocholine cytidylyltransferase present in rat liver cytosol was activated almost 30-fold when assayed in the presence of liposomes containing 60 mole % dioleoyl phosphatidylethanolamine (DOPE). During the assay, some of the DOPE was degraded to lysoPE and oleic acid. Whereas cytidylyltransferase activity was not affected when assayed in the presence of liposomes containing lysoPE, liposomes containing oleic acid activated the enzyme. Activation by oleic acid could be eliminated by the addition of fatty acid-free bovine serum albumin (BSA) to the assay. When cytidylyltransferase activity was measured in the presence of both BSA and liposomes containing DOPE, enzyme activity was increased almost 20-fold, as compared with assays performed in the absence of added lipid. The 1.5-fold difference in cytidylyltransferase activity observed when cytosol was assayed with DOPE containing liposomes in the absence or presence of BSA (30-fold stimulation vs 20-fold stimulation) cannot be explained by the loss of activation attributable to oleic acid alone. Activation of the enzyme in the presence of liposomes containing DOPE and oleic acid is several-fold greater than the sum of the activations caused by the individual compounds. These data suggest that PE and oleic acid act synergistically in activating the cytidylyltranferase.     

The effects of air pollution and climatic factors on atmospheric corrosion of marble under field exposure

The atmospheric corrosion of marble was evaluated in terms of SO₂ concentration as air pollution and climatic factors such as rainfall, relative humidity, temperature and so on under the field exposure. Marble of calcite type (CaCO₃) was exposed to outdoor atmospheric environment with and without a rain shelter at four test sites in the southern part of Vietnam for 3-month, 1- and 2-year periods from July 2001 to September 2003. The thickness loss of marble was investigated gravimetrically. X-ray diffraction and X-ray fluorescent methods were applied to study corrosion products on marble. The corrosion product of marble was only gypsum (CaSO₄ · 2H₂O) and was washed out by rain under the unsheltered exposure condition. It was found that the most substantial factors influencing the corrosion of marble were rainfall, SO₂ concentration in the air and relative humidity. Based on the results obtained, we estimated the dose-response functions for the atmospheric corrosion of marble in the southern part of Vietnam.     

Corrosion protection of molybdate doped polypyrrole film prepared in succinic acid solution

ABSTRACT

Polypyrrole (PPy) was prepared on the mild steel substrate by electrochemical polymerisation in the solution containing pyrrole monomer and succinic acid. The mild steel surface could be passivated before and during electropolymerisation by molybdate. The morphology and structure of the PPy film were studied with SEM. The typical cauliflower structure of PPy was observed. Raman and IR spectroscopy showed that the obtained PPy was in an oxidised state. The thermal stability of PPy was investigated by the thermal gravimetric analysis, showing that PPy was stable at higher than 480°C. The electrochemical property of the PPy film was performed by open circuit potential, polarisation curves (I/E), and electrochemical impedance spectroscopy. The corrosion behaviour of mild steel (CT3) with PPy film in solution NaCl 3% was studied.

This paper is part of a supplementary issue from the 17th Asia-Pacific Corrosion Control Conference (APCCC-17).     

钢渣对水溶液中砷的吸附动力学和热力学特性试验

以炼钢厂固体废弃物钢渣为材料,通过批量平衡吸附法,并结合宏观热力学和动力模型应用,分析和研究了钢渣对水溶As(III)的吸附特征。结果表明钢渣在吸附As(III)过程中,初始阶段吸附量迅速增加,随着浓度的增加,吸附逐渐趋于饱和,最后达到平衡,具有"快速吸附、缓慢平衡"的特点。钢渣吸附材料具有极高的最大吸附容量,高达3.58×104mg/kg。钢渣对As(III)的吸附均符合Langmuir和Freundlich吸附等温线,其中钢渣对As(III)的吸附特征与Freundlich等温吸附方程吻合性最好,相关系数(R2)达到0.99以上。钢渣对As(III)的吸附动力学数据均符合一级动力学方程、Elovich方程和双常数方程,拟合优度用相关系数(R2)为0.92~0.98,相比较而言,钢渣对As(III)的吸附以Elovich方程为最佳模型。     

Comparison of particle-phase polycyclic aromatic hydrocarbons and their variability causes in the ambient air in Ho Chi Minh City, Vietnam and in Osaka, Japan, during 2005-2006

A comparative study of polycyclic aromatic hydrocarbons (PAHs) associated with particulate matter (TSP) in the ambient air in an urban area in Ho Chi Minh City, Vietnam and in Osaka, Japan was carried out from 2005 to 2006. The objective of this study was to investigate the environmental levels, emission sources, seasonal variations and health risk of eleven PAHs in the two cities, especially Ho Chi Minh City where air pollution is becoming a serious concern. The results showed that the concentrations of TSP and total PAHs were significantly higher in Ho Chi Minh City than levels in Osaka. The concentrations of 5- and 6-ring PAHs (BeP, BbF, BkF, BaP, BghiP and InP) were much higher in TSP samples in Ho Chi Minh City than in Osaka, accounting for 82% and 51% of total PAHs, respectively. These PAHs are known to be highly carcinogenic and mutagenic in humans. Vehicular emission is suggested as one of the main pollution sources of PAHs in both cities. Motorcycles and gasoline automobiles are suggested as the main emission sources of PAHs in Ho Chi Minh City, whereas diesel automobiles are the primary source in Osaka. Seasonal variations of PAHs were observed in this study; higher concentrations of PAHs were found in the rainy season (May-December) and lower concentrations corresponded to the dry season (February-April) in Ho Chi Minh City, while higher concentrations of PAHs were observed in the winter (November-January) in Osaka. The number of sunshine hours was an important meteorological factor affecting seasonal variations of PAHs in Ho Chi Minh City, while the temperature was a main factor causing the variations of PAHs in Osaka. The high BaP equivalent concentration of 5- and 6-ring PAHs even in the ambient air is an alarming signal for harmfulness to human health and environmental quality in Ho Chi Minh City.