A study of surface changes of wood-polypropylene composites as the result of exterior weathering

Outdoor applications of composites raised questions about their durability. In this study, the effects of outdoor weathering on the properties of wood-polypropylene composites with and without pigments were examined. The composites were placed outdoors for one year, and their colour changes were evaluated after 1, 3, 6, 9 and 12 months of weathering. The weathering resulted in considerable colour fading of the composites. Composites containing darker colour pigments had better colour stability. Scanning electron microscopy analysis revealed that surface cracks caused by weathering in a wood-polypropylene composite having a higher polypropylene content were less abundant, and the deterioration of the surface layer was lower compared to composites containing less polymer. Measurements of melting temperatures by differential scanning calorimetry gave a consistent picture of polypropylene degradation in the surface layer. After weathering, a decrease in Charpy impact strength was found for composites characterised by higher moisture absorption.     

The synthesis,characterization, and weathering behavior of polycarbonates derived from bis(P-hydroxyphenyl) dimethylsilane (BPSI)

Polycarbonates and copolycarbonates based on BPSi and BPA were easily made using the standard interfacial technique. Molecular weight and NMR data indicate that up to 4 mol % of the BPSi decomposes during polymerization via a base-catalyzed rearrangement of BPSi to arylsiloxanes. Oxygen index studies show an increased flame resistance with increasing BPSi monomer content. DSC measurements show a decrease in glass transition with BPSi monomer concentration while TGA shows an increase in char residue with BPSi monomer content. In addition, TGA indicates no change in either thermal or thermooxidative stability with the relative BPSi/BPA concentrations. Outdoor weathering of BPSi PC and BPA PC films indicates that BPSi PC is ca. 5 times more weathering resistant than BPA PC. This latter result can be attributed to a combination of BPSi PC's lower UV absorptivity, higher water repellency, and lower likelihood for side chain photooxidation. © 1993 John Wiley & Sons, Inc.     

Perylene-based profluorescent nitroxides for the rapid monitoring of polyester degradation upon weathering: An assessment

A profluorescent nitroxide possessing an isoindoline nitroxide moiety linked to a perylene fluorophore was developed to monitor radical mediated degradation of melamine-formaldehyde crosslinked polyester coil coatings in an industry standard accelerated weathering tester. Trapping of polyester-derived radicals (most likely C-radicals) that are generated during polymer degradation leads to fluorescent closed-shell alkoxy amines, which was used to obtain time-dependent degradation profiles to assess the relative stability of different polyesters towards weathering. The nitroxide probe couples excellent thermal stability and satisfactory photostability with high sensitivity and enables detection of free radical damage in polyesters under conditions that mimic exposure to the environment on a time scale of hours rather than months or years required by other testing methods. There are indications that the profluorescent nitroxide undergoes partial photo-degradation in the absence of polymer-derived radicals. Unexpectedly, it was also found that UV-induced fragmentation of the NO–C bond in closed-shell alkoxy amines leads to regeneration of the profluorescent nitroxide and the respective C-radical. The maximum fluorescence intensity that could be achieved with a given probe concentration is therefore not only determined by the amount of polyester radicals formed during accelerated weathering, but also by the light-driven side reactions of the profluorescent nitroxide and the corresponding alkoxy amine radical trapping products. Studies to determine the optimum probe concentration in the polymer matrix revealed that aggregation and re-absorption effects lowered the fluorescence intensity at higher concentrations of the profluorescent nitroxide, but too low probe concentrations, where these effects would be avoided, were not sufficient to trap the amount of polyester radicals formed upon weathering. The optimized experimental conditions were used to assess the impact of temperature and UV irradiance on polymer degradation during accelerated weathering.     

水库下伏采空区渗流场耦合模拟分析

基于扰动情况下岩体应力场与渗流场相互作用机理,确定了应力场环境下岩体渗流参数的计算公式以及耦合模型中渗透体积力的加载方程,采用有限元分析软件ANSYS,运用物理环境耦合方法,介绍了水库下伏扰动岩体渗流场模拟分析的方法及流程,并对某库区下伏岩体渗流场进行了模拟分析,通过对该库区下伏采空区渗流场进行分析,对库区及采空区提出了处理建议.     

麦饭石调节溶液pH值的影响因素

为了寻求麦饭石调节溶液pH值作用最佳效果,采用室内试验方法,研究了麦饭石调节溶液pH值作用的影响因素,发现经风化作用后的麦饭石调节溶液pH值作用效果优于未风化的麦饭石。风化后的麦饭石中的Al3+易于从硅酸盐矿物中析出,是麦饭石能调节溶液pH值并优于未风化的麦饭石原因。随着麦饭石粒度的减小其调节溶液pH值作用能力提高。该研究对麦饭石矿产资源的进一步开发利用具有一定的参考意义。     

乌江流域沉积岩风化过程中稀土元素的富集与释放

以乌江流域石灰岩、白云质灰岩、白云岩、硅质岩、页岩和砂岩等沉积岩的13条风化剖面为对象，运用R型分层聚类分析和质量平衡计算方法，研究了这些岩石风化过程中稀土元素（REE）的富集与释放及其对植物生长和河水REE分布的影响，目的是为河水物质来源研究和为农业生产提供依据。结果表明：（1）乌江流域石灰土中REE的富集程度显著高于各自母岩、黄壤、上陆壳（UCC）、中国土壤（CS）和世界土壤（WS）；（2）沉积岩风化过程中REE的富集特征和机制可能与母岩中REE分布特征以及风化剖面中有机质、铁（氢）氧化物和粘土矿物的吸附有关；（3）沉积岩风化过程中释放的REE可为植物吸收利用；（4）石灰岩等沉积岩风化过程中REE和F。等元素的释放对河水溶解态REE的分布有重要影响。     

Sample temperatures during outdoor and laboratory weathering exposures

Effective exposure temperatures (T_eff) in Arizona were calculated from hourly or 10-min parsed irradiation data along with ambient, black panel, and sample temperatures. The T_eff represents a constant temperature that creates the same amount of photodegradation as the naturally varying temperature and provides a benchmark temperature for making lifetime predictions from accelerated laboratory exposures. The annual ambient and black panel T_eff at a Wittmann, Arizona site were 30 °C and 42 °C, respectively, assuming that the photodegradation has an activation energy (E_a) of 21 kJ/mol (5 kcal/mol). T_eff was only weakly dependent on E_a over the range of 10-40 kJ/mol (3-10 kcal/mol). Samples exposed as van sunroofs were found to have T_eff that were offset from the black panel temperatures by a constant amount for the entire year. Thus, measurements of sample and black panel need to be made for only a few weeks to determine the offset and give the annual sample T_eff if the annual black panel T_eff is known. Light-colored samples probably are better compared with the ambient temperatures. Sample temperatures in xenon arc exposures usually are higher than the outdoor T_eff, so Arrhenius temperature corrections need to be carried out to relate accelerated to outdoor exposures. Temperatures in xenon arc exposure tests often correspond more closely to maximum temperatures that samples might encounter for only a few hours per year.