玻璃纤维增强建筑用聚乙烯树脂复合材料的性能

采用剥离测试方法来表征制得的玻璃纤维增强建筑用聚乙烯树脂复合材料的界面黏结强度,并对其进行红外光谱、接触角、微观组织测试与分析。研究结果表明:采用浸润剂处理可以使玻璃表面生成新基团;浸润剂能够提高玻璃表面接触角,从而更易与树脂形成浸润状态,由此改善玻璃和树脂的界面结合状态,实现界面黏结特性的显著优化。在剥离测试中发现经浸润剂处理后,玻璃可以和树脂之间形成更强的界面结合作用;树脂从玻璃表面发生剥离之后,形成了光滑的玻璃片,同时还有部分纵横交错的划痕。     

DOPO‐Based Phosphorus‐Containing Methacrylic (Co)Polymers: Glass Transition Temperature Investigation

A two‐step synthetic procedure is designed for preparing new flame‐retardant methacrylic monomers containing 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO) as a substituent side group. DOPO and methacrylate moieties are linked by linear aliphatic hydrocarbon spacers (3 to 11 carbon atoms). Copolymerization with methyl methacrylate is carried out leading to copolymers containing between 2 and 10 wt% phosphorus. All homo‐ and copolymers exhibit a unique glass transition temperature (T_g ). A new group contribution for DOPO‐based substituent is extracted that leads to reasonable estimations of T_g s of other published polymers. The Fox equation provides a good estimation of T_g s for most copolymers and for physical blends of poly(methyl methacrylate) (PMMA) and DOPO. When using monomers having three and four carbon atoms in the hydrocarbon spacer, the T_g of copolymers remains close to that of PMMA over a wide range of composition.     

Hydrolysis-resistant polyurethane elastomers synthesized from hydrophobic bio-based polyfarnesene diol

Hydrolytic stability is an essential requirement for polyurethanes (PUs) that are used in highly humid and aqueous environments. In this study, hydrolysis-resistant PU elastomers (PUEs) are synthesized based on hydrophobic bio-based polyfarnesene diol (PFD), which contains unique “bottle brushes” structure (with long branched hydrocarbon side chains). The effect of hard segment (HS) content, ranging from 30 to 50%, on the morphology and properties of PUEs is investigated by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, scanning electron microscopy, tensile, water absorption, and contact angle measurements. The results show that there are prominent phase separations in the synthesized PUEs. The PUEs show a three-stage degradation process and two T_g, one is at about −66 °C and the other 61 °C, which are related to the soft segment and HS, respectively. Water contact angles of PUEs increase from 98.6 to 105.2° with the increasing of PFD structural unit fraction. After being immersed in deionized water for 30 days, PUEs show no significant degradation of both tensile strength and elongation at break, and mass changes of all samples are less than 0.5%. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47673.     

地下水穿透情形下玻璃固化体的蚀变研究

玻璃固化体在高放废物处置库中的长期处置行为，是处置库安全评价的关键环节之一。本研究模拟极端情形下，地下水穿透包装容器与固化体接触后，固化体中元素的浸出和蚀变行为。结果表明，地下水与固化体接触后，各元素的浸出浓度迅速增大，在200 d后逐渐下降并趋于稳定；温度对固化体中不同元素浸出速率的影响不同，B和Si的浸出速率随温度的增加而增大，U和Re的浸出速率随温度的降低而增大；固化体蚀变程度随温度的升高而加重，但其蚀变层的形成会阻滞元素在其中的扩散，客观上降低了固化体蚀变速率；富Si处置环境有利于抑制固化体中元素的浸出。     

Ductile-brittle transition mechanisms of amorphous glass subjected to taper grinding experiment

Taper grinding experiments were conducted in this paper to investigate the continuous and complete ductile-brittle transition process of two kinds of amorphous glass: high purity fused silica (HPFS) which is silica rich glass and soda-lime silica glass (SLSG) which is low silica glass. The grinding force, ground surface morphology, surface roughness, and subsurface damage depth induced during different stages of taper grinding were all analyzed. A mathematical model describing the cutting force of a grit and micro-crack length was established to clarify the ductile-brittle transition mechanisms of isotropic material. The model revealed that material removal mechanisms and grinding force were mainly determined by the crack equivalent length in front of the grit and its equivalent cutting force. The ground surface roughness and subsurface damage depth were mainly affected by the cutting force of the grit and length of cracks behind it. The ductile machinability of SLSG was better than that of HPFS due to the bonding of metallic atoms in SLSG with nonbridging oxygens, as well as their packing into free volume in SiO₂ network.     

Non-linear dissolution mechanisms of sodium calcium phosphate glasses as a function of pH in various aqueous media

Phosphate glasses for bioresorbable implants display dissolution rates that vary significantly with composition, however currently their mechanisms of dissolution are not well understood. Based on this systematic study we present new insights into these mechanisms. Two-stage dissolution was observed, with time dependence initially parabolic and later linear, and a two-stage model was developed to describe this behaviour. Dissolution was accelerated by lower Ca concentration in the glass, and lower pH in the dissolution medium. A new dissolution mechanism is proposed, involving an initial stage where diffusion-controlled formation of a conversion layer occurs. Once the conversion layer is stabilised, layer dissolution reactions become rate-limiting. Under this mechanism the transition time is sensitive to the nature of the conversion layer and solution conditions. These results reveal the dependence of P₂O₅–CaO–Na₂O glass dissolution on solution pH, and provide new insight into the dissolution mechanisms, particularly regarding the transition between the two dissolution stages.     

Preparation and electrochemical characterization of Ti-based amorphous metallic glass with high strength

Ti-based amorphous metallic glasses have excellent mechanical, physical, and chemical properties, which is an important development direction and research hotspot of metal composite reinforcement. As a stable, simple, efficient, and large-scale preparation technology of metallic powders, the gas atomization process provides an effective way of preparing amorphous metallic glasses. In this study, the controllable fabrication of a Ti-based amorphous powder, with high efficiency, has been realized by using gas atomization. The scanning electron microscope, energy-dispersive spectrometer, and X-ray diffraction are used to analyze surface morphology, element distribution, and phase structure, respectively. A microhardness tester is used to measure the mechanical property. An electrochemical workstation is used to characterize corrosion behavior. The results show that as-prepared microparticles are more uniform and exhibit good amorphous characteristics. The mechanical test shows that the hardness of amorphous powder is significantly increased as compared with that before preparation, which has the prospect of being an important part of engineering reinforced materials. Further electrochemical measurement shows that the corrosion resistance of the as-prepared sample is also significantly improved. This study has laid a solid foundation for expanding applications of Ti-based metallic glasses, especially in heavy-duty and corrosive domains.     

Deformation-induced bonding of polymer films below the glass transition temperature

Bonding between polymers through interdiffusion of macromolecules is a well-known mechanism of polymer adhesion. A new polymer bonding mechanism in the solid state, taking place at ambient temperatures well below the glass transition value (T_g), has been recently reported; in this mechanism, bulk plastic compression of polymer films held in contact led to adhesion over timescales of the order of a fraction of a second. In this study, we prepared various blends of plasticized polymer films with desirable ductility from amorphous and semicrystalline powders of hydroxypropyl methylcellulose and polyvinyl alcohol derivatives; then, we observed the bonding of these polymers at ambient temperatures, up to 80 K below T_g, purely through mechanical deformation. The deformation-induced bonding of the polymer films studied in this work led to interfacial fracture toughnesses in the range of 1.0–21.0 J/m² when bulk plastic strains between 3% and 30% were imposed across the films. Scanning electron microscopy observation of the debonded interfaces also confirmed that bonding was caused by deformation-induced macromolecular mobilization and interpenetration. These results expand the range of applicability of sub-T_g, solid-state, deformation-induced bonding processes.     

Conversion kinetics of container glass batch melting

Understanding the batch-to-glass conversion process is fundamental to optimizing the performance of glass-melting furnaces and ensuring that furnace modeling can correctly predict the observed outcome when batch materials or furnace conditions change. To investigate the kinetics of silica dissolution, gas evolution, and primary foam formation and collapse, we performed X-ray diffraction, thermal gravimetry, feed expansion tests, and evolved gas analysis of batch samples heated at several constant heating rates. We found that gas evolving reactions, foaming, and silica dissolution depend on the thermal history of the batch in a similar manner: the kinetic parameters of each process were linear functions of the square root of the heating rate. This kinetic similarity reflects the stronger-than-expected interdependence of these processes. On the basis of our results, we suggest that changes in furnace operating conditions, such as firing or boosting, influence the melting rate less than what one would expect without consideration of batch conversion kinetics.