A unified treatment of axisymmetric adhesive contact problems using the harmonic potential function method

A unified treatment of axisymmetric adhesive contact problems is provided using the harmonic potential function method for axisymmetric elasticity problems advanced by Green, Keer, Barber and others. The harmonic function adopted in the current analysis is the one that was introduced by Jin et al. (2008) to solve an external crack problem. It is demonstrated that the harmonic potential function method offers a simpler and more consistent way to treat non-adhesive and adhesive contact problems. By using this method and the principle of superposition, a general solution is derived for the adhesive contact problem involving an axisymmetric rigid punch of arbitrary shape and an adhesive interaction force distribution of any profile. This solution provides analytical expressions for all non-zero displacement and stress components on the contact surface, unlike existing ones. In addition, the newly derived solution is able to link existing solutions/models for axisymmetric non-adhesive and adhesive contact problems and to reveal the connections and differences among these solutions/models individually obtained using different methods at various times. Specifically, it is shown that Sneddon’s solution for the axisymmetric punch problem, Boussinesq’s solution for the flat-ended cylindrical punch problem, the Hertz solution for the spherical punch problem, the JKR model, the DMT model, the M-D model, and the M-D-n model can all be explicitly recovered by the current general solution.     

Processable polyisoimide polymer blends for application as thermally stable adhesives for composites and advanced metal alloys

Polyimides are effective thermally stable bonding agents for substrates including titanium, aluminum alloys, steel alloys, metal matrix composites, and polymer/fiber composites with good tolerance toward elevated temperature and humidity. Problems associated with polyimide adhesives, including high processing temperatures and pressures and high melt viscosity, can be partially or totally alleviated by use of blends of polyisoimides. During thermal processing, the polyisoimides are isomerized to their polyimide modifications.     

用含螺环原碳酸酯的预聚物改性环氧树脂的研究

合成了一个新的螺环原碳酸酯单体，３，９ 二羟甲基 ３’，９’ 二苯基 １，５，７，１１ 四氧杂螺环［５，５］十一烷，它与二苯甲烷二异氰酸酯（ＭＤＩ）反应生成了低分子量预聚物，用该预聚物对环氧树脂进行改性，可以减少残留在树脂基体中的环氧基团，这说明该预聚物与环氧树脂之间发生了共聚固化反应．基体的Ｔｇ和热稳定性随预聚物加入量的增加而降低，但改性环氧树脂的粘接强度则随预聚物的加入量的增加而增加，螺环基团上的取代基对改性环氧树脂基体也有一定的影响，作者对上述试验观察到的现象进行了讨论．     

基于同步辐射X射线相衬显微CT技术的竹木复合材料胶合界面特征研究

第三代同步辐射光源X射线相位衬度显微CT能获得样品内部结构的边缘增强图像,实现对低Z材料成像。利用上海同步辐射光源X射线相衬显微成像技术,实现了竹木复合材料中EPI和MUF胶合界面和胶黏剂渗透特征的无损探测,并基于这些特征分析了几种不同加工工艺对胶黏剂在木材和竹材中渗透的影响。该技术为人造板工艺解剖学研究提供了一种重要无损检测手段。     

Preparation, characterization and adhesive properties of di- and tri-hydroxy benzoyl chitosan nanoparticles

Modified chitosans with 3,4-di-hydroxy benzoyl groups (CS-DHBA) and 3,4,5-tri-hydroxy benzoyl groups (CS-THBA) were synthesized and their nanoparticles were prepared via ionic crosslinking by tripolyphosphate (TPP). The chemical structure and degree of substitution (DS) of di-and tri-hydroxy benzoyl chitosans are determined by FTIR and 1H-NMR spectroscopy. The morphology of particles, size distribution and zeta potential of nanoparticles were studied using transmission electron microscopy (TEM) and dynamic light scattering (DLS), respectively. The mean diameters of particles of CS-DHBA and CS-THBA nanoparticles were 144 nm and 112 nm, respectively. It was found that the particles size decreased slightly with decreasing the degree of substitution and increasing degree of deacetylation (DD), due to increasing of ionic crosslinking of ammonium ions and polyanions of tripolyphosphate. The TEM photographs of CS-DHBA show that these particles are spherical in shape, but the particles of CS-THBA show some aggregation. In addition, the solubility and the mechanical properties of the prepared modified chitosans and their nanoparticles were evaluated for bio-adhesive and biomedical application. The results of solubility tests indicated that, the CS-DHBA and CS-THBA have higher solubility at pH > 7 comparing to CS. Also the CS-DHBA, CS-THBA and their nanoparticles showed a significant adhesive capacity and enhanced tensile strength and tensile modulus.     

木质素活化改性制备酚醛树脂胶黏剂研究进展

木质素由于化学结构与苯酚相似,通过活化改性可部分替代苯酚制备木质素改性酚醛树脂胶黏剂。既可降低成本、达到生物质资源高效利用的目的,并且制备的木质素改性酚醛树脂胶黏剂有毒残余较低,具有环保意义,是合成制备生物质高分子材料的重要途径。本文综述了国内外研究人员在木质素活化改性制备酚醛树脂胶黏剂研究领域的最新进展,重点介绍了化学改性、物理改性、生物改性等木质素活化改性方法,比较了不同改性产物制备酚醛树脂胶黏剂的性能,并对影响木质素活化改性制备酚醛树脂胶黏剂实现工业化应用的主要因素进行了分析。     

可光固化星形超支化聚酯的合成与表征

描述了基于季戊四醇和１，２，４ 苯三甲酸酐，经由甲基丙烯酸缩水甘油酯和甲基丙烯酸酐改性的系列超支化聚酯的“发散”合成方法，即合成反应从“中心核”开始，逐步向外扩展，控制链增长，每个分子形成具有大约８，１２和１６个甲基丙烯酸酯双键的超支化臂。这种星形聚酯分子具有三维球状结构，不会产生分子链间的缠结，在辐射固化涂层和粘合剂等领域具有广阔的应用前景．     

Inhibation of crystal growth during drying in gels derived from a cheap,mixed metal oxide precursor

The influence of addition of small amounts of either citric acid or lactic acid on the formation of crystalline matter in dried gels derived from a multi-component industrial sol–gel silica precursor has been studied. The sols were water-based and had formic acid as the main acid constituent. A pronounced decrease in the extent of crystallization was observed for both acids, with citric acid being more effective than lactic acid. The results are discussed based on the complexation behavior of the corresponding acids under the studied conditions, and the complexation behavior in solution can be directly linked to the extent of crystallization in the dried gels. However, the sol–gel kinetics followed that expected for a purely silica-based sol, which suggests that the kinetics is mainly controlled by the silica portion of the sol. The results are suggested to be of importance for the industrial use of these sols as binders, as pronounced crystallization in the gels upon drying may lead to mechanical stresses, and thus to a decreased binder performance.     

基于Norland紫外固化胶的热光开关器件

采用新型聚合物材料Norland紫外固化胶（NOA）制备了聚合物M-Z型热光开关器件。对NOA薄膜材料的光学性质进行了表征,采用感应耦合等离子体（ICP）方法制备出形貌良好的波导器件。测得在1 550 nm波长下,长2.2 cm的直波导插入损耗为8.3 dB。在电极上施加直流信号,测得热光开关的消光比为11 dB,驱动功率为85 mW。引入直流偏置网络,获得了器件的开关特性曲线,测得开关器件的上升时间为1.085 ms,下降时间为489.5μs。实验结果表明：NOA材料在热光开关及其它聚合物光波导集成器件的制备中具有很大的应用潜力。     

Fabrication of Photoprocessable Materials via Photopolymerization Using an Acid-Induced Photocleavable Platinum-Acetylide Crosslinker

Photopolymerization and photoprocessing are core technologies for molding and tuning polymer materials. However, they are incompatible with single materials owing to their contradictory photoreactivity. Herein, an acid-induced photocleavable crosslinker, a platinum–acetylide complex covered by permethylated cyclodextrins, enables the fabrication of photoprocessable materials via photopolymerization with N-(2-hydroxyethyl)acrylamide. The polymer networks are molded by 365 nm irradiation as well as softened and degraded by a cooperative reaction with HCl as an acidic additive under 365 nm UV light, or 470 nm visible light in the presence of a photosensitizer. Moreover, the crosslinker is applied to a photoadhesive triggered by 365 nm irradiation. The adhesion is detachable on-demand through acid-induced photodegradation with the same wavelength and intensity of irradiation. Thus, acid-induced photocleavage allows the integration of light-induced molding and processing under various lights of various wavelengths, opening up new strategies for polymer technologies.