纳米AT13陶瓷喷涂层结合强度的分形维数表征

应用分形维数对微弧等离子喷涂纳米AT13涂层的界面进行研究，结果表明：随喷涂电流的增加，纳米AT13涂层的界面分维不断增大，其结合强度也不断提高；随着氩气压力的增加，纳米AT13涂层的界面分维和结合强度都先增大后减小；界面分维D可用于表征涂层结合强度σ，σ随D的增大而增大，且ln(σ)与D之间呈近似线性关系：ln(σ)=17.6D-26.2.     

Formaldehyde‐Free Wood Adhesives from Decayed Wood

Summary: Extensive studies using mussel adhesive protein as a formaldehyde‐free, strong, and water‐resistant adhesive model revealed that a combination of a polymer with catechol moieties and a polymer with amino groups could serve as a strong and water‐resistant wood adhesive. This study demonstrated that the treatment of abundant and readily available brown‐rot‐fungus‐decayed wood with NaBH₄ followed by mixing with polyethylenimine resulted in a formaldehyde‐free, strong, and water‐resistant wood adhesive.

Lignin is demethylated by brown‐rot fungi and then reduced using NaBH₄.     

新型金属-树脂间粘接性单体的合成与应用

甲基丙烯酰氧癸基硫脲嘧啶羧酸酯;粘接性单体;复合树脂;牙用合金;粘接性能     

Flexural Properties of Glass Fibre Reinforced Composite with Partially Biodegradable Polymer Matrix

Summary: The aim of this study was to evaluate flexural properties of a partially biodegradable glass fibre reinforced composite after water immersion and dehydration. In addition water sorption and solubility was determined. E-glass fibres were preimpregnated with a biodegradable biopolymer of poly(hydroxyproline) amide (PA). The preimpregnated fibres were then further-impregnated with Bis-GMA–TEGDMA-resin and light polymerized (n = 6). There was also specimen made of plain polymer and FRC without PA. After water immersion and/or dehydration, the specimens were tested by the three-point bending test. The flexural strength and Young's modulus was increased in most cases after water immersion and dehydration except for PA containing specimens. The water sorption was <50 µg/mm³ for all studied specimens and solubility was 20 µg/mm³ for specimens without PA and 35 µg/mm³ for specimens with PA.     

Introducing flexibility in urea–formaldehyde resins: Copolymerization with polyetheramines

Adhesives obtained by copolymerizing urea, formaldehyde, and difunctional polyetheramine with different molecular weights (230, 600, 900, and 2000 g mol⁻¹) are presented as a more resilient alternative to conventional urea–formaldehyde resins. Urea and polyetheramine contents were varied and the resulting resins characterized by FTIR, ¹³C‐NMR, and TGA. These resins were used for production of agglomerated cork panels, an application that demands that the binder system is flexible. Polyetheramine with molecular weight 900 g mol⁻¹ yielded the most promising agglomerated cork panel, with remarkable flexibility, good tensile strength, and with the E1 formaldehyde content specification for wood‐based panels used in construction, according to European Standard EN 12460‐5. These new thermoset adhesives have demonstrated to be capable of being used in systems where conventional formaldehyde‐based resins do not perform well due to inherent high rigidity. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 1834–1843     

Alumina additives for fast iron‐mediated AGET ATRP of MMA using onium salt as ligand

Three kinds of alumina (acidic, neutral, and basic Al₂O₃) were effective as additives for the control and rate enhancement of iron‐mediated AGET (activators generated by electron transfer) ATRP (atom transfer radical polymerization) of methyl methacrylate (MMA) in the presence of limited amount of air, using FeCl₃·6H₂O as the catalyst, tetrabutylammonium bromide or tetra‐n‐butylphosphonium bromide as the ligand, ethyl 2‐bromoisobutyrate as the initiator, and ascorbic acid as the reducing agent. The conversion could be up to 83.9% in the case of basic Al₂O₃ and 75.3% with neutral Al₂O₃ only in 13 h, respectively, whereas no polymer could be obtained even in 50 h without additives. The polymers obtained with neutral and basic Al₂O₃ had controlled molecular weights and low M_w/M_n values (～1.2). Tacticities of the as‐prepared PMMA in the presence of these three kinds of Al₂O₃ were consistent with that obtained from conventional free‐radical polymerization of MMA. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Synthesis and characterization of four alkyl 2‐cyanoacrylate monomers and their precursors for use in latent fingerprint detection

Four novel cyanoacrylates, 2‐cyanoethyl 2‐cyanoacrylate, 1‐cyanoethyl 2‐cyanoacrylate, trideuteromethyl 2‐cyanoacrylate and pentadeuteroethyl 2‐cyanoacrylate have been synthesized using a Diels‐Alder protection/deprotection route involving anthracene. The common route for the synthesis of alkyl 2‐cyanoacrylates was found to be unsatisfactory for the production of small quantities of the targeted cyanoacrylates, which have potential as reagents for the mid‐infrared spectral imaging of fingerprints on difficult surfaces. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010     

Antimicrobial modified hydroxyapatite composite dental bite by stereolithography

This study is aimed at the synthesis of antimicrobial hydroxyapatite (HAP)‐based composites for dental application by stereolithography (SLA). A micron‐sized commercial HAP was modified by methacrylate and quaternary ammonium salt, and, then, it was used in different amounts (namely 2.5, 5, and 10 wt%) as filler for a photocurable custom made resin for SLA. Thermal stability, microstructure, and particles size of the pristine (HAP) and modified HAP (mHAP) were evaluated by thermogravimetric analysis (TGA), X‐ray diffraction (XRD), and particle size analyser (CILAS). The suitability of each formulation for stereolithography process was assessed by measuring viscosity, degree of conversion (DC%) by Fourier transform infrared spectroscopy (FTIR), glass transition temperature, and thermal stability. Photo‐cured specimens for physical, mechanical, and antimicrobial testing were built by SLA. The flexural strength of the samples was measured using a 3‐point bending test method, and the fractured surface was analysed by scanning electron microscopy (SEM). The antimicrobial activity of samples was investigated against some standard microorganisms (Staphylococcus aureus, Escherichia coli, and Candida albicans), as representative Gram positive and Gram negative bacteria and fungus, respectively. The flexural strength increased with a filler content up to 5% and slightly decreased for higher content. SEM analysis confirmed the presence of uniformly distributed HAP. The incorporation of mHAP reduced the bacterial and fungal growth in dose‐dependent manner in comparison with the neat samples. Finally, a prototype of dental bite was built by SLA.     

Synthesis,photopolymerization, and adhesive properties of hydrolytically stable phosphonic acid‐containing (meth)acrylamides

Three novel dental monomers containing phosphonic acid groups ( 1a and 2a , based on diethyl amino(phenyl)methylphosphonate and 3a based on diethyl 1‐aminoheptylphosphonate) were synthesized in two steps: the reaction of α‐aminophosphonates with acryloyl chloride (for monomers 1a and 3a ) or methacryloyl chloride (for 2a ) to give monomers with phosphonate groups, and the hydrolysis of phosphonate groups by using trimethyl silylbromide. Their (and the intermediates') structures were confirmed by FTIR, ¹H, ¹³C, and ³¹P NMR spectroscopy. All the monomers dissolve well in water (1<pH<2) and are hydrolytically stable. Their homo‐ and copolymerizations with 2‐hydroxyethyl methacrylate (HEMA) and HEMA/glycerol dimethacrylate were investigated with photo‐DSC. Thermal polymerization of the new monomers in water or in ethanol/water solution was investigated, giving polymers in good yields. X‐ray diffraction results showed only dicalcium phosphate dehydrate formation upon interaction of 1a ‐ 3a with hydroxyapatite indicating its strong decalcification and that monomer‐Ca salts are highly soluble. Some results were also compared to those with a bisphosphonic acid‐containing methacrylamide ( 4a ) previously reported; and the influence of monomer structure on polymerization/adhesive properties is discussed. These properties, especially hydrolytic stability and good rates of polymerization, make these new monomers suitable candidates as components of dental adhesive mixtures. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 511–522     

Non-slipping adhesive contact between mismatched elastic spheres: A model of adhesion mediated deformation sensor

A generalized JKR model is established for non-slipping adhesive contact between two dissimilar elastic spheres subjected to a pair of pulling forces and a mismatch strain. We discuss the full elastic solution to the problem as well as the so-called non-oscillatory solution in which tension and shear tractions along the contact interface is decoupled from each other. The model indicates that the mismatch strain has significant effect on the contact area and the pull-off process. Under a finite pulling force, a pair of adhering spheres is predicted to break apart spontaneously at a critical mismatch strain. This study suggests an adhesion mediated deformation sensing mechanism by which cells and molecules can detect mechanical signals in the environment via adhesive interactions.