Improvement of adhesion and paint ability of EVA copolymers with different vinyl acetate contents by treatment with UV-ozone

The surface modifications produced by UV-ozone treatment of two ethylene-vinyl acetate (EVA) copolymers containing 12 and 20 wt% vinyl acetate (EVA12 and EVA20 respectively) were studied. The treatment with UV-ozone improved the wettability of both EVAs due to the creation of new carbon–oxygen moieties. The extent of these modifications increased with increasing length of the treatment and the modifications produced in EVA20 were produced for shorter lengths of treatment. The UV-ozone treatment also created roughness and heterogeneities on the EVA surfaces. Whereas roughness formation prevailed on the UV-ozone treated EVA12, important ablation was dominant on the treated EVA20. T-peel strength values in joints made with polychloroprene adhesive increased when the EVAs were treated with UV-ozone. Short length of UV-ozone treatment (1 min) produced higher T-peel strength in joints made with EVA20 whereas higher T-peel strength values in joints made with EVA12 were obtained after treatment for 5–7.5 min in which a cohesive failure into a weak boundary layer on the treated EVA surface was found. Furthermore, the adhesion of UV-ozone treated EVA20 to acrylic paint increased. Finally, the ageing resistance of the treated EVA/polychloroprene adhesive joints was good and the surface modifications on the UV-ozone treated EVAs lasted for 24 h after treatment at least.     

Assessment of local strain field in adhesive layer of an unsymmetrically repaired CFRP panel using digital image correlation

The present study focuses on experimental investigation of through the thickness displacement and strain field in thin adhesive layer in single sided (unsymmetrical) patch repaired CFRP (carbon fiber reinforced polymer) panel under tensile load. Digital image correlation (DIC) technique is employed to acquire the displacement and strain (longitudinal, peel and shear) field. Experimental determination of shear transfer length based on shear strain field obtained from DIC is introduced to estimate the optimum overlap length which is an essential parameter in patch design for the repair of CFRP structures. Further, DIC experiment with magnified optics is performed to get an insight into complex and localized strain field over thin adhesive layer especially at critical zones leading to damage initiation. The failure mechanism, load displacement behavior, damage initiation and propagation are closely monitored using DIC. The influence of patch edge tapering on strain distribution in adhesive layer is also investigated. The DIC successfully captures the global and localized strain field at critical zones over thin adhesive layer and further helps in monitoring the damage based on strain anomalies. Strains are found to have maximum magnitude at the patch overlap edge and the shear strain level in adhesive layer is higher than the peel strain. Normal tapering increases the peel strain and has negligible influence on shear strain level in adhesive layer. The recommended overlap length is found to be consistent with the recommendation in the literature. Whole field strain pattern and the overlap length obtained from experiment are further compared with the finite element analysis results and they appear to be in good coherence.     

微波复合介质基板性能研究

采用微扰法、螺旋圆柱谐振法和带状线谐振法分别对聚四氟树脂复合精细电子陶瓷微波复合介质的复介电常数进行了测量与误差分析。基于扫描电子显微镜 (SEM )观察 ,从微观上解释了辊压工艺对介质介电性能一致性改善的原因。研究了不同的表面处理方法对基板金属化剥离强度的影响规律。     

ANALYTICAL SOLUTIONS FOR PEELING USING BEAM-ON-FOUNDATION MODEL AND COHESIVE ZONE

When fibrillation occurs during peeling, the normal stress in the adhesive may gradually reduce to zero at the peel front. The shear stress also reduces to zero. Classical beam-spring (or beam-on-elastic-foundation) models do not yield solutions that have these properties. With the use of a beam-on-foundation model combined with a cohesive zone in the neighborhood of the peel front, these properties can be satisfied. In order to obtain analytical solutions, peel tests are considered in which the backing has a small slope and is linearly elastic in the adhered region, and the traction law is assumed to be piecewise linear. Cases are considered with only normal stresses in the adhesive (mode I), only shear stresses (mode II), and both stresses coupled (mixed-mode behavior). Analytical solutions are obtained for displacements of the backing, forces in the backing, and stresses between the adhesive and the backing.     

A numerical analysis of the elastic-plastic peel test

The adhesive fracture energy, G_c, is determined from two types of elastic-plastic peel tests (i.e. the single-arm 90° and T-peel methods) and a linear-elastic fracture-mechanics (LEFM) test method (i.e. the tapered double-cantilever beam, TDCB method). A rubber-toughened epoxy adhesive, with both aluminium-alloy and steel substrates, has been used in the present work to manufacture the bonded joints. The peel tests are then modelled using numerical methods. The overall approach to modelling the elastic-plastic peel tests is to employ a finite-element analysis (FEA) approach and to model the crack advance through the adhesive layer via a node-release technique, based upon attaining a critical plastic strain in the element immediately ahead of the crack tip. It is shown that this ‘critical plastic strain fracture model (CPSFM)’ results in predicted values of the steady-state peel loads which are in excellent agreement with the experimentally-measured values. Also, the resulting values of G_c, as determined using the FEA CPSFM approach, have been found to be in excellent agreement with values from previously-reported analytical and direct-measurement methods. Further, it has been found that the calculated values of G_c are independent of whether a standard LEFM test or an elastic-plastic peel test method is employed. Therefore, it has been demonstrated that the value of the adhesive fracture energy, G_c, is independent of the geometric parameters studied and the value of G_c is indeed a characteristic of the joint, in this case for cohesive fracture through the adhesive layer. Finally, it is noted that the FEA CPSFM approach promises considerable potential for the analysis of peel tests which involve very extensive plastic deformation of the peeling arm and for analysing, and predicting, the performance of more complex adhesively-bonded geometries which involve extensive plastic deformation of the substrates.     

Characterization and application of propylene grafted hydrogenated dicyclopentadiene hydrocarbon resin

Hydrocarbon resins, which are defined as low molecular weight, amorphous, and thermoplastic polymers, are widely used as tackifiers for various types of adhesives, as processing aids in rubber compounds, and as modifiers for paint and ink products, and for use in plastics polymers such as isotactic polypropylene. Recently, the quantities of the hydrocarbon resin׳ raw materials which are the side products from naphtha cracking process have decreased because of light-feed cracking such as gas cracking, so new raw materials for hydrocarbon resin production are essential. To be satisfied with the previously mentioned factors, the substitution of hydrocarbon resin raw materials with renewable resources is a worthy consideration. Moreover, new hydrocarbon resin having high adhesion performance, low specific gravity, and good compatibility with various polymers has been requested in various adhesives.To meet those requests, in this study, propylene instead of side product from naphtha cracking as main raw material of hydrocarbon resin were partially used. The propylene serves as a new, sustainable raw material and was successfully grafted onto dicyclopentadiene. The reaction of the propylene with dicyclopentadiene was confirmed because, according to NMR and FT-IR analyses, a pendant methyl-propylene group exists in the structure of the propylene-grafted, hydrogenated dicyclopentadiene hydrocarbon resin. To establish an optimal production condition regarding the propylene-grafted, hydrogenated dicyclopentadiene hydrocarbon resin, numerous experiments were conducted according to the mole ratio of the raw materials and the polymerization temperature. The propylene-grafted, hydrogenated dicyclopentadiene hydrocarbon resin that was manufactured according to optimal conditions results in a lower specific gravity and a high molecular weight, whereby the advantages of the adhesion properties of an SIS-based pressure-sensitive-adhesive are exploited. When the propylene-grafted, hydrogenated dicyclopentadiene hydrocarbon resin was formulated with the SIS-based pressure-sensitive-adhesive, both the heat stability and the shear-adhesion strength are sound.     

Preparation of pressure-sensitive adhesives from tung oil via Diels-Alder reaction

In this study, tung oil was polymerized with a dimaleimide (4,4’-methylene-bis(N-phenylmaleimide) (MPMI) and two diacrylates (poly(propylene glycol) diacrylate (PPGDA) and bisphenol A glycerolate diacrylate (BPAGDA) via Diels-Alder reaction (DA reaction) to prepare pressure-sensitive adhesives (PSAs). On the one hand, the polymer of tung oil and MPMI was readily prepared however it was too rigid to serve as a PSA. On the other hand, the polymerization of tung oil with PPGDA or BPAGDA resulted in PSAs with peel strengths ranging from 0.1 to 0.2 N cm⁻¹ and loop tacks ranging from 0.4 to 0.5 N. Nevertheless, tung oil reacted readily with acrylic acid to form adducts (TOAA) with lower content of conjugated diene groups than those of tung oil. The use of TOAAs instead of tung oil to polymerize PPGDA failed to increase the peel strength of the resulting PSAs. However, polymerizations of TOAAs with BPAGDA resulted in PSAs with much higher peel strengths and much higher loop tacks than the polymerization of tung oil with BPAGDA. In addition, the introduction of a small amount of MPMI in the polymerization of TOAA and PPGDA significantly shortened the curing time.     

Evaluation of the Chemical Composition and Antioxidant Activity of the Peel Oil of Citrus nobilis

Peel oil of Citrus nobilis (Lour) was analyzed for determining its chemical composition. Fourteen identified components accounted for 99.1% (GC) and 100.0% (FID) of the total oil. Major component of the oil was limonene (76.8%-GC and 86.2%-FID). Essential oil was also evaluated for its antioxidant activity in four complementary test systems namely; β-carotene/linoleic acid, DPPH radical scavenging, reducing power and metal chelating activities. In the first system, antioxidant activity increased with the increasing concentration. At 20.0 mg.ml^?1 concentration, antioxidant property of the oil was 96.8% ± 0.2 and as strong as the positive controls BHT and α-tocopherol. Scavenging effect of the oil was superior to the positive controls BHT and α-tocopherol at 1.5 mg.ml^?1 concentration (96.4% ± 0.1). Reducing power and chelating effect of the essential oil increased with the increasing concentration.     

石榴皮提取物体外抗氧化活性比较研究

研究石榴皮提取物的体外抗氧化作用。采用羟自由基(.OH)、超氧阴离子自由基(.O2-)、2,2-二苯代苦味酰基自由基(DPPH.)的生成体系,研究石榴皮提取物及绿茶多酚、没食子酸为对照,对自由基的清除能力和对小鼠肝组织匀浆脂质过氧化抑制作用。结果表明:石榴皮提取物对羟自由基、超氧阴离子、DPPH.的半清除率分别为I:C50=71.37 mg/mL、SC50=557.55 mg/mL、DC50=31.98 mg/mL;没食子酸对这3种自由基的半清除率分别为I:C50=51.85 mg/mL、SC50=289.2 mg/mL、DC50=37.65 mg/mL;绿茶多酚对这3种自由基的半清除率分别为:IC50=66.67 mg/mL、SC50=1043.91 mg/mL、DC50=22.48 mg/mL。石榴皮提取物对小鼠肝组织匀浆的脂质过氧化半抑制率EC50=5.21 mg/mL、没食子酸半抑制率EC50=22.82 mg/mL、绿茶多酚半抑制率EC50=3.47 mg/mL。研究表明石榴皮提取物较没食子酸和绿茶多酚具有良好的清除自由基及抑制脂质过氧化的能力。石榴皮提取物能有效清除羟自由基、超氧阴离子自由基、DPPH.自由基,抑制脂质过氧化作用,具有进一步研究和开发价值。     

Influence of the interfacial composition on the adhesion between aggregates and bitumen: Investigations by EDX, XPS and peel tests

The study of the adhesion between aggregates and bitumen is necessary to enhance the lifetime of the roads. The purpose of this work concerns the interaction between the mineralogy of the aggregates and the adhesion force measured at the interface between bitumen and aggregate. The adhesion of bitumen was studied according to the mineralogy of the aggregates, which were made of dolomite rock or granite. A method was developed to measure the fracture energy during the peeling of the bitumen layer from the aggregate surface. The specific manufacturing of the samples ensured reproducible measurements using a constant thickness of the bitumen layer and by introducing a strengthened and flexible membrane into the bulk of bitumen. The peeling results demonstrated that the locus of the failure varied according to the mineralogy of the aggregate. The failure was cohesive during the peeling of the dolomite/bitumen system while the failure was partly interfacial concerning the granite/bitumen system. The interface between bitumen and minerals was characterized, before and after peeling. In case of the granite, the detection of sulfur by X-ray Photoelectron Spectroscopy (XPS) highlighted only the bitumen residues and allowed identifying the mineral compounds that weaken the interface between bitumen and granite. Finally, XPS analyses showed that the alkali feldspars of the granite induced a weak interface with bitumen.