Adhesion Properties of Acrylic Copolymers Modified with Si-Containing Copolymer

We made clear the cause of the increase in peel strength of pressure sensitive (PS) adhesives as a function of contact time, and investigated how to modify PS adhesives to maintain a low and constant peel strength for a long time. It was found that polar groups in the adhesive orient to the interface between the adhesive and the (stainless steel) metal substrate (SUS 304) so as to minimize interfacial free energy during adhesion, and the orientation increased affinity between the adhesive and the metal material and increased the peel strength as a result. The use of modifier which contained both P(MMA-co-SiMA) and PDMS showed an excellent modification effect, although modification with only PDMS or P(MMA-co-SiMA) was not sufficient. It was suggested that PDMS which migrated to the surface was extended uniformly over the surface by PDMS segments of P(MMA-co-SiMA) and that the enriched layer of PDMS on the adhesive surface worked as a barrier to prevent the orientation of polar groups in bulk. Therefore, low and constant peel strength could be achieved.     

Effects of surface modification by oxygen plasma on peel adhesion of pressure‐sensitive adhesive tapes

Surfaces of poly(isobutylene) (PIB) and poly(butylacrylate) (PBA) pressure‐sensitive adhesive tapes were treated by oxygen plasma, and effects of surface modification on their adhesive behavior were investigated from the viewpoint of peel adhesion. The peel adhesion between PIB and PBA pressure‐sensitive adhesive tapes and stainless steel has been improved by the oxygen plasma treatment. The surface‐modification layer was formed on PIB and PBA pressure‐sensitive adhesive surfaces by the oxygen plasma treatment. The oxygen plasma treatment led to the formation of functional groups such as various carbonyl groups. The treated layer was restricted to the topmost layer (50–300 nm) from the surface. The GPC curves of the oxygen plasma‐treated PBA adhesive were less changed. Although a degradation product of 1–3% was formed in the process of the oxygen plasma treatment of the PIB adhesive. There are differences in the oxygen plasma treatment between the PIB and PBA adhesives. A close relationship was recognized between the amount of carbonyl groups and peel adhesion. Therefore, the carbonyl groups formed on the PIB and PBA adhesive surfaces may be a main factor to improve the peel adhesion between the PIB and PBA adhesive and stainless steel. The peel adhesion could be controlled by changing the carbonyl concentration on the PIB and PBA adhesive surfaces. We speculate that the carbonyl groups on the PIB and PBA adhesive surface might provide an interaction with a stainless steel surface. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1392–1401, 2000     

Investigation of Polyimidesiloxanes for Use as Adhesives by Electron Spectroscopy for Chemical Analysis

Angle-dependent electron spectroscopy for chemical analysis (ESCA) was used to examine the air facing surface (20–100 Å thick) composition of polyimidesiloxanes with different processing variations, and of varying polydimethylsiloxane (PDMS) content and block length (number of PDMS repeat unit varies from 1 to 9). Polyimide was clearly detected (due to the nitrogen content) in the 20–100 Å surface regions. This shows that a small amount of PDMS and short PDMS segment lengths in polyimidesiloxanes give a surface region with both PDMS and polyimide present. The surface composition, particularly that in the ca. 100 Å region, was correlated to the peel strength of polyimidesiloxane melt pressed to a metal substrate. Our results suggest that both PDMS and polyimide are essential components to rendering a needed peel strength. PDMS, having a good diffusive ability, readily reaches the substrate upon being pressed, achieving intimate contact, while imide groups interact with the substrate, presumably through chemical bonding; these two factors act synergistically to result in a high peel strength. In addition, the interaction mechanism and the failure mechanism involved in bonding polyimidesiloxane and metal substrate were also elucidated based on the ESCA results.     

G／Epoxy复合材料胶接强度研究

使用G／Epoxy作为底材研究了垫板、结构胶黏剂厚度和底材表面处理对拉伸剪切强度的影响。使用光学显微镜观察了断口形貌。结果表明加垫板能减小试验过程中由于加载偏心引起剥离应力,测试结果较大;结构胶黏剂的厚度和底材表面处理对拉伸剪切强度影响十分明显,随着厚度的增大而减小,经打磨表面裸露出纤维的试样拉伸剪切强度很低。结构胶黏剂厚度较小时以内聚破坏为主,随着厚度的增加破坏模式转变为粘接破坏。     

The Effect of PEEK Fibres and Powder on Joints Made with a High Temperature Adhesive

High temperature adhesives typically exhibit low levels of peel strength since they tend to be more brittle than typical toughened adhesives used for lower temperature applications. It was found that incorporating thermoplastic fibres or powder into the bondline of a joint made with a high temperature epoxy-based adhesive resulted in significant improvements in peel strength. Poly(ether ether ketone) (PEEK) fibres and powder were incorporated into the adhesive resin and used in aluminium joints. These were tested in peel and single lap shear using a range of fibre lengths, orientations and volume fractions. It was seen that large increases in peel strength could be achieved but that lap shear strength was degraded with most types of modification. However, some modifications resulted in significant increases in peel strength with limited decrease in lap shear strength. These improved properties have been achieved using physical modifications rather than chemical alteration of the resin.     

Effects of nitrogen plasma treatment of pressure-sensitive adhesive layer surfaces on their peel adhesion behavior

The influence of the surface modification of pressure-sensitive adhesive tapes on their adhesion behavior has been investigated. PBA [poly(butyl acrylate)] and PIB [poly(isobutylene)] adhesives were chosen as pressure-sensitive adhesives and nitrogen plasma was used for the surface modification of the adhesives. The peel force of PBA or PIB adhesive/stainless steel joints was evaluated. The nitrogen plasma treatment showed large effects on the adhesion behavior of both the PBA and the PIB adhesives. The peel force for the PBA adhesive/stainless steel joint decreased by 57 times as a result of the nitrogen plasma treatment and that for the PIB adhesive/stainless steel joint increased by 2.2 times. There are essential differences in the modification reactions caused by the nitrogen plasma between the PBA and PIB adhesives. For the PBA adhesive, cross-linking reactions occurred among the PBA polymer chains and the surface was hardened. For the PIB adhesive, degradation reactions occurred and products with a low molecular weight were formed on the surface. These differences are due to the different responses of the PBA and PIB adhesives towards the nitrogen plasma. The mechanism of the changes in adhesion behavior caused by the nitrogen plasma is discussed.     

Design of experiments for optimization a biodegrable adhesive based on ramon starch (Brosimum alicastrum Sw.)

In this work, a Central Composite Design (CCD) and Response Surface Methodology (RSM) were used to study the effect of starch content, hydrolyzing agent (NaOH) content, temperature and cooking period on peel strength and shear strength of biodegradable adhesives based on Ramon (Brosimum alicastrum Sw.) and Corn (Zea mays L.) starch. Scribe® paper was used as substrate or adherent. The CCD consisted of 36 experiments (including 12 central points). The second-order regression models of the response surface method, used to predict the response variables, exhibited a high correlation between the data obtained and the predicted data, and were thus considered reliable to optimize the mechanical properties for peel strength and shear strength of the Ramon starch adhesives. Starch content, hydrolyzing agent content and the cooking temperature of the adhesives proved to be the most significant factors affecting peel strength and shear strength of the adhesives of both the Ramon and corn starch. Moreover, the interactions of Starch-NaOH and Starch-Temperature were found to be the most significant in the adhesive properties in both adhesives. The mechanical properties (peel strength and shear strength) of both adhesives increased until reaching approximately their temperatures of gelatinization (T _{RAMON GEL} = 83 °C, T _{GEL CORN} = 72 °C). At higher temperatures, the mechanical properties of the adhesives diminished. The results of this study show that the adhesive prepared with the Ramon starch presents adhesive properties similar to those of an adhesive prepared with corn starch. This would imply that the Ramon starch is a viable alternative to substitute corn starch in industrial applications not relating to food production.     

Preparation of high peel strength and high anti-aging epoxy adhesive that used for bonding aluminum alloy without surface treatment

In the case of bonding of aluminum alloy, surface pretreatment have been widely adopted for adherends so as to achieve superior adhesive performance. However, the strict surface treatment of the aluminum alloy cannot be implemented without special equipment and the mechanical properties, corrosion resistance and aging resistance of the common adhesives cannot meet the demand without surface treatment. Here, acrylic oligomer modified by carboxyl terminated organosilicon and nano alumina were used to modify an epoxy formulation based on a classical DGEBA monomer to produce a high peel strength epoxy adhesive that can be used without surface pretreatment. The peel strength and the shear strength of the adhesive could reach 7.18?N/cm and 18.75?MPa, respectively, and could be well maintained under ?70?°C and 100?°C. The novel adhesive also has good heat aging resistance, water resistance and artificial seawater resistance. SEM and XPS were used to investigate mechanism of aging resistance of modified adhesives without surface treatment.     

Adhesion at Poly(Butylacrylate)-Poly(Dimethylsiloxane) Interfaces

We present an investigation of the adhesion modulation mechanisms of silica-like nanoparticles (MQ resins) incorporated in polydimethylsiloxane (PDMS) elastomers and acrylic adhesives. The Johnson-Kendall-Roberts (JKR) test has been used to gain information on the both zero velocity and the velocity dependence of the adhesive strength, avoiding as much as possible contributions to the adhesive strength of bulk dissipation in the adhesive (which is not the case with peel tests). As the incorporation of the MQ resins into the elastomers deeply affects their own mechanical properties, the loading and unloading curves of small poly(butylacrylate) (PBA) lenses on either PDMS elastomers, adsorbed PDMS and pure MQ resin layers are compared in a systematic manner. The PBA chains are observed to have a neat affinity for the MQ resin nanoparticles. When MQ resins are present at the interface, they tend to prevent facture propagation, thus producing a larger deformation of the PBA lens. The modulation of adhesion is then dominated by the corresponding dissipation inside the acrylic adhesive.     

Adhesion at Poly(Butylacrylate)–Poly(Dimethylsiloxane) Interfaces

We present an investigation of the adhesion modulation mechanisms of silica-like nanoparticles (MQ resins) incorporated in polydimethylsiloxane (PDMS) elastomers and acrylic adhesives. The Johnson-Kendall-Roberts (JKR) test has been used to gain information on the both zero velocity and the velocity dependence of the adhesive strength, avoiding as much as possible contributions to the adhesive strength of bulk dissipation in the adhesive (which is not the case with peel tests). As the incorporation of the MQ resins into the elastomers deeply affects their own mechanical properties, the loading and unloading curves of small poly(butylacrylate) (PBA) lenses on either PDMS elastomers, adsorbed PDMS and pure MQ resin layers are compared in a systematic manner. The PBA chains are observed to have a neat affinity for the MQ resin nanoparticles. When MQ resins are present at the interface, they tend to prevent facture propagation, thus producing a larger deformation of the PBA lens. The modulation of adhesion is then dominated by the corresponding dissipation inside the acrylic adhesive.     

Influence of Dioctyl Maleate Concentration on Performance Behavior of Water Based Pressure-sensitive Adhesives via Reversible Addition–Fragmentation Chain Transfer Emulsion Polymerization

Reversible addition–fragmentation chain transfer (RAFT)-mediated polymerization was successfully applied for the synthesis of pressure-sensitive adhesives (PSAs) of predetermined molar mass and of low polydispersity index (PDI). The performances of the adhesives were investigated by testing tack, peel, and shear resistance on seven different substrates (coated paper, uncoated paper, polyethylene terephthalate (PET), biaxially oriented polyethylene terephthalate (BOPP), aluminum strip, low linear density polyethylene (LLDPE), and low density polyethylene (LDPE). The influence of monomer composition on the adhesive performance was evaluated by varying the molar ratio of butyl acrylate (BA)/dioctyl maleate (DOM) while keeping the molar ratio of acrylic acid (AA) and 2-hydroxy ethyl acrylate (2-HEA) constant. As the DOM content increased, shear, peel strength, and loop tack were found to increase. It was noted that the adhesive properties of PSAs can be tailored by incorporating small amounts of hydrophobic DOM into the PSAs, which significantly increases the peel and shear strength of the resulting PSAs. Carboxyl terminated bifunctional trithiocarbonate RAFT agent possess the strong potential to polymerize hydrophobic DOM in aqueous phase and exhibit better living character with PDI less than 1.5.     

Interphases in the Adhesive Bonding of Fluoropolymers

Strong and durable adhesive bonds may be made between polytetrafluoroethylene (PTFE) and either cyanoacrylate (CA) or epoxy adhesives, if the PTFE surface is modified by the use of a “primer” such as triphenylphosphine (TPP) or diaminodiphenylmethane (DDM). The primer mixes with the PTFE surface, and the modified surface is then capable of forming an interphase, tens to hundreds of nanometers thick, where interpenetration of the adhesive and adherend occurs. Using CA adhesives, PTFE/CA/PTFE block compression shear bond strength (ASTM D4501-85) of over 10 MPa can be achieved, with failure occurring cohesively. Initial work with epoxy adhesives indicates that the use of DDM primer gives adhesive bonds comparable in strength with those produced by modification of the fluoropolymer surface by sodium naphthalenide.     

Addition of Silica to Polyurethane Adhesives

The influence of the addition of silica (Aerosil-200) (5-25 wt%) to polyurethane adhesives on their adhesion properties with non-chlorinated and surface-chlorinated rubbers has been studied. The chlorinating agent was Trichloroisocyanuric acid (TIC) in 2-butanone solution at a concentration of between 1 and 9 wt%. In general, silica produced an increase in the adhesive viscosity and an improvement of green (immediate) peel strength (especially with chlorinated rubber). The best results were obtained for a silica content of 10-20 wt%. However, the addition of silica did not improve the peel strength after a thermal ageing process. Polyurethane adhesives containing silica undergo an improvement in their resistance to degradation by chlorine on the rubber surface. On the other hand, the chlorination of silica produces the rupture of Si-O bonds and the formation of Si-H and Si-Cl groups. Furthermore, the stirring speed (directly related to the dispersion) of silica into the adhesive is an important parameter which affects the viscosity and peel strength. A stirring speed of 1000 rpm gives the best silica dispersion.     

Addition of Silica to Polyurethane Adhesives

The influence of the addition of silica (Aerosil-200) (5-25 wt%) to polyurethane adhesives on their adhesion properties with non-chlorinated and surface-chlorinated rubbers has been studied. The chlorinating agent was Trichloroisocyanuric acid (TIC) in 2-butanone solution at a concentration of between 1 and 9 wt%. In general, silica produced an increase in the adhesive viscosity and an improvement of green (immediate) peel strength (especially with chlorinated rubber). The best results were obtained for a silica content of 10-20 wt%. However, the addition of silica did not improve the peel strength after a thermal ageing process. Polyurethane adhesives containing silica undergo an improvement in their resistance to degradation by chlorine on the rubber surface. On the other hand, the chlorination of silica produces the rupture of Si-O bonds and the formation of Si-H and Si-Cl groups. Furthermore, the stirring speed (directly related to the dispersion) of silica into the adhesive is an important parameter which affects the viscosity and peel strength. A stirring speed of 1000 rpm gives the best silica dispersion.     

Sensitivity and Optimization of Peel Strength Based on Composition of Adhesives for Footwear Industry

In order to contribute to the research and development of adhesives for the footwear industry, this paper aims to develop a model capable to predict and optimize the peel strength from the composition of adhesives. The proposed approach is based on three stages: experimental planning of measurements, global sensitivity analysis for uncertainty propagation, and optimization procedure. The design variables are the weight percentages of the solid raw material constituents such as polyurethane, resins, and additives of the adhesive joint. Considering the experimental results obtained for Taguchi design points as input/output patterns, an artificial neural network (ANN) is developed based on supervised evolutionary learning. Using the developed ANN a global sensitivity analysis procedure is implemented and the variability of the structural response of adhesive joint is studied. The optimal solution for adhesives composition for maximum peel strength is investigated based on ANN model and using a genetic algorithm. The proposed approach is able to predict the optimal peel strength including its sensitivity to uncertainties. The results show that the sensitivities of design variables belonging to polyurethane and additive groups are important for optimal adhesive joint. The optimal peel strength based on proposed approach is consistent with the experimental testing data.     

Effect of Cross-Linking on Tack and Peel Strength of Polymers

In this work the influence of cross-linking on the adhesive fracture energy and the peel strength is studied choosing polydimethylsiloxane (PDMS) as a model polymer. A series of samples was prepared by electron-beam irradiation which covers the whole range from a viscoelastic liquid to a cross-linked rubber. The mechanical behaviour of these PDMS samples was characterized by mechanical spectroscopy. Tack measurements with an instrument described elsewhere⁵ and peel measurements show that the adhesive fracture energy after short contact times as a measure of tack and the peel strength have a pronounced maximum in the range above the gel point, where the PDMS consists of a very loose and imperfect network and a high fraction of soluble polymer. In this range debonding is connected with the formation of fibrillar structures within the polymer.     

Effect of adhesive thickness and surface roughness on the shear strength of aluminium one-component polyurethane adhesive single-lap joints for automotive applications

Adhesively bonded technology is now widely accepted as a valuable tool in mechanical design, allowing the production of connections with a very good strength‐to‐weight ratio. The bonding may be made between metal–metal, metal–composite or composite–composite. In the automotive industry, elastomeric adhesives such as polyurethanes are used in structural applications such as windshield bonding because they present important advantages in terms of damping, impact, fatigue and safety, which are critical factors. For efficient designs of adhesively bonded structures, the knowledge of the relationship between substrates and the adhesive layer is essential. The aim of this work, via an experimental study, is to carry out and quantify the various variables affecting the strength of single-lap joints (SLJs), especially the effect of the surface preparation and adhesive thickness. Aluminium SLJs were fabricated and tested to assess the adhesive performance in a joint. The effect of the bondline thickness on the lap-shear strength of the adhesives was studied. A decrease in surface roughness was found to increase the shear strength of the SLJs. Experimental results showed that rougher surfaces have less wettability which is coherent with shear strength tests. However, increasing the adhesive thickness decreased the shear strength of SLJs. Indeed, a numerical model was developed to search the impact of increasing adhesive thickness on the interface of the adherend.     

Surface Modification of Epoxy Resin with Silicone-containing Block Copolymers

In order to improve oil and water repellency, silicone-containing block copolymers, composed of methylmethacrylate (MMA), glycidylmethacrylate (GMA), and polydimethylsiloxanemethacrylate (SMA), were blended in an epoxy resin. It was expected that the low surface energy dimethylsiloxane segments would adsorb and orient at the exterior of the resin to make a thin surface phase and the glycidyl groups would mesh with the epoxy resin by primary bonding. The techniques of X-ray photoelectron spectroscopy (ESCA), dynamic contact angle (DCA) and peel strength measurements of pressure sensitive adhesives were used to characterize the modified epoxy resin surface phases. The amount of Si_2p obtained via angular dependent ESCA investigation in the near surface region of the modified resin increased with decreasing sampling depth. With an increase in modifier content, both the amount of Si_2p and O_1s also increased. Both advancing and receding contact angles for an aluminum plate coated with modified resin, measured by dipping into and out of water, increased with the addition of these modifiers. The peel strength of a pressure sensitive adhesive tape affixed to the modified epoxy resin decreased dramatically with increasing modifier content. It was found that these copolymers were good surface modifiers to improve oil and water repellency and that they acted as release agents.     

Surface modification using bio‐inspired adhesive polymers based on polyaspartamide derivatives

The catechol functional group of dopamine (3,4‐dihydroxyphenethylamine) has the ability to form strong adhesive bonds to inorganic and organic surfaces in aqueous environments. In this study, novel adhesive polyaspartamides containing catechol pendant groups were synthesized from polysuccinimide through successive aminolysis reactions with quantitative dopamine and ethylenediamine. The adhesion and crosslinking of dopamine‐modified polyaspartamide in aqueous alkaline media was used successfully to modify the surface of various materials (including synthetic polymers, metals, metal oxides, ceramics) using a simple immersion method. Contact angle measurements, SEM and X‐ray photoelectron spectroscopy of the modified surfaces were used to verify the surface coating on a variety of materials with very different inherent wetting properties. These novel biocompatible polymers have potential industrial and biomedical applications as adhesives or coating materials for functional surface modification. Copyright © 2011 Society of Chemical Industry     

Polyester Polyol-Based Polyurethane Adhesive; Effect of Treatment on Rubber Surface

Polyester polyols were synthesized using vegetable oil fatty acids having different characteristics (mainly in terms of hydroxyl functionality) and epoxy resin, using triethylamine as a catalyst. Polyols were characterized by the FTIR spectroscopy. Polyurethane adhesives were synthesized from it and used in bonding rubber. Treatment of sulphuric acid on the non-polar styrene butadiene rubber (SBR) surface was studied for the bond strength improvement via an increase in wettability of the rubber surface. Wettability was found by measuring the contact angle using Goniometer. Bond strength was evaluated by a 180° T-peel test. The surface modification and mode of bond failure were studied by Scanning Electron Microscopy (SEM). The synthesized polyurethane adhesives were compared with the commercial adhesive.