Viscoelastic Windows of Pressure-Sensitive Adhesives

A viscoelastic window (VW) concept has been proposed to identify different types of pressure-sensitive adhesives (PSA's). Such viscoelastic windows are constructed from the values of dynamic storage modulus: G' and dynamic loss modulus G' at frequencies of 10^-2 and 10² rad/sec. These frequencies are chosen because the range covers most of the time scales corresponding to the uses of PSA's at different application rates in performance tests. A four quadrant concept has also been recommended to categorize different types of PSA's based on the location of their VW's on the log-log cross plot of G' and G'. It was found that for most PSA's, the range of G' and G' at room temperature within these selected frequencies falls between 10³ and 10⁶ Pascals. The proposed four-quadrants (top-left hand quadrant of high G' and low G', top-right hand quadrant of high G' and high G', lower left hand quadrant of low G' and low G', and lower right-hand quadrant of low G' and high G') correspond respectively to (1) non-PSA or release coatings (2) high shear PSA's, (3) removable PSA's and medical PSA's and (4) quick and cold stick PSA's. It was also observed that the VW's of general purpose permanent PSA's occupy the central region which straddles part of the four quadrants.     

Miscibility and Probe Tack of Acrylic Pressure Sensitive Adhesives—Acrylic Copolymer/Tackifier Resin Systems

Miscibility between acrylic copolymers and tackifier resins are investigated in terms of phase diagrams, and the probe tack of the blends are measured as a function of both temperature and rate of separation in order to obtain the master curves. It is found that the probe tack of the pressure sensitive adhesives are closely related to the miscibility between the components. The master curves of the miscible blends shift along the X(rate)-axis according to the change of T_g of the bulk materials with a gradual variation of the peak heights. However, those of the immiscible blends will not shift along the X(rate)-axis, but the magnitude will decrease with increase of a dispersed phase.     

PSA performances and viscoelastic properties of SIS‐based PSA blends with H‐DCPD tackifiers

Hotmelt pressure sensitive adhesives (PSAs) usually contain styrenic block copolymers like styrene–isoprene–styrene (SIS), SBS, SEBS, tackifier, oil, and additives. These block copolymers individually reveal no tack. Therefore, a tackifier is a low molecular weight material with high glass transition temperature (T_g), and imparts the tacky property to PSA. The SIS block copolymer with different diblocks was blended with hydrogenated dicyclopentadiene (H‐DCPD tackifier), which has three kinds of T_g. PSA performance was evaluated by probe tack, peel strength, and shear adhesion failure temperature. PSA is a viscoelastic material, so that its performance is significantly related to the viscoelastic properties of PSAs. We tested the viscoelastic properties by dynamic mechanical analysis and the thermal properties by differential scanning calorimeter to investigate the relation between viscoelastic properties and PSA performance. © 2006 Wiley Periodicals, Inc. J Appl PolymSci 102: 2839–2846, 2006     

层间接触条件对沥青路面高温性能的影响研究

应用BISAR软件计算了不同层间接触条件下的沥青面层剪应力,通过直剪试验测定了洒布不同粘层材料的复合马歇尔试件的抗剪强度,并采用车辙试验测定复合式车辙板的DS和总变形量.研究结果表明:完全光滑的层间接触条件大幅提高了沥青面层的最大剪应力,加速沥青面层发生剪切破坏而出现车辙;粘层提高了层间抗剪强度,不同的粘层材料对层间接触条件的改善效果不同;高抗剪强度的层间接触能提高复合式车辙板的高温性能.     

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.     

Adhesion of a rigid punch to a confined elastic layer revisited

The adhesion of a punch to a linear elastic, confined layer is investigated. Numerical analysis is performed to determine the equivalent elastic modulus in terms of layer confinement. The size of the layer relative to the punch radius and its Poisson’s ratio are found to affect the layer stiffness. The results reveal that the equivalent modulus of a highly confined layer depends on its Poisson’s ratio, whereas, in contrast, an unconfined layer is only sensitive to the extent of the elastic film. The solutions of the equivalent modulus obtained from the simulations are fitted by an analytical function that, subsequently, is utilized to deduce the energy release rate for detachment of the punch via linear elastic fracture mechanics. The energy release rate strongly varies with layer confinement. Regimes for stable and unstable crack growth can be identified that, in turn, are correlated to interfacial stress distributions to distinguish between different detachment mechanisms.     

分子质量调节剂对丙烯酸酯乳液压敏胶性能的影响

采用预乳化半连续聚合法,合成了丙烯酸酯乳液压敏胶。探讨了叔十二烷基硫醇、2,4-二苯基-4-甲基-1-戊烯、乙二醇以及异丙醇等分子质量调节剂对压敏胶聚合稳定性、黏度、初粘性、持粘性和180o剥离强度的影响。结果表明,叔十二烷基硫醇和异丙醇对压敏胶的性能影响较大,2,4-二苯基-4-甲基-1-戊烯和乙二醇的影响较小;随分子质量调节剂用量增大,压敏胶的初粘性增大,持粘性和180o剥离强度先增大后降低,黏度先降低后又增大;加入2,4-二苯基-4-甲基-1-戊烯和异丙醇的乳液压敏胶聚合稳定性随分子质量调节剂用量增大而变差,加入叔十二硫醇的乳液压敏胶的聚合稳定性则随用量增大先变差后又增强,而乙二醇则与之相反。     

电子制造服务产业需求协同模型的构建与应用

运用象限分析法,以价值链为切入点,对电子制造服务产业需求管理中的主要指标,销售额比率、生产频率、生产时间进行分析.通过纵向分析历史数据,计算出客户平均的周需求量与销售比率,同时确定产品在需求协同模型中的位置,计算出生产频率和被均衡化的需求量.归纳了四大需求类型并建立适用于中国电子制造服务产业的需求协同模型.     

The influence of loose and semianchored siloxane polymer chains on the tack of crosslinked silicone rubber

The influence of addition of nonreactive silicone oil or semianchored silicone polymer on crosslinked poly(dimethylsiloxane) (PDMS) rubber–rubber adhesion was studied. The additives can be considered either a tackifier, or connector molecules, able to cross the interface and entangle. In both cases, it influences the tack of the elastomers. An additional variable is the molecular weight of the additive, which affects the reptation of the polymer chains. Polymer–polymer demixing, which is the result of thermodynamic incompatibility of mixed polymers is another factor that influences tack. It causes the free chains to appear at the surface forming a layer of oil, which actually destroys the tack of the PDMS samples. The resulting tack phenomena as a function of oil, respectively semianchored silicone polymer chains, are very much dependent on the transient nature of the polymer reptation: in many cases the polymers need very long time periods to obtain equilibrium in interphase crossing, or oil sweats out of the crosslinked polymers, forming a liquid layer between the two phases resulting in a low tack value, due to hydrodynamic wetting alone. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of molecular weight of epoxidized‐natural rubber on viscosity and tack of pressure‐sensitive adhesives

The effect of molecular weight of rubber on viscosity and loop tack of rubber‐adhesives were studied using two grades of epoxidized‐natural rubber, i.e., ENR 25 and ENR 50. Coumarone–indene resin, gum rosin, and petro resin were used as tackifiers. Toluene was used as the solvent throughout the experiment. The adhesive was coated on polyethylene terephthalate (PET) substrate using a SHEEN hand coater. Viscosity was determined by a HAAKE Rotary Viscometer, whereas loop tack was measured by a Llyod Adhesion Tester operating at 10 cm/min. Results show that viscosity increases gradually upto a critical molecular weight of 6.8 × 10⁴ and 3.9 × 10⁴ for ENR 25 and ENR 50, respectively, before a rapid increase in viscosity is observed. Loop tack indicates maximum value at the respective critical molecular weights for the three tackifiers investigated suggesting the culmination of wettability. For both rubbers, loop tack increases with coating thickness due to the concentration effect of adhesive. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010