Relevant bibliographies by topics / Pressure-sensitive adhesives

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Pressure-sensitive adhesives'

Author: Grafiati
Published: 4 June 2021
Last updated: 29 July 2024

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Journal articles on the topic "Pressure-sensitive adhesives"

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Creton, Costantino. "Pressure-Sensitive Adhesives: An Introductory Course." MRS Bulletin 28, no. 6 (June 2003): 434–39. http://dx.doi.org/10.1557/mrs2003.124.

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AbstractSelf-adhesive materials are called, in the adhesives trade, “pressure-sensitive adhesives” (PSAs). PSAs are designed to stick on almost any surface by simple contact under light pressure. This special class of adhesives does not undergo any physical transformation or chemical reaction during the bonding process. Because of this, the rheological properties of the adhesive must be finely tuned for the application, combining a carefully chosen polymer architecture and monomer composition with the proper addition of small molecules called tackifying resins. PSAs are soft, deformable solids and, depending on the formulation, easily form bridging fibrils between two surfaces upon debonding. They are safe to use and easy to handle and thus are increasingly replacing more conventional types of adhesives. In this article, we review both the primary material characteristics of PSAs and the main physical principles that make them work effectively.
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Xu, Chen, and Yong Shen. "Biomass-sourced polymers for pressure-sensitive adhesive applications." E3S Web of Conferences 394 (2023): 01008. http://dx.doi.org/10.1051/e3sconf/202339401008.

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Pressure-sensitive adhesives are self-adhesive chemical products that have gradually supplanted traditional glues in recent years. Most of the commercially available pressure-sensitive adhesives are derived from petrochemical resources. The increasing attention to environmental protection, coupled with the introduction of stringent regulations and rising oil prices, has led to widespread attention being paid to the development of sustainable pressure-sensitive adhesives from biomass sources. This paper summarizes the biomass-sourced pressure-sensitive adhesives and their modification methods that have been reported in recent years as promising alternatives to petrochemical resources.
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Crosby, Alfred J., and Kenneth R. Shull. "Adhesive failure analysis of pressure-sensitive adhesives." Journal of Polymer Science Part B: Polymer Physics 37, no. 24 (December 15, 1999): 3455–72. http://dx.doi.org/10.1002/(sici)1099-0488(19991215)37:24<3455::aid-polb7>3.0.co;2-3.

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Kuo, Chung-Feng Jeffrey, Wei Lun Lan, Jui-Wen Wang, John-Ber Chen, and Pin-Hua Lin. "Hot-melt pressure-sensitive adhesive for seamless bonding of nylon fabric Part II: Process parameter optimization for seamless bonding of nylon fabric." Textile Research Journal 89, no. 12 (July 31, 2018): 2294–304. http://dx.doi.org/10.1177/0040517518790970.

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This study develops hot melt pressure sensitive adhesives (HMPSAs) for the seamless bonding of nylon fabric, using butyl acrylate as the main monomer material and mixing the functional monomer for polymerization. It is combined with 2-10phr diphenyl (2,4,6-trimethylbenzoyl) phosphine oxide for the photoinitiator and ultraviolet irradiation is used to make a pre-polymer. The effects of butyl acrylate content, type of functional monomer, and 2-10phr diphenyl (2,4,6-trimethylbenzoyl) phosphine oxide content on the molecular weight of acrylate pre-polymer are discussed, following the Taguchi method. The pre-polymer is then mixed with the reactive diluent glycidyl methacrylate blend and with 2-10phr diphenyl (2,4,6-trimethylbenzoyl) phosphine oxide, coated on a release film, irradiated by ultraviolet light, and cured into hot melt pressure sensitive adhesives. The adhesive properties of hot melt pressure sensitive adhesive bonding on nylon include the peel strength, the shear strength, adhesive warpage, adhesive color difference, and adhesive overflow, which are discussed following the Taguchi method and the elimination and choice translating reality method for multi-quality analysis. Hot melt pressure sensitive adhesives are implemented by optimization parameters for practical validation. The results show that the peel strength of hot melt pressure sensitive adhesives is 1.495 kg/cm, the shear strength of hot melt pressure sensitive adhesives is 14.326 kg/cm2, adhesive warpage is 0.93 mm, adhesive color difference is 1.66, and adhesive overflow is 0.97 mm. The performance of HMPSAs in this study is enhanced effective.
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Mozelewska, Karolina, and Adrian Krzysztof Antosik. "Influence of Silicone Additives on the Properties of Pressure-Sensitive Adhesives." Materials 15, no. 16 (August 19, 2022): 5713. http://dx.doi.org/10.3390/ma15165713.

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Research was carried out on the influence of various silicone compounds on the properties of pressure-sensitive adhesives. Silicone-based pressure-sensitive adhesives have good self-adhesive properties and are used in many different industries. However, their thermal resistance is relatively low. In order to improve this property, modifications were made to these adhesives. Compositions were tested, such as viscosity or thermogravimetric analysis, as well as tests of finished products in the form of self-adhesive tapes, i.e., peel adhesion, tack, cohesion at room and elevated temperature, SAFT test (Shear Adhesive Failure Temperature), pot-live (viscosity) and shrinkage. During the tests, an increase in thermal resistance (225 °C), lower shrinkage (0.08%), and lower viscosity was achieved (16.5 Pas), which is a positive phenomenon in the technology of pressure-sensitive adhesives. Thanks to this research, the properties of silicone self-adhesive adhesives have been significantly improved.
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Czech, Zbigniew, Robert Pełech, Agnieszka Kowalczyk, Arkadiusz Kowalski, and Rafał Wróbel. "Electrically conductive acrylic pressure-sensitive adhesives containing carbon black." Polish Journal of Chemical Technology 13, no. 4 (January 1, 2011): 77–81. http://dx.doi.org/10.2478/v10026-011-0053-2.

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Electrically conductive acrylic pressure-sensitive adhesives containing carbon black Acrylic pressure-sensitive adhesives (PSA) are non electrical conductive materials. The electrical conductivity is incorporated into acrylic self-adhesive polymer after adding electrically conductive additives like carbon black, especially nano carbon black. After an addition of electrical conductive carbon black, the main and typical properties of pressure-sensitive adhesives such as tack, peel adhesion and shear strength, are deteriorated. The investigations reveals that the acrylic pressure-sensitive adhesives basis must be synthesised with ameliorated initial performances, like high tack, excellent adhesion and very good cohesion. Currently, the electrical conductive solvent-borne acrylic PSA containing carbon black are not commercially available on the market. They are promising materials which can be applied for the manufacturing of diverse technical high performance self-adhesive products, such as broadest line of special electrically conductive sensitive tapes.
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Antosik, Adrian Krzysztof, Karolina Mozelewska, and Konrad Gziut. "Influence of UV on the self-adhesive properties of silicone pressure-sensitive adhesives." Polimery 68, no. 1 (January 19, 2023): 19–24. http://dx.doi.org/10.14314/polimery.2023.1.3.

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The paper presents the results of research on the UV radiation influence on the self-adhesive properties of silicone adhesives. The adhesives were obtained by cross-linking commercial resins (PSA 590, Q2-7566) at the temperature of 110°C, using different amounts (0–3 wt%) of bis(2,4-dichlorobenzoyl) peroxide. Self-adhesive properties of adhesives such as adhesion, tack, and durability before and after aging were determined. The adhesives showed stable self-adhesive properties, however, the PSA 590 adhesive had a higher maximum operating temperature than the Q2-7566 adhesive.
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Mobley, L. W. "Pressure Sensitive Polyurethane Adhesives." Journal of Cellular Plastics 27, no. 1 (January 1991): 47–48. http://dx.doi.org/10.1177/0021955x9102700155.

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Comyn, John. "Pressure-sensitive adhesives technology." International Journal of Adhesion and Adhesives 17, no. 4 (November 1997): 382. http://dx.doi.org/10.1016/s0143-7496(97)00034-1.

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Antosik, Adrian Krzysztof, Artur Grajczyk, Marzena Półka, Magdalena Zdanowicz, John Halpin, and Marcin Bartkowiak. "Influence of Talc on the Properties of Silicone Pressure-Sensitive Adhesives." Materials 17, no. 3 (February 1, 2024): 708. http://dx.doi.org/10.3390/ma17030708.

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The article describes new silicone self-adhesive adhesives modified with the addition of talc. The obtained self-adhesive materials were characterized to determine their adhesive properties (adhesion, cohesion, and adhesion) and functional properties (pot life of the composition, shrinkage, and thermal properties of adhesives). Novel materials exhibited high thermal resistance above 225 °C while maintaining or slightly reducing other values (adhesion, cohesion, shrinkage, and tack). Selected composition: T 0.1 was used to prepare self-adhesives in industrial-scale production. Moreover, conducted test results revealed that the addition of talc delayed the thermal decomposition of the adhesive and provided reduced intensity of smoke emissions during combustion as well as the flammability of the adhesive layer.
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Dissertations / Theses on the topic "Pressure-sensitive adhesives"

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Akogyeram, Samuel. "Bonding and debonding mechanism of pressure sensitive adhesives." Thesis, Brunel University, 2010. http://bura.brunel.ac.uk/handle/2438/12765.

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Pressure-sensitive adhesives (PSAs) are complex macromolecular-based blend formulations that, in dry form will adhere permanently to diverse surfaces with the application of mere finger pressure. This thesis addresses the bonding and debonding mechanisms of coated films of different commercially available PSAs by systemically investigating the film characteristics on multiple levels. The methods implemented involve a novel procedure in investigating viscoelastic properties with Dynamic Mechanical Analysis, film surface chemistry with Time-of-flight Secondary Ion Mass Spectrometry and film morphology, modulus and bonding characteristics with Atomic Force Microscope. The theoretical aspect invoked rubber elasticity, viscoelasticity and thermodynamic concepts in representation of film morphology with corresponding adhesion nature. The results indicate that the bonding and debonding behaviour of PSA films are of a viscoelastic nature, dictated mainly by two fundamental morphological elements. These elements are; (1) the formation of phase-separated self-assembly of polystyrene-richcopolymer nano-domains within the adhesive matrix and (2) the inter-linking of the nanodomains by elastically active elastomer segments into a physical crosslinked network system that is highly efficient in dissipating large strain energy. These morphological factors are manifested through a profound contribution to the peel strength of the adhesive films when either coated at high temperatures or annealed. Increasing the content of the polystyrene endblock-tackifier in the adhesive blend formulation increased the PSA’s performance sensitivity to the film coating temperature. Meanwhile increasing the cis-C=C bond concentration in the formulation reduced the film’s performance sensitivity to coating temperature, as polydienes are premised to promote the entropy-elasticity of the film matrix by contributing to the nano-domain interconnections. This thesis generates many qualitative similarities, despite the significantly different adhesive blends investigated and hopefully the results reported here are more universal than one might expect.
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Roberge, Stephane. "Styrenebutyl acrylate mini-emulsion-based pressure sensitive adhesives." Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/27022.

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Adhesives are defined as substances capable of holding at least two surfaces together. A class of adhesives called pressure-sensitive adhesives (or PSAs) is characterized by instantaneous adhesion upon application of light pressure. In order to develop new application-specific products and improve existing processes, there is a need to identify the factors that influence the performance of PSAs. Operating conditions like feed composition, temperature, and solid content will affect latex properties such as copolymer composition, molecular weight distribution (MWD) and particle size distribution (PSD). Those latex properties can in turn affect the performance of the adhesive. Because of environmental concerns and government regulations to substitute solvent-based systems by water-borne products, there is a growing interest in producing such PSAs by emulsion (or mini-emulsion) polymerization. Mini-emulsions allow for improved control over the PSD compared to conventional emulsion polymerizations. Coupled with control over the MWD and copolymer composition, mini-emulsions could offer the possibility of tailoring the desired properties of PSAs. It was of interest in this thesis, to measure the effect of varying particle size and copolymer composition on adhesive properties. Based on this primary objective, a series of styrene/butyl acrylate mini-emulsion copolymerizations were carried out in a 1.2L stainless steel reactor. (Abstract shortened by UMI.)
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Jovanovic, Renata. "Butyl acrylatevinyl acetate emulsion-based pressure sensitive adhesives." Thesis, University of Ottawa (Canada), 2004. http://hdl.handle.net/10393/29120.

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Pressure-sensitive adhesives (PSAs) are adhesives that bond upon application of light pressure. With applications ranging from everyday home and office supplies to bioelectrodes and spaces shuttle parts, PSAs are among the fastest growing adhesive markets. Emulsion polymerization is increasingly used for the production of PSAs due to its higher environmental compliance as well as other advantages (e.g. lower energy consumption, lower capital costs...) compared to other technologies. However, there is a considerable lack of the integration of different areas of knowledge required for the production of PSAs using this technology. Process conditions (e.g. feed composition, temperature, solids content...) are only one area of interest. These conditions will result in inherent polymer properties (e.g. composition, molecular weight distribution, particle size distribution, gel content...), which govern final product properties (e.g. loop tack, peel and shear strength). Better understanding of each area separately (e.g. process parameters, inherent polymer properties, final product properties) and finally, their integration will lead to the improvement of existing and development of new emulsion-based products and processes. In this work, the above-mentioned three areas of PSA production were investigated for butyl acrylate/vinyl acetate emulsion-based polymers. The objectives were to investigate different variables affecting polymerization process, polymer and adhesive properties. The ultimate objective was to develop empirical models that will incorporate these variables to enable better prediction of the PSA properties. The knowledge gained during building of empirical models could later be used for development of mechanistic ones. In this work a screening design was used first to manipulate eight different process variables in order to generate a wide range of inherent polymer properties and final PSA properties. The properties obtained ranged from good, to moderate and to less desirable. However, the major obstacle in this step was the presence of different modes of failure for the same type of adhesive tests. Under these conditions, modeling was not possible due to the lack of a uniform failure mode in all PSA tests. (Abstract shortened by UMI.)
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Nasiri, Anahita. "The Use of Lignin in Pressure Sensitive Adhesives and Starch-Based Adhesives." Thesis, Université d'Ottawa / University of Ottawa, 2019. http://hdl.handle.net/10393/39853.

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After cellulose, lignin is the second most abundant natural polymer in the world. It has multiple functional groups, providing great potential for polymer production. In this project, we explored the use of this renewable and valuable resource in two different adhesive applications to displace petroleum-based additives, thereby providing a more sustainable and “green” product. In this regard, two types of lignin, water-soluble (Amalin LPH) and non-water-soluble lignin (Amalin HPH) provided by the British Columbia Research Institute (BCRI) were used. In the first case, lignin was added to a pressure-sensitive adhesive (PSA) formulation via in-situ seeded semi-batch emulsion polymerization. It was seen that lignin does not readily take part in the polymerization reaction; rather, its presence results in reaction inhibition. Therefore, Amalin LPH lignin was modified via acrylation to overcome this issue. In another modification approach, maleic anhydride was used to produce maleated Amalin HPH lignin. Both the acrylated and maleated lignins were used in butyl acrylate/methyl methacrylate emulsion copolymerizations to produce PSA films. A series of controlled experiments with different lignin loadings was conducted. Adhesive properties of the PSA films were measured and compared with the corresponding acrylic base case formulation. The incorporation of lignin in the PSA formulation was a “green” solution to conventional PSA production and led to a simultaneous increase in tack and shear strength. Further characterization of the latex films via transmission electron microscopy (TEM) showed that lignin was successfully incorporated into the polymer particles. It also showed that the use of maleated lignin at a higher concentration led to a core-shell morphology. In the second application, unmodified Amalin LPH lignin was used to create a starch-based adhesive through the Stein-Hall process, a two-step process involving a “carrier” portion and a “slurry” portion. Several formulations with lignin loadings up to 35 wt% distributed in varying ratios in the carrier and slurry portions were prepared. It was shown that the addition of lignin to the starch-based adhesive formulation increases the water-resistance of the adhesive. Therefore, lignin addition is a solution for a common issue in starch-based adhesives, their lack of water-resistance due to the high affinity of starch toward water. Lignin incorporation solely in the slurry portion significantly increased the strength of the glued joints in a paper board adhesive test. The use of lignin as a renewable replacement of petroleum-based components in two different adhesive formulations was demonstrated successfully. This research strongly suggests that lignin can be used as a high value-added property modifier in adhesive applications.
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Dastjerdi, Zahra. "Cellulose Nanocrystals: Renewable Property Modifiers for Pressure Sensitive Adhesives." Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/36649.

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Pressure sensitive adhesives (PSAs) are polymeric materials with versatile applications in industrial and consumer products such as protective films, product labels, masking tape, and sticky notes, to name a few applications. World demand for emulsion–based products is on the rise due to worldwide legislation on solvent emissions. In order to completely replace emulsion-based PSAs with their solvent-based counterpart, the property modification of emulsion-based PSAs is required. The use of nanomaterials to modify polymer properties is well established. The aim of this thesis was to use cellulose nanocrystals (CNCs) as property modifiers for emulsion-based PSAs. CNCs are recognized as a highly efficient reinforcement nanofiller. Owing to their environmentally friendly characteristics, low density, high aspect ratio, non-toxicity, and abundant availability, the application of CNCs in composite materials is gaining increasing attention. In this thesis, the inclusion of CNCs in emulsion-based PSAs was carried out through in situ emulsion polymerization and blending technique. To the best of our knowledge, there is limited information about the synthesis of CNC/PSAs nanocomposites via in situ emulsion polymerization and the evaluation of their mechanical performance. The addition of CNCs to the polymerization formulation caused latex instability due to the negatively charged surfaces of the CNCs. After numerous attempts to overcome the stability issues, a stable polymerization formulation and protocol were developed. CNC/PSAs were synthesized via in situ seeded-semi batch emulsion polymerization, which is a common commercial production pathway for PSAs. The mechanical performance of the resulting PSA nanocomposite films, namely, shear strength, tack, and peel strength, was evaluated at several CNC loadings. All three PSA adhesive properties were simultaneously enhanced with increasing CNC loading. The inclusion of CNCs into the films increased their hydrophilicity. Consequently, the PSA films’ improved wettability on a stainless steel substrate imparted greater tack and peel strength. The blending of the CNCs with a base latex also led to improved adhesive properties. However, the property modification through blending was not as effective as that for the CNC/PSA films synthesized via in situ emulsion polymerization. Thus, CNCs are safe nanomaterials that have been shown to provide remarkable property enhancement of emulsion-based PSA films at low loadings (1wt%).
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Viney, R. D. "Structure-property relationships in water-borne pressure-sensitive adhesives." Thesis, University of Manchester, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.488267.

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Wang, Tao. "Interfacial control in colloidal nanocomposites for pressure-sensitive adhesives." Thesis, University of Surrey, 2008. http://epubs.surrey.ac.uk/882/.

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This work developed various two-phase colloidal nanomaterials from aqueous dispersions and applied them as pressure-sensitive adhesives. A fundamental understanding of the nano-scale interfacial friction and the macro-scale viscoelasticity and adhesive properties of these nanomaterials was developed via various existing models.
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Zhao, Boxin Pelton Robert H. "The interactions of pressure sensitive adhesive with paper surfaces." *McMaster only, 2004.

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Kadioglu, Ferhat. "Quasi-static and dynamic behaviour of a structural pressure-sensitive adhesive." Thesis, University of Bristol, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311379.

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Errington, Nicola. "Structure-property relationships in water-borne, crosslinked, acrylic pressure-sensitive adhesives." Thesis, University of Manchester, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.594755.

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Five series of acrylic water-borne pressure-sensitive adhesives (PSA's) were prepared with controlled particle morphologies, including core-shell and continually-varying composition. All latex adhesives were prepared at 50 % solids content by emulsion polymerisation of n-butyl acrylate (BA) and acrylic acid (AA) as the main monomers and 1,6-hexanediol diacrylate (HDA) as a crosslinking agent. Seed particles of poly(butyl acrylate) (PBA) were grown by an in-situ batch process to produce a particle of diameter 110 nm. Direct growth of these particles by a semi-continuous process under monomerstarved conditions was employed to give a final particle diameter of approximately 310 nm. Preliminary investigations were aimed at preparation of a latex with a narrow particle size distribution and a low level of coagulum. Initial work using 2-ethylhexyl acrylate (EHA) as the main monomer was not successful because a stable 50 % solids latex could not be produced with controlled particle growth. Hence a formulation was developed using BA and AA. Three series of latexes were prepared with a core-shell particle morphology. Series 1 involved the investigation of the level of crosslinker in the core, at fixed 45:55 core:shell weight ratio, with HDA levels ranging from 0 to 37.5 mol%. Series 2 investigated the volume fraction of crosslinked core (containing 33.3 mol% HDA) over the range 55:45 to 15:85 core:shell weight ratio. Series 3 investigated the effects of the thickness of a crosslinked shell (9.1 mol% HDA) for core-shell particles with a noncrosslinked core (at 55:45, 75:25 and 90:10 core:shell weight ratios). Series 4 latexes were prepared using power-feed processes, one linear power-feed and three based on Series 1 and 2 core-shell adhesive compositions. An additional latex was prepared with a particle profile in which the composition changed linearly with particle radius. Series 5 adhesives were blends of two latexes, such that the mixture had the same composition as Series 2 core-shell adhesives and consisted of the 'core' of the core-shell adhesive blended with a latex with the same composition as the shell of the respective core-shell adhesive. Latex preparation was controlled and monitored by measuring the particle size and the conversion of monomer to polymer at intervals during the preparation. Thermal properties of the adhesives were investigated for thick film samples by dynamic mechanical analysis {DMA}to measure the glass transition temperature {Tg}. Differential scanning calorimetry {DSC}was also used to measure Tgfor comparison. DMA showed two Tg's corresponding to the core and the shell. As the level of crosslinker was increased, the two Tg's became more discrete due to the Tg of the crosslinked phase increasing. The magnitude of the peaks in loss tangent {tan 5} for the core and shell material changed in accordance with the ratio of core:shell. Power-feed adhesives showed a broad glass transition region, which spanned the regions between the Tg's of the equivalent core-shell adhesive. The peaks in tan 5 for the blended systems were more discrete than for the equivalent core-shell adhesives. Adhesive properties were assessed using shear resistance and 1800 peel adhesion tests. Static shear tests were inadequate for testing highly-crosslinked adhesives; hence a dynamic shear resistance test was developed. In comparison to a uniform {noncrosslinked} poly(butyl acrylate-eo-acrylic acid} (PBAlAA) latex, inclusion of crosslinker led to vastly reduced peel adhesion. However, as the level of crosslinker was increased in the Series 1 adhesives, both the peel adhesion and the shear resistance increased. Series 2 and 3 latexes showed that the peel adhesion increases as the amount of non-crosslinked phase is increased. Series 2 adhesives exhibited a maximum in the shear resistance, while Series 3 adhesives showed a decreased in shear resistance as amount of non-crosslinked! ehe core was increased. Adhesive properties of Series 4 power-feed latex polymers showed no dependence on overall crosslink density, but revealed that there is a dependence on the distribution of crosslinker through the particle.
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Books on the topic "Pressure-sensitive adhesives"

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Welch, Mary F., Joseph F. Healey, Carol G. Bowman, and Dawn J. Trebec. Pressure sensitive tapes. Cleveland: Freedonia Group, 2001.

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Benedek, Istvan. Pressure-sensitive adhesives technology. New York: Marcel Dekker, 1997.

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1941-, Benedek Istvan, ed. Pressure-sensitive adhesives and applications. 2nd ed. New York: Marcel Dekker, 2004.

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Donatas, Satas, ed. Handbook of pressure sensitive adhesive technology. 3rd ed. Warwick, R.I: Satas & Assoc., 1999.

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Donatas, Satas, ed. Handbook of pressure sensitive adhesive technology. 2nd ed. New York: Van Nostrand Reinhold, 1989.

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1941-, Benedek Istvan, ed. Developments in pressure-sensitive products. 2nd ed. Boca Raton, FL: Taylor & Francis, 2006.

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1941-, Benedek Istvan, and Feldstein Mikhail M, eds. Technology of pressure-sensitive adhesives and products. Boca Raton, FL: CRC Press, 2009.

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Babington, Mary F., Jennifer L. Mapes, and Rachel M. Stehle. Private companies in the pressure sensitive tape industry. Cleveland: Freedonia Group, 1999.

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Johnston, John. Pressure sensitive adhesive tapes: A guide to their function, design, manufacture, and use. Northbrook. Ill: Pressure Sensitive Tape Council, 2000.

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Benedek, Istvan. Development and manufacture of pressure-sensitive products. New York: M. Dekker, 1999.

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Book chapters on the topic "Pressure-sensitive adhesives"

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Paul, Charles W. "Pressure-Sensitive Adhesives (PSAs)." In Handbook of Adhesion Technology, 341–72. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-01169-6_15.

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Paul, Charles W., and Eric Silverberg. "Pressure-Sensitive Adhesives (PSAs)." In Handbook of Adhesion Technology, 373–407. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-55411-2_15.

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Sobieski, Loretta A., and Thomas J. Tangney. "Silicone Pressure Sensitive Adhesives." In Handbook of Pressure Sensitive Adhesive Technology, 508–17. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_18.

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Paul, Charles W., and Eric Silverberg. "Pressure-Sensitive Adhesives (PSAs)." In Handbook of Adhesion Technology, 1–36. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-42087-5_15-2.

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Satas, Donatas. "Acrylic Adhesives." In Handbook of Pressure Sensitive Adhesive Technology, 396–456. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_15.

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Butler, G. L. "Natural Rubber Adhesives." In Handbook of Pressure Sensitive Adhesive Technology, 260–94. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_11.

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Temin, Samuel C. "Pressure-Sensitive Adhesives for Tapes and Labels." In Handbook of Adhesives, 641–63. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-0671-9_38.

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Satas, Donatas. "Pressure Sensitive Adhesives and Adhesive Products in the United States." In Handbook of Pressure Sensitive Adhesive Technology, 1–23. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_1.

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Hickman, A. D. "Styrene/Butadiene Latex-Based Adhesives." In Handbook of Pressure Sensitive Adhesive Technology, 295–316. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_12.

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Chu, Sung Gun. "Viscoelastic Properties of Pressure Sensitive Adhesives." In Handbook of Pressure Sensitive Adhesive Technology, 158–203. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4757-0866-0_8.

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Conference papers on the topic "Pressure-sensitive adhesives"

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Szymberski, Mike. "Pressure Sensitive Adhesives." In SAE 2001 World Congress. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2001. http://dx.doi.org/10.4271/2001-01-0844.

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Cunningham, Gilbert. "Contribution from pressure-sensitive adhesives." In Electronic Imaging: Science & Technology, edited by Rudolf L. van Renesse. SPIE, 1996. http://dx.doi.org/10.1117/12.235450.

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Huang, Hao, Abhijit Dasgupta, and E. Mirbagheri. "Mechanical behavior of pressure-sensitive adhesives (PSAs)." In 2017 16th IEEE Intersociety Conference on Thermal and Thermomechanical Phenomena in Electronic Systems (ITherm). IEEE, 2017. http://dx.doi.org/10.1109/itherm.2017.7992644.

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Dickinson, J. T. "Photon-Emission From Peeling Pressure Sensitive Adhesives." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by E. R. Menzel. SPIE, 1988. http://dx.doi.org/10.1117/12.945431.

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Zhao, Boxin, Robert Pelton, and Vasiliki Bartzoka. "Peeling Pressure Sensitive Tape from Paper." In Advances in Paper Science and Technology, edited by S. J. I’Anson. Fundamental Research Committee (FRC), Manchester, 2005. http://dx.doi.org/10.15376/frc.2005.2.827.

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The ability of adhesives to bond paper and paperboard is critical for most packaging and converting operations. Despite the huge body of literature describing both paper and adhesives technologies, there are only a few research papers describing paper/adhesive interactions. Described herein are the results of a systematic investigation of pressure sensitive adhesive (PSA) peeling from paper. The peel force versus peel distance curve depends upon the failure mode. A constant force is observed when the PSA cleanly separates from paper (i.e. interfacial failure) at low peel rate. By contrast, at high peeling rates, in the paper failure domain, the peel force climbs to a maximum and then relaxes to a steady-state value. The maximum peel force, which we call the peak force, corresponds to the fracture of the top layer of fibres during the initiation of paper delamination whereas the steady-state peel force occurs during the propagation of paper delamination. To characterize the range of behaviors it is necessary to conduct a series of peeling experiments over an extended range of peel rates. The results are best analyzed by plotting the peak peel force versus the peel rate on logarithmic axes giving what we call a peel map. For a broad range of tape/paper combinations, peel maps have similar shapes. The interfacial failure domain consists of a linear segment with a positive slope. This line intersects with a horizontal line segment at higher peel rates, corresponding to the paper failure domain. Principal component analysis, a multivariate statistical analysis, of a large set of peel maps was used to reveal the influence of paper properties on peeling. The peak peel forces in the paper failure domain correlated with standard paper properties linked to z-directional strength. The slopes of the peel maps in the interfacial domain were independent of paper properties but were sensitive to adhesive rheology. The absolute location of the interfacial segment of the peel map mainly was sensitive to the chemical composition of the paper surface and secondarily related to surface roughness. Water contact angles on paper were not good predictors of adhesion. Finally, we illustrate the utility of peak peel force in the paper failure domain as a measure of paper surface strength.
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D’Amore, Alberto, and Luigi Grassia. "Timescales and properties of PSA (pressure sensitive adhesives)." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738490.

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Feldstein, M. M., M. B. Novikov, B. E. Gdalin, Alberto D’Amore, Domenico Acierno, and Luigi Grassia. "RELAXATION TIMES FEATURED FOR POLYMERIC PRESSURE SENSITIVE ADHESIVES." In IV INTERNATIONAL CONFERENCE TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2008. http://dx.doi.org/10.1063/1.2988975.

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Lamanna, Giuseppe, Luciana Sartore, and Alessandro Basile. "Structure and mechanics of soft PSAs (pressure sensitive adhesives)." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876891.

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Nishiguchi, K., K. Maeda, and S. Okazawa. "FULL EULERIAN FINITE ELEMENT ANALYSIS OF PRESSURE-SENSITIVE ADHESIVES." In 10th World Congress on Computational Mechanics. São Paulo: Editora Edgard Blücher, 2014. http://dx.doi.org/10.5151/meceng-wccm2012-18882.

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Huang, Hao, Abhijit Dasgupta, Ehsan Mirbagheri, and Srini Boddapati. "Mechanical Characterization of Assemblies Bonded With Pressure-Sensitive Adhesives (PSAs)." In ASME 2015 International Technical Conference and Exhibition on Packaging and Integration of Electronic and Photonic Microsystems collocated with the ASME 2015 13th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ipack2015-48707.

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The focus of this paper is on the stress-strain behavior and creep response of a pressure-sensitive adhesive (PSA) with and without carrier layers. This study consists of two phases. The first phase focuses on understanding of the effects of fabrication profiles, including bonding pressure, bonding temperature, bonding time, and aging time, on the PSA joint strength. This part of the study is used to identify an acceptable bonding and aging conditions for manufacturing a robust PSA bonded assembly. Specimens fabricated with this selected set of bonding process conditions are then used for mechanical characterization. The second phase focuses on the assembly’s mechanical behavior (stress-strain behavior and the creep curves) under different loading conditions, including loading stress, loading rate, and loading temperature. The mechanical behavior of PSA bonded assemblies is affected not only by the loading conditions, but also by the assembly architecture. The mechanical behaviors and failure modes of PSAs with and without carrier layers are compared. The reasons for these differences are also discussed.
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Reports on the topic "Pressure-sensitive adhesives"

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Steven J. Severtson. Development of Screenable Pressure Sensitive Adhesives. Office of Scientific and Technical Information (OSTI), November 2003. http://dx.doi.org/10.2172/819519.

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Foster, Mark D. Surface Segregation of Tackifier in Pressure Sensitive Adhesives. Fort Belvoir, VA: Defense Technical Information Center, October 1995. http://dx.doi.org/10.21236/ada304011.

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Steven J. Severtson. Development of Recycling Compatible Pressure-Sensitive Adhesives and Coatings. Office of Scientific and Technical Information (OSTI), February 2010. http://dx.doi.org/10.2172/975049.

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Foster, Mark D., and Seung-ho Moon. Nanomechanical Study of Model Pressure Sensitive Adhesives by Scanning Probe Microscopy. Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada429212.

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Rakesh Gupta. Energy Efficienct Processes for Making Tackifier Dispersions used to make Pressure Sensitive Adhesives. Office of Scientific and Technical Information (OSTI), July 2006. http://dx.doi.org/10.2172/918086.

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Edwards, H. W., M. F. Kostrzewa, and G. P. Looby. Environmental Research Brief: Pollution prevention assessment for a Manufacturer of pressure-sensitive adhesive tape. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/111854.

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Bruce. L52273 Internal Repair of Pipelines. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), December 2005. http://dx.doi.org/10.55274/r0010287.

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External, corrosion-caused loss of wall thickness is the most common cause of repair for gas transmission pipelines. To prevent an area of corrosion damage from causing a pipeline to rupture, the area containing the corrosion damage must be reinforced. Since corrosion is a time dependent process, as pipelines become older, more repairs are required. Repair methods that can be applied from the inside of a gas transmission pipeline (i.e., trenchless methods) are an attractive alternative to conventional repair methods since pipeline excavation is precluded. This is particularly true for pipelines in environmentally sensitive and highly populated areas. Hydrostatic pressure testing was conducted on pipe sections with simulated corrosion damage repaired with glass fiber-reinforced composite liners, carbon fiber-reinforced composite liners, weld deposition, an adhesively bonded steel patch, and adhesively bonded/helically wound steel strip. To benchmark pipeline material performance, additional pipe sections were evaluated in the virgin and in the corrosion damaged/un-repaired conditions. Three repair technologies exhibited burst pressures that were greater than the burst pressures of the un-repaired pipe sections: adhesively bonded/helically wound steel strip repair exhibited the highest performance with burst pressures ranging from 0.4% to 144% higher; carbon fiber-reinforced liner repair had burst pressures ranging from 4% to 17% higher; and glass fiber-reinforced liner repair had burst pressures ranging from 1% to 7% higher. Two repair technologies exhibited burst pressures that were lower than the burst pressures of the un-repaired pipe sections: adhesively bonded steel patch repair was 1% lower and weld deposition repair was10% lower.
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Synthesis, Characterization, to application of water soluble and easily removable cationic pressure sensitive adhesives. Office of Scientific and Technical Information (OSTI), January 2004. http://dx.doi.org/10.2172/828196.

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Synthesis, characterization and application of water-soluble and easily removable cationic pressure-sensitive adhesives. Quarterly technical report. Office of Scientific and Technical Information (OSTI), September 1999. http://dx.doi.org/10.2172/761025.

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