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Relevant bibliographies by topics / Polymer Pair

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Academic literature on the topic 'Polymer Pair'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Polymer Pair"

1

Ptak, Anita, and Adrianna Łukaszyk. "INFLUENCE OF CONTACT TIME WITH LUBRICANTON POLYMER-POLYMER SLIDING PAIR INTERACTION." Tribologia 308, no. 2 (2024): 87–93. http://dx.doi.org/10.5604/01.3001.0054.8431.

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This paper presents tribological investigations of pairs of same-type construction polymers: PET, PA6, andPOM, which for different durations were in contact with a lubricant. Hydraulic oil HLP 68, used for heavilyloaded drive systems, was the lubricant. Test samples were subjected to storage in this lubricating mediumfor different lengths of time: ranging from no storage to 2 weeks of storage. The static friction coefficient,which has a significant bearing on the startup of systems, was studied. Furthermore, investigations aimed atidentifying the phenomena involved in the interaction of the po

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An, Changwei, Jun Zhang, and Xianqi Guan. "CO₂ Adsorption Based on Porphyrin Based Porous Organic Polymers." Journal of Physics: Conference Series 2463, no. 1 (2023): 012057. http://dx.doi.org/10.1088/1742-6596/2463/1/012057.

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Abstract In order to efficiently catalyze the cycloaddition reaction of CO2 and epoxy alkanes under mild environment and no catalyst, this paper designed and synthesized two kinds of porphyrin based porous organic polymers—porphyrin based porous organic polymer containing carboxyl group (ppop-cooh) and porphyrin based porous organic polymer containing quaternary ammonium salt ion pair. Quaternary ammonium salt cation anion pair nucleophilic groups and metal active centers were introduced into the polymer by pre- and post-modification respectively. The chemical structure and pore structure of t

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Ptak, Anita, and Zuzanna Łuksza. "Using Standstill Time to Evaluate the Startup in Polymer Pair Systems." Polymers 15, no. 24 (2023): 4696. http://dx.doi.org/10.3390/polym15244696.

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The subject of polymer–polymer pair interaction is highly important, bearing in mind that such pairs are used in the construction of machines and equipment, among other uses. Considering that the characteristics of polymer–polymer sliding pairs (e.g., the load limit value and advantageous parameter, PV) differ from those of polymer–metal pairs, the subject is particularly interesting and has been little explored so far. Hence, the present study presents one of the areas of the effects of standstill time (intrinsically characteristic of polymeric materials) on the startup parameters in sliding

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Seo, Y., and H. Kim. "Reactive Compatibilized Polymer-Polymer Interface : Amorphous and Semi-crystalline Polymer Pair." International Journal of Material Forming 1, S1 (2008): 795–98. http://dx.doi.org/10.1007/s12289-008-0295-6.

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C., BHATTACHARYYA, N. BHATTACHARYYA S., and M. MANDAL B. "Poly(vinyl propionate) and Poly(ethyl acrylate)- A Miscible Polymer Pair." Journal of Indian Chemical Society Vol. 63, Jan 1986 (1986): 157–60. https://doi.org/10.5281/zenodo.6255725.

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Department of Physical Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Calcutta-700 092 A new miscible polymer pair, <em>viz. </em>poly(vinyl propionate) (PVPr) and poly(ethyl acrylate) (PEA) is reported. Blends of these polymers form clear films, clear solutions in common solvents and have single glass transition temperatures. Miscibility of these two polymers in binary combinations with poly(methyl acrylate) (PMA) or poly(vinyl acetate) (PVA) was also examined. Differential scanning calorimetry (D.S.C.) reveals that PVPr+PVA, PEA +PVA, PMA+PVPr and PMA +PEA are immisc

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KUJAWA, Maciej, and Wojciech WIELEBA. "THE INFLUENCE OF A CONSTANT STATE OF DEFORMATION ON THE FRICTION COEFFICIENT IN SELECTED THERMOPLASTICS (POLYMER–STEEL PAIR)." Tribologia, no. 4 (August 31, 2017): 39–45. http://dx.doi.org/10.5604/01.3001.0010.5992.

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The effect of tensile deformation on polymer structures and their mechanical properties is described in various papers. However, the majority of articles are focused on high deformation (a few hundred percentiles) at increased temperature. It causes changes in orientation and the crystallinity ratio. The authors of this paper asses the influence of strain (max. 50%) on hardness and the coefficient of friction (polymer–steel A1 couple) for selected polymers. The deformation was conducted at room temperature and maintained during tests. There was a significant reduction (up to 50%) of hardness a

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Dell, Zachary E., and Kenneth S. Schweizer. "Intermolecular structural correlations in model globular and unconcatenated ring polymer liquids." Soft Matter 14, no. 45 (2018): 9132–42. http://dx.doi.org/10.1039/c8sm01722k.

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We employ the field theoretic polymer integral equation theory to construct a segment-level theory for the pair structure and thermodynamics of dense liquids of simple globule and ring polymers. We find that the partially interpenetrating behavior of rings is reflected in a deeper correlation hole and in a limited number of neighbors, in stark contrast to chains.

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Albrecht, Ken, Yuki Hirabayashi, Masaya Otake, et al. "Polymerization of a divalent/tetravalent metal-storing atom-mimicking dendrimer." Science Advances 2, no. 12 (2016): e1601414. http://dx.doi.org/10.1126/sciadv.1601414.

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The phenylazomethine dendrimer (DPA) has a layer-by-layer electron density gradient that is an analog of the Bohr atom (atom mimicry). In combination with electron pair mimicry, the polymerization of this atom-mimicking dendrimer was achieved. The valency of the mimicked atom was controlled by changing the chemical structure of the dendrimer. By mimicking a divalent atom, a one-dimensional (1D) polymer was obtained, and by using a planar tetravalent atom mimic, a 2D polymer was obtained. These poly(dendrimer) polymers could store Lewis acids (SnCl2) in their unoccupied orbitals, thus indicatin

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Gowda, Ravikumar R., та Eugene Y. X. Chen. "Chemoselective Lewis pair polymerization of renewable multivinyl-functionalized γ-butyrolactones". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 375, № 2101 (2017): 20170003. http://dx.doi.org/10.1098/rsta.2017.0003.

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Multivinyl-functionalized γ-butyrolactones, γ-vinyl-γ-methyl-α-methylene-γ-butyrolactone ( γ VMMBL) and γ-allyl-γ-methyl-α-methylene-γ-butyrolactone ( γ AMMBL), have been synthesized from biorenewable ethyl levulinate and effectively polymerized by Lewis pairs consisting of an organic N -heterocyclic carbene Lewis base and a strong organo-Lewis acid E(C 6 F 5 ) 3 (E = Al, B). This Lewis pair polymerization is quantitatively chemoselective, proceeds exclusively via polyaddition across the conjugated α-methylene double bond without participation of the γ-vinyl or γ-allyl double bond, and produce

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Zhang, Liwei, Heping Zheng, and Huilin Xie. "Molecular Dynamics Study on Interfacial Strengthening Mechanisms of Ettringite/Polymer Nanocomposites." Buildings 13, no. 12 (2023): 2976. http://dx.doi.org/10.3390/buildings13122976.

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Compared with polymer-modified ordinary-Portland-cement-based materials, research on cement materials based on polymer-modified sulfoaluminate is still in the preliminary stage and lacks an understanding of the mechanism of the interaction interface. The aim of this work is to study the bond performance of ettringite, the main hydration product of sulfoaluminate cement, with various types of polymers using molecular dynamics methods. Steered molecular dynamics were used to simulate the separation of polyamide (PA), polyethylene glycol (PEG), polyacrylic acid (PAA) and polypropylene (PP) from e

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Dissertations / Theses on the topic "Polymer Pair"

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Stolwijk, Nicolaas A. "Ionic transport and pair formation in polymer electrolytes." Universitätsbibliothek Leipzig, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-181807.

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Stolwijk, Nicolaas A. "Ionic transport and pair formation in polymer electrolytes." Diffusion fundamentals 20 (2013) 20, S. 1, 2013. https://ul.qucosa.de/id/qucosa%3A13585.

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Deng, Guodong. "SYNTHESIS AND CHARACTERIZATION OF IONICALLY CROSS-LINKED NETWORKS THROUGH THE USE OF ION-PAIR COMONOMERS." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1534124831858723.

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Li, Cheng. "Synthesis of ionically crosslinked polyelectrolytes by homopolymerization of an ion-pair comonomer." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1532382224656914.

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Bayrak, Pehlivan İlknur. "Functionalization of polymer electrolytes for electrochromic windows." Doctoral thesis, Uppsala universitet, Fasta tillståndets fysik, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-204437.

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Saving energy in buildings is of great importance because about 30 to 40 % of the energy in the world is used in buildings. An electrochromic window (ECW), which makes it possible to regulate the inflow of visible light and solar energy into buildings, is a promising technology providing a reduction in energy consumption in buildings along with indoor comfort. A polymer electrolyte is positioned at the center of multi-layer structure of an ECW and plays a significant role in the working of the ECW. In this study, polyethyleneimine: lithium (bis(trifluoromethane)sulfonimide (PEI:LiTFSI)-based p

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Yin, Yijing. "An Experimental Study on PEO Polymer Electrolyte Based All-Solid-State Supercapacitor." Scholarly Repository, 2010. http://scholarlyrepository.miami.edu/oa_dissertations/440.

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Supercapacitors are one of the most important electrochemical energy storage and conversion devices, however low ionic conductivity of solid state polymer electrolytes and the poor accessibility of the ions to the active sites in the porous electrode will cause low performance for all-solid-state supercapacitors and will limit their application. The objective of the dissertation is to improve the performance of all-solid-state supercapactor by improving electrolyte conductivity and solving accessibility problem of the ions to the active sites. The low ionic conductivity (10-8 S/cm) of poly(eth

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Clark, Anthony. "Properties of Effective Pair Potentials that Map Polymer Melts onto Liquids of Soft Colloid Chains." Thesis, University of Oregon, 2013. http://hdl.handle.net/1794/13005.

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The ability to accurately represent polymer melts at various levels of coarse graining is of great interest because of the wide range of time and length scales over which relevant process take place. Schemes for developing effective interaction potentials for coarse-grained representations that incorporate microscopic level system information are generally numerical and thus suffer from issues of transferability because they are state dependent and must be recalculated for different system and thermodynamic parameters. Numerically derived potentials are also known to suffer from representabil

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Takahashi, Masakuni. "Elucidation of the Dominant Factor in Electrochemical Materials Using Pair Distribution Function Analysis." Doctoral thesis, Kyoto University, 2021. http://hdl.handle.net/2433/263748.

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京都大学<br>新制・課程博士<br>博士(人間・環境学)<br>甲第23287号<br>人博第1002号<br>京都大学大学院人間・環境学研究科相関環境学専攻<br>(主査)教授内本喜晴, 教授田部勢津久, 准教授戸﨑充男<br>学位規則第4条第1項該当<br>Doctor of Human and Environmental Studies<br>Kyoto University<br>DFAM

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Amram, Bruno. "Etude, par dichroisme infrarouge, de l'orientation de reseaux d'elastomeres etires." Paris 6, 1988. http://www.theses.fr/1988PA066023.

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Le dichroisme ir permet d'obtenir sans marquage et sans hypothese sur l'axe de chaine le second moment de la fonction d'orientation de reseaux de polyisoprenes etires uniaxialement. La relaxation de la phase amorphe est predominante dans le caoutchouc naturel

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Caucheteux, Isabelle. "Solutions de polymeres pres d'une paroi solide : etude experimentale de l'adsorption par une technique de fluorescence induite par une onde evanescente." Paris 6, 1988. http://www.theses.fr/1988PA066124.

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Books on the topic "Polymer Pair"

1

Vieth, W. R. Membrane systems: Analysis and design : applications in biotechnology, biomedicine, and polymer science. Hanser Publishers, 1988.

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Vieth, W. R. Membrane systems: Analysis and design : applications in biotechnology, biomedicine, and polymer science. J. Wiley, 1994.

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Abraham, Tamir, ed. Mixing and excess thermodynamic properties: A literature source book : supplement 2. Elsevier, 1986.

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Binder and Polymer Assisted Powder Processing. Asm International, 2020.

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Radiation technology for polymers. 2nd ed. Taylor & Francis, 2010.

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Drobny, Jiri George. Radiation Technology for Polymers. Taylor & Francis Group, 2002.

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Drobny, Jiri George. Radiation Technology for Polymers. Taylor & Francis Group, 2010.

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Drobny, Jiri George. Radiation Technology for Polymers. Taylor & Francis Group, 2010.

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Radiation Technology for Polymers. CRC Press LLC, 2020.

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Radiation Technology for Polymers Third Edition. Taylor & Francis Group, 2020.

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Book chapters on the topic "Polymer Pair"

1

Bharti, Sarita, and Selvaraj Senthilvelan. "Transmission Efficiency and Surface Damage of Polymer–Polymer Gear Pair Under Wet Lubrication." In Lecture Notes in Mechanical Engineering. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0550-5_77.

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Jerome, R., G. Broze, and Ph Teyssie. "Association of the Ion Pair End-Groups of Halato Telechelic Polymers in Nonpolar Solvents." In Microdomains in Polymer Solutions. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2123-1_14.

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Fuchiwaki, Masaki. "Micro Pump Driven by a Pair of Conducting Polymer Soft Actuators." In Soft Actuators. Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54767-9_31.

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Rosenfield, H. D., and R. Barton. "Pair-Density Function of Nano-Scale Morphology in Oriented Polymer Fibers: Applicati on to Nomex Aramid." In Advances in X-Ray Analysis. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5377-9_58.

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Sokołowska, Joanna Julia, and Bogumiła Chmielewska. "Carbon Footprint and CO2 Emissions in the Concrete-Polymer Composites Technology." In Springer Proceedings in Materials. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-72955-3_14.

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AbstractIn the building materials industry, similarly to other industry sectors, the quantification of greenhouse gas emissions is undertaken, enabling the identification of GHG sources both for individual production processes and in total – for specific material solutions and products. While recently a lot of attention is paid to analyze carbon footprint of ordinary concrete and development of low-emission cements with significantly reduced Portland clinker content, the issue of GHG quantification in the context of concrete-like polymer composites (including concretes with polymer binders e.g

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Gooch, Jan W. "Lone Pair." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7006.

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Gooch, Jan W. "Metameric Pair." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7363.

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Gooch, Jan W. "Inert Pair." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6291.

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Gooch, Jan W. "Ion Pair." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_6460.

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Gooch, Jan W. "Bonding Pair." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1490.

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Conference papers on the topic "Polymer Pair"

1

LaBerge, Kelsen, Robert Handschuh, Stephen Berkebile, and Gary Roberts. "Hybrid Gear Performance Under Loss-of-Lubrication Conditions." In Vertical Flight Society 73rd Annual Forum & Technology Display. The Vertical Flight Society, 2017. http://dx.doi.org/10.4050/f-0073-2017-12144.

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Hybrid composite gear technology is being investigated to increase power density in rotorcraft drive systems. These gears differ from conventional steel gears in that the structural web material is replaced with a lightweight carbon fiber composite. Past studies have focused on performance of this technology under normal operating conditions, however, for this technology to be viable it must also withstand adverse conditions. The study presented here evaluates the performance of hybrid gears under loss-of-lubrication conditions in NASA Glenn Research Center’s Contact Fatigue Test Facility. Two

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Shaw, S. S., and K. S. Sorbie. "Synergistic Properties of Phosphonate and Polymeric Scale Inhibitor Blends for Barium Sulphate Scale Inhibition." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-3867.

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Abstract Inorganic barium sulphate is one of the most difficult types of scale to inhibit in oil and gas production systems, due to its physical hardness and its chemical and thermal stability. Barium sulphate scale is most commonly inhibited using either phosphonate or polymeric scale inhibitors (SIs) deployed at sub-stoichiometric concentrations. What is much less well known in the oil industry is the effect of using combinations of two (or more) SIs synergistically for enhanced scale inhibition performance. In this paper, we present a series of static barium sulphate inhibition efficiency (

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Roy, Soma, and Michael H. Azarian. "Friction and Wear Behavior of Polymer-Gold Contact Pairs in a Micromechanical Switching Element Under Fretting Load." In 2024 IEEE 69th Holm Conference on Electrical Contacts (HOLM). IEEE, 2024. https://doi.org/10.1109/holm56222.2024.10768511.

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Hwang, Ho-Sang, Bum-Kyoung Seo, and Kune-Woo Lee. "Strippable Core-Shell Polymer Emulsion for Decontamination of Radioactive Surface Contamination." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40193.

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In this study, the core-shell composite polymer for decontamination from the surface contamination was synthesized by the method of emulsion polymerization and blends of polymers. The strippable polymer emulsion is composed of the poly(styrene-ethyl acrylate) [poly(St-EA)] composite polymer, poly(vinyl alcohol) (PVA) and polyvinylpyrrolidone (PVP). The morphology of the poly(St-EA) composite emulsion particle was core-shell structure, with polystyrene (PS) as the core and poly(ethyl acrylate) (PEA) as the shell. Core-shell polymers of styrene (St)/ethyl acrylate (EA) pair were prepared by sequ

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Chen, Ray T., Lev Sadovnik, Zong J. Sun, Daniel Robinson, and Tomasz Jannson. "Polymer waveguide modulator." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.fu4.

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We report the first colinear single-mode polymer waveguide modulator that can be formed on any smooth surface—including semiconductors, conductors, and insula tors—regardless of its conductivity and refractive index. The tunability of polymer film allows us to shift the guiding layer from step index profile to graded-index profile. The phase-matching condition for optical power transfer is achieved through current injection. A 34 dB extinction ratio was observed with an injection current density of ~10 μA/μm2. Unlike that of the conventional dual-channel coupler, the asymmetry of the colinear

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Park, M. K. "Enriched pair tunneling effect and feep fracture of synthetic metal-polymer." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834825.

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De Sio, Antonietta, Ephraim Sommer, Filippo Troiani, et al. "Coherent ultrafast polaron pair formation in a conjugated polymer at room temperature." In CLEO: QELS_Fundamental Science. OSA, 2016. http://dx.doi.org/10.1364/cleo_qels.2016.fw4n.2.

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Chen, Ray T., Lev Sadovnik, Daniel Rabinson, Tomasz Jannson, and Joanna Jannson. "Heterostructure collinear graded index polymer waveguide modulator." In Integrated Photonics Research. Optica Publishing Group, 1991. http://dx.doi.org/10.1364/ipr.1991.thj2.

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We are reporting a novel graded index (GRIN) collinear asymmetrical polymer waveguide modulator. Disparity of the waveguide pair provides us with a much larger dynamic range of phase matching condition suitable for single-mode waveguide to multi-mode waveguide coupling. Formation of a universal polymer waveguide was made possible by tuning the guiding layer index profile from stepped index to graded index through a mass perturbation method.

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Gu, Wenting, Peng Cheng, Arindam Ghosh, et al. "A Polymer-Based Microfluidic Resistive Sensor for Detecting Distributed Loads." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-87672.

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This paper reports on a polymer-based microfluidic resistive sensor for detecting distributed loads. The sensor is comprised of a polymer rectangular microstructure with an embedded electrolyte-filled microchannel and an array of electrodes aligned along the microchannel length. Electrolyte solution in the microchannel serves as impedance transduction. Distributed loads acting on the polymer microstructure give rise to different deflection along the microstructure length, which is recorded as the resistance change in electrolyte solution. This sensor can detect distributed loads by monitoring

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Prakash, M. B. Nanda, G. Thejas Urs, H. T. Anand, and R. Somashekar. "Pair correlation studies of CdCl2 doped PVA polymer films using X-ray data." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872766.

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Reports on the topic "Polymer Pair"

1

Percec, V., and D. Tomazos. Transformation of a Monotropic Mesophase into an Enantiotropic Mesophase by Copolymerization of the Parent Polymers' Monomer Pair Containing Constitutional Isomeric Mesogenic Side Groups. Preprint. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada208782.

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