Academic literature on the topic 'Poly(acrylate) networks'

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Journal articles on the topic "Poly(acrylate) networks"

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Rault, J., A. Lucas, R. Neffati, and M. Monleón Pradas. "Thermal Transitions in Hydrogels of Poly(ethyl acrylate)/Poly(hydroxyethyl acrylate) Interpenetrating Networks." Macromolecules 30, no. 25 (1997): 7866–73. http://dx.doi.org/10.1021/ma970344i.

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Mellal, T., M. Habchi, and B. Dali Youcef. "Effect of nature and degree of crosslinking agent of poly(hydroxy-butyl-methacrylate-co-2-ethyl-hexyl-acrylate) networks on the swelling properties in nematic liquid crystal 5CB." Revista Mexicana de Física 66, no. 5 Sept-Oct (2020): 617. http://dx.doi.org/10.31349/revmexfis.66.617.

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We experimentally measured the effect of nature and concentration of crosslinker on the photopolymerized time of the poly(hydroxy-butyl-methacrylate-co-2-ethyl-hexyl-acrylate)/5CB system. Initial mixtures are composed of monofunctional monomers hydroxy-butyl-methacrylate (HBMA) and 2-ethyl-hexyl-acrylate (2-EHA), and one of the three bifunctional monomers, poly-propylene-glycol-di-acrylate (PPGDA), tri-propylene-glycol-di-acrylate (TPGDA), or 1,6-hexane-diol-di-acrylate (HDDA), and 2-hydroxy-2-methylpropiophenone (Darocur 1173) as a photoinitiator. The copolymers were elaborated via UV irradia
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Li, Lei, Huaming Wang, Xibin Shen, et al. "Nanocomposites of Poly(n-Butyl Acrylate) with Fe3O4: Crosslinking with Hindered Urea Bonds, Reprocessing and Related Functional Properties." Polymers 16, no. 18 (2024): 2638. http://dx.doi.org/10.3390/polym16182638.

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In this contribution, we reported the synthesis of the nanocomposites of poly(n-butyl acrylate) with Fe3O4 nanoparticles (NPs) via dynamic crosslinking of poly(n-butyl acrylate)-grafted Fe3O4 NPs with hindered urea bonds (HUBs). Towards this end, the surfaces of Fe3O4 NPs were grafted with poly(n-butyl acrylate-ran-2-(3-tert-butyl-3-ethylureido)ethyl acrylate) chains [denoted as Fe3O4-g-P(BA-r-TBEA)] via living radical polymerization. Thereafter, 1,2-bis(tert-butyl)ethylenediamine was used as a crosslinker to afford the organic–inorganic networks with variable contents of Fe3O4 NPs and crossli
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Andreopoulos, A. G. "Properties of poly(2-hydroxyethyl acrylate) networks." Biomaterials 10, no. 2 (1989): 101–4. http://dx.doi.org/10.1016/0142-9612(89)90040-9.

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Yan, Liang, Duc-Truc Pham, Philip Clements та ін. "β-Cyclodextrin- and adamantyl-substituted poly(acrylate) self-assembling aqueous networks designed for controlled complexation and release of small molecules". Beilstein Journal of Organic Chemistry 13 (7 вересня 2017): 1879–92. http://dx.doi.org/10.3762/bjoc.13.183.

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Three aqueous self-assembling poly(acrylate) networks have been designed to gain insight into the factors controlling the complexation and release of small molecules within them. These networks are formed between 8.8% 6A-(2-aminoethyl)amino-6A-deoxy-6A-β-cyclodextrin, β-CDen, randomly substituted poly(acrylate), PAAβ-CDen, and one of the 3.3% 1-(2-aminoethyl)amidoadamantyl, ADen, 3.0% 1-(6-aminohexyl)amidoadamantyl, ADhn, or 2.9% 1-(12-aminododecyl)amidoadamantyl, ADddn, randomly substituted poly(acrylate)s, PAAADen, PAAADhn and PAAADddn, respectively, such that the ratio of β-CDen to adamanty
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G�mez Ribelles, J. L., M. Monle�n Pradas, G. Gallego Ferrer, et al. "Poly(methyl acrylate)/poly(hydroxyethyl acrylate) sequential interpenetrating polymer networks. Miscibility and water sorption behavior." Journal of Polymer Science Part B: Polymer Physics 37, no. 14 (1999): 1587–99. http://dx.doi.org/10.1002/(sici)1099-0488(19990715)37:14<1587::aid-polb4>3.0.co;2-u.

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Campillo-Fernández, Alberto J., Manuel Salmerón Sánchez, Roser Sabater i Serra, José María Meseguer Dueñas, Manuel Monleón Pradas, and José Luis Gómez Ribelles. "Water-induced (nano) organization in poly(ethyl acrylate-co-hydroxyethyl acrylate) networks." European Polymer Journal 44, no. 7 (2008): 1996–2004. http://dx.doi.org/10.1016/j.eurpolymj.2008.04.032.

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Mpoukouvalas, Anastasia, Wenwen Li, Robert Graf, Kaloian Koynov, and Krzysztof Matyjaszewski. "Soft Elastomers via Introduction of Poly(butyl acrylate) “Diluent” to Poly(hydroxyethyl acrylate)-Based Gel Networks." ACS Macro Letters 2, no. 1 (2012): 23–26. http://dx.doi.org/10.1021/mz300614m.

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Frisch, Harry L., Linfu Wang, Weiyu Huang, Yao He Hua, Han X. Xiao, and Kurt C. Frisch. "Interpenetrating polymer networks from polyurethanes and poly(methyl acrylate)." Journal of Applied Polymer Science 43, no. 3 (1991): 475–79. http://dx.doi.org/10.1002/app.1991.070430308.

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Meseguer Dueñas, J. M., D. Torres Escuriola, G. Gallego Ferrer, et al. "Miscibility of Poly(butyl acrylate)−Poly(butyl methacrylate) Sequential Interpenetrating Polymer Networks." Macromolecules 34, no. 16 (2001): 5525–34. http://dx.doi.org/10.1021/ma002046i.

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Dissertations / Theses on the topic "Poly(acrylate) networks"

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Deng, Guodong. "Self-Assembly of Poly(Ethylene Oxide)-Block-Poly(Ethyl Acrylate)-Block-Polystyrene with Phenolic Resins." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1399044329.

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Wu, Dung-Han, and 吳東翰. "The Interpenetrating Polymer Networks Based on Poly(ethylene glycol) methyl ether acrylate and Gelatin." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/38382815217819986749.

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碩士<br>大同大學<br>化學工程研究所<br>93<br>This article describes the synthesis of interpenetrating polymer networks (IPNs) based on Poly(ethylene glycol) methyl ether acrylate (PEGMEA) and gelatin,which were crosslinked sequentially using N,N’-methylene bisacrylamide (NMBA) and glutaraldehyde, respectively。 Various samples were prepared by taking varying amounts of PEGMEA and gelatin in the initial feed。 Sequential IPNs were prepared by first polymerizing and crosslinking PEGMEA in the presence of gelatin using redox initiators (Ammonium Peroxydisulfate and N,N,N'',N''''- tetramethylethylenediamine) and
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Yan, Liang. "Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging." Thesis, 2016. http://hdl.handle.net/2440/103611.

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Polymer networks are promising biomaterials for drug delivery as they have porous structures and are often biocompatible. The general aspects of the host-guest complexation capability of polymer networks containing cyclodextrins as well as their application in drug delivery are considered in Chapter 1. The introduction of cyclodextrins into polymer networks has the potential to improve drug loading capacity and modulate subsequent drug release behavior due to the host-guest complexation by cyclodextrins of drug molecules. Thus, Chapter 2 and Chapter 3 are concerned with new research on water s
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Huang, Chia Sheng, and 黃家聖. "Interpenetrating network membranes of poly (2-hydroxylethyl meth-acrylate) (poly HEMA) and poly (vinyl alcohol) (PVA) in various ratios were prepared by UV radiation and treated with glutaraldehyde (GA). From the spectral change of FTIR, the hydroxyl grou." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/33056050865582555044.

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碩士<br>長庚大學<br>化工與材料工程研究所<br>93<br>Interpenetrating network membranes of poly (2-hydroxylethyl meth- acrylate) (poly HEMA) and poly (vinyl alcohol) (PVA) in various ratios were prepared by UV radiation and treated with glutaraldehyde (GA). From the spectral change of FTIR, the hydroxyl groups disappeared and an acetal ring and ether linkage were formed for the reaction between the hydroxyl groups of PVA and GA. From the stress-strain curve, it was found that the tensile strength and elongation increased with PVA content on the PVA / poly (HEMA) membranes. After crosslinking with GA, the membran
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Book chapters on the topic "Poly(acrylate) networks"

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Babić, Marija M., and Simonida Lj Tomić. "Semi-interpenetrating Networks Based on (Meth)acrylate, Itaconic Acid, and Poly(vinyl Pyrrolidone) Hydrogels for Biomedical Applications." In Interpenetrating Polymer Network: Biomedical Applications. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-0283-5_10.

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Grainger, D. W., and H. Yu. "NOVEL THERMO-RESPONSIVE AMPHIPHILIC POLY N-ISOPROPYLACRYL-AMIDE-CO-SODIUM ACRYLATE-CO-N-N-ALKYLACRYLAMIDE NETWORKS." In Advances in Drug Delivery Systems, 6. Elsevier, 1994. http://dx.doi.org/10.1016/b978-0-444-82027-3.50054-7.

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Mark, James E., Dale W. Schaefer, and Gui Lin. "Copolymers and Interpenetrating Networks." In The Polysiloxanes. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780195181739.003.0010.

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Random copolymers are prepared by the copolymerization of a mixture of cyclic oligomers. Although the resulting polymer can be quite blocky (figure 8.1), taking the reaction to equilibrium can give a polymer that is essentially random in its chemical sequencing. One reason for preparing copolymers is to introduce functional species, such as hydrogen or vinyl side groups, along the chain backbone to facilitate cross linking. Another reason is the introduction of sufficient chain irregularity to make the polymer inherently noncrystallizable. Specific examples of comonomers include imides, peryle
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