Relevant bibliographies by topics / Crosslinking

Academic literature on the topic 'Crosslinking'

Author: Grafiati
Published: 4 June 2021
Last updated: 28 July 2024

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Journal articles on the topic "Crosslinking"

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Sun, Licheng. "Crystal crosslinking." Nature Chemistry 7, no. 9 (August 17, 2015): 684–85. http://dx.doi.org/10.1038/nchem.2323.

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Leccisotti, Antonio. "Transepithelial crosslinking." Journal of Cataract & Refractive Surgery 38, no. 9 (September 2012): 1706. http://dx.doi.org/10.1016/j.jcrs.2012.07.011.

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NAKAYAMA, Yasuharu. "Crosslinking Agent." Journal of the Japan Society of Colour Material 96, no. 2 (February 20, 2023): 58–63. http://dx.doi.org/10.4011/shikizai.96.58.

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Partschefeld, C., J. Schreiner, U. Schwarzenbolz, and T. Henle. "Studies on Enzymatic Crosslinking of Casein Micelles." Czech Journal of Food Sciences 27, Special Issue 1 (June 24, 2009): S99—S101. http://dx.doi.org/10.17221/938-cjfs.

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The aim of our study was to gain insights into the reactions occurring in casein micelles during enzymatic modification with microbial transglutaminase (mTG). Therefore, UHT-treated milk was incubated with varying amounts of mTG and the caseins were analysed using different analytical methods. Regarding the casein species, it was observed that β -casein was crosslinked to a higher extent than the α-caseins. From this it can be suggested that β-casein is mainly located in the outer space of the micellar structure and therefore better accessible to mTG than α-caseins, which are located predominantly in the interior. Furthermore, it was demonstrated by gel-permeation chromatography and RP-HPLC that the caseins are fixed within the micellar structure, by what the ratio of extramicellar casein decreased. We conclude that an isopeptide network in the outer β -casein rich “shell” of the micelle is formed by mTG, which is responsible for the increased micellar stability.
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Warburton, Linnea, and Boris Rubinsky. "Freezing-modulated-crosslinking: A crosslinking approach for 3D cryoprinting." Bioprinting 27 (August 2022): e00225. http://dx.doi.org/10.1016/j.bprint.2022.e00225.

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Lloyd, Sarah M., and Yupeng He. "Exploring Extracellular Matrix Crosslinking as a Therapeutic Approach to Fibrosis." Cells 13, no. 5 (March 2, 2024): 438. http://dx.doi.org/10.3390/cells13050438.

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The extracellular matrix (ECM) provides structural support for tissues and regulatory signals for resident cells. ECM requires a careful balance between protein accumulation and degradation for homeostasis. Disruption of this balance can lead to pathological processes such as fibrosis in organs across the body. Post-translational crosslinking modifications to ECM proteins such as collagens alter ECM structure and function. Dysregulation of crosslinking enzymes as well as changes in crosslinking composition are prevalent in fibrosis. Because of the crucial roles these ECM crosslinking pathways play in disease, the enzymes that govern crosslinking events are being explored as therapeutic targets for fibrosis. Here, we review in depth the molecular mechanisms underlying ECM crosslinking, how ECM crosslinking contributes to fibrosis, and the therapeutic strategies being explored to target ECM crosslinking in fibrosis to restore normal tissue structure and function.
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Wang, Yuan-Xia, Chen-Chen Wang, Ying Shi, Li-Zhi Liu, Nan Bai, and Li-Fu Song. "Effects of Dynamic Crosslinking on Crystallization, Structure and Mechanical Property of Ethylene-Octene Elastomer/EPDM Blends." Polymers 14, no. 1 (December 30, 2021): 139. http://dx.doi.org/10.3390/polym14010139.

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The dynamic crosslinking method has been widely used to prepare rubber/plastic blends with thermoplastic properties, and the rubber phase is crosslinked in these blends. Both polyolefin elastomer (POE) and ethylene-propylene-diene monomer rubber (EPDM) can be crosslinked, which is different from usual dynamic crosslinking components. In this paper, dynamic crosslinked POE/EPDM blends were prepared. For POE/EPDM blends without dynamic crosslinking, EPDM can play a nucleation role, leading to POE crystallizing at a higher temperature. After dynamic crosslinking, the crosslinking points hinder the mobility of POE chains, resulting in smaller crystals, but having too many crosslinking points suppresses POE crystallization. Synchrotron radiation studies show that phase separation occurs and phase regions form in non-crosslinked blends. After crosslinking, crosslinking points connecting EPDM and part of POE chains, enabling more POE to enter the EPDM phase and thus weakening phase separation, indicates that dynamic crosslinking improves the compatibility of POE/EPDM, also evidenced by a lower β conversion temperature and higher α conversion temperature than neat POE from dynamic mechanical analysis. Moreover, crosslinking networks hinder the crystal fragmentation during stretching and provide higher strength, resulting in 8.3% higher tensile strength of a 10 wt% EPDM blend than neat POE and almost the same elongation at break. Though excessive crosslinking points offer higher strength, they weaken the elongation at break.
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Zeng, Fanwei, Xing Guo, Li Sun, Xuelian He, Zuoxiang Zeng, and Zhen Liu. "Non-isothermal crosslinking of ethylene vinyl acetate initiated by crosslinking agents: kinetic modelling." RSC Advances 12, no. 24 (2022): 15623–30. http://dx.doi.org/10.1039/d2ra01994a.

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The kinetic parameter Ea of EVA crosslinking reaction initiated by a peroxide crosslinking agent showed irregular changes in the early stage of crosslinking, and increase with the increase of conversion rate α in the later stage of crosslinking.
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Hu, Zhenhua, Zhouyang Xiang, Tao Song, and Fachuang Lu. "Effects of crosslinking degree on the coating properties of arabinoxylan." BioResources 14, no. 1 (November 8, 2018): 70–86. http://dx.doi.org/10.15376/biores.14.1.70-86.

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Arabinoxylan (AX) was extracted from sugarcane bagasse and modified through crosslinking with glutaraldehyde (GA). The effects of crosslinking degree on the rheological and coating properties of glutaraldehyde crosslinked arabinoxylan (GAX) were investigated. To better evaluate the degree of crosslinking, the crosslink index was used to represent the degree of crosslinking for the GAX in this study. The viscosity of the GAX solution increased when the degree of crosslinking increased, and the solution demonstrated non-Newtonian flow behavior. A high degree of crosslinking was detrimental to the film and coating properties of the GAX. At an optimum degree of crosslinking, the tensile strength of the GAX films increased by approximately 170% and 60% compared with that of the AX and GAX with the highest degree of crosslinking, respectively; the tensile strength of the GAX-coated paper increased by approximately 15% compared with that of the GAX with the highest degree of crosslinking. When calcium carbonate was mixed with the paper coating adhesives, the GAX showed comparable coating properties to that of polyvinyl alcohol, demonstrating its potential to substitute petroleum-based paper coating adhesives.
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Fukumori, Kenzo. "Crosslinking of Rubbers." Seikei-Kakou 30, no. 4 (March 20, 2018): 142–45. http://dx.doi.org/10.4325/seikeikakou.30.142.

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Dissertations / Theses on the topic "Crosslinking"

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Haleem, Asad Bilal. "Crosslinking nucleophilic dyes on cotton." Thesis, University of Leeds, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250890.

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Thompson, Corrine P. "Chemical models of crosslinking polymers." Thesis, University of Surrey, 1995. http://epubs.surrey.ac.uk/844286/.

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Low molecular weight compounds were used to model the reaction between a range of substituted methyl-ketones with hydrazides in comparison to amines. The reactions were studied by 1H-NMR spectroscopy at three pH values, in order to establish structure-reactivity relationships and pH control of the reaction. The information gained was used to design four acrylate monomers containing a terminal methyl-ketone moiety. The monomers were incorporated into a methyl methacrylate and n-butyl acrylate polymer backbone at low concentrations. The methyl-ketone group was expected to engage in crosslinking reactions with a water-soluble dihydrazide crosslinker. Tests were performed to show the effect on polymer film properties when such a reaction occurs. Swelling studies were carried out to show the extent of reaction in polymer samples through calculation of the average molecular weight between crosslinks. Mc. An introduction to emulsion polymers and their application in binder compositions is given in chapter 1. Several condensation processes known to occur between carbonyl- and amino-functional groups in different structures, and under different conditions, are also outlined. The experimental procedures and analytical techniques used throughout the research are described in chapter 2. In chapters 3 and 4, model systems were used to determine details of the condensation process (in a dilute aqueous environment) and control of the reaction by pH. This knowledge was applied in chapter 5 to the design of polymer systems which may be crosslinked through such condensations. The resulting systems were compared to a commercially available crosslinking emulsion polymer composition to test their relative performance. These various aspects are discussed at the end of the thesis with suggestions for further research.
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Sisson, Thomas Michael 1966. "Crosslinking polymerization in supramolecular assemblies." Diss., The University of Arizona, 1997. http://hdl.handle.net/10150/282566.

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Supramolecular assemblies are composed of noncovalently associated molecules which organize in water to yield 2-D and 3-D architectures. Crosslinking polymerization of supramolecular assemblies provides an effective means to modify their chemical and physical properties. Two methods of characterizing crosslinked polymeric assemblies were developed. These techniques rely on experimentally observed changes in polymer solubility and assembly stability in the presence of nonionic surfactants. The results show an inefficient crosslinking mechanism in organized media compared to isotropic polymerization. Two models rationalizing the inefficient crosslinking observed in organized media were proposed. Symmetrical crosslinking agents were synthesized to test the models. These results suggest intramolecular memorialization is an important process in the efficiency of crosslinking. The polymerization of a heterobifunctional lipid with two polymerizable groups in the same acyl chain separated by a six carbon spacer yielded a novel linear ladder-like polymer architecture. The two reactive groups are in regions of different polarity allowing for the simultaneous, selective, and sequential polymerization depending on the initiation chemistry employed. A second heterobifunctional lipid was designed and synthesized with a longer spacer between the two reactive groups. Polymerization of vesicles gave stable polymeric vesicles. The results from the crosslinking and redox polymerization studies on 2-D assemblies were applied to the inverted hexagonal and bicontinuous cubic phases. Phase behavior is characterized before and after crosslinking polymerization principally by variable temperature ³¹NMR. γ-Initiated polymerization of bis-lipids was studied to evaluate their sensitivity to ionizing radiation. The reactive moiety effects the initial rate of polymerization, extent of polymerization, and inhibition by oxygen. A preliminary investigation of polymerizable ion-paired amphiphiles (IPA) showed polymerization methods commonly used for zwitterionic lipids can be applied to IPA. This is the first report of polymerization of reactive groups in the anionic acyl chain of an ion-paired amphiphile.
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Bewsher, Alan. "New crosslinking methods for functionalised oligomers." Thesis, Lancaster University, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.335350.

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Bajomo, Michael A. "Smart crosslinking of water soluble polymers." Thesis, Imperial College London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526402.

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Tabtiang, Arunee. "Irradiation crosslinking of oriented plasticised PVC compounds." Thesis, Loughborough University, 1995. https://dspace.lboro.ac.uk/2134/12433.

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Plasticised polyvinyl chloride (PPVC) compounds were biaxially stretched, annealed in the drawn state and subsequently exposed to electron beam irradiation. During sample irradiation the crosslinking reaction was promoted by a radiation sensitising monomer, trimethylolpropanetrimethacrylate (TMPTMA), included in the PVC compound formulations. The influence of stabiliser type and level, TMPTMA level and irradiation dose on the network structure produced was investigated. A tin stabiliser, Stanclere TL, was selected for this study as it promoted the crosslinking reaction and it showed no interfering peaks in the wide angle x-ray diffraction (WAXD) traces which were used to follow the development of structural order. The appearance of gel, the material insoluble in THF, in irradiated oriented samples proved that a crosslinked structure was created. The gel formation increased with TMPTMA level and irradiation dose. The gel content was found to affect mechanical properties at elevated temperatures and produced an increase in the area shrinkage temperature. Sample thickness and the plasticiser content were found to have a major effect upon gel formation. The thicker the sample was, the smaller the quantity of gel that was formed. Samples containing 46.5phr plasticiser showed greater gel content than samples containing 25phr plasticiser as a result of the higher molecular mobility in the more plasticised samples. It was also found that the orientation of the film decreased the efficiency of network formation in PVC formulations with a 46.5phr plasticiser content but no significant change in gel content could be detected in those containing 25phr plasticiser. Tensile properties and impact strength at room temperature were slightly improved in irradiated samples. The modified structure resulted in an improvement in tensile strength and penetration resistance at higher temperatures and an increased area shrinkage temperature. Crosslinking did not affect room temperature recovery or crystalline orientation; however irradiation crosslinking reduced crystallinity.
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Sarker, Dipak Kumar. "Control of protein foam stability by crosslinking." Thesis, University of East Anglia, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309907.

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Rueda, de la Garza Gabriela. "The effects of crosslinking in polymer miscibility." Thesis, Imperial College London, 1988. http://hdl.handle.net/10044/1/47234.

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Briceno, Garcia Ruben Dario. "Crosslinking of ethylene copolymers from epoxy chemistry." Thesis, Lyon, INSA, 2014. http://www.theses.fr/2014ISAL0037.

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La plupart des couches d'isolation de câbles pour la moyenne tension "MV" et haute tension "HV" sont fabriquées en polyéthylène réticulé (XLPE) par voie peroxyde. L'impact des sous-produits de réaction sur les propriétés et la nécessité d'une étape de dégazage au cours du processus sont les principaux problèmes liés à cette technologie. Cette étude se concentre sur le développement d'une méthode de réticulation alternative sans les problèmes liés aux sous-produits. Des copolymères d’éthylène/époxy ont été réticulés thermiquement en utilisant un agent aminoacide pour créer des liaisons covalentes entre les fonctions époxydes. L’influence de différents paramètres sur la cinétique de réaction tels que la température de réticulation, les proportions aminoacide/époxy, la taille des particules de l’aminoacide et la teneur en époxy dans les copolymères a été étudiée par techniques de caractérisation telles que : rhéologie dynamique, spectrométrie FTIR, microscopie à balayage électronique et calorimétrie différentielle. En outre, l'étude de la structure du réseau avant et pendant un vieillissement thermique a été effectuée par différentes techniques (mesures de gonflement, spectroscopie FTIR, propriétés de traction et thermoporosimétrie) sur deux types de réseaux : un pré-contraint et un autre non-contraint. Enfin, une caractérisation des propriétés électriques par spectroscopie diélectriques et mesures de claquage électrique a été faite. Les résultats concernant les cinétiques de réaction, les propriétés thermomécaniques et le comportement électrique ont montré que la formulation développée dans cette étude peut être utilisée pour une application de câble
Most of insulation layers of cables for medium voltage “MV” and high voltage “HV” applications are made of crosslinked polyethylene (XLPE) by peroxide technology. The impact of reaction by-products on properties and the consequential need of a degassing stage during the process are the main problems related to this technology. This study focuses on the development of an alternative crosslinking method without by-products issues. Epoxy-ethylene copolymers were thermally crosslinked by using an amino-acid agent to create covalent cross-links between epoxide functions. Influence of several parameters on kinetic reactions such as crosslinking temperature, amino acid/epoxy proportions, size particle of amino acid and epoxy content in copolymers were studied by characterization techniques such as: dynamic rheology, FTIR spectrometry, SEM microscopy and differential calorimetry. In addition, study of the network structure before and during a thermal aging was done on a pre-constrained and a non-constrained network by different techniques (swelling ratio measurement, FTIR spectroscopy, tensile properties and thermoporosimetry analysis). Finally, a characterization of electrical properties by dielectric spectroscopy and breakdown measurements was done. Results related to reaction kinetic, thermo-mechanical properties and electrical behavior have shown that the developed formulation can be used for cable application
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Trimukhe, K. D. "Crosslinking reactions of chitosan and their applications." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2007. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2625.

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Books on the topic "Crosslinking"

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Bhattacharya, Amit, James W. Rawlins, and Paramita Ray, eds. Polymer Grafting and Crosslinking. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470414811.

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1946-, Bhattacharya Amit, Ray Paramita, and Gujarat Bhavnagar, eds. Polymer grafting and crosslinking. Hoboken, N.J: John Wiley, 2009.

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Güven, O., ed. Crosslinking and Scission in Polymers. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-1924-2.

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Aziz, T. Crosslinking of low-density polythylene. Manchester: UMIST, 1997.

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Leon, G. Crosslinking of low-density polyethylene. Manchester: UMIST, 1996.

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NATO Advanced Study Institute on "Advanced Methods of Determination of Crosslinking and Scission in Polymers and their Effects on Mechanical Properties" (1988 Kemer, Kemer Bucağı, Antalya İli, Turkey). Crosslinking and scission in polymers. Dordrecht: Kluwer Academic Publishers, 1990.

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Güven, O. Crosslinking and Scission in Polymers. Dordrecht: Springer Netherlands, 1990.

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Carbone, Nicholas. Photochemical Crosslinking Reactions in Polymers. [New York, N.Y.?]: [publisher not identified], 2012.

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Kamenov, Ognian. Additive incorporation in the polyethylene orientation-crosslinking process. Ottawa: National Library of Canada, 1996.

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Ajit, Singh, and Atomic Energy of Canada Limited., eds. Crosslinking of commercial polyethylenes by 10 MeV electrons. Pinawa, Man: AECL, Whiteshell Laboratories, 1995.

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Book chapters on the topic "Crosslinking"

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Gooch, Jan W. "Crosslinking." In Encyclopedic Dictionary of Polymers, 183. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3123.

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Hernández-Ortiz, Julio César, and Eduardo Vivaldo-Lima. "Crosslinking." In Handbook of Polymer Synthesis, Characterization, and Processing, 187–204. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118480793.ch9.

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Gooch, Jan W. "Crosslinking Agent." In Encyclopedic Dictionary of Polymers, 183. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3124.

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Gooch, Jan W. "Crosslinking Agents." In Encyclopedic Dictionary of Polymers, 183. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3125.

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Gooch, Jan W. "Crosslinking Index." In Encyclopedic Dictionary of Polymers, 183. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_3126.

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Jipa, S., and T. Zaharescu. "1.1 Crosslinking." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I, 93–107. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_7.

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Gooch, Jan W. "Radiation Crosslinking." In Encyclopedic Dictionary of Polymers, 606. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9728.

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Gooch, Jan W. "Self-Crosslinking." In Encyclopedic Dictionary of Polymers, 652. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10432.

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Goethals, Ron. "Crosslinking Technologies." In The Global Cable Industry, 215–48. Weinheim, Germany: WILEY-VCH GmbH, 2021. http://dx.doi.org/10.1002/9783527822263.ch8.

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Chodák, Ivan. "Crosslinking of polypropylene." In Polymer Science and Technology Series, 128–34. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4421-6_18.

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Conference papers on the topic "Crosslinking"

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Mendez, Antonio J., and Robert M. Gagliardi. "Lasercom crosslinking for satellite clusters." In Photonics West 2001 - LASE, edited by G. Stephen Mecherle. SPIE, 2001. http://dx.doi.org/10.1117/12.430799.

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Lei, Cuiyue, and P. E. Clark. "Crosslinking of Guar and Guar Derivatives." In SPE Annual Technical Conference and Exhibition. Society of Petroleum Engineers, 2004. http://dx.doi.org/10.2118/90840-ms.

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Milne, Peter J., and Rod G. Zika. "Crosslinking of collagen gels: photochemical measurements." In OE/LASE '92, edited by Jean-Marie Parel. SPIE, 1992. http://dx.doi.org/10.1117/12.137413.

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Croutxe-Barghorn, Celine, Olivier Soppera, and Daniel-Joseph Lougnot. "Microlens array fabrication through crosslinking photopolymerization." In Symposium on Micromachining and Microfabrication, edited by Sing H. Lee and J. Allen Cox. SPIE, 1999. http://dx.doi.org/10.1117/12.360531.

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Clark, P. E., M. Balakrishnan, and L. Sundram. "Crosslinking of Hydroxypropyl Guar With Metal Ions." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1993. http://dx.doi.org/10.2118/25208-ms.

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Verga, Daniela, Florian Hamon, Florent Poyet, Sophie Bombard, and Marie-Paule Teulade-Fichou. "Trapping quadruplexes with highly specific crosslinking agents." In XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414193.

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Caronia, Paul J., Jeffrey M. Cogen, and Peter Dluzneski. "Novel polymer crosslinking chemistries for cable insulation." In 2014 IEEE Electrical Insulation Conference (EIC). IEEE, 2014. http://dx.doi.org/10.1109/eic.2014.6869416.

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Redmond, Robert W., Irene E. Kochevar, Michael C. McCormack, and William G. Austen. "Clinical Potential of Light-Activated Tissue Crosslinking." In CLEO: Applications and Technology. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/cleo_at.2015.aw3j.2.

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Lei, Cuiyue, and Peter E. Clark. "Fracturing-Fluid Crosslinking at Low Polymer Concentration." In SPE Annual Technical Conference and Exhibition. Society of Petroleum Engineers, 2005. http://dx.doi.org/10.2118/96937-ms.

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Levy, Ilan, Tzur Paldi, and Oded Shoseyov. "ENGINEERING CARBOHYDRATE-BINDING MODULES FOR POLYSACCHARIDE CROSSLINKING." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.477.

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Reports on the topic "Crosslinking"

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McMillen, D. F., and R. Malhotra. Mitigating crosslinking reactions through preconversion strategies. Final report. Office of Scientific and Technical Information (OSTI), July 1994. http://dx.doi.org/10.2172/119893.

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McMillen, D. F., and R. Malhotra. Cleavage and crosslinking of polymeric coal structures during pyrolysis. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/7296882.

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Thompson, Aidan Patrick, John G. Curro, Dana R. Rottach, Gary Stephen Grest, Joanne L. Budzien, and David Chi S. Lo. Constitutive models for rubber networks undergoing simultaneous crosslinking and scission. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/877144.

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Wagener, Kenneth, Hector Zuluaga, and Paula Delgado. Polycarbosilane Elastomers via Chain-Internal and Chain-End Latent Crosslinking. Fort Belvoir, VA: Defense Technical Information Center, August 2007. http://dx.doi.org/10.21236/ada474165.

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Mattei-Sosa, Jose, Victor Medina, Chris Griggs, and Veera Gude. Crosslinking graphene oxide and chitosan to form scalable water treatment membranes. Engineer Research and Development Center (U.S.), July 2019. http://dx.doi.org/10.21079/11681/33263.

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McMillen, D. F., and R. Malhotra. Cleavage and crosslinking of polymeric coal structures during pyrolysis. Final report. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/10169100.

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Van Buskirk, Caleb Griffith. Crosslinking of SAVY-4000 O-rings as a Function of Aging Conditions. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1392792.

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Usachenko, S. I., and E. M. Bradbury. Histone-DNA contacts in structure/function relationships of nucleosomes as revealed by crosslinking. Office of Scientific and Technical Information (OSTI), December 1998. http://dx.doi.org/10.2172/334246.

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DE Belle, Ian. Cloning and Characterization of Active Egr-1 Target Genes by In Vivo Crosslinking. Fort Belvoir, VA: Defense Technical Information Center, May 2001. http://dx.doi.org/10.21236/ada395170.

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10

DE Belle, Ian. Cloning and Characteristics of Active Egr-1 Target Genes by In Vivo Crosslinking. Fort Belvoir, VA: Defense Technical Information Center, May 2003. http://dx.doi.org/10.21236/ada417973.

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