Academic literature on the topic 'Carbohydrates polymer'

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Journal articles on the topic "Carbohydrates polymer"

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Bowen, P. T., and T. M. Keinath. "Sludge Conditioning: Effects of Sludge Biochemical Composition." Water Science and Technology 17, no. 4-5 (April 1, 1985): 505–15. http://dx.doi.org/10.2166/wst.1985.0155.

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Variations in response of three different sludges to conditioning with organic polyelectrolytes were evaluated with respect to the carbohydrate, protein and lipid content of the sludges. These biochemicals comprise the surfaces of most sludges. The difference in the concentration of these compounds is intrinsic to the sludge type. Polymer Index (PI) , a measure of minimum polymer dose required to achieve maximum dewaterability, was statistically related to each of the three components. Carbohydrate content correlated most strongly with PI. As carbohydrate content increases, PI was found to decrease indicating better polymer performance. Biopolymers, which are composed mainly of carbohydrates may surround the cells forming a highly reactive surface. These exocellular materials also promote bioflocculation. Both actions result in a lower polymer requirement for destabilizing the sludge. Protein and lipid were not observed to have strong correlation with PI. Cellular surfaces and structures are composed of these components. The low correlation indicates these components are less favored than carbohydrates for polymer interaction.
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Krishnaveni Manubolu, Sreenivasulu Munna, and Chandrasekhar Kothapalli Bonnoth. "A Study on Extraction and Characterization of Vigna mungo Polymer." International Journal of Research in Pharmaceutical Sciences 12, no. 3 (July 1, 2021): 1870–78. http://dx.doi.org/10.26452/ijrps.v12i3.4787.

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The aim of work is to extract and characterize the Vigna mungo polymer solvent using acetone and ethanol. Natural polymers contribution towards formulation of dosage forms is appreciable as they are biocompatible, biodegradable and safe. So extraction and characterization of Vigna mungo polymer helps in the interaction studies of preformulation. In this present study, various physicochemical characters like phytochemical screening, viscosity, particle size analysis, and flow characteristics were determined. Further characterization performed using FTIR and XRD. Vigna mungo polymer obtained using acetone was taken into further studies of evaluation because of more product yield and less particle size. FTIR results revealed existence of carbohydrate nature. X-ray diffractogram presented degree of crystallinity 26.4%. And phytochemical screening of the extracted polymer indicated presence of mucilage and carbohydrates using ruthenium red and molisch's test. Statistical analysis of data was performed using two way ANOVA using Graphpad prism 5 software was used to compare Vigna mungo polymer extracted using acetone and ethanol. Physicochemical parameters experimental data found to be statistical significance two way ANOVA (P < 0.05).
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Kerzner, B., H. R. Sloan, H. J. McClung, C. C. Chidi, A. H. Ailabouni, and C. Seckel. "Absorption of glucose polymers from canine jejunum deprived of pancreatic amylase." American Journal of Physiology-Gastrointestinal and Liver Physiology 250, no. 6 (June 1, 1986): G824—G829. http://dx.doi.org/10.1152/ajpgi.1986.250.6.g824.

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We evaluated the absorption of glucose polymers in canine jejunal Thiry-Vella fistulas proven to be free of pancreatic amylase. Medium-length oligomers with degrees of polymerization of 6 through 10 glucose units (DP 6–10) and long-chain material (DPavg23) were isolated from a cornstarch hydrolysate. We perfused 90, 180, and 360 mg/dl solutions of glucose, DP 6–10, and DPavg23 at 0.4, 1.9, and 3.4 ml/min. At all perfusion rates carbohydrate absorption decreased as the chain length of the oligomers increased, and these differences persisted even at the slowest perfusion rate employed. In two additional animals the fistulas were perfused at 3.4 ml/min with the three test carbohydrates at concentrations of 90, 180, 225, 270, 315, 360, 405, and 450 mg/dl. At this flow rate, the assimilative process of DP 6–10 and the long-chain fraction appeared to be saturated at carbohydrate concentrations above 360 mg/dl, whereas the absorption of glucose was linearly related to concentration throughout the range studied. With both groups of polymers, the fluid emerging from the fistula was virtually free of glucose, a finding that suggests that polymer digestion, not glucose absorption, is the rate-limiting step for polymer assimilation.
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Flo, Trude H., Liv Ryan, Lars Kilaas, Gudmund Skjåk-Bræk, Robin R. Ingalls, Anders Sundan, Douglas T. Golenbock, and Terje Espevik. "Involvement of CD14 and β2-Integrins in Activating Cells with Soluble and Particulate Lipopolysaccharides and Mannuronic Acid Polymers." Infection and Immunity 68, no. 12 (December 1, 2000): 6770–76. http://dx.doi.org/10.1128/iai.68.12.6770-6776.2000.

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ABSTRACT Lipopolysaccharide (LPS) and related bacterial products can be recognized by host inflammatory cells in a particulate, bacterium-bound form, as well as in various soluble, released forms. In the present study we have compared the mechanisms used by LPS, detoxified LPS (DLPS), and mannuronic acid polymers (M-polymers), in solution or covalently linked to particles, in stimulating monocytes to tumor necrosis factor (TNF) production. The addition of recombinant LPS binding protein (LBP) and/or soluble CD14 (sCD14) enhanced the production of TNF from monocytes stimulated with soluble LPS, DLPS, or M-polymer, but did not affect the response to M-polymer or DLPS attached to particles. Treatment of monocytes with antibody to CD14, CD18, or CD11b showed that CD14, but not CR3 (CD11b/CD18), mediated monocyte TNF production in response to the soluble antigens. In contrast, anti-CD14, anti-CD11b and anti-CD18 monoclonal antibodies all inhibited the response to the particulate stimuli. On the other hand, B975, a synthetic analog of Rhodobacter capsulatus lipid A, completely abrogated the monocyte TNF response induced by LPS but did not affect the TNF induction by DLPS or M-polymer, either in soluble or particulate forms. These data demonstrate that the engagement of immune receptors by bacterial products such as LPS, DLPS, and M-polymer is dependent upon the presentation form of their constituent carbohydrates, and that factors such as aggregation state, acylation, carbohydrate chain length, and solid versus liquid phase of bacterial ligands influence the mechanisms used by cells in mediating proinflammatory responses.
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Tan, Jin, Chenguang Wang, Qi Zhang, and Longlong Ma. "Synthesis and Characterization of Furans and Levulinates Polymers: Derived from Cellulosic Carbohydrates via Aldol Condensation." E3S Web of Conferences 53 (2018): 03011. http://dx.doi.org/10.1051/e3sconf/20185303011.

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Aldol condensation between furans and levulinates shows a selective route for the polymers production. In this work, the influences of mole ratio between furans and levulinates as well as substrate species on the formation of polymers structure were investigated. The characterization of gel permeation chromatography and 13C nuclear magnetic resonance to the synthesized polymers suggested that the mole ratio between furans and levulinates, and substrate species exhibited a great effect on the structure of polymers. Higher mole ratios between furans and levulinates resulted in the aggravated polymerization. EMF-EL polymers showed larger molecular weight distribution compared with FFA-EL/LA polymers. This investigation further provides other key factors to the decision of polymer structure.
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Ribeiro, Jessica P. M., Patrícia V. Mendonça, Jorge F. J. Coelho, Krzysztof Matyjaszewski, and Arménio C. Serra. "Glycopolymer Brushes by Reversible Deactivation Radical Polymerization: Preparation, Applications, and Future Challenges." Polymers 12, no. 6 (June 1, 2020): 1268. http://dx.doi.org/10.3390/polym12061268.

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The cellular surface contains specific proteins, also known as lectins, that are carbohydrates receptors involved in different biological events, such as cell–cell adhesion, cell recognition and cell differentiation. The synthesis of well-defined polymers containing carbohydrate units, known as glycopolymers, by reversible deactivation radical polymerization (RDRP) methods allows the development of tailor-made materials with high affinity for lectins because of their multivalent interaction. These polymers are promising candidates for the biomedical field, namely as novel diagnostic disease markers, biosensors, or carriers for tumor-targeted therapy. Although linear glycopolymers are extensively studied for lectin recognition, branched glycopolymeric structures, such as polymer brushes can establish stronger interactions with lectins. This specific glycopolymer topology can be synthesized in a bottlebrush form or grafted to/from surfaces by using RDRP methods, allowing a precise control over molecular weight, grafting density, and brush thickness. Here, the preparation and application of glycopolymer brushes is critically discussed and future research directions on this topic are suggested.
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Motoyanagi, Jin, Minh Nguyen, Tomonari Tanaka, and Masahiko Minoda. "Protecting Group-Free Synthesis of Glycopolymer-Type Amphiphilic Macromonomers and Their Use for the Preparation of Carbohydrate-Decorated Polymer Particles." Biomolecules 9, no. 2 (February 19, 2019): 72. http://dx.doi.org/10.3390/biom9020072.

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Polymer particles modified with carbohydrates on their surfaces are of significant interest, because their specific recognition abilities to biomolecules are valuable for developing promising materials in biomedical fields. Carbohydrate-decorated core-shell polymer particles are expected to be efficiently prepared by dispersion polymerization using a glycopolymer-based amphiphilic macromonomer as both a polymeric steric stabilizer and a monomer. To create glycopolymer-type macromonomers, we propose a new strategy combining living cationic polymerization of an alkynyl-functionalized vinyl ether (VE), and the click reaction for the preparation of glycopolymers having a polymerizable terminal group, and investigate their dispersion copolymerization with styrene for generating carbohydrate-decorated polymer particles. This study deals with (i) the synthesis of block copolymer-type amphiphilic macromonomers bearing a methacryloyl group at the α-terminus, and pendant alkynyl groups by living cationic polymerization of alkynyl-substituted VE (VEEP), (ii) the derivatization of maltose-carrying macromonomers by click chemistry of the pendant alkynyl groups of the precursor macromonomers with maltosyl azide without any protecting/deprotecting processes, and (iii) the preparation of maltose-decorated (Mal-decorated) polymer particles through the dispersion copolymerization of glycopolymer-type macromonomers with styrene in polar media. Moreover, this study concerns the specific interactions of the resultant polymer particles with the lectin concanavalin A (Con A).
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Massicotte, D., F. Peronnet, G. Brisson, K. Bakkouch, and C. Hillaire-Marcel. "Oxidation of a glucose polymer during exercise: comparison with glucose and fructose." Journal of Applied Physiology 66, no. 1 (January 1, 1989): 179–83. http://dx.doi.org/10.1152/jappl.1989.66.1.179.

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The purpose of this study was to compare the oxidation of 13C-labeled glucose, fructose, and glucose polymer ingested (1.33 g.kg-1 in 19 ml.kg-1 water) during cycle exercise (120 min, 53 +/- 2% maximal O2 uptake) in six healthy male subjects. Oxidation of exogenous glucose and glucose polymer (72 +/- 15 and 65 +/- 18%, respectively, of the 98.9 +/- 4.7 g ingested) was similar and significantly greater than exogenous fructose oxidation (54 +/- 13%). A transient rise in plasma glucose concentration was observed with glucose ingestion only. However, plasma insulin levels were similar with glucose and glucose polymer ingestions and significantly higher than with water or fructose ingestion. Plasma free fatty acid and glycerol responses to exercise were blunted with carbohydrate ingestion. However, fat utilization was not significantly different with water (82 +/- 14 g), glucose (60 +/- 3 g), fructose (59 +/- 11 g), or glucose polymer ingestion (60 +/- 8 g). Endogenous carbohydrate utilization was significantly lower with glucose (184 +/- 22 g), glucose polymer (187 +/- 31 g), and fructose (211 +/- 18 g) than with water (239 +/- 30 g) ingestion. Plasma volume slightly increased with water ingestion (7.4 +/- 4.5%), but the decrease was similar with glucose (-7.6 +/- 5.1%) and glucose polymer (-8.2 +/- 4.6%), suggesting that the rate of water delivery to plasma was similar with the two carbohydrates.(ABSTRACT TRUNCATED AT 250 WORDS)
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Parang, Keykavous. "Polymer-Supported reagents for methylphosphorylation and phosphorylation of carbohydrates." Bioorganic & Medicinal Chemistry Letters 12, no. 14 (July 2002): 1863–66. http://dx.doi.org/10.1016/s0960-894x(02)00266-4.

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Redgwell, R. J., V. Trovato, and D. Curti. "Cocoa bean carbohydrates: roasting-induced changes and polymer interactions." Food Chemistry 80, no. 4 (April 2003): 511–16. http://dx.doi.org/10.1016/s0308-8146(02)00320-5.

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Dissertations / Theses on the topic "Carbohydrates polymer"

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Yuwen, Jing. "Polymer-Based Photoactive Surface for the Efficient Immobilization of Nanoparticles, Polymers, Graphene and Carbohydrates." PDXScholar, 2011. https://pdxscholar.library.pdx.edu/open_access_etds/413.

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This thesis focuses on developing a new photocoupling surface, base on polyallyamine (PAAm), to increase the efficiency of the photocoupling agent perfluorophenyl azide (PFPA) in the immobilization of nanoparticles, carbohydrates and graphene. Extensive studies have been carried out in our lab on the covalent immobilization of polymers and graphene using PFPA-functionalized surfaces. Here we show that PAAm-based PFPA surface can be used to efficiently immobilize not only graphene and polymers but also nanomaterials and small molecules. This was accomplished by first silanizing silicon wafers with PFPA-silane followed by attaching a thin film of PAAm by UV radiation. Treating the PAAm surface with N-hydroxysuccinimide-derivatized PFPA (PFPA-NHS) yielded the PAAm-PFPA surface. The functionalized surfaces were characterized by ellipsometry (layer thickness), contact angle (surface tension), and ATR-FTIR. The PAAm surface was further characterized by determining the density of amino groups on the surface. The PAAm-PFPA surfaces were subsequently used to covalently immobilize polymers, nanomaterials, carbohydrates and graphene by a simple procedure of coating the molecules or materials on the PAAm-PFPA surface followed by UV irradiation. The resulting surfaces were characterized using ellipsometry, AFM, optical microscopy. The attached carbohydrates were further evaluated using lectins, i.e., carbohydrate-binding proteins.
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Moore, Martin. "New Dipolar Cycloaddition reactions of a Carbohydrate-derived Vinyl Sulfoxide Alkyne Equivalent and a Polymer-supported Alkyne with Azides." Connect to online version at OhioLINK ETD Connect to online version at Digital.Maag, 1998. http://hdl.handle.net/1989/4782.

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Kantchev, Assen B. "Part 1, Oligosaccharide synthesis on a hyperbranched polymer as soluble support ; Part 2, Photoresponsive conformational equilibria of chiral, helically folded dendrons /." The Ohio State University, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486572165275834.

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Abeylath, Thotaha Wijayahewage Sampath Chrysantha. "Glyconanobiotics : novel carbohydrated nanoparticle polymers." [Tampa, Fla] : University of South Florida, 2007. http://purl.fcla.edu/usf/dc/et/SFE0001948.

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Gaitonde, Vishwanath Venkatesh. "Carbohydrate-Based Synthetic Methodology and Polymer Development." University of Toledo / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1438939333.

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Liu, Xiaohong. "Synthesis and Characterization of Carbohydrate-conjugated Polyesters and Polyurethanes." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1491433530882435.

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Mazzoccoli, Jason Paul. "ULTRASONICATION OF POLYSACCHARIDE MATERIALS." Cleveland, Ohio : Case Western Reserve University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1262572128.

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Thesis (Doctor of Philosophy)--Case Western Reserve University, 2010
Department of Chemical Engineering Title from PDF (viewed on 2010-05-25) Includes abstract Includes bibliographical references and appendices Available online via the OhioLINK ETD Center
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Taylor, Leeanne R. "Rational design of glycosaminoglycan mimics using N-alkyl-N,N-linked urea oligomer containing polymers." University of Cincinnati / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1406819426.

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Benjamin, Michael. "Synthesis, Characterization, and Determination of Relaxivities for Glycoamido-DTPA Polymers for Use as MRI Contrast Agents." University of Cincinnati / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1154109396.

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Pan, Yining. "Immobilized Viologen Polymer for Use in Direct Carbohydrate Fuel Cells." BYU ScholarsArchive, 2013. https://scholarsarchive.byu.edu/etd/3524.

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Glucose and other carbohydrates are some of the most abundant renewable energy sources in the world. The oxidation of carbohydrates in a fuel cell allows their chemical energy to be converted directly into electrical energy. Viologen has been indentified and shows promising ability as an electron-transfer catalyst or mediator for carbohydrate oxidation in an alkaline carbohydrate fuel cell. Building on the previous results, the objective of this work was to develop an immobilization chemistry of viologen onto an electrode and to investigate the catalytic activity for carbohydrate oxidation in direct carbohydrate fuel cells.The immobilization was achieved by electropolymerizing a novel viologen monomer onto an electrode surface. The novel viologen monomer, which functions as a monosubstituted viologen, was synthesized and isolated in-house. Gold-plated nickel wire and graphite disks were used as the substrates for the electropolymerization. SEM, EDAX, XPS and water-contact-angle measurement were used to verify the formation of the coating on the gold and graphite surfaces. The catalytic activity of the immobilized viologen on graphite disk surface was examined using a fuel-cell-like device. The test was operated within the desired pH range for an operating fuel cell; it was found that the immobilized viologen polymer has a low catalytic activity toward oxidizing carbohydrates. In addition, the electrochemical properties of the novel viologen monomer were investigated by the method of cyclic voltammetry, as well as for that of two aminoviologens synthesized in-house. Redox potentials, diffusion coefficients, and heterogeneous electron-transfer rate constants were determined.
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Books on the topic "Carbohydrates polymer"

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Kalia, Susheel. Polysaccharide Based Graft Copolymers. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013.

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Symposium on Industrial Polysaccharides (1992 Washington, D.C.). Carbohydrates and carbohydrate polymers: Analysis, biotechnology, modification, antiviral, biomedical and other applications. Mount Prospect, IL: ATL Press, 1993.

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Paulsen, Berit S., ed. Bioactive Carbohydrate Polymers. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-015-9572-8.

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Scholz, Carmen. Polymers from renewable resources: Carbohydrates and agroproteins. Washington, D.C: American Chemical Society, 2000.

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Ito, Ryouichi. Handbook of carbohydrate polymers: Development, properties and applications. New York: Nova Science Publishers, 2010.

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Edgar, Kevin J. Polysaccharide materials: Performance by design. Washington, DC: American Chemical Society, 2009.

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Edgar, Kevin J. Polysaccharide materials: Performance by design. Washington, DC: American Chemical Society, 2009.

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Engineered carbohydrate-based materials for biomedical applications: Polymers, surfaces, dendrimers, nanoparticles, and hydrogels. Hoboken, N.J: Wiley, 2011.

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J, Cristóbal López, and SpringerLink (Online service), eds. Reactivity Tuning in Oligosaccharide Assembly. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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Edgar, Kevin J., Charles M. Buchanan, and Thomas Heinze. Polysaccharide materials: Performance by design. Washington DC: American Chemical Society, 2009.

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Book chapters on the topic "Carbohydrates polymer"

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Nishimura, Shin-Ichiro. "Solution and Polymer-Supported Synthesis of Carbohydrates." In Carbohydrate-Based Drug Discovery, 129–36. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527602437.ch5.

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Babooram, Keshwaree, and Ravin Narain. "Carbohydrates and their Roles in Biological Recognition Processes." In Polymer Adhesion, Friction, and Lubrication, 545–74. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118505175.ch13.

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Jong, L. "Reinforcement Effect of Soy Protein and Carbohydrates in Polymer Composites." In ACS Symposium Series, 86–108. Washington, DC: American Chemical Society, 2008. http://dx.doi.org/10.1021/bk-2008-0999.ch006.

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Gooch, Jan W. "Carbohydrates." In Encyclopedic Dictionary of Polymers, 116. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1920.

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Gooch, Jan W. "Carbohydrates." In Encyclopedic Dictionary of Polymers, 880. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13314.

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Dräger, Gerald, Andreas Krause, Lena Möller, and Severian Dumitriu. "Carbohydrates." In Handbook of Biodegradable Polymers, 155–93. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527635818.ch7.

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Gooch, Jan W. "Carbohydrate." In Encyclopedic Dictionary of Polymers, 116. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1919.

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Gooch, Jan W. "Carbohydrate." In Encyclopedic Dictionary of Polymers, 880. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13313.

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Yang, Jun, and Yixiang Xu. "Functional Carbohydrate Polymers: Prebiotics." In Polymers for Food Applications, 651–91. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-94625-2_24.

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Farrukh, Sarah, Kiran Mustafa, Arshad Hussain, and Muhammad Ayoub. "Synthesis and Applications of Carbohydrate-Based Hydrogels." In Polymers and Polymeric Composites: A Reference Series, 1491–514. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-77830-3_49.

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Conference papers on the topic "Carbohydrates polymer"

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Rosenberg, E., and Robert A. Kellner. "IR-ATR spectroscopic determination of the diffusion coefficients of carbohydrates in polymer matrices." In Luebeck - DL tentative, edited by Herbert M. Heise, Ernst H. Korte, and Heinz W. Siesler. SPIE, 1992. http://dx.doi.org/10.1117/12.56394.

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Xuan, Trinh Anh, Phan Nghia Trung, Bui Long Dinh, Takumi Yamaguchi, and Koichi Kato. "Preparation of water-soluble glycoconjugated poly(acrylamide) for NMR analyses of carbohydrate-carbohydrate interactions." In PROCEEDINGS OF PPS-29: The 29th International Conference of the Polymer Processing Society - Conference Papers. American Institute of Physics, 2014. http://dx.doi.org/10.1063/1.4873797.

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Aldisi, Zulfa, Nabil Zouari, Samir Jaoua, Maria Dittrich, Hamad Al-Kuwari, and Tomaso Bontognali. "Characterization of the Extracellular Polymeric Substances (EPS) of Virgibacillus Strains capable of Mediating the Formation of High Mg-Calcite and Protodolomite." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0026.

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The origin of dolomite –a common carbonate mineral– is the subject of an ongoing debate. It has been proposed that extracellular polymeric substances (EPS) excreted by microbes contain specific organic molecules that facilitate the incorporation of magnesium in the carbonate minerals. We characterized the EPS produced under different conditions by measuring total carbohydrate (TCHO), total protein (TP) content and by (FTIR) analysis. We report the formation of Mgcarbonates with a mol% Mg higher than 41%, exclusively in association with EPS, rich in carbohydrates (TCHO > than 75% of the total EPS mass). Moreover, FTIR analysis of these EPS revealed the presence of protein secondary structures (e.g., β-sheets) known to favor mineral nucleation. These results suggest that some organic molecules with specific functional groups (e.g., carboxyl and hydroxyl groups) may be of key importance for overcoming the kinetic barriers that else prevent the incorporation of Mg into carbonate minerals, a crucial step for the formation of dolomite in natural environments.
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Helmholz, Heike, Peter Thiesen, and Bernd Niemeyer. "SILICA- AND POLYMER-BASED LECTIN ADSORBENTS FOR GLYCOCONJUGATE SEPARATION." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.390.

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Allavudeen, S. Sulthan, and Duraikkannu Loganathan. "TOWARDS ENZYMATIC OLIGOSACCHARIDE SYNTHESIS ON POLYMER-SUPPORT: DEVELOPMENT OF A BIOMIMETIC APPROACH." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.611.

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Sletmoen, Marit, Gudmund Skjak-Braek, and Bjorn T. Stokke. "SINGLE-MOLECULAR PAIR ALGE4 EPIMERASE-MANNURONAN INTERACTIONS AND POLYMER ELASTICITY DETERMINED BY AFM." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.557.

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Hedenetz, A. G., B. Schwarz, P. Olf, F. M. Unger, and W. Schmid. "TOWARDS THE SYNTHESIS OF THE SECONDARY CELL WALL POLYMER (SCWP) OF BACILLUS STEAROTHERMOPHILUS STRAIN PV72/p6." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.555.

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Yamada, Kuriko, Susumu Nishiguchi, Atsushi Toda, Kenji Monde, and Shin-Ichiro Nishimura. "EFFICIENT SYNTHESIS OF OLIGOSACCHARIDE DERIVATIVES USING IMMOBILIZED GLYCOSYLTRANSFERASES AND WATER-SOLUBLE PRIMER POLYMERS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.651.

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Yamane, Shintarou, Norimasa Iwasaki, Tokifumi Majima, Tatsuya Masuko, Tadanao Funakoshi, Akio Minami, and Shin-ichiro Nishimura. "REASIBILITY OF ALGINATE-BASED CHITOSAN HYBRID BIOMATERIAL FOR A SCAFFOLD IN CARTILAGE TISSUE ENGINEERING: EVALUATION OF CHONDROCYTE ADHESION TO NEW POLYMER FIBERS." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.804.

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Haraguchi, Soichi, Tina Pastoor, William Guy Bradley, and Akiko Tanaka. "Abstract B29: Improving the efficacy of dendritic cell-based human papillomavirus vaccines in mice using a natural lignin-carbohydrate complex and/or synthetic lignin-like polyphenol polymers." In Abstracts: AACR Special Conference: Tumor Immunology and Immunotherapy: A New Chapter; December 1-4, 2014; Orlando, FL. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/2326-6074.tumimm14-b29.

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Reports on the topic "Carbohydrates polymer"

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Yuwen, Jing. Polymer-Based Photoactive Surface for the Efficient Immobilization of Nanoparticles, Polymers, Graphene and Carbohydrates. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.413.

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