Academic literature on the topic 'Poly(vinyl amine-co-vinyl amide) (PVAm)'
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Journal articles on the topic "Poly(vinyl amine-co-vinyl amide) (PVAm)"
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Seifert, Susan, Frank Simon, Giesela Baumann, Michael Hietschold, Andreas Seifert, and Stefan Spange. "Adsorption of Poly(vinyl formamide-co-vinyl amine) (PVFA-co-PVAm) Polymers on Zinc, Zinc Oxide, Iron, and Iron Oxide Surfaces." Langmuir 27, no. 23 (2011): 14279–89. http://dx.doi.org/10.1021/la203479n.
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Ashtiani, Saeed, Mehdi Khoshnamvand, Chhabilal Regmi, and Karel Friess. "Interfacial Design of Mixed Matrix Membranes via Grafting PVA on UiO-66-NH2 to Enhance the Gas Separation Performance." Membranes 11, no. 6 (2021): 419. http://dx.doi.org/10.3390/membranes11060419.
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In this study, defect-free facilitated transport mixed matrix membrane (MMM) with high loading amount of UiO-66-NH2 nanoparticles as metal–organic frameworks (MOFs) was fabricated. The MOFs were covalently bonded with poly (vinyl alcohol) (PVA) to incorporate into a poly (vinyl amine) (PVAm) matrix solution. A uniform UiO-66-NH2 dispersion up to 55 wt.% was observed without precipitation and agglomeration after one month. This can be attributed to the high covalent interaction at interfaces of UiO-66-NH2 and PVAm, which was provided by PVA as a functionalized organic linker. The CO2 permeability and CO2/N2 and selectivity were significantly enhanced for the fabricated MMM by using optimal fabrication parameters. This improvement in gas performance is due to the strong impact of solubility and decreasing diffusion in obtained dense membrane to promote CO2 transport with a bicarbonate reversible reaction. Therefore, the highest amount of amine functional groups of PVAm among all polymers, plus the abundant amount of amines from UiO-66-NH2, facilitated the preferential CO2 permeation through the bicarbonate reversible reaction between CO2 and –NH2 in humidified conditions. XRD and FTIR were employed to study the MMM chemical structure and polymers–MOF particle interactions. Cross-sectional and surface morphology of the MMM was observed by SEM-EDX and 3D optical profilometer to detect the dispersion of MOFs into the polymer matrix and explore their interfacial morphology. This approach can be extended for a variety of polymer–filler interfacial designs for gas separation applications.
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Wittke, Ralph, Dierk Knittel, Robert Kaufmann, and Eckhard Schollmeyer. "Modification of Poly(ethylene terephthalate) Surfaces by Linear Poly(vinyl amine)." Zeitschrift für Naturforschung A 64, no. 9-10 (2009): 653–57. http://dx.doi.org/10.1515/zna-2009-9-1018.
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The feasibility of fixing linear poly(vinyl amine) (PVAm) onto the surface of a poly(ethylene terephthalate) (PET) foil is shown. Pretreatment of the PET foil for PVAm anchoring is UV irradiation generated by an excimer lamp (λ = 222 nm). Thereby newly formed COOH-groups are able to build up in situ an ionic double layer with PVAm by proton transfer. The properties of the modified PET foil like wetting performance and electric conductivity are significantly improved by this treatment.
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Sansatsadeekul, Jitlada, and Katanchalee Mai-Ngam. "Reversible Self-Assembling of Comb-Like Functionalized Dextran Surfactant Polymers as an SPR-Sensing Surfaces." Advanced Materials Research 747 (August 2013): 225–29. http://dx.doi.org/10.4028/www.scientific.net/amr.747.225.
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Novel surface plasmon resonance (SPR) sensing surfaces were developed from the perspective of reversible self-assembling of the mixed dextran surfactant polymers onto SPR gold chips. Two comb-like dextran surfactant polymers, which are different in their dextran molecular weight (MW) distribution and the presence of amine functional groups, and their characterization were synthesized. These structurally well-defined surfactant polymers include a bimodal amine dextran surfactant polymer and a monomodal dextran surfactant polymer. The bimodal one consists of poly (vinyl amine) (PVAm) backbone with amine functionalized high MW dextran, non-functionalized low MW dextran and hydrophobic hexyl pendant groups. Allyl high MW dextran aldonic acid and low MW dextran aldonic acid chains with various ratios were sequentially attached to PVAm. The unreacted amine groups on the backbone were further grafted with hexanoic acid and the allyl groups on the high MW dextran were finally converted to amine. The monomodal surfactant polymer, PVAm with non-functionalized low MW dextran and hexyl branches, was synthesized and characterized using similar procedures, except with the absence of allyl high MW dextran aldonic acid and the amine functionalization. The molecular compositions of the surfactant polymers were determined by FTIR and 1H-NMR. Surface active properties at the air-water interface were determined using tensiometer. Reduction in water contact angles was observed on the surfactant treated surfaces. Reversible self-assembling of the synthesized surfactant polymers on SPR gold chip surface was monitored using SPR analysis. Reproducibility of the mixed surfactant assembling process was preliminarily confirmed by a consistent increase in reflectivity change, while no detectable changes in the reflectivity under a 1-h buffer flow indicated stability of the absorbed surfactant layer. Moreover, a simple, quick flow of a basis regeneration solution completely removed the adsorbed surfactant from the surface. Our preliminary investigation also exhibited that the regenerated SPR gold chip was effectively reusable.
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Schulze, Katja, Annette Koch, Alke Petri-Fink, et al. "Uptake and Biocompatibility of Functionalized Poly(vinylalcohol) Coated Superparamagnetic Maghemite Nanoparticles by Synoviocytes In Vitro." Journal of Nanoscience and Nanotechnology 6, no. 9 (2006): 2829–40. http://dx.doi.org/10.1166/jnn.2006.484.
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Superparamagnetic iron oxide nanoparticles (SPION) were coated with either Polyvinyl alcohol (PVA) or Vinyl alcohol/vinyl amine copolymer and further functionalized with the fluorochromes Cy3.5 or Texas Red. A colloidally stable suspension of nanoparticles was incubated on sheep synovial cells in vitro for 3, 24, 72, and 120 hours. Nanoparticle internalization into synoviocytes as well as biocompatibility was visualized using light, fluorescence and confocal microscopy and fluorochrome labeled cells were quantified by flow cytometry. Data were analyzed by ANOVA factorial tests. Amino-PVA-SPION alone was detectable in cytoplasmic endosome-like structures after 3 hours of incubation but resulted in early cell death after 24 hours. Although amino-PVA-Cy3.5- SPION and PVA-TexasRed-SPION were taken up more slowly and less intensely, both labeled more than 80% of the cells in culture, but did not significantly change cell morphology or vitality at any time of evaluation in comparison to control cells. Results indicate that functionalized amino PVA- coated SPION are biocompatible, were successfully internalized by synoviocytes and hold promise for future biomedical applications utilizing magnetic drug targeting in joint disease.
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Shu, Xiaobo, Liping Wan, and Mubai Duan. "Persistent inhibition performance of amine polymers to inhibit clay swelling." Journal of Polymer Engineering 38, no. 4 (2018): 323–31. http://dx.doi.org/10.1515/polyeng-2016-0428.
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AbstractClay hydration and swelling can cause shale instability in the drilling of oil and gas wells. The persistent inhibition performance of polyether amine (PEA) and poly(vinyl alcohol-g-dimethyl aminopropyl methacrylamide) (PVA-g-DMAPMA) as amine clay inhibitors has been investigated through hot rolling dispersion test, bulk hardness test, and bentonite inhibition test. The micro-mechanism has also been explained by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscope (SEM), and X-ray diffraction (XRD) analyses. Through the interaction of PEA and PVA-g-DMAPMA, the PEA can enter into clay platelets to exclude water molecules from entering and hydrating the clay, and the PVA-g-DMAPMA can affect the surface of clay minerals to prevent further intrusion of water molecules. Due to the effect of multiple cationic sites, both PEA and PVA-g-DMAPMA can maintain persistent clay inhibition and are less susceptible to reversing the adsorption.
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Hassan, Mohammad, Ahmed Abukmail, Alaa Hassiba, Kenneth Mauritz, and Ahmed Elzatahry. "PVA/Chitosan/Silver Nanoparticles Electrospun Nanocomposites: Molecular Relaxations Investigated by Modern Broadband Dielectric Spectroscopy." Nanomaterials 8, no. 11 (2018): 888. http://dx.doi.org/10.3390/nano8110888.
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In this study, we used broadband dielectric spectroscopy to analyze polymer nanofibers of poly(vinyl alcohol)/chitosan/silver nanoparticles. We also studied the effect of incorporating silver nanoparticles in the polymeric mat, on the chain motion dynamics and their interactions with chitosan nanofibers, and we calculated the activation energies of the sub-Tg relaxation processes. Results revealed the existence of two sub-Tg relaxations, the first gets activated at very low temperature (−90 °C) and accounts for motions of the side groups within the repeating unit such as –NH2, –OH, and –CH2OH in chitosan and poly(vinyl alcohol). The second process gets activated around −10 °C and it is thought to be related to the local main chain segments’ motions that are facilitated by fluctuations within the glycosidic bonds of chitosan. The activation energy for the chitosan/PVA/AgNPs nanocomposite nanofibers is much higher than that of the chitosan control film due to the presence of strong interactions between the amine groups and the silver nanoparticles. Kramers–Krönig integral transformation of the ε′′ vs. f spectra in the region of the chitosan Tg helped resolve this relaxation and displayed the progress of its maxima with increasing temperature in the regular manner.
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Hellstern, Daniel, Katja Schulze, Bernhard Schöpf, et al. "Systemic Distribution and Elimination of Plain and with Cy3.5 Functionalized Poly(vinyl alcohol) Coated Superparamagnetic Maghemite Nanoparticles After Intraarticular Injection in Sheep In Vivo." Journal of Nanoscience and Nanotechnology 6, no. 9 (2006): 3261–68. http://dx.doi.org/10.1166/jnn.2006.482.
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PVA coated and fluorescent dye (Cy3.5) functionalized vinyl alcohol/vinyl amine copolymer coated superparamagnetic iron oxide nanoparticles (SPION) were evaluated for systemic distribution and elimination after intraarticular injection in sheep. Observation was done at 3, 24, 72, and 120 hours after injection using light microscopy, fluorescent microscopy, and confocal microscopy. No pathologic influence of SPION on the tissue harvested could be seen. A significantly increased iron content could be identified in the kidneys, lymph nodes, and spleen after injection of SPION. No particles were detected in the liver, the urinary, and the gall bladder. No positive fluorescent signal could be attributed to SPION throughout the organs. Our results indicated that the iron component of the SPION is possible to be incorporated into the physiologic iron metabolism after reabsorption in the proximal tubule system of the kidney and that concentration levels of Cy3.5 are too low to be detected throughout the body.
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Sutekin, Semiha Duygu, Mehtap Sahiner, Selin Sagbas Suner, Sahin Demirci, Olgun Güven, and Nurettin Sahiner. "Poly(Vinylamine) Derived N-Doped C-Dots with Antimicrobial and Antibiofilm Activities." C 7, no. 2 (2021): 40. http://dx.doi.org/10.3390/c7020040.
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Nitrogen-doped carbon dots (N-doped C-dots) was synthesized by using poly(vinyl amine) (PVAm) as a nitrogen source and citric acid (CA) as a carbon source via the hydrothermal method. Various weight ratios of CA and PVAm (CA:PVAm) were used to synthesize N-doped C-dots. The N-doped C-dots revealed emission at 440 nm with excitation at 360 nm and were found to increase the fluorescence intensity with an increase in the amount of PVAm. The blood compatibility studies revealed no significant hemolysis for N-doped C-dots that were prepared at different ratios of CA:PVAm for up to 500 μg/mL concentration with the hemolysis ratio of 1.96% and the minimum blood clotting index of 88.9%. N-doped C-dots were found to be more effective against Gram-positive bacteria than Gram-negative bacteria, with the highest potency on Bacillus subtilis (B. subtilis). The increase in the weight ratio of PVAm in feed during C-dots preparation from 1 to 3 leads to a decrease of the minimum bactericidal concentration (MBC) value from 6.25 to 0.75 mg/mL for B. subtilis. Antibiofilm ability of N-doped C-dots prepared by 1:3 ratio of CA:PVAm was found to reduce %biofilm inhibition and eradication- by more than half, at 0.78 mg/mL for E. coli and B. subtilis generated biofilms and almost destroyed at 25 mg/mL concentrations.
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Arikibe, Joachim Emeka, Roselyn Lata, and David Rohindra. "Synthesis, Preparation and Characterization of Amine-Induced Bacterial Cellulose-Poly(Vinyl Alcohol) Semi-Interpenetrating Network Hydrogel." Key Engineering Materials 841 (May 2020): 238–42. http://dx.doi.org/10.4028/www.scientific.net/kem.841.238.
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Bacterial cellulose (BC) was synthesized using Gluconacetobacter xylinus (BCRC 14182). Synthesized BC was powdered and dissolved in Bis(ethylenediamine) copper (II) hydroxide (Cuen) solution to introduce the amine (NH2) group onto the BC network to yield modified BC (mBC) which was then blended with poly (vinyl alcohol) (PVA) and subsequently crosslinked with genipin (Gp). Pristine, modified and crosslinked hydrogels were studied using Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM) and swelling behavior in water. FTIR revealed a distortion on the BC network chain via a reduction in the absorption of OH peak of mBC and the emergence of peaks at 1587 and 1560 cm-1 attributed to N-H stretching of the induced NH2 group. SEM confirmed the 3-D fibril and porous structure of BC which became distorted after modification and crosslinking. The hydrogels showed equilibrium water content of 86.5%, 67.5%, 66.7% and 33.0 % for BC, PVA, mBC-PVA and mBC-PVA-Gp, respectively. The decreased swelling in mBC-PVA-Gp indicated that genipin was able to crosslink the modified BC.
Dissertations / Theses on the topic "Poly(vinyl amine-co-vinyl amide) (PVAm)"
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Salem, Tarek Sayed Mohamed. "Plasma-based surface modifications of polyester fabrics and their interaction with cationic polyelectrolytes and anionic dyes." Doctoral thesis, Universitätsbibliothek Chemnitz, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-83580.
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Plasma-based surface modifications offer many interesting possibilities for the production of high value-added polymeric materials. In this work, different plasma-based synthetic concepts were employed to endow poly(ethylene terephthalate) (PET) fabrics with accessible amine functionalities. These concepts were compared to find out the appropriate engineering methods, which can be further accepted by textile industries to overcome the limited reactivity of PET fabric surfaces, while the bulk characteristics are kept unaffected. Amine functionalities were introduced onto the surface of PET fabrics using either low-pressure ammonia plasma treatment or coating oxygen plasma-treated PET fabric with cationic polyelectrolytes. Two different cationic polyelectrolytes were used in this study namely poly(diallyldimethylammonium chloride) as an example of strong polyelectrolytes and poly(vinyl amine-co-vinyl amide) as an example of weak polyelectrolytes. The modified surfaces were characterized by a combination of various surface-sensitive techniques such as X-ray photoelectron spectroscopy (XPS), electrokinetic measurements and time-dependent contact angle measurements. Furthermore, the amine functionalities introduced by different surface modifications were used for the subsequent immobilization of various classes of anionic dyes to evaluate the efficiency of different surface modifications. Color strength (K/S) and fastness measurements of colored fabrics were also explored. Their results can be taken as a measure of the extent of the interaction between different modified surfaces and anionic dyes. Finally, it was demonstrated that anchoring poly(vinyl amine-co-vinyl amide) layer onto PET fabric surfaces modified with low-pressure oxygen plasma is an efficient approach to improve coloration behavior and to overcome different problems related to PET fabrics coloration, such as coloration of PET/wool blend fabric with a single class of dyes. This is a crucial step towards the substrate independent surface coloration, which becomes dependent on the properties of the top layer rather than chemical structure of the fibers.
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Salem, Tarek Sayed Mohamed. "Plasma-based surface modifications of polyester fabrics and their interaction with cationic polyelectrolytes and anionic dyes." Doctoral thesis, 2011. https://monarch.qucosa.de/id/qucosa%3A19664.
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Plasma-based surface modifications offer many interesting possibilities for the production of high value-added polymeric materials. In this work, different plasma-based synthetic concepts were employed to endow poly(ethylene terephthalate) (PET) fabrics with accessible amine functionalities. These concepts were compared to find out the appropriate engineering methods, which can be further accepted by textile industries to overcome the limited reactivity of PET fabric surfaces, while the bulk characteristics are kept unaffected. Amine functionalities were introduced onto the surface of PET fabrics using either low-pressure ammonia plasma treatment or coating oxygen plasma-treated PET fabric with cationic polyelectrolytes. Two different cationic polyelectrolytes were used in this study namely poly(diallyldimethylammonium chloride) as an example of strong polyelectrolytes and poly(vinyl amine-co-vinyl amide) as an example of weak polyelectrolytes. The modified surfaces were characterized by a combination of various surface-sensitive techniques such as X-ray photoelectron spectroscopy (XPS), electrokinetic measurements and time-dependent contact angle measurements. Furthermore, the amine functionalities introduced by different surface modifications were used for the subsequent immobilization of various classes of anionic dyes to evaluate the efficiency of different surface modifications. Color strength (K/S) and fastness measurements of colored fabrics were also explored. Their results can be taken as a measure of the extent of the interaction between different modified surfaces and anionic dyes. Finally, it was demonstrated that anchoring poly(vinyl amine-co-vinyl amide) layer onto PET fabric surfaces modified with low-pressure oxygen plasma is an efficient approach to improve coloration behavior and to overcome different problems related to PET fabrics coloration, such as coloration of PET/wool blend fabric with a single class of dyes. This is a crucial step towards the substrate independent surface coloration, which becomes dependent on the properties of the top layer rather than chemical structure of the fibers.
Book chapters on the topic "Poly(vinyl amine-co-vinyl amide) (PVAm)"
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Steiner, G., and C. Zimmerer. "Poly(vinyl amine) (PVAm)." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_118.
Full textConference papers on the topic "Poly(vinyl amine-co-vinyl amide) (PVAm)"
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Hossain, Mohammad K., Samira N. Shaily, Hadiya J. Harrigan, and Terrie Mickens. "Processing of Biodegradable Polymer Composite Using Soy Protein-Based Resin and Nanoclay." In ASME 2016 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/imece2016-67809.
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A completely biodegradable composite was fabricated from an herbal polymer, soy protein concentrate (SPC) resin. Soy protein was modified by adding 30 wt% of glycerol and 5 wt% of poly vinyl alcohol (PVA) to enhance its mechanical as well as thermal property. 3%, 5%, 10%, and 20% nanoclay (NC) were infused into the system. To evaluate its mechanical properties, crystallinity, thermal properties, bonding interaction, and morphological evaluation, tensile, X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR) tests, and optical microscopy (OM) and scanning electron microscopy (SEM) evaluation were performed. Tensile tests showed that the addition of nanoclay improved the mechanical properties of the modified resin. Soy protein is hydrophilic due to the presence of amino acids that contain various polar groups such as amine, carboxyl, and hydroxyl. As a result, polar nanoclay particles that are exfoliated can be evenly dispersed in the SPC resin. From experimental results, it is clear that adding of nanoclay with SPC resin significantly increased the stiffness of the SPC resin. A combination of 5% clay, 30% glycerol, and 5% PVA with the modified SPC resulted in the maximum stress of 18 MPa and Young modulus of 958 MPa. The modified SPC showed a reduced failure strain as well. X-ray diffraction curves showed an improvement of crystallinity of the prepared resin with increasing amount of nanoclay. Interaction among soy, glycerol, PVA, and nanoclay was clearly demonstrated from the FTIR analysis. Optical microscopy (OM) and scanning electron microscopy (SEM) micrographs revealed rougher surface in the nanoclay infused SPC samples compared to that of the neat one. SEM evaluation revealed rougher fracture surface in the NC infused samples.