Relevant bibliographies by topics / Polyethylene oxide

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Polyethylene oxide'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 July 2024

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Journal articles on the topic "Polyethylene oxide"

1

Koksal, E., R. Ramachandran, P. Somasundaran, and C. Maltesh. "Flocculation of oxides using polyethylene oxide." Powder Technology 62, no. 3 (September 1990): 253–59. http://dx.doi.org/10.1016/0032-5910(90)80112-c.

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Sharma, Swati, Nitu Bhaskar, Surjasarathi Bose, and Bikaramjit Basu. "Biomimetic porous high-density polyethylene/polyethylene-grafted-maleic anhydride scaffold with improved in vitro cytocompatibility." Journal of Biomaterials Applications 32, no. 10 (April 5, 2018): 1450–63. http://dx.doi.org/10.1177/0885328218766742.

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A major challenge for tissue engineering is to design and to develop a porous biocompatible scaffold, which can mimic the properties of natural tissue. As a first step towards this endeavour, we here demonstrate a distinct methodology in biomimetically synthesized porous high-density polyethylene scaffolds. Co-extrusion approach was adopted, whereby high-density polyethylene was melt mixed with polyethylene oxide to form an immiscible binary blend. Selective dissolution of polyethylene oxide from the biphasic system revealed droplet–matrix-type morphology. An attempt to stabilize such morphology against thermal and shear effects was made by the addition of polyethylene- grafted-maleic anhydride as a compatibilizer. A maximum ultimate tensile strength of 7 MPa and elastic modulus of 370 MPa were displayed by the high-density polyethylene/polyethylene oxide binary blend with 5% maleated polyethylene during uniaxial tensile loading. The cell culture experiments with murine myoblast C2C12 cell line indicated that compared to neat high-density polyethylene and high-density polyethylene/polyethylene oxide, the high-density polyethylene/polyethylene oxide with 5% polyethylene- grafted-maleic anhydride scaffold significantly increased muscle cell attachment and proliferation with distinct elongated threadlike appearance and highly stained nuclei, in vitro. This has been partly attributed to the change in surface wettability property with a reduced contact angle (∼72°) for 5% PE- g-MA blends. These findings suggest that the high-density polyethylene/polyethylene oxide with 5% polyethylene- grafted-maleic anhydride can be treated as a cell growth substrate in bioengineering applications.
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Gao, Renjin, Jiafang Li, Jianrong Xia, Qi Lin, and Liwei Wang. "Influence of polyethylene oxide (PEO) on the performance of Chinese lacquer films." BioResources 17, no. 4 (August 10, 2022): 5622–31. http://dx.doi.org/10.15376/biores.17.4.5622-5631.

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The Chinese lacquer composite films were prepared by modifying raw lacquer with polyethylene oxide. The film was characterized via Fourier-transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. The infrared spectra confirmed the interaction between the polyethylene oxide and urushiol. The heat-resistance of the film was found to have decreased due to the presence of polyethylene oxide via thermogravimetric analysis. Additional pores and wrinkles were observed in the scanning electron microscopy image of polyethylene oxide modified lacquer films. The mechanical properties were tested according to the national standard. The results indicated that the gloss and flexibility of the modified film was enhanced by the presence of polyethylene oxide. When the ratio of polyethylene oxide was 3%, the gloss was increased from 59.8 to 81.6 and the flexibility changed from 15 mm to 1 mm. The alkaline-resistance, hardness, and adhesion were also increased via the modification of polyethylene oxide.
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Ali, Nasar, Dorina Chipara, Karen Lozano, James Hinthorne, and Mircea Chipara. "Polyethylene oxide—fullerene nanocomposites." Applied Surface Science 421 (November 2017): 220–27. http://dx.doi.org/10.1016/j.apsusc.2016.11.166.

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Ohno, Hiroyuki, and Takahiro Tsukuda. "Electron-transfer reaction of polyethylene oxide-modified myoglobin in polyethylene oxide oligomers." Journal of Electroanalytical Chemistry 341, no. 1-2 (December 1992): 137–49. http://dx.doi.org/10.1016/0022-0728(92)80480-r.

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Liu, Huan, and Baoqi Zuo. "Sound absorption property of PVA/PEO/GO nanofiber membrane and non-woven composite material." Journal of Industrial Textiles 50, no. 4 (March 6, 2019): 512–25. http://dx.doi.org/10.1177/1528083719832857.

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Blend films based on polyvinyl alcohol/polyethylene oxide (70/30 wt%) undoped and doped with different concentration of graphene oxide were prepared by spiral vane electrospinning. Characteristic properties of the blend films were investigated by using X-ray diffraction and scanning electron microscopy. The sound absorption performance of the compositions (nanofiber membranes and needle punched non-woven fabric) was tested by an impedance tube. The sound absorption performance of non-woven fabric has greatly improved after combining with thin nanofiber membranes. With addition of graphene oxide, the fibers were intertwined in a loop and form a network, the areal density and surface roughness of the nanofiber membrane are reduced. Composites containing polyvinyl alcohol/polyethylene oxide nanofiber membranes and composites containing polyvinyl alcohol/polyethylene oxide/graphene oxide nanofiber membranes exhibited different sound absorption properties in different frequency bands. When the fiber coefficient of variation was small, the average sound absorption coefficient of the composite material was high. However, composites containing both polyvinyl alcohol/polyethylene oxide and polyvinyl alcohol/polyethylene oxide/graphene oxide nanofiber membranes had similar sound absorption properties, and the average sound absorption coefficient was greater than that of polyvinyl alcohol/polyethylene oxide composites.
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Eljali, Ahmed, Irwana Nainggolan, Shahrir Hashim, Tulus Ikhsan Nasution, and Nur Zurihan Abd Wahab. "Fabrication of Chitosan-Polyethylene Oxide Polymeric Thin Film Using Electrochemical Deposition for Detection of Volatile Organic Compounds." Key Engineering Materials 744 (July 2017): 359–63. http://dx.doi.org/10.4028/www.scientific.net/kem.744.359.

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This study focused on the fabrication of chitosan-polyethylene oxide sensitive thin film. The polyethylene oxide was used as an additive to enhance the electrical properties of chitosan towards ethanol and methanol gases. The chitosan-polyethylene oxide sensitive film was fabricated using electrochemical deposition technique to deposit a thin film of the sensitive blend on the printed circuit board surface. The sensitive blend electrical (I-V) properties were tested using a specific developed test chamber. Ethanol and methanol volatile organic compound gases were chosen in this work to study the thin sensing properties of the chitosan-polyethylene oxide film. The analyzed data demonstrated that chitosan-polyethylene oxide sensitive film was capable to detect the VOC gas molecules and showed that the sensitive blend was significantly selective to ethanol over methanol gas with output values of 0.31 µA and 0.023 µA respectively. Atomic force microscopy test was used to characterize the morphology and roughness of the pure chitosan and chitosan-polyethylene oxide sensitive films.
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Iutynska, G. O. "BIODEGRADATION AND ANTIMICROBIAL ACTIVITY OF GUANIDINE-CONTAINING POLYETHYLENE OXIDE HYDROGEL." Biotechnologia Acta 13, no. 4 (August 31, 2020): 60–70. http://dx.doi.org/10.15407/biotech13.04.060.

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Thompson, Andre L., Lydia M. Mensah, and Brian J. Love. "The effect of cisplatin on the nanoscale structure of aqueous PEO–PPO–PEO micelles of varying hydrophilicity observed using SAXS." Soft Matter 15, no. 19 (2019): 3970–77. http://dx.doi.org/10.1039/c9sm00071b.

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Miqdad, Husam, and Ibrahim Abdel-Rahman. "THE ACTIVATION ENERGY OF PURE POLYETHYLENE OXIDE AND POLYETHYLENE OXIDE DISPERSED WITH IODINE." Journal of Southwest Jiaotong University 57, no. 6 (December 30, 2022): 614–19. http://dx.doi.org/10.35741/issn.0258-2724.57.6.57.

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The activation energy of thin films polymers made of pure polyethylene oxide (PEO) andPEOdoped with 0.1 % by weight iodine were investigated. The observed physical constants of the cast thin films, such as the activation energy were determined. The films were prepared by the casting method using electricity. This study investigated the variation of the activation energy of thin films of pure (PEO) andPEOdoped with 0.1 % wt. iodine with a frequency in the range of 200-800 kHz and with the temperature in the range of 30-55°C. The results proved that there is a significant change in the values of the activation energy (Ea) of both thin films being studied with the variation of frequency and temperature. It was found that the values of the (Ea) of the prepared thin films decrease withPEOdoped with 0.1 % wt. iodine. The Ea values for both thin films studied decrease with the increase in frequency and temperature.
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Dissertations / Theses on the topic "Polyethylene oxide"

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Archambault, Jacques Gérard. "Protein adsorption to polyethylene oxide-grafted surfaces /." *McMaster only, 2002.

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Couture, Lorraine. "Adsorption of polyethylene oxide on latex particles." Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=59265.

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Layer thickness measurements are used to investigate polymer adsorption and possible conformations of adsorbed polymer.
In a first step, photon correlation spectroscopy (PCS) is used to monitor the layer thickness at different ratios of polyethylene oxide (PEO) per polystyrene (PS) latex spheres. Comparison of the polymer concentration at which the equilibrium layer thickness was attained with the concentration where the adsorption isotherm reached its plateau leads to a proposed three step adsorption process. Kinetic studies of the layer thickness build-up also support this mechanism. Polymer polydispersity and the effect of anchored end groups on layer thickness are found to be in agreement with theoretical predictions.
In a second step, a rheological investigation of PEO coated polystyrene-butadiene (PSB) latex spheres was performed. The influence of coating on the second virial coefficient was determined. Comparison of the layer thickness as measured by viscosity and PCS shows the relative importance of the latex polydispersity for the two methods.
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Segouin, Frances H. "Crystallization kinetics of poly(ethylene oxide) /." Online version of thesis, 1994. http://hdl.handle.net/1850/11678.

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Unsworth, Larry David Brash J. L. "Protein adsorption to chemisorbed polyethylene oxide thin films." *McMaster only, 2005.

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Fitzgerald, Paul A. "Solution behaviour of polyethylene oxide, nonionic gemini surfactants." Connect to full text, 2002. http://setis.library.usyd.edu.au/adt/public_html/adt-NU/public/adt-NU20031219.162500/index.html.

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FitzGerald, Paul Anthony. "Solution Behaviour of Polyethylene Oxide, Nonionic Gemini Surfactants." Thesis, The University of Sydney, 2002. http://hdl.handle.net/2123/504.

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In recent years there has been increasing interest in novel forms of surfactants. Of particular interest are gemini surfactants, which consist of two conventional surfactants joined by a spacer at the head groups, as they exhibit lower critical micelle concentrations than can be achieved by conventional surfactants. In this work, the self-assembly behaviour of several nonionic gemini surfactants with polyethylene oxide head groups (GemnEm, where n (= 20) is the number of carbons per tail and m (= 10, 15, 20 and 30) is the number of ethylene oxides per head group) were investigated. The Critical Micelle Concentrations (CMCs) were measured using a fluorescence probe technique. The CMCs are all ~2 x 10?7 M, with almost no variation with m. The CMCs are several orders of magnitude lower than conventional C12Em nonionic surfactants. The mixing behaviour of the gemini surfactants with conventional surfactants was also studied. They obeyed ideal mixing behaviour with both ionic and nonionic surfactants. Micelle morphologies were studied using Small Angle Neutron Scattering. The gemini surfactants with the larger head groups (i.e. Gem20E20 and Gem20E30) formed spherical micelles. Gem20E15 showed strong scattering at low Q, characteristic of elongated micelles. As the temperature was increased towards the cloud point, the scattering approached the Q-1 dependence predicted for infinite, straight rods. The existence of anisotropic micelles was supported by the viscosity of Gem20E15, which increases by several orders of magnitude on heating towards its cloud point. Phase behaviour was determined using Diffusive Interfacial Transport coupled to near-infrared spectroscopy. Much of the behaviour of these systems is similar to conventional nonionic surfactants. For example, Gem20E10 forms a dilute liquid isotropic phase (W) coexisting with a concentrated lamellar phase (La) at around room temperature and forms a sponge phase at higher temperatures. This is similar to the behaviour of C12E3 and C12E4. The other surfactants studied are all quite soluble in water and form liquid isotropic and hexagonal phases from room temperature. At higher concentrations Gem20E15 formed a cubic and then a lamellar phase while Gem20E20 formed a cubic phase and then an intermediate phase. This is also comparable to the phase behaviour of conventional nonionic surfactants except the intermediate phase, which is often only observed for surfactant systems with long alkyl tails.
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FitzGerald, Paul Anthony. "Solution Behaviour of Polyethylene Oxide, Nonionic Gemini Surfactants." University of Sydney. Chemistry, 2002. http://hdl.handle.net/2123/504.

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In recent years there has been increasing interest in novel forms of surfactants. Of particular interest are gemini surfactants, which consist of two conventional surfactants joined by a spacer at the head groups, as they exhibit lower critical micelle concentrations than can be achieved by conventional surfactants. In this work, the self-assembly behaviour of several nonionic gemini surfactants with polyethylene oxide head groups (GemnEm, where n (= 20) is the number of carbons per tail and m (= 10, 15, 20 and 30) is the number of ethylene oxides per head group) were investigated. The Critical Micelle Concentrations (CMCs) were measured using a fluorescence probe technique. The CMCs are all ~2 x 10?7 M, with almost no variation with m. The CMCs are several orders of magnitude lower than conventional C12Em nonionic surfactants. The mixing behaviour of the gemini surfactants with conventional surfactants was also studied. They obeyed ideal mixing behaviour with both ionic and nonionic surfactants. Micelle morphologies were studied using Small Angle Neutron Scattering. The gemini surfactants with the larger head groups (i.e. Gem20E20 and Gem20E30) formed spherical micelles. Gem20E15 showed strong scattering at low Q, characteristic of elongated micelles. As the temperature was increased towards the cloud point, the scattering approached the Q-1 dependence predicted for infinite, straight rods. The existence of anisotropic micelles was supported by the viscosity of Gem20E15, which increases by several orders of magnitude on heating towards its cloud point. Phase behaviour was determined using Diffusive Interfacial Transport coupled to near-infrared spectroscopy. Much of the behaviour of these systems is similar to conventional nonionic surfactants. For example, Gem20E10 forms a dilute liquid isotropic phase (W) coexisting with a concentrated lamellar phase (La) at around room temperature and forms a sponge phase at higher temperatures. This is similar to the behaviour of C12E3 and C12E4. The other surfactants studied are all quite soluble in water and form liquid isotropic and hexagonal phases from room temperature. At higher concentrations Gem20E15 formed a cubic and then a lamellar phase while Gem20E20 formed a cubic phase and then an intermediate phase. This is also comparable to the phase behaviour of conventional nonionic surfactants except the intermediate phase, which is often only observed for surfactant systems with long alkyl tails.
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Howard, Matthew A. Neau Steven H. "The application of polyethylene oxide (PolyOx®) and methoxypolyethylene glycol (Carbowax Sentry®) in the production of extruded-spheronized beads with a high drug load." Diss., UMK access, 2004.

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Thesis (Ph. D.)--School of Pharmacy and Dept. of Chemistry. University of Missouri--Kansas City, 2004.
"A dissertation in pharmaceutical sciences and chemistry." Advisor: Steven H. Neau. Typescript. Vita. Description based on contents viewed Feb. 24, 2006; title from "catalog record" of the print edition. Includes bibliographical references (leaves 129-141). Online version of the print edition.
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Olsen, Adam Paul Flagan Richard C. Kornfield Julia A. "Scanning activity gravimetric analysis (SAGA) of aqueous polyethylene oxide /." Diss., Pasadena, Calif. : Caltech, 2006. http://resolver.caltech.edu/CaltechETD:etd-05262006-133416.

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Mohammadi, Hadi. "On the Melting and Crystallization of Linear Polyethylene, Poly(ethylene oxide) and Metallocene Linear Low-Density Polyethylene." Diss., Virginia Tech, 2018. http://hdl.handle.net/10919/84921.

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The crystallization and melting behaviors of an ethylene/1-hexene copolymer and series of narrow molecular weight linear polyethylene and poly(ethylene oxide) fractions were studied using a combination of ultra-fast and conventional differential scanning calorimetry, optical microscopy, small angle X-ray scattering, and wide angle X-ray diffraction. In the case of linear polyethylene and poly(ethylene oxide), the zero-entropy production melting temperatures of initial lamellae of isothermally crystallized fractions were analyzed in the context of the non-linear Hoffman-Weeks method. Using the Huggins equation, limiting equilibrium melting temperatures of 141.4 ± 0.8oC and 81.4 ± 1.0oC were estimated for linear polyethylene and poly(ethylene oxide), respectively. The former and the latter are about 4oC lower and 12.5oC higher than these predicted by Flory/Vrij and Buckley/Kovacs, respectively. Accuracy of the non-linear Hoffman-Weeks method was also examined using initial lamellar thickness literature data for a linear polyethylene fraction at different crystallization temperatures. The equilibrium melting temperature obtained by the Gibbs-Thomson approach and the C2 value extracted from the initial lamellar thickness vs. reciprocal of undercooling plot were similar within the limits of experimental error to those obtained here through the non-linear Hoffman-Weeks method. In the next step, the Lauritzen-Hoffman (LH) secondary nucleation theory was modified to account for the effect of stem length fluctuations, tilt angle of the crystallized stems, and temperature dependence of the lateral surface free energy. Analysis of spherulite growth rate and wide angle X-ray diffraction data for 26 linear polyethylene and 5 poly(ethylene oxide) fractions revealed that the undercooling at the regime I/II transition, the equilibrium fold surface free energy, the strength of the stem length fluctuations and the substrate length at the regime I/II transition are independent of chain length. The value of the equilibrium fold surface free energy derived from crystal growth rate data using the modified Lauritzen-Hoffman theory matches that calculated from lamellar thickness and melting data through the Gibbs-Thomson equation for both linear polyethylene and poly(ethylene oxide). Larger spherulitic growth rates for linear polyethylene than for poly(ethylene oxide) at low undercooling is explained by the higher secondary nucleation constant of poly(ethylene oxide). While the apparent friction coefficient of a crystallizing linear polyethylene chain is 2 to 8 times higher than that of a chain undergoing reptation in the melt state, the apparent friction coefficient of a crystallizing poly(ethylene oxide) chain is about two orders of magnitude lower. This observation suggests that segmental mobility on the crystal phase plays a significant role in the crystal growth process. In case of the statistical ethylene/1-hexene copolymer, the fold surface free energies of the copolymer lamellae at the time of crystallization and melting increase with increasing undercooling, approaching the same magnitude at high undercooling. As a result of this temperature dependence, the experimental melting vs. crystallization temperature plot is parallel to the Tm = Tc line and the corresponding Gibbs-Thomson plot is non-linear. This behavior is attributed to the fact that longer ethylene sequences form a chain-folded structure with lower concentration of branch points on the lamellar surface at lower undercooling, while shorter ethylene sequences form lamellar structures at higher undercooling exhibiting a higher concentration of branch points on the lamellar surface. Branch points limit the ability of lamellar structures to relax their kinetic stem-length fluctuations during heating prior to melting.
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Books on the topic "Polyethylene oxide"

1

Scheiner, Bernard J. Dewatering of mineral waste using the flocculant polyethylene oxide. [Avondale, MD]: U.S. Dept. of the Interior, Bureau of Mines, 1985.

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United States. Bureau of Mines. Dewatering of Mineral Waste Using the Flocculant Polyethylene Oxide. S.l: s.n, 1985.

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United States. Bureau of Mines. Infrared Examination of Ion-Exchanged Montmorillonite Treated with Polyethylene Oxide. S.l: s.n, 1986.

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Webb, S. W. An infrared examination of ion-exchanged montmorillonite treated with polyethylene oxide. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1986.

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Smelley, Annie G. Large-scale dewatering of phosphatic clay waste from northern Florida. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1985.

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Watson, Pamela J. Improved drilling of coal measure rocks for underground mine void detection and exploration programs. Washington, D.C: U.S. Dept. of the Interior, Bureau of Mines, 1991.

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Sharma, Sandeep K. Dewatering of Alaska placer effluent using PEO. Washington, D.C. (810 7th St., N.W., Washington 20241-0001): U.S. Dept. of the Interior, Bureau of Mines, 1992.

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Sharma, Sandeep K. Dewatering of Alaska placer effluent using PEO. Washington, DC: U.S. Dept. of the Interior, Bureau of Mines, 1992.

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Watson, Pamela J. Improved drilling of coal measure rocks for underground mine void detection and exploration programs. Washington, DC: Bureau of Mines, United States Dept. of the Interior, 1991.

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Stanley, D. A. Flocculation and dewatering of montmorillonite modified by ion exchange. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1986.

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Book chapters on the topic "Polyethylene oxide"

1

Gooch, Jan W. "Polyethylene Oxide." In Encyclopedic Dictionary of Polymers, 560. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9082.

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Car, Anja. "Polyethylene Oxide." In Encyclopedia of Membranes, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_480-2.

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Steiner, G., and C. Zimmerer. "Polyethylene oxide (PEO)." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I, 840–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_92.

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Braun, Hans-Georg, Evelyn Meyer, and Mingtai Wang. "Dendritic Growth of Polyethylene Oxide on Patterned Surfaces." In Polymer Crystallization, 238–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/3-540-45851-4_13.

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Grainger, David, Teruo Okano, and Sung Wan Kim. "Surface Characteristics of Polyethylene Oxide-Polystyrene Multiblock Copolymers." In Advances in Biomedical Polymers, 229–47. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1829-3_21.

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Martin, Lawrence M., and Ali R. Rajabi-Siahboomi. "Applications of Polyethylene Oxide (POLYOX) in Hydrophilic Matrices." In Hydrophilic Matrix Tablets for Oral Controlled Release, 123–41. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1519-4_5.

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Hall, Mark, and Michael Read. "Hot-Melt Extrusion of Ethylcellulose, Hypromellose and Polyethylene Oxide." In Hot-Melt Extrusion: Pharmaceutical Applications, 145–75. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9780470711415.ch7.

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Peng, Yaoli, Long Liang, and Wencheng Xia. "Coal flotation improvement through hydrophobic flocculation induced by polyethylene oxide." In XVIII International Coal Preparation Congress, 1003–8. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-40943-6_157.

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Shariatinia, Zahra, and Iraj Kohsari. "Fabrication of Antibacterial Electrospun Chitosan-Polyethylene Oxide Nanocomposite Nanofibrous Mats." In Eco-friendly and Smart Polymer Systems, 19–22. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45085-4_5.

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Michalczyk, A., and W. Borchard. "Determination of the Thermodynamic Properties of the System Polyethylene Oxide/Water." In Integration of Fundamental Polymer Science and Technology—3, 100–104. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1115-4_9.

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Conference papers on the topic "Polyethylene oxide"

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Hahne, Steffen, Bernd Ploss, Kensuke Yoshida, and Takeo Furukawa. "Nonlinear conductivity of ion-complexed polyethylene oxide." In 2010 10th IEEE International Conference on Solid Dielectrics (ICSD). IEEE, 2010. http://dx.doi.org/10.1109/icsd.2010.5567943.

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Kubyshkina, Elena, B. L. G. Jonsson, and Mikael Unge. "Electronic properties of magnesium oxide - polyethylene interface." In 2016 IEEE International Conference on Dielectrics (ICD). IEEE, 2016. http://dx.doi.org/10.1109/icd.2016.7547734.

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Nechaev, A. I., P. V. Khramtsov, and S. A. Zamorina. "Polyethylene glycol-based modification of graphene oxide." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069205.

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YU. YURKOV, G., D. A. BARANOV, and L. V. GOROBINSKII. "SYNTHESIS OF CERIUM OXIDE NANOPARTICLES IN POLYETHYLENE MATRIX." In Proceedings of the International Conference on Nanomeeting 2007. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812770950_0076.

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Sönmez, Maria, Laurentia Alexandrescu, Mihai Georgescu, Florentina Dana Gurau, Denisa Ficai, Anton Ficai, Roxana Trusca, Oprea Ovidiu, Lavinia Ardelean Ioana, and Doina Constantinescu. "Influence of Calcium Oxide on Thermal and Mechanical Properties of Recycled Polyethylene Terephtalate / Polyethylene Mixture." In The 4th World Congress on New Technologies. Avestia Publishing, 2018. http://dx.doi.org/10.11159/icnfa18.135.

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Higaki, T., T. Tachibana, Y. Kimura, T. Maemoto, S. Sasa, and M. Inoue. "Flexible zinc oxide thin-film transistors using oxide buffer layers on polyethylene napthalate substrates." In 2011 International Meeting for Future of Electron Devices, Kansai (IMFEDK). IEEE, 2011. http://dx.doi.org/10.1109/imfedk.2011.5944860.

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Khanbareh, H., S. van der Zwaag, and W. A. Groen. "Piezoelectric and pyroelectric properties of lead titanate-polyethylene oxide composites." In ELECTROCERAMICS XIV CONFERENCE. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4901656.

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Staii, Cristian. "Scanning Conductance Microscopy of Carbon Nanotubes and Polyethylene Oxide Nanofibers." In ELECTRIC PROPERTIES OF SYNTHETIC NANOSTRUCTURES: XVII International Winterschool/Euroconference on Electronic Properties of Novel Materials. AIP, 2004. http://dx.doi.org/10.1063/1.1812057.

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PINHEIRO GIGLIO, LEONARDO, MARCELO GANZAROLLI DE OLIVEIRA, and SCHEILA DAIANA FAUSTO ALVES. "TOPICAL NITRIC OXIDE-RELEASING POLYETHYLENE TEREPHTHALATE MESH INCREASES DERMAL VASODILATION." In XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil: Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51473.

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"Action Mechanisms of Comb-Type Superplasticizers Containing Grafted Polyethylene Oxide Chains." In SP-195: The Sixth Canmet/ACI Conference on Superplasticizers and Other Chemical Admixtures in Concrete. American Concrete Institute, 2000. http://dx.doi.org/10.14359/9906.

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Reports on the topic "Polyethylene oxide"

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Lell, R., K. Grimm, R. McKnight, R. Shaefer, and INL. ZPPR-20 phase D : a cylindrical assembly of polyethylene moderated U metal reflected by beryllium oxide and polyethylene. Office of Scientific and Technical Information (OSTI), September 2006. http://dx.doi.org/10.2172/929227.

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Selser, James C. A study of the relationship between lithium ion transport and structure and dynamic behavior in polyethylene oxide-melt/LiClO4 battery electrolytes. Office of Scientific and Technical Information (OSTI), July 2009. http://dx.doi.org/10.2172/958302.

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You might also be interested in the extended bibliographies on the topic 'Polyethylene oxide' for particular source types:
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