Academic literature on the topic 'Polyethylene'

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Journal articles on the topic "Polyethylene"

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Yurkin, A. A., I. D. Simonov-Emelyanov, P. V. Surikov, and N. L. Shembel. "EFFECT OF POLYETHYLENE MOLECULAR MASS CHARACTERISTICS ON SLIP EFFECT." Fine Chemical Technologies 11, no. 5 (October 28, 2016): 91–93. http://dx.doi.org/10.32362/2410-6593-2016-11-5-91-93.

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The rheological properties of polyethylene with different molecular weight characteristics were studied. Difference of molecular weight characteristics was found on the basis of melt flow index, and slip effect in the molten polyethylene flow was studied. The presence of slip effect is found in case of flowing polyethylene with a higher molecular weight in contrast to polyethylene with lower molecular weight at different temperatures. Changes of the slip effect parameters upon mixing polyethylenes with very much different molecular weight characteristics were studied.
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Kuleznev, V. N., P. V. Surikov, V. D. Sevruk, and T. A. Sineva. "A Comparative Investigation of the Rheological Properties in Shear and Tension of Tube-Grade Polymodal Polyethylene Melts." International Polymer Science and Technology 41, no. 10 (October 2014): 31–34. http://dx.doi.org/10.1177/0307174x1404101006.

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Melts of bimodal (tube) polyethylenes relax considerably more rapidly than normal monomodal specimens. At exit from an l/d = 20 capillary, a melt of bimodal polyethylene behaves like an unrelaxed melt, whereas normal polyethylene does not manage to relax entirely even at exit from an l/d = 30 capillary. The obtained results point to one of the reasons for the high durability of polyethylene tubes with a bimodal molecular weight distribution.
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Yahaya, O. T., D. C. Obadiah, O. E. Oladele, C. Obi, O. J. Edache, J. A. Haruna, and F. D. Oripelaye. "EFFECTS OF SOIL SOLARIZATION ON FUNGAL AND BACTERIAL POPULATIONS ASSOCIATED WITH AMARANTHIS VIRIDIS L. (AFRICAN SPINACH) IN LAGOS, NIGERIA." African Journal of Health, Safety and Environment 2, no. 2 (November 5, 2021): 133–53. http://dx.doi.org/10.52417/ajhse.v2i2.168.

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Soil solarization is increasingly used to control soil-borne pathogens because it is environment-friendly. However, performance varied geographically, necessitating experimental trials before its introduction. This study assessed the effects of solarization on soil-borne bacteria and fungi, growth, and proximate composition of Amaranthus viridis (African spinach) in Lagos, Nigeria. Two raised beds were solarized for six weeks with a transparent and black polyethylene sheet, and a non-solarized (control) bed was equally made. The vegetable seeds were planted and their growths were recorded for four weeks. Soil samples at 15-20cm deep and leaves were obtained for microbiological and proximate analysis, respectively. The mean temperature of transparent xxpolyethylene’s soil was 45.33 oC, black polyethylene (35 oC), and non-solarized (33.50 oC). The mean height and width of transparent polyethylene’s A. viridis were 24 and 3cm, black polyethylene (19 and 2.2 cm), and non-solarized (17 and 1.6cm). The transparent polyethylene’s soil had 3100 and 250 cfu/g bacterial and fungal colonies, black polyethylene (3200 and 1900 cfu/g), and non-solarized (37000 and 1900 cfu/g), respectively. The proximate contents of the transparent polyethylene’s A. viridis were (70 moisture, 10 ash, 4.24 protein, 1.45 fat and 9.94 % fibre), black polyethylene (73.35 moisture, 8.36 ash, 3.1% protein, 1.23 fat, and 6.77 % fibre), and non-solarized (76.09 moisture, 5.91 protein, 3.15 ash, 1.31 fat and 6.75 % fibre). Overall, statistical differences (p ≤ 0.05) existed between the solarized and non-solarized and between transparent and black polyethylene (transparent>black>non-solarized). Thus, solarization could be an effective strategy for controlling soil-borne bacteria and fungi of A. viridis in the area studied.
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Wang, Yang, Guowei Feng, Nan Lin, Huiqing Lan, Qiang Li, Dichang Yao, and Jing Tang. "A Review of Degradation and Life Prediction of Polyethylene." Applied Sciences 13, no. 5 (February 27, 2023): 3045. http://dx.doi.org/10.3390/app13053045.

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After around 50 years of development, the key substance known as polyethylene has been extremely influential in a variety of industries. This paper investigates how polyethylene materials have been used in the domains of water, packaging, and medicine to advance contemporary society in order to comprehend the physical and chemical alterations that polyethylene undergoes after being subjected to long-term environmental variables (e.g., temperature, light, pressure, microbiological factors, etc.). For the safe operation of polyethylene materials, it has always been of the utmost importance to evaluate polyethylene’s service life effectively. This paper reviews some of the most common literature journals on the influence of environmental factors on the degradation process of polyethylene materials and describes methods for predicting the lifetime of degradable polyethylene materials using accelerated aging tests. The Arrhenius equation, the Ozawa–Flynn–Wall (OFW) method, the Friedman method, the Coats–Redfern method, the Kissinger method and Kissinger–Akahira–Sunose (KAS) method, Augis and Bennett’s method, and Advanced Isoconversional methods are all discussed, as well as the future development of polyethylene.
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Ivakhnenko, Tatiana E. "Modern Technologies in the Customs Examination of Polymers." Вестник Российской таможенной академии, no. 4 (2022): 63–76. http://dx.doi.org/10.54048/20727240_2022_04_063.

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The article discusses the features of using the two most effective methods for the physicochemical analysis of polymers: IR-spectrometry and differential scanning calorimetry, and draws conclusions regarding the prospects for using the nuclear magnetic resonance method to identify polyethylene for customs purposes. Polyethylene in primary forms makes up a significant share in the import of polymer raw materials to the Russian Federation. A significant difference in import duty rates for sub-items, including polyethylenes in primary forms, differing in physical and chemical characteristics, causes a high risk of false declaration of these goods. Features of the classification of polyethylenes in accordance the Commodity Nomenclature of Foreign Economic Activity of the Eurasian Economic Union determine the need to identify such indicators as the qualitative chemical composition, the presence and ratio of copolymer units in the polymer, density, structure of the polymer, etc. Of particular importance is the need to identify the type of polyethylene. To identify the characteristics by which polyethylene can be attributed to one of the types that are important for the classification of polymer raw materials in accordance with the Commodity Nomenclature of Foreign Economic Activity of the Eurasian Economic Union, it is necessary to carry out consistent identification using a complex of modern high-tech methods of physical and chemical research.
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Bashir, Z., and J. A. Odell. "Polyethylene-polyethylene microfibrillar composites." Journal of Materials Science 28, no. 4 (January 1, 1993): 1081–89. http://dx.doi.org/10.1007/bf00400896.

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Yuan, Shi-Fang, Luyao Wang, Yi Yan, Tian Liu, Zygmunt Flisak, Yanping Ma, and Wen-Hua Sun. "4,4′-Dimethoxybenzhydryl substituent augments performance of bis(imino)pyridine cobalt-based catalysts in ethylene polymerization." RSC Advances 12, no. 25 (2022): 15741–50. http://dx.doi.org/10.1039/d2ra01547a.

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Employing ligands with 4,4′-dimethoxybenzhydryl groups, the cobalt precatalysts display high activities toward ethylene polymerization and produce highly linear polyethylenes, the high density polyethylene (HDPE).
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Grigoryeva, O., A. Fainleib, J. Grenet, and J. M. Saiter. "Reactive Compatibilization of Recycled Polyethylenes and Scrap Rubber in Thermoplastic Elastomers: Chemical and Radiation-Chemical Approach." Rubber Chemistry and Technology 81, no. 5 (November 1, 2008): 737–52. http://dx.doi.org/10.5254/1.3548229.

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Abstract Reactive compatibilization of recycled low- or high-density polyethylenes (LDPE and HDPE, respectively) and ground tire rubber (GTR) via chemical interactions of pre-functionalized components in their blend interface has been carried out. Polyethylene component was functionalized with maleic anhydride (MAH); as well, the rubber component was modified via functionalization with MAH or acrylamide (AAm) using chemically or irradiation (γ-rays) induced grafting techniques. The grafting degree and molecular mass distribution of the functionalized polymers have been measured via FTIR and Size Exclusion Chromatography (SEC) analyses, respectively. Additional coupling agents such as p-phenylene diamine (PDA) and polyamide fiber were used for producing some thermoplastic elastomer (TPE). Thermoplastic elastomer materials based on synthesized reactive polyethylenes and GTR as well as ethylene-propylenediene monomer rubber (EPDM) were prepared by dynamic vulcanization of the rubber phase inside thermoplastic (polyethylene) matrix and their phase structure, and main properties have been studied using DSC, DMTA and mechanical testing. As a result, high performance thermoplastic elastomers based on functionalized polyethylene and ground rubber with improved mechanical properties have been developed.
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English, A. D., P. Smith, and D. E. Axelson. "Polyethylene/deutero-polyethylene phase behaviour." Polymer 26, no. 10 (September 1985): 1523–26. http://dx.doi.org/10.1016/0032-3861(85)90087-4.

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Zong, Kening, Yanhui Hou, Xiaobei Zhao, Yali Sun, Binyuan Liu, and Min Yang. "Slurry Homopolymerization of Ethylene Using Thermostable α-Diimine Nickel Catalysts Covalently Linked to Silica Supports via Substituents on Acenaphthequinone-Backbone." Polymers 14, no. 17 (September 5, 2022): 3684. http://dx.doi.org/10.3390/polym14173684.

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Four supported α-diimine nickel(II) catalysts covalently linked to silica via hydroxyl functionality on α-diimine acenaphthequinone-backbone were prepared and used in slurry polymerizations of ethylene to produce branched polyethylenes. The catalytic activities of these still reached 106 g/molNi·h at 70 °C. The life of the supported catalyst is prolonged, as can be seen from the kinetic profile. The molecular weight of the polyethylene obtained by the 955 silica gel supported catalyst was higher than that obtained by the 2408D silica gel supported catalyst. The melting points of polyethylene obtained by the supported catalysts S-C1-a/b are all above 110 °C. Compared with the homogeneous catalyst, the branching numbers of the polyethylenes obtained by the supported catalysts S-C1-a/b is significantly lower. The polyethylenes obtained by supported catalyst S-C1-a/b at 30–50 °C are free-flowing particles, which is obviously better than the rubber-like cluster polymer obtained from homogeneous catalyst.
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Dissertations / Theses on the topic "Polyethylene"

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Khan, Mohammad Ashraf. "Surface properties of high density polyethylene and cross-linked polyethylene." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/mq52587.pdf.

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Bottomley, L. "Heterogeneous polyethylene alloys." Thesis, Brunel University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235021.

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Butler, M. F. "Deformation of polyethylene." Thesis, University of Cambridge, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.597170.

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In order to characterise deformation as completely and unambiguously as possible it is desirable to eliminate the possibility of sample relaxation by performing measurements in-situ, during deformation. The bulk of the thesis describes a comprehensive series of investigations into the mechanical behaviour of a range of oriented and unoriented commercial grade polyethylenes deformed in tension and compression over a range of temperatures. High intensity synchrotron X-rays and fast electronic area detectors were used to enable the two-dimensional wide-angle X-ray scattering (WAXS) and small-angle X-ray scattering (SAXS) patterns, which reveal information about the molecular and lamellar deformation respectively, to be measured simultaneously during deformation. In addition, the load-extension curve was measured at the same time as the X-ray scattering patterns. Sample relaxation was completely eliminated and for the first time the micro- and macroscopic deformation was precisely and unambiguously correlated. The use of a range of samples, with varying molecular weights, branch densities, branch types, lamellar thicknesses and percentage crystallinities, enabled a study to be made of the influence of microstructural variables (as well as experimental conditions such as deformation temperature) on the mechanical properties. A study was also performed on the mechanical properties of thin solution-cast PE films made from the same commercial grades used for the bulk samples. Crazing mechanisms were observed using optical and transmission electron microscopy. It was found that that results could be rationalised in terms of the degree of entanglement of the chains and the ease by which these entanglements were overcome during deformation. Increasing the entanglement density by increasing the molecular weight or by the incorporation of short chain branches increased the toughness of the films. As for the bulk samples, branch length was unimportant.
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Kay, Christopher James. "Polyethylene block copolymers." Thesis, University of Warwick, 2014. http://wrap.warwick.ac.uk/62620/.

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Chapter 1 introduces the concept of polyethylene (PE) end-functionalisation as a route to block copolymers, reviews the different literature methods for their synthesis this way, and compares the advantages and disadvantages of each. Finally, an existing method which makes use of PE terminated with a styrene derivative is identified as having fewer disadvantages than most literature procedures. Further investigation of the mechanism is proposed. Chapter 2 focusses on the different types of so-called dormant state formed in Ziegler-Natta catalysed olefin polymerisations, and in particular on the dormancy occurring after styrene insertion. Copolymerisations of ethylene with styrene, allylbenzene and 4-phenyl-1-butene in the presence of hydrogen are undertaken, and evidence for the presence of a dormant state or simply competitive rates of hydrogenation vs ethylene insertion is discussed. Increasing styrene concentration beyond that used by Chung is found to yield PE capped at both chain ends with styrene. A new mechanism – Catalytic Hydride Initiated Polymerisation (CHIP) – is consistent with these new observations. Chapter 3 focusses on extending the application of the CHIP mechanism to the synthesis of new examples of end-functional PE. Copolymerisations of ethylene with α-methylstyrene and related monomers 1,3/1,4-diisopropenylbenzene, α-methylstyrene dimer and limonene in the presence of hydrogen are investigated, resulting in the successful synthesis of a range of PE examples initiated with each comonomer. The effects of hydrogen pressure and comonomer concentration are also discussed. The advantages of CHIP are discussed, and the synthesis of end-functionalised PE incorporating DIB is studied in detail. An α-methylstyrene like end group is present at the start of the PE chains. Chapter 4 describes the free-radical copolymerisation of the new functionalised PE with acrylate monomers. Observations are consistent with a new reversible termination mechanism similar to nitroxide mediated polymerisation. The products are characterised by NMR, GPC, DLS, TEM and DSC, and the evidence is found to be consistent with the presence of block copolymers. Chapter 5 details the experimental procedures used to carry out the work in this thesis.
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Green, Christopher Duncan. "Polyethylene-montmorillonite nanocomposites." Thesis, University of Southampton, 2008. https://eprints.soton.ac.uk/65001/.

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Nanocomposite materials are currently attracting much interest due to their possibility of global property improvement – mechanical strength, toughness, electrical breakdown strength, electrical erosion resistance and flame retardancy. In order to disperse montmorillonite clay (MMT) into polyethylene (PE), the clay sheets need to be rendered organophilic. Masterbatches with a high level (~40 %wt) of organomodified clay can then be dispersed into a host by a simple mechanical process. Two chemically different masterbatches were purchased: Nanoblend 2101 from PolyOne Corp. and C30PE from Nanocor Inc. These were let down using a RandcastleTM single screw extruder with a patented mixing device to provide elongational flow. Wide angle X-ray diffraction was used together with transmission electron microscopy to evaluate the particle dispersion, which consisted of intercalated clay organised in clusters up to one micron in diameter. The performance of these materials was assessed in terms of AC ramp breakdown statistics, dielectric spectroscopy, dynamic and tensile mechanical properties. Nanoblend masterbatch consistently improved the breakdown statistics, more than overcoming the inherent demerit of extrusion, which mildly aged the unfilled material (as confirmed by Raman spectroscopy.) On the other hand, even low loading levels of Nanocor could result in reduced breakdown strength and increased scatter. Furthermore, both sets of materials demonstrated large dielectric losses at power frequencies and poorer performance under mechanical tension. These materials would therefore require considerable development before they could confidently be used commercially. The nature of the PE-MMT interactions was examined by investigating the crystallisation kinetics and resulting morphologies with differential scanning calorimetry and scanning electron microscopy. By varying the masterbatch type, loading level and crystallisation temperature, it was possible to study a wide range of supercrystalline morphologies using a permanganic etching technique. This is a useful contribution to the field of nanocomposites research. It is known that the morphologies of polymers can affect their mechanical properties and electrical treeing behaviour, and so it is possible that controlled crystallisation could provide a route toward designer materials with optimised behaviour.
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Hanna, Paul R. W. "Studies on the rotational moulding of nanoclay filled polyethylene and polyethylene." Thesis, Queen's University Belfast, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.601653.

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Oluz, Zehra. "Additives For Photodegradable Polyethylene." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12614537/index.pdf.

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Polyethylene (PE) is one of the most popular polymers used in daily life. However, saturated hydrocarbons cannot absorb the energy of light reaching to earth, so degradation process is rather slow which in return cause disposal problems. On the other hand, it was observed that in presence of oxygen and impurities in the polymer matrix, degradation can be rendered to shorter time intervals. This study covers investigation of effect of three different additives in UV induced oxidative degradation of polyethylene. In this work vanadium (III) acetylacetonate, serpentine and Cloisite 30B were used as additives both together and alone to follow photodegradation of polyethylene. Amount of vanadium (III) acetylacetonate was kept constant at 0.2 wt%, while serpentine and Cloisite 30B were used between 1 and 4 wt%. All compositions were prepared by using Brabender Torque Rheometer, and shaped as thin films by compression molding. Samples were irradiated by UV light up to 500 hours. Mechanical and spectroscopic measurements were carried out in certain time intervals to monitor the degradation. It can be concluded that all combinations of three additives showed the fastest degradation behavior compared to pure PE. In the absence of vanadium (III) acetylacetonate the degradation was slowed and fluctuations were observed in the residual percentage strain at break values. There was not a significant change in tensile strength of all samples. Carbonyl index values followed by FTIR were always in increasing manner. Thermal properties were also investigated by DSC Thermograms and they did not change significantly.
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Blacker, Richard. "Electrostatic phenomena in polyethylene." Thesis, Loughborough University, 1990. https://dspace.lboro.ac.uk/2134/10330.

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Measurement of the electrostatic nature of materials is an essential step towards understanding the underlying processes and to the eventual modification of charge behaviour. Indirect monitoring was achieved by resistivity measurements, however, this approach is limited to studying the material and not the electrostatic charge and is, in general, not a satisfactory method. Electrostatic field meters allowed the electrical behaviour of polyethylene to be monitored; its charge accumulation and decay processes were accurately monitored, thus giving a good information base for material modification later in the programme. The use of a data-logging system (based on the Apple//e computer) allowed the manipulation and long term storage of information, whilst giving improved presentation of results. High Density Polyethylene is an intrinsically insulating polymer whose electrostatic properties can be greatly modified by the use of internal antistats. Such additives migrate to a surtace and become effective [at reducing surtace resistivity] over a period of time depending on the diffusivity of the antistat species, and on the external atmospheric conditions, particularly humidity. The effusion of antistat onto a surface was monitored by surtace analysis techniques including X-ray photoelectron scattering, goniometry and infra-red spectroscopy, however, whilst such techniques offered a direct indication of the surtace state and the effect of any surtace modification, electrostatic testing was found to be the most sensitive technique for following antistat action. It is possible to tailor individual antistats to specific applications, however such usage provides only specific protection (fast acting but short lived, or slow acting but long lived). Two single antistat species were combined, and a synergistic effect was obtained for fast acting and long lived systems. It was found that antistats operate by welting (coating) an insulating surtace, and then absorbing atmospheric water vapour, thus lowering the surtace resistivity. Complete surtace coverage is not possible over an HDPE surtace due to its low surtace energy (28mNm'1), however, more complete surtace coverage was achieved by surtace oxidation [raising the polar surlace energy). Natural HDPE is not readily susceptible to surface oxidation; therefore oxidation treatment had only a limited effect. An addition of the fully compatible polymer LLDPE raised the oxidation level and allowed more complete antistat coverage, thereby improving antistatic activity and raising the level of protection gained by using a standard level of antistat. A patent is being taken out covering the use of LLDPE in conjunction with mixed antistat systems.
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Chiloyan, Vazrik. "Polyethylene fiber drawing optimization." Thesis, Massachusetts Institute of Technology, 2011. http://hdl.handle.net/1721.1/68829.

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Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2011.
"June 2011." Cataloged from PDF version of thesis.
Includes bibliographical references (p. 33).
Polymer fiber drawing creates fibers with enhanced thermal conductivity and strength compared to bulk polymer because drawing aligns the molecular chains. I optimize the polymer fiber drawing method in order to achieve polymer fibers that are drawn to lengths exceeding 1cm and develop a method to cut and store them for future experimental purposes. With lengths exceeding 1cm, starting with lengths near 0.5mm, these fibers undergo very large tensile deformations. This ensures the fibers obtained have been ultra drawn, and the polymer chains have aligned, thus enhancing the tensile strength and thermal conductivity of the fiber. By storing these fibers, I can perform experimental measurements in the future to obtain thermal conductivity values for polyethylene fibers and notice the effect of aligning the molecular chains.
by Vazrik Chiloyan.
S.B.
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Clark, Darren Cameron. "Dual monomer grafting of styrene and maleic anhydride onto polyethylene, effect of polyethylene microstructure." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0020/NQ54405.pdf.

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Books on the topic "Polyethylene"

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Kissin, Yury V. Polyethylene. München: Carl Hanser Verlag GmbH & Co. KG, 2012. http://dx.doi.org/10.3139/9781569905210.

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Services, Chemical Intelligence, ed. Polyethylene. Dunstable: Chemical Intelligence Services, 1993.

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Clark, Becky, and William G. Baumgartner. Polyethylene. Cleveland, OH: Freedonia Group, Inc., 1998.

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Kissin, Yury V. Polyethylene. München, Germany: Carl Hanser Verlag GmbH & Co. KG, 2020. http://dx.doi.org/10.1007/978-1-56990-832-7.

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Thomas, Jince, Sabu Thomas, and Zakiah Ahmad, eds. Crosslinkable Polyethylene. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0514-7.

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Ita, Paul A., Aaron Hackle, and A. M. Zaper. World polyethylene. Cleveland: Freedonia Group, 1999.

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Ita, Paul A., and Pam Safarek. World polyethylene. Cleveland, Ohio: Freedonia Group, 1997.

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Weizer, William P., and Kelly Misch. Polyethylene terephthalate resins. Cleveland: Freedonia Group, 1999.

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Mertens, Fiona C. Polyethylene modified asphalt. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1992.

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Bottomley, Leslie. Heterogeneous polyethylene alloys. Uxbridge: Brunel University, 1988.

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Book chapters on the topic "Polyethylene"

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Bährle-Rapp, Marina. "Polyethylene." In Springer Lexikon Kosmetik und Körperpflege, 436. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_8103.

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Gooch, Jan W. "Polyethylene." In Encyclopedic Dictionary of Polymers, 559. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9069.

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Gooch, Jan W. "Polyethylene." In Encyclopedic Dictionary of Polymers, 560. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9080.

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Gooch, Jan W. "Polyethylene." In Encyclopedic Dictionary of Polymers, 560. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9081.

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Baker, Ian. "Polyethylene." In Fifty Materials That Make the World, 163–68. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78766-4_31.

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Peacock, Andrew J., and Allison Calhoun. "Polyethylene." In Polymer Chemistry, 267–83. München: Carl Hanser Verlag GmbH & Co. KG, 2006. http://dx.doi.org/10.3139/9783446433434.018.

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Kurtz, Steven, and Michael Manley. "Polyethylene." In Essentials in Total Hip Arthroplasty, 55–61. Boca Raton: CRC Press, 2024. http://dx.doi.org/10.1201/9781003524014-7.

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Kissin, Yury V. "Educational Minimum: Manufacture, Structure, and Mechanical Properties of Polyethylene Resins." In Polyethylene, 1–33. München: Carl Hanser Verlag GmbH & Co. KG, 2012. http://dx.doi.org/10.3139/9781569905210.001.

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Kissin, Yury V. "Melt Index and Melt Flow Ratio of Polyethylene Resin." In Polyethylene, 35–55. München: Carl Hanser Verlag GmbH & Co. KG, 2012. http://dx.doi.org/10.3139/9781569905210.002.

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Kissin, Yury V. "Melting Point of Polyethylene Resin." In Polyethylene, 57–72. München: Carl Hanser Verlag GmbH & Co. KG, 2012. http://dx.doi.org/10.3139/9781569905210.003.

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Conference papers on the topic "Polyethylene"

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Dirix, Y., D. Zurbru¨gg, A. Becker, and H. Schmotzer. "Serum Absorption and Ageing of Polyethylenes During a Hip Simulator Study: Comparison Between Conventional and Crosslinked UHMWPE." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-63415.

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Highly crosslinked polyethylenes have been developed as an alternative bearing material for total joint replacements with an improved wear resistance. These polyethylenes are also expected to have an enhanced oxidative stability during shelf ageing compared to γ-sterilized, conventional polyethylene due to the reduced content of free radicals.
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Walker, R. C., A. Meddeb, S. Perini, E. Furman, R. Rajagopalan, M. Lanagan, W. H. H. Woodward, T. Person, and S. Sengupta. "High-temperature polarization analysis of polyethylene and polyethylene-semicon bilayers." In 2022 IEEE Conference on Electrical Insulation and Dielectric Phenomena (CEIDP). IEEE, 2022. http://dx.doi.org/10.1109/ceidp55452.2022.9985362.

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Ito, T., M. Osono, Y. Ehara, T. Sakai, K. Sato, and M. S. A. A. Hammam. "Effects of chlorinated polyethylene on the partial discharge resistance of polyethylene." In Conference on Electrical Insulation & Dielectric Phenomena - Annual Report 1985. IEEE, 1985. http://dx.doi.org/10.1109/ceidp.1985.7728313.

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Peng Yang, Yoshimichi Ohki, and Fuqiang Tian. "Analysis on thermally stimulated currents in polyethylene-terephthalate and polyethylene-naphthalate." In 2014 International Symposium on Electrical Insulating Materials (ISEIM). IEEE, 2014. http://dx.doi.org/10.1109/iseim.2014.6870804.

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Ulrych, Jiri, Radek Polansky, and Josef Pihera. "Dielectric analysis of polyethylene terephthalate (PET) and polyethylene naphthalate (PEN) films." In 2014 15th International Scientific Conference on Electric Power Engineering (EPE). IEEE, 2014. http://dx.doi.org/10.1109/epe.2014.6839429.

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Stancu, Cristina, Petru V. Notingher, Valentin Ionita, Virgil Marinescu, and Denis Panaitescu. "Polyethylene-based magnetic composites." In 2014 International Conference on Applied and Theoretical Electricity (ICATE). IEEE, 2014. http://dx.doi.org/10.1109/icate.2014.6972596.

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Wang, Yang, Kai Wu, David Cubero, Donal Mackernan, David Coker, and Nick Quirke. "Electron trapping in polyethylene." In 2013 IEEE International Conference on Solid Dielectrics (ICSD). IEEE, 2013. http://dx.doi.org/10.1109/icsd.2013.6619710.

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Richaud, Emmanuel, Bruno Fayolle, Bruno Flaconnèche, and Jacques Verdu. "Biodiesel permeability in polyethylene." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738433.

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"Activation of polyethylene granules." In Chemical technology and engineering. Lviv Polytechnic National University, 2021. http://dx.doi.org/10.23939/cte2021.01.143.

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Richaud, Emmanuel. "Biodiesel Permeability in Polyethylene." In SAE 2012 World Congress & Exhibition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2012. http://dx.doi.org/10.4271/2012-01-0747.

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Reports on the topic "Polyethylene"

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Serduke, F., and M. Gerassimenko. Modeling of steel spheres impacting polyethylene. Office of Scientific and Technical Information (OSTI), July 1999. http://dx.doi.org/10.2172/14797.

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Kalb, P. D., and P. Colombo. Polyethylene solidification of low-level wastes. Office of Scientific and Technical Information (OSTI), February 1985. http://dx.doi.org/10.2172/5847886.

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Braegelmann, Peter. Printability and Mechanical Properties of Polyethylene and Polyethylene/Nylon Blend Parts Made by Selective Laser Sintering. Office of Scientific and Technical Information (OSTI), September 2022. http://dx.doi.org/10.2172/1887106.

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Kyser, E. A. Acid solution absorption of extruded polyethylene foam. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/10143063.

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Coe, Joshua Damon, Eric Brown, Carl Mcelhinney Cady, Carl A. Carlson, Bradford Edwin Clements, Dana Mcgraw Dattelbaum, K. Fezzaa, et al. Equation of State and Damage in Polyethylene. Office of Scientific and Technical Information (OSTI), October 2017. http://dx.doi.org/10.2172/1398944.

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Kyser, E. A. Acid solution absorption of extruded polyethylene foam. Office of Scientific and Technical Information (OSTI), January 1993. http://dx.doi.org/10.2172/6622519.

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Crissman, J. M., F. W. Wang, C. M. Guttman, J. R. Maurey, H. L. Wagner, B. M. Fanconi, and D. L. VanderHart. Reference standard polyethylene resins and piping materials :. Gaithersburg, MD: National Bureau of Standards, 1987. http://dx.doi.org/10.6028/nbs.ir.87-3506.

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Crissman, J. M. Reference standard polyethylene resins and piping materials :. Gaithersburg, MD: National Bureau of Standards, 1988. http://dx.doi.org/10.6028/nbs.ir.88-3705.

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Rogers, C. E. Stress Cracking of Polyethylene in Organic Liquids. Fort Belvoir, VA: Defense Technical Information Center, February 1986. http://dx.doi.org/10.21236/ada165733.

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Cassella, K., W. Overton, M. Lyman, S. Urbin, J. George, K. Paulsen, K. Arasteh, et al. Bioremediation of Polyethylene Terephthalate with Ideonella sakaiensis. Office of Scientific and Technical Information (OSTI), July 2023. http://dx.doi.org/10.2172/1992582.

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