Relevant bibliographies by topics / Nylon 6

Academic literature on the topic 'Nylon 6'

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Published: 4 June 2021
Last updated: 9 March 2023

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Journal articles on the topic "Nylon 6"

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Abdel-Gawad, Ahmed M., Adham R. Ramadan, Araceli Flores, and Amal M. K. Esawi. "Fabrication of Nylon 6-Montmorillonite Clay Nanocomposites with Enhanced Structural and Mechanical Properties by Solution Compounding." Polymers 14, no. 21 (October 22, 2022): 4471. http://dx.doi.org/10.3390/polym14214471.

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Melt compounding has been favored by researchers for producing nylon 6/montmorillonite clay nanocomposites. It was reported that high compatibility between the clay and the nylon6 matrix is essential for producing exfoliated and well-dispersed clay particles within the nylon6 matrix. Though solution compounding represents an alternative preparation method, reported research for its use for the preparation of nylon 6/montmorillonite clay is limited. In the present work, solution compounding was used to prepare nylon6/montmorillonite clays and was found to produce exfoliated nylon 6/montmorillonite nanocomposites, for both organically modified clays with known compatibility with nylon 6 (Cloisite 30B) and clays with low/no compatibility with nylon 6 (Cloisite 15A and Na+-MMT), though to a lower extent. Additionally, solution compounding was found to produce the more stable α crystal structure for both blank nylon6 and nylon6/montmorillonite clays. The process was found to enhance the matrix crystallinity of blank nylon6 samples from 36 to 58%. The resulting composites were found to possess comparable mechanical properties to similar composites produced by melt blending.
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Tanaka, Nobuyuki. "Porosity control in nylon-6/nylon-6, 6 membranes." Macromolecular Symposia 102, no. 1 (January 1996): 429–31. http://dx.doi.org/10.1002/masy.19961020150.

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Brooke, G. M., J. A. Hugh MacBride, S. Mohammed, and M. C. Whiting. "Versatile syntheses of oligomers related to nylon 6, nylon 4 6 and nylon 6 6." Polymer 41, no. 17 (August 2000): 6457–71. http://dx.doi.org/10.1016/s0032-3861(99)00875-7.

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Liu, Fei F., E. Keith Marchildon, and Kimberley B. McAuley. "Modeling Equilibrium Behavior of Nylon 6, Nylon 6,6 and Nylon 6/6,6 Copolymer." Macromolecular Reaction Engineering 13, no. 2 (February 7, 2019): 1800078. http://dx.doi.org/10.1002/mren.201800078.

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Liu, Fei F., and Kim B. McAuley. "Improved Kinetic Rate Constants for Nylon 6, Nylon 6,6, and Nylon 6/6,6 Copolymer." Macromolecular Reaction Engineering 14, no. 1 (November 11, 2019): 1900037. http://dx.doi.org/10.1002/mren.201900037.

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Yeh, Jen Taut, Chuen Kai Wang, Zhi Wei Liu, Chi Hui Tsou, and Tai Chin Chiang. "Preparation and Characterization of Nylon 6/Nylon 6 Clay Fibers." Advanced Materials Research 476-478 (February 2012): 763–66. http://dx.doi.org/10.4028/www.scientific.net/amr.476-478.763.

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The drawing, tenacity and thermal properties of nylon 6 (NY6)/nylon 6 clay (NYC) composite fiber specimens prepared at varying NYC contents and drawing temperatures were investigated. The achievable draw ratio (Dra) values of NY6x(NYC)y as-spun fiber specimens initially increase in conjunction with NYC content, and then approach a maximum value, as their NYC contents and drawing temperature approach the 0.5 wt% and 120 oC, respectively. The percentage crystallinity (Xc) values of NY6x(NYC)y as-spun fiber specimens increased significantly, as their NYC contents increased from 0 to 2 wt%. The thermal property were performed on NY6x(NYC)y resins and/or fiber specimens to determine the optimum NYC content and possible deformation mechanisms accounting for the interesting drawing properties found above.
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Pae, Youlee. "Structure and properties of polyimide-g-nylon 6 and nylon 6-b-polyimide-b-nylon 6 copolymers." Journal of Applied Polymer Science 99, no. 1 (2005): 300–308. http://dx.doi.org/10.1002/app.22480.

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Ahn, Tae Oan, Sung Chul Hong, Han Mo Jeong, and Jung Ho Kim. "Nylon 6-polyethersulfone-nylon 6 block copolymer: synthesis and application as compatibilizer for polyethersulfone/nylon 6 blend." Polymer 38, no. 1 (January 1997): 207–15. http://dx.doi.org/10.1016/s0032-3861(96)00450-8.

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Araújo, Edcleide Maria, Renê Anísio da Paz, Tomás Jefférson Alves de Mélo, Amanda Melissa Damião Leite, Renata Barbosa, and Edson Noriyuki Ito. "Use of Brazilian Clay in Nylon 6 with Different Molecular Weight Nanocomposites." Materials Science Forum 660-661 (October 2010): 777–83. http://dx.doi.org/10.4028/www.scientific.net/msf.660-661.777.

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The effect of nylon 6 (Ny6) molecular weight on the development of polymer/layered silicates nanocomposites prepared by the melt intercalation technique was studied in this work. The nylon6/organoclay nanocomposites were prepared in the counter-rotational twin screw extruder. The results of torque rheometry showed that the presence of organoclay in the nylon 6 increased the torque. The results of X-ray diffraction (XRD) and transmission electron microscopy (TEM) showed exfoliated and/or partially exfoliated structures.
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Li, Yue Ling, Xin Min Hao, Ya Fei Guo, Xiao Chen, Yuan Yang, and Jian Ming Wang. "Study on the Acid Resistant Properties of Bio-Based Nylon 56 Fiber Compared with the Fiber of Nylon 6 and Nylon 66." Advanced Materials Research 1048 (October 2014): 57–61. http://dx.doi.org/10.4028/www.scientific.net/amr.1048.57.

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The new kind of bio-based nylon 56 fiber has been synthesized by adipic acid and 1,5-pentanediamine, which was prepared by fermenting a variety of starch in straw. The resistance of the nylon 56 fiber to acid need to be studied because the problem of nylon fabrics often encounter reactions of chemical reagents in their processing, finishing and dressing. The factors of acid concentration, temperature and time affect the mechnical behavior of the fibers of nylon 56 ,nylon6 and nylon 66. Strength of all three nylon fibers have obvious decrease if treated in acetic acid concentration of 10 g/L, while have a straight line down if treated in acetic acid concentration of 100 g/L as time increases until to a half falling down at 120 minutes. Bio-based nylon 56 fibers treated in acetic acid concentration of 100 g/L for 30 minutes have a sharp reduction and almost lost its function at 50 minutes.
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Dissertations / Theses on the topic "Nylon 6"

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Xu, Xiaolin. "Cellulose fiber reinforced nylon 6 or nylon 66 composites." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/26487.

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Thesis (Ph.D)--Polymer, Textile and Fiber Engineering, Georgia Institute of Technology, 2009.
Committee Chair: John D. Muzzy; Committee Co-Chair: Youjiang Wang; Committee Member: Art Ragauskas; Committee Member: Donggang Yao; Committee Member: Karl Jacob. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Mukai, Uchu. "Mechanical properties of PDMS-nylon-6 diblock copolymer and its blends with homo nylon-6." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/11454.

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Srinivas, Srivatsan. "Crystallization behavior of nylon 6/6 and it's [sic] blends with poly(vinyl pyrrolidone) /." This resource online, 1992. http://scholar.lib.vt.edu/theses/available/etd-09192009-040352/.

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Mohan, Anushree. "Modification of Nylon 6 Structure via Nucleation." NCSU, 2009. http://www.lib.ncsu.edu/theses/available/etd-07092009-181421/.

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For nearly two decades inclusion compounds (ICs) have been formed by threading polymer chains into the cyclic starches, cyclodextrins (CDs). Non-covalently bonded crystalline ICs have been formed by threading CDs, onto guest nylon-6 (N6) chains. When excess N6 is employed, non-stoichiometric (n-s)-N6-CD-ICs with partially uncovered and dangling N6 chains result. We have been studying the constrained crystallization of the N6 chains dangling from (n-s)-N6-CD-ICs in comparison with bulk N6 samples, as a function of N6 molecular weights, lengths of uncovered N6 chains, and the CD host used. While the crystalline CD lattice is stable to ~ 300° C, the uncovered and dangling, yet constrained, N6 chains may crystallize below, or be molten above ~225° C. In the IC channels formed with host α- and γ-CDs containing 6 and 8 glucose units, respectively, single and pairs of side-by-side N6 chains can be threaded and included. In the α-CD-ICs the ~ 0.5nm channels are separated by ~ 1.4nm, while in γ-CD-ICs the ~ 1nm channels are ~ 1.7 nm apart, with each γ-CD channel including two N6 chains. The constrained dangling chains in the dense (n-s)-N6-CD-IC brushes crystallize faster and to a greater extent than those in bulk N6 melts, and this behavior is enhanced as the molecular weights/chain lengths of N6 are increased. Furthermore, when added at low concentrations (n-s)-N6-CD-ICs serve as effective nucleating agents for the bulk crystallization of N6 from the melt. Because of the biodegradable/bioabsorbable nature of CDs, (n-s)-polymer-CD-ICs can provide environmentally favorable, non-toxic nucleants for enhancing the melt crystallization of polymers and improving their properties.
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Rotter, George Edmund. "Polymerization and crystal formation of nylon 6." Case Western Reserve University School of Graduate Studies / OhioLINK, 1990. http://rave.ohiolink.edu/etdc/view?acc_num=case1054928542.

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Gaglione, Anthony. "Multiscale Modeling of an Industrial Nylon-6 Leacher." Thesis, Virginia Tech, 2007. http://hdl.handle.net/10919/31149.

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This thesis presents a multiscale model of an industrial nylon-6 leacher. We develop several models at various spatial scales and implement them together in a simplistic, efficient way to develop an overall leacher model. We solve dynamic transport differential equations using the finite-volume method and method of lines in an in-house-developed FORTRAN program. We use the ODEPACK package of ordinary differential equation (ODE) solvers to solve our system of coupled ODEs. Our multiscale model performs transport, thermodynamic, physical property, and mass-transfer calculations at a finite-volume scale. We introduce two additional scales: a mesoscale, in which we perform computational fluid dynamic (CFD) simulations, and a molecular scale. Our CFD simulations solve for turbulent properties of fluid flowing over a packed bed. We incorporate the turbulent diffusivity of the fluid into our finite-volume leacher model. We perform molecular simulations and use the conductor-like screening model-segment activity coefficient (COSMO-SAC) model to generate solubility predictions of small, cyclic oligomers in water and ε-caprolactam. Additionally, we develop an extension of COSMO-SAC to model polymer species, which we refer to as Polymer-COSMO-SAC, and apply it to solve liquid-liquid equilibrium equations. We present a unique methodology to apply COSMO-based models to polymer species, which shows reasonable results for nylon-6. Because of the computational intensity of our Polymer-COSMO-SAC liquid-liquid equilibrium algorithm, we generate pre-computed tables of equilibrium predictions that we may import into our leacher model. Our integration of multiscale models maximizes efficiency and feasibility with accuracy.

We are able to use our multiscale models to estimate necessary parameters, but we need to fit two mass-transfer related parameters to industrial data. We validate our model against the plant data and find average-absolute errors in the final mass percent of ε-caprolactam and cyclic dimer in polymer chips of 25.0% and 54.7%, respectively. Several plant data sets are suspected outliers and we believe an unforeseen equilibrium limitation may cause this discrepancy. If we remove these outlying data sets, we then find average-absolute errors of 7.5% and 19.3% for ε-caprolactam and cyclic dimer, respectively. We then use our validated model to perform application and sensitivity studies to gain critical insight into the leacherâ s operating conditions.


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Kegel, Mark Steven, and n/a. "Fibres from recycled post consumer PET/nylon 6 blends." Swinburne University of Technology, 2006. http://adt.lib.swin.edu.au./public/adt-VSWT20070606.111448.

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The objective of this project was to develop blends based upon post consumer RPET and N6, and to evaluate the suitability of these blends to form fibres for the end use in carpet fibre. In the work carried out it was found it is possible to spin RPET/N6 biconstituent fibres over a wide range of blend ratios. All the blends studied have diminished physical properties when compared to those of pure RPET and N6. The processability of these blends also deteriorated due to the large increases in normal forces which manifests in extrusion equipment as die swell that often results in melt fracture. It has been shown that the morphology of the fibre controls the degree of decay in properties and die swell at the spinnerette. The blends that are rich in one phase, with the secondary phase distributed as elongated fibrils have shown better physical performance and improved processing compared to the blends 70/30 � 30/70, which have poorer properties and increased die swell due to there co-continuous morphology. In quiescent studies, the physical properties of the blends have had little deviation from those predicted using a rule of mixtures line. In and around the 50% RPET blend, die swell was observed to be extreme and this makes fibre spinning difficult. It was found that this was caused by a loss in viscosity in the blends and a general increase in normal forces in response to applied shear. The die swell phenomenon is a rheological characteristic of the blends, which was inevitably caused by internal capillary flow of one component in the other. IR spectroscopy has shown that there is little to no in-situ compatibilisation occurring during simple melt processing. However, it was found that significant interfacial compatibilisation could be achieved through solid stating N6/RPET blends. The FTIR spectra for solid state blends in figure 4.51 has shown absorbency in the 3300 cm-1 region after all free N6 was removed. This indicates that in-situ compatibilisation has occurred between the phases in the solid stating process and it is a time dependent reaction. The Burgers and Koltunov models can be used to predict the creep behaviour of the fibre blends studied. The Burgers model provides greater accuracy for longer-term exposure to stress. From the thermal results, the solid stating process significantly affects the melting and crystallisation out of the melt and the ultimate level of crystallinity. The contribution of the copolymer in these changes appears to be small. The physical strength of the fibres made on the laboratory line was only marginally lower than those made on a factory line. The morphology of the mid-range blends is co-continuous and that of the N6 and RPET rich blends is dispersed droplet morphology. Based on the finding, a N6 rich blends and in particular the 10% RPET blend is the most suitable for further commercial development as its processing, physical performance and post spinning processing closely resemble the pure N6 currently in use. It has provided performance and consistency throughout the processing and testing we have conducted.
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Srinivas, Srivatsan. "Crystallization behavior of nylon 6/6 and its blends with poly(vinyl pyrrolidone)." Thesis, Virginia Tech, 1992. http://hdl.handle.net/10919/44859.

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This thesis presents the results of a study on the blends of an aliphatic crystallizable polyamide (nylon 6/6) and trace quantities of a polar non-crystallizable diluent (poly(vinylpyrrolidone)). This study is based on the preliminary findings of Keith et al. who reported striking morphological changes in nylon 6/6 upon addition of small amounts of poly(vinylpyrrolidone) (PVP). The melting behavior of pure nylon 6/6 was also studied during the course of this investigation. The melting behavior of nylon 6/6 was studied using a differential scanning calorimeter (DSC). Samples were isothermally crystallized at various temperatures from the melt. Subsequent DSC analysis showed the presence of three distinct melting endotherms. The behavior of these three endotherms was studied as a function of the crystallization temperature (TC), annealing time, and DSC heating rate. X-ray studies (small and wide angle) and hot stage optical microscopy studies were also carried out to determine the cause of the multiple endotherms. The influence of addition of PVP on the crystal morphology of nylon 6/6 was studied using DSC, x-ray and hot stage photomicroscopy. The addition of PVP has a dramatic effect on the spherulitic morphology of nylon. The addition of PVP to nylon caused a striking reduction in the nucleation density of spherulites, modification of lamellar organization in spherulites (as evidenced by the occurrence of banding), and modification of interlamellar spacings.
Master of Science
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Kegel, Mark. "Fibres from recycled post consumer PET/nylon 6 blends." Australasian Digital Thesis Program, 2006. http://adt.lib.swin.edu.au/public/adt-VSWT20070606.111448/index.html.

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Thesis (PhD) - Swinburne University of Technology, Industrial Research Institute Swinburne - 2006.
A thesis submitted to Industrial Research Institute Swinburne in fulfilment of the requirements for the degree of Doctor of Philosophy, Swinburne University of Technology - 2006. Typescript. "July 2006". Includes bibliographical references (p. 147-156).
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Saman, Mansor Mohamad. "Study of the conductivity of Nylon 6/ABS blends." Thesis, Sheffield Hallam University, 1999. http://shura.shu.ac.uk/20318/.

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In this research project the study was conducted on conductivity of acrylonitrile butadiene styrene (ABS)/Nylon 6 blend with carbon black as conductive filler. Three different blends of ABS/carbon black, Nylon 6/carbon black and ABS/Nylon 6/carbon black with various compositions were prepared by mixing together by using a single screw extruder. Each compound was reblended to achieve homogeneous mixture and the effect of processing was studied. Conductivity of the low resistance of blends were obtained by measuring sheet resistance using four-point probe as according to ASTM F 1529. The sheet resistance could only be detected for ABS/carbon black 20 wt % and above, and ABS/Nylon 6 with 80:20 ratio with 10 wt % of carbon black. Whereas, for Nylon 6/carbon black blends and the others high resistance of blends, their resistances were measured by Teraohmeter according to ASTM D 257 method. Percolation threshold (critical volume fraction) of the blends was studied to find actual conductive filler contents to avoid deterioration of mechanical properties. In this case, tensile tests were conducted according to ASTM D 638 to establish their mechanical properties. Meanwhile, scanning electron microscopy (SEM) was used to study the morphology of blended polymers, interface of polymer/carbon black and aggregation phenomenon between carbon black and polymers. The correlation between conductivity, mechanical properties and morphological characterisation of all the blends was studied. The results show that, the addition of carbon black up to 10%, increases conductivity and tensile strength of ABS/carbon black and Nylon 6/carbon black blends. Conductivity continues to increase with further addition of carbon black, but at the expense of tensile strength reduction due to the effect of brittle nature of carbon black. By adding ABS in ABS/Nylon 6/carbon black blends, conductivity increases, whereas tensile strength decreases. However, tensile strength of ABS/Nylon 6/carbon black blends were too low to compare with individual polymer blended with carbon black, due to immiscibility between ABS and Nylon 6. Reblending the compound for the third time increases conductivity and mechanical properties due to increase in homogeneity and uniform distribution of carbon black dispersion. Both ABS and conductive carbon black absorb moisture that can effect the properties of compound. Drying of the compound will remove moisture which will result in improvements in conductivity and tensile strength.
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Books on the topic "Nylon 6"

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Hashim, Kamaruddin. Compatibilization of poly(vinylidene fluoride)/nylon 6 blends by intermolecular association. 1996.

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Krüssmann, Helmut, Gerhard Heidemann, Sudhir Dugal, and Giselher Valk. Untersuchungen Zum Mechanismus der Thermooxidation und Zur Stabilisierung Von Nylon 6. VS Verlag fur Sozialwissenschaften GmbH, 2013.

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Book chapters on the topic "Nylon 6"

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Gooch, Jan W. "Nylon 6." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8039.

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Gooch, Jan W. "Nylon 6." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8043.

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Gooch, Jan W. "Nylon 6/6." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8040.

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Bährle-Rapp, Marina. "Nylon-6 bis Nylon-11." In Springer Lexikon Kosmetik und Körperpflege, 380. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_7035.

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Gooch, Jan W. "Nylon 6/6 Salt." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8041.

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Deopura, B. L., and A. K. Mukherjee. "Nylon 6 and nylon 66 fibres." In Manufactured Fibre Technology, 318–59. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5854-1_13.

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Gooch, Jan W. "Nylon 4/6." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8037.

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Gooch, Jan W. "Nylon 6/T." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8042.

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Gooch, Jan W. "Nylon 6/10." In Encyclopedic Dictionary of Polymers, 494. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8044.

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Gooch, Jan W. "Nylon 6/12." In Encyclopedic Dictionary of Polymers, 495. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_8045.

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Conference papers on the topic "Nylon 6"

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Ishii, S., H. Suzuki, Y. Morisawa, H. Sato, S. Yamamoto, Y. Ozaki, C. Otani, T. Uchiyama, and H. Hoshina. "Vibrational spectra of nylon-6, nylon-6/6, nylom-11 and nylon-12 studied by terahertz spectroscopy." In 2012 37th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2012). IEEE, 2012. http://dx.doi.org/10.1109/irmmw-thz.2012.6380372.

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Shaffer, Derek, Cody Reinstadtler, John T. Roth, and Ihab Ragai. "Analysis of Cryogenically Treated Sheet Nylon 6/6." In ASME 2017 12th International Manufacturing Science and Engineering Conference collocated with the JSME/ASME 2017 6th International Conference on Materials and Processing. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/msec2017-3039.

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When manufacturing polymer and rubber products, the parts are frequently exposed to cryogenic temperatures after molding or forming in order to improve the ability to remove excess material and flash. However, there has been very little investigation into the effect that cryogenic temperatures may have on polymers. As such, the goal of the research described herein is to examine the effect of this type of treatment on the properties of one such polymer, Nylon 6/6. More specifically, the temperature of the environment surrounding Nylon 6/6 is decreased at two different rates into the cryogenic temperature range, allowed to soak, and then returned to ambient. Whereupon the material properties of the treated Nylon are compared to baseline. This testing demonstrates that the exposure to the cold environment resulted in a decrease in the yield and ultimate tensile strength of the Nylon while leaving the area reduction and strain after necking roughly unchanged. Examination of the surface condition of the treated specimens did not bring to light corresponding cracking from the treatments, thereby indicated that the resultant change in mechanical behavior is likely caused by structural changes within the Nylon. Additional testing of the Nylon, with respect to frequency response, further demonstrated that exposure to cryogenic temperatures resulted in decreases in the Nylon’s natural response at the structure’s dominate mode. These initial findings indicate that the conventional technique of lowering a part’s temperature to enhance the ability to remove flash does, in fact, result in measurable changes in the mechanical behavior of the Nylon product.
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Azizo, Amar Shafrin, Mohd Dzul Hakim Wirzal, Muhammad Roil Bilad, and Abdull Rahim Mohd Yusoff. "Assessment of nylon 6, 6 nanofibre membrane for microalgae harvesting." In THE 2ND INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY 2017 (ICAST’17). Author(s), 2017. http://dx.doi.org/10.1063/1.5005365.

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Sreelatha, K. "Optical characterization of semiconducting nylon 6 films." In LIGHT AND ITS INTERACTIONS WITH MATTER. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4898243.

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Crippa, Giuseppe, and Piermaria Davoli. "Comparative Fatigue Resistance of Fiber Reinforced Nylon 6 Gears." In ASME 1992 Design Technical Conferences. American Society of Mechanical Engineers, 1992. http://dx.doi.org/10.1115/detc1992-0083.

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Abstract The fatigue-life diagrams of injection-molded nylon 6 gears with different reinforcements are presented for various lubrication modes (dry, grease, splash oil lubrication) and for different meshing combinations (plastic/plastic and steel/plastic gears). Tests have been carried out with a properly designed back-to-back rig; results are compared with previous experiments, performed with unreinforced nylon 6 gears. Tested gears have been 232 (70 in unreinforced nylon and 162 in differently filled polyamides). More than 700·106 cycles have been totalised. From test data, and from the “matrix” of gear/pinion material combination, the capabilities of differently reinforced nylon 6 gears for fatigue and wear resistance have been outlined. These capabilities are the basis for a proper material selection in plastic gear design.
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Prabhakaran, Rajesh, Marianna Kontopoulou, Gene Zak, Phil Bates, and Bobbye Baylis. "Laser Transmission Welding of Glass Reinforced Nylon 6." In SAE 2003 World Congress & Exhibition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2003. http://dx.doi.org/10.4271/2003-01-1133.

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Bouchard, Benjamin J., and Daniel S. Leydon. "Blow Moldable Nylon 6 for Air Induction Components." In International Congress & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1995. http://dx.doi.org/10.4271/950231.

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Mahadevegowda, Amoghavarsha, Colin Johnston, and Patrick S. Grant. "Nylon-6 based nanocomposite films for capacitor applications." In 2017 IEEE 17th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2017. http://dx.doi.org/10.1109/nano.2017.8117497.

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Schutte, Juan, Johan Potgieter, Steven Dirven, and Xiaowen Yuan. "The effects of electrospinning collection surface modification on nylon 6-6 placement." In 2017 24th International Conference on Mechatronics and Machine Vision in Practice (M2VIP). IEEE, 2017. http://dx.doi.org/10.1109/m2vip.2017.8211509.

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LEW, THOMAS, and K. RAI. "Biaxially oriented nylon-6 as a long duration material." In International Balloon Technology Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1991. http://dx.doi.org/10.2514/6.1991-3659.

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Reports on the topic "Nylon 6"

1

Veith, C. A., and R. E. Cohen. Synthesis of Poly(dimethylsiloxane) - Nylon 6 Diblock Copolymers. Fort Belvoir, VA: Defense Technical Information Center, December 1989. http://dx.doi.org/10.21236/ada216850.

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2

Beyer, Frederick L., and Christopher Ziegler. Wide-Angle X-Ray Scattering Characterization of the Morphology of Nylon 6 6 Obturator Materials. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada426285.

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3

Ostermayer, David, Frederick L. Beyer, Peter G. Dehmer, and Melissa A. Klusewitz. Measurement of V50 Behavior of a Nylon 6-Based Polymer-Layered Silicate Nanocomposite. Fort Belvoir, VA: Defense Technical Information Center, September 2001. http://dx.doi.org/10.21236/ada399371.

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4

Johnson, C. G., and L. J. Mathias. 13C and 15N Solid-State NMR of Copolymers of Nylon 6 and 7: Observation of a Stable Pseudohexagonal Phase. Fort Belvoir, VA: Defense Technical Information Center, June 1993. http://dx.doi.org/10.21236/ada265799.

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