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Journal articles on the topic 'Nylon 6'

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Author: Grafiati

Published: 4 June 2021

Last updated: 9 March 2023

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Park, Wan-Woo, Jong-Yoon Lee, Bong-Yeon Kim, Young Jun Kim, and Young Tai Yoo. "Thermal and Biodegradation Behavior of Nylon 4 and Nylon 4/6 Copolymers." Polymer Korea 41, no. 4 (July 31, 2017): 624–31. http://dx.doi.org/10.7317/pk.2017.41.4.624.

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12

Brooke, Gerald M., S. Mohammed, and Mark C. Whiting. "The synthesis of oligomers related to nylon 4 6 and nylon 6 6." Polymer 40, no. 3 (January 1999): 773–88. http://dx.doi.org/10.1016/s0032-3861(98)00079-2.

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13

Zhao, Zhudi, Wenxue Yu, Yanhua Liu, Jianqiao Zhang, and Zhenjie Shao. "Isothermal crystallization behaviors of nylon-6 and nylon-6/montmorillonite nanocomposite." Materials Letters 58, no. 5 (February 2004): 802–6. http://dx.doi.org/10.1016/j.matlet.2003.07.016.

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14

Yeh, Jen-Long, Jen-Feng Kuo, and Chuh-Yung Chen. "Studies on crystallization kinetics of nylon 6-polyoxypropylene-nylon 6 copolymers." Journal of Polymer Research 4, no. 2 (April 1997): 81–89. http://dx.doi.org/10.1007/s10965-006-0011-5.

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15

Li, Juan, Zhengping Fang, Lifang Tong, Aijuan Gu, and Fu Liu. "Polymorphism of nylon-6 in multiwalled carbon nanotubes/nylon-6 composites." Journal of Polymer Science Part B: Polymer Physics 44, no. 10 (2006): 1499–512. http://dx.doi.org/10.1002/polb.20808.

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16

Wu, Tzong-Ming, Erh-Chiang Chen, and Chien-Shiun Liao. "Polymorphic behavior of nylon 6/saponite and nylon 6/montmorillonite nanocomposites." Polymer Engineering & Science 42, no. 6 (June 2002): 1141–50. http://dx.doi.org/10.1002/pen.11018.

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17

Yeh, Jen-Long, Jen-Feng Kuo, and Chuh-Yung Chen. "Morphology and properties of nylon 6-polyoxypropylene-nylon 6 block copolymers." Materials Chemistry and Physics 37, no. 2 (March 1994): 161–69. http://dx.doi.org/10.1016/0254-0584(94)90087-6.

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18

Ning, Xin, and Hatsuo Ishida. "RIM-pultrusion of nylon-6 and rubber-toughened nylon-6 composites." Polymer Engineering and Science 31, no. 9 (May 1991): 632–37. http://dx.doi.org/10.1002/pen.760310903.

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19

Li, Yuying, and Xiao Hu. "Polymorphism of nylon-6 in nylon-6/nanoclay/functionalized polyolefin blends." Journal of Polymer Science Part B: Polymer Physics 45, no. 12 (2007): 1494–502. http://dx.doi.org/10.1002/polb.21167.

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20

Bates, P. J., C. Dyck, and M. Osti. "Vibration welding of nylon 6 to nylon 66." Polymer Engineering and Science 44, no. 4 (2004): 760–71. http://dx.doi.org/10.1002/pen.20068.

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21

Wei, Wei, Jen Taut Yeh, Xin Ling Wang, Peng Li, and Wei Wei. "Removal of Cd(II) from Aqueous Solution by Electrospun Nylon 6 Nanofibrous Nonwoven Containing Attapulgite." Advanced Materials Research 332-334 (September 2011): 1295–99. http://dx.doi.org/10.4028/www.scientific.net/amr.332-334.1295.

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The attapulgite powders modified by silicane coupling agent are loaded onto the surface of nylon 6 nanofibers by immersing the nylon 6 electrospun fiber nonwoven in a bath containing modified attapulgite dispersion under ultrasonicating. The nylon6 nanofibrous nonwoven containing attapulgite nano particles was explored as “nano adsorbent” to remove Cd (II) ions from Cd (II) aqueous solution. The effects of various parameters on adsorption properties, such as contact time, pH values of Cd (II) solution and initial Cd (II) concentration were investigated.

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22

Thongpin, Chanchai, Kullanith Chaemprasith, Jakapan Teeralertpanich, Parisara Saensuk, and Nontawat Kritape. "In Situ Reinforcement of PLA Using Nylon 6 in PLA/Nylon 6 Extrudate Blend via Twin-Screw Extrusion." Key Engineering Materials 659 (August 2015): 428–35. http://dx.doi.org/10.4028/www.scientific.net/kem.659.428.

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This research was aimed to study the possibility of in-situ reinforcement of PLA by elongated Nylon 6 in PLA/Nylon 6 blend during elongating of PLA/Nylon extrusion. PLA was melt blending with Nylon 6 in a twin screw extruder with various compositions i.e. 5, 10, 15 and 20 % of Nylon 6. The extrudate was drawn after leaving extrusion orifice die of 3 mm in diameter, with the pulling speed of 12 cycles per minute. The extrudate gauge length 15 cm were used to perform tension test in order to investigate tensile properties. The blending between PLA and Nylon 6 with 11 phr of benzene sulfonamide (BSA), based on Nylon 6, as a plasticizer was also investigated at the same PLA/Nylon 6 blend ratios. The extrusion used conditions were also the same. Tension was also performed onto the extrudates with the gauge length 15 cm. Thermal degradation was also investigated. The SEM micrographs of blends in the longitudinal direction of PLA/Nylon 6 extrudate showed elongated of Nylon 6 in PLA matrix phase. The elongated of Nylon 6 phase in PLA matrix phase was found very clear in the plasticized blends. This phenomenon clearly occurred for the blends composition of both 95/5 and 90/10, with and without plasticizer. The results also showed that Young’s modulus of the blends with 5 % Nylon 6 was increased about 10 % whereas at 10 % nylon 6, the modulus was not significantly different from neat PLA. With the addition of plasticizer, nylon 6 was elongated more than that in the blend with un-plasticized Nylon 6. Due to the lack in interfacial adhesion, shown by SEM micrograph, tensile strength was found to be decreased. As expected, the elongation at break under tension was increased with the content of nylon 6. This was due to the toughening effect of elongated Nylon 6. Thermal stability, notified by degradation temperature of PLA, Td, was found to be improved. This was due to the high thermal stability of nylon 6. The results from the research can inform that the elongated nylon 6 phase in PLA matrix can perform as fibrous reinforcement. At high content of nylon 6, i.e. 15 and 20 %, the elongation of nylon 6 was rather difficult due to the less matrix phase and low shearing between PLA and nylon 6. Phase compatibility improvement could be the factor to improve the in-situ reinforcement.

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23

Gonsalves, K. E., X. Chen, and T. K. Wong. "Synthesis, characterization and biodegradation test of nylon 2/6 and nylon 2/6/6." Journal of Materials Chemistry 1, no. 4 (1991): 643. http://dx.doi.org/10.1039/jm9910100643.

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24

Dijkstra, K., and R. J. Gaymans. "Nylon-6/rubber blends." Journal of Materials Science 29, no. 12 (June 1994): 3231–38. http://dx.doi.org/10.1007/bf00356668.

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25

Dijkstra, K., A. Van Der Wal, and R. J. Gaymans. "Nylon-6-rubber blends." Journal of Materials Science 29, no. 13 (July 1994): 3489–96. http://dx.doi.org/10.1007/bf00352054.

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26

Dijkstra, K., and G. H. Ten Bolscher. "Nylon-6/rubber blends." Journal of Materials Science 29, no. 16 (August 1994): 4286–93. http://dx.doi.org/10.1007/bf00414212.

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27

Lai, Chiu-Chun, Bo-Sien Yu, Hao-Wen Lo, Wei-Feng Teng, Lung-Chang Liu, and Chien-Ming Chen. "Synthesis and properties of low-crystallinity nylon 6 with high transparency and low hygroscopicity containing adipic acid." Modern Physics Letters B 34, no. 07n09 (March 18, 2020): 2040005. http://dx.doi.org/10.1142/s0217984920400059.

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In this research, a series of amorphous nylons 6 were prepared by introducing adipic acid and different structure amines into the copolymerization with caprolactam. The effects including thermal properties, crystallinity, dynamic mechanical properties, optical properties, and water absorption of different copolymerization structure and copolymerization ratio on the properties of nylon 6 were investigated. The results show the melting point and thermal cracking temperature Td 5 of nylon 6 are, respectively, between 179[Formula: see text]C and 217[Formula: see text]C and 278[Formula: see text]C to 336[Formula: see text]C. Nylon 6 structure introducing a methyl side chain is more effective than a meta-benzene ring, a meta-cycloalkyl, and bicycloalkyl groups, so CAMM and CAI have the lowest crystallinity.

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28

Scully, Kevin, and Rabin Bissessur. "Decomposition kinetics of nylon-6/graphite and nylon-6/graphite oxide composites." Thermochimica Acta 490, no. 1-2 (June 2009): 32–36. http://dx.doi.org/10.1016/j.tca.2009.01.029.

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29

Fong, H. "Generation of electrospun fibers of nylon 6 and nylon 6-montmorillonite nanocomposite." Polymer 43, no. 3 (February 2002): 775–80. http://dx.doi.org/10.1016/s0032-3861(01)00665-6.

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30

Li, Lei, Leon M. Bellan, Harold G. Craighead, and Margaret W. Frey. "Formation and properties of nylon-6 and nylon-6/montmorillonite composite nanofibers." Polymer 47, no. 17 (August 2006): 6208–17. http://dx.doi.org/10.1016/j.polymer.2006.06.049.

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31

Zhao, Zhudi, Weitao Zheng, Wenxue Yu, Hongwei Tian, and Hujie Li. "Unusual Crystallization Behavior in Nylon-6 and Nylon-6/Montmorillonite Nanocomposite Films." Macromolecular Rapid Communications 25, no. 14 (July 21, 2004): 1340–44. http://dx.doi.org/10.1002/marc.200400168.

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32

Cooper, Sharon J., Edward D. T. Atkins, and Mary J. Hill. "Temperature-Induced Changes in Lamellar Crystals of Monodisperse Nylon 6 and Nylon 6 6 Oligoamides." Macromolecules 31, no. 25 (December 1998): 8947–56. http://dx.doi.org/10.1021/ma981158v.

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33

USUKI, Arimitsu, Masaya KAWASUMI, Yoshitsugu KOJIMA, Akane OKADA, Toshio KURAUCHI, Tadao OGAWA, and Toshimi ARAGA. "Molecular Structure of Nylon in Nylon 6-Clay Hybrid." KOBUNSHI RONBUNSHU 52, no. 5 (1995): 299–304. http://dx.doi.org/10.1295/koron.52.299.

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34

Choy, C. L., W. P. Leung, and E. L. Ong. "Thermal expansivity of oriented nylon-6 and nylon-6,6." Polymer 26, no. 6 (June 1985): 884–88. http://dx.doi.org/10.1016/0032-3861(85)90132-6.

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35

Enlow, Elizabeth M., Jennifer L. Kennedy, Alexander A. Nieuwland, James E. Hendrix, and Stephen L. Morgan. "Discrimination of Nylon Polymers Using Attenuated Total Reflection Mid-Infrared Spectra and Multivariate Statistical Techniques." Applied Spectroscopy 59, no. 8 (August 2005): 986–92. http://dx.doi.org/10.1366/0003702054615142.

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Nylons are an important class of synthetic polymers, from an industrial, as well as forensic, perspective. A spectroscopic method, such as Fourier transform infrared (FT-IR) spectroscopy, is necessary to determine the nylon subclasses (e.g., nylon 6 or nylon 6,6). Library searching using absolute difference and absolute derivative difference algorithms gives inconsistent results for identifying nylon subclasses. The objective of this study was to evaluate the usefulness of peak ratio analysis and multivariate statistics for the identification of nylon subclasses using attenuated total reflection (ATR) spectral data. Many nylon subclasses could not be distinguished by the peak ratio of the N–H vibrational stretch to the sp3 C–H2 vibrational stretch intensities. Linear discriminant analysis, however, provided a graphical visualization of differences between nylon subclasses and was able to correctly classify a set of 270 spectra from eight different subclasses with 98.5% cross-validated accuracy.

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36

Anand, Anoop, Narendhara Kumar, Rahul Harshe, and Makarand Joshi. "Glass/epoxy structural composites with interleaved nylon 6/6 nanofibers." Journal of Composite Materials 51, no. 23 (December 7, 2016): 3291–98. http://dx.doi.org/10.1177/0021998316682603.

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Nylon 6/6 nanofibers of diameter 80–100 nm were electrospun on bidirectional E-glass fabric. The fabric with nanofibers on one surface was used to fabricate glass/epoxy structural composites, through resin film infusion. Mechanical properties of composites with interleaved nylon 6/6 nanofibers were found to be substantially improved from that of the control specimens fabricated under identical conditions, but without nanofibers. Compressive strength of composites showed over 30% increase, while interlaminar shear strength improved by 17% with nylon nanofibers of an areal density as low as 0.4 gsm. Residual compressive strength of laminates after a low-velocity impact event also showed a promising improvement with interleaved electrospun nanofibers.

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37

Ding, Hong, and F. W. Harris. "Synthesis and characterization of novel nylon 6-b-polyimide-b-nylon 6 copolymers." Pure and Applied Chemistry 67, no. 12 (January 1, 1995): 1997–2004. http://dx.doi.org/10.1351/pac199567121997.

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38

Nguyễn, Loan, Sung-Moon Choi, Dong-Hun Kim, Nak-Kyung Kong, Phil-Jung Jung, and Soo-Young Park. "Preparation and characterization of nylon 6 compounds using the nylon 6-grafted GO." Macromolecular Research 22, no. 3 (February 4, 2014): 257–63. http://dx.doi.org/10.1007/s13233-014-2046-5.

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39

Yeh, Jen-Taut, Chuen-Kai Wang, Zhi-Wei Liu, Peng Li, Chi-Hui Tsou, Yu-Ching Lai, and Fang-Chang Tsai. "Drawing and ultimate tensile properties of nylon 6/nylon 6 clay composite fibers." Polymer Engineering & Science 52, no. 6 (March 27, 2012): 1348–55. http://dx.doi.org/10.1002/pen.22185.

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40

Usuki, Arimitsu, Yoshitsugu Kojima, Masaya Kawasumi, Akane Okada, Yoshiaki Fukushima, Toshio Kurauchi, and Osami Kamigaito. "Synthesis of nylon 6-clay hybrid." Journal of Materials Research 8, no. 5 (May 1993): 1179–84. http://dx.doi.org/10.1557/jmr.1993.1179.

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It was found that montmorillonite cation exchanged for 12-aminolauric acid (12-montmorillonite) was swollen by ∊-caprolactam to form a new intercalated compound. Caprolactam was polymerized in the interlayer of montmorillonite, a layer silicate, yielding a nylon 6-clay hybrid (NCH). The silicate layers of montmorillonite were uniformly dispersed in nylon 6. The carboxyl end groups of 12-aminolauric acid in 12-montmorillonite initiated polymerization of ∊-caprolactam, and as 12-montmorillonite content became larger, the molecular weight of nylon was reduced. From the result of end-group analysis, carboxyl end groups were more than amino end groups. The difference between the carboxyl and the amino end groups was attributed to ammonium cations (-NH3+) of nylon molecules, because the difference agreed with the anion site concentration of the montmorillonite in NCH. It is suggested that the ammonium cations in nylon 6 interact with the anions in montmorillonite.

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41

Lou, Ching Wen, Po Ching Lu, Hsuan Mao Yeh, and Jia Horng Lin. "Manufacturing Technique and Stab-Resistance Evaluation of Three-Dimensional Nylon 6/LPET Compound Nonwoven Fabrics." Advanced Materials Research 910 (March 2014): 170–73. http://dx.doi.org/10.4028/www.scientific.net/amr.910.170.

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This study aims to examine the influence of the temperatures of heat treatment on the puncture-resistance of Nylon6/LPET compound nonwoven fabrics. Polyamide 6 (Nylon 6) fibers and low-melting-point polyester (LPET) fibers are combined and undergo a heat treatment to make three-dimensional (3-D) Nylon 6/LPET compound nonwoven fabrics through a nonwoven process. The nonwoven fabrics are tested for their dynamic puncture resistance, constant rate puncture resistance, and impact strength. The experiment results show that when thermally treated at a high temperature, the compound nonwoven fabrics are rendered with a lower dynamic puncture resistance and a lower constant rate puncture resistance, but a greater impact strength.

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42

Dijkstra, K., J. ter Laak, and R. J. Gaymans. "Nylon-6/rubber blends: 6. Notched tensile impact testing of nylon-6/(ethylene-propylene rubber) blends." Polymer 35, no. 2 (January 1994): 315–22. http://dx.doi.org/10.1016/0032-3861(94)90696-3.

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43

Kim, Jong J., and S. W. Seo. "Crystallization Kinetics of Nylon 6." Textile Research Journal 64, no. 7 (July 1994): 427–31. http://dx.doi.org/10.1177/004051759406400709.

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44

Li, Hong, and James A. Donovan. "Salt embrittlement of Nylon 6." Engineering Fracture Mechanics 101 (March 2013): 91–95. http://dx.doi.org/10.1016/j.engfracmech.2012.07.028.

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45

Gupta, Mool C., and Rajbahadur R. Pandey. "γ-Irradiation of Nylon 6." Journal of Polymer Science Part A: Polymer Chemistry 26, no. 2 (February 1988): 491–502. http://dx.doi.org/10.1002/pola.1988.080260213.

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46

Chavarria, F., and D. R. Paul. "Comparison of nanocomposites based on nylon 6 and nylon 66." Polymer 45, no. 25 (November 2004): 8501–15. http://dx.doi.org/10.1016/j.polymer.2004.09.074.

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47

Kang, Tae-Kyu, Yang Kim, Won-Jei Cho, and Chang-Sik Ha. "Effects of amorphous nylon on the properties of nylon 6." Polymer Testing 16, no. 4 (August 1997): 391–401. http://dx.doi.org/10.1016/s0142-9418(96)00059-1.

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48

Verma, Anu, B. L. Deopura, and A. K. Sengupta. "A study on blends of nylon-6 and nylon-66." Journal of Applied Polymer Science 31, no. 3 (February 20, 1986): 747–62. http://dx.doi.org/10.1002/app.1986.070310301.

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49

Hasegawa, Naoki, Hirotaka Okamoto, Makoto Kato, Arimistu Usuki, and Norio Sato. "Nylon 6/Na–montmorillonite nanocomposites prepared by compounding Nylon 6 with Na–montmorillonite slurry." Polymer 44, no. 10 (May 2003): 2933–37. http://dx.doi.org/10.1016/s0032-3861(03)00215-5.

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50

Usuki, Arimitsu, Akihiko Koiwai, Yoshitsugu Kojima, Masaya Kawasumi, Akane Okada, Toshio Kurauchi, and Osami Kamigaito. "Interaction of nylon 6-clay surface and mechanical properties of nylon 6-clay hybrid." Journal of Applied Polymer Science 55, no. 1 (January 3, 1995): 119–23. http://dx.doi.org/10.1002/app.1995.070550113.

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