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Wiki Education Foundation-supported course assignment
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This article was the subject of a Wiki Education Foundation-supported course assignment, between 28 August 2018 and 6 December 2018. Further details are available on the course page. Student editor(s): Amc0124.
Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 05:31, 17 January 2022 (UTC)
Melting points
editI have added the melting point range for the family as found at http://www.machinedesign.com/BDE/materials/bdemat2/bdemat2_29.html to the page. I realise that this is a family of compounds, but people generally think of a single substance called 'Nylon' and as such I would consider it to be useful to have a rough indication of the melting temperatures on this page.
PA 6 and 66 draw
editAbout PA 6.6:
"Since each monomer in this copolymer has the same reactive group on both ends, the direction of the amide bond reverses between each monomer..."
And about PA 6:
"The peptide bond within the caprolactam is broken with the exposed active groups on each side being incorporated into two new bonds as the monomer becomes part of the polymer backbone. In this case, all amide bonds lie in the same direction..."
So, were the chains PA 6 / 66 drawn (http://en.wikipedia.org/wiki/Image:Nylon6_and_Nylon_66.png) correctly? In there, both amide group are in the same direction. I would like to know...
Thanks!
Nylon 510 section not really about Nylon 510
editThe section Nylon 510 was tagged a few days ago as not citing any sources. This is true, but there is another problem as well. Of 13 sentences, only the first is really about Nylon 510, and the third mentions PA 510 as one item in a list. The rest of the section is really a collection of miscellaneous points about other polyamides which should be moved elsewhere in the article. So some serious re-organization is needed here, especially for the material in this section. Dirac66 (talk) 01:17, 2 March 2020 (UTC)
Petroleum product
editOne could read the entire lead, and much of the article, before discovering that nylon is made from petroleum. There are innumerable sources for this; here's one.[1] The word oil is mentioned first 2,300 words into the article (but not described as its manufacturing origin), crude oil 4,700 words in, and petroleum is mentioned not once in the entire article. Where nylon comes from, is one of the five-W questions to be answered by any encyclopedic or journalistic article about nylon, which means high up in the lead, probably in the WP:LEADSENTENCE, and prominently in the body of the article. I don't plan to make changes to this article as I'm busy elsewhere, but hopefully some regulars or others here will attend to this. Thanks, Mathglot (talk) 22:11, 9 November 2020 (UTC)
References
- ^ Islam, M. R.; Chhetri, A. B.; Khan, M. M. (25 January 2011). "9.9 Theoretical Comparison Between Nylon and Silk". The Greening of Petroleum Operations: The Science of Sustainable Energy Production. Hoboken, NJ: John Wiley & Sons. p. 397. ISBN 978-0-470-92290-3. OCLC 927404049. Retrieved 9 November 2020.
- The first sentence says "Nylon is a synthetic polymer", and the linked article on synthetic polymers starts off with "Synthetic polymers are derived from petroleum oil". Seems that none of our other articles on specific thermoplastics mention petroleum in the intro. – Thjarkur (talk) 23:06, 30 December 2020 (UTC)
- Thanks for pointing this out. In the linked article, I have now changed "derived from petroleum oil" to "often derived from petroleum oil", since there are many exceptions. Dirac66 (talk) 01:58, 31 December 2020 (UTC)
Yugandhar
editHis is a good person and he is a seicentist and he has a youtube channel and subscribe and support him Thank you 160.238.75.58 (talk) 15:06, 16 February 2022 (UTC)
Naylon
editEasy naylon information Please 2409:4041:2CB1:65D7:0:0:C849:6014 (talk) 06:10, 4 September 2022 (UTC)
Images
editThe images of N-6 and N-6,6 are difficult to parse and not very useful. I'm a chemist and even though I've worked with both, I had to study the diagrams far longer than if they'd simply been -((CH2-)5-C(=O)-NH-)x and -(C(=O)(CH2)4-C(=O)NH(CH2)6)-NH)-x (or even better with the structural skeleton in 2D rather than on a line. As far as I can see, the only advantage is "oooh! red, blue, white and green|gray balls!" I see no advantage in suggesting that the alternate carbonyl oxygens are "trans" oriented (since they rotate freely). These depictions are useful to who? Nobody, I think. My guess is that they replaced more useful depictions because they were "ball and stick" but actually convey less information, in a sense. There's no use in depicting what is fundamentally a linear polymer in 3D projection. I also note that neither the images nor their caption indicate what the various ball colors signify. Replace these depictions with the corresponding chemical structure (it might also be useful to mention what values the repeat unit typically has; i.e. x = nnn - nnnnn.98.17.180.146 (talk) 09:11, 4 November 2024 (UTC)