<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(11)</volume><submitter>Peng L</submitter><pubmed_abstract>The characteristics of pure α- and β-form of the cyclic dimer (1,8-diazacyclotetradecane-2,9-dione) were systematically and integrally investigated during this study. The results showed that the α-form could dissolve and rapidly transform into the β-form in methanol, and in caprolactam solution at a lower temperature, an interesting transition occurred and formed co-precipitates, which refract colourful light under PLM. However, these dimers can aggregate in water, and they are then transformed into multi-slice layers and compact structures. The detailed transition behaviours between the two forms were further measured by FT-IR, XRD and DSC by varying the temperature from 25°C to 360°C, respectively, which showed that there are two endothermic transitions over the course of the heating programme. At a temperature of approximately 242°C, the β crystals were initially converted into α crystals, and then they melted when the temperature reached over 345°C. A video recorded under a light microscope also showed that the sublimation of the β cyclic dimer occurred after the transition. However, the α-form might sublimate at temperatures lower than 150°C when mixed with volatile matter.</pubmed_abstract><journal>Royal Society open science</journal><pagination>180957</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6281911</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The crystal-form transition behaviours and morphology changes in a polyamide 6 cyclic dimer.</pubmed_title><pmcid>PMC6281911</pmcid><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Jiang F</pubmed_authors><pubmed_authors>Peng S</pubmed_authors><pubmed_authors>Yi C</pubmed_authors><pubmed_authors>Peng L</pubmed_authors></additional><is_claimable>false</is_claimable><name>The crystal-form transition behaviours and morphology changes in a polyamide 6 cyclic dimer.</name><description>The characteristics of pure α- and β-form of the cyclic dimer (1,8-diazacyclotetradecane-2,9-dione) were systematically and integrally investigated during this study. The results showed that the α-form could dissolve and rapidly transform into the β-form in methanol, and in caprolactam solution at a lower temperature, an interesting transition occurred and formed co-precipitates, which refract colourful light under PLM. However, these dimers can aggregate in water, and they are then transformed into multi-slice layers and compact structures. The detailed transition behaviours between the two forms were further measured by FT-IR, XRD and DSC by varying the temperature from 25°C to 360°C, respectively, which showed that there are two endothermic transitions over the course of the heating programme. At a temperature of approximately 242°C, the β crystals were initially converted into α crystals, and then they melted when the temperature reached over 345°C. A video recorded under a light microscope also showed that the sublimation of the β cyclic dimer occurred after the transition. However, the α-form might sublimate at temperatures lower than 150°C when mixed with volatile matter.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2022-02-09T08:18:18.265Z</modification><creation>2019-03-27T00:13:08Z</creation></dates><accession>S-EPMC6281911</accession><cross_references><pubmed>30564398</pubmed><doi>10.1098/rsos.180957</doi></cross_references></HashMap>