Ellen J. Quane, Niels Elders, Anna S. Newman, Sophia van Mourik, Neal S. J. Williams, Keimpe J. van den Berg, Anthony J. Ryan, Oleksandr O. Mykhaylyk
{"title":"Correction to “Synthesis, Morphology, and Particle Size Control of Acidic Aqueous Polyurethane Dispersions”","authors":"Ellen J. Quane, Niels Elders, Anna S. Newman, Sophia van Mourik, Neal S. J. Williams, Keimpe J. van den Berg, Anthony J. Ryan, Oleksandr O. Mykhaylyk","doi":"10.1021/acs.macromol.5c00418","DOIUrl":null,"url":null,"abstract":"The originally published Table 2 is incorrect. The sample names were entered in the wrong order such that they matched up with the incorrect corresponding parameters. This mistake has been resolved in the corrected Table 2 below: <i>R</i> is the geometric mean particle radius with multiplicative standard deviation σ*. The proportion of PU distributed as supramolecular structures is quantified by ϕ<sub>2</sub>/ϕ<sub>tot</sub>. <i>R</i><sub>g</sub> gives the radius of gyration of these structures, and ν is a structural parameter that indicates solubilization of these polymer-like structures. The caption to the originally published Figure 7 refers to the tables incorrectly. The first reference should be made to Table 1 and not to Table S1. The second reference should be made to Table 2 and not to Table 1. The value ϕ<sub>2</sub>/ϕ<sub>tot</sub> is given in Table 2, as specified in the corrected caption below: Corrected Figure 7 caption: Relationship between the acid (COOH) content in the original PU formulation (Table 1) and the fraction of PU in supramolecular structures formed by (H<sub>12</sub>MDI)<sub><i>n</i>+1</sub>DMPA<sub><i>n</i></sub> molecules, measured by SAXS (Table 2, ϕ<sub>2</sub>/ϕ<sub>tot</sub>) for PUD samples synthesized with polyether (soft segment) of <i>M</i><sub>n</sub> = 650 g mol<sup>–1</sup> (blue circles), 1000 g mol<sup>–1</sup> (green squares), and 2000 g mol<sup>–1</sup> (red triangles). This article has not yet been cited by other publications.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"15 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00418","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The originally published Table 2 is incorrect. The sample names were entered in the wrong order such that they matched up with the incorrect corresponding parameters. This mistake has been resolved in the corrected Table 2 below: R is the geometric mean particle radius with multiplicative standard deviation σ*. The proportion of PU distributed as supramolecular structures is quantified by ϕ2/ϕtot. Rg gives the radius of gyration of these structures, and ν is a structural parameter that indicates solubilization of these polymer-like structures. The caption to the originally published Figure 7 refers to the tables incorrectly. The first reference should be made to Table 1 and not to Table S1. The second reference should be made to Table 2 and not to Table 1. The value ϕ2/ϕtot is given in Table 2, as specified in the corrected caption below: Corrected Figure 7 caption: Relationship between the acid (COOH) content in the original PU formulation (Table 1) and the fraction of PU in supramolecular structures formed by (H12MDI)n+1DMPAn molecules, measured by SAXS (Table 2, ϕ2/ϕtot) for PUD samples synthesized with polyether (soft segment) of Mn = 650 g mol–1 (blue circles), 1000 g mol–1 (green squares), and 2000 g mol–1 (red triangles). This article has not yet been cited by other publications.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.