Formation of linear and crosslinked polyurethane nanoparticles that self-assemble differently in acetone and in water
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61389013%3A_____%2F17%3A00472825" target="_blank" >RIV/61389013:_____/17:00472825 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/17:10368992
Result on the web
<a href="http://dx.doi.org/10.1016/j.porgcoat.2017.03.003" target="_blank" >http://dx.doi.org/10.1016/j.porgcoat.2017.03.003</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.porgcoat.2017.03.003" target="_blank" >10.1016/j.porgcoat.2017.03.003</a>
Alternative languages
Result language
angličtina
Original language name
Formation of linear and crosslinked polyurethane nanoparticles that self-assemble differently in acetone and in water
Original language description
For the first time, stable water-borne polyurethane dispersions (PUDs) leading to mechanically strong polyurethane (PU) coatings were prepared without any chain extender. Elimination of this step and using of water-crosslinking gives promising applications of PUDs as biomaterials and production on an industrial scale. The PU system consists of polycarbonate macrodiol (PCD), (2,2-bis(hydroxymethyl)) propionic acid (DMPA), 1,6-diisocyanatohexane (HDI) and N,N-diethylethanamine (TEA). Fourier transform infrared spectroscopy (FTIR), dynamic mechanical thermal analysis (DMTA), static light scattering (SLS), dynamic light scattering (DLS) and atomic force microscopy (AFM) enabled the study of the assembly of the PU chains/nanoparticles into supramolecular structures in acetone and in water. In acetone, the self-assembly of isocyanate-terminated pre-polymer chains occurs in the form of either PU solutions (linear PUs) or PU dispersions (crosslinked PUs). Due to a phase inversion, spherical linear or water-crosslinked PU dispersions are formed after water addition. The isocyanate-to-total hydroxyl ratio is very important. A slight isocyanate (NCO) excess of 1.05 leads to linear rod-like nanoparticles in acetone followed by a core-shell structure after water addition. An isocyanate excess of 1.5 leads to compact sphere or microgel particles initially crosslinked by moisture in acetone, and the final crosslinking and phase inversion occurs after water addition. The chain lengths of the linear PUs and the mesh sizes in PU networks increase with the PCD:DMPA ratio. Thus, the design of PU nanoparticles with desired sizes, shapes and crosslink densities is possible. Unlike the substantially different shapes, sizes and compactness of PUs in acetone, all PUDs in water are spherical nanoparticles with an average diameter from 21 to 72 nm, a zeta potential from -40 to -65 mV and a size-dispersity index from 0.05 to 0.22.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10404 - Polymer science
Result continuities
Project
<a href="/en/project/GA13-06700S" target="_blank" >GA13-06700S: Multifunctional highly elastic polymeric materials with controlled biodegradability</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Progress in Organic Coatings
ISSN
0300-9440
e-ISSN
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Volume of the periodical
106
Issue of the periodical within the volume
May
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
9
Pages from-to
119-127
UT code for WoS article
000399521700014
EID of the result in the Scopus database
2-s2.0-85014856823