2017
DOI: 10.1007/s10965-017-1412-3
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Synthesis and characterization of nanosized polylactic acid/TiO2 particle brushes by azeotropic dehydration polycondensation of lactic acid

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Cited by 11 publications
(4 citation statements)
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“…12 This charge is developed due to the presence of external siloxane groups on the HNT surface, 53 whereas a zeta potential value of À28.2 mV for PLA was due to the presence of carboxylic anionic groups at the polymer chain ends. 54,55 The zeta potential value of HP 1 is comparable with HNT, which indicated the effective and complete intercalation of PLA chains into HNT due to the lower concentration of HNT in the bionanocomposites. As a result, there was no PLA available without intercalation to effectively alter the negative charge arising from the carboxylic anionic groups at the chain ends of PLA.…”
Section: Dls and Zeta Potential Analysismentioning
confidence: 94%
“…12 This charge is developed due to the presence of external siloxane groups on the HNT surface, 53 whereas a zeta potential value of À28.2 mV for PLA was due to the presence of carboxylic anionic groups at the polymer chain ends. 54,55 The zeta potential value of HP 1 is comparable with HNT, which indicated the effective and complete intercalation of PLA chains into HNT due to the lower concentration of HNT in the bionanocomposites. As a result, there was no PLA available without intercalation to effectively alter the negative charge arising from the carboxylic anionic groups at the chain ends of PLA.…”
Section: Dls and Zeta Potential Analysismentioning
confidence: 94%
“…The residue left after TGA analysis was 12.2% which is much more than the amount of ZnO nanoparticles. But this is observed in degradation of many hybrid materials . This also means that the catalyst is thermally stable and can be used comfortably for reactions temperatures upto 250 °C.…”
Section: Resultsmentioning
confidence: 99%
“…The −OH group at 1627, 1630, and 1630 cm –1 on pristine TiO 2 -NP1, TiO 2 -NP2, and TiO 2 -NP3 shifted to 1635, 1627, and 1627 cm –1 , respectively, while the −CO of lactic acid at 1719–1720 cm –1 basically disappeared. This indicated that the −OH on TiO 2 NPs interacted with the −CO of lactic acid to form a grafted structure of lactic acid on TiO 2 -NPs. , Therefore, lactic acid was adsorbed onto TiO 2 NPs via complexation between the carboxyl group of lactic acid and the hydroxyl group on the particle surface. The order of oxygen content following TiO 2 -NP1 > TiO 2 -NP2 > TiO 2 -NP3 (Table S6) was in line with their order of adsorption capacity for both l -histidine and lactic acid (Figure a–c), further indicating that the hydroxyl group on TiO 2 NPs was an important adsorption site for these organic constituents.…”
Section: Resultsmentioning
confidence: 99%