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https://hdl.handle.net/10442/19025
Εξειδίκευση τύπου : | Άρθρο σε επιστημονικό περιοδικό |
Τίτλος: | Closely Packed Core-Shell Micelle Structures of Double Hydrophilic Miktoarm Star Copolymers at the Air-Water Interface |
Δημιουργός/Συγγραφέας: | Zhang, Yu Wen, Gangyao Giaouzi, Despoina [EL] Πίσπας, Στέργιος[EN] Pispas, Stergios Li, Jian |
Ημερομηνία: | 2024-04-03 |
Γλώσσα: | Αγγλικά |
ISSN: | 0743-7463 1520-5827 |
DOI: | 10.1021/acs.langmuir.4c00437 |
Άλλο: | 38567402 |
Περίληψη: | The aggregation behavior of amphiphilic block copolymers at the air-water interface has been extensively studied, but less attention was given to that of star copolymers. In this work, we studied the interfacial aggregation behavior of two double hydrophilic pH- and temperature-responsive miktoarm star copolymers of poly[di(ethylene glycol) methyl ether methacrylate]-poly[2-(dimethylamino)ethyl methacrylate] (PDEGMA3-PDMAEMA3 and PDEGMA4-PDMAEMA7, the subscripts denote arm numbers) with different molecular weights. The effects of subphase pH and temperature on the monolayer isotherms and hysteresis curves of the two star copolymers and the morphologies of their Langmuir-Blodgett (LB) films were studied by the Langmuir film balance technique and atomic force microscopy, respectively. At the air-water interface, the two star copolymers tend to form closely packed micelles. These micelles exhibit a core-shell structure, where the small hydrophobic core consists of cross-linker of ethylene glycol dimethacrylate (EGDMA) and the carbon backbones of PDEGMA and PDMAEMA arms and the short hydrophilic shell is composed of di(ethylene glycol) and tertiary amine side groups. With increasing subphase pH, the surface pressure versus molecular area isotherms shift toward larger mean molecular areas as a result of the enhanced interface adsorption of nonprotonated tertiary amine groups. The isotherm shift of PDEGMA3-PDMAEMA3 monolayers is primarily attributed to high density of tertiary amine groups in the shells, while that of PDEGMA4-PDMAEMA7 is mainly attributed to high density of di(ethylene glycol) groups in the shells. The hysteresis degrees in the monolayers of the two copolymers under alkaline and neutral conditions are greater than those under acidic conditions due to the decreased protonation degree of the tertiary amine groups. At 10 °C, the mobility of the shells is poor and the isotherms are located on the right. Above the lower critical solution temperature, di(ethylene glycol) groups contract, which causes a slight shift of the isotherms toward smaller mean molecular areas. |
Τίτλος πηγής δημοσίευσης: | Langmuir : the ACS journal of surfaces and colloids |
Θεματική Κατηγορία: | [EL] Φυσική και θεωρητική χημεία[EN] Physical and theoretical chemistry |
Λέξεις-Κλειδιά: | Alcohols Copolymers Interfaces Isotherms Monolayers |
Κάτοχος πνευματικών δικαιωμάτων: | © 2024 American Chemical Society |
Ηλεκτρονική διεύθυνση στον εκδότη (link): | https://doi.org/10.1021/acs.langmuir.4c00437 |
Εμφανίζεται στις συλλογές: | Ινστιτούτο Θεωρητικής και Φυσικής Χημείας (ΙΘΦΧ) - Επιστημονικό έργο
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