Role of the Polymer Microstructure in Controlling Colloidal and Thermo-Responsive Properties of Nano-Objects Prepared Via RAFT Polymerization in a Non-polar Medium

被引:3
作者
Gardoni, Gianmaria [1 ]
Manfredini, Nicolo [1 ]
Bagnato, Giulia [1 ]
Sponchioni, Mattia [1 ]
Moscatelli, Davide [1 ]
机构
[1] Politecn Milan, Dept Chem Mat & Chem Engn Giulio Natta, I-20131 Milan, Italy
关键词
DISPERSION POLYMERIZATION; RADICAL POLYMERIZATION; DRUG-DELIVERY; COPOLYMER; NANOPARTICLES; TRANSITION; VESICLES; WORMS; SIZE;
D O I
10.1021/acs.langmuir.3c01065
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
After having demonstrated their potential in biomedicalapplications,thermo-responsive block copolymers that are able to self-assembleinto nano-objects in response to temperature modifications are becomingmore and more appealing in other sectors, such as the oil and gasand lubricant fields. Reversible addition-fragmentation chaintransfer (RAFT) polymerization-induced self-assembly has been demonstratedas a valuable strategy for producing nano-objects from modular blockcopolymers in non-polar media, required for the mentioned applications.Although the influence of the nature and size of the thermo-responsiveblock of these copolymers on the properties of the nano-objects isextensively studied in the literature, the role of the solvophilicblock is often neglected. In this work, we elucidate the role of themain microstructural parameters, including those of the solvophilicportion, of block copolymers produced by RAFT polymerization in thehydrocarbon blend decane/toluene 50:50 v/v on the thermo-responsivebehavior and colloidal properties of the resulting nano-objects. Twolong-aliphatic chain monomers were employed for the synthesis of fourmacromolecular chain transfer agents (macroCTAs), with increasingsolvophilicity according to the number of units (n) or length of the alkyl side chain (q). Subsequently,the macroCTAs were chain-extended with different repeating units ofdi(ethylene glycol) methyl ether methacrylate (p),leading to copolymers that are able to self-assemble below a criticaltemperature. We show that this cloud point can be tuned by actingon n, p, and q.On the other hand, the colloidal stability, expressed in terms ofarea of the particle covered by each solvophilic segment, is onlya function of n and q, which providesa way for controlling the size distribution of the nano-objects andto decouple it from the cloud point.
引用
收藏
页码:10133 / 10144
页数:12
相关论文
共 52 条
[1]   Mechanistic Insights for Block Copolymer Morphologies: How Do Worms Form Vesicles? [J].
Blanazs, Adam ;
Madsen, Jeppe ;
Battaglia, Giuseppe ;
Ryan, Anthony J. ;
Armes, Steven P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (41) :16581-16587
[2]   Evaluating the potential of natural surfactants in the petroleum industry: the case of hydrophobins [J].
Blesic, Marijana ;
Dichiarante, Valentina ;
Milani, Roberto ;
Linder, Markus ;
Metrangolo, Pierangelo .
PURE AND APPLIED CHEMISTRY, 2018, 90 (02) :305-314
[3]   In situ cross-linking in RAFT-mediated emulsion polymerization: Reshaping the preparation of cross-linked block copolymer nano-objects by polymerization-induced self-assembly [J].
Cao, Junpeng ;
Tan, Yingxin ;
Dai, Xiaocong ;
Chen, Ying ;
Zhang, Li ;
Tan, Jianbo .
POLYMER, 2021, 230
[4]   Tunable Degradation Behavior of PEGylated Polyester-Based Nanoparticles Obtained Through Emulsion Free Radical Polymerization. [J].
Colombo, Claudio ;
Dragoni, Luca ;
Gatti, Simone ;
Pesce, Ruggiero M. ;
Rooney, Thomas R. ;
Mavroudakis, Evangelos ;
Ferrari, Raffaele ;
Moscatelli, Davide .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2014, 53 (22) :9128-9135
[5]   Principles and Characteristics of Polymerization-Induced Self-Assembly with Various Polymerization Techniques [J].
Cornel, Erik Jan ;
Jiang, Jinhui ;
Chen, Shuai ;
Du, Jianzhong .
CCS CHEMISTRY, 2021, 3 (04) :2104-2125
[6]   Reversible-deactivation radical polymerization (Controlled/living radical polymerization): From discovery to materials design and applications [J].
Corrigan, Nathaniel ;
Jung, Kenward ;
Moad, Graeme ;
Hawker, Craig J. ;
Matyjaszewski, Krzysztof ;
Boyer, Cyrille .
PROGRESS IN POLYMER SCIENCE, 2020, 111
[7]   RAFT-Mediated Polymerization-Induced Self-Assembly [J].
D'Agosto, Franck ;
Rieger, Jutta ;
Lansalot, Muriel .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2020, 59 (22) :8368-8392
[8]   The self-assembly and thermoresponsivity of poly(isoprene-b-methyl methacrylate) copolymers in non-polar solvents [J].
Day, Daniel M. ;
Hutchings, Lian R. .
EUROPEAN POLYMER JOURNAL, 2021, 156
[9]   Shear-induced alignment of block copolymer worms in mineral oil [J].
Derry, Matthew J. ;
Mykhaylyk, Oleksandr O. ;
Armes, Steven P. .
SOFT MATTER, 2021, 17 (39) :8867-8876
[10]   Polymerization-induced self-assembly of block copolymer nanoparticles via RAFT non-aqueous dispersion polymerization [J].
Derry, Matthew J. ;
Fielding, Lee A. ;
Armes, Steven P. .
PROGRESS IN POLYMER SCIENCE, 2016, 52 :1-18