Carboxyl-Functionalized Nanoparticles Produced by Pulsed Plasma Polymerization of Acrylic Acid

被引:16
|
作者
Pleskunov, Pavel [1 ]
Nikitin, Daniil [1 ]
Tafiichuk, Renata [1 ]
Shelemin, Artem [1 ]
Hanus, Jan [1 ]
Khalakhan, Ivan [2 ]
Choukourov, Andrei [1 ]
机构
[1] Charles Univ Prague, Dept Macromol Phys, Fac Math & Phys, V Holesovickach 2, Prague, Czech Republic
[2] Charles Univ Prague, Dept Surface & Plasma Sci, Fac Math & Phys, V Holesovickach 2, Prague, Czech Republic
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2018年 / 122卷 / 14期
关键词
ATMOSPHERIC-PRESSURE; ION CHEMISTRY; SURFACES; DEPOSITION; COATINGS; CULTURE; CELLS; FILMS; ENERGY;
D O I
10.1021/acs.jpcb.8b01648
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carboxyl-enriched and size-selected polymer nano particles (NPs) may prove to be very useful in biomedical applications for linker-free binding of biomolecules and their transport to cells. In this study, we report about the synthesis of such NPs by low-pressure low-temperature pulsed plasma polymerization of acrylic acid. Gas aggregation duster source was adapted to operate plasma with a constant pulse period of SO mu s and with varying duty cyde. The NPs were produced with the size ranging from 31 +/- 5 to 93 +/- 4 nm and with retention of the carboxyl groups ranging from 4.0 to 12.0 atom %. Two regimes of the NP formation were identified. In the large duty cycle regime, the NP growth was interfered with by positive ion bombardment which resulted in the ion-driven detachment of the carboxyl species and in the formation of carboxyl-deficient NPs. In the small duty cycle regime, the NP growth was accompanied by the radical-driven chain propagation with the attachment of intact monomer molecules. Improved efficacy of the monomer retention resulted in increased concentration of the carboxyl groups.
引用
收藏
页码:4187 / 4194
页数:8
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