Thermoswitchable Janus Gold Nanoparticles with Stimuli-Responsive Hydrophilic Polymer Brushes

Langmuir ◽  
2016 ◽  
Vol 32 (17) ◽  
pp. 4297-4304 ◽  
Author(s):  
Xiaoqin Niu ◽  
Fen Ran ◽  
Limei Chen ◽  
Gabriella Jia-En Lu ◽  
Peiguang Hu ◽  
...  

2008 ◽  
Vol 41 (21) ◽  
pp. 8152-8158 ◽  
Author(s):  
Smrati Gupta ◽  
Mukesh Agrawal ◽  
Petra Uhlmann ◽  
Frank Simon ◽  
Ulrich Oertel ◽  
...  


2019 ◽  
Author(s):  
Yanchun Tang ◽  
Kohzo Ito ◽  
Hideaki Yokoyama

In this study, we prepared ultrafiltration membranes with a decoupled responses of filtration property to temperature and pH. The membrane preparation method was developed based on our previous work. We utilized methanol-supercritical carbon dioxide (methanol-scCO<sub>2</sub>) selective swelling method to introduce nanopores to block copolymers containing poly(diethylene glycol) methyl ether methacrylate (PMEO<sub>2</sub>MA), poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) and polystyrene (PS) blocks. Formation of the mesoporous barrier layer with PS being the mechanically stable part of the matrix was driven by selective swelling of the PMEO<sub>2</sub>MA-b-PDMAEMA domains. Due to the selective swelling of PMEO<sub>2</sub>MA or PDMAEMA domains to introduce pores, the interior of the pores are covered with PMEO<sub>2</sub>MA or PDMAEMA blocks after pore formation. The PMEO<sub>2</sub>MA-b-PDMAEMA polymer brushes are naturally attached on the pore walls and worked as functional gates. PMEO<sub>2</sub>MA is a non-toxic, neutral thermo-responsive polymer with LCST at 26 ᴼC. PDMAEMA is a typical weak polyelectrolyte with pK<sub>a</sub> value at 7.0-7.5 and also a thermo-responsive polymer revealed a LCST of 20-80 °C in aqueous solution. Therefore, these membranes were expected to have multi dimensions as function of the combination of temperature and pH. Moreover, to understand the detail of the temperature and pH depended conformation transitions of PMEO<sub>2</sub>MA-b-PDMAEMA brushes, those diblock copolymers were end-tethered on flat substrates and analyzed via neutron reflectivity (NR).



2012 ◽  
Vol 24 (41) ◽  
pp. 5559-5563 ◽  
Author(s):  
Christoph Tonhauser ◽  
Ali A. Golriz ◽  
Christian Moers ◽  
Rebecca Klein ◽  
Hans-Jürgen Butt ◽  
...  


Polymers ◽  
2018 ◽  
Vol 10 (10) ◽  
pp. 1084
Author(s):  
Kaimin Chen ◽  
Lan Cao ◽  
Ying Zhang ◽  
Kai Li ◽  
Xue Qin ◽  
...  

Stimuli-responsive nanoparticles are among the most popular research topics. In this study, two types of core-shell (polystyrene with a photoiniferter (PSV) as the core and diblock as the shell) polymer brushes (PSV@PNIPA-b-PAA and PSV@PAA-b-PNIPA) were designed and prepared using surface-initiated photoiniferter-mediated polymerization (SI-PIMP). Moreover, their pH- and temperature-stimuli responses were explored by dynamic light scattering (DLS) and turbidimeter under various conditions. The results showed that the conformational change was determined on the basis of the competition among electrostatic repulsion, hydrophobic interaction, hydrogen bonding, and steric hindrance, which was also confirmed by protein adsorption experiments. These results are not only helpful for the design and synthesis of stimuli-responsive polymer brushes but also shed light on controlled protein immobilization under mild conditions.



2009 ◽  
Vol 42 (13) ◽  
pp. 4817-4828 ◽  
Author(s):  
Yuquan Zou ◽  
Nicholas A. A. Rossi ◽  
Jayachandran N. Kizhakkedathu ◽  
Donald E. Brooks


Nanomaterials ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 591 ◽  
Author(s):  
Monika Zygo ◽  
Miroslav Mrlik ◽  
Marketa Ilcikova ◽  
Martina Hrabalikova ◽  
Josef Osicka ◽  
...  

This study reports the utilization of controlled radical polymerization as a tool for controlling the stimuli-responsive capabilities of graphene oxide (GO) based hybrid systems. Various polymer brushes with controlled molecular weight and narrow molecular weight distribution were grafted from the GO surface by surface-initiated atom transfer radical polymerization (SI-ATRP). The modification of GO with poly(n-butyl methacrylate) (PBMA), poly(glycidyl methacrylate) (PGMA), poly(trimethylsilyloxyethyl methacrylate) (PHEMATMS) and poly(methyl methacrylate) (PMMA) was confirmed by thermogravimetric analysis (TGA) coupled with online Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Various grafting densities of GO-based materials were investigated, and conductivity was elucidated using a four-point probe method. Raman shift and XPS were used to confirm the reduction of surface properties of the GO particles during SI-ATRP. The contact angle measurements indicated the changes in the compatibility of GOs with silicone oil, depending on the structure of the grafted polymer chains. The compatibility of the GOs with poly(dimethylsiloxane) was also investigated using steady shear rheology. The tunability of the electrorheological, as well as the photo-actuation capability, was investigated. It was shown that in addition to the modification of conductivity, the dipole moment of the pendant groups of the grafted polymer chains also plays an important role in the electrorheological (ER) performance. The compatibility of the particles with the polymer matrix, and thus proper particles dispersibility, is the most important factor for the photo-actuation efficiency. The plasticizing effect of the GO-polymer hybrid filler also has a crucial impact on the matrix stiffness and thus the ability to reversibly respond to the external light stimulation.



2004 ◽  
Vol 25 (14) ◽  
pp. 1298-1302 ◽  
Author(s):  
Anthony M. Granville ◽  
William J. Brittain


2003 ◽  
Vol 42 (24) ◽  
pp. 2751-2754 ◽  
Author(s):  
Kohji Ohno ◽  
Kyoungmoo Koh ◽  
Yoshinobu Tsujii ◽  
Takeshi Fukuda


Soft Matter ◽  
2015 ◽  
Vol 11 (24) ◽  
pp. 4830-4839 ◽  
Author(s):  
Lichun Song ◽  
Hui Sun ◽  
Xiaolu Chen ◽  
Xia Han ◽  
Honglai Liu

This work reports on the aqueous stimuli-responsive behaviors of an ABA triblock copolymer, a BAB triblock copolymer, an AB diblock copolymer and citrate-based gold nanoparticles decorated with AB diblock copolymers.



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