Temperature-triggered switchable nanofibrous membranes are successfully fabricated from a mixture of cellulose acetate (CA) and poly(N-isopropylacrylamide) (PNIPAM) by employing a single-step direct electrospinning process. These hybrid CA-PNIPAM membranes demonstrate the ability to switch between two wetting states viz. superhydrophilic to highly hydrophobic states upon increasing the temperature. At room temperature (23 °C) CA-PNIPAM nanofibrous membranes exhibit superhydrophilicity, while at elevated temperature (40 °C) the membranes demonstrate hydrophobicity with a static water contact angle greater than 130°. Furthermore, the results here demonstrate that the degree of hydrophobicity of the membranes can be controlled by adjusting the ratio of PNIPAM in the CA-PNIPAM mixture.
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http://dx.doi.org/10.1002/marc.201500037 | DOI Listing |
Talanta
January 2022
The Key Laboratory of Space Applied Physics and Chemistry, Ministry of Education, Northwestern Polytechnical University, Xi'an, 710129, PR China. Electronic address:
In this work, based on the dual catalytic properties of copper (Cu) particles for methanol oxidation and persulfate initiated radical polymerization, a temperature-controlled catalytic electrode, defined the PNIPAM-Cu@CP, was constructed by electrodepositing Cu particles on a carbon paper electrode and triggering the polymerization of the temperature-sensitive polymer N-isopropylacrylamide (PNIPAM) on the surface of the electrode, which is expected to be applicated in the micro-direct methanol fuel cell (DMAC) for detection of methanol crossover and also has temperature recognition and high-temperature self-protection functions. Cu particles and PNIPAM were characterized by X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM) for their specific structure and morphology. The cyclic voltammetry (CV) results showed the proposed electrode as a temperature-controlled switch-like methanol sensor, has a wide linear range (1-300 mM and 300-1200 mM), excellent sensitivity (72.
View Article and Find Full Text PDFActa Biomater
December 2021
Institute of Physical Chemistry and Electrochemistry, Leibniz Universität Hannover, Callinstr. 3A, 30167 Hannover, Germany. Electronic address:
Thermally "switchable" poly(glycidyl ether) (PGE) brushes constitute effective coatings for the temperature-triggered harvest of confluent cell sheets. Based on a simple "grafting-to" approach, such coatings can be tethered to various applied plastic culture substrate materials. Herein, we elucidate the self-assembly of PGE brushes with tunable grafting densities up to 0.
View Article and Find Full Text PDFPolymers (Basel)
December 2020
Polymer Competence Center Leoben GmbH, Roseggerstrasse 12, 8700 Leoben, Austria.
The pronouncedly low thermal conductivity of polymers in the range of 0.1-0.2 W m K is a limiting factor for their application as an insulating layer in microelectronics that exhibit continuously higher power-to-volume ratios.
View Article and Find Full Text PDFActa Biomater
March 2020
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Shanghai Belt and Road Joint Laboratory of Advanced Fiber and Low-dimension Materials (Donghua University), College of Materials Science and Engineering, Donghua University, 2999 North Renmin Road, Shanghai 201620, PR China. Electronic address:
Cartilage defect repair remains a great clinical challenge due to the limited self-regeneration capacity of cartilage tissue. Surgical treatment of injured cartilage is rather difficult due to the narrow space in the articular cavity and irregular defect area. Herein, we designed and fabricated chondrogenic and physiological-temperature-triggered shape-memory ternary scaffolds for cell-free cartilage repair, where the poly (glycerol sebacate) (PGS) networks ensured elasticity and shape recovery, crystallized poly (1,3-propylene sebacate) (PPS) acted as switchable phase, and immobilized bioactive kartogenin (KGN) endowed the scaffolds with chondrogenic capacity.
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