scholarly journals Superhydrophilic Coating with Antibacterial and Oil-Repellent Properties via NaIO4-Triggered Polydopamine/Sulfobetaine Methacrylate Polymerization

Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2008
Author(s):  
Hsiu-Wen Chien ◽  
Hong-Yu Lin ◽  
Chau-Yi Tsai ◽  
Tai-Yu Chen ◽  
Wei-Nian Chen

Superhydrophilic coatings have been widely used for the surface modification of membranes or biomedical devices owing to their excellent antifouling properties. However, simplifying the modification processes of such materials remains challenging. In this study, we developed a simple and rapid one-step co-deposition process using an oxidant trigger to fabricate superhydrophilic surfaces based on dopamine chemistry with sulfobetaine methacrylate (SBMA). We studied the effect of different oxidants and SBMA concentrations on surface modification in detail using UV–VIS spectrophotometry, dynamic light scattering, atomic force microscopy, X-ray photoelectron spectroscopy, and surface plasmon resonance. We found that NaIO4 could trigger the rate of polymerization and the optimum ratio of dopamine to SBMA is 1:25 by weight. This makes the surface superhydrophilic (water contact angle < 10°) and antifouling. The superhydrophilic coating, when introduced to polyester membranes, showed great potential for oil/water separation. Our study provides a complete description of the simple and fast preparation of superhydrophilic coatings for surface modification based on mussel-inspired chemistry.

2017 ◽  
Vol 95 (5) ◽  
pp. 605-611 ◽  
Author(s):  
Lei Wang ◽  
Shaoqing Wen ◽  
Zhanxiong Li

A series of novel amphiphilic ABA-type poly(tridecafluorooctylacrylate)-poly(ethylene glycol)-poly(tridecafluorooctylacrylate) (henceforth referred to as p-TDFA-PEG-p-TDFA) triblock oligomers were successfully synthesized via atom transfer radical polymerization (ATRP) using well-defined Br-PEG-Br as macroinitiator and copper as catalyst. The block oligomers were characterized by Fourier transform infrared (FTIR) spectroscopy and 1H and 19F nuclear magnetic resonances (NMR). Gel permeation chromatography (GPC) showed that the block oligomers have been obtained with narrow molecular weight distributions of 1.22–1.33. X-ray photoelectron spectroscopy (XPS) was carried out to confirm the attachment of p-TDFA-PEG-p-TDFA onto the silicon substrate, together with the chemical compositions of p-TDFA-PEG-p-TDFA. The wetabilities of the oligomer films were measured by water contact angles (CAs). Water CAs of p-TDFA-PEG-p-TDFA film were measured and their morphologies were tested by atomic force microscopy (AFM). The result showed that the CAs of the oligomer films, which possess fluoroalkyl groups assembled on the outer surface, increase after heating due to the migration of fluoroalkyl groups and the resulted microphase separation of the p-TDFA-PEG-p-TDFA.


Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 848 ◽  
Author(s):  
Qi Zhao ◽  
Feipeng Wang ◽  
Kaizheng Wang ◽  
Guibai Xie ◽  
Wanzhao Cui ◽  
...  

In this work, fluorocarbon film was deposited on silicon (P/100) substrate using polytetrafluoroethylene (PTFE) as target material at elevated sputtering temperature. Field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) were employed to investigate the surface morphology as well as structural and chemical compositions of the deposited film. The surface energy, as well as the polar and dispersion components, were determined by water contact angle (WCA) measurement. The experimental results indicated that increasing sputtering temperature effectively led to higher deposition rate, surface roughness and WCA of the film. It was found that the elevated temperature contributed to increasing saturated components (e.g., C–F2 and C–F3) and decreasing unsaturated components (e.g., C–C and C–CF), thus enhancing the fluorine-to-carbon (F/C) ratio. The results are expected aid in tailoring the design of fluorocarbon films for physicochemical properties.


2013 ◽  
Vol 634-638 ◽  
pp. 353-356
Author(s):  
Chao Lin Miao ◽  
Hui Wang

Surface modification of microporous polypropylene membrane was performed by grafting polymerization of acrylamide.The morphological and microstructure changes of the membrane surface were confirmed by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy and atomic force microscopy. The results indicate that the pore size of the grafted membrane was reduced.


2003 ◽  
Vol 796 ◽  
Author(s):  
Jing Tang ◽  
Henrik Birkedal ◽  
Eric W. McFarland ◽  
Galen D. Stucky

ABSTRACTCdSe/CdS core/shell quantum dots have been synthesized and assembled onto pre-functionalized gold surfaces by either hydrogen bonding or covalent bonds through different functional groups. Control of the conditions during the deposition process allows producing a high coverage of quantum dots via molecular linkages. The quantum-dot surface is highly photoactive and is used in a surface sensitized Schottky barrier photovoltaic structure as the photoreception component. Atomic force microscopy (AFM) and X-ray photoelectron Spectroscopy (XPS) are used to characterize and confirm the morphology and linkage of the assemblies on Au surfaces. The electron transfer from the quantum-dot layer to the Schottky barrier device is examined by measuring the current-voltage (IV) curve of such photovoltaic devices under simulated sun light.


Technologies ◽  
2021 ◽  
Vol 9 (2) ◽  
pp. 36
Author(s):  
Ibrahim Cisse ◽  
Sarah Oakes ◽  
Shreen Sachdev ◽  
Marc Toro ◽  
Shin Lutondo ◽  
...  

Polyethersulfone (PES) films are widely employed in the construction of membranes where there is a desire to make the surface more hydrophilic. Therefore, UV photo-oxidation was studied in order to oxidize the surface of PES and increase hydrophilicity. UV photo-oxidation using low pressure mercury lamps emitting both 253.7 and 184.9 nm radiation were compared with only 253.7 nm photons. The modified surfaces were characterized using X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and water contact angle (WCA) measurements. Both sets of lamps gave similar results, showing an increase of the oxygen concentration up to a saturation level of ca. 29 at.% and a decrease in the WCA, i.e., an increase in hydrophilicity, down to ca. 40°. XPS detected a decrease of sp2 C-C aromatic group bonding and an increase in the formation of C-O, C=O, O=C-O, O=C-OH, O-(C=O)-O, and sulphonate and sulphate moieties. Since little change in surface roughness was observed by AFM, the oxidation of the surface caused the increase in hydrophilicity.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Luís C. Almeida ◽  
Tânia Frade ◽  
Rui D. Correia ◽  
Yu Niu ◽  
Gang Jin ◽  
...  

AbstractWe report a straightforward and reproducible electrochemical approach to develop polydopamine-ethanolamine (ePDA-ETA) films to be used as immunosensing interfaces. ETA is strongly attached to polydopamine films during the potentiodynamic electropolymerization of dopamine. The great advantage of the electrochemical methods is to generate the oxidized species (quinones), which can readily react with ETA amine groups present in solution, with the subsequent incorporation of this molecule in the polymer. The presence of ETA and its effect on the electrosynthesis of polydopamine was accessed by cyclic voltammetry, ellipsometry, atomic force microscopy, FTIR and X-ray photoelectron spectroscopy. The adhesive and biocompatible films enable a facile protein linkage, are resilient to flow assays, and display intrinsic anti-fouling properties to block non-specific protein interactions, as monitored by real-time surface plasmon resonance, and confirmed by ellipsometry. Immunoglobulin G (IgG) and Anti-IgG were used in this work as model proteins for the affinity sensor. By using the one-step methodology (ePDA-ETA), the lower amount of immobilized biorecognition element, IgG, compared to that deposited on ePDA or on ETA post-modified film (ePDA/ETA), allied to the presence of ETA, improved the antibody-antigen affinity interaction. The great potential of the developed platform is its versatility to be used with any target biorecognition molecules, allowing both optical and electrochemical detection.


2012 ◽  
Vol 3 ◽  
pp. 267-276 ◽  
Author(s):  
Stella Kiel ◽  
Olga Grinberg ◽  
Nina Perkas ◽  
Jerome Charmet ◽  
Herbert Kepner ◽  
...  

This work describes a general method for the preparation of salt nanoparticles (NPs) made from an aqueous solution of ionic compounds (NaCl, CuSO4 and KI). These nanoparticles were created by the application of ultrasonic waves to the aqueous solutions of these salts. When the sonication was carried out in the presence of a glass microscope slide, a parylene-coated glass slide, or a silicon wafer the ionic NPs were embedded in these substrates by a one-step, ultrasound-assisted procedure. Optimization of the coating process resulted in homogeneous distributions of nanocrystals, 30 nm in size, on the surfaces of the substrates. The morphology and structure of each of the coatings were characterized by physical and chemical methods, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). After 24 h of leaching into water the nanoparticles of the inorganic salts were still present on the slides, and complete leaching of nanoparticles occurred only after 96 h. A mechanism of the ultrasound-assisted coating is proposed.


2019 ◽  
Vol 19 (6) ◽  
pp. 3495-3504
Author(s):  
Guocheng Song ◽  
Jing Li ◽  
Junrong Yu ◽  
Yan Wang ◽  
Jing Zhu ◽  
...  

In the present paper, Phenolphthalein poly(ether sulfone) (PES-C) nanofibrous membranes were prepared via solution-blowing technology and polyvinylpyrrolidone (PVP) which would be converted to stable gels by reaction with potassium persulfate (K2S2O8) was immobilized on the surface of nanofibers. The influence factors such as PVP concentration and depositing time were optimized to obtain the composite nanofibrous membranes. The membranes were characterized by Scanning electron microscopy (SEM), Fourier transform infrared (FTIR), Wide-angle X-ray diffraction (WAXD), X-ray photoelectron spectroscopy (XPS) and Water contact angles (WCA), etc. The hydrophilicity of the composite membrane was significantly enhanced by immobilizing Polyvinylpolypyrrolidone (PVPP) on the surface of nanofibers. Furthermore the filtration experiment of starch suspension and oil-water separation test were executed and the anti-fouling properties of the modified membranes were evaluated with the flux recovery ratio (FRR%). The results showed that membranes with PVPP-modified had a more excellent and stability antifouling performances compared with the original membranes. Generally, this work provides a simple and useful method to improve anti-fouling properties of PES-C nanofibrous membranes which had great potential application in microfiltration.


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