Surface tension of melt polymer brushes and diblock copolymers

Langmuir ◽  
1993 ◽  
Vol 9 (8) ◽  
pp. 2215-2219 ◽  
Author(s):  
D. R. M. Williams
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).


MRS Advances ◽  
2016 ◽  
Vol 1 (27) ◽  
pp. 1971-1976
Author(s):  
Troels Røn ◽  
Irakli Javakhishvili ◽  
Søren Hvilsted ◽  
Katja Jankova ◽  
Seunghwan Lee

ABSTRACTFor biological and mechanical systems involving moving parts, surface slipperiness is often a critical attribute for their optimal functions. Surface grafting with hydrophilic polymers is a powerful means to render materials slippery in aqueous environment. In “inverted grafting-to approach”, the hydrophilic polymer chains of amphiphilic diblock copolymers dispersed within a poly(dimethylsiloxane) (PDMS) network are selectively segregated upon exposure to aqueous solution. This allows formation of extremely stable brush-like polymer layers. Tribological application of inverted grafting-to approach was successfully demonstrated with PDMS-block-poly(acrylic acid) (PDMS-b-PAA) dispersed within thin PDMS films on PDMS blocks by showing friction coefficients (µ) of ca 10-2 to 10-3, depending on the load, pH and buffer salinity in the absence of other external re-supply of PAA chains. Further manipulations of the thin PDMS film incorporating PDMS-b-PAA to optimize the tribological properties are presented. Lastly, first trials to employ PAA-grafted PDMS surface to generate in-vitro mucosae model are also presented and discussed.


2013 ◽  
Vol 800 ◽  
pp. 428-431
Author(s):  
Yang Yang ◽  
Chun Cheng Zuo ◽  
Yu Xin Zuo ◽  
Ying Yu

The formation process of diblock copolymer brushes, formed by the adsorption of flexible chains on the surface is studied by Molecular Dynamic simulations. The surface adsorption density has been distinguished, depending on the various chain structures and counterions. The mode was considered as size ratio of A-block lengths to the the chain length, B-block carries the positive charge, and add counterions to the system. The result shows that the surface adsorption density is affected strongly by ratio of A-block length to the chain length, inhibited by the counterions, which is qualitatively consistent with experiments. These initial findings can be used as a guide for the preparation of actual diblock polymer brushes on metal crystal surfaces membranes by the adsorption approach.


Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1228 ◽  
Author(s):  
Chun-Na Yan ◽  
Lin Xu ◽  
Qing-Di Liu ◽  
Wei Zhang ◽  
Rui Jia ◽  
...  

Well-defined polymer brushes attached to nanoparticles offer an elegant opportunity for surface modification because of their excellent mechanical stability, functional versatility, high graft density as well as controllability of surface properties. This study aimed to prepare hybrid materials with good dispersion in different solvents, and to endow this material with certain fluorescence characteristics. Well-defined diblock copolymers poly (styrene)-b-poly (hydroxyethyl methyl acrylate)–co-poly (hydroxyethyl methyl acrylate- rhodamine B) grafted silica nanoparticles (SNPs-g-PS-b-PHEMA-co-PHEMA-RhB) hybrid materials were synthesized via surface-initiated activators regenerated by electron transfer atom transfer radical polymerization (SI-ARGET ATRP). The SNPs surfaces were modified by 3-aminopropyltriethoxysilane (KH-550) firstly, then the initiators 2-Bromoisobutyryl bromide (BIBB) was attached to SNPs surfaces through the esterification of acyl bromide groups and amidogen groups. The synthetic initiators (SNPs-Br) were further used for the SI-ARGET ATRP of styrene (St), hydroxyethyl methyl acrylate (HEMA) and hydroxyethyl methyl acrylate-rhodamine B (HEMA-RhB). The results indicated that the SI-ARGET ATRP initiator had been immobilized onto SNPs surfaces, the Br atom have located at the end of the main polymer chains, and the polymerization process possessed the characteristic of controlled/“living” polymerization. The SNPs-g-PS-b-PHEMA-co-PHEMA-RhB hybrid materials show good fluorescence performance and good dispersion in water and EtOH but aggregated in THF. This study demonstrates that the SI-ARGET ATRP provided a unique way to tune the polymer brushes structure on silica nanoparticles surface and further broaden the application of SI-ARGET ATRP.


2013 ◽  
Vol 705 ◽  
pp. 143-149 ◽  
Author(s):  
Yang Yang ◽  
Chun Cheng Zuo ◽  
Yu Xin Zuo ◽  
Ying Yu

We use molecular dynamics simulations method to investigate the behavior characteristics of AB diblock copolymers that are adsorbed on a planar surface. Adsorption density has been distinguished, depending on the adsorption manner of A-block on the (100) surface and formation of brushes. It is examined in detail that conformational behavior of the brushes affects the adsorption density. In addition, we make a comparison of linear brush with length ratio of the A-block to the chain, in the cases of the fixed length of chain and the fixed length of A-block, respectively. The result shows that the adsorption density is strongly affected by the length ratio of the A-block to the chain. And our findings can be used as a guide for fabrication and preparation of actual synthetic polymer brushes on a solid surface by the approach of physical adsorption.


2001 ◽  
Vol 707 ◽  
Author(s):  
Aaron M. Forster ◽  
S. Michael Kilbey

ABSTRACTWe have used the surface forces apparatus to measure the structural and frictional force profiles between opposing, solvated brush layers as a function of temperature. Two different polyvinylpyridine-polystyrene [PVP-PS] diblock copolymers were used to make PS brushes. The molecular weights (in thousands) of these PVP-PS materials were [114/103]k, [30/70]k, respectively. Structural and frictional force profiles in toluene and cyclohexane were measured, and the cyclohexane experiments were conducted at temperatures ranging from the theta-point to 50 C. In toluene the PS brushes needed to be compressed to ∼1/5th of their equilibrium height before frictional forces were measured, but this onset of frictional forces was detected at a much lower level of compression in near-theta cyclohexane. In cyclohexane the structural force profiles were basically insensitive to the temperature change, but the frictional forces depended strongly on the solvent temperature. When the cyclohexane temperature was raised, the onset of frictional forces decreased toward the good-solvent onset. We also discuss the dependence of frictional force on shearing parameters.


2001 ◽  
Vol 710 ◽  
Author(s):  
Aaron M. Forster ◽  
S. Michael Kilbey

ABSTRACTWe have used the surface forces apparatus to measure the structural and frictional force profiles between opposing, solvated brush layers as a function of temperature. Two different polyvinylpyridine-polystyrene [PVP-PS] diblock copolymers were used to make PS brushes. The molecular weights (in thousands) of these PVP-PS materials were [114/103]k, [30/70]k, respectively. Structural and frictional force profiles in toluene and cyclohexane were measured, and the cyclohexane experiments were conducted at temperatures ranging from the theta-point to 50°C. In toluene the PS brushes needed to be compressed to ∼1/5th of their equilibrium height before frictional forces were measured, but this onset of frictional forces was detected at a much lower level of compression in near-theta cyclohexane. In cyclohexane the structural force profiles were basically insensitive to the temperature change, but the frictional forces depended strongly on the solvent temperature. When the cyclohexane temperature was raised, the onset of frictional forces decreased toward the good-solvent onset. We also discuss the dependence of frictional force on shearing parameters.


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