scholarly journals Synthesis, Hydrophilicity and Micellization of Coil–Brush Polystyrene-b-(polyglycidol-g-polyglycidol) Copolymer—Comparison with Linear Polystyrene-b-Polyglycidol

Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 253
Author(s):  
Mariusz Gadzinowski ◽  
Maciej Kasprów ◽  
Teresa Basinska ◽  
Stanislaw Slomkowski ◽  
Łukasz Otulakowski ◽  
...  

In this paper, an original method of synthesis of coil–brush amphiphilic polystyrene-b-(polyglycidol-g-polyglycidol) (PS-b-(PGL-g-PGL)) block copolymers was developed. The hypothesis that their hydrophilicity and micellization can be controlled by polyglycidol blocks architecture was verified. The research enabled comparison of behavior in water of PS-b-PGL copolymers and block–brush copolymers PS-b-(PGL-g-PGL) with similar composition. The coil–brush copolymers were composed of PS-b-PGL linear core with average DPn of polystyrene 29 and 13 of polyglycidol blocks. The DPn of polyglycidol side blocks of coil–b–brush copolymers were 2, 7, and 11, respectively. The copolymers were characterized by 1H and 13C NMR, GPC, and FTIR methods. The hydrophilicity of films from the linear and coil–brush copolymers was determined by water contact angle measurements in static conditions. The behavior of coil–brush copolymers in water and their critical micellization concentration (CMC) were determined by UV-VIS using 1,6-diphenylhexa-1,3,5-trien (DPH) as marker and by DLS. The CMC values for brush copolymers were much higher than for linear species with similar PGL content. The results of the copolymer film wettability and the copolymer self-assembly studies were related to fraction of hydrophilic polyglycidol. The CMC for both types of polymers increased exponentially with increasing content of polyglycidol.

2012 ◽  
Vol 1376 ◽  
Author(s):  
Haydee Vargas-Villagran ◽  
Elvia Teran-Salgado ◽  
Maraolina Dominguez-Diaz ◽  
Osvaldo Flores ◽  
Bernardo Campillo ◽  
...  

ABSTRACTIn this research, we describe the electrospinning processing of polylactic acid (PLA) and the influence of silver nanoparticles on the morphology and microstructure of produced non woven membranes thus produced. The PLA was electrospun from a chloroform solution and a filamentary and granular morphology was obtained, the filaments having an average diameter of 1.25 μm, When silver nanoparticles (of ca. 12 nm size) were incorporated, the filaments diameter was reduced to an average of 0.65 μm, and the density of beads was also reduced. The membranes were rather amorphous, as revealed by X-ray scattering, presumably due to the quenching process associated with the electrospinning process. Water contact angle measurements showed that silver nanoparticles induced significant hidrophobicity in the membranes as neat PLA membrane had a contact angle of 54° and PLA/Ag membrane exhibited an angle of 115°.


2017 ◽  
Vol 89 (1) ◽  
pp. 141-152 ◽  
Author(s):  
Ioanna-Georgia Athanasoulia ◽  
Petroula A. Tarantili

AbstractThe effect of incorporation of poly(ethylene glycol) (PEG) on thermomechanical and hydrophilicity properties of poly(L-lactic acid) (PLLA) was investigated. PEG/PLLA blends, containing 10, 20, 30 and 40 wt% PEG, were prepared by melt-extrusion in a co-rotating twin-screw extruder. By DSC analysis, it was observed that the Tg of PLLA phase in PEG/PLLA blends decreased accompanied by a significant decrease in Tcc and increase in their melting enthalpy. Therefore, the addition of PEG enhances the crystallization ability of PLLA phase due to its lubricating effect which increased mobility of PLLA chains. From TGA it was observed that low concentrations of PEG (10 & 20 wt%) increase the Tonset of thermal degradation, probably due to improved heat resistance of the crystalline phase. At higher PEG content, the Tonset decreases, as the lubricating effect becomes the controlling mechanism for the initiation of degradation process. Decrease in tensile strength and modulus was recorded especially in PLLA blends with PEG content higher than 20 wt%. The elongation at break decreases reaching a maximum at 20 wt% PEG and then dropped again. To investigate the effect of PEG on the wetting ability of PLLA, water contact angle measurements were performed. The results indicate that the introduction of PEG lowers the contact angle values in PEG/PLLA film surfaces, as compared to pure PLLA, suggesting improved hydrophilic properties.


2019 ◽  
Vol 10 (4) ◽  
pp. 77-94
Author(s):  
Sashivinay Kumar Gaddam ◽  
Aruna Palanisamy

A novel cottonseed oil-based ionizable polyol was introduced as ionic soft segment in waterborne polyurethane dispersion (PUD) synthesis. The ionizable polyol was synthesized by ring opening of epoxidized cottonseed oil (ECSO) with 4-aminobenzoic acid (PABA) and blended with hydroxylated cottonseed oil polyol (HCSO) in different weight ratios to develop a series of mixed polyols having different hydroxyl numbers viz., 146, 130 and 114 mg KOH/g. Three different PUDs were synthesized using the mixed polyols, isophorone diisocyanate, and 3-aminopropyltriethoxysilane. The chemical structure, thermo-mechanical properties, and surface properties of cured PUD films were examined using Fourier-transform infrared spectroscopy (FTIR), Dynamic mechanical thermal analysis (DMTA), universal testing machine (UTM) and contact angle measurements respectively. The effect of Si–O–Si cross-linking network density, which increases with an increase in OH values of the mixed polyol was also investigated. All the PUDs prepared in this study exhibited good storage stability (>4 months), and the average particle sizes of PUDs ranged from 18 to 124 nm. The highest hydroxyl mixed polyol derived PUD film (PUD-35 film) exhibited high thermal stability, mechanical strength; Tg value, water contact angle value, chemical, and abrasion resistance properties due to the extended siloxane cross-link network structure. The introduction of ionizable polyol into the soft segment led to an improvement in hard and soft segment phase mixing of PUDs, and this strategy could enrich the exploration of new synthetic methodologies in the field of bio-based PUD manufacturing.


Chemija ◽  
2018 ◽  
Vol 29 (3) ◽  
Author(s):  
Kamilė Vonžodaitė ◽  
Eglė Balčiūnaitė ◽  
Rasa Alaburdaitė ◽  
Edita Paluckienė

Layers of copper sulfides, CuxS, on the surface of a polypropylene film were formed by the sorption–diffusion method using two reducing agents – hydroquinone and hydroxylamine sulfate. The formed copper sulfide layers were investigated by UV/VIS, X-ray diffraction (XRD) and water contact angle measurements (WCA). The investigations confirmed that a layer of nonstoichiometric copper sulfide was formed on the surface of the polypropylene film. The water contact angle measurements revealed the change in adhesive properties of the samples after each treatment stage.


1997 ◽  
Vol 51 (12) ◽  
pp. 1905-1909 ◽  
Author(s):  
Oliver M. R. Chyan ◽  
Junjun Wu ◽  
Jin-Jian Chen

The hydrogen termination process on a Si(100) surface has been studied by multiple internal reflection infrared spectroscopy (MIR-IS) and contact-angle measurements. Three main silicon hydride absorption peaks at 2087, 2104, and 2114 cm−1 were found to gradually increase with the hydrofluoric (HF) acid etching. Eventually, a constant peak height was reached as an indication of complete hydrogen termination. Integration of all the surface hydrides absorption peaks (2000 to 2200 cm−1) provides direct quantitative evaluation of the hydrogen termination process. On the other hand, water contact-angle data were shown to consistently lag behind the IR measurement in determining the extent of hydrogen termination on the silicon surface. Analysis of the surface free energy of HF-etched silicon surfaces indicates that the degree of the hydrogen termination determined by water contact-angle measurements is subjected to inaccuracies due to the preferential hydrogen-bonding interaction between the water and silicon surface oxide.


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