Syntheses and interfacial characterization of graft copolymers from styrene and 2-hydroxyethyl methacrylate that comprise either trunks or branches

1995 ◽  
Vol 73 (11) ◽  
pp. 1757-1764 ◽  
Author(s):  
Hidekazu Yoshida ◽  
Shinichi Itsuno ◽  
Koichi. Ito
Keyword(s):  
Graft Copolymer ◽  
Graft Copolymers ◽  
Micelle Formation ◽  
Hydroxyethyl Methacrylate ◽  
H Nmr ◽  
Copolymer Films ◽  
Angle Measurements ◽  
Contact Angle Measurements ◽  
Copolymer Micelle ◽  
End Capping

Polystyrene (PS) and poly(2-hydroxyethyl methacrylate) (PHEMA) macromonomers with either p-vinylbenzyl or methacrylate end groups were prepared by living anionic polymerizations of styrene and 2-(trimethylsilyloxy)ethyl methacrylate, respectively, followed by appropriate end-capping. They were radically copolymerized with 2-hydroxyethyl methacrylate and styrene, respectively, to afford PS-g-PHEMA and PHEMA-g-PS, having PS trunks with PHEMA branches or the reverse architecture. 1H NMR spectra of the graft copolymers in deuterated methanol showed their micelle formation with PS and PHEMA chains as the core and the shell, respectively. In chloroform the reverse micelles were observed. Contact angle measurements of water on the graft copolymer films revealed that PS chains were generally dominant on the free surface. The films either cast from methanol or after immersion into water, however, were apparently wettable, indicating dominant PHEMA chains on the surface. Keywords: styrene, 2-hydroxyethyl methacrylate, graft copolymer, micelle formation, wettability.

Synthesis and characterization of amphiphilic graft copolymers with hydrophobic poly(α-methylstyrene) backbone and hydrophilic poly(n-vinylpyrrolidone) side chains

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Fatima Zohra Sebba ◽  
Seghier Ould Kada ◽  
Mohamed Benaicha ◽  
Nerjesse Nemiche
Keyword(s):  
Graft Copolymer ◽  
Graft Copolymers ◽  
Radical Copolymerization ◽  
Side Chains ◽  
Free Radical Copolymerization ◽  
Good Efficiency ◽  
Molecular Weights ◽  
Grafting Reaction ◽  
Viscosity Variation ◽  
End Capping

AbstractIn this study, 2-oxopropylmethacrylate-terminated poly(N-vinyl-2- pyrrolidone) is produced by cationic polymerization using HClO4 as an initiator. Termination (end capping) step is accomplished using 2- hydroxypropylmethacrylate (2HPMA) and the polymer product has different chain lengths of molecular weight averages ranging from 672 to 3049 g/mol. The study also synthesised amphipathic graft copolymers having hydrophobic poly(α- methylstyrene) as a backbone chain and hydrophilic poly(N-vinyl-2-pyrrolidone) (PVP) as side chains of various lengths. The copolymer synthesis was accomplished by free radical copolymerization of ω-oxopropylmethacrylate PVP in the presence of α-methyl styrene initiated with benzoyl peroxide. Measurements of the dynamic viscosity of the polymer solution (20% weight of macromonomers in ethanol) show that the viscosity is proportional to the average molecular weights M̅n . However, a reverse behaviour of the viscosity variation with regard to M̅n is observed for graft copolymer samples. The viscosity variation with respect to the graft copolymer mass must be due to steric effects, which are strongly pronounced in grafted copolymer chains. Appearance of the number of side chains attached to poly(α-methylstyrene) backbone reveals that the grafting reaction has occurred with good efficiency.

scholarly journals Improvement of Thermal and Mechanical Properties of Vietnam Deproteinized Natural Rubber via Graft Copolymerization with Methyl Methacrylate

2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Thi Nhan Nguyen ◽  
Hieu Nguyen Duy ◽  
Dung Tran Anh ◽  
Thuong Nghiem Thi ◽  
Thu Ha Nguyen ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Natural Rubber ◽  
Methyl Methacrylate ◽  
Graft Copolymer ◽  
Graft Copolymerization ◽  
Graft Copolymers ◽  
Thermal And Mechanical Properties ◽  
H Nmr ◽  
Tert Butyl Hydroperoxide ◽  
Deproteinized Natural Rubber

In this study, we investigated the improvement of the thermal and mechanical properties of Vietnam deproteinized natural rubber (DPNR) via graft copolymerization of methyl methacrylate (MMA). The graft copolymerization was achieved successfully in latex stage using tert-butyl hydroperoxide (TBHPO) and tetra-ethylenepentamine (TEPA) as radical initiators at 30°C. By grafting with various MMA feeds and initiator concentration of 6.6×10−5 mol/g-rubber, the highest grafting efficiency and conversion were achieved at MMA of 15 wt.% per kg of rubber, 68% and 90%, respectively. The structure of grafted copolymers was characterized by 1H NMR, FTIR-ATR, and GPC, and thermal properties were investigated through DSC and TGA measurements. These showed that graft copolymers were more stable and rigid than DPNR. Storage modulus (G′) of graft copolymer was found to double that of DPNR, which contributed to the formation of graft copolymer. After sulfur vulcanization, the mechanical properties of DPNR-graft-PMMA, such as tensile strength, tear strength, and hardness, were improved significantly. Curing behaviors of the graft copolymers were found to be remarkably better than virgin DPNR.

Nanostructured Polymer Brushes With Reversibly Changing Properties

2002 ◽  
Vol 727 ◽  
Author(s):  
Denys Usov ◽  
Manfred Stamm ◽  
Sergiy Minko ◽  
Christian Froeck ◽  
Andreas Scholl ◽  
...  
Keyword(s):  
Polymer Brushes ◽  
Phase Segregation ◽  
Water Contact ◽  
Angle Measurements ◽  
Nanostructured Polymer ◽  
Contact Angle Measurements ◽  
Vertical Segregation ◽  
Oxygen Plasma Etching ◽  
Grafting From ◽  
Photoemission Electron

AbstractWe investigated the interplay between different mechanisms of the lateral and vertical segregation in the synthesized via “grafting from” approach symmetric A/B (where A and B are poly(styrene-co-2,3,4,5,6-pentafluorostyrene) and poly(methylmethacrylate), respectively) polymer brushes upon exposure to different solvents. We used X-ray photoemission electron spectroscopy and microscopy (X-PEEM), AFM, water contact angle measurements, and oxygen plasma etching to study morphology of the brushes. The ripple morphology after toluene (nonselective solvent) revealed elongated lamellar-like domains of A and B polymers alternating across the surface. The dimple-A morphology consisting of round clusters of the polymer A was observed after acetone (selective solvent for B). The top layer was enriched with the polymer B showing that the brush underwent both the lateral and vertical phase segregation. A qualitative agreement with predictions of SCF theory was found.

Wrinkling Poly(trimethylene 2,5-Furanoate) Free-standing Films: Nanostructure Formation and Physical Properties

2020 ◽  
Author(s):  
Michelina Soccio ◽  
Nadia Lotti ◽  
Andrea Munari ◽  
Esther Rebollar ◽  
Daniel E Martínez-Tong
Keyword(s):  
Irradiation Time ◽  
Polymer Surface ◽  
Laser Source ◽  
Free Standing ◽  
Force Microscopy ◽  
Nanostructure Formation ◽  
Physicochemical Changes ◽  
Angle Measurements ◽  
Atomic Force ◽  
Contact Angle Measurements

<p>Nanostructured wrinkles were developed on fully bio-based poly(trimethylene furanoate) (PTF) films by using the technique of Laser Induced Periodic Surface Structures (LIPSS). We investigated the effect of irradiation time on wrinkle formation using an UV pulsed laser source, at a fluence of 8 mJ/cm2. It was found that the pulse range between 600 and 4800 pulses allowed formation of periodic nanometric ripples. The nanostructured surface was studied using a combined macro- and nanoscale approach. We evaluated possible physicochemical changes taking place on the polymer surface after irradiation by infrared spectroscopy, contact angle measurements and atomic force microscopy. The macroscopic physicochemical properties of PTF showed almost no changes after nanostructure formation, differently from the results previously found for the terephthalic counterparts, as poly(ethyleneterephthalate), PET, and poly(trimethyleneterephthalate), PTT. The surface mechanical properties of the nanostructured PTF were found to be improved, as evidenced by nanomechanical force spectroscopy measurements. In particular, an increased Young’s modulus and higher stiffness for the nanostructured sample were measured. <br></p>

scholarly journals Adhesion Studies during Generative Hybridization of Textile-Reinforced Thermoplastic Composites via Additive Manufacturing

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3888
Author(s):  
Johanna Maier ◽  
Christian Vogel ◽  
Tobias Lebelt ◽  
Vinzenz Geske ◽  
Thomas Behnisch ◽  
...  
Keyword(s):  
Additive Manufacturing ◽  
Polyamide 6 ◽  
Thermoplastic Composites ◽  
Efficient Production ◽  
Angle Measurements ◽  
Small Series ◽  
Contact Angle Measurements ◽  
Static Tensile ◽  
Pre Treatment ◽  
Manufacturing Technologies

Generative hybridization enables the efficient production of lightweight structures by combining classic manufacturing processes with additive manufacturing technologies. This type of functionalization process allows components with high geometric complexity and high mechanical properties to be produced efficiently in small series without the need for additional molds. In this study, hybrid specimens were generated by additively depositing PA6 (polyamide 6) via fused layer modeling (FLM) onto continuous woven fiber GF/PA6 (glass fiber/polyamide 6) flat preforms. Specifically, the effects of surface pre-treatment and process-induced surface interactions were investigated using optical microscopy for contact angle measurements as well as laser profilometry and thermal analytics. The bonding characteristic at the interface was evaluated via quasi-static tensile pull-off tests. Results indicate that both the bond strength and corresponding failure type vary with pre-treatment settings and process parameters during generative hybridization. It is shown that both the base substrate temperature and the FLM nozzle distance have a significant influence on the adhesive tensile strength. In particular, it can be seen that surface activation by plasma can significantly improve the specific adhesion in generative hybridization.

scholarly journals Epoxy/alumina composite coating on welded steel 316L with excellent wear and anticorrosion properties

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Maryama Hammi ◽  
Younes Ziat ◽  
Zakaryaa Zarhri ◽  
Charaf Laghlimi ◽  
Abdelaziz Moutcine
Keyword(s):  
Electrochemical Behaviour ◽  
Sem Analysis ◽  
Water Contact ◽  
Welded Steel ◽  
Melted Zone ◽  
Angle Measurements ◽  
Contact Angle Measurements ◽  
Alumina Composite ◽  
The Cost ◽  
Good Contrast

AbstractThe main purpose of this study is to elaborate anticorrosive coatings for the welded steel 316L, since this later is widely used in industrial field. Hence, within this work we have studied the electrochemical behaviour of different zones of the welded steel 316 in 1 M HCl media. The macrography study of the welded steel has revealed the different areas with a good contrast. We have stated three different zones, namely; melted zone (MZ), heat affected zone (HAZ) and base metal zone (BM). Impedance studies on welded steel 316L were conducted in 1 M HCl solution, coating of Epoxy/Alumina composite was applied on different zones, in order to reveal the anti-corrosion efficiency in each zone. Scanning electron microscopy (SEM) analysis was undertaken in order to check how far the used coating in such aggressive media protects the studied zones and these findings were assessed by water contact angle measurements. The choice of this coating is based on the cost and the safety. We concluded that the Epoxy/Alumina composite has a good protecting effect regarding welded steel in aggressive media.

scholarly journals Synthesis and Characterization of Polyphosphazenes Modified with Hydroxyethyl Methacrylate and Lactic Acid

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Evelyn Carolina Martínez Ceballos ◽  
Ricardo Vera Graziano ◽  
Gonzalo Martínez Barrera ◽  
Oscar Olea Mejía
Keyword(s):  
Lactic Acid ◽  
Ring Opening ◽  
Room Temperature ◽  
Block Structure ◽  
Ring Opening Polymerization ◽  
Synthesis And Characterization ◽  
Poly Lactic Acid ◽  
Hydroxyethyl Methacrylate ◽  
H Nmr

Poly(dichlorophosphazene) was prepared by melt ring-opening polymerization of the hexachlorocyclotriphosphazene. Poly[bis(2-hydroxyethyl-methacrylate)-phosphazene] and poly[(2-hydroxyethyl-methacrylate)-graft-poly(lactic-acid)-phosphazene] were obtained by nucleophilic condensation reactions at different concentrations of the substituents. The properties of the synthesized copolymers were assessed by FTIR,1H-NMR and31P-NMR, thermal analysis (DSC-TGA), and electron microscopy (SEM). The copolymers have a block structure and show twoTg's below room temperature. They are stable up to a temperature of 100°C. The type of the substituents attached to the PZ backbone determines the morphology of the polymers.

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