scholarly journals The polymerisation of oligo(ethylene glycol methyl ether) methacrylate from a multifunctional poly(ethylene imine) derived amide: a stabiliser for the synthesis and dispersion of magnetite nanoparticles

2014 ◽  
Vol 5 (2) ◽  
pp. 524-534 ◽  
Author(s):  
Aaron Kleine ◽  
Cem L. Altan ◽  
U. Ecem Yarar ◽  
Nico A. J. M. Sommerdijk ◽  
Seyda Bucak ◽  
...  
Keyword(s):  
Ethylene Glycol ◽  
Methyl Ether ◽  
Magnetite Nanoparticles ◽  
Ethylene Imine ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

Magnetite nanoparticles stabilized with polymeric bilayer of poly(ethylene glycol) methyl ether–poly(ɛ-caprolactone) copolymers

Polymer ◽  
2008 ◽  
Vol 49 (18) ◽  
pp. 3950-3956 ◽  
Author(s):  
Siraprapa Meerod ◽  
Gamolwan Tumcharern ◽  
Uthai Wichai ◽  
Metha Rutnakornpituk
Keyword(s):  
Ethylene Glycol ◽  
Methyl Ether ◽  
Magnetite Nanoparticles ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

The role of hydrogen bonding in alginate/poly(acrylamide-co-dimethylacrylamide) and alginate/poly(ethylene glycol) methyl ether methacrylate-based tough hybrid hydrogels

RSC Advances ◽  
2015 ◽  
Vol 5 (71) ◽  
pp. 57678-57685 ◽  
Author(s):  
Zhi Wei Low ◽  
Pei Lin Chee ◽  
Dan Kai ◽  
Xian Jun Loh
Keyword(s):  
Hydrogen Bonding ◽  
Elastic Modulus ◽  
Ethylene Glycol ◽  
Methyl Ether ◽  
Poly Ethylene Glycol ◽  
Hybrid Hydrogels ◽  
Poly Ethylene ◽  
Glycol Methyl Ether ◽  
Poly Acrylamide

Hybrid hydrogels, with an elastic modulus and compressive toughness of 350 kPa and 70 J m−3, was synthesized and reported here.

The Influences of Monomer Structure and Solvent on the Radical Copolymerization of Tertiary Amine and PEGylated Methacrylates

2021 ◽  
Author(s):  
Priscila Quiñonez-Angulo ◽  
Robin Hutchinson ◽  
Angel Licea-Claverie ◽  
Enrique Saldivar ◽  
Ivan Zapata-Gonzalez
Keyword(s):  
Ethylene Glycol ◽  
Methyl Ether ◽  
Tertiary Amine ◽  
Radical Copolymerization ◽  
Poly Ethylene Glycol ◽  
Ethyl Methacrylate ◽  
Monomer Structure ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

Tertiary Amine Methacrylates (TAMAs), such as 2-(N,N-diethylamino)ethyl methacrylate (DEAEMA) and 2-(N,N-dimethylamino)ethyl methacrylate (DMAEMA), and PEGylated (macro)monomers, such as 2-ethoxyethyl methacrylate (EEMA1) and poly(ethylene glycol) methyl ether methacrylates with 9 and...

Control the Surface Wettability of Thermo-Responsive Poly(Ethylene Glycol Methyl Ether methacrylate-co-Triethylene Glycol Methyl Ether Methacrylate) Thin Film by Varying Temperature

2021 ◽  
Vol 873 ◽  
pp. 53-58
Author(s):  
Yang Yi Chen ◽  
Min Pan ◽  
Shan Hong Hu ◽  
Qi Huan ◽  
Chu Yang Zhang
Keyword(s):  
Thin Film ◽  
Ethylene Glycol ◽  
Methyl Ether ◽  
Triethylene Glycol ◽  
Surface Wettability ◽  
Molar Ratio ◽  
Poly Ethylene Glycol ◽  
Vis Spectroscopy ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

The surface wettability of thermo-responsive random poly (ethylene glycol methyl ether methacrylate-co-triethylene glycol methyl ether methacrylate), abbreviated as P(MEOMA-co-MEO3MA), was investigated in thin film. UV-Vis spectroscopy shows that the LCST of P(MEOMA-co-MEO3MA) with molar ratios of 0:20, 6:14 and 9:11 were 43°C, 32 oC and 25 oC, respectively. LCST shifts towards lower temperature when molar ratio of MEOMA increases. ATR-FTIR indicates that P(MEOMA-co-MEO3MA) thin film experienced a collapse when the temperature passes its LCST. The contact angle of the paraffin oil on the film decreases 15o when the temperature is above its LCST, which confirms the surface wettability can be controlled. Atomic force microscopy shows the surface of the swollen thin film becomes rougher when above it LCST.

scholarly journals Hybrid Mesoporous Silica Nanoparticles Grafted with 2-(tert-butylamino)ethyl Methacrylate-b-poly(ethylene Glycol) Methyl Ether Methacrylate Diblock Brushes as Drug Nanocarrier

Molecules ◽  
2020 ◽  
Vol 25 (1) ◽  
pp. 195 ◽  
Author(s):  
Abdullah M Alswieleh ◽  
Abeer M Beagan ◽  
Bayan M Alsheheri ◽  
Khalid M Alotaibi ◽  
Mansour D Alharthi ◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Ethylene Glycol ◽  
Silica Nanoparticles ◽  
Methyl Ether ◽  
Diblock Copolymer ◽  
Mesoporous Silica Nanoparticles ◽  
Poly Ethylene Glycol ◽  
Ethyl Methacrylate ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

This paper introduces the synthesis of well-defined 2-(tert-butylamino)ethyl methacrylate-b-poly(ethylene glycol) methyl ether methacrylate diblock copolymer, which has been grafted onto mesoporous silica nanoparticles (PTBAEMA-b-PEGMEMA-MSNs) via atom transfer radical polymerization (ATRP). The ATRP initiators were first attached to the MSN surfaces, followed by the ATRP of 2-(tert-butylamino)ethyl methacrylate (PTBAEMA). CuBr2/bipy and ascorbic acid were employed as the catalyst and reducing agent, respectively, to grow a second polymer, poly(ethylene glycol) methyl ether methacrylate (PEGMEMA). The surface structures of these fabricated nanomaterials were then analyzed using Fourier Transform Infrared (FTIR) spectroscopy. The results of Thermogravimetric Analysis (TGA) show that ATRP could provide a high surface grafting density for polymers. Dynamic Light Scattering (DLS) was conducted to investigate the pH-responsive behavior of the diblock copolymer chains on the nanoparticle surface. In addition, multifunctional pH-sensitive PTBAEMA-b-PEGMEMA-MSNs were loaded with doxycycline (Doxy) to study their capacities and long-circulation time.

Control of the water compatibility and shape recovery of polyurethane using the graft polymerization of poly(ethylene glycol) methyl ether acrylate

2020 ◽  
Vol 52 (5) ◽  
pp. 453-468
Author(s):  
Yong-Chan Chung ◽  
Ha Youn Kim ◽  
Jae Won Choi ◽  
Byoung Chul Chun
Keyword(s):  
Low Temperature ◽  
Ethylene Glycol ◽  
Methyl Ether ◽  
Shape Recovery ◽  
Graft Polymerization ◽  
Vapor Permeability ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene ◽  
Low Temperature Flexibility ◽  
Glycol Methyl Ether

Graft polymerization of poly(ethylene glycol) methyl ether acrylate (PEGA) onto polyurethane (PU) was conducted to improve its water compatibility, tensile mechanical strength, shape memory, and low-temperature flexibility properties, as well as to control its water vapor permeability (WVP). Control PUs containing free poly(PEGA) were also prepared to compare with the poly(PEGA)-grafted PUs. The water compatibility of PU notably improved due to the grafting of poly(PEGA) based on water contact angle results. The soft segment melting temperature and glass transition temperature were not changed with the increase in the PEGA content. The tensile strength of PU sharply increased due to the grafting of poly(PEGA), whereas the free poly(PEGA) in the control PUs did not cause a similar increase. The maximum strain of PU was not affected by the grafting of poly(PEGA). The shape recovery at 0°C significantly increased compared with the unmodified PU. The low-temperature flexibility of PU improved, and the WVP through the PU membrane was reduced by the grafting of poly(PEGA) onto PU.

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