Home About us Contact
|
Home About us Contact | ||
|
|
||
Ethyleneglycol Dimethacrylate (ethyleneglycol + dimethacrylate)
Selected AbstractsSynthesis, characterization, and antimicrobial properties of novel quaternary amine methacrylate copolymersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008Supriya Punyani Abstract A novel amine methacrylate monomer trimethylolpropane trimethacrylate,piperazine,ethyleneglycol dimethacrylate (TMPTMA-PPZ-EGDMA) was synthesized by amination of trimethylolpropane trimethacrylate (TMPTMA) with excess of piperazine (PPZ) followed by reaction with ethyleneglycol dimethacrylate (EGDMA). Copolymerization of TMPTMA-PPZ-EGDMA with 2-hydroxyethyl methacrylate (HEMA) was carried out by free radical polymerization using ammonium persulfate (APS) and N,N,N,,N,-tetramethyl ethylenediamine (TEMED) as a redox initiator. The copolymers obtained were then quaternized with 1-iodooctane. The monomers were characterized by FTIR and 1H NMR spectral studies. The molecular weights and polydispersity values of the monomers were determined with gel permeation chromatography. Quaternized copolymers containing more than 20% amine methacrylate monomer showed microporosity in the range of 9.9,10.4 ,m. The antibacterial activity of the quaternized copolymers against Escherichia coli and Staphylococcus aureus was studied using UV,vis spectrophotometer and scanning electron microscopy. Quaternized copolymers showed broad-spectrum contact-killing antibacterial properties without releasing any active agent as checked by iodide selective ion meter. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Biocompatibility investigation and urea removal from blood by urease-immobilized HEMA incorporated poly(ethyleneglycol dimethacrylate) microbeadsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2003F. Ayhan Abstract The biocompatibility of modified and urease-immobilized poly(ethyleneglycol dimethacrylate/2-hydroxyethylmetacrylate) [poly(EGDMA/HEMA)] microbeads was tested through blood compatibility tests. Twelve percent HEMA incorporated nonporous particles of 105,125 ,m were used in the research. Hydroxyl groups on microbeads were chemically modified by following a three-step procedure that is composed of activation, spacer-arm incorporation (hexamethylene diamine) and, finally, glutaraldehyde bounding. Enzyme urease was immobilized on microbead surfaces, and adsorption of blood proteins in serum and plasma, blood coagulation time, and leukocyte and platelet adhesion were tested. Incubation of 1.5 cc of biological fluid with 100 mg of urease-immobilized poly(EGDMA/HEMA) microbeads at room temperature shows that protein adsorption on surfaces occurs, but protein content after treatment was in the range of healthy people. Adsorbed albumin and total globulin amounts per gram of microbeads is much greater than fibrinogen. Immobilization of urease reduced the protein adsorption and blood coagulation times compared with those of modified microbeads. Prothrombin time (PT) was not altered much, whereas poly(EGDMA/HEMA) microbeads induced a significant increase of activated partial thromboplastin time (APTT). The platelet and leukocyte adhesion slightly increased with the modification of poly(EGDMA/HEMA) and decreased with the introduction of urease. When blood samples were treated with urease-immobilized microbeads, BUN values of patients were lowered to almost acceptable amounts. © 2002 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 64B: 13,18, 2003 [source] Synthesis and properties of methacrylate-based networked polymers having ionic liquid structuresJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 20 2010Kozo Matsumoto Abstract Methacrylate-based networked polymers having ionic liquid structures were prepared by radical copolymerization of methyl methacrylate (MMA) with multifunctional crosslinkers: ethyleneglycol dimethacrylate (EGDMA), trimethylolpropane trimethacrylate (TMPTMA), or triethyleneglycol dimethacrylate (TEGDMA), in the presence of 1-ethyl-3-methylethyl-1-imidazolium bis(trifluoromethane)sulfonyl imide (EMImTFSI). The fundamental physical properties of several film samples prepared by varying the monomer composition and ionic liquid content were investigated. The obtained materials became turbid with increasing crosslinker content and ionic liquid content. Their ionic conductivity increased with increasing ionic liquid content, while it was almost independent of the crosslinker content. EGDMA-derived materials and TMPTMA-derived materials showed higher ionic conductivity than TEGDMA-derived materials. TMPTMA-derived materials showed higher thermal stability than EGDMA or TEGDMA-derived materials. EGDMA and TMPTMA-derived materials were stiffer than the TEGDMA-derived materials. The elastic modulus of the film samples increased but the film became more brittle with the increase of crosslinker content. Scanning electron microscopy and atomic force microscopy observation revealed that phase separation of networked polymers and ionic liquid occurred in the highly crosslinked samples, and the phase separation structures became larger in scale with the increase of crosslinking density. This phase separation was considered to have a strong effect on the mechanical properties of the film samples. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 [source] Synthesis of glyco-microspheres via a thiol-ene coupling reactionJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 20 2009Wenfang Gu Thiol-ene click chemistry was employed to form microspheres with sugar groups with high bioactivity and efficient binding of Concanavalin A. Two systems were investigated , a microsphere prepared from ethyleneglycol dimethacrylate, which contained excess vinyl functionalities as a natural result of the preparation process, and the commercially available Wang microsphere, which had to be modified with acryloylchloride to generate pendant vinyl groups. [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.] [source] Influence of the cross-linking density on the main dielectric relaxation of poly(methyl acrylate) networksPOLYMER ENGINEERING & SCIENCE, Issue 10 2005J.M. Meseguer Dueñas A series of polymer networks of varying cross-linking density was prepared by copolymerization of methyl acrylate and ethyleneglycol dimethacrylate. The aim of this work is to study the influence of cross-linking on the conformational mobility of the polymer chains using dielectric relaxation spectroscopy (DRS) in the temperature range of the main dielectric relaxation. As expected, the temperature range in which glass transition takes place became wider with increasing crosslinking density. DRS results were analyzed using the Havriliak-Negami equation. Master Cole-Cole arcs could be drawn for all the networks. The arcs become more symmetric as cross-linking density increases, as a consequence of the different effect of cross-links on large and small scale mobility. The conformational mobility that produces the main relaxation is drastically reduced when the cross-linking density increases what reduces the relaxation strength, but it also gives a qualitative change of behavior, as shown by the temperature dependence of the relaxation strength. In the loosely cross-linked networks the relaxation strength decreases monotonously as temperature increases, as in the main dielectric relaxation of linear polymers. Nevertheless, in highly cross-linked networks the curve of relaxation strength against temperature presents a maximum. POLYM. ENG. SCI., 45:1336,1342, 2005. © 2005 Society of Plastics Engineers [source] | ||||||||||