High-Temperature Homopolymerization of Ethyl Acrylate andn-Butyl Acrylate:  Polymer Characterization

2005 ◽  
Vol 38 (18) ◽  
pp. 7619-7628 ◽  
Author(s):  
Congling Quan ◽  
Masoud Soroush ◽  
Michael C. Grady ◽  
Joan E. Hansen ◽  
William J. Simonsick
Keyword(s):  
High Temperature ◽  
Butyl Acrylate ◽  
Ethyl Acrylate ◽  
Polymer Characterization ◽  
Acrylate Polymer

scholarly journals Design, Preparation, and Evaluation of a Novel Elastomer with Bio-Based Diethyl Itaconate Aiming at High-Temperature Oil Resistance

Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1897
Author(s):  
Hui Yang ◽  
Haijun Ji ◽  
Xinxin Zhou ◽  
Weiwei Lei ◽  
Liqun Zhang ◽  
...  
Keyword(s):  
High Temperature ◽  
Butyl Acrylate ◽  
Glycidyl Methacrylate ◽  
Average Molecular Weight ◽  
Ethyl Acrylate ◽  
Number Average Molecular Weight ◽  
Elongation At Break ◽  
Oil Resistance ◽  
Monomer Ratio ◽  
Preparation And Evaluation

A novel elastomer poly(diethyl itaconate-co-butyl acrylate-co-ethyl acrylate-co-glycidyl methacrylate) (PDEBEG) was designed and synthesized by redox emulsion polymerization based on bio-based diethyl itaconate, butyl acrylate, ethyl acrylate, and glycidyl methacrylate. The PDEBEG has a number average molecular weight of more than 200,000 and the yield is up to 96%. It is easy to control the glass transition temperature of the PDEBEG, which is ranged from −25.2 to −0.8 °C, by adjusting the monomer ratio. We prepared PDEBEG/CB composites by mixing PDEBEG with carbon black N330 and studied the oil resistance of the composites. The results show that the tensile strength and the elongation at break of the composites with 10 wt% diethyl itaconate can reach up to 14.5 MPa and 305%, respectively. The mechanical properties and high-temperature oil resistance of the composites are superior to that of the commercially available acrylate rubber AR72LS.

scholarly journals Polar poly(n-butyl acrylate)-g-polyacrylonitrile elastomer with high temperature elasticity and healability as flexible electronic substrate

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Yuzhu Zheng ◽  
Deli Xu ◽  
Shiyou Tian ◽  
Manli Li ◽  
Wenwen Wang ◽  
...  
Keyword(s):  
High Temperature ◽  
Graft Copolymer ◽  
Butyl Acrylate ◽  
Uniaxial Tensile ◽  
Uniaxial Tensile Test ◽  
Self Healing ◽  
Chemical Structures ◽  
Flexible Electronic ◽  
Ag Nanowires ◽  
Cyano Groups

AbstractIn this work, graft copolymer poly (n-butyl acrylate)-g-polyacrylonitrile with poly (n-butyl acrylate) as backbones and polyacrylonitrile as side chains (PnBA-g-PAN) was synthesized by macromonomer method and emulsion polymerization. The macromonomer was synthesized by atom transfer radical polymerization and end-group modification. The chemical structures and thermal properties of macromonomer and graft copolymer were investigated by FTIR, GPC, NMR and TGA, etc. The mechanical properties of graft copolymer elastomer was also measured by uniaxial tensile test. Rheological properties at different temperature and mechanical property demonstrated that graft copolymer elastomer possessed elasticity until 180 oC because of cyclization of cyano groups. Ag nanowires@PnBA-g-PAN composite elastomer was developed, and the resulted material exhibited autonomic healing property on account of segments’ flexibility and dynamic interaction between Ag nanowires (AgNWs) and cyano groups. This is a general method for generation of elastomer with high temperature elasticity and fast self-healing. The composite elastomer has potential application in flexible electronic conductor.

The Influence of Purification of Ethyl Acrylate on the Properties of Cement Matrix

2010 ◽  
Vol 150-151 ◽  
pp. 1143-1151
Author(s):  
Chau Lee ◽  
Nian Fu Wang ◽  
Meng Xun Xiem
Keyword(s):  
Hydrogen Peroxide ◽  
Early Stage ◽  
Setting Time ◽  
Ethyl Acrylate ◽  
Cement Matrix ◽  
Strength Development ◽  
Final Setting Time ◽  
Before And After ◽  
Analysis Of Performance ◽  
Acrylate Polymer

This research mainly probes into the analysis of performance and assessment that ethyl acrylate polymer is applied to the cement matrix. The result shows that, before and after the purification, ethyl acrylate can increase the flowability of modified mortar, and with the increasing the dosage of polymer, the flowability is getting better. But if the dosage of hydrogen peroxide used to remove the residua alcohol is excessive, it is easy to cause high mortar viscosity, and that is unfavorable to the flowability. According to the setting time of the mortar under normal consistency, the result shows that the ethyl acrylate before the purification, has retarding effects on both initial and final setting time. With the increasing the dosage of polymer, it takes longer for both setting time. Besides, because hydrogen peroxide has accelerative effect, the purified ethyl acrylate can shorten the setting time of initial and final setting time. However, over dosage of hydrogen peroxide can easily lead to poor strength development in later stage. Using purified ethyl acrylate can overcome the shortcoming of lower strength of 3、7- day early stage. when hydrogen peroxide consumption is 0.5% of the total amount of acid and alcohol, the ethyl acrylate has the positive effect on improving the compressive strength. Finally, among the comprehensive assessments of the mortar testing results, EH0.5-0.1 has the significant effect of modification.

Dermal oncogenicity bioassays of acrylic acid, ethyl acrylate, and butyl acrylate

1984 ◽  
Vol 14 (2-3) ◽  
pp. 115-120 ◽  
Author(s):  
Linval R. DePass ◽  
Edward H. Fowler ◽  
Daniel R. Meckley ◽  
Carrol S. Weil
Keyword(s):  
Acrylic Acid ◽  
Butyl Acrylate ◽  
Ethyl Acrylate

Controlling the morphology of glyco-nanoparticles in water using block copolymer mixtures: the effect on cellular uptake

2015 ◽  
Vol 6 (45) ◽  
pp. 7812-7820 ◽  
Author(s):  
Aydan Dag ◽  
Hongxu Lu ◽  
Martina Stenzel
Keyword(s):  
Block Copolymer ◽  
Ethylene Glycol ◽  
Cellular Uptake ◽  
Methyl Ether ◽  
Butyl Acrylate ◽  
Diblock Copolymers ◽  
Ethyl Acrylate ◽  
Poly Ethylene Glycol ◽  
Poly Ethylene ◽  
Glycol Methyl Ether

Poly[(2-(α-d-mannosyloxy)ethyl acrylate)-block-(n-butyl acrylate)], P(ManA-b-BA), and poly[poly(ethylene glycol) methyl ether acrylate]-block-(n-butyl acrylate)], P(OEGMEA-b-BA) diblock copolymers were mixed at various ratios to generate self-assembled structures of different morphologies.

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