scholarly journals Investigation of the paint curing mechanism

2021 ◽  
Vol 57 ◽  
pp. 667-671
Author(s):  
Alexandr Sukhodolya ◽  
Tatiana Cherepnina ◽  
Irina Kostyuk ◽  
Viktor Klimenko
Keyword(s):  
1971 ◽  
Vol 9 (8) ◽  
pp. 2283-2289 ◽  
Author(s):  
Vladimir Ivanovich Kurachenkov ◽  
Leonid Andreevich Igonin

Author(s):  
Zuowei Chen ◽  
Liquan Wang ◽  
Jiaping Lin ◽  
Lei Du

High-temperature phthalonitrile resins have a wide range of applications, and understanding their curing mechanism is of great importance for academic research and engineering applications. However, the actual curing mechanism is...


2013 ◽  
Vol 5 (4) ◽  
pp. 479 ◽  
Author(s):  
In-Su Lee ◽  
Sung-Ae Son ◽  
Bock Hur ◽  
Yong-Hoon Kwon ◽  
Jeong-Kil Park

2017 ◽  
Vol 115 ◽  
pp. 186-196 ◽  
Author(s):  
Muhammad Irfan ◽  
Abid Riaz Ahmed ◽  
Karl Kolter ◽  
Roland Bodmeier ◽  
Andriy Dashevskiy

2020 ◽  
Vol 165 ◽  
pp. 03026
Author(s):  
Zhang Yuping ◽  
Wang Zilong ◽  
Zheng Yifeng

The curing mechanism and research status of inorganic soil solidifying agent, organic soil solidifying agent, ionic soil solidifying agent, bioenzyme soil solidifying agent and compound soil solidifying agent were reviewed, and the application of soil solidifying agent in water conservancy and road engineering was introduced. Several suggestions are put forward for the problems existing in soil stabilizer.


2008 ◽  
Vol 62 (10) ◽  
pp. 1129-1136 ◽  
Author(s):  
Liang Li ◽  
Qili Wu ◽  
Shanjun Li ◽  
Peiyi Wu

In this work, the isothermal curing process of diglycidyl ether of bisphenol A(DGEBA) cured with 4,4′-diaminodiphenylmethane (DDM) was monitored in situ by mid-infrared (MIR) and near-infrared (NIR) spectroscopy. With the help of generalized two-dimensional (2D) correlation analysis, the results obtained showed that, during curing, the change of amine and epoxy groups was simultaneous, taking place prior to the change of hydroxyl groups, followed by the change of CH2/CH groups, resulting from the ring-opening reaction of epoxy groups. In addition, 2D MIR×NIR hetero-spectral correlation analysis and second-derivative analysis were also employed, by means of which direct evidence of the curing mechanism could be obtained and obscure NIR band assignments in the overlapped CH combination region could be made.


2012 ◽  
Vol 20 (8) ◽  
pp. 673-682
Author(s):  
Ying Yu ◽  
Min Zhi Rong ◽  
Ming Qiu Zhang

Nano-sized SiO2 particles grafted with hyperbranched aromatic polyamide were employed as fillers for fabricating epoxy based composites. The hyperbranched aromatic polyamide was selected because its terminal amine groups could take part in the curing reaction of epoxy resin and covalently connect silica nanoparticles with the matrix. The experimental results proved the occurrence of this reaction, and indicated that the presence of the grafted SiO2 in epoxy does not change the overall curing mechanism of epoxy. In comparison to the composites filled with untreated nano-SiO2 particles, the composites with the grafted nano-SiO2 exhibited significantly improved sliding wear resistance and reduced frictional coefficient owing to the strong filler/matrix interfacial bonding. Moreover, hyperbranched aromatic polyamide grafted nano-SiO2 was more effective to enhance tribological properties of epoxy than linear polymers grafted versions.


2002 ◽  
Vol 10 (3) ◽  
pp. 237-248 ◽  
Author(s):  
Baochun Guo ◽  
Weiwen Fu ◽  
Demin Jia ◽  
Qinghua Qiu ◽  
Lei Wang

The cure characteristics of bisphenol A dicyanate-novolac epoxy resin blends were investigated by gel time determination and dynamic DSC. The effects of the proportion on the structures of cured blends were investigated by FTIR. In situ FTIR was utilized to study the curing mechanism and curing kinetics. The results indicated the distinct catalytic effects of the novolac epoxy resin on the curing of bisphenol A dicyanate. Due to considerable amounts of unepoxidized phenol present in the novolac epoxy resin, the reactions between phenol and cyanate disturbed the formation of the co-reaction products. The curing reactions of the blends indicated by in situ FTIR did not follow the Bauer mechanism totally. A composite mechanism of triazine-epoxy insertion and epoxy-cyanate reaction indwells in the systems. The authors suggest that most of the oxazolidinone present in the blends is formed by isomerization of oxazoline rather than by insertion of epoxy into isocyanurate. The amount of epoxy resin in the blend did not alter the curing mechanism, but had significant effects on the kinetic behaviour.


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