Properties of Polyurethane Coatings Based on Linseed Oil Phosphate Ester Polyol

2018 ◽  
Vol 6 (7) ◽  
pp. 737-745 ◽  
Author(s):  
A. Abolins ◽  
V. Yakushin and D. Vilsone
2018 ◽  
Vol 43 (1) ◽  
pp. 92-100 ◽  
Author(s):  
Vladimir Yakushin ◽  
Arnis Abolins ◽  
Dzintra Vilsone ◽  
Irina Sevastyanova

2011 ◽  
Vol 686 ◽  
pp. 528-532 ◽  
Author(s):  
Jian Bing Chen ◽  
Qiang Guo ◽  
Jin Liang Sun ◽  
Xian Li Shao ◽  
Zhi Jun Nie

The waterborne polyurethane coatings modified by linseed oil were prepared in a method of ammonolysis. The influence of reaction time and temperature of the linseed oil ammonolysis on structure and properties of the waterborne polyurethane coatings was investigated and discussed. It has been shown in this work that the preferred ammonolysis temperature would be 102~118°C, the reaction time could be about 80 min, and structure of the modified waterborne polyurethane was analysed by FTIR. The touch-dry time of the modified waterborne polyurethane with drier would be shorter than that of non-modified waterborne polyurethane, normally in a week, and the stability of the modified waterborne polyurethane coating in water could stand for 3 months under room temperature. The TGA results of the coatings showed that the weight loss started at about 294°C.


2019 ◽  
Author(s):  
James Ewen ◽  
Carlos Ayestaran Latorre ◽  
Arash Khajeh ◽  
Joshua Moore ◽  
Joseph Remias ◽  
...  

<p>Phosphate esters have a wide range of industrial applications, for example in tribology where they are used as vapour phase lubricants and antiwear additives. To rationally design phosphate esters with improved tribological performance, an atomic-level understanding of their film formation mechanisms is required. One important aspect is the thermal decomposition of phosphate esters on steel surfaces, since this initiates film formation. In this study, ReaxFF molecular dynamics simulations are used to study the thermal decomposition of phosphate esters with different substituents on several ferrous surfaces. On Fe<sub>3</sub>O<sub>4</sub>(001) and α-Fe(110), chemisorption interactions between the phosphate esters and the surfaces occur even at room temperature, and the number of molecule-surface bonds increases as the temperature is increased from 300 to 1000 K. Conversely, on hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>, most of the molecules are physisorbed, even at high temperature. Thermal decomposition rates were much higher on Fe<sub>3</sub>O<sub>4</sub>(001) and particularly α-Fe(110) compared to hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>. This suggests that water passivates ferrous surfaces and inhibits phosphate ester chemisorption, decomposition, and ultimately film formation. On Fe<sub>3</sub>O<sub>4</sub>(001), thermal decomposition proceeds mainly through C-O cleavage (to form surface alkyl and aryl groups) and C-H cleavage (to form surface hydroxyls). The onset temperature for C-O cleavage on Fe<sub>3</sub>O<sub>4</sub>(001) increases in the order: tertiary alkyl < secondary alkyl < primary linear alkyl ≈ primary branched alkyl < aryl. This order is in agreement with experimental observations for the thermal stability of antiwear additives with similar substituents. The results highlight surface and substituent effects on the thermal decomposition of phosphate esters which should be helpful for the design of new molecules with improved performance.</p>


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