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One of the concerns for biolubricants is the improvement of their oxidation resistance. In this paper the oxidative behavior of seven different types of biobased lubricants basestocks is examined. The aim was to study their relative oxidation stability and also to investigate their response to various antioxidants. The renewable lubricants were treated with four antioxidant additives at a concentration of 0.5% wt. and a comparative assessments of the latters' effectiveness in suppressing the oxidation rate was carried out. Alterations in the acid value were examined as well as relative changes of the oxidized samples by FTIR spectroscopy. The oxidation stability was assessed by employing a Rapid Small Scale Oxidation Test (RSSOT) apparatus according to the accelerated oxidation stability standard method ASTM D7545/EN16091. RSSOT is a relatively new method and thus the behaviour of biobased lubricants and antioxidant agents in this accelerated method has not been thoroughly examined.

This study investigates the effectiveness of seven phenolic compounds, including pyrogallol (PY), butylated hydroxytoluene (BHT), 2,5-di-tert-butylhydroquinone (DTBHQ), 4-tert-Butylcatechol (TBC), 2,5-bis(dimethylaminomethyl) hydroquinone, 2,5-bis(piperidinomethyl) hydroquinone and 2,5-bis(morpholinomethyl) hydroquinone on the oxidation stability of sunflower and soybean oil methyl esters. The seven phenolic compounds were dissolved in the base fuels at the same concentration levels, i.e., 200, 600, 800, 1000 and 1200 ppm. The oxidation stability measurements were carried out by employing a Rancimat accelerated oxidation unit according to EN 14214. Additionally, the antioxidant activity of the above mentioned compounds was also determined in a RSSOT apparatus (Rapid Small Scale Oxidation Test) according to ASTM D7545.

In this study, the transesterification process of 4 different vegetable oils (sunflower, rapeseed, olive oil and used frying oil) took place utilizing ethanol, in order to characterize the ethyl esters and their blends with diesel fuel obtained as fuels for internal combustion engines. All ethyl esters were synthesized using calcium ethoxide as a heterogeneous solid base catalyst. The ester preparation involved a two-step transesterification reaction, followed by purification. The effects of the mass ratio of catalyst to oil, the molar ratio of ethanol to oil, and the reaction temperature were studied on conversion of sunflower oil to optimize the reaction conditions in both stages. The rest of the vegetable oils were converted to ethyl esters under optimum reaction parameters. The optimal conditions for first stage transesterification were an ethanol/oil molar ratio of 12:1, catalyst amount (3.5%), and 80 °C temperature, whereas the maximum yield of ethyl esters reached 80.5%.