Lubricant Composition
a technology of lubricant composition and composition, which is applied in the field of lubricant composition, can solve the problems of compound being incapable of satisfying the recently increased demand for stabilizing properties, deteriorating operability at a low temperature, and becoming inferior, and achieve excellent stabilizing properties, excellent rust prevention properties, and excellent stability
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example 1
[0122]10.1 g of 1,4-bis(4-aminophenoxy)benzene was dissolved in a mixed solvent of 100 ml of pyridine and 100 ml of AK-225 (mixture of CF3CF2CHCl2 and CClF2CF3CHClF), followed by slow dropping of 209.0 g of acid fluoride (n=11) at a room temperature, and by stirring overnight under a condition ranging from the room temperature to 40° C.
[0123]50 ml of methanol was added and stirred, followed by subsequent neutralization with a saturated NaHCO3 water solution.
[0124]The reaction product was extracted by AK-225 (mixture of CF3CF2CHCl2 and CClF2CF3CHClF), and washed by a saturated NaCl water solution. The AK-225 was distilledly removed by an evaporator, to obtain a light yellow and highly viscous liquid (C-2).
[0125]With analysis of a chemical structure of C-2 by NMR, it was revealed that it had a structure of Formula (I), and n=11, m=1, and k=3. In view of the starting materials of synthesis, Y is supposed to be 0 (oxygen atom).
[0126]10 g of the obtained light yellow and highly viscous l...
example 2
[0132]10.1 g of 1,4-bis(4-aminophenoxy)benzene was dissolved in a mixed solvent of 100 ml of pyridine and 100 ml of AK-225, followed by slow dropping of 101.0 g of acid fluoride (n=40) at a room temperature, and by stirring overnight under a condition ranging from the room temperature to 40° C.
[0133]50 ml of methanol was added and stirred, followed by subsequent neutralization with a saturated NaHCO3 water solution.
[0134]The reaction product was extracted by AK-225, and washed by a saturated NaCl water solution. The AK-225 was distilledly removed by an evaporator, to obtain a light yellow and highly viscous liquid (C-3).
[0135]With analysis of a chemical structure of C-3 by NMR, it was revealed that it had a structure of Formula (I), and n=40, m=1, and k=3. In view of the starting materials of synthesis, Y is supposed to be 0 (oxygen atom).
[0136]1 g of the obtained light yellow and highly viscous liquid (C-3) was added into 199 g of the base oil (A-1) used in Example 1, followed by s...
example 3
[0138]3 g of bis[4-(aminophenoxy)phenyl]sulfone was dissolved in a mixed solvent of 100 ml of pyridine and 100 ml of AK-225, followed by slow dropping of 209.0 g of acid fluoride (n=11) at a room temperature, and by stirring overnight under a condition ranging from the room temperature to 40° C.
[0139]50 ml of methanol was added and stirred, followed by subsequent neutralization with a saturated NaHCO3 water solution.
[0140]The reaction product was extracted by AK-225, and washed by a saturated NaCl water solution. The AK-225 was distilledly removed by an evaporator, to obtain a light yellow and highly viscous liquid (C-4).
[0141]With analysis of a chemical structure of C-4 by NMR, it was revealed that it had a structure of Formula (I), and n=11, m=2, and k=3. In view of the starting materials of synthesis, Y's are supposed to be an SO2 group and O (oxygen atom).
[0142]6 g of the obtained light yellow and highly viscous liquid (C-4) was added into 194 g of the base oil (A-1) used in Exa...
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