Modified polyamide composition containing at least one phenolic compound
A phenolic compound and compound technology, applied in the field of polyamide composition, can solve problems such as the degradation of mechanical properties of polyamide matrix
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Embodiment 1
[0056] Example 1: Synthesis of polymers comprising units of formula (I)
[0057] The following were charged to a well stirred reactor: 141 g (1.5 mol) phenol and 276 g (1.5 mol) laurylaldehyde. Then 4.9 g of 50% aqueous NaOH were added as catalyst. The temperature is raised to 100-110°C to obtain a homogeneous liquid medium. The medium is kept at 100-110° C. for 14 h. Unreacted reactants and formed water were removed by vacuum distillation (1-10 mbar, 120°C). 56 g of distillate were obtained. The obtained product was a viscous orange-yellow liquid (311 g) at 80°C.
[0058] The product is in CDCl 3 pass in 1 H NMR characterization: Multiplets at 7.3 / 6.9 / 4.8 / 0.8-2.2.
Embodiment 2
[0059] Example 2: Synthesis of polymers comprising units of formula (I) and units of formula (II)
[0060] Synthesized by basic catalysis. 94 g (1 mol) of phenol, 138.2 g (0.75 mol) of lauryl aldehyde and 60.8 g (0.75 mol) of a 37% by weight HCOH solution were charged to the well-stirred reactor. Then 3.3 g of 50% aqueous NaOH were added as catalyst. The temperature is raised to 90-100° C. and the water introduced and formed is distilled continuously. The medium is kept at 90-100°C for 6h. The medium has two phases. The reaction medium is concentrated under vacuum (10 mbar) at 90°C. Some solids separated. The product obtained was a viscous orange liquid (195 g) at 80°C.
[0061] The product is in CDCl 3 pass in 1 H NMR characterization: Multiplets at 8.8 / 6.8-5.4 / 4.8 / 2.2-0.5.
Embodiment 3
[0062] Example 3: Synthesis of polymers comprising units of formula (I) and units of formula (II)
[0063] Synthesized by acid catalysis. Charge the following materials into a well stirred reactor:
[0064] - Phenol: 94g (1mol)
[0065] -1 wt% oxalic acid
[0066] The temperature was raised to 100°C. A mixture of 138.2 g (0.75 mol) of laurylaldehyde and 60.8 g (0.75 mol) of a 37% by weight solution of HCOH was then poured in over several hours. The medium was kept at 100°C for 5h. The reaction is completed by gradually raising the temperature to 150-180°C over several hours. The reaction medium is concentrated under vacuum (10 mbar) within a temperature window of 100-150°C. The product obtained was a viscous orange liquid (195 g) at 80°C.
[0067] The product is in CDCl 3 pass in 1 H NMR characterization: Multiplets at 8.8 / 6.8-5.4 / 4.8 / 2.2-0.5.
[0068] Both types of resins have a number average molecular weight (Mn) of about 2000-2200 g / mol. This corresponds to an...
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