Preparation method of phenolic emulsifier, emulsified bitumen and its application
A technology of emulsified asphalt and emulsifier, which is applied in the preparation of organic compounds, chemical instruments and methods, and the preparation of amino hydroxyl compounds. simple effect
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Embodiment 1
[0036] Get 10.13g (0.1mol) of diethylenetriamine and join in the reactor that 10ml of absolute ethanol and 15ml of dioxane are housed, slowly add 8.3g (0.1mol) of 37% formaldehyde solution after heating up to 10°C . React at 4 room temperature for 2h, then cool to 0°C to obtain an intermediate product, then add 20.6g (0.1mol) of octylphenol, raise the temperature to 80°C for 5h under reflux. The solvent was distilled off under reduced pressure to obtain a yellow viscous liquid, which was the final product, and the yield obtained by liquid chromatography was 90.2%. Save it for asphalt experiments.
[0037] The intermediate product was separated and purified by column 1 H-NMR and IR detection, the results are as follows:
[0038] 1 H-NMR (400MHz, CDCl 3 , δ, ppm): δ5.23(s, 2H), 2.81-2.60(m, 3*CH 2 , 6H), 2.4(m, 3H), 1.53(t, J=8.4Hz J=16.0, J=7.6Hz, 2H);
[0039] IR (neat): 3323cm -1 , 3213cm -1 , 1651cm -1 , 1180cm -1 , 1123cm -1 .
[0040] The final product is sepa...
Embodiment 2
[0049] Take 21.94g (0.15mol) of triethylenetetramine and add it into a reactor filled with 50ml of toluene, and slowly add 10.6g (0.1mol) of benzaldehyde solution after raising the temperature to 40°C. After reacting at 40°C for 5h, cool to 0°C to obtain an intermediate product, then add 23.4g (0.1mol) of decylphenol, raise the temperature to 120°C for 5h under reflux, and the yield obtained by liquid chromatography is 87.9% . The solvent was distilled off under reduced pressure to obtain a yellow viscous liquid, which was the final product, which was reserved for asphalt experiment.
[0050] The intermediate product was separated and purified by column 1 H-NMR and IR detection, the results are as follows:
[0051] 1 H-NMR (400MHz, CDCl 3 , δ, ppm) δ8.11(s, 1H), 7.62(d, J=7.6Hz, 2H), 7.29(t, J=7.6, J=15.6, J=8.0Hz, 3H), 3.67(t, J=15.2, J=7.6Hz, 2H), 2.85-2.57(m, 5*CH 2 , 10H), 2.35(m, 4H);
[0052] IR (neat): 3321cm -1 , 3217cm -1 , 1648cm -1 , 1596cm -1 , 1511cm -...
Embodiment 3
[0061] Take 17.5g (0.12mol) of triethylenetetramine and add it into a reactor filled with 50ml of water, and slowly add 12.45g of 37%-40% (0.15mol) formaldehyde solution after raising the temperature to 30°C. After reacting at 30°C for 2h, cool to 25°C to obtain an intermediate product, then add 26.2g (0.1mol) of dodecylphenol, then increase the temperature to 110°C for reflux reaction for 7h, the yield obtained by liquid chromatography was 96.5%. The solvent was distilled off under reduced pressure to obtain a yellow viscous liquid, which was the final product, which was reserved for asphalt experiment.
[0062] The intermediate product was separated and purified by column 1 H-NMR and IR detection, the results are as follows:
[0063] 1 H-NMR (400MHz, CDCl 3 , δ, ppm) δ5.32(s, 2H), 2.82-2.56(m, 5*CH 2 , 10H), 2.38(m, 4H), 1.53(t, J=7.6Hz J=14.8, J=7.2Hz, 2H);
[0064] IR (neat): 3321cm -1 , 3207cm -1 , 1644cm -1 , 1185cm -1 , 1118cm -1 .
[0065] The final product...
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