Branched polyacrylamide and preparation method thereof
A technology of polyacrylamide and acrylamide, which is applied in the preparation of carboxylic acid amide, chemical instruments and methods, and the preparation of organic compounds, etc., which can solve the problem of the decrease of the flow resistance of polymers, the loss of polymer solution viscosity, and the decrease of solution viscosity, etc. problems, to achieve excellent mechanical shear resistance, easy industrial production, and mild reaction conditions
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Embodiment 1
[0034] The synthesis of embodiment 1 branched polyacrylamide
[0035] (1) Synthesis of branched functional monomers
[0036] Put a 1000ml single-necked round-bottom flask into an oil bath, add 0.1mol of diethylenetriamine and 0.5mol of methyl acrylate, dimethyl sulfoxide as a solvent, and react under uniform stirring in an ice bath for 6 hours, then add 1.0mol of The transesterification reaction of ethylenediamine occurred at 80°C. After 6 hours, a diaphragm vacuum pump was used to distill under reduced pressure for 4 hours, and all dimethyl sulfoxide and excess unreacted ethylenediamine were distilled out under reduced pressure. Then add 0.5 mol of maleic anhydride in dimethyl sulfoxide solution to the flask, heat to 80° C. and react for 6 hours, then distill off the dimethyl sulfoxide under reduced pressure to obtain a white branched functional monomer sample.
[0037] (2) Synthesis of branched polyacrylamide
[0038] Acrylamide 1000g, branched functional monomer 0.05g, di...
Embodiment 2
[0039] Structural characterization of embodiment 2 branched functional monomer
[0040] figure 1 It is the hydrogen nuclear magnetic resonance spectrum figure of the branched functional monomer synthesized, and the functional monomer uses D 2 O is dissolved, and TMS is used as an internal standard. In the target molecule, each hydrogen atom corresponds to the following:
[0041] The proton displacement δ is: methyl group (3.250), methylene group adjacent to amide group (around 3.407 and 3.628), methylene group adjacent to tertiary amine (2.773), CH 2 =CH double bond (around 5.885 and 6.567).
[0042] From the analysis of the spectrogram data, it can be seen that the product is a branched functional monomer.
Embodiment 3
[0043] The structural characterization of embodiment 3 branched polyacrylamide
[0044] figure 2 It is the infrared spectrum of branched polyacrylamide, and it is known from the analysis of the spectrum: 3430 cm -1 is the hydroxyl stretching vibration peak, 2920 cm -1 The stretching vibration peak of methylene, 1650cm -1 is the stretching vibration peak of amide and secondary amide; 1450 cm -1 is the hydrocarbon bending vibration peak; 1350 cm -1 is the bending vibration absorption peak generated by the hydroxyl group.
[0045] Various functional groups of the polymer were analyzed by infrared spectroscopy, and the results showed that the synthesized polymer had the characteristics of branched polyacrylamide.
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