Dithiocarboxylic-terminated polyamidoamine dentritic polymer as well as preparation method and use thereof
A dithiocarboxylic acid and amine dendrimer technology is applied in the field of preparation of dithiocarboxylic acid functionalized polyamide-amine dendrimer, which can solve the problems of large dosage, insufficient acid resistance, environment pollution by fly ash, etc. Achieve the effect of strong resistance to acid-base shock, good acid-base shock resistance, and low dosage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0048] Embodiment 1: Preparation of hexamethylenediamine core polyamide amine end-capped by sodium dithiocarboxylate
[0049] Slowly add 143.00 g (20%, 0.05 mol) of 0-generation polyamide amine (Hexaethylenediamine core, 0 generation, PAMAM dendrimer; The following abbreviation H-PAMAM (NH 2 ) 4 ) methanol solution, lower the temperature to 5°C, slowly add 65g NaOH (40%, 0.65 mol) aqueous solution dropwise, and control the dropping rate so that the temperature is 8 ), the yield was 90.97%.
[0050] The nuclear magnetic resonance spectrum of gained dendrimers is as follows: 13 C NMR (D 2 O): δ26.55; 28.48; 34.23; 36.53; 50.13; 53.28; 56.32; 175.89; 211.82. Its chemical formula is: (CH 2 ) 6 {N[CH 2 CH 2 CONH CH 2 CH 2 N(CSSNa) 2 ] 2} 2 .
Embodiment 2
[0051] Example 2: Preparation of butanediamine core polyamide-amine terminated by ammonium dithiocarboxylate
[0052] Slowly add 136.00 g (20%, 0.05 mol) of 0-generation polyamide-amine (Butanediamine core, 0 generation, PAMAM dendrimer ; The following abbreviation is B-PAMAM(NH 2 ) 4 ) methanol solution, cool down to 5°C, slowly add 40.93g of ammonia water (27%, 0.65 mol) dropwise, and control the dropping rate so that the temperature is 4 ) 8 ), the yield was 91.01%.
[0053] The nuclear magnetic resonance spectrum of gained dendrimers is as follows: 13 C NMR (D 2 O): δ26.98; 33.96; 35.57; 51.26; 54.32; 57.81; 176.77; 213.43. Its chemical formula is: (CH 2 ) 4 {N[CH 2 CH 2 CONH CH 2 CH 2 N(CSSNH 4 ) 2 ] 2} 2 .
Embodiment 3
[0054] Embodiment 3: Preparation of ethylenediamine core polyamide-amine end-capped by sodium dithiocarboxylate
[0055] Slowly add 129.00 g (20%, 0.05 mol) of 0-generation polyamide amine (Ethylenediamine core, 0 generation, PAMAM dendrimer; The following abbreviation E-PAMAM (NH 2 ) 4 ) methanol solution, lower the temperature to 5°C, slowly add 75.00g NaOH (40%, 0.75 mol) aqueous solution dropwise, and control the dropping rate so that the temperature is 8 ), the yield was 90.43%.
[0056] The nuclear magnetic resonance spectrum of gained dendrimers is as follows: 13 C NMR (D 2 O): δ34.02; 36.13; 50.91; 51.26; 56.54; 175.84; 212.48. Its chemical formula is: (CH 2 ) 2 {N[CH 2 CH 2 CONH CH 2 CH 2 N(CSSNa) 2 ] 2} 2 .
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 