N-methyl, N-carboxymethyl dithio amidocarbonic acid chelating resin and its preparing method
A technology of carboxymethyldithiocarbamic acid and carboxymethylthiocarbamic acid, which is applied in the field of chelating resin and its synthesis, can solve the problem that the number of resin functional groups needs to be increased, and the selectivity has not been further studied and prepared. Complicated conditions and other issues, to achieve the effect of stable performance, easy synthesis, and wide application prospects
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[0022] Example 1
[0023] (a) Suspension polymerization.
[0024] Styrene monomer is added to a certain amount of dilute sodium hydroxide solution or the monomer is directly filtered through a resin column containing a strong base anion exchange resin to remove the polymerization inhibitor.
[0025] In a 1000 mL beaker, add 210 g of styrene, 26 g of divinylbenzene, and 140 g of liquid paraffin, and stir well before use.
[0026] In a 1000mL three-necked flask, add 600g of distilled water and raise the temperature to 40°C, then add 6g of gelatin, stir to completely dissolve, and at the same time warm up to 50°C, add 2mL of methine blue, stir evenly, add the above styrene, divinylbenzene and liquid For the wax mixture, add 4.0g initiator benzoyl peroxide; adjust the appropriate stirring speed to make the oil bead size suitable, gradually increase the temperature to 80℃ at a speed of 1℃ / 6min, keep it for 4h, and then gradually increase the temperature to 85℃ Insulate for 3h, 90°C for...
Example Embodiment
[0035] Example 2
[0036] The synthesis steps of another embodiment of the present invention are as follows:
[0037] (a) Use styrene as monomer, divinylbenzene as crosslinking agent, liquid wax as porogen, magnesium carbonate as dispersant, benzoyl peroxide as initiator, suspension polymerization method, low synthesis Cross-linked macroporous polystyrene-divinylbenzene copolymer, using steam distillation or ethanol extraction as a solvent to remove the residual porogen in the resin pores, and then air drying to obtain low cross-linked macroporous polystyrene -Divinylbenzene resin, that is, white balls.
[0038] The amount of crosslinking agent is 4% of the total amount of monomer and crosslinking agent, the amount of porogen is 40% of the weight of monomer, and the degree of crosslinking of low-crosslinking macroporous polystyrene is 2%.
[0039] (b) Soak the white ball in chloromethyl ether 4 times its weight, add 20% of the weight of the white ball zinc chloride as a catalyst, ...
Example Embodiment
[0041] Example 3
[0042] The specific steps are the same as in Example 2, except that the amount of crosslinking agent in step (a) is 12% of the total amount of monomer and crosslinking agent, and the amount of porogen is 60% of the weight of monomer, low crosslinking macroporous polystyrene The degree of crosslinking is 6%. In step (b), the chloromethylation reaction is carried out at a temperature of 45°C. The functional group content of the prepared N-methyl, N-carboxymethyl dithiocarbamic acid chelating resin is 2.19 mmol / g.
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