POLYMERIZATION INHIBITOR FOR N-VINYL PYRROLIDONE MONOMER AND USE THEREOF

Abstract

Disclosed is a polymerization inhibitor of N-vinyl pyrrolidone monomers and use thereof. The polymerization inhibitor is selected from an inorganic weak acid potassium salt and/or an organic acid potassium salt. The polymerization inhibitor is added to N-vinyl pyrrolidone monomers, and is sealed and preserved under the protection of inert gas, wherein the addition amount of the polymerization inhibitor is 0.005-0.2% by mass with respect to the mass of the N-vinyl pyrrolidone monomers. Directly adding the polymerization inhibitor into the N-vinyl pyrrolidone monomers in proportion can inhibit the self-polymerization of the N-vinyl pyrrolidone monomers, and hence extend the shelf life. The chromaticity and toxicity of the monomers can be reduced to a great extent. The polymerization inhibitor can be used directly during solution polymerization without being removed, and does not affect the chromaticity of a polymerization solution.

Claims

1. (canceled)

2. (canceled)

3. A method comprising: using a polymerization inhibitor in preservation or transportation of N-vinyl pyrrolidone monomers, wherein the polymerization inhibitor is selected from inorganic weak acid potassium salt and/or organic acid potassium salt.

4. The method according to claim 3, wherein a polymerization inhibitor is added into the N-vinyl pyrrolidone monomers, and then seal and preservation are carried out under the protection of inert gas.

5. The method according to claim 4, wherein the addition amount of the polymerization inhibitor is 0.005-0.2% by mass with respect to the mass of the N-vinyl pyrrolidone monomers.

6. The method according to claim 5, wherein the addition amount of the polymerization inhibitor is 0.01-0.15% by mass with respect to the mass of the N-vinyl pyrrolidone monomers.

7. The method according to claim 4, wherein the preservation temperature is 120 C. or less.

8. The method according to claim 7, wherein the preservation temperature is 15-40 C.

9. The method according to claim 3, wherein the polymerization inhibitor is one or more selected from the group consisting of potassium carbonate, potassium acetate, potassium propionate, potassium oxalate, potassium citrate and potassium tartrate.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0016] The technical solution of the present invention will be clearly and completely described hereinafter with reference to the examples of the present invention. Obviously, the described examples are only a part of the examples of the present invention, but not all of the examples.

[0017] Examples 1 to 7 are used to illustrate the inhibitor of the N-vinyl pyrrolidone monomers of the present invention and use thereof.

EXAMPLE 1

[0018] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.100.002 g of potassium carbonate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 120 C. oven. Take a bottle out every 10 minutes from the oven to test the self-polymerization. Self-polymer was detected at the 90th minute but the sample was colorless and transparent liquid. The specific results were shown in Table 1.

EXAMPLE 2

[0019] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.02500.0005 g of potassium acetate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 120 C. oven. Take a bottle out every 20 minutes from the oven to test the self-polymerization. Self-polymer was detected at the 300th minute but the sample was still colorless and transparent liquid. The specific results were shown in Table 1.

EXAMPLE 3

[0020] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.02500.0005 g of potassium acetate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 40 C. oven. Take a bottle out every 10 days from the oven to test the self-polymerization. Self-polymer was detected at the 190th day but the sample was still light yellow transparent liquid. The specific results were shown in Table 2.

EXAMPLE 4

[0021] A group of brown reagent bottles with the same capacity were filled with 2000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.100.005 g of potassium propionate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 40 C. oven. Take out a bottle every 10 days from the oven to test the self-polymerization. Self-polymer was detected at the 150th day but the sample was still colorless and transparent liquid with a chromaticity <50 Haze. The specific results were shown in Table 2.

EXAMPLE 5

[0022] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.02500.0005 g of potassium acetate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 25 C. stability test box (simulating room temperature). Take out a bottle every 30 days (one month) from the box to test the self-polymerization. Self-polymerization was detected at the 10th month (not detected at the 9th month), but the sample was light yellow transparent liquid with a chromaticity of 50 Haze. The specific results were shown in Table 3.

[0023] EXAMPLE 6

[0024] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly-produced N-vinyl pyrrolidone monomers respectively, 0.0500.005 g of potassium acetate was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 25 C. stability test box (simulating room temperature). Take a bottle out every 30 days (one month) from the box to test the self-polymerization. Self-polymer was detected at the 10th month, but the sample was a light yellow transparent liquid with a chromaticity of 125 Haze. The specific results were shown in Table 3.

EXAMPLE 7

[0025] A group of brown reagent bottles with the same capacity were filled with 2000.5 g of newly-produced N-vinyl pyrrolidone monomers respectively, 0.0500.005 g of potassium acetate and 0.0500.005g of potassium citrate were respectively added at the same time, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 25 C. stability test box (simulating room temperature). Take a bottle out every 30 days (one month) from the box to test the self-polymerization. Self-polymer was detected at the 10th month, but the sample was a light yellow transparent liquid with a chromaticity of 100 Haze. The specific results were shown in Table 3.

CONTROL EXAMPLE 1

[0026] Taking the same experimental condition as in Example 1, a group of brown reagent bottles were filled with pure N-vinyl pyrrolidone, then were sealed after air was removed by introducing nitrogen, which were used as a blank control group in which the self-polymerization was detected. In the blank control group, the self-polymerization was detected at the 50th minute, and the sample with self-polymer was colorless and transparent liquid. The specific results were shown in Table 1.

CONTROL EXAMPLE 2

[0027] Taking the same experimental conditions as in Example 3, a group of brown reagent bottles were filled with pure N-vinyl pyrrolidone, and then were sealed after air was removed by introducing nitrogen, On the 10th day of heating test, self-polymerization has taken place, but the viscosity was relatively small, and the sample was colorless liquid.

[0028] The specific results were shown in Table 2.

EXAMPLE 3

[0029] A group of brown reagent bottles with the same capacity were filled with 100 0.5 g of newly produced N-vinyl pyrrolidone monomers respectively, then 0.100.01 g of sodium hydroxide was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a 40 C. oven. Take a bottle out every 10 days from the oven to test the self-polymerization. Self-polymer was detected at the 50th day, a sample of which is yellow transparent liquid with a chromaticity of 400 Haze. The specific results were shown in Table 2.

CONTROL EXAMPLE 4

[0030] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly produced N-vinyl pyrrolidone monomers respectively, 0.100.01 g of sodium hydroxide was respectively added, and then the bottles were sealed after air was removed by introducing bubbled nitrogen. These bottles were shaken evenly and placed in a stability test box at 25 C. Take a bottle out every 30 days from the oven to test the self-polymerization. Self-polymer was detected at the 7th month (180210 days) but the sample was yellow transparent liquid with a chromaticity of 250 Haze. The specific results were shown in Table 3.

CONTROL EXAMPLE 5

[0031] A group of brown reagent bottles with the same capacity were filled with 1000.5 g of newly-produced N-vinyl pyrrolidone monomers respectively, bubbled nitrogen was introduced to remove air, and 0.38 mL 26.5% ammonia water was added respectively, then the bottles were sealed. These bottles were shaken evenly and placed in a stability test box at 25 C. Take a bottle out every 30 days from the oven to test the self-polymerization. Self-polymer was detected at the 4th month (90120 days), but the sample was colorless and transparent liquid with a chromaticity <50 Haze. The specific results were shown in Table 3.

[0032] Usage Example

[0033] The N-vinyl pyrrolidone monomers (from Example 5, that is added with 0.025% potassium acetate and preserved at room temperature for 10 months) were used to synthesiz PVP according to the current PVP K30 polymerization process with a solvent of purified water. After polymerization, a K value of 31.5 was detected, and the polymerization solution was colorless and transparent.

[0034] The following tables 1, 2 and 3 record the corresponding data of examples and control examples at 120 C., 40 C. and 25 C., respectively.

TABLE-US-00001 TABLE 1 Time of self- Polymerization polymerization Items inhibitor Dosage detected Color Example 1 Potassium 0.1% The 90th minute colorless carbonate Example 2 Potassium 0.025% The 300th minute colorless acetate Control The 50th minute colorless example 1

TABLE-US-00002 TABLE 2 Time of self- Polymerization polymerization Monomer Items inhibitor Dosage detected chromaticity Example 3 Potassium 0.025% The 190th day 50 Haze acetate Example 4 Potassium 0.1% The 150th day <50 Haze propionate Control The 10th day <50 Haze example 2 Control Sodium 0.1% The 50th day 400 Haze example 3 hydroxide

TABLE-US-00003 TABLE 3 Time of self- Polymerization polymerization Monomer Items inhibitor Dosage detected chromaticity Example 5 Potassium 0.025% The 10th month 50 Haze acetate Example 6 Potassium 0.05% The 10th month 125 Haze acetate Example 7 Potassium 0.05% + The 10th month 100 Haze acetate + 0.05% potassium citrate Control Sodium 0.1% The 7th month 250 Haze example 4 hydroxide Control Ammonia 0.1% The 4th month <50 Haze example 5

[0035] From the data in Tables 1 to 3, it can be seen that the polymerization inhibitor of the present invention can effectively inhibit the self-polymerization of N-vinyl pyrrolidone monomers, with less do dosage, high efficiency, wide temperature range of polymerization inhibition effect, and better effect within the preferred condition range. In addition, as can be seen from the usage example, the polymerization inhibitor does not substantially affect the color of the N-vinyl pyrrolidone monomers, the polymerization rate during solution polymerization, and the chromaticity of the polymerization solution after use.

[0036] Examples of the present invention have been described hereinbefore, and the above description is exemplary, not exhaustive, and the present invention is not limited to the disclosed examples. Many modifications and variations will be apparent to those ordinary skilled in the art without departing from the scope and spirit of the illustrated examples.