A METHOD FOR PREPARING BIOBASED NYLON: POLYLACTAM

Abstract

The invention relates to a preparation method of green nylon poly butyrolactams, the biological materials of GABA in vacuum under the condition of high temperature melt decomposition and purified butyrolactams, then by vacuum polymerization of green nylon poly butyrolactams. Compared with the prior art, the invention is prepared by biological method for the synthesis of a wide range of sources, to solve the problem of raw material supply PA4 for mass production, reduce the cost of reaction, and the reaction condition is simple, easy to implement simplified synthesis steps, from the laboratory to the transformation of industrial production.

Claims

1. a method for preparing green nylon poly butyrolactams, characterized in that the method is the biological materials of GABA in vacuum under the condition of high temperature melt decomposition and purified butyrolactams, then by vacuum polymerization of green nylon poly butyrolactams.

2. according to claim 1, a method for preparing green nylon poly (amide) is described: (1) high temperature melting: gamma aminobutyric acid in nitrogen atmosphere, stirring, and then at 200-225 DEG C. under the high temperature conditions of full melting, get a small amount of water in the micro yellow oily liquid; (2) vacuum purification: the preparation of a small yellow oily liquid containing a small amount of water in the vacuum drying chamber at a temperature of 70 DEG C., so that after the evaporation of water to produce a purified yellow oily liquid; (3): the catalyst is added to vacuum polymerization of purified butyrolactams, nitrogen removal in the reactor air, oil bath is heated to 50 DEG C., stirring until the continuous reaction, catalyst and butyrolactams complete reaction, then adding initiator, polymerization conditions remain unchanged, 815 h will continue to reflect, at last the reaction product is water and acetone cleaning and drying, the white solid product of nylon 4.

3. According to claim 2 a green nylon poly butyrolactams preparation method of the 2, which is characterized in that the gamma aminobutyric acid is converted from biomass by fermentation, followed by glutamic acid decarboxylase enzyme conversion and extract purified.

4. According to claim 2 a green nylon poly butyrolactams preparation method of the 2, The whole reaction process is under the condition that nitrogen rate is 3-5 ml/min.

5. According to claim 2 a green nylon poly butyrolactams preparation method of the 2, which is characterized in that the process of the vacuum polymerization, butyrolactams, catalyst, initiator ratio of 1:(0.25-0.375):(0.5-0.75).

6. according to the requirements of claim 2, a method for preparing green nylon poly (amide) is characterized in that the catalyst is sodium hydroxide or potassium hydroxide.

7. according to the requirements of claim 2, a method for the preparation of a green nylon poly (ether amide) is characterized in that the initiator is benzoyl chloride or decyl chloride (two).

8. according to the requirements of claim 2, a method for the preparation of a green nylon poly (ether amide) is described.

9. according to claim 2, a process for the preparation of a green nylon poly (amide) is characterized in that: (2) the purity of the intermediate product obtained by the method is higher than 99.6%.

10. according to claim 2, a method for preparing green nylon poly (amide) is characterized in that: (3) the molecular weight of the white solid product nylon ( ) is above 10 thousand.

Description

BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

[0025] FIG. 1 shows the infrared spectrum of -aminobutyric acid;

[0026] FIG. 2 is an infrared spectrum of butyrolactam obtained in Example 1;

[0027] FIG. 3 is a nuclear magnetic resonance spectrum of butyrolactam obtained in Example 1;

[0028] FIG. 4 is an infrared spectrum of PA4 obtained in Example 2;

[0029] FIG. 5 is an X-ray diffraction pattern of PA4 obtained in Example 2;

[0030] FIG. 6 is a nuclear magnetic resonance spectrum of PA4 obtained in Example 2;

[0031] FIG. 7 is a nuclear magnetic resonance spectrum of PA4 obtained in Example 5.

DETAILED DESCRIPTION OF THE INVENTION

[0032] The invention will now be described in detail with reference to the accompanying figures and examples.

Embodiment 1

[0033] (1) high temperature melting: 80 g of -aminobutyric acid was added in 500 ml three-necked flask. The -aminobutyric acid as evenly spread evenly, close to the inner wall of the flask. A magnetic stirrer rotor was then thrown into three-necked flasks, which place in a magnetic stirring oil bath. Three-necked flasks were connected to nitrogen tanks, condensing equipment and thermometers, respectively, and adjusted to a nitrogen rate of 3 ml/min. First, the heating temperature was set at 190 C. to melt -aminobutyric acid. The temperature was raised to 190 C. and then incubated for 20 minutes. The temperature was raised 5 C. every 10 minutes until 225 C., and the mixture was incubated for 1 hour. After that, turn off the heating power, until mixture natural cooling. Place the resulting liquid in a glass instrument and store in a cool place.

[0034] (2) Vacuum purification: The prepared liquid was placed in a vacuum oven at 70 C. and the water was evaporated for 24 hours to obtain about 50 g purified yellowish oily liquid (butyrolactam). The infrared spectrum and the nuclear magnetic resonance spectrum of the prepared butyrolactam are shown in FIG. 2-3. Infrared spectrum showed three characteristic peaks (750 cm.sup.1, 1250 cm.sup.1 and 1500 cm.sup.1), which indicate that the material is -aminobutyric acid (FIG. 1). The characteristic peaks of 720 cm.sup.1, 1280 cm.sup.1 and 1600 cm.sup.1 in FIG. 2 indicated that the material is -butyrolactam; The characteristic peaks at 2.2, 2.35, and 3.4 indicate that the substance is -butyrolactam.

[0035] Decompression polymerization: 20 g butyrolactam and 5 g sodium were placed in 500 ml four-necked flask. A magnetic stirrer rotor was then thrown into four-necked flasks, which place in a magnetic stirring oil bath. Four bottlenecks were connected nitrogen tank, condensing equipment, constant pressure funnel and thermometer respectively, and then adjust the nitrogen rate of 3 ml/min. The mixture was reacted for 3 hour at 50 C. with stirring, and then added 10 g of benzoyl chloride. After the reaction was carried out for 8 hours in above condition, the polymer was capped by adding 120 ml formic acid. The product was then rinsed three times using the mixture of water and acetone (1:1; v:v), and the unreacted monomer was washed off. The final PA4 product was dried as a white solid product and weighed about 10 g.

Embodiment 2

[0036] (1) high temperature melting: 100 g of -aminobutyric acid was added in 500 ml three-necked flask. The -aminobutyric acid as evenly spread evenly, close to the inner wall of the flask. A magnetic stirrer rotor was then thrown into three-necked flasks, which place in a magnetic stirring oil bath. Three-necked flasks were connected to nitrogen tanks, condensing equipment and thermometers, respectively, and adjusted to a nitrogen rate of 5 ml/min. The heating temperature was set at 220 C. to melt -aminobutyric acid. The reaction was carried out for 2-3 hours until the water in the water pipe is no longer increased. Then turn off the heating power, until its natural cooling. Place the resulting liquid in a glass instrument and store in a cool place.

[0037] (2) Vacuum purification: The prepared liquid was placed in a vacuum oven at 70 C. and the water was evaporated for 36 hours to obtain about 65 g of the purified yellowish oily liquid (butyrolactam).

[0038] (3) Decompression polymerization: 30 g of butyrolactam and 7.5 g of potassium hydroxide were placed in a 500 ml three-necked flask. A magnetic stirrer rotor was then thrown into three-necked flasks, which place in a magnetic stirring oil bath. The three-necked flask was connected to a condensing apparatus, constant pressure funnel and vacuum distillation unit, and adjust the nitrogen rate of 5 ml/min. The oil bath temperature was set at 50 C., and after 5 h of stirring, 15 g of sebacic acid chloride was added. Keep the polymerization conditions unchanged, the reaction was carried out for 10 hours, and then turned off the heating power, until mixture natural cooling. The reaction product was washed three times using the mixture of water and acetone (1:1; v:v), and the unreacted monomer was washed off. The final PA4 product was dried as a white solid product and weighed about 15 g.

[0039] PA4 solid (10 g) obtained by polymerization was subjected to two-step solid polycondensation under nitrogen atmosphere to increase the molecular weight. The molecular weight of PA4 was remarkably increased detecting by the viscosity method. The infrared spectrum, X-ray diffraction spectrum and nuclear magnetic resonance spectrum of the obtained PA4 are shown in FIG. 4-6. Some characteristic peaks was identified, such as the characteristic peaks at 730 cm.sup.1, 1000 cm.sup.1 and 1580 cm.sup.1 in FIG. 4; the characteristic peaks at 13, 17, 27, 29, 31, 42, 44, 52 in FIG. 3; the characteristic peaks at 2.2, 2.35, 3.4 in FIG. 6. The above results indicated that the substance is PA4.

Embodiment 3

[0040] Butyactam (30 g) obtained by vacuum purification process in Example 2 was placed in a 500-ml three-necked flask and added 10 g of potassium hydroxide. A magnetic stirrer rotor was then thrown into three-necked flasks, which place in a magnetic stirring oil bath at 50 C. The three-necked flask was connected to a condensing apparatus, constant pressure funnel and vacuum distillation unit, and adjust the nitrogen rate of 5 ml/min. The mixture was reacted with stirring until the potassium hydroxide and butyrolactam were consuming completely. Then add 22 g benzoyl chloride, and maintain the same polymerization conditions to react 15 h. Turn off the heating power, until mixture natural cooling. The reaction product was washed twice with a mixture of water and methanol in a volume ratio of 1:1 and then washed twice with a large amount of acetone, and the unreacted monomer was washed off. The final PA4 product was dried as a white solid product and weighed about 15 g.

Embodiment 4

[0041] (1) 5.2 g of -aminobutyric acid was dissolved in 250 ml of toluene, and then 15 g of Al.sub.2O.sub.3 was added. The whole reaction was carried out in a 500-ml three-necked flask and heated to 80 C. using an induction cooker for 8 h. After the completion of the reaction, the whole glass apparatus was cooled to room temperature. The catalyst was filtered, and the product obtained by filtration was washed with the toluene and chloroform mixture (1:1; v:v). The solvent was removed by rotary evaporation to obtain the yellow liquid oily butyrolactam.

[0042] (2) Decompression polymerization: 20 g of butyrolactam and 5 g of sodium were placed in a 500 ml four-necked flask. A magnetic stirrer rotor was then thrown into four-necked flasks, which place in a magnetic stirring oil bath. Four bottlenecks were connected nitrogen tank, condensing equipment, constant pressure funnel and thermometer respectively, and then adjust the nitrogen rate of 3 ml/min. The reaction was carried out for 6 h with stirring at 70 C. Then, 10 g of benzoyl chloride was added and keep the above polymerization conditions for 10 hours. Polymer was capped by adding 120 ml of formic acid. The reaction product was washed twice with a mixture of water and acetone in a volume ratio of 1:1, and the unreacted monomer was washed off. The final PA4 product was dried as a white solid product and weighed about 8 g.

Embodiment 5

[0043] Take 50 g of butyrolactam prepared by chemical process in a four-necked flask and added 13 g of sodium. A magnetic stirrer rotor was then thrown into four-necked flasks, which place in a magnetic stirring oil bath. Four bottlenecks were connected nitrogen tank, condensing equipment, constant pressure funnel and thermometer respectively, and then adjust the nitrogen rate of 4 ml/min. The reaction was carried out for 3 h with stirring at 50 C. Then, 26 g of benzoyl chloride was added and dissolved it in tetrahydrofuran. Keep the above polymerization conditions for 15 hours, and the polymer was capped by adding 120 ml of formic acid. The reaction product was washed three times with a mixture of water and acetone in a volume ratio of 1:1, and the unreacted monomer was washed off. The final PA4 product was dried as a white solid product and weighed about 28 g. The NMR spectrum of the obtained PA4 is shown in FIG. 7. The characteristic peaks of 2.2, 2.35, and 3.4 at FIG. 7 indicated that the product is PA4.