CN112876820B - Polyethylene terephthalate composite material - Google Patents

Abstract

The invention discloses a polyethylene terephthalate composite material. It is made of polyethylene terephthalate, sodium lignosulfonate and benzoxazine; the mass fraction of polyethylene terephthalate is 70-99, sodium lignosulfonate The parts by mass of benzoxazine are 1-30, and the parts by mass of benzoxazine are 1-30; the three materials are dried; the dried polyethylene terephthalate, benzoxazine and wood Sodium sulfonate is melted and blended to obtain a blended composite material; the blended composite material is injection-molded to obtain a composite material spline; the composite material spline is heated and solidified; and cooled to normal temperature. The polyethylene terephthalate composite material of the invention has high thermal stability and flame retardancy, and has wide application prospects in the fields of film sheets, packaging bottles, electronic appliances, auto parts, mechanical equipment and the like.

Description

A kind of polyethylene terephthalate composite material

technical field

The invention relates to a composite material, specifically a polyethylene terephthalate composite material with high thermal stability and flame retardancy.

Background technique

Polyethylene terephthalate is an important engineering plastic. Due to its excellent physical and mechanical properties, polyethylene terephthalate is widely used in film sheets, packaging bottles, electronic appliances, auto parts and mechanical equipment. However, polyethylene terephthalate is highly flammable, it exhibits severe dripping behavior when burned, and the flame spreads rapidly as a result. This high fire risk seriously threatens the safety of people's lives and property. In order to improve the flame retardant properties of polyethylene terephthalate, adding flame retardants is an effective method. However, due to the low carbon-forming properties of polyethylene terephthalate, common flame retardants cannot significantly improve its thermal stability and carbon-forming properties, so the problems of low melt dripping and low flame retardant properties do not exist. can be effectively resolved. Therefore, how to effectively improve the carbon-forming properties of polyethylene terephthalate is still one of the difficulties faced in improving its flame retardant properties. An effective solution to this problem is valuable for improving the flame retardant properties of polyethylene terephthalate and expanding its application fields.

SUMMARY OF THE INVENTION

To overcome the above-mentioned problems in the prior art, the present invention provides a polyethylene terephthalate composite material.

In order to achieve the above object, a kind of technical scheme that the present invention solves its technical problem adopts is:

The composite material is mainly made of polyethylene terephthalate, sodium lignosulfonate and benzoxazine.

In the composite material, the mass fraction of polyethylene terephthalate is 70-99, the mass fraction of sodium lignosulfonate is 1-30, and the mass fraction of benzoxazine is 1-30.

In the composite material, the mass fraction of polyethylene terephthalate is 80-90, the mass fraction of sodium lignosulfonate is 10-20, and the mass fraction of benzoxazine is 10-20.

The mass ratio of benzoxazine and sodium lignosulfonate in the composite material is 0.5-2.

The benzoxazine is a compound with a six-membered oxazine ring structure containing nitrogen and oxygen in the molecule.

The composite material is prepared in the following manner:

1) drying treatment with polyethylene terephthalate, benzoxazine and sodium lignosulfonate;

2) melt blending the dried polyethylene terephthalate, benzoxazine and sodium lignosulfonate in step 1) to obtain a blended composite material;

3) injection molding the obtained blended composite material in step 2) to obtain a composite material spline;

4) heating and curing the composite material splines obtained in step 3) to obtain a polyethylene terephthalate composite material.

The drying treatment temperature in the step 1) is 80° C. and the time is 8 hours.

In the blended composite material obtained in the step 2), the mass fraction of polyethylene terephthalate is 70-99, the mass fraction of sodium lignosulfonate is 1-30, and the mass of benzoxazine is 1-30. The number of copies is 1 to 30.

In the blended composite material obtained in the step 2), the mass fraction of polyethylene terephthalate is 80-90, the mass fraction of sodium lignosulfonate is 10-20, and the mass of benzoxazine The number of copies is 10 to 20.

The melt blending in the step 2) adopts a torque rheometer, the temperature is 270° C., the rotor speed is 60 rpm, and the time is 2 minutes.

The injection molding in the step 3) uses an injection molding machine, the temperature of the injection zone is 255°C, the temperature of the template zone is 45°C, and the pressure holding time is 2 minutes.

The heating and curing process in the step 4) is as follows: setting a step temperature control for treatment, specifically, heat treatment at 120-140° C. for 1-3 hours, heat-treatment at 150-170° C. for 1-3 hours, and heat treatment at 180-200° C. for 1-3 hours. Heat treatment for 1 to 3 hours, 210 to 230°C for 0.5 to 2 hours, 240 to 260°C for 10 to 60 minutes, and then cooled to room temperature.

Preferably, the heating and curing process in the step 4) is: setting a step temperature control for treatment, specifically heat treatment at 130°C for 2 hours, heat treatment at 160°C for 2 hours, heat treatment at 190°C for 2 hours, and heat treatment at 220°C for 2 hours. Heat treatment for 1 hour, heat treatment at 250°C for 0.5 hours, and then cool to room temperature.

The beneficial effects that the present invention has are as follows:

The raw materials benzoxazine and sodium lignosulfonate used in the present invention can effectively improve the carbon-forming ability of polyethylene terephthalate, thereby improving the burning and dripping behavior and resistance of polyethylene terephthalate. It has high flammability and simple preparation method, and has broad application prospects in the fields of film sheets, packaging bottles, electronic appliances, auto parts and mechanical equipment.

Detailed ways

The present invention will be further described in detail below in conjunction with specific embodiments.

In the embodiment of the present invention, polyethylene terephthalate, benzoxazine (6,6'-(propane-2,2-diyl)bis(3-phenyl-3,4-dihydro-2H- benzo[e][1,3]oxazine)) and sodium lignosulfonate are commercially available materials.

Thermal stability performance test method: using a thermogravimetric analyzer (NETZSCH, TG 209F1), temperature range: room temperature to 650°C, heating rate: 10°C/min, nitrogen atmosphere.

Flame retardant performance test method: use oxygen index analyzer (Suzhou Phoenix, PX-01-005), test according to national standard GB/T 2406.2-2009; use UL94 vertical and horizontal combustion tester (Suzhou Phoenix, PX-03-001 ), tested according to the national standard GB/T 2408-2008.

Example 1

1) Weigh 27 g of polyethylene terephthalate and 3 g of benzoxazine, and dry in a drying oven at 80° C. for 8 hours to obtain dry benzoxazine and polyethylene terephthalate.

2) adding the dry polyethylene terephthalate and benzoxazine obtained in the step 1) into a torque rheometer to carry out melt blending, the temperature is 270 ° C, the rotor speed is 60 rev/min, and the time is 2 minutes; The blended composite material is taken out and cooled to normal temperature to obtain a blended composite material of polyethylene terephthalate and benzoxazine.

3) adding the blended composite material of polyethylene terephthalate and benzoxazine obtained in step 2) into a micro injection molding machine for injection molding, the temperature of the injection zone is 255°C, and the temperature of the template zone is 45°C, The pressure holding time was 2 minutes to obtain a composite spline of polyethylene terephthalate and benzoxazine.

4) heating and curing the blended composite material strip of polyethylene terephthalate and benzoxazine obtained in step 3), heat-treated at 130° C. for 2 hours, heat-treated at 160° C. for 2 hours, and 190° C. Heat treatment at 220°C for 2 hours, 220°C for 1 hour, 250°C for 0.5 hours, and cooled to room temperature.

The thermal stability performance test results are shown in Table 1.

The flame retardant performance test results are shown in Table 2.

Example 2

1) Weigh 27 g of polyethylene terephthalate, 2 g of benzoxazine, and 1 g of sodium lignosulfonate, and dry in a drying oven at 80° C. for 8 hours to obtain dry polyethylene terephthalate. , benzoxazine and sodium lignosulfonate.

2) adding the dry polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 1) into a torque rheometer and melt blending, temperature 270° C., rotor rotating speed 60 rev/ minutes, time 2 minutes; take out the blended composite material, and cool to normal temperature to obtain a blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

3) adding the blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 2) into a micro injection molding machine for injection molding, the injection zone temperature is 255 ° C, and the template The zone temperature was 45°C, and the pressure holding time was 2 minutes to obtain a composite spline of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

4) heating and curing the composite material strips of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 3), heat treatment at 130° C. for 2 hours, and heat treatment at 160° C. 2 hours, heat treatment at 190°C for 2 hours, heat treatment at 220°C for 1 hour, heat treatment at 250°C for 0.5 hours, and cooling to room temperature.

The thermal stability performance test results are shown in Table 1.

The flame retardant performance test results are shown in Table 2.

Example 3

1) Weigh 27 g of polyethylene terephthalate, 1.5 g of benzoxazine, 1.5 g of sodium lignosulfonate, and dry in a drying oven at 80° C. for 8 hours to obtain dry polyethylene terephthalate. Alcohol esters, benzoxazines and sodium lignosulfonate.

2) adding the dry polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 1) into a torque rheometer and melt blending, temperature 270° C., rotor rotating speed 60 rev/ minutes, time 2 minutes; take out the blended composite material, and cool to normal temperature to obtain a blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

3) adding the blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 2) into a micro injection molding machine for injection molding, the injection zone temperature is 255 ° C, and the template The zone temperature was 45°C, and the pressure holding time was 2 minutes to obtain a composite spline of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

4) heating and curing the composite material strips of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 3), heat treatment at 130° C. for 2 hours, and heat treatment at 160° C. 2 hours, heat treatment at 190°C for 2 hours, heat treatment at 220°C for 1 hour, heat treatment at 250°C for 0.5 hours, and cooling to room temperature.

The thermal stability performance test results are shown in Table 1.

The flame retardant performance test results are shown in Table 2.

Example 4

1) Weigh 27 g of polyethylene terephthalate, 1 g of benzoxazine, 2 g of sodium lignosulfonate, and dry in a drying oven at 80° C. for 8 hours to obtain dry polyethylene terephthalate , benzoxazine and sodium lignosulfonate.

2) adding the dry polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 1) into a torque rheometer and melt blending, temperature 270° C., rotor rotating speed 60 rev/ minutes, time 2 minutes; take out the blended composite material, and cool to normal temperature to obtain a blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

3) adding the blended composite material of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 2) into a micro injection molding machine for injection molding, the injection zone temperature is 255 ° C, and the template The zone temperature was 45°C, and the pressure holding time was 2 minutes to obtain a composite spline of polyethylene terephthalate, benzoxazine and sodium lignosulfonate.

4) heating and curing the composite material strips of polyethylene terephthalate, benzoxazine and sodium lignosulfonate obtained in step 3), heat treatment at 130° C. for 2 hours, and heat treatment at 160° C. 2 hours, heat treatment at 190°C for 2 hours, heat treatment at 220°C for 1 hour, heat treatment at 250°C for 0.5 hours, and cooling to room temperature.

The thermal stability performance test results are shown in Table 1.

The flame retardant performance test results are shown in Table 2.

Example 5

1) Weigh 27g of polyethylene terephthalate, 3g of sodium lignosulfonate, and dry at 80°C for 8 hours in a drying oven to obtain dry polyethylene terephthalate and sodium lignosulfonate .

2) The dry polyethylene terephthalate and sodium lignosulfonate obtained in step 1) were added to a torque rheometer for melt blending, the temperature was 270° C., the rotor speed was 60 rev/min, and the time was 2 minutes. ; Take out the blended composite material and cool it to normal temperature to obtain a blended composite material of polyethylene terephthalate and sodium lignosulfonate.

3) adding the blended composite material of polyethylene terephthalate and sodium lignosulfonate obtained in step 2) into a micro injection molding machine for injection molding, the temperature of the injection zone is 255°C, and the temperature of the template zone is 45°C , the pressure holding time was 2 minutes, and the composite material splines of polyethylene terephthalate and sodium lignosulfonate were obtained.

4) heating and curing the composite material strips of polyethylene terephthalate and sodium lignosulfonate obtained in step 3), heat-treated at 130° C. for 2 hours, heat-treated at 160° C. for 2 hours, and heat-treated at 190° C. for 2 hours. Heat treatment at 220°C for 2 hours, heat treatment at 220°C for 1 hour, heat treatment at 250°C for 0.5 hours, and cool to room temperature.

The thermal stability performance test results are shown in Table 1.

The flame retardant performance test results are shown in Table 2.

Table 1

Note: Control is pure polyethylene terephthalate.

It can be seen from Table 1 that:

Compared with pure polyethylene terephthalate, the carbon residues of polyethylene terephthalate composites added with benzoxazine and sodium lignosulfonate at 650 °C were significantly increased. Example 2 had the highest amount of carbon residue at 650°C, which was higher than that of Example 1 and Example 5 at 650°C, and was also higher than that of Example 3 and Example 4 at 650°C. It shows that the two materials of sodium lignosulfonate and benzoxazine have synergistic effect and are related to the ratio.

Table 2

sample Limiting oxygen index (%) Vertical combustion class UL-94 Example 1 25.5 V-2 Example 2 26.4 V-1 Example 3 24.8 V-2 Example 4 24.6 V-2 Example 5 23.1 V-2 control 21.8 NR

Note: Control is pure polyethylene terephthalate.

It can be seen from Table 2 that:

The limiting oxygen index of Example 2 is the highest, which is higher than the limiting oxygen index of Example 1 and Example 5, and also higher than that of Example 3 and Example 4. The vertical combustion level of Example 2 reaches V-1 level, which is better than other examples. It shows that the two materials of sodium lignosulfonate and benzoxazine have synergistic effect on flame retardancy and it is related to the ratio.

The above embodiments are only used to explain the present invention, but not to limit the protection scope of the present invention. Any equivalent changes or modifications made within the spirit of the present invention and the protection scope of the claims are deemed to be within the protection scope of the present invention.

Claims (9)

1. A polyethylene terephthalate composite material is characterized in that: the composite material is mainly prepared from polyethylene glycol terephthalate, sodium lignosulfonate and benzoxazine;

the mass ratio of benzoxazine to sodium lignosulfonate in the composite material is 2.

2. The polyethylene terephthalate composite material according to claim 1, wherein: the composite material comprises, by mass, 70-99 parts of polyethylene glycol terephthalate, 1-30 parts of sodium lignosulfonate and 1-30 parts of benzoxazine.

3. The polyethylene terephthalate composite material according to claim 2, wherein: the composite material comprises, by mass, 80-90 parts of polyethylene glycol terephthalate, 10-20 parts of sodium lignosulfonate and 10-20 parts of benzoxazine.

4. The polyethylene terephthalate composite material according to claim 1, wherein: the benzoxazine is a compound with a six-membered oxazine ring structure containing nitrogen and oxygen in the molecule.

5. The polyethylene terephthalate composite material according to claim 1, wherein: the composite material is prepared by adopting the following steps:

1) drying polyethylene glycol terephthalate, benzoxazine and sodium lignosulfonate;

2) carrying out melt blending on the polyethylene terephthalate, the benzoxazine and the sodium lignosulfonate which are dried in the step 1) to obtain a blended composite material;

3) performing injection molding on the blended composite material obtained in the step 2) to obtain a composite material sample strip;

4) heating and curing the composite material sample strip obtained in the step 3).

6. The polyethylene terephthalate composite material according to claim 5, wherein: the drying treatment temperature in the step 1) is 80 ℃, and the drying treatment time is 8 hours.

7. The polyethylene terephthalate composite material according to claim 5, wherein: the mass parts of the polyethylene glycol terephthalate, the sodium lignosulfonate and the benzoxazine in the blending composite material obtained in the step 2) are 70-99, 1-30 and 1-30 respectively.

8. The polyethylene terephthalate composite material according to claim 5, wherein: the blending composite material obtained in the step 2) comprises, by mass, 80-90 parts of polyethylene glycol terephthalate, 10-20 parts of sodium lignosulfonate and 10-20 parts of benzoxazine.

9. The polyethylene terephthalate composite material according to claim 5, wherein: the heating and curing process in the step 4) comprises the following steps: and step temperature control is arranged for processing, and specifically, the heat treatment is carried out for 1-3 hours at 120-140 ℃, for 1-3 hours at 150-170 ℃, for 1-3 hours at 180-200 ℃, for 0.5-2 hours at 210-230 ℃ and for 10-60 minutes at 240-260 ℃ in sequence, and then the mixture is cooled to the normal temperature.