Method of manufacturing high temperature resistant composite materials

Abstract

Methods of manufacturing high-temperature composite materials using carbon nanotube to improve the efficiency of insulation applied to propulsion systems for aerospace equipment including 5 steps: step 1: select necessary materials and equipment, step 2: disperse MW-CNTs in the polar solution, step 3: distribute MW-CNTs evenly in the resin, step 4: eliminate residual solvents, step 5: curing phenolic resin composites.

Claims

1. A method of manufacturing heat-resistant composite material comprising: Step 1: providing a phenolic resin of 100% purity having a molecular weight of approximately 124,137, and equipment for manufacturing process including a vacuum stirring tank, an ultrasonic vibrating tank, a vacuum heating chamber and an autoclave; Step 2: dispersing MW-CNTs in a polar solvent with a concentration of 100%, the mass ratio of the polar solvent is between 1:10 and 1:20; Step 3: distributing MW-CNTs evenly in the phenolic resin, wherein this step is performed by using a method of magnetic stirring and ultrasonic vibration at a frequency of 20-40 kHz for 30-60 minutes; Step 4: eliminating residual solvents by performing a method of evaporating from open surfaces in a vacuum furnace to form a phenolic resin composite; Step 5: curing the phenolic resin composite in an autoclave at a pressure of 690 kPa, which consists of 3 phases: keep the temperature at 70° C. for 1.5 hours, keep the temperature at 100° C. for 1 hour, and keep the temperature at 140° C. for 4 hours.

2. The method of manufacturing heat-resistant composite material according to claim 1, wherein at Step 2: dispersing MW-CNTs in the polar solution, wherein the mass ratio of the polar solvent is 1:14.

3. The method of manufacturing heat-resistant composite material according to claim 1, wherein at Step 3: dispersing MW-CNTs in the phenolic resin, is as follows: the mass ratio of the polar solvent containing MW-CNTs prepared in Step 3 that is added to the phenolic resin is 1:10; the polar solvent containing MW-CNTs added to the phenolic resin is magnetic vacuum stirred for 3 to 7 hours at a speed of 60-100 rpm at a temperature of 40-50° C.; and the polar solvent containing MW-CNTs added to the phenolic resin is then subjected to ultrasonic vibration at 20-40 kHz for 30-60 minutes.

4. The method of manufacturing heat-resistant composite material according to claim 1, wherein at the step of eliminating residual solvents by the method of evaporating from open surfaces in the vacuum furnace, the step is performed at temperatures of 50-70° C. for 3-5 days.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1: Figure showing the steps taken;

(2) FIG. 2: Surface of the samples after fire resistance test;

(3) FIG. 3: Heat-spreading rate of samples;

(4) FIG. 4: Thermal conductivity of samples;

(5) FIG. 5: Surface of samples after ablation test;

(6) FIG. 6: Cross-sectional image (side) of samples after ablation test;

(7) FIG. 7: Diagram determining the ablation index of materials;

(8) FIG. 8: Diagram determining the mass loss according to temperature (thermal stability) of materials; and

DETAILED DESCRIPTION OF THE INVENTION

(9) According to one aspect of the invention, the method of manufacturing composite materials is proposed by using CNTs to improve the efficiency of the insulation.

(10) Step 1: Select Necessary Materials and Equipment

(11) Select liquid phenolic materials with high purity and specific density. It is best when the selected liquid phenolic resin material has a purity of 100% and a molecular weight of approximately 124,137.

(12) At the same time, prepare the required equipment for the manufacturing process. At least, the following equipment is required: vacuum stirring tank, ultrasonic vibrating tank, vacuum heating chamber and autoclave.

(13) Step 2: Dilute MW-CNTs in the Polar Solution

(14) At this step, dilute MW-CNTs in the polar solution, whereby MWCNT is dispersed in a polar solution of 100% concentration with an appropriate equivalent mass ratio.

(15) The dispersion of MW-CNTs is better if done in polar solvent with an equivalent mass ratio between [1:10] and [1:20], preferably 1:14.

(16) The solution used at this step may be polar solvent such as acetone, ethanol, methanol, etc.

(17) After dispersing MW-CNTs in this solution, a polar solution with MW-CNTs disperses is obtained, the intermediate mixture is used to further disperse MW-CNTs in phenolic resin from the next step.

(18) Step 3: Distribute MW-CNTs Evenly in the Resin

(19) At this step, it is possible to disperse MW-CNTs by methods such as magnetic vacuum stirring and ultrasonic vibration. The purpose is to facilitate the uniform distribution of MW-CNTs in phenolic resin solution.

(20) According to an invention implementation plan, the dispersion of MWCNT by magnetic vacuum stirring is done as follows:

(21) The polar solvent solution containing MWCNT prepared in step 3 is added to the phenolic resin at the appropriate rate. It provides better results if the ratio reaches [1:10].

(22) The homogeneous solution is stirred in a magnetic vacuum and then ultrasonic vibrated.

(23) The process of stirring in a magnetic vacuum is carried out in a vacuum vessel (the mixture is put into the flask and vacuumed to 0 mbar. The system is then placed on a magnetic induction heating stove and it is continued to perform the magnetic stirring process. The process can last from 3-7 h at 60-100 rpm at a temperature of 40-50° C.

(24) Ultrasonic vibrations provide better results if performed at 20-40 kHz (preferably 37 kHz) for 30-60 minutes.

(25) At the end of this step, a mixture of liquid phenolic resin and MW-CNT particles are distributed evenly.

(26) Step 4: Remove the Residual Solvent

(27) At this step, remove the residual solvent in the solution after step 3 by the method of evaporating from open surfaces in a vacuum furnace.

(28) The mixture is placed in a device with a large open surface and kept in a vacuum environment at a specified temperature and time. The method gives better results when done at temperatures of 50-70° C. for 3-5 days.

(29) Implementing the method of eliminating residual solvents at the above-mentioned temperature and time still ensures the retention of phenolic resin components, while evaporating the amount of polar solvent.

(30) Step 5: Curing Phenolic Resin Composites

(31) After obtaining the solvent-reducing MW-CNTs homogeneous mixture, which is of high purity, the curing process forms the shape of the material to be used.

(32) Curing is a hardening process of plastics based on circuit development and cross-linking under defined pressure temperature conditions.

(33) According to standard curing process for phenolic resin in autoclave, at 690 kPa, there are 3 stages: Keep the temperature at 70° C. for 1.5 hours Keep the temperature at 100° C. for 1 hour Keep the temperature at 140° C. for 4 hours.

EXAMPLES

(34) At a specific aspect, to compare the ability to increase the efficiency of the insulation, the author conducted tests on four types of materials, including: Phenolic resin material, hereinafter called “Materials (a)”. Material (a) is added with carbon fibers (CFs) which are cut from mat material, with a length of 30 mm, a thickness of 0.27 mm—This material is applied to fabricate insulation layer by ablation mechanism according to the previous plan, and is currently being applied, hereinafter referred to as “Materials (b)”. Material (a) combined with C-fibers mat (with a size of 50×50×0.27 mm). This material is being applied to fabricate insulation according to the ablation mechanism of the Russian propulsion system, hereinafter referred to as “Materials (c)”. Materials (c) combined with MW-CNTs, hereinafter referred to as “Materials (d)”.

(35) The authors offer a number of tests that are conducted to compare the four types of materials mentioned above: Fire resistance test: The sample is exposed to C.sub.4H.sub.10 gas flame at a temperature of 1300° C. for 30 seconds according to ASTM E84-11. Observing the surface near the flame position, and determine the area of the heat-spreading zone, hereinafter referred to as “test (1)”. Thermal conductivity test: Hereinafter referred to as the “test (2)”. Ablation test: The sample is exposed to the flame of oxygen—kerosene at 2300° C. Determine the surface temperature where exposed directly to the flame and the time the sample is penetrated by the flame, hereinafter referred to as the “test (3)”. Thermal stability test: The test is for determining ablation rate according to the temperatures from 100-800° C., hereinafter referred to as the “test (4)”. Tensile test at room temperature: Hereinafter referred to as the “test (5)”.

(36) The result of the test is given as follows:

(37) Test (1): Fire Resistance Test:

(38) Sample Surface State:

(39) Refer to FIG. 2, at sample (c) and sample (d), cracks develop on the surface of phenolic resin, instead of causing plastic flow. Meanwhile, the structure of sample a) and b) is almost destroyed. Thus, it can be commented that the reinforced carbon content can reduce the number of cracks for phenolic resin when exposed to fire. The development of cracks can be limited by adding CNTs and evenly distributed CFs (mat).

(40) It can be explained as follows: If the sample has low thermal conductivity, cracks easily appear due to stress concentration. However, the increased amount of C can help reduce the appearance of cracks by increasing the thermal conductivity of the material. Mat-type CFs results in better thermal conductivity than rag-type CFs, due to its evenly distributed, layered structure. Heat spreading ability: Refer to FIG. 3, notice that in the material (a), there is a large temperature difference between the front and back of the sample under the effect of a heat source of 1300° C. Composites with more CFs have a lower temperature difference between the two sides because the CF component has good thermal conductivity. After adding CNTs to CF/phenolic composites, the material gives the best properties. This shows that CNT has the ability to increase the thermal conductivity for phenolic matrix composites.

(41) Test (2): Thermal Conductivity Test: Refer to FIG. 4, showing that composites with reinforced C have higher thermal conductivity. In addition, the type and arrangement also affect the ability of heat absorption, dispersion and heat transfer, thus affecting thermal conductivity. Materials (c) and (d) have a higher thermal conductivity than material (b) despite having the same CF content. The difference here is because the shredded CFs are not continuous, leaving lots of space between them. The mat-type CFs has a more continuous structure than CFs in composite. In addition, the appearance of CNTs also caused the difference in thermal conductivity between materials (c) and (d) because CNT has a large surface area, therefore, with only a small amount of CNTs also help increase the contact area and heat conduction through the composite.

(42) Test (3): Ablation Test: Evaluation of ablation rate: Refer to FIGS. 5 and 6, it can be seen that material (a) has the largest ablation rate. In materials (b), (c), (d), due to the addition of component C, the rate decreases.

(43) In material (a), thermal destruction is concentrated near the flame torch. In materials (b), (c) and (d), the heat destruction area spreads out and is easy to observe. At sample (a), carbon black concentrated at the flame contact position in the front of the sample. However, there is a small amount on the back. At samples (b), (c), soot is available on both the front and the back of the sample. Especially with the mat-type CF sample, the amount of soot on the front and back is almost the same. It is easy to comment that the faster the combustion rate is, the less trace of oxidation is left, while the sign of oxidation can be seen in (c) and (d). The soot status on both sides of the sample shows that the material has a low ablation rate. Evaluation of ablation time: Refer to FIG. 7, the sample (a) is most susceptible to be destructed due to the heat concentrated in a narrower area. Samples (b), (c), (d) are more difficult to be damaged due to their higher thermal conductivity, easily transfer and diffuse heat away from flame.

(44) Test (4): Thermal Stability Test: Refer to FIG. 7: the results show that the addition of CFs increases the thermal stability of materials (2), (3), (4). CFs and CNTs reduce the decomposition rate of materials at high temperatures. It is possible to identify that the addition of CFs and CNTs can reduce the ablation rate of phenolic resin composites.

(45) Test (5): Tensile Test at Room Temperature: FIG. 8 showing the influence of CNTs content by weight on the tensile strength of the material: the results show that the increase in MW-CNT content helped to increase the properties of the final composite.

(46) Through the tests, it can be concluded, with a sample size of 50×50×10 mm: Thermal conductivity: Material (a)<(b)<(c)<(d) Thermal stability: Materials (d)>(c)>(b)>(a).

(47) Accordingly, it was found that the increase in MWCNT content contributes to increase the properties of composites (d).

(48) The addition of CNT content of 0.5% helps to significantly increase the properties of the ablative materials used for manufacturing the insulation of propulsion system for aerospace equipment.

(49) The invention is described in detail by using the options described above. However, it is clear that, the invention is not limited to the plan described in the invention description. An invention may be made in moderation that is not outside the scope of the invention determined by the protection claim points. So what is described in the patent description is for illustrative purposes only, and will not impose any restrictions on the invention.