PIEZOELECTRIC POLYLACTIC ACID MATERIAL AND PREPARATION METHOD AND APPLICATION THEREOF

Abstract

A piezoelectric polylactic acid material is has a layered stacking structure, and a porous structure is formed between stacked layers. The piezoelectric polylactic acid material has a piezoelectric constant of 5.2-35.3 pC/N, has the ability to efficiently catalyze dye/pigment degradation, and can be used in the fields of dye/pigment degradation and tooth whitening. A preparation method for the piezoelectric polylactic acid composite material is also provided.

Claims

1. A piezoelectric polylactic acid material, wherein the microstructure of the piezoelectric polylactic acid material is a layered stacking structure, and a porous structure is formed between stacked layers.

2. The piezoelectric polylactic acid material according to claim 1, wherein the piezoelectric polylactic acid material has a piezoelectric constant of 5.2-35.3 pC/N.

3. The piezoelectric polylactic acid material according to claim 1, wherein the piezoelectric polylactic acid material is prepared by the following method: subjecting poly(L-lactic acid), poly(D-lactic acid) and a pore-forming agent to melting and blending at 170-220 C. to obtain a blend; and then removing the pore-forming agent to obtain the piezoelectric polylactic acid material, wherein the pore-forming agent has good compatibility with the polylactic acid.

4. The piezoelectric polylactic acid material according to claim 3, wherein the pore-forming agent is a polymer or a small molecule having good compatibility with the polylactic acid; preferably, the pore-forming agent is selected from any one of polyethylene glycol, polyvinyl acetate, polymethyl methacrylate, polyhydroxybutyric acid, tributyl citrate, or dioctyl phthalate.

5. The piezoelectric polylactic acid material according to claim 3, wherein the ratio of the poly(L-lactic acid) to the poly(D-lactic acid) to the pore-forming agent is as follows: 30-70 parts by weight of the poly(L-lactic acid), 30-70 parts by weight of the poly(D-lactic acid) and 10-50 parts by weight of the pore-forming agent; further, in the preparation method of the piezoelectric polylactic acid material, the raw material further comprises a compatibilizer, and the use amount of the compatibilizer is 0.1-0.6 part by weight, preferably 0.3-0.4 part by weight; further, the compatibilizer is an amphiphilic compound having good compatibility with both the polylactic acid and the pore-forming agent; preferably, the compatibilizer is any one of a polyethylene oxide-propylene oxide-ethylene oxide block copolymer, a polyethylene oxide-propylene oxide block copolymer, a polyethylene oxide-lactic acid-ethylene oxide block copolymer, and a polyethylene oxide-butyl acrylate block copolymer; further, the poly(L-lactic acid) has a weight-average molecular weight of 1*10.sup.4-5*10.sup.6 g/mol and an optical purity of equal to or greater than 90%; and the poly(D-lactic acid) has a weight-average molecular weight of 1*10.sup.4-5*10.sup.6 g/mol and an optical purity of equal to or greater than 90%.

6. The piezoelectric polylactic acid material according to claim 3, wherein in the preparation method of the piezoelectric polylactic acid material, the pore-forming agent is removed by the following method: placing the blend in a solvent capable of dissolving the pore-forming agent but not capable of dissolving the polylactic acid, and conducting full etching to remove the pore-forming agent; and further, the solvent is selected from one of water, ethanol, acetone, cyclohexane, n-hexane, dichloromethane, or trichloromethane.

7. A preparation method of the piezoelectric polylactic acid material according to claim 1, wherein the preparation method comprises: subjecting poly(L-lactic acid), poly(D-lactic acid) and a pore-forming agent to melting and blending at 170-220 C. to obtain a blend; and then removing the pore-forming agent to obtain the piezoelectric polylactic acid material, wherein the pore-forming agent has good compatibility with the polylactic acid.

8. Use of a piezoelectric polylactic acid material in tooth whitening, dye/pigment degradation, piezoelectric sensing, ultrasonic imaging, in vivo drivers, or implantable piezoelectric devices for induced regeneration of tissues, wherein the piezoelectric polylactic acid material is the piezoelectric polylactic acid material according to claim 1.

9. A tooth whitening material, wherein the tooth whitening material is a piezoelectric polylactic acid material, and the piezoelectric polylactic acid material is the piezoelectric polylactic acid material according to claim 1.

10. A tooth whitening product, wherein the tooth whitening product is a tooth whitening agent or a tooth whitening instrument containing the piezoelectric polylactic acid whitening material according to claim 1; further, the tooth whitening agent is a piezoelectric polylactic acid material or a tooth whitening composition containing a piezoelectric polylactic acid material; further, the tooth whitening agent is in a form of a powder, a liquid, a gum, a gel, a paste, or a fiber; further, the tooth whitening composition containing a piezoelectric polylactic acid material is a toothpaste, a tooth powder, a gum, a chew gum, a gel, a tooth cleaning solution, a tooth scrub, a mouthwash, or a medical floss containing piezoelectric polylactic acid; further, the tooth whitening instrument is a tooth whitening instrument prepared by adding a piezoelectric polylactic acid material; and the tooth whitening instrument is a toothbrush, a tooth socket, or a tooth support prepared by adding a piezoelectric polylactic acid material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] FIG. 1 is a schematic diagram showing a piezoelectric catalytic degradation mechanism of a piezoelectric polylactic acid powdered material having the ability to efficiently catalyze dye/pigment degradation provided by the present disclosure. From the schematic diagram, it can be seen that an SC-PLA powdered material with a layered stacking structure can achieve a piezoelectric effect under the action of mechanical vibration, and then generate reactive oxidation species (such as .Math.OH and .Math.O.sub.2.sup.) having strong oxidation in water to catalyze dye/pigment degradation.

[0041] FIG. 2 shows scanning electron microscope (SEM) images of SC-PLA powdered materials prepared in Comparative Example 1 (FIG. 2a and FIG. 2a), Example 1 (FIG. 2b and FIG. 2b) and Comparative Example 2 (FIG. 2c and FIG. 2c) of the present disclosure.

[0042] FIG. 3 shows a diagram (ultraviolet spectrum in an upper figure of FIG. 3) showing concentration changes of a pigment at different ultrasonic times when an SC-PLA powdered material prepared in Example 1 is used in an IC pigment degradation experiment and corresponding physical images (in a lower figure of FIG. 3). From the figure, it can be seen that with the increase of the ultrasonic time, an ultraviolet characteristic peak (at a wavelength of about 600 nm) of an IC pigment gradually becomes weak. When the ultrasonic time reaches 30 min, the pigment is basically completely degraded (the degradation efficiency is up to 98%), and an aqueous solution becomes colorless and transparent.

[0043] FIG. 4 shows the whitening ability of the SC-PLA powdered material prepared in Example 1 of the present disclosure for a stained bovine tooth. Specific steps are as follows: 0.5 g of the SC-PLA powder was evenly smeared on the surface of the wet tooth (the tooth was stained with a mixed liquid of coffee, tea and cola for a week), an electric toothbrush (with a vibration frequency of 30,000 Hz) was used for a brushing experiment, and photos were taken every 30 min for recording.

DESCRIPTION OF THE EMBODIMENTS

[0044] According to the present disclosure, a pore-forming agent having good compatibility with poly(L-lactic acid) and poly(D-lactic acid) is introduced. On the one hand, PLLA and PDLA molecular chains are endowed with good activity ability in a blending process, and the formation of a perfect lamellar crystal stacking structure is promoted while the crystallinity is improved, so that piezoelectric properties of a powdered material are improved. On the other hand, in a crystallization process, the pore-forming agent is removed from lamellar crystals to form a lamellar stacking phase separation structure, followed by etching with an optional solvent to form a lamellar stacking porous structure, so that the powder is endowed with more excellent piezoelectric properties.

[0045] Examples are provided below to describe the present disclosure in detail. However, it shall be noted that the following examples are merely used for further explaining the present disclosure, and cannot be understood as limitations of the protection scope of the present disclosure. Some non-essential improvements and adjustments made by a person skilled in the art according to the content of the present disclosure still fall within the protection scope of the present disclosure.

[0046] It is worth noting that (1) all parts of materials used in the following examples and comparative examples of the present disclosure are parts by weight; (2) scanning electron microscope photos of products obtained in the following examples and comparative examples and a d.sub.33 coefficient of materials (the d.sub.33 coefficient is one of coefficients commonly used for characterizing piezoelectric properties of a material, and a larger d.sub.33 coefficient indicates stronger piezoelectric properties of a material) are measured by an American FE-SEM scanning electron microscope and a ZJ-3 piezoelectric tester, respectively; and (3) a pigment degradation experiment of the products obtained the following examples and comparative examples includes the following specific steps: 0.2 g of a sample is added into 100 mL of an indigo carmine (IC) dye aqueous solution with a concentration of 5 mg/L and then subjected to ultrasonic vibration at a frequency of 20 kHz and a power of 50 W for 30 min, and concentration changes of a pigment in the aqueous solution are measured by an ultraviolet spectrophotometer, where the ultraviolet spectrophotometer used is UV-3600 produced by Shimadzu of Japan.

Example 1

[0047] PLLA and PDLA having a weight-average molecular weight of 2.0*10.sup.5 g/mol and 1.5*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 40 parts of a PEG (with an Mw of 10,000 g/mol) pore-forming agent, 0.3 part of a PEO-PLA-PEO compatibilizer, 30 parts of the PLLA and 30 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 200 C. for 6 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in deionized water for selective etching of a PEG phase, and then dried to obtain a layered porous polylactic acid powder.

[0048] The powder has a d.sub.33 coefficient of 35.3 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 98%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 94%.

Example 2

[0049] PLLA and PDLA having a weight-average molecular weight of 1.0*10.sup.4 g/mol and 2.5*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 30 parts of a PVAc pore-forming agent, 0.6 part of a PEO-PPO-PEO compatibilizer, 42 parts of the PLLA and 28 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 190 C. for 3 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in cyclohexane for selective etching of a PVAc phase, and then dried to obtain a layered porous polylactic acid powder.

[0050] The powder has a d.sub.33 coefficient of 22.8 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 93%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 90%.

Example 3

[0051] PLLA and PDLA having a weight-average molecular weight of 1.0*10.sup.5 g/mol and 4.0*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 10 parts of a PMMA pore-forming agent, 0.5 part of a PEO-PBA compatibilizer, 63 parts of the PLLA and 27 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 180 C. for 5 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in acetone for selective etching of a PMMA phase, and then dried to obtain a layered porous polylactic acid powder.

[0052] The powder has a d.sub.33 coefficient of 5.2 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 82%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 78%.

Example 4

[0053] PLLA and PDLA having a weight-average molecular weight of 5.0*10.sup.5 g/mol and 3.0*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 20 parts of a PHB pore-forming agent, 0.2 part of a PEO-PPO compatibilizer, 32 parts of the PLLA and 48 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 210 C. for 4 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in dichloromethane for selective etching of a PHB phase, and then dried to obtain a layered porous polylactic acid powder.

[0054] The powder has a d.sub.33 coefficient of 10.6 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 87%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 83%.

Example 5

[0055] PLLA and PDLA having a weight-average molecular weight of 5.0*10.sup.4 g/mol and 1.0*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 20 parts of a TBC pore-forming agent, 30 parts of the PLLA and 30 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 170 C. for 8 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in ethanol for selective etching of a TBC phase, and then dried to obtain a layered porous polylactic acid powder.

[0056] The powder has a d.sub.33 coefficient of 30.7 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 96%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 92%.

Example 6

[0057] PLLA and PDLA having a weight-average molecular weight of 3.0*10.sup.5 g/mol and 1.0*10.sup.4 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 30 parts of a DOP pore-forming agent, 21 parts of the PLLA and 49 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 180 C. for 9 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in ethanol for selective etching of a DOP phase, and then dried to obtain a layered porous polylactic acid powder.

[0058] The powder has a d.sub.33 coefficient of 17.2 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 91%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 88%.

Example 7

[0059] PLLA and PDLA having a weight-average molecular weight of 4.0*10.sup.5 g/mol and 2.0*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 50 parts of a PEG (with an Mw of 10,000 g/mol) pore-forming agent, 0.1 part of a PEO-PPO compatibilizer, 25 parts of the PLLA and 25 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 190 C. for 10 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in deionized water for selective etching of a PEG phase, and then dried to obtain a layered porous polylactic acid powder.

[0060] The powder has a d.sub.33 coefficient of 28.9 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 95%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 91%.

Example 8

[0061] PLLA and PDLA having a weight-average molecular weight of 2.5*10.sup.5 g/mol and 5.0*10.sup.4 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 20 parts of a PVAc pore-forming agent, 0.4 part of a PEO-PBA compatibilizer, 40 parts of the PLLA and 40 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 220 C. for 7 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in cyclohexane for selective etching of a PVAc phase, and then dried to obtain a layered porous polylactic acid powder.

[0062] The powder has a d.sub.33 coefficient of 13.8 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 89%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 84%.

Comparative Example 1

[0063] PLLA and PDLA having a weight-average molecular weight of 2.0*10.sup.5 g/mol and 1.5*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 40 parts of a PEO (with an Mw of 30,000 g/mol) pore-forming agent, 0.3 part of a PEO-PLA-PEO compatibilizer, 30 parts of the PLLA and 30 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 200 C. for 6 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in deionized water for selective etching of a PEO phase, and then dried to obtain a layered porous polylactic acid powder.

[0064] The powder has a d.sub.33 coefficient of 0.3 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 5%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 1%.

Comparative Example 2

[0065] PLLA and PDLA having a weight-average molecular weight of 2.0*10.sup.5 g/mol and 1.5*10.sup.5 g/mol, respectively, were subjected to vacuum drying at a vacuum degree of less than 900 Pa at 60 C. until the water content was less than 200 ppm. 40 parts of a PEG (with an Mw of 10,000 g/mol) pore-forming agent, 0.3 part of a PEO-PLA-PEO compatibilizer, 30 parts of the PLLA and 30 parts of the PDLA were uniformly mixed by physical stirring. A resulting mixture was added into a torque rheometer, subjected to melting and blending at a temperature of 230 C. for 6 min, and then cooled to obtain an SC-PLA initial powder. The initial powder was placed in deionized water for selective etching of a PEG phase, and then dried to obtain a layered porous polylactic acid powder. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 98%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 94%.

[0066] The powder has a d.sub.33 coefficient of 0.8 pC/N. When the powder is used in an IC pigment degradation experiment, the degradation efficiency of the pigment is 8%. After the powder is used in the pigment degradation experiment for 10 times, the degradation efficiency of the pigment is 2%.

[0067] Performance Test:

[0068] In the present disclosure, the microstructure of the composite materials obtained in Example 1 and Comparative Examples 1-2 is tested, and results are as shown in FIG. 2. From FIG. 2a and FIG. a, it can be seen that in Comparative Example 1, the PEO (with an Mw of 30,000 g/mol) pore-forming agent used has poor compatibility with the PLA matrix, phase separation from the PLA matrix is conducted in a melt state to obtain an island-like porous structure, and the powder has large powder particles and uneven size, so that the structure has little effect of improving the piezoelectric properties, and the d.sub.33 coefficient is only 0.3 pC/N. In Example 1 (FIG. b and FIG. b), the PEG (with an Mw of 10,000 g/mol) pore-forming agent used has good compatibility with the PLA matrix (the blend has a homogeneous structure in a molten state), and phase separation is conducted after the PLA matrix is crystallized to form a layered stacking structure, so that the finally obtained powder has excellent piezoelectric properties, and the d.sub.33 coefficient is as high as 35.5 pC/N. In Comparative Example 2, the PEG (with an Mw of 10,000 g/mol similar to that in Example 1) pore-forming agent used has good compatibility with the PLA matrix, but the processing temperature is as high as 230 C. (very close to the melting point of SC-PLA), and the layered porous structure of the powder is almost destroyed, so that the piezoelectric properties are greatly reduced, and the d.sub.33 coefficient is only 0.8 pC/N.