CN113956488A - PBAT-based self-reinforced elastomer and preparation method and application thereof - Google Patents
PBAT-based self-reinforced elastomer and preparation method and application thereof Download PDFInfo
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Abstract
The invention discloses a PBAT-based self-reinforced elastomer, a preparation method and an application thereof, wherein the self-reinforced elastomer is prepared from the following components in parts by weight: PBAT 19-80 parts, polyether 19-80 parts, and catalyst 0.01-0.05 part. The invention prepares the block copolymer of PBAT and polyether by one step through an ester exchange method. The copolymer has the characteristic of an elastomer, and if stressed during use, the microstructure of the copolymer generates oriented microfibers along the stress direction, so that the copolymer is converted into a self-reinforced elastomer in situ. The self-reinforced elastomer does not need to prepare fibers separately in advance, does not need to compound the fibers and a matrix, does not need an organic solvent, and has simple required equipment and preparation process. According to the invention, the elastomer and the PLA are melted and blended to exist in the composite material in a dispersed phase form, so that the composite material can be toughened, and the tensile strength of the composite material can be improved.
Description
Technical Field
The invention belongs to the technical field of polymers, and particularly relates to a PBAT-based self-reinforced elastomer, and a preparation method and application thereof.
Background
In 1975, capatii and Porter first proposed the concept of self-reinforced composites and first applied to the preparation of polyethylene self-reinforced composites. In the self-reinforced composite material, the reinforcing phase and the base phase belong to the same homologous compound or have the same molecular structure. The highly anisotropic reinforcing phase acts as a bearing force, and the reinforcing phase is bonded by the base phase having lower isotropy or anisotropy. The preparation method of the self-reinforced composite material mainly comprises an impregnation hot-pressing method, a skin-core structure fiber hot-pressing method, an apposition method and a wrapping method. The basic principle is to select the reinforcing phase and the base phase with the same chemical structure and different melting points and create a temperature processing window, heat treatment is carried out in the temperature processing window, the matrix with the low melting point is melted and the reinforcing body is impregnated or coated, and the matrix is solidified after cooling down to bond the reinforcing phase, thereby preparing the self-reinforcing material.
Chinese patent publication nos. CN105368022A and CN109593216A both disclose a self-reinforcing material prepared by impregnation hot pressing. The method comprises the steps of carrying out melt spinning on a polymer to obtain nascent fiber, and stretching to obtain polymer stretched fiber. And finally, after the polymer drawn fiber passes through the low-melting-point polymer solution, drying the polymer drawn fiber by hot air, carrying out hot pressing and cooling, thus obtaining the composite material. Chinese patent publication nos. CN104001428A, CN104888621A, CN104888621A and CN104801205A all disclose a self-reinforced hollow fiber membrane prepared by a skin-core structure fiber hot pressing method. The method is to prepare the hollow braided tube reinforcement and then prepare the membrane casting solution. And finally, uniformly coating the casting solution on the surface of the hollow braided tube through a co-extrusion spinning head, and then immersing the hollow braided tube into a coagulating bath for forming through an air gap under the traction of a godet roller to obtain the hollow fiber membrane. Chinese patent publication No. CN108265566A discloses a self-reinforced para-aramid paper prepared by using an isotopologue method. The method comprises the steps of mixing, defibering and dispersing aramid chopped fibers, pulp, fibrid and aramid nano fibers to prepare uniform suspension, papermaking and forming, squeezing, drying and further carrying out hot pressing on a hot press to obtain the aramid paper. Alper et al prepared polycaprolactone self-reinforced composite materials by a supramolecular chemical method in which inclusion methods are used to form host-guest structures. The method is characterized in that an acetone solution of polycaprolactone and an aqueous solution of cyclodextrin are mixed under certain conditions, and a hydrophobic inner cavity of the cyclodextrin can wrap single polycaprolactone high-molecular chains to form a bead string shape. At the moment, the polymer chain of the polycaprolactone is changed into a straight chain structure from an entangled state or a random winding state, and the regularity of the molecular chain is greatly improved. After the cyclodextrin is removed, the straightened structure of the macromolecular chain is maintained, at which point the polymer exhibits a higher mechanical strength [ Gurarslan, A.; shen, j.; tonelli, A.E., Behavior of Poly (ε -Caprolactone) S (PCLs) Coalesc from the same Stoichimetric Urea addition Compounds and the same Use as Nucleavants for crystallization PCL catalysts: macromolecules 2012, 45(6), 2835-.
In the self-reinforced material preparation technology, the reinforced fiber needs to be prepared firstly, then the reinforced fiber and the resin are compounded, the preparation process is complex, the equipment requirement is high, part of the technology even needs to be added with an organic solvent, the problem of cost increase caused by solvent recovery exists, and the risk of environmental pollution exists.
Polylactic acid (PLA) is a novel biodegradable material with the largest yield and the widest application range at present. It has the advantages of excellent degradation performance, high mechanical strength, good processing performance and the like, but the application of the material in many fields is limited due to the problem of brittle texture. Poly (butylene adipate terephthalate) (PBAT) has both excellent degradability and ductility of aliphatic polyesters and good mechanical properties and high temperature resistance of aromatic polyesters. The PBAT and the PLA are usually used for blending modification, so that the toughness of the PLA can be improved, and the processability of the PBAT can be improved, but the PBAT serving as a tough material generally reduces the strength of a blend. Therefore, while the PBAT is toughened, the impact strength and the elongation at break of the PBAT/PLA composite material are improved by adding the bisoxazoline, the isocyanate, the styrene-acrylate-epoxy acrylate copolymer and the like as chain extenders in Chinese patents CN103589124A and CN 111718566A. In the Chinese patent CN113429762A, talcum powder is added as a nano filler for blending modification, so that the strength of the PLA/PBAT composite material is improved. Chinese patent CN104194294A discloses a PLA/PBAT composite material, a preparation method and application thereof, so as to improve the mechanical strength of the PLA/PBAT material; the preparation method of the composite material comprises the following steps: placing PLA and PBAT into a vacuum drying oven, and drying for 8-16 hours at 70-100 ℃; putting the hyperbranched triazine, the PLA, the PBAT, the stearic acid, the calcium stearate and the antioxidant into an internal mixer according to the weight part ratio for uniformly mixing; and putting the extruded mixed material into a tablet machine for tabletting to prepare the PLA/PBAT composite material, wherein the tensile strength of the composite material is 24-25.44 MPa, and the elongation at break of the composite material is 20.19-69.86%. Chinese patent CN111040395A discloses a PBAT/PLA composite material added with nano lanthanum oxide, epoxy compound and citrate plasticizer, which greatly improves the tensile strength and elongation at break of the composite material.
However, the technology for preparing the PLA composite material has the problem of complex formula and process, and even if other auxiliary agents are added, the improvement of the tensile strength and the elongation at break of the composite material is very limited.
Disclosure of Invention
The purpose of the invention is as follows: the invention aims to solve the technical problem of providing a PBAT-based self-reinforced elastomer, and a preparation method and application thereof.
The invention also aims to solve the technical problem of providing a preparation method of the PLA/PBAT-based elastomer blend, wherein the PBAT-based elastomer is used for modifying PLA, the process is simple, and the strength and the toughness of the material are improved.
The technical scheme is as follows: in order to solve the problems of the prior art, the invention provides a PBAT-based self-reinforced elastomer, which is prepared from the following components in parts by weight: PBAT 19-80 parts, polyether 19-80 parts, and catalyst 0.01-0.05 part.
Wherein the polyether is one or more of bifunctional polyethers such as polyethylene oxide, ethylene oxide/propylene oxide copolymer, polytetrahydrofuran, polypropylene glycol or epichlorohydrin-tetrahydrofuran copolyether.
Wherein the PBAT is a conventional commercial product.
Wherein the catalyst is one or more of esterification catalysts such as n-butyl titanate, antimony trioxide, alkoxy aluminum, titanium oxide, or antimony acetate.
The invention also comprises a preparation method of the PBAT-based self-reinforced elastomer, which comprises the following steps: under the protection of nitrogen, PBAT, polyether and a catalyst are put into a reaction kettle to be heated, after the PBAT, the polyether and the catalyst are melted, a stirring and vacuum pump is started, ester exchange reaction is carried out at constant temperature, and after the reaction is finished, the copolymer is prepared.
Wherein the transesterification reaction temperature is 200-280 ℃.
Wherein the vacuum degree is 50-500 Pa.
The invention also provides the use of PBAT-based self-reinforced elastomers for toughening or/and reinforcing PLA.
The invention also provides a preparation method of the PLA/PBAT-based elastomer blend, which comprises the following steps:
(1) preparation of PBAT-based elastomer: heating PBAT, polyether and a catalyst in a reaction kettle, melting, starting a stirring and vacuum pump, performing ester exchange reaction at a constant temperature, and preparing a copolymer, namely the PBAT-based elastomer after the reaction is finished;
(2) preparation of PLA/PBAT-based elastomer blends: and placing the PLA and the PBAT-based elastomer into a hopper of a double-screw extruder with a dryer, and extruding by the extruder to obtain the PLA/PBAT-based elastomer blend.
The polyether is bifunctional polyether, preferably one or more of polyethylene oxide, ethylene oxide/propylene oxide copolymer, polytetrahydrofuran, polypropylene glycol or epichlorohydrin-tetrahydrofuran copolyether.
Wherein the catalyst is one or more of esterification catalysts such as n-butyl titanate, antimony trioxide, alkoxy aluminum, titanium oxide, or antimony acetate.
Wherein in the step (1), the PBAT is 19-80 parts, the polyether is 19-80 parts, and the catalyst is 0.01-0.05 part by weight.
Wherein in the step (2), the PLA 60-90 parts and the PBAT-based elastomer 10-40 parts are calculated according to the weight parts.
Wherein, the first zone to the sixth zone and the head temperature of the double-screw extruder in the step (2) are 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃.
Wherein the extrusion speed of the twin-screw extruder in the step (2) is 80-150 revolutions per minute.
The invention carries out ester exchange reaction after adding catalyst into PBAT and bifunctional polyether, and the butanediol on the PBAT molecular chain is replaced by the polyether and is embedded into the PBAT molecular chain, thus preparing the block copolymer of PBAT and polyether. The copolymer has the characteristic of an elastomer, and if stressed during use, the microstructure of the copolymer generates oriented microfibers along the stress direction, so that the copolymer is converted into a self-reinforced elastomer in situ.
Has the advantages that: compared with the prior art, the invention has the following advantages: the self-reinforced elastomer is used as one of self-reinforced materials, fibers do not need to be prepared independently in advance, the fibers do not need to be compounded with a matrix, an organic solvent is not needed, and required equipment and a preparation process are simple. The self-reinforced elastomer prepared by the invention can be directly used in a common high polymer melt blending production line in the processes of modification, processing and molding. The elastomer and the PLA are melted and blended to be present in the composite material in a dispersed phase form, so that the composite material can be toughened, and the tensile strength of the composite material can be improved. The PLA/PBAT-based elastomer blend prepared by the invention can be directly used in a common thermoplastic polymer material production line, can obtain a material with fiber reinforcement characteristics without increasing the process flow, and has strong applicability and wider application.
Drawings
FIG. 1 is a scanning electron micrograph of a self-reinforced elastomer prepared according to example 3.
Detailed Description
Other reagents of PBAT of the present invention and the like are commercially available products.
The invention is further described below with reference to the figures and examples.
EXAMPLE 1 preparation of self-reinforcing elastomer
Under the protection of nitrogen, 80 parts of PBAT, 19 parts of polytetrahydrofuran and 0.01 part of n-butyl titanate are put into a reaction kettle and heated to 240 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 50Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
EXAMPLE 2 preparation of self-reinforced Elastomers
Under the protection of nitrogen, 60 parts of PBAT, 39.9 parts of ethylene oxide/propylene oxide copolymer and 0.03 part of antimony trioxide are placed into a reaction kettle and heated to 280 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 100Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
EXAMPLE 3 preparation of self-reinforced Elastomers
Under the protection of nitrogen, 50 parts of PBAT, 49.9 parts of polyethylene oxide and 0.03 part of alkoxy aluminum are put into a reaction kettle and heated to 200 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 500Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
EXAMPLE 4 preparation of self-reinforced Elastomers
Under the protection of nitrogen, 30 parts of PBAT, 59.9 parts of polypropylene glycol and 0.04 part of titanium oxide are put into a reaction kettle and heated to 200 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 300Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
EXAMPLE 5 preparation of self-reinforcing Elastomers
Under the protection of nitrogen, 19 parts of PBAT, 80 parts of epichlorohydrin-tetrahydrofuran copolyether and 0.05 part of antimony acetate are put into a reaction kettle and heated to 260 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 50Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
Comparative example 1
Under the protection of nitrogen, 50 parts of PBAT, 49.9 parts of polyoxypropylene tetraol and 0.03 part of alkoxy aluminum are put into a reaction kettle and heated to 200 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 500Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
Comparative example 2
Under the protection of nitrogen, 80 parts of polybutylene terephthalate (PBT), 19 parts of polytetrahydrofuran and 0.01 part of n-butyl titanate are put into a reaction kettle and heated to 240 ℃, after melting, a stirring and vacuum pump is started, ester exchange reaction is carried out at a constant temperature of 50Pa of vacuum degree, and after the reaction is finished, the copolymer is prepared.
The results of mechanical property tests of the copolymers prepared in examples 1 to 5 and the copolymers prepared in comparative examples 1 to 2 are shown in Table 1.
The test method of the mechanical property is GB/T1040-2006 (standard method for measuring the tensile property of plastics).
TABLE 1
As can be seen from Table 1, the tensile strength and tensile strain at break of the copolymer obtained in comparative example 1 are lower than those of the copolymer obtained in example 3. This is because the polyoxypropylene tetraol in comparative example 1 is not a bifunctional polyether, and crosslinking or grafting occurs during the esterification reaction, resulting in no fiber generation during stretching. The reason why the tensile strength of the copolymer obtained in comparative example 2 is smaller than that of example 1 is that the tensile strength is larger because the PBT in the copolymer obtained in comparative example 2 is an aromatic polyester having a very high rigidity, but the tensile strength at break is smaller because no fiber is generated during the drawing. The copolymers prepared in examples 1 to 5 have fibers formed due to the presence of the polyether glycol blocks and no crosslinking or grafting reaction during the esterification reaction, thereby increasing the tensile strain at break and the tensile strength of the copolymer, and enabling the copolymer to have better mechanical strength and greater tensile strain. Scanning electron microscope analysis was performed on the adipic acid/butylene terephthalate glycol copolymer obtained in example 3. As can be seen in fig. 1, a is the microstructure when unstressed, in which case no fibres are present in the material. b and c are microstructures when the stress is gradually increased, the material gradually generates oriented fibers in the same direction as the stress under the action of the stress, and the fiber structure is more obvious along with the increase of the stress.
Example 6
PLA and the PBAT self-reinforced elastomer prepared in example 1 were uniformly blended at a ratio of 90: 10 and then fed into a twin-screw extruder, and the temperatures of the first zone to the sixth zone and the head of the extruder were set to 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃, 180 ℃ respectively. Extruding at the speed of 130r/min, drawing and granulating to obtain the PLA/PBAT-based elastomer blend. The performance parameters of the blends are shown in Table 2.
Example 7
PLA and the PBAT self-reinforced elastomer prepared in example 2 were uniformly blended at a ratio of 80: 20 and then fed into a twin-screw extruder, and the temperatures of the first zone to the sixth zone and the head of the extruder were set to 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃, 180 ℃ respectively. Extruding at the speed of 110r/min, drawing and granulating to obtain the PLA/PBAT-based elastomer blend. The performance parameters of the blends are shown in Table 2.
Example 8
PLA and the PBAT self-reinforced elastomer prepared in example 3 were uniformly blended at a ratio of 70: 30 and then fed into a twin-screw extruder, and the temperatures of the first zone to the sixth zone and the head of the extruder were set to 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃, 180 ℃ respectively. Extruding at the speed of 100r/min, drawing and granulating to obtain the PLA/PBAT-based elastomer blend. The performance parameters of the blends are shown in Table 2.
Example 9
PLA and the PBAT self-reinforced elastomer prepared in example 4 were uniformly blended at a ratio of 60: 40, and then fed into a twin-screw extruder, and the temperatures of the first zone to the sixth zone and the head of the extruder were set to 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃, 180 ℃ respectively. Extruding at the speed of 100r/min, drawing and granulating to obtain the PLA/PBAT-based elastomer blend. The performance parameters of the blends are shown in Table 2.
Comparative example 3
PLA and PBAT are evenly blended according to the mass ratio of 90: 10 and then added into a double-screw extruder, and the temperatures of a first zone to a sixth zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 130r/min, drawing, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 4
PLA and PBAT are evenly blended according to the mass ratio of 80: 20 and then added into a double-screw extruder, and the temperatures of a first zone to a sixth zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 110r/min, drawing strips, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 5
PLA and PBAT are evenly blended according to the mass ratio of 70: 30 and then added into a double-screw extruder, and the temperatures of a first zone to a sixth zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 100r/min, drawing strips, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 6
PLA and PBAT are evenly blended according to the mass ratio of 60: 40 and then added into a double-screw extruder, and the temperatures of a first zone to a sixth zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 90/min, drawing strips, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 7
PLA, PBAT and polyglyceryl diacetate are evenly blended according to the mass ratio of 90: 10: 5 and then added into a double-screw extruder, and the temperatures of a first zone, a second zone, a third zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 130r/min, drawing, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 8
PLA, PBAT and nano calcium carbonate (nano-CaCo3) are evenly blended according to the mass ratio of 80: 20: 5, then added into a double-screw extruder, and the temperatures of a first zone, a second zone, a third zone and a machine head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 110r/min, drawing strips, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
Comparative example 9
PLA, PBAT and a compatibilizer DT are evenly blended according to the mass ratio of 70: 30: 0.3 and then added into a double-screw extruder, and the temperatures of a first zone, a second zone, a third zone and a head of the extruder are respectively set to be 100 ℃, 150 ℃, 170 ℃, 180 ℃, 190 ℃ and 180 ℃. Extruding at the speed of 100r/min, drawing strips, and granulating to obtain the PLA/PBAT composite material. The performance parameters of the PLA/PBAT composite are shown in Table 2.
The mechanical properties of the PLA/PBAT-based elastomer blends prepared in examples 6-9 and the composites prepared in comparative examples 3-9 were tested, and the results are shown in table 2.
The test method of the mechanical property is GB/T1040-2006 (standard method for measuring the tensile property of plastics).
TABLE 2 Properties of PLA/PBAT-based elastomer blends and mechanical Properties of PLA/PBAT composites
As can be seen from Table 2, comparative examples 3 to 6 are smaller in both tensile strength and tensile strain at break than the copolymers obtained in examples 6 to 9. The tensile strength and the elongation at break of the pure PLA are reduced along with the increase of the content of the PBAT, because the tensile strength and the elongation at break of the composite material are reduced to a certain extent by only adding the toughness material PBAT in the comparative examples 3-6, but the tensile strength of the composite material is reduced compared with the tensile strength of the pure PLA, and the compatibility between the PLA and the PBAT is poor. The copolymers obtained in examples 6 to 9 have a fiber structure formed therein under stress due to the presence of the polyether glycol block and no crosslinking or grafting reaction during the esterification reaction, thereby increasing the elongation at break and tensile strength of the copolymer. In comparative examples 7-9, other additives were added to ensure the tensile strength of the composite to some extent, and the elongation at break was improved using PBAT, but the tensile strength and elongation at break were still much lower than the copolymers prepared in examples 6-9.
Claims (9)
1. The PBAT-based self-reinforced elastomer is characterized by comprising the following components in parts by weight: PBAT 19-80 parts, polyether 19-80 parts, and catalyst 0.01-0.05 part.
2. The PBAT-based self-reinforced elastomer of claim 1, wherein the polyether is a difunctional polyether.
3. The PBAT-based self-reinforced elastomer of claim 1, wherein the polyether is one or more of polyethylene oxide, ethylene oxide/propylene oxide copolymer, polytetrahydrofuran, polypropylene glycol, or epichlorohydrin-tetrahydrofuran copolyether.
4. The PBAT-based self-reinforced elastomer of claim 1, wherein the catalyst is an esterification catalyst.
5. The PBAT-based self-reinforced elastomer of claim 1, in which the catalyst is one or more of n-butyl titanate, antimony trioxide, aluminum alkoxide, titanium oxide or antimony acetate.
6. The method for preparing the PBAT-based self-reinforced elastomer of any one of claims 1 to 5, comprising the steps of: under the protection of nitrogen, PBAT, polyether and a catalyst are put into a reaction kettle to be heated, after the PBAT, the polyether and the catalyst are melted, a stirring and vacuum pump is started, ester exchange reaction is carried out at constant temperature, and after the reaction is finished, the copolymer is prepared.
7. The method of claim 6, in which the transesterification temperature is 200 to 280 ℃.
8. The method for preparing the PBAT-based self-reinforced elastomer according to claim 6, wherein the vacuum degree is 50-500 Pa.
9. Use of the PBAT-based self-reinforced elastomer of any of claims 1 to 5 for toughening or/and reinforcing polylactic acid.
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| CN113897043A (en) | 2022-01-07 |
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