The present disclosure relates to a polybutylene terephthalate resin composition, a method of preparing the same, and a molded article including the same, and more particularly to a polybutylene terephthalate resin composition exhibiting an excellent physical property balance between mechanical properties and flame retardancy even without a halogen-based flame retardant, a method of preparing the polybutylene terephthalate resin composition and a molded article including the polybutylene terephthalate resin composition.
To realize weight reduction and reduce manufacturing costs, research is actively being conducted to replace automobile component materials with plastic in the automobile field.
Among plastics, polyester resin is widely used as a material for automobile components and is evaluated as having the potential to replace aluminum or steel. Among polyester resins as materials for automobile components, research into the application of a polybutylene terephthalate resin to various automobile components is being actively conducted due to the excellent high rigidity and heat resistance of the polybutylene terephthalate resin.
However, to apply a polybutylene terephthalate resin as a material for electronic components, especially connector parts, it is necessary to develop a flame retardant composite material containing a non-halogenated flame retardant.
A metal salt phosphorus-based flame retardant is mainly used as a non-halogenated flame retardant for a polybutylene terephthalate resin composite material, but, when compared to when using a halogen-based flame retardant, it is difficult to realize the same degree of mechanical rigidity and flame retardancy. Accordingly, there is an urgent need for the development of a polybutylene terephthalate resin composition having excellent mechanical rigidity and flame retardancy while including a non-halogenated flame retardant.
The background description provided herein is for the purpose of generally presenting context of the disclosure. Unless otherwise indicated herein, the materials described in this section are not prior art to the claims in this application and are not admitted to be prior art, or suggestions of the prior art, by inclusion in this section.
Therefore, the present disclosure has been made in view of the above problems, and it is one object of the present disclosure to provide a polybutylene terephthalate resin composition capable of realizing a physical property balance between mechanical strength and flame retardancy suitable for an automobile component material, and a method of preparing the polybutylene terephthalate resin composition.
It is another object of the present disclosure to provide a molded article manufactured using the polybutylene terephthalate resin composition.
The above and other objects can be accomplished by the present disclosure described below.
In accordance with an aspect of the present disclosure, the above and other objects can be accomplished by the provision of a polybutylene terephthalate resin composition, including: polybutylene terephthalate; an aluminum salt of diethyl phosphinic acid; melamine polyphosphate; and a silica-containing reinforcing agent, wherein the polybutylene terephthalate resin composition satisfies Equation 1:
where a represents a tensile strength (MPa) of the polybutylene terephthalate resin composition measured according to ISO 527, and b represents a flow index (g/10 min) of the polybutylene terephthalate resin composition measured at 265° C. under a load of 2.16 kg according to ISO 1133.
II) In I), the silica-containing reinforcing agent may include 50% by weight or more, specifically 50 to 70% by weight, preferably 50 to 65% by weight, more preferably 50 to 60% by weight, of silica.
III) In I) or II), when a content of the polybutylene terephthalate is c and a content of the silica-containing reinforcing agent is d, the polybutylene terephthalate resin composition may satisfy 0.5d≤c≤2d.
Here, the content may mean % by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent, or, as needed, may mean % by weight based on 100% by weight of a total of one or more selected from among melamine cyanurate, polyethylene, a processability improver and a heat-resistant additive as well as the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent.
IV) In I) to III), the polybutylene terephthalate may be included in an amount of 15 to 65% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may further include a processability improver and a heat-resistant additive, and the polybutylene terephthalate may be included in an amount of 15 to 65% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent, the processability improver and the heat-resistant additive.
V) In I) to IV), the polybutylene terephthalate may have an intrinsic viscosity (η) of 0.5 to 1.25 dl/g measured according to ASTM D2857.
VI) In I) to V), the silica-containing reinforcing agent may be included in an amount of 10 to 50% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may further include a processability improver and a heat-resistant additive, and the silica-containing reinforcing agent may be included in an amount of 10 to 50% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent, the processability improver and the heat-resistant additive.
VII) In I) to VI), the aluminum salt of diethyl phosphinic acid may be included in an amount of 5 to 35% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may further include a processability improver and a heat-resistant additive, and the aluminum salt of diethyl phosphinic acid may be included in an amount of 5 to 35% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent, the processability improver and the heat-resistant additive.
VIII) In I) to VII), the melamine polyphosphate may be included in an amount of 0.1 to 10% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, and the silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may further include a processability improver and a heat-resistant additive, and the melamine polyphosphate may be included in an amount of 0.1 to 10% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent, the processability improver and the heat-resistant additive.
IX) In I) to VIII), the polybutylene terephthalate resin composition may further include melamine cyanurate in an amount of 0.1 to 10% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent and the melamine cyanurate; or the polybutylene terephthalate resin composition may further include melamine cyanurate, a processability improver and a heat-resistant additive, and the processability improver and the heat-resistant additive may be included in an amount of 0.1 to 10% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent, the melamine cyanurate, the processability improver and the heat-resistant additive.
X) In I) to IX), the resin composition may further include a processability improver in an amount of 0.001 to 3% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent and the processability improver.
XI) In I) to X), the resin composition may further include a heat-resistant additive in an amount of 0.001 to 3% by weight based on 100% by weight of a total of the polybutylene terephthalate, the aluminum salt of diethyl phosphinic acid, the melamine polyphosphate, the silica-containing reinforcing agent and the heat-resistant additive.
In accordance with another aspect of the present disclosure, there is provided a method of preparing a polybutylene terephthalate resin composition, the method including: kneading and extruding polybutylene terephthalate; an aluminum salt of diethyl phosphinic acid; melamine polyphosphate; and a silica-containing reinforcing agent, wherein the polybutylene terephthalate resin composition satisfies Equation 1:
where a represents a tensile strength (MPa) of the polybutylene terephthalate resin composition measured according to ISO 527, and b represents a flow index (g/10 min) of the polybutylene terephthalate resin composition measured at 265° C. under a load of 2.16 kg according to ISO 1133. XIII) In accordance with yet another aspect of the present disclosure, there is provided a molded article including the above-described polybutylene terephthalate resin composition.
XIV) In XIII), the molded article may be an automotive electronic component.
As apparent from the above description, a polybutylene terephthalate resin composition according to the present disclosure can provide an excellent physical property balance between mechanical strength and flame retardancy at a level equivalent to or higher than that of a polyester resin composite material containing a halogen-based flame retardant, has excellent processability due to excellent flowability, and can be provided as a material for automotive electronic components.
That is, a molded article made of the polybutylene terephthalate resin composition according to the present disclosure can exhibit a high level of physical property balance between mechanical properties such as tensile strength and flame retardancy.
Therefore, the polybutylene terephthalate resin composition according to the present disclosure and a molded article including the same can be widely used in the field of automobile components requiring the same.
Hereinafter, the present disclosure will be described in more detail to aid in understanding of the present disclosure.
The terms and words which are used in the present specification and the appended claims should not be construed as being confined to common meanings or dictionary meanings but should be construed as having meanings and concepts matching the technical spirit of the present disclosure in order to describe the present disclosure in the best fashion.
The present inventors confirmed that a balance of physical properties of mechanical strength and flame retardancy at a level suitable for an automobile component material can be realized by adjusting the type and content of a non-halogenated flame retardant, thus completing the present disclosure.
The polybutylene terephthalate resin composition according to the present disclosure includes polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent.
When a is a tensile strength (MPa) measured by ISO 527 and b is a flow index (g/10 min) measured according to ISO 1133 under a load of 2.16 kg at 265° C., a/b of the polybutylene terephthalate resin composition may satisfy, for example, 7.76 to 45, specifically 7.76 to 40, preferably 7.77 to 40. When the ranges are satisfied, the property balance among rigidity, flame retardancy and processability can be provided.
In an embodiment of the present disclosure, a may be 130 or more, or 130 to 165, and b may be 4 to 20, or 4 to 18.
Hereinafter, each component of the polybutylene terephthalate resin composition of the present disclosure is described in detail.
In one embodiment of the present disclosure, as the polybutylene terephthalate, polybutylene terephthalate obtained by polycondensation through direct esterification or transesterification of 1,4-butanediol and terephthalic acid or dimethyl terephthalate may be used.
In one embodiment of the present disclosure, to increase the impact strength of the polybutylene terephthalate resin composition, a copolymer obtained by copolymerizing the polybutylene terephthalate and an impact strength enhancing compound such as polytetramethylene glycol, polyethylene glycol, polypropylene glycol, aliphatic polyester, and aliphatic polyamide or a modified polybutylene terephthalate obtained by mixing the polybutylene terephthalate and the impact strength enhancing compound may be used.
In an embodiment of the present disclosure, the intrinsic viscosity (η) of the polybutylene terephthalate measured according to ASTM D2857 may be, for example, 0.5 to 1.25 dl/g, preferably 0.5 to 1.25 dl/g, more preferably 0.52 to 1 dl/g. When the intrinsic viscosity of the polybutylene terephthalate is within the ranges, a polybutylene terephthalate resin composition in which a property balance between mechanical property and moldability is excellent may be obtained.
In an embodiment of the present disclosure, the polybutylene terephthalate may be included in an amount of 15 to 65% by weight, 25 to 58% by weight, preferably 40 to 58% by weight, more preferably 40 to 55% by weight, even more preferably 45 to 55% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may include a processability improver and a heat-resistant additive and the polybutylene terephthalate may be included in an amount of 15 to 65% by weight, 25 to 58% by weight, preferably 40 to 58% by weight, more preferably 40 to 55% by weight, even more preferably 45 to 55% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, a processability improver and a heat-resistant additive. When the polybutylene terephthalate is included within the ranges, a polybutylene terephthalate resin composition having an excellent property balance among processability, specific gravity and mechanical property may be provided.
In an embodiment of the present disclosure, the reinforcing agent may be, for example, glass fiber, and the reinforcing agent may be used in combination with other inorganic fibers.
Here, the inorganic fiber may include one or more selected from carbon fiber, basalt fiber, and natural fiber such as kenaf or hemp.
In an embodiment of the present disclosure, the cross-section of the reinforcing agent may have a shape such as a circle, a rectangle, an oval, a dumbbell, or a rhombus. The reinforcing agent may have an average diameter of 8 to 20 μm, or 10 to 15 μm and an average length of 2 to 6 mm, or 2 to 4 mm.
Here, the average diameter and average length of the reinforcing agent may be measured by methods commonly used in the art. For example, the reinforcing agent may be observed with a scanning electron microscope (SEM), and an average diameter and average length of 10 to 30 strands of the reinforcing agent may be respectively measured.
During a fiber production or post-treatment process, the reinforcing agent may be treated with a sizing agent, and the sizing agent may include a processing improver, a coupling agent, and a surfactant.
The processing improver is mainly used to form good strands, and the coupling agent improves adhesion between the reinforcing agent and the polybutylene terephthalate resin. When the coupling agent is appropriately selected and used in consideration of the types of the polybutylene terephthalate resin and the reinforcing agent, excellent physical properties may be imparted to the polybutylene terephthalate resin composition.
Methods of using the coupling agent may include a method of directly treating with a reinforcing agent, a method of adding to an organic matrix, and the like, and to sufficiently exhibit the performance of the coupling agent, the content thereof should be appropriately selected.
Examples of the coupling agent include amine-based coupling agents, acrylic coupling agents, and silane-based coupling agents such as γ-aminopropyltriethoxysilane, γ-aminopropyltrimethoxysilane, N-(beta-aminoethyl) γ-aminopropyltriethoxysilane, γ-methacryloxypropyl triethoxysilane, γ-glycidoxypropyl trimethoxysilane, and β (3,4-epoxyethyl) γ-aminopropyl trimethoxysilane.
In particular, the reinforcing agent of the present disclosure contains preferably silica. In this case, rigidity and mechanical property can be provided.
In the reinforcing agent, the silica may be included in an amount of, for example, 50% by weight or more, specifically 50 to 70% by weight, preferably 50 to 65% by weight, more preferably 50 to 60% by weight. When these ranges are satisfied, an excellent balance between rigidity and mechanical property may be provided.
Specifically, as shown in the following examples and comparative examples, it can be confirmed that, when silica is added in a non-appropriate content, for example when 48% by weight of a reinforcing agent is added as an alternative, flame retardancy is excellent, but a balance between physical properties is not provided due to poor tensile strength and flow index (see Comparative Example 4).
In the present disclosure, the content of silica in the reinforcing agent may be measured or confirmed using X-Ray Fluorescence spectrometry (XRF).
In an embodiment of the present disclosure, the silica-containing reinforcing agent may be included in an amount of 10 to 50% by weight, preferably 15 to 50% by weight, more preferably 20 to 50% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may include a processability improver and a heat-resistant additive, and the silica-containing reinforcing agent may be included in an amount of 10 to 50% by weight, preferably 15 to 50% by weight, more preferably 20 to 50% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, a processability improver and a heat-resistant additive.
The non-halogenated flame retardant according to the present disclosure may include an aluminum salt of diethyl phosphinic acid and melamine polyphosphate, may provide flame retardant effect during extrusion and injection molding of the polybutylene terephthalate resin composition, and may sufficiently provide a flame retardant effect even when the polybutylene terephthalate resin composition is stored for a long time.
The aluminum salt of diethyl phosphinic acid can improve the flame retardancy of a composition by forming a char on the surface of a polymer.
In an embodiment of the present disclosure, the aluminum salt of diethyl phosphinic acid may be a commercially available product.
The aluminum salt of diethyl phosphinic acid may be included, for example, in an amount of 5 to 35% by weight, 10 to 30% by weight, specifically 10 to 25% by weight, preferably 10 to 20% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may include a processability improver and a heat-resistant additive, and the aluminum salt of diethyl phosphinic acid may be included in an amount of 5 to 35% by weight, 10 to 30% by weight, specifically 10 to 25% by weight, preferably 10 to 20% by weight based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, a processability improver and a heat-resistant additive. When these ranges are satisfied, The flame retardancy of the composition may be improved by forming a char on a polymer surface.
When the melamine polyphosphate is used together with the aluminum salt of diethyl phosphinic acid described above, the melamine polyphosphate and the aluminum salt of diethyl phosphinic acid form a char on a polymer surface together, thereby enhancing a protection effect against combustion.
In an embodiment of the present disclosure, a commercially available product may be used as the melamine polyphosphate.
The melamine polyphosphate may be included in an amount of, for example, 0.1 to 10% by weight, specifically 0.1 to 5% by weight, preferably 1 to 5% by weight, more preferably 2 to 4% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent; or the polybutylene terephthalate resin composition may include a processability improver and a heat-resistant additive, and the melamine polyphosphate may be included in an amount of, for example, 0.1 to 10% by weight, specifically 0.1 to 5% by weight, preferably 1 to 5% by weight, more preferably 2 to 4% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, a processability improver and a heat-resistant additive. When these ranges are satisfied, a char may be sufficiently formed on a polymer surface, thereby improving the flame retardancy of the composition.
According to an embodiment of the present disclosure, melamine cyanurate may be included. In this case, an inert gas may be generated, thereby improving flame retardancy.
The melamine cyanurate may be included in an amount of, for example, 0.1 to 10% by weight, specifically 0.1 to 4.5% by weight, preferably 0.1 to 3.5% by weight, more preferably 1 to 3.5% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent and melamine cyanurate; or the polybutylene terephthalate resin composition may include a processability improver and a heat-resistant additive and may be included in an amount of, for example, 0.1 to 10% by weight, specifically 0.1 to 4.5% by weight, preferably 0.1 to 3.5% by weight, more preferably 1 to 3.5% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, melamine cyanurate, a processability improver and a heat-resistant additive.
The processability improver according to the present disclosure may be olefin wax, and serves to help the polybutylene terephthalate resin composition maintain excellent releasability and injection properties.
The olefin wax may be a polymer having a low melt viscosity and may be an oily solid having sliding properties and plasticity. For example, the olefin wax may include at least one selected from polyethylene wax and polypropylene wax, and commercially available olefin wax may be used.
For example, polyethylene may be used as the processability improver. Specifically, polyethylene having a drop point of 100 to 120° C., a melting point (mp) of 95 to 115° C., a density (23° C.) of 0.9 to 1.0 g/cm3, and an absolute viscosity (120° C.) of 350 to 450 mm2/s may be used. In this case, releasability and injection moldability may be effectively provided.
In the present disclosure, a dropping point indicates the temperature at which a lubricant transitions from a semi-solid to a liquid according to ASTM D566, KS M 2033. More specifically, a sample is placed in a specified cup having a diameter of 100 mm and the sample is heated according to the specified conditions. Then, a temperature at which grease drops is measured. In this case, the temperature represents a dropping point.
In the present disclosure, melting point may be measured using a differential scanning calorimeter 2920 (DSC 2920, TA Co.). As a specific example of measuring melting point, after a DSC is equilibrated at a temperature of 0° C., the temperature is increased to 180° C. at a rate of 20° C./min, the temperature is reduced to −60° C. at a rate of 20° C./min, and then the temperature is increased to 180° C. at a rate of 10° C./min. At this time, in the second temperature increase section, a melting point is obtained from the top region of an endothermic curve.
In the present disclosure, a density may be measured, for example, according to the measurement method of ASTM D1505.
In the present disclosure, an absolute viscosity may be measured using an absolute viscometer manufactured by Brookfield. As a specific measurement example, an absolute viscosity may be measured according to ASTM D1986-14 method using the absolute viscometer LVT 230 manufactured by Brookfield.
Specifically, polyethylene having a drop point of 105 to 115° C., a melting point (mp) of 100 to 110° C., a density (23° C.) of 0.95 to 1.0 g/cm3, and an absolute viscosity (120° C.) of 380 to 420 mm2/s may be used as the processability improver.
Specifically, polyethylene wax having a drop point of 108 to 112° C., a melting point (mp) of 102 to 106° C., a density (23° C.) of 0.95 to 0.98 g/cm3, and an absolute viscosity (120° C.) of 400 to 420 mm2/s may be used as the processability improver.
In an embodiment of the present disclosure, a commercially available product may be used as the processability improver. For example, products such as LC102N may be used.
In an embodiment of the present disclosure, the processability improver may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 3% by weight, more preferably 0.01 to 3% by weight, most preferably 0.01 to 1% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent and a processability improver; or the polybutylene terephthalate resin composition may include melamine cyanurate and may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 3% by weight, more preferably 0.01 to 3% by weight, most preferably 0.01 to 1% by weight, based on 100% by weight of a total of a processability improver, polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, polyethylene, a silica-containing reinforcing agent and melamine cyanurate. When the ranges are satisfied, excellent releasability and injection moldability may be sufficiently provided.
Specifically, the resin composition may include polyethylene. This polyethylene may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 3% by weight, more preferably 0.01 to 3% by weight, most preferably 0.01 to 1% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent and polyethylene; or the polybutylene terephthalate resin composition may include polyethylene, melamine cyanurate and a heat-resistant additive and may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 3% by weight, more preferably 0.01 to 3% by weight, most preferably 0.01 to 1% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, polyethylene, a silica-containing reinforcing agent, polyethylene, melamine cyanurate and a heat-resistant additive.
The heat-resistant additive according to the present disclosure may provide an antioxidant effect at high temperature during extrusion and injection molding of the polybutylene terephthalate resin composition.
The heat-resistant additive may be, for example, one or more selected from a hindered phenolic compound, a phosphite compound and a phosphonite compound.
As the hindered phenolic compound, a commercially available product may be used.
Examples of the hindered phenolic compound include octadeeyl-3-(4-hydroxy-3,5-ditert-butylphenyl) propionate, tetrabis[methylene-3-(3,5-di-tert-butyl-4-hydroxyphenyl) propionate]methane, 1,3,5-tri-methyl-2,4,6-tris(3,5-di-tertbutyl-4-hydroxybenzyl)benzene, pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate and the like, and it is preferred to use pentaerythritol tetrakis (3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate.
Examples of the phosphite compound include triphenyl phosphite, tris(monyl phenyl) phosphite, triisodecyl phosphite, diphenyl-isooctyl-phosphite, bis(2,6-di-tert-butyl-4-methylphenyl)pentaerythritol diphosphite, tris(2,4-di-tert-butylphenyl) phosphite and the like, and it is preferred to use tris(2,4-di-tert-butylphenyl) phosphite.
As the phosphonite compound, a compound represented by Formula 1 below may be used:
where R1 and R2 are each independently alkyl, aryl, alkylaryl, specifically C1-C30M alkyl, C6-C30 aryl or alkylaryl, and Ar is an aryl group such as phenyl, naphthyl, biphenyl or terphenyl.
As another example, the heat-resistant additive may be a mixture of a compound represented by Formula 2 below and a compound represented by Formula 3 below.
When the compound represented by Formula 2 below is mixed with the compound represented by Formula 3 below, a density of, for example, 530 g/l or more, specifically 530-630 g/l, is preferred to provide an antioxidant effect at high temperature.
Here, the density may be a value measured using a method and equipment commonly used in this technical field.
In an embodiment of the present disclosure, a commercially available product may be used. For example, a product such as B-225 may be used.
In an embodiment of the present disclosure, the heat-resistant additive may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 2% by weight, more preferably 0.01 to 2% by weight, even more preferably 0.1 to 2% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent and a heat-resistant additive. When the ranges are satisfied, thermal stability may be provided during processing at high temperature.
The heat-resistant additive may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 2% by weight, more preferably 0.01 to 2% by weight, even more preferably 0.1 to 2% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, melamine cyanurate and a heat-resistant additive.
The heat-resistant additive may be included in an amount of, for example, 0.001 to 3% by weight, preferably 0.05 to 2% by weight, more preferably 0.01 to 2% by weight, even more preferably 0.1 to 2% by weight, based on 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, melamine cyanurate, polyethylene and a heat-resistant additive.
The polybutylene terephthalate resin composition according to the present disclosure may include polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent, and, when the content of the polybutylene terephthalate is c and the content of the silica-containing reinforcing agent is d, may satisfy correlation 0.5d≤c≤2d, specifically correlation d≤c≤2d, preferably correlation 1.3d≤c≤1.8d. When these ranges are satisfied, rigidity and excellent physical property balance between mechanical property and flame retardancy may be provided.
In this description, unless otherwise specified, “content” is given in % by weight. Specifically, the content of each of c and d may be % by weight included in 100% by weight of a total of polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, a silica-containing reinforcing agent, a processability improver and a heat-resistant additive.
Here, c may be, for example, an integer of 35 to 58, preferably an integer of 40 to 58, more preferably an integer of 40 to 55, even more preferably an integer of 45 to 50. When these ranges are satisfied, rigidity and excellent physical property balance between mechanical property and flame retardancy may be provided.
In addition, d may be, for example, an integer of 10 to 50, preferably an integer of 15 to 50, more preferably an integer of 20 to 50. When these ranges are satisfied, rigidity and excellent physical property balance between mechanical property and flame retardancy may be provided.
In an embodiment of the present disclosure, the polybutylene terephthalate resin composition may include 15 to 65% by weight of polybutylene terephthalate; 10 to 50% by weight of a silica-containing reinforcing agent; 5 to 35% by weight of an aluminum salt of diethyl phosphinic acid; 0.1 to 10% by weight of melamine polyphosphate; 0 to 10% by weight of melamine cyanurate; 0.001 to 3% by weight of a heat-resistant additive; and 0.001 to 3% by weight of a processability improver.
As another example, the polybutylene terephthalate resin composition may include 35 to 58% by weight of polybutylene terephthalate; 15 to 50% by weight of a silica-containing reinforcing agent; 10 to 25% by weight of an aluminum salt of diethyl phosphinic acid; 0.1 to 5% by weight of melamine polyphosphate; 0 to 4.5% by weight of melamine cyanurate; 0.001 to 3% by weight of a heat-resistant additive; and 0.001 to 3% by weight of a processability improver.
As another example, the polybutylene terephthalate resin composition may include 40 to 58% by weight of polybutylene terephthalate; 20 to 50% by weight of a silica-containing reinforcing agent; 10 to 20% by weight of an aluminum salt of diethyl phosphinic acid; 1 to 5% by weight of melamine polyphosphate; 0.1 to 10% by weight of melamine cyanurate; 0.05 to 2% by weight of a heat-resistant additive; and 0.05 to 3% by weight of a processability improver. When these ranges are satisfied, rigidity and excellent physical property balance between mechanical property and flame retardancy may be provided.
The polybutylene terephthalate resin composition may include, for example, one or more additives selected from among a UV stabilizer, a pigment and a colorant in an amount of, for example, 0.01 to 5 parts by weight, preferably 0.5 to 2 parts by weight, more preferably 1 to 2 parts by weight, based on 100 parts by weight of the polybutylene terephthalate resin composition. Within the ranges, the inherent characteristics of the additives may be exhibited without affecting the physical properties of the resin composition.
The polybutylene terephthalate resin composition according to the present disclosure may be prepared by a method known in the art. For example, the polybutylene terephthalate resin composition may be prepared in the form of pellets by a method of melt-extruding a mixture of components and additives in an extruder, and the pellets may be used to manufacture injection-molded articles and extrusion-molded articles.
In one embodiment of the present disclosure, the pellets are extruded at a temperature of 240 to 280° C. In addition, when injecting the pellets, the temperature of a mold is preferably 80 to 120° C. When the mold temperature is 80° C. or less, appearance may be deteriorated. When the mold temperature is higher than 120° C., the pellets may stick to the mold, reducing releasability and increasing cooling rate.
A method of preparing the polybutylene terephthalate resin composition of the present disclosure may include, for example, a step of kneading and extruding polybutylene terephthalate, an aluminum salt of diethyl phosphinic acid, melamine polyphosphate, and a silica-containing reinforcing agent and the above-described melanin cyanurate as needed.
In the step of kneading and extruding, the screw rotation speed of an extruder may be, for example, 150 to 330 rpm, 150 to 300 rpm, or 200 to 250 rpm. When these ranges are satisfied and as the screw rotation speed is small, rigidity and processability may be improved.
The transport amount per hour (F/R) of the polybutylene terephthalate resin composition fed into the extruder is characterized as being 70 kg/hr or less, preferably 60 kg/hr or less, more preferably 50 kg/hr or less, even more preferably 45 to 55 kg/hr. Within these ranges, rigidity and a physical property balance between processability and specific gravity may be realized.
In accordance with another embodiment of the present disclosure, a molded article made of the above-described polybutylene terephthalate resin composition is provided.
The molded article may be, for example, an automotive electronic component.
Specifically, the molded article may be an automotive connector.
The molded article may have a tensile strength of 130 MPa or more, or 135 to 165 MPa measured according to ISO 527.
The molded article may have a flow index of 4 to 20 g/10 min, or 4 to 18 g/min measured at 265° C. under a load of 2.16 kg according to ISO 1133.
A 0.8 mm specimen of the molded article may have a flame retardancy (burning time/5 ea) of 50 seconds or less measured according to UL 94.
In describing the polybutylene terephthalate resin composition of the present disclosure, the method of preparing the polybutylene terephthalate resin composition and a molded article made of the polybutylene terephthalate resin composition, it is stated that other conditions or equipment not explicitly described can be appropriately selected within ranges commonly practiced in the art and are not particularly limited.
Hereinafter, examples of the present disclosure will be described in detail so that those skilled in the art in the technical field to which the present disclosure belongs can easily practice the present disclosure. However, the present disclosure can be implemented in many different forms and is not limited to examples to be described below.
In an embodiment of the present disclosure, components used to prepare a polybutylene terephthalate resin composition were as follows:
The respective components were mixed according to the contents shown in Table 1 below. The physical properties of the prepared composition were measured in the following manners and are shown in Table 1 below.
Next, the mixture was supplied at 50 kg/hr, and the screw rotation speed of an extruder was 250 rpm. Here, extrusion was performed at 250° C. using a twin-screw extruder with a screw diameter of 45 mm, and the extruded product was produced in the form of pellets.
The produced pellets were dried at 100° C. for 4 hours or more, and then extruded at 80° C. to manufacture a specimen with a size of 2.5 mm×50 mm×90 mm. The physical properties of the manufactured specimen were measured in the following manners and are shown in Table 1 below.
(The sum of the components shown in the table is 100% by weight.)
As shown in Table 1, it was confirmed that Examples 1 to 3 including all the components according to the present disclosure had a flow index of 4 to 18 g/10 min and a tensile strength of 135 to 160 MPa, required a total time of 13.9 to 34 seconds when burned with flame retardancy V-0, and exhibited a balance between physical properties such as rigidity, processability and flame retardancy. Here, the calculated a/b values were 7.77 to 40, which was confirmed to be within the appropriate range.
On the other hand, it can be seen that, in the case of Comparative Example 1 in which aromatic phosphate and Teflon were used together, tensile strength and flow index are decreased. In this case, it can be seen that the calculated a/b value is also less than 7.76.
Since tensile strength was poor and a flow index could not be measured, the a/b calculation value could not be calculated either.
In addition, it was confirmed that in the case of Comparative Example 2 in which an aluminum salt of diethyl phosphinic acid was added alone and melamine polyphosphate and melamine cyanurate were not added, tensile strength and flow index were decreased.
In addition, it was confirmed that, in the case of Comparative Example 3 in which the content of an aluminum salt of diethyl phosphinic acid in the composition of Example 1 was reduced and polybutylene terephthalate was additionally added as much as the reduced content, tensile strength and flow index were excellent, but flame retardancy could not be measured.
In addition, it can be seen that, in the case of Comparative Example 4 having the same composition as in Example 2 except that a reinforcing agent in which the content of silica is less than an appropriate range, flame retardancy is excellent, but tensile strength and flow index are poor. In this case, it can be seen that the a/b calculation value is also less than 7.76.
In addition, it can be seen that, in the case of Comparative Example 5 having the same composition as in Example 2 except that polybutylene terephthalate was additionally added as much as the reduced reinforcing agent content, flow index is excellent, but tensile strength and flame retardancy are poor. In this case, it can be seen that the a/b calculation value is also less than 7.76.
Further, it can be confirmed that, in the case of Comparative Example 6 having the same composition as in Example 2 except that the content of an aluminum salt of diethyl phosphinic acid and the content of melamine cyanurate were changed, flame retardancy is poor. In this case, it can be seen that the a/b calculation value is also less than 7.76.
In conclusion, when the polybutylene terephthalate resin composition disclosed in the present disclosure includes polybutylene terephthalate, a silica-containing reinforcing agent, a flame retardant, a heat-resistant component, and the like in a specific composition ratio, the physical property balance between processability, specific gravity, rigidity, and flame retardancy can be realized. Accordingly, the polybutylene terephthalate resin composition of the present disclosure can be used as a substitute for polyester resin composite materials containing a halogen-based flame retardant, and can be suitably used in the manufacture of automotive parts.
Number | Date | Country | Kind |
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10-2022-0117051 | Sep 2022 | KR | national |
10-2023-0087762 | Jul 2023 | KR | national |
This application is a National Phase entry pursuant to 35 U.S.C. § 371 of International Application No. PCT/KR2023/009651, filed on Jul. 7, 2023, and claims the benefit of and priority to Korean Patent Application No. 10-2022-0117051, filed on Sep. 16, 2022, and Korean Patent Application No. 10-2023-0087762, filed on Jul. 6, 2023, in the Korean Intellectual Property Office, the disclosures of which are incorporated herein by reference in their entirety as if fully set forth herein.
Filing Document | Filing Date | Country | Kind |
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PCT/KR2023/009651 | 7/7/2023 | WO |