JPH0329673B2 - - Google Patents

Description

[Detailed description of the invention]

[Industrial Application Field] The present invention relates to a container coated with a heat-shrinkable film made of a block copolymer having excellent impact resistance, low-temperature stretchability, shrinkage characteristics, and environmental damage resistance. [Conventional technology] Shrink packaging has recently been used particularly for food packaging because it can neatly eliminate the bagging and wrinkles that were unavoidable with conventional packaging technology, and it can also quickly wrap products tightly or irregularly shaped items. is increasing. Conventionally, vinyl chloride resin has been mainly used as a material for shrink wrapping films, sheets, etc. because it satisfies required properties such as low-temperature shrinkability, transparency, and mechanical strength. However, vinyl chloride resin has hygienic problems due to vinyl chloride monomer and plasticizers.
There is a strong demand for alternatives due to the problem of hydrogen chloride generation during incineration. On the other hand, block copolymer resins made of vinyl aromatic hydrocarbons and conjugated dienes do not have the above problems and have good transparency and impact resistance, so they are widely used as materials for food packaging containers. It is being done. [Problems to be Solved by the Invention] However, conventionally known block copolymers are unsuitable as materials for heat-shrinkable packaging because of their high stretching temperatures and high shrinkage temperatures. For example, JP-A-49-102494 and JP-A-49-
Publication No. 108177 describes a packaging film obtained by biaxially stretching a block copolymer having a styrene hydrocarbon content of 50 to 95% by weight, and a composition in which the block copolymer is blended with a styrene resin. However, such a film cannot achieve sufficient shrinkage unless the heat shrinkage temperature is about 100°C or higher. Methods for improving the low-temperature shrinkability of such block copolymers are also disclosed in JP-A-50-6673 and JP-A-55-5544.
This is attempted in the Publication No. In the former method, by applying the tubular method to a linear copolymer, simultaneous biaxial orientation is achieved through expansion stretching in a temperature range where effective high degree of orientation occurs, resulting in good low-temperature heat shrinkability. This is a method of manufacturing film. however,
In this method, expansion and stretching is started in a very limited temperature range depending on the butadiene content of the raw resin, and the temperature in the stretching zone from the expansion start point to the expansion end point is strictly controlled. Unless a gradient is provided, a film having the desired low-temperature heat shrinkability cannot be obtained, and therefore it has the disadvantage that it is difficult to implement easily. In the latter method, a styrene-butadiene block copolymer with a styrene content of 20-50% is added to a styrene-butadiene block copolymer with a styrene content of 65-90%.
This method produces a biaxially stretched film with low-temperature shrinkability by blending the two by weight; however, if the kneading conditions of both components are poor, sufficient low-temperature shrinkability cannot be achieved, and the kneading method requires advanced techniques. This method has the disadvantage that it requires a lot of time and is difficult to implement. [Means for Solving the Problems] In view of the current situation, the present inventors have conducted intensive studies on a method for easily obtaining block copolymer films, sheets, etc. with excellent low-temperature shrinkability. The vinyl aromatic hydrocarbon polymer block constituting the copolymer may be a block copolymer having a molecular weight within a certain range, or such a block copolymer may be combined with a low molecular weight vinyl aromatic hydrocarbon polymer or a normal high molecular weight vinyl aromatic polymer. It was discovered that a composition containing a group hydrocarbon polymer can be stretched at a relatively low temperature, and the purpose was achieved.
Applications were filed for Japanese Patent Application No. 56-63325 and Japanese Patent Application No. 56-95314. Subsequently, the present inventors further investigated the improvement and found that a short-chain vinyl aromatic hydrocarbon polymer portion having a vinyl aromatic hydrocarbon unit number within a specific range was present in the block copolymer chain. As a result, films and sheets with excellent moldability and impact resistance can be obtained, and heat-shrinkable films and sheets with good low-temperature stretchability and excellent shrinkage characteristics and environmental damage resistance can be obtained. I found out that it can be done. An object of the present invention is to provide a film-covered container coated with such a heat-shrinkable film in which cracks do not occur in the covering film after heat-shrink wrapping. That is, the present invention has (1) a polymer block mainly composed of at least one vinyl aromatic hydrocarbon and a polymer block mainly composed of at least one conjugated diene,
Moreover, the number average molecular weight of the vinyl aromatic hydrocarbon polymer block is 10,000 to 100,000, and the number of vinyl aromatic hydrocarbon units in the block copolymer chain is in the range of 2 to about 30. Part content is 3-30%, weight ratio of vinyl aromatic hydrocarbon and conjugated diene is 60:
A heat-shrinkable film made by uniaxially or biaxially stretching a block copolymer with a ratio of 40 to 95:5 and a number average molecular weight of 20,000 to 500,000. (2) Metal, porcelain, glass, polyethylene, polypropylene, polybutene. Polyolefin resins such as polymethacrylic acid ester resins, polycarbonate resins, polyester resins such as polyethylene terephthalate and polybutylene terephthalate, polyamide resins, polystyrene, rubber modified high impact polystyrene (HIPS), styrene-acrylonitrile copolymer Coalescence, styrene-maleic anhydride copolymer, acrylonitrile-butadiene-styrene copolymer (ABS), methacrylic acid ester-butadiene-styrene copolymer (MBS), polyvinyl chloride resin, polyvinylidene chloride resin, phenol The present invention relates to a film-covered container formed by heat-shrinking a container using at least one member selected from resin, urea resin, melamine resin, epoxy resin, unsaturated polyester resin, and silicone resin as a constituent material. The present invention will be explained in detail below. The block copolymer used in the present invention has at least one, preferably two or more, vinyl aromatic hydrocarbon-based polymer blocks and at least one conjugated diene-based polymer block. It is a block copolymer. Here, the polymer block mainly composed of vinyl aromatic hydrocarbons is a polymer block in which the content of vinyl aromatic hydrocarbons exceeds 50% by weight, preferably 70% by weight or more. Specific examples include a homopolymer block or a polymer block composed of a vinyl aromatic hydrocarbon homopolymer portion and a copolymer portion of a vinyl aromatic hydrocarbon and a conjugated diene. Furthermore, a polymer block mainly composed of a conjugated diene is a polymer block in which the content of conjugated diene is 50% by weight or more, preferably 70% by weight or more, and includes a conjugated diene homopolymer block, a vinyl aromatic hydrocarbon Specific examples thereof include a copolymer block of conjugated diene and a conjugated diene, or a polymer block consisting of a combination thereof. The vinyl aromatic hydrocarbon content of the block copolymer used in the present invention is 60 to 95% by weight, preferably
It is 65 to 90% by weight, more preferably 70 to 88% by weight. If the vinyl aromatic hydrocarbon content is less than 60% by weight, the film will have poor tensile strength and rigidity, making it unsuitable for use as a heat-shrinkable film. Moreover, if it exceeds 95% by weight, it is not preferable because impact resistance is poor. The greatest feature of the present invention is that the vinyl aromatic hydrocarbon polymer block contained in the block copolymer chain has a number average molecular weight of 10,000 to 100,000, preferably
15,000 to 80,000, more preferably 20,000 to 60,000, and a short chain vinyl aromatic hydrocarbon polymer portion having a number of vinyl aromatic hydrocarbon units in the range of 2 to about 30 is present in the block copolymer chain. Moreover, the content of the short-chain vinyl aromatic hydrocarbon polymer portion is 3 to 30%, preferably 5 to 25%, and more preferably 7 to 20%. If the number average molecular weight of the vinyl aromatic hydrocarbon polymer block is less than 10,000, the tensile strength and rigidity will be poor, and if it exceeds 100,000, the low-temperature stretchability and shrinkage properties will be poor, which is not preferred. Furthermore, if the content of the short-chain vinyl aromatic hydrocarbon polymer portion is less than 3%, the low-temperature stretchability, shrinkage characteristics, and environmental damage resistance will be poor, and if it exceeds 30%, the tensile strength and rigidity will be poor. Undesirable. In the present invention, the number average molecular weight of the vinyl aromatic hydrocarbon polymer block contained in the block copolymer chain refers to the oxidative decomposition of the block copolymer (LMKOLTHOFF, et al., J. Polym. Sci. 1,
429 (1946)) was measured by gel permeation chromatography (GPC). ” refers to the value calculated according to the method described in the publication by Kodansha). The calibration curve for GPC is created using standard polystyrene commercially available for GPC. In addition, in the present invention, the short-chain vinyl aromatic hydrocarbon polymer portion in which the number of vinyl aromatic hydrocarbon units in the block copolymer chain ranges from 2 to about 30 is defined as:
In GPC (using an ultraviolet absorption photometer detector set to an absorption wavelength of 254 nm in the detection part) of a component obtained by ozonolysis of a block copolymer (Japan Rubber Association Journal, 54 (9) 564 (1981)), The molecular weight corresponding to each count number was determined from a calibration curve created using standard polystyrene and polystyrene oligomer, and the molecular weight corresponding to the styrene dimer was calculated from the component corresponding to the styrene dimer.
Components corresponding to styrene (decomposition products that undergo oxidation have hydroxyl groups and butadiene residues, so styrene
The 30-mer is treated as corresponding to an oxidative decomposition product with a molecular weight of 4000) (hereinafter referred to as the short-chain vinyl aromatic hydrocarbon polymer portion). The content of the short-chain vinyl aromatic hydrocarbon polymer portion is the content of the short-chain vinyl aromatic hydrocarbon compound relative to the total peak area in the gel permeation chromatogram of the component obtained by ozonolysis of the block copolymer. Refers to the ratio of the area of a part. In the present invention, the presence of a short-chain vinyl aromatic hydrocarbon polymer portion improves low-temperature stretchability.
Shrinkage characteristics, environmental damage resistance, etc. are improved, but since the short-chain vinyl aromatic hydrocarbon polymer part is incorporated into the block copolymer chain, it cannot be extracted with solvents, etc., and it has a low molecular weight. It is superior to mixtures of vinyl aromatic hydrocarbon polymers in terms of non-extractability. In the block copolymer used in the present invention,
There is no particular restriction on the molecular weight of a polymer block mainly composed of conjugated dienes, but generally the number average molecular weight is
500-200000, preferably 1000-100000.
Further, the number average molecular weight of the block copolymer as a whole is 20,000 to 500,000, preferably 50,000 to 300,000.
It is. Particularly preferred block copolymers in the present invention include short chain vinyl aromatic hydrocarbon polymer portions having a range of 2 to about 30 vinyl aromatic hydrocarbon units in the block copolymer chain and vinyl aromatic hydrocarbon units in the chain. The weight ratio to the part containing 1 aromatic hydrocarbon unit is 0.1/1 to 2.5/1, preferably 0.2/1 to 2/1.
1, more preferably a block copolymer with a ratio of 0.4/1 to 1.5/1. A block copolymer having such a weight ratio or a block copolymer composition containing the same has excellent extrusion processability and stretch formability, and it is easy to obtain a film or sheet with a uniform thickness. The weight ratio of the short-chain vinyl aromatic hydrocarbon polymer portion and the portion containing one vinyl aromatic hydrocarbon unit in the chain is determined by the gel permeation of the component obtained by ozonolysis of the block copolymer. It can be determined by comparing the area of the short-chain vinyl aromatic hydrocarbon polymer portion with the area of the portion corresponding to one vinyl aromatic hydrocarbon unit in the chromatogram. The block copolymer used in the present invention is basically produced by a known method of block copolymerizing a conjugated diene and a vinyl aromatic hydrocarbon using an anionic polymerization initiator such as an organolithium compound in a hydrocarbon solvent. However, the number average molecular weight of the vinyl aromatic hydrocarbon polymer block, the content of the short chain vinyl aromatic hydrocarbon polymer portion, and the vinyl aromatic hydrocarbon content are manufactured so that they are within the ranges specified in the present invention. Conditions must be set. The content of the short chain vinyl aromatic hydrocarbon polymer portion is determined by the copolymer composition ratio of vinyl aromatic hydrocarbon and conjugated diene,
It can be adjusted within the range specified by the present invention by adjusting the monomer concentration in the polymerization system, adjusting the copolymerization reactivity ratio by using an ether compound or amine compound, and the polymerization temperature. (B) (A-B) _o (B) A(-B-A) _o (C) B(-A-B) _o (In the above formula, A is a polymer block mainly composed of vinyl aromatic hydrocarbons. , B is a polymer block mainly composed of conjugated diene. The boundary between A block and B block does not necessarily need to be clearly distinguished. n is an integer of 1 or more, and generally 1 to 5. ) or the general formula, (d) [(B _- A)- _o ]- _{n+2 n+2 X} (F) [( _{B-A)- o B} ]- _n+2 is the same as
represents, for example, a residue of a coupling agent such as silicon tetrachloride or tin tetrachloride, or a residue of an initiator such as a polyfunctional organolithium compound. m and n are integers of 1 or more. Generally, it is an integer from 1 to 5. ) or any mixture of these block copolymers can be used. In the present invention, vinyl aromatic hydrocarbons include styrene, 0-methylstyrene, p-methylstyrene, p-tert-butylstyrene, 1,3-dimethylstyrene, α-methylstyrene, vinylnaphthalene, vinylanthracene, etc. However, styrene is a particularly common one.
These may be used not only alone, but also as a mixture of two or more. The conjugated diene is a diolefin having a pair of conjugated double bonds, for example 1.3
-butadiene, 2-methyl-1,3-butadiene (isoprene), 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 1,3-hexadiene, etc., but particularly common ones include Examples include 1,3-butadiene and isoprene.
These may be used not only alone, but also as a mixture of two or more. The block copolymer used in the present invention may be modified with hydroxyl groups by hydrogenation, halogenation, hydrogen halogenation, epoxidation, or chemical reaction within a range that does not impair its basic properties such as low-temperature shrinkability and rigidity. Modifications such as introduction of functional groups such as thiol groups, nitrile groups, sulfonic acid groups, carboxyl groups, and amino groups may also be performed. The block copolymer used in the present invention is used as a film molding material either alone or as a block copolymer composition in which components other than the block copolymer are added to the block copolymer depending on the purpose. can. The block copolymer composition used in the present invention includes the block copolymer defined in the present invention,
A block copolymer resin of a vinyl aromatic hydrocarbon and a conjugated diene with a vinyl aromatic hydrocarbon content of 60 to 95% by weight outside the range specified in the present invention, a vinyl aromatic hydrocarbon content of less than 60% by weight Block copolymer elastomers of vinyl aromatic hydrocarbons and conjugated dienes, polymers of the vinyl aromatic hydrocarbon monomers described above, and other vinyl monomers such as ethylene, propylene, butylene. , vinyl chloride, vinylidene chloride, vinyl acetate, acrylic esters such as methyl acrylate, methacrylic esters such as methyl methacrylate, copolymers with acrylonitrile, etc.
The composition contains 2 to 70% by weight, preferably 5 to 50% by weight of at least one polymer selected from rubber modified high impact styrenic resins (HIPS). By blending these polymers into the block copolymer defined in the present invention, rigidity, impact resistance, etc. can be improved. Various additives can be added to the block copolymer used in the present invention or the block copolymer composition containing the above polymers depending on the purpose. Suitable additives include 30 parts by weight or less of coumaron-indene resins, terpene resins, softeners such as oils, and plasticizers. Further, various stabilizers, pigments, antiblocking agents, antistatic agents, lubricants, etc. can also be added. In addition, examples of antiblocking agents, lubricants, and antistatic agents include fatty acid amide, ethylene bisstearamide, sorbitan monostearate, saturated fatty acid esters of fatty alcohols, and pentaerythritol fatty acid esters, and as ultraviolet absorbers. , pt-butylphenyl salicylate, 2-(2'-hydroxy-
5′-methylphenyl)benzotriazole, 2-
(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole, 2,
5-bis-[5'-t-butylbenzoxazolyl-
(2)] Thiophene and other compounds described in "Practical Handbook of Additives for Plastics and Rubber" (Kagaku Kogyo Co., Ltd.) can be used. These are generally 0.01 to 5
It is used in an amount of 0.1 to 2% by weight, preferably 0.1 to 2% by weight. To obtain a heat-shrinkable uniaxially or biaxially stretched film from the block copolymer or block copolymer composition described above, the block copolymer or block copolymer composition is processed through a conventional T-die or annular die. It is extruded into a flat or tube shape at 150 to 250°C, preferably 170 to 220°C, and the resulting unstretched product is uniaxially or biaxially stretched. For example, in the case of uniaxial stretching, in the case of a film or sheet, it is stretched in the extrusion direction using a calendar roll, etc., or in the direction perpendicular to the extrusion direction using a tenter, etc., and in the case of a tube shape, it is stretched in the extrusion direction of the tube or in the circumferential direction. Stretch. In the case of biaxial stretching, in the case of a film or sheet, the extruded film or sheet is stretched in the longitudinal direction with a metal roll, etc., and then stretched in the transverse direction with a tenter, etc., and in the case of a tube shape, the extruded film or sheet is stretched in the longitudinal direction with a tenter, etc. They are stretched simultaneously or separately in the circumferential direction of the tube, that is, in the direction perpendicular to the tube axis. In the present invention, it is preferable to stretch at a stretching temperature of 60 to 110°C, preferably 80 to 100°C, and a stretching ratio of 1.5 to 8 times, preferably 2 to 6 times, in the longitudinal and/or transverse directions. If the stretching temperature is less than 60°C, breakage occurs during stretching, making it difficult to obtain a desired heat-shrinkable film, and if it exceeds 110°C, it is difficult to obtain a film with good shrinkage properties. The stretching ratio is selected within the above range to correspond to the shrinkage ratio required depending on the application, but if the stretching ratio is less than 1.5 times, the heat shrinkage ratio is low and it is not suitable for heat-shrinkable packaging.
Further, a stretching ratio exceeding 8 times is not preferable in terms of stable production in the stretching process. In the case of biaxial stretching, the stretching ratios in the machine direction and the transverse direction may be the same or different. After uniaxial stretching or biaxial stretching, the heat-shrinkable film is then heated to 60 to 105°C, preferably 80 to 95°C, immediately after cooling if necessary.
for a short time, e.g. 3-60 seconds, preferably 10-40 seconds.
It is also possible to carry out a heat treatment for a second to prevent natural shrinkage at room temperature. Heat-shrinkable films are obtained in this way, but when these are used as heat-shrinkable packaging materials or heat-shrinkable label materials, the heat shrinkage rate at 80°C in the stretching direction must be 15% or more. Preferably 20~
It is preferable to set it to 70%, more preferably 30 to 80%. If the heat shrinkage rate at 80℃ in the stretching direction is less than 15%, the shrinkage characteristics are poor, so it is necessary to adjust the process to a high and uniform temperature in the shrink packaging process, or to heat it for a long time. This is undesirable because it becomes impossible to package such products and shrink-wrapping processing capacity decreases. In addition, in the present invention, the heat shrinkage rate at 80°C refers to uniaxial stretching or biaxial stretching.
This is the heat shrinkage rate in each stretching direction of a molded product when an axially stretched film or the like is immersed for 5 minutes in a heating medium such as 80°C hot water, silicone oil, or glycerin that does not inhibit the properties of the molded product. Furthermore, the uniaxially stretched or biaxially stretched heat-shrinkable film of the present invention has a tensile modulus in the stretching direction of 5000 Kg/cm ² or more, preferably 7000 Kg/cm 2 or more, and more preferably 7000 Kg/cm ² or more.
It is preferable that the weight is 10000 Kg/cm ² or more as a heat-shrinkable packaging material. Tensile modulus in stretching direction is 5000
Kg/cm ² or more is preferable because it allows normal packaging without causing sagging during the shrink packaging process. When the uniaxially stretched or biaxially stretched film used in the present invention is used as a heat-shrinkable packaging material, it is heated at a temperature of 150 to 300°C, preferably 180 to 250°C for several seconds to achieve the desired heat shrinkage rate. Heat shrinkage can be achieved by heating for several minutes, preferably 1 to 60 seconds, more preferably 2 to 30 seconds. The heat-shrinkable film defined in the present invention is superior in terms of hygiene compared to conventional vinyl chloride resin-based films, and its properties can be utilized for a variety of applications, such as packaging for fresh foods, frozen foods, and confectionery; It can be used for packaging clothing, stationery, toys, etc. Particularly preferred applications include printing characters or designs on a uniaxially stretched film of the block copolymer or block copolymer composition defined in the present invention, and then printing the film on plastic molded products, metal products, glass containers, porcelain, etc. It can be used as a so-called heat-shrinkable label material, which is used by being brought into close contact with the surface of a package by heat-shrinking. In particular, the uniaxially stretched heat-shrinkable film specified in the present invention has excellent shrinkage characteristics and environmental damage resistance, so it has a low thermal expansion coefficient, as well as a heat-shrinkable label material for plastic molded products that deform when heated to high temperatures. Materials such as metals, porcelain,
Glass, polyolefin resins such as polyethylene, polypropylene, and polybutene, polymethacrylate resins, polycarbonate resins,
It can be suitably used as a heat-shrinkable label material for containers using at least one member selected from polyester resins such as polyethylene terephthalate and polybutylene terephthalate, and polyamide resins. In addition to the above-mentioned resins, examples of materials constituting plastic containers in which the heat-shrinkable block copolymer film defined in the present invention can be used include polystyrene, rubber-modified high-impact polystyrene (HIPS), and styrene-acrylonitrile. Polymer, styrene-maleic anhydride copolymer, acrylonitrile-butadiene-styrene copolymer (ABS), methacrylic acid ester-butadiene-
Styrene copolymer (MBS), polyvinyl chloride resin, polyvinylidene chloride resin, phenolic resin, urea resin, melamine resin, epoxy resin,
Examples include unsaturated polyester resins and silicone resins. These plastic containers may be a mixture of two or more resins or may be a laminate. In addition, when using a heat-shrinkable film obtained by uniaxially stretching the block copolymer or block copolymer composition defined in the present invention as a heat-shrinkable label material, 80% in the direction orthogonal to the stretching direction is used. The heat shrinkage rate at °C is preferably less than 15%, preferably 10% or less, more preferably 5% or less. Therefore, in the present invention, substantially uniaxial stretching for heat-shrinkable labels means stretching in the stretching direction.
Stretching is performed so that the heat shrinkage rate at 80°C is 15% or more and the heat shrinkage rate at 80°C in the direction orthogonal to the stretching direction is less than 15%. In addition, in the present invention, the thickness of the film is generally 10
~200μ, preferably 30-100μ. [Examples] In order to explain the present invention in more detail, Examples of the present invention are shown below, but it goes without saying that the content of the present invention is not limited to these Examples. Examples 1 to 9 and Comparative Examples 1 to 6 The block copolymers shown in Table 1 were produced using n-butyllithium as a catalyst in a cyclohexane solvent according to a conventional method. The content of short-chain polystyrene moieties was controlled by adjusting the monomer composition ratio and monomer addition rate in the copolymerization reaction of butadiene and styrene. Each block copolymer contains 2,6-di-
0.5% by weight each of tert-butyl-4-methylphenol and trisnonylphenyl phosphorite were added. The obtained block copolymer was formed into a sheet with a thickness of 0.25 mm at 200°C using a 40 mmφ extruder, and then uniaxially stretched horizontally to a thickness of about 5 times using a tenter.
A 60μ film was prepared. At this time, the temperature in the tenter was set at the lowest temperature at which a uniaxially stretched film could be stably produced from each block copolymer without breaking during stretching. Examples 1 to 9 of the present invention
The film was a good film with less unevenness in thickness compared to the comparative example. Next, the tensile modulus of each block copolymer and heat-shrinkable film in the stretching direction, puncture strength, and heat shrinkage rate at 80°C in the stretching direction were measured. As a result, it was revealed that the heat-shrinkable film of the present invention exhibits good rigidity, impact resistance, and shrinkage rate. All of these heat-shrinkable films had a heat shrinkage rate of 5% or less at 80°C in the direction orthogonal to the stretching direction. Also, both
It was a transparent film with a haze of 7% or less. Next, after printing letters and patterns on the heat-shrinkable film of each block copolymer obtained as described above, the stretched direction is the circumferential direction, and the non-stretched direction is the longitudinal direction. A cylindrical heat-shrinkable label was produced using a shrink label automatic machine, placed over a glass bottle, and passed through a shrink tunnel controlled at a temperature of approximately 220°C to heat-shrink it. The time taken to pass through the shrink tunnel was controlled so that each heat-shrinkable label was in tight contact with the glass bottle surface, but labels with a lower heat shrinkage rate at 80°C took a longer time. In addition, the heat-shrinkable films of Comparative Examples 2, 3, and 5 had low rigidity;
A good coated product could not be obtained. When the environmental damage resistance of each of the heat-shrinkable film coated glass bottles obtained in this way was investigated, it was found that all the heat-shrinkable film coated products defined in the present invention had good performance. .

【table】

【table】

【table】

[Table] Examples 10 to 12 A block copolymer composition was prepared according to the formulation method shown in Table 2, and then a uniaxially stretched film was produced in the same manner as described above. Table 2 shows the performance of each film obtained. In addition, the heat shrinkage rate at 80°C in the direction orthogonal to the stretching direction for each uniaxially stretched film is 5% or less, and the haze is 9% for each film.
It was below. Examples 13 to 16 The same block copolymers as in Examples 2, 6, and 9 and the same block copolymer composition as in Example 12 were
After forming into a sheet shape using a mmφ extruder, a biaxial stretching device is used to double the width by 3 times in both the vertical and horizontal directions.
A biaxially stretched film with a thickness of about 40 μm was produced by axial stretching. Table 3 shows the performance of each biaxially stretched film obtained.
It was shown to.

【table】

【table】

[Table] Examples 17-20 Block copolymers of Examples 1 and 2, Example 11
Uniaxially stretched films having a thickness of approximately 40 μm were prepared using the block copolymer compositions of 1 and 12 in the same manner as described above. Next, after printing letters and patterns on these films, a cylindrical heat-shrinkable label is made with the stretched direction in the circumferential direction and the non-stretched direction in the longitudinal direction, and it is made into an impact-resistant material. It was placed over a cylindrical cup made of polystyrene, and then passed through a shrink tunnel controlled at a temperature of 180 to 200°C to shrink it. As a result, all of these heat-shrinkable labels were in tight contact with the cup surface of the packaged product without any stickiness or wrinkles, and were not easily peeled off.
In addition, the printed letters and patterns had a colorful finish with no local deformation, and the cup of the packaged product was not deformed by heating at all. Examples 21-29 The heat-shrinkable labels of Examples 1-9 were placed over containers molded from polypropylene, polycarbonate, polybutylene terephthalate, and nylon 66, respectively, instead of glass bottles, and heat-shrinked. When the environmental damage resistance of each heat-shrinkable label covering the container was examined, good performance was found in all cases. [Effects of the Invention] The heat-shrinkable film defined in the present invention has excellent shrinkability at low temperatures or in a short period of time even at high temperatures, so it does not deteriorate or deform when heated at high temperatures for a long period of time in the shrink packaging process. Suitable for packaging containers such as plastic containers.
Further, the heat-shrinkable film defined in the present invention has excellent impact resistance and can be used as a coating for containers such as glass bottles that are likely to have fragments scattered when broken. Furthermore, the heat-shrinkable film defined by the present invention has excellent environmental damage resistance, and is difficult to break even if a container covered with the heat-shrinkable film defined by the present invention is left in an outdoor environment with severe temperature changes. It has the following characteristics. In particular, when the container to be coated is made of materials such as metal, porcelain, glass, or polyester resin, which have very different properties such as thermal expansion coefficient and water absorption, conventional heat-shrinkable films cannot be used. The film had the drawback of poor environmental damage resistance after coating, and cracks easily formed in the film. However, when using the heat-shrinkable film defined in the present invention, there is no such problem and it can be Withstands being left in the natural environment. Therefore, the heat-shrinkable film defined in the present invention takes advantage of these advantages,
It can be particularly suitably used for applications such as labels for containers made of the above-mentioned materials.

Claims (1)

[Scope of Claims] 1. A polymer block comprising at least one vinyl aromatic hydrocarbon-based polymer block and at least one conjugated diene-based polymer block, and further comprising a vinyl aromatic hydrocarbon polymer block. The number average molecular weight of
The content of short-chain vinyl aromatic hydrocarbon polymer moieties in the range of 30 is 3~30%, the weight ratio of vinyl aromatic hydrocarbon and conjugated diene is 60:40~95:5, and the number average molecular weight is 20000. A heat-shrinkable film made by uniaxially or biaxially stretching a block copolymer having a molecular weight of ~500,000. Polycarbonate resin, polyethylene terephthalate,
Polyester resins such as polybutylene terephthalate, polyamide resins, polystyrene, rubber-modified high-impact polystyrene (HIPS), styrene-acrylonitrile copolymers, styrene-maleic anhydride copolymers, acrylonitrile-butadiene-styrene copolymers ( ABS), methacrylic acid ester-butadiene-styrene copolymer (MBS), polyvinyl chloride resin, polyvinylidene chloride resin, phenol resin, urea resin, melamine resin, epoxy resin, unsaturated polyester resin, silicone resin at least 1
A film-covered container made by heat-shrinking a container using seeds as a constituent material.