WO2001081455A1 - Colored pigment master batch and blow molding method using the same - Google Patents
Colored pigment master batch and blow molding method using the same Download PDFInfo
- Publication number
- WO2001081455A1 WO2001081455A1 PCT/JP2001/003269 JP0103269W WO0181455A1 WO 2001081455 A1 WO2001081455 A1 WO 2001081455A1 JP 0103269 W JP0103269 W JP 0103269W WO 0181455 A1 WO0181455 A1 WO 0181455A1
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- WIPO (PCT)
- Prior art keywords
- molding
- pigment
- temperature
- thermoplastic elastomer
- blow
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/0005—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor characterised by the material
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C2049/7879—Stretching, e.g. stretch rod
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/08—Biaxial stretching during blow-moulding
- B29C49/087—Means for providing controlled or limited stretch ratio
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/42394—Providing specific wall thickness
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/10—Polymers of propylene
- B29K2023/12—PP, i.e. polypropylene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
- B29K2105/0032—Pigments, colouring agents or opacifiyng agents
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/26—Scrap or recycled material
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2421/00—Characterised by the use of unspecified rubbers
Definitions
- the present invention relates to a coloring method for obtaining a blow-molded article having a woodgrain appearance.
- the present invention relates to a pigment mass batch and a blow molding method using the same.
- the color pigment master patch of the present invention uses a specific thermoplastic elastomer as the resin, so that it does not require any further adjustment of the blow molding conditions. In addition to the appearance of a wood grain pattern, it is possible to easily recycle molding burrs produced when manufacturing blow molded articles.
- resin molded products having a striped appearance such as wood grain or marble pattern have a certain degree of dispersion of the striped pigment in the molding base resin through the plasticizing process and extrusion process of the molding material. It is manufactured by dry-lending a batch of coloring masters that does not occur, and forming the pigment dispersion spots into a design appearance.
- the marble appearance is represented by light and shade stripes of the pigment for the stripe pattern including the inside of the product, and the woodgrain appearance is represented by streaks appearing on the product surface.
- the process of creating a wood grain pattern with stripes on the product surface is as follows: (1) Driving and plasticizing and extruding a wood pigment master patch and a base color pigment master batch as the base color on the molding base resin; (2) The extrusion process The pigment mass for wood grain melted in the evening, the batch becomes an island and is gradually extruded while being pulled toward the wall of the extrusion channel. (3) When it reaches near the wall surface with large shear stress, the molten wood pigment mass in the evening Batch islands are stretched to create continuous, long streaks; ⁇ pigments appear as streaks on the surface of the extruded part; ⁇ ⁇ elongation remaining more than a certain depth from the part The missing wood pigment is concealed by the base color pigment and is not observed from the table. As a result, only the surface streaks are observed.
- the carrier resin used in the wood pigment pigment batches has a high melting point of engineering plastic (engineering plastic) such as polyester, polyamide, and acrylic resins. Resin or partially crosslinked olefin resin is used.
- engineering plastic engineering plastic
- these are used as a woodgrain pigment master batch, but it is difficult to obtain a clear striped pattern, and the molding conditions They are often used at the expense of
- An object of the present invention is to provide blow molding using a polyolefin resin, particularly polypropylene, which has been slow to develop and spread as a wood-grain furniture, under the conditions of blow molding and mechanical properties of the blow molding machine. It is an object of the present invention to provide a colored pigment masterbatch that is highly recyclable and has high recyclability, and a method for producing a blow-molded article having a woodgrain appearance using the colored pigment masterpatch.
- the inventor of the present invention has proposed as a pigmented masterbatch for obtaining a wood grain pattern by a blow molding method: (1) to make streaks having a wood grain appear without a large change in molding conditions; The streaks clearly appear on the product surface under the molding conditions. 2 The recyclability of the molding burs is good. That is, when the recycled material is mixed, the residual grain of the recycled material. Colors are re-dispersed quickly and color change does not occur for each molding. (3) There is a characteristic that physical properties do not deteriorate, that is, pinch-off strength does not easily decrease and impact performance does not decrease.
- the pigment is a pigment property compatible with the blow molding properties
- it is a crystalline thermoplastic elastomer having a specific vicat softening point and a specific crystal melting point.
- a thermoplastic elastomer with an MFR (melt-to-mouth ratio) ratio of at least a specified value to the base resin is used as a carrier resin in a colored pigment master batch, or a specific vitreous is used.
- Carrier tree in color pigment masterbatch for blow molding It has been found that the above object can be achieved by using it as a fat. The present invention has been completed based on such findings.
- the present invention provides a colored pigment master batch comprising a pigment and a carrier resin, which has a higher vicat softening point than the melting temperature of the molded base resin (base resin to be blow molded), and A crystalline thermoplastic elastomer having a crystalline melting point at least 20 ° C higher than the melting temperature of the base resin, and has a MFR (melt flow rate) ratio (thermoplastic elastomer) to the molding base resin.
- the present invention provides a colored pigment master batch for blow molding, characterized in that a thermoplastic elastomer having a MFR of one or more (MFR of the molding base resin) of 5 or more is used as a carrier resin. .
- the present invention provides a colored pigment master batch comprising a pigment and a carrier resin, which has a higher vicat softening point than the melting temperature of the molding base resin, and has a higher melting point than the melting temperature of the molding base resin.
- Amorphous thermoplastic elastomers with an outflow temperature of at least 20 ° C higher than the molded base resin, and the MFR (melt flow rate) ratio of the molded base resin An object of the present invention is to provide a color pigment masterbatch for blow molding, characterized in that a thermoplastic elastomer having an MFR / MFR of the molding base resin of 5 or more is used as a carrier resin.
- the present invention relates to a professional molding method for obtaining a molded article having streak-like colored stripes by using the colored pigment master patch for professional molding, and a blow molded article molded using the same. Is provided. BEST MODE FOR CARRYING OUT THE INVENTION
- the coloring pigment master patch of the present invention uses the above specific thermoplastic elastomer as a carrier resin.
- the reason that Toma-ichi is excellent in blow molding suitability is as follows.
- 2Since it is a material with rubber-like properties, it is easily deformed even at the stage without flowability (exceeding the vicat softening point, below the crystal melting point or below the outflow starting temperature), and the pigment dissolves out.
- the masterbatch itself can be stretched and crushed moderately while keeping the weight low. As a result, when the melting temperature is exceeded, the masterbatch does not elute without delay, and the graininess of the wood grain is likely to appear.
- the soft segment portion of the thermoplastic elastomer has high compatibility with the whole resin and contributes to the physical properties as a modifier. This is a characteristic that contributes to preventing a decrease in pinch-off strength and impact strength.
- the thermoplastic elastomer which is a carrier resin in the batch of the coloring pigment master of the present invention, is a specific crystalline thermoplastic elastomer or a special thermoplastic elastomer. It is a constant amorphous thermoplastic elastomer. Crystalline thermoplastic elastomers and amorphous thermoplastic elastomers are broadly classified mainly by the properties of the hard segment portion. The crystalline thermoplastic elastomer and the amorphous thermoplastic elastomer have individual characteristics, but in the present invention, the vicat softening point, the melting temperature (the crystal melting point or the outflow starting temperature) are used. The type of the thermoplastic elastomer is not particularly limited as long as the properties of the MFR are compatible.
- the thermoplastic elastomer must have a vicat softening point higher than the melting temperature of the molded base resin. This is because the pigment master batch, which uses the molding material and thermoplastic elastomer injected into the hopper as the carrier resin, has a large frictional force during the process of being transported in a solid state through the plasticized cylinder. Since the materials move by rubbing due to the crushing force, solid properties that maintain sufficient wear resistance and rigidity until the molding material melts above the melting temperature are required. After passing through the solid transport section, the temperature inside the cylinder gradually rises above the vicat softening point of the thermoplastic elastomer, and the elastic strength of the thermoplastic elastomer begins to decrease significantly. You.
- the heater set temperature under the hopper should be lower than the vicat softening point of the thermoplastic elastomer, and the subsequent temperature up to the plasticized cylinder outlet should be the thermoplasticity. It is preferable to gradually increase the temperature in the temperature range from the vicat softening point of the elastomer to the crystal melting point or outflow starting temperature.
- thermoplastic elastomer contained in the pigment masterbatch has a higher vicat softening point than the heater set point below the hopper, resulting in a plasticized silicone. It is necessary to have a crystal melting point or outflow starting temperature higher than the outlet temperature. Although this temperature condition range is wide depending on the molding material and mechanical characteristics, as described above, the thermoplastic elastomer can adjust the temperature characteristics, so that the pigment master can be used as required. Batches can be manufactured. The vicat softening point is measured according to ASTM D155.
- the melting temperature of the thermoplastic elastomer is the melting point of the crystal in the case of the crystalline thermoplastic elastomer, and the melting temperature is clear in the case of the amorphous thermoplastic elastomer. Therefore, in general, the outflow temperature measured using a Koka type flow tester is used as the melting temperature. Furthermore, while using the melting temperature as a guide, the suitability of the plasticized state is determined by the melting state of the thermoplastic elastomer at the outlet of the plasticizing cylinder of the blow molding machine and the deformation state of the master batch. Judgment will be made.
- the crystallizing melting point or outflow starting temperature of the thermoplastic elastomer is higher than the melting temperature of the base resin by 20 ° C or more, as viewed from a general blow plasticizing temperature profile. It was determined to be necessary. In the present invention, even if the crystal melting point or outflow starting temperature of the thermoplastic elastomer is higher than the melting temperature of the molding base resin, if the temperature difference is less than 20 ° C, a clear grain pattern or stripe pattern is obtained. A disadvantage arises that the coloring pigment is difficult to obtain.
- the crystal melting point is measured using a differential scanning calorimeter.
- the MFR of thermoplastic elastomer For the MFR of thermoplastic elastomer, the MFR measurement conditions specified for the molding base resin used (for example, polypropylene: 230 t, load: 2.16 kg (21.2 1.) ), High-density polyethylene: 190, load 2.16 kg (2.1.2 N))), the ratio of MFR of thermoplastic elastomer to MFR of molding base resin to MFR ( The MFR of the thermoplastic elastomer / the MFR of the molding base resin) is required to be 5 or more, preferably 10 or more, particularly preferably 20 or more. The upper limit of the MFR ratio is not limited, but if it is larger than necessary, the size of the drawdown increases during molding. If the MFR ratio is less than 5, there is a disadvantage that the pigment is hardly exposed or stretched. The MFR of the molding base resin will be described later. MFR was measured in accordance with ASTD 1238.
- the carrier resin in the coloring pigment masterbatch of the present invention is made of a thermoplastic elastomer having the above-mentioned properties, and the thermoplastic elastomer is a polyester-based elastomer, Polyurethane elastomers, polyurethane elastomers, polyolefin elastomers, etc. are preferred, and polyester elastomers are particularly preferred.
- the polyester-based elastomer include perprene P (manufactured by Toyobo Co., Ltd., polyester using an aliphatic polyether. Polyether type), perprene S (manufactured by Toyobo Co., Ltd., fatty acid).
- the configuration of the colored pigment master batch of the present invention is as follows: thermoplastic elastomer having the above-mentioned properties: 1 to 99.9% by weight 0 / o, olefin resin: 0 to 70% by weight, pigment: 1 to 70% by weight 0-20% by weight of other additives Can be Other additives include lubricants, modified thermoplastic resins, and the like.
- the content of the heat-friendly plastic Heras Tomah in the colored pigment master in patches rather to preferred are 2 0-9 0 weight 0/0, 4 0-7 0% by weight and particularly preferred arbitrariness.
- the pigment component contained in one batch of the coloring pigment master is preferably from 10 to 50% by weight, particularly preferably from 20 to 40% by weight.
- the olefin resin is not essential, it contributes to the improvement of the kneading property when producing a mass batch.
- the coloring pigment masterbatch for wood grain in the molding material as 0.1 to 5% by weight as a pigment, a sufficiently satisfactory wood grain appearance can be obtained.
- the amount of one batch of the coloring pigment master varies depending on the use of the blow molded product and the difference in the hiding power of the base color pigment. However, in the case of a normal wood grain appearance product, 0.3% by weight of the pigment is used. A sufficient grain feeling can be obtained by adding a certain amount.
- the molding base resin is not particularly limited as long as it is a thermoplastic resin and can be blow-molded.
- polyolefin, polystyrene, polycarbonate, polyacetal, polyester, poly- Amides and the like can be mentioned, and polyolefin is particularly suitable for molding.
- the resin properties are not particularly limited as long as they can be blow-molded, but if the MFR is too high, it is disadvantageous for blow molding.
- the MFR [230 t, load 2.16 kg (2.1.2 N)] is preferably 0.1 to 5 g / 10 minutes, especially 0.1 to 5 g. 2 g / 10 minutes is preferred.
- the MFR was measured in accordance with ASTM D1238.
- thermoplastic elastomer (carrier resin) in one batch of the colored pigment mass is crystalline
- the plasticizing extruder of the blow molding machine is used. Temperature of molding material including molding base resin and coloring pigment master patch at the tip Is adjusted so that it is not less than the vicat softening point of the thermoplastic elastomer in the masterbatch and not more than the crystal melting point, and the temperature-adjusted molding material is sent to an extrusion head, and the molding material is After heating to a temperature higher than the crystal melting point of the thermoplastic elastomer in the masterbatch and extruding from the extrusion head, a blow-molded product is manufactured, while the carrier of the coloring pigment masterpatch is manufactured.
- the temperature of the molding material containing the molding base resin and the coloring pigment masterbatch at the tip of the plasticizing extruder of the blow molding machine is adjusted to the following value.
- the thermoplastic elastomer in the masterbatch is adjusted to have a vicat softening point or higher and a flow start temperature or lower, and the temperature-adjusted molding material is extruded.
- the molding material is extruded from the extrusion head to form a blow molded product.
- the temperature at the tip of the plasticizing extruder is determined when the crystalline thermoplastic elastomer is used as the carrier resin. 5) ° C ⁇ (Crystal melting point-5) The temperature is about ° C. The reason is that if the temperature is close to the crystal melting point of the thermoplastic elastomer, the fluidity of the thermoplastic elastomer is small, but it is difficult to disperse or split, and the pigment is released from the carrier resin. It is because it can suppress.
- the molding material is delivered to the extrusion head.
- the stretched, crushed, or appropriately split and deformed carrier resin has extremely high thermal responsiveness, so the inside of the extruded head is lower than the crystalline melting point of the thermoplastic elastomer. If the temperature is high, the molten state And the viscosity drops rapidly. However, if the latent heat of crystallization is large, the time must be adjusted or the temperature in the extrusion head must be increased.
- the carrier resin having reduced viscosity is easily pulled out to the wall side of the blow mold having high shear stress, so that streaks are likely to appear on the surface layer of the molded product. Even if the molten colored masterbatch is extruded into the wall side in an island shape, it is easily stretched due to shear stress.
- thermoplastic elastomer for example, a general polyester-based elastomer having a PBT (polybutylene terephthalate) -based hard segment and a polyether-based soft segment is used.
- PBT polybutylene terephthalate
- the vitreous softening point, crystal melting point and melt viscosity can be adjusted according to the fraction to be synthesized. Can be.
- a base color pigment to be a backgrain (base) having a wood grain pattern to the molding material.
- the base color pigment may be added as is, but is preferably added as a master—batch.
- the base color pigment it is preferable to use the same pigment as the wood grain pigment except for the color tone, and the pigment can be obtained by kneading the pigment with the carrier resin.
- the carrier resin of one batch of the base color pigment master those having a melting temperature lower than the melting temperature of the molded base resin are preferable. For example, low density polyethylene, high density polyethylene, linear low Density polyethylene, polypropylene and the like.
- the addition amount of the base color pigment mass batch should be 1 to 10% by weight in the molding material as a pigment. And 1 to 3% by weight are particularly preferred. As described above, the amount of the coloring pigment master patch added can be 0.1 to 5% by weight in the molding material as a pigment.
- molding burrs are generated on one outer periphery of a cavity of a molding die.
- the molding burrs are subjected to crushing treatment or re-belleting, added to a molding material in a predetermined amount, and recycled.
- the amount of the pigment master batch added is generally subtracted from the amount of the residual pigment contained in the recycled material, but the amount of the pigment that causes the grain to appear as in this blow molding is generally used.
- the total pigment in the blow-molded body with the grain pattern obtained is 2.5% by weight.
- There is a total of 2.75% by weight of the pigment, 0.5)% by weight and the newly added pigment (base + grain 1.5)% by weight.
- the final pigment component ratio is 3% by weight, which satisfies the above expression, and the final base pigment component ratio converges to a constant value.
- the first molded article after the second recycling especially the fourth molded article after the fourth recycling, can obtain a professional molded article having a uniform grain and a good wood grain pattern. I understand.
- the pigment component ratio of the base color obtained by the above calculation is the final pigment component ratio when the recycling material is continuously added at a fixed ratio. It does not become. In other words, in the process where the final pigment component ratio is not reached, the pigment component ratio in the product will continue to change, and the base color (base color) of the product will change due to the effect of the pigment dissolved in the molding material. become. In the case of this blow molding, a colored pigment that appears each time a wood grain pattern is added.Since the pigment in one batch does not dissolve into the molding material, the colored pigment component contained in the recycled material is dissolved. As a result, the base color of the product changes.
- the final base color tint is added each time based on the final wood grain pigment component rate contained in the product.
- the pigment having a component ratio that is obtained by subtracting the component ratio of the woodgrain pigment master batch to be used becomes the color shade formed by mixing with the base color pigment.
- This grain is that the wood grain coloring pigment remaining in the recycled material is the coloring pigment of the present invention. If redispersion is reliable in the molding material during molding, such as in a masterbatch, and redispersibility is poor, as in the case of conventional wood-grain coloring pigments, the final tint may be different from expected. And the tint will continue to change.
- the coloring pigment master patch of the present invention employs a thermoplastic elastomer having extremely good deformability as described above as the carrier resin. Since the carrier resin is easily split or miniaturized to release the pigment, the pigment residue in the carrier resin hardly occurs.
- Pigments separated from the carrier resin are rapidly dispersed in the molding base resin, so that color unevenness and accumulation unevenness due to uneven distribution of the pigment do not occur.
- the base color of the molded article approaches a constant color by repeating the recycling a certain number of times.
- recycle molding is repeated at least a certain number of times in proportion to the recycling material addition rate until the base color of the product becomes stable. It is necessary to produce a large number of products before the color becomes stable, so that a certain amount of defective products cannot be prevented.
- the recycled material needs to have the same pigment component concentration in each recycled material, it is necessary to store a certain amount of the recycled material in the recycled material and manage it. This problem It requires some contrivance to resolve it. That is, at the beginning of blow molding, in molding a molding material to which no recycled material is added, only a pigment component equivalent to the above-described color pigment for producing a wood grain pattern is used as a base color pigment for the base color.
- a master batch is formed using a carrier resin with the same dispersibility as the carrier resin of the master batch, and the wood-grain pigment master batch is prepared based on the above-mentioned planned addition ratio of the recycled material to the molding material.
- the final pigment component ratio included in the calculated product is subtracted from the color pigment component ratio for the wood grain, and then added. By doing so, a product having a pigment component ratio equal to the final pigment component ratio can be formed from the initial stage of production.
- the recycling material can be treated and the addition of the recycling material is started, the addition of the well-dispersed wood grain pigment masterbatch is stopped, and the addition of the specified coloring pigment masterbatch is started. change.
- the base color of the product molded in this way can be molded without causing a color change from the first molding. Furthermore, there is no need to separate and manage recycled materials for each recycling.
- the good dispersibility of the color of the color pigment that gives a wood grain pattern is an important performance for stably recycling molding burrs.
- a product having a wood grain appearance can be manufactured at low cost in the same manner as in general molding.
- Molding resin, coloring pigment (pigment for wood grain) Master batch and base The masters shown in Tables 2 and 3 were used as a single batch of black pigment master.
- E-150 GK is block polypropylene made by Idemitsu Petrochemical Co., Ltd.
- the mastergrain pigment for wood grain shown in Examples 1 to 4 and Comparative Example 1 had a thermoplastic elastomer, a polyolefin, a pigment component, and a ratio of other additives of 45% by weight and 20% by weight, respectively. %, were from 3 0 wt 0/0, 5% by weight.
- thermoplastic elastomer is a polyester-based thermoplastic elastomer manufactured by Toyobo Co., Ltd.
- Example 1 is Perprene P_150B
- Examples 2 and 3 are Perprene P-280B
- Example 4 is perprene S-301
- Comparative Example 1 is vertrene P_80C.
- Polyolefin is a low density polyethylene.
- Denatured polypropylene is poly evening click H- 1 0 0 0 F of Idemitsu Petrochemical Co.
- the commercially available pigment used in Comparative Example 2 is a wood grain pigment that uses a partially crosslinked polyolefin as a carrier resin and is generally used in extrusion molding, and has been used in blow molding. .
- Table 3 shows the combinations and amounts of wood pigment and base pigment used.
- the mold used for the molding was a flat rectangular bottle mold with a capacity of 1.8 liters, with one side having a grain and one side having no grain.
- the molding machine used was a V8 type blow molding machine (accumulator type) manufactured by Nippon Steel Corporation.
- the molding conditions shown in Table 4 were set based on the condition that there was no unmelted wood grain pigment on the extruded parison, and the pigment was hardened to form an island.
- the extrusion volume of the molding material for forming one bottle with a capacity of 1.8 liters was 0.2 to 0.25 liter, and the blow-up ratio was 2 to 3 times. Average wall thickness of molded product is 2-3 mm, weight is 170 g-18 0 g.
- the evaluation of the grain and recyclability of the bottles obtained by blow molding was based on the evaluation of the grain feeling when the streaks ( ⁇ ) appeared on the entire container. Those with low sensation or low clarity are indicated by ⁇ , and those that do not serve as a seam are indicated by X.
- 100% of the pulverized material obtained by pulverizing the molded bottle was molded again under the same conditions except that the pigment mass for wood grain was not added, and the wood grain color was obtained. ⁇ when there is no uneven spots and when there is a slight shade of color
- MFR The unit of MFR shown in Table 2 is g / 10 minutes, the softening point of Vicat is measured in accordance with ASTMD155, and the crystal melting point is measured using a differential scanning calorimeter. Measured, MFR is ASTMD 1 2 3
- the temperatures C1 to C3 mean the resin temperature at the tip of the plasticizing extruder at and near the part connected to the extrusion head, and in the order of C1, C2 and C3. Close to the resin supply port.
- the tip of the plasticizing extruder is also called the melt extrusion section of the extruder.
- the temperature of D1 to D3 means the resin temperature of the air head (extrusion head), and the molding material is extruded through the head in the order of D1, D2 and D3. We reach machine exit.
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- Medicinal Chemistry (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/018,012 US6720377B2 (en) | 2000-04-17 | 2001-04-17 | Color pigment master batch and blow molding method using the same |
| EP01919972A EP1201702A4 (en) | 2000-04-17 | 2001-04-17 | COLOR PIGMENT CONCENTRATE AND THEIR USE IN THE BLOW MOLDING PROCESS |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000-115040 | 2000-04-17 | ||
| JP2000115040A JP2001294671A (ja) | 2000-04-17 | 2000-04-17 | 着色顔料マスターバッチ及びこれを用いたブロー成形法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2001081455A1 true WO2001081455A1 (en) | 2001-11-01 |
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ID=18626752
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2001/003269 Ceased WO2001081455A1 (en) | 2000-04-17 | 2001-04-17 | Colored pigment master batch and blow molding method using the same |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6720377B2 (ja) |
| EP (1) | EP1201702A4 (ja) |
| JP (1) | JP2001294671A (ja) |
| TW (1) | TWI222456B (ja) |
| WO (1) | WO2001081455A1 (ja) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001294671A (ja) | 2000-04-17 | 2001-10-23 | Idemitsu Petrochem Co Ltd | 着色顔料マスターバッチ及びこれを用いたブロー成形法 |
| JP2003119352A (ja) * | 2001-10-16 | 2003-04-23 | Idemitsu Petrochem Co Ltd | 着色顔料マスターバッチ組成物及び成形方法 |
| JP4895207B2 (ja) * | 2002-05-09 | 2012-03-14 | 宇部興産株式会社 | 合成樹脂製品粉砕物の再利用方法 |
| DE60334210D1 (de) * | 2002-05-09 | 2010-10-28 | Ube Industries | Verfahren zur wiederverwendung von zerkleinertem kunstharzprodukt |
| WO2019050032A1 (ja) * | 2017-09-11 | 2019-03-14 | 積水化成品工業株式会社 | 熱可塑性エラストマー組成物、発泡粒子及び発泡成形体 |
| JP7829277B2 (ja) * | 2020-11-11 | 2026-03-13 | 積水成型工業株式会社 | ブロー容器の製造方法 |
| CN112590106B (zh) * | 2020-12-08 | 2023-01-24 | 曼盛包装(上海)有限公司 | 一种全回料制备带有大理石纹路塑料奖牌的方法 |
| CN114806208A (zh) * | 2022-04-28 | 2022-07-29 | 盛嘉伦橡塑(河源)有限公司 | 热塑性弹性体匀纹材料及其制备方法、热塑性弹性体制品 |
| CN115505205A (zh) * | 2022-09-28 | 2022-12-23 | 梁锡 | 仿木纹日用品微发泡注塑材料的配方及制作方法 |
| CN116199996B (zh) * | 2022-09-30 | 2024-09-03 | 珠海格力电器股份有限公司 | 颗粒注塑料、具有自然纹理的注塑件及其制备方法 |
| CN115850986A (zh) * | 2022-12-19 | 2023-03-28 | 济宁金筑工贸有限公司 | 一种仿真篱笆支撑架及其复合材料 |
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| JP2001294671A (ja) | 2000-04-17 | 2001-10-23 | Idemitsu Petrochem Co Ltd | 着色顔料マスターバッチ及びこれを用いたブロー成形法 |
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- 2001-04-17 US US10/018,012 patent/US6720377B2/en not_active Expired - Fee Related
- 2001-04-17 WO PCT/JP2001/003269 patent/WO2001081455A1/ja not_active Ceased
- 2001-04-17 EP EP01919972A patent/EP1201702A4/en not_active Withdrawn
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| JPH01108268A (ja) * | 1987-10-21 | 1989-04-25 | Dainichiseika Color & Chem Mfg Co Ltd | 熱可塑性エラストマー用着色剤組成物 |
| JPH0268374A (ja) * | 1988-09-02 | 1990-03-07 | Iwao Hishida | 熱可塑性樹脂成形品の模様現出用着色剤 |
| JPH05278099A (ja) * | 1992-03-31 | 1993-10-26 | Sumika Color Kk | 黒色系ポリエステル中空成形体、ならびに、黒色系ポリエステル中空成形体用マスターバッチおよび着色ペレット |
| JPH0811753A (ja) * | 1994-06-29 | 1996-01-16 | Kyoraku Co Ltd | 自動車用外板の製造方法 |
| JPH08319419A (ja) * | 1995-05-26 | 1996-12-03 | Satoshi Sanzen | 合成樹脂用模様着色材料及びその製造方法並びに着色模様を有する合成樹脂成形体 |
| JPH10324751A (ja) * | 1997-05-26 | 1998-12-08 | Nippon Porikemu Kk | マスターバッチ |
| US6046265A (en) * | 1998-01-21 | 2000-04-04 | General Electric Company | Crystalline resin compositions having a special effect surface appearance |
| JP2000033925A (ja) * | 1998-07-22 | 2000-02-02 | Toppan Printing Co Ltd | 延伸ポリプロピレン容器 |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2001294671A (ja) | 2001-10-23 |
| EP1201702A1 (en) | 2002-05-02 |
| US20030040556A1 (en) | 2003-02-27 |
| US6720377B2 (en) | 2004-04-13 |
| TWI222456B (en) | 2004-10-21 |
| EP1201702A4 (en) | 2002-11-13 |
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