US20030209826A1 - Process for producing molded article - Google Patents
Process for producing molded article Download PDFInfo
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- US20030209826A1 US20030209826A1 US10/465,751 US46575103A US2003209826A1 US 20030209826 A1 US20030209826 A1 US 20030209826A1 US 46575103 A US46575103 A US 46575103A US 2003209826 A1 US2003209826 A1 US 2003209826A1
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- Prior art keywords
- mold
- molding material
- liquid molding
- molded article
- contact angle
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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
- B29C67/00—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
- B29C67/24—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00 characterised by the choice of material
- B29C67/246—Moulding high reactive monomers or prepolymers, e.g. by reaction injection moulding [RIM], liquid injection moulding [LIM]
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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
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
- B29C33/60—Releasing, lubricating or separating agents
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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
- B29C33/00—Moulds or cores; Details thereof or accessories therefor
- B29C33/56—Coatings, e.g. enameled or galvanised; Releasing, lubricating or separating agents
- B29C33/60—Releasing, lubricating or separating agents
- B29C33/62—Releasing, lubricating or separating agents based on polymers or oligomers
- B29C33/64—Silicone
Abstract
A process for producing a molded article comprised of polyurethane is provided, comprising the steps of pouring or injecting a liquid molding material into a mold under the condition that the contact angle between the liquid molding material and the inner surface of the mold is adjusted to not more than 30° by applying the surface-treating agent to the inner surface of the mold, and curing the liquid molding material. A surface-treating agent is also provided which reduces the contact angle between the liquid molding material and a flat plate made of the same material as the mold to not more than 30°. when the surface-treating agent is applied to the flat plate and the liquid molding material is dropped thereon.
Description
- The present invention is directed to a process for producing a molded article, and more particularly to a process for producing a molded article, capable of producing a molded article having a shape accurately corresponding to the shape of an inner surface of a mold, and a surface-treating agent used in the process.
- When a molded article is produced by pouring or injecting a liquid molding material into a mold, and curing the liquid molding material, a mold releasing agent has been hitherto applied to the inner surface of the mold in order to easily release a molded article from the mold.
- However, when a mold releasing agent is applied to the inner surface of a mold having a complicated shape on its inner surface, and a molded article is produced, the surface properties of the molded article are sometimes deteriorated because so-called surface void, i.e. surface defect caused by insufficient filling of the liquid starting materials and/or foams into the mold having a complicated shape on its inner surface is generated.
- An object of the present invention is to provide a process for producing a molded article, capable of producing a molded article having a shape accurately corresponding to the shape of an inner surface of a mold, without the generation of defects which lower the surface properties of a molded article, such as surface void on the surface of the molded article.
- The above and other objects of the present invention will be apparent from the following description.
- The present invention is directed to the following:
- [1] a process for producing a molded article comprising,
- (A) pouring or injecting a liquid molding material into a mold in the presence of a surface-treating agent comprising a contact angle-reducing substance under the condition that the contact angle between the liquid molding material and the inner surface of the mold is not more than 30°, and
- (B) curing the liquid molding material;
- [2] a surface-treating agent used in a process for producing a molded article comprising pouring or injecting a liquid molding material into a mold and curing the liquid molding material, comprising a contact angle-reducing substance which reduces the contact angle between the liquid molding material and a flat plate made of the same material as the mold to not more than 30°, when the liquid molding material containing the surface-treating agent is dropped on the flat plate, or when the surface-treating agent is applied to the flat plate and the liquid molding material is dropped thereon;
- [3] a method for reducing surface voids during molding, comprising using the above surface-treating agent; and
- [4] use of the above surface-treating agent for reducing surface voids.
- Typical examples of the liquid molding materials are resins such as polyurethanes, epoxy resins, phenolic resins, polyesters, urea resins, olefinic resins such as polyethylenes and polypropylenes, and styrenic resins; rubbers such as natural rubbers, isoprene rubbers, chloroprene rubbers, styrene-butadiene rubbers, butadiene rubbers, acrylonitrile-butadiene rubbers, ethylene-propylene rubbers, butyl rubbers, and acrylic rubbers.
- The liquid molding materials can be those which are foamed during molding to give a foamed molded article. The liquid molding materials which give a foamed molded article include self-foamable polyurethanes, foamable olefinic resins, foamable styrene resins, or the like. When the olefinic resins, the styrene resins, or the like are used, there can be employed a process comprising foaming pre-foamed resin particles, or a process comprising impregnating a foaming agent into those resins, and thereafter molding and foaming the resins in a mold.
- The process of the present invention exhibits excellent effects for liquid molding materials, particularly polyurethanes, the surface properties of which are easily deteriorated during molding. Typical examples of the polyurethanes are, for instance, polyether polyurethanes, polyester polyurethanes, and the like.
- The starting materials for the polyurethane are not particularly limited, and known ones can be used. It is desired that the starting materials for the polyurethane are a polyol solution and an isocyanate prepolymer. The polyol solution comprises a polyol component, such as a polyether-polyol or a polyester-polyol, a chain extender, water, a foam stabilizer (a surfactant), and, as occasion demands, a catalyst. The isocyanate prepolymer can be prepared from a polyol component such as a polyether-polyol or a polyester-polyol, and a polyisocyanate component such as methylenediphenyl diisocyanate or a modified compound thereof. The polyether-polyol, the polyester-polyol, the chain extender, the foam stabilizer (a surfactant), the catalyst, the polyisocyanate component, and the isocyanate prepolymer may be those which are known. The contact angle-reducing substance can be contained in the isocyanate prepolymer and/or the polyol solution, and it is desired that the contact angle-reducing substance is contained in the isocyanate prepolymer. The content of the contact angle-reducing substance in the isocyanate prepolymer is preferably 0.1 to 7% by weight, more preferably 0.1 to 5% by weight.
- The polyurethane foam containing the contact angle-reducing substance can be produced by reacting the polyol component with components such as the polyisocyanate component, the isocyanate prepolymer, and as occasion demands, water, a chain extender, a foam stabilizer (a surfactant), a catalyst, and the like, in the presence of the contact angle-reducing substance.
- In the present invention, one of the major features resides in that the liquid molding material is poured or injected into a mold in the presence of a surface-treating agent comprising a contact angle-reducing substance under the condition that the contact angle between the liquid molding material and the inner surface of the mold is not more than 30°, and the liquid molding material is cured. When molded under this condition, there can be exhibited an excellent effect that a molded article having a shape accurately corresponding to the shape of the inner surface of a mold can be produced, without the generation of surface voids in the molded article. The reasons why this excellent effect is exhibited are not clear, but it is presumably based on the following. When the contact angle between the liquid molding material and the inner surface of the mold is reduced to not more than 30°, the wettability of the mold by the liquid molding material is improved, and thereby the friction between the liquid molding material and the mold is reduced. As a result, the liquid molding material can flow into the mold to follow the complicated shape of the inner surface of the mold. It is desired that the contact angle between the liquid molding material and the inner surface of the mold is not more than 23°, particularly not more than 21°, from the viewpoint of the reducing surface voids of the resulting molded article.
- It is desired that the surface-treating agent comprises a contact angle-reducing substance, which reduces the contact angle between the liquid molding material and a flat plate made of the same material as the mold to not more than 30° when the liquid molding material containing the surface-treating agent is dropped on the flat plate, or when the surface-treating agent is applied to the flat plate and the liquid molding material is dropped thereon. When this surface-treating agent is used, surface voids during molding can be reduced. More concretely, when the surface-treating agent is used, there can be exhibited an excellent effect that a molded article having a shape accurately corresponding to the shape of the inner surface of the mold can be easily produced without the generation of surface voids in the resulting molded article. The reasons why this excellent effect is exhibited are not clear, but it is presumably based on the following. The wettability of the mold by the liquid molding material is improved by the surface-treating agent, and thereby the friction between the liquid molding material and the mold is reduced. As a result, the liquid molding material can flow into the mold to follow the complicated shape of the inner surface of the mold. It is desired that the contact angle between the surface-treating agent and the inner surface of the mold is not more than 23°, particularly not more than 21°.
- The contact angle can be determined in accordance with the following procedures.
- 1) The measurement atmosphere is kept windless at 25° C. and 55% RH.
- 2) As the flat plate made of the same material as the mold, an aluminum plate [average roughness Ra: 0.2-0.4 μm] is horizontally arranged. Thereafter, a silicone mold releasing agent is sprayed on its surface, and sufficiently wiped off with a waste cloth.
- 3) A given surface-treating agent is uniformly sprayed in the amount of 10 g/m2 on the silicone mold releasing agent-sprayed surface (surface-treating agents which are solid at 25° C. are previously heated to a temperature not lower than their melting points to melt and then sprayed).
- 4) The liquid molding material previously degassed by evacuation is collected with a syringe, and one droplet is dropped on the flat plate from the height of 10 cm from the surface of the flat plate in a manner so that the droplet of the liquid molding material has the weight of 0.10±0.02 g.
- 5) The time at which the droplet reaches the surface of the flat plate is counted as zero second. The change of the droplet is observed in accordance with the passage of time from the sideways direction of the droplet with a microscope as a CCD camera. After 60 seconds passed, the contact angle between the droplet and the flat plate is measured.
- Examples of the contact angle-reducing substance include at least one compound selected from the group consisting of esters, ethers and amides, each having a boiling point of not less than 50° C., preferably not less than 100° C. at normal pressure, in particular a boiling point of not less than 100° C. at normal pressure and a boiling point of not more than 300° C. under the pressure of 0.133 kPa. Among the contact angle-reducing substances, those having vapor pressures of a level which does not completely evaporate within the working hours are preferable.
- Examples of the ester having a boiling point of not less than 50° C. include alkyl stearates wherein an alcohol residue moiety of the ester has 1 to 22 carbon atoms, such as ethyl stearate and butyl stearate; alkyl acetates wherein an alcohol residue moiety of the ester has 4 to 22 carbon atoms, such as decyl acetate and octadecyl acetate; alkyl oleates wherein an alcohol residue moiety of the ester has 1 to 22 carbon atoms, such as methyl oleate and butyl oleate; and other alkyl esters of fatty acids wherein the fatty acid residue moiety of the ester has an alkyl group of 2 to 21 carbon atoms, and the alcohol residue moiety of the ester has 1 to 22 carbon atoms, such as butyl propionate, butyl 2-ethylhexanoate, ethyl decanoate and methyl linoleate. Those esters can be used alone or in an admixture thereof. Among them, from the viewpoints of imparting an excellent effect of suppressing generation of surface voids to a resulting molded article and thus improving its appearance (design), alkyl esters of fatty acids, formed from a fatty acid and a monohydric alcohol, such as ethyl stearate, butyl stearate, decyl acetate, octadecyl acetate, methyl oleate and butyl acetate, can be suitably used. Further, it is desired that the fatty acid has 2 to 22 carbon atoms, preferably 2 to 18 carbon atoms, and that the monohydric alcohol has 1 to 22 carbon atoms, preferably 1 to 18 carbon atoms. Moreover, it is desired that the total number of carbon atoms of the fatty acid and the monohydric alcohol is 10 to 40, preferably 12 to 36. In addition, from the viewpoint of yellowing resistance of the resulting molded article, alkyl esters of saturated fatty acids, such as butyl stearate and octadecyl acetate, can be particularly suitably used.
- The ester having a boiling point of not less than 50° C. may be a symmetric ether or asymmetric ether. Examples thereof include dioctyl ether, dibutyl ether, dihexyl ether, didecyl ether, butyl hexyl ether, and the like. Those esters may be used alone or in an admixture thereof. Among them, from the viewpoints of imparting an excellent effect of suppressing generation of surface voids to a resulting molded article and thus improving its appearance (design), dioctyl ether, and the like can be suitably used.
- The content of the contact angle-reducing substance in the surface-treating agent may be appropriately adjusted so that the contact angle between the liquid molding material and the flat plate is reduced to not more than 30°, preferably not more than 23°, more preferably not more than 21°. Incidentally, the contact angle-reducing substance itself can be solely used as the surface-treating agent, since the contact angle between the liquid molding material and the flat plate can be reduced to not more than 30°, even when the contact angle-reducing substance is used alone as the surface-treating agent.
- The surface-treating agent may contain a mold releasing agent such as a silicone compound or a wax as occasion demands, in addition to the contact angle-reducing substance. The surface-treating agent containing the contact angle-reducing substance and the mold releasing agent can be desirably used by applying it to the inner surface of the mold during the production of various molded articles because this surface-treating agent suppresses the generation of surface voids, and improves the appearance (design) of the molded article.
- The silicone compound can be suitably used in the present invention because the silicone compound is excellent in liquidity and releasing properties, and moreover is durable for repetitious use. Typical examples of the silicone compound include dimethyl silicone oil, and modified silicone oils such as alkyl-modified silicone oils and higher fatty acid-modified silicone oils, or those diluted with a solvent, those prepared into aqueous emulsions, and the like. Concretely, there can be cited dimethyl silicone oil having a viscosity of 30 to 5000 mm2/s at 25° C. Those silicone compounds can be used alone or in an admixture thereof.
- The wax can be suitably used because it is inexpensive. Examples of the wax include mineral oils, olefinic waxes, paraffin waxes, and the like. Those waxes can be used alone or in admixture thereof. Among them, the mineral oils and paraffin waxes each having a molecular weight of not less than 300 are preferable.
- Among the mold releasing agents, the silicone compounds are more preferable from the viewpoint of the releasing property.
- The content of the mold releasing agent in the surface-treating agent cannot be absolutely determined because it differs depending upon their kinds. However, it is desired that the content is usually not less than 5% by weight, preferably not less than 10% by weight, more preferably not less than 30% by weight, from the viewpoint of exhibiting sufficient releasing properties. Also, it is desired that the content is not more than 95% by weight, preferably not more than 90% by weight, from the viewpoint of exhibiting sufficient surface properties.
- The surface-treating agent can be applied to the inner surface of the mold, or it can be contained in the liquid molding material.
- When the surface-treating agent is applied to the inner surface of the mold, an outsole of shoe soles made of a polyurethane foam having complicated shapes particularly in the bottom surface can be formed in a shape exactly conforming to the mold without the generation of defects which impair the surface properties of the molded article, such as surface void.
- The method for applying the surface-treating agent to the inner surface of the mold includes, for instance, a method of coating, spraying, dipping, or the like, without limiting the present invention to those methods above.
- When the surface-treating agent is applied to the inner surface of the mold, the mold is filled with the liquid molding material thereafter, and can be molded under given molding conditions suitable for the kinds of the liquid molding material, and the like. It is desired that the amount of the surface-treating agent applied to the inner surface of the mold is 3 to 30 g/m2 from the viewpoints of imparting sufficient surface properties to a resulting molding article and preventing cracking and dulling of the surface.
- When the surface-treating agent is contained in the liquid molding material, a midsole of shoe soles, made of a polyurethane foam and particularly having a complicated shape in the side surfaces can be molded in a shape exactly conforming to the mold without the generation of the defects which impair the surface properties of the molded article, such as surface void.
- When the surface-treating agent is contained in the liquid molding material, the content of the surface-treating agent in the liquid molding material differs depending upon the kinds of the liquid molding material. However, it is desired that the content is adjusted so that the contact angle between the liquid molding material and the flat plate made of the same material as the mold is not more than 30°. For instance, it is desired that the content of the contact angle-reducing substance in the liquid molding material is 0.05 to 3.5% by weight, preferably 0.25 to 1% by weight.
- When the surface-treating agent is contained in the liquid molding material, the liquid molding material is filled in the mold, and can be molded under given molding conditions suitable for the kinds of the liquid molding material.
- The materials of the mold which can be used in the present invention are not particularly limited. Examples of such materials include iron, stainless steel, copper, aluminum, aluminum alloys, epoxy resins, phenolic resins, and the like. In addition, the shapes of the inner surface of the mold are not particularly limited, and any arbitrary shape can be selected as long as the inner surface has a shape well corresponding to the shape of the desired molded article.
- When the liquid molding material is molded in a mold, it is desirable to previously apply a mold releasing agent to the inner surface of the mold by means of coating, spraying, dipping, or the like in order to improve its releasing property. The mold releasing agent includes dimethyl silicone oil, mineral oils, paraffin waxes, and the like, without intending to limit the present invention to those exemplified above.
- Thus, a molded article having a given shape can be obtained by molding and subsequent demolding. The resulting molded article has excellent surface properties because the generation-of harmful defects such as surface void is suppressed even when the molded article has a complicated shape in its inner surface.
- Especially, when the molded article is a molded article made of a polyurethane foam, the above-mentioned effects are exhibited even more excellently. Particularly, the above effects are even more remarkably exhibited for the polyurethane foam for shoe soles having complicated shapes in the bottom surface or side surfaces.
- In general, the shoe soles can be classified into outsoles used in sandals and men's shoes, and midsoles used in sports shoes. The effects according to the present invention can be remarkably exhibited particularly in midsoles used within a low density region.
- From the viewpoint of reducing surface voids, the density of the polyurethane foam is preferably not less than 0.15 g/cm3 and less than 0.30 g/cm3, and more preferably not less than 0.20 g/cm3 and less than 0.30 g/cm3.
- (Preparation of Liquid Molding Material for Polyether Polyurethane Foam)
- In a mixer (Model “DH-2.5,” manufactured by Tokushu Kika Kogyo K. K.) were previously stirred 50 parts by weight of a polyol solution [trade name: “EDDYFOAM AS-2045,” manufactured by Kao Corporation], comprising polypropylene glycol, a chain extender, water and a foam stabilizer (a surfactant), and 50 parts by weight of an isocyanate prepolymer [trade name: “EDDYFOAM B-6009N,” manufactured by Kao Corporation], main constituents of which were polypropylene glycol and 4,4-diphenylmethane diisocyanate, and the resulting mixture was evacuated in a desiccator.
- The resulting liquid mixture was used to measure a contact angle in accordance with the following method for measurement of a contact angle. As a result, the contact angle was found to be 43°.
- The viscosity of this liquid mixture gradually increases. Therefore, the time period from the previous stirring of the polyol solution and the isocyanate prepolymer to the measurement of the contact angle was adjusted to four minutes.
- (Preparation of Liquid Molding Material for Polyester Polyurethane Foam)
- In a mixer (Model “DH-2.5,” manufactured by Tokushu Kika Kogyo K. K.) were previously stirred 50 parts by weight of a polyol solution [trade name: “EDDYFOAM AS-1210U,” manufactured by Kao Corporation], comprising a polyester-polyol, a chain extender, water and a foam stabilizer (a surfactant), and 50 parts by weight of an isocyanate prepolymer [trade name: “EDDYFOAM B-2009,” manufactured by Kao Corporation], main constituents of which were a polyester-polyol and 4,4-diphenylmethane diisocyanate, and the resulting mixture was evacuated in a desiccator.
- The resulting liquid mixture was used to measure a contact angle in accordance with the following method for measurement of a contact angle. As a result, the contact angle was found to be 46°.
- The viscosity of this liquid mixture gradually increases. Therefore, the time period from the previous stirring of the polyol solution and the isocyanate prepolymer to the measurement of the contact angle was adjusted to four minutes.
- [Measurement of Contact Angle]
- 1) The measurement atmosphere is kept windless at 25° C. and 55% RH.
- 2) As the flat plate made of the same material as the mold, an aluminum plate [average roughness Ra: 0.2-0.4 μm] is horizontally arranged. Thereafter, a silicone mold releasing agent [trade name: “PURAPOWER 2060,” manufactured by Kao Corporation] is sprayed on its surface, and sufficiently wiped off with a waste cloth.
- 3) A given surface-treating agent is uniformly sprayed in the amount of 10 g/m2 on the silicone mold releasing agent-sprayed surface (surface-treating agents which are solid at 25° C. are previously heated to a temperature of not lower than their melting points to melt and then sprayed).
- 4) The liquid molding material previously degassed by evacuation is collected with a syringe [Model “SS-02S,” manufactured by TERUMO CORPORATION], and one droplet is dropped on the flat plate from the height of 10 cm from the surface of the flat plate in a manner so that the droplet of the liquid molding material has the weight of 0.10±0.02 g.
- 5) The time at which the droplet reaches the surface of the flat plate is counted as zero second. The change of the droplet is observed in accordance with the passage of time from the sideways direction of the droplet with a microscope [Product No. “VH-6200,” manufactured by KEYENCE CORPORATION] as a CCD camera. After 60 seconds passed, the contact angle between the droplet and the flat plate is measured.
- [Production of Molded Articles Made of Polyether Polyurethane Foam]
- There was used a mold for testing made of aluminum having an inner surface for forming on the tiptoe portion a sole pattern having 127 projections for antislipping wherein each of their height, width and length is about 5 mm, respectively, and wherein each vertical cross section of the projections was triangular. The temperature of the mold was adjusted to 50°±2° C. A mold releasing agent (trade name: “PURAPOWER 2060,” manufactured by Kao Corporation) was sprayed on the inner surface, and wiped off with a waste cloth.
- A surface-treating agent shown in Table 1 was used, and sprayed on the mold releasing agent-sprayed surface with a spray gun so that the amount of the surface treatment agent applied was 10 g/m2. The contact angle between the liquid molding material and the surface-treating agent-sprayed surface was measured in accordance with the above method for measurement of a contact angle. The results are shown in Table 1.
- One tank of a pouring-type low-pressure foaming machine was charged with an isocyanate prepolymer [trade name: “EDDYFOAM B-6009N,” manufactured by Kao Corporation], and the liquid temperature was adjusted to 40° C., and the other tank thereof was charged with a liquid mixture prepared by mixing 100 parts by weight of a polyol composition solution [trade name: “EDDYFOAM AS-2045,” manufactured by Kao Corporation] and 2 parts by weight of a catalyst [trade name: “EDDYFOAM AS-651-60C,” manufactured by Kao Corporation], and the liquid temperature was adjusted to 40° C.
- The isocyanate prepolymer was admixed with the liquid mixture, and the resulting mixture was stirred using this low-pressure foaming machine, so that an isocyanate index was 98. The resulting mixture was poured into the mold mentioned above to allow foaming. After 5 minutes passed from the pouring, the foamed product was taken out from the mold, to give a molded article made of a polyurethane foam. Each of the resulting molded articles had a density of about 0.65 g/cm3 and hardness (Asker C) of 80±2.
- Next, the shape transfer ratio of the resulting molded article made of a polyurethane foam was evaluated in accordance with the following method. The results are shown in Table 1.
- [Shape Transfer Ratio]
- In order to determine whether or not a molded article having a shape accurately corresponding to the shape of the inner surface of the mold is obtained, the shape transfer ratio was obtained in accordance with the following method.
- The case where not less than 50% of the projections for antislipping of the molded article was lacked at its tip portion was evaluated as Score −3, and the number of the lacked projections is defined as “p”; the case where not less than 30% and less than 50% of the projections for antislipping of the molded article was lacked at its tip portion was evaluated as Score −2, and the number of the lacked projections is defined as “q”; the case where less than 30% of the projections for antislipping of the molded article was lacked at its tip portion was evaluated as Score −1, and the number of the lacked projections is defined as “r”; and the case where no lacked portions were observed was evaluated as Score 0, and the number of no lacked projections is defined as “s” (the total number of p+q+r+s is 127. The shape transfer ratio was calculated in accordance with the following equation:
- [Shape Transfer Ratio]=[381+(−3)×p+(−2)×q+(−1)×r+0×s]÷3.81
- [Production of Molded Articles Made of Polyester Polyurethane Foam]
- The same procedures as in Examples 1 to 4 were carried out except that an isocyanate prepolymer [trade name: “EDDYFOAM B-2009,” manufactured by Kao Corporation], and 100 parts by weight of a polyol solution [trade name: “EDDYFOAM AS-1210,” manufactured by Kao Corporation] and 1.5 parts by weight of a catalyst [trade name: “EDDYFOAM AS-651-60C,” manufactured by Kao Corporation], instead of the isocyanate prepolymer, the polyol solution and the catalyst used in Examples 1 to 4, to produce a molded article made of a polyurethane foam. Each of the resulting molded articles had a density of about 0.60 g/cm3 and hardness (Asker C) of 80±2.
- The shape transfer ratio of the resulting molded article made of a polyurethane foam was evaluated in the same manner as above. The results are shown in Table 1.
TABLE 1 Contact Angle Shape Kind of Composition of Sur- after Transfer Example Polyurethane face-Treating Agent 60 sec Ratio No. Foam (% by weight) (° C.) (%) Example 1 Ether Butyl stearate (100) 18 93.5 Polyurethane 2 Ether Ethyl stearate (100) 17 94.6 Polyurethane 3 Ether Octadecyl (100) 17 95.5 Polyurethane stearate 4 Ether Dioctyl ether (100) 17 97.7 Polyurethane Comp. Ex. 1 Ether None 43 34.9 Polyurethane 2 Ether EMULGEN (100) 32 50.3 Polyurethane 903*1 3 Ether Linseed oil (100) 31 57.5 Polyurethane 4 Ether Lard (100) 31 44.6 Polyurethane Example 5 Ester Butyl stearate (100) 21 86.3 Polyurethane 6 Ester Ethyl stearate (100) 23 83.6 Polyurethane 7 Ester Octadecyl (100) 22 83.6 Polyurethane stearate 8 Ester Dioctyl ether (100) 22 90.2 Polyurethane Comp. Ex. 5 Ester None 46 30.3 Polyurethane 6 Ester EMULGEN (100) 34 46.3 Polyurethane 903*1 7 Ester Linseed oil (100) 34 53.3 Polyurethane 8 Ester Lard (100) 35 42.1 Polyurethane - As is clear from the results shown in Table 1, it can be seen that all of the molded articles obtained in each Example have extremely high shape transfer ratios of because a contact angle-reducing substance showing a contact angle of not more than 30° is used.
- [Production of Molded Articles Made of Polvether Polyurethane Foam]
- The same procedures as in Examples 1 to 4 were carried out except that spraying of the mold releasing agent on the mold for testing was omitted and that surface-treating agents shown in Table 2, which were previously admixed together at 25° C., were used, to produce a molded article made of a polyurethane foam. Each of the resulting molded articles had a density of about 0.65 g/cm3 and hardness (Asker C) of 80±2.
- The releasing property after production of the molded article made of a polyurethane foam was evaluated in accordance with the following method. The shape transfer ratio of the resulting molded article made of a polyurethane foam was evaluated in the same manner as above. The results are shown in Table 2.
- [Releasing Property after Production]
- The condition when taking out the resulting molded article from the mold was determined based on the following criteria:
⊚: the molded article not being entirely stuck to the inner surface of the mold at all; ∘: the molded article being slightly stuck to the inner surface of the mold without posing any problems; and x: the molded article being stuck to the mold, thereby making it impossible to take out the molded article from the mold. - [Production of Molded Articles Made of Polyester Polyurethane Foam]
- The same procedures as in Examples 5 to 8 were carried out except that spraying of the mold releasing agent on the mold for testing was omitted and that the surface-treating agents shown in Table 2, which were previously admixed together at 25° C. were used, to produce a molded article made of a polyurethane foam. Each of the resulting molded articles had a density of about 0.65 g/cm3 and hardness (Asker C) of 80±2.
- The releasing property after production and the shape transfer ratio of the resulting molded article made of a polyurethane foam were evaluated in the same manner as above. The results are shown in Table 2.
- In Table 2, the following mold releasing agents were used: Mold releasing agent A: [trade name: “SUPER OIL B,” manufactured by NOF Corporation]; Mold releasing agent B: dimethyl silicone oil [trade name: “TSF-451-50,” manufactured by Toshiba Silicone Co., Ltd.]; Mold releasing agent C: dimethyl silicone oil [trade name: “TSF-451-300,” manufactured by Toshiba Silicone Co., Ltd.]; Mold releasing agent D: a blend of silicone compounds [trade name: “PURAPOWER 20conc 60,” manufactured by Kao Corporation].
TABLE 2 Releas- Shape Kind of Composition of Sur- ing Transfer Example Polyurethane face-Treating Agent Proper- Ratio No. Foam (% by weight) ty (%) Example 9 Ether Butyl stearate (10) ⊚ 70.3 Polyurethane Mold releasing (90) agent A 10 Ether Butyl stearate (20) ⊚ 95.0 Polyurethane Mold releasing (80) agent A 11 Ether Butyl stearate (50) ⊚ 96.3 Polyurethane Mold releasing (50) agent A 12 Ether Butyl stearate (80) ∘ 92.5 Polyurethane Mold releasing (20) agent A 13 Ether Butyl stearate (20) ∘ 92.3 Polyurethane Mold releasing (80) agent A 14 Ether Butyl stearate (20) ⊚ 96.3 Polyurethane Mold releasing (80) agent B 15 Ether Butyl stearate (20) ⊚ 92.8 Polyurethane Mold releasing (80) agent C 16 Ether Butyl stearate (20) ⊚ 89.3 Polyurethane Mold releasing (80) agent D 17 Ether Dioctyl ether (20) ∘ 93.6 Polyurethane Mold releasing (80) agent A 18 Ether Dioctyl ether (20) ⊚ 98.5 Polyurethane Mold releasing (80) agent B 19 Ether Dioctyl ether (20) ⊚ 95.3 Polyurethane Mold releasing (80) agent C 20 Ether Dioctyl ether (20) ⊚ 91.6 Polyurethane Mold releasing (80) agent D Comp. Ex. 9 Ether Mold releasing (100) ⊚ 33.6 Polyurethane agent A 10 Ether Mold releasing (100) ⊚ 35.6 Polyurethane agent B 11 Ether Mold releasing (100) ⊚ 38.3 Polyurethane agent C 12 Ether Mold releasing (100) ⊚ 34.2 Polyurethane agent D Example 21 Ester Butyl stearate (20) ⊚ 83.3 Polyurethane Mold releasing (80) agent A 22 Ester Dioctyl ether (20) ⊚ 84.6 Polyurethane Mold releasing (80) agent A - As is clear from the results shown in Table 2, it can be seen that each of the molded articles made of a polyurethane foam obtained in each Example has an extremely high shape transfer ratio, and also has excellent releasing properties after molding because the contact angle-reducing substance showing a contact angle of not more than 30° is used.
- There was used a mold made of aluminum having a shape corresponding to a molded article having a length of 255 mm, a width of 90 mm, a height of 30 mm, and a thickness of 5 mm, and also having 20 projections wherein each of length, width, and height is 20 mm, 20 mm, and 2 mm, respectively, as a design of its side surface. The temperature of the mold was adjusted to 70°±2° C. A mold releasing agent (trade name: “PURAPOWER 2060,” manufactured by Kao Corporation) was sprayed on the inner surface, and wiped off with a waste cloth.
- A contact angle-reducing substance shown in Table 3 was added to an isocyanate prepolymer [trade name: “EDDYFOAM B-3021,” manufactured by Kao Corporation]. One tank of a pouring-type low-pressure foaming machine was charged with the resulting mixture, and the liquid temperature was adjusted to 35° C. The other tank thereof was charged with a liquid mixture prepared by mixing 100 parts by weight of a polyol solution [trade name: “EDDYFOAM AS-6-52U,” manufactured by Kao Corporation], 1.3 parts by weight of a catalyst [trade name: “EDDYFOAM AS-651-60C,” manufactured by Kao Corporation], 2 parts by weight of a crosslinking agent [trade name: “EDDYFOAM AS-60E,” manufactured by Kao Corporation], 0.5 parts by weight of a foam stabilizer (a surfactant) [trade name: “EDDYFOAM AS-11S,” manufactured by Kao Corporation], and the liquid temperature was adjusted to 40° C.
- The isocyanate prepolymer was admixed with the liquid mixture and stirred using this low-pressure foaming machine so that an isocyanate index was 100. The resulting mixture was poured into the mold mentioned above to allow foaming. After 5 minutes passed from the pouring, the foamed product was taken out from the mold, to give a molded article made of a polyurethane foam. Each of the resulting molded articles had a density of about 0.28 g/cm3 and hardness (Asker C) of 60±2.
- Next, the shape transfer ratio of the resulting molded article made of a polyurethane foam was evaluated in accordance with the following method. The results are shown in Table 3.
- When the upper portion of the projections is lacked in the length of not less than 2 mm during the molding of the molded article, its length is measured, and a sum (T) of length of all surface voids is calculated, and the shape transfer ratio is calculated from the following equation:
- Shape Transfer Ratio=(400+T)÷400×100
- The evaluation is made on the following criteria:
[Criteria] ∘: the transfer ratio being not less than 95 (extremely excellent appearance); Δ: the transfer ratio being not less than 92.5 and less than 95 (good appearance); and x: the transfer ratio being less than 92.5 (poor appearance). -
TABLE 3 Contact Angle- Reducing Substance Evaluation of and Amount Thereof Shape Transfer Example [Content in Isocyanate Pre- Ratio No. polymer (% by weight)] (%) Example 23 Butyl stearate (0.5) ∘ 24 Butyl stearate (1) ∘ 25 Butyl stearate (5) ∘ 26 Ethyl stearate (1) ∘ Comp. Ex. 13 Octyl phthalate (1) x 14 Octyl phthalate (5) x 15 None x - As is clear from the above results shown in Table 3, it can be seen that all of the molded articles made of a polyurethane foam obtained in Examples 23 to 26 have high shape transfer ratios because the contact angle-reducing substance is added thereto.
- Industrial Applicability
- According to the process of the present invention, there can be exhibited an effect that a molded article having a shape accurately corresponding to the shape of the inner surface of the mold can be produced without the generation of lowering surface properties such as surface void on the surface of the molded article.
- Therefore, the process of the present invention can be suitably employed when producing a molded article used, for instance, for shoe soles.
Claims (9)
1. A process for producing a molded article made of a polyurethane comprising,
(A) pouring or injecting a liquid molding material into a mold under the condition that the contact angle between the liquid molding material and the inner surface of the mold is adjusted to not more than 30° by applying the surface-treating agent to the inner surface of the mold, and
(B) curing the liquid molding material.
2. The process according to claim 1 , wherein the molded article is a shoe sole made of a polyurethane foam.
3. The process according to claim 1 , wherein the contact angle-reducing substance is an ester prepared from a fatty acid and a monohydric alcohol.
4. The process according to claim 1 , wherein the contact angle between the liquid molding material and the inner surface of the mold is adjusted to not more than 23°.
5. The process according to claims 1, wherein a mold releasing agent is applied to the inner surface of the mold prior to pouring or injecting the liquid molding material in the mold.
6. A surface-treating agent used for applying the surface-treating agent to the inner surface of the mold in a process for producing a molded article comprising pouring or injecting a liquid molding material into a mold and curing the liquid molding material, comprising a contact angle-reducing substance which reduces the contact angle between the liquid molding material and a flat plate made of the same material as the mold to not more than 30°, when the surface-treating agent is applied to the flat plate and the liquid molding material is dropped thereon.
7. The surface-treating agent of claim 6 , wherein the molded article is a shoe sole made of a polyurethane foam.
8. A method for reducing surface voids during molding, comprising using the surface-treating agent as defined in claim 6 .
9. A method for reducing surface voids during molding, comprising using the surface-treating agent as defined in claim 7.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/465,751 US20030209826A1 (en) | 1998-04-28 | 2003-06-20 | Process for producing molded article |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11909598 | 1998-04-28 | ||
JP10/119095 | 1998-04-28 | ||
US09/674,149 US6607687B1 (en) | 1998-04-28 | 1999-04-27 | Process for producing molded article |
US10/465,751 US20030209826A1 (en) | 1998-04-28 | 2003-06-20 | Process for producing molded article |
Related Parent Applications (2)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP1999/002259 Division WO1999055510A1 (en) | 1998-04-28 | 1999-04-27 | Process for producing molded article |
US09/674,149 Division US6607687B1 (en) | 1998-04-28 | 1999-04-27 | Process for producing molded article |
Publications (1)
Publication Number | Publication Date |
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US20030209826A1 true US20030209826A1 (en) | 2003-11-13 |
Family
ID=14752787
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US09/674,149 Expired - Fee Related US6607687B1 (en) | 1998-04-28 | 1999-04-27 | Process for producing molded article |
US10/465,751 Abandoned US20030209826A1 (en) | 1998-04-28 | 2003-06-20 | Process for producing molded article |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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US09/674,149 Expired - Fee Related US6607687B1 (en) | 1998-04-28 | 1999-04-27 | Process for producing molded article |
Country Status (5)
Country | Link |
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US (2) | US6607687B1 (en) |
EP (1) | EP1075369A1 (en) |
KR (1) | KR100595954B1 (en) |
CN (1) | CN100368172C (en) |
WO (1) | WO1999055510A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190030964A1 (en) * | 2016-01-29 | 2019-01-31 | Compagnie Generale Des Etablissements Michelin | Electrically conductive mold release for non-pneumatic tires |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN103228414B (en) | 2010-09-30 | 2015-12-16 | 陶氏环球技术有限责任公司 | The container minimizing the defect in reactive polyurethane flow process is modified |
CN104985824A (en) * | 2015-05-14 | 2015-10-21 | 孟凡英 | High polymer material one-dimensional pore manufacturing method |
Citations (4)
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US4151661A (en) * | 1976-09-27 | 1979-05-01 | Nihon Soflan Chemical & Engineering Co. Ltd. | Shoe soles and method for manufacturing the same |
US4157990A (en) * | 1976-02-10 | 1979-06-12 | Henkel Inc. | Lubricating and anti-tack compositions useful in the shaping of thermoplastics containing mixed esters and esters of C32-72 monoalcohols with C18-72 monoacids |
US5635580A (en) * | 1993-09-29 | 1997-06-03 | Hoya Corporation | Process for the production of polyurethane lens |
US5670553A (en) * | 1995-08-25 | 1997-09-23 | Imperial Chemical Industries Plc | Internal mold release compositions |
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JPS5542091A (en) | 1978-09-19 | 1980-03-25 | Sanyo Electric Co Ltd | Method and device for storing and indicating reservation data for timer |
US5326505A (en) * | 1992-12-21 | 1994-07-05 | Johnson & Johnson Vision Products, Inc. | Method for treating an ophthalmic lens mold |
JPH0760811A (en) | 1993-08-27 | 1995-03-07 | Japan Synthetic Rubber Co Ltd | Manufacture of push button member |
JPH07214587A (en) | 1994-02-08 | 1995-08-15 | Asahi Chem Ind Co Ltd | Surface hydrophilic synthetic resin molding |
JPH07329099A (en) | 1994-06-03 | 1995-12-19 | Sumitomo Bayer Urethane Kk | Manufacture of polyurethane resin molded product |
US5849209A (en) * | 1995-03-31 | 1998-12-15 | Johnson & Johnson Vision Products, Inc. | Mold material made with additives |
US5690865A (en) | 1995-03-31 | 1997-11-25 | Johnson & Johnson Vision Products, Inc. | Mold material with additives |
JP3118415B2 (en) * | 1996-04-23 | 2000-12-18 | 良和 藤 | Cement admixture and its manufacturing method |
JPH10128861A (en) | 1996-10-29 | 1998-05-19 | Nikon Corp | Manufacture of plastic lens |
-
1999
- 1999-04-27 CN CNB998055999A patent/CN100368172C/en not_active Expired - Fee Related
- 1999-04-27 US US09/674,149 patent/US6607687B1/en not_active Expired - Fee Related
- 1999-04-27 KR KR1020007011890A patent/KR100595954B1/en not_active IP Right Cessation
- 1999-04-27 WO PCT/JP1999/002259 patent/WO1999055510A1/en active IP Right Grant
- 1999-04-27 EP EP99917199A patent/EP1075369A1/en not_active Withdrawn
-
2003
- 2003-06-20 US US10/465,751 patent/US20030209826A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4157990A (en) * | 1976-02-10 | 1979-06-12 | Henkel Inc. | Lubricating and anti-tack compositions useful in the shaping of thermoplastics containing mixed esters and esters of C32-72 monoalcohols with C18-72 monoacids |
US4151661A (en) * | 1976-09-27 | 1979-05-01 | Nihon Soflan Chemical & Engineering Co. Ltd. | Shoe soles and method for manufacturing the same |
US5635580A (en) * | 1993-09-29 | 1997-06-03 | Hoya Corporation | Process for the production of polyurethane lens |
US5670553A (en) * | 1995-08-25 | 1997-09-23 | Imperial Chemical Industries Plc | Internal mold release compositions |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20190030964A1 (en) * | 2016-01-29 | 2019-01-31 | Compagnie Generale Des Etablissements Michelin | Electrically conductive mold release for non-pneumatic tires |
Also Published As
Publication number | Publication date |
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EP1075369A1 (en) | 2001-02-14 |
CN100368172C (en) | 2008-02-13 |
WO1999055510A1 (en) | 1999-11-04 |
KR100595954B1 (en) | 2006-07-03 |
US6607687B1 (en) | 2003-08-19 |
KR20010043029A (en) | 2001-05-25 |
CN1298338A (en) | 2001-06-06 |
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