JP2000084943A - Insulating mold and molding method using the same - Google Patents
Insulating mold and molding method using the sameInfo
- Publication number
- JP2000084943A JP2000084943A JP25680898A JP25680898A JP2000084943A JP 2000084943 A JP2000084943 A JP 2000084943A JP 25680898 A JP25680898 A JP 25680898A JP 25680898 A JP25680898 A JP 25680898A JP 2000084943 A JP2000084943 A JP 2000084943A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- insulating layer
- molding
- heat insulating
- heat
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- 239000000178 monomer Substances 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 description 1
- KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- 229940065472 octyl acrylate Drugs 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- GYDSPAVLTMAXHT-UHFFFAOYSA-N pentyl 2-methylprop-2-enoate Chemical compound CCCCCOC(=O)C(C)=C GYDSPAVLTMAXHT-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- AYEFIAVHMUFQPZ-UHFFFAOYSA-N propane-1,2-diol;prop-2-enoic acid Chemical compound CC(O)CO.OC(=O)C=C AYEFIAVHMUFQPZ-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 102220259718 rs34120878 Human genes 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- WLOQLWBIJZDHET-UHFFFAOYSA-N triphenylsulfonium Chemical compound C1=CC=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 WLOQLWBIJZDHET-UHFFFAOYSA-N 0.000 description 1
- 239000012953 triphenylsulfonium Substances 0.000 description 1
- 125000000391 vinyl group Chemical class [H]C([*])=C([H])[H] 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Moulds For Moulding Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、複雑な3次元形状
においても高外観を達成できる断熱金型及びそれを用い
た成形方法に関する。更に詳しくは、成形される熱可塑
性樹脂組成物の優れた特性を損なうことなく、複雑な3
次元形状においても高外観が達成でき、かつ極めて短期
間で作成が可能な断熱金型およびそれを用いた成形方法
に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat-insulating mold capable of achieving a high appearance even in a complicated three-dimensional shape, and a molding method using the same. More specifically, a complex 3D composition can be used without impairing the excellent properties of the thermoplastic resin composition to be molded.
The present invention relates to a heat-insulating mold capable of achieving a high appearance even in a three-dimensional shape and capable of being produced in an extremely short time, and a molding method using the same.
【0002】[0002]
【従来の技術】熱可塑性樹脂を射出成形方法やブロー成
形法等を用いて成形する場合、金型の型表面転写性を向
上し、成形品の光沢に優れ、またウエルドライン、フロ
ーマーク、ジェッティング等の外観不良を低減した外観
の高品位化が常に要求されている。従来、これらの外観
不良を改良するためには塗装等の後加工が一般に行われ
ているが、近年、成形品使用後のリサイクルや、塗装時
の環境問題、さらにはコストダウンのために、塗装レス
化の要求が非常に大きい。2. Description of the Related Art When molding a thermoplastic resin by an injection molding method or a blow molding method, the mold surface transferability of a mold is improved, the gloss of a molded product is excellent, and a weld line, a flow mark, a jet mark, and the like are obtained. There is always a demand for a high-quality appearance with reduced appearance defects such as filming. Conventionally, post-processing such as painting is generally performed to improve these appearance defects, but in recent years, painting has been carried out for recycling after use of molded products, environmental problems at the time of painting, and cost reduction. There is a great demand for less
【0003】成形時に金型の型表面転写性を向上し、成
形品の光沢に優れ、ウエルドライン、フローマーク、ジ
ェッティング等の外観不良を低減した高品位の外観を有
する成形品を得るためには、一般に高い金型温度や樹脂
温度、高い射出圧力、高速射出等の成形条件の最適化が
行われ、それによりある程度までは目的を達成すること
ができる。In order to improve the mold surface transferability of a mold during molding, obtain a molded article having excellent gloss and excellent appearance with reduced appearance defects such as weld lines, flow marks and jetting. In general, the molding conditions such as high mold temperature and resin temperature, high injection pressure, high-speed injection and the like are optimized, thereby achieving the object to some extent.
【0004】これらの成形条件の中で、最も影響が大き
い成形条件が金型温度であり、金型温度を高くすること
が高外観な成形品を得る上では特に好ましい。しかし、
金型全体の温度を高くすることは、溶融した熱可塑性樹
脂を成形品を取り出せる温度まで金型内で冷却するため
に必要な冷却時間が長くなり、生産効率を低下させる。
従って、金型全体の温度を高くすることなく高外観の成
形品を得る方法や金型温度を高くしても生産効率を低下
させない成形法が要求される。[0004] Among these molding conditions, the one having the greatest influence is the mold temperature, and it is particularly preferable to increase the mold temperature in order to obtain a molded article having a high appearance. But,
Increasing the temperature of the entire mold increases the cooling time required for cooling the molten thermoplastic resin in the mold to a temperature at which the molded product can be taken out, thereby lowering production efficiency.
Therefore, there is a demand for a method of obtaining a molded article having a high appearance without increasing the temperature of the entire mold, and a molding method which does not lower the production efficiency even if the mold temperature is increased.
【0005】近年これらの要求に対して、例えば、金型
に加熱用と冷却用の冷却管を設けて、成形工程に応じ
て、熱媒体と冷媒体を交互に循環させて加熱、冷却する
方法が行われている。しかしこの方法では熱エネルギー
の消費量が高く、生産効率も向上しない。一方、金型壁
面に熱伝導率の小さい物質で断熱層を設けることによ
り、成形時に金型表面部分のみを局所的に高温とし、金
型表面の転写性を向上する方法が古くから提案されてお
り、例えば、USP3544518号やWO89/10
823号が開示されている。しかしながらUSP354
4518号の断熱層は具体的にはポリエチレンテレフタ
レートフィルムであり、成形体が複雑な3次元形状を有
する場合には十分な対応ができない欠点がある。WO8
9/10823号も同様に、ポリイミドの板状物を断熱
層として使用しており、金型の表面形状が複雑である場
合には対応が困難であるという欠点があった。かかる問
題を解決すべく特開平7−80187号公報では、直鎖
型ポリイミド前駆体溶液を金型壁面に塗布、加熱を繰り
返してポリイミド断熱層を形成する方法が示されてい
る。この方法は3次元形状を有する金型壁面にも対応で
きるが、直鎖型ポリイミド前駆体溶液を金型壁面に塗
布、加熱を数回繰り返さなければならず、断熱金型の作
製期間が極めて長くなる欠点があった。更に、金型形状
が複雑な場合には機械加工等による寸法の調整を行う必
要があるが、複雑な3次元形状を有する金型の場合には
その対応も十分できないとの欠点を有していた。In response to these demands in recent years, for example, a method of heating and cooling by providing a cooling pipe for heating and cooling in a mold and alternately circulating a heat medium and a cooling medium in accordance with a molding process. Has been done. However, this method consumes high heat energy and does not improve production efficiency. On the other hand, a method of improving the transferability of the mold surface by providing a heat insulating layer with a material having a low thermal conductivity on the mold wall surface to locally heat only the mold surface during molding and improving the mold transferability has been proposed for a long time. For example, US Pat. No. 3,544,518 and WO 89/10
No. 823 is disclosed. However, USP 354
The heat insulating layer of No. 4518 is specifically a polyethylene terephthalate film, and has a drawback that it cannot sufficiently cope with a case where the molded article has a complicated three-dimensional shape. WO8
Similarly, Japanese Patent Application No. 9/10823 uses a polyimide plate as a heat insulating layer, and has a drawback that it is difficult to cope with a complicated mold surface shape. To solve this problem, Japanese Patent Application Laid-Open No. 7-80187 discloses a method of forming a polyimide heat insulating layer by repeatedly applying a linear polyimide precursor solution to a mold wall surface and heating the mold. Although this method can be applied to a mold wall having a three-dimensional shape, it is necessary to apply a linear polyimide precursor solution to the mold wall and repeat heating several times. There were disadvantages. Further, when the shape of the mold is complicated, it is necessary to adjust the dimensions by machining or the like, but in the case of a mold having a complicated three-dimensional shape, there is a drawback that it is not possible to cope with the problem. Was.
【0006】[0006]
【発明が解決しようとする課題】本発明は、成形される
熱可塑性樹脂組成物の優れた特性を損なうことなく、複
雑な3次元形状においても高外観が達成でき、かつ極め
て短期間で作成が可能な断熱金型およびそれを用いた成
形方法の提供を目的とするものである。本発明者らは、
上記目的を達成せんとして鋭意検討した結果、金属から
なる主金型の金型表面における任意の部位に断熱層を組
み込んだ断熱金型において、かかる断熱層を3次元造形
法により作製し、かつかかる断熱層の厚みをかかる対応
する部位における成形品肉厚に対して特定の範囲とする
ことにより、上記目的を達成できることを見出し、さら
に検討を重ねて本発明を完成した。SUMMARY OF THE INVENTION The present invention can achieve a high appearance even in a complicated three-dimensional shape without impairing the excellent properties of the thermoplastic resin composition to be molded, and can be produced in a very short time. It is an object of the present invention to provide a possible heat-insulating mold and a molding method using the same. We have:
As a result of intensive studies to achieve the above object, in a heat-insulating mold in which a heat-insulating layer is incorporated at an arbitrary position on the mold surface of a metal main mold, such a heat-insulating layer is produced by a three-dimensional molding method, and It has been found that the above object can be achieved by setting the thickness of the heat insulating layer to a specific range with respect to the thickness of the molded product at the corresponding portion, and the present inventors have further studied and completed the present invention.
【0007】[0007]
【課題を解決するための手段】本発明は、熱可塑性樹脂
組成物の成形時に使用する金型の主金型の中に断熱層を
組み込み、主金型が該熱可塑性樹脂組成物のTgよりも
低い温度で保持され、断熱層が組み込まれた部分の金型
キャビティ表面温度の成形時における最高温度がTg+
1〜Tg+50℃の範囲となる成形方法において使用す
る断熱金型であって、断熱層を組み込む金型キャビティ
部分における、該断熱層の厚みが成形品肉厚に対して
0.01〜2倍の範囲にあり、更に該断熱層が3次元造
形法により造形された、熱伝導率1.0W/m・K以下
の合成樹脂組成物からなる断熱層であることを特徴とす
る断熱金型に関するものである。SUMMARY OF THE INVENTION According to the present invention, a heat insulating layer is incorporated in a main mold of a mold used for molding a thermoplastic resin composition, and the main mold has a Tg of the thermoplastic resin composition. Is maintained at a low temperature, and the maximum temperature at the time of molding of the mold cavity surface temperature of the portion where the heat insulating layer is incorporated is Tg +
A heat-insulating mold used in a molding method in the range of 1 to Tg + 50 ° C., wherein the thickness of the heat-insulating layer in a mold cavity portion incorporating the heat-insulating layer is 0.01 to 2 times the thickness of the molded product. A heat insulating layer comprising a synthetic resin composition having a thermal conductivity of 1.0 W / m · K or less, wherein the heat insulating layer is formed by a three-dimensional forming method. It is.
【0008】本発明で用いられる3次元造形法は、通
常、積層造形法と呼ばれ、ラピッドプロトタイピングに
よる試作品やラピッドツーリングによる成形用の型を短
期間に安価に製造する手法としてよく知られるものであ
る。The three-dimensional molding method used in the present invention is generally called an additive manufacturing method, and is well known as a method of manufacturing a prototype by rapid prototyping or a mold for rapid tooling at a low cost in a short period of time. Things.
【0009】ここで用いる3次元造形法としては、複雑
な3次元形状を有する断熱層を容易に造形できる光造形
法、粉末焼結法、インクジェット法、樹脂押出し法、シ
ート切断法等が挙げられる。得られた造形物を断熱層と
して用いる上で好ましい3次元造形法としては、複雑な
3次元形状を有する断熱層を短時間に造形するととも
に、造形物を構成する材料の耐熱性が高く、且つ熱伝導
率が低いこと求められることから、光造形法が特に好ま
しい。As the three-dimensional molding method used here, there are an optical molding method, a powder sintering method, an ink-jet method, a resin extrusion method, a sheet cutting method, etc., which can easily form a heat insulating layer having a complicated three-dimensional shape. . As a preferable three-dimensional shaping method for using the obtained modeled object as a heat insulating layer, a heat insulating layer having a complicated three-dimensional shape is formed in a short time, and the material constituting the modeled object has high heat resistance, and Since low thermal conductivity is required, stereolithography is particularly preferred.
【0010】この3次元造形法について基本的な造形プ
ロセスを簡単に説明する。一般に3次元造形法で用いら
れる積層造形用材料としては、樹脂、紙、金属粉末など
が挙げられ、特に光硬化性樹脂については、射出成形用
金型として使用することを前提として材料的な改質が加
えられている。3次元造形法では、3次元CADを用い
て造形物の形状データが作成され、3次元造形法で使用
可能なフォーマットに変換された後、任意の積層厚さに
分割された断面形状を光造形法、粉末焼結法、インクジ
ェット法、樹脂押出し法、シート切断法等により積層す
ることで3次元造形物を得ることができる。A basic modeling process of the three-dimensional molding method will be briefly described. In general, examples of the material for lamination molding used in the three-dimensional molding method include resin, paper, metal powder, and the like. In particular, a photocurable resin is materially modified on the assumption that it is used as a mold for injection molding. Quality is added. In the three-dimensional printing method, the shape data of a formed object is created using three-dimensional CAD, converted into a format usable in the three-dimensional printing method, and then the cross-sectional shape divided into an arbitrary layer thickness is optically formed. A three-dimensional structure can be obtained by laminating by a method, a powder sintering method, an inkjet method, a resin extrusion method, a sheet cutting method, or the like.
【0011】本発明でいう主金型とは、金型全体の構成
をいい、断熱層部分を組み込む対象となるものをいう。
主金型は金属からなり、したがって熱伝導率の良好な材
料からなるものである。本発明の効果は、主金型を構成
する金属の熱伝導率が基本的に良好であり、一方特定部
位における断熱層の熱伝導率が低いことにより達成でき
るものである。本発明の断熱層は、3次元造形法により
造形されるため、金属からなる主金型の金型表面の任意
に選ばれた高外観を要求される3次元形状がいかなる複
雑な3次元形状を有していても、短期間に安価に製造す
ることができる。In the present invention, the main mold refers to the entire structure of the mold, and is the one into which the heat insulating layer is incorporated.
The main mold is made of a metal and therefore of a material having good thermal conductivity. The effect of the present invention can be achieved by the fact that the metal constituting the main mold has basically good thermal conductivity, while the thermal conductivity of the heat insulating layer at a specific portion is low. Since the heat-insulating layer of the present invention is formed by a three-dimensional forming method, any three-dimensional shape requiring an arbitrarily selected high appearance of the metal surface of the main die made of metal can have any complicated three-dimensional shape. Even if it has, it can be manufactured at a low cost in a short time.
【0012】尚、本発明でいう光造形法とは、従来公知
の光造形法のいずれも対象とするものであり、例えば、
光硬化性樹脂の液面の上から光を照射し、液面で樹脂を
硬化させ、テーブルを特定のピッチで降下させることに
より積層を行う自由液面法、及び透明の容器に入った光
硬化性樹脂を容器の下側から光を照射し積層を行う規制
液面法のいずれの方法も使用することが可能である。更
にかかる光造形は金型の主金型に直接光造形物を造形す
ることも可能であるし、主金型の入れ子に直接光造形物
を造形し、かかる入れ子部分を主金型に組み込む構造、
また通常に光造形した造形型を、主金型の中に組み込む
構造のいずれの方法を使用することもできる。The stereolithography method according to the present invention is intended for any conventionally known stereolithography method.
A free liquid level method in which light is irradiated from above the liquid surface of the photocurable resin, the resin is cured at the liquid surface, and the table is lowered at a specific pitch for lamination, and photocuring in a transparent container Any of the regulated liquid level methods in which the conductive resin is irradiated with light from the lower side of the container to perform lamination can be used. Further, in such an optical molding, it is also possible to directly mold the optical molded article on the main mold of the mold, or to directly mold the optical molded article on the nest of the main mold and incorporate the nested portion into the main mold. ,
In addition, any method of a structure in which a molding die usually formed by stereolithography is incorporated in a main mold can be used.
【0013】また本発明は、光造形に使用する硬化を誘
因する光として可視光、紫外光、赤外光、近赤外光及び
特にそれらのレーザー光を使用し、かかる光に反応して
硬化する光硬化性樹脂とからなる造形システムを主たる
対象とするが、更に電子線、X線、高エネルギー粒子線
等のエネルギー線を使用し、かかるエネルギー線に反応
し硬化する物質を用いる造形システムにおいても有効に
使用することが可能である。また化学物質に反応し硬化
する物質に、該化学物質の反応単位を正確に位置決めし
て投射する造形方法、及びマスクを介して上記の光、エ
ネルギー線、及び化学物質を投影する、いわゆるリソグ
ラフィー手法を用いる造形システムにおいても有効に使
用できるものである。最も好ましく使用できるものは、
作製期間及び装置、光源の取り扱いなどの点から紫外光
のレーザー光であるが、場合によってはより精密な積層
が可能な、赤外光、近赤外光による光造形も有用であ
る。Further, the present invention uses visible light, ultraviolet light, infrared light, near-infrared light and especially those laser lights as light for inducing curing used in stereolithography, and cures in response to such light. The main object is a molding system composed of a photo-curable resin, and an electron beam, an X-ray, and an energy beam such as a high-energy particle beam. Can also be used effectively. Also, a molding method for accurately positioning and projecting a reaction unit of the chemical substance on a substance which reacts and cures with the chemical substance, and a so-called lithography method of projecting the light, energy rays and the chemical substance through a mask. It can also be used effectively in a modeling system using. The most preferably used ones are
Ultraviolet laser light is used from the viewpoints of the production period, the device, the handling of the light source, and the like. However, in some cases, stereolithography using infrared light or near-infrared light, which enables more precise lamination, is also useful.
【0014】本発明の断熱層は、かかる熱伝導率が1.
0W/m・K以下の合成樹脂組成物であれば特に限定さ
れるものではない。かかる積層造形用材料の具体的例の
1つとしては、合成樹脂が光造形法により造形された熱
伝導率が1.0W/m・K以下の光硬化性樹脂を好まし
く挙げることができる。この光硬化性樹脂は、重合性の
ビニル系化合物、エポキシ系化合物等のいずれでもよ
く、単官能性化合物及び多官能性化合物のいずれのモノ
マー及びまたはオリゴマーが用いられる。これらの単官
能性化合物及び多官能性化合物は、特に限定されるもの
ではなく、以下に光硬化性樹脂の代表的なものを挙げ
る。The heat insulating layer of the present invention has such a thermal conductivity of 1.
There is no particular limitation as long as the synthetic resin composition is 0 W / m · K or less. As a specific example of such a material for lamination molding, a photocurable resin having a thermal conductivity of 1.0 W / m · K or less obtained by molding a synthetic resin by stereolithography can be preferably exemplified. The photocurable resin may be any of a polymerizable vinyl compound and an epoxy compound, and any monomer or oligomer of a monofunctional compound and a polyfunctional compound is used. These monofunctional compounds and polyfunctional compounds are not particularly limited, and typical examples of the photocurable resin are given below.
【0015】重合性のビニル系化合物の代表的な例とし
て、単官能性化合物としては、イソボルニルアクリレー
ト、イソボルニルメタクリレート、ジンクロペンテニル
アクリレート、ボルニルアクリレート、ボルニルメタク
リレート、2−ヒドロキシエチルアクリレート、2−ヒ
ドロキシプロピルアクリレート、プロピレングリコール
アクリレート、ビニルピロリドン、アクリルアミド、酢
酸ビニル、スチレン等が挙げられる。As typical examples of the polymerizable vinyl compound, monofunctional compounds include isobornyl acrylate, isobornyl methacrylate, zinclopentenyl acrylate, bornyl acrylate, bornyl methacrylate, and 2-hydroxyethyl acrylate. , 2-hydroxypropyl acrylate, propylene glycol acrylate, vinyl pyrrolidone, acrylamide, vinyl acetate, styrene and the like.
【0016】多官能性化合物としては、トリメチロール
プロパントリアクリレート、EO変性トリメチロールプ
ロパントリアクリレート、エチレングリコールジアクリ
レート、テトラエチレングリコールジアクリレート、
1,4−ブタンジオールジアクリレート、1,6−ヘキ
サンジオールジアクリレート、ネオペンチルグリコール
ジアクリレート、ジシクロペンテニルジアクリレート、
ポリエステルジアクリレート、ジアリルフタレート等が
挙げられる。Examples of the polyfunctional compound include trimethylolpropane triacrylate, EO-modified trimethylolpropane triacrylate, ethylene glycol diacrylate, tetraethylene glycol diacrylate,
1,4-butanediol diacrylate, 1,6-hexanediol diacrylate, neopentyl glycol diacrylate, dicyclopentenyl diacrylate,
Examples include polyester diacrylate and diallyl phthalate.
【0017】かかる単官能性化合物及び/又は多官能性
化合物の1種類以上を単独または混合物の形で使用する
ことができる。One or more of such monofunctional compounds and / or polyfunctional compounds can be used alone or in the form of a mixture.
【0018】当該光硬化性樹脂で使用されるビニル系化
合物の重合開始剤としては、光重合開始剤及び熱重合開
始剤が用いられるが、光重合開始剤としては、2,2−
ジメトキシ−2−フェニルアセトフェノン、1−ヒドロ
キシシクロヘキシルフェニルケトン、アセトフェノン、
ベンゾフェノン、キサントン、フルオレノン、ベズアル
デヒド、フルオレン、アントラキノン、トリフェニルア
ミン、カルバゾール、3−メチルアセトフェノン、ミヒ
ラーケトン等が代表的なものとして挙げることができる
が、これらに限定されるものではなく、又これらの開始
剤は1種または2種以上を組み合わせて使用することも
できる。さらに必要に応じてアミン系化合物等の増感剤
を併用することも可能である。As the polymerization initiator of the vinyl compound used in the photocurable resin, a photopolymerization initiator and a thermal polymerization initiator are used, and as the photopolymerization initiator, 2,2-
Dimethoxy-2-phenylacetophenone, 1-hydroxycyclohexylphenyl ketone, acetophenone,
Benzophenone, xanthone, fluorenone, bezaldehyde, fluorene, anthraquinone, triphenylamine, carbazole, 3-methylacetophenone, Michler's ketone, and the like can be given as typical examples, but are not limited thereto. Initiators can be used alone or in combination of two or more. If necessary, a sensitizer such as an amine compound can be used in combination.
【0019】また熱重合開始剤としては、ベンゾイルパ
ーオキサイド、t−ブチルパーオキシベンゾエート、ジ
クミルパーオキサイド、ジイソプロピルパーオキシジカ
ーボネート、t−ブチルパーオキサイド、アゾビスイソ
ブチロニトリル等が代表的なものとして挙げられること
ができる。本発明で使用される重合開始剤又は熱重合開
始剤の使用量は、ビニル系化合物に対してそれぞれ0.
1〜10重量%である。Typical thermal polymerization initiators include benzoyl peroxide, t-butylperoxybenzoate, dicumyl peroxide, diisopropylperoxydicarbonate, t-butyl peroxide, azobisisobutyronitrile and the like. Can be mentioned. The amount of the polymerization initiator or the thermal polymerization initiator used in the present invention is preferably 0.1 to 0.1 based on the vinyl compound.
1 to 10% by weight.
【0020】エポキシ系化合物の代表的な例としては、
水素添加ビスフェノールAジグリシジルエーテル、3,
4−エポキシシクロヘキシルメチル−3,4−エポキシ
シクロヘキサンカルボキシレート、2−(3,4−エポ
キシシクロヘキシル−5,5−スピロ−3,4−エポキ
シ)シクロヘキサン−m−ジオキサン、ビス(3,4−
エポキシシクロヘキシルメチル)アジペート等が挙げら
れる。これらのエポキシ系化合物を用いる場合には、ト
リフェニルスルホニウムヘキサフルオロアンチモネード
等のエネルギー活性カチオン開始剤が用いられる。Typical examples of epoxy compounds include:
Hydrogenated bisphenol A diglycidyl ether, 3,
4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, 2- (3,4-epoxycyclohexyl-5,5-spiro-3,4-epoxy) cyclohexane-m-dioxane, bis (3,4-
(Epoxycyclohexylmethyl) adipate and the like. When these epoxy compounds are used, an energy-active cation initiator such as triphenylsulfonium hexafluoroantimonide is used.
【0021】当該光硬化性樹脂には、必要に応じて、レ
ベリング剤、界面活性剤、有機高分子化合物、有機可塑
剤、有機系充填剤、及び無機充填剤等を配合してもよ
い。ここで有機系充填剤としては、架橋ポリスチレン粒
子、架橋ポリメチルメタクリレート粒子、架橋シリコー
ン粒子、及び全芳香族ポリアミド粒子の粒子状充填剤の
他、全芳香族ポリエステル繊維及び全芳香族ポリアミド
繊維等の繊維状充填剤をあげることができる。If necessary, a leveling agent, a surfactant, an organic polymer compound, an organic plasticizer, an organic filler, an inorganic filler, and the like may be added to the photocurable resin. Here, as the organic filler, other than the particulate filler of crosslinked polystyrene particles, crosslinked polymethyl methacrylate particles, crosslinked silicone particles, and wholly aromatic polyamide particles, wholly aromatic polyester fibers and wholly aromatic polyamide fibers, etc. Fibrous fillers can be mentioned.
【0022】また無機充填剤としては、ガラスビーズ、
アルミナ粒子、タルク粒子、ガラスフレーク、マイカ、
グラファイト、シリカ粒子、ワラストナイト、各種ウイ
スカー等を挙げることができる。かかる有機系充填剤及
び無機充填剤は、平均粒径は0.3〜50μmであり、
好ましくは1〜30μmの平均粒径の場合である。平均
粒径がかかる範囲内の場合には、硬化処理前の溶液の粘
度を適度に保つと同時に、造形物の精度を十分に保つこ
とができる。尚かかる観点からワラストナイト、ウイス
カー、全芳香族ポリエステル繊維等の繊維状充填剤にお
いては、上記平均粒径は繊維長の範囲を示すものとす
る。As the inorganic filler, glass beads,
Alumina particles, talc particles, glass flakes, mica,
Examples include graphite, silica particles, wollastonite, and various whiskers. Such organic fillers and inorganic fillers have an average particle size of 0.3 to 50 μm,
Preferably, the average particle diameter is 1 to 30 μm. When the average particle size is within such a range, the viscosity of the solution before the curing treatment can be kept at an appropriate level, and at the same time, the precision of the molded article can be sufficiently maintained. From such a viewpoint, in the case of fibrous fillers such as wollastonite, whiskers and wholly aromatic polyester fibers, the above average particle size indicates the range of the fiber length.
【0023】本発明で使用するウイスカーとしては例え
ば、ホウ酸アルミニウムウイスカー、チタン酸カリウム
ウイスカー、水酸化硫酸マグネシウムウイスカー、酸化
チタンウイスカー、酸化亜鉛ウイスカー等を挙げること
ができる。ウイスカーの繊維径としては、0.3〜1μ
mの範囲を満足するものが好ましく、より好ましくは、
0.3〜0.7μmの範囲である。The whiskers used in the present invention include, for example, aluminum borate whiskers, potassium titanate whiskers, magnesium hydroxide sulfate whiskers, titanium oxide whiskers, and zinc oxide whiskers. The fiber diameter of whiskers is 0.3-1μ
m is preferably satisfied, more preferably,
It is in the range of 0.3 to 0.7 μm.
【0024】またマイカ、タルク、ガラスフレーク等の
板状の充填剤においては、かかる厚みが薄い方が好まし
く、例えばガラスフレークにおいては特に好ましくは、
ゾル−ゲル法等により作成された平均厚みが2μm以下
のものが使用される。In the case of a plate-like filler such as mica, talc, glass flake, etc., it is preferable that the thickness is small. For example, in the case of glass flake, particularly preferable is:
Those having an average thickness of 2 μm or less prepared by a sol-gel method or the like are used.
【0025】上記の有機系充填剤及び無機充填剤の配合
量は光硬化性樹脂組成物において、5〜70容量%、よ
り好ましくは20〜65容量%、特に好ましくは30〜
60容量%の場合である。The amount of the organic filler and the inorganic filler is 5 to 70% by volume, more preferably 20 to 65% by volume, and particularly preferably 30 to 70% by volume in the photocurable resin composition.
This is the case of 60% by volume.
【0026】当該光硬化性樹脂としては、前記ビニル系
化合物、エポキシ系化合物を単独にあるいは併用混合し
て使用してもよく、さらに必要に応じて他の成分を配合
してもよいが、各成分の混合方法は特に限定されるもの
ではない。As the photocurable resin, the above-mentioned vinyl compounds and epoxy compounds may be used alone or in combination with each other. Further, if necessary, other components may be blended. The method of mixing the components is not particularly limited.
【0027】当該光硬化性樹脂は、硬化時すると非常に
剛性が高く、表面硬度も高く、且つ耐熱性に優れてお
り、射出成形法やブロー成形法の断熱層として特に好ま
しい。The photocurable resin has extremely high rigidity when cured, has a high surface hardness, and has excellent heat resistance, and is particularly preferable as a heat insulating layer in an injection molding method or a blow molding method.
【0028】本発明において、断熱層として用いられる
合成樹脂の熱伝導率を1.0W/m・K以下にする必要
がある。かかる値が1.0W/m・Kより大きい場合
は、断熱層の保温効果が低く、金型表面での急速な冷却
固化を抑制することが困難となる。より好ましくは0.
05〜0.7W/m・Kであり、特に好ましくは0.1
〜0.6W/m・Kの場合である。In the present invention, the thermal conductivity of the synthetic resin used as the heat insulating layer needs to be 1.0 W / m · K or less. If the value is greater than 1.0 W / m · K, the heat insulating effect of the heat insulating layer is low, and it is difficult to suppress rapid cooling and solidification on the mold surface. More preferably, 0.
05 to 0.7 W / m · K, particularly preferably 0.1
0.60.6 W / m · K.
【0029】本発明においては、断熱層が組み込まれた
金型キャビティ部分における成形品肉厚に対する断熱層
の厚みを0.01〜2倍の範囲とする必要がある。より
好ましくは0.02〜1倍の範囲である。かかる値が
0.01未満であると、断熱層が薄すぎるために断熱層
を通して熱が主金型に逃げてしまうため保温効果が低
く、金型表面での急速な冷却固化を抑制することが困難
となる。一方、かかる値が2を越えると反対に成形中に
熱可塑性樹脂から断熱層に蓄積された熱が主金型に逃げ
にくくなり、断熱層表面温度の低下する時間、すなわち
冷却時間が必要以上に長くなるため好ましくない。尚、
本発明においては、成形品肉厚に対応する断熱層の厚み
において、実質的に本発明の目的を損なわない範囲で、
一部の部分が本発明で特定する範囲を超えることを妨げ
るものではない。一部の部分としては、全体の面積の1
0%以下を目安とする。また成形品の厚みとしては、一
般に射出成形法やブロー成形法等で成形可能な厚みが使
用できるが、好ましくはかかる成形品の厚みが0.5m
m〜20mmの場合が好ましい。In the present invention, the thickness of the heat-insulating layer must be in the range of 0.01 to 2 times the thickness of the molded product in the mold cavity where the heat-insulating layer is incorporated. More preferably, it is in the range of 0.02 to 1 times. When the value is less than 0.01, heat escapes to the main mold through the heat insulating layer because the heat insulating layer is too thin, so that the heat retaining effect is low, and rapid cooling and solidification on the mold surface can be suppressed. It will be difficult. On the other hand, if the value exceeds 2, on the contrary, the heat accumulated in the heat insulating layer from the thermoplastic resin during molding becomes difficult to escape to the main mold, and the time during which the heat insulating layer surface temperature decreases, that is, the cooling time becomes longer than necessary. It is not preferable because it becomes longer. still,
In the present invention, in the thickness of the heat insulating layer corresponding to the thickness of the molded product, within a range that does not substantially impair the object of the present invention,
It does not prevent some portions from exceeding the range specified in the present invention. As a part, 1 of the total area
The standard is 0% or less. As the thickness of the molded product, a thickness that can be generally molded by an injection molding method, a blow molding method, or the like can be used, but preferably the thickness of the molded product is 0.5 m
m to 20 mm is preferred.
【0030】本発明の目的とする外観の良好な成形品を
得るためには、熱可塑性樹脂組成物が金型表面に接触し
てから熱可塑性樹脂組成物に成形時の圧力が十分に加わ
るまでの間、金型キャビティにおける断熱層表面温度の
最高温度が熱可塑性樹脂のTg以上となることが必要で
あり、すなわち熱可塑性樹脂を成形する際における断熱
層表面の最高温度が当該熱可塑性樹脂組成物のTgに対
して、Tg+1〜Tg+50℃の範囲とする必要があ
る。更にその後に断熱層表面温度がTg以下の温度にな
ることが必要である。尚本発明でTgとは、ガラス転移
温度のことをいい、かかる温度はDSC(示差走査熱量
測定)により10℃/分の昇温速度で測定される値であ
る。断熱層表面の最高温度がTg+1℃よりも低い場合
には、熱可塑性樹脂が金型表面に接触してから熱可塑性
樹脂に射出圧力を十分に加えても、金型の型表面転写性
を向上することが困難となり、Tg+50℃を越えると
逆に熱可塑性樹脂が金型表面に接触してから熱可塑性樹
脂に射出圧力等の成形時の圧力を十分に加えることによ
り金型の型表面転写性は向上するものの、溶融した熱可
塑性樹脂を金型内で成形品を取り出せる温度まで冷却す
るために必要な冷却時間が長くなり、生産効率が低下し
実用的でなく好ましくない。In order to obtain a molded article having a good appearance which is the object of the present invention, it is required that the thermoplastic resin composition is brought into contact with the surface of the mold until the pressure during molding is sufficiently applied to the thermoplastic resin composition. It is necessary that the maximum temperature of the heat insulating layer surface temperature in the mold cavity be equal to or higher than the Tg of the thermoplastic resin, that is, the maximum temperature of the heat insulating layer surface during molding of the thermoplastic resin is determined by the thermoplastic resin composition. It is necessary to be in the range of Tg + 1 to Tg + 50 ° C. with respect to Tg of the product. Further, it is necessary that the surface temperature of the heat-insulating layer thereafter becomes lower than Tg. In the present invention, Tg means a glass transition temperature, and such a temperature is a value measured by DSC (differential scanning calorimetry) at a heating rate of 10 ° C./min. When the maximum temperature of the heat-insulating layer surface is lower than Tg + 1 ° C., the mold surface transferability of the mold is improved even if the injection pressure is sufficiently applied to the thermoplastic resin after the thermoplastic resin comes into contact with the mold surface. If the temperature exceeds Tg + 50 ° C., on the contrary, the thermoplastic resin comes into contact with the mold surface and then the molding pressure such as the injection pressure is sufficiently applied to the thermoplastic resin to transfer the mold surface. However, the cooling time required for cooling the molten thermoplastic resin to a temperature at which the molded article can be taken out of the mold increases, and the production efficiency decreases, which is not practical and not preferable.
【0031】本発明の断熱金型およびそれを用いた成形
方法は、熱可塑性樹脂組成物の成形を対象とするもので
あり、熱可塑性樹脂組成物については特に限定されるも
のではない。しかしながら本発明の効果をより好ましく
発揮し得るのは非晶性熱可塑性樹脂を主とする熱可塑性
樹脂組成物の場合である。The heat insulating mold of the present invention and the molding method using the same are intended for molding a thermoplastic resin composition, and the thermoplastic resin composition is not particularly limited. However, the effects of the present invention can be more preferably exerted in the case of a thermoplastic resin composition mainly containing an amorphous thermoplastic resin.
【0032】ここで非晶性熱可塑性樹脂を主とすると
は、少なくとも組成物中の樹脂成分を100重量%とし
た場合、非晶性熱可塑性樹脂が50重量%以上含有され
る場合をいう。非晶性熱可塑性樹脂としては、スチレン
系樹脂、アクリル樹脂、ポリカーボネート樹脂、非晶性
ポリエステル樹脂、非晶性ポリアリレート樹脂、ポリエ
ーテルスルホン樹脂、変性ポリフェニレンオキサイド樹
脂をあげることができる。本発明のスチレン系樹脂とし
ては、例えばポリスチレン、スチレン・ブタジエン・ス
チレン共重合体(SBS)、水添スチレン・ブタジエン
・スチレン共重合体(水添SBS)、水添スチレン・イ
ソプレン・スチレン共重合体(SEPS)、耐衝撃性ポ
リスチレン(HIPS)、アクリロニトリル・スチレン
共重合体(AS樹脂)、アクリロニトリル・ブタジエン
・スチレン共重合体(ABS樹脂)、メチルメタクリレ
ート・ブタジエン・スチレン共重合体(MBS樹脂)、
メチルメタクリレート・アクリロニトリル・ブタジエン
・スチレン共重合体(MABS樹脂)、アクリロニトリ
ル・エチレンプロピレン系ゴム・スチレン共重合体(A
ES樹脂)又はこれらの混合物が挙げられる。Here, the expression "mainly composed of an amorphous thermoplastic resin" means a case where at least the resin component in the composition is 100% by weight and the amount of the amorphous thermoplastic resin is 50% by weight or more. Examples of the amorphous thermoplastic resin include a styrene resin, an acrylic resin, a polycarbonate resin, an amorphous polyester resin, an amorphous polyarylate resin, a polyether sulfone resin, and a modified polyphenylene oxide resin. Examples of the styrene resin of the present invention include polystyrene, styrene / butadiene / styrene copolymer (SBS), hydrogenated styrene / butadiene / styrene copolymer (hydrogenated SBS), and hydrogenated styrene / isoprene / styrene copolymer (SEPS), impact-resistant polystyrene (HIPS), acrylonitrile / styrene copolymer (AS resin), acrylonitrile / butadiene / styrene copolymer (ABS resin), methyl methacrylate / butadiene / styrene copolymer (MBS resin),
Methyl methacrylate / acrylonitrile / butadiene / styrene copolymer (MABS resin), acrylonitrile / ethylene propylene rubber / styrene copolymer (A
(ES resin) or a mixture thereof.
【0033】本発明のアクリル樹脂は、メチルメタクリ
レートを主成分とするものであり、メチルメタクリレー
ト単独の重合体、もしくはその共重合体である。かかる
共重合体の共重合成分としてはメチルアクリレート、エ
チルアクリレート、プロピルアクリレート、イソプロピ
ルアクリレート、ブチルアクリレート、アミルアクリレ
ート、ヘキシルアクリレート、オクチルアクリレート、
2−エチルヘキシルアクリレート、シクロヘキシルアク
リレート、ドデシルアクリレート、オクタデシルアクリ
レート、フェニルアクリレート、ベンジルアクリレート
等のアクリル酸アルキルエステル、またエチルメタクリ
レート、プロピルメタクリレート、イソプロピルメタク
リレート、ブチルメタクリレート、アミルメタクリレー
ト、ヘキシルメタクリレート、オクチルメタクリレー
ト、2−エチルヘキシルメタクリレート、シクロヘキシ
ルメタクリレート、ドデシルメタクリレート、オクタデ
シルメタクリレート、フェニルメタクリレート、ベンジ
ルメタクリレート等のメタクリル酸アルキルエステルを
挙げることができる。The acrylic resin of the present invention contains methyl methacrylate as a main component, and is a polymer of methyl methacrylate alone or a copolymer thereof. Examples of the copolymer component of the copolymer include methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, amyl acrylate, hexyl acrylate, octyl acrylate,
Acrylic alkyl esters such as 2-ethylhexyl acrylate, cyclohexyl acrylate, dodecyl acrylate, octadecyl acrylate, phenyl acrylate, and benzyl acrylate, and ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl methacrylate, amyl methacrylate, hexyl methacrylate, octyl methacrylate, 2- Examples thereof include alkyl methacrylates such as ethylhexyl methacrylate, cyclohexyl methacrylate, dodecyl methacrylate, octadecyl methacrylate, phenyl methacrylate, and benzyl methacrylate.
【0034】本発明でいうポリカーボネート樹脂とは、
二価フェノールとカーボネート前駆体をホスゲン法、溶
融法により反応させて得られる芳香族ポリカーボネート
樹脂、またはこれらの方法により得られるプレポリマー
を固相重合法により重合度を上げて得られる芳香族ポリ
カーボネート樹脂、及び二価フェノールと一酸化炭素及
び酸素とを、もしくは二酸化炭素とをパラジウム系触媒
等の存在下反応させて得られる芳香族ポリカーボネート
樹脂、及び更にかかる方法により得られたプレポリマー
を溶融法、固相重合法等の方法により重合度を上げたこ
とにより得られる芳香族ポリカーボネート樹脂である。
ここで用いる二価フェノールとしては例えば2,2−ビ
ス(4−ヒドロキシフェニル)プロパン(以下ビスフェ
ノールAという)、ビス(4−ヒドロキシフェニル)メ
タン、1,1−ビス(4−ヒドロキシフェニル)エタ
ン、2,2−ビス(4−ヒドロキシ−3,5−ジメチル
フェニル)プロパン、2,2−(4−ヒドロキシ−3−
メチルフェニル)プロパン、ビス(4−ヒドロキシフェ
ニル)スルフォン等が挙げられる。好ましい二価フェノ
ールはビス(4−ヒドロキシフェニル)アルカン系であ
り、ビスフェノールAが特に好ましい。カーボネート前
駆体としてはカルボニルハライド、カルボニルエステ
ル、ハロホルメート等が挙げられ、具体的にはホスゲ
ン、ジフェニルカーボネート、二価フェノールのジハロ
ホルメート等が挙げられる。ポリカーボネート樹脂を製
造するに当り、上記二価フェノールを単独で用いても又
は二種以上を併用してもよく、またポリカーボネート樹
脂は三官能以上の多官能性芳香族化合物を共重合した分
岐ポリカーボネート樹脂であっても、二種以上のポリカ
ーボネート樹脂の混合物であってもよい。The polycarbonate resin in the present invention is:
An aromatic polycarbonate resin obtained by reacting a dihydric phenol and a carbonate precursor by a phosgene method, a melting method, or an aromatic polycarbonate resin obtained by increasing the degree of polymerization of a prepolymer obtained by these methods by a solid phase polymerization method , And an aromatic polycarbonate resin obtained by reacting dihydric phenol with carbon monoxide and oxygen, or carbon dioxide in the presence of a palladium-based catalyst or the like, and a prepolymer obtained by such a method, It is an aromatic polycarbonate resin obtained by increasing the degree of polymerization by a method such as solid phase polymerization.
Examples of the dihydric phenol used here include 2,2-bis (4-hydroxyphenyl) propane (hereinafter referred to as bisphenol A), bis (4-hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, 2,2-bis (4-hydroxy-3,5-dimethylphenyl) propane, 2,2- (4-hydroxy-3-
Methylphenyl) propane, bis (4-hydroxyphenyl) sulfone and the like. Preferred dihydric phenols are bis (4-hydroxyphenyl) alkanes, with bisphenol A being particularly preferred. Examples of the carbonate precursor include carbonyl halide, carbonyl ester, and haloformate, and specific examples include phosgene, diphenyl carbonate, and dihaloformate of a dihydric phenol. In producing the polycarbonate resin, the above dihydric phenols may be used alone or in combination of two or more, and the polycarbonate resin is a branched polycarbonate resin obtained by copolymerizing a trifunctional or higher polyfunctional aromatic compound. Or a mixture of two or more polycarbonate resins.
【0035】尚本発明でいう熱可塑性樹脂組成物には、
熱可塑性樹脂単体も含むものである。The thermoplastic resin composition according to the present invention includes:
It also includes a single thermoplastic resin.
【0036】本発明の断熱金型は、断熱層の表面に断熱
層単独に比してより平滑な表面や3次元造形のみでは不
十分となりやすい微細な模様、凹凸等を成形品表面に付
与することを目的として金属層を設けてもよい。金属層
としては、断熱金型に直接、化学メッキ及び/又は電気
メッキ等の方法及び金属板を張りつける方法等で作成す
ることができる。更に金属層に微細な模様、凹凸をつけ
ることも可能である。またかかる金属層の厚みは特に限
定されるものではないが、尚金属層を設ける場合は10
0μm以下とすることが好ましい。100μmを超える
と断熱層の効果が希薄となり、高外観を要求する部分の
金型表面の温度が高温になり難くなるからである。特に
2〜50μmの厚みが好ましい。The heat-insulating mold of the present invention imparts a smoother surface to the surface of the heat-insulating layer, or a fine pattern, unevenness, or the like, which tends to be insufficient with only three-dimensional molding, as compared with the heat-insulating layer alone. A metal layer may be provided for the purpose. The metal layer can be formed by a method such as chemical plating and / or electroplating or a method of attaching a metal plate directly to the heat insulating mold. Furthermore, it is also possible to provide fine patterns and irregularities on the metal layer. The thickness of the metal layer is not particularly limited.
It is preferable that the thickness be 0 μm or less. If the thickness exceeds 100 μm, the effect of the heat-insulating layer is diminished, and the temperature of the mold surface in a portion requiring high appearance is unlikely to become high. Particularly, a thickness of 2 to 50 μm is preferable.
【0037】本発明の断熱金型及びそれを用いた成形方
法は主に射出成形法やブロー成形法について使用できる
他、ガスアシスト成形法や射出圧縮成形法、超高速射出
成形法等の特殊な射出成形法においても同様に使用でき
る。The heat-insulating mold and the molding method using the same according to the present invention can be used mainly for injection molding and blow molding, and special molding methods such as gas-assist molding, injection compression molding and ultra-high-speed injection molding. The same can be used in the injection molding method.
【0038】[0038]
【発明の実施の形態】以下に実施例を挙げて更に説明す
る。実施例において用いる熱可塑性樹脂、各金型、及び
3次元造形法と造形された断熱層は次の通りである。 熱可塑性樹脂:ガラス繊維30%強化芳香族ポリカーボネート樹脂 Tg:149℃(ビスフェノールAの重合体であり、芳香族ポリ カーボネート樹脂の粘度平均分子量23,500) 主金型 :鋼材(S55C)熱伝導率20W/m・K 3次元造形法:光造形装置 SOLIFORM−500A(帝人製機) 断熱層 :光硬化性樹脂 TSR−753(帝人製機) 熱伝導率0.50W/m・KDESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be further described below with reference to examples. The thermoplastic resin used in the examples, the respective molds, and the three-dimensional molding method and the formed heat insulating layer are as follows. Thermoplastic resin: Glass fiber 30% reinforced aromatic polycarbonate resin Tg: 149 ° C. (A polymer of bisphenol A, viscosity average molecular weight of aromatic polycarbonate resin 23,500) Main mold: Steel material (S55C) Thermal conductivity 20 W / m · K Three-dimensional modeling: Stereolithography device SOLIFORM-500A (Teijin machine) Thermal insulation layer: Photo-curable resin TSR-753 (Teijin machine) Thermal conductivity 0.50 W / m · K
【0039】[実施例1〜3、比較例1〜5] (1)サンプルの成形 図5及び図6に示す入れ子式であるドアハンドル金型の
ハンドル意匠面に、光造形法を用いて作製した表1に示
した厚みの断熱層に化学メッキ処理を施したものを図5
〜図7に示す要領で組み込みんだ断熱金型を用いて、ガ
ラス繊維30%強化ポリカーボネート樹脂を、射出成形
機[住友重機械工業(株)SG−150U]により表1
に示す各シリンダー温度、金型温度、及び成形サイクル
で図1〜図4に示すドアハンドル成形品を成形した。尚
かかる断熱層部分の作製は全ての場合において5時間以
内に可能であった。また、引張り試験片の中央にウエル
ドを発生させるウエルドダンベル金型のウエルド部に、
光造形法を用いて作製した表1に示した断熱層に化学メ
ッキ処理を施したものを組み込んだ断熱金型を用いて、
表1に示した成形品厚みのウエルド試験片を作成した。
金型の両端から充填したウエルド有りダンベル成形品と
片端から樹脂を充填したウエルド無しダンベル成形品を
成形し、ウエルド強度保持率を算出した。この場合もか
かる断熱層は全ての場合において5時間以内に製作が可
能であった。尚、表中断熱層が0mmとは、断熱層を設
けない金型を用いて、上記成形品を成形した場合を示
す。[Examples 1 to 3 and Comparative Examples 1 to 5] (1) Molding of Samples The nested door handle mold shown in FIGS. FIG. 5 shows a heat-insulating layer having the thickness shown in Table 1 subjected to chemical plating.
Using a heat-insulating mold incorporated in the manner shown in FIG. 7, a glass fiber 30% reinforced polycarbonate resin was molded using an injection molding machine [Sumitomo Heavy Industries, Ltd. SG-150U].
The door handle molded products shown in FIGS. 1 to 4 were molded at each cylinder temperature, mold temperature, and molding cycle shown in FIG. The production of such a heat insulating layer was possible within 5 hours in all cases. Also, in the weld part of the weld dumbbell mold that generates weld in the center of the tensile test piece,
Using a heat-insulating mold that incorporates the heat-insulating layer shown in Table 1 produced by stereolithography and subjected to chemical plating,
Weld test pieces having the thickness of the molded product shown in Table 1 were prepared.
A dumbbell molded product with a weld filled from both ends of the mold and a dumbbell molded product without a weld filled with resin from one end were molded, and the weld strength retention was calculated. Also in this case, such a heat insulating layer could be manufactured within 5 hours in all cases. In addition, the case where the heat insulating layer is 0 mm in the table indicates a case where the above-mentioned molded article is formed using a mold having no heat insulating layer.
【0040】(2)断熱層表面温度の測定 断熱層表面温度を断熱層の裏側より金型表面部分に接触
した熱電対を用いて最高温度を測定した。(2) Measurement of Surface Temperature of Heat Insulating Layer The maximum temperature of the surface temperature of the heat insulating layer was measured using a thermocouple in contact with the surface of the mold from the back side of the heat insulating layer.
【0041】(3)転写性(表面粗さ)の測定 ドアハンドル成形品のハンドル意匠面を三次元表面粗さ
形状測定機(東京精密製サーフコム1400A−3DF
−12)を用いて表面粗さ(中心点平均値)を測定し
た。表面粗さは、0.2μm以下が好ましい。(3) Measurement of Transferability (Surface Roughness) The handle design surface of the door handle molded product was measured using a three-dimensional surface roughness shape measuring machine (Surfcom 1400A-3DF manufactured by Tokyo Seimitsu).
-12) was used to measure the surface roughness (center point average value). The surface roughness is preferably 0.2 μm or less.
【0042】(4)ウエルド強度(引張り強度保持率) ウエルド有りダンベル成形品とウエルド無しダンベル成
形品を用いて引張り強度を測定し、ウエルドの有無によ
る引張り強度保持率を下記式(1)に従い算出した。引
張り強度保持率は80%以上が好ましい。(4) Weld strength (retention rate of tensile strength) Tensile strength is measured using a dumbbell molded product with a weld and a dumbbell molded product without a weld, and the tensile strength retention with or without a weld is calculated according to the following equation (1). did. The tensile strength retention is preferably 80% or more.
【0043】[0043]
【数1】 (Equation 1)
【0044】(5)成形サイクル ドアハンドル成形品を射出成形する際、熱可塑性樹脂を
射出充填後、金型から成形品を取り出せる温度(当該熱
可塑性樹脂のTg以下)まで冷却された後、成形品を取
り出すまでに要する時間を測定した。今回対象とするサ
ンプルにおいては、成形サイクルは100秒以下が生産
効率を低下させず実用的で好ましい。(5) Molding cycle In injection molding of a door handle molded product, after injection filling with a thermoplastic resin, the molded product is cooled to a temperature at which the molded product can be taken out of the mold (Tg of the thermoplastic resin or less). The time required to remove the article was measured. In the present sample, a molding cycle of 100 seconds or less is practical and preferable without reducing the production efficiency.
【0045】[0045]
【表1】 [Table 1]
【0046】表1から示されるように、実施例1〜3は
比較例1〜3に比べて、表面粗さが極めて小さく転写性
に格段に優れるとともに、ウエルド強度においても良好
であることがわかる。すなわち、特定の断熱層厚みであ
る必要があることがわかる。また比較例4に示すように
断熱層を設けず金型温度を高温にした場合、及び比較例
5に示すように断熱層表面の最高温度が50℃を越える
場合は成形サイクルが大変長くなり、本発明が比較例4
〜5との比較においても、成形サイクルが短く、生産効
率を低下させず実用的で好ましいことがわかる。As shown in Table 1, Examples 1 to 3 have extremely small surface roughness and excellent transferability, and are excellent in weld strength, as compared with Comparative Examples 1 to 3. . That is, it is understood that it is necessary to have a specific heat insulating layer thickness. Further, when the mold temperature was increased without providing the heat insulating layer as shown in Comparative Example 4, and when the maximum temperature of the heat insulating layer surface exceeded 50 ° C. as shown in Comparative Example 5, the molding cycle became very long, Comparative Example 4
Also in comparison with Nos. To 5, it can be seen that the molding cycle is short and practical and preferable without reducing the production efficiency.
【0047】[0047]
【発明の効果】本発明の断熱金型は、複雑な3次元形状
においても高外観を達成できるものでり、複雑な形状に
おいても転写性、光沢度に優れ、ウエルド強度が高い成
形品を得ることが可能であり、且つ従来製造し難かった
断熱層を短期間且つ安価に製造することができることか
ら、その工業的利用価値は極めて大きい。According to the heat-insulating mold of the present invention, a high appearance can be achieved even in a complicated three-dimensional shape, and a molded product having excellent transferability, glossiness and high weld strength can be obtained even in a complicated shape. Since it is possible to produce the heat insulating layer, which has been difficult to produce conventionally, in a short period of time and at low cost, its industrial value is extremely large.
【図1】評価サンプルの1つであるドアハンドル成形品
の概略を示した側面図である。FIG. 1 is a side view schematically showing a door handle molded product which is one of evaluation samples.
【図2】評価サンプルの1つであるドアハンドル成形品
の概略を示した正面図である。FIG. 2 is a front view schematically showing a door handle molded product which is one of the evaluation samples.
【図3】評価サンプルの1つであるドアハンドル成形品
の図2にしめす一点鎖線における切断面の概略を示した
図(取り付け用の腕の短い側をみた側面図)である。FIG. 3 is a schematic view (a side view of the short side of the mounting arm) of a door handle molded product, which is one of the evaluation samples, taken along a dashed line in FIG.
【図4】評価サンプルの1つであるドアハンドル成形品
の概略を示した裏面図である。FIG. 4 is a rear view schematically showing a molded door handle, which is one of the evaluation samples.
【図5】ドアハンドル成形金型におけるドアハンドル入
れ子部分の概略を示した正面図である。かかる入れ子は
金型の固定側に取り付けられ成形が行われる。FIG. 5 is a front view schematically showing a door handle nest portion in the door handle molding die. The nest is attached to the fixed side of the mold to perform molding.
【図6】ドアハンドル入れ子部分の概略を示した側面図
である。入れ子は金型と同一の鋼材により形成される。
かかる入れ子部分に金型鋼材により作成されたスペーサ
ー、次に光造形により造形されメッキが施された断熱層
があり、更に金型鋼材により作成された固定枠を入れ子
にネジ止めすることにより入れ子部分に固定される。FIG. 6 is a side view schematically showing a door handle nesting portion. The nest is formed of the same steel material as the mold.
The nested portion has a spacer made of a mold steel material, and then has a heat insulation layer formed by optical molding and plated, and furthermore, a fixing frame made of the mold steel material is screwed into the nest to form a nested portion. Fixed to
【図7】スペーサー、断熱層、固定枠の関係の概要を示
した斜視図である。スペーサーは固定枠の上部にあるネ
ジにより固定できる構造としている。FIG. 7 is a perspective view showing an outline of a relationship between a spacer, a heat insulating layer, and a fixed frame. The spacer has a structure that can be fixed with screws at the top of the fixing frame.
1 評価サンプルの1つであるドアハンドル本体 2 ドアハンドルのハンドル意匠面(金型の対応する
部分に断熱層を設置) 3 切断面の箇所を示す一点鎖線 4 金型固定側入れ子本体 5 断熱層及びスペーサーを固定するための固定枠
(金型鋼材と同一材) 6 スペーサー(金型鋼材と同一材、濃いトーンの部
分) 7 光造形により作成された断熱層(薄いトーンの部
分) 8 固定枠固定用のネジ及びネジ穴 9 スペーサー固定用のネジ及びネジ穴Reference Signs List 1 Door handle main body, one of evaluation samples 2 Handle design surface of door handle (heat insulating layer is installed on corresponding part of mold) 3 One-dot chain line indicating cut surface 4 Mold fixing side nesting main body 5 Heat insulating layer And a fixing frame for fixing the spacer (same material as the mold steel material) 6 Spacer (same material as the mold steel material, dark tone portion) 7 Thermal insulation layer created by stereolithography (light tone portion) 8 Fixed frame Screws and screw holes for fixing 9 Screws and screw holes for fixing spacer
Claims (7)
金型の主金型の中に断熱層を組み込み、主金型が該熱可
塑性樹脂組成物のTgよりも低い温度で保持され、断熱
層が組み込まれた部分の金型キャビティ表面温度の成形
時における最高温度がTg+1〜Tg+50℃の範囲と
なる成形方法において使用する断熱金型であって、断熱
層を組み込む金型キャビティ部分における、該断熱層の
厚みが成形品肉厚に対して0.01〜2倍の範囲にあ
り、更に該断熱層が3次元造形法により造形された、熱
伝導率1.0W/m・K以下の合成樹脂組成物からなる
断熱層であることを特徴とする断熱金型。1. A heat insulating layer is incorporated in a main mold of a mold used for molding a thermoplastic resin composition, and the main mold is held at a temperature lower than Tg of the thermoplastic resin composition. A heat insulating mold used in a molding method in which a maximum temperature of a mold cavity surface temperature of a part in which a layer is incorporated during molding is in a range of Tg + 1 to Tg + 50 ° C. The thickness of the heat insulating layer is in the range of 0.01 to 2 times the thickness of the molded product, and the heat insulating layer is formed by a three-dimensional forming method, and has a thermal conductivity of 1.0 W / m · K or less. A heat insulating mold comprising a heat insulating layer made of a resin composition.
1に記載の断熱金型。2. The heat insulating mold according to claim 1, wherein the three-dimensional forming method is an optical forming method.
又は2のいずれか1項に記載の断熱金型。3. A heat insulating layer having a metal layer on a surface thereof.
Or the heat-insulating mold according to any one of 2.
メッキにより作成された請求項3に記載の断熱金型。4. The heat insulating mold according to claim 3, wherein the metal layer is formed by chemical plating and / or electroplating.
樹脂を主とする樹脂組成物である請求項1〜4のいずれ
か1項に記載の断熱金型。5. The heat-insulating mold according to claim 1, wherein the thermoplastic resin composition is a resin composition mainly composed of an amorphous thermoplastic resin.
熱金型を用いた、高外観部分を有する成形品を得るため
の成形方法。6. A molding method for obtaining a molded article having a high appearance portion, using the heat-insulating mold according to any one of claims 1 to 5.
gより20〜60℃低い温度で保持されるとともに、断
熱層の組み込まれた部位の成形時における最高温度が、
Tg+10〜Tg+30℃の範囲に達する条件で成形行
うことを特徴とする請求項6に記載の高外観部分を有す
る成形品を得るための成形方法。7. The thermoplastic resin composition according to claim 7, wherein the main mold of the mold is a thermoplastic resin composition.
g is maintained at a temperature lower by 20 to 60 ° C., and the maximum temperature at the time of molding the part where the heat insulating layer is incorporated is:
The molding method for obtaining a molded article having a high appearance portion according to claim 6, wherein the molding is performed under a condition of reaching Tg + 10 to Tg + 30 ° C.
Priority Applications (1)
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JP25680898A JP2000084943A (en) | 1998-09-10 | 1998-09-10 | Insulating mold and molding method using the same |
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JP25680898A JP2000084943A (en) | 1998-09-10 | 1998-09-10 | Insulating mold and molding method using the same |
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Publication Number | Publication Date |
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JP2000084943A true JP2000084943A (en) | 2000-03-28 |
Family
ID=17297735
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JP25680898A Pending JP2000084943A (en) | 1998-09-10 | 1998-09-10 | Insulating mold and molding method using the same |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002321226A (en) * | 2001-04-26 | 2002-11-05 | Araco Corp | Mold and method for manufacturing the same |
US6932610B2 (en) | 2002-12-02 | 2005-08-23 | Ono & Co., Ltd. | Process for producing an artificial bone model and an artificial bone model produced by the process |
JP2006321711A (en) * | 2005-04-20 | 2006-11-30 | Trial Corp | Microsphere used for selective laser sintering, method for producing the same, molding by selective laser sintering, and method for producing the same |
JP2008528342A (en) * | 2005-02-04 | 2008-07-31 | ザ プロクター アンド ギャンブル カンパニー | Process for forming a container by stretch blow molding, and container formed by the process |
JP2017001220A (en) * | 2015-06-06 | 2017-01-05 | 株式会社シントー | Laminate molding form block and injection molding method using form block |
JP2018048312A (en) * | 2016-09-20 | 2018-03-29 | ナガセケムテックス株式会社 | Patterning material for three-dimensional photo-molding and casting method using the same |
-
1998
- 1998-09-10 JP JP25680898A patent/JP2000084943A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002321226A (en) * | 2001-04-26 | 2002-11-05 | Araco Corp | Mold and method for manufacturing the same |
US6932610B2 (en) | 2002-12-02 | 2005-08-23 | Ono & Co., Ltd. | Process for producing an artificial bone model and an artificial bone model produced by the process |
JP2008528342A (en) * | 2005-02-04 | 2008-07-31 | ザ プロクター アンド ギャンブル カンパニー | Process for forming a container by stretch blow molding, and container formed by the process |
JP2006321711A (en) * | 2005-04-20 | 2006-11-30 | Trial Corp | Microsphere used for selective laser sintering, method for producing the same, molding by selective laser sintering, and method for producing the same |
JP2017001220A (en) * | 2015-06-06 | 2017-01-05 | 株式会社シントー | Laminate molding form block and injection molding method using form block |
JP2018048312A (en) * | 2016-09-20 | 2018-03-29 | ナガセケムテックス株式会社 | Patterning material for three-dimensional photo-molding and casting method using the same |
JP7051336B2 (en) | 2016-09-20 | 2022-04-11 | ナガセケムテックス株式会社 | Patterning material for 3D stereolithography and casting method using it |
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