JP7637400B2 - Abrasive grain - Google Patents
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- JP7637400B2 JP7637400B2 JP2020155977A JP2020155977A JP7637400B2 JP 7637400 B2 JP7637400 B2 JP 7637400B2 JP 2020155977 A JP2020155977 A JP 2020155977A JP 2020155977 A JP2020155977 A JP 2020155977A JP 7637400 B2 JP7637400 B2 JP 7637400B2
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- abrasive grains
- thermoplastic
- polyethylene oxide
- soluble polyethylene
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- 239000006061 abrasive grain Substances 0.000 title claims description 43
- 229920005989 resin Polymers 0.000 claims description 35
- 239000011347 resin Substances 0.000 claims description 35
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 21
- 229920001169 thermoplastic Polymers 0.000 claims description 20
- 229920005992 thermoplastic resin Polymers 0.000 claims description 20
- 239000004416 thermosoftening plastic Substances 0.000 claims description 20
- 239000011342 resin composition Substances 0.000 claims description 15
- -1 polyethylene Polymers 0.000 claims description 10
- 229920001225 polyester resin Polymers 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 229920005604 random copolymer Polymers 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 238000002074 melt spinning Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 230000005611 electricity Effects 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000004626 polylactic acid Substances 0.000 description 2
- 238000006748 scratching Methods 0.000 description 2
- 230000002393 scratching effect Effects 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- PFBWBEXCUGKYKO-UHFFFAOYSA-N ethene;n-octadecyloctadecan-1-amine Chemical compound C=C.CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC PFBWBEXCUGKYKO-UHFFFAOYSA-N 0.000 description 1
- ZJOLCKGSXLIVAA-UHFFFAOYSA-N ethene;octadecanamide Chemical compound C=C.CCCCCCCCCCCCCCCCCC(N)=O.CCCCCCCCCCCCCCCCCC(N)=O ZJOLCKGSXLIVAA-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920006111 poly(hexamethylene terephthalamide) Polymers 0.000 description 1
- 229920002961 polybutylene succinate Polymers 0.000 description 1
- 239000004631 polybutylene succinate Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、熱可塑性樹脂によって構成される砥粒に関するものである。 The present invention relates to abrasive grains made of thermoplastic resin.
成形物としては、金型の内部に合成樹脂材料を充填して成形する射出成形、トランスファ成形でできる樹脂成形物、溶融金属を型に流し込んで成形される鋳物、あるいは3Dプリンターを用いて造形した樹脂製の成形等の種々の成形物が挙げられ、これらの成形物には、不要なバリが付着していることから、バリを取り除く作業(いわゆるバリ取り)が行われている。バリ取り作業としては、砥粒が用いられ、砥粒を対象物に吹きつける、砥粒を対象物に接する状態で流動させる、容器中に対象物と砥粒を入れて一緒にかき回す等により行われる。 Molded products include various types of molded products, such as injection molding, in which a synthetic resin material is filled into a mold, resin molded products made by transfer molding, castings formed by pouring molten metal into a mold, and resin molded products created using a 3D printer. Since these molded products have unwanted burrs attached to them, a process to remove the burrs (known as deburring) is carried out. Abrasive grains are used for the deburring process, and the grains are sprayed onto the object, the grains are made to flow in contact with the object, or the object and grains are placed in a container and stirred together.
バリ取り用の砥粒としては、ガラス、スチール、アルミナ、また、熱硬化性樹脂や熱可塑性樹脂などの合成樹脂等の各種素材からなるものが使用されており、対象物の素材等に応じて適宜選択されているが、砥粒の硬度や形状によって、対象物の表面に傷をつける恐れがあった。また、バリ取り時には、摩擦によって砥粒が損傷すると、バリ取り作業効率が低下することになる。また、摩擦により静電気が発生すると、砥粒が対象物に張り付いてしまい、効果的にバリ取りが行えないという問題がある。特許文献1には、バリ取り用投射材に帯電防止剤を含有させることによって、この問題に対処することが提案されている。 Abrasive grains for deburring are made of various materials such as glass, steel, alumina, and synthetic resins such as thermosetting resins and thermoplastic resins, and are selected appropriately depending on the material of the object, but there is a risk of scratching the surface of the object depending on the hardness and shape of the abrasive grains. Furthermore, if the abrasive grains are damaged by friction during deburring, the efficiency of the deburring work will decrease. Furthermore, if static electricity is generated by friction, the abrasive grains will stick to the object, making it difficult to deburr effectively. Patent Document 1 proposes addressing this problem by incorporating an antistatic agent into the deburring shot material.
本発明は、対象物の表面等を傷つけることなく、また、繰り返しの作業による摩擦に対して損傷しにくく耐久性を有し、さらに、作業時の摩擦によって帯電しにくい砥粒を提供することを課題とする。 The objective of the present invention is to provide abrasive grains that do not damage the surface of the object, are durable and resistant to damage caused by friction during repeated work, and are also resistant to charging due to friction during work.
本発明者らは、上記課題を解決するため検討した結果、本発明に到達した。すなわち、本発明は、樹脂組成物を構成する樹脂として母体となる熱可塑性樹脂(A)に、重量平均分子量が5万~900万である熱可塑性水溶性ポリエチレンオキサイド系樹脂が配合されてなる樹脂組成物により構成され、
前記熱可塑性水溶性ポリエチレンオキサイド系樹脂が、エチレンオキサイドのみからなる重合体あるいはポリエチレンオキサイド・プロピレンオキサイドランダム共重合体のいずれかであり、
直径が50μm~3000μm、長さが0.05mm~10mmであるペレット状物からなることを特徴とする砥粒を要旨とする。
The present inventors have conducted research to solve the above problems and arrived at the present invention. That is, the present invention is a resin composition comprising a thermoplastic resin (A) as a base resin constituting the resin composition and a thermoplastic water-soluble polyethylene oxide resin having a weight average molecular weight of 50,000 to 9,000,000 blended therein,
the thermoplastic water-soluble polyethylene oxide resin is either a polymer consisting of ethylene oxide alone or a polyethylene oxide-propylene oxide random copolymer,
The gist of the invention is an abrasive grain characterized by being made of pellet-shaped material having a diameter of 50 μm to 3000 μm and a length of 0.05 mm to 10 mm.
以下、本発明について詳細に説明する。
本発明の用砥粒は、樹脂製等の成形物を作成した際に生成されるバリを取り除く際や、成形物の表面を研磨する等において用いるものであり、熱可塑性樹脂(A)に、熱可塑性水溶性ポリエチレンオキサイド系樹脂が配合されてなる樹脂組成物により構成される。
The present invention will be described in detail below.
The abrasive grains of the present invention are used for removing burrs generated during the production of molded articles made of resin or the like, and for polishing the surfaces of molded articles, and are composed of a resin composition in which a thermoplastic resin (A) is blended with a thermoplastic water-soluble polyethylene oxide-based resin.
熱可塑性樹脂(A)は、樹脂組成物を構成する主体となる樹脂であり、ポリエステル系樹脂またはポリアミド系樹脂を好ましく用いる。 The thermoplastic resin (A) is the main resin that constitutes the resin composition, and polyester-based resin or polyamide-based resin is preferably used.
ポリエステル系樹脂としては、分子内にエステル結合を有するものであれば特に限定されるものではなく、例えば芳香族ポリエステルでは、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリプロピレンテレフタレート等が挙げられ、また、脂肪族ポリエステルでは、例えばポリ乳酸、ポリブチレンサクシネート、ポリカプロラクタン等が挙げられる。また、本発明における目的を阻害しない範囲であれば、上記したポリエステルに他のジカルボン酸成分、ジオール成分あるいはオキシカルボン酸成分等を共重合してもよく、あるいは上記したポリエステル同士のブレンドや、上記したポリエステルと共重合したポリエステルとをブレンドしたものであってもよい。共重合できる他の成分としては、ジカルボン酸では、例えば、イソフタル酸、ナフタレンジカルボン酸、5-ナトリウムスルホイソフタル酸、無水フタル酸、セバシン酸、アジピン酸、コハク酸等が挙げられ、ジオール成分では、エタンジオール、プロパンジオール、1,4-ブタンジオール、1,5-ペンタンジオール、1,6-ヘキサンジオール、シクロヘキサンジメタノール等が挙げられる。ポリエステル系樹脂の相対粘度は、耐久性を考慮して、好ましくは1.4以上であり、より好ましくは1.5以上である。 The polyester resin is not particularly limited as long as it has an ester bond in the molecule. For example, aromatic polyesters include polyethylene terephthalate, polybutylene terephthalate, polypropylene terephthalate, etc., and aliphatic polyesters include polylactic acid, polybutylene succinate, polycaprolactone, etc. In addition, the above-mentioned polyesters may be copolymerized with other dicarboxylic acid components, diol components, or oxycarboxylic acid components, etc., as long as the purpose of the present invention is not hindered. Alternatively, the above-mentioned polyesters may be blended with each other, or may be blends of polyesters copolymerized with the above-mentioned polyesters. Examples of other components that can be copolymerized include dicarboxylic acids such as isophthalic acid, naphthalenedicarboxylic acid, 5-sodium sulfoisophthalic acid, phthalic anhydride, sebacic acid, adipic acid, and succinic acid, and diol components such as ethanediol, propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, and cyclohexanedimethanol. Taking durability into consideration, the relative viscosity of the polyester resin is preferably 1.4 or more, and more preferably 1.5 or more.
ポリアミド系樹脂としては、分子内にアミド基を有するものであれば特に限定されるものではなく、例えばナイロン6、ナイロン66、ナイロン69、ナイロン46、ナイロン610、ナイロン1010、ナイロン11、ナイロン12、ナイロン6T、ナイロン9T、ポリメタキシレンアジパミドやこれら各成分を共重合したものやブレンドしたもの等が挙げられる。ポリアミド系樹脂の相対粘度は、耐久性を考慮して、好ましくは2.5以上であり、より好ましくは3.0以上である。 The polyamide resin is not particularly limited as long as it has an amide group in the molecule, and examples thereof include nylon 6, nylon 66, nylon 69, nylon 46, nylon 610, nylon 1010, nylon 11, nylon 12, nylon 6T, nylon 9T, polymetaxylene adipamide, and copolymers or blends of these components. The relative viscosity of the polyamide resin is preferably 2.5 or more, more preferably 3.0 or more, taking durability into consideration.
本発明の砥粒を構成する樹脂組成物は、前記した熱可塑性樹脂(A)に熱可塑性水溶性ポリエチレンオキサイド系樹脂が配合されてなるものである。熱可塑性水溶性ポリエチレンオキサイド系樹脂の配合量は、樹脂組成物中に1~15質量%であることが好ましい。より好ましくは1~12質量%である。熱可塑性水溶性ポリエチレンオキサイドの配合量を1質量%以上とすることにより、摩擦帯電効果を効果的に発揮することができる。一方、配合量を15質量%以下とすることにより、良好な強度を有する砥粒となる。 The resin composition constituting the abrasive grains of the present invention is obtained by blending the thermoplastic water-soluble polyethylene oxide resin with the thermoplastic resin (A) described above. The blend amount of the thermoplastic water-soluble polyethylene oxide resin in the resin composition is preferably 1 to 15% by mass. More preferably, it is 1 to 12% by mass. By making the blend amount of the thermoplastic water-soluble polyethylene oxide 1% by mass or more, the triboelectric charging effect can be effectively exerted. On the other hand, by making the blend amount 15% by mass or less, the abrasive grains have good strength.
樹脂組成物を構成する樹脂として母体となる熱可塑性樹脂(A)への分散性を考慮し、熱可塑性水溶性ポリエチレンオキサイド系樹脂の重量平均分子量は、5万~900万のものを用いる。重量平均分子量が5万~900万の熱可塑性水溶性ポリエチレンオキサイド系樹脂は、砥粒を製造するにあたっての溶融押出機内で、熱可塑性樹脂(A)と良好に混合でき、熱可塑性樹脂(A)中に良好に分散する。なお、重量平均分子量50万を超える熱可塑性水溶性ポリエチレンオキサイド系樹脂を混合する場合は、温度300℃以上に設定すると、母体となるポリエステル系樹脂中に良好に分散する。また、重量平均分子量50万以下の熱可塑性水溶性ポリエチレンオキサイド系樹脂を混同する場合は、300℃以下であって、熱可塑性樹脂(A)が溶融する温度に設定すればよく、300℃以下の温度において、母体となるポリエステル系樹脂中に良好に分散する。
Considering the dispersibility in the thermoplastic resin (A) that is the base resin for constituting the resin composition, the thermoplastic water-soluble polyethylene oxide resin has a weight-average molecular weight of 50,000 to 9,000,000. The thermoplastic water-soluble polyethylene oxide resin with a weight-average molecular weight of 50,000 to 9,000,000 can be mixed well with the thermoplastic resin (A) in the melt extruder for producing the abrasive grains, and disperses well in the thermoplastic resin (A). When mixing a thermoplastic water-soluble polyethylene oxide resin with a weight-average molecular weight of more than 500,000, the temperature is set to 300°C or higher, and the thermoplastic water-soluble polyethylene oxide resin disperses well in the base polyester resin. When mixing a thermoplastic water-soluble polyethylene oxide resin with a weight-average molecular weight of 500,000 or less, the temperature is set to 300°C or lower, at which the thermoplastic resin (A) melts, and the thermoplastic resin disperses well in the base polyester resin at a temperature of 300°C or lower.
熱可塑性水溶性ポリエチレンオキサイド系樹脂としては、エチレンオキサイドのみによって構成される樹脂、または、エチレンオキシドとプロピレンオキシドとがランダム共重合してなるエチレンオキサイド・プロピレンオキサイドランダム共重合体である。
The thermoplastic water-soluble polyethylene oxide resin is a resin composed only of ethylene oxide , or an ethylene oxide-propylene oxide random copolymer obtained by random copolymerization of ethylene oxide and propylene oxide .
熱可塑性樹脂(A)中に混合してなる熱可塑性水溶性ポリエチレンオキサイド系樹脂が、共存物の影響を受けにくい非イオン性ポリマーであるため、熱可塑性樹脂(A)との相溶性に優れ良好に分散するため、砥粒の強度を良好に維持することができ、また、母体である熱可塑性樹脂(A)中に熱可塑性水溶性ポリエチレンオキサイド系樹脂均一に分散しているため、砥粒表面においてスリップ剤としても機能すると考えられ、摩擦帯電性と強度とのバランスに優れたものとなると推測する。 The thermoplastic water-soluble polyethylene oxide resin mixed into the thermoplastic resin (A) is a non-ionic polymer that is not easily affected by coexisting substances, and therefore has excellent compatibility with the thermoplastic resin (A) and disperses well, allowing the strength of the abrasive grains to be well maintained. In addition, since the thermoplastic water-soluble polyethylene oxide resin is uniformly dispersed in the parent thermoplastic resin (A), it is believed to function as a slip agent on the abrasive grain surface, resulting in an excellent balance between triboelectric charging properties and strength.
なお、本発明において、樹脂組成物には、本発明の効果を損なわない範囲であれば、必要に応じて例えば熱安定剤、結晶化剤、顔料、酸化防止剤、抗菌剤、香料、可塑剤、染料、界面活性剤等の各種添加剤を添加することができる。また、強度を高めるために、脂肪酸アミド類、例えばメタキシリレンビスステアリルアミド、メタキシリレンビスオレイルアミド、キシレンビスステアリン酸アミド、エチレンビスステアリルアミド、エチレンビスステアリン酸アミド等を添加してもよい。 In the present invention, various additives such as heat stabilizers, crystallizing agents, pigments, antioxidants, antibacterial agents, fragrances, plasticizers, dyes, and surfactants can be added to the resin composition as needed, so long as the effects of the present invention are not impaired. In addition, fatty acid amides such as metaxylylene bisstearylamide, metaxylylene bisoleylamide, xylene bisstearic acid amide, ethylene bisstearylamide, and ethylene bisstearic acid amide may be added to increase strength.
本発明の砥粒は、上記した熱可塑性樹脂(A)を主体として、熱可塑性水溶性ポリエチレンオキサイド系樹脂が特定量配合した樹脂組成物により構成されるが、熱可塑性水溶性ポリエチレンオキサイド系樹脂を含まない熱可塑性樹脂と複合したものであってよい。 The abrasive grains of the present invention are composed of a resin composition mainly composed of the above-mentioned thermoplastic resin (A) and a specific amount of thermoplastic water-soluble polyethylene oxide resin, but may be composited with a thermoplastic resin that does not contain a thermoplastic water-soluble polyethylene oxide resin.
本発明の砥粒は、前記した樹脂組成物により構成され、直径が50μm~3000μm、長さが0.05mm~10mmであるペレット状物である。直径は、ペレット状物の軸方向に直行する方向における径であり、軸方向に直行する方向の断面形状は、円形であっても、異形であっても、また、中空部を有したものであってもよい。なお、軸方向に直行する面の形状が異形の場合は、長径と短径の平均径が50~3000μmの範囲であればよい。また、軸方向に直行する面に中空部を有する場合は、外径を直径とみなす。長さは、ペレット状物の軸方向の長さである。砥粒の直径および長さを上記範囲とすることにより、取り扱い性が良好で、適度な強度を有する砥粒となる。なお、砥粒の好ましい直径は100μm~1500μm、長さは0.1mm~10mmである。 The abrasive grains of the present invention are pellet-shaped objects made of the resin composition described above, and have a diameter of 50 μm to 3000 μm and a length of 0.05 mm to 10 mm. The diameter is the diameter in a direction perpendicular to the axial direction of the pellet-shaped object, and the cross-sectional shape in the direction perpendicular to the axial direction may be circular, irregular, or may have a hollow portion. If the shape of the surface perpendicular to the axial direction is irregular, the average diameter of the major axis and minor axis may be in the range of 50 to 3000 μm. If the surface perpendicular to the axial direction has a hollow portion, the outer diameter is regarded as the diameter. The length is the length in the axial direction of the pellet-shaped object. By setting the diameter and length of the abrasive grains in the above ranges, the abrasive grains have good handleability and appropriate strength. The preferred diameter of the abrasive grains is 100 μm to 1500 μm, and the preferred length is 0.1 mm to 10 mm.
本発明の砥粒は、バリ取り用として好ましく用いられるものであり、対象物の表面に傷をつけることなく、作業効率が向上するものであることから、研磨用としても好ましく用いることもできる。 The abrasive grains of the present invention are preferably used for deburring, and because they improve work efficiency without scratching the surface of the object, they can also be preferably used for polishing.
本発明の砥粒を得る方法としては、例えば、前記した樹脂組成物をモノフィラメント糸条となるように溶融紡出して、得られたモノフィラメントを所定の長さに切断することにより得ることができる。モノフィラメントを得る際に、主体となる熱可塑性樹脂(A)を配向結晶化させることによって、良好な強度を有し、耐久性を有する砥粒を得ることができる。 The abrasive grains of the present invention can be obtained, for example, by melt-spinning the resin composition described above into a monofilament thread and cutting the obtained monofilament to a predetermined length. When obtaining the monofilament, the thermoplastic resin (A), which is the main component, is oriented and crystallized, thereby making it possible to obtain abrasive grains having good strength and durability.
具体的には、熱可塑性樹脂(A)からなるチップに、所定量の熱可塑性水溶性ポリエチレンオキサイド系樹脂をブレンドし、溶融混合した後、溶融紡糸する。次いで、溶融紡糸により得られた糸条を冷却し、油剤を付与し、あるいは付与せず、一旦未延伸糸として巻き取った後あるいはいったん巻き取ることなく、引き続いて延伸を施す。溶融紡糸後の糸条の冷却は、室温での冷却、冷却風の吹付けによる冷却、水浴中に通すことによる冷却のいずれでもよい。延伸にあたっての延伸倍率2~8倍とし、熱延伸を施す。熱延伸の加熱手段としては、温水バス中で熱延伸するか、加熱ローラを用いて熱延伸する。熱延伸後は、巻取り操作を連続して行い、モノフィラメントを得、得られたモノフィラメントのフィラメント軸方向に、所定の長さに切断することによって、本発明の砥粒を得ることができる。 Specifically, a predetermined amount of thermoplastic water-soluble polyethylene oxide resin is blended with chips made of thermoplastic resin (A), melt-mixed, and then melt-spun. The filament obtained by melt spinning is then cooled, and an oil agent is applied or not applied, and the filament is wound up as an undrawn filament, and then drawn, either without being wound up or without being drawn. The filament after melt spinning may be cooled at room temperature, by blowing cooling air, or by passing through a water bath. The filament is hot-drawn at a draw ratio of 2 to 8 times. As a heating means for hot drawing, hot drawing is performed in a hot water bath or by using a heated roller. After hot drawing, a winding operation is continuously performed to obtain a monofilament, and the abrasive grain of the present invention can be obtained by cutting the obtained monofilament to a predetermined length in the filament axis direction.
本発明によれば、対象物の表面等を傷つけにくく、繰り返しの摩擦に対して損傷しにくく耐久性を有し、かつ、バリ取りや表面研磨による作業時の摩擦によって帯電しにくく、作業効率の良い砥粒を提供することができる。 The present invention provides abrasive grains that are less likely to scratch the surface of an object, are resistant to damage from repeated friction, are durable, and are less likely to become charged due to friction during work such as deburring or surface polishing, resulting in good work efficiency.
本発明を実施例に基づいて説明する。なお、本発明は、実施例に限定するものではない。 The present invention will be described based on examples. Note that the present invention is not limited to the examples.
実施例1
重量平均分子量100万のポリエチレンオキサイド・プロピレンオキサイドランダム共重合体(明成化学工業株式会社製、商品名 アルコックス 品番EP-10)5質量%とポリエチレンテレフタレート樹脂チップ95質量%とを混合し、溶融紡糸温度を295℃とし、1.0mmφ×4Hの紡糸口金から溶融紡糸した。紡糸した糸条を50℃の水浴中で冷却した後、巻き取ることなく、速度20m/minで90℃の温浴中で延伸し、さらに巻き取ることなく、120℃の乾熱雰囲気中で総延伸倍率が5.3倍となるように延伸し巻き取った。繊度560dtex(直径0.225mm)のモノフィラメントを得た。得られたモノフィラメントを0.5mm~5mmの長さにカットして、実施例1の砥粒を得た。
Example 1
5% by mass of polyethylene oxide-propylene oxide random copolymer (manufactured by Meisei Chemical Industry Co., Ltd., trade name Alcox, product number EP-10) having a weight average molecular weight of 1,000,000 and 95% by mass of polyethylene terephthalate resin chips were mixed, and melt-spun at a melt spinning temperature of 295°C from a 1.0 mmφ×4H spinneret. The spun thread was cooled in a water bath at 50°C, and then stretched in a hot bath at 90°C at a speed of 20 m/min without winding, and then stretched and wound in a dry heat atmosphere at 120°C to a total stretch ratio of 5.3 times without winding. A monofilament having a fineness of 560 dtex (diameter 0.225 mm) was obtained. The obtained monofilament was cut to a length of 0.5 mm to 5 mm to obtain the abrasive grain of Example 1.
実施例2
重量平均分子量20万のポリエチレンオキサイド(明成化学工業株式会社製、商品名 アルコックス 品番R-400)2.5質量%とポリアミド6樹脂チップ97.5質量%とを混合し、溶融紡糸温度を265℃とし、1.9mmφ×14Hの紡糸口金から溶融紡糸した。紡糸した糸条を25℃の水浴中で冷却した後、巻き取ることなく、速度30m/minで80℃の温浴中で延伸し、さらに巻き取ることなく、175℃の雰囲気中で総延伸倍率が4.8倍となるように延伸し巻き取った。繊度1858dtex(直径0.45mm)のモノフィラメントを得た。得られたモノフィラメントを0.5mmから5mmにカットして、実施例2の砥粒を得た。
Example 2
2.5% by mass of polyethylene oxide (manufactured by Meisei Chemical Industry Co., Ltd., trade name Alcox, product number R-400) with a weight average molecular weight of 200,000 and 97.5% by mass of polyamide 6 resin chips were mixed, and melt-spun at a melt spinning temperature of 265°C from a 1.9mmφ×14H spinneret. The spun thread was cooled in a water bath at 25°C, and then stretched in a warm bath at 80°C at a speed of 30m/min without winding, and then stretched and wound in an atmosphere at 175°C to a total stretch ratio of 4.8 times without winding. A monofilament with a fineness of 1858dtex (diameter 0.45mm) was obtained. The obtained monofilament was cut to 0.5mm to 5mm to obtain the abrasive grains of Example 2.
比較例1
実施例1において、ポリエチレンテレフタレート樹脂チップのみを用いたこと以外は、実施例1と同様にして、繊度560dtex(直径0.225mm)のモノフィラメントを得た。得られたモノフィラメントを0.5mm~5mmの長さにカットして比較例1の砥粒を得た。
Comparative Example 1
A monofilament having a fineness of 560 dtex (diameter 0.225 mm) was obtained in the same manner as in Example 1, except that only polyethylene terephthalate resin chips were used in Example 1. The obtained monofilament was cut to a length of 0.5 mm to 5 mm to obtain the abrasive grains of Comparative Example 1.
比較例2
実施例2において、ポリアミド6樹脂チップのみを用いたこと以外は、実施例2と同様にして、繊度1879dtex(直径0.453mm)のモノフィラメントを得た。得られたモノフィラメントを0.5mm~5mmにカットして比較例2の砥粒を得た。
Comparative Example 2
A monofilament having a fineness of 1879 dtex (diameter 0.453 mm) was obtained in the same manner as in Example 2, except that only polyamide 6 resin chips were used in Example 2. The obtained monofilament was cut to 0.5 mm to 5 mm to obtain the abrasive grains of Comparative Example 2.
得られた実施例1、2および比較例1、2の砥粒を用いて、バリ取り試験を行い、評価した。 The obtained abrasive grains of Examples 1 and 2 and Comparative Examples 1 and 2 were used to conduct deburring tests and were evaluated.
<バリ取り試験>
バリ取りをする成形品として、3Dプリンターを用いて成形した長さ8cm、幅1cm、厚さ2mmの棒状の成形品を準備した。成形品は、ポリ乳酸樹脂(ユニチカ(株)製のテラマック3Dプリンター用フィラメント)を使用して造形したものである。
<Deburring test>
A rod-shaped molded product with a length of 8 cm, a width of 1 cm, and a thickness of 2 mm was prepared using a 3D printer as the molded product to be deburred. The molded product was made using polylactic acid resin (Terramac 3D printer filament manufactured by Unitika Ltd.).
次いで、3Dプリンターにより造形した成形品に対してバリ取りを行った。プラスチック容器に砥粒20gを入れた。攪拌機(東洋精機製作所製)の先端箇所に成形品を取り付け、撹拌機に取り付けた成形品を、容器内の砥粒中にて382rpmの回転速度で4時間回転させ、成形品のバリ取りを行った。 Next, the molded product created using the 3D printer was deburred. 20 g of abrasive grains were placed in a plastic container. The molded product was attached to the tip of a mixer (manufactured by Toyo Seiki Seisakusho), and the molded product attached to the mixer was rotated in the abrasive grains in the container at a rotation speed of 382 rpm for 4 hours to deburr the molded product.
バリ取り試験後、成形品の状態を確認し、成形品の表面に傷をつけることなく、バリが良好に取れているか否かの確認し(バリ取り効果)、また、バリ取り試験後の砥粒について、静電気が発生していないか(摩擦帯電性)および砥粒の表面状態を確認して、砥粒に損傷がないか(摩耗耐久性)を確認し、評価した。 After the burr removal test, the condition of the molded product was checked to see if the burrs had been successfully removed without damaging the surface of the molded product (burr removal effect). In addition, after the burr removal test, the abrasive grains were checked to see if static electricity had been generated (frictional charging property) and the surface condition of the abrasive grains was checked to see if there was any damage to the abrasive grains (abrasion resistance), and were then evaluated.
実施例1、2の砥粒を用いてバリ取り試験を行った成形品は、いずれも良好にバリが取れており、成形品表面に傷はなかった。また、砥粒は、静電気の発生はわずかであり、作業効率が良好であるものと評価できた。バリ取り試験後の砥粒の表面には、削れた箇所は一部であり、繰り返し使用でき、耐久性が良好であると評価できた。 All molded products that underwent burr removal tests using the abrasive grains of Examples 1 and 2 had burrs removed successfully, and there were no scratches on the surfaces of the molded products. The abrasive grains also generated only a small amount of static electricity, and were evaluated as having good work efficiency. After the burr removal test, only a few areas of the abrasive grain surface were chipped, and the products were evaluated as being suitable for repeated use and having good durability.
一方、比較例1、2の砥物においては、バリ取り試験により得られた成形体は、いずれも良好にバリが取れており、成形品表面に傷はなかったが、砥粒は、静電気が発生しており、成形品の表面の一部に張り付いていた。また、バリ取り試験後の砥粒の表面には、削れた箇所が多くみられた。
On the other hand, in the case of the abrasives of Comparative Examples 1 and 2, the burrs of the molded products obtained in the deburring test were all well removed, and there were no scratches on the surfaces of the molded products, but the abrasive grains generated static electricity and stuck to some of the surfaces of the molded products. In addition, many chipped areas were observed on the surfaces of the abrasive grains after the deburring test.
Claims (4)
前記熱可塑性水溶性ポリエチレンオキサイド系樹脂が、エチレンオキサイドのみからなる重合体あるいはポリエチレンオキサイド・プロピレンオキサイドランダム共重合体のいずれかであり、
直径が50μm~3000μm、長さが0.05mm~10mmであるペレット状物からなることを特徴とする砥粒。 The resin composition is constituted by a resin composition in which a thermoplastic water-soluble polyethylene oxide resin having a weight average molecular weight of 50,000 to 9,000,000 is blended with a thermoplastic resin (A) that is a base resin constituting the resin composition,
the thermoplastic water-soluble polyethylene oxide resin is either a polymer consisting of ethylene oxide alone or a polyethylene oxide-propylene oxide random copolymer,
The abrasive grains are characterized in that they are pellet-shaped with a diameter of 50 μm to 3000 μm and a length of 0.05 mm to 10 mm.
4. A deburring abrasive, comprising the abrasive according to claim 1, which is used for deburring.
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| JP2001277124A (en) | 2000-01-26 | 2001-10-09 | Bridgestone Corp | Blasting material and blasting process |
| JP2003220559A (en) | 2002-01-23 | 2003-08-05 | Toray Ind Inc | Projectile material |
| JP2004035760A (en) | 2002-07-04 | 2004-02-05 | Nippon Polypenco Ltd | Polyamide resin blast material |
| JP2009291870A (en) | 2008-06-04 | 2009-12-17 | Unitica Fibers Ltd | Abrasive material |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001277124A (en) | 2000-01-26 | 2001-10-09 | Bridgestone Corp | Blasting material and blasting process |
| JP2003220559A (en) | 2002-01-23 | 2003-08-05 | Toray Ind Inc | Projectile material |
| JP2004035760A (en) | 2002-07-04 | 2004-02-05 | Nippon Polypenco Ltd | Polyamide resin blast material |
| JP2009291870A (en) | 2008-06-04 | 2009-12-17 | Unitica Fibers Ltd | Abrasive material |
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