JP2006182883A - Silicone emulsion composition and releasing agent - Google Patents
Silicone emulsion composition and releasing agent Download PDFInfo
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- JP2006182883A JP2006182883A JP2004376851A JP2004376851A JP2006182883A JP 2006182883 A JP2006182883 A JP 2006182883A JP 2004376851 A JP2004376851 A JP 2004376851A JP 2004376851 A JP2004376851 A JP 2004376851A JP 2006182883 A JP2006182883 A JP 2006182883A
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- 239000000839 emulsion Substances 0.000 title claims abstract description 91
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 60
- 239000004094 surface-active agent Substances 0.000 claims abstract description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000002245 particle Substances 0.000 claims abstract description 16
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 11
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 7
- 239000000470 constituent Substances 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 12
- 125000006353 oxyethylene group Chemical group 0.000 claims description 11
- 239000006082 mold release agent Substances 0.000 claims description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 238000000465 moulding Methods 0.000 claims description 3
- 238000003860 storage Methods 0.000 abstract description 9
- 238000002156 mixing Methods 0.000 abstract description 5
- -1 polyoxyethylene Polymers 0.000 description 37
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 12
- 238000000926 separation method Methods 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 8
- 238000004945 emulsification Methods 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- LTSWUFKUZPPYEG-UHFFFAOYSA-N 1-decoxydecane Chemical compound CCCCCCCCCCOCCCCCCCCCC LTSWUFKUZPPYEG-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000000084 colloidal system Substances 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 229920002545 silicone oil Polymers 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000002518 antifoaming agent Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 238000004065 wastewater treatment Methods 0.000 description 3
- UWOVWIIOKHRNKU-UHFFFAOYSA-N 2,6-diphenyl-4-(2,4,6-triphenylpyridin-1-ium-1-yl)phenolate Chemical compound [O-]C1=C(C=2C=CC=CC=2)C=C([N+]=2C(=CC(=CC=2C=2C=CC=CC=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=C1C1=CC=CC=C1 UWOVWIIOKHRNKU-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000005215 alkyl ethers Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000314 lubricant Substances 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
- 150000002739 metals Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、離型剤等の用途に好適なシリコーンエマルジョン組成物およびそれを用いた離型剤に係り、さらに詳しくは、高濃度安定性および配合作業性を改善したシリコーンエマルジョン組成物およびそれを用いた離型剤に関する。 The present invention relates to a silicone emulsion composition suitable for use as a mold release agent and the like, and a mold release agent using the same, and more specifically, a silicone emulsion composition with improved high-concentration stability and compounding workability and the same. It relates to the release agent used.
金属やゴム・プラスチックなどの製品を成形する際の金型用離型剤として使用するため、オルガノポリシロキサンを乳化剤により水中に均一に分散させたシリコーンエマルジョン組成物が種々提案されている。 Various silicone emulsion compositions in which organopolysiloxane is uniformly dispersed in water using an emulsifier have been proposed for use as a mold release agent for molding products such as metals, rubber and plastics.
例えば、特許文献１では、ジメチルポリシロキサンの水性エマルジョンにポリオキシエチレンアルキルフェニルエーテル硫酸ナトリウムを添加した組成物が、また、特許文献２では、環状ジメチルポリシロキサンと乳化剤と水からなるシリコーンエマルジョン組成物が提案されている。 For example, in Patent Document 1, a composition in which sodium polyoxyethylene alkylphenyl ether sulfate is added to an aqueous emulsion of dimethylpolysiloxane, and in Patent Document 2, a silicone emulsion composition comprising cyclic dimethylpolysiloxane, an emulsifier and water. Has been proposed.
しかしながら、これらのシリコーンエマルジョン組成物は、機械的安定性に乏しく、機械的剪断力が加わった場合にはそのエマルジョン形態が破壊され易いという欠点があった。 However, these silicone emulsion compositions have a drawback that they have poor mechanical stability, and the emulsion form is easily destroyed when mechanical shearing force is applied.
これらの問題を解決させるため、すなわち、例えばこれらのシリコーンエマルジョン組成物をアルミニウムダイキャスト成形用離型剤として使用する場合、組成物を数十倍の水で希釈し、この希釈液をギアポンプにより送液して金型内壁に吹き付け、金型内壁表面にオルガノポリシロキサンの油膜を均一に形成させるとともに、余剰の希釈液は回収してギアポンプにより繰り返し送液する方法が一般に採用されているが、この過程でエマルジョン破壊が起こり、金型に均一に塗布することができなくなるという問題があった。また、このように希釈液を循環させて使用する設備においては、エアーの巻き込みによる泡立ちが大きいという問題もあった。 In order to solve these problems, that is, when, for example, these silicone emulsion compositions are used as a mold release agent for aluminum die casting, the composition is diluted with several tens of times of water, and this diluted solution is sent by a gear pump. In general, a method is used in which an oil film of organopolysiloxane is uniformly formed on the inner wall surface of the mold and sprayed on the inner wall of the mold, and the excess dilution liquid is collected and repeatedly fed by a gear pump. There was a problem that emulsion breakage occurred in the process and it was impossible to uniformly apply to the mold. In addition, the equipment that circulates the diluent as described above has a problem that foaming due to entrainment of air is large.
かかる問題を解決するため、ジメチルポリシロキサンと、ポリオキシエチレン高級アルコールエーテルと、ポリオキシエチレン高級アルコールエーテル硫酸塩および水からなるシリコーンエマルジョン組成物（特許文献３）が提案されている。しかしながら、このような組成物では、エマルジョンの安定性、特に希釈時の機械的、経時的安定性は十分でなく、さらにエマルジョン溶液に発生する泡の除去の為に使用する消泡剤や、装置の汚れ成分によりその安定性は著しく低下する傾向にあった。この問題を解決するためには、界面活性剤量を増やすという対策がとられている。 In order to solve this problem, a silicone emulsion composition (Patent Document 3) composed of dimethylpolysiloxane, polyoxyethylene higher alcohol ether, polyoxyethylene higher alcohol ether sulfate and water has been proposed. However, with such a composition, the stability of the emulsion, particularly the mechanical and time-dependent stability at the time of dilution, is not sufficient, and further, an antifoaming agent or apparatus used for removing bubbles generated in the emulsion solution Due to the soil components, the stability tended to decrease significantly. In order to solve this problem, measures are taken to increase the amount of the surfactant.
また、ポリオルガノシロキサンとアニオン性乳化剤と多価アルコールおよび水からなる組成物が特許文献４に提案されているが、泡立ちを抑制するためのもので、高濃度、高界面活性剤組成物の粘度、安定性に関するものではなかった。 A composition comprising a polyorganosiloxane, an anionic emulsifier, a polyhydric alcohol, and water is proposed in Patent Document 4, but it is for suppressing foaming, and has a high concentration and a high viscosity of the surfactant composition. It was not about stability.
このように、エマルジョン組成物の安定性などの特性を向上させるためには、界面活性剤の量を増やすことが有効であるため、各種界面活性剤の配合量を増やす検討が行なわれている。しかし、界面活性剤量の増加は、エマルジョン溶液の増粘、特にチクソトロピック性を持つような粘性化をもたらす。このような流動性の低下は、計量性、仕込み性分散性などの作業性を著しく低下させる。さらには、乳化に必要以上の過剰な界面活性剤は、エマルジョン自体の破壊や、エマルジョン層と水層に別れるような層分離といったような均一性不良によるエマルジョン溶液の安定性を低下させてしまう問題を持っていた。これらの問題を解消するためには、エマルジョンの濃度を下げるという方法が一般的に用いられている。しかし、濃度を下げたものは、コンパクト性に欠け輸送保管のコストアップや外装容器の増加をもたらす、さらに外装容器の増加は廃棄に伴う環境負荷も増大させることとなる。このため、高濃度で安定性、作業性に優れるエマルジョンが広く求められている。
上述したように、金型用離型剤に使用するため各種のシリコーンエマルジョン組成物が提案されているが、機械的安定性、金型への付着性、廃液の排水処理性などの特性を付加したエマルジョンにおいては、高濃度での流動性や安定性において十分なものは未だ得られていない。 As mentioned above, various silicone emulsion compositions have been proposed for use in mold release agents, but they add properties such as mechanical stability, adhesion to molds, and wastewater drainage treatment. In the obtained emulsion, sufficient fluidity and stability at a high concentration have not yet been obtained.
本発明はこのような従来の事情に対処すべくなされたもので、十分な流動性を有し、かつ、自体の保存安定性に優れたシリコーンエマルジョン組成物、およびこれを用いた離型剤を提供することを目的としている。 The present invention has been made to cope with such a conventional situation. A silicone emulsion composition having sufficient fluidity and excellent in storage stability itself, and a mold release agent using the same are disclosed. It is intended to provide.
本発明者らは、上記目的達成のため検討した結果、界面活性剤の濃度が高い高濃度エマルジョンに対し、特定のアルキレンオキサイド誘導体を添加することが低粘性および安定性に有効であり、十分な流動性を有し、かつ、自体の保存安定性に優れたシリコーンエマルジョン組成物が得られることを見出し、本発明を完成するに至った。 As a result of investigations to achieve the above object, the present inventors have found that adding a specific alkylene oxide derivative to a high-concentration emulsion having a high surfactant concentration is effective for low viscosity and stability, and is sufficient. It has been found that a silicone emulsion composition having fluidity and excellent storage stability can be obtained, and the present invention has been completed.
即ち本発明は、
（Ａ）（Ａ−１）平均重合度が５〜1000のオルガノポリシロキサン；40〜60重量％、（Ａ−２）界面活性剤；（Ａ−１）のオルガノポリシロキサンに対し12〜20重量％、（Ａ−３）水；残部を主要構成成分とする、粒径が100〜300nmの乳化エマルジョン組成物100重量部に、
（Ｂ）下記式（１）で示されるアルキレンオキサイド誘導体１〜13重量部を配合したことを特徴とするシリコーンエマルジョン組成物である。
That is, the present invention
(A) (A-1) Organopolysiloxane having an average degree of polymerization of 5 to 1000; 40 to 60% by weight, (A-2) surfactant; 12 to 20% by weight based on the organopolysiloxane of (A-1) %, (A-3) water; 100 parts by weight of an emulsified emulsion composition having a particle size of 100 to 300 nm, with the balance being the main constituent,
(B) A silicone emulsion composition comprising 1 to 13 parts by weight of an alkylene oxide derivative represented by the following formula (1).
R1O-[（AO）m（EO）n]-R2 （１）
（式中、AOは炭素数３〜４のオキシアルキレン基、EOはオキシエチレン基、ｍおよびｎはそれぞれ前記オキシアルキレン基、オキシエチレン基の平均付加モル数で、０≦ｍ≦25、４≦ｎ≦100、３ｍ≦ｎである。炭素数３〜４のオキシアルキレン基、オキシエチレン基はブロック状に付加してもランダム状に付加してもよい。R1、R2は、同一もしくは異なっていてもよい炭素数１〜４の炭化水素基又は水素原子である。）
R 1 O-[(AO) m (EO) n ] -R 2 (1)
(In the formula, AO is an oxyalkylene group having 3 to 4 carbon atoms, EO is an oxyethylene group, m and n are average addition moles of the oxyalkylene group and oxyethylene group, and 0 ≦ m ≦ 25, 4 ≦ n ≦ 100 and 3m ≦ n The oxyalkylene group and oxyethylene group having 3 to 4 carbon atoms may be added in a block shape or in a random shape, and R 1 and R 2 may be the same or different. It is a C1-C4 hydrocarbon group or hydrogen atom that may be present.)
本発明のシリコーンエマルジョン組成物は、濃度、界面活性剤含有量が高いにも関わらず、低粘度で安定性に優れたものとなる。 The silicone emulsion composition of the present invention has a low viscosity and excellent stability despite its high concentration and high surfactant content.
また、本発明の離型剤は、上記のような高濃度で界面活性剤を多く含むにも関わらず、低粘性および安定性に優れるシリコーンエマルジョン組成物であるので、各種界面活性剤を用いて希釈時の機械安定性、塗布性、離型特性、排水処理性などの特性をもたせた離型剤、特にアルミニウムダイキャスト成形のような用途において、輸送、保管時のコンパクト性、外装容器の廃棄量の軽減性に優れたものとなる。 In addition, since the release agent of the present invention is a silicone emulsion composition excellent in low viscosity and stability despite containing a large amount of surfactant at a high concentration as described above, various surfactants are used. Release agent with properties such as mechanical stability at dilution, coating properties, release properties, wastewater treatment properties, especially aluminum die cast molding, compactness during transportation and storage, disposal of outer containers It will be excellent in quantity reduction.
以下、本発明の実施の形態について説明する。本発明は、（Ａ）成分である特定の乳化エマルジョン組成物に対し、（Ｂ）成分の式（１）で示されるアルキレンオキサイド誘導体を配合することを特徴とするシリコーンエマルジョン組成物であり、先ず（Ｂ）成分について説明する。 Hereinafter, embodiments of the present invention will be described. The present invention is a silicone emulsion composition characterized in that an alkylene oxide derivative represented by formula (1) of the component (B) is blended with a specific emulsified emulsion composition as the component (A). (B) A component is demonstrated.
（Ｂ）成分のアルキレンオキサイド誘導体は、（Ａ）成分のエマルジョン溶液の粘度を下げるとともに、組成物に安定性を持たせる成分である。本発明で用いるアルキレンオキサイド誘導体は、下記式（１）で示されるものである。 The alkylene oxide derivative (B) is a component that lowers the viscosity of the emulsion solution (A) and provides stability to the composition. The alkylene oxide derivative used in the present invention is represented by the following formula (1).
R1O-[（AO）m（EO）n]-R2 （１）
ここで、AOは炭素数３〜４のオキシアルキレン基であり、具体的には、オキシプロピレン基、オキシブチレン基、オキシイソブチレン基、オキシトリメチレン基、オキシテトラメチレン基などが挙げられる。好ましくは、オキシプロピレン基、オキシブチレン基が挙げられる。ｍは炭素数３〜４のオキシアルキレン基の平均付加モル数であり、０≦ｍ≦25、好ましくは０≦ｍ≦10である。また、ｎはオキシエチレン基の平均付加モル数であり、４≦ｎ≦100、好ましくは10≦ｎ≦70である。炭素数３〜４のオキシアルキレン基が25を超えると減粘性がなく安定性が低下する。またオキシエチレン基が４未満あるいは100を超えると、減粘性がない。
R 1 O-[(AO) m (EO) n ] -R 2 (1)
Here, AO is an oxyalkylene group having 3 to 4 carbon atoms, and specific examples include an oxypropylene group, an oxybutylene group, an oxyisobutylene group, an oxytrimethylene group, and an oxytetramethylene group. Preferably, an oxypropylene group and an oxybutylene group are mentioned. m is the average number of added moles of an oxyalkylene group having 3 to 4 carbon atoms, and 0 ≦ m ≦ 25, preferably 0 ≦ m ≦ 10. N is the average number of moles of oxyethylene group added, and 4 ≦ n ≦ 100, preferably 10 ≦ n ≦ 70. When the number of oxyalkylene groups having 3 to 4 carbon atoms exceeds 25, there is no viscosity reduction and the stability is lowered. If the oxyethylene group is less than 4 or more than 100, there is no viscosity reduction.
炭素数３〜４のオキシアルキレン基とオキシエチレン基の割合は、３ｍ≦ｎであり、好ましくは５ｍ≦ｎである。３ｍ＞ｎでは、減粘性がない。オキシエチレン基および炭素数３〜４のオキシアルキレン基の付加する順序は特に指定はない。また、オキシエチレン基と炭素数３〜４のオキシアルキレン基はブロック状に付加していてもランダム状に付加していても良い。ブロック状には２段階ブロックのみならず、３段以上のブロックも含まれる。好ましくはランダム状に付加されている物が挙げられる。 The ratio of the oxyalkylene group having 3 to 4 carbon atoms and the oxyethylene group is 3 m ≦ n, preferably 5 m ≦ n. At 3 m> n, there is no viscosity loss. The order of adding the oxyethylene group and the oxyalkylene group having 3 to 4 carbon atoms is not particularly specified. Further, the oxyethylene group and the oxyalkylene group having 3 to 4 carbon atoms may be added in a block shape or in a random shape. The block shape includes not only two-stage blocks but also three-stage blocks or more. The thing added preferably at random is mentioned.
R1およびR2は炭素数１〜４の炭化水素基もしくは水素原子で、炭化水素基としては、メチル基、エチル基、ｎ-プロピル基、イソピロピル基、n-ブチル基、sec-ブチル基、tert-ブチル基などが挙げられる。好ましくはメチル基、エチル基である。炭素数が５以上の炭化水素基では親水性が低下し、減粘性が劣る。本発明に用いるアルキレンオキサイド誘導体は公知の方法で製造することができる。例えば、水酸基を有している化合物にエチレンオキサイドを付加重合した後、ハロゲン化アルキルをアルカリ触媒の存在化にエーテル反応させることによって得られる。 R 1 and R 2 are each a hydrocarbon group having 1 to 4 carbon atoms or a hydrogen atom, and examples of the hydrocarbon group include a methyl group, an ethyl group, an n-propyl group, an isopropyl group, an n-butyl group, a sec-butyl group, Examples thereof include a tert-butyl group. A methyl group and an ethyl group are preferred. Hydrocarbon groups having 5 or more carbon atoms have poor hydrophilicity and poor viscosity. The alkylene oxide derivative used in the present invention can be produced by a known method. For example, it can be obtained by addition-polymerizing ethylene oxide to a compound having a hydroxyl group and then ether-reacting an alkyl halide in the presence of an alkali catalyst.
本発明に用いるアルキレンオキシド誘導体は、直鎖状が好ましいが、ポリエチレングリコールトリオールのように部分的な分岐があっても良い。 The alkylene oxide derivative used in the present invention is preferably linear, but may be partially branched like polyethylene glycol triol.
本発明において、（Ｂ）アルキレンオキシド誘導体の配合量は（Ａ）成分の乳化エマルジョン組成物100重量部に対し、１〜13重量部が好ましい。更に好ましくは３〜1２重量部である。１重量部未満では減粘性がなく、13重量部を超えて配合すると減粘性がないとともにエマルジョンの安定性を損なうためである。 In the present invention, the blending amount of the (B) alkylene oxide derivative is preferably 1 to 13 parts by weight per 100 parts by weight of the emulsified emulsion composition of the component (A). More preferably, it is 3 to 12 parts by weight. This is because if it is less than 1 part by weight, there is no viscosity reduction, and if it exceeds 13 parts by weight, there is no viscosity reduction and the stability of the emulsion is impaired.
（Ａ）成分の乳化エマルジョン組成物は、（Ａ−１）平均重合度が５〜1000のオルガノポリシロキサン；40〜60重量％、（Ａ−２）界面活性剤；（Ａ−１）のオルガノポリシロキサンに対し12〜20重量％、（Ａ−３）水；残部を主要構成成分とする、粒径が100〜300nmのエマルジョン組成物であれば特に限定はなく、一般的に用いられる乳化方法により製造することができる。例えば、特開平５−２９５２６４号公報に示される乳化組成物およびそれに類する乳化組成物に界面活性剤を添加し（Ａ）成分組成としたものがより安定性が高いものとして好適に用いられる。さらに、この種のシリコーンエマルジョン組成物に通常配合される成分、例えば防腐剤；防黴剤；防錆剤；キレート剤；着色剤；鉱物油；パラミチン酸、ステアリン酸等の高級脂肪酸；増粘剤；アルミニウム粉末、黒鉛等の無機粉末等を、本発明の効果を阻害しない範囲で適宜配合したものであっても良い。 The emulsified emulsion composition of component (A) comprises (A-1) an organopolysiloxane having an average degree of polymerization of 5 to 1000; 40 to 60% by weight, (A-2) a surfactant; 12 to 20% by weight based on polysiloxane, (A-3) water; Emulsification method generally used without particular limitation as long as it is an emulsion composition having a remainder as a main constituent and a particle size of 100 to 300 nm Can be manufactured. For example, a composition obtained by adding a surfactant to an emulsion composition disclosed in JP-A-5-295264 and an emulsion composition similar thereto is preferably used as having a higher stability. In addition, components usually incorporated in this type of silicone emulsion composition, such as preservatives; antifungal agents; rust inhibitors; chelating agents; coloring agents; mineral oils; higher fatty acids such as paramitic acid and stearic acid; An inorganic powder such as aluminum powder or graphite may be appropriately blended within a range not impairing the effects of the present invention.
（Ａ）成分のシリコーンエマルジョン組成物は、（Ａ−１）〜（Ａ−３）各成分を、ホモミキサー、コロイドミル、ラインミキサー、ホモジナイザー等の乳化機を用いて乳化することにより製造することができる。 The (A) component silicone emulsion composition is manufactured by emulsifying each component (A-1) to (A-3) using an emulsifier such as a homomixer, colloid mill, line mixer, or homogenizer. Can do.
エマルジョンの粒径はその平均粒径100〜300nmが好ましく、更に好ましくが150〜250nm である。100nm未満のものはは、製造が困難であるとともに、増粘が激しくなる。また300nmを超えると十分な安定性が得られない。 The average particle size of the emulsion is preferably 100 to 300 nm, more preferably 150 to 250 nm. Those having a thickness of less than 100 nm are difficult to produce and increase in viscosity. Further, if it exceeds 300 nm, sufficient stability cannot be obtained.
平均粒径とは、一般的な粒度測定装置により測定されて得られる平均粒子径やメジアン径を示し、例えばCOULTER（株）製；LS230の場合、屈折率を1.45に設定して得られたデータの平均粒子径に代表される値である。 The average particle diameter means an average particle diameter or median diameter obtained by measuring with a general particle size measuring apparatus. For example, in the case of LS230, data obtained by setting the refractive index to 1.45. It is a value represented by the average particle diameter of
（Ａ−１）成分のオルガノポリシロキサンは、平均重合度が５〜1000、好ましくは30〜600のものであって、基本的に直鎖状のシロキサン骨格を有するものである。若干の分岐を有していてもよいが、分子全体が直鎖状の構造からなるものが好ましい。平均重合度が５未満では、離型剤としての効果が十分でなく、平均重合度が1000を越えると、粘度が大きくなりすぎるために乳化が困難になる。 The (A-1) component organopolysiloxane has an average degree of polymerization of 5 to 1000, preferably 30 to 600, and basically has a linear siloxane skeleton. Although it may have some branches, it is preferable that the whole molecule has a linear structure. If the average degree of polymerization is less than 5, the effect as a mold release agent is not sufficient, and if the average degree of polymerization exceeds 1000, the viscosity becomes too high and emulsification becomes difficult.
分子中のケイ素原子に結合する有機基としては、メチル基、エチル基、n-プロピル基、イソプロピル基、n-ブチル基、イソブチル基、n-ブチル基、イソブチル基、t-ブチル基、n-ペンチル基、イソペンチル基、n-ヘキシル基、n-オクチル基、2-エチルへキシル基、n-デシル基、イソデシル基、n-ドデシル基、イソドデシル基、n-テトラデシル基、n-ヘキサデシル基、n-オクタデシル基等の炭素数１〜24の直鎖または分岐状のアルキル基、；シクロヘキシル基等の炭素数４〜７のシクロアルキル基；ビニル基、アリル基等の炭素数２〜８のアルケニル基；2-フェニルエチル基、2-フェニルプロピル基等の、アリール基がフェニル基または低級アルキル基（炭素数４以下）置換フェニル基で、アルキル基が低級アルキル（炭素数４以下）基であるアラルキル基；フェニル基、トリル基等の低級アルキル基（炭素数4以下）置換フェニル基等のアリール基；およびこれらの基の炭化水素に結合した水素原子がハロゲン原子、シアノ基、アミノ基等で置換された基、例えばクロロメチル基、3,3,3-トリフルオロプロピル基、シアノメチル基、N-（2-アミノエチル）-3-アミノプロピル基、3-アミノプロピル基等が例示される。また、ケイ素原子に結合するその他の基として、アルコキシ基、水酸基、水素原子等を部分的に含んでいてもよい。なかでも、炭素数１〜18の直鎖もしくは分岐状のアルキル基もしくは2-フェニルプロピル基置換フェニル基の単独もしくは2種以上の混合物が好ましい。 Examples of the organic group bonded to the silicon atom in the molecule include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, n-butyl group, isobutyl group, t-butyl group, n- Pentyl group, isopentyl group, n-hexyl group, n-octyl group, 2-ethylhexyl group, n-decyl group, isodecyl group, n-dodecyl group, isododecyl group, n-tetradecyl group, n-hexadecyl group, n A linear or branched alkyl group having 1 to 24 carbon atoms such as an octadecyl group; a cycloalkyl group having 4 to 7 carbon atoms such as a cyclohexyl group; an alkenyl group having 2 to 8 carbon atoms such as a vinyl group or an allyl group Aralkyl in which the aryl group is a phenyl group or a lower alkyl group (4 or less carbon atoms) substituted phenyl group, and the alkyl group is a lower alkyl (4 or less carbon atoms) group, such as a 2-phenylethyl group or 2-phenylpropyl group; An aryl group such as a phenyl group, a tolyl group or other lower alkyl group (4 or less carbon atoms) substituted phenyl group; and the hydrogen atom bonded to the hydrocarbon of these groups is substituted with a halogen atom, a cyano group, an amino group, or the like; Examples thereof include chloromethyl group, 3,3,3-trifluoropropyl group, cyanomethyl group, N- (2-aminoethyl) -3-aminopropyl group, 3-aminopropyl group and the like. Moreover, as other groups couple | bonded with a silicon atom, the alkoxy group, a hydroxyl group, a hydrogen atom, etc. may be included partially. Of these, a linear or branched alkyl group having 1 to 18 carbon atoms or a phenyl group substituted with a 2-phenylpropyl group alone or a mixture of two or more thereof is preferable.
本発明のシリコーンエマルジョン組成物を離型剤として使用する場合、1分子中のケイ素原子に結合する有機基の少なくとも50モル％がメチル基であることが離型性の点で好ましい。 When the silicone emulsion composition of the present invention is used as a release agent, it is preferable from the viewpoint of releasability that at least 50 mol% of organic groups bonded to silicon atoms in one molecule are methyl groups.
（Ａ−１）成分のオルガのポリシロキサンは、製造のしやすさ、取り扱い性、コンパクト性から４０〜６０重量％であることが好ましい。 The (A-1) component Olga polysiloxane is preferably 40 to 60% by weight in view of ease of production, handleability, and compactness.
（Ａ−２）界面活性剤は、（Ａ−１）成分のオルガノポリシロキサンを乳化する成分とエマルジョン組成物に機械的安定性、金型への付着性、廃液の排水処理性などの特性を付与するための成分である。通常（Ａ−１）成分の乳化用界面活性剤成分と乳化物に特性を付与するための追添加用界面活性剤成分からなる。乳化用の界面活性剤としては、（Ａ−１）成分のオルガノポリシロキサンの乳化に適した界面活性剤および量であれば特に指定はないが、機械乳化よりエマルジョンを製造する場合、界面活性剤としては、ポリオキシエチレンアルキルエーテルが好適に用いられる。本発明においては、炭素数８〜24のアルキル基（例えば、エチルヘキシル基、ノニル基、デシル基、イソデシル基、ラウリル基、テトラデシル基、セチル基、ステアリル基等）を有し、かつ、エチレンオキサイドの付加モル数が２〜20であるものが好ましく使用される。これらのポリオキシエチレンアルキルエーテルは、１種を単独で使用してもよく、２種以上を混合して使用してもよい。また、乳化重合によりエマルジョンを製造する場合、ドデシルベンゼンスルホン酸やアルキル硫酸塩、アルキルポリエーテル硫酸塩などのアニオン系界面活性剤が用いられる。その量は（Ａ−１）成分に対し５〜10重量％が一般的に用いられる。 (A-2) Surfactant has characteristics such as mechanical stability, adhesion to mold, wastewater treatment of waste liquid, and the like in the emulsion composition and the component emulsifying the organopolysiloxane of component (A-1). It is a component for imparting. Usually, it comprises a surfactant component for emulsification of component (A-1) and a surfactant component for additional addition for imparting characteristics to the emulsion. The surfactant for emulsification is not particularly specified as long as it is a surfactant and an amount suitable for emulsification of the organopolysiloxane of component (A-1), but when producing an emulsion from mechanical emulsification, the surfactant As such, polyoxyethylene alkyl ether is preferably used. In the present invention, it has an alkyl group having 8 to 24 carbon atoms (for example, ethylhexyl group, nonyl group, decyl group, isodecyl group, lauryl group, tetradecyl group, cetyl group, stearyl group, etc.) and ethylene oxide. Those having an added mole number of 2 to 20 are preferably used. These polyoxyethylene alkyl ethers may be used alone or in a combination of two or more. In the case of producing an emulsion by emulsion polymerization, an anionic surfactant such as dodecylbenzene sulfonic acid, alkyl sulfate, or alkyl polyether sulfate is used. The amount is generally 5 to 10% by weight based on the component (A-1).
安定性などの特性を付与する界面活性剤としては、その目的および効果により適宜選択されたものであれば特に指定はないが、ノニオン、アニオン、カチオン、両性などの界面活性剤を単独あるいは2種類以上を組み合わせて用いたものである。機械乳化で得られたエマルジョンにはアニオン系あるいは両性界面活性剤が単独あるいは２種類以上を組み合わせて用いられる。また、乳化重合で得られたエマルジョンにはノニオン系の界面活性剤を単独あるいは２種類以上を組み合わせて用いられる。 The surfactant imparting characteristics such as stability is not particularly specified as long as it is appropriately selected depending on the purpose and effect, but nonionic, anionic, cationic, amphoteric and other surfactants may be used alone or in two types. The above is used in combination. In the emulsion obtained by mechanical emulsification, an anionic or amphoteric surfactant is used alone or in combination of two or more. In addition, nonionic surfactants may be used alone or in combination of two or more in the emulsion obtained by emulsion polymerization.
特にアニオン系とノニオン系を併用した場合、単一系で製造したエマルジョンによりも、安定性が大きく向上する。さらに、ノニオン系にアニオン系を併用するとイオン性が付与でき、排水処理の際の吸着剤への吸着性が向上し、エマルジョンの処理性が大幅に向上する。また、アニオン系にノニオンを併用すると、被着体への濡れ性、レべリング性、乾燥後の被着体表面の白化性を大幅に低減できるなどのメリットが得られる。 In particular, when an anionic system and a nonionic system are used in combination, the stability is greatly improved even by an emulsion produced in a single system. Further, when an anionic system is used in combination with a nonionic system, ionicity can be imparted, the adsorptivity to the adsorbent during wastewater treatment is improved, and the processability of the emulsion is greatly improved. In addition, when a nonion is used in combination with an anionic system, there are obtained merits such as wettability to an adherend, leveling properties, and whiteness of the adherend surface after drying can be greatly reduced.
追添加用界面活性剤の量は、（Ａ−１）のオルガノポリシロキサンに対し界面活性剤の総量が12〜20重量％になるよう調整することが好ましい。12重量％未満では機械安定性などの効果が十分でなく、20重量％を超えると粘度が高くなりすぎ、取り扱い性が悪くなるとともに、エマルジョンの安定性も低下する。 The amount of the surfactant for additional addition is preferably adjusted so that the total amount of the surfactant is 12 to 20% by weight based on the organopolysiloxane (A-1). If it is less than 12% by weight, the effects such as mechanical stability are not sufficient, and if it exceeds 20% by weight, the viscosity becomes too high, handling becomes worse, and the stability of the emulsion is also lowered.
本発明のシリコーンエマルジョン組成物は、オルガノポリシロキサンおよび界面活性剤が高濃度であっても、低粘度であり、保存時に均一性を損なう層分離などがない安定性なものである。計量、配合などの作業性を損なうことなく、界面活性剤濃度を増加できるので、希釈使用時の機械安定性などの特性を向上させた製品を生産性の低下がなく適用することができる。また、高濃度であるため、輸送、保管に有利であるとともに、外装容器も軽減できるので、外装容器の廃棄にともなう環境負荷も軽減することができる。また、粘性が低いのでそのままでも容易に使用できる。本組成物は、そのままあるいは水で希釈して金型用離型剤として有効に使用されるが、その他、電線の芯線の引抜きやアイロン掛けの際の潤滑剤、ゴム・プラスチック製品あるいは家具などの艶出剤、繊維に撥水性や柔軟性などを付与するための繊維処理剤、塗料成分、化粧料成分、医薬品成分などの用途にも適宜使用することができる。 The silicone emulsion composition of the present invention has a low viscosity even when the organopolysiloxane and the surfactant are high in concentration, and is stable without layer separation that impairs uniformity during storage. Since the surfactant concentration can be increased without impairing workability such as weighing and blending, a product with improved characteristics such as mechanical stability at the time of dilution can be applied without lowering the productivity. In addition, since the concentration is high, it is advantageous for transportation and storage, and the outer container can be reduced, so that the environmental load due to disposal of the outer container can also be reduced. Moreover, since the viscosity is low, it can be used easily as it is. This composition is effectively used as a mold release agent as it is or diluted with water, but also as a lubricant, rubber / plastic product, furniture, etc. It can also be used as appropriate for applications such as polishes, fiber treatment agents for imparting water repellency and flexibility to fibers, paint components, cosmetic ingredients, and pharmaceutical ingredients.
本発明を実施例によりさらに詳細に説明するが、本発明はこれらの実施例に限定されるものではない。なお、以下の記載において「部」及び「％」はそれぞれ「重量部」及び「重量％」を意味し、また、粘度は25℃における測定値である。
実施例１
下記式で表されるオルガノポリシロキサン（粘度700mPa、シリコーンオイルAと表記）47.5部に、ポリオキシエチレン（3）デシルエーテル1.5部、ポリオキシエチレン（15）デシルエーテル3.0部及び水5.0部を添加し均一に混合した後、コロイドミル乳化器を用いて乳化した（ミル乳化物１）。
Examples The present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples. In the following description, “parts” and “%” mean “parts by weight” and “% by weight”, respectively, and the viscosity is a measured value at 25 ° C.
Example 1
Polyoxyethylene (3) decyl ether 1.5 parts, polyoxyethylene (15) decyl ether 3.0 parts and water 5.0 parts are added to 47.5 parts of an organopolysiloxane represented by the following formula (viscosity 700 mPa, expressed as silicone oil A) After uniform mixing, the mixture was emulsified using a colloid mill emulsifier (mill emulsion 1).
このミル乳化物のエマルジョン粒径を、COULTREER（株）製 LS230を用い屈折率を1.45に設定して測定したところ、粒径が236nmであった。 The emulsion particle size of this mill emulsion was measured using COLSREER LS230 with a refractive index of 1.45. The particle size was 236 nm.
このミル乳化物１にポリオキシエチレン（2）ラウリルエーテル硫酸ナトリウム27%aq. 1.0部（固形分0.3部）、ラウリル硫酸トリエタノールアミン40%aq. 4.2部（固形分1.7部）、ヤシ油脂肪酸アミドプロピルジメチル酢酸ベタイン30%aq. 4.2部（固形分1.3部）、ポリエチレングリコール（平均分子量2000）9.2部及び水24.4部を添加し均一に混合してシリコーンエマルジョン組成物を得た。 In this mill emulsion 1, polyoxyethylene (2) sodium lauryl ether sulfate 27% aq. 1.0 part (solid part 0.3 part), lauryl sulfate triethanolamine 40% aq. 4.2 part (solid part 1.7 part), coconut oil fatty acid Amidepropyldimethylacetate betaine 30% aq. 4.2 parts (solid content 1.3 parts), polyethylene glycol (average molecular weight 2000) 9.2 parts and water 24.4 parts were added and mixed uniformly to obtain a silicone emulsion composition.
以下、ミル乳化物１を用いて、表２〜４に示す組成で、実施例２〜６及び比較例１〜９、11、14のシリコーンエマルジョン組成物も同様にして調製した。
実施例７
下記式で表されるオルガノポリシロキサン（粘度1500mPa、シリコーンオイルBと表記）42.7部に、ポリオキシエチレン（3）デシルエーテル1.3部、ポリオキシエチレン（15）デシルエーテル2.6部及び水4.5部を添加し均一に混合した後、コロイドミル乳化器を用いて乳化し（ミル乳化物２）、このミル乳化物のエマルジョン粒径を、COULTREER（株）製 LS230を用い屈折率を1.45に設定して測定したところ、粒径が229nmであった。
Hereinafter, using the mill emulsion 1, the silicone emulsion compositions of Examples 2 to 6 and Comparative Examples 1 to 9, 11, and 14 having the compositions shown in Tables 2 to 4 were similarly prepared.
Example 7
Add 41.3 parts of organopolysiloxane (viscosity 1500 mPa, silicone oil B) represented by the following formula with 1.3 parts of polyoxyethylene (3) decyl ether, 2.6 parts of polyoxyethylene (15) decyl ether and 4.5 parts of water After mixing uniformly, emulsify using a colloid mill emulsifier (mill emulsion 2), and measure the emulsion particle size of this mill emulsion using COLSREER LS230 with a refractive index of 1.45. As a result, the particle size was 229 nm.
このミル乳化物２にラウリル硫酸トリエタノールアミン40%aq. 3.7部（固形分1.5部）、ヤシ油脂肪酸アミドプロピルジメチル酢酸ベタイン30%aq. 3.7部（固形分1.１部）、ポリエチレングリコール（平均分子量400）4.1部及び水37.4部を添加し均一に混合して、シリコーンエマルジョン組成物を得た。 This mill emulsion 2 was mixed with lauryl sulfate triethanolamine 40% aq. 3.7 parts (solid content 1.5 parts), coconut oil fatty acid amidopropyldimethylacetate betaine 30% aq. 3.7 parts (solid content 1.1 parts), polyethylene glycol ( 4.1 parts of average molecular weight 400) and 37.4 parts of water were added and mixed uniformly to obtain a silicone emulsion composition.
以下、ミル乳化物２を用いて、表２に示す組成で、実施例８のシリコーンエマルジョン組成物も同様にして調製した。
比較例10
シリコーンオイルB 32.1部に、ポリオキシエチレン（3）デシルエーテル1.0部、ポリオキシエチレン（15）デシルエーテル2.0部及び水4.3部を添加し均一に混合した後、コロイドミル乳化器を用いて乳化した。このミル乳化物のエマルジョン粒径を、COULTER（株）製 LS230を用い屈折率を1.45に設定して測定したところ、粒径が497nmであった（ミル乳化物３）。さらにラウリル硫酸トリエタノールアミン40%aq. 4.1部（固形分1.6部）、ヤシ油脂肪酸アミドプロピルジメチル酢酸ベタイン30%aq. 4.1部（固形分1.2部）及び水52.4部を添加し均一に混合して、シリコーンエマルジョン組成物を得た。
Hereinafter, using the mill emulsion 2, the silicone emulsion composition of Example 8 having the composition shown in Table 2 was also prepared in the same manner.
Comparative Example 10
To 32.1 parts of silicone oil B, 1.0 part of polyoxyethylene (3) decyl ether, 2.0 parts of polyoxyethylene (15) decyl ether and 4.3 parts of water were added and mixed uniformly, and then emulsified using a colloid mill emulsifier. . The emulsion particle size of this mill emulsion was measured using an LS230 manufactured by COULTER Co., Ltd. and the refractive index was set to 1.45. The particle size was 497 nm (mill emulsion 3). Furthermore, add 40 parts aq. Lauryl sulfate 40% aq. 4.1 parts (solid content 1.6 parts), coconut oil fatty acid amidopropyldimethylacetate 30% aq. 4.1 parts solids 1.2 parts solid and 52.4 parts water and mix uniformly. Thus, a silicone emulsion composition was obtained.
以下、ミル乳化物３を用いて、表４に示す組成で、比較例12、13のシリコーンエマルジョン組成物も同様にして調製した。 Hereinafter, the silicone emulsion compositions of Comparative Examples 12 and 13 were similarly prepared using the mill emulsion 3 with the compositions shown in Table 4.
実施例１及び２のシリコーンエマルジョン組成物に関して、表１の一般特性を調べた。また防錆性、ペインタブル性、離型性は下記方法により評価した。
・防錆性
150mlのガラス瓶にシリコーンエマルジョン組成物を130ml入れ、長さ3cm、直径2.5mmの軟鉄製の釘３本を沈め、50℃オーブンに48時間静置し、次のように防錆性をチェックした。
○：全く錆びの発生無し。
△：部分的に錆びの発生がやや認められる。
×：ほぼ全面に錆びの発生があり、錆びの沈降もある。
・ペインタブル性
シリコーンエマルジョン組成物を、水で50倍に希釈し、簡易型スプレーガンを用いてクレーコート紙に均一に吹き付け、室温で乾燥後、油性の太書き用マジックインキで定規を使って等間隔で紙を引き、線のかすれた具合いを、次のように判定した。
○：線のかすれは全く無く均一にマジックインキが付着している。
△：部分的に僅かに線のかすれがあり、やや不均一なマジックインキの付着となっている。
×：マジックインキのかすれが大。
・離型性
内径5cm×5cm、深さ5mmであり、底を鏡面仕上げした金型に、水で5倍希釈したシリコーンエマルジョン組成物を吹き付け、約350℃に予熱し、電気炉で約750℃で熔融させたアルミニウムの湯を該金型に注ぎ込み、除冷後、金型からアルミニウム片を引きはがし、はがれ程度で離型性を評価した。
○：型汚れ性良好
△：やや型汚れ性が悪い
×：型離れが困難
The general properties of Table 1 were investigated for the silicone emulsion compositions of Examples 1 and 2. Moreover, rust prevention property, paintability, and releasability were evaluated by the following methods.
・ Rust prevention
130ml of the silicone emulsion composition was placed in a 150ml glass bottle, 3 soft iron nails with a length of 3cm and a diameter of 2.5mm were submerged, and allowed to stand in an oven at 50 ° C for 48 hours.
○: No rusting.
Δ: Some rusting is slightly observed.
X: Rust is generated almost on the entire surface, and there is also rust settling.
・ Paintable The silicone emulsion composition is diluted 50 times with water, sprayed evenly on clay-coated paper using a simple spray gun, dried at room temperature, and using a ruler with oil-based thick ink magic ink etc. Paper was drawn at intervals, and the degree of faint lines was determined as follows.
○: There is no fading of the lines at all and the magic ink is uniformly attached.
(Triangle | delta): There is a slight blur of a line partially, and it has adhered slightly non-uniform magic ink.
×: The fading of the magic ink is large.
・ Releasability Inner diameter 5cm × 5cm, depth 5mm, mold with mirror finished bottom, sprayed with 5 times diluted silicone emulsion with water, preheated to about 350 ℃, about 750 ℃ in electric furnace The molten aluminum was poured into the mold, and after cooling, the aluminum piece was peeled off from the mold, and the releasability was evaluated by the degree of peeling.
○: Good mold stain △: Slightly poor mold stain ×: Difficult to separate
また全ての実施例、比較例について下記に示す方法で各種特性を評価した。また平均粒子径はコロイドミルのミルギャップ値及び加圧窒素量を調整する事で制御した。
・泡切れ性
200gの組成物を泡立て、250CCとしたものを300CCのガラス瓶に入れ、25℃に室内に1日3日放置し、その泡切れ性を見た。
泡切れ性を、以下に示す基準によりチェックした。
（評価基準）
◎ ：５時間以内
○ ：２４時間以内
× ：３日以内
××：３以上
・機械安定性
シリコーンエマルジョン組成物を有効成分濃度が1.0%になるように水で希釈し、次いで、この希釈液300gを底面積約55cm2の500mlビーカーに入れ、ホモミキサーを用い8000rpmの回転速度で10分間撹拌した。その間、希釈液の泡立ちに伴い、ジーイー東芝シリコーン（株）製消泡剤TSA772（下記式で表されるシリコーンオイルＣ、シリコーンオイルＤ及び二酸化珪素粉をベースとする有効成分25%のシリコーンエマルジョン）を添加し（添加量：水で2倍に希釈した消泡剤液を希釈液300gに対して80ppm量添加）、泡消しを行った。その後、希釈液表面の泡が完全に消えるまでビーカーを静置し、泡が消えた時点のエマルジョンの状態を目視にて測定し、以下に示す判断基準により評価した。
Moreover, various characteristics were evaluated by the method shown below about all the Examples and the comparative examples. The average particle size was controlled by adjusting the mill gap value of the colloid mill and the amount of pressurized nitrogen.
・ Fabricity
200 g of the composition was foamed and 250 CC was put into a 300 CC glass bottle and left in a room at 25 ° C. for 3 days a day, and the foaming property was observed.
The defoaming property was checked according to the following criteria.
(Evaluation criteria)
◎: Within 5 hours ○: Within 24 hours ×: Within 3 days XX: 3 or more • Machine stability The silicone emulsion composition is diluted with water so that the active ingredient concentration is 1.0%, and then 300 g of this diluted solution Was placed in a 500 ml beaker having a bottom area of about 55 cm 2 and stirred for 10 minutes at a rotation speed of 8000 rpm using a homomixer. Meanwhile, anti-foaming agent TSA772 manufactured by GE Toshiba Silicone Co., Ltd. (silicone emulsion of 25% active ingredient based on silicone oil C, silicone oil D and silicon dioxide powder represented by the following formula) accompanied with foaming of the diluent Was added (addition amount: 80 ppm amount of antifoam solution diluted twice with water with respect to 300 g of the diluted solution) to eliminate bubbles. Thereafter, the beaker was allowed to stand until the bubbles on the surface of the diluent completely disappeared, and the state of the emulsion when the bubbles disappeared was visually measured and evaluated according to the following criteria.
（評価基準）
◎ ：液表面に干渉膜がなくオイル浮きほとんど認められなかった。
○ ：液表面に僅かな干渉膜もしくは底面積の１％未満に相当するオイル状物の浮きが認められた。
△ ：液表面に干渉膜もしくは底面積の１〜５％未満に相当するオイル状物浮きが認められた。
× ：底面積の５〜３０％未満に相当するオイル状物浮きが認められた。
××：底面積の３０％以上に相当するオイル状物浮きが認められた。
・保存安定性
300mlの寸胴のガラス瓶に底から液面の高さが100mmとなるようにシリコーンエマルジョン組成物を入れ、50℃オーブンに4週間静置し、水層、油層の分離あるいは凝固物の発生の有無等を確認した。
（評価基準）
◎：油の分離、表層のクリーミングがなく、排水分離による底部の水層の発生が０〜１mm未満
○：油の分離、表層のクリーミングがなく、排水分離による底部の水層の発生が１〜2mm未満
△：油の分離、表層のクリーミングがなく、排水分離による底部の水層の発生が2〜5mm未満
×：油の分離、表層のクリーミング、排水分離による底部の水層の発生が５mm以上の少なくともいずれか一つが発生
・コンパクト性
シリコーン成分含効率からコンパクト性を以下の基準で判断した。
◎：60〜80％
○：40〜60％
×：10〜40％
これらの結果をシリコーンエマルジョン組成物の組成とともに表２〜４に示す。
(Evaluation criteria)
A: There was no interference film on the liquid surface, and almost no oil floated.
○: A slight interference film on the liquid surface or an oily substance corresponding to less than 1% of the bottom area was observed to float.
Δ: An interference film or an oily substance floating corresponding to less than 1 to 5% of the bottom area was observed on the liquid surface.
X: Oily substance floating corresponding to less than 5 to 30% of the bottom area was observed.
Xx: Oily substance floating corresponding to 30% or more of the bottom area was observed.
・ Storage stability
Put the silicone emulsion composition in a glass bottle with a 300ml cylinder so that the liquid level is 100mm from the bottom, and leave it in an oven at 50 ℃ for 4 weeks. It was confirmed.
(Evaluation criteria)
◎: No oil separation or surface creaming, generation of bottom water layer by drainage separation is less than 0 to 1 mm ○: No oil separation, surface layer creaming, bottom water layer generation by drainage separation 1 Less than 2mm △: No oil separation or surface creaming, generation of bottom water layer by drainage separation is less than 2-5mm ×: Oil separation, surface creaming, bottom water layer generation by drainage separation is 5mm or more Generation of at least one of the above and compactness Compactness was judged from the silicone component content efficiency according to the following criteria.
A: 60-80%
○: 40-60%
×: 10-40%
These results are shown in Tables 2 to 4 together with the composition of the silicone emulsion composition.
表から明らかなように各実施例のシリコーンエマルジョン組成物は保存安定性の良好なエマルジョンであった。 As is clear from the table, the silicone emulsion composition of each example was an emulsion having good storage stability.
Claims (4)
（Ｂ）下記式（１）で示されるアルキレンオキサイド誘導体１〜13重量部を配合したことを特徴とするシリコーンエマルジョン組成物。
R1O-[（AO）m（EO）n]-R2 （１）
（式中、AOは炭素数３〜４のオキシアルキレン基、EOはオキシエチレン基、ｍおよびｎはそれぞれ前記オキシアルキレン基、オキシエチレン基の平均付加モル数で、０≦ｍ≦25、４≦ｎ≦100、３ｍ≦ｎである。炭素数３〜４のオキシアルキレン基、オキシエチレン基はブロック状に付加してもランダム状に付加してもよい。R1、R2は、同一もしくは異なっていてもよい炭素数１〜４の炭化水素基又は水素原子である。） (A) (A-1) Organopolysiloxane having an average degree of polymerization of 5 to 1000; 40 to 60% by weight, (A-2) surfactant; 12 to 20% by weight based on the organopolysiloxane of (A-1) %, (A-3) water; 100 parts by weight of an emulsified emulsion composition having a particle size of 100 to 300 nm, with the balance being the main constituent,
(B) A silicone emulsion composition comprising 1 to 13 parts by weight of an alkylene oxide derivative represented by the following formula (1).
R 1 O-[(AO) m (EO) n ] -R 2 (1)
(In the formula, AO is an oxyalkylene group having 3 to 4 carbon atoms, EO is an oxyethylene group, m and n are average addition moles of the oxyalkylene group and oxyethylene group, and 0 ≦ m ≦ 25, 4 ≦ n ≦ 100 and 3m ≦ n The oxyalkylene group and oxyethylene group having 3 to 4 carbon atoms may be added in a block shape or in a random shape, and R 1 and R 2 may be the same or different. It is a C1-C4 hydrocarbon group or hydrogen atom that may be present.)
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006182882A (en) * | 2004-12-27 | 2006-07-13 | Ge Toshiba Silicones Co Ltd | Silicone emulsion composition and releasing agent |
| JP2013079298A (en) * | 2011-10-01 | 2013-05-02 | Nof Corp | Asphalt mixture adhesion preventing agent |
| JP2013087164A (en) * | 2011-10-14 | 2013-05-13 | Nof Corp | Antiadhesive agent for asphalt mixture |
| JP2013185018A (en) * | 2012-03-06 | 2013-09-19 | Nof Corp | Anti-adhesive agent for asphalt mixture |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01301757A (en) * | 1988-05-30 | 1989-12-05 | Shin Etsu Chem Co Ltd | Silicon emulsion composition |
| JPH10306020A (en) * | 1997-03-04 | 1998-11-17 | Shiseido Co Ltd | Emulsion composition |
| JPH11148012A (en) * | 1997-11-17 | 1999-06-02 | Shin Etsu Chem Co Ltd | Silicone emulsion |
| JP2001139449A (en) * | 1999-11-15 | 2001-05-22 | Shiseido Co Ltd | Water-in-oil type emulsified cosmetic of low viscosity having high water-phase content |
| JP2002069189A (en) * | 2000-08-24 | 2002-03-08 | Ge Toshiba Silicones Co Ltd | Polyorganosiloxane emulsion and cosmetics containing the same |
| JP2002188055A (en) * | 2000-12-20 | 2002-07-05 | Ge Toshiba Silicones Co Ltd | Silicon emulsion |
| JP2002363408A (en) * | 2001-06-04 | 2002-12-18 | Shin Etsu Chem Co Ltd | Method for producing organopolysiloxane emulsion |
| JP2003275845A (en) * | 2002-03-25 | 2003-09-30 | Ge Toshiba Silicones Co Ltd | Emulsion composition for aluminum diecast releasing |
| JP2006182882A (en) * | 2004-12-27 | 2006-07-13 | Ge Toshiba Silicones Co Ltd | Silicone emulsion composition and releasing agent |
-
2004
- 2004-12-27 JP JP2004376851A patent/JP4717435B2/en active Active
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01301757A (en) * | 1988-05-30 | 1989-12-05 | Shin Etsu Chem Co Ltd | Silicon emulsion composition |
| JPH10306020A (en) * | 1997-03-04 | 1998-11-17 | Shiseido Co Ltd | Emulsion composition |
| JPH11148012A (en) * | 1997-11-17 | 1999-06-02 | Shin Etsu Chem Co Ltd | Silicone emulsion |
| JP2001139449A (en) * | 1999-11-15 | 2001-05-22 | Shiseido Co Ltd | Water-in-oil type emulsified cosmetic of low viscosity having high water-phase content |
| JP2002069189A (en) * | 2000-08-24 | 2002-03-08 | Ge Toshiba Silicones Co Ltd | Polyorganosiloxane emulsion and cosmetics containing the same |
| JP2002188055A (en) * | 2000-12-20 | 2002-07-05 | Ge Toshiba Silicones Co Ltd | Silicon emulsion |
| JP2002363408A (en) * | 2001-06-04 | 2002-12-18 | Shin Etsu Chem Co Ltd | Method for producing organopolysiloxane emulsion |
| JP2003275845A (en) * | 2002-03-25 | 2003-09-30 | Ge Toshiba Silicones Co Ltd | Emulsion composition for aluminum diecast releasing |
| JP2006182882A (en) * | 2004-12-27 | 2006-07-13 | Ge Toshiba Silicones Co Ltd | Silicone emulsion composition and releasing agent |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006182882A (en) * | 2004-12-27 | 2006-07-13 | Ge Toshiba Silicones Co Ltd | Silicone emulsion composition and releasing agent |
| JP2013079298A (en) * | 2011-10-01 | 2013-05-02 | Nof Corp | Asphalt mixture adhesion preventing agent |
| JP2013087164A (en) * | 2011-10-14 | 2013-05-13 | Nof Corp | Antiadhesive agent for asphalt mixture |
| JP2013185018A (en) * | 2012-03-06 | 2013-09-19 | Nof Corp | Anti-adhesive agent for asphalt mixture |
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