JPH01181739A - Mold release agent - Google Patents
Mold release agentInfo
- Publication number
- JPH01181739A JPH01181739A JP63006584A JP658488A JPH01181739A JP H01181739 A JPH01181739 A JP H01181739A JP 63006584 A JP63006584 A JP 63006584A JP 658488 A JP658488 A JP 658488A JP H01181739 A JPH01181739 A JP H01181739A
- Authority
- JP
- Japan
- Prior art keywords
- mold release
- release agent
- lecithin
- water
- fractionation
- 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.)
- Granted
Links
- 239000006082 mold release agent Substances 0.000 title claims abstract description 39
- 235000010445 lecithin Nutrition 0.000 claims abstract description 30
- 239000000787 lecithin Substances 0.000 claims abstract description 30
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims abstract description 29
- 229940067606 lecithin Drugs 0.000 claims abstract description 29
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims abstract description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- 108090000790 Enzymes Proteins 0.000 claims abstract description 16
- 102000004190 Enzymes Human genes 0.000 claims abstract description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000005194 fractionation Methods 0.000 claims abstract description 11
- 238000011282 treatment Methods 0.000 claims abstract description 10
- 238000005805 hydroxylation reaction Methods 0.000 claims abstract description 5
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 4
- 230000033444 hydroxylation Effects 0.000 claims abstract description 4
- 239000012528 membrane Substances 0.000 claims abstract description 4
- 238000005904 alkaline hydrolysis reaction Methods 0.000 claims description 3
- 239000007921 spray Substances 0.000 abstract description 17
- 238000000034 method Methods 0.000 abstract description 8
- 239000003925 fat Substances 0.000 abstract description 5
- 239000000839 emulsion Substances 0.000 abstract description 4
- 239000003513 alkali Substances 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 229940088598 enzyme Drugs 0.000 description 14
- 239000007789 gas Substances 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000003380 propellant Substances 0.000 description 10
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- 229940083466 soybean lecithin Drugs 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 description 5
- 244000068988 Glycine max Species 0.000 description 5
- 235000010469 Glycine max Nutrition 0.000 description 5
- 102000015439 Phospholipases Human genes 0.000 description 5
- 108010064785 Phospholipases Proteins 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 235000008429 bread Nutrition 0.000 description 5
- 240000002791 Brassica napus Species 0.000 description 4
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000443 aerosol Substances 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 235000013305 food Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- -1 propylene glycol unsaturated fatty acid ester Chemical class 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 102000002322 Egg Proteins Human genes 0.000 description 3
- 108010000912 Egg Proteins Proteins 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 235000013345 egg yolk Nutrition 0.000 description 3
- 210000002969 egg yolk Anatomy 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 235000015067 sauces Nutrition 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 235000013311 vegetables Nutrition 0.000 description 3
- JQWAHKMIYCERGA-UHFFFAOYSA-N (2-nonanoyloxy-3-octadeca-9,12-dienoyloxypropoxy)-[2-(trimethylazaniumyl)ethyl]phosphinate Chemical compound CCCCCCCCC(=O)OC(COP([O-])(=O)CC[N+](C)(C)C)COC(=O)CCCCCCCC=CCC=CCCCCC JQWAHKMIYCERGA-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000003915 liquefied petroleum gas Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000011837 pasties Nutrition 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 150000004965 peroxy acids Chemical class 0.000 description 2
- 229960004063 propylene glycol Drugs 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000467686 Eschscholzia lobbii Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229940099578 hydrogenated soybean lecithin Drugs 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(a)産業上の利用分野
本発明は、特定のレシチンを水に分散させてなる離型剤
に関する。このものは噴射ガスを用いな(でも容易にス
プレーできるなどの利点がある。DETAILED DESCRIPTION OF THE INVENTION (a) Industrial Application Field The present invention relates to a mold release agent comprising a specific lecithin dispersed in water. This product has the advantage of not using propellant gas (but can be easily sprayed).
(b)従来の技術 離型剤は、食品用として、鉄板焼き用、製菓用。(b) Conventional technology Mold release agents are used for food, teppanyaki, and confectionery.
製パン用、天板用等に用いられる他、工業用として、ゴ
ム製品、プラスチック製品等に用いられている。そして
、これらの離型剤にはレシチンを用いることが知られて
いる。In addition to being used for bread making, baking sheets, etc., it is also used for industrial purposes such as rubber products and plastic products. It is known that lecithin is used as a mold release agent.
例えば、鉄板焼き用油として、スパッタリング現象抑制
の目的で植物性液状油にレシチンとプロピレングリコー
ル不飽和脂肪酸エステルを添加、溶解することを特徴と
する方法(特開昭54−103405号公報)、食用油
脂にレシチンとポリグリセリン脂肪酸エステル単独また
は、ポリグリセリン脂肪酸エステルと他の乳化剤を組み
合わせて配合することを特徴とする方法(特開昭62−
181738号公報)等がある。For example, as an oil for teppanyaki, a method characterized by adding and dissolving lecithin and propylene glycol unsaturated fatty acid ester in vegetable liquid oil for the purpose of suppressing sputtering phenomenon (Japanese Patent Application Laid-open No. 103405/1983), A method characterized by blending lecithin and polyglycerin fatty acid ester alone or in combination with polyglycerin fatty acid ester and other emulsifiers in oil and fat (JP-A-1982-1999)
181738), etc.
一方、これらの離型剤をスプレーする方法としては、ポ
ンプスプレーによるもの(非エアゾル型)、噴射ガスを
用いるもの(エアゾル型)などがあるが、従来のレシチ
ンを配合した離型剤はいずれもレシチンを油脂に溶解し
たものであり、油脂の粘度が高いため、ポンプスプレー
ではスプレー性が悪く、殆どの場合、噴射ガスを用いる
方法が採用されていた。即ちこれは離型剤を圧力容器に
入れ、フロンガス、液化石油ガス、亜酸化窒素ガス、窒
素ガス、炭酸ガス等のガスを封入する方法である。On the other hand, there are methods for spraying these mold release agents, such as pump spray (non-aerosol type) and propellant gas (aerosol type), but conventional mold release agents containing lecithin do not Lecithin is dissolved in oil and fat, and because the oil has a high viscosity, it has poor sprayability with a pump spray, and in most cases, a method using propellant gas has been adopted. That is, this is a method in which a mold release agent is placed in a pressure vessel and a gas such as chlorofluorocarbon gas, liquefied petroleum gas, nitrous oxide gas, nitrogen gas, or carbon dioxide gas is sealed therein.
(C)発明が解決しようとする課題
しかし、噴射ガス使用にあたっては、食品用途の場合は
、スプレー効果の他、食品衛生上、法規上、さらには安
全上の配慮が必要であり、これまで十分納得のゆくもの
は見出されていない。例えば、噴射ガスとして液化石油
ガスを用いた場合、この離型剤を火気のある場所で使用
すると火災の危険を伴う。(C) Problems to be solved by the invention However, when using propellant gas for food applications, in addition to the spray effect, consideration must be given to food hygiene, legal regulations, and safety. Nothing satisfactory has been found. For example, when liquefied petroleum gas is used as the propellant gas, there is a risk of fire if this mold release agent is used in a place with open flames.
また、工業用途の場合、圧力容器充填タイプのスプレー
式離型剤は、コスト面で不利であるばかりでなく、安価
な工業用スプレー式離型剤は、トルエン等の溶剤を使っ
ている場合が多(、作業者にとって有害であった。Furthermore, in the case of industrial applications, spray mold release agents filled in pressure vessels are not only disadvantageous in terms of cost, but also inexpensive industrial spray mold release agents often use solvents such as toluene. It was harmful to the workers.
スプレー性を改善するために、従来の離型剤に水を添加
し乳液タイプにしたものも試みられているが、この製品
を熱フライパンや熱鉄板上に噴射すると、水の飛びばね
が起こり、危険である等の欠点があった。In order to improve sprayability, attempts have been made to add water to conventional mold release agents to create an emulsion type, but when this product is sprayed onto a hot frying pan or hot iron plate, water splashes and springs occur. It had drawbacks such as being dangerous.
(d)課題を解決するための手段
本発明の口約は、噴射ガスを用いることなく容易にスプ
レーでき、しかも十分良好な離型効果を示す、安全で風
味の良い離型剤を提供することにある。(d) Means for Solving the Problems The purpose of the present invention is to provide a safe and flavorful mold release agent that can be easily sprayed without using propellant gas and exhibits a sufficiently good mold release effect. It is in.
本発明者らは鋭意研究の結果、水に分散可能なレシチン
を調製し、これを水に分散させれば、上記の目的が達成
されることを見い出し、これに基づいて本発明を完成し
た。As a result of intensive research, the present inventors found that the above object could be achieved by preparing water-dispersible lecithin and dispersing it in water, and based on this, completed the present invention.
即ち本発明は水に分散可能な動植物レシチンと水とから
なる離型剤に係るものである。That is, the present invention relates to a mold release agent comprising water and animal/vegetable lecithin that is dispersible in water.
、゛ 上記の水に分散可能な動植物レシチンとは、例え
ば卵黄、牛脳、大豆、菜種等のレシチンを原料とし、こ
れにアルコール分別、アセトン分別、膜分別、酵素処理
、ヒドロキシル化、アルカリ加水分解、および水素添加
から選ばれる一種または二種以上の工程、望ましくは酵
素処理を含む工程を経て製造される動植物レシチンであ
る。,゛ The above-mentioned water-dispersible animal and plant lecithin is made from lecithin from egg yolk, cow brain, soybean, rapeseed, etc., and is subjected to alcohol fractionation, acetone fractionation, membrane fractionation, enzyme treatment, hydroxylation, and alkaline hydrolysis. , and hydrogenation, preferably including enzyme treatment.
なお、上記の原料は、これらに限定されるものではない
。Note that the above raw materials are not limited to these.
また、アルコール分別、アセトン分別、膜分別。Also, alcohol separation, acetone separation, membrane separation.
酵素処理、ヒドロキシル化、アルカリ加水分解。Enzyme treatment, hydroxylation, alkaline hydrolysis.
水素添加の各工程は、いずれも常法によって行うことが
でき、なんら特別の手段は必要としない。Each step of hydrogenation can be carried out by conventional methods and does not require any special means.
酵素処理工程で用いる酵素は、リパーゼ、ホスホリパー
ゼ等の加水分解酵素であり、この処理によって、動植物
レシチンの水分散能は著しく高まる。本発明においては
、従ってこの酵素処理工程の採用が望ましい。もっとも
その他の工程のうち少なくとも一種を経て得られるレシ
チンであれば、本発明の目的を達することができるので
、酵素処理工程は必須ではない。The enzyme used in the enzyme treatment step is a hydrolytic enzyme such as lipase or phospholipase, and this treatment significantly increases the water dispersibility of animal and plant lecithin. Therefore, in the present invention, it is desirable to adopt this enzyme treatment step. However, as long as the lecithin is obtained through at least one of the other steps, the purpose of the present invention can be achieved, so the enzyme treatment step is not essential.
なお、レシチンの他、合成乳化剤を配合することも可能
であるが、本発明で用いる水分散性レシチンは十分な離
型効果を持っているので、単独で水に分散させて用いる
ことの方が望ましい。また、若干の油分添加も可能だが
、例えば食品用途としてフライパン上の飛びはね、スプ
レー性、低カロリー性などを考慮した場合には、50%
以下、望ましくは10%以下が良い。In addition to lecithin, it is also possible to blend a synthetic emulsifier, but since the water-dispersible lecithin used in the present invention has a sufficient mold release effect, it is better to use it alone by dispersing it in water. desirable. It is also possible to add a small amount of oil, but for example, when considering splashing on frying pans, sprayability, low calorie properties, etc. for food applications, 50%
It is preferably 10% or less.
本発明の離型剤はプロペラ攪拌、ホモミキサー攪拌等に
より、レシチンを水に0.1〜50χ、望ましくは0.
1〜35χ分散させることによって製造することができ
る。The mold release agent of the present invention is prepared by adding lecithin to water by 0.1 to 50x, preferably 0.1 to 50x, by stirring with a propeller or a homomixer.
It can be manufactured by dispersing 1 to 35χ.
このもののスプレーに当たっては、とくに噴射ガスを必
要としないので、ハンドスプレー等のポンプスプレー式
の非エアゾル型容器に充填して使用することができる。Since no particular propellant gas is required for spraying this product, it can be used by filling a pump spray type non-aerosol type container such as a hand sprayer.
なお、この離型剤を、噴射ガスを用いるエアゾル型容器
に充填することは何ら差し支えなく、本発明はそのよう
な形態を排除するものではない。Note that there is no problem in filling this mold release agent into an aerosol type container using a propellant gas, and the present invention does not exclude such a form.
(e)実施例
実施例1
表−1に示した組成を有し、ハンドスプレー容器に充填
した離型剤は、スプレーの広がり、粒子の細かさとも良
好でフライパン上のはねかえりもほとんどなかった。ま
た、火気に向かって噴射しても、安全で、全く問題がな
かった。(e) Examples Example 1 The mold release agent having the composition shown in Table 1 and filled in a hand spray container had good spray spread and particle fineness, and had almost no splashing on the frying pan. Moreover, it was safe and there were no problems even when sprayed into fire.
表−1
なお粉末状酵素処理大豆レシチンの製造法は以下のとお
りである。Table 1 The method for producing powdered enzyme-treated soybean lecithin is as follows.
ペースト状大豆レシチンから溶剤を用いてトリグリセリ
ドを除去した粉末状大豆レシチン20gを温水180g
に分散させ、ホモミキサーで均一に懸濁する。IN水酸
化カリウム水溶液を適当量加えpHを8.0に調整し、
1M塩化カルシウム水溶液を0.2請l添加する。20g of powdered soybean lecithin, which is obtained by removing triglycerides from pasty soybean lecithin using a solvent, in 180g of warm water.
and homogeneously suspend using a homomixer. Add an appropriate amount of IN potassium hydroxide aqueous solution and adjust the pH to 8.0.
Add 0.2 liters of 1M calcium chloride aqueous solution.
50℃に加温後ホスホリパーゼAの酵素源とじて豚パン
クレアチン(和光純薬工業■製)を0.2g添加し、攪
拌しつつ反応を行う。反応中、適量のIN水酸化カリウ
ム水溶液を加えつつpHを8.0〜9.0に維持する。After heating to 50°C, the enzyme source of phospholipase A was removed, 0.2 g of pork pancreatin (manufactured by Wako Pure Chemical Industries, Ltd.) was added, and the reaction was carried out with stirring. During the reaction, the pH is maintained at 8.0 to 9.0 while adding an appropriate amount of IN potassium hydroxide aqueous solution.
8時間後に塩酸を加えpHを7.0にし反応を終了する
。After 8 hours, hydrochloric acid was added to adjust the pH to 7.0 to complete the reaction.
このものは酸価66、過酸化物価0、アセトン不溶分9
7χである。This product has an acid value of 66, a peroxide value of 0, and an acetone insoluble content of 9.
It is 7χ.
実施例2
表−2に示した組成を有し、ハンドスプレー容器に充填
した離型剤は、スプレーの広がり、粒子の細かさとも良
好で、フライパンのはねかえりもほとんどなかった。ま
た、火気に向かって噴出しても安全で、全く問題がなか
った。Example 2 A mold release agent having the composition shown in Table 2 and filled into a hand spray container had good spray spread and particle fineness, and almost no frying pan splashing. It was also safe to spray into fire, and there were no problems at all.
表−2
なお、ペースト状酵素処理大豆レシチンの製造法は以下
のとおりである。Table 2 The method for producing paste-like enzyme-treated soybean lecithin is as follows.
ペースト状レシチン40gを温水160gに分散させ、
ホモ、ミキサーで乳化する。IN水酸化ナトリウム水溶
液を、適量加え、pHを8.0に調整し、1n塩化力゛
N、−
ルシウム水溶液を0.2w+1添加する。50℃に加温
後ホスホリパーゼA(ノボインダストリー社製 レシタ
ーゼl0L) 0.02m1を添加し、攪拌しつつ反応
を行う。反応中、適量の水酸化ナトリウム水溶液を添加
しつつ、pHを8.0〜9.0に維持する。6時間後適
当量の塩酸を加えpHを7.0に調整し、反応を停止す
る。濃縮・乾燥を行い18gの酵素処理レシチンを得る
。Disperse 40g of paste lecithin in 160g of warm water,
Homo, emulsify with a mixer. Add an appropriate amount of IN sodium hydroxide aqueous solution to adjust the pH to 8.0, and add 0.2w+1 of 1N chloride aqueous solution. After heating to 50° C., 0.02 ml of phospholipase A (Lecitase 10L, manufactured by Novo Industries) is added, and the reaction is carried out with stirring. During the reaction, the pH is maintained at 8.0 to 9.0 while adding an appropriate amount of aqueous sodium hydroxide solution. After 6 hours, an appropriate amount of hydrochloric acid is added to adjust the pH to 7.0 to stop the reaction. Concentration and drying are performed to obtain 18 g of enzyme-treated lecithin.
このものは酸価65、過酸化物価O、アセトン不溶分5
5にである。This product has an acid value of 65, a peroxide value of O, and an acetone insoluble content of 5.
It's on 5th.
実施例3
表−3に示した組成を有し、ハンドスプレー容器に充填
した離型剤は、スプレーの広がり、粒子の細かさとも良
好で、フライパンのはねかえりもほとんどなかった。ま
た、火気に向かって噴射しても安全で、全(問題がなか
った。Example 3 The mold release agent having the composition shown in Table 3 and filled into a hand spray container had good spray spread and particle fineness, and almost no frying pan splashing. It is also safe to spray into fire, and there were no problems.
表−3
なお、アセトン分別処理卵黄レシチンの製造法は以下の
とおりである。Table 3 The method for producing acetone fractionated egg yolk lecithin is as follows.
卵黄500gをヘキサン:エタノール=70:302.
5Kgに加え、ホモミキサーで1時間分散させた後静置
しヘキサン層をとる。脱溶剤して、卵黄油123gを得
た。このものにアセトン615gを加え、ホモミキサー
で30工程を2回繰り返した。その後5℃、24時間静
置し不溶部を得る。これを乾燥させてアセトン分別処理
卵黄レシチン34gを得た。500g of egg yolk was mixed with hexane:ethanol = 70:302.
In addition to 5 kg, the mixture was dispersed for 1 hour using a homomixer, then left to stand and a hexane layer was taken. The solvent was removed to obtain 123 g of egg yolk oil. 615 g of acetone was added to this mixture, and 30 steps were repeated twice using a homomixer. Thereafter, the mixture was allowed to stand at 5° C. for 24 hours to obtain an insoluble portion. This was dried to obtain 34 g of acetone fractionated egg yolk lecithin.
このものは、酸価16、過酸個物価0、アセトン不溶分
99%である。This product has an acid value of 16, a peracid content value of 0, and an acetone insoluble content of 99%.
実施例4
表−4に示した組成を有し、ハンドスプレー容器に充填
した離型剤を、製パン用型に噴霧塗布したところ、スプ
レー性は均一で良好であった。Example 4 When a mold release agent having the composition shown in Table 4 and filled in a hand spray container was sprayed onto a baking mold, the sprayability was uniform and good.
対照として市販の離型油(植物性液状油にレシチンとプ
ロピレン−グリコール不飽和脂肪酸エステルを添加、溶
解したもの。以下同様)をハンドスプレーに充填してス
プレーしようと試みたが、油の粒子は広がらず、線状に
噴出され、均一に塗布できなかった。As a control, I filled a hand sprayer with commercially available mold release oil (vegetable liquid oil with lecithin and propylene-glycol unsaturated fatty acid ester added and dissolved; the same applies hereinafter) and tried spraying it, but the oil particles It did not spread and was sprayed in a linear pattern, making it impossible to apply it evenly.
表−4
なお、アルコール分別酵素処理菜種レシチンの製造法は
以下のとおりである。Table 4 The method for producing alcohol-fractionated enzyme-treated rapeseed lecithin is as follows.
エタノール分画処理により得た精製高純度菜種レシチン
20gを温水180gに分散させ、ホモミキサーで均一
に懸濁する。 IN水酸化ナトリウム水溶液を適当量加
えpHを8.0に調整し、IM塩化カルシーウム水溶液
を0.2ml添加する。50℃に加温後ホスホリパーゼ
A(シグマ社製 ホスホリパーゼAi)を50+ig添
加し、攪拌しつつ反応を行う。反応中通量のIN水酸化
ナトリウム水溶液を加えつつ、pHを8.0〜9.0に
維持する。4時間後に塩酸を加え、pHを7.0にし反
応を停止してアルコール分別酵素処理菜種レシチン19
gを得る。20 g of purified high-purity rapeseed lecithin obtained by ethanol fractionation treatment is dispersed in 180 g of warm water and homogeneously suspended using a homomixer. Add an appropriate amount of IN aqueous sodium hydroxide solution to adjust the pH to 8.0, and add 0.2 ml of IM aqueous calcium chloride solution. After heating to 50° C., 50+ig of phospholipase A (phospholipase Ai, manufactured by Sigma) was added, and the reaction was carried out with stirring. The pH is maintained between 8.0 and 9.0 while adding the same amount of IN sodium hydroxide solution during the reaction. After 4 hours, hydrochloric acid was added to adjust the pH to 7.0 to stop the reaction, and alcohol fractionation and enzyme-treated rapeseed lecithin 19
get g.
このものは、酸価71、過酸個物価0、アセトン不溶分
98%である。This product has an acid value of 71, a peracid content value of 0, and an acetone insoluble content of 98%.
実施例5
表−5に示した組成を有し、ハンドスプレー容器に充填
した離型剤を、金型に噴霧塗布したところ、スプレー性
は均一で良好であった。Example 5 When a mold release agent having the composition shown in Table 5 and filled in a hand spray container was sprayed onto a mold, the sprayability was uniform and good.
表−5
なお、ヒドロキシル化水添大豆レシチンの製造法は以下
のとおりである。Table 5 The method for producing hydroxylated hydrogenated soybean lecithin is as follows.
ペースト状大豆レシチン3Kgを61のアセトンで3回
攪拌して、中性脂肪、脂肪酸等を除去して、主としてリ
ン脂質からなる沈澱物を得、乾燥する。3 kg of pasty soybean lecithin is stirred three times with 61 g of acetone to remove neutral fats, fatty acids, etc. to obtain a precipitate mainly consisting of phospholipids, which is then dried.
この高純度大豆レシチン(ヨウ素価85) 200gを
2倍量のヘキサンに溶解し、乳酸と過酸価水素を加え常
法によりヒドロキシル化反応を行い、ヒドロキシル化高
純度大豆レシチン(ヨウ素価33)を得た。Dissolve 200g of this high-purity soybean lecithin (iodine value 85) in twice the amount of hexane, add lactic acid and hydrogen peroxide value, and carry out a hydroxylation reaction using a conventional method to obtain hydroxylated high-purity soybean lecithin (iodine value 33). Obtained.
このちの300gを2倍量のベンゼン/エタノール=5
71に溶解し、22オートクレーブ中で、触媒として1
0χパラジウムカーボン2χ、水素圧20Kg /C1
1” 、温度50℃、・反応時間4時間の条件で水素添
加し、触媒を濾別後、溶剤を留去して、ヒドロキシル化
水素添加高純度大豆レシチン180g (ヨウ素価3)
を得た。Double the amount of benzene/ethanol for the next 300g = 5
71 as a catalyst in a 22 autoclave.
0χ palladium carbon 2χ, hydrogen pressure 20Kg/C1
1", temperature: 50°C, reaction time: 4 hours. After filtering off the catalyst, the solvent was distilled off to obtain 180 g of hydroxylated and hydrogenated high-purity soybean lecithin (iodine value: 3).
I got it.
実施例6
実施例1〜3の離型剤を用い、簿焼卵を焼き、フライパ
ンからの剥離性を評価した。フライパンは150℃に加
熱し、本発明の離型剤を均一にスプレーした。数秒加熱
することによって水分を蒸散させ、レシチンの極薄い膜
を作った後、卵液を入れて焼いた。Example 6 Using the mold release agents of Examples 1 to 3, hard-boiled eggs were fried, and the releasability from the frying pan was evaluated. The frying pan was heated to 150° C. and sprayed uniformly with the mold release agent of the present invention. After heating for a few seconds to evaporate the water and create an extremely thin film of lecithin, egg wash was added and baked.
対照として、フライパンに何も塗布しない場合および大
豆白絞油を塗布した場合についても同様の操作を行った
。As a control, the same operation was performed when nothing was applied to the frying pan and when soybean white squeezed oil was applied.
実施例1〜3の離型剤を用いた場合、および、大豆白絞
油を塗布した場合は、いずれも良好な剥離性を示したが
、何も塗布しない場合は、卵がフライパンにこびりつき
、はがすことができなかった。また繰り返し薄焼卵を焼
く際の作業性は大豆白絞油の場合に比べ、実施例1〜3
の場合の方がはるかに良好で簡便であった。When the mold release agents of Examples 1 to 3 were used and when soybean white squeezed oil was applied, both showed good releasability, but when nothing was applied, the eggs stuck to the frying pan, and I couldn't peel it off. In addition, the workability when repeatedly baking thinly baked eggs was higher than that in Examples 1 to 3 compared to using soybean white oil.
was much better and simpler.
実施例7
実施例1〜3の離型剤を用い、実施例6と同様にして、
市販のタレ付焼肉を焼いた(但しフライパンは200℃
に加熱した)。実施例1〜3の離型剤を用いた場合と、
大豆白絞油を塗布した場合は、タレによる若干のこげつ
きはあるものの、良好な剥離性を示したが、何も塗布し
ない場合は、肉全体がフライパンにこびりつき、はがす
ことができなかった。また、タレによるこげつきができ
た後、さらに離型剤を加えて肉を焼(とき、大豆白絞油
の場合に比べて、実施例1〜3の離型剤は、すぐれた離
型作用を示した。Example 7 Using the mold release agents of Examples 1 to 3, in the same manner as Example 6,
I grilled commercially available yakiniku with sauce (however, the frying pan was heated to 200℃).
). When using the mold release agents of Examples 1 to 3,
When soybean white squeezed oil was applied, good peelability was exhibited, although there was some scorching due to the sauce, but when nothing was applied, the entire meat stuck to the frying pan and could not be peeled off. In addition, when the meat is grilled by adding a mold release agent after the meat is charred by the sauce, the mold release agents of Examples 1 to 3 have a superior mold release effect compared to the case of soybean oil. Indicated.
実施例8
実施例4の離型剤を用い、表−6の処方でパンを焼いた
。なお生地は直埋法によって作り、200℃、40分間
で焼き上げた。Example 8 Using the mold release agent of Example 4, bread was baked according to the recipe shown in Table 6. The dough was made by the direct burying method and baked at 200°C for 40 minutes.
表−6
対照として焼型に何も塗布しない場合および市販の離型
油をハケで塗布した場合についても同様の操作で、パン
を焼いた。Table 6 As a control, bread was baked in the same manner in cases where nothing was applied to the baking mold and cases where commercially available mold release oil was applied with a brush.
実施例4の離型剤を用いる場合と、市販の離型油をハケ
で塗布した場合は型をさかさにし軽く衝激を与えるのみ
で、容易にパンを取り出すことができたが、何も塗布し
ない場合は、パンを取り出すことができなかった。また
、実施例4の離型剤は、市販の離型油をハケで塗る場合
に比べ、作業性が著しく優れており、大量生産にも適し
ていた。When using the mold release agent of Example 4 and when applying commercially available mold release oil with a brush, it was possible to easily take out the bread by simply inverting the mold and giving it a slight impact, but when nothing was applied If not, the bread could not be taken out. Furthermore, the mold release agent of Example 4 had significantly better workability than the case where commercially available mold release oil was applied with a brush, and was suitable for mass production.
実施例9
実施例5の離型剤をアルミニウム製の金型に噴霧塗布し
た後、数秒加熱して水を蒸散させ、レシチンのご(薄い
膜を作り、ここに樹脂を流し込む注形法により、スチレ
ン系樹脂を成型した。硬化後、固化物を取り出した。対
照として、レシチンをトルエンに5χ溶解させた離型剤
を用いてスチレン系樹脂を製造した。両者は、離型性に
差はなく、良好であった。しかし、対照品は激しいトル
エンの蒸散があって、作業者の労働環境上問題があるの
に対し、実施例5の離型剤を用いた場合は、環境を全く
汚染せず、作業を快適に行うことができた。Example 9 The mold release agent of Example 5 was sprayed onto an aluminum mold, heated for a few seconds to evaporate the water, and then molded with lecithin (a thin film was created and the resin was poured into it by a casting method). A styrene resin was molded. After curing, the solidified product was taken out. As a control, a styrene resin was manufactured using a mold release agent prepared by dissolving lecithin in toluene by 5x. There was no difference in mold release properties between the two. However, the control product caused severe toluene evaporation, which caused problems in the working environment of workers, whereas the mold release agent of Example 5 did not pollute the environment at all. I was able to work comfortably.
(f)発明の効果
本発明の離型剤はレシチンと水とからなっており、従来
のもののように油脂を含んでいない。そのため製品の粘
度が低く、と(に噴射ガスを用いたり、乳液の状態にし
なくてもスプレー適性の優れたものとなる。また粘度を
下げるために用いられていたトルエン、酢酸エチルなど
の溶剤も不要になる。従って本発明の離型剤は噴射ガス
、乳液タイプおよび溶剤の使用に伴う種々の欠点が排除
され、レシチンの離型効果を最大限に発揮できるという
利点を持っている。(f) Effects of the Invention The mold release agent of the present invention consists of lecithin and water and does not contain fats and oils unlike conventional agents. Therefore, the viscosity of the product is low, making it suitable for spraying without using propellant gas or making it into an emulsion. Also, solvents such as toluene and ethyl acetate, which were used to lower the viscosity, can be used. Therefore, the mold release agent of the present invention has the advantage of eliminating various drawbacks associated with the use of propellant gases, emulsion types, and solvents, and maximizing the mold release effect of lecithin.
Claims (2)
型剤。(1) A mold release agent consisting of water and animal and plant lecithin that is dispersible in water.
、アセトン分別、膜分別、酵素処理、ヒドロキシル化、
アルカリ加水分解および水素添加から選ばれる一種また
は二種以上の工程を経て得られるものである請求項1記
載の離型剤。(2) Animal and plant lecithins that are dispersible in water are subjected to alcohol fractionation, acetone fractionation, membrane fractionation, enzyme treatment, hydroxylation,
The mold release agent according to claim 1, which is obtained through one or more steps selected from alkaline hydrolysis and hydrogenation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63006584A JPH084448B2 (en) | 1988-01-13 | 1988-01-13 | Release agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63006584A JPH084448B2 (en) | 1988-01-13 | 1988-01-13 | Release agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01181739A true JPH01181739A (en) | 1989-07-19 |
JPH084448B2 JPH084448B2 (en) | 1996-01-24 |
Family
ID=11642374
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63006584A Expired - Fee Related JPH084448B2 (en) | 1988-01-13 | 1988-01-13 | Release agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH084448B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5587009A (en) * | 1995-06-12 | 1996-12-24 | Ecolab Inc. | Adhesive release agent applied to surface for improved cleaning |
EP1013265A2 (en) * | 1998-12-22 | 2000-06-28 | DIANORM G. Maierhofer GmbH | Skin care dispersion composition |
-
1988
- 1988-01-13 JP JP63006584A patent/JPH084448B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5587009A (en) * | 1995-06-12 | 1996-12-24 | Ecolab Inc. | Adhesive release agent applied to surface for improved cleaning |
EP1013265A2 (en) * | 1998-12-22 | 2000-06-28 | DIANORM G. Maierhofer GmbH | Skin care dispersion composition |
EP1013265A3 (en) * | 1998-12-22 | 2001-07-04 | DIANORM G. Maierhofer GmbH | Skin care dispersion composition |
Also Published As
Publication number | Publication date |
---|---|
JPH084448B2 (en) | 1996-01-24 |
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