JP2000119692A - Detergent for resin and cleaning method for resin discharging device - Google Patents
Detergent for resin and cleaning method for resin discharging deviceInfo
- Publication number
- JP2000119692A JP2000119692A JP10289451A JP28945198A JP2000119692A JP 2000119692 A JP2000119692 A JP 2000119692A JP 10289451 A JP10289451 A JP 10289451A JP 28945198 A JP28945198 A JP 28945198A JP 2000119692 A JP2000119692 A JP 2000119692A
- Authority
- JP
- Japan
- Prior art keywords
- component
- resin
- cleaning
- detergent
- compound
- 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.)
- Withdrawn
Links
- 229920005989 resin Polymers 0.000 title claims abstract description 62
- 239000011347 resin Substances 0.000 title claims abstract description 62
- 238000004140 cleaning Methods 0.000 title claims description 33
- 238000000034 method Methods 0.000 title claims description 13
- 239000003599 detergent Substances 0.000 title abstract description 25
- 238000007599 discharging Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 6
- 239000012459 cleaning agent Substances 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract description 5
- 125000002947 alkylene group Chemical group 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract 1
- 238000004821 distillation Methods 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 150000008282 halocarbons Chemical class 0.000 description 6
- 239000000499 gel Substances 0.000 description 5
- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 238000011109 contamination Methods 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229920002050 silicone resin Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 230000000779 depleting effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 2
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000002440 industrial waste Substances 0.000 description 2
- -1 organic acid esters Chemical class 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- ZIKLJUUTSQYGQI-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxypropoxy)propane Chemical compound CCOCC(C)OCC(C)OCC ZIKLJUUTSQYGQI-UHFFFAOYSA-N 0.000 description 1
- KIAMPLQEZAMORJ-UHFFFAOYSA-N 1-ethoxy-2-[2-(2-ethoxyethoxy)ethoxy]ethane Chemical compound CCOCCOCCOCCOCC KIAMPLQEZAMORJ-UHFFFAOYSA-N 0.000 description 1
- JONNRYNDZVEZFH-UHFFFAOYSA-N 2-(2-butoxypropoxy)propyl acetate Chemical compound CCCCOC(C)COC(C)COC(C)=O JONNRYNDZVEZFH-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- CKCGJBFTCUCBAJ-UHFFFAOYSA-N 2-(2-ethoxypropoxy)propyl acetate Chemical compound CCOC(C)COC(C)COC(C)=O CKCGJBFTCUCBAJ-UHFFFAOYSA-N 0.000 description 1
- IZZVHOPLTANRPW-UHFFFAOYSA-N 2-(2-propan-2-yloxyethoxy)ethyl acetate Chemical compound CC(C)OCCOCCOC(C)=O IZZVHOPLTANRPW-UHFFFAOYSA-N 0.000 description 1
- LEDYRHPAPPWTNW-UHFFFAOYSA-N 2-(2-propan-2-yloxypropoxy)propyl acetate Chemical compound C(C)(=O)OCC(OCC(C)OC(C)C)C LEDYRHPAPPWTNW-UHFFFAOYSA-N 0.000 description 1
- GWQAFGZJIHVLGX-UHFFFAOYSA-N 2-(2-propoxyethoxy)ethyl acetate Chemical compound CCCOCCOCCOC(C)=O GWQAFGZJIHVLGX-UHFFFAOYSA-N 0.000 description 1
- UFBBZQDFWTVNGP-UHFFFAOYSA-N 2-(2-propoxypropoxy)propyl acetate Chemical compound CCCOC(C)COC(C)COC(C)=O UFBBZQDFWTVNGP-UHFFFAOYSA-N 0.000 description 1
- SGQLKNKVOZVAAY-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethyl acetate Chemical compound CCCCOCCOCCOCCOC(C)=O SGQLKNKVOZVAAY-UHFFFAOYSA-N 0.000 description 1
- ZYTRLHRQWPTWNT-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propyl acetate Chemical compound CCCCOC(C)COC(C)COC(C)COC(C)=O ZYTRLHRQWPTWNT-UHFFFAOYSA-N 0.000 description 1
- NVSCAPMJFRYMFK-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethyl acetate Chemical compound CCOCCOCCOCCOC(C)=O NVSCAPMJFRYMFK-UHFFFAOYSA-N 0.000 description 1
- ZZHKLWVSWMWRFF-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]propane Chemical compound CCOCCOCCOC(C)C ZZHKLWVSWMWRFF-UHFFFAOYSA-N 0.000 description 1
- JDNLDGRWNMIHQC-UHFFFAOYSA-N 2-[2-(2-ethoxypropoxy)propoxy]propyl acetate Chemical compound CCOC(C)COC(C)COC(C)COC(C)=O JDNLDGRWNMIHQC-UHFFFAOYSA-N 0.000 description 1
- WZDMGBHDHARVNN-UHFFFAOYSA-N 2-[2-(2-propan-2-yloxyethoxy)ethoxy]ethyl acetate Chemical compound CC(C)OCCOCCOCCOC(C)=O WZDMGBHDHARVNN-UHFFFAOYSA-N 0.000 description 1
- XTXCPMSLGCQIHT-UHFFFAOYSA-N 2-[2-(2-propan-2-yloxypropoxy)propoxy]propyl acetate Chemical compound C(C)(=O)OCC(OCC(OCC(C)OC(C)C)C)C XTXCPMSLGCQIHT-UHFFFAOYSA-N 0.000 description 1
- ONPJEOPZOXVCDK-UHFFFAOYSA-N 2-[2-(2-propoxyethoxy)ethoxy]ethyl acetate Chemical compound CCCOCCOCCOCCOC(C)=O ONPJEOPZOXVCDK-UHFFFAOYSA-N 0.000 description 1
- GVNDORYZXGHHCM-UHFFFAOYSA-N 2-[2-(2-propoxypropoxy)propoxy]propyl acetate Chemical compound CCCOC(C)COC(C)COC(C)COC(C)=O GVNDORYZXGHHCM-UHFFFAOYSA-N 0.000 description 1
- IPJXGXLWHUYXCS-UHFFFAOYSA-N 2-[2-[2-(2-ethoxyethoxy)ethoxy]ethoxy]propane Chemical compound CCOCCOCCOCCOC(C)C IPJXGXLWHUYXCS-UHFFFAOYSA-N 0.000 description 1
- VQAJOWJEGHKRHX-UHFFFAOYSA-N CCOCC(C)OCC(C)OC(C)C Chemical compound CCOCC(C)OCC(C)OC(C)C VQAJOWJEGHKRHX-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Landscapes
- Details Or Accessories Of Spraying Plant Or Apparatus (AREA)
- Coating Apparatus (AREA)
- Detergent Compositions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、樹脂吐出装置のミ
キシング部およびノズル部などに付着した、未硬化状態
の2液硬化型樹脂成分を洗浄するための洗浄剤、及び該
洗浄剤を用いた樹脂吐出装置の洗浄方法に関するもので
ある。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cleaning agent for cleaning an uncured two-component curable resin component adhered to a mixing portion and a nozzle portion of a resin discharge device, and to use the cleaning agent. The present invention relates to a method for cleaning a resin discharge device.
【0002】[0002]
【従来の技術】従来、2液硬化型樹脂の吐出装置の洗浄
には、塩化メチレンなどのハロゲン化炭化水素類が用い
られていたが、ハロゲン化炭化水素類は、オゾン層を破
壊する原因物質として指摘され、その利用に大きく制限
があり、一部のハロゲン化炭化水素類は人体に対する安
全性に懸念がある。そのため、ハロゲン化炭化水素類の
代替洗浄剤として、セロソルブ類やカルビトール系溶剤
類、石油系炭化水素、N−メチル−2ピロリドン、有機
酸エステルなどを含む混合系洗浄剤などが用いられてい
る。2. Description of the Related Art Conventionally, halogenated hydrocarbons such as methylene chloride have been used for cleaning a two-part curable resin discharge device. Halogenated hydrocarbons are substances causing ozone layer destruction. It is pointed out that its use is greatly restricted, and some halogenated hydrocarbons are concerned about safety to the human body. For this reason, mixed detergents containing cellosolves, carbitol solvents, petroleum hydrocarbons, N-methyl-2-pyrrolidone, organic acid esters, and the like have been used as substitutes for halogenated hydrocarbons. .
【0003】[0003]
【発明が解決しようとする課題】ハロゲン化炭化水素類
の代替洗浄剤として、上記のごとき様々なものが使用さ
れているが、石油系炭化水素には引火点が低いものがあ
り、セロソルブ類やピロリドン系溶剤には人体への安全
性が懸念されるので、取扱いに注意を要する。また、こ
れらの洗浄剤を用いた洗浄後の廃液には、洗浄剤と汚染
物質である樹脂液とが混在している。従って、これらの
廃液は、通常、産業廃棄物として処理・回収されるが、
揮発性の高い洗浄剤を100%回収するのは難しく、一
部回収されずにそのまま大気中に放出される場合が多か
った。更に、上記ハロゲン化炭化水素代替洗浄剤は、特
定の樹脂、例えばシリコーン系樹脂に対する洗浄力が低
いという欠点がある。Various substitutes as described above have been used as substitutes for halogenated hydrocarbons. However, some petroleum hydrocarbons have low flash points, such as cellosolves and the like. The pyrrolidone-based solvent needs to be handled with care because there is concern about safety to the human body. Further, in the waste liquid after cleaning using these cleaning agents, the cleaning agent and the resin liquid as a contaminant are mixed. Therefore, these waste liquids are usually treated and collected as industrial waste,
It is difficult to recover 100% of a highly volatile cleaning agent, and in many cases, it is released to the atmosphere as it is without being partially recovered. Further, the above-mentioned halogenated hydrocarbon substitute cleaning agent has a drawback that the cleaning power for a specific resin, for example, a silicone resin is low.
【0004】本発明は、2液硬化型樹脂成分による汚染
に対する汎用の洗浄であって、シリコーン系等の2液硬
化型樹脂成分に対しても優れた洗浄力を発揮し得て、し
かも人体に対して安全で取扱も容易であり、オゾン層破
壊物質に該当しない洗浄剤を提供することを目的とす
る。[0004] The present invention is a general-purpose cleaning method against contamination by a two-component curable resin component, and can exert an excellent detergency on a two-component curable resin component such as a silicone resin. An object of the present invention is to provide a cleaning agent which is safe and easy to handle and does not correspond to an ozone depleting substance.
【0005】[0005]
【課題を解決するための手段】本発明は、この様な従来
の問題点に着目してなされたものであって、洗浄作用を
有する各種化合物の中から特定のグリコールエーテルと
そのアセテート化合物とを用いれば、シリコーン系を含
む広範囲の2液硬化型樹脂成分に対して洗浄力を発揮し
得ることを見出したことに基づき成し遂げられたもので
ある。DISCLOSURE OF THE INVENTION The present invention has been made in view of such conventional problems, and is intended to provide a specific glycol ether and its acetate compound among various compounds having a detergency. It has been accomplished based on the finding that, when used, a detergency can be exerted on a wide range of two-component curable resin components including silicones.
【0006】即ち、本願の樹脂用洗浄剤は、未硬化状態
の2液硬化型樹脂成分用の洗浄剤であって、該洗浄剤
が、以下の一般式(1):That is, the resin detergent of the present invention is a detergent for an uncured two-component curable resin component, and the detergent has the following general formula (1):
【0007】[0007]
【化3】 Embedded image
【0008】[式中、R1及びR3はそれぞれ独立に炭素
数1〜3のアルキル基、R2は水素原子またはメチル
基、nは2〜3の整数を表す]で示される(a)成分の
単一化合物からなることを特徴とする。Wherein R 1 and R 3 are each independently an alkyl group having 1 to 3 carbon atoms, R 2 is a hydrogen atom or a methyl group, and n is an integer of 2 to 3 (a) It is characterized by consisting of a single compound of the components.
【0009】この一般式(1)で表される化合物は、ウ
レタン樹脂、エポキシ樹脂の他、シリコーン系の2液硬
化型樹脂の未硬化状態の成分による汚染に対する洗浄性
にも優れており、且つ人体に対して安全で取扱も容易で
あって、オゾン層破壊物質に該当しない。そして、樹脂
吐出装置等における洗浄時にこの化合物が樹脂成分中に
混入しても、少量であれば樹脂の硬化阻害をもたらすこ
ともない。また、この洗浄剤は(a)成分の単一化合物
よりなるため、使用後の廃液を単に蒸留処理により回収
するだけで、上記用途に再利用が可能となるという利点
を有している。更に、この一般式(2)で表される
(a)成分の化合物は水酸基を分子内に含まないので、
樹脂吐出装置等における洗浄時にこの化合物が樹脂成分
中に混入しても樹脂の硬化に悪影響を与えることはな
い。The compound represented by the general formula (1) is excellent in cleaning properties against contamination by an uncured component of a silicone two-component curable resin in addition to urethane resin and epoxy resin, and It is safe for the human body and easy to handle, and does not fall under ozone depleting substances. Even if this compound is mixed into the resin component at the time of cleaning in a resin discharge device or the like, a small amount of the compound does not inhibit the curing of the resin. In addition, since this detergent is composed of a single compound of the component (a), it has the advantage that it can be reused for the above-mentioned applications simply by collecting waste liquid after use by distillation. Further, since the compound of the component (a) represented by the general formula (2) does not contain a hydroxyl group in the molecule,
Even if this compound is mixed into the resin component at the time of cleaning in a resin discharge device or the like, it does not adversely affect the curing of the resin.
【0010】また、本願の樹脂用洗浄剤は、上記(a)
成分に加えて、以下の一般式(2)[0010] Further, the resin detergent of the present invention comprises the above (a)
In addition to the components, the following general formula (2)
【0011】[0011]
【化4】 Embedded image
【0012】[式中、R1は炭素数2〜4のアルキル
基、R2は水素原子またはメチル基、nは2〜3の整数
を表す]で示される(b)成分を更に含有していてもよ
い。この一般式(2)で表される(b)成分の化合物も
水酸基を分子内に含まないので、樹脂吐出装置等におけ
る洗浄時にこの化合物が樹脂成分中に混入しても樹脂の
硬化に悪影響を与えることはない。Wherein R 1 is an alkyl group having 2 to 4 carbon atoms, R 2 is a hydrogen atom or a methyl group, and n is an integer of 2 to 3). You may. Since the compound of the component (b) represented by the general formula (2) also does not contain a hydroxyl group in the molecule, even if this compound is mixed into the resin component during cleaning in a resin discharge device or the like, it adversely affects the curing of the resin. I will not give.
【0013】上記(b)成分を併用する場合には、前記
(a)成分の含有量が50重量%以上100重量%未
満、前記(b)成分の含有量が0重量%より大きく50
重量%以下であることが好ましい。(a)成分及び
(b)成分の含有量がこの範囲を外れると、シリコーン
系樹脂等に対する洗浄力を発揮させることができず、洗
浄剤としての汎用性が低くなるので好ましくない。When the component (b) is used in combination, the content of the component (a) is 50% by weight or more and less than 100% by weight, and the content of the component (b) is more than 0% by weight and 50% by weight.
It is preferable that the content be not more than weight%. If the contents of the component (a) and the component (b) are out of this range, it is not preferable because the detergency for the silicone resin or the like cannot be exerted and the versatility as a detergent is reduced.
【0014】また、本発明の樹脂吐出装置の洗浄方法
は、2液硬化型樹脂の吐出装置のミキシング部およびノ
ズル部などに付着した、未硬化状態の2液硬化型樹脂成
分を洗浄するための方法であって、上記のいずれかの洗
浄剤を用いて樹脂吐出装置のミキシング部およびノズル
部などを洗浄するものである。この方法で洗浄を行え
ば、洗浄剤が2液硬化樹脂成分に混入しても樹脂の硬化
阻害などの悪影響を及ぼすことが少なく、従って、洗浄
剤の混入に対する特別の配慮を必要としない。Further, the method for cleaning a resin discharge device of the present invention is a method for cleaning an uncured two-component curable resin component adhered to a mixing portion and a nozzle portion of a two-liquid curable resin discharge device. A method for cleaning a mixing section, a nozzle section, and the like of a resin discharge device using any of the above-described cleaning agents. If the cleaning is carried out by this method, even if the detergent is mixed into the two-component cured resin component, adverse effects such as inhibition of curing of the resin are less likely to occur, and therefore, no special consideration is required for the mixing of the detergent.
【0015】[0015]
【発明の実施の形態】本発明の洗浄剤が適用対象とする
汚染物は、例えば、ウレタン系樹脂、エポキシ系樹脂、
シリコーン系樹脂などの2液硬化型樹脂成分である。BEST MODE FOR CARRYING OUT THE INVENTION Contaminants to which the cleaning agent of the present invention is applied include, for example, urethane resins, epoxy resins,
It is a two-component curable resin component such as a silicone resin.
【0016】本発明の洗浄剤によって、これらの未硬化
樹脂成分あるいは混合前の各樹脂成分が付着した、金属
部品、ガラス部品または、樹脂吐出装置のミキシング部
およびノズル部などを洗浄することができる。The cleaning agent of the present invention can clean metal parts, glass parts, mixing parts and nozzle parts of a resin discharge device to which these uncured resin components or each resin component before mixing adhere. .
【0017】本発明の洗浄剤に用いられる(a)成分の
化合物は、炭素数1〜3のアルキル基で両端を封鎖した
アルキレンオキシド、即ち、一般式(1)で示される化
合物である。かかる化合物として、具体的には、ジエチ
レングリコールジメチルエーテル、ジエチレングリコー
ルジエチルエーテル、トリエチレングリコールジメチル
エーテル、ジプロピレングリコールジメチルエーテル、
ジプロピレングリコールジエチルエーテル、ジプロピレ
ングリコールイソプロピルエチルエーテル、ジエチレン
グリコールイソプロピルエチルエーテル、トリエチレン
グリコールジエチルエーテル、トリエチレングリコール
イソプロピルエチルエーテル等が挙げられる。The compound of the component (a) used in the detergent of the present invention is an alkylene oxide whose both ends are blocked with an alkyl group having 1 to 3 carbon atoms, that is, a compound represented by the general formula (1). As such a compound, specifically, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, dipropylene glycol dimethyl ether,
Examples thereof include dipropylene glycol diethyl ether, dipropylene glycol isopropyl ethyl ether, diethylene glycol isopropyl ethyl ether, triethylene glycol diethyl ether, and triethylene glycol isopropyl ethyl ether.
【0018】これらの化合物を組み合わせて使用して
も、2液硬化型樹脂の未硬化状態の成分による汚染に対
する洗浄性、人体および環境への安全性に優れ、取扱が
容易であり、さらに、洗浄剤が樹脂成分中に混入しても
樹脂の硬化阻害をもたらす可能性が少ないという本発明
の利点は成し遂げられるが、蒸留回収による再利用可能
性に鑑み、これらを単独で用いることが好ましい。Even when these compounds are used in combination, the two-part curable resin has excellent detergency against contamination by uncured components, is excellent in safety to human bodies and the environment, is easy to handle, and is easy to handle. Although the advantage of the present invention that the possibility of inhibiting the curing of the resin is small even when the agent is mixed in the resin component is achieved, it is preferable to use these alone in view of the reusability by distillation recovery.
【0019】本発明の洗浄剤に用いられる(b)成分の
化合物は、炭素数2〜4のアルキル基およびアセチル基
で末端を封鎖したアルキレンオキシド、即ち、一般式
(2)で示される化合物である。かかる化合物として、
具体的にはジエチレングリコールモノエチルエーテルア
セテート、ジエチレングリコールモノプロピルエーテル
アセテート、ジエチレングリコールモノイソプロピルエ
ーテルアセテート、ジエチレングリコールモノブチルエ
ーテルアセテート、トリエチレングリコールモノエチル
エーテルアセテート、トリエチレングリコールモノプロ
ピルエーテルアセテート、トリエチレングリコールモノ
イソプロピルエーテルアセテート、トリエチレングリコ
ールモノブチルエーテルアセテート、ジプロピレングリ
コールモノエチルエーテルアセテート、ジプロピレング
リコールモノプロピルエーテルアセテート、ジプロピレ
ングリコールモノイソプロピルエーテルアセテート、ジ
プロピレングリコールモノブチルエーテルアセテート、
トリプロピレングリコールモノエチルエーテルアセテー
ト、トリプロピレングリコールモノプロピルエーテルア
セテート、トリプロピレングリコールモノイソプロピル
エーテルアセテート、トリプロピレングリコールモノブ
チルエーテルアセテートが挙げられる。The compound of component (b) used in the detergent of the present invention is an alkylene oxide whose terminal is blocked with an alkyl group having 2 to 4 carbon atoms and an acetyl group, that is, a compound represented by the general formula (2). is there. As such a compound,
Specifically, diethylene glycol monoethyl ether acetate, diethylene glycol monopropyl ether acetate, diethylene glycol monoisopropyl ether acetate, diethylene glycol monobutyl ether acetate, triethylene glycol monoethyl ether acetate, triethylene glycol monopropyl ether acetate, triethylene glycol monoisopropyl ether acetate , Triethylene glycol monobutyl ether acetate, dipropylene glycol monoethyl ether acetate, dipropylene glycol monopropyl ether acetate, dipropylene glycol monoisopropyl ether acetate, dipropylene glycol monobutyl ether acetate,
Examples thereof include tripropylene glycol monoethyl ether acetate, tripropylene glycol monopropyl ether acetate, tripropylene glycol monoisopropyl ether acetate, and tripropylene glycol monobutyl ether acetate.
【0020】上記一般式(1)に於いて、n=1の化合
物については引火点が低いため、洗浄時、蒸留時等の取
扱い上の安全性、人体への安全性等が懸念されるので好
ましくない。また、nが4以上の場合には洗浄性が劣る
ので好ましくない。アルキル基R1の炭素数が5以上に
なると、引火点は高くなるので人体への危険性や引火、
爆発などの可能性は低減されるが、洗浄性は低下してし
まうので好ましくない。その上、沸点も高くなるので、
単独で用いる場合には蒸留再生時に多大の負荷がかかる
ために好ましくない。成分(a)のみからなる場合、洗
浄剤を回収、再利用するための蒸留は、公知の常法に従
って、減圧蒸留法などにより、洗浄剤の成分である化合
物の沸点に鑑みて条件を適宜設定して行うとよい。In the above general formula (1), since the compound having n = 1 has a low flash point, there is concern about the safety in handling during washing, distillation, etc., the safety to the human body, and the like. Not preferred. On the other hand, when n is 4 or more, it is not preferable because the cleaning property is poor. When the number of carbon atoms in the alkyl group R 1 is 5 or more, the flash point becomes higher, which may cause danger to the human body,
Although the possibility of an explosion or the like is reduced, the cleaning property is reduced, which is not preferable. In addition, the boiling point will be higher,
When used alone, it is not preferable because a great load is applied at the time of regeneration by distillation. When only the component (a) is used, the distillation for recovering and reusing the detergent is carried out by a vacuum distillation method or the like according to a known ordinary method, and conditions are appropriately set in view of the boiling point of the compound which is a component of the detergent. It is good to do it.
【0021】上記一般式(2)に於いても、n=1の化
合物については引火点が低いため、洗浄時等の取扱い上
の安全性、人体への安全性等が懸念されるので好ましく
ない。また、nが4以上の場合には洗浄性が劣るので好
ましくない。In the above general formula (2), too, the compound having n = 1 has a low flash point, so that safety in handling at the time of washing and the like, safety to the human body, and the like are not preferred. . On the other hand, when n is 4 or more, it is not preferable because the cleaning property is poor.
【0022】本発明の洗浄剤を用いて洗浄を行う際に
は、当該洗浄液を常温で使用しても洗浄効果は得られる
が、場合により40℃程度まで加温したり、ブラッシン
グ、超音波などの物理的操作を併用することで洗浄性の
向上が期待できる。When cleaning is performed using the cleaning agent of the present invention, the cleaning effect can be obtained even when the cleaning liquid is used at room temperature. However, in some cases, the cleaning liquid is heated to about 40 ° C., brushing, ultrasonic waves, or the like. By using the physical operations described above in combination, it is expected that the cleaning property can be improved.
【0023】[0023]
【実施例】[実験例1]溶解性実験 2液硬化性樹脂であるウレタン系樹脂(第一工業製薬
(株)社製、エイムフレックスEF-243)、エポキシ系樹
脂(日本ペルノックス(株)社製、エポキシペルノック
スME)及びシリコーンゲル(日本ペルノックス(株)社
製、SE−8019H)のそれぞれの1mlを、表1に
示す配合比で調製した実施例および比較例の各洗浄剤1
00mlに加えて攪拌し、1分間攪拌した後室温で1日
放置後の溶解状態を観察した。溶解状態は目視にて評価
した。その結果を以下の表1に示す。EXAMPLES [Experimental Example 1] Solubility Experiment Urethane-based resin (Aimflex EF-243, manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) which is a two-pack curable resin, epoxy-based resin (Nippon Pernox Co., Ltd.) And Epoxy Pernox ME) and 1 ml each of a silicone gel (SE-8019H, manufactured by Nippon Pernox Co., Ltd.) were prepared at the compounding ratios shown in Table 1.
After stirring for 1 minute, the solution was allowed to stand at room temperature for 1 day, and the dissolved state was observed. The dissolution state was evaluated visually. The results are shown in Table 1 below.
【0024】[0024]
【表1】 [Table 1]
【0025】表1の実施例1〜3から明らかなように、
ジプロピレングリコールジメチルエーテル:ジエチレン
グリコールモノブチルエーテルアセテート=50:50
及び(a)成分のジプロピレングリコールジメチルエー
テルが50重量%より多い配合比では、ウレタン系樹
脂、エポキシ系樹脂のみならず、シリコーンゲルに対し
ても良好な洗浄性を示すことが分かる。また、実施例4
及び5から明らかなように、(a)成分であるジプロピ
レングリコールジメチルエーテル又はジエチレングリコ
ールジエチルエーテル単独の洗浄剤も、ウレタン系樹
脂、エポキシ系樹脂のみならず、シリコーンゲルに対し
て良好な洗浄性を示すことが分かる。As is clear from Examples 1 to 3 in Table 1,
Dipropylene glycol dimethyl ether: diethylene glycol monobutyl ether acetate = 50:50
Also, it can be seen that when the mixing ratio of the dipropylene glycol dimethyl ether of the component (a) is more than 50% by weight, good detergency is exhibited not only for urethane resins and epoxy resins, but also for silicone gels. Example 4
As is clear from FIGS. 5 and 5, the detergent of dipropylene glycol dimethyl ether or diethylene glycol diethyl ether alone as the component (a) also shows good detergency not only for urethane resins and epoxy resins but also for silicone gels. You can see that.
【0026】これに対して、モノエーテルを使用した比
較例1及び2では、特にシリコーンゲルに対する洗浄性
に劣ることが分かる。また、比較例3及び4の洗浄剤
は、(a)成分及び(b)成分を含んではいるものの、
(a)成分の比率が50重量%より小さいため、特にシ
リコーンゲルに対する洗浄性に劣っていることが分か
る。On the other hand, Comparative Examples 1 and 2 using the monoether are inferior in cleaning properties, especially for silicone gel. Further, although the detergents of Comparative Examples 3 and 4 contain the component (a) and the component (b),
Since the ratio of the component (a) is less than 50% by weight, it can be seen that the detergency to silicone gel is particularly poor.
【0027】[実験例2]洗浄性実験ディスペンサーを
使用し、実験例1で用いた2液性ウレタン樹脂成分の混
合および吐出を3秒に一回の割合で1時間行った後、表
2に示す実施例および比較例に係る各洗浄液を500m
l流し、ディスペンサー内部を洗浄した。洗浄後、樹脂
液輸送チューブ内を観察して、内部の残存物量から残存
状態を評価した。この結果を表2に示す。[Experimental Example 2] The two-liquid urethane resin component used in Experimental Example 1 was mixed and discharged at a rate of once every 3 seconds for one hour using a cleaning dispenser. Each cleaning liquid according to the example and the comparative example shown in FIG.
1 to wash the inside of the dispenser. After the washing, the inside of the resin liquid transport tube was observed, and the remaining state was evaluated based on the amount of the residue inside. Table 2 shows the results.
【0028】[0028]
【表2】 [Table 2]
【0029】表2より明らかなとおり、実施例1及び4
洗浄剤を用いると、2液性ウレタン樹脂成分の残存物量
が殆ど残らず、これらの洗浄剤の洗浄性は良好であるこ
とが分かる。これに対して、比較例1の洗浄剤では残存
物が多く、比較例5及び3の洗浄剤でも残存物が少し残
った。As is clear from Table 2, Examples 1 and 4
When a detergent is used, almost no residual amount of the two-component urethane resin component remains, which indicates that these detergents have good detergency. In contrast, the detergent of Comparative Example 1 had a large amount of residue, and the detergents of Comparative Examples 5 and 3 also had a small amount of residue.
【0030】[実験例3]硬化阻害性実験 2液性ウレタン樹脂(サンユレジン(株)社製UF-820)
の樹脂成分液(オリゴマー)15gに、表3に示す各洗
浄剤をそれぞれ樹脂に対して0.5重量%(75mg)
及び5重量%(750mg)となるように加え、1分間
攪拌後、60℃に加温して硬化させた後の樹脂の状態を
観察した。この結果を表3に示す。[Experimental Example 3] Curing inhibition test Two-part urethane resin (UF-820 manufactured by Sanyuresin Co., Ltd.)
Each of the detergents shown in Table 3 was added to 15 g of the resin component liquid (oligomer) in 0.5% by weight (75 mg) based on the resin.
And after stirring for 1 minute, heated to 60 ° C. and cured to observe the state of the resin. Table 3 shows the results.
【0031】[0031]
【表3】 [Table 3]
【0032】表3に示されるとおり、比較例に係る、分
子内に水酸基を持つアルコールやグリコールモノエーテ
ルに比べて、実施例6および4の洗浄剤は、樹脂の硬化
に対する影響が少なかった。従って、かなりの量が樹脂
成分に混入しても、本発明の洗浄剤が樹脂硬化の阻害を
もたらすことはないことが明らかになった。As shown in Table 3, the cleaning agents of Examples 6 and 4 had less influence on the curing of the resin than the alcohols and glycol monoethers having a hydroxyl group in the molecule according to Comparative Examples. Therefore, it has been clarified that even if a considerable amount is mixed in the resin component, the cleaning agent of the present invention does not cause inhibition of resin curing.
【0033】[0033]
【発明の効果】以上説明したように、本発明の樹脂用洗
浄剤は、2液硬化型樹脂の未硬化状態の成分による汚染
に対する洗浄性に優れている。また、人体に対して安全
で取扱も容易であって、オゾン層破壊物質に該当しな
い。そして、水酸基を分子内に含まない化合物を用いて
いるので、樹脂吐出装置等における洗浄時にこの化合物
が樹脂成分中に混入しても硬化阻害をもたらす可能性が
極めて少ない。As described above, the resin cleaner of the present invention is excellent in cleaning performance against contamination by the uncured components of the two-pack curable resin. In addition, it is safe for the human body and easy to handle, and does not fall under the category of ozone depleting substances. Further, since a compound containing no hydroxyl group in the molecule is used, there is very little possibility that curing inhibition will be caused even if this compound is mixed into a resin component during cleaning in a resin discharge device or the like.
【0034】また、本発明の成分(a)のみからなる洗
浄剤は、所定温度での蒸留を行うだけで洗浄剤を回収で
きるので、回収率は良好であり、係る蒸留処理に格段の
コストや設備を必要としない点において有利である。回
収された洗浄剤は元の洗浄剤と同等の洗浄効果を期待で
きるので反復使用も可能であり、従って、環境汚染の原
因となる産業廃棄物を減じることにつながる。Further, since the detergent comprising only the component (a) of the present invention can be recovered only by distillation at a predetermined temperature, the recovery rate is good, and the cost and cost for the distillation treatment are remarkable. This is advantageous in that no equipment is required. The recovered cleaning agent can be expected to have the same cleaning effect as the original cleaning agent, so that it can be used repeatedly, thus reducing the amount of industrial waste causing environmental pollution.
【0035】更に、本発明の洗浄剤は、2液硬化樹脂成
分に混入しても樹脂の硬化阻害などの悪影響を及ぼすこ
とないので、洗浄剤の混入に対する特別の配慮を必要と
しない。Further, since the cleaning agent of the present invention does not adversely affect the curing of the resin even when mixed into the two-component cured resin component, no special consideration is required for mixing the cleaning agent.
【0036】加えて、本発明の樹脂吐出装置の洗浄方法
によれば、上記の洗浄剤をもちるため、樹脂の吐出装置
のミキシング部およびノズル部などに付着した未硬化状
態の2液硬化型樹脂成分を効率よく洗浄することができ
る。In addition, according to the method for cleaning a resin discharge device of the present invention, since the above-mentioned cleaning agent is used, the uncured two-liquid curing type adhered to the mixing portion and the nozzle portion of the resin discharge device. The resin component can be efficiently washed.
Claims (3)
浄剤であって、該洗浄剤が、 以下の一般式(1): 【化1】 [式中、R1及びR3はそれぞれ独立に炭素数1〜3のア
ルキル基、R2は水素原子またはメチル基、nは2〜3
の整数を表す]で示される(a)成分の単一化合物から
なることを特徴とする洗浄剤。1. A cleaning agent for a two-component curable resin component in an uncured state, wherein the cleaning agent has the following general formula (1): [Wherein, R 1 and R 3 are each independently an alkyl group having 1 to 3 carbon atoms, R 2 is a hydrogen atom or a methyl group, and n is 2 to 3
Which represents an integer of the formula (a).
子またはメチル基、nは2〜3の整数を表す]で示され
る(b)成分を更に含有し、前記(a)成分の含有量が
50重量%以上100重量%未満、前記(b)成分の含
有量が0重量%より大きく50重量%以下であることを
特徴とする洗浄剤。2. A compound of the component (a) according to claim 1 and a compound represented by the following general formula (2): Wherein R 1 is an alkyl group having 2 to 4 carbon atoms, R 2 is a hydrogen atom or a methyl group, and n is an integer of 2 to 3). A) a cleaning agent, wherein the content of the component is 50% by weight or more and less than 100% by weight, and the content of the component (b) is more than 0% by weight and 50% by weight or less.
部およびノズル部などに付着した、未硬化状態の2液硬
化型樹脂成分を洗浄するための方法であって、請求項1
又は2に記載の洗浄剤を用いて該樹脂吐出装置のミキシ
ング部およびノズル部などを洗浄することを特徴とする
洗浄方法。3. A method for cleaning an uncured two-liquid curable resin component adhered to a mixing portion and a nozzle portion of a two-liquid curable resin discharge device, the method comprising:
Or a cleaning method for cleaning a mixing section, a nozzle section, and the like of the resin discharge device using the cleaning agent according to 2.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10289451A JP2000119692A (en) | 1998-10-12 | 1998-10-12 | Detergent for resin and cleaning method for resin discharging device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10289451A JP2000119692A (en) | 1998-10-12 | 1998-10-12 | Detergent for resin and cleaning method for resin discharging device |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000119692A true JP2000119692A (en) | 2000-04-25 |
Family
ID=17743443
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP10289451A Withdrawn JP2000119692A (en) | 1998-10-12 | 1998-10-12 | Detergent for resin and cleaning method for resin discharging device |
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JP (1) | JP2000119692A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011057777A (en) * | 2009-09-08 | 2011-03-24 | Adeka Corp | Detergent composition for silicone staining and cleaning method using the same |
JP2011111464A (en) * | 2009-11-24 | 2011-06-09 | Dai Ichi Kogyo Seiyaku Co Ltd | Detergent composition for two-pack curable resin |
JP2012052024A (en) * | 2010-09-01 | 2012-03-15 | Arakawa Chem Ind Co Ltd | Detergent composition for optical molding resin molded product |
-
1998
- 1998-10-12 JP JP10289451A patent/JP2000119692A/en not_active Withdrawn
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011057777A (en) * | 2009-09-08 | 2011-03-24 | Adeka Corp | Detergent composition for silicone staining and cleaning method using the same |
JP2011111464A (en) * | 2009-11-24 | 2011-06-09 | Dai Ichi Kogyo Seiyaku Co Ltd | Detergent composition for two-pack curable resin |
JP2012052024A (en) * | 2010-09-01 | 2012-03-15 | Arakawa Chem Ind Co Ltd | Detergent composition for optical molding resin molded product |
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