JP2001031997A - Solvent composition - Google Patents

Solvent composition

Info

Publication number
JP2001031997A
JP2001031997A JP11206786A JP20678699A JP2001031997A JP 2001031997 A JP2001031997 A JP 2001031997A JP 11206786 A JP11206786 A JP 11206786A JP 20678699 A JP20678699 A JP 20678699A JP 2001031997 A JP2001031997 A JP 2001031997A
Authority
JP
Japan
Prior art keywords
weight
solvent composition
cleaning
dichloro
present
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP11206786A
Other languages
Japanese (ja)
Inventor
Takeshi Hanada
毅 花田
Masaaki Tsuzaki
真彰 津崎
Toshio Miki
寿夫 三木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AGC Inc
Original Assignee
Asahi Glass Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP11206786A priority Critical patent/JP2001031997A/en
Publication of JP2001031997A publication Critical patent/JP2001031997A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a novel solvent composition which has excellent detergency and can be used in a wide range of cleaning uses. SOLUTION: A solvent composition comprises 10 to less than 35 wt.% dichloropentafluoropropane and more than 65 to 90 wt.% CF3-[O-CF (CF3)- CF2]n-(O-CF2)m-O-CF3 (wherein m is an integer of 0-6; and n is an integer of 0-6, provided that m=n=0 is excluded). The dichloropentafluoropropane is preferably 3, 3-dichloro-1,1,1,2,2-pentafluoropropane and/or 1,3-dichloro-1,1,2,2,3- penta-fluoropropane.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、ジクロロペンタフ
ルオロプロパンと特定のパーフルオロポリエーテルを特
定割合で含む溶剤組成物に関する。この溶剤組成物は、
プラスチック、金属、ガラス、セラミックス、繊維など
の固体表面を洗浄するための洗浄溶剤組成物等として使
用できる。
The present invention relates to a solvent composition containing dichloropentafluoropropane and a specific perfluoropolyether in a specific ratio. This solvent composition is
It can be used as a cleaning solvent composition for cleaning solid surfaces such as plastics, metals, glasses, ceramics, and fibers.

【0002】[0002]

【従来の技術】従来、各種脱脂洗浄、フラックス洗浄、
塵埃洗浄等には、不燃性、化学的及び熱的安定性に優れ
る1,1−ジクロロ−1―フルオロエタンやジクロロペ
ンタフルオロプロパン(以下、R225とも記す。)等
が使用されている。また、それらにメタノールやエタノ
ールなどのアルコール類や炭化水素等を加え、溶解力を
高めた混合溶剤も使用されている。
2. Description of the Related Art Conventionally, various degreasing cleaning, flux cleaning,
For dust cleaning and the like, 1,1-dichloro-1-fluoroethane and dichloropentafluoropropane (hereinafter, also referred to as R225), which are excellent in nonflammability, chemical and thermal stability, are used. In addition, mixed solvents having increased dissolving power by adding alcohols such as methanol and ethanol, hydrocarbons, and the like to them are also used.

【0003】特に、R225及びその混合物は、金属、
プラスチック、エラストマー等の基材を侵しにくく、各
種の汚れを選択的に溶解する等の特徴を有するため、各
種精密機械部品や電子部品、これらの電子部品を実装し
たプリント基板、光学部品等の産業分野の洗浄に広く使
用されている。
In particular, R225 and mixtures thereof include metals,
Since it has the characteristics of hardly invading base materials such as plastics and elastomers and selectively dissolving various stains, it can be used for various precision machine parts and electronic parts, printed circuit boards mounted with these electronic parts, optical parts, etc. Widely used for cleaning in the field.

【0004】[0004]

【発明が解決しようとする課題】R225及びその混合
物は、洗浄性が良好で乾燥性にも優れるが、一部のプラ
スチックやゴム材質に対して影響を与え、特にアクリル
樹脂等に対しては影響が強いため、これらの高分子材料
を含む部品の洗浄には使用できなかった。
R225 and its mixture have good cleaning properties and excellent drying properties, but have an effect on some plastics and rubber materials, especially on acrylic resins. Therefore, it cannot be used for cleaning parts containing these polymer materials.

【0005】本発明は、R225の洗浄力を維持したま
ま、これらの高分子材料への影響がない溶剤を提供する
ことを目的とする。
An object of the present invention is to provide a solvent which does not affect these polymer materials while maintaining the detergency of R225.

【0006】[0006]

【課題を解決するための手段】本発明者は鋭意検討の結
果、R225と特定のパーフルオロポリエーテルを混合
した場合、R225の洗浄力を維持したまま、アクリル
樹脂等の高分子材料への影響がない溶剤が得られること
を見出した。
Means for Solving the Problems As a result of diligent studies, the present inventor has found that when R225 and a specific perfluoropolyether are mixed, the effect of R225 on a polymer material such as an acrylic resin while maintaining the detergency of R225 is maintained. It has been found that a solvent free of the above can be obtained.

【0007】すなわち、本発明は、(1)ジクロロペン
タフルオロプロパンと(2)下記式1で表されるパーフ
ルオロポリエーテルを含む組成物であって、(1)/
(2)の割合が10重量%以上35重量%未満/65重
量%超90重量%以下であることを特徴とする溶剤組成
物を提供する。ただし、式1においてmは0〜6の整
数、nは0〜6の整数であり、m=n=0は除く。
That is, the present invention provides a composition comprising (1) dichloropentafluoropropane and (2) a perfluoropolyether represented by the following formula (1):
A solvent composition characterized in that the ratio of (2) is 10% by weight or more and less than 35% by weight / more than 65% by weight and 90% by weight or less. However, in Formula 1, m is an integer of 0 to 6, n is an integer of 0 to 6, and m = n = 0 is excluded.

【0008】[0008]

【化2】 Embedded image

【0009】[0009]

【発明の実施の形態】本発明における(1)成分のR2
25とは、分子式C3HCl25で表されるジクロロペ
ンタフルオロプロパンの1種又は2種以上の混合物を意
味する。R225の好ましいものは、3,3−ジクロロ
−1,1,1,2,2−ペンタフルオロプロパン(以
下、R225caとも記す。)及び1,3−ジクロロ−
1,1,2,2,3−ペンタフルオロプロパン(以下、
R225cbとも記す。)から選ばれる少なくとも1種
である。R225が、R225ca及びR225cbの
混合物である場合の混合割合は、特に限定されないが、
例えば、R225ca/R225cbの割合が1〜99
重量%/1〜99重量%であり、好ましくは40〜50
重量%/50〜60重量%である。
BEST MODE FOR CARRYING OUT THE INVENTION The component (1) of the present invention, R2
25 means one or a mixture of two or more dichloropentafluoropropanes represented by the molecular formula C 3 HCl 2 F 5 . Preferred examples of R225 include 3,3-dichloro-1,1,1,2,2-pentafluoropropane (hereinafter, also referred to as R225ca) and 1,3-dichloro-.
1,1,2,2,3-pentafluoropropane (hereinafter, referred to as
Also referred to as R225cb. ) Is at least one member selected from the group consisting of: The mixing ratio when R225 is a mixture of R225ca and R225cb is not particularly limited,
For example, the ratio of R225ca / R225cb is 1-99.
% By weight / 1 to 99% by weight, preferably 40 to 50%.
% By weight / 50-60% by weight.

【0010】本発明において、(2)成分の式1で表さ
れるパーフルオロポリエーテルとしては、特定のnとm
を有する単独の化合物であってもよく、nとmが異なる
複数種類の混合物であってもよい。通常は、沸点が50
〜65℃の範囲のものが好ましく採用され得る。具体的
には、アウジモント社(イタリー)の製品「Galde
n SV 55」(商品名)(沸点:56℃)などが挙
げられる。
In the present invention, as the perfluoropolyether represented by the formula (1) of the component (2), specific n and m
Or a mixture of a plurality of types in which n and m are different. Usually, the boiling point is 50
Those having a temperature range of -65 ° C can be preferably employed. Specifically, the product "Galde" of Audimont (Italy)
n SV 55 "(trade name) (boiling point: 56 ° C).

【0011】本発明の溶剤組成物は、本発明の目的を阻
害しない範囲で上記R225及び上記特定のパーフルオ
ロポリエーテル以外の化合物を含有してもよい。
The solvent composition of the present invention may contain a compound other than R225 and the specific perfluoropolyether as long as the object of the present invention is not impaired.

【0012】主として溶解性を調整するためには、例え
ば以下に挙げる化合物の1種又は2種以上を0.1〜5
0重量%、好ましくは0.1〜40重量%、さらに好ま
しくは0.1〜20重量%の範囲で本発明の組成物中へ
配合できる。
In order to mainly control the solubility, for example, one or more of the following compounds may be used in an amount of 0.1 to 5%.
0% by weight, preferably 0.1 to 40% by weight, more preferably 0.1 to 20% by weight can be incorporated into the composition of the present invention.

【0013】n−ペンタン、2−メチルペンタン、2,
2−ジメチルプロパン、n−ヘキサン、3−メチルペン
タン、2,2−ジメチルブタン、2,3−ジメチルブタ
ン、n−ヘプタン、2−メチルヘキサン、3−メチルヘ
キサン、2,3−ジメチルペンタン、2,4−ジメチル
ペンタン、n−オクタン、2,2,3−トリメチルペン
タン、2,2,4−トリメチルペンタン、シクロペンタ
ン、シクロヘキサン、メチルシクロヘキサン、エチルシ
クロヘキサン等の炭化水素類。ジクロロメタン、シス−
1,2−ジクロロエチレン、トランス−1,2−ジクロ
ロエチレン、トリクロロエチレン、テトラクロロエチレ
ン等の塩素化炭化水素類。1−ブロモプロパン等の臭素
化炭化水素類。アセトン、メチルエチルケトン、メチル
ブチルケトン、メチルイソブチルケトン等のケトン類。
ジエチルエーテル、メチルセロソルブ、テトラヒドロフ
ラン、1,4−ジオキサン等のエーテル類。
N-pentane, 2-methylpentane, 2,
2-dimethylpropane, n-hexane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, n-heptane, 2-methylhexane, 3-methylhexane, 2,3-dimethylpentane, Hydrocarbons such as 2,4-dimethylpentane, n-octane, 2,2,3-trimethylpentane, 2,2,4-trimethylpentane, cyclopentane, cyclohexane, methylcyclohexane, and ethylcyclohexane. Dichloromethane, cis-
Chlorinated hydrocarbons such as 1,2-dichloroethylene, trans-1,2-dichloroethylene, trichloroethylene, and tetrachloroethylene. Brominated hydrocarbons such as 1-bromopropane. Ketones such as acetone, methyl ethyl ketone, methyl butyl ketone and methyl isobutyl ketone;
Ethers such as diethyl ether, methyl cellosolve, tetrahydrofuran, and 1,4-dioxane;

【0014】2,2−ジクロロ−1,1,1−トリフル
オロエタン、1,1−ジクロロ−1−フルオロエタン等
の塩素化フッ素化炭化水素類。酢酸メチル、酢酸エチ
ル、酢酸プロピル、酢酸ブチル等のエステル類。メタノ
ール、エタノール、1−プロパノール、2−プロパノー
ル、1−ブタノール、2−ブタノール、イソブタノー
ル、t−ブタノール等のアルコール類。
Chlorinated fluorinated hydrocarbons such as 2,2-dichloro-1,1,1-trifluoroethane and 1,1-dichloro-1-fluoroethane. Esters such as methyl acetate, ethyl acetate, propyl acetate and butyl acetate. Alcohols such as methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutanol and t-butanol.

【0015】主として安定性を高めるために、例えば以
下に挙げる化合物の1種又は2種以上を0.001〜5
重量%の範囲で本発明の組成物中へ配合できる。
In order to mainly improve the stability, for example, one or more of the following compounds are added in an amount of 0.001 to 5
It can be incorporated into the composition of the present invention in the range of weight%.

【0016】ニトロメタン、ニトロエタン、ニトロプロ
パン、ニトロベンゼン等のニトロ化合物類。ジエチルア
ミン、トリエチルアミン、イソプロピルアミン、n−ブ
チルアミン等のアミン類。フェノール、o−クレゾー
ル、m−クレゾール、p−クレゾール、チモール、p−
t−ブチルフェノール、t−ブチルカテコール、カテコ
ール、イソオイゲノール、o−メトキシフェノール、ビ
スフェノールA、サリチル酸イソアミル、サリチル酸ベ
ンジル、サリチル酸メチル、2,6−ジ−t−ブチル−
p−クレゾール等のフェノール類。2−(2’−ヒドロ
キシ−5’−メチルフェニル)ベンゾトリアゾール、2
−(2’−ヒドロキシ−3’−t−ブチル−5’−メチ
ルフェニル)−5−クロロベンゾトリアゾール、1,
2,3−ベンゾトリアゾール、1−[(N,N−ビス−
2−エチルヘキシル)アミノメチル]ベンゾトリアゾー
ル等のベンゾトリアゾール類。
Nitro compounds such as nitromethane, nitroethane, nitropropane and nitrobenzene. Amines such as diethylamine, triethylamine, isopropylamine and n-butylamine. Phenol, o-cresol, m-cresol, p-cresol, thymol, p-
t-butylphenol, t-butylcatechol, catechol, isoeugenol, o-methoxyphenol, bisphenol A, isoamyl salicylate, benzyl salicylate, methyl salicylate, 2,6-di-t-butyl-
Phenols such as p-cresol. 2- (2'-hydroxy-5'-methylphenyl) benzotriazole, 2
-(2'-hydroxy-3'-t-butyl-5'-methylphenyl) -5-chlorobenzotriazole, 1,
2,3-benzotriazole, 1-[(N, N-bis-
Benzotriazoles such as 2-ethylhexyl) aminomethyl] benzotriazole.

【0017】本発明の溶剤組成物は、R225及び上記
特定のパーフルオロポリエーテルを特定の割合で含むた
め、洗浄される物品の材質、例えば軟質塩化ビニル、ポ
リカーボネート、ABS樹脂、アクリル樹脂等のプラス
チック類や、ニトリルゴム等のゴム類への影響がなく、
しかも引火性がない優れたものである。さらに本発明の
溶剤組成物は、従来のR225と同程度の溶解力を有
し、各種用途に幅広く好適に使用できる。
Since the solvent composition of the present invention contains R225 and the above-mentioned specific perfluoropolyether in a specific ratio, the material of the article to be washed, for example, plastic such as soft vinyl chloride, polycarbonate, ABS resin, acrylic resin, etc. And no impact on rubbers such as nitrile rubber,
Moreover, it is excellent without flammability. Further, the solvent composition of the present invention has the same dissolving power as conventional R225, and can be used widely and suitably for various uses.

【0018】こうした具体的な用途としては、ガラス、
セラミックス、プラスチック、ゴム、金属製各種物品等
に付着した油、フラックス、インキ、塵埃等の洗浄剤、
ドライクリーニング用溶剤等が挙げられる。特にIC部
品、電気機器、精密機械、光学レンズ等の洗浄剤や塵埃
除去剤として好適である。洗浄方法としては、手拭き、
浸漬、スプレー、揺動、超音波洗浄又はこれらを組み合
せた方法等を採用すればよい。
Examples of such specific applications include glass,
Cleaning agents for oil, flux, ink, dust, etc. attached to ceramics, plastics, rubber, various metal products, etc.
And a solvent for dry cleaning. In particular, it is suitable as a cleaning agent and a dust removing agent for IC parts, electric equipment, precision instruments, optical lenses, and the like. Washing methods include hand wiping,
Immersion, spraying, rocking, ultrasonic cleaning, or a combination thereof may be employed.

【0019】[0019]

【実施例】以下、実施例及び比較例を挙げて、さらに具
体的に説明するが、本発明はこれらによって限定されな
い。各例において、(2)成分としてのPFPE−1
は、アウジモント社(イタリー)の製品「Galden
SV 55」(商品名)(沸点:56℃)である。例
1〜例5及び例8〜例12は実施例であり、例6〜例7
及び例13〜例14は比較例である。
EXAMPLES The present invention will be described more specifically below with reference to examples and comparative examples, but the present invention is not limited thereto. In each case, PFPE-1 as the component (2)
Is a product of Audimont (Italy) "Galden
SV 55 "(trade name) (boiling point: 56 ° C). Examples 1 to 5 and 8 to 12 are working examples, and Examples 6 to 7
Examples 13 and 14 are comparative examples.

【0020】(例1〜例7)表1の溶剤組成物を用いて
アクリル樹脂(X)、ニトリルゴム(Y)への適合性試
験を行った。すなわち、各高分子材料X、Yのテストピ
ース(25mm×30mm×3mm)を、加熱し沸騰し
ている表1の溶剤組成物中に5分間浸漬した。浸漬後の
テストピースを目視観察し、外観変化(◎:変化なし、
×:割れ又は部分的溶解が発生)を判定した。結果を表
1に示す。評価の結果は、Xへの適合性をX欄に、Yへ
の適合性をY欄に示す。また、表1において、R225
(ca:cb)とは、R225caとR225cbの混
合物を示す。また重量%欄の括弧内の数字は、R225
ca:R225cbの重量%を示す。
(Examples 1 to 7) Using the solvent compositions shown in Table 1, compatibility tests with acrylic resin (X) and nitrile rubber (Y) were performed. That is, a test piece (25 mm × 30 mm × 3 mm) of each of the polymer materials X and Y was immersed in a heated and boiling solvent composition of Table 1 for 5 minutes. The test piece after immersion was visually observed, and the appearance changed (:: no change,
X: cracking or partial dissolution occurred). Table 1 shows the results. The results of the evaluation are shown in column X for compatibility with X and in column Y for compatibility with Y. In Table 1, R225
(Ca: cb) indicates a mixture of R225ca and R225cb. The number in parenthesis in the weight% column is R225.
ca: indicates the weight% of R225cb.

【0021】[0021]

【表1】 [Table 1]

【0022】(例8〜例14)表2の溶剤組成物を用い
て金属加工油の洗浄試験を行った。すなわち、SUS−
304のテストピース(25mm×30mm×2mm)
を、金属加工油A:ダフニカットAS40H(出光興産
社製)、B:ダフニカットAS30D(出光興産社
製)、C:ダフニカットAS25F(出光興産社製)中
に浸漬して金属加工油を付着させた。該金属加工油を付
着させたテストピースを、40℃に加温した表2の溶剤
組成物中に5分間浸漬して洗浄した。金属加工油の除去
度(◎:良好に除去可、△:微量残存、×:かなり残
存)を判定した結果を表2に示す。なお、表2において
R225(ca:cb)とは、R225caとR225
cbの混合物を示す。また重量%欄の括弧内の数字は、
R225ca:R225cbの重量%を示す。金属加工
油A、B、Cの除去度は、表2のA欄(金属加工油
A)、B欄(金属加工油B)、C欄(金属加工油C)に
それぞれ示した。
(Examples 8 to 14) Using the solvent compositions shown in Table 2, a cleaning test of metal working oil was performed. That is, SUS-
304 test pieces (25 mm x 30 mm x 2 mm)
Was immersed in a metal working oil A: Daphnicut AS40H (manufactured by Idemitsu Kosan Co., Ltd.), B: Daphnicut AS30D (manufactured by Idemitsu Kosan Co., Ltd.), and C: Daphnicut AS25F (manufactured by Idemitsu Kosan Co., Ltd.) to adhere the metal working oil. The test piece to which the metal working oil was attached was washed by immersing it in the solvent composition of Table 2 heated to 40 ° C. for 5 minutes. Table 2 shows the results of determination of the degree of metalworking oil removal (除去: good removal, Δ: trace remaining, ×: considerable remaining). In Table 2, R225 (ca: cb) means R225ca and R225.
2 shows a mixture of cb. Also, the number in parentheses in the weight% column is
R225ca: indicates the weight% of R225cb. The degrees of removal of the metal working oils A, B, and C are shown in Table 2, column A (metal working oil A), column B (metal working oil B), and column C (metal working oil C).

【0023】[0023]

【表2】 [Table 2]

【0024】[0024]

【発明の効果】本発明の溶剤組成物は、R225と特定
のパーフルオロポリエーテルを特定の割合で含むことを
特徴とし、アクリル樹脂等の高分子材料に対しての影響
がなく、さらに油等の汚れに対する優れた溶解性を有す
るため、幅広い洗浄用途に使用できる利点がある。
The solvent composition according to the present invention is characterized by containing R225 and a specific perfluoropolyether in a specific ratio, has no influence on a polymer material such as an acrylic resin, and further has no influence on an oil or the like. It has the advantage of being able to be used for a wide range of cleaning applications because of its excellent solubility in soil.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4H003 DA05 DA14 DA15 DA16 DB02 DB03 DC03 ED26 ED29 FA15 4H006 AA03 AA05 AB70 GP01 GP20 4K053 PA03 QA04 QA05 QA07 RA08 RA36 RA38 RA41 TA13  ──────────────────────────────────────────────────続 き Continued on front page F term (reference) 4H003 DA05 DA14 DA15 DA16 DB02 DB03 DC03 ED26 ED29 FA15 4H006 AA03 AA05 AB70 GP01 GP20 4K053 PA03 QA04 QA05 QA07 RA08 RA36 RA38 RA41 TA13

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】(1)ジクロロペンタフルオロプロパンと
(2)下記式1で表されるパーフルオロポリエーテルを
含む組成物であって、(1)/(2)の割合が10重量
%以上35重量%未満/65重量%超90重量%以下で
あることを特徴とする溶剤組成物。ただし、式1におい
てmは0〜6の整数、nは0〜6の整数であり、m=n
=0は除く。 【化1】
1. A composition containing (1) dichloropentafluoropropane and (2) a perfluoropolyether represented by the following formula 1, wherein the ratio of (1) / (2) is 10% by weight or more and 35% by weight. Less than 90% by weight / less than 65% by weight / less than 90% by weight. However, in Formula 1, m is an integer of 0 to 6, n is an integer of 0 to 6, and m = n
= 0 is excluded. Embedded image
【請求項2】ジクロロペンタフルオロプロパンが3,3
−ジクロロ−1,1,1,2,2−ペンタフルオロプロ
パン及び/又は1,3−ジクロロ−1,1,2,2,3
−ペンタフルオロプロパンである請求項1記載の溶剤組
成物。
2. The method according to claim 1, wherein the dichloropentafluoropropane is 3,3.
-Dichloro-1,1,1,2,2-pentafluoropropane and / or 1,3-dichloro-1,1,2,2,3
The solvent composition according to claim 1, which is -pentafluoropropane.
JP11206786A 1999-07-21 1999-07-21 Solvent composition Pending JP2001031997A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004514025A (en) * 2000-11-08 2004-05-13 ソルヴェイ Solvent composition
US9705056B2 (en) 2012-02-09 2017-07-11 Dow Corning Corporation Gradient polymer structures and methods
EP3831918A4 (en) * 2018-07-27 2022-04-13 Central Glass Company, Limited Solvent composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004514025A (en) * 2000-11-08 2004-05-13 ソルヴェイ Solvent composition
US9705056B2 (en) 2012-02-09 2017-07-11 Dow Corning Corporation Gradient polymer structures and methods
EP3831918A4 (en) * 2018-07-27 2022-04-13 Central Glass Company, Limited Solvent composition

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