JPH0231754B2 - TAIDENBOSHISEISENJOEKI - Google Patents
TAIDENBOSHISEISENJOEKIInfo
- Publication number
- JPH0231754B2 JPH0231754B2 JP21223782A JP21223782A JPH0231754B2 JP H0231754 B2 JPH0231754 B2 JP H0231754B2 JP 21223782 A JP21223782 A JP 21223782A JP 21223782 A JP21223782 A JP 21223782A JP H0231754 B2 JPH0231754 B2 JP H0231754B2
- Authority
- JP
- Japan
- Prior art keywords
- general formula
- group
- carbon atoms
- antistatic
- surfactant
- 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.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 claims description 33
- 239000004094 surface-active agent Substances 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 238000004140 cleaning Methods 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000013543 active substance Substances 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical group 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 3
- 125000004185 ester group Chemical group 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- -1 polyoxyethylene group Polymers 0.000 claims description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- 230000003068 static effect Effects 0.000 description 14
- 230000000694 effects Effects 0.000 description 11
- 230000005611 electricity Effects 0.000 description 7
- 239000011241 protective layer Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000010248 power generation Methods 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 238000003745 diagnosis Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 230000007257 malfunction Effects 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 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
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Landscapes
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は増感紙汚染性がなく且つすぐれた帯電
防止性を有する帯電防止性洗浄液に関するもので
ある。
通常レントゲンフイルムは増感紙間に挾まれ撮
影される。この取扱いの際、即ちレントゲンフイ
ルムの増感紙間に入れる時、又はレントゲンフイ
ルムを増感紙間から取り出す時に増感紙〜レント
ゲンフイルム間の摩擦、剥離帯電により静電気が
発生し、この静電気が放電する事によりレントゲ
ンフイルムをかぶらせる故障が起きる事がある
(「スタチツクマーク故障」と呼ぶ)。この静電気
は特に低湿条件下(例えば冬季、除湿された部屋
等)で発生しやすい。この放電によるスタチツク
マーク故障が発生すると診断上重大な誤りをおか
す危険性が生じる。従つて従来静電気発生を防止
するため、アンチスタチツクsolutionとか、AS
クリーナーと称し市販されているX線増感紙用帯
電防止液を増感紙表面にガーゼ等を用いて塗布す
る方法がとられてきた。
これらの帯電防止液に用いられている素材とし
ては、たとえば特開昭56−28263号に見られるよ
うな、ポリオキシエチレン−ポリオキシプロピレ
ン・第1級アルコールアルコキシレート・第2級
アルコールアルコキシレートのうち少なくとも2
種類を混合したものが使用されていた。
しかしながらこれらの帯電防止液は、色々な種
類のレントゲンフイルムに対して、必ずしも有効
でなく、あるフイルムに対しては帯電防止効果は
あつても、他のフイルムについてはほとんどその
機能を有しないという欠点があつた。さらに、ぬ
りつけ直後では静電気発生防止効果はあつても、
上記混合界面活性剤が増感紙に塗布され何回も繰
り返し使用されていると、この効果が無くなり、
増感紙〜レントゲンフイルム間の摩擦剥離帯電に
より静電気が発生し、これが放電する事により、
スタチツクマーク故障が生ずるという欠点があつ
た。
このようなスタチツク故障は、診断上重大な誤
りをおかす恐れがあるので、絶対に発生させては
ならないものである。又、このような静電気発生
を防止する薬品は、世の中ですでに数多く知られ
ているが、きわめて微量な化学物質により、その
性質が大きく動いてしまう写真フイルムと接触す
るような系では、使える薬品はきわめて限定さ
れ、従つて、本発明の目的の増感紙に対しての効
果的な静電気防止効果を有する帯電防止液は、今
まで見い出されていなかつたのである。
そこで、本発明の目的は、
第一に、あらゆるレントゲンフイルムに対し、
優れた帯電防止効果を有する帯電防止液を提供す
る事にある。
第二に、増感紙等に対し、高い保持性を有する
帯電防止液を提供する事にある。
第三に、写真性に何ら悪影響を及ぼさない帯電
防止液を提供する事にある。
第四に、増感紙表面に付着した手アカ、現像
液、口紅等の汚れを容易に拭き取る事ができる帯
電防止液を提供する事にある。
第五に、皮膚への刺激のない帯電防止液を提供
する事にある。
第六に、経時安定性の優れた帯電防止液を提供
する事にある。
第七に、多量の有機溶剤を含有しない帯電防止
液を提供する事にある。
第八に、増感紙汚染性(界面活性剤が増感紙に
塗布されると増感紙保護層表面から保護層内部
に、更には蛍光層まで浸透し、保護層、蛍光層に
存在する物質と作用し、長期間使用しているうち
に増感紙が黄色に変色してしまう現象)のない帯
電防止液を提供する事にある。
本発明のこれらの目的は下記一般式()で表
わされる界面活性剤の少なくとも1つと、下記一
般式()で表わされる界面活性剤及び下記一般
式()で表わされるフツ素化炭化水素系界面活
性剤から選ばれる少なくとも1つの界面活性剤と
を含有する帯電防止性洗浄液に於て、一般式
()で表わされる界面活性剤及び/又は一般式
()で表わされるフツ素化炭化水素系界面活性
剤に対する一般式()で表わされる界面活性剤
の重量比が5/95乃至50/50であり、かつ該洗浄
液中の界面活性剤濃度が0.5乃至5.0重量%である
事を特徴とする帯電防止性洗浄液により達成され
た。
一般式()
但し、a、b及びcは整数を表わし、a+c=
4乃至160、b=10乃至45である。
一般式()
但し、R、R1は炭素数3乃至12の脂肪族炭化
水素基、Aは炭素数3乃至5の脂肪族炭化水素
基、Mは水素原子、アルカリ金属原子又は4級ア
ンモニウム基、を表わす。
一般式()
RF−A−X
但し、RFは少なくとも3個の沸素原子を含有
する部分沸素化または全沸素化炭化水素を表わ
し、Aは化学結合手または二価の脂肪族、芳香族
または混合脂肪族−芳香族基を表わし、これは酸
素原子、エステル基またはアミド基の異種原子で
中断されたものを含む。Xは(−CH2CH2O)oR3
(ここに、R3は水素原子又は炭素数1乃至5のア
ルキル基を表わし、nは5〜20の整数を表わし、
このポリオキシエチレン基は一つまたはそれ以上
のイソプロピレンオキシ基で中断されていてもよ
い)、
(ここに、Alkは炭素数1乃至5の低級アルキレ
ン基を表わし、R4は炭素数1乃至5の低級アル
キル基を表わす)、−SO3M、−OSO3Mまたは−
COOMを表わす(ここに、Mは一般式()の
Mと同じ意味を表わす)。
一般式()で表わされる界面活性剤及び/又
は一般式()で表わされるフツ素化界面活性剤
に対する一般式()で表わされる界面活性剤の
重量比は5/95乃至50/50であるが特に好ましく
は10/90乃至30/70である。
即ち、界面活性剤の全重量の70乃至90%は一般
式()で表わされる界面活性剤であることが好
ましい。
又、本発明の帯電防止性洗浄液中での界面活性
剤の全重量は0.5乃至5.0%であるが、特に1.0〜
3.0%であることが好ましい。
一般式()に於て、Mとしてはアルカリ金属
原子、特にナトリウム又はカリウムであることが
好ましい。
一般式()に於て、Aの中を異種原子で中断
する場合のエステル基としては−COO−基を、
アミド基としては−CONR2−、−SO2NR2−(こ
こに、R2は水素原子または炭素数1乃至5のア
ルキル基を表わす)を挙げられる。
次に本発明に使用する代表的な化合物例を示
す。
一般式−で表わされる化合物例
一般式−で表わされる化合物例
フツ素化炭化水素系界面活性剤の具体例
これらの化合物のうち主要なものについては市
販されており、それらを使うと便利である。
一般式−の市販品例としては、プルロニツク
L−44(旭電化工業製)等が挙げられる。
一般式−の例としては、スルホン酸系界面活
性剤のうち、特公昭52−25250に記載されている
化合物が挙げられる。
フツ素化炭化水素系界面活性剤の市販品の例と
しては、メガフアクF−110(大日本インキ)等が
挙げられる。
本発明の帯電防止液に特徴的な事としては、相
手となるレントゲンフイルムを選ばずに、その帯
電防止効果を発揮する点にある。
レントゲンフイルムは、その表面層において各
種性能を満足させるため、種々の添加剤を使用し
ており、その表面状態は各レントゲンフイルムメ
ーカー毎、各レントゲンフイルム品種毎に大きく
異なつているのが実状である。
その為にこれらのフイルムが増感紙との間で摩
擦や剥離を受けた時にはその帯電性も各フイルム
によつて大きく異なつているというように考えら
れる。しかし驚くべき事に本発明の帯電防止液に
おいては、各フイルムに依らず優れた帯電防止効
果を発揮した。
この効果は、本発明の特徴である2種類以上の
界面活性剤の混合の結果、その相乗作用として発
現したものである。
すなわち、本2種類以上の界面活性剤の混合に
より、静電気故障の2つの要因である発電性、漏
洩性(表面抵抗率測定で評価できる)の両方が著
しく改善されたのである。これは他の帯電防止液
には見られない特徴である。
さらに通常は、多種類の界面活性剤を混合する
場合には、しばしばそれらの相溶性、表面配向性
等のちがいから、塗布時にはじいたりむらが生じ
たり、発泡したりする事が見られるが、本発明の
2種類以上の界面活性剤の混合系では、このよう
なトラブルは見られず、きわめてきれいに均一に
塗布できるのも特徴である。
本発明の帯電防止液はこのようにすぐれた性能
を有しており、X線増感紙の他、スタチツク故障
の発生する個所、例えば搬送系ローラー部等に於
いてもすぐれた帯電防止効果を示した。
又レントゲン感材以外の感材例えばカラー感
材、印刷用感材等へも本発明の技術を適用できる
と考える。
又本発明の帯電防止液の増感紙への塗布方法と
しては、ガーゼ等にしみ込ませて増感紙表面を拭
くとか、スプレーで増感紙表面に吹き付ける等の
方法がある。
以下に実施例を挙げて本発明を更に説明する
が、本発明はこれら実施例に限定されるものでは
ない。
実施例 1
〔1〕 帯電防止液の評価方法
1−1) 帯電防止性テスト
Hi Screen Standard(化成オプトニク
ス(株)保護層ポリエチレンテレフタレート
(PET)…以下スクリーンAという
Hi Screen Standard(化成オプトニツ
クス(株)保護層DAC)…以下スクリーンB
という
LT−(化成オプトニクス(株)保護層
DAC)
…以下スクリーンCという
の3種の増感紙に各種帯電防止液(3重量%
水溶液)をガーゼに1c.c.しみ込ませて塗布し
室温放置、2時間乾燥させた。次いで25℃、
25%RHに3時間調湿した後表面抵抗率の測
定を行なつた。
表面抵抗率の測定は、帯電防止液塗布済増
感紙の試験片を電極間隔0.14cm、長さ10cmの
真チユウ製電極(試験片と接する部分はステ
ンレス製)に挾み、タケダ理研製絶縁計
(TR−8651)で1分値を測定した。(表面抵
抗率は、その値が小さい程帯電防止効果は大
きい。)
スタチツクマーク発生試験は、帯電防止性
テストで作成した試料を用い、帯電防止液を
塗布した面に未露光レントゲンフイルムを挾
みゴムローラーでこすり、次いでこのレント
ゲンフイルムを増間紙間より取り出し現像す
る。この際スタチツクマークの全く発生しな
かつた場合○、一部発生した場合△、全面発
生した場合×とする。
1−2) 発電性テスト
前記のスクリーンA,B,Cに、前述の方
法で各種帯電防止液を塗布後、25℃、25%
RHの室内で3時間調湿する。この時発電性
の相手物質として選定したレントゲンフイル
ム〔〔Fuji X−ray Film;RX(NIF)〕富士
写真フイルム(株)製…(フイルム−A)及び
〔EK.X−ray Film;XRP(NIF)〕イースマ
ン・コダツク社製…(フイルム−B)も同様
に調湿しておく。
発電性テスト法は直径10cm、長さ10cmの2
本のローラーに、帯電防止液を塗布したスク
リーンを幅7cmに切つて貼り付け、スプリン
グテンシヨン2Kg2個でフリーローラーを駆
動ローラー側に押し付ける。
次にローラーを20m/minのスピードで回
転させ、先ほど相手物質として選んだレント
ゲンフイルムを2cm×25cmの大きさに切つ
て、回転しているローラーの間に挿入し、ロ
ーラーでしごかれて出て来たレントゲンフイ
ルムをフアラデーケージ(330PF)で受け、
この時の帯電量(クーロン)をタケダ理研製
絶縁計(TR−8651)で測定する。
1−3) 増感紙に対する保持性試験
Hi Screen Standardに上記と同様に各種
帯電防止液を塗布する。25℃、25%RHに3
時間調湿後表面抵抗率を測定し、次いでその
試験片を片面ネルで10回こすり再び表面抵抗
率を測定し表面抵抗率の悪化具合で判断し
た。
〔2〕 下記処方〔〕〜〔〕及び比較例に示
す帯電防止性液を調液した。
The present invention relates to an antistatic cleaning liquid that does not cause intensifying screen staining and has excellent antistatic properties. Normally, X-ray film is sandwiched between intensifying screens and images are taken. During this handling, that is, when the X-ray film is placed between the intensifying screens or when the X-ray film is taken out from between the intensifying screens, static electricity is generated due to friction between the intensifying screen and the X-ray film and charging when peeled off, and this static electricity is discharged. This may cause a malfunction that causes the X-ray film to become covered (referred to as a "static mark malfunction"). This static electricity is particularly likely to occur under low humidity conditions (for example, in winter, in a dehumidified room, etc.). If a static mark failure occurs due to this discharge, there is a risk of making a serious error in diagnosis. Therefore, in order to prevent the generation of static electricity, anti-static solutions and AS
A method has been adopted in which a commercially available antistatic liquid for X-ray intensifying screens called cleaner is applied to the surface of the intensifying screen using gauze or the like. The materials used in these antistatic liquids include polyoxyethylene-polyoxypropylene, primary alcohol alkoxylate, and secondary alcohol alkoxylate, as seen in JP-A No. 56-28263. at least 2 of them
A mixture of types was used. However, these antistatic liquids are not necessarily effective against various types of X-ray films, and have the disadvantage that although they may have an antistatic effect on some types of film, they have almost no effect on other films. It was hot. Furthermore, even though it is effective in preventing static electricity generation immediately after application,
If the above mixed surfactant is applied to an intensifying screen and used repeatedly, this effect will disappear,
Static electricity is generated due to frictional peeling between the intensifying screen and the X-ray film, and as this discharges,
The disadvantage was that static mark failures occurred. Such static failures should never occur because they may cause serious errors in diagnosis. In addition, there are many chemicals already known in the world that can prevent the generation of static electricity, but there are only a few chemicals that can be used in systems that come into contact with photographic film, whose properties can be greatly affected by extremely small amounts of chemicals. is extremely limited, and therefore, no antistatic liquid has been found so far that has an effective antistatic effect on the intensifying screen that is the object of the present invention. Therefore, the purpose of the present invention is, firstly, to
An object of the present invention is to provide an antistatic liquid having an excellent antistatic effect. The second objective is to provide an antistatic liquid that has high retention properties for intensifying screens and the like. The third object is to provide an antistatic liquid that does not have any adverse effect on photographic properties. Fourthly, it is an object of the present invention to provide an antistatic liquid that can easily wipe off stains such as hand marks, developer, lipstick, etc. adhering to the surface of an intensifying screen. Fifth, it is to provide an antistatic liquid that does not irritate the skin. Sixthly, it is possible to provide an antistatic liquid with excellent stability over time. Seventhly, it is an object to provide an antistatic liquid that does not contain a large amount of organic solvent. Eighth, intensifying screen staining (when a surfactant is applied to an intensifying screen, it penetrates from the surface of the intensifying screen protective layer to the inside of the protective layer and even to the fluorescent layer, and is present in the protective layer and fluorescent layer. The purpose of the present invention is to provide an antistatic liquid that does not interact with substances and cause an intensifying screen to turn yellow after long-term use. These objects of the present invention include at least one surfactant represented by the following general formula (), a surfactant represented by the following general formula (), and a fluorinated hydrocarbon interface represented by the following general formula (). In an antistatic cleaning liquid containing at least one surfactant selected from active agents, a surfactant represented by the general formula () and/or a fluorinated hydrocarbon interface represented by the general formula () A charging method characterized in that the weight ratio of the surfactant represented by the general formula () to the active agent is 5/95 to 50/50, and the surfactant concentration in the cleaning liquid is 0.5 to 5.0% by weight. Achieved by preventive cleaning fluid. General formula () However, a, b and c represent integers, and a+c=
4 to 160, b=10 to 45. General formula () However, R and R 1 represent an aliphatic hydrocarbon group having 3 to 12 carbon atoms, A represents an aliphatic hydrocarbon group having 3 to 5 carbon atoms, and M represents a hydrogen atom, an alkali metal atom, or a quaternary ammonium group. General formula () R F -A-X However, R F represents a partially or fully fluorinated hydrocarbon containing at least three fluorine atoms, and A is a chemical bond or a divalent aliphatic hydrocarbon. , represents an aromatic or mixed aliphatic-aromatic group, including those interrupted by a heteroatom of an oxygen atom, an ester group or an amide group. X is (-CH 2 CH 2 O) o R 3
(Here, R 3 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, n represents an integer of 5 to 20,
This polyoxyethylene group may be interrupted by one or more isopropyleneoxy groups), (Here, Alk represents a lower alkylene group having 1 to 5 carbon atoms, and R 4 represents a lower alkyl group having 1 to 5 carbon atoms), -SO 3 M, -OSO 3 M or -
COOM (here, M has the same meaning as M in general formula ()). The weight ratio of the surfactant represented by the general formula () to the surfactant represented by the general formula () and/or the fluorinated surfactant represented by the general formula () is from 5/95 to 50/50. is particularly preferably from 10/90 to 30/70. That is, it is preferable that 70 to 90% of the total weight of the surfactant be the surfactant represented by the general formula (). Further, the total weight of the surfactant in the antistatic cleaning liquid of the present invention is 0.5 to 5.0%, particularly 1.0 to 5.0%.
Preferably it is 3.0%. In the general formula (), M is preferably an alkali metal atom, particularly sodium or potassium. In the general formula (), when A is interrupted by a heteroatom, the ester group is -COO-,
Examples of the amide group include -CONR2- and -SO2NR2- (wherein R2 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms). Next, typical examples of compounds used in the present invention are shown. Examples of compounds represented by the general formula - Examples of compounds represented by the general formula - Specific examples of fluorinated hydrocarbon surfactants Most of these compounds are commercially available and are convenient to use. Examples of commercially available products of the general formula - include Pluronic L-44 (manufactured by Asahi Denka Kogyo). Examples of the general formula - include compounds described in Japanese Patent Publication No. 52-25250 among sulfonic acid surfactants. Examples of commercially available fluorinated hydrocarbon surfactants include Megafuac F-110 (Dainippon Ink). A characteristic feature of the antistatic liquid of the present invention is that it exhibits its antistatic effect regardless of the type of X-ray film to be used. X-ray film uses various additives in its surface layer to satisfy various performance requirements, and the reality is that the surface condition differs greatly between each X-ray film manufacturer and each X-ray film type. . For this reason, when these films are subjected to friction or peeling from the intensifying screen, it is thought that the charging properties vary greatly depending on the film. However, surprisingly, the antistatic liquid of the present invention exhibited excellent antistatic effects regardless of the type of film. This effect is produced as a result of the synergistic effect of mixing two or more types of surfactants, which is a feature of the present invention. In other words, by mixing two or more types of surfactants, both power generation performance and leakage performance (which can be evaluated by surface resistivity measurement), which are two causes of electrostatic failure, were significantly improved. This is a feature not found in other antistatic liquids. Furthermore, when many types of surfactants are mixed, repellency, unevenness, and foaming are often observed during application due to differences in their compatibility, surface orientation, etc. The mixed system of two or more types of surfactants of the present invention is free from such troubles and is characterized by being able to be applied extremely cleanly and uniformly. The antistatic liquid of the present invention has excellent performance as described above, and has an excellent antistatic effect not only in X-ray intensifying screens but also in locations where static failures occur, such as the rollers of the conveyance system. Indicated. It is also believed that the technology of the present invention can be applied to photosensitive materials other than X-ray photosensitive materials, such as color photosensitive materials and printing photosensitive materials. The antistatic liquid of the present invention can be applied to the intensifying screen by soaking it in gauze or the like and wiping the surface of the intensifying screen, or by spraying it onto the surface of the intensifying screen. The present invention will be further explained below with reference to Examples, but the present invention is not limited to these Examples. Example 1 [1] Evaluation method of antistatic liquid 1-1) Antistatic property test Hi Screen Standard (Kasei Optonics Co., Ltd.) Protective layer polyethylene terephthalate (PET)...hereinafter referred to as screen A Hi Screen Standard (Kasei Optonics Co., Ltd.) )Protective layer DAC)…Screen B below
LT- (Kasei Optonics Co., Ltd. protective layer)
DAC)...Three types of intensifying screens, hereinafter referred to as screen C, were coated with various antistatic liquids (3% by weight).
Aqueous solution) was soaked in 1 c.c. of gauze and applied, left at room temperature, and dried for 2 hours. Then 25℃,
After adjusting the humidity to 25% RH for 3 hours, the surface resistivity was measured. To measure the surface resistivity, a test piece of an intensifying screen coated with an antistatic liquid is held between Machiyu electrodes (the part in contact with the test piece is made of stainless steel) with an electrode spacing of 0.14 cm and a length of 10 cm. The 1-minute value was measured using a meter (TR-8651). (The smaller the value of surface resistivity, the greater the antistatic effect.) The static mark generation test uses the sample prepared for the antistatic property test, and an unexposed X-ray film is placed on the surface coated with antistatic liquid. The X-ray film is then rubbed with a rubber roller and then taken out from between the interspersed sheets and developed. In this case, if the static mark did not occur at all, it was evaluated as ○, if it occurred partially, it was evaluated as △, and if it occurred all over the area, it was evaluated as ×. 1-2) Power generation test After applying various antistatic liquids to the screens A, B, and C using the method described above, heat the screens at 25℃ and 25%.
Humidify in a RH room for 3 hours. At this time, X-ray films [[Fuji X-ray Film; RX (NIF)] manufactured by Fuji Photo Film Co., Ltd. (Film-A) and [EK. )] Manufactured by Easman Kodatsu Co., Ltd. (Film-B) is also humidity-controlled in the same way. The power generation test method is 2 with a diameter of 10 cm and a length of 10 cm.
Cut a 7cm wide screen coated with antistatic liquid and paste it on the book roller, then press the free roller against the drive roller using two 2kg spring tensioners. Next, rotate the rollers at a speed of 20 m/min, cut the X-ray film you previously selected as the target material into pieces of 2 cm x 25 cm, insert them between the rotating rollers, and squeeze them out. The received X-ray film is received in a Faraday cage (330PF),
Measure the amount of charge (coulombs) at this time using a Takeda Riken insulation meter (TR-8651). 1-3) Retention test on intensifying screen Apply various antistatic liquids to Hi Screen Standard in the same manner as above. 3 to 25℃, 25%RH
After adjusting the humidity for a period of time, the surface resistivity was measured, and then the test piece was rubbed with a flannelette on one side 10 times, and the surface resistivity was measured again, and the degree of deterioration of the surface resistivity was judged. [2] Antistatic liquids shown in the following formulations [] to [] and comparative examples were prepared.
【表】【table】
【表】
上記の如く、本発明の帯電防止液は、優れた発
電防止性能、高い保持性を示すものである。
尚、処方−〜(本発明)については、いず
れも写真性、増感紙汚染性、液の経時安定性につ
いては問題なかつた。[Table] As described above, the antistatic liquid of the present invention exhibits excellent power generation prevention performance and high retention properties. Regarding the formulations (invention), there were no problems with regard to photographic properties, intensifying screen staining, and stability of the liquid over time.
Claims (1)
少なくとも1つと、下記一般式()で表わされ
る界面活性剤及び下記一般式()で表わされる
フツ素化炭化水素系界面活性剤から選ばれる少な
くとも1つの界面活性剤とを含有する帯電防止性
洗浄液に於て、一般式()で表わされる界面活
性剤及び/又は一般式()で表わされるフツ素
化炭化水素系界面活性剤に対する一般式()で
表わされる界面活性剤の重量比が5/95乃至50/
50であり、かつ該洗浄液中の界面活性剤濃度が
0.5乃至5.0重量%である事を特徴とする帯電防止
性洗浄液。 一般式() 但し、a、b及びcは整数を表わしa+c=4
乃至160、b=10乃至45である。 一般式() 但し、R、R1は炭素数3乃至12の脂肪族炭化
水素基、Aは炭素数3乃至5の脂肪族炭化水素
基、Mは水素原子、アルカリ金属原子又は4級ア
ンモニウム基、を表わす。 一般式() RF−A−X 但し、RFは少なくとも3個の沸素原子を含有
する部分沸素化または全沸素化炭化水素を表わ
し、Aは化学結合手または二価の脂肪族、芳香族
または混合脂肪族−芳香族基を表わし、これは酸
素原子、エステル基またはアミド基の異種原子で
中断されたものを含む。Xは(−CH2CH2O)oR3
(ここに、R3は水素原子又は炭素数1乃至5のア
ルキル基を表わし、nは5〜20の整数を表わし、
このポリオキシエチレン基は一つまたはそれ以上
のイソプロピレンオキシ基で中断されていてもよ
い)、 (ここに、Alkは炭素数1乃至5の低級アルキレ
ン基を表わし、R4は炭素数1乃至5の低級アル
キル基を表わす)、−SO3M、−OSO3Mまたは−
COOMを表わす(ここにMは一般式()のM
と同じ意味を表わす)。[Scope of Claims] 1 At least one surfactant represented by the following general formula (), a surfactant represented by the following general formula (), and a fluorinated hydrocarbon interface represented by the following general formula () In an antistatic cleaning liquid containing at least one surfactant selected from active agents, a surfactant represented by the general formula () and/or a fluorinated hydrocarbon interface represented by the general formula () The weight ratio of the surfactant represented by the general formula () to the active agent is 5/95 to 50/
50, and the surfactant concentration in the cleaning solution is
An antistatic cleaning liquid characterized by having a content of 0.5 to 5.0% by weight. General formula () However, a, b and c represent integers and a+c=4
b=10 to 160, and b=10 to 45. General formula () However, R and R 1 represent an aliphatic hydrocarbon group having 3 to 12 carbon atoms, A represents an aliphatic hydrocarbon group having 3 to 5 carbon atoms, and M represents a hydrogen atom, an alkali metal atom, or a quaternary ammonium group. General formula () R F -A-X However, R F represents a partially or fully fluorinated hydrocarbon containing at least three fluorine atoms, and A is a chemical bond or a divalent aliphatic hydrocarbon. , represents an aromatic or mixed aliphatic-aromatic group, including those interrupted by a heteroatom of an oxygen atom, an ester group or an amide group. X is (-CH 2 CH 2 O) o R 3
(Here, R 3 represents a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, n represents an integer of 5 to 20,
This polyoxyethylene group may be interrupted by one or more isopropyleneoxy groups), (Here, Alk represents a lower alkylene group having 1 to 5 carbon atoms, and R 4 represents a lower alkyl group having 1 to 5 carbon atoms), -SO 3 M, -OSO 3 M or -
Represents COOM (here M is M in the general formula ()
(expresses the same meaning as ).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21223782A JPH0231754B2 (en) | 1982-12-03 | 1982-12-03 | TAIDENBOSHISEISENJOEKI |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21223782A JPH0231754B2 (en) | 1982-12-03 | 1982-12-03 | TAIDENBOSHISEISENJOEKI |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59102975A JPS59102975A (en) | 1984-06-14 |
| JPH0231754B2 true JPH0231754B2 (en) | 1990-07-16 |
Family
ID=16619231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21223782A Expired - Lifetime JPH0231754B2 (en) | 1982-12-03 | 1982-12-03 | TAIDENBOSHISEISENJOEKI |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0231754B2 (en) |
-
1982
- 1982-12-03 JP JP21223782A patent/JPH0231754B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59102975A (en) | 1984-06-14 |
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