JPH0227386B2 - XSENZOKANSHOTAIDENBOSHISEISENJOEKI - Google Patents
XSENZOKANSHOTAIDENBOSHISEISENJOEKIInfo
- Publication number
- JPH0227386B2 JPH0227386B2 JP4413480A JP4413480A JPH0227386B2 JP H0227386 B2 JPH0227386 B2 JP H0227386B2 JP 4413480 A JP4413480 A JP 4413480A JP 4413480 A JP4413480 A JP 4413480A JP H0227386 B2 JPH0227386 B2 JP H0227386B2
- Authority
- JP
- Japan
- Prior art keywords
- antistatic
- ray
- intensifying
- intensifying screen
- 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.)
- Expired - Lifetime
Links
- 239000007788 liquid Substances 0.000 claims description 26
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 7
- -1 alkylammonium carboxylic acid betaine compound Chemical class 0.000 claims description 7
- 229960003237 betaine Drugs 0.000 claims description 7
- 238000004140 cleaning Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 description 18
- 230000003068 static effect Effects 0.000 description 12
- 239000011241 protective layer Substances 0.000 description 11
- 229920005994 diacetyl cellulose Polymers 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 238000011109 contamination Methods 0.000 description 7
- 230000005611 electricity Effects 0.000 description 6
- 239000002736 nonionic surfactant Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002280 amphoteric surfactant Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 239000006224 matting agent Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000003745 diagnosis Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 230000007257 malfunction Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 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
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 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
- 238000003756 stirring Methods 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
Landscapes
- Conversion Of X-Rays Into Visible Images (AREA)
- Detergent Compositions (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X線増感紙用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監紙間に挟まれ撮
影される。この取扱いの際、即ちレントゲンフイ
ルムを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こる事がある
(「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sclution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公昭35−
16425に見られるごときポリエチレンオキサイド、
ポリプロピレンオキサイド等のポリアルキレング
リコール系非イオン性界面活性剤が多く使用され
ていた。しかしながらこれらの帯電防止液は処理
直後では静電気発生防止効果はあつたが、次のよ
うな重大な欠点を有する事が判明した。即ち上記
非イオン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、更には螢光
層まで浸透し、保護層、螢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
に変色してしまう事がある。(これを「増感紙汚
染」と呼ぶ)。この汚染された増感紙を使用して
レントゲンフイルムを撮影し、現像すると増感紙
汚染された個所がレントゲンフイルムに減感マー
クとしてうつり、診断上重大な誤りをおかす危険
性がある。この増感紙汚染は、特に増感紙保護層
にジアセチルセルロース(以下「DAC」と略
す。)を使用している場合顕著に現われ、しかも
この汚染はいかにあとから拭いてもとれないもの
である。
又、帯電防止液として前記の如き非イオン界面
活性剤を使用すると増感紙保護層がDACの場合、
恐らく界面活性剤がDAC中にしみ込むという同
様の理由から帯電防止効果が経時により減退する
という欠点がある。
本発明の目的は第一に増感紙汚染性のないレン
トゲン増感紙用帯電防止液を提供する事にある。
第二にあらゆるレントゲンフイルムに対しすぐ
れた帯電防止効果を有するレントゲン増感紙用帯
電防止液を提供する事にある。
第三に増感紙に対し高い保持性を有するレント
ゲン増感紙用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レント
ゲン増感紙用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レントゲン増感紙用
帯電防止液を提供する事にある。
第六に経時安定性のすぐれたレントゲン増感紙
用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レントゲン
増感紙用帯電防止液を提供する事にある。
第八に写真性に何ら悪影響を及ぼさないレント
ゲン増感紙用帯電防止液を提供する事にある。
これらの目的は下記に示す両性界面活性剤の少
なくとも1種を主要構成成分として含有せしめた
帯電防止性洗浄液によつて達成される事を見い出
した。
すなわち、
アルキルアンモニウムカルボン酸ベタイン化合
物及びアルキルアンモニウムスルホン酸ベタイン
化合物から選ばれる少なくとも1つの化合物を
0.1〜20重量%含有する帯電防止性洗浄液。
次に本発明に使用する代表的な化合物例を示
す。
本発明に使用する両性界面活性剤は疎水基とし
て炭素数が6〜20のアルキル基又はアルケニル基
を有し、又アニオン性基としてはカルボキシル基
もしくはスルホン基が好ましいが、特に好ましい
ものはカルボキシルベタインである。
本発明に使用するこれら両性界面活性剤は通常
の方法で容易に合成できるが例えばジヤーナル
オブ ズイ アメリカン ケミカル ソサイエテ
ー第69巻、2095頁(1947年発行)および特公昭50
−5048明細書に記載されている方法で容易に合成
できる。
合成例(化合物1)
N−ドデジルN,N−ジメチルアミンの合成
ドデシルアミン1moleをエタノール300mlに溶
解させ、これに85%のフオルミツクアシツド260
mlを30〜40℃に保ちながら滴下する。次に同温下
で37%ホルムアルデヒド210mlを滴下する。滴下
終了後炭酸ガスの発生がなくなるまで還流する。
冷却し苛性ソーダで中和後トルエンを加え二層に
分離させ、上層を蒸留する。N−ドデシルN,N
−ジメチルアミン170g(収率80%、b、p94
℃/1mm)が得られる。
N−ドデシルN,N′−ジメチル−α−カルボ
ン酸ベタインの合成
N−ドデシルN,N′−ジメチルアミンを常法
によりモノクロル酢酸ソーダ水溶液と70〜80℃4
〜5時間かきまぜるとα−カルボン酸ベタインが
得られる。この粗成物はアセトンから再結晶する
ことにより精製する。
上記界面活性剤は帯電防止液中0.1〜20重量%、
好ましくは1〜10重量%含有される。
本発明の帯電防止液には界面活性剤としては
又はに属するもののみであることが好ましいが
必要に応じて、他の界面活性剤を併用する事もで
きる。他の界面活性剤としてはカチオン、アニオ
ン、非イオン界面活性剤が挙げられるが先に説明
したように非イオン界面活性剤は本発明の界面活
性剤に対し10重量%未満である事が好ましく、更
に5重量%以下である事が好ましい。又カチオ
ン、アニオン界面活性剤では本発明の界面活性剤
に対し50重量%以下である事が好ましく、更に20
重量%以下である事が好ましい。
これら界面活性剤としては
非イオン界面活性剤
C8H17O(CH2CH2O)5H、
C10H21O(CH2CH2O)5H、
アニオン界面活性剤
The present invention relates to an antistatic cleaning liquid for X-ray intensifying screens that does not cause intensifying screen contamination and has excellent antistatic properties. Normally, the X-ray film is placed between two pieces of paper and 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 static electricity is generated when the film is peeled off and this static electricity is discharged. This may cause a malfunction that causes the X-ray film to overlap (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 sclution, 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. For example, the materials used in these antistatic liquids include
Polyethylene oxide, such as that found in 16425,
Polyalkylene glycol nonionic surfactants such as polypropylene oxide have been widely used. However, although these antistatic liquids were effective in preventing the generation of static electricity immediately after treatment, it was found that they had the following serious drawbacks. That is, when the above nonionic surfactant is applied to the intensifying screen,
It penetrates from the surface of the protective layer of the intensifying screen into the inside of the protective layer and even to the fluorescent layer, and interacts with the substances present in the protective layer and fluorescent layer, causing the screen to turn yellow after long-term use. There are things I end up doing. (This is called "intensifying screen contamination.") If an X-ray film is photographed using this contaminated intensifying screen and then developed, the contaminated area of the intensifying screen will be transferred to the X-ray film as a desensitization mark, and there is a risk of making a serious error in diagnosis. This contamination of the intensifying screen is particularly noticeable when diacetyl cellulose (hereinafter referred to as "DAC") is used for the protective layer of the intensifying screen, and this contamination cannot be removed no matter how much you wipe it afterwards. . In addition, if a nonionic surfactant such as the one mentioned above is used as an antistatic liquid, if the protective layer of the intensifying screen is DAC,
The drawback is that the antistatic effect decreases over time, probably for the same reason that the surfactant soaks into the DAC. The first object of the present invention is to provide an antistatic liquid for X-ray intensifying screens that does not cause intensifying screen contamination. The second object is to provide an antistatic liquid for X-ray intensifying screens that has an excellent antistatic effect on all kinds of X-ray films. The third object is to provide an antistatic liquid for X-ray intensifying screens that has high retention properties for intensifying screens. Fourthly, the hand marks and developer that adhered to the surface of the intensifying screen,
To provide an antistatic liquid for an X-ray intensifying screen that can easily wipe off stains from lipstick, etc. The fifth object is to provide an antistatic liquid for X-ray intensifying screens that does not irritate the skin. The sixth object is to provide an antistatic liquid for X-ray intensifying screens that has excellent stability over time. The seventh object is to provide an antistatic liquid for X-ray intensifying screens that does not contain a large amount of organic solvent. The eighth object is to provide an antistatic liquid for X-ray intensifying screens that does not have any adverse effect on photographic properties. It has been found that these objects can be achieved by an antistatic cleaning liquid containing at least one of the following amphoteric surfactants as a main component. That is, at least one compound selected from an alkylammonium carboxylic acid betaine compound and an alkylammonium sulfonic acid betaine compound.
Antistatic cleaning liquid containing 0.1 to 20% by weight. Next, typical examples of compounds used in the present invention are shown. The amphoteric surfactant used in the present invention has an alkyl group or an alkenyl group having 6 to 20 carbon atoms as a hydrophobic group, and a carboxyl group or a sulfone group is preferable as an anionic group, and a particularly preferable one is carboxyl betaine. It is. These amphoteric surfactants used in the present invention can be easily synthesized by conventional methods.
of Zui American Chemical Society Vol. 69, p. 2095 (published in 1947) and Special Publication of the 1970s
It can be easily synthesized by the method described in -5048 specification. Synthesis Example (Compound 1) Synthesis of N-dodecyl N,N-dimethylamine Dissolve 1 mole of dodecylamine in 300 ml of ethanol, and add 85% Formic Acid 260 to this.
ml dropwise while keeping it at 30-40℃. Next, 210 ml of 37% formaldehyde is added dropwise at the same temperature. After the addition is complete, the mixture is refluxed until no carbon dioxide gas is generated.
After cooling and neutralizing with caustic soda, toluene is added to separate into two layers, and the upper layer is distilled. N-dodecyl N,N
-dimethylamine 170g (yield 80%, b, p94
℃/1mm) is obtained. Synthesis of N-dodecyl N,N'-dimethyl-α-carboxylic acid betaine N-dodecyl N,N'-dimethylamine was mixed with an aqueous monochloroacetic acid aqueous solution at 70-80℃4 by a conventional method.
Stirring for ~5 hours yields alpha-carboxylic acid betaine. This crude product is purified by recrystallization from acetone. The above surfactant is 0.1 to 20% by weight in the antistatic liquid,
Preferably it is contained in an amount of 1 to 10% by weight. It is preferable that the antistatic liquid of the present invention contains only surfactants belonging to or, but other surfactants may be used in combination if necessary. Examples of other surfactants include cationic, anionic, and nonionic surfactants, but as explained above, the amount of nonionic surfactants is preferably less than 10% by weight based on the surfactant of the present invention. Furthermore, it is preferably 5% by weight or less. In addition, for cationic and anionic surfactants, it is preferable that the amount is 50% by weight or less, and more preferably 20% by weight or less, based on the surfactant of the present invention.
It is preferable that it is less than % by weight. These surfactants include nonionic surfactants C 8 H 17 O (CH 2 CH 2 O) 5 H, C 10 H 21 O (CH 2 CH 2 O) 5 H, anionic surfactant
カチオン界面活性剤
等が挙げられる。
又これら界面活性剤の他必要に応じてマツト剤
等他物質を含有せしめる事ができる。マツト剤と
してはSiO2等が挙げられる。マツト剤の添加量
は界面活性剤に対し0.001〜10重量%、更に0.01
〜1重量%である事が好ましい。
本発明の界面活性剤は本来水溶性があるが必要
に応じて、メタノール、エタノール等の有機溶剤
を添加する事ができる。しかしX線増感紙用帯電
防止性洗浄液は、一般には暗室等の密室で使用さ
れる場合が多いので好ましくは有機溶剤の添加は
避けた方が良い。
帯電防止効果だけを期待する場合にはカチオ
ン、アニオン、非イオン両性タイプの界面活性剤
の中に有効なものも見い出されたがしかしながら
我々の研究では本発明の目的全てを満足する界面
活性剤は、この膨大な数の界面活性剤のうち本発
明の界面活性剤のみであつた。
又本発明に使用する界面活性剤に特徴的な事と
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。従つてその帯電性も各フイル
ムによつて大きく異な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界面活性剤にお
いては各フイルムに依らずすぐれた帯電防止効果
を発揮した。
これは他の界面活性剤ではみられない特徴であ
る。
本発明の帯電防止液は、その表面保護層のバイ
ンダーがDACから成る増感紙に対して極めて有
利に用いることが出来る。
本発明の界面活性剤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。
なお、実施例における接着テストは以下の方法
により行なつた。
(1) 増感紙汚染テスト
一般カセツテにLT−(化成オプトニクス
(株)製保護層DAC増感紙)をはり、増感紙表面
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し2時間乾
燥させた。次いで30℃、80%RHに1時間調湿
した後、RXレントゲンフイルム(富士写真フ
イルム(株)製)をはさみ5分間放置し、次いでレ
ントゲンフイルムを入れ換え5分間放置する。
このようにして2000枚のレントゲンフイルムを
処理し、増感紙の汚染具合を目視で判定する。
全く汚染されてない場合〇、一部汚染された場
合△、全面汚染された場合×とする。
(2) 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(以下
「PET」と略す))
Hi Screen Standard(化成オプトニクス
(株)保護層DAC)
LT−(化成オプトニクス(株)保護層
DAC)
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)に挟み、タケダ理研製絶縁計(TR−
8651)で1分間測定した。(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挟みゴム
ローラーでこすり、次いでこのレントゲンフイ
ルムを増感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
〇、一部発生した場合△、全面発生した場合×
とする。
(3) 増感紙に対する保持性試験
Hi Screen Standard(保護層DAC、PET)
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。
実施例 cationic surfactant etc. In addition to these surfactants, other substances such as matting agents can be contained as necessary. Examples of the matting agent include SiO 2 and the like. The amount of matting agent added is 0.001 to 10% by weight relative to the surfactant, and further 0.01% by weight.
The content is preferably 1% by weight. Although the surfactant of the present invention is originally water-soluble, an organic solvent such as methanol or ethanol can be added as necessary. However, since antistatic cleaning liquids for X-ray intensifying screens are generally used in closed rooms such as darkrooms, it is preferable to avoid adding organic solvents. When antistatic effects are desired, some cationic, anionic, and nonionic amphoteric surfactants have been found to be effective, but our research has shown that there are no surfactants that satisfy all of the objectives of the present invention. Among this huge number of surfactants, only the surfactant of the present invention was found. A characteristic feature of the surfactant used in the present invention is that it exhibits its antistatic effect regardless of the X-ray film used. X-ray film uses various additives in its surface layer to satisfy various performances, and the surface condition varies depending on each X-ray film manufacturer.
The reality is that each X-ray film type differs greatly. Therefore, it is thought that the charging properties vary greatly depending on each film. However, surprisingly, the surfactant of the present invention exhibited an excellent antistatic effect regardless of the type of film. This is a feature not found in other surfactants. The antistatic liquid of the present invention can be extremely advantageously used in an intensifying screen in which the binder of the surface protective layer is DAC. The surfactant 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 failure occurs, such as in the conveyor system rollers. 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. Note that the adhesion test in the examples was conducted by the following method. (1) Intensifying screen contamination test LT- (Kasei Optonics)
A protective layer DAC intensifying screen (manufactured by Co., Ltd.) was applied, and 1 c.c. of various antistatic liquids (3% by weight aqueous solution) soaked in gauze was applied to the surface of the intensifying screen and left at room temperature to dry for 2 hours. After adjusting the humidity to 30° C. and 80% RH for 1 hour, RX X-ray film (manufactured by Fuji Photo Film Co., Ltd.) was placed and left for 5 minutes, then the X-ray film was replaced and left for 5 minutes.
In this way, 2,000 pieces of X-ray film were processed, and the degree of contamination of the intensifying screen was visually determined.
If it is not contaminated at all, mark it as 〇, if it is partially contaminated, mark it as △, and if it is completely contaminated, mark it as ×. (2) Antistatic property test Hi Screen Standard (Kasei Optonics
Protective Layer Polyethylene Terephthalate Co., Ltd. (hereinafter abbreviated as "PET") Hi Screen Standard (Kasei Optonics Co., Ltd.)
Protective Layer DAC Co., Ltd.) LT- (Kasei Optonics Co., Ltd. Protective Layer
Gauze was soaked with 1 c.c. of various antistatic liquids (3% by weight aqueous solution) and applied to three types of intensifying screens (DAC), and left at room temperature to dry for 2 hours. Then 25℃, 25%
After adjusting the humidity to RH for 3 hours, the surface resistivity was measured. To measure the surface resistivity, a test piece of intensifying screen coated with antistatic liquid was sandwiched between Machiyu electrodes (the part in contact with the test piece was made of stainless steel) with an electrode spacing of 0.14 cm and a length of 10 cm, and a Takeda Riken insulation meter was used. (TR-
8651) for 1 minute. (The smaller the surface resistivity value is, the greater the antistatic effect is.) The static mark generation test uses a sample prepared for the antistatic property test, and an unexposed X-ray film is sandwiched between the surface coated with the antistatic liquid. After rubbing with a rubber roller, the X-ray film is then taken out from between the intensifying screens and developed. At this time, if static marks do not occur at all, 〇, if some static marks occur, △, if they occur all over, ×
shall be. (3) Retention test on intensifying screen Hi Screen Standard (protective layer DAC, PET)
Apply various antistatic liquids in the same manner as above. twenty five
After adjusting the humidity to 25% RH for 3 hours, the surface resistivity was measured, and then the test piece was rubbed 10 times with a flannel on one side, the surface resistivity was measured again, and the degree of deterioration of the surface resistivity was judged. Example
【表】
〓C13H27COONa
10部〓
[Table] 〓C 13 H 27 COONa
10 copies〓
Claims (1)
合物及びアルキルアンモニウムスルホン酸ベタイ
ン化合物から選ばれる少なくとも1つの化合物を
0.1〜20重量%含有することを特徴とするX線増
感紙用帯電防止性洗浄液。1 At least one compound selected from an alkylammonium carboxylic acid betaine compound and an alkylammonium sulfonic acid betaine compound.
An antistatic cleaning liquid for X-ray intensifying screens characterized by containing 0.1 to 20% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4413480A JPH0227386B2 (en) | 1980-04-04 | 1980-04-04 | XSENZOKANSHOTAIDENBOSHISEISENJOEKI |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4413480A JPH0227386B2 (en) | 1980-04-04 | 1980-04-04 | XSENZOKANSHOTAIDENBOSHISEISENJOEKI |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56141375A JPS56141375A (en) | 1981-11-05 |
| JPH0227386B2 true JPH0227386B2 (en) | 1990-06-15 |
Family
ID=12683149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4413480A Expired - Lifetime JPH0227386B2 (en) | 1980-04-04 | 1980-04-04 | XSENZOKANSHOTAIDENBOSHISEISENJOEKI |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0227386B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9381147B2 (en) * | 2014-10-20 | 2016-07-05 | Johnson & Johnson Consumer Inc. | Compositions comprising zwitterionic ester ammonioalkanoates |
| US9943816B2 (en) * | 2014-10-20 | 2018-04-17 | Eastman Chemical Company | Amphoteric ester sulfonates |
| US9533951B2 (en) | 2014-10-20 | 2017-01-03 | Eastman Chemical Company | Heterocyclic amphoteric compounds |
| US11414380B2 (en) | 2015-09-17 | 2022-08-16 | Eastman Chemical Company | Amphoteric compounds |
| US9993408B2 (en) | 2015-09-17 | 2018-06-12 | Johnson & Johnson Consumer Inc. | Compositions comprising zwitterionic alkyl-alkanoylamides and/or alkyl alkanoates |
-
1980
- 1980-04-04 JP JP4413480A patent/JPH0227386B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56141375A (en) | 1981-11-05 |
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