JPS58141220A - Treatment of microporous cellulosic film - Google Patents
Treatment of microporous cellulosic filmInfo
- Publication number
- JPS58141220A JPS58141220A JP2211982A JP2211982A JPS58141220A JP S58141220 A JPS58141220 A JP S58141220A JP 2211982 A JP2211982 A JP 2211982A JP 2211982 A JP2211982 A JP 2211982A JP S58141220 A JPS58141220 A JP S58141220A
- Authority
- JP
- Japan
- Prior art keywords
- film
- treatment
- plasma
- microporous
- gas
- 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
Links
Landscapes
- Treatments Of Macromolecular Shaped Articles (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は鋼111蝋維嵩或に酪酸繊維索等の繊維索系d
導体↓ジなる倣細多孔注フィルムの孔の性質會本買的に
夏えることなく親水性を付与する処理力法に関するもの
でるる。さらに砕しく云えば繊繊嵩鋳尋体よジなる微細
多孔性フィルムの表面に4周波励起によるグラズマ処理
金行ってフィルムの孔の性質1に実質的に変えることな
く、フィルムに親水性全付与する方法に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention provides fiber cable systems such as steel 111 wax fibers or butyric acid fiber cables.
This article concerns the processing power method that imparts hydrophilicity without commercially increasing the properties of the pores in the conductor ↓ imitative microporous injection film. More specifically, the surface of a microporous film such as a fiber bulk casting body is subjected to a glazma treatment using four-frequency excitation to completely impart hydrophilic properties to the film without substantially changing the pore properties of the film. It's about how to do it.
硝rhIt稙m系或は酪酸繊維系等の稙維累誘尋体より
なる倣km多孔社フィルムは近時、精密p適用等りノイ
ルメーメf4アとし−C%方面で巾広く1更用−gtt
ているが、本末、疎水性でめるため、これに親水性を付
与するのに、グリセリン、トリア七テ/、ヒドリキシノ
ロビルセルローズ、或ハトリドンX−100勢の界面活
性剤t−湿@嗣として飄m腺液VC癌加するか、I!l
麟恢にこれらの湿潤剤で二次処理管行っている。The imitation km porosha film made of filamentous dielectric material such as nitrate rhItm type or butyric acid fiber type has recently been widely used in the precision p application, etc.
However, since it is hydrophobic, a surfactant such as glycerin, tri-7, hydrixinolobil cellulose, or Hatridon X-100 is used to give it hydrophilicity. As a successor, will I add VC cancer? l
Secondary treatment pipes are often treated with these wetting agents.
しかしこれらの湿潤剤は仮処理液およびPlfL等に移
行し、こ扛らの液に悪影響を与えるので好ましくない。However, these wetting agents are undesirable because they migrate into the temporary treatment liquid, PlfL, etc. and have an adverse effect on these liquids.
これらの感影醤を防ぐため、実際使用時にはめらかしめ
予備洗浄を行っているのが通例でるるか、手間がかかる
し、又、完全にこれら湿潤剤を除去することに極めて困
−である。さらにはかかる湿潤剤の存在は滴れの不均一
性の原因となり或は経時的にこれら湿#l剤が変化し几
り、次lから揮散して親水性を劣化させる等多くの欠点
がめった。In order to prevent these wetting agents from forming, it is customary to perform pre-smoothing and pre-cleaning before actual use, which is time-consuming and extremely difficult to completely remove these wetting agents. . Furthermore, the presence of such wetting agents causes non-uniformity of dripping, or these wetting agents change and cool down over time, and evaporate from the next step, resulting in a deterioration of hydrophilicity, and many other drawbacks are rare. .
本発明者らはこの様な従来法の欠点t−a服し、簡単な
操作で多孔性7−トのもつ孔の性質を損なわず親水性の
みt付与し得る方法を開発するために鋭意研究を重ね九
結米、繊維素系fiL細多孔性フィルム表面に?161
i11波励起によるノラズマ処理を施して親水性τ1・
1与嘔ぜ得ることと見出し、此の知見に基づいて本発明
ftなすに至つ几。即ち本発明はフ1ルム表面に高崗波
励起によるノラズマ処理を施rことVCよ、)でフィル
ムに親水at−付与さぜることを符値とする繊繕素糸砿
細多孔性フィルムの処’1力hx懺旨とするものでりる
Oノラズマは大別して千両グラツマ(熱グラツマ)と非
乎鈎!うでマ(低温ノラズマ)に分類4扛るが、本°尾
明に他用するのは非平衡グラツマに属する低温ノラノマ
でめ9、処理の対象となるフ4Jレムに対して熱的影曽
が少ないという利点があるO即ら0すl −I Tor
r (/J//ス圧力においてAmm電電J’を印加す
ることによってノラズマを形成し、こnt−処理対尿物
の六面に作用させることによって表面版′繊を何うもの
でるる。The present inventors have overcome the drawbacks of such conventional methods and have conducted extensive research in order to develop a method that can impart only hydrophilicity to porous materials without impairing their pore properties through simple operations. Layer nine knots on the surface of the cellulose-based fiL microporous film? 161
Hydrophilic τ1・
Based on this finding, we have come up with the present invention. That is, the present invention is directed to the production of a finely porous film made of finely woven fibers, whose surface is subjected to a nolasma treatment by high-frequency excitation (also known as VC) to impart hydrophilicity to the film. The thing that makes the place '1 power hx summary is Riru O Norazuma can be roughly divided into senryo guratsuma (thermal guratsuma) and non-harvest! Although it is classified as Udema (low-temperature Norasma)4, it is also used for low-temperature Norasma belonging to non-equilibrium Glatumas9, and it has a thermal effect on F4J Rem, which is the target of treatment. O, which has the advantage of having less
By applying an Amm electric current J' at a pressure of /J//, a nolasma is formed, and by acting on six sides of the nt-treated urine, the surface plate' fibers are produced.
放置の形式にμ内6μ電極力式、外部IIL惨方式等・
檜々の万人がbるが、外部電極方式が好ましい。For the left type, μ internal 6μ electrode force type, external IIL type, etc.
There are many types of cypresses, but the external electrode method is preferable.
jスtよ黒磯//ス、就中アルコ゛/、ヘリウム、窒素
等の小1I5Bガスを使用する。For example, a small 1I5B gas such as Kuroiso gas, especially alcohol, helium, or nitrogen, is used.
ノラズマ処理の脅長は改質の効果が、数十オングストロ
ーム〃1ら数十オングストロームの深さの表向層に止り
、フィルムの本質的な特性金変えないという利点かめる
。又、処理時間は他の処理乗件によっであるs1変るが
、通常10秒〜60秒4にと考えればよい。The advantage of NORAZMA treatment is that the modification effect is limited to the surface layer at a depth of several tens of angstroms to several tens of angstroms and does not change the essential properties of the film. Further, the processing time varies by a certain amount s1 depending on other processing conditions, but it is generally considered to be 10 seconds to 60 seconds4.
このグラツマ処理によって繊維単糸微細多孔性フィルム
の透装置、破裂強匿、・譬ノルポイント等の値は殆んど
変らず、外部も変化しない、付与された親水性も折開し
て保存しておけば3t月経過後も変らず、120℃、3
0分のオートクレーブ処理後でも充分その親水性に保几
れうる。又、105℃、2時間の熱風乾燥後でも常温に
戻せはでの親水性は保持されている。Due to this Glatsma treatment, the permeability, rupture resistance, and nodal point values of the single fiber microporous film hardly change, and the external properties do not change either. If you leave it there, it will not change even after 3t months have passed, and the temperature will remain at 120℃, 3
Its hydrophilicity can be maintained sufficiently even after autoclaving for 0 minutes. Further, even after hot air drying at 105° C. for 2 hours, the hydrophilicity is maintained even when the temperature is returned to room temperature.
次に添付図面に匠って本発明の実NI一様の一例奢説明
する。第1図は本発明方法′を実施するのに好適なグラ
ツマ処理装置の概略説明図でろって、ノラズマ反応器l
の内部には被処理物2が装入される。バルブ3を開けて
A璧ポンノ9で規定真壁l1(12は真空針)に減圧し
乍ら流量y4節弁4を制御してガス((5μガス♂ンベ
シ一定量流す。Next, an example of the actual NI uniformity of the present invention will be explained with reference to the accompanying drawings. FIG. 1 is a schematic explanatory diagram of a Glazma treatment apparatus suitable for carrying out the method of the present invention.
The object to be processed 2 is placed inside the chamber. Open the valve 3 and reduce the pressure to the specified true wall l1 (12 is the vacuum needle) with the A valve 9, while controlling the flow rate y4 and the control valve 4 to flow a constant amount of gas ((5μ gas ♂).
このガスは簡向波コイル6によって励起さ扛、゛これに
上って被処理物2σグラズマ処理される。七の恢、がス
は排田口lOから排出される。図において8は電流計、
11はfi1m調節器でめる。This gas is excited by the simple wave coil 6, and the object to be treated is subjected to 2σ glasma treatment. In the seventh case, the gas is discharged from the discharge port IO. In the figure, 8 is an ammeter,
11 is set using the fi1m adjuster.
此の処理には王としてアルゴンガスが使われたかヘリウ
ムや窒素がス尋不活性ガスなら同様に便用可能でめる。Argon gas was used as the primary gas for this process, but helium and nitrogen gases can also be used as well if they are inert gases.
真空度は1〜Q、1torr又20〜50ワ2トの電力
が用いられ7t。The degree of vacuum is 1 to Q, 1 torr, and the power of 20 to 50 watts is 7 tons.
本発明によって処理された繊維素系微細多孔性フィルム
を工たとえ湿114削を師卯していなくても優れた親水
性を良好に保持するので清浄な多孔性フィルムが潜られ
る。又、oJ塑性を保持するため、県別(7たグリセリ
ン等も本発明の処理によってその抽出皺が少なくなると
いう効果も賛さnる。Even if the cellulose-based microporous film treated according to the present invention is processed, it retains excellent hydrophilicity even if it is not subjected to wet abrasion, resulting in a clean porous film. In addition, in order to maintain oJ plasticity, the treatment of the present invention also praises the effect of reducing the extraction wrinkles of glycerin and the like.
爽−例1
試験I 試験■
硝化綿 35部 35部アセトン
140 140エメノール 12 U
120n−!タノール 1t)0
100区−■ 試験…
水 12部 1
2gグリセリン03
上表の様な浴液(試験11試−U)をそれぞれガラス板
よVctL砥し、温[30℃、種数70饅の−9で約1
時間乾沫後、ガラス板より剥ぎ取り、枠につけて113
0℃、1時間のIii鎌t;rTりた。得られた)(ル
ムt5 tar X 10国に切り、図面に示すゾラズ
マ処理器の台7上におき、アルゴンガス40 =rl/
rnln (D割で流し争う、真空ボンノ9で0゜75
torr 4C排気後、高向波電源8をオンにし、電力
を50ワツトに設定し、111%コ1ルに13.56
kllklzのl116Itd波電流を印加し、グラズ
マ會発生させた。Refreshing Example 1 Test I Test ■ Nitrified cotton 35 parts 35 parts acetone
140 140 Emenol 12 U
120n-! Tanol 1t) 0
100th Ward-■ Exam...Wednesday 12th part 1
2g Glycerin 03 The bath solution as shown in the above table (Test 11 Test-U) was polished to VctL on a glass plate, and the temperature [30℃, species number 70 rice cake -9] was about 1
After drying for a while, peel it off from the glass plate and attach it to the frame.
It was heated at 0°C for 1 hour. (obtained) (lum t5 tar
rnln (0°75 with vacuum bonno 9, competing with D discount)
After exhausting torr 4C, turn on the high wave power source 8, set the power to 50 watts, and set the power to 13.56 to 111%.
A 1116Itd wave current of kllklz was applied to generate a glasma interaction.
処理時間は10秒、30秒、60秒に変えて行った。規
定時間処理し皮後、A11lll波電流の印加を停止し
、処理器を開放してフィルムをとり出し九〇実験しリ2
・ 緘 験 m 試 験 ■二o’Fa
t綿 1.5 % 1.5 s三酢
鍍−1,51,5
エタノール l(J 10礪化
メルン 40 40水
1.5 1.
5グリtリン 00.5
上表の様な命取(試験繊、試験■〕tそれぞれガラス根
土に眞姑し、麺[25℃ 製置50−の甲で#’−J
1時藺放蝋恢、ガラス仮より刺ざ堆り、枠qこつげて1
(llj℃、1時間の転線tOった。得らt′した〕1
ルムt″5cmXlOmに切り、図囲に示すグラズマ処
堰器の台上ICkき アルゴンガス50Jy’p i
nの割で流し乍ら0.5 torr VC排気後、^−
波電電61ikfンし、電力に50ワツトに設定し、篩
電コづルに13.56 Mllzのl1li同波電流を
印加し、lシlマを発生さぜた。処理時間は10秒、3
0秒、1)Oしに哀えて(’TりたJ現冗時間処理し友
後、^11Il政の印加を停止し、処虐蟲を開放してフ
ィルムtと9出した。The treatment time was changed to 10 seconds, 30 seconds, and 60 seconds. After processing for the specified time, stop applying the A11llll wave current, open the processor, take out the film, and conduct 90 experiments.
t Cotton 1.5% 1.5 s Sansuzu-1,51,5 Ethanol l (J 10 Silicated melan 40 40 Water
1.5 1.
5 Grit phosphorus 00.5 Death as shown in the table above (test fiber, test)
At 1 o'clock, the wax was made, the glass was pierced, and the frame was fixed. 1
(llj℃, 1 hour transition line tO was obtained. Obtained t')] 1
Cut the lumen to 5cmXlOm and use the argon gas 50Jy'pi on the bench IC of the Glazma treatment weir shown in the figure.
After draining 0.5 torr VC as compared to n, ^-
A wave electric current of 61 ikf was turned on, the power was set to 50 watts, and a 11li wave current of 13.56 Mllz was applied to the sieve electric coil to generate an l simmer. Processing time is 10 seconds, 3
0 seconds, 1) After processing the current situation for a while, I stopped applying the power, released the torture insects, and released films t and 9.
実験例3
夾−例1.夾験例2の谷試料金直極25鳥vczr抜き
、25℃の蒸藺水土に浮ばせて完全に漬れる1での時間
(秒)を測定した。又、一部の試料を1100℃−2時
間熱風帖塊処理、及びl 20C−工O分間π−iクレ
ープ処理した故、1川じ−j定會イ了 ラ 7Co
結束を 第 l 表ンこ示す 。Experimental Example 3 - Example 1. The 25 bird vczr of the valley test sample of Experimental Example 2 was removed, floated on steamed rice water soil at 25°C, and the time (seconds) required for it to be completely immersed was measured. In addition, some of the samples were subjected to hot air blast treatment at 1100°C for 2 hours and π-i crepe treatment for 120C to 0 minutes, so that the results were not satisfied.
The binding is shown in Table 1.
14 1 表
実−例4
火験しIJ l 、爽−例2の各試料の一般物性を測定
し友。細末t−MZ表に73<す。14 1 Table - Example 4 The general physical properties of each sample of Example 2 were measured using a fire test. The fine powder t-MZ table shows 73<.
第 2 表
実験例5
300114三角フラスコに水1t)OLjt−加え、
直往47九試料1枚をとり、精秤したものを入れ、密栓
した。121C−30分のオートクレー!処理した後、
水中に#付したグリセリンの量をガスクロ1トゲラフイ
ーによって定量分析した。その結果を次に示す。Table 2 Experimental Example 5 Add 1 ton of water to a 300114 Erlenmeyer flask,
One 479 sample was taken, accurately weighed, and sealed. 121C-30 minutes autoclay! After processing,
The amount of #-marked glycerin in water was quantitatively analyzed using gas chromatography. The results are shown below.
試料:実験例1の試験用
抽出量:
グラズマ禾処理品 3・9/φ47%グラズマ処境
品 0.5す/φ47へ(30秒シSample: Test extraction amount of Experimental Example 1: Glazma-treated product 3.9/φ47% Glazma-treated product 0.5s/to φ47 (30 seconds cycle)
第1図は本発明を実施するi&置の概略説明図でわる・ Figure 1 is a schematic explanatory diagram of an i &
Claims (1)
によるグラズマ処理を施すことを%黴とする繊維S承倣
祷多孔注フィルムの処理力法。A processing power method for a porous film that imitates fiber S, in which a microporous film made of fiber A is subjected to glazma treatment by frequency excitation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2211982A JPS58141220A (en) | 1982-02-16 | 1982-02-16 | Treatment of microporous cellulosic film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2211982A JPS58141220A (en) | 1982-02-16 | 1982-02-16 | Treatment of microporous cellulosic film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58141220A true JPS58141220A (en) | 1983-08-22 |
Family
ID=12073994
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2211982A Pending JPS58141220A (en) | 1982-02-16 | 1982-02-16 | Treatment of microporous cellulosic film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58141220A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60221441A (en) * | 1984-04-18 | 1985-11-06 | Bridgestone Corp | Production of polar foamed products |
EP0788833A1 (en) * | 1996-02-12 | 1997-08-13 | Conte S.A. | Process for increasing the wettability of a porous body and device for carrying out the process |
WO2002046282A1 (en) * | 2000-12-07 | 2002-06-13 | Exxonmobil Oil Corporation | Plasma treated porous film |
DE102008020197A1 (en) * | 2008-04-15 | 2009-10-22 | Gelita Ag | Fast wettable, hydrocolloid-containing material, process for its preparation and its use |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5342185A (en) * | 1976-09-28 | 1978-04-17 | Sekisui Chem Co Ltd | Manufacture of separating membrane |
-
1982
- 1982-02-16 JP JP2211982A patent/JPS58141220A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5342185A (en) * | 1976-09-28 | 1978-04-17 | Sekisui Chem Co Ltd | Manufacture of separating membrane |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60221441A (en) * | 1984-04-18 | 1985-11-06 | Bridgestone Corp | Production of polar foamed products |
EP0788833A1 (en) * | 1996-02-12 | 1997-08-13 | Conte S.A. | Process for increasing the wettability of a porous body and device for carrying out the process |
FR2744649A1 (en) * | 1996-02-12 | 1997-08-14 | Conte | METHOD FOR INCREASING THE WETABILITY OF A POROUS BODY AND DEVICE FOR IMPLEMENTING THE PROCESS |
US6074534A (en) * | 1996-02-12 | 2000-06-13 | Conte Sa | Method of increasing the wettability of a porous body |
WO2002046282A1 (en) * | 2000-12-07 | 2002-06-13 | Exxonmobil Oil Corporation | Plasma treated porous film |
DE102008020197A1 (en) * | 2008-04-15 | 2009-10-22 | Gelita Ag | Fast wettable, hydrocolloid-containing material, process for its preparation and its use |
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