JPH06258607A - Dissolving and washing liquid for pitch, pine resin and the like - Google Patents
Dissolving and washing liquid for pitch, pine resin and the likeInfo
- Publication number
- JPH06258607A JPH06258607A JP6610993A JP6610993A JPH06258607A JP H06258607 A JPH06258607 A JP H06258607A JP 6610993 A JP6610993 A JP 6610993A JP 6610993 A JP6610993 A JP 6610993A JP H06258607 A JPH06258607 A JP H06258607A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- pitch
- dissolving
- hydrocarbon
- dissolution
- 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- Withdrawn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
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ピッチ,パラフィン,
松ヤニ,グリース,ワックス等を溶解して除去するピッ
チ、松ヤニ等の溶解洗浄液。The present invention relates to pitch, paraffin,
Dissolving and cleaning solution for pitch, pine tar, etc. that dissolves and removes pine tar, grease, wax, etc.
【0002】[0002]
【従来の技術】レンズ,プリズム,ミラー等の光学素子
の加工においては、光学素子を治具にセットして行って
いるが、この治具への仮止め接着のため、ピッチ,パラ
フィン,松ヤニ等の接着剤が使用されている。また、光
学素子の磨き皿にはピッチを用いることにより光学素子
を高精度に加工することもなされている。一方、金物や
プラスチックの切削には切削油が使用されていると共
に、これらの製造においてはグリース,ワックス等の油
剤が付着する。このように各種製品の製造や加工の際に
は接着剤,油剤が付着するため、これらを除去する必要
があり、これらの溶解洗浄液として用いられている。2. Description of the Related Art In the processing of optical elements such as lenses, prisms and mirrors, the optical elements are set on a jig, but pitch, paraffin and pine resin are used for temporary fixing to the jig. Etc. adhesives are used. Further, it is also possible to process the optical element with high precision by using a pitch in the polishing plate of the optical element. On the other hand, cutting oil is used for cutting metal objects and plastics, and oil agents such as grease and wax adhere to them in the production thereof. As described above, since adhesives and oils adhere during the manufacture and processing of various products, it is necessary to remove them, and they are used as a dissolving and cleaning solution for these.
【0003】かかる溶解洗浄液としてはトリクレンが用
いられていたが、塩素系溶剤のため毒性が強く、健康上
および環境汚染上、取扱いに注意を要する問題があっ
た。このためトリクレンの代替剤を使用する必要があ
り、特公昭51−29195号公報には、N−メチルピ
ロリドンを用いてピッチ状の重合物質を除去する方法が
記載されている。Although trichlene has been used as such a dissolution cleaning liquid, it has a strong toxicity because it is a chlorine-based solvent, and there is a problem that it must be handled with care for health and environmental pollution. For this reason, it is necessary to use a trichlene substitute, and Japanese Patent Publication No. 51-29195 discloses a method of removing a pitch-like polymerized substance using N-methylpyrrolidone.
【0004】[0004]
【発明が解決しようとする課題】しかしながら本発明者
がN−メチルピロリドンを用いてピッチの溶解を試みた
ところ、100%溶解することは困難であった。すなわ
ちN−メチルピロリドン100ml中に2.1gのピッ
チ団子を投入し、28KHz,1.2KWの超音波振動
を加えながら溶解させたところ、15分間経過しても溶
解が50%程度しかできず、その後、継続処理してもピ
ッチ団子が膨潤するだけであった。これに対し、トリク
レン100mlを用いて同様な処理を行ったところ、約
2.5分後にピッチ団子の100%が溶解した。以上の
ことから、N−メチルピロリドンはある程度の溶解力を
有しているが、それ以上の溶解力を増大させることがで
きないことが判明した。However, when the present inventors tried to dissolve pitch using N-methylpyrrolidone, it was difficult to dissolve 100%. That is, when 2.1 g of pitch dumpling was put into 100 ml of N-methylpyrrolidone and dissolved while applying ultrasonic vibration of 28 KHz and 1.2 KW, dissolution was only about 50% even after 15 minutes, After that, even if the treatment was continued, the pitch dumpling only swelled. On the other hand, when the same treatment was performed using 100 ml of trichlene, 100% of the pitch dumplings were dissolved after about 2.5 minutes. From the above, it was found that N-methylpyrrolidone has a certain degree of dissolving power, but cannot further increase the dissolving power.
【0005】また、N−メチルピロリドンはプラスチッ
ク材料に対してのアタック性が強く、プラスチックを使
用した部品に対しての洗浄には不向きとなっている。し
かも、N−メチルピロリドンは高親水性を有しており、
水吸収により経時的に劣化して、洗浄力が低下するばか
りでなく、悪臭を発する問題も有している。Further, N-methylpyrrolidone has a strong attack property on a plastic material, and is not suitable for cleaning parts made of plastic. Moreover, N-methylpyrrolidone has high hydrophilicity,
Not only does it deteriorate over time due to water absorption and the detergency decreases, but it also has the problem of giving off a bad odor.
【0006】本発明は上記事情を考慮してなされたもの
であり、N−メチルピロリドンよりも溶解力が大きく、
トリクレンに匹敵する溶解洗浄力を有し、しかも被洗浄
物へのアタック性がなく、安全に使用することが可能な
接着剤の溶解洗浄液を提供することを目的とする。The present invention has been made in consideration of the above circumstances, and has a larger dissolving power than N-methylpyrrolidone,
An object of the present invention is to provide a solution for cleaning and dissolving an adhesive, which has a solution cleaning power comparable to that of trichlene, has no attack on an object to be cleaned, and can be safely used.
【0007】[0007]
【課題を解決するための手段および作用】本発明の溶解
洗浄液は、アロマティック系炭化水素,シクロパラフィ
ン系炭化水素またはパラフィン系炭化水素の内のいずれ
か1種を有効成分として含有することを特徴とする。ま
た本発明においてはアロマティック系炭化水素,シクロ
パラフィン系炭化水素,パラフィン系炭化水素の内の少
なくとも2種を混合して有効成分としたことを特徴とし
ている。後者の混合物の場合においては、溶解洗浄対象
の接着剤に応じて合目的に、その配合が行われる。ま
た、混合物においては、他の溶剤を混合することもでき
る。Means and Actions for Solving the Problems The dissolution cleaning solution of the present invention is characterized by containing any one of aromatic hydrocarbons, cycloparaffinic hydrocarbons or paraffinic hydrocarbons as an active ingredient. And Further, the present invention is characterized in that at least two kinds of aromatic hydrocarbons, cycloparaffinic hydrocarbons and paraffinic hydrocarbons are mixed and used as an active ingredient. In the case of the latter mixture, the compounding is appropriately performed depending on the adhesive to be dissolved and washed. In addition, other solvents can be mixed in the mixture.
【0008】アロマティック系炭化水素はベンゼン環に
アルキル基が結合した石油由来の化合物であり、結合す
るアルキル基の数に応じて、化1,化2,化3に示す3
種に大別される。化1,化2,化3において、R1 ,R
2 ,R3 はいずれもCn H2n+1であり、化1におけるn
は1〜30、化2におけるnは10≦n≦30、化3に
おけるnは10≦n≦30である。2以上のアルキル基
が結合する化2,化3においてR1 =R2 ,R1 =R2
=R3 であるか、R1 ≠R2 ,R1 ≠R2 ≠R3 であ
る。アルキル基の炭素数nは溶解洗浄対象物に応じて適
宜選定される。Aromatic hydrocarbons are petroleum-derived compounds in which an alkyl group is bonded to a benzene ring, and are represented by Chemical formula 1, Chemical formula 2, and Chemical formula 3 depending on the number of alkyl groups bonded.
It is roughly divided into species. In Chemical formula 1, Chemical formula 2, and Chemical formula 3, R 1 , R
2 and R 3 are both C n H 2n + 1 , and n in the chemical formula 1
Is 1 to 30, n in Chemical formula 2 is 10 ≦ n ≦ 30, and n in Chemical formula 3 is 10 ≦ n ≦ 30. In Chemical formula 2 and Chemical formula 3 in which two or more alkyl groups are bonded, R 1 = R 2 , R 1 = R 2
= R 3 , or R 1 ≠ R 2 and R 1 ≠ R 2 ≠ R 3 . The carbon number n of the alkyl group is appropriately selected according to the object to be dissolved and washed.
【0009】[0009]
【化1】 [Chemical 1]
【0010】[0010]
【化2】 [Chemical 2]
【0011】[0011]
【化3】 [Chemical 3]
【0012】シクロパラフィン系炭化水素も石油由来の
化合物であり、アルキル基の結合数に応じて化4,化
5,化6に示す3種に大別される。化4,化5,化6に
おいて、R1 ,R2 ,R3 はいずれもCn H2n+1であ
り、化4におけるnは1〜30、化5および化6におけ
るnは10≦n≦30である。また、化5および化6に
おいてはR1 =R2 ,R1 =R2 =R3 であるか、R1
≠R2 ,R1 ≠R2 ≠R3である。このシクロパラフィ
ン系炭化水素においても、アルキル基と炭素数nは溶解
洗浄対象物に応じて適宜、選定される。Cycloparaffinic hydrocarbons are also petroleum-derived compounds and are roughly classified into three types shown in Chemical formula 4, Chemical formula 5, and Chemical formula 6 according to the number of alkyl group bonds. In Chemical Formula 4, Chemical Formula 5, and Chemical Formula 6, R 1 , R 2 , and R 3 are all C n H 2n + 1 , n in Chemical Formula 4 is 1 to 30, and n in Chemical Formula 5 and Chemical Formula 6 is 10 ≦ n. ≦ 30. Further, in Chemical formulas 5 and 6, R 1 = R 2 , R 1 = R 2 = R 3 or R 1
≠ R 2 , R 1 ≠ R 2 ≠ R 3 . Also in this cycloparaffin hydrocarbon, the alkyl group and the carbon number n are appropriately selected according to the object to be dissolved and washed.
【0013】[0013]
【化4】 [Chemical 4]
【0014】[0014]
【化5】 [Chemical 5]
【0015】[0015]
【化6】 [Chemical 6]
【0016】パラフィン系炭化水素は化学式Cn H2n+2
を有し、10≦n≦17の石油由来の化合物が使用され
る。一方、洗浄対象となる接着剤におけるピッチは重油
精製後の残留カスであり、単純なアロマティック系,パ
ラフィン系ではなく、極性を有した各種モノマー,オリ
ゴマー,ポリマーの混合物である。これに対し、上述し
た炭化水素化合物は極性のバランスが良く、これにより
塩素系溶剤と同等あるいはそれ以上強力にピッチを溶解
することができる。かかる作用は他の油剤であるパラフ
ィン,松ヤニ,グリース,ワックス等に対しても有効で
あり、これらを十分に溶解することができる。Paraffinic hydrocarbons have the chemical formula C n H 2n + 2
And petroleum-derived compounds with 10 ≦ n ≦ 17 are used. On the other hand, the pitch in the adhesive to be cleaned is a residual residue after heavy oil refining, and is not a simple aromatic system or paraffin system but a mixture of various polar monomers, oligomers and polymers. On the other hand, the above-mentioned hydrocarbon compound has a good balance of polarities, which allows the pitch to be dissolved as strongly as or more strongly than the chlorine-based solvent. This action is also effective for other oil agents such as paraffin, pine resin, grease, wax, etc., and these can be sufficiently dissolved.
【0017】[0017]
【実施例】溶解洗浄液として、いずれも石油由来のアロ
マティック系炭化水素,シクロパラフィン系炭化水素お
よびパラフィン系炭化水素を用意し、溶解洗浄対象物と
してピッチ,松ヤニ,パラフィン,密ロウを用意し、以
下の手順で溶解試験を行った。この場合、アロマティッ
ク系炭化水素としては、炭素数14,平均分子量15
6、パラフィン系炭化水素としては炭素数15,平均分
子量174、シクロパラフィン系炭化水素としては炭素
数12,平均分子量130の各化合物を溶解洗浄液とし
て使用した。[Embodiment] All of the petroleum-derived aromatic hydrocarbons, cycloparaffinic hydrocarbons, and paraffinic hydrocarbons were prepared as dissolution cleaning liquids, and pitch, pine resin, paraffin, and wax were prepared as dissolution cleaning objects. The dissolution test was conducted in the following procedure. In this case, the aromatic hydrocarbon has 14 carbon atoms and an average molecular weight of 15
6. Each compound having a carbon number of 15 and an average molecular weight of 174 as a paraffinic hydrocarbon and having a carbon number of 12 and an average molecular weight of 130 as a cycloparaffinic hydrocarbon was used as a dissolution cleaning liquid.
【0018】まず、K級2号および3号のピッチを1:
1の比率で混合し、円錐台形状のピッチ塊2.1gを注
型してピッチの溶解用試料とした。また、松ヤニ,パラ
フィン,密ロウは0.25gの塊として溶解用試料とし
た。これらを溶解槽内に投入し、各溶解洗浄液による溶
解試験を行った。図2はピッチ塊2.1gの溶解試験を
示し、ビーカー1内に常温の溶解洗浄液2を100ml
投入し、このビーカー1を超音波槽3の常温の水槽4に
浸漬する。超音波槽3内には28KHz,1.2KWの
出力を有した超音波振動板5が設けられている。このよ
うにセットした後、超音波振動を作用させた状態でビー
カー1内に2.1gのピッチ塊6を投入して溶解させ
る。溶解は1分経過毎における残留ピッチ塊6の重量を
測定しながら100%溶解させるまでの時間を計測し
た。First, the K-class No. 2 and No. 3 pitches are set to 1:
The mixture was mixed at a ratio of 1 and 2.1 g of a truncated cone-shaped pitch lump was cast to obtain a pitch melting sample. In addition, pine resin, paraffin and beeswax were used as a sample for dissolution in the form of a mass of 0.25 g. These were put into a dissolution tank, and a dissolution test was performed using each dissolution cleaning solution. FIG. 2 shows a dissolution test of 2.1 g of pitch lump, and 100 ml of room temperature dissolution cleaning liquid 2 is placed in the beaker 1.
Then, the beaker 1 is put into the ultrasonic bath 3 and is immersed in the normal temperature water bath 4. Inside the ultrasonic tank 3, an ultrasonic diaphragm 5 having an output of 28 KHz and 1.2 KW is provided. After setting in this way, 2.1 g of pitch lumps 6 are put into the beaker 1 while being subjected to ultrasonic vibration to be melted. For the dissolution, the time required for 100% dissolution was measured while measuring the weight of the residual pitch lumps 6 every 1 minute.
【0019】図3は松ヤニ,パラフィン,密ロウの溶解
試験を示し、試験管7内に溶解洗浄液2を充填して超音
波槽3の水槽4に浸漬する。水槽4は常温であり、超音
波槽3内には28KHz,1.2KWの出力の超音波振
動板5が設けられている。この試験においても超音波振
動を作用させた状態で、それぞれの試験管7に松ヤニ
8,パラフィン9,密ロウ10の各試料0.25gを投
入して完全溶解までの時間を測定した。FIG. 3 shows a dissolution test of pine resin, paraffin, and beeswax. The test tube 7 is filled with the dissolution cleaning liquid 2 and immersed in the water tank 4 of the ultrasonic tank 3. The water tank 4 is at room temperature, and an ultrasonic vibration plate 5 having an output of 28 KHz and 1.2 KW is provided in the ultrasonic tank 3. Also in this test, 0.25 g of each sample of pine resin 8, paraffin 9, and beeswax 10 was put into each test tube 7 while ultrasonic vibration was applied, and the time until complete dissolution was measured.
【0020】図1は図2に示す操作によりピッチ塊6を
溶解した場合の完全溶解までの時間をプロットした特性
図であり、特性曲線Aは上述したパラフィン系炭化水
素、特性曲線Bは上述したアロマティック系炭化水素、
特性曲線Cは同じく〔アロマティック系炭化水素:上述
したシクロパラフィン系炭化水素〕=50:50の混合
液、、特性曲線Dはパラフィン系炭化水素としてn−テ
トラデカンを用いた場合、特性曲線Eは比較例としての
トリクレンをそれぞれ示す。同図からアロマティック系
炭化水素(B)がトリクレンと同等の溶解力を有すると
共に、アロマティック系炭化水素とシクロパラフィン系
炭化水素の混合液(C)、パラフィン系炭化水素(Aお
よびD)がこれに続く溶解力を有しており、いずれも短
時間で完全溶解できることを示している。なお、シクロ
パラフィン系炭化水素を単体として使用したデータを記
載してしないが、混合液の溶解力を示す特性曲線Cから
判るように、シクロパラフィン系炭化水素単体でも、十
分な溶解力を有するものである。FIG. 1 is a characteristic diagram plotting the time until complete dissolution when the pitch mass 6 is dissolved by the operation shown in FIG. 2, the characteristic curve A being the above-mentioned paraffinic hydrocarbon, and the characteristic curve B being the above-mentioned. Aromatic hydrocarbons,
Characteristic curve C is the same as [aromatic hydrocarbon: cycloparaffinic hydrocarbon described above] = 50: 50, and characteristic curve D is the case where n-tetradecane is used as paraffinic hydrocarbon, characteristic curve E is Each of trichlene as a comparative example is shown. From the figure, the aromatic hydrocarbon (B) has the same dissolving power as trichlene, and the mixed liquid (C) of the aromatic hydrocarbon and the cycloparaffinic hydrocarbon and the paraffinic hydrocarbons (A and D) are It has the following dissolving power and shows that they can be completely dissolved in a short time. Although the data using the cycloparaffinic hydrocarbon as a simple substance is not described, as can be seen from the characteristic curve C showing the dissolving power of the mixed solution, the cycloparaffinic hydrocarbon alone has a sufficient dissolving power. Is.
【0021】表1は松ヤニ,パラフィン,密ロウを図2
に示す操作で完全溶解までに要する時間を測定した結果
を示す。溶解洗浄液の種類によって時間の大小はあるも
のの、いずれも完全溶解が可能となっている。Table 1 shows pine resin, paraffin and beeswax.
The results of measuring the time required for complete dissolution by the procedure shown in are shown below. Although the amount of time required varies depending on the type of dissolution cleaning solution, it is possible to completely dissolve them.
【0022】この溶解試験においても、シクロパラフィ
ン系炭化水素単体の溶解試験を行っていないが、アロマ
ティック系炭化水素:シクロパラフィン系炭化水素=4
9:51の混合液が、松ヤニ,パラフィン,密ロウのい
ずれをも溶解することからシクロパラフィン系炭化水素
単体でも十分な溶解力を有している。Even in this dissolution test, the dissolution test of the cycloparaffinic hydrocarbon alone was not conducted, but aromatic hydrocarbon: cycloparaffinic hydrocarbon = 4
Since the 9:51 mixed solution dissolves all of pine resin, paraffin, and beeswax, cycloparaffinic hydrocarbon alone has a sufficient dissolving power.
【0023】これらに加えて、本発明においては、アロ
マティック系炭化水素,パラフィン系炭化水素およびシ
クロパラフィン系炭化水素を混合しても、上述した溶解
洗浄対象物を同様に強力に溶解できることが判明してい
る。これらの混合液の場合には、溶解洗浄対象物に応じ
て、混合する化合物およびその混合比率を合目的に選択
することができる。In addition to these, in the present invention, it has been found that even if aromatic hydrocarbons, paraffin hydrocarbons and cycloparaffin hydrocarbons are mixed, the above-mentioned object to be dissolved and cleaned can be similarly strongly dissolved. is doing. In the case of these mixed liquids, the compound to be mixed and the mixing ratio thereof can be appropriately selected according to the object to be dissolved and washed.
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【発明の効果】以上のとおり本発明の溶解洗浄液はピッ
チ,松ヤニ,パラフィン,グリース,ワックス等の油剤
を完全溶解することができるため、トリクレンなどの塩
素系溶剤の代替用洗浄液として有用な用途を有してい
る。As described above, the dissolution cleaning solution of the present invention is capable of completely dissolving oil agents such as pitch, pine resin, paraffin, grease, wax, etc., and is therefore useful as a cleaning solution as a substitute for chlorine-based solvents such as trichlene. have.
【図1】ピッチ塊の溶解特性図。FIG. 1 is a dissolution characteristic diagram of pitch lumps.
【図2】ピッチの溶解試験を示す断面図。FIG. 2 is a cross-sectional view showing a pitch dissolution test.
【図3】松ヤニ等の溶解試験を示す断面図。FIG. 3 is a cross-sectional view showing a dissolution test of pine resin.
Claims (5)
とを特徴とするピッチ、松ヤニ等の溶解洗浄液。1. A solution for cleaning pitch, pine resin, etc., characterized by containing an aromatic hydrocarbon.
ことを特徴とするピッチ、松ヤニ等の溶解洗浄液。2. A solution for cleaning pitch, pine resin, etc., which contains cycloparaffinic hydrocarbon.
特徴とするピッチ、松ヤニ等の溶解洗浄液。3. A dissolution cleaning solution for pitch, pine resin, etc., characterized by containing paraffinic hydrocarbons.
フィン系炭化水素,パラフィン系炭化水素の内の少なく
とも2種を混合したことを特徴とするピッチ、松ヤニ等
の溶解洗浄液。4. A dissolution cleaning solution for pitch, pine resin, etc., characterized by mixing at least two kinds of aromatic hydrocarbons, cycloparaffinic hydrocarbons, and paraffinic hydrocarbons.
フィン系炭化水素,パラフィン系炭化水素の内の少なく
とも1種と溶液とを混合したことを特徴とするピッチ、
松ヤニ等の溶解洗浄液。5. A pitch characterized by mixing a solution with at least one of aromatic hydrocarbons, cycloparaffinic hydrocarbons, and paraffinic hydrocarbons,
A solution for dissolving and cleaning pine resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6610993A JPH06258607A (en) | 1993-03-02 | 1993-03-02 | Dissolving and washing liquid for pitch, pine resin and the like |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6610993A JPH06258607A (en) | 1993-03-02 | 1993-03-02 | Dissolving and washing liquid for pitch, pine resin and the like |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06258607A true JPH06258607A (en) | 1994-09-16 |
Family
ID=13306400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6610993A Withdrawn JPH06258607A (en) | 1993-03-02 | 1993-03-02 | Dissolving and washing liquid for pitch, pine resin and the like |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06258607A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08254602A (en) * | 1995-03-16 | 1996-10-01 | Japan Energy Corp | Cleaning agent for optical component |
-
1993
- 1993-03-02 JP JP6610993A patent/JPH06258607A/en not_active Withdrawn
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08254602A (en) * | 1995-03-16 | 1996-10-01 | Japan Energy Corp | Cleaning agent for optical component |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5503681A (en) | Method of cleaning an object | |
KR0145061B1 (en) | Method and apparatus for cleaning | |
JPH06503685A (en) | Methods and compositions for cleaning contaminants containing esters of terpenes and monobasic acids | |
JP3256630B2 (en) | Cleaning method | |
JPH02255385A (en) | Terpene-base solvent for cleaning of photo-polymer printing plate | |
JPS62234530A (en) | Solvent mixture | |
JP3203285B2 (en) | Method for producing low-corrosion polyarylene sulfide | |
JPH06258607A (en) | Dissolving and washing liquid for pitch, pine resin and the like | |
JPH06240295A (en) | Dissolving and cleansing fluid for pitch, colophonium or the like | |
JP3939774B2 (en) | Ternary mixture of solvents and their use in removing oily substances | |
JP4530382B2 (en) | Washing liquid composition for wax and pitch | |
JPH06128592A (en) | Composition for dissolving wax | |
JP4530381B2 (en) | Cleaning liquid composition | |
WO2017126652A1 (en) | Liquid detergent composition for removing sludge and hard films formed in system containing heavy hydrocarbon or element imparting polarity to molecule, and cleaning method using same | |
JP3319930B2 (en) | Alkylsulfosuccinate-containing compositions that significantly reduce the interfacial tension between various substances and water | |
JPH09191007A (en) | Photoresist removing liquid | |
KR102022857B1 (en) | Composition for removing styrene-acrylonitrile resin and recovering method of organic solvent contained in the same | |
JPH0978095A (en) | Cleaning composition and cleaning | |
RU1801974C (en) | Bitumen-polymer composition for protective coating of metal | |
RU2101337C1 (en) | Industrial means for removing remains of petroleum and petroleum products from surface | |
JP2003514103A (en) | Cleaning composition | |
JP3582886B2 (en) | Cleaning agent for optical parts | |
JPH09125092A (en) | Cleansing composition and cleansing | |
JP2921665B2 (en) | How to treat plastic waste | |
CN112859553A (en) | Vanadium oxide corrosion-inhibition fluorine-containing stripping liquid, preparation method and application thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A300 | Withdrawal of application because of no request for examination |
Free format text: JAPANESE INTERMEDIATE CODE: A300 Effective date: 20000509 |