CN104195560A - Anhydrous tetramethyl ammonium hydroxide stripping solution - Google Patents

Anhydrous tetramethyl ammonium hydroxide stripping solution Download PDF

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Publication number
CN104195560A
CN104195560A CN201410457193.3A CN201410457193A CN104195560A CN 104195560 A CN104195560 A CN 104195560A CN 201410457193 A CN201410457193 A CN 201410457193A CN 104195560 A CN104195560 A CN 104195560A
Authority
CN
China
Prior art keywords
tetramethylammonium hydroxide
stripping solution
organic solvent
aqueous stripping
ammonium hydroxide
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
CN201410457193.3A
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Chinese (zh)
Inventor
曹大妹
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.)
KUNSHAN SIGO MICROELECTRONICS MATERIALS Co Ltd
Original Assignee
KUNSHAN SIGO MICROELECTRONICS MATERIALS 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 KUNSHAN SIGO MICROELECTRONICS MATERIALS Co Ltd filed Critical KUNSHAN SIGO MICROELECTRONICS MATERIALS Co Ltd
Priority to CN201410457193.3A priority Critical patent/CN104195560A/en
Publication of CN104195560A publication Critical patent/CN104195560A/en
Pending legal-status Critical Current

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  • Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)

Abstract

The invention relates to an anhydrous tetramethyl ammonium hydroxide stripping solution, which is mainly composed of tetramethyl ammonium hydroxide, propyl gallate and an organic solvent at the ratio of (3-7):3:17, wherein the organic solvent is formed by mixing one or two organic solvents and is dimethyl sulfoxide and/or an E200 solvent. A preparation method of the anhydrous tetramethyl ammonium hydroxide stripping solution comprises the following steps of 1, preparing a tetramethylammonium hydroxide/propyl gallate mixed solution; 2, mixing the mixed solution obtained in the step (1) and other organic solvents, and stirring for 30 minutes under ventilating; and 3, filtering the mixed solution obtained in the step 2 to be 0.2mu m. The use temperature of the anhydrous tetramethyl ammonium hydroxide stripping solution is 40-60 DEG C.

Description

Tetramethylammonium hydroxide is without aqueous stripping solution
Technical field
The present invention relates to dry etching field, specifically Tetramethylammonium hydroxide is without aqueous stripping solution.
Background technology
Metal etch (etching) is by materials'use chemical reaction or physical shock effect and the technology removing.Metal etch technology can be divided into wet etching (wet etching) and dry etching (dry etching) two classes.
Conventionally indication metal etch also claims photochemistry metal etch (photochemical etching); after referring to make a plate, develop by exposure; protective membrane that will metal etch region is removed; in the time of metal etch, contact chemical solution; reach the effect of dissolved corrosion, form effect concavo-convex or hollow out moulding.Can be used to the earliest manufacture the printing such as copperplate, photo zincography embossing plate, be also used in widely weight reduction (Weight Reduction) instrument panelling, nameplate and traditional processing method are difficult to the processing of the thin type workpiece of processing etc.; Develop through constantly improvement and processing unit, can also be used for the processing of aviation, machinery, chemical industry electronics sheet parts precision metallic etching products, especially on manufacture of semiconductor, metal etch indispensable technology especially.
Technical in aluminum metal dry etching, often has resistates and occurs, these resistatess form through high temperature after metal adds gas to add photoresist material, and aluminum metal also can be subject to dry etching gas corrosion simultaneously.Also there is no at present a kind of special Tetramethylammonium hydroxide that effective especially dry etching is used afterwards to aluminum metal without aqueous stripping solution.
Summary of the invention
The present invention, just for above technical problem, provides a kind of special Tetramethylammonium hydroxide that effective especially dry etching is used afterwards to aluminum metal without aqueous stripping solution.
Tetramethylammonium hydroxide, without aqueous stripping solution, is mainly made up of Tetramethylammonium hydroxide, Tenox PG, organic solvent, and wherein, the ratio between each component is Tetramethylammonium hydroxide: Tenox PG: organic solvent=3~7:3:17.Organic solvent forms for one or both organic solvents mix.Organic solvent is dimethyl sulfoxide (DMSO).Organic solvent is E200 solvent.
The present invention also provides the preparation method of Tetramethylammonium hydroxide without aqueous stripping solution, comprises the following steps: 1, preparation Tetramethylammonium hydroxide/Tenox PG mixing solutions; 2, the mixing solutions in step 1 is mixed with other organic solvent, ventilate and stir 30 minutes; 3, the mixing solutions in step 2 is filtered through 0.2 μ m.Tetramethylammonium hydroxide is 40 DEG C~60 DEG C without the use temperature of aqueous stripping solution.Wherein, step 1, step 2 all need be carried out in the tempering tank of nonmetal single material.
Tetramethylammonium hydroxide of the present invention mainly contains without the beneficial effect of aqueous stripping solution:
1, can not cause aluminum metal to damage.
2, formula is simple, easily mixes.
3, use temperature is easily controlled.
4, there is no the danger of burning or blast.
Embodiment
Below in conjunction with specific embodiment, the invention will be further described.
Embodiment 1
Tetramethylammonium hydroxide and Tenox PG are prepared into Tetramethylammonium hydroxide/Tenox PG mixing solutions in the ratio of 1:1, in the pure PE tempering tank with ventilation installation, Tetramethylammonium hydroxide/Tenox PG mixing solutions is mixed in the ratio of 1:2 with dimethyl sulfoxide (DMSO), ventilate and stir after 30 minutes, after 0.2 μ m filters, carry out the anhydrous of dry etching and peel off.
Through test, it is very obvious that this Tetramethylammonium hydroxide is peeled off effect without aqueous stripping solution to aluminum metal dry-etching residue, and owing to being anhydrous formulations, therefore can not cause the corrosion of aluminium.
Embodiment 2
Tetramethylammonium hydroxide and Tenox PG are prepared into Tetramethylammonium hydroxide/Tenox PG mixing solutions in the ratio of 7:3, in the pure PE tempering tank with ventilation installation, Tetramethylammonium hydroxide/Tenox PG mixing solutions, dimethyl sulfoxide (DMSO), E200 solution are mixed in the ratio of 7:8:5, ventilate and stir after 30 minutes, after 0.2 μ m filters, carry out the anhydrous of dry etching and peel off.
Through test, it is very obvious that this Tetramethylammonium hydroxide is peeled off effect without aqueous stripping solution to aluminum metal dry-etching residue, and owing to being anhydrous formulations, therefore can not cause the corrosion of aluminium.

Claims (7)

1. Tetramethylammonium hydroxide, without aqueous stripping solution, is mainly made up of Tetramethylammonium hydroxide, Tenox PG, organic solvent, and wherein, the ratio between each component is Tetramethylammonium hydroxide: Tenox PG: organic solvent=3~7:3:17.
2. Tetramethylammonium hydroxide, without aqueous stripping solution, is characterized in that described organic solvent forms for one or both organic solvents mix according to claim 1.
3. Tetramethylammonium hydroxide, without aqueous stripping solution, is characterized in that described organic solvent is dimethyl sulfoxide (DMSO) according to claim 1.
4. Tetramethylammonium hydroxide, without aqueous stripping solution, is characterized in that described organic solvent is E200 solvent according to claim 1.
5. Tetramethylammonium hydroxide, without aqueous stripping solution, is characterized in that described Tetramethylammonium hydroxide is 40 DEG C~60 DEG C without the use temperature of aqueous stripping solution according to claim 1.
6. Tetramethylammonium hydroxide, without the preparation method of aqueous stripping solution, mainly comprises the following steps: 1, preparation Tetramethylammonium hydroxide/Tenox PG mixing solutions; 2, the mixing solutions in step 1 is mixed with other organic solvent, ventilate and stir 30 minutes; 3, the mixing solutions in step 2 is filtered through 0.2 μ m.
7. Tetramethylammonium hydroxide, without the preparation method of aqueous stripping solution, is characterized in that described step 1, step 2 all carry out in the tempering tank of nonmetal single material according to claim 6.
CN201410457193.3A 2014-09-10 2014-09-10 Anhydrous tetramethyl ammonium hydroxide stripping solution Pending CN104195560A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410457193.3A CN104195560A (en) 2014-09-10 2014-09-10 Anhydrous tetramethyl ammonium hydroxide stripping solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410457193.3A CN104195560A (en) 2014-09-10 2014-09-10 Anhydrous tetramethyl ammonium hydroxide stripping solution

Publications (1)

Publication Number Publication Date
CN104195560A true CN104195560A (en) 2014-12-10

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106773563A (en) * 2016-12-27 2017-05-31 昆山欣谷微电子材料有限公司 Tetrapropyl amine bromide is without aqueous stripping solution

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003140364A (en) * 2001-11-02 2003-05-14 Mitsubishi Gas Chem Co Inc Resist removing solution for copper wiring board
CN1444103A (en) * 2002-03-12 2003-09-24 三菱瓦斯化学株式会社 Optical photoresist stripping composition and cleaning composition
CN1873543A (en) * 2005-05-12 2006-12-06 东京应化工业株式会社 Stripping liquid for photoresist
CN101286016A (en) * 2007-04-13 2008-10-15 安集微电子(上海)有限公司 Low etching photoresist cleaning agent
CN101384694A (en) * 2006-02-15 2009-03-11 马林克罗特贝克公司 Stabilized, non-aqueous cleaning compositions for microelectronics substrates

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003140364A (en) * 2001-11-02 2003-05-14 Mitsubishi Gas Chem Co Inc Resist removing solution for copper wiring board
CN1444103A (en) * 2002-03-12 2003-09-24 三菱瓦斯化学株式会社 Optical photoresist stripping composition and cleaning composition
CN1873543A (en) * 2005-05-12 2006-12-06 东京应化工业株式会社 Stripping liquid for photoresist
CN101384694A (en) * 2006-02-15 2009-03-11 马林克罗特贝克公司 Stabilized, non-aqueous cleaning compositions for microelectronics substrates
CN101286016A (en) * 2007-04-13 2008-10-15 安集微电子(上海)有限公司 Low etching photoresist cleaning agent

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106773563A (en) * 2016-12-27 2017-05-31 昆山欣谷微电子材料有限公司 Tetrapropyl amine bromide is without aqueous stripping solution

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Application publication date: 20141210