JPH1053568A - Purification and recovery of tetraalkylammonium hydroxide from waste developer liquor - Google Patents

Abstract

PROBLEM TO BE SOLVED: To industrially advantageously purify and recover a high-purity tetraalkylammonium hydroxide reusable in the photolithography process from a waste liquor containing a tetraalkylammonium hydroxide used as a positive- type resist developer. SOLUTION: A waste liquor containing a tetraalkylammonium hydroxide is treated with activated carbon to adsorb the impurities in the waste liquor to the activated carbon and remove them. Alternatively, the waste liquor is neutralized to remove the resultant insolubilized deposits, and then treated with activated carbon to adsorb the impurities in the waste liquor to the activated carbon and remove them; the resultant waste liquor is subjected to electrodialysis in an electrolytic bath using a cation exchange membrane.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for purifying and recovering tetraalkylammonium hydroxide from a developing waste solution. More specifically, the present invention relates to tetraalkylammonium hydroxide-containing waste liquid used as a positive resist developer in a photolithography process in the manufacture of integrated circuits such as ICs and LSIs, TFTs for liquid crystals, and printed circuit boards. The present invention relates to a method for purifying and recovering alkyl ammonium.

[0002]

2. Description of the Related Art In the manufacture of semiconductor integrated circuits such as ICs and LSIs, and thin film transistors TFT for liquid crystal, lithography techniques, particularly photolithography techniques using light, are employed to form fine patterns. That is, a method of applying a photoresist on a substrate such as a silicon wafer, exposing a predetermined circuit, and then performing development and etching. There are two types of photoresist, a positive type and a negative type, and the positive type is increasingly used for fine circuits because of its excellent dimensional accuracy and resolution. As the positive photoresist developing solution, an organic alkali aqueous solution, particularly a tetraalkylammonium hydroxide aqueous solution is used because it dislikes metal ions.

The waste liquid after use in the development of a positive photoresist contains a photoresist component such as a novolak resin dissolved with tetraalkylammonium hydroxide, a trace amount of a solvent, a surfactant and the like. Therefore, this development waste liquid causes water pollution and cannot be discarded as it is, and is disposed of through various processing steps.
There is a need to reduce or utilize waste liquid as the amount used increases. As a method of treating a tetraalkylammonium hydroxide-containing waste liquid used for the development of a positive photoresist, a method of reducing the waste liquid by distillation of the waste liquid or concentration by a reverse osmosis membrane is known.

Further, as a method of recovering and reusing the tetraalkylammonium hydroxide in the waste liquid, the waste liquid is subjected to a neutralization treatment to insolubilize the alkali-dissolved resist, and the insolubilized precipitate is filtered by various filtration methods. A method of filtering and separating is known. For example, a method in which the separated filtrate is supplied to an anode chamber of an electrolytic cell partitioned by an ion exchange membrane, and a tetraalkylammonium hydroxide aqueous solution is recovered from a cathode chamber and reused (Japanese Patent Laid-Open No. 4-228587). Has been proposed. In addition, lower organic substances which are residues of the resist solvent or the surfactant contained in the waste liquid are oxidatively decomposed by hydrogen peroxide, ultraviolet light or ozone (Japanese Patent Laid-Open No. 5-1 / 1993).
No. 7889) or a method of recovering high-purity tetraalkylammonium hydroxide by performing anodizing decomposition by an electrolytic method (Japanese Patent Laid-Open No. 5-106074).

[0005]

However, the conventional waste liquid containing tetraalkylammonium hydroxide is neutralized,
In a method of obtaining a tetraalkylammonium hydroxide by performing electrolysis using an ion exchange membrane after separating the insolubilized resist, it is not possible to completely remove the remaining organic substances. Furthermore, it is extremely difficult to completely remove residual organic matter even if it is decomposed by a chemical or electrolytic oxidation. In addition, as the method described above is used to obtain high-purity tetraalkylammonium hydroxide with less impurities, the purification cost increases. In addition, it has been difficult to remove metal ions such as Na, K, and Ca which are inevitably mixed when collecting the waste liquid.

In view of the above situation, an object of the present invention is to eliminate the drawbacks of the conventional method for treating a tetraalkylammonium hydroxide-containing waste liquid, and to recover a tetraalkylammonium hydroxide-containing waste liquid of high purity that can be reused. An object of the present invention is to provide a method for industrially advantageously purifying and recovering tetraalkylammonium hydroxide.

[0007]

Means for Solving the Problems In order to solve the above-mentioned problems, the present inventors have made intensive studies and, as a result, concentrated and cooled a tetraalkylammonium hydroxide-containing waste solution used as a positive resist developing solution. It has been found that the above object can be achieved by crystallizing tetraalkylammonium hydroxide and recovering it as crystals.
Further, a means for neutralizing the tetraalkylammonium hydroxide-containing waste liquid to remove insoluble precipitates,
By incorporating means for performing electrodialysis in an electrolytic cell using a cation exchange membrane and the above-described method of concentrating and cooling, it has been found that tetraalkylammonium hydroxide with higher purity can be advantageously obtained.

Thus, according to the present invention, a tetraalkylammonium hydroxide-containing waste liquid used as a positive resist developer is treated with activated carbon to remove impurities in the waste liquid by adsorption. A method for purifying and recovering alkyl ammonium is provided.

Further, according to the present invention, a waste solution containing tetraalkylammonium hydroxide used as a positive resist developing solution is neutralized to remove insolubilized precipitates,
Next, a method for purifying and recovering tetraalkylammonium hydroxide is provided, wherein the method is treated with activated carbon to adsorb and remove impurities in the waste liquid, and electrodialysis is performed in an electrolytic cell using a cation exchange membrane. Is done.

[0010]

BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the purification and recovery method of the present invention will be described in detail. In the first method of the present invention,
As shown in the chart of FIG. 1, the wastewater containing tetraalkylammonium hydroxide is preferably concentrated, then treated with activated carbon to adsorb impurities and filtered to recover and recover the tetraalkylammonium hydroxide.

In the second method of the present invention, as shown in the chart of FIG. 2, the waste liquid containing tetraalkylammonium hydroxide is preferably concentrated, neutralized, decanted, and the supernatant liquid is decanted. The mixture is treated with activated carbon to adsorb impurities, removed by filtration or other means, and then subjected to electrodialysis in an electrolytic cell using a cation exchange membrane to purify and recover the tetraalkylammonium hydroxide.

In the first method of the present invention, it is preferable to first concentrate the tetraalkylammonium hydroxide-containing waste liquid used as the positive photoresist developer. The waste liquid of the photoresist developer generally contains about 0.1 to 2.0% by weight of a tetraalkylammonium hydroxide, which is concentrated to about 30 to 50% by weight to be used in the next activated carbon treatment step. Adsorption efficiency can be increased. Concentration is generally from normal pressure to 30-60 Torr
Heating is performed at 40 to 70 ° C. under reduced pressure of r. The concentration device is not particularly limited, and a normal evaporator or the like can be used.

The concentrated tetraalkylammonium hydroxide-containing waste liquid is treated with activated carbon to adsorb the photoresist components and a small amount of solvent, surfactant and the like in the tetraalkylammonium hydroxide-containing waste liquid. The activated carbon used is not particularly limited, and those generally known as adsorbents can be used. Specific examples thereof include powdered and granular coconut shell activated carbon,
Coal-based activated carbon, soft granular coal and the like can be mentioned. The amount of activated carbon used is usually 0.001 to 0.2 times (weight ratio) the amount of the concentrated waste liquid containing tetraalkylammonium hydroxide. The tetraalkylammonium hydroxide is recovered in the filtrate by filtering the mixture of the waste liquid containing tetraalkylammonium hydroxide and activated carbon. The filtrate can crystallize and recover the tetraalkylammonium hydroxide in the filtrate by, for example, concentrating and cooling.

In the second method of the present invention, the wastewater containing tetraalkylammonium hydroxide is neutralized to remove insoluble precipitates, and then subjected to adsorption treatment with activated carbon and filtration as in the first method. Then, the filtrate containing the tetraalkylammonium hydroxide is subjected to electrodialysis. Second
In the above method, the waste liquid containing tetraalkylammonium hydroxide can be concentrated if necessary to increase the content of tetraalkylammonium hydroxide to about 5 to 50% by weight, and then transferred to the neutralization step. By concentrating, the subsequent electrodialysis can be performed with higher efficiency.

The acid used for neutralization is not particularly limited. However, when a tetraalkylammonium hydroxide is reused in a photolithography process, even if a small amount of an acid component remains, it may affect semiconductor devices and the like. Therefore, it is preferable to avoid inorganic anions such as chloride ions, sulfate ions, and nitrate ions, and metal-containing acids.
Preferred acids include carbon dioxide and carbonic acid.

By the neutralization treatment with carbon dioxide or carbon dioxide, the tetraalkylammonium hydroxide in the waste liquid becomes a carbonate or a bicarbonate, and a resist component such as a novolak resin in the waste liquid is insolubilized and precipitated. The components that have become insolubilized and precipitated are removed by solid-liquid separation means such as decantation and filtration. The tetraalkylammonium hydroxide salt-containing liquid from which the insolubilized precipitate has been removed is subjected to adsorption treatment with activated carbon and filtration as in the first method.

Next, the filtrate containing the tetraalkylammonium hydroxide salt is subjected to electrodialysis. By electrodialysis, the tetraalkylammonium hydroxide carbonate or bicarbonate is converted to high purity tetraalkylammonium hydroxide. Electrodialysis can be performed using an electrolytic cell having an anode compartment and a cathode compartment partitioned by a cation exchange membrane. When a solution containing a tetraalkylammonium hydroxide salt is supplied to the anode compartment, high-purity hydroxylation can be performed. Tetraalkylammonium is formed in the cathode compartment.

As the cation exchange membrane for partitioning the anode chamber and the cathode chamber, a cation exchange membrane made of a fluororesin is preferably used. As the anode, a platinum group metal or its oxide is formed on titanium or another gold-resistant substrate. An electrode, a magnetite electrode or the like is used, and as the cathode, an alkali-resistant metal such as nickel or stainless steel is preferably used. Electrodialysis is performed at a temperature of 5 to 80 ° C. and a current density of 1 to 30 A /
It is preferable to carry out at about dm ² . After performing the electrodialysis, the tetraalkylammonium hydroxide-containing liquid can be, for example, concentrated and further cooled to crystallize the tetraalkylammonium hydroxide, which can be recovered as crystals.

[0019]

EXAMPLES Hereinafter, the purification and recovery methods of the present invention will be described specifically with reference to Examples. Example 1 (Purification and recovery processes shown in the chart of FIG. 1) In an LSI manufacturing process, image exposure was performed using a novolak resin as a positive photoresist, and tetramethylammonium hydroxide (TMAH) aqueous solution was used as a developing solution. After development, waste solution containing TMAH (TMAH concentration 0.5% by weight)
Was concentrated under reduced pressure at a liquid temperature of 60 ° C. and 40 torr to obtain a brown liquid.

As a result of the analysis, the concentration of TMAH in the concentrate was 2
0.6% by weight, metal ion concentration: Na 4.02pp
m, K 2.86 ppm, Fe 0.34 ppm, Ca4.
01 ppm and Si 30.6 ppm. When the absorbance was measured to measure organic residues such as resist residues, a red absorption wavelength of 420 nm and a yellow absorption wavelength of 3 were measured.
The absorbance at 50 nm and the absorbance wavelength of the benzene ring at 280 nm are 3.636, 10.456 and 2 respectively.
7.706.

Further, in order to measure the total organic residue in the concentrate, the solution was acidified with hydrochloric acid, extracted with chloroform, stripped of chloroform, and weighed. The amount of the organic residue was 432 ppm. . 14.8 g of granular activated carbon (Tsurumi Coal GL-30 coal system) was added to 210.3 g of this brown concentrated liquid [the amount of activated carbon / the amount of concentrated waste liquid (weight ratio) = 0.07], and the temperature was 4. The liquid was stirred for 0 hours. Thereafter, the mixture was filtered through a filter paper (qualitative filter paper 5C) to separate the activated carbon and the filtrate, and a colorless and transparent filtrate (2
00.6 g).

The TMAH concentration in the obtained filtrate was 18.4.
Weight%, and the metal ion concentration is Na 3.62 p
pm, K2.03ppm, Fe0.63ppm, Ca
2.080 ppm and 20.30 ppm of Si. The absorbance was 0.054 at a red absorption wavelength of 420 nm, 0.153 at a yellow absorption wavelength of 350 nm, and 0.759 at a benzene ring absorption wavelength of 280 nm. The organic residue content by a chloroform extraction method was 54 ppm. TMA
The adsorption treatment with activated carbon and filtration were performed in the same manner as described above, except that the amount of activated carbon added to the above-mentioned concentrated liquid of the H-containing waste liquid was changed as shown in Table 1 below. The analysis results of the obtained filtrate were as shown in the following Table 1 (Run No. 1, 3).

[0023]

[Table 1]

Example 2 (Purification and recovery process shown in the chart of FIG. 2) Waste liquid containing tetramethylammonium hydroxide (TMAH) used as a positive photoresist developer in an LSI manufacturing process (the one treated in Example 1) Was concentrated under reduced pressure at a liquid temperature of 60 ° C. and 40 torr to obtain a brown concentrated liquid.

As a result of the analysis, the concentration of TMAH in the concentrate was 2
0.8 wt%, metal ion concentration is Na 3.88 pp
m, K 3.06 ppm, Fe 0.42 ppm, Ca4.
30 ppm and 38.64 ppm of Si. When an absorbance measurement was performed to measure an organic residue such as a resist residue, the absorbance at a red absorption wavelength of 420 nm, the yellow absorption wavelength of 350 nm, and the absorption wavelength of a benzene ring at 280 nm were 2.963 and 11.485, respectively. And 25.868.

Further, in order to measure the total organic residue in the concentrate, the solution was acidified with hydrochloric acid, extracted with chloroform, stripped of chloroform, and weighed. The amount of the organic residue was 396 ppm. . Carbon dioxide was injected into the above concentrated solution to neutralize to pH 8.2.
Near the end of the neutralization, the soluble resist was insolubilized and a precipitate was formed. The supernatant was filtered through a Teflon filter having a pore size of 0.1 μm to separate and separate insoluble organic substances by filtration.

To 330.5 g of the filtrate, 9.9 g of granular activated carbon (Tsurumi Coal GL-30 coal system) was added.
[Activated carbon amount / concentrated waste liquid amount (weight ratio) = 0.03], the liquid was stirred at room temperature for 2 hours. Thereafter, the mixture was filtered through a filter paper (qualitative filter paper 5C), and the activated carbon and the filtrate were separated to obtain 321.6 g of a colorless and transparent filtrate. Then, having a anode and a cathode of the pair of 1 dm ^2, a cation exchange membrane (Nafion 324,
The filtrate was subjected to electrodialysis using a filter press type electrolytic cell partitioned into an anode chamber and a cathode chamber (manufactured by DuPont). A platinum-coated titanium electrode was used as the anode, and a nickel electrode was used as the cathode. The electrolysis was performed at an electrolysis temperature of 50 ° C. and a current density of 20 A / dm ² .

After completion of the electrolysis, the obtained catholyte is a colorless and transparent solution.
1.03% by weight. Further, the catholyte is treated with a solution concentration of 60.
And concentrated under reduced pressure of 40 torr.
A solution by weight was obtained. The concentrated liquid was cooled to 2 ° C. to crystallize white crystals, and solid-liquid separation was performed by centrifugation to obtain white crystals of TMAH. The crystallinity was 40.8%. The white crystals were dissolved in ultrapure water to obtain a colorless and transparent solution having a concentration of 20.80% by weight.

As a result of analyzing this solution, the metal ion concentration was found to be 3.40 ppm for Na, 2.84 ppm for K, and
0.1 ppm or less, Ca 0.68 ppm, Si 26.8
It was 4 ppm. The absorbance is 420 nm of red absorption wavelength.
0.020 at yellow absorption wavelength 350 nm,
It was 0.086 at an absorption wavelength of 280 nm of the benzene ring. Further, the content of the organic residue by the chloroform extraction method was 14 ppm.

Comparative Example 1 (Purification and recovery processes shown in the chart of FIG. 3) An electrolytic dialysate was obtained by performing exactly the same operation as in Example 2 except that the activated carbon treatment was not performed. After the electrolysis, the obtained catholyte was analyzed, and the TMAH concentration was 20.86% by weight.

As a result of analyzing this solution, the metal ion concentration was found to be 3.63 ppm of Na, 2.82 ppm of K,
0.1 ppm or less, Ca 0.80 ppm, Si 36.3
It was 3 ppm. The absorbance is 420 nm of red absorption wavelength.
0.102, 0.363 at 350 nm yellow absorption wavelength,
It was 1.386 at an absorption wavelength of 280 nm of a benzene ring. The organic residue content by a chloroform extraction method was 78 ppm.

[0032]

According to the method of the present invention, the waste liquid containing tetraalkylammonium hydroxide used as a positive resist developing solution is subjected to adsorption treatment with activated carbon, whereby the residual organic substances in the waste liquid can be almost completely removed. Thus, high-purity tetraalkylammonium hydroxide that can be reused in the photolithography process can be industrially advantageously recovered. In particular, between the concentration step and the activated carbon treatment step, neutralization of the tetraalkylammonium hydroxide-containing concentrated waste liquid and removal of insolubilized precipitates are performed, and electrodialysis is performed after the activated carbon treatment step, whereby higher purity is obtained. Can be recovered.

[Brief description of the drawings]

FIG. 1 is a chart showing an example (Example 1) of a purification and recovery process according to the method of the present invention.

FIG. 2 is a chart showing another example (Example 2) of a purification and recovery process according to the method of the present invention.

FIG. 3 is a chart showing an example of a purification and recovery process (Comparative Example 1) according to a conventional technique.

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[Procedure amendment]

[Submission date] October 25, 1996

[Procedure amendment 1]

[Document name to be amended] Statement

[Correction target item name] 0007

[Correction method] Change

[Correction contents]

[0007]

[Means for Solving the Problems]

[Procedure amendment 2]

[Document name to be amended] Statement

[Correction target item name] 0016

[Correction method] Change

[Correction contents]

By the neutralization treatment with carbon dioxide or carbon dioxide, the tetraalkylammonium hydroxide in the waste liquid becomes a carbonate or bicarbonate, and the resist component such as a novolak resin in the waste liquid is insolubilized and precipitated. The components that have become insolubilized and precipitated are removed by solid-liquid separation means such as decantation and filtration. The tetraalkylammonium hydroxide salt-containing liquid from which the insolubilized precipitate has been removed is subjected to adsorption treatment with activated carbon and filtration as in the first method.

Continued on the front page (51) Int.Cl. ⁶ Identification number Agency reference number FI Technical indication G03F 7/26 C02F 1/46 103 (72) Inventor Koichi Wada 5-1 Okawacho, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture Showa Inside the Production Engineering Center of Electric Works Co., Ltd. (72) Norio Moriya 5-1 Okawacho, Kawasaki-ku, Kawasaki City, Kanagawa Prefecture Showa Inside of the Production Engineering Center Showa Electric Works Co., Ltd. 13-9 Showa Denko K.K.

Claims (2)

[Claims] 1. A method for purifying and recovering tetraalkylammonium hydroxide, comprising treating a wastewater containing tetraalkylammonium hydroxide used as a positive resist developer with activated carbon to adsorb and remove impurities in the wastewater. . 2. A waste solution containing tetraalkylammonium hydroxide used as a positive resist developing solution is neutralized to remove insolubilized precipitates, and then treated with activated carbon to adsorb and remove impurities in the waste solution. And a method for purifying and recovering tetraalkylammonium hydroxide, further comprising performing electrodialysis in an electrolytic cell using a cation exchange membrane.