JPH09227316A - Antifungal composition - Google Patents

Antifungal composition

Info

Publication number
JPH09227316A
JPH09227316A JP8038003A JP3800396A JPH09227316A JP H09227316 A JPH09227316 A JP H09227316A JP 8038003 A JP8038003 A JP 8038003A JP 3800396 A JP3800396 A JP 3800396A JP H09227316 A JPH09227316 A JP H09227316A
Authority
JP
Japan
Prior art keywords
water glass
quaternary ammonium
ammonium salt
caulking agent
compound
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Withdrawn
Application number
JP8038003A
Other languages
Japanese (ja)
Inventor
Hitoshi Kitamura
仁史 北村
Masahiro Kondo
正博 近藤
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.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP8038003A priority Critical patent/JPH09227316A/en
Publication of JPH09227316A publication Critical patent/JPH09227316A/en
Withdrawn legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain an antifungal composition capable of retaining stable antifungal effect over a long period by combinedly using water glass and a specific compound. SOLUTION: This antifungal composition is obtained by combining water glass with an isopropyl alcohol-based thiazolylsulfamide compound or combining water glass with a quaternary ammonium salt. Water glass free from Ag is preferably used as the water glass. For example, 2-(4-thiazolyl-1H benzimidazole is used as the isopropylalcohol-based thiazolylsulfamide. The water glass is used in an amount of about 0.5-3.0wt.% based on caulking agent and the sulfamide compound is used in an amount of about 0.5-2.0wt.%. The quaternary ammonium salt includes benzabenzalkonium chloride or benzethonium chloride. The quaternary ammonium salt is added in an amount of 0.5-2.0wt.% based on a caulking agent.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、コーキング剤等に
配合して使用される防かび剤組成物に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a fungicide composition which is used by being mixed with a caulking agent or the like.

【0002】[0002]

【従来の技術】建物の外壁や内壁などにおいて壁材等の
間に生じる隙間にコーキング剤を充填することによっ
て、隙間を埋めると共に水の浸入を防ぐようにしてい
る。しかしコーキング剤にかびが生えると汚れて外観が
悪くなると共にコーキング剤の劣化が著しくなって防水
性にも問題が生じる。
2. Description of the Related Art A caulking agent is filled in a gap formed between wall materials on an outer wall or an inner wall of a building so as to fill the gap and prevent water from entering. However, if the caulking agent becomes moldy, the caulking agent becomes dirty and the appearance is deteriorated, and the caulking agent is significantly deteriorated to cause a problem in waterproofness.

【0003】そこで従来からコーキング剤に水ガラスを
防かび剤として配合することによって、コーキング剤に
かびが生えることを防ぐようにしている。
Therefore, conventionally, water glass is added to a caulking agent as an antifungal agent to prevent the caulking agent from growing mold.

【0004】[0004]

【発明が解決しようとする課題】しかし水ガラスは水に
溶けやすいために溶出速度が速く、長期の間にコーキン
グ剤中から消失し、防かび効果を長く保持することがで
きないという問題があった。本発明は上記の点に鑑みて
なされたものであり、長期に亘って安定した防かび効果
を持続する防かび剤組成物を提供することを目的とする
ものである。
However, since water glass is easily dissolved in water, its elution rate is high, and it disappears from the caulking agent over a long period of time, and there is a problem that the antifungal effect cannot be maintained for a long time. . The present invention has been made in view of the above points, and it is an object of the present invention to provide a fungicide composition which maintains a stable antifungal effect for a long period of time.

【0005】[0005]

【課題を解決するための手段】本発明の請求項1に係る
防かび剤組成物は、水ガラスとイソプロピルアルコール
系チアゾリルスルファミド化合物とを主成分とすること
を特徴とするものである。また本発明の請求項2に係る
防かび剤組成物は、水ガラスと4級アンモニウム塩とを
主成分とすることを特徴とするものである。
The fungicide composition according to claim 1 of the present invention is characterized by containing water glass and an isopropyl alcohol thiazolylsulfamide compound as main components. . The fungicide composition according to claim 2 of the present invention is characterized by containing water glass and a quaternary ammonium salt as main components.

【0006】[0006]

【発明の実施の形態】以下、本発明の実施の形態を説明
する。請求項1の発明は、無機系防かび剤である水ガラ
スと、有機系防かび剤であるイソプロピルアルコール
(以下IPAと略称)系チアゾリルスルファミド化合物
とを配合して防かび剤組成物を調製することを特徴とす
る。水ガラスとしてはAg入りのものを使用することも
できるが、人体に対する安全上、Ag無し水ガラスを用
いるのが好ましい。またIPA系チアゾリルスルファミ
ド化合物としては、例えば2−(4−チアゾリル)−1
H−ベンズイミダゾール〔2−(4−Thiazolyl )−1H
−benzimidazol〕を用いることができる。
Embodiments of the present invention will be described below. The invention of claim 1 is an antifungal composition comprising water glass as an inorganic antifungal agent and isopropyl alcohol (hereinafter abbreviated as IPA) type thiazolylsulfamide compound as an organic antifungal agent. Is prepared. As the water glass, it is possible to use Ag-containing glass, but it is preferable to use Ag-free water glass from the viewpoint of safety for the human body. Examples of the IPA-based thiazolyl sulfamide compound include 2- (4-thiazolyl) -1
H-benzimidazole [2- (4-Thiazolyl) -1H
-Benzimidazole] can be used.

【0007】この防かび剤組成物はコーキング剤に対し
て1〜5重量%の添加量で配合するのが好ましい。添加
量が1重量%未満では防かび効果を十分に得ることが難
しく、また防かび効果は5重量%の添加で十分であり、
これ以上添加するとコストの面で不利になる。また、こ
の防かび剤組成物において、水ガラスとIPA系チアゾ
リルスルファミド化合物の配合比率は、コーキング剤に
対して水ガラスの添加量が0.5〜3.0重量%の範囲
に、IPA系チアゾリルスルファミド化合物の添加量が
0.5〜2.0重量%の範囲になるように設定するのが
好ましい。即効性重視であれば水ガラスの配合比率を少
なくし、効果の持続性(冗長性)重視であれば水ガラス
の配合比率を多くするのがよい。
The antifungal composition is preferably added in an amount of 1 to 5% by weight based on the caulking agent. If the amount added is less than 1% by weight, it is difficult to obtain a sufficient fungicidal effect, and addition of 5% by weight is sufficient for the antifungal effect.
Adding more than this is disadvantageous in terms of cost. Further, in this antifungal composition, the mixing ratio of water glass and the IPA-based thiazolylsulfamide compound is such that the addition amount of water glass to the caulking agent is in the range of 0.5 to 3.0% by weight. It is preferable to set the amount of the IPA-based thiazolyl sulfamide compound added to be in the range of 0.5 to 2.0% by weight. If the immediate effect is important, the blending ratio of water glass should be reduced, and if the effect persistence (redundancy) is emphasized, the blending ratio of water glass should be increased.

【0008】ここで、水ガラスとIPA系チアゾリルス
ルファミド化合物を比較すると、水ガラスはIPA系チ
アゾリルスルファミド化合物よりも水に溶出し易く、I
PA系チアゾリルスルファミド化合物は水よりも溶出し
難く、水ガラスを単独で使用すると短期間に溶出して残
存率が低くなると共に、IPA系チアゾリルスルファミ
ド化合物を単独で使用すると効果が出るまでに長期の期
間が必要である。一方、上記のような無機系の水ガラス
と有機系のIPA系チアゾリルスルファミド化合物から
なる防かび剤組成物にあっては、溶出し易い水ガラスと
溶出し難いIPA系チアゾリルスルファミド化合物は混
在した状態で共にコーキング剤の表面に溶出してくるこ
とになるために、水ガラスの溶出速度はIPA系チアゾ
リルスルファミド化合物に引きずられて遅くなり、また
IPA系チアゾリルスルファミド化合物の溶出速度は水
ガラスに引きずられて速くなり、この結果、水ガラスと
IPA系チアゾリルスルファミド化合物の配合による相
乗効果で、初期から長期に亘るまで防かび剤組成物をコ
ーキング剤の表面に溶出させることができ、長期に亘っ
て安定して防かび効果を発揮させることができるもので
ある。
A comparison between water glass and the IPA-based thiazolyl sulfamide compound shows that water glass is more easily eluted into water than the IPA-based thiazolyl sulfamide compound.
PA-based thiazolylsulfamide compounds are more difficult to elute than water, and when water glass is used alone, it elutes in a short period of time and the residual rate is low, and when IPA-based thiazolylsulfamide compounds are used alone, it is effective. It takes a long time to get out. On the other hand, in the fungicide composition comprising the above inorganic water glass and the organic IPA thiazolyl sulfamide compound, the water glass which is easily eluted and the IPA thiazolyl sulfamide which is difficult to be eluted Since the de-compounds will be eluted together on the surface of the caulking agent in a mixed state, the elution rate of water glass will be slowed down by the IPA-based thiazolylsulfamide compound, and the IPA-based thiazolylsul The elution speed of the famid compound is increased by being dragged by water glass, and as a result, the synergistic effect of the combination of water glass and the IPA-based thiazolylsulfamide compound results in caulking of the fungicide composition from the initial stage to the long term. The agent can be eluted on the surface of the agent and can stably exhibit the antifungal effect over a long period of time.

【0009】また請求項2の発明は、無機系防かび剤で
ある水ガラスと、有機系防かび剤である4級アンモニウ
ム塩とを配合して防かび剤組成物を調製することを特徴
とする。水ガラスとしてはAg入りのものを使用するこ
ともできるが、人体に対する安全上、Ag無し水ガラス
を用いるのが好ましい。4級アンモニウム塩としては塩
化ベンザルコニウムや塩化ベンゼトニウムなどを用いる
ことができる。
The invention of claim 2 is characterized in that an antifungal composition is prepared by mixing water glass which is an inorganic antifungal agent and a quaternary ammonium salt which is an organic antifungal agent. To do. As the water glass, it is possible to use Ag-containing glass, but it is preferable to use Ag-free water glass from the viewpoint of safety for the human body. As the quaternary ammonium salt, benzalkonium chloride, benzethonium chloride or the like can be used.

【0010】この防かび剤組成物はコーキング剤に対し
て1〜5重量%の添加量で配合するのが好ましい。添加
量が1重量%未満では防かび効果を十分に得ることが難
しく、また防かび効果は5重量%の添加で十分であり、
これ以上添加するとコストの面で不利になる。また、こ
の防かび剤組成物において、水ガラスと4級アンモニウ
ム塩の配合比率は、コーキング剤に対して水ガラスの添
加量が0.5〜3.0重量%の範囲に、4級アンモニウ
ム塩の添加量が0.5〜2.0重量%の範囲になるよう
に設定するのが好ましい。
The antifungal composition is preferably added in an amount of 1 to 5% by weight based on the caulking agent. If the amount added is less than 1% by weight, it is difficult to obtain a sufficient fungicidal effect, and addition of 5% by weight is sufficient for the antifungal effect.
Adding more than this is disadvantageous in terms of cost. In this antifungal composition, the mixing ratio of water glass and quaternary ammonium salt is such that the addition amount of water glass to the caulking agent is in the range of 0.5 to 3.0% by weight. It is preferable to set the addition amount of 0.5 to 2.0% by weight.

【0011】ここで、水ガラスと4級アンモニウム塩を
比較すると、4級アンモニウム塩はは水ガラスに比べて
水に溶出し易く、水ガラスは4級アンモニウム塩に比べ
て水に溶出し難くい。そしてこのような無機系の水ガラ
スと有機系の4級アンモニウム塩からなる防かび剤組成
物にあっては、溶出し易い4級アンモニウム塩と溶出し
難い水ガラスは混在した状態で共にコーキング剤の表面
に溶出してくることになるために、4級アンモニウム塩
の溶出速度は水ガラスに引きずられて遅くなり、また水
ガラスの溶出速度は4級アンモニウム塩に引きずられて
速くなり、この結果、水ガラスと4級アンモニウム塩の
配合による相乗効果で、初期から長期に亘るまで防かび
剤組成物をコーキング剤の表面に溶出させることがで
き、長期に亘って安定して防かび効果を発揮させること
ができるものである。
Here, comparing the water glass and the quaternary ammonium salt, the quaternary ammonium salt is easier to elute in water than water glass, and the water glass is less likely to elute in water than the quaternary ammonium salt. . In the fungicide composition comprising such an inorganic water glass and an organic quaternary ammonium salt, the caulking agent is a mixture of the quaternary ammonium salt that is easily eluted and the water glass that is difficult to be eluted. The elution rate of the quaternary ammonium salt is slowed by the water glass because it is eluted on the surface of the water, and the elution rate of the water glass is increased by the quaternary ammonium salt. By the synergistic effect of the combination of water glass and quaternary ammonium salt, the fungicide composition can be eluted on the surface of the caulking agent from the beginning to the long term, and the fungicidal effect is stably exhibited for a long term. It can be done.

【0012】[0012]

【実施例】以下本発明を実施例によって具体的に説明す
る。 (実施例1)シリコンコーキング剤(東芝シリコーン社
製「トスシール381」)97.5gに、日本硝子繊維
社製のAg無し水ガラス粉末2.0gとIPA系チアゾ
リルスルファミド化合物(ナック社製「NACS NA
−1」)0.5gからなる防かび剤組成物を添加し、常
温・常湿下でニーダを用いて約3分間攪拌することによ
って混練した。次にこの防かび剤入りのシリコンコーキ
ング剤を金属ベラで約2mmの厚みにプレート状に塗り
延ばし、そのまま約3日間室温で養生させた。その後、
これを3cm×3cmの大きさにカットし、テストサン
プルピースとした。
The present invention will be described below in detail with reference to examples. (Example 1) 97.5 g of a silicone caulking agent ("Tosseal 381" manufactured by Toshiba Silicone Co., Ltd.), 2.0 g of Ag-free water glass powder manufactured by Nippon Glass Fiber Co., Ltd., and an IPA-based thiazolyl sulfamide compound (manufactured by Nac) "NACS NA
-1 ") 0.5 g of the fungicide composition was added, and the mixture was kneaded by stirring with a kneader at room temperature and normal humidity for about 3 minutes. Then, the anti-fungal agent-containing silicone caulking agent was spread on a plate with a metal spatula to a thickness of about 2 mm, and allowed to cure at room temperature for about 3 days. afterwards,
This was cut into a size of 3 cm × 3 cm to prepare a test sample piece.

【0013】(実施例2)シリコンコーキング剤97.
0gに、水ガラス粉末2.0gとIPA系チアゾリルス
ルファミド化合物1.0gからなる防かび剤組成物を加
えるようにした他は、実施例1と同様にした。 (実施例3)シリコンコーキング剤97.0gに、水ガ
ラス粉末2.5gとIPA系チアゾリルスルファミド化
合物0.5gからなる防かび剤組成物を添加するように
した他は、実施例1と同様にした。
(Example 2) Silicon caulking agent 97.
The same procedure as in Example 1 was carried out except that 0 g was added with a fungicide composition consisting of 2.0 g of water glass powder and 1.0 g of IPA-based thiazolylsulfamide compound. (Example 3) Example 1 was repeated except that a fungicide composition consisting of 2.5 g of water glass powder and 0.5 g of IPA-based thiazolylsulfamide compound was added to 97.0 g of a silicone caulking agent. Same as.

【0014】(実施例4)シリコンコーキング剤97.
0gに、水ガラス粉末2.5gと4級アンモニウム塩で
ある塩化ベンザルコニウム0.5gからなる防かび剤組
成物を添加するようにした他は、実施例1と同様にし
た。 (実施例5)シリコンコーキング剤97.0gに、水ガ
ラス粉末2.0gと4級アンモニウム塩である塩化ベン
ザルコニウム1.0gからなる防かび剤組成物を添加す
るようにした他は、実施例1と同様にした。
(Example 4) Silicon caulking agent 97.
The same procedure as in Example 1 was carried out except that 0 g of the fungicide composition consisting of 2.5 g of water glass powder and 0.5 g of quaternary ammonium salt benzalkonium chloride was added. (Example 5) Except that a fungicide composition consisting of 2.0 g of water glass powder and 1.0 g of quaternary ammonium salt benzalkonium chloride was added to 97.0 g of a silicone caulking agent. Same as Example 1.

【0015】(比較例1)防かび剤を添加しないシリコ
ンコーキング剤をそのまま用いた。 (比較例2)シリコンコーキング剤97.0gに、水ガ
ラス粉末3.0gを添加するようにした他は、実施例1
と同様にした。
(Comparative Example 1) A silicon caulking agent containing no fungicide was used as it was. Comparative Example 2 Example 1 was repeated except that 3.0 g of water glass powder was added to 97.0 g of silicon caulking agent.
Same as.

【0016】(比較例3)シリコンコーキング剤97.
0gに、IPA系チアゾリルスルファミド化合物3.0
gを添加するようにした他は、実施例1と同様にした。 (比較例4)シリコンコーキング剤97.0gに、塩化
ベンザルコニウム3.0gを添加するようにした他は、
実施例1と同様にした。
(Comparative Example 3) Silicon caulking agent 97.
0 g of the IPA-based thiazolyl sulfamide compound 3.0
Same as Example 1 except that g was added. (Comparative Example 4) 3.0 g of benzalkonium chloride was added to 97.0 g of a silicon caulking agent,
It was the same as in Example 1.

【0017】上記の実施例1〜5及び比較例1〜4で得
たテストサンプルピースを用い、MIL規格に準拠して
初期品及び10年経過相当品について、かび抵抗試験を
おこなった。結果を表1に示す。尚、表1においてかび
抵抗試験の評価は、「0」:菌発生なし、「1」:わず
かに発生、「2」:少し発生、「3」:中間的発生、
「4」:激しく発生、である。
Using the test sample pieces obtained in the above Examples 1 to 5 and Comparative Examples 1 to 4, a mold resistance test was carried out on an initial product and a product equivalent to 10 years old according to the MIL standard. The results are shown in Table 1. In Table 1, the mold resistance test was evaluated as follows: "0": No bacterial development, "1": Slight development, "2": Slight development, "3": Intermediate development,
"4": Violent occurrence.

【0018】[0018]

【表1】 [Table 1]

【0019】表1にみられるように、水ガラスとイソプ
ロピルアルコール系チアゾリルスルファミド化合物から
なる防かび剤組成物を用いた実施例1〜3及び、水ガラ
スと4級アンモニウム塩からなる防かび剤組成物を用い
た実施例4〜5のものでは、初期から10年経過に至る
まで、長期間に亘って防かび効果が持続するものであっ
た。
As shown in Table 1, Examples 1 to 3 using a fungicide composition composed of water glass and an isopropyl alcohol thiazolyl sulfamide compound, and a composition composed of water glass and a quaternary ammonium salt were used. In Examples 4 to 5 using the fungicide composition, the antifungal effect lasted for a long period from the initial stage to 10 years.

【0020】[0020]

【発明の効果】上記のように請求項1の発明は、水ガラ
スとイソプロピルアルコール系チアゾリルスルファミド
化合物を防かび剤として併用するようにしたので、両成
分の相乗効果で長期に亘って安定した防かび効果を持続
させることができるものである。
As described above, according to the invention of claim 1, since water glass and the isopropyl alcohol thiazolyl sulfamide compound are used together as a fungicide, the synergistic effect of both components can be exerted for a long time. It is possible to maintain a stable antifungal effect.

【0021】また請求項2の発明は、水ガラスと4級ア
ンモニウム塩を防かび剤として併用するようにしたの
で、両成分の相乗効果で長期に亘って安定した防かび効
果を持続させることができるものである。
According to the second aspect of the present invention, since water glass and a quaternary ammonium salt are used together as an antifungal agent, a stable antifungal effect can be maintained for a long period of time by the synergistic effect of both components. It is possible.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 水ガラスとイソプロピルアルコール系チ
アゾリルスルファミド化合物とを主成分とすることを特
徴とする防かび剤組成物。
1. A fungicide composition comprising water glass and an isopropyl alcohol-based thiazolylsulfamide compound as main components.
【請求項2】 水ガラスと4級アンモニウム塩とを主成
分とすることを特徴とする防かび剤組成物。
2. A fungicide composition comprising water glass and a quaternary ammonium salt as main components.
JP8038003A 1996-02-26 1996-02-26 Antifungal composition Withdrawn JPH09227316A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8038003A JPH09227316A (en) 1996-02-26 1996-02-26 Antifungal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8038003A JPH09227316A (en) 1996-02-26 1996-02-26 Antifungal composition

Publications (1)

Publication Number Publication Date
JPH09227316A true JPH09227316A (en) 1997-09-02

Family

ID=12513408

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8038003A Withdrawn JPH09227316A (en) 1996-02-26 1996-02-26 Antifungal composition

Country Status (1)

Country Link
JP (1) JPH09227316A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11170444A (en) * 1997-12-08 1999-06-29 Try Company:Kk Packaging body
JP2000070345A (en) * 1998-09-02 2000-03-07 Kanehiro:Kk Antibacterial sheet and antibacterial tape
EP1290943A1 (en) * 2001-09-07 2003-03-12 Air Liquide Santé (International) Preservative for coating compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11170444A (en) * 1997-12-08 1999-06-29 Try Company:Kk Packaging body
JP2000070345A (en) * 1998-09-02 2000-03-07 Kanehiro:Kk Antibacterial sheet and antibacterial tape
EP1290943A1 (en) * 2001-09-07 2003-03-12 Air Liquide Santé (International) Preservative for coating compositions

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