JPS61235034A - Binder composition for casting mold - Google Patents
Binder composition for casting moldInfo
- Publication number
- JPS61235034A JPS61235034A JP7594285A JP7594285A JPS61235034A JP S61235034 A JPS61235034 A JP S61235034A JP 7594285 A JP7594285 A JP 7594285A JP 7594285 A JP7594285 A JP 7594285A JP S61235034 A JPS61235034 A JP S61235034A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- weight
- parts
- casting mold
- curing
- 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
- Mold Materials And Core Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は改良された自硬性鋳型用粘結剤組成物に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an improved self-hardening binder composition for molds.
従来よりフルフリルアルコールや芳香族アルコールに対
し、芳香族ジアルデヒドを混合し、鋳型用粘結剤に使用
し高強度を得ることは公知の事実である(特開昭57−
124543号公報)。しかし、芳香族ジアルデヒドは
フラン樹脂に対する溶解性に問題があった。更に芳香族
ジアルデヒドは、その製造が難しく、汎用的には問題が
ある。It is a well-known fact that aromatic dialdehyde is mixed with furfuryl alcohol or aromatic alcohol and used as a binder for molds to obtain high strength (Japanese Unexamined Patent Application Publication No. 1983-1999).
124543). However, aromatic dialdehydes have a problem in solubility in furan resins. Furthermore, aromatic dialdehydes are difficult to produce and are problematic for general use.
また、フラン系粘結剤にtl[あるいは澱粉類等を利用
することは公知の事実であるが、硬化速度や鋳型強度が
低下する欠点があった。Furthermore, although it is a well-known fact that tl [or starches, etc.] can be used as a furan-based binder, there is a drawback that the curing speed and mold strength are reduced.
本発明者らは糖類での硬化速度や鋳型強度の低下を改良
すべく鋭意研究の結果、[8あるいは澱粉等の分子内に
1つあるいは2つ以上のα−ジオールを含存する化合物
を酸化して得られるところの分子内に1つあるいは2つ
以上のアルデヒド基を有する化合物を、フラン系樹脂あ
るいはフェノール系樹脂等の酸硬化型樹脂に混合あるい
は反応させることにより、硬化速度が速く、鋳型の表面
安定性に優れた強度の高い鋳型用粘結剤組成物が得られ
ることを見出し本発明に至った。The present inventors have conducted intensive research to improve the curing speed and mold strength reduction caused by sugars. By mixing or reacting a compound having one or more aldehyde groups in the molecule with an acid-curing resin such as a furan-based resin or a phenol-based resin, the curing speed is fast and the mold is The inventors have discovered that a binder composition for molds with excellent surface stability and high strength can be obtained, leading to the present invention.
即ち、本発明は、酸硬化型樹脂に、糖類あるいは澱粉か
ら得られる分子内に1つあるいは2つ以上のアルデヒド
基を有する化合物を混合あるいは反応させてなることを
特徴とする酸硬化型鋳型用粘結剤組成物を提供するもの
である。That is, the present invention provides a method for use in acid-curing molds, which is made by mixing or reacting an acid-curing resin with a compound having one or more aldehyde groups in the molecule obtained from saccharides or starch. A binder composition is provided.
本発明に用いられるアルデヒド基を有する化合物は、酸
硬化型樹脂100重量部に対し、好ましくは2〜50重
量部、更に好ましくは5〜20重量部の量で混合もしく
は反応させる。The compound having an aldehyde group used in the present invention is preferably mixed or reacted in an amount of 2 to 50 parts by weight, more preferably 5 to 20 parts by weight, based on 100 parts by weight of the acid-curing resin.
又、本発明の鋳型用粘結剤組成物に対し、γ−アミノプ
ロピルトリエトキシシラン、γ−(2−アミノエチル)
アミノプロピルメチルジメトキシシラン等の公知の各種
シランカップリング剤又は水を1〜20重量%好ましく
は5〜15重量%添加しても良い。Furthermore, for the mold binder composition of the present invention, γ-aminopropyltriethoxysilane, γ-(2-aminoethyl)
Various known silane coupling agents such as aminopropylmethyldimethoxysilane or water may be added in an amount of 1 to 20% by weight, preferably 5 to 15% by weight.
尚、糖類あるいは澱粉等を酸化する際に、アルデヒド基
だけでなく、ケトン基やカルボキシル基が同時に生成す
る。これら副生物の混入は特に大幅に硬化速度や鋳型強
度に悪影響を与えるものではないが、これらケトン基及
びカルボキシル基の生成量は30当量%以下であること
が好ましい。又、アルデヒド基は2つ以上あることが好
ましい。In addition, when oxidizing sugars, starch, etc., not only aldehyde groups but also ketone groups and carboxyl groups are generated at the same time. Although the inclusion of these by-products does not particularly significantly adversely affect the curing rate or mold strength, it is preferable that the amount of these ketone groups and carboxyl groups produced is 30 equivalent % or less. Moreover, it is preferable that there are two or more aldehyde groups.
本発明で用いるIIi類や澱粉類としては、グルコース
、ガラクトース、ショ糖、果糖、麦芽糖などの単糖類、
少#M類、多糖類等、又、デキストリン、可溶性澱粉、
トウモロコシ澱粉、サツマイモ澱粉、コメ澱粉、コムギ
澱粉などの天然澱粉及び加工澱粉等のいかなる糖や澱粉
でも良い。又、これらの糖や澱粉を酸化する際に用いら
れる酸化剤としては、過沃素酸、四酢酸鉛、クロム酸、
過酸化水素、硝酸、酸素等が用いられる。Examples of class IIi and starches used in the present invention include monosaccharides such as glucose, galactose, sucrose, fructose, and maltose;
Small #Ms, polysaccharides, etc., dextrin, soluble starch,
Any sugar or starch may be used, including natural starches such as corn starch, sweet potato starch, rice starch, and wheat starch, and modified starches. In addition, the oxidizing agents used to oxidize these sugars and starches include periodic acid, lead tetraacetate, chromic acid,
Hydrogen peroxide, nitric acid, oxygen, etc. are used.
本発明において、Iii類や澱粉等の分子内に1つある
いは2つ以上のα−ジオールを含有する化合物を酸化し
て得られる分子内に1つあるいは2つ以上の反応性の高
いアルデヒド基を含有する化合物を、酸硬化型樹脂に混
合あるいは反応させて用いることにより、鋳型造型時の
粘結剤硬化反応において、上記反応性の高いアルデヒド
を硬化反応に組み込むことにより、硬化速度が速くなり
、鋳型強度が高く、表面安定性の優れた鋳型が得られる
ものである。In the present invention, one or more highly reactive aldehyde groups are added in the molecule obtained by oxidizing a compound containing one or more α-diols in the molecule, such as Group III or starch. By mixing or reacting the contained compound with an acid-curing resin, the curing speed can be increased by incorporating the highly reactive aldehyde into the curing reaction in the binder curing reaction during mold making. A mold with high mold strength and excellent surface stability can be obtained.
以下、実施例により、本発明を更に詳細に説明する。尚
、実施例では酸硬化型樹脂としてフラン樹脂を用いた。Hereinafter, the present invention will be explained in more detail with reference to Examples. In the examples, furan resin was used as the acid-curable resin.
製造例1
ビーカー中に過沃素酸50重量部と水200重量部の混
合水溶液を入れ、これにコーンスターチ40重量部を加
えて攪拌反応した後、濾過水洗し目的とする化合物(^
)を得た。Production Example 1 A mixed aqueous solution of 50 parts by weight of periodic acid and 200 parts by weight of water was placed in a beaker, 40 parts by weight of cornstarch was added thereto, stirred and reacted, filtered and washed with water to obtain the desired compound (^
) was obtained.
実施例1〜4、比較例1
10℃において、鋳物砂100重量部に対し、硬化触媒
としてパラトルエンスルホン酸の75%水溶液を0.4
重量部加え、1分間混合した後、上記化合物(^)を酸
硬化型樹脂に、表1に示す配合割合で混合溶解した粘結
剤組成物を1.0重量部加え、更に1分間混合した。こ
の混練砂で50mmφX50mmhの試験片を作成した
後、その鋳型強度及び表面安定性を測定した。Examples 1 to 4, Comparative Example 1 At 10°C, 0.4% of a 75% aqueous solution of para-toluenesulfonic acid was added as a curing catalyst to 100 parts by weight of foundry sand.
After adding parts by weight and mixing for 1 minute, 1.0 parts by weight of a binder composition prepared by mixing and dissolving the above compound (^) in the acid-curing resin at the compounding ratio shown in Table 1 was added and further mixed for 1 minute. . A test piece of 50 mmφ x 50 mmh was prepared from this kneaded sand, and its mold strength and surface stability were measured.
結果を表1に示す。又、化合物(A)を添加しない系を
比較例1として示した。The results are shown in Table 1. Moreover, a system in which compound (A) was not added was shown as Comparative Example 1.
尚、試験片の強度は圧縮強度を測定し、表面安定性は試
験片を10メツシユのふるい上に乗せ、ロータツブ振動
機で2分間処理し、処理前後の重量比から求めた。The strength of the test piece was determined by measuring the compressive strength, and the surface stability was determined by placing the test piece on a 10-mesh sieve, treating it with a rotary tube vibrator for 2 minutes, and determining the weight ratio before and after the treatment.
表 1
実施例5〜8、比較例2〜6
25℃において、鋳物砂100重量部に対し、硬化触媒
としてパラトルエンスルホン酸の75%水溶液を0.4
5重量部加え、1分間混合した後、上記化合物(A)を
酸硬化型樹脂に、表2に示す配合割合で混合溶解した粘
結剤組成物を1,0重量部加え、更に1分間混合した。Table 1 Examples 5 to 8, Comparative Examples 2 to 6 At 25°C, 0.4% of a 75% aqueous solution of para-toluenesulfonic acid was added as a curing catalyst to 100 parts by weight of foundry sand.
After adding 5 parts by weight and mixing for 1 minute, 1.0 parts by weight of a binder composition prepared by mixing and dissolving the above compound (A) in the acid-curing resin at the mixing ratio shown in Table 2 was added, and further mixed for 1 minute. did.
この混練砂で50mmφx50mmbの試験片を作成し
た後、その鋳型強度を測定した。A test piece of 50 mmφ x 50 mmb was prepared from this kneaded sand, and its mold strength was measured.
結果を表2に示す。又、化合物(A)を混合しない系と
糖を混合溶解した系を比較例2〜6として示した。The results are shown in Table 2. Moreover, a system in which compound (A) was not mixed and a system in which sugar was mixed and dissolved were shown as Comparative Examples 2 to 6.
表 2
表2から明らかな如く、化合物(A)を混合溶解するこ
とにより硬化速度及び24時間放置強度とも著しく改善
される。Table 2 As is clear from Table 2, by mixing and dissolving compound (A), both the curing speed and the 24-hour standing strength are significantly improved.
製造例2
ビーカー中に過沃素酸50重量部と水200重量部の混
合水溶液を入れ、これにデキストリン40重量部を加え
て攪拌反応した後、濾過水洗し目的とする化合物(B)
を得た。Production Example 2 A mixed aqueous solution of 50 parts by weight of periodic acid and 200 parts by weight of water was placed in a beaker, 40 parts by weight of dextrin was added thereto, stirred and reacted, filtered and washed with water to obtain the target compound (B).
I got it.
実施例9〜12、比較例7
25℃において、鋳物砂100重量部に対し、硬化触媒
としてパラトルエンスルホン酸の75%水溶液を0.4
5重量部加え、1分間混合した後、上記化合物(B)を
酸硬化型樹脂に、表3に示す配合割合で混合溶解した粘
結剤組成物を1.0重量部加え、更に1分間混合した。Examples 9 to 12, Comparative Example 7 At 25°C, 0.4% of a 75% aqueous solution of para-toluenesulfonic acid was added as a curing catalyst to 100 parts by weight of foundry sand.
After adding 5 parts by weight and mixing for 1 minute, 1.0 parts by weight of a binder composition prepared by mixing and dissolving the above compound (B) in the acid-curing resin at the mixing ratio shown in Table 3 was added, and further mixed for 1 minute. did.
この混練砂で50m+*φx50mn+hの試験片を作
成した後、その鋳型強度を測定した。A test piece of 50 m + *φ x 50 mn + h was prepared from this kneaded sand, and its mold strength was measured.
結果を表3に示す。又、化合物(B)を混合しない系を
比較例7として示した。The results are shown in Table 3. Moreover, a system in which compound (B) was not mixed was shown as Comparative Example 7.
表 3
製造例3
ビーカー中に過沃素酸50重量部と水200重量部の混
合水溶液を入れ、これにブドウ糖40重量部を加えて攪
拌反応した後、濾過し目的とする化合物(C)を得た。Table 3 Production Example 3 A mixed aqueous solution of 50 parts by weight of periodic acid and 200 parts by weight of water was placed in a beaker, 40 parts by weight of glucose was added thereto, stirred and reacted, and then filtered to obtain the target compound (C). Ta.
実施例13〜16、比較例8
25℃において、鋳物砂100重量部に対し、硬化触媒
としてパラトルエンスルホン酸の75%水溶液を0.4
5重量部加え、1分間混合した後、上記化合物(C)を
酸硬化型樹脂に、表4に示す配合割合で混合溶解した粘
結剤組成物を1.0重量部加え、更に1分間混合した。Examples 13 to 16, Comparative Example 8 At 25°C, 0.4% of a 75% aqueous solution of para-toluenesulfonic acid was added as a curing catalyst to 100 parts by weight of foundry sand.
After adding 5 parts by weight and mixing for 1 minute, 1.0 parts by weight of a binder composition prepared by mixing and dissolving the above compound (C) in the acid-curing resin at the mixing ratio shown in Table 4 was added, and further mixed for 1 minute. did.
どの混練砂で50mttrφX50mmbの試験片を作
成した後、その鋳型強度を測定した。A test piece of 50 mttrφ×50 mmb was prepared using any of the mixed sands, and the mold strength thereof was measured.
結果を表4に示す。又、化合物(C)を混合しない系を
比較例8として示した。The results are shown in Table 4. Moreover, a system in which compound (C) was not mixed was shown as Comparative Example 8.
表 4Table 4
Claims (1)
子内に1つあるいは2つ以上のアルデヒド基を有する化
合物を混合あるいは反応させてなることを特徴とする酸
硬化型鋳型用粘結剤組成物。1. A binder composition for acid-curing molds, which is made by mixing or reacting an acid-curing resin with a compound having one or more aldehyde groups in the molecule obtained from saccharides or starch. thing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7594285A JPS61235034A (en) | 1985-04-10 | 1985-04-10 | Binder composition for casting mold |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7594285A JPS61235034A (en) | 1985-04-10 | 1985-04-10 | Binder composition for casting mold |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61235034A true JPS61235034A (en) | 1986-10-20 |
Family
ID=13590788
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7594285A Pending JPS61235034A (en) | 1985-04-10 | 1985-04-10 | Binder composition for casting mold |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61235034A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013133131A1 (en) * | 2012-03-09 | 2013-09-12 | 花王株式会社 | Binder composition for producing template, and method for producing template |
WO2020070819A1 (en) * | 2018-10-03 | 2020-04-09 | 花王株式会社 | Binder composition for forming mold |
CN112512722A (en) * | 2018-08-24 | 2021-03-16 | 花王株式会社 | Binder composition for mold making |
-
1985
- 1985-04-10 JP JP7594285A patent/JPS61235034A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013133131A1 (en) * | 2012-03-09 | 2013-09-12 | 花王株式会社 | Binder composition for producing template, and method for producing template |
JP2013212536A (en) * | 2012-03-09 | 2013-10-17 | Kao Corp | Binder composition for producing template |
CN112512722A (en) * | 2018-08-24 | 2021-03-16 | 花王株式会社 | Binder composition for mold making |
CN112512722B (en) * | 2018-08-24 | 2023-02-28 | 花王株式会社 | Binder composition for mold making |
WO2020070819A1 (en) * | 2018-10-03 | 2020-04-09 | 花王株式会社 | Binder composition for forming mold |
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