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JPS6338254B2 - - Google Patents
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JPS6338254B2 - - Google Patents

Info

Publication number
JPS6338254B2
JPS6338254B2 JP55500148A JP50014879A JPS6338254B2 JP S6338254 B2 JPS6338254 B2 JP S6338254B2 JP 55500148 A JP55500148 A JP 55500148A JP 50014879 A JP50014879 A JP 50014879A JP S6338254 B2 JPS6338254 B2 JP S6338254B2
Authority
JP
Japan
Prior art keywords
core
mold
cores
silicate
binder
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.)
Expired
Application number
JP55500148A
Other languages
Japanese (ja)
Other versions
JPS55501134A (en
Inventor
Ingumaaru Aaranzuberii
Raashuueritsuku Petashon
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.)
AARUSERU AIAARU AB
Original Assignee
AARUSERU AIAARU AB
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
Priority claimed from SE7907450A external-priority patent/SE429509B/en
Application filed by AARUSERU AIAARU AB filed Critical AARUSERU AIAARU AB
Publication of JPS55501134A publication Critical patent/JPS55501134A/ja
Publication of JPS6338254B2 publication Critical patent/JPS6338254B2/ja
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
    • B22C1/18Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents
    • B22C1/186Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of inorganic agents contaming ammonium or metal silicates, silica sols
    • B22C1/188Alkali metal silicates

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Mold Materials And Core Materials (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Description

請求の範囲 1 結着材としてケイ酸ナトリウム又はケイ酸カ
リウムを用いた粒状及び/又は繊維状物質の鋳物
用コア又は型を製造する方法において、ケイ酸ナ
トリウム又はカリウムを物質の重量を基に計算し
て1―3%の量でその物質の混合物に添加し、シ
リコーン油、シリコーン乳剤及びシリコネートよ
りなる群から選ばれた少なくとも1種の界面活性
物質を物質の重量を基に計算して0.1%を越えな
い量で添加し、コア又は型を110―180℃に加熱す
ることを特徴とする鋳物用コア又は型の製造方
法。
Claim 1: A method for manufacturing a foundry core or mold of granular and/or fibrous material using sodium silicate or potassium silicate as a binder, in which the sodium or potassium silicate is calculated based on the weight of the material. and at least one surfactant selected from the group consisting of silicone oils, silicone emulsions and siliconates in an amount of 1-3% to the mixture of substances, and 0.1% calculated on the weight of the substances. A method for manufacturing a foundry core or mold, which comprises adding the core or mold to a temperature of 110-180°C.

2 コア箱を使用し、該コア箱を110―180℃に加
熱することを特徴とする特許請求の範囲第1項に
記載の方法。
2. The method according to claim 1, characterized in that a core box is used and the core box is heated to 110-180°C.

3 コアに110―180℃の温度の熱風を送風するこ
とを特徴とする特許請求の範囲第1―2項のいず
れかに記載の方法。
3. The method according to any one of claims 1 to 2, characterized in that hot air at a temperature of 110 to 180° C. is blown onto the core.

4 コアにCO2を送風し、熱風を補足的に送風し
てもしなくてもよいことを特徴とする特許請求の
範囲第1―2項のいずれかに記載の方法。
4. The method according to any one of claims 1 to 2, characterized in that CO 2 is blown into the core, and hot air may or may not be blown supplementarily.

5 コア又は型をコアと型剤でそれぞれ形成し、
それにエステル硬化剤を添加したことを特徴とす
る特許請求の範囲第2―4項のいずれかに記載の
方法。
5. Forming a core or a mold with a core and a molding agent, respectively,
The method according to any one of claims 2 to 4, characterized in that an ester curing agent is added thereto.

6 ケイ酸ナトリウム又はカリウムのモル比
SiO2/Na2Oが2―3であることを特徴とする前
記特許請求の範囲のいずれかに記載の方法。
6 Molar ratio of sodium or potassium silicate
Process according to any of the preceding claims, characterized in that SiO 2 /Na 2 O is 2-3.

明細書 本発明は、結着材としてケイ酸ナトリウム又は
ケイ酸カリウムを用いて粒状及び/又は繊維状物
質の鋳物用コア又は型を製造する方法に関する。
Description The present invention relates to a method for producing foundry cores or molds of granular and/or fibrous material using sodium or potassium silicate as a binder.

ケイ酸ナトリウム又はケイ酸カリウムは、以下
ケイ酸アルカリと呼ぶが、鋳物工業において例え
ば砂の型やコアの製造において長い間使用されて
きた。型やコアは室温において混合硬化剤によつ
て又はCO2を送風することにより冷却される。し
かしながら、そのように製造することは、十分な
強度を得るのに比較的高い結着剤の含有量が必要
である。その上、結着剤としてケイ酸カリウムを
使用することは、いくつかの他の不利益を伴な
い、そのうち次のものが特に挙げられる。
Sodium or potassium silicates, hereinafter referred to as alkali silicates, have long been used in the foundry industry, for example in the production of sand molds and cores. The mold or core is cooled at room temperature with a mixed curing agent or by blowing CO 2 . However, such manufacturing requires a relatively high binder content to obtain sufficient strength. Moreover, the use of potassium silicate as a binder is associated with several other disadvantages, among which are mentioned the following:

型やコアの耐火度の減少。 Reduced fire resistance of molds and cores.

鋳造後の型やコアの不十分な崩壊。 Insufficient collapse of the mold or core after casting.

使用した型やコア物質(成形砂)の低回収率。 Low recovery of used molds and core material (molding sand).

これらの不利益が型又はコアの製造においてケ
イ酸アルカリの利用を従来制限してきた。
These disadvantages have traditionally limited the use of alkali silicates in the manufacture of molds or cores.

有機結着剤、一般に樹脂を用いたコアの製造に
おいては、硬化剤として作用する物質(例えばあ
る酸)を混合しそしてその上コア箱又はコアを
250〜300℃の温度に加熱する。
In the manufacture of cores using organic binders, generally resins, a substance that acts as a curing agent (for example, an acid) is mixed and the core box or core is
Heat to a temperature of 250-300 ° C.

この方法で製造したコアは、コアの製造時とそ
の後の鋳造中の両方において実質的なガス発生を
起し、そのためにそのような鋳物工場の環境を都
合の悪いものにする。その上、そのようなコアの
製造には多くのエネルギーを必要とする。
Cores made in this manner exhibit substantial gas evolution both during core manufacture and subsequent casting, thereby rendering the environment in such foundries inhospitable. Moreover, the production of such cores requires a lot of energy.

本発明は前述の不利益を減らす目的を持ち、そ
して結着剤としてケイ酸ナトリウム又はケイ酸カ
リウムを用いて粒状及び/又は繊維状物質の鋳物
用コア又は型を製造する方法に関する。本発明は
界面活性物質をその物質の混合の際に添加し、そ
してコア又は型を110〜180℃に加熱することを実
質的に特徴とする。
The present invention has the aim of reducing the aforementioned disadvantages and relates to a method for producing foundry cores or molds of granular and/or fibrous material using sodium or potassium silicate as binder. The invention is essentially characterized in that the surface-active substance is added during mixing of the substances and the core or mold is heated to 110-180°C.

本発明に従つて界面活性物質を型物質に添加し
そしてコア又は型を110〜180℃に加熱することに
より、従来使用された量に比べケイ酸アルカリの
添加量を減少することが可能であり、それによつ
て型又はコアの強度や表面硬度を低下させること
はない。このことは型とコアを一層楽々と取扱い
そして保管することができそして型とコアは、鋳
造中熱や機械的応力に対し十分な抵抗を示すこと
も意味する。ケイ酸アルカリ含有量が少ないの
で、鋳造後の崩壊は非常に良好である。その上
に、鋳造は環境を保護する、というのは、健康に
とつて有害なガスがほとんど生じないからであ
る。コア製造時の輻射熱は適度であり、そしてエ
ネルギー消費量は少ない。その迅速な手順のた
め、その方法はとりわけ連続生産を可能にする。
By adding surface-active substances to the mold material according to the invention and heating the core or mold to 110-180°C, it is possible to reduce the amount of alkali silicate added compared to the amounts used previously. , thereby not reducing the strength or surface hardness of the mold or core. This also means that the mold and core can be handled and stored more easily and that the mold and core exhibit sufficient resistance to heat and mechanical stress during casting. Due to the low alkali silicate content, the disintegration after casting is very good. Moreover, casting protects the environment, since it produces very few gases that are harmful to health. The radiant heat during core manufacturing is moderate and energy consumption is low. Due to its rapid procedure, the method particularly allows continuous production.

SiO2/Na2O比(モル比)が0.5〜3.5の比較的
少量の液体ケイ酸アルカリと、界面活性剤、シリ
コーン油、シリコーン乳剤又はシリコネート
(siliconate)の形をとつた界面活性物質とが結着
されるべき型又はコア物質に添加される。
A relatively small amount of liquid alkali silicate with a SiO 2 /Na 2 O ratio (molar ratio) of 0.5 to 3.5 and a surfactant in the form of a surfactant, silicone oil, silicone emulsion or siliconate are used. Added to the mold or core material to be bound.

結着剤の量を最小限に維持しそして鋳造後の最
適な崩壊を成しとげることができるために、例え
ば多少の添加剤を伴なうケイ酸ナトリウムが使用
され、添加剤は: (a) シリコーン油、シリコーン乳剤及びシリコネ
ートよりなる群から選ばれた少なくとも1種の
界面活性物質。
In order to be able to keep the amount of binder to a minimum and achieve optimal disintegration after casting, for example sodium silicate with some additives is used, the additives being: (a ) At least one surfactant selected from the group consisting of silicone oil, silicone emulsion and siliconate.

(b) 糖誘導体の形をとる崩壊剤と界面活性化形成
剤で、通常ケイ酸ナトリウム溶液に安定に維持
するために処理されるものである。前記糖誘導
体とは、糖から誘導可能な糖に類似する一群の
物質を意味し、例えば、グルコースホスフエー
ト、グルコサン、グリコセミド
(glycosemide)、グリカール、チオアセター
ル、グルコフラノース、グルコピラノース、グ
ルコネート、ラクタイト、ラクツロース、ソル
ビツト、キシリツト等が挙げられる。
(b) Disintegrants and surfactant-forming agents in the form of sugar derivatives, which are usually treated to keep them stable in sodium silicate solutions. The sugar derivatives refer to a group of substances similar to sugars that can be derived from sugars, such as glucose phosphate, glucosan, glycosemide, glycal, thioacetal, glucofuranose, glucopyranose, gluconate, lactite, Examples include lactulose, sorbitol, xylitol, and the like.

本発明を以下に本発明を使用する実施例を用い
てより詳細に述べる。ケイ酸アルカリの従来の通
常量は、砂の量に基づいて計算して3〜5%以上
であることが認められる。
The present invention will be described in more detail below using examples in which the invention is used. It is observed that the conventional usual amount of alkali silicate is 3-5% or more, calculated on the basis of the amount of sand.

(1) 砂と砂の量に基づいて計算して1.5%のケイ
酸ナトリウム(比が2.7)と0.015%のシリコー
ン乳剤の混合物を作つた。高さ50mmで直径50mm
の円筒形の検体をこの混合物で作つた。検体を
150℃に加熱し、冷却後圧力試験を行なつた。
500〜600N/cm2の圧縮強さが得られた。シリコ
ーンを添加しない零点試験(シリコーン乳剤を
添加しない以外上記と同様にして行つた比較試
験)ではわずかに80〜90N/cm2の圧縮強さを生
じたにすぎなかつた。
(1) A mixture of 1.5% sodium silicate (ratio 2.7) and 0.015% silicone emulsion was made, calculated based on the amount of sand and sand. Height 50mm and diameter 50mm
A cylindrical specimen was made from this mixture. sample
It was heated to 150°C, and after cooling, a pressure test was conducted.
Compressive strengths of 500-600 N/cm 2 were obtained. A zero point test without the addition of silicone (a comparative test conducted in the same manner as above except without the addition of silicone emulsion) produced a compressive strength of only 80 to 90 N/cm 2 .

2%のケイ酸ナトリウム含有量と0.02%のシ
リコーン乳剤においては、約800N/cm2の圧縮
強さが得られ、一方零点試験では約550N/cm2
を生じた。
For a 2% sodium silicate content and 0.02% silicone emulsion, a compressive strength of about 800 N/cm 2 is obtained, while in the zero point test it is about 550 N/cm 2
occurred.

(2) コア箱を自動車物質用鋳物工場のコア・シユ
ーター(shooter)で150℃に加熱した。コア混
合物(mix)を砂(平均粒径0.25mm)と上記に
よる結着剤の2.5%とで作つた。コア混合物を
機械に充填し、コアを良好な充填度が得られる
ような圧力、通常400〜700kPa(4―7Kg/cm2
で撃つた。コアは箱中で、厚み(10―50mm)に
よつて20―60秒で熱硬化しその後鋳造にすぐ使
えた。
(2) The core box was heated to 150°C in a core shooter of an automotive material foundry. A core mix was made of sand (average particle size 0.25 mm) and 2.5% of the binder as described above. The core mixture is filled into the machine and the pressure is such that a good degree of core filling is obtained, usually 400-700kPa (4-7Kg/cm 2 ).
I shot it with The core was heat cured in the box in 20-60 seconds depending on the thickness (10-50 mm) and was then ready for casting.

(3) コアの製造は上記に従つて行なわれた。しか
しながら今回コアはより厚くなつており、従つ
てその上熱風(110―150℃)をコア箱に送風し
た。この方法で、60秒以下で完全に満足すべき
コアを製造することができた。
(3) Core manufacturing was performed as described above. However, this time the core was thicker, so hot air (110-150°C) was also blown into the core box. In this way, a completely satisfactory core could be produced in less than 60 seconds.

(4) (3)に従つてコアの製造を行なつた。しかしな
がら、ここでは熱風をCO2ガスに代えた。この
方法でも又完全に満足すべきコアを製造でき
た。従来、上記のケイ酸アルカリ含有量におい
てはこれは不可能であつた。
(4) The core was manufactured according to (3). However, here the hot air was replaced with CO2 gas. This method also produced completely satisfactory cores. Hitherto, this has not been possible with the above alkali silicate contents.

(5) (3)に従つてコアの製造を行なつた、しかし熱
風の一部をCO2に代えた。完全に満足すべきコ
アが得られた。
(5) The core was manufactured according to (3), but some of the hot air was replaced with CO 2 . A completely satisfactory core was obtained.

(6) (4)に従つてコアの製造を行なつた。しかしな
がら、ここでは、結着剤は49゜Be(ここで単位
“゜Be”はボーメ比重計の示度であつて、比重
の尺度として用いられる単位“ボーメ度”を意
味する)、比2.7の純ケイ酸ナトリウム3%と1
%の糖誘導体とで、即ち、結着剤の全量は4%
であつた。コアは良好な表面硬度を示した。し
かしながら、鋳造後の崩壊は上記による(2)、
(3)、(4)のそれよりもいく分悪かつた。
(6) The core was manufactured according to (4). However, here the binder is 49°Be (where the unit "°Be" refers to the Baume hydrometer reading and the unit "Baume degrees" used as a measure of specific gravity), with a ratio of 2.7. Pure sodium silicate 3% and 1
% sugar derivative, i.e. the total amount of binder is 4%
It was hot. The core showed good surface hardness. However, the collapse after casting is due to the above (2),
It was somewhat worse than (3) and (4).

(7) (3)に従つてコアの製造を行なつた、しかし普
通の種類のエステル硬化剤を7―10%添加し
た。この結果コアはより迅速にすつかり乾燥
し、このことは、大きな型/コアの製造におい
て、価値がある。
(7) The core was prepared according to (3), but with the addition of 7-10% ester hardener of the usual type. As a result, the core soaks and dries more quickly, which is valuable in the manufacture of large molds/cores.

実験によつて、界面活性物質は物質の重量を
基に計算して0.1%を越えるべきではなく、好
ましくは0.0001―0.1%の範囲内にあるべきで
あることがわかつた。
Experiments have shown that the surfactant should not exceed 0.1%, calculated on the weight of the material, and should preferably be in the range 0.0001-0.1%.

JP55500148A 1978-12-21 1979-12-21 Expired JPS6338254B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE7813194 1978-12-21
SE7907450A SE429509B (en) 1979-09-07 1979-09-07 VIEW TO PREPARE A CASTERY OR FORM OF CORN-SHAPE AND / OR FIBROSE MATERIALS WITH SODIUM SILICATE OR CALCIUM SILICATE AS BINDING AGENT

Publications (2)

Publication Number Publication Date
JPS55501134A JPS55501134A (en) 1980-12-18
JPS6338254B2 true JPS6338254B2 (en) 1988-07-29

Family

ID=26657178

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55500148A Expired JPS6338254B2 (en) 1978-12-21 1979-12-21

Country Status (7)

Country Link
JP (1) JPS6338254B2 (en)
DE (1) DE2953426C2 (en)
FI (1) FI64525C (en)
GB (1) GB2048735B (en)
IT (1) IT1126678B (en)
NO (1) NO151921C (en)
WO (1) WO1980001254A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0824996B2 (en) * 1989-10-31 1996-03-13 宇部興産株式会社 Water-soluble core and method for producing the same
GB9324561D0 (en) * 1993-11-30 1994-01-19 Borden Uk Ltd Foundry binder
US6139619A (en) * 1996-02-29 2000-10-31 Borden Chemical, Inc. Binders for cores and molds
BR9710858A (en) 1996-06-25 1999-08-17 Borden Chem Inc Bonding agent for cores and molds
DE102007051850B4 (en) 2007-10-30 2025-08-28 Ask Chemicals Gmbh Process for the production of casting moulds for metal processing using a moulding material mixture with improved flowability
DE102012103705A1 (en) 2012-04-26 2013-10-31 Ask Chemicals Gmbh Method for producing molds and cores for casting metal, and molds and cores produced by this method

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3424600A (en) * 1965-05-26 1969-01-28 Abram Moiseevich Liass Liquid mixes for foundry cores and moulds and method of manufacturing foundry cores and moulds from same
GB1165949A (en) * 1966-10-18 1969-10-01 Mitsubishi Heavy Ind Ltd Method for Making a Mould using Manganese Carbonate
GB1366705A (en) * 1971-07-09 1974-09-11 Foseco Int Hardening of refractory/sodium silicate

Also Published As

Publication number Publication date
DE2953426C2 (en) 1987-03-12
GB2048735B (en) 1983-03-09
FI793967A7 (en) 1980-06-22
FI64525B (en) 1983-08-31
DE2953426T1 (en) 1980-12-18
NO151921B (en) 1985-03-25
IT1126678B (en) 1986-05-21
JPS55501134A (en) 1980-12-18
IT7928350A0 (en) 1979-12-21
GB2048735A (en) 1980-12-17
NO151921C (en) 1985-07-10
FI64525C (en) 1983-12-12
NO794187L (en) 1980-06-24
WO1980001254A1 (en) 1980-06-26

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