JPS5848266B2 - Wet treatment method for water glass-based foundry sand - Google Patents
Wet treatment method for water glass-based foundry sandInfo
- Publication number
- JPS5848266B2 JPS5848266B2 JP4965276A JP4965276A JPS5848266B2 JP S5848266 B2 JPS5848266 B2 JP S5848266B2 JP 4965276 A JP4965276 A JP 4965276A JP 4965276 A JP4965276 A JP 4965276A JP S5848266 B2 JPS5848266 B2 JP S5848266B2
- Authority
- JP
- Japan
- Prior art keywords
- water glass
- sand
- caustic soda
- foundry sand
- treatment method
- 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
Links
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 title claims description 41
- 239000004576 sand Substances 0.000 title claims description 32
- 235000019353 potassium silicate Nutrition 0.000 title claims description 30
- 238000000034 method Methods 0.000 title claims description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 75
- 239000002699 waste material Substances 0.000 claims description 14
- 239000011230 binding agent Substances 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 40
- 235000011121 sodium hydroxide Nutrition 0.000 description 23
- 239000004115 Sodium Silicate Substances 0.000 description 11
- 229910052911 sodium silicate Inorganic materials 0.000 description 11
- 238000004090 dissolution Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000003513 alkali Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000012670 alkaline solution Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000010922 glass waste Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Molds, Cores, And Manufacturing Methods Thereof (AREA)
Description
【発明の詳細な説明】
本発明はCO2プロセス鋳型廃砂、ダイカル法鋳型廃砂
など鋳物砂に水硝子を粘結剤として、添加して鋳型とし
て使用した水ガラス系鋳物砂廃砂をアルカリ溶液で湿式
溶解洗滌し、再生利用に供するための処理方法に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention utilizes water glass waste foundry sand, which is used as a mold by adding water glass as a binder to foundry sand such as CO2 process foundry waste sand and Dical method foundry waste sand, to an alkaline solution. The present invention relates to a processing method for wet dissolving and cleaning and recycling.
近年、鋳物廃砂は、省資源環境保全の立場から単に無害
化して廃棄することは経済的でなく、再生利用の方向が
クローズアップされつつある。In recent years, from the standpoint of resource conservation and environmental conservation, it is not economical to simply detoxify and dispose of foundry waste sand, and recycling is becoming more and more popular.
鋳物廃砂としては水ガラスなど無機系を結合剤としたも
の、樹脂、油脂など有機系を結合剤としたものがあるが
、特に水ガラスを結合剤とする場合の廃砂再生にあたっ
ては種々の検討が必要である。There are two types of foundry waste sand: those using inorganic binders such as water glass, and those using organic binders such as resins and oils. Needs consideration.
すなわち、水ガラス系鋳型は珪砂に水ガラスを添加した
鋳型材からなっているが、添加された水ガラスはアルカ
リ可溶型の珪酸塩である。That is, the water glass mold is made of a mold material in which water glass is added to silica sand, and the added water glass is an alkali-soluble silicate.
この水ガラスがCO2硬化型のように造型時に化学変化
しても、鋳型が溶湯によって熱影響をうけてもなおほと
んどはNa2CO, , Na2 S i03,Na2
0−msio2などのアルカリ可溶性の塩として付着存
在することは廃砂が水にふれて、かなりpHの高い排水
を徐々に漏出することから明らかである。Even if this water glass changes chemically during molding, as in the case of a CO2-curing type, even if the mold is thermally affected by the molten metal, most of the water glass will still be Na2CO, , Na2 Si03, Na2
It is clear that the waste sand is present as an alkali-soluble salt such as 0-msio2 because when it comes into contact with water, wastewater with a considerably high pH gradually leaks out.
従来から水硝子系鋳物廃砂の処理方法としては、高温加
熱による焼成方法があるが装置の稼動費、設備費が高く
、また付着アルカリ塩を酸で中和する方法があるが、中
和は十分にされにくくゲル化した−(St02)n−の
残存など問題点が多い。Conventional methods for treating water glass-based foundry waste sand include firing at high temperatures, but this requires high equipment operating costs and equipment costs.Also, there is a method of neutralizing adhering alkali salts with acid, but neutralization is difficult. There are many problems such as the residual -(St02)n- which is difficult to gel and remains.
これら従来の処理方法は廃砂を再生利用する面と付着し
たアルカリの効果的な除去とアルカリの再生という面か
ら必ずしも十分ではない。These conventional treatment methods are not necessarily sufficient in terms of recycling waste sand, effectively removing attached alkali, and regenerating alkali.
本発明は上述の実態をふまえ、その欠点を解消したもの
であって、水ガラス系の鋳型廃砂をカセイソーダとケイ
酸ソーダの混合アルカリ溶蔽と接触させ、廃砂に付着し
たアルカリを効果的に洗滌することを特徴としている。The present invention has been developed based on the above-mentioned circumstances and has solved the drawbacks, by bringing water glass-based foundry waste sand into contact with a mixed alkaline solution of caustic soda and sodium silicate, and effectively removing the alkali attached to the waste sand. It is characterized by cleaning.
すなわち本発明者らはガラス系鋳型廃砂の湿式洗浄剤と
して多種の酸、アルカリを選定し、効果的な処理剤、処
理条件を見出すべく実験検討した結果、第3図に示すよ
うに、カセイソーダのみを洗滌剤として使用しても十分
その効果は認められるか、処理時間の短縮をはかればそ
の所要量も多くなり、処理剤コストがかかるなどの不利
益が発生し、一万カセイソーダの濃度すなわち所要量を
できるだけ低くするとともに、ケイ酸ソーダを共存させ
た混合アルカリ溶液とすることにより洗浄効果に有利で
あることを見出した。That is, the present inventors selected various acids and alkalis as wet cleaning agents for glass mold waste sand, and as a result of conducting experimental studies to find effective treatment agents and treatment conditions, as shown in Figure 3, caustic soda Is it sufficiently effective to use only 10,000 caustic soda as a cleaning agent?If you try to shorten the processing time, the amount required will increase, resulting in disadvantages such as increased processing agent cost. That is, it has been found that it is advantageous for the cleaning effect to reduce the required amount as much as possible and to use a mixed alkaline solution in which sodium silicate coexists.
すなわち(第1図及び第3図)の実験データの比較で明
らかなように、たとえば廃砂に含まれる付着アルカリを
100℃ですべて溶解除去させる時間を4時間とすれ(
!カセイソーダ5%、ケイ酸ソーダ5%の混合アルカリ
で洗浄すればよいが、カセイソーダのみでは63%の濃
度が必要であり、またカセイソーダ5%、ケイ酸ソーダ
5%では溶解時間は4時間であるが、カセイソーダ5%
では6.5時間を要する。In other words, as is clear from the comparison of the experimental data in (Figures 1 and 3), for example, if the time to dissolve and remove all the attached alkali contained in the waste sand at 100°C is set to 4 hours (
! It is sufficient to wash with a mixed alkaline mixture of 5% caustic soda and 5% sodium silicate, but with caustic soda alone a concentration of 63% is required, and with 5% caustic soda and 5% sodium silicate, the dissolution time is 4 hours. , caustic soda 5%
It will take 6.5 hours.
上述のようにカセイソーダ単独よりもケイ酸ソーダを共
存させる方が溶解速度を促進させる効果がある。As mentioned above, the coexistence of sodium silicate is more effective in accelerating the dissolution rate than the use of caustic soda alone.
すなわち処理時間が短縮されてまた、カセイソーダ所要
量も少なくてすむなどの利がある。That is, the processing time is shortened and the amount of caustic soda required is also reduced.
また第2図に示したように100゜C付近の高い処理濃
度ではケイ酸ソーダを共存させたカセイソーダ溶液はカ
セイソーダ単独と同様の溶解除去効果を示した。Further, as shown in FIG. 2, at a high treatment concentration near 100 DEG C., a caustic soda solution containing sodium silicate exhibited the same dissolution and removal effect as caustic soda alone.
以上述べたカセイソーダとケイ酸ソーダの混合アルカリ
溶蔽による廃砂上のアルカリ性物質の除去は、ゲル化の
進んだシリカ分一( S 102 ) n一のカセイソ
ーダによる溶解作用と付着ケイ酸ソーダと溶解剤として
のケイ酸ソーダの親和性増大による溶解の作用効果が相
乗的に働いていると推定される。The above-mentioned removal of alkaline substances on waste sand by mixed alkali dissolution of caustic soda and sodium silicate is achieved by the dissolving action of highly gelled silica fraction (S102) n1 by caustic soda, the adhering sodium silicate, and the dissolving agent. It is presumed that the effect of dissolution due to increased affinity of sodium silicate as a compound works synergistically.
なお、これら混合アルカリ溶液に公知の活性剤を少量添
加し、廃砂への浸透性向上による溶解除去効果をはかる
ことはいうまでもない。It goes without saying that a small amount of a known activator may be added to these mixed alkaline solutions to improve the dissolution and removal effect by improving the permeability to the waste sand.
使用される溶解剤としてのカセイソーダは一般の工業用
のものでよく、またケイ酸ソーダも一般に多用されてい
るSiO2/Na20のモル比が1.8〜3.5のもの
で十分でのる。The caustic soda used as a dissolving agent may be a general industrial one, and the commonly used sodium silicate with a SiO2/Na20 molar ratio of 1.8 to 3.5 is sufficient.
カセイソーダとケイ酸ソーダの量比は第1図に示したよ
うに目標とする処理時間によって異なるが、NaOH/
(NaOH+ Na 2 0 − n S t 02
)重量比が0. 1〜0. 9望ましくは0.5であり
、NaOH+Na2o−nSio2合量の水溶肢中の濃
度は5〜15重量%、望ましくはio重量%前後である
。The ratio of amounts of caustic soda to sodium silicate varies depending on the target treatment time, as shown in Figure 1.
(NaOH+ Na20-n S t 02
) weight ratio is 0. 1~0. 9 is preferably 0.5, and the concentration of the total amount of NaOH+Na2o-nSio2 in the aqueous limb is 5 to 15% by weight, preferably around io% by weight.
処理温度は高い方がよく、50〜200℃であるが、特
に100°C〜110℃が望ましい。The higher the treatment temperature, the better, from 50 to 200°C, and particularly preferably from 100°C to 110°C.
加圧溶解を採用すれば更に高温で溶解でき、処理速度も
速いことはいうまでもないが加圧操作など装置面、操作
面で必ずしも適正とはいいがたい面が残されている。It goes without saying that if pressurized melting is used, melting can be carried out at higher temperatures and the processing speed is faster, but there are still aspects such as pressurized operation that are not necessarily appropriate in terms of equipment and operation.
次に本発明の実施例を示す。Next, examples of the present invention will be shown.
実施例 1
新砂(三つ子山珪砂)100部に対して、S i0 2
/Na20モル数2.3の水硝子5部を加えて混練し、
CO2ガスで硬化させた試験片を実体鋳物における熱影
響を考慮して、1000℃に設定した電気炉で2時間加
熱焼或したのち、破砕して古砂を作或した。Example 1 S i0 2 for 100 parts of new sand (triplet mountain silica sand)
/Na20 mol number 2.3 5 parts of water glass was added and kneaded,
Taking into consideration the thermal effect on actual casting, the test piece hardened with CO2 gas was heated and baked in an electric furnace set at 1000°C for 2 hours, and then crushed to produce old sand.
一方、温度計、供液器、攪拌器を取付けた内容積2lの
セペラブルフラスコに水酸化ナトリウム、水酸化ナトリ
ウム+水硝子、あるいは水硝子容蔽を入れマントルヒー
タで所定の温度に設定したのち上述の古砂を入れ、10
0rpmでプロペラ攪拌機を回転しな゛がら、古砂表面
に付着した水硝子を溶解させた。On the other hand, put sodium hydroxide, sodium hydroxide + water glass, or a water glass container into a separable flask with an internal volume of 2 liters equipped with a thermometer, liquid donor, and stirrer, and set the temperature to the specified temperature using a mantle heater. Add the old sand mentioned above, 10
While rotating the propeller stirrer at 0 rpm, water glass adhering to the surface of the old sand was dissolved.
ついで、溶出水硝子量を定量するための溶液を一定時間
毎に採取した。Then, a solution for quantifying the amount of dissolved water glass was sampled at regular intervals.
採取した溶液は急玲したのち、沢過し、腋中のS io
2を重量法で定量し、古砂を投入する前の溶液中のS
i0 2定量値をブランクとして求めておき、その差分
を溶出SiO2とし水硝子換算し、上述古砂に付着させ
た水硝子量を100として除去率を算出した。After steeping the collected solution, strain it and remove it from the armpit.
2 was determined gravimetrically, and S in the solution before adding old sand was determined.
The i0 2 quantitative value was obtained as a blank, the difference was converted into water glass as eluted SiO2, and the removal rate was calculated by setting the amount of water glass attached to the old sand as 100.
セパラブルフラスコ内で再生処理した古砂はP過により
固液分離したのち、水洗を十分に行ない再生砂を回収し
た。The recycled sand in the separable flask was separated into solid and liquid by P filtration, and then thoroughly washed with water to recover the recycled sand.
実施例 2
第4図は実施例1と同様の鋳物砂及びNaOH5wt%
Na2 0 2. 3 S t02 5 w t%の水
溶液を容積3lの攪拌機付オートクレープ内に仕込み、
加圧昇温しで得られた水硝子除去速度である。Example 2 Figure 4 shows the same foundry sand and NaOH5wt% as in Example 1.
Na2 0 2. 3 S t02 A 5 wt% aqueous solution was placed in a 3 liter autoclave with a stirrer,
This is the water glass removal rate obtained by pressurizing and heating.
溶解速度に及ぼす温度の影響は大きく、加圧昇温する程
短時間で水硝子が除去された。The effect of temperature on the dissolution rate was large, and the higher the pressure and temperature, the faster the water glass was removed.
上述の実験方法で実施した実験結果を添付図面に示す第
1図はNaOHとNa20 ・2.38iO2の混合率
を変化させて、上述の方法により作或した古砂に付着す
る水硝子を100%除去するに要する時間を求めたもの
である。Figure 1 shows the experimental results carried out using the above-mentioned experimental method in the accompanying drawings. By varying the mixing ratio of NaOH and Na20.2.38iO2, water glass adhering to the old sand produced by the above-mentioned method was reduced to 100%. This is the time required for removal.
10%N a 2 0・23Si02水硝子溶液では1
2時間の処理でも100%除去することは困難であった
。1 in 10% Na20.23Si02 water-glass solution
It was difficult to remove 100% even after 2 hours of treatment.
第2図は処理温度と付着水硝子の除去率の関係を実験検
討したものであり、除去に対する温度の影響は指数函数
的に影響があり、本発明の処理温度は煮沸状態に近い程
効果が大きいことが明らかである。Figure 2 shows an experimental study of the relationship between the treatment temperature and the removal rate of attached water glass.The effect of temperature on removal is exponential, and the closer the treatment temperature of the present invention is to the boiling state, the more effective it is. It is clear that it is large.
第3図は100%除去するための所要時間とNaOH水
溶液濃度の関係を示したものである。FIG. 3 shows the relationship between the time required for 100% removal and the NaOH aqueous solution concentration.
なお、上述の処理により100%付着水硝子を除去した
再生砂を100%用いて、690k9のストラップの鋳
込み試験を行なった結果は新砂による製品と同様良好な
ものであった。A casting test was conducted on a 690k9 strap using 100% recycled sand from which 100% of the adhering water glass had been removed by the above treatment, and the results were as good as those made of new sand.
第1図は付着水硝子を100%除去するための所要時間
とカ性ソーダ・水ガラス混合液のTotal濃度との関
係を示す線図。
第2図は処理温度と付着水硝子除去率との関係を示す線
図。
第3図は付着水硝子を100%除去するための所要時間
とカ性ソーダ濃度の関係を示す線図である。FIG. 1 is a diagram showing the relationship between the time required to remove 100% of adhering water glass and the total concentration of the caustic soda/water glass mixture. FIG. 2 is a diagram showing the relationship between treatment temperature and adhering water glass removal rate. FIG. 3 is a diagram showing the relationship between the time required to remove 100% of the attached water glass and the caustic soda concentration.
Claims (1)
( NaOH+Na20−n s i 02)重量比(
但し、nはモル比で1.8〜3.5)が0.1〜0.9
をなすNaOH+Na20−nSiO2の5〜15重量
パーセントの混合アルカリ水溶液と50〜200℃で接
触させることを特徴とする。 水硝子系鋳物砂の湿式処理方法。[Claims] 1. Waste foundry sand using a water glass binder is mixed with HaOH/
(NaOH+Na20-ns i02) Weight ratio (
However, n is a molar ratio of 1.8 to 3.5) is 0.1 to 0.9
It is characterized in that it is brought into contact with a mixed alkaline aqueous solution of 5 to 15 weight percent of NaOH+Na20-nSiO2 at 50 to 200°C. Wet treatment method for water glass-based foundry sand.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4965276A JPS5848266B2 (en) | 1976-04-30 | 1976-04-30 | Wet treatment method for water glass-based foundry sand |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4965276A JPS5848266B2 (en) | 1976-04-30 | 1976-04-30 | Wet treatment method for water glass-based foundry sand |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS52133023A JPS52133023A (en) | 1977-11-08 |
| JPS5848266B2 true JPS5848266B2 (en) | 1983-10-27 |
Family
ID=12837114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4965276A Expired JPS5848266B2 (en) | 1976-04-30 | 1976-04-30 | Wet treatment method for water glass-based foundry sand |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5848266B2 (en) |
-
1976
- 1976-04-30 JP JP4965276A patent/JPS5848266B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS52133023A (en) | 1977-11-08 |
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