JPH0144102B2 - - Google Patents
Info
- Publication number
- JPH0144102B2 JPH0144102B2 JP60055268A JP5526885A JPH0144102B2 JP H0144102 B2 JPH0144102 B2 JP H0144102B2 JP 60055268 A JP60055268 A JP 60055268A JP 5526885 A JP5526885 A JP 5526885A JP H0144102 B2 JPH0144102 B2 JP H0144102B2
- Authority
- JP
- Japan
- Prior art keywords
- flotation
- feldspar
- peo
- per
- added
- 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
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Description
<産業上の利用分野>
本発明は陶石から浮遊選鉱法によつて長石を分
離し、他の有用成分たる粘土及び石英をより効率
良く回収する方法に関するものである。
陶石は窯業原料として重要な材料であるが、通
常の陶石には耐火度に悪影響を及びす長石が相当
含まれている為に、該長石を分離除去する必要が
ある。
<従来の技術>
陶石の脱長石浮選の一方法として本発明者等は
先に特願昭59−97194号(特開昭60−241951号公
報参照)にて示した二段浮選方法を開発した。こ
の二段浮選方法はまず粘土浮選を行い、次いで長
石浮選を行うという方法である。しかしこの二段
浮選方法に於いては、粘土浮選の工程中にかなり
多くの長石が浮鉱中に巻込まれるので、それを少
なくする為にpHを調節し、強酸性領域あるいは
強アルカリ領域で選鉱を行うと長石の巻込みは減
少するものの、粘土の回収率が低くなるという欠
点がある事を確認した。
<発明が解決しようとする問題点>
本発明は、陶石の脱長石浮選に於いて、粘土の
回収率を低下せしめる事なく長石を十分に分離す
る事が出来る様な方法を提供せんとするものであ
る。
<問題点を解決する為の手段>
本発明では粘土の回収率を下げる事なく、長石
を十分に分離する為に、pHの調整を行うと共に、
陽イオン型捕集剤の一種であるアルキルアミンと
共に、陶土やクレー質の凝集剤その他に用いられ
ているポリエチレンオキサイドを陶石粉末スラリ
ーに添加して浮選を行う方法を提供せんとするも
のである。
即ち、本発明はpH3以下に調整した陶石粉末の
スラリーに対し、1回当りにアルキルアミンを陶
石の乾量1トン当り10〜35gと、ポリエチレンオ
キサイドを10%パルプ濃度のスラリー1当り1
〜4mgを、3〜5回に渡り添加することを特徴と
する陶石の浮遊選鉱による長石分離方法の様に強
酸側で行う方法、並びにpH10以上に調整した陶
石粉末のスラリーに対し、1回当りにアルキルア
ミンを陶石の乾量1トン当り50〜100gと、ポリ
エチレンオキサイドを10%パルプ濃度のスラリー
1当り2〜8mgを、3〜5回に渡り添加するこ
とを特徴とする陶石の浮遊選鉱による長石分離方
法の様に強アルカリ側で行う方法に係るものであ
る。
なお本発明で用いるアルキルアミン(以下
COACという)としては、アルキルアミンやジア
ミン等のアルキルアミンの塩酸塩、酢酸塩、ある
いはアルキルアミンと石油スルホン酸との当量比
の混合物を用いるものとし、又ポリエチレンオキ
サイド(以下PEOという)は非イオン性の水溶
性高分子化合物で、HO―(CH2CH2O)o―
CH2CH2OHの一般式で示されるもので、その概
観は顆粒状である。このPEOは平均分子量430〜
480万と極めて大きな分子量を有し、水溶性では
あるが、即水に溶解はしないので本発明では、こ
のPEO0.1g程度を水面に分散させ、一昼夜膨潤
させたものを所定濃度に希釈して用いる様にし
た。
次に本発明のpH調整は硫酸と水酸化ナトリウ
ムを用いて行い、かつ起泡剤としてはパインオイ
ルを用いた。
<実施例及び作用>
熊本県天草郡天草町産の陶石(SiO2 74.32重量
%、Al2O3 16.26重量%、Na2O 2.67重量%、
K2O3.59重量%)をボールミル粉砕し、第1表に
示す様な粒度分布の原土を得た。
<Industrial Application Field> The present invention relates to a method for separating feldspar from chinastone by a flotation method and recovering clay and quartz, which are other useful components, more efficiently. Pottery stone is an important material as a raw material for ceramics, but since ordinary pottery stone contains a considerable amount of feldspar, which has a negative effect on fire resistance, it is necessary to separate and remove the feldspar. <Prior art> As a method for flotation to remove feldspar from pottery stone, the present inventors previously proposed a two-stage flotation method in Japanese Patent Application No. 59-97194 (see Japanese Patent Application Laid-open No. 60-241951). developed. This two-stage flotation method involves first performing clay flotation and then performing feldspar flotation. However, in this two-stage flotation method, a considerable amount of feldspar is entrained in the floating ore during the clay flotation process, so in order to reduce this, the pH is adjusted and Although beneficiation reduces the inclusion of feldspar, it has been confirmed that it has the disadvantage of lowering the recovery rate of clay. <Problems to be Solved by the Invention> The present invention aims to provide a method that can sufficiently separate feldspar without reducing the recovery rate of clay in feldspar-free flotation of pottery stone. It is something to do. <Means for solving the problems> In the present invention, in order to sufficiently separate feldspar without reducing the recovery rate of clay, pH is adjusted and
The purpose is to provide a method for flotation by adding polyethylene oxide, which is used as a flocculant for china clay and clay, to a chinastone powder slurry along with an alkylamine, which is a type of cationic scavenger. be. That is, in the present invention, for a slurry of chinastone powder adjusted to pH 3 or less, alkylamine is added at a rate of 10 to 35 g per ton of dry weight of chinastone, and polyethylene oxide is added at a rate of 10 to 35 g per 1 ton of slurry having a pulp concentration of 10%.
A method of separating feldspar by flotation of china stone, which is characterized by adding ~4 mg over 3 to 5 times, and a method performed on the strong acid side, and a slurry of china stone powder adjusted to a pH of 10 or more, A pottery stone characterized by adding 50 to 100 g of alkylamine per ton of dry weight of pottery stone and 2 to 8 mg of polyethylene oxide per 1 ton of slurry having a pulp concentration of 10% over 3 to 5 times. This relates to a method of separating feldspar using flotation, which is carried out on the strongly alkaline side. Note that the alkylamine used in the present invention (hereinafter referred to as
As COAC), hydrochloride or acetate of alkylamine such as alkylamine or diamine, or a mixture of alkylamine and petroleum sulfonic acid in an equivalent ratio is used, and polyethylene oxide (hereinafter referred to as PEO) is a nonionic A water-soluble polymer compound with HO―(CH 2 CH 2 O) o ―
It has the general formula CH 2 CH 2 OH, and its appearance is granular. This PEO has an average molecular weight of 430~
It has an extremely large molecular weight of 4.8 million, and although it is water-soluble, it does not dissolve immediately in water, so in the present invention, about 0.1 g of this PEO is dispersed on the water surface, swelled overnight, and then diluted to a predetermined concentration. I decided to use it. Next, pH adjustment in the present invention was performed using sulfuric acid and sodium hydroxide, and pine oil was used as a foaming agent. <Examples and effects> Pottery stone from Amakusa-cho, Amakusa-gun, Kumamoto Prefecture (SiO 2 74.32% by weight, Al 2 O 3 16.26% by weight, Na 2 O 2.67% by weight,
K 2 O (3.59% by weight) was ground in a ball mill to obtain raw soil with a particle size distribution as shown in Table 1.
【表】
この第1表に示す原土を用い、フアーレンワル
ド型浮選機の500c.c.セルに所定重量の原土、所定
pHの水溶液を入れ2分間撹拌した。この時のパ
ルプ濃度は10%とし、pHの測定は実験終了後に
行つた。
上記2分間撹拌した後、CAOC、PEOそして
起泡剤としてのパインオイルの順に添加し、各試
薬添加後2分間、2分間、1分間撹拌した後10分
間浮選をおこなつたその後の2回目以降の繰返し
浮選は、COAC、PEOの順に添加し、それぞれ
試薬添加後2分間撹拌し10分間浮選を行うという
操作を繰返した。
浮選産物は乾燥秤量後、X線粉末法により鉱物
組成を定量し、浮遊率、実収率を求めた。
又比較の為に起泡剤の他はCOACのみを添加し
た場合の実験も同様に行つた。
第1図に酸性領域に於けるpHと浮鉱中の鉱物
組成、浮遊率の関係を現わすグラフを示す。この
第1図よりPEO添加によつて浮鉱中の粘土の含
有率が若干低下し、長石の含有率が少し増加する
傾向があるが、全体の浮遊率は相当増加している
事が判る。またpHが増すにつれ浮鉱への長石の
混入が増加しかつ浮鉱中の粘土含有率が減少する
事が判る。次に第2図には同じく酸性側に於ける
各鉱物の実収率を示すが、この第2図よりPEO
添加により長石及び石英の浮鉱中への混入が若干
増えるが、粘土の実収率は30%以上改善されてい
る事が判る。以上第1図及び第2図から酸性側に
於いてはpH3以下が好ましい事が判る。
次に第3図にpH=2の場合にPEOの添加量を
1回当り2mg/で、COACの添加量を変化させ
た場合の各鉱物のニユートン分離効率を、又第4
図には同じくpH=2の場合にCOACの添加量を
1回当り25g/tでPEOの添加量を変化させた場合
の各鉱物のニユートン分離効率を示す。この第3
図及び第4図より酸性側に於けるCOACは1回当
り10〜35g/tが、又PEOは1回当り1〜4mg/
が好ましい事、更に他に行つた実験より上記量を
3〜5回添加すると望ましい事が判つた。
次に第5図にアルカリ側のpHと浮鉱中の鉱物
組成、浮遊率の関係を現わすグラフを、又第6図
に同じくアルカリ側に於けるpHと実収率との関
係を現わすグラフを示すが、この第5図よりpH
が高くなるにつれ全体的に浮遊率が減少して行く
傾向があること、特にPEO添加の場合にはpHが
10を越える範囲では浮遊率の減少が急激である事
が判る。これはpH10以上では非解離のアミンが
増加する為と考えられる。
しかしpHが高くなるにつれ浮遊物中の粘土の
含有率は上昇しており、PEOの添加によりpH10
以上の領域に於いて粘土の含有率が著しいことが
判る。又第6図の各成分の実収率からもPEO添
加の効果がある事が判る。以上の第5図及び第6
図よりpH10以上が粘土の回収率を維持しつゝ、
長石の混入を抑えるのに適しているといえる。
次に第7図にpH=10.4〜10.7で、PEOを1回
当り4mg/で1回添加と一定にし、COACの添
加量を変化させた場合の各鉱物のニユートン分離
効率を、又第8図にはpH9.9〜10.4でCOACを1
回当り50g/tで4回添加と一定にし、PEOの添加
量を変化させた場合の各鉱物のニユートン分離効
率を示すが、この第7図及び第8図よりアルカリ
側に於けるCOACは1回当り50〜100g/tが、又
PEOは1回当り2〜8mg/が好ましい事、更に
他に行つた実験より上記1回当量を3〜5回添加
すると望ましい事が判つた。
<発明の効果>
以上述べて来た如く、本発明によればCOACと
PEOを併用し、pHを3以下の強酸性側又は10以
上の強アルカリ側に調整する事により粘土の実収
率を高く維持しながら、粘土と長石とをより良く
選択分離する事が出来るという効果がある。[Table] Using the raw soil shown in Table 1, a specified weight of raw soil was placed in a 500 c.c. cell of a Fahrenwald type flotation machine.
A pH aqueous solution was added and stirred for 2 minutes. The pulp concentration at this time was 10%, and the pH was measured after the experiment was completed. After stirring for the above 2 minutes, CAOC, PEO, and pine oil as a foaming agent were added in this order, and after addition of each reagent, the mixture was stirred for 2 minutes, 2 minutes, and 1 minute, and then flotation was performed for 10 minutes. Subsequent flotation was repeated by adding COAC and PEO in this order, stirring for 2 minutes after each reagent addition, and flotating for 10 minutes. After drying and weighing the flotation product, the mineral composition was determined by the X-ray powder method, and the flotation rate and actual yield were determined. For comparison, an experiment was also conducted in which only COAC was added in addition to the foaming agent. Figure 1 shows a graph showing the relationship between pH, mineral composition in floating ore, and floating rate in an acidic region. It can be seen from Figure 1 that the clay content in the floating ore tends to decrease slightly and the feldspar content increases slightly due to the addition of PEO, but the overall floating rate increases considerably. It is also seen that as the pH increases, the amount of feldspar mixed into the floating ore increases and the clay content in the floating ore decreases. Next, Figure 2 shows the actual yield of each mineral on the acidic side.
Although the addition of feldspar and quartz into the floating ore slightly increases, it is clear that the actual yield of clay has been improved by more than 30%. From the above figures 1 and 2, it can be seen that on the acidic side, pH 3 or less is preferable. Next, Figure 3 shows the Newtonian separation efficiency of each mineral when the amount of PEO added is 2 mg/time and the amount of COAC added is changed when pH = 2.
The figure also shows the Newtonian separation efficiency of each mineral when the amount of COAC added was 25 g/t per time and the amount of PEO added was changed when pH = 2. This third
From the figure and Figure 4, COAC on the acidic side is 10 to 35 g/t, and PEO is 1 to 4 mg/t per dose.
It has been found from other experiments that it is preferable to add the above amount 3 to 5 times. Next, Figure 5 is a graph showing the relationship between pH on the alkaline side, mineral composition in floating ore, and floating rate, and Figure 6 is a graph showing the relationship between pH and actual yield on the alkaline side. However, from this figure 5, pH
The overall floating rate tends to decrease as the pH increases, especially when PEO is added.
It can be seen that the floating rate decreases rapidly in the range exceeding 10. This is thought to be due to an increase in undissociated amines at pH 10 or higher. However, as the pH increases, the content of clay in the suspended solids increases, and by adding PEO,
It can be seen that the content of clay is significant in the above areas. Also, it can be seen from the actual yield of each component in Figure 6 that the addition of PEO has an effect. Figures 5 and 6 above
The figure shows that pH 10 or higher maintains the clay recovery rate.
It can be said that it is suitable for suppressing the contamination of feldspar. Next, Figure 7 shows the Newtonian separation efficiency of each mineral when pH = 10.4 to 10.7, PEO was added at a constant rate of 4 mg/time, and the amount of COAC added was varied, and Figure 8 1 COAC at pH 9.9-10.4
The Newtonian separation efficiency of each mineral is shown when the amount of PEO added is varied, with the addition constant at 50 g/t per time, four times. From Figures 7 and 8, COAC on the alkaline side is 1. 50~100g/t per cycle, and
It has been found from other experiments that it is preferable to add PEO in an amount of 2 to 8 mg/time, and that it is desirable to add the above-mentioned equivalent amount 3 to 5 times. <Effects of the invention> As described above, according to the present invention, COAC and
By using PEO in combination and adjusting the pH to a strongly acidic side of 3 or less or a strong alkaline side of 10 or more, clay and feldspar can be better selectively separated while maintaining a high clay yield. There is.
第1図は酸性側に於ける浮遊率と浮鉱中の各鉱
物組成を示すグラフ、第2図は同じく各鉱物の実
収率を示すグラフ、第3図及び第4図は同じくそ
れぞれCOAC及びPEOの添加量を変えた場合の
各鉱物のニユートン分離効率を示すグラフ、第5
図はアルカリ側に於ける浮遊率と浮鉱中の各鉱物
組成を示すグラフ、第6図は同じく各鉱物の実収
率を示すグラフ、第7図及び第8図は同じくそれ
ぞれCOAC及びPEOの添加量を変えた場合の各
鉱物のニユートン分離効率を示すグラフ。
Figure 1 is a graph showing the flotation rate on the acidic side and the composition of each mineral in floating ore, Figure 2 is a graph showing the actual yield of each mineral, and Figures 3 and 4 are COAC and PEO, respectively. Graph showing the Newtonian separation efficiency of each mineral when the amount of addition is changed, 5th
The figure is a graph showing the flotation rate on the alkali side and the composition of each mineral in the floating ore, Figure 6 is a graph showing the actual yield of each mineral, and Figures 7 and 8 are the same, respectively, with the addition of COAC and PEO. A graph showing the Newtonian separation efficiency of each mineral when the amount is changed.
Claims (1)
し、1回当りにアルキルアミンを陶石の乾量1ト
ン当り10〜35gと、ポリエチレンオキサイドを10
%パルプ濃度のスラリー1当り1〜4mgを、3
〜5回に渡り添加することを特徴とする陶石の浮
遊選鉱による長石分離方法。 2 pH10以上に調整した陶石粉末のスラリーに
対し、1回当りにアルキルアミンを陶石の乾量1
トン当り50〜100gと、ポリエチレンオキサイド
を1%パルプ濃度のスラリー1当り2〜8mg
を、3〜5回に渡り添加することを特徴とする陶
石の浮遊選鉱による長石分離方法。[Claims] 1. For a slurry of china stone powder adjusted to pH 3 or less, 10 to 35 g of alkylamine per 1 ton of dry weight of china stone and 10 to 35 g of polyethylene oxide are added per ton of dry weight of china stone.
1 to 4 mg per slurry with a pulp concentration of 3
A method for separating feldspar by flotation of pottery stone, which is characterized in that it is added five times. 2 Add alkylamine to the slurry of chinastone powder adjusted to pH 10 or higher by adding 1 dry amount of chinastone at a time.
50-100g per ton and 2-8mg of polyethylene oxide per slurry with 1% pulp concentration.
A method for separating feldspar by flotation of pottery stone, characterized by adding the following three to five times.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60055268A JPS61212351A (en) | 1985-03-18 | 1985-03-18 | Separating method for feldspar by floatation of pottery stone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60055268A JPS61212351A (en) | 1985-03-18 | 1985-03-18 | Separating method for feldspar by floatation of pottery stone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61212351A JPS61212351A (en) | 1986-09-20 |
| JPH0144102B2 true JPH0144102B2 (en) | 1989-09-26 |
Family
ID=12993855
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60055268A Granted JPS61212351A (en) | 1985-03-18 | 1985-03-18 | Separating method for feldspar by floatation of pottery stone |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61212351A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9923259B2 (en) | 2013-08-15 | 2018-03-20 | Ooo Siemens | Device for radio-frequency power coupling and method of using the device |
-
1985
- 1985-03-18 JP JP60055268A patent/JPS61212351A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9923259B2 (en) | 2013-08-15 | 2018-03-20 | Ooo Siemens | Device for radio-frequency power coupling and method of using the device |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61212351A (en) | 1986-09-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |