JPS6022953A - Flotation collector - Google Patents

Flotation collector

Info

Publication number
JPS6022953A
JPS6022953A JP58131749A JP13174983A JPS6022953A JP S6022953 A JPS6022953 A JP S6022953A JP 58131749 A JP58131749 A JP 58131749A JP 13174983 A JP13174983 A JP 13174983A JP S6022953 A JPS6022953 A JP S6022953A
Authority
JP
Japan
Prior art keywords
flotation collector
flotation
oxide
acid
deriv
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
Application number
JP58131749A
Other languages
Japanese (ja)
Inventor
Yoshikazu Ogura
義和 小倉
Yasunobu Mizuno
水野 康伸
Nobuhiro Ueshima
伸宏 上嶋
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.)
Neos Co Ltd
Original Assignee
Neos Co 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 Neos Co Ltd filed Critical Neos Co Ltd
Priority to JP58131749A priority Critical patent/JPS6022953A/en
Publication of JPS6022953A publication Critical patent/JPS6022953A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain flotation collector having high dressing effect by adding polyalkylene oxide deriv. having a specified mol.wt. and contg. a specified proportion of propylene oxide to a flotation collector. CONSTITUTION:A polyalkylene oxide deriv. having 400-200,000 average mol.wt. contg. >=5mol propylene oxide in a molecule is added to a flotation collector. Said polyalkylene oxide deriv. is obtd. by adding propylene oxide to a compd. having active H. Examples of the compd. having active H are alcohols, phenols, carboxylic acids, amines, alkanolamines, mercaptans, amides, amino-acids, etc. The amt. to be used of the flotation collector is 0.01-2wt%. The flotation collector has superior dressing effect for several ores (e.g. chalcocite). When it is used as a flotation collector for pulverized coal, superior deashing rate is attained.

Description

【発明の詳細な説明】[Detailed description of the invention]

浮遊選鉱法IJ 、 m物や石炭の選別法としζ古くか
ら知られている。これは通常、鉱石類を細粉し、水スラ
リーとした接、選鉱4iに入れ、捕収剤、起泡剤、揚台
によっては調整剤を入れ、攪拌し、空気を吹き込むこと
によって、目的とする物質を泡に(J着さμ、適当な方
法で隼める方法である。。 411収剤は鉱物中の選別物質の表面を辣水竹に1Jる
ことにJ、す、泡に(=Jるし易く(するIfIj公を
b′、)bのであり、従来、)アンセー1−、ア)1j
1−ルジチA−ノAスノ」−1〜、ブA尿素誘導体、1
指1坊醇まだは王の塩等が、J、く用いられでおり、ま
たlx炭等にJ3いCは安IIII/eF軽油1.幻油
、へ重油谷のI−1油留分が使用されでさた。 捕収剤トニ曹請される性能は、高い回収率を達成ηるこ
と、10れた選別効果を右づることおJ、び後の1lf
2水上稈に、1メいC優れた脱水率を小りこと貿(−あ
る。従来、これらの性能を仝で満足づる捕収剤/!:l
!?ることi、(困ガl−あっ−USJ、り改1>され
〕= J+li IIy剤の開発が要望されている。1
木発明LL、It!i化ノ゛11ピレンiJ!導体を用
いC優れた選別効果をイj4る汀選捕収剤を提供づる魚
にある。 即ち、本発明にL1分子中に酸化ノ′1−Iピレンを巳
)しル以1有し、平均分子量が40 (’)・〜200
00Oのポリアルキレンオキシド誘導体を含有づる浮選
捕収剤を提供り−る。 本発明におい−(、ポリアル:ルンΔ−1ニシド誘導体
は、種々の活性水素基と酸化ゾ[1ピレンまたは酸化)
”L1ピレンと酸化土チレンをイ」加重合さμることに
よって得られる。活性水素をイ1リ−る化合物としく’
 kl、ノノルゴJ−ル類、フェノール類、カルボン酸
類、アミン類、ノ′ルカノールアミン類、メルカプタン
類、アミド類、その他ノIミノ酸類、グリコ」−ル類、
ノノミノノ1ノール類等が例示される。 アル」−ル類としては、1価アル」−ル、例えばメタノ
ール、エタノール、イソプロパツール等の低級ア、ルコ
ールからラウリルj′ル]−ル、ステアリルアルコール
、A°レイルアルコール等の8級アルコール、シクロヘ
キリノール、アビエチン酸等のli残基を有づ゛るアル
コール、ジエーチールヘキサノールのごとぎ側鎖を右り
るアルコール、2級アル]−ルの他、多価アルコール、
例えばエチレングリコール、プロピレングリ−1−ル、
1タンジー1−ル、ヘキリ゛ンジオール、グリセリン、
ジグリヒリン、ソルビタン、ペンタエリスリ1−−ル、
ツルじッ1−、シュークロ1−ス、セル1,1−ス、澱
粉、ポリ酢酸ビニル部分ケン化物、ポリグリレリン、ジ
ペンタエリスリ1〜−ル等、またはぞれらの部分土スア
ル類、例えばモノグリレリド、ソルビタン七ツノノルキ
レー1−1等が例示される。。 ノコノール類どし−(は、)Jノール、クレゾール、ア
ルキルノ1ノール、ノ1−ルノ、I−ノール、スヂレン
化フ」ノール、レゾルシン、ノ入イドに1−1ノン、ビ
L1ガ[l−ル、)−フェノール類およびぞれらの11
\ルマリン縮含物等が例示される。 カルボン酸としCは、酢酸、ラウリン酸、Aレイン醇、
リノール酸、リシノール酸、フェニルn1酸、鉄酸、二
1ハク酸、アジピン酸、フタル酸、タイマー酸、1−リ
メリ1〜M、トリメシン酸、ビ[1メリ]−酸等の他、
ilクリル酸、メタクリル酸、無水lレイン酸等の重合
性カルボン酸残基を含む重合体、ポリカルボン酸またば
その部分子−ス)゛ル化物等が例示される。 アミン類どしては、1級アミン、例えばtツメデルアミ
ン、LノTデルアミン、Aクヂルアミンンウリルノ7ミ
ン、牛脂アミン、アニリン、I・ルイジン、ヘンシルア
ミン、り1−1ルノlニリン1.α−フェニルエチルア
ミン等、2級アミン、例えばジエチルアミン、メヂルス
ノアリルj7ミン、N−メチルノアニリン、しルホリン
等、ポリアミン、例えば」−ヂレンジアミン、1″ロビ
レンジノ7ミン、へ:1−υメチレンジアミン、フJ−
ニレンジノ7ミン、ベンジジン、グアニジン、ジ、■、
ブレン1−リアミン、1〜すLチレン71〜ラミン、ペ
ンタエチレンヘギ1Jミン等のはか、■ブレンイミンの
重合にJ、っ−C得られるポリ上ブレンイミン等が例示
される。 ノフルカノールノ7ミンとしては、モノ−しタノールj
ノミン、ジェタノールアミン、1ヘリエタノールアミン
等、d3 J:び七ノー丁ヂルプL1パノールアミン等
のしノアルニ1ニルアルカノールアミンよい。 アミドどしくは、ラウリン酸j′ミド、ステアリン酎ア
ミド、Aレイン酸アミド等が例示される。 メルカプタンとしくは、ラウリルメルカプタン、ドデシ
ルノ」−ルメルノJブタン等がある1。 上記活性水素をイソする化合物は親水性の強い物?ff
のほうがりfましい。rlに々fまり,い活1〈1水素
含イ]化合物は,ポリ77ミン類、特に分子(nの比較
的^いポリ1ブ−レンーrミンC゛ある。ポリ上プレン
イミンは多数の分岐を右するポリ」−ブレンイミンが好
ましく、分子品は300〜1 0 0 0 00 ’t
 ’I?iに6 0 0−・I’ 0 0 0 0が好
ましい。 酸化1′l[ビlノン、は、1分子中に0[ル以上、3
1、り好ましくはT (’)以Fであり、高申合庶の場
合はさらに酸化」ルンを句加しkbのぐあつ−( bJ
、い、、酸化f目ピレンと酸化[−ブーレンのJU干合
陣をゆ用4るlLlは、1 1.1ツク共重合体(・あ
つ(もく、、l:たランダムJ(j?!合体であってら
よい。 ポリilルー11ノンAキシド誘導体の分子(i5は、
m1′ノ分子吊が400・〜2 0 0 0 0 0程
麿、特に好よ
Flotation method IJ has been known for a long time as a method of sorting minerals and coal. This is usually achieved by grinding ores into a fine powder, making a water slurry, placing it in a beneficiation machine, adding a collecting agent, a foaming agent, and a conditioning agent depending on the platform, stirring, and blowing air. This is a method of solidifying the substance to be mixed into foam (J) using an appropriate method. = J is easy to do (if Ij public is b',) b, and conventionally) Answer 1-, A) 1j
1-Rujiti A-noAsuno''-1~, BuA urea derivative, 1
King's salt etc. are often used in J and J, and J3 and C are AIII/eF diesel oil 1. The I-1 oil fraction from Hejuyu Valley was used for the phantom oil. The performance of the scavenger is to achieve a high recovery rate, to obtain a good sorting effect, and to obtain the following 1lf.
2. There is a small trade in water culm with excellent dehydration efficiency.
! ? There is a demand for the development of a compound IIy.
Wood invention LL, It! i-based 11pyrene iJ! It is possible to use a conductor to provide a scavenging agent that has an excellent sorting effect. That is, in the present invention, the L1 molecule contains at least 1) 1-I pyrene oxide, and the average molecular weight is 40(')-200.
A flotation collector containing a 00O polyalkylene oxide derivative is provided. In the present invention, polyal:run Δ-1 niside derivatives have various active hydrogen groups and oxidized zo[1 pyrene or oxidized]
It is obtained by polymerizing L1 pyrene and oxidized earth tyrene. As a compound that contains active hydrogen.
kl, nonolols, phenols, carboxylic acids, amines, norkanolamines, mercaptans, amides, other amino acids, glycols,
Examples include nonominononol and the like. Examples of alcohols include monohydric alcohols, such as lower alcohols such as methanol, ethanol, and isopropanol, and octahydric alcohols such as lauryl alcohol, stearyl alcohol, and A° rail alcohol. , cyclohexylnol, alcohols with li residues such as abietic acid, alcohols with a right side chain such as diethylhexanol, secondary alcohols, polyhydric alcohols,
For example, ethylene glycol, propylene glycol,
1 tanzyl, hexylene diol, glycerin,
diglyhirin, sorbitan, pentaerythrol,
Tsuruji 1-, sucrose 1-su, cell 1,1-su, starch, partially saponified polyvinyl acetate, polyglyrelin, dipentaerythryl 1--ol, etc., or partial earth compounds thereof, such as monoglyleride, sorbitan Examples include Nanatsunonorkyre 1-1. . Noconols - (ha) J-nor, cresol, alkyl-1-nor, no-1-luno, I-nol, styrenated phenols, resorcinol, 1-1-1-1 non, bi-L1-[l- )-phenols and their respective 11
\Lumarin condensate etc. are exemplified. Carboxylic acid, C is acetic acid, lauric acid, A rhein,
In addition to linoleic acid, ricinoleic acid, phenyl n1 acid, ferric acid, 21-huccinic acid, adipic acid, phthalic acid, timer acid, 1-limeri 1 to M, trimesic acid, bi[1-meri]-acid, etc.
Examples include polymers containing polymerizable carboxylic acid residues such as il-acrylic acid, methacrylic acid, and linic anhydride; polycarboxylic acids; Examples of amines include primary amines, such as T-thumedelamine, L-T-delamine, A-tallowamine, tallow amine, aniline, I-luidine, hensylamine, and l-1-1 l-niline. α-Phenylethylamine, etc., secondary amines, such as diethylamine, methylsnoallylj7mine, N-methylnoaniline, sulfoline, etc., polyamines, such as ``-dilenediamine, 1''robylenediamine, to:1-υ methylenediamine, −
Nylendino7mine, benzidine, guanidine, di,■,
Examples include brene 1-liamine, 1~suL tyrene 71~ramin, pentaethylene hegyene 1J amine, etc.; As noflukanol, monotanol j
Nomin, jetanolamine, 1-heliethanolamine, etc., d3 J: 1-helialkanolamine, such as L1 panolamine, etc. are suitable. Examples of amides include lauric acid j'amide, stearic acid amide, and Aleic acid amide. Examples of mercaptans include lauryl mercaptan and dodecyl-lumerno-J butane. Is the compound that isolates active hydrogen mentioned above highly hydrophilic? ff
It's more frightening. The active 1〈1hydrogen-containing〉compounds that are highly active in rl include poly77mines, especially molecules (n) of relatively relatively poly1-butene-rmine C.Polypreimine has a large number of branches. Preferably, poly'-blenimine has a molecular weight of 300 to 100000't.
'I? It is preferable that i is 600-.I'00000. Oxidation 1'l [vinone, 0 [l or more, 3] in one molecule
1, preferably T (') to F, and in the case of high-grade combinations, add the oxidation ``run'' to kb no guatsu-( bJ
Using the JU combination of oxidized f-th pyrene and oxidized [-bourene, 4 lLl is 1 1.1 Tsuk copolymer (・atsu(moku,, l: random J(j? !It would be good if it was a combination. Molecule of polyil-11 non-A oxide derivative (i5 is
The molecular weight of m1' is about 400 to 2000000, which is particularly favorable.

【ノくはり 0 0 0−・1 0 0 
0 0 0て゛ある。1!1られにポリj′ル.ルンA
1ーシト手合体のLI L L3は10Lスト、好;L
しくは6以下である。 本発明捕収剤の使用■)は、被抽収物質である金属微粉
末の、あるいは鉱r1微粉末の粒度にJ、って異なるが
、0.01〜2重量%であり、粒度200メツシユパス
60〜80%の場合には06.05〜1屯吊%でよい。 J:た他の捕収剤と渥「゛て使用してもよい。 本発明浮jハ捕収剤は種々の鉱物、例えば輝銅鉱、黄銅
鉱、iv!1i銀鉱、硫銅錫鉱、硫砒銅鉱、硫安鉛鉱、
輝水鉛鉱、等の硫化鉱物を含む鉱石ヤ)、赤銅鉱、錫h
、赤亜鉛鉱、軟マンガン鉱、白安鉱、砒華、金紅石、l
−1矢等の酸化鉱物を含む鉱石や、菱i11!鉛鉱、菱
マンガン斯い白雲11、マグネザイ1へ、方解石1、ス
トIIンチウム鉱、バストネリ−イ1−等のN2M鉱物
を含む鉱r1や、ホタル石、氷晶イコ等のフッ素含イ1
鉱物の鉱石等に使用りることができるが、(i機微粉末
の浮選捕収剤として使用した11)は、従来の捕収剤に
比べ優れた1112灰率を得ることが′Cきる。 さらにrj炭機微粉末1史用した場合、浮選6炭微粉末
を水スラリー炭どしCf1I!川りる際の分散安定f1
に寄りし、あるいは得られ/=7’i炭微粉末全微粉末
とし“(使用りる際には、これが安定剤としCも奇’J
 Jるため、混炭油に使用りる際の活性剤の使用h1を
減ら・jことが1■能となる。 以上、実施例をあげC木ブを明を説明りる。 実施例゛1 200メツシー+ 66%パスのオーン旧にわ)砕しI
ご)4化銅鉱11(銅と1)(0、56%含+r ) 
ヲ20中串%含むスラリー2.5kgをクー1−1\−
1ネI賀ノボ汀)へ別に入れ、12 (、) Orpm
−(゛5分間版拌後、表 ′1に示り木′ブifi l
!IJ浮選捕収剤0 、 L−,3’X+ (!添加し
〕、次いぐ120 Orpm (゛5分間博J’l’ 
l、 IJ oこのスラリーに起泡剤(バーrンAイル
)を0.1!i鱈入れ、120 Orpmで1η打を継
続しイfがら、空気を入れ()7′)パを行ない、1;
1られた浮)バフ11ス中の銅含右111を測定しIこ
。結果を表−′1に;): ’J’ 、、同様(、二従
来般に使用され(いる浮jバ捕収剤(J−〕い(浬選を
11ない、)1」ス中の銅−含右吊を測定した1、結末
を同じく表−1に小り、。 実施例2 200メツシユパス< 100%)に粉砕した微粉珪砂
(Si 02として87.4%含有)を20%含むスラ
リー2.5kgをウニムコ2i製ラボ浮選機に入れ、1
200rpIllで5分間1殿拌後、表−2に承り本発
明浮選捕取剤0.5%を添加し7、同じ<1200rp
mで5分間撹拌後、4−ノブ−ルー2−ペンタノール(
起泡剤)を0.15に入れ、攪拌(1200rpI11
)を継続しながら、空気を入れて浮選を行なった。浮選
後のゾール中のs+ 02含有ff1(%)を表−2に
承り。同様にして従来の浮選捕取剤を0.5%使用し、
4選を行な・)た結果を同じく表−2に示】。 実施例3 大同病く原炭)をボールミルで微粉砕し、200メツシ
ュア8%パスのものを得た。この微粉炭250(J (
灰分11.6%)をつ1ム」社製ラボ浮選機に入れ、水
2250gを加え、1.200rpmで10分間攪拌し
、スラリーを得た9、該スラリーに本発明浮選捕収剤を
石炭に対し0.1重色%加え、120Orpmで3分間
攪拌し、4−メチル−2−ペンタノール(起泡剤)0.
2xiを2回に分り°C加え、これを1200rlll
llC攪拌し4丁がら空気を入れ(浮選選別した。泡を
容器に移し、ブノナーL1−1−〇石炭を濾過した。−
過後のケーキ中の含水量および灰分を測定した。含水量
は濾取含水イコ炭微粉末を105〜110 ”Cの高温
乾燥機に1時間入れて乾燥した時の乾燥前後の巾雀差C
表ねり(%)。灰分はJIS M8812に従つη測定
した。結果を表−3に示1゜なお、上記の測定(J石炭
収率95〜96%で得られたbのの評1曲である。
[Nokhari 0 0 0-・1 0 0
There is 0 0 0. 1! 1 poly j' le. Run A
1-shito hand combination LI L L3 is 10L strike, good; L
Or less than 6. Use of the collecting agent of the present invention (1) is 0.01 to 2% by weight, depending on the particle size of the metal fine powder or ore r1 fine powder that is the substance to be extracted, and the particle size is 200 mesh pass. In the case of 60 to 80%, 06.05 to 1 ton suspension % may be sufficient. The scavenging agent of the present invention may be used in combination with other scavengers. Copper ore, ammonium sulfate,
Ore containing sulfide minerals such as molybdenite, cuprite, tin
, red zinc ore, soft manganese ore, white beanite, arsenic, goldstone, l
Ore containing oxidized minerals such as -1 arrow and rhombus i11! Lead ore, rhodochrosite, such as Baiyun 11, magnesite 1, calcite 1, stylinium ore, bastnerii 1-containing N2M minerals, and fluorine-containing minerals such as fluorite and ice crystals 1.
Although it can be used for mineral ores, etc., (11) used as a flotation collector for fine powder can obtain a superior 1112 ash rate compared to conventional collectors. Furthermore, when rj charcoal fine powder 1 is used, flotation 6 charcoal fine powder is mixed into water slurry charcoal Cf1I! Dispersion stability f1 when walking in a river
or obtained/=7'i fine charcoal powder and all fine powder (when used, this is used as a stabilizer and C is also odd'J
Therefore, it is possible to reduce the amount of activator used when used in mixed coal oil. Above, the details of the C tree will be explained by giving examples. Example ゛1 200 Metsushi + 66% Pass Orn Old Niwa) Shattered I
) Copper tetrahide 11 (copper and 1) (contains 0.56% +r)
Cool 2.5 kg of slurry containing 20%
Separately into 1 page (1 page), 12 (,) Orpm
- (After stirring the plate for 5 minutes, as shown in Table 1)
! IJ flotation collector 0, L-, 3'X+ (! added), then 120 Orpm (5 minutes
l, IJ oAdd 0.1 of a foaming agent (Burn Ail) to this slurry! i Put in the cod, continue to make 1 η strokes at 120 Orpm, then add air () 7') and perform Pa, 1;
1) Measure the copper content 111 in the buff 11 bath. The results are shown in Table 1; The results of the copper-containing suspension measurements are also shown in Table 1. Example 2 Slurry containing 20% of finely divided silica sand (containing 87.4% as Si02) pulverized to 200 mesh passes <100%) Put 2.5 kg into the Unimuco 2i laboratory flotation machine,
After stirring at 200 rpm for 5 minutes, 0.5% of the flotation trapping agent of the present invention was added according to Table 2, and the same <1200 rpm was added.
After stirring for 5 minutes at m, 4-knob-2-pentanol (
Add foaming agent) to 0.15 and stir (1200 rpI11
), air was introduced and flotation was performed. Table 2 shows the s+02 content ff1 (%) in the sol after flotation. Similarly, using 0.5% of the conventional flotation capture agent,
The results of the four selections are also shown in Table 2]. Example 3 Raw coal (Raw coal) was pulverized in a ball mill to obtain 200 mesh 8% pass coal. This pulverized coal 250 (J (
(Ash content: 11.6%) was placed in a laboratory flotation machine manufactured by TSU 1M Co., Ltd., 2250 g of water was added thereto, and the mixture was stirred at 1.200 rpm for 10 minutes to obtain a slurry. was added to coal in an amount of 0.1%, stirred at 120 rpm for 3 minutes, and 0.1% of 4-methyl-2-pentanol (foaming agent) was added.
Add 2xi in 2 times at °C and heat it to 1200rllll.
ILC was stirred and air was introduced into the four cylinders (flotation and sorting was carried out. The foam was transferred to a container and the Bunonar L1-1-0 coal was filtered.-
The moisture content and ash content in the cake after filtration were measured. The water content is determined by the difference in width C before and after drying when the filtered water-containing Icochar fine powder is placed in a high-temperature dryer at 105 to 110 C for 1 hour and dried.
Surface level (%). The ash content was measured by η according to JIS M8812. The results are shown in Table 3. Note that this is an evaluation of the above measurement (B obtained with a coal yield of 95 to 96%).

Claims (1)

【特許請求の範囲】 1、1分子中に酸化ブUピレンを5;しル以上含む平均
分子量400〜200000のポリアルキレンオキシド
誘導体を含む浮選捕収剤。 2、 ポリアルギレンAキシド誘導体がアミノ基をイ1
りる化合物に、酸化ブ1」ピレンを付加Mることによっ
て得られるものCある第1項記載の浮”lIIMi収剤
。 3、7ミノ化合物がポリアルルンイミンひある第2項記
載の浮選捕収剤。 4、 ポリilルキレンAキシド誘尋体が耐化ブ(」ピ
レン残基を10以トイiする第1■口記載の淫選捕収剤
[Scope of Claims] 1. A flotation collector containing a polyalkylene oxide derivative having an average molecular weight of 400 to 200,000 and containing at least 5 mm of butyrene oxide in each molecule. 2. Polyargylene A oxide derivative has an amino group
The flotation agent according to item 1, which is obtained by adding pyrene oxide to a compound containing 3,7 mino, and the flotation agent according to item 2, where the compound is polyarrunimine. Collecting agent. 4. The selective collecting agent described in Part 1, in which the polyil alkylene A oxide derivative contains 10 or more pyrene residues.
JP58131749A 1983-07-18 1983-07-18 Flotation collector Pending JPS6022953A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58131749A JPS6022953A (en) 1983-07-18 1983-07-18 Flotation collector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58131749A JPS6022953A (en) 1983-07-18 1983-07-18 Flotation collector

Publications (1)

Publication Number Publication Date
JPS6022953A true JPS6022953A (en) 1985-02-05

Family

ID=15065288

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58131749A Pending JPS6022953A (en) 1983-07-18 1983-07-18 Flotation collector

Country Status (1)

Country Link
JP (1) JPS6022953A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6161658A (en) * 1984-08-29 1986-03-29 ザ ダウ ケミカル カンパニー Frother composition for recovering valuable minerals from ore and flotation method
JPS6174659A (en) * 1984-08-29 1986-04-16 ザ ダウ ケミカル カンパニー Frother composition and froth flotation method for recovering crude coal or coal
JPH01119278A (en) * 1987-10-30 1989-05-11 Yamato Sewing Mach Co Ltd Method and apparatus for finely adjusting corner measuring position in automatic bead sewing machine
US5037534A (en) * 1989-09-14 1991-08-06 J. M. Huber Corporation Flotation aid and process for removal of impurities from silicate minerals
US5180511A (en) * 1989-09-14 1993-01-19 J.M. Huber Corporation Flotation aid and process for removal of impurities from silicate minerals
WO2011096479A1 (en) * 2010-02-04 2011-08-11 住友金属鉱山株式会社 Method for separating arsenic mineral from copper material with high arsenic content
JP2013525237A (en) * 2010-03-19 2013-06-20 オムヤ・デイベロツプメント・アー・ゲー Floss flotation method for separating silicates and alkaline earth metal carbonates using a scavenger comprising at least one hydrophobically modified polyalkyleneimine
CN108554645A (en) * 2018-02-28 2018-09-21 许宝林 A kind of foaming agent of energy conservation and environmental protection, clean and effective

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6161658A (en) * 1984-08-29 1986-03-29 ザ ダウ ケミカル カンパニー Frother composition for recovering valuable minerals from ore and flotation method
JPS6174659A (en) * 1984-08-29 1986-04-16 ザ ダウ ケミカル カンパニー Frother composition and froth flotation method for recovering crude coal or coal
JPH0139822B2 (en) * 1984-08-29 1989-08-23 Dow Chemical Co
JPH0141099B2 (en) * 1984-08-29 1989-09-04 Dow Chemical Co
JPH01119278A (en) * 1987-10-30 1989-05-11 Yamato Sewing Mach Co Ltd Method and apparatus for finely adjusting corner measuring position in automatic bead sewing machine
JPH0246228B2 (en) * 1987-10-30 1990-10-15 Yamato Sewing Machine Mfg
US5037534A (en) * 1989-09-14 1991-08-06 J. M. Huber Corporation Flotation aid and process for removal of impurities from silicate minerals
US5180511A (en) * 1989-09-14 1993-01-19 J.M. Huber Corporation Flotation aid and process for removal of impurities from silicate minerals
WO2011096479A1 (en) * 2010-02-04 2011-08-11 住友金属鉱山株式会社 Method for separating arsenic mineral from copper material with high arsenic content
JP2013525237A (en) * 2010-03-19 2013-06-20 オムヤ・デイベロツプメント・アー・ゲー Floss flotation method for separating silicates and alkaline earth metal carbonates using a scavenger comprising at least one hydrophobically modified polyalkyleneimine
CN108554645A (en) * 2018-02-28 2018-09-21 许宝林 A kind of foaming agent of energy conservation and environmental protection, clean and effective

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