Market Survey on Copper - Indian Bureau of Mines

Market Survey on Copper - Indian Bureau of Mines Market Survey on Copper - Indian Bureau of Mines

13.02.2013 Views

c) Flotation Reagents The most important reagents in copper ore flotation are collectors, frothers, pH regulators and depressants. i) Collectors: The reagents which create the hydrophobic surfaces on minerals are called collectors. They are hetropolar organic compounds, i.e. collector molecule contains a non-polar hydrocarbon group and a polar (charged) group. The non-polar hydrocarbon radical has pronounced waterrepellant properties whereas polar group has affinity for water. The collectors absorb on the mineral surface with non-polar end oriented outwards. It is this orientation which imparts hydrophobicity to the mineral particles. The most widely used collectors for sulphide flotation are xanthates (sulphydryl type) which have polar bivalent sulphur. The other sulphur- bearing collectors are thiono carbonates, dithiophosphates (Aerofloat) and pthilocarbonitides. The dithiophosphates are not as widely used as xanthates, but are still important reagents in sulphide flotation. They have pentavalent phosphorus in polar group. Sodium ethyl xanthate has a typical structure. The reaction of xanthate with oxidation product of sulphide surface through ion exchange process is considered to be a major adsorption mechanism for flotation of sulphides. However, a high degree of surface oxidation accompanied by formation of sulphates readily reacts with xanthates. As the metal xanthates so formed scale off the mineral surface, the solubility of copper, lead, silver and mercury in xanthate is very low whereas solubility of iron and zinc xanthates is much higher. There fore sphalerite activation by copper sulphate is necessary. The alkali earth metal xanthates (Ca, Ba, Mg) are very soluble and they have no collector action on the minerals of such metals nor on oxides, silicates or alumino-silicates. This phenomenon permits extremely selective flotation of sulphides from gangue minerals. Xanthates are normally used in weakly alkaline pulps, since they decompose in acid media and at high pH hydroxyl ions can displace xanthate ions from the mineral surface. Sodium isopropyl xanthate is the universal collector used in the copper flotation plants. Sodium isopropyl xanthate is often replaced by amyl xanathate as it yields pyrite-rich copper concentrate suitable for flash smelting. The performance of combination of two or more xanthates/collectors has been found much superior to those of individual collectors and therefore copper flotation plants are employing combination of two to four collectors. ii) Frothers: When the mineral surface has been rendered hydrophobic by the use of a collector, stability of bubble attachment especially at the pulp surface depends to a considerable extent on the efficiency of the frother. Frothers are generally surface-active hetropolar organic reagents capable of being adsorbed on air-water interface. When frother molecules react with water, the water dipoles combine readily with polar groups and hydrate them. But there is practically no reaction with the non-polar hydrocarbon group, the tendency being to force the latter into the airphase. Thus, hetropolar structure 34

of frother molecule leads to its adsorption i.e. molecules concentrate in the surface layer with non-polar groups oriented towards the air and polar group towards the water. Frothing action is due to the ability of frother to adsorb on the air-water interface, because of its surface activity and to reduce the surface tension, thus, stabilising the air bubble. Frother must be to some extent soluble in water. The acids, amines and alcohols are the most widely used frothers since they have practically no collection properties. Pine oil which contains aromatic alcohols has been widely used as frother in copper ore flotation plants. Cresol (cresylic acid: CH3C6 H4OH) is also widely used. A wide range of synthetic frothers, based mainly on high molecular weight alcohols is now in use in many plants. A typical synthetic frother is Dowfroth-250, which is being widely used in copper flotation plants. Combination of two or more frothers is also reported to give better performance. iii) Regulators: Regulators or modifiers are widely used in copper ore flotation to modify the action of collector either by intensifying or reducing its water repellent effect on the mineral surface. They, thus, make collector action more selective towards certain minerals. Regulators can be classified as activators, depressants, dispersants and pH modifiers. iv) Activators: These reagents modify the mineral surfaces so as to make them hydrophobic and susceptible to collector action. Activators are generally soluble salts which ionize in solution and the ions then react with the mineral surface. Activators are occasionally used in copper flotation. Oxide minerals of copper like azurite, malachite, etc. sluggishly float with collectors and need large dosages. Such minerals are activated by use of sodium sulphide or sodium hydrosulphide. The sodium sulphide should be added in stages and its amount should be carefully controlled, as excess amount depresses even activated oxide minerals and also the sulphide minerals. v) Depressants: Depressants are employed to ensure selective flotation by rendering certain minerals hydrophilic (water avid), preventing their flotation. There are many types of depressants and their actions are complex. Cyanides are widely used in copper-zinc and copper pyrite separation. Sodium cyanide is more commonly used depressant. The depressing action of cyanide depends on its concentration, pH value and length of xanthenes hydrocarbon chain. Depressing effect of cyanide ion increases with pH. It is maximum (100%) at pH 13 and minimum (0.06%) at pH

c) Flotati<strong>on</strong> Reagents<br />

The most important reagents in copper ore flotati<strong>on</strong> are collectors,<br />

frothers, pH regulators and depressants.<br />

i) Collectors: The reagents which create the hydrophobic surfaces <strong>on</strong><br />

minerals are called collectors. They are hetropolar organic compounds, i.e.<br />

collector molecule c<strong>on</strong>tains a n<strong>on</strong>-polar hydrocarb<strong>on</strong> group and a polar<br />

(charged) group. The n<strong>on</strong>-polar hydrocarb<strong>on</strong> radical has pr<strong>on</strong>ounced waterrepellant<br />

properties whereas polar group has affinity for water. The collectors<br />

absorb <strong>on</strong> the mineral surface with n<strong>on</strong>-polar end oriented outwards. It is this<br />

orientati<strong>on</strong> which imparts hydrophobicity to the mineral particles.<br />

The most widely used collectors for sulphide flotati<strong>on</strong> are xanthates<br />

(sulphydryl type) which have polar bivalent sulphur. The other sulphur- bearing<br />

collectors are thi<strong>on</strong>o carb<strong>on</strong>ates, dithiophosphates (Aer<strong>of</strong>loat) and<br />

pthilocarb<strong>on</strong>itides. The dithiophosphates are not as widely used as xanthates,<br />

but are still important reagents in sulphide flotati<strong>on</strong>. They have pentavalent<br />

phosphorus in polar group. Sodium ethyl xanthate has a typical structure.<br />

The reacti<strong>on</strong> <strong>of</strong> xanthate with oxidati<strong>on</strong> product <strong>of</strong> sulphide surface<br />

through i<strong>on</strong> exchange process is c<strong>on</strong>sidered to be a major adsorpti<strong>on</strong> mechanism<br />

for flotati<strong>on</strong> <strong>of</strong> sulphides. However, a high degree <strong>of</strong> surface oxidati<strong>on</strong><br />

accompanied by formati<strong>on</strong> <strong>of</strong> sulphates readily reacts with xanthates. As the<br />

metal xanthates so formed scale <strong>of</strong>f the mineral surface, the solubility <strong>of</strong> copper,<br />

lead, silver and mercury in xanthate is very low whereas solubility <strong>of</strong> ir<strong>on</strong> and<br />

zinc xanthates is much higher. There fore sphalerite activati<strong>on</strong> by copper<br />

sulphate is necessary. The alkali earth metal xanthates (Ca, Ba, Mg) are very<br />

soluble and they have no collector acti<strong>on</strong> <strong>on</strong> the minerals <strong>of</strong> such metals nor <strong>on</strong><br />

oxides, silicates or alumino-silicates. This phenomen<strong>on</strong> permits extremely<br />

selective flotati<strong>on</strong> <strong>of</strong> sulphides from gangue minerals. Xanthates are normally<br />

used in weakly alkaline pulps, since they decompose in acid media and at high<br />

pH hydroxyl i<strong>on</strong>s can displace xanthate i<strong>on</strong>s from the mineral surface.<br />

Sodium isopropyl xanthate is the universal collector used in the copper<br />

flotati<strong>on</strong> plants. Sodium isopropyl xanthate is <strong>of</strong>ten replaced by amyl xanathate<br />

as it yields pyrite-rich copper c<strong>on</strong>centrate suitable for flash smelting. The<br />

performance <strong>of</strong> combinati<strong>on</strong> <strong>of</strong> two or more xanthates/collectors has been<br />

found much superior to those <strong>of</strong> individual collectors and therefore copper<br />

flotati<strong>on</strong> plants are employing combinati<strong>on</strong> <strong>of</strong> two to four collectors.<br />

ii) Frothers: When the mineral surface has been rendered hydrophobic by<br />

the use <strong>of</strong> a collector, stability <strong>of</strong> bubble attachment especially at the pulp<br />

surface depends to a c<strong>on</strong>siderable extent <strong>on</strong> the efficiency <strong>of</strong> the frother.<br />

Frothers are generally surface-active hetropolar organic reagents capable <strong>of</strong><br />

being adsorbed <strong>on</strong> air-water interface. When frother molecules react with<br />

water, the water dipoles combine readily with polar groups and hydrate them.<br />

But there is practically no reacti<strong>on</strong> with the n<strong>on</strong>-polar hydrocarb<strong>on</strong> group, the<br />

tendency being to force the latter into the airphase. Thus, hetropolar structure<br />

34

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