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08‐02‐2018

Introduction
 Waste electric and electronic equipment (WEEE) has been taken into
consideration not only by the government but also by the public due to
their hazardous material contents.
Electronic Waste Management
 Currently, the main options for the treatment of electronic waste are
Recovery of Metals from Electronic Waste reuse, remanufacturing, and recycling, as well as incineration &
landfilling.
BRAJESH KUMAR DUBEY  Recycling of electronic waste is an important subject not only from the
DEPARTMENT OF CIVIL ENGINEERING point of waste treatment but also from the recovery aspect of valuable
materials

Introduction Process Description


 Still quite limited due to the heterogeneity of the materials  Recycling of E-Waste can be broadly divided into three steps

 The metal content is around 28- 30% (copper: 10–20%, lead: 1–5%,
nickel: 1–3% precious metals like silver, platinum and gold are also
present in the electronic scrap to a total of 0.3–0.4%)

 The other materials are plastics 19%, bromine 4%, glass and ceramics Disassembly Upgrading Refining
49%.Besides these inorganic elements, the other important organic
compounds are also found in circuit boards like isocyanates, phosgene,
acrylic and phenolic resins (Ludwig et al., 2003)

A schematic flowsheet showing the options for recovery of


metals from E-Scrap (Adapted from Yazıcı and Deveci, 2009). Process Description
 Disassembly: Selectively disassembly, targeting on singling out hazardous or
E Scrap
valuable components for special treatment, is an indispensable process in recycling
of E-Waste.
Manual
Dismantling  Upgrading: Using mechanical processing and/or metallurgical processing to up-
grade desirable materials content (preparing materials for refining process).
Size
Reduction  Refining: Recovered materials are retreated or purified by using chemical
• Gravity, Magnetic, (metallurgical) process.
Physical Electrostatic and Eddy-
Separation Current separation Base and Precious  Pyrometallurgical
Metals (Cu, Au,  Hydrometallurgical
Hydrometallurgy/ Ag, Pd)
Pyrometallurgy  Biometallurgical

Electrometallurgy

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Existing E-Waste Recycling Techniques CRT Recycling


 CRT Recycling  Two major constituents of CRT comprises of glass components ( funnel
 Glass to glass Recycling glass, panel glass, solder glass, neck) and non-glass components (viz.,
plastics, steel, copper, electron gun, phosphor coating).
 Glass to Lead Recycling
 Metal recovery
 CRT glass components consists of SiO2, NaO, CaO, coloring, oxidizing
 Precious metal recovery
and X-ray protection components (K2O, MgO, ZnO, BaO, PbO) and lead
 Pyrometallurgical and hydrometallurgical Processing (Pb).
 Biometallurgical process
 Recovery of metals from mobile phones (case study)  The glass-to-glass and glass-to-lead recycling, being the two technology
route available at present for CRT.

Glass to Glass recycling Glass to Lead recycling


 After the separation of metals, whole glass is ground  In these process, metallic lead (Pb) and Copper (Cu) are
into cullet without isolating the panel and funnel glass separated and recovered from the CRT glass through a smelting
and the said cullet is used for manufacturing new CRT process.

 The recovered CRT glasses processed in the lead smelter also


 Disadvantage associated to unknown lead composition acts as a fluxing agent in the smelting process.
in mixed grinding cullet on account of varied CRT glass
compositions depending on the manufacturer and its
 This process is automated with high overall throughput and cost
origin
effective as compared with the glass-to-glass recycling process,

Metal Recovery
 Ferrous components are separated either by a permanent magnet
or electromagnet
 Metals such as aluminum and copper from non-metallic
materials are separated in eddy current separator FEW EXAMPLES (METAL RECOVERY
 Removal of the non-recyclable materials (e.g., epoxy resin and PROCESS)
fiber glass) is done to enhance the value of recyclable material
 Post-separation provides higher metal concentration in lesser
volume, thereafter the enriched metal content can then be sold
and transported to an appropriate recycling facility for further
processing

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Huei-Chia-Dien Company's physical separation Union Miniere Company's copper-smelting flowsheet for recycling of scrap
flowsheet for recycling of scrap IC boards. IC board

Slag (further treated


Eddy Current Aluminum in Blast Furnace ) Precious metal
Primary crusher Air Classifier Plastic
Separator refinery (Au, Ag,
Scrap IC UM Olen Pt, Pd, Rh, Ru)
Non-Ferrous (Fe)
board Plant
Cu
Iron (Fe) Smelter
Magnetic Magnetic Magnetic Copper
Iron (Fe)
separator Separator Separator
Cu
Non-Ferrous (Fe) Heavy Sulphuric acid plant pellation
Furnace Special Metals
H2SO4 (In, Se, Te)
Hammer Mill Cyclone Light Dust
Fiber Glass, Resin

PYROMETALLURGICAL PROCESS

Process flow chart for the technology developed for precious metals at CSIR-NML, Jamshedpur (Cui and Zhang,
2008)

Introduction Process Description (Noranda Process)


 Pyrometallurgical process includes incineration, smelting in a  Materials entering the reactor are immersed in a molten metal
plasma arc furnace or blast furnace, drossing, sintering and melting bath (1250 ◦C) which is churned by a mixture of supercharged
and reactions in a gas phase at high temperatures. air (up to 39% oxygen).
 Traditional method to recover non-ferrous metals as well as
precious metals from electronic waste in the past two decades.  The resulting of agitated oxidation zone converts impurities
 In the process, the crushed scraps are burned in a furnace or in a including iron, lead and zinc into oxides which become fixed in
molten bath to remove plastics a silica-based slag.
 Refractory oxides form a slag phase together with some metal
oxides  The slag is cooled and milled to recover more metals before
disposal

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Process Description Noranda process


 The copper matte containing precious metals is removed and
transferred to the converters.

 After an upgrading in the converters, liquid blister copper is


refined in anode furnaces and cast into anodes with purity of
99.1%.

 The remaining 0.9% contains the precious metals, including


gold, silver, platinum and palladium, along with other
Cui and Zhang 2008
recoverable metals, such as selenium, tellurium, and nickel

Rönnskår Smelter Rönnskår Smelter


 Another application for pyrometallurgical process to recover  In Kaldo reactor, blended feed material with E-Waste
metals from E-waste is practiced at the Boliden Ltd, Sweden. and lead concentrates is charged by skip hoist.
 Also known as Rönnskår Smelter.
 In these process, scraps can be fed into the process in different
 An oxygen lance supplies the needed O2 for combustion
steps depending on their purities.
with an oil-oxygen burner
 High copper containing scrap is fed into Converting process
directly
 Low grade E-Waste is fed into Kaldo Furnace  Off-gases are subjected to additional combustion air at
around 1200◦C in post-combustion.

Rönnskår Smelter Schematic Diagram for the Rönnskår Smelter

 Mixed copper alloy is sent to the copper converting for


recovery of metals (Cu, Ag, Au, Pd, Ni, Se, and Zn)

 Remaining dusts (containing Pb, Sb, In and Cd) are


sent to other operations for metal recovery

APME (Association of Plastics Manufacturers in Europe) Report, 2000

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Umicore’s Precious Metal Refining Umicore’s Precious Metal Refining Process


Process (Hoboken, Belgium) ( Hoboken, Belgium)
 The first step in the precious metals operations (PMO) is  The Base Metals Operations process by-products from the PMO.
smelting by using an IsaSmelt furnace.  The main processing steps are lead blast furnace, lead refinery and
 The smelter separates precious metals in a copper bullion from special metals plant.
mostly all other metals concentrated in a lead slag, which is  Transforms them into impure lead bullion, nickel species, copper
further treated at the Base Metals Operations (BMO). matte and depleted slag
 The copper bullion is then treated by copper-leaching and  The impure lead bullion, collecting most of the nonprecious metals,
electrowinning and precious metals refinery for copper and is further treated in the lead refinery (Harris process)
precious metals recovery

Umicore’s Precious Metal Refining Umicore’s Precious Metal Refining


Process (Hoboken, Belgium) Process (Hoboken, Belgium)
 Special metals (indium, selenium, tellurium) residues were
generated in the lead refining process.
 Sulfur is converted into SO2 which is transformed to
 Pure metals are recovered in a special metals refinery.
sulfuric acid in the “contact” plant.

 An emission control system is installed at Umicore’s IsaSmelt


process
 Hygienic gases and process gases are cooled with energy recovery
and cleaned using some techniques, such as bag house filters,  Emissions from the plant are well below the European
electrofilters, and scrubbers
limits (Hageluken ,2007).

Recovery of Gold from E-Scrap(Dunn et Recovery of Gold from E-Scrap(Dunn et


al.,1991: US Patent, US5004500 . al.,1991: US Patent, US5004500 .
 The gold scrap reacted with chlorine at a temperature with  Then ammonium hydroxide and nitric acid were used
the range of about 300–7000C to form a mixture respectively for washing the metallic gold/silver chloride
containing metallic gold, silver chloride, and other metal mixture to dissolve the silver chloride and the traces of
chlorides. metallic silver from the metallic gold

 The mixture was washed with air-sparged hydrochloric  It should be pointed out that Dunn’s processing is
acid to dissolve the impurity metal chlorides other than developed for refining high grade gold materials that
silver chloride forming a metallic gold/silver chloride contain more than 80% of gold.
mixture.

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Perspectives on Pyrometallurgical Recovery of Perspectives on Pyrometallurgical Recovery of


Metals from E-Waste Metals from E-Waste
 Ceramic components and glass in the E-Waste increases the amount of slag
 It is clear that the traditional technology, pyrometallurgy has been from blast furnaces which enhances the loss of precious metals and base
used for recovery of precious metals from waste electronic metals from the scrap.
equipment in practice for years.
 Only partial separation of metals can be achieved using pyrometallurgy,
 However, most methods involving pyrometallurgical processing of
electronic waste give rise to the following limits. resulting in a limited upgrading of the metal value

 Integrated smelters cannot recover aluminum and iron as metals.  Hydrometallurgical techniques and/or electrochemical processing are
subsequently necessary
 The presence of halogenated flame retardants (HFR) in the smelter feed  Precious metals stay for a long time in the pyrometallurgical process and
can lead to the formation of dioxins unless special installations and
measures are present are obtained at the very end of the process

Introduction
 Hydrometallurgical method is more exact, more
predictable and more easily controlled.
HYDROETALLURGICAL PROCESS
 Consist of a series of acid or caustic leaches of
solid material

Introduction Cyanide Leaching


 Solutions are then subjected to separation and purification
procedures such as precipitation of impurities, solvent  It is an electrochemical process utilized in the mining
extraction, adsorption and ion-exchange to isolate and industries for more than one century.
concentrate the metals of interest  The overall reactions are
4Au + 8 CN- = 4Au(CN)2- + 4e
O2 + 2H2O +4e = 4OH-
 Final treatment by electro-refining process, chemical reduction  Maximum dissolution of gold, silver, palladium, and platinum
or crystallization for metal recovery. in cyanide solution can be obtained at pH 10–10.5.
 The order of activity for noble metals is Au>Ag>Pd>Pt

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Halide leaching Halide leaching


 The use of halide (fluorine, chlorine, bromine, iodine and  Chlorination rates are favored by low pH, high chloride and
astatine) systems for gold dissolution pre-dates cyanidation. chlorine levels, increased temperatures, and high surface areas.

 Gold forms both Au(I) and Au(III) complexes with chloride,  The first step is dissolving gold into aqua regia and the
bromide and iodide depending on the solution chemistry reaction involved in these process are:
conditions 2HNO3 +6HCl → 2NO + 4H2O + 3Cl2
2Au + 11HCl + 3HNO3→ 2HAuCl4 +3NOCl + 6H2O
 Only chlorine/chloride has been applied industrially on a
significant scale

Limitation Thiourea leaching


 Chloride leaching of gold is more difficult to apply than  The research on using of thiourea ((NH2)2CS) as a gold
cyanide extraction for two major reasons: extraction agent has shown considerable promise in recovery
of gold from ores.
 Special stainless steel and rubber-lined equipment is required to resist
the highly corrosive acidic and oxidizing conditions  In acidic conditions, thiourea dissolves gold, forming a
cationic complex.
 Chlorine gas is highly poisonous and must be controlled to avoid any
health risk.  The reaction is rapid and gold extractions of up to 99% can be
achieved

Thiourea leaching Limitation


 The anodic reactions are
 Its commercial application has been hindered by
Au + 2CS(NH2)2→ Au(CS(NH2)2)2+ + e
the following three factors
Pyper and Hendrix summarized that,
 It is more expensive than cyanide
 The rate of leaching is contingent upon thiourea and oxidant  Its consumption in gold processing is high because
concentrations thiourea is readily oxidized in solution
 The use of ferric ion in sulfuric acid is the most effective system;
 The gold recovery step requires more development.
 The ferric ion ties up thiourea in iron–thiourea complexes;

 The rate of gold dissolution is strongly determined by pH.

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Thiosulfate leaching Thiosulfate leaching


 Gold dissolution in ammoniacal thiosulfate solution is an  Depending on the concentration of S2O32−, Cu(NH3)2+ converts to
electrochemical reaction catalyzed by the presence of cupric Cu(S2O3)35− ions and likewise for Au(NH3)2+ .
ions.
 It was proposed that Cu(NH3)42+ species present in solution  Both the Cu(S2O3)35− species and the Cu(NH3)2+ species in solution
acquires electrons on the cathodic portion of the gold surface are then oxidized to Cu(NH3)42+ with oxygen.
and is directly reduced to Cu(NH3)2+.
Au + 5S2O32− +Cu(NH3)42+ → Au(S2O3)23− +4NH3 +Cu(S2O3)35−
 At the same time, either ammonia or thiosulfate ions react
2Cu(S2O3)35− +8NH3 +1/2O2 +H2O → 2Cu(NH3)42+ +2OH− +6S2O32−
with Au+ ions on the anodic surface of gold and enter the
solution to form either Au(NH3)2+ or Au(S2O3)23−.

Thiosulfate leaching Thiosulfate leaching


(Advantages/Disadvantages) (Advantages/Disadvantages)
 It can be seen that the gold thiosulfate complex is fairly stable  The process is generally slow
once it has formed.
 pH of 9–10 is generally preferred at ambient temperature
because thiosulfate appears to be less prone to degradation in  High reagent consumption renders most thiosulfate
this region and Cu(II)-ammonia complex is also stable. systems uneconomical, in spite of their potential
 The principal problem with thiosulfate leaching is the high environmental benefits
consumption of reagent during extraction.
 A loss of up to 50% of thiosulfate in ammoniacal thiosulfate  At present, no simple and affordable method for
solutions containing copper was also observed. recovering gold from thiosulfate leach solutions exists

Types of Mechanism
 Cementation

MECHANISM OF EXTRACTION OF  Solvent extraction


PRECIOUS METAL FROM LEACHING
SOLUTION  Adsorption on activated carbon

 Ion exchange

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Cementation Cementation
 Since the 1890s, Zinc cementation has been used to  The major reactions are
recover gold from cyanide solutions on a commercial 2Au(CN)2− +2e → 2Au + 4CN−
scale.
Zn + 4CN−→ Zn(CN)42− +2e
 The process is actually called the Merill-Crowe process  Cementation of gold is practically constant over
the pH range 8–11.
 The major reactions are the cathodic deposition of gold  Impurities such as lead, copper, nickel, arsenic,
and anodic corrosion of zinc. antimony and sulfur are most deleterious for gold
cementation.

Cementation Cementation
 Awadalla and Ritcey (1991) reported that the recovery
 It is observed that gold ion can be reduced effectively to
of gold from thiourea, thiosulfate or thiocyanate
metallic gold from acidic solutions of thiourea by the
solutions by reduction-precipitation with a stabilized
addition of SBH even at ambient temperature.
form of sodium borohydride (SBH).

 This result indicates that thiourea can be used as not only


 Sodium borohydride containing 12% by weight NaBH4
an alternative leachant for gold bearing materials but also
and 40% NaOH.
a stripping agent for gold from loaded solvents and
resins.

Solvent Extraction
 Extraction of gold from thiosulfate solutions with alkyl
phosphorus esters was studied by (Zhao et al., 1997).

Recovery of precious metals from  The addition of ammonia has a strong influence on the
solutions by solvent extraction extraction of gold from thiosulfate solutions with alkyl
phosphorus esters.
 The extraction mechanism in the presence or absence of
ammonia should be considered separately

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Solvent Extraction Activated Carbon


 For the system with no ammonia, the extraction reaction is  Mechanism and kinetic of adsorption of gold from solutions onto
iNa+ +2Au+ +jS2O32− +OH− +mTBP(o) = NaiAu2(S2O32−)j(OH−)·mTBP(o) activated carbon have been investigated by many researchers.

 The addition of ammonia into thiosulfate solutions, the extraction reaction is  For solid/liquid adsorption processes, two isothermal expressions
iNa+ +2Au+ +jS2O32− +OH− +2NH3 +mTBP(o) = NaiAu2(S2O32−)j(OH−)(NH3)2·mTBP](o) are well known
Q = Qmax bC/(1 + bC)
Where i (i = 3–5) varies with j (j = 2–3), and the TBP coefficients m in the two Q is the quantity of solute adsorbed per unit weight of carbon, Qmax is
equations are in the ranges of 1.5–2.5 and 6–9 respectively. the maximum sorption capacity, C is the equilibrium concentration of
the adsorbate in solution and b is the adsorption equilibrium constant

Activated Carbon Ion Exchange


 Another expression is the Freundlich isotherm  Commercial IEX resins employing small quaternary ammonium
moieties (strong base resins) have been successful in recovering
where K and n (0 < n < 1) are Freundlich constants. gold from thiosulfate liquors.

 A Freundlich-type multicomponent isotherm was developed by  Thomas et al.2001 observed almost full recovery of gold and silver
Sheindorf et al., (1981)
using strong base resins.
= ∑
where aij is defined as competition coefficient (aii = 1), Ki = qmiAi and Ki
can be determined from the mono-component system  Aqua regia leaching can be used (Sheng and Etsell, 2007) for
recovery of gold from computer chips due to its flexibility, ease and
low capital requirement

Recovery of Metals from PCB Scrap


Hydrometallurgical Process
PCB Scrap

Electrodeposition in
Sn HCl
recovery for
Dissolution in H2SnO3
1.5M HCl solution
Sn precipitation as

Shredding
Leaching
in 1-6M
HNO3
metastannic acid
Sn+4HNO3=
H2SnO3
+4NO2+H2O
Filtration HN03
regeneration
Bio-metallurgical
for reuse
Neutralization
by NaOH

Electrodepositi
on of Cu and
Process
electrodepositi
on of PbO2

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Introduction Introduction
 The understanding of the biochemical processes involved in  At present, research and development is in progress for a
the treatments of metals has been subject to growing number of metals such as copper, nickel, cobalt, zinc, gold,
investigations for the last 20 years. and silver.

 Materials and minerals industry due to the great interest shown  Microbes are employed for structural functions and catalytic
by major international companies for this new technology. functions.

 One of the most promising technologies.  Microbes are two types both Prokaryote and Eukaryote

Classification Classification of Bioleaching


• Bioleaching has been
successfully applied in recovery Direct leaching
of metals from metallic sulfides,
which are the major bearing
Bioleaching
Bio-metallurgy

minerals for many base and


Indirect Leaching Thiosulfate
precious metals.
Bioleaching Pathway
• Biosorption process is a passive
physico-chemical interaction
Polysulfide
Biosorption Pathway
between the charged surface
groups of micro-organisms and
ions in solution, in which living
as well as dead organisms can be
used.

Bioleaching (Direct) Bioleaching (Indirect Method)


 An example of mechanism of bacteria by Metal-Sulphide  In indirect action mechanism, ferric ion (Fe3+) is the oxidizing
action. agent for minerals.
 Role of organisms is simply regeneration of Fe3+ from Fe2+ .
 In direct action mechanism, microorganisms will directly MS + 2Fe3+→ M2+ +2Fe2+ +S0
oxidize minerals and solubilize metals 2Fe2+ +0.5O2 +2H+→ 2Fe3+ +H2O
MS + H2SO4 +0.5O2→ MSO4 +S0 +H2O
S0 +1.5O2 +H2O → H2SO4  According to their research, metal sulfides are leached via two
different reaction mechanisms: the thiosulfate and the polysulfide
pathways.

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Thiosulfate Leaching Polysulfide Pathway


 The thiosulfate mechanism is exclusively based on the  The polysulfide mechanism allows for a dissolution by
oxidative attack of iron(III) ions on the acid-insoluble metal an attack of iron(III) ions and/or by protons.
sulfides FeS2, MoS2 and WS2.
 Main sulfur intermediate is thiosulfate.
 The main sulfur intermediate is polysulfide
FeS2 +6Fe3+ +3H2O → S2O32− +7Fe2+ +6H+ MS + Fe3+ +H+→ M2+ +0.5H2Sn +Fe2+ (n≥ 2)
S2O32− +8Fe3+ +5H2O → 2SO42− +8Fe2+ +10H+ 0.5H2Sn +Fe3+→ 0.125S8 +Fe2+ +H+
0.125S8 +1.5O2 +H2O → SO42− +2H+

Bioleaching Bioleaching of Metals from E-Waste


 In both pathways, the main role of leaching bacteria consists of  Dust collected from shredding processes of electronic scrap
regeneration of iron(III) ions. was used in the investigation (Brandl et al., 2001).
 Thus, the acidophilic iron(II) ion oxidizers control the redox
potential in their environment.  The leaching experiments was performed by using a mixed
 These is determined mainly by the iron(III)/iron(II) ratio in leaching culture of Thiobacillus ferrooxidans and T. thiooxidans.
solutions.
 Main drivers are iron-oxidizing microorganisms mesophilic or
thermophilic  Two steps process are introduced to reduce the toxic effects
on microorganism.

Bioleaching of Metals from E-Waste Bioleaching of Metals from E-Waste


 In the first stage, biomass was produced in the absence of  At higher concentration, metal mobilization was
electronic scrap. reduced.

 Then electronic scrap was added in different concentrations and


the cultures were incubated for an additional time period  Pb and Sn were not detected in the leachate.

 The leaching results confirmed that at scrap concentrations of 5  It is proposed that Pb precipitated as PbSO4 and Sn
and 10 g/L, respectively, Thiobacilli were able to leach more precipitated probably as SnO.
than 90% of the available Al, Cu, Ni, and Zn

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Bioleaching of Metals from E-Waste Biosorption


 The bioleaching mechanism of copper from printed circuit  Biosorbents are prepared from the naturally abundant
boards shreds by A. ferrooxidans has been also investigated by and/or waste biomass of algae, fungi or bacteria.
(Choi et al., 2004)

 Acid condition favors the biosorption of precious metals


 In the leaching process, Fe2(SO4)3 formed by A. ferrooxidans
oxidizes the elemental copper contained in PCBs to cupric ion from solution, especially for the adsorption on bacteria.
Fe2(SO4)3 +Cu → Cu2+ +2Fe2+ +3SO42−
 Researches on biosorption of precious metals mainly
focused on gold.

Biosorption Biosorption
 The biomass may be used in its “natural state” or modified.  The major advantage of using chitosan is that the
amino sites of chitosan are easily protonated in
 Biosorption by chitosan derivatives provides an alternative for acid media
recovery of precious metals from solution due to the fact that
relatively higher adsorption capacities.
 Accentuating the electrostatic forces often
 Chitosan is a deacetylated derivative of chitin implicated in the initial stages of sorption

 Second most abundant biopolymer on earth after cellulose

Biosorption Mechanism of Biosorption


 Freely suspended microbial biomass has disadvantages  Biosorption of precious metals from solutions can be
due to small particle size, low mechanical strength and simplified as chemical sorption mechanisms and
difficulty in biomass/effluent separation. physical sorption mechanisms.
 Chemical sorption mechanisms include complexation,
 Immobilized biomass particles in packed- or fluidized- chelation, micro precipitation and microbial reduction.
bed reactors minimize these disadvantages  Physical sorption mechanisms generally involve
electrostatic forces and ion exchange.

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Hybrid Technology Hybrid Technology


 Generally biological leaching is a cost effective technique  Hybrid technique is proposed, involving combination
but time consuming of chemical (safer chemicals) and biological leaching,
so that both will complement each other.
 Complete recovery of metal alone by biological leaching is
not possible in most of the cases (Ren et al.,2009).  Can reasonably enhance the efficiency of metal
extraction from their ores or any other source like E
 Chemical leaching is comparatively rapid and efficient but it waste
has its own environmental issues

Hybrid Technology Flow Chart of Hybrid Technology


 Hybrid combination employed for the extraction
of Zn, Cd, Pb and Cu involving EDTA (Wasay et
Mixture of Metal
al., 1998) with either A. ferrooxidans (Cheikh et metals
M
Isolated

al., 2010), Bacterial strain DSM 9103 Microorganism


Ligand Metal
(Satroutdinov et al., 2000) or Shewanella association

putrefaciens (Dobbin et al., 1995)

Adapted from Pant et al., 2012

Conclusion Conclusion
 Recycling of electronic waste is an important subject not  Traditional technology, pyrometallurgy has encountered some
only from the point of waste treatment but also from the challenges from environmental considerations.
recovery of valuable metals
 Thermal processing of E-Waste provides an approach for
recovery of energy if a comprehensive emission control system
 The value distribution for different electronic scrap samples is installed.
shows that for cell phones, calculators, and printed circuit
board scraps, the precious metals make up more than 70%
 Leaching of gold by thiourea may be the most realistic
of the value
substitute

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Conclusion
 Biotechnology has been one of the most promising
technologies in metallurgical processing.

 Biosorption based process offers a number of advantages Hazardous and Other Wastes (Management and
including low operating costs, minimization of the volume Transboundary Movement) Rules, 2016.
of chemical and biological sludge to be handled and high
efficiency in detoxifying effluents
 The scope of hybrid technology can be examined for metal
extraction

Hazardous and Other Wastes (Management


and Transboundary Movement) Rules, 2016 Exception
 Came into force from 1st day of October, 2016.  Waste-water and exhaust gases as covered under the
provisions of the Water (Prevention and Control of Pollution)
Act, 1974 and the Air (Prevention and Control of Pollution)
 Applicable to every manufacturer, producer, consumer, Act, 1981
bulk consumer, collector, dealers, e-retailer, refurbisher,
dismantler and recycler involved in manufacture, sale,  Wastes arising out of the operation from ships beyond five
transfer, purchase, collection, storage and processing of kilometres of the relevant baseline as covered under the
E-Waste or electrical and electronic equipment provisions of the Merchant Shipping Act, 1958
(Schedule 1)

Exception Objectives of the rules


90

 Radio-active wastes as covered under the provisions of  To Minimize illegal recycling and to promote safe recovery
operations by channelizing E-waste to registered E-waste
the Atomic Energy Act, 1962
recyclers.
 Extended Responsibilities to producers to manage the system of E-
 Bio-medical wastes covered under the Bio-Medical waste collection/take back and channelizing to a registered
Wastes (Management and Handling) Rules, 1998. dismantler/recycler
 Reduce Hazardous substances in Electrical and Electronic
components.
 Wastes covered under the Municipal Solid Wastes  To regulate the generation, collection, storage, transportation,
(Management and Handling) Rules, 2000 import, export etc.

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About the rules About the rules


 These rule have 6 chapters, 8 schedules and 11  The producer of electrical and electronic equipment's is
responsible for the entire life cycle of its own branded
forms. product and in particular the environmentally sound end-of-
 Procedure for Authorization of producers, life management and facilitating collection and take back
dismantlers, collection agencies, and recyclers.
 Liability of producers, collection agencies, transporter,
 Procedure for registration/renewal of registration dismantlers and recyclers
of recyclers
 Reduction of hazardous substances used in E- equipment

Responsibilities of the occupier for


management of hazardous and other
93
wastes
 Prevention
 Minimization
Responsibilities
 Reuse,
 Recycling
 Recovery, utilization including co-processing;
 Safe disposal.

Responsibilities Responsibilities…
95 96

 Responsibilities of the producer: The producer of electrical and electronic  Obtaining an authorization from the concerned State Pollution Control Board or
equipment shall be responsible for Pollution Control Committee in accordance with the procedure under rule 9.
 Collection of e-waste generated during manufacturing, from the 'end of life' of  Maintaining records in Form 2 of the e-waste handled and make such
their products with the principle of 'Extended Producer Responsibility‘ " records available for scrutiny by the State Pollution Control Board (SPCB) or the
 Should ensure collection and channelization by authorizing collection Pollution Control Committee concerned.
agencies  Filing annual returns in Form 3 to the State Pollution Control Board or
 Setting up collection centers or take back systems either individually or Pollution Control Committee concerned, on or before the 30th day of June.
collectively  Responsibilities of collection centers:
 Financing and organizing a system individually or by joining a scheme  Obtain an authorization in accordance with the procedure under rule 9 from
 Providing contact details and creating awareness about hazards through the SPCB or PCC.
Image courtesy:
publications, advertisements, posters etc. MINISTRY OF
ENVIRONMENT,  Ensure that the e-waste collected is stored in a secured manner till it
 Affixing a visible, legible symbol given, on the products to prevent e-waste
FOREST
NOTIFICATION 201 is sent to registered dismantler(s) or recycler(s), no damage is caused to the
from being dropped in garbage. environment during storage and transportation of E-Waste.

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97
Responsibilities… 98
Responsibilities…
 File annual returns in Form 3 to the SPCB or PCC before 30th June.  Ensure that Processes do not have any adverse effect on the health and the
 Maintain records of the e-waste handled in Form 2. environment in accordance with guidelines published by CPCB from time to time.
 Responsibilities of bulk consumer:  Ensure that dismantled e-waste are segregated, non-recyclable/non- recoverable
 Consumers or Bulk consumers of electrical and electronic equipment shall ensure that e-waste components sent to the registered recycling facilities for recovery of materials;
generated by them is channelized to authorized collection center(s) or registered dismantler(s) or  File a return in Form 3 to SPCB or the PCC
recycler(s) or is returned to the pick-up or take back services provided by the producers.
 Do not process any e-waste for recovery or refining, unless he is
 Shall maintain records of e-waste generated by them in Form 2 and disposal through registered
registered with SPCB as a recycler.
recycler in Form 3
 Responsibilities of recycler:
 Responsibilities of dismantler:
 Obtain authorization and registration and ensure that the facility and recycling
 Obtain authorization and registration from SPCB with the procedure under the rules 9 & 11;
processes are in accordance with the guidelines.
 Ensure that no damage is caused to the environment during storage and transportation of e-
waste;  make available all records and file annual returns in Form 3 to SPCB or PCC.

Responsibilities of State Pollution Control


Board/ Pollution Control Committee Responsibilities of Central Pollution Control Boards
99 100

 Coordinated with State Pollution Control Boards/ Committees of Union


SPCBs/PCCs has been assigned the following duties: territories.
 Preparation of inventories of e-waste.
 Preparation of Guidelines for Environmentally Sound Management of e-
 Granting Authorization and Registration. waste.
 Monitoring of compliance of authorization and registration  Conducting assessment of e-waste generation and processing.
conditions.
 Documentation, compilation of data on e-waste and uploading on websites
 Maintaining information on the conditions imposed for of Central Pollution Control Board.
authorization.
 Recommendation of standards and specifications for processing and
 Taking action against violations of the standards and guidelines.
recycling e-waste
 Ensure that collection center should not store e-waste for a period
 Conducting training & awareness programs
exceeding one hundred and eighty days.
 Submit Annual Report to the Ministry of Environment & Forests

102

TOP E-WASTE
MANAGEMENT COMPANIES
E Waste Management in India IN INDIA

17
08‐02‐2018

Address:
B-41/1, Peenya
Industrial Area, 3rd Stg,
Peenya Industrial Area,
Bengaluru, Karnataka
560058
Phone: 080 2836 0902
Delhi
Gurgaon (Haryana)
Address:
Mumbai
Plot No.37,APIIC
Kolkata
Industrial Park,IDA
Hyderabad
Mankhal, Mankhal
Chennai
Industrial Development
Bangalore
Area, Malikdanguda,
Kerala
Telangana 501359
Phone:1800 419 0161
103 104

Steps followed by the company for Unit details


recycling
105 106

 Unit : M/s. Earth Sense Recycle Pvt Ltd.


Recycling efficiency is to recover up to 98% of
recyclable products and dispose off the remaining hazardous  Head Quarters: Chennai
waste through TSDF. (Hazardous Waste Transportation and
Disposal Services)  Capacity (MTA): 2160
 Units locations: Andhra Pradesh (1,800 MTA) ,
Maharashtra (360 MTA), and 4 more.
 Collection center locations: Trivandrum, Coimbatore,
Kolkata, Bengaluru.

Delhi
KARNATAKA Hyderabad
TAMIL NADU
UTTAR PRADESH

Delhi
Hyderabad

ADDRESS: H-59 Sector 63, Noida, UP 201301,


P: +91-120-4087100 F: +91-120-4087101
107 108

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Attero’s Clean E-India


109 110

Attero’s recycling, is the only unit which does  Attero is a NASA recognized technology innovator,
the complete e-waste management process with promoting eco-friendly reuse and recycling E waste.
 Wide range of services, include country-wide pick up,
its end to end e-cycling plant, zero dumping collection, tracking, logistics management, recovery,
refurbishment, e-waste recycling and disposal.
technology.

Recycling Solutions Recycling Solutions


111

 Attero’s Recycling technology aims to take today’s waste and turn  Battery recycling: Furnace smelting , treatment with
it into conflict-free, sustainable resources for tomorrow. alloys are the technologies involved. Attero recycles
 Mobile phone recycling: Scanned and updated in the system, all types of batteries classified as e-waste by the EPA.
separating components which can be used again in different
 PCB recycling: Printed circuit boards Component
industries, such as electronics, plating, jewelry, automotive and art
foundries. Removal Machine which separates components.
 Display unit recycling: Cathode Ray Tubes (CRT) contain lead,  I.T Goods recycling: Includes desktops, laptops,
glass which can be recovered and reused. The process involves servers to printers, scanners, copiers etc
glass cutting, heating & air blow. Using Magnetic Separator,
ferrous metals removed

Unit details
113

 Unit: M/s. Attero Recycling Pvt. Ltd


 Capacity (MTA): 12000 Address:
Tech Logic, Unit II,
 Location: Uttarakhand Shed No.36, 2nd
Main, 
Ranganathapura, 
 Collection center locations: Delhi, Hyderabad, Bangalore,
India 560 044
Bengaluru.
 E-mail: cleaneindia@gmail.com

114

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Ramakrishna Dalmia
Wing, 4th Floor,
PHD House, 4/2, Siri Greenscape Eco Management:
511-512, Elegance Tower Jasola
Institutional Area, Non-Hierarchical Commercial
August Kranti Center
Marg, New Delhi 110 New Delhi – 110025
016, India Phone: +911140515662
Tel: +91-11-2685 5487,
4287 8418

115 116

Action plan followed in


recycling
118

 Collection of disposed Zinc, Brass, Copper, lead etc.


 Recovery starts with the separation of containing metals from
other materials,
 Typically by magnetics, sink-float, or hand sorting etc.
 Pretreatment, Melting, Refining etc. are the processes
WEST BENGAL
followed up by the J S Pigments in recycling E waste for
ODISHA environmental sustainability
ASSAM
117 MADHYA PRADESH

Unit details
119 120

 Unit: M/s. J.S. Pigments Pvt. Ltd.


 Head Quarters: Kolkata
 Capacity (MTA): 600 MTA
 Units locations: Kolkata
 Collection center locations: West Bengal, Odisha, Assam,
Madhya Pradesh
 E-mail: jspigments@gmail.com

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08‐02‐2018

Processes involved Unit details


121 122

 Recycling is being done by simply tossing the right matter in the right bin.
 REMOVAL OF COVER: Remove the main cover by taking out the screws. Place it in  Unit: M/s Hi- Tech Recycling India Pvt Ltd.
waste container.  Head Quarters: Maharashtra
 REMOVAL OF CABLE ASSEMBLIES AND WIRING: Discard the component with  Capacity (MTA): 500
cable assembly attached in the appropriate waste container.  Units locations: Maharashtra
 DISMANTLING OF REAR PANEL: Place the fasteners in the metals waste container  Collection center locations: Pune
 REMOVAL OF PC BOARDS: PCB’s consist of sheet metal brackets, metal stand offs  Website: www.hitechrecycling.in
disassembled and placing into waste container.
 DISMANTLING OF OTHER COMPONENTS: Power Supplies, Keyboards,
Displays, Hard Drives, Speakers etc

Cutting edge technology, highly advanced techniques with a team of diligent


professionals.
123 124

 Following are the steps involved in e-waste handling: Collection of e-


waste material from premises and safe transportation to our factory
premises.
 Sorting
 Identify Usefulness
 Identify hazardousness
 Dismantling
 Segregation
 Treatment / Disposal

Unit details
125

 Unit: Earth E-Waste Management Pvt. Ltd


Electronic Waste Management
 Head Quarters: Gujarat
Recovery of Metals from Electronic Waste
 Capacity (MTA): 6000
 Units locations: Gujarat End of Week - 3
 Collection center locations: Surat
 E-mail: info@eemplindia.com

21

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