| Literature DB >> 31203937 |
Fulvio Ardente1, Cynthia E L Latunussa2, Gian Andrea Blengini3.
Abstract
Although the amount of waste photovoltaic (PV) panels is expected to grow exponentially in the next decades, little research on the resource efficiency of their recycling has been conducted so far. The article analyses the performance of different processes for the recycling of crystalline silicon PV waste, in a life cycle perspective. The life cycle impacts of the recycling are compared, under different scenarios, to the environmental benefits of secondary raw materials recovered. Base-case recycling has a low efficiency and, in some cases, not even in line with legislative targets. Conversely, high-efficient recycling can meet these targets and allows to recover high quality materials (as silicon, glass and silver) that are generally lost in base-case recycling. The benefits due to the recovery of these materials counterbalance the larger impacts of the high-efficiency recycling process. Considering the full life cycle of the panel, the energy produced by the panel grants the most significant environmental benefits. However, benefits due to high-efficient recycling are relevant for some impact categories, especially for the resource depletion indicator. The article also points out that thermal treatments are generally necessary to grant the high efficiency in the recycling. Nevertheless, these treatments have to be carefully assessed since they can be responsible for the emissions of air pollutants (as hydrogen fluoride potentially released from the combustion of halogenated plastics in the panel's backsheet). The article also identifies and assesses potential modifications to the high-efficiency recycling process, including the delocalisation of some treatments for the optimisation of waste transport and the introduction of pyrolysis in the thermal processing of the waste. Finally, recommendations for product designers, recyclers and policymakers are discussed, in order to improve the resource efficiency of future PV panels.Entities:
Keywords: Critical raw material (CRM); Crystalline silicon photovoltaic panel (c-Si PV); E-waste; Life Cycle Assessment (LCA); Secondary raw material (SRM); Waste Electrical and Electronic Equipment (WEEE)
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Year: 2019 PMID: 31203937 PMCID: PMC6591708 DOI: 10.1016/j.wasman.2019.04.059
Source DB: PubMed Journal: Waste Manag ISSN: 0956-053X Impact factor: 7.145
Fig. 1Input and output flows for FRELP recycling process for c-Si PV waste (with dashed parts as modified from Latunussa et al., 2016). Transport between the processes is highlighted with an asterisk (*).
Fig. 2Input and output flows for a baseline recycling process for c-Si PV waste.
Fig. 3Impact assessment (Part 1): Comparison of FRELP process with baseline recycling process for c-Si PV waste (with TPT backsheet).
Fig. 4Impact assessment (Part 2): Comparison of FRELP process with baseline recycling process for c-Si PV waste (with TPT backsheet).
Summary of main features related to materials recycling in the FRELP and baseline processes.
| Material | Recycling rate [%] | Detail of material output | Potentially substituted material | |||
|---|---|---|---|---|---|---|
| Baseline | FRELP | Baseline | FRELP | Baseline | FRELP | |
| Aluminium | 92% | 94% | Aluminium scraps from panel frames, separated by manual dismantling | Aluminium scraps from frames and internal connectors, separated to high purity by automated dismantling and further processed | Secondary aluminium, equivalent in quality to primary material | Secondary aluminium, equivalent in quality to primary material |
| Copper | 72% | 90% | Copper scraps from cables | Copper scraps from cables and from interior parts of the PV panel | Secondary copper, equivalent to primary material | Secondary copper, equivalent to primary material |
| Glass | 9% | 88% | Glass scraps | Glass scraps separated through a highly selective process in order to maintain high purity. Antimony in glass is assumed to be lost. | Glass for medium-low quality applications | Glass for medium-high quality applications (e.g. production of flat glass). |
| Silicon | – | 95% | – | Silicon separated by acid leaching to obtain high purity SRM | – | Metallurgical grade silicon metal |
| Silver | – | 94% | – | Silver separated by electrolysis on graphite rods | – | Secondary silver equivalent to primary material |
Comparison of the impacts of FRELP process, for PV panels with different backsheets, and detail of incineration (step 9).
| Impact category | Unit | Incineration (FRELP step 9) | FRELP (full process) | ||||
|---|---|---|---|---|---|---|---|
| KPK | PPE | TPT | KPK | PPE | TPT | ||
| Climate change | [kg CO2 eq] | 1492.5 | 1489.7 | 1477.6 | 462.7 | 462.4 | 461.0 |
| Ozone depletion | [kg CFC-11 eq] | 4.4E-06 | 1.1E-06 | 3.1E-06 | 3.3E-05 | 3.2E-05 | 3.3E-05 |
| Human toxicity, cancer effects | [CTUh] | 1.4E-06 | 1.2E-06 | 1.3E-06 | 1.4E-05 | 1.4E-05 | 1.4E-05 |
| Human toxicity, non-cancer effects | [CTUh] | 1.1E-06 | 8.5E-07 | 1.0E-06 | 1.6E-05 | 1.6E-05 | 1.6E-05 |
| Human toxicity (ReCiPe) | [kg 1,4-DB eq] | 711.8 | 6.9 | 437.7 | 380.0 | 302.5 | 349.9 |
| Particulate matter | [kg PM2.5 eq] | 0.02 | 0.02 | 0.02 | 0.10 | 0.10 | 0.10 |
| Ionising radiation HH | [kg U235 eq] | 3.1 | 0.7 | 2.2 | 32.1 | 31.8 | 32.0 |
| Photochemical ozone formation | [kg NMVOC eq] | 0.4 | 0.3 | 0.4 | 3.0 | 3.0 | 3.0 |
| Acidification | [molc H+ eq] | 0.3 | 0.3 | 0.3 | 2.7 | 2.7 | 2.7 |
| Acidification (EDIP) | [m2] | 295.7 | 2.9 | 181.8 | 64.6 | 32.4 | 52.1 |
| Terrestrial eutrophication | [molc N eq] | 1.5 | 1.4 | 1.5 | 12.2 | 12.2 | 12.2 |
| Freshwater eutrophication | [kg P eq] | 0.0019 | 0.0011 | 0.0016 | 0.0539 | 0.0538 | 0.0539 |
| Marine eutrophication | [kg N eq] | 0.13 | 0.12 | 0.13 | 1.10 | 1.09 | 1.09 |
| Freshwater ecotoxicity | [CTUe] | 16.1 | 13.3 | 15.0 | 255.6 | 255.3 | 255.4 |
| Mineral depletion | [kg Sb eq] | 0.0001 | 0.0001 | 0.0001 | 0.004 | 0.004 | 0.004 |
| Cumulative energy demand, non-renewable | [MJ] | 313.5 | 65.0 | 216.9 | 3085.4 | 3058.1 | 3074.8 |
Fig. 5Comparison of the impacts and benefits of PV panels in different life cycle stages.
Fig. 6Comparison of transport in the FRELP process standard (as in Fig. 1) and in the improved scenario for decentralised treatments.
Impacts of scenarios for decentralised process.
| Impact category | Unit | (A) FRELP | (B.1) FRELP decentralised | (B.2) FRELP decentralised | Variations (compared to scenario A) | |
|---|---|---|---|---|---|---|
| (300 km) | (500 km) | B.1 | B.2 | |||
| Climate change | [kg CO2 eq] | 4.6E+02 | 3.9E+02 | 4.0E+02 | −15% | −14% |
| Ozone depletion | [kg CFC-11 eq] | 3.3E-05 | 2.2E-05 | 2.2E-05 | −34% | −31% |
| Human toxicity, cancer effects | [CTUh] | 1.4E-05 | 1.0E-05 | 1.0E-05 | −28% | −26% |
| Human toxicity, non-cancer effects | [CTUh] | 1.6E-05 | 1.1E-05 | 1.1E-05 | −32% | −30% |
| Human toxicity (ReCiPe) | [kg 1,4-DB eq] | 3.5E+02 | 2.5E+02 | 2.6E+02 | −28% | −26% |
| Particulate matter | [kg PM2.5 eq] | 1.0E-01 | 8.1E-02 | 8.2E-02 | −19% | −18% |
| Ionising radiation HH | [kg U235 eq] | 3.2E+01 | 2.5E+01 | 2.5E+01 | −22% | −21% |
| Photochemical ozone formation | [kg NMVOC eq] | 3.0E+00 | 2.7E+00 | 2.7E+00 | −10% | −10% |
| Acidification | [molc H+ eq] | 2.7E+00 | 2.4E+00 | 2.4E+00 | −10% | −10% |
| Acidification (EDIP) | [m2] | 5.2E+01 | 4.9E+01 | 4.9E+01 | −7% | −6% |
| Terrestrial eutrophication | [molc N eq] | 1.2E+01 | 1.1E+01 | 1.1E+01 | −8% | −8% |
| Freshwater eutrophication | [kg P eq] | 5.4E-02 | 4.7E-02 | 4.8E-02 | −12% | −11% |
| Marine eutrophication | [kg N eq] | 1.1E+00 | 1.0E+00 | 1.0E+00 | −9% | −8% |
| Freshwater ecotoxicity | [CTUe] | 2.6E+02 | 1.9E+02 | 2.0E+02 | −24% | −23% |
| Abiotic depletion potential (mineral) | [kg Sb eq] | 4.4E-03 | 2.3E-03 | 2.4E-03 | −47% | −45% |
| Cumulative energy demand, non-renewable | [MJ] | 3.1E+03 | 2.0E+03 | 2.1E+03 | −35% | −32% |
Comparison of the impacts of FRELP process with pyrolysis scenario.
| Impact category | FRELP | Pyrolysis scenario | |||
|---|---|---|---|---|---|
| Impact | Benefit | Impact | Benefit | ||
| Climate change | [kg CO2 eq] | 461.0 | −2,398.3 | 361.3 | −2,365.6 |
| Ozone depletion | [kg CFC-11 eq] | 0.00003 | −0.00016 | 0.00004 | −0.00016 |
| Human toxicity, cancer effects | [CTUh] | 0.00001 | −0.00062 | 0.00001 | −0.00062 |
| Human toxicity, non-cancer effects | [CTUh] | 0.00002 | −0.00021 | 0.00001 | −0.00021 |
| Human toxicity (ReCiPe) | [kg 1,4-DB eq] | 349.9 | −5135.2 | 290.7 | −5203.6 |
| Particulate matter | [kg PM2.5 eq] | 0.1 | −1.4 | 0.1 | −1.4 |
| Ionising radiation HH | [kg U235 eq] | 32.0 | −586.4 | 30.4 | −582.2 |
| Photochemical ozone formation | [kg NMVOC eq] | 3.0 | −6.1 | 3.8 | −6.0 |
| Acidification | [molc H+ eq] | 2.7 | −15.1 | 2.7 | −15.0 |
| Acidification (EDIP) | [m2] | 52.1 | −214.7 | 32.5 | −213.8 |
| Terrestrial eutrophication | [molc N eq] | 12.2 | −22.5 | 12.0 | −22.3 |
| Freshwater eutrophication | [kg P eq] | 0.054 | −1.6 | 0.1 | −1.6 |
| Marine eutrophication | [kg N eq] | 1.095 | −2.0 | 1.1 | −2.0 |
| Freshwater ecotoxicity | [CTUe] | 255.4 | −8,055.6 | 246.3 | −8,048.1 |
| Mineral depletion | [kg Sb eq] | 0.004 | −4.8 | 0.004 | −4.8 |
| CED Non-renewable | [MJ] | 3,074.8 | −28,286.3 | 2,899.4 | −28,863.9 |