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R&D & Battery Recycling

Engineering non-destructive lithium-ion battery recycling

Most recycling today discards the cathode's crystal structure to recover the metals; direct recycling avoids this by relithiating the structure in place instead.

See the technology comparison

In active R&D, not yet commercialized

The battery industry's growth is often framed as an unambiguous climate win. The manufacturing and end-of-life reality is more complicated: virgin active material is mined and refined globally, and the two conventional recycling routes in wide use today, pyrometallurgical smelting and hydrometallurgical leaching, are themselves energy- and reagent-intensive, and both destroy the cathode's crystal structure to get at the metals inside it.

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Technology overview

Three recycling routes, compared

A literature-based comparison of the two conventional routes against direct recycling, the approach HSCR is engineering.

FeaturePyrometallurgicalHydrometallurgicalDirect Recycling
Lithium recovery0–10% (lost to slag)90–95%95–99%
Manganese recovery10–20% (mostly to slag)90–95%n/a (retained in the active material)
Feedstock toleranceHigh (mixed/low-purity feed OK)Medium (needs sorting)Low (needs high-purity input)
Energy intensity~2–4 kWh/kg feed (furnace)~0.3–0.6 kWh/kg feed~0.4–0.7 kWh/kg feed
Cathode crystal structureDestroyedDestroyedPreserved (relithiated in place)

Based on published literature. HSCR's own process is in development; process-specific performance data will be published once verified. Cf. Roy et al., Carbon Energy, 2024, on the energy and reagent intensity of conventional recycling routes.

Process flow

The same six pretreatment steps. Then a very different path.

Built from our internal process model (Sheets 2–7): every route starts with the same collection-to-black-mass pretreatment. What happens after that is where direct recycling's advantage comes from.

Shared pretreatment: every route starts here

  1. 01Collection & discharge
  2. 02Dismantling (casing / BMS)
  3. 03Electrolyte removal
  4. 04Shredding
  5. 05Delamination & classification (foil vs. active-material separation)
  6. 06Binder removal → black mass

then the routes diverge

Pyrometallurgical

12 steps total
  1. 07Carbothermic smelting (furnace)
  2. 08Alloy re-leach (acid dissolution)
  3. 09Impurity removal
  4. 10Solvent extraction
  5. 11Precursor co-precipitation
  6. 12Lithiation & calcination

New cathode, Li/Mn mostly lost to slag

Hydrometallurgical

11 steps total
  1. 07Acid leaching (H₂SO₄ + H₂O₂)
  2. 08Impurity removal
  3. 09Solvent extraction
  4. 10Precursor co-precipitation
  5. 11Lithiation & calcination

New cathode, structure rebuilt from scratch

Direct Recycling

8 steps total
  1. 07Cathode AM isolation (binder & conductive-carbon residue removed)
  2. 08Relithiation (Li dosing, no dissolution)

Regenerated cathode, structure preserved

Step counts are process stages from our internal techno-economic model (Sheets 2–7), not a timing or cost claim. Pyrometallurgical smelting still requires the same acid-leach and re-synthesis chain as hydrometallurgy for its alloy output, which is why it has the most stages of the three rather than the fewest. Direct Recycling carries one step Pyro/Hydro don't need: isolating pure cathode active material from graphite, binder, and conductive carbon before relithiation, because it needs a high-purity feed where the other two routes can process the whole black mass together.

What's actually being preserved

Structure, at the atomic scale

Molecular-dynamics simulations from the founder's own research, the same class of atomistic modeling used to understand why structure-preserving recycling is chemically different from dissolve-and-resynthesize.

These are materials-science simulations of battery electrochemistry, not recordings of HSCR's recycling process. They illustrate the crystal structure the technology aims to preserve, not the recycling steps themselves.
The cathode's layered crystal structure

The cathode's layered crystal structure

A molecular-dynamics view of a layered oxide cathode lattice, the ordered structure that took significant energy to build in the first place, and the thing leaching and smelting both break apart to get at the metals.

Lithium intercalating between graphite layers

Lithium intercalating between graphite layers

A lithium ion moving into a graphite anode lattice during charge, the same layered-insertion mechanism direct recycling relies on to redose lithium back into a degraded cathode without dissolving it first.

Anode–electrolyte interface

Anode–electrolyte interface

A graphite anode lattice alongside the surrounding electrolyte species, the same class of atomistic modeling (ReaxFF MD) used to study how these materials behave, rather than treating them as an undifferentiated feedstock stream.

Why this matters

What the model projects

Modeled techno-economic estimates for HSCR's own process, from a worked example run of our internal model.

Modeled estimates from HSCR's internal techno-economic model, not measured lab results. These figures come from a worked example run of the model, not from a physical pilot; real performance data will replace them once the process is lab-verified.

≥ 99%

Battery-grade purity achieved (modeled, NMC batch)

≥ 98%

Battery-grade purity achieved (modeled, LFP batch)

≈ $13/kg (modeled)

Net value modeled per kg of feedstock processed (NMC)

≈ $8/kg (modeled)

Net value modeled per kg of feedstock processed (LFP)

Feedstock

What we accept

Chemistries accepted

NMCLFPNCALCO

Formats accepted

CylindricalPouchPrismatic

Status

IP and regulatory status

Patent & IP status

Proprietary process. Patent filing in preparation. IP protection in progress.

Regulatory status

Regulatory and environmental authorizations (e.g. state pollution-control board approvals) will be pursued once the process is finalized.

Lab capability

Facility details to follow.

Compare the routes

Run your own feedstock through all three routes

Enter a feed mass and chemistry to see step count, recovery, energy intensity, and modeled net value side by side for Pyrometallurgical, Hydrometallurgical, and Direct Recycling.

Step counts and literature-band ranges apply to any chemistry. The two $/kg figures below are exact outputs of our internal model for the one worked run of each route (NMC through Hydrometallurgical, LFP through Direct Recycling); every other pairing shows the same literature band Sheet 10 of that model uses, not an invented number.

Pyrometallurgical

12 steps
Li recovery
0–10% (lost to slag)
Mn recovery
10–20% (mostly to slag)
Feedstock tolerance
High (mixed/low-purity feed OK)
Final purity
n/a (alloy output feeds back into hydrometallurgical re-leach)
Energy intensity
2–4 kWh/kg feed

Net value, per kg feed

Route-dependent, not modeled for NMC in our worked example (Pyro wasn't routed in this run either).

Hydrometallurgical

11 steps
Li recovery
90–95%
Mn recovery
90–95%
Feedstock tolerance
Medium (needs Sheet 1B sorting)
Final purity
≥98% target
Energy intensity
0.3–0.6 kWh/kg feed

Net value, per kg feed

$13.11/kg

Direct Recycling

8 steps
Li recovery
95–99%
Mn recovery
n/a (retained in the active material)
Feedstock tolerance
Low (needs high-purity input)
Final purity
90–97% (method dependent)
Energy intensity
0.4–0.7 kWh/kg feed

Net value, per kg feed

Route-dependent, not modeled for NMC in our worked example.

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There's a live remote research-internship role on this work: Research Intern: R&D, Lithium-ion Battery Recycling.

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FAQ

Technical FAQ

Chemistries: NMC, LFP, NCA, LCO. Formats: Cylindrical, Pouch, Prismatic.