Knowledge Base
People conflate these two. They shouldn't. A hydrotreater (HDT) removes heteroatoms and saturates olefins. A hydrocracker (HCR) does that and breaks carbon-carbon bonds to convert heavy to light. Which one you need depends entirely on what you want out the other end.
One-line distinction: HDT changes the chemistry of your feed; HCR changes the boiling range. If you need the product lighter, it's HCR.
| Feed / Goal | Unit | Why |
|---|---|---|
| Naphtha desulfurization to < 1 ppmS for reformer | Naphtha HDT (NHT) | Sulfur poisons Pt/Re reformer; no conversion needed |
| Kerosene/jet sweetening to JP-8 or Jet A spec | Kerosene HDT | Mercaptan removal, saturation, limited hetero removal |
| ULSD production (ULSD 15 ppmS, Euro VI 10 ppm) | Diesel HDT (DHT) / ULSD HDT | Deep HDS, some aromatic sat; no cracking |
| Heavy diesel aromatics saturation for cetane lift | DHT with dearom stage (2-stage) | HDA catalyst in 2nd stage |
| VGO to naphtha + distillates (max gasoline or max distillate) | Hydrocracker (HCR) | Real bond breaking; conversion > 40% |
| Atmospheric resid or vacuum resid upgrade | Residue Hydrocracker (RDS, LC-Finer, H-Oil) | High pressure, ebullated bed; CCR-tolerant |
| FCC feed pretreat (lower S, N, and CCR) | FCC Feed HDT (FFHT/VGOHT) | Kills S and N ahead of catalytic cracker; no cracking wanted |
| Renewable diesel / SAF from triglycerides (FOG, UCO) | Renewable HDT (Hydrotreated Esters & Fatty Acids, HEFA) | Decarboxylation / HDO; isomerization downstream |
| Parameter | HDT (typical) | HCR (typical) |
|---|---|---|
| Reactor WABT | 600 - 720 F | 700 - 780 F (single stage) / 750 - 830 F (2nd stage) |
| Reactor pressure | 500 - 1200 psig (distillate HDT) 600 - 900 psig (naphtha) | 1500 - 2500 psig (mild HCR) 2000 - 3000 psig (full HCR) |
| H2 partial pressure | 400 - 900 psia | 1500 - 2500 psia |
| H2 consumption | 100 - 400 SCF/BBL | 1500 - 2500 SCF/BBL (often 2000+) |
| LHSV | 1.5 - 4.0 hr-1 | 0.4 - 2.0 hr-1 |
| Cycle length | 24 - 48 months | 18 - 36 months; 2nd stage is the shorter |
| Catalyst | CoMo (HDS-selective) / NiMo (HDN, HDA) | NiMo/NiW + zeolite or amorphous SiO2-Al2O3 cracking |
| Conversion (to lower boiling range) | < 5 vol% | 30 - 95 vol% |
| Product slate | Same as feed, cleaner | Lighter than feed (naphtha, kero, diesel, LPG) |
| Metallurgy | 1-1/4 Cr - 1/2 Mo (reactor), CS piping post-reactor | 2-1/4 Cr - 1 Mo - 1/4 V (reactor); SS 347/321 internals |
Feed + H2 cross over the catalyst. Heteroatom-removal reactions dominate:
R-S-R' + 2H2 -> RH + R'H + H2SR-N + H2 -> R-H + NH3 - requires higher T/P, ring saturation first.R-O-H + H2 -> RH + H2O - important on renewable/biobased feeds.organic-Ni/V + H2 -> Ni/V sulfides on guard bed.ArH + 3H2 -> cycloparaffin - exothermic, limited thermodynamically above 700 F.All mild exotherms (10-25 F per stage). No significant C-C bond cleavage. Carbon skeleton is preserved.
Everything HDT does plus bifunctional cracking:
Exotherm is large: typical 40-80 F per bed, managed by H2 quench between beds. Conversion is tunable via reactor temperature. Runaway risk is real; emergency depressuring is a required safeguard.
| Service | Catalyst | Rationale |
|---|---|---|
| Straight HDS (naphtha, distillate) | CoMo on gamma-Al2O3 | Highest HDS activity per H2 mole |
| Deep HDS + HDN + HDA (ULSD, kero) | NiMo on gamma-Al2O3 | Better on refractory S and N; higher H2 consumption |
| Resid HDM + HDS guard | NiMo on alumina with large pore/macropore structure | Metal accommodation, diffusion limited |
| Single-stage max-distillate HCR | NiMo + amorphous SiO2-Al2O3 | Lower acidity = lower gas yield, more diesel |
| Single-stage max-gasoline HCR | NiW/NiMo + Y-zeolite | High acidity, high conversion to light product |
| Mild HCR on VGO (10-40% conv) | NiMo on amorphous support | Extend cycle, moderate conversion |
| HEFA (renewable diesel) | NiMo pretreat + Pt/Pd dewaxing | HDO then iso for cloud point spec |
Hydrogen partial pressure controls aromatic saturation equilibrium and catalyst coking rate. At HDT pressures (400-900 psia H2), you can't push HDA past about 50% on a heavy feed - thermodynamics caps it. At HCR pressures (1500-2500 psia), you can push past 95% HDA and break the aromatic rings.
Pressure also controls cycle length. Every 100 psia of H2 partial pressure buys roughly 3-6 months of cycle on distillate HDT, more on HCR. Every dollar spent on compressor work buys cycle length back.
If someone proposes either unit, get these numbers from the engineering package before you approve:
HDT is cheap, small, and reliable - but it does not break bonds. HCR is expensive, large, runs hot, and is metallurgically demanding - but it turns heavy into light. Pick the cheaper unit that meets the actual product spec; don't spend HCR money for an HDT problem. And when you do need HCR, build the H2 plant and the metallurgy at full spec the first time. Retrofits are brutal.
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