Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sulfur trioxide | HCID 24682 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Benzenesulfonic Acid | HCID 7371 | — |
Reaction Steps
A fifty-fifty (50/50) hexane mixture by volume of polypropyl benzene alkylates was charged to a continuous sulfonation unit. 20% sulfur trioxide (SO3) by weight in sulfuric acid (H2SO4) was charged to the unit. Spent sulfuric acid (H2SO4) was continuously removed in a two phase non-aqueous system leaving a polypropenyl benzene sulfonic acid product containing 7.4% by weight residual sulfuric acid (H2SO4). At this stage, water was added to dilute the residual sulfuric acid (H2SO4) to 85% by weight, including the sulfuric acid (H2SO4) generated from unused sulfur trioxide (SO3). The aqueous phase was separated from the resultant two phase aqueous-organic system, leaving the organic phase containing 0.98% by weight sulfuric acid (H2SO4). Hexane was added to the organic phase followed by addition of Calcium Carbonate (CaCO3). The resulting mixture was treated with SX-5W oil to reduce the viscosity of the sulfonic acid and also make a 30% by weight active product sulfonate. The product mixture was heated at 215° F. to strip the hexane. The hexane-stripped product was filtered to yield a sulfonic acid and oil product mixture containing less than 0.4%* by weight sulfuric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04321214 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-0317588913f247cea9f9377a803c17d1 |
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| Source note | uspto-grants-1982_03 |
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