Extraction of hydrocarbons from hydrocarbon-containing materials and/or processing of hydrocarbon-containing materials
A method of extracting hydrocarbon-containing organic matter from a hydrocarbon-containing material includes the steps of providing a first liquid comprising a turpentine liquid; contacting the hydrocarbon-containing material with the turpentine liquid to form an extraction mixture; extracting the hydrocarbon material into the turpentine liquid; and separating the extracted hydrocarbon material from a residual material not extracted.
1. A method for increasing flowability of viscous or immobile hydrocarbon-containing materials in an underground formation, flow line, or storage tank comprising contacting a hydrocarbon-containing material selected from oil (tar) sands, oil shale, natural gas, petroleum gas, heavy crude oil and/or crude oil with a non-aqueous turpentine liquid in an underground formation, flow line, or storage tank;
forming a mixture of non-aqueous turpentine liquid and hydrocarbon-containing material having decreased viscosity; and
causing said mixture to flow as a one-phase liquid in said underground formation, flow line, or storage tank; and
wherein said non-aqueous turpentine liquid comprises α-terpineol, β-terpineol, or a combination thereof.
2. The method of claim 1 , wherein said contacting and forming of said mixture decreases the viscosity of the hydrocarbon-containing material.
3. The method of claim 1 , wherein said contacting takes place in situ in an underground formation.
4. The method of claim 3 , wherein said contacting is performed at an extraction site.
5. The method of claim 1 , wherein said non-aqueous turpentine liquid is further comprised natural turpentine, synthetic turpentine, mineral turpentine, pine oil, α-pinene, β-pinene, y-terpineol, terpene resins, α-terpene, β-terpene, y-terpene, geraniol, 3-carene, dipentene (p-mentha-1,8-diene), nopol, pinane, 2-pinane hydroperoxide, terpin hydrate, 2-pinanol, dihydromycenol, isoborneol, p-menthan-8-ol, α-terpinyl acetate, citronellol, p-menthan-8-yl acetate, 7-hydroxydihydrocitronellal, menthol, anethole, camphene; p-cymene, anisaldeyde, 3,7-dimethyl-1,6-octadiene, isobornyl acetate, ocimene, alloocimene, alloocimene alcohols, 2-methoxy-2,6-dimethyl-7,8-epoxyoctane, camphor, citral, 7-methoxydihydro-citronellal, 10-camphorsulphonic acid, cintronellal, menthone, and mixtures thereof.
6. The method of claim 1 , wherein the turpentine liquid comprises at least about 50% by volume α-terpineol and at least about 20% by volume β-terpineol.
7. The method of claim 1 , wherein the turpentine liquid comprises α-terpineol and β-terpineol, wherein the ratio of α-terpineol to β-terpineol is at least about 1.3:1.
8. The method of claim 1 , wherein the turpentine liquid comprises α-terpineol and β-terpineol, wherein the ratio of α-terpineol to β-terpineol is at least about 2:1.
9. The method of claim 1 , wherein the turpentine liquid comprises at least about 30% by volume α-terpineol and at least about 15% β-terpineol.
10. The method of claim 1 , wherein said turpentine liquid comprises:
about 40-60% α-terpineol,
about 30-40% β-terpineol,
about 5-20% β-pinene, and
about 0-10% p-cymene.
11. The method of claim 1 , wherein said contacting is performed in situ in a naturally occurring geological formation of oil (tar) sands, oil shale, natural gas, petroleum gas, heavy crude oil and/or crude oil.
12. The method of claim 1 , wherein said contacting occurs in an oil reservoir and forms a homogeneous one-phase liquid comprising said mixture of non-aqueous turpentine liquid and hydrocarbon-containing material having decreased viscosity.