1. A method for removing a turpentine liquid and solvent-associated liquids trapped within pores of a material having API gravity of more than 10\xb0 that has been treated with turpentine liquid, comprising the steps of:
a) providing a solvent-extracting composition,
b) contacting said material having API gravity of more than 10\xb0 that has been treated with turpentine liquid with said solvent-extracting composition such that said solvent-extracting composition penetrates into pores of the material,
c) forming a recovery mixture, wherein the recovery mixture comprises at least a portion of the turpentine liquid and solvent-associated liquids extracted into the solvent-extracting composition; and
d) separating the recovery mixture from any residual material containing non-extracted material from the material having API gravity of more than 10\xb0 that has been treated with said turpentine liquid that is not extracted into the solvent-extracting composition.
2. The method of claim 1, further comprising the step of:
separating the recovery mixture into a first portion and a second portion, the first portion comprising a turpentine liquid product stream that includes at least a portion of the turpentine liquid and any solvent-associated liquids extracted from the pores of the material, the second portion comprising at least a portion of the solvent-extracting composition.
3. The method of claim 1, wherein said turpentine liquid further comprises a second liquid selected from an alkane, an aromatic, an aliphatic amine, an aromatic amine, carbon bisulfide, a solvent manufactured in petroleum refining, a decant oil, a light cycle oil, naphtha, a solvent manufactured in dry distilling coal, a solvent manufactured in fractionating liquefied coal, benzene, naphthalene, toluene, pentane, heptane, hexane, benzene, toluene, xylene, naphthalene, anthracene, tetraline, triethylamine, aniline, carbon bisulfide, or a mixture thereof.
4. The method of claim 1, wherein said turpentine liquid is selected from the group consisting of natural turpentine, synthetic turpentine, mineral turpentine, pine oil, alpha-pinene, beta-pinene, alpha-terpineol, beta-terpineol, gamma-terpineol, 3-carene, anethole, dipentene (p-mentha-1,8-diene), terpene resins, alpha-terpene, beta-terpene, gamma terpene, nopol, pinane, camphene, p-cymene, anisaldehyde, 2-pinane hydroperoxide, 3,7-dimethyl-1,6-octadiene, isobornyl acetate, terpin hydrate, ocimene, 2-pinanol, dihydromyrcenol, isoborneol, alloocimene, alloocimene alcohols, geraniol, 2-methoxy-2,6-dimethyl-7,8-epoxyoctane, camphor, p-menthan-8-ol, alpha-terpinyl acetate, citral, citronellol, 7-methoxydihydrocitronellal, 10-camphorsulphonic acid, p-menthene, p-menthan-8-yl acetate, citronellal, 7-hydroxydihydrocitronellal, menthol, menthone, polymers thereof, and mixtures thereof.
5. The method of claim 4, wherein said turpentine liquid comprises alpha-terpineol, alpha-pinene, beta-pinene, p-cymene, or a combination thereof.
6. The method of claim 1, wherein said solvent-extracting composition comprises an alcohol, an organic compound with a hydroxyl functional group, an organic or inorganic solvent, or a combination thereof.
7. The method of claim 1, wherein said solvent-extracting composition comprises one or more acyclic or cyclic alcohols.
8. The method of claim 1, wherein said solvent-extracting composition comprises methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, 1-Pentanol, 3-Methyl-1-butanol, 2-Methyl-1-butanol, 2,2-Dimethyl-1-propanol, 3-Pentanol, 2-Pentanol, 3-Methyl-2-butanol, 2-Methyl-2-butanol, hexanol, 1-Hexanol, 2-Hexanol, 3-Hexanol, 2-Methyl-1-pentanol, 3-Methyl-1-pentanol, 4-Methyl-1-pentanol, 2-Methyl-2-pentanol, 3-Methyl-2-pentanol, 4-Methyl-2-pentanol, 2-Methyl-3-pentanol, Tertiary 3-Methyl-3-pentanol, Primary 2,2-Dimethyl-1-butanol, 2,3-Dimethyl-1-butanol, 3,3-Dimethyl-1-butanol, 2,3-Dimethyl-2-butanol, 3,3-Dimethyl-2-butanol, 2-Ethyl-1-butanol, lower aliphatic alcohols, benzene, toluene, methyl ethyl ketone (MEK), furfural, tetrahydrofuran (THF), acetone, hydrofluoric acid, hexane, xylene, or a mixture thereof.
9. The method of claim 1, wherein said solvent-extracting composition comprises methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, hexanol, or a mixture thereof.
10. The method of claim 3, wherein said solvent-extracting composition comprises an alcohol, an organic compound with a hydroxyl functional group, an organic or inorganic solvent, or a combination thereof and the ratio of alcohol, the organic compound with a hydroxyl functional group, andor the organic or inorganic solvent in the solvent-extracting composition to the second liquid is greater than or equal to about 1:1 by volume.
12. The method of claim 1, wherein said material is contacted with said solvent-extracting composition in a ratio range of about 1:6 to 6:1 by weight.
13. The method of claim 12, wherein the material is contacted with said solvent-extracting composition in a ratio of about 1:4 to 2:1 by weight.
14. The method of claim 12, wherein the material is contacted with said solvent-extracting composition in a ratio of about 1:3 to 1:1 by weight.
15. The method of claim 1, wherein the amount of the solvent-extracting composition in said recovery mixture is about 10 to about 2500 wt. % of the material.
16. The method of claim 15, wherein the amount of the solvent-extracting composition in said recovery mixture is about 30 to about 200 wt. % of the material.
17. The method of claim 16, wherein the amount of the solvent-extracting composition in said recovery mixture is about 50 to about 150 wt. % of the material.
18. The method of claim 17, wherein the amount of the solvent-extracting composition in said recovery mixture is about 100 wt. % of the material.
19. The method of claim 1, wherein said contacting is carried out at a temperature within the range of about 2\xb0 C. to about 400\xb0 C.
20. The method of claim 19, wherein said contacting is carried out at a temperature within the range of about 15\xb0 C. to about 150\xb0 C.
21. The method of claim 1, wherein said material is contacted with said solvent-extracting composition for 1 to 300 minutes.
22. The method of claim 21, wherein said material is contacted with said solvent-extracting composition for 5 to 60 minutes.
23. The method of claim 1, wherein said contacting step (b) is repeated 1 to 10 times before performing step (c).
24. The method of claim 1, wherein said solvent-extracting composition comprises at least 10% alcohol.
25. The method of claim 1, wherein said solvent-extracting composition comprises at least 50% alcohol.
26. The method of claim 1, wherein said solvent-extracting composition comprises at least 90% alcohol.
27. The method of claim 1, wherein said contacting extracts at least 50% of turpentine liquid and any solvent-associated liquids contained within said material before said contacting.
28. The method of claim 27, wherein said contacting extracts at least 80% of turpentine liquid and any solvent-associated liquids contained within said material before said contacting.
29. The method of claim 1, wherein said contacting further comprises boiling and refluxing said solvent-extracting composition.
30. The method of claim 1, wherein said method comprises contacting said material with a substantially non-aqueous solvent-extracting composition.
31. The method of claim 1, wherein said method does not involve the use of water or an emulsion.
32. The method of claim 1, wherein said method does not involve the use of salt or salt solution.
33. The method of claim 1, wherein said solvent-extracting composition comprises a surfactant.
34. The method of claim 1, wherein said solvent-extracting composition is surfactant-free or substantially surfactant-free.
35. The method of claim 1, wherein said solvent-extracting composition is micelle-free or substantially micelle-free.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
1. A seed of soybean cultivar 6114011, wherein a representative sample of seed of said cultivar was deposited under ATCC Accession No. PTA-______.
2. A soybean plant, or a part thereof, produced by growing the seed of claim 1.
3. A tissue culture of cells produced from the plant of claim 2, wherein said cells of the tissue culture are produced from a plant part selected from the group consisting of leaf, pollen, embryo, cotyledon, hypocotyl, meristematic cell, root, root tip, pistil, anther, flower, stem, pod and petiole.
4. A protoplast produced from the plant of claim 2.
5. A protoplast produced from the tissue culture of claim 3.
6. A soybean plant regenerated from the tissue culture of claim 3, wherein the plant has all of the morphological and physiological characteristics of cultivar 6114011.
7. A method for producing an F1 hybrid soybean seed, wherein the method comprises crossing the plant of claim 2 with a different soybean plant and harvesting the resultant F1 hybrid soybean seed.
8. A hybrid soybean seed produced by the method of claim 7.
9. A hybrid soybean plant, or a part thereof, produced by growing said hybrid seed of claim 8.
10. A method of producing an herbicide resistant soybean plant wherein the method comprises transforming the soybean plant of claim 2 with a transgene wherein the transgene confers resistance to an herbicide selected from the group consisting of imidazolinone, sulfonylurea, glyphosate, glufosinate, L-phosphinothricin, triazine and benzonitrile.
11. An herbicide resistant soybean plant produced by the method of claim 10.
12. A method of producing an insect resistant soybean plant wherein the method comprises transforming the soybean plant of claim 2 with a transgene that confers insect resistance.
13. An insect resistant soybean plant produced by the method of claim 12.
14. The soybean plant of claim 13, wherein the transgene encodes a Bacillus thuringiensis endotoxin.
15. A method of producing a disease resistant soybean plant wherein the method comprises transforming the soybean plant of claim 2 with a transgene that confers disease resistance.
16. A disease resistant soybean plant produced by the method of claim 15.
17. A method of producing a soybean plant with modified fatty acid metabolism or modified carbohydrate metabolism wherein the method comprises transforming the soybean plant of claim 2 with a transgene encoding a protein selected from the group consisting of phytase, fructosyltransferase, levansucrase, \u03b1-amylase, invertase and starch branching enzyme or encoding an antisense of stearyl-ACP desaturase.
18. A soybean plant having modified fatty acid metabolism or modified carbohydrate metabolism produced by the method of claim 17.
19. A method of introducing a desired trait into soybean cultivar 6114011 wherein the method comprises:
(a) crossing a 6114011 plant, wherein a representative sample of seed was deposited under ATCC Accession No. PTA-______, with a plant of another soybean cultivar that comprises a desired trait to produce progeny plants wherein the desired trait is selected from the group consisting of male sterility, herbicide resistance, insect resistance, modified fatty acid metabolism, modified carbohydrate metabolism, modified seed yield, modified oil percent, modified protein percent, modified lodging resistance, modified shattering, modified iron-deficiency chlorosis and resistance to bacterial disease, fungal disease or viral disease;
(b) selecting one or more progeny plants that have the desired trait to produce selected progeny plants;
(c) crossing the selected progeny plants with the 6114011 plants to produce backcross progeny plants;
(d) selecting for backcross progeny plants that have the desired trait and all of the physiological and morphological characteristics of soybean cultivar 6114011 listed in Table 1; and
(e) repeating steps (c) and (d) three or more times in succession to produce selected fourth or higher backcross progeny plants that comprise the desired trait and all of the physiological and morphological characteristics of soybean cultivar 6114011 listed in Table 1.
20. A soybean plant produced by the method of claim 19, wherein the plant has the desired trait and all of the physiological and morphological characteristics of soybean cultivar 6114011 listed in Table 1.
21. The soybean plant of claim 20, wherein the desired trait is herbicide resistance and the resistance is conferred to an herbicide selected from the group consisting of imidazolinone, sulfonylurea, glyphosate, glufosinate, L-phosphinothricin, triazine and benzonitrile.
22. The soybean plant of claim 20, wherein the desired trait is insect resistance and the insect resistance is conferred by a transgene encoding a Bacillus thuringiensis endotoxin.
23. The soybean plant of claim 20, wherein the desired trait is modified fatty acid metabolism or modified carbohydrate metabolism and said desired trait is conferred by a nucleic acid encoding a protein selected from the group consisting of phytase, fructosyltransferase, levansucrase, \u03b1-amylase, invertase and starch branching enzyme or encoding an antisense of stearyl-ACP desaturase.