Process for the recovery of oleaginous compounds and nutrients from biomass

1. A method for obtaining an oleaginous composition and recycling nutrients from biomass, comprising:

(a) obtaining an feedstock comprising said biomass and water;

(b) heating the feedstock in a closed reaction vessel to a first temperature between about 250° C. and about 360° C. and holding at said first temperature for a time between 0 minutes and about 90 minutes;

(c) cooling the feedstock of (b) to a temperature between ambient temperature and about 150° C.;

(d) acidifying the cooled feedstock of (c) to a pH from about 3.0 to less than 6.0 to produce an acidified composition;

(e) heating the acidified composition of (d) to a second temperature of between about 40° C. and about 150° C. and holding the acidified composition at said second temperature for between 0 minutes and about 45 minutes;

(f) adding to the acidified composition of (e) a volume of a solvent approximately equal in volume to the water in said acidified composition to produce a solvent extraction composition, wherein said solvent is sparingly soluble in water, but oleaginous compounds are at least substantially soluble in said solvent;

(g) heating the solvent extraction composition in closed reaction vessel to a third temperature of between about 60° C. and about 150° C. and holding at said third temperature for a period of between about 15 minutes and about 45 minutes;

(h) separating the solvent extraction composition into at least an organic phase and an aqueous phase;

(i) removing the organic phase from said aqueous phase;

(j) removing the solvent from the organic phase to obtain an oleaginous composition;

(k) and treating the aqueous phase to recover nitrogen and phosphorus.

2. The method of claim 1 , wherein phosphorus is recovered by precipitation with at least one of a calcium salt, a ferrous salt, a ferric salt and an aluminum salt.

3. The method of claim 1 , wherein nitrogen is recovered by adjusting the pH of the aqueous phase to a pH between about 8 and about 11; heating the pH adjusted aqueous phase to a temperature between about 40° C. and about 100° C. to produce ammonia gas; and collecting the ammonia gas.

4. The method of claim 3 , wherein the pH adjusted aqueous phase is heated to a temperature between about 80° C. and about 100° C.

5. The method of claim 1 , wherein said nitrogen and phosphorus are recovered by adjusting the pH of the aqueous phase to a pH between about 8 and about 11 with at least one of calcium oxide, calcium hydroxide and calcium carbonate to precipitate phosphorus; separating said precipitate; heating the pH adjusted aqueous phase to a temperature between about 40° C. and about 100° C. to produce ammonia gas; and collecting said ammonia gas.

6. The method of 1 , further comprising pretreating said feedstock prior to heating to said first temperature by heating said feedstock to a pretreatment temperature of between about 80° C. and about 220° C. and holding at said pretreatment temperature for between about 5 minutes and about 60 minutes to produce a pretreated feedstock.

7. The method of claim 6 , further comprising removing water from said pretreated feedstock and treating the water to recover nitrogen and phosphorus.

8. The method of claim 7 , wherein phosphorus is recovered by precipitation with at least one of a calcium salt, a ferrous salt, a ferric salt and an aluminum salt.

9. The method of claim 8 , wherein nitrogen is recovered by adjusting the pH of the water to a pH between about 8 and about 11, heating the pH adjusted water to a temperature between about 40° C. and about 100° C. to produce ammonia gas, and collecting said ammonia gas.

10. The method of claim 9 , wherein the pH adjusted water is heated to a temperature between about 80° C. and about 100° C.

11. The method of claim 6 , wherein said nitrogen and phosphorus is recovered by adjusting the pH of the water to a pH between about 8 and about 11 with at least one of calcium oxide, calcium hydroxide and calcium carbonate to precipitate phosphorus; separating said precipitate; heating the pH adjusted water to a temperature between about 40° C. and about 100° C. to produce ammonia gas; and collecting said ammonia gas.