Compositions and methods for separating fluids

Patent metadata

Field	Value
Publication number	US-2018065125-A1
Application number	US-201615551941-A
Country	US
Kind code	A1
Filing date	Feb 19, 2016
Priority date	Feb 20, 2015
Publication date	Mar 8, 2018
Grant date	—

Abstract

A method of separating a fluid containing oil and water into an oil phase and a water phase comprising contacting the fluid with supported magnetic nanoparticles. The supported magnetic nanoparticles can be recovered after being used in a separation process to conduct subsequent separation operations on a fluid.

First claim

1 . A method of separating a composition containing oil and water, the method comprising:
contacting a composition containing oil and water with supported magnetic nanoparticles to cause the oil and water to be at least partially separated into an oil phase and a water phase, where the supported magnetic nanoparticles comprise functionalized nanoparticle bonded to a support material.

2 . The method of claim 1 wherein the functionalized nanoparticles comprise a magnetic metal chosen from iron, cobalt, nickel, manganese, or a combination of two or more thereof.

3 . The method of claim 2 , wherein the functionalized nanoparticles comprise particles chosen from Fe 3 O 4 , Fe 2 O 3 , Fe 2 TiO 4 , CoPt, fcc phase FePt, fct phase FePt, FeCo, MnAl, MnBi, Ni3Fe, FeS, CoFe 2 O 4 , MnFe 2 O 4 , or a combination of two or more thereof

4 . The method of claim 2 , wherein the functionalized nanoparticles are functionalized by stabilization of the nanoparticles with a C 7 -C 30 organic fatty acid.

5 . The method of claim 4 , wherein the fatty acid is chosen from lauric acid, oleic acid, stearic acid, myristic acid, hexadecanoic acid, palmitic acid, or a combination of two or more thereof.

6 . The method of claim 1 , wherein the functionalized nanoparticles comprise magnetic nanoparticles encapsulated in a polymer matrix.

7 . The method of claim 6 , wherein the polymer matrix comprises an organic polymer matrix comprising a polymer or copolymer of a vinyl aromatic, a vinyl halide, an alpha monoolefin, an acrylonitrile, an acrylate, an amide, an acrylamide, an ester, or a combination of two or more thereof.

8 . The method of claim 6 , wherein the polymer matrix is derived from a silicon hydride-containing polyorganohydrosiloxane of the general formula:
M 1 a M 2 b D 1 c D 2 d T 1 e T 2 f Q j
wherein: M 1 =R 1 R 2 R 3 SiO 1/2 ; M 2 =R 4 R 5 R 6 SiO 1/2 ; D 1 =R 7 R 8 SiO 2/2 ; D 2 =R 9 R 10 SiO 2/2 ; T 1 =R 11 SiO 3/2 ; T 2 =R 12 SiO 3/2 ; Q=SiO 4/2 ; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , and R 12 are aliphatic, aromatic or fluoro monovalent hydrocarbon having from 1 to 60 carbon atoms; at least one of R 4 , R 9 , R 12 is hydrogen; and the subscript a, b, c, d, e, f, and j are zero or positive subject to the following limitations: 2≦a+b+c+d+e+f+j≦6000, and b+d+f>0.

9 . The method of claim 6 , wherein the polymer matrix comprises a functional group chosen from a hydride; a carboxyl group, an alkoxy functional group, an epoxy functional group, a triaz-1-yn-2-ium functional group, an anhydride group, a mercapto group, an acrylate, an alkyl, an olefinic, a dienyl, or a combination of two or more thereof.

10 . The method of claim 6 , wherein the polymer matrix comprises a functional group chosen from —S i —H; —Si(CH 2 ) n COOR 13 , —Si(CH 2 nSi(OR 14 ) 3 , —Si(OR 15 ) 1-3 , —S i (CH 2 ) n -epoxy, —Si—(CH 2 ) n —N—N≡N, etc. where R 13 , R 14 , and R 15 is chosen from hydrogen, hydrocarbyl, substituted hydrocarbyl, or a combination of two or more thereof, and n is chosen from 1 to 26.

11 . The method of claim 10 , wherein the polymer matrix comprises a polysiloxane.

12 . The method of claim 11 , wherein the polysiloxane is formed from a hydrosiloxane and a vinyl silicon compound.

13 . The method of claim 6 wherein the polymer matrix has a ratio of polymer to metal of from about 1:1000 to about 100:1.

14 . The method of any of claims 1 wherein the nanoparticles have a particle size of from about 1 to about 100 nanometers.

15 . The method of any of claims 1 wherein the support material is chosen from silicon, a silicate such as a sodium silicate, a borosilicate, or a calcium aluminum silicates, clay, silicate, silica, starch, carbon, alumina, titania, calcium carbonate, barium carbonate, zirconia, metal oxide, carbon nanotubes, synthetic and natural zeolites, polymeric resins in bead or fibrous form, or mixtures of two or more thereof.

16 . The method of any of claims 1 wherein the metal loading ranges from about 0.001 to 20 percent by weight of the support material.

17 . The method of any of claims 1 wherein the metal loading ranges from about 0.05 to about 5 percent by weight of the support material.

18 . The method of any of claims 1 , wherein the support material comprises a functional group chosen from a group such as silanol, alkoxy, acetoxy, silazane, oximino-functional silyl group, hydroxyl, acyloxy, ketoximino, amine, aminoxy, alkylamide, hydrogen, allyl, an aliphatic olefinic group, aryl, hydrosulfide, or a combination of two or more thereof.

19 . The method of any of claims 1 , wherein the support material comprises a functional group chosen from —Si—CH═CH 2 , —Si—OH, —Si—(CH 2 ) n C≡CH, —Si—(CH 2 ) n —NH 2 , —Si—(CH 2 ) n —OH, —Si—(CH 2 ) n —SH, or a combination of two or more thereof, and n is 1-26.

20 . The method of any of claims 1 wherein the metal-containing polymer matrix is covalently bonded to the support material via a hydrophobic functional group attached to the support material.

21 . The method of claim 20 , wherein the hydrophobic group is chosen from an alkyldisilazane, a vinyl-containing silazane, or a combination thereof.

22 . The method of any of claims 1 , wherein the composition containing oil and water is at a temperature of from about 1° C. to about 1000° C.

23 . The method of any of claims 1 further comprising:
applying a magnetic field to the water phase and removing the oil phase from the composition.

24 . The method of claim 23 , wherein the step of removing the oil phase comprises decanting the oil phase from the composition.

25 . The method of claim 23 further comprising removing the supported magnetic particles from the water phase.

26 . The method of claim 25 further comprising washing the supported magnetic particles that were removed from the water phase.

27 . The method of claim 25 further comprising reusing the supported magnetic particles that were removed from the water phase in a subsequent operation to separate a composition comprising oil and water.

28 . The method of any of claims 1 , wherein the composition is a water-in-oil emulsion.

29 . The method of any of claims 1 , wherein the composition is an oil-in-water emulsion.

30 . The method of any of claims 1 , wherein the oil is chosen from a crude oil, a crude oil distillate, bitumen, a crude oil-light oil blend, a vegetable oil, an animal oil, a synthetic oil, or a combination of two or more thereof.

31 . A solid demulsifier comprising:
functionalized magnetic metal nanoparticles covalently bonded to a support, wherein the functionalized magnetic nanoparticles comprise nanoparticles that exhibit magnetic properties, and said nanoparticles are encapsulated in a polymer matrix and/or are functionalized by stabilization of the nanoparticles with a C 7 -C 30 organic fatty acid.

32 . An emulsion comprising:
an oil, water, and a solid demulsifier, wherein the solid demulsifier comprises functionalized magnetic metal nanoparticles covalently bonded to a support, wherein the functionalized magnetic nanoparticles comprise nanoparticles that exhibit magnetic properties.

33 . The emulsion of claim 32 , wherein said nanoparticles are encapsulated in a polymer matrix and/or are

Assignees

• Momentive Performance Mat Inc

Inventors

• Komati Srinivas

Classifications

• B03C1/002 Primary

  High gradient magnetic separation (acting directly on the substance being separated B03C1/025; acting on the medium containing the substance being separated B03C1/32) · CPC title

• B03C1/01

  by addition of magnetic adjuvants · CPC title

• C08G77/50

  by carbon linkages · CPC title

• C10G33/02

  with electrical or magnetic means · CPC title

• C07C57/03

  Monocarboxylic acids · CPC title