WO2011100183A1 - Water-in-oil emulsion compositions and methods for making and using the same - Google Patents

Water-in-oil emulsion compositions and methods for making and using the same Download PDF

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Publication number
WO2011100183A1
WO2011100183A1 PCT/US2011/023866 US2011023866W WO2011100183A1 WO 2011100183 A1 WO2011100183 A1 WO 2011100183A1 US 2011023866 W US2011023866 W US 2011023866W WO 2011100183 A1 WO2011100183 A1 WO 2011100183A1
Authority
WO
WIPO (PCT)
Prior art keywords
silicon
group
containing polymer
copolymer
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2011/023866
Other languages
English (en)
French (fr)
Inventor
Haunn-Lin Chen, (Tony)
Douglas A. Cywar
Matthew J. Davis
Morris Lewellyn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cytec Technology Corp
Original Assignee
Cytec Technology Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cytec Technology Corp filed Critical Cytec Technology Corp
Priority to CN201180009227.7A priority Critical patent/CN102869437B/zh
Priority to EA201290785A priority patent/EA022770B1/ru
Priority to BR112012019681A priority patent/BR112012019681A2/pt
Priority to CA2789608A priority patent/CA2789608A1/en
Priority to JP2012552911A priority patent/JP6306819B2/ja
Priority to US13/578,271 priority patent/US20160185613A1/en
Priority to EP11708601.7A priority patent/EP2533886B1/en
Priority to AU2011216038A priority patent/AU2011216038B2/en
Priority to ES11708601.7T priority patent/ES2675099T3/es
Priority to AP2012006425A priority patent/AP2012006425A0/xx
Publication of WO2011100183A1 publication Critical patent/WO2011100183A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00Compounds of aluminium
    • C01F7/02Aluminium oxide; Aluminium hydroxide; Aluminates
    • C01F7/04Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom
    • C01F7/06Preparation of alkali metal aluminates; Aluminium oxide or hydroxide therefrom by treating aluminous minerals or waste-like raw materials with alkali hydroxide, e.g. leaching of bauxite according to the Bayer process
    • C01F7/0646Separation of the insoluble residue, e.g. of red mud
    • C01F7/0653Separation of the insoluble residue, e.g. of red mud characterised by the flocculant added to the slurry
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/54Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
    • C02F1/56Macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/54Silicon compounds

Definitions

  • Bauxite is the basic raw material for almost all manufactured aluminum compounds. In the course of production of aluminum compounds, bauxite can be refined to aluminum hydroxide by the Bayer process, the Sinter process, and combinations thereof. Bauxites are typically classified according to their main mineralogical constituents as gibbsitic, boehmitic and diasporic. The mineralogical composition of bauxite can impact the method of processing.
  • the Sinter process often requires another step where a desilication additive such as lime is added to the green liquor to remove soluble silica species from the liquor.
  • a desilication additive such as lime is added to the green liquor to remove soluble silica species from the liquor.
  • the slurry is treated with flocculants and fed to a desilication settler to remove insoluble desilication products that include sodium aluminosilicates and calcium aluminosilicates.
  • the settled solids from the flocculation procedure known as mud, are withdrawn from the bottom of the mud settler and passed through a countercurrent washing circuit for recovery of sodium aluminate and soda.
  • the red mud and/or aluminate liquor may contain sodium
  • the suspended solids are preferably separated at a relatively fast rate if the overall process is to be efficient.
  • Efficient removal of suspended solids from process streams in processes to produce alumina has been addressed in a variety of maimers, including, but not limited to: employing polyacrylates as flocculants; using combinations of polyacrylates and starch in Bayer alumina recovery circuits; using polyacrylamide within the mud settler; treating different stages in the Bayer alumina recovery circuit with different flocculant compositions; removing suspended solids from Bayer alumina process streams by contacting and mixing a Bayer process stream with hydroxamated polymers; and using blends of hydroxamated polymer emulsions with polyacrylate emulsions to remove suspended solids from Bayer alumina process streams.
  • the silicon-containing polymer is generally configured to enhance flocculation of suspended solids in a process for digesting Bauxite ore.
  • Examples of silicon-containing polymers include polymers having pendant silane groups, e.g., silicon-containing pendant groups, of the Formula (I) attached thereto: -Si(OR) 3 (I)
  • each R is independently hydrogen, C 1-20 alkyl, C 2-20 alkenyl, C 6-12 aryl, C 7-20 aralkyl, a group I metal ion, a group II metal ion, or NR' 4 + ; where each R' is independently hydrogen, C 1-20 alkyl, C 2-20 alkenyl, C 6-12 aryl, and C 7-20 aralkyl; and where R and R' are each independently unsubstituted, or hydroxy-substituted.
  • R groups include lower alkyl groups, e.g., C 1-6 alkyl groups and C 1 . 3 alkyl groups; phenyl, benzyl, Na + , K + , and NH 4 + .
  • substituted alkyl or aryl groups can advantageously be employed.
  • the silicon-containing polymer may have at least 10%, 12%, 15%, or 20% of monomeric units having an -Si(OR) 3 group.
  • High content of -Si(OR) 3 groups present in the flocculant composition may increase the flocculation benefit of the flocculant composition.
  • the aqueous solution including the silicon-containing polymer may be made in a variety of manners.
  • a polymer backbone is synthesized by solution
  • the silicon-containing polymers can be made by polymerizing a monomer containing the group -Si(OR) 3 of Formula (1), or by
  • aminopropyltriethoxysilane p-aminophenyltriethoxysilane, 3-(m-aminophenoxypropyl)- trimethoxysilane, ⁇ -aminobutyltriethoxylsilane, and the like.
  • Other functional groups can be added to the polymer by reacting it with amines, alcohols, and other compounds.
  • the amount of the fu st recurring unit is at least about S % , preferably at least about 8 %, by number based on total number of recurring units in the polymer.
  • the polymer can comprise further recurrent units derived from vinyl monomers such as styrene, alkyl vinyl ether and N-vinylpyrrolidone.
  • the amount of the second recurring unit is at least about 8% e.g., at least about 10%, by number based on total number of recurring units in the polymer.
  • a 1 and A 2 are each independently a direct bond or an organic connecting group comprising from about 1 to about 20 carbons;
  • R “ H, optionally substituted C 1 -C 20 alkyl, optionally substituted C 6 -C 12 aryl, optionally substituted C 7 -C 20 aralkyl, optionally substituted C 2 -C 20 alkenyl, Group I metal ion, Group II metal ion, or NR 1 4 , where each R 1 is independently selected from H, optionally substituted C 1 -C 20 alkyl, optionally substituted C 6 -C 12 aryl, optionally substituted C 7 -C 20 aralkyl, and optionally substituted C 2 -C 20 alkenyl.
  • polymer PI may be used herein to refer to polymers comprising a recurring unit of the structure (I), optionally a recurring unit of the structure (II), and a recurring unit of the structure (III).
  • the polymer PI comprises recurring units of the structure (I) in which R" is a Group I metal ion (e.g., Na), a Group (II) metal ion (e.g., K) and/or NR ⁇ (e.g., ammonium).
  • R" is a Group I metal ion (e.g., Na), a Group (II) metal ion (e.g., K) and/or NR ⁇ (e.g., ammonium).
  • the amounts of recurring unit in the polymer PI may vary over a broad range.
  • the polymer PI comprises at least about 8 mole percent, preferably at least about 15 mole percent of recurring units of the structure (I), based on total moles of recurring units in the polymer
  • Q is optionally substituted C 1 -C 20 alkyl, optionally substituted C 6 -C 12 aryl, optionally substituted C 7 -C 20 aralkyl, or optionally substituted C 2 -C 20 alkenyl.
  • the aqueous solution including the silicon-containing polymer is intermixed with surfactant and oil at amounts and ratios sufficient to form a water-in-oil emulsion. While the weight ratio of the aqueous phase to hydrocarbon phase may vary widely, weight ratios in the range of about 4:1 to about 1 :1 are typically suitable.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Hydrology & Water Resources (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Colloid Chemistry (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
PCT/US2011/023866 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods for making and using the same Ceased WO2011100183A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
CN201180009227.7A CN102869437B (zh) 2010-02-12 2011-02-07 油包水乳液组合物及其制备和使用方法
EA201290785A EA022770B1 (ru) 2010-02-12 2011-02-07 Эмульсионные композиции "вода-в-масле", способ их получения и применения
BR112012019681A BR112012019681A2 (pt) 2010-02-12 2011-02-07 métodos para fazer uma composição em emulsão água em óleo e para floculação, e, composição em emulsão água em óleo
CA2789608A CA2789608A1 (en) 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods for making and using the same
JP2012552911A JP6306819B2 (ja) 2010-02-12 2011-02-07 油中水エマルジョン組成物およびそれの製造および使用方法
US13/578,271 US20160185613A1 (en) 2010-02-12 2011-02-07 Water-in-Oil Emulsion Compositions and Methods for Making and Using the Same
EP11708601.7A EP2533886B1 (en) 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods for making and using the same
AU2011216038A AU2011216038B2 (en) 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods for making and using the same
ES11708601.7T ES2675099T3 (es) 2010-02-12 2011-02-07 Composiciones de emulsión de agua en aceite y métodos de preparación y uso de las mismas
AP2012006425A AP2012006425A0 (en) 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods formaking and using the same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US30397210P 2010-02-12 2010-02-12
US61/303,972 2010-02-12

Publications (1)

Publication Number Publication Date
WO2011100183A1 true WO2011100183A1 (en) 2011-08-18

Family

ID=44226012

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2011/023866 Ceased WO2011100183A1 (en) 2010-02-12 2011-02-07 Water-in-oil emulsion compositions and methods for making and using the same

Country Status (12)

Country Link
US (1) US20160185613A1 (enExample)
EP (1) EP2533886B1 (enExample)
JP (1) JP6306819B2 (enExample)
CN (1) CN102869437B (enExample)
AP (1) AP2012006425A0 (enExample)
BR (1) BR112012019681A2 (enExample)
CA (1) CA2789608A1 (enExample)
EA (1) EA022770B1 (enExample)
ES (1) ES2675099T3 (enExample)
SA (1) SA111320188B1 (enExample)
TR (1) TR201809462T4 (enExample)
WO (1) WO2011100183A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220380662A1 (en) * 2021-05-25 2022-12-01 Shell Oil Company Hydraulic fracturing fluid

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106749829B (zh) * 2016-12-27 2018-04-10 广州市斯洛柯高分子聚合物有限公司 一种超分散剂及其制备方法
CN107573450B (zh) * 2017-09-21 2020-12-18 东华大学 一种分散染料墨水用聚羧酸盐类分散剂及其制备方法和应用
EP4251571A1 (en) * 2020-11-26 2023-10-04 Kemira OYJ Method for producing coagulant aluminium salts

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3734873A (en) 1970-12-15 1973-05-22 Nalco Chemical Co Rapid dissolving water-soluble polymers
US4698178A (en) * 1984-10-03 1987-10-06 Th. Goldschmidt Ag Use of polyoxyalkylene-polysiloxane copolymers with silicon-linked, long-chain alkyl radicals as emulsifiers for the preparation of water/oil emulsions
GB2315757A (en) * 1996-07-31 1998-02-11 Gen Electric Dilution stable antifoam emulsion concentrate
US5883181A (en) * 1993-11-24 1999-03-16 Cytec Technology Corp. Multimodal emulsions and processes for preparing multimodal emulsions
US6814873B2 (en) 2002-07-22 2004-11-09 Cytec Technology Corp. Method of preventing or reducing aluminosilicate scale in a bayer process
US20080257827A1 (en) 2007-04-20 2008-10-23 Qi Dai Use of silicon-containing polymers to improve red mud flocculation in the bayer process

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5264027A (en) * 1992-08-11 1993-11-23 Wacker Silicones Corporation Detergent resistant compositions
CA2177157A1 (en) * 1993-11-24 1995-06-01 Huann-Lin Chen Multimodal emulsions and processes for preparing multimodal emulsions
JP3693208B2 (ja) * 1997-03-04 2005-09-07 東北リコー株式会社 孔版印刷用w/o型エマルションインキ
CN101658736B (zh) * 2005-02-25 2013-05-29 Cytec技术有限公司 异羟肟酸化聚合物的水包油包水乳液及其使用方法
CN1986644A (zh) * 2005-12-21 2007-06-27 汉高股份两合公司 稳定的硅烷化聚合物乳液及其制备方法和应用

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3734873A (en) 1970-12-15 1973-05-22 Nalco Chemical Co Rapid dissolving water-soluble polymers
US4698178A (en) * 1984-10-03 1987-10-06 Th. Goldschmidt Ag Use of polyoxyalkylene-polysiloxane copolymers with silicon-linked, long-chain alkyl radicals as emulsifiers for the preparation of water/oil emulsions
US5883181A (en) * 1993-11-24 1999-03-16 Cytec Technology Corp. Multimodal emulsions and processes for preparing multimodal emulsions
GB2315757A (en) * 1996-07-31 1998-02-11 Gen Electric Dilution stable antifoam emulsion concentrate
US6814873B2 (en) 2002-07-22 2004-11-09 Cytec Technology Corp. Method of preventing or reducing aluminosilicate scale in a bayer process
US20080257827A1 (en) 2007-04-20 2008-10-23 Qi Dai Use of silicon-containing polymers to improve red mud flocculation in the bayer process

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220380662A1 (en) * 2021-05-25 2022-12-01 Shell Oil Company Hydraulic fracturing fluid
US11739257B2 (en) * 2021-05-25 2023-08-29 Shell Usa, Inc. Hydraulic fracturing fluid

Also Published As

Publication number Publication date
CA2789608A1 (en) 2011-08-18
AU2011216038A1 (en) 2012-08-30
EP2533886A1 (en) 2012-12-19
BR112012019681A2 (pt) 2016-05-03
JP6306819B2 (ja) 2018-04-04
TR201809462T4 (tr) 2018-07-23
CN102869437A (zh) 2013-01-09
JP2013519506A (ja) 2013-05-30
AP2012006425A0 (en) 2012-08-31
EP2533886B1 (en) 2018-04-11
EA201290785A1 (ru) 2013-01-30
US20160185613A1 (en) 2016-06-30
SA111320188B1 (ar) 2015-06-10
EA022770B1 (ru) 2016-02-29
ES2675099T3 (es) 2018-07-06
CN102869437B (zh) 2015-10-21

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