NO123112B - - Google Patents

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Info

Publication number: NO123112B
Authority: NO; Norway
Prior art keywords: water; flotation; reaction; residue; solution
Prior art date: 1966-04-30

Application number

NO167888A

Other languages

English (en)

Norwegian (no)

Inventor

W Lehmann

H Siemann

H Tretter

Original Assignee

Bayer Ag

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.)

1966-04-30

Filing date

1967-04-26

Publication date

1971-09-27

1967-04-26 Application filed by Bayer Ag filed Critical Bayer Ag

1971-09-27 Publication of NO123112B publication Critical patent/NO123112B/no

Links

239000008396 flotation agent Substances 0.000 claims description 19
239000002351 wastewater Substances 0.000 claims description 15
238000006243 chemical reaction Methods 0.000 claims description 14
125000003277 amino group Chemical group 0.000 claims description 13
150000002170 ethers Chemical class 0.000 claims description 10
229920005862 polyol Polymers 0.000 claims description 9
150000003077 polyols Chemical class 0.000 claims description 9
239000000835 fiber Substances 0.000 claims description 8
239000000945 filler Substances 0.000 claims description 8
-1 sulfhydryl compound Chemical class 0.000 claims description 8
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
238000005956 quaternization reaction Methods 0.000 claims description 6
238000011084 recovery Methods 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
125000001033 ether group Chemical group 0.000 claims description 5
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 5
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 4
XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 claims description 4
125000004966 cyanoalkyl group Chemical group 0.000 claims description 4
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
229920000768 polyamine Polymers 0.000 claims description 4
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
239000001301 oxygen Substances 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
229920000233 poly(alkylene oxides) Polymers 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
239000002699 waste material Substances 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
229920001515 polyalkylene glycol Polymers 0.000 claims 1
239000000243 solution Substances 0.000 description 27
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
239000007864 aqueous solution Substances 0.000 description 16
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
230000000694 effects Effects 0.000 description 10
238000005188 flotation Methods 0.000 description 10
239000007795 chemical reaction product Substances 0.000 description 8
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 7
238000003756 stirring Methods 0.000 description 7
150000001412 amines Chemical class 0.000 description 6
239000002253 acid Substances 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
229920001223 polyethylene glycol Polymers 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 4
239000000047 product Substances 0.000 description 4
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 3
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 3
238000001816 cooling Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
UYBWIEGTWASWSR-UHFFFAOYSA-N 1,3-diaminopropan-2-ol Chemical compound NCC(O)CN UYBWIEGTWASWSR-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
150000002924 oxiranes Chemical class 0.000 description 2
238000004806 packaging method and process Methods 0.000 description 2
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
239000002994 raw material Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 2
NSQSYCXRUVZPKI-UHFFFAOYSA-N 3-(2-aminoethylamino)propanenitrile Chemical compound NCCNCCC#N NSQSYCXRUVZPKI-UHFFFAOYSA-N 0.000 description 1
KRPRVQWGKLEFKN-UHFFFAOYSA-N 3-(3-aminopropoxy)propan-1-amine Chemical compound NCCCOCCCN KRPRVQWGKLEFKN-UHFFFAOYSA-N 0.000 description 1
QPIOXOJERGNNMX-UHFFFAOYSA-N 3-(3-aminopropylsulfanyl)propan-1-amine Chemical compound NCCCSCCCN QPIOXOJERGNNMX-UHFFFAOYSA-N 0.000 description 1
NBYAQKGCTNTFGK-UHFFFAOYSA-N 3-[1-(3-aminopropoxy)-2,2-dimethylpropoxy]propan-1-amine Chemical compound NCCCOC(C(C)(C)C)OCCCN NBYAQKGCTNTFGK-UHFFFAOYSA-N 0.000 description 1
BGMWVSZXPICMNL-UHFFFAOYSA-N 3-[2,3-bis(3-aminopropoxy)propoxy]propan-1-amine Chemical compound NCCCOCC(OCCCN)COCCCN BGMWVSZXPICMNL-UHFFFAOYSA-N 0.000 description 1
POTQBGGWSWSMCX-UHFFFAOYSA-N 3-[2-(3-aminopropoxy)ethoxy]propan-1-amine Chemical compound NCCCOCCOCCCN POTQBGGWSWSMCX-UHFFFAOYSA-N 0.000 description 1
AGWNPPHYGKSJKF-UHFFFAOYSA-N 3-[2-(3-aminopropylsulfanyl)ethylsulfanyl]propan-1-amine Chemical compound NCCCSCCSCCCN AGWNPPHYGKSJKF-UHFFFAOYSA-N 0.000 description 1
CJCOYIXVZLLXHJ-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)phenoxy]propan-1-amine Chemical compound NCCCOC1=CC=C(OCCCN)C=C1 CJCOYIXVZLLXHJ-UHFFFAOYSA-N 0.000 description 1
XUSNPFGLKGCWGN-UHFFFAOYSA-N 3-[4-(3-aminopropyl)piperazin-1-yl]propan-1-amine Chemical compound NCCCN1CCN(CCCN)CC1 XUSNPFGLKGCWGN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
229920002873 Polyethylenimine Polymers 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
235000011187 glycerol Nutrition 0.000 description 1
TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
DILRJUIACXKSQE-UHFFFAOYSA-N n',n'-dimethylethane-1,2-diamine Chemical compound CN(C)CCN DILRJUIACXKSQE-UHFFFAOYSA-N 0.000 description 1
WOVJRSMTQMZAJS-UHFFFAOYSA-N n,n'-bis(3-aminopropyl)hexane-1,6-diamine Chemical compound NCCCNCCCCCCNCCCN WOVJRSMTQMZAJS-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
238000004064 recycling Methods 0.000 description 1
230000035939 shock Effects 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/32—Epoxy compounds containing three or more epoxy groups
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/24—Treatment of water, waste water, or sewage by flotation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21F—PAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
- D21F1/00—Wet end of machines for making continuous webs of paper
- D21F1/66—Pulp catching, de-watering, or recovering; Re-use of pulp-water
- D21F1/70—Pulp catching, de-watering, or recovering; Re-use of pulp-water by flotation

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Hydrology & Water Resources (AREA)
Engineering & Computer Science (AREA)
Environmental & Geological Engineering (AREA)
Water Supply & Treatment (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Paper (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Epoxy Resins (AREA)

NO167888A 1966-04-30 1967-04-26 NO123112B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEF0049081		1966-04-30

Publications (1)

Publication Number	Publication Date
NO123112B true NO123112B (de)	1971-09-27

Family

ID=7102715

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO167888A NO123112B (de)	1966-04-30	1967-04-26

Country Status (8)

Country	Link
US (1)	US3575797A (de)
AT (1)	AT275312B (de)
CH (1)	CH487299A (de)
DE (1)	DE1546290A1 (de)
FI (1)	FI45254C (de)
GB (1)	GB1179493A (de)
NO (1)	NO123112B (de)
SE (1)	SE326368B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE816132A (fr) *	1973-06-11	1974-12-10		Nouveaux polymeres d'ionenes et procedes pour leur preparation
DE2436386C2 (de) *	1974-07-29	1982-09-23	Basf Ag, 6700 Ludwigshafen	Verwendung stickstoffhaltiger Kondensationsprodukte
DE2733973A1 (de) *	1977-07-28	1979-02-15	Basf Ag	Wasserloesliche, vernetzte stickstoffhaltige kondensationsprodukte
FI89729C (fi) *	1992-04-14	1993-11-10	Keskuslaboratorio	Foerfarande foer separering och aotervinning av pigment
PE20100438A1 (es) *	2008-06-05	2010-07-14	Georgia Pacific Chemicals Llc	Composicion de suspension acuosa con particulas de materiales valiosos e impurezas
WO2010101745A1 (en)	2009-03-04	2010-09-10	Dow Global Technologies Inc.	Thermosettable composition containing a glycidylether based on trimethyolpropane octadecaethoxilate
CN113402000A (zh) *	2021-05-10	2021-09-17	中海油(天津)油田化工有限公司	一种油田含油污水处理用浮选剂及其制备方法

1966
- 1966-04-30 DE DE19661546290 patent/DE1546290A1/de active Pending
1967
- 1967-04-18 FI FI671141A patent/FI45254C/fi active
- 1967-04-25 US US633383A patent/US3575797A/en not_active Expired - Lifetime
- 1967-04-26 NO NO167888A patent/NO123112B/no unknown
- 1967-04-26 SE SE05910/67A patent/SE326368B/xx unknown
- 1967-04-27 CH CH602567A patent/CH487299A/de not_active IP Right Cessation
- 1967-04-28 GB GB09654/67A patent/GB1179493A/en not_active Expired
- 1967-04-28 AT AT404367A patent/AT275312B/de active

Also Published As

Publication number	Publication date
FI45254B (de)	1971-12-31
GB1179493A (en)	1970-01-28
AT275312B (de)	1969-10-27
SE326368B (de)	1970-07-20
US3575797A (en)	1971-04-20
FI45254C (fi)	1972-04-10
DE1546290A1 (de)	1970-02-26
CH487299A (de)	1970-03-15

Publication	Publication Date	Title
US4144123A (en)	1979-03-13	Incorporating a crosslinked polyamidoamine condensation product into paper-making pulp
US3855158A (en)	1974-12-17	Resinous reaction products
DE69829410T2 (de)	2006-04-13	Verfahren zur aufbereitung von nassfestem papier
US3899388A (en)	1975-08-12	Treating compositions
FI64179B (fi)	1983-06-30	Vattenloesliga amidgrupper innehaollande polyaminer och deras anvaendning
US3893885A (en)	1975-07-08	Auxiliaries for the manufacture of paper
US3753931A (en)	1973-08-21	Polyether amines their production and use
JPS6351177B2 (de)	1988-10-13
US3215654A (en)	1965-11-02	Process for preparing aqueous solutions of alkylated aminopolyamide-epichlorohydrin resins and use of same as retention aids
US4066494A (en)	1978-01-03	Nitrogenous condensation products used as retention aids in papermaking
US3694390A (en)	1972-09-26	Epoxidized polyamide resin forming stable aqueous solutions of high concentration
US4250112A (en)	1981-02-10	Polyalkylenepolyamines containing quaternary dialkylammonium groups
KR840002011A (ko)	1984-06-11	경화성 폴리(옥사졸리돈 및 우레탄) 조성물 및 그 제법
NO123112B (de)	1971-09-27
NL8103917A (nl)	1982-04-01	Gemodificeerd aminopolyol, werkwijze voor de bereiding hiervan en werkwijze voor de bereiding van stijf polyurethanschuim op basis van het aminopolyol.
US4198269A (en)	1980-04-15	Quaternary ammonium salts of epihalohydrin polymers as additives for fibrous cellulosic materials
EP0763073B1 (de)	2000-01-19	Nassfeste harzzusammensetzung und verfahren für ihre herstellung
US3715335A (en)	1973-02-06	Linear polyester backbone quaternary ammonium polyelectrolytes
CA1218664A (en)	1987-03-03	Ammonium polyamidoamines
US3086961A (en)	1963-04-23	Water-soluble dibasic acid-polyalkylenepolyamine-alkylene glycol crosslinked polymer
US4156775A (en)	1979-05-29	Quaternary ammonium salts of epihalohydrin polymers as additives for fibrous materials
FI64178B (fi)	1983-06-30	Amidgrupper innehaollande vattenloesliga icke-sjaelvtvaerbindande polyaminer och deras anvaendning
US4673729A (en)	1987-06-16	Paper auxiliary from condensation product of aliphatic polyol-ether-amine and compound polyfunctional toward amino groups
US3372085A (en)	1968-03-05	Water-soluble polyalkylenepolyamine/urethane resins and application thereof in production of wet strength paper
US3702351A (en)	1972-11-07	Cationic thermosetting resins containing the reaction product of a carboxyl terminated polyester with an epoxy amine adduct treated with epichlorohydrin