NO127403B - - Google Patents

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Info

Publication number: NO127403B
Authority: NO; Norway
Prior art keywords: polyamines; polyamine; acid; alkylene; solution
Prior art date: 1968-01-05

Application number

NO6924A

Other languages

English (en)

Norwegian (no)

Inventor

Iii J Longoria

Original Assignee

Dow Chemical Co

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.)

1968-01-05

Filing date

1969-01-03

Publication date

1973-06-18

1969-01-03 Application filed by Dow Chemical Co filed Critical Dow Chemical Co

1973-06-18 Publication of NO127403B publication Critical patent/NO127403B/no

Links

229920000768 polyamine Polymers 0.000 claims description 39
239000002738 chelating agent Substances 0.000 claims description 13
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 9
229920001281 polyalkylene Polymers 0.000 claims description 9
239000003381 stabilizer Substances 0.000 claims description 9
-1 alkylene imine Chemical class 0.000 claims description 8
229920000642 polymer Polymers 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
230000015556 catabolic process Effects 0.000 claims description 7
238000006731 degradation reaction Methods 0.000 claims description 6
238000002845 discoloration Methods 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 5
229910052783 alkali metal Inorganic materials 0.000 claims description 4
150000001340 alkali metals Chemical group 0.000 claims description 3
239000000243 solution Substances 0.000 description 11
239000000126 substance Substances 0.000 description 5
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
229920002873 Polyethylenimine Polymers 0.000 description 3
239000002253 acid Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
229910001385 heavy metal Inorganic materials 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
230000006641 stabilisation Effects 0.000 description 3
238000011105 stabilization Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000013522 chelant Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000006260 foam Substances 0.000 description 2
150000002466 imines Chemical class 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
150000003624 transition metals Chemical class 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
FSVCELGFZIQNCK-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)glycine Chemical compound OCCN(CCO)CC(O)=O FSVCELGFZIQNCK-UHFFFAOYSA-N 0.000 description 1
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
JYXGIOKAKDAARW-UHFFFAOYSA-N N-(2-hydroxyethyl)iminodiacetic acid Chemical compound OCCN(CC(O)=O)CC(O)=O JYXGIOKAKDAARW-UHFFFAOYSA-N 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000012496 blank sample Substances 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
238000010538 cationic polymerization reaction Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
235000019441 ethanol Nutrition 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000007863 gel particle Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
239000003607 modifier Substances 0.000 description 1
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 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229960003330 pentetic acid Drugs 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000333 poly(propyleneimine) Polymers 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000013055 pulp slurry Substances 0.000 description 1
239000000523 sample Substances 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
239000010865 sewage Substances 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
239000004753 textile Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/175—Amines; Quaternary ammonium compounds containing COOH-groups; Esters or salts thereof
- G—PHYSICS
- G04—HOROLOGY
- G04F—TIME-INTERVAL MEASURING
- G04F5/00—Apparatus for producing preselected time intervals for use as timing standards

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Paper (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO6924A 1968-01-05 1969-01-03 NO127403B (zh)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US69583568A	1968-01-05	1968-01-05

Publications (1)

Publication Number	Publication Date
NO127403B true NO127403B (zh)	1973-06-18

Family

ID=24794657

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO6924A NO127403B (zh)	1968-01-05	1969-01-03

Country Status (11)

Country	Link
US (1)	US3577556A (zh)
BE (1)	BE726474A (zh)
CH (1)	CH514647A (zh)
DE (1)	DE1900308A1 (zh)
DK (1)	DK122188B (zh)
FI (1)	FI48846C (zh)
FR (1)	FR1604456A (zh)
GB (1)	GB1214123A (zh)
NL (1)	NL6900083A (zh)
NO (1)	NO127403B (zh)
SE (1)	SE354869B (zh)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2402702A1 (fr) *	1977-09-13	1979-04-06	Air Liquide	Procede d'epoxydation d'huiles
US4602108A (en) *	1984-08-01	1986-07-22	Ethyl Corporation	Alkyl amine color inhibitor
JPH0657240B2 (ja) *	1985-10-31	1994-08-03	アイコ−株式会社	脱臭剤
US5808150A (en) *	1997-08-14	1998-09-15	Concept Sciences, Inc.	Stabilization of hydroxylamine solutions
EP0924293B2 (en) †	1997-11-24	2009-11-11	The Procter & Gamble Company	Use of a crystal growth inhibitor to reduce fabric abrasion
CN102741310B (zh)	2010-01-08	2016-04-27	亨斯迈石油化学有限责任公司	胺氧化的抑制

1968
- 1968-01-05 US US695835A patent/US3577556A/en not_active Expired - Lifetime
- 1968-12-30 SE SE17990/68A patent/SE354869B/xx unknown
- 1968-12-30 FI FI683752A patent/FI48846C/fi active
- 1968-12-31 FR FR1604456D patent/FR1604456A/fr not_active Expired
1969
- 1969-01-03 NO NO6924A patent/NO127403B/no unknown
- 1969-01-03 NL NL6900083A patent/NL6900083A/xx unknown
- 1969-01-03 BE BE726474D patent/BE726474A/xx unknown
- 1969-01-03 DK DK5469AA patent/DK122188B/da unknown
- 1969-01-03 GB GB615/69A patent/GB1214123A/en not_active Expired
- 1969-01-03 DE DE19691900308 patent/DE1900308A1/de active Pending
- 1969-01-06 CH CH8269A patent/CH514647A/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
FR1604456A (zh)	1971-11-08
FI48846B (zh)	1974-09-30
NL6900083A (zh)	1969-07-08
SE354869B (zh)	1973-03-26
BE726474A (zh)	1969-07-03
GB1214123A (en)	1970-12-02
DK122188B (da)	1972-01-31
FI48846C (fi)	1975-01-10
CH8269A4 (zh)	1971-12-15
US3577556A (en)	1971-05-04
CH514647A (de)	1971-12-15
DE1900308A1 (de)	1969-09-04

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