CS226911B1 - Polymere polydonor komplexons and method of their manufacture polymere polydonor - Google Patents

Polymere polydonor komplexons and method of their manufacture polymere polydonor Download PDF

Info

Publication number: CS226911B1
Authority: CS; Czechoslovakia
Prior art keywords: polydonor; alkyl; polymeric; optionally; atoms
Prior art date: 1981-10-28

Application number

CS817919A

Other languages

Czech (cs)

English (en)

Inventor

Jaroslav Kahovec

Zdenek Matejka

Josef Tomasek

Original Assignee

Jaroslav Kahovec

Zdenek Matejka

Josef Tomasek

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.)

1981-10-28

Filing date

1981-10-28

Publication date

1984-04-16

1981-10-28 Application filed by Jaroslav Kahovec, Zdenek Matejka, Josef Tomasek filed Critical Jaroslav Kahovec

1981-10-28 Priority to CS817919A priority Critical patent/CS226911B1/cs

1982-10-19 Priority to DD82244155A priority patent/DD233034A3/de

1982-10-28 Priority to GB08230876A priority patent/GB2115422B/en

1982-10-28 Priority to DE19823240006 priority patent/DE3240006A1/de

1982-10-29 Priority to CA000414533A priority patent/CA1187250A/en

1982-10-29 Priority to US06/437,619 priority patent/US4407978A/en

1984-04-16 Publication of CS226911B1 publication Critical patent/CS226911B1/cs

Links

238000000034 method Methods 0.000 title claims description 4
238000004519 manufacturing process Methods 0.000 title claims 2
229920000642 polymer Polymers 0.000 claims abstract description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
125000000217 alkyl group Chemical group 0.000 claims abstract description 9
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims abstract description 7
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
239000012442 inert solvent Substances 0.000 claims abstract description 3
150000003512 tertiary amines Chemical class 0.000 claims abstract description 3
-1 polyethylene Polymers 0.000 claims description 9
229920002873 Polyethylenimine Polymers 0.000 claims description 6
125000000896 monocarboxylic acid group Chemical group 0.000 claims description 5
239000004698 Polyethylene Substances 0.000 claims description 4
239000004793 Polystyrene Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
150000004676 glycans Chemical class 0.000 claims description 4
229920000058 polyacrylate Polymers 0.000 claims description 4
229920000573 polyethylene Polymers 0.000 claims description 4
229920000193 polymethacrylate Polymers 0.000 claims description 4
229920001282 polysaccharide Polymers 0.000 claims description 4
239000005017 polysaccharide Substances 0.000 claims description 4
229920002223 polystyrene Polymers 0.000 claims description 4
230000004048 modification Effects 0.000 claims description 3
238000012986 modification Methods 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 2
150000001875 compounds Chemical class 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 abstract description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
229910052760 oxygen Inorganic materials 0.000 abstract 1
239000001301 oxygen Substances 0.000 abstract 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
239000010949 copper Substances 0.000 description 20
239000000047 product Substances 0.000 description 12
229910052757 nitrogen Inorganic materials 0.000 description 11
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 10
229910052802 copper Inorganic materials 0.000 description 10
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
238000001179 sorption measurement Methods 0.000 description 10
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 8
238000002329 infrared spectrum Methods 0.000 description 8
239000000203 mixture Substances 0.000 description 8
229960003330 pentetic acid Drugs 0.000 description 8
UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 7
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 6
RAZLJUXJEOEYAM-UHFFFAOYSA-N 2-[bis[2-(2,6-dioxomorpholin-4-yl)ethyl]azaniumyl]acetate Chemical compound C1C(=O)OC(=O)CN1CCN(CC(=O)O)CCN1CC(=O)OC(=O)C1 RAZLJUXJEOEYAM-UHFFFAOYSA-N 0.000 description 5
150000001408 amides Chemical class 0.000 description 5
150000007942 carboxylates Chemical class 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
229920002678 cellulose Polymers 0.000 description 4
239000001913 cellulose Substances 0.000 description 4
150000002148 esters Chemical group 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
229910001385 heavy metal Inorganic materials 0.000 description 3
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
FCKYPQBAHLOOJQ-UHFFFAOYSA-N Cyclohexane-1,2-diaminetetraacetic acid Chemical compound OC(=O)CN(CC(O)=O)C1CCCCC1N(CC(O)=O)CC(O)=O FCKYPQBAHLOOJQ-UHFFFAOYSA-N 0.000 description 2
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
RUSUZAGBORAKPY-UHFFFAOYSA-N acetic acid;n'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCNCCNCCN RUSUZAGBORAKPY-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
DEFVIWRASFVYLL-UHFFFAOYSA-N ethylene glycol bis(2-aminoethyl)tetraacetic acid Chemical compound OC(=O)CN(CC(O)=O)CCOCCOCCN(CC(O)=O)CC(O)=O DEFVIWRASFVYLL-UHFFFAOYSA-N 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
150000002739 metals Chemical class 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
RAEOEMDZDMCHJA-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-[2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]ethyl]amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CCN(CC(O)=O)CC(O)=O)CC(O)=O RAEOEMDZDMCHJA-UHFFFAOYSA-N 0.000 description 1
POLIXZIAIMAECK-UHFFFAOYSA-N 4-[2-(2,6-dioxomorpholin-4-yl)ethyl]morpholine-2,6-dione Chemical compound C1C(=O)OC(=O)CN1CCN1CC(=O)OC(=O)C1 POLIXZIAIMAECK-UHFFFAOYSA-N 0.000 description 1
229920001661 Chitosan Polymers 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
238000005642 Gabriel synthesis reaction Methods 0.000 description 1
101100383120 Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) cdcH gene Proteins 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
239000003929 acidic solution Substances 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
238000005576 amination reaction Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
125000006159 dianhydride group Chemical group 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
238000009854 hydrometallurgy Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
125000001841 imino group Chemical group [H]N=* 0.000 description 1
NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
229910021645 metal ion Inorganic materials 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000007747 plating Methods 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
239000002594 sorbent Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000002351 wastewater Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/10—Acylation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines

Landscapes

Chemical & Material Sciences (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Solid-Sorbent Or Filter-Aiding Compositions (AREA)

CS817919A 1981-10-28 1981-10-28 Polymere polydonor komplexons and method of their manufacture polymere polydonor CS226911B1 (en)

Priority Applications (6)

Application Number	Priority Date	Filing Date	Title
CS817919A CS226911B1 (en)	1981-10-28	1981-10-28	Polymere polydonor komplexons and method of their manufacture polymere polydonor
DD82244155A DD233034A3 (de)	1981-10-28	1982-10-19	Polymere polydonorkomplexone und verfahren zu ihrer gewinnung
GB08230876A GB2115422B (en)	1981-10-28	1982-10-28	A polymeric polydonor complexon and the method for preparation thereof
DE19823240006 DE3240006A1 (de)	1981-10-28	1982-10-28	Polymere polydonorkomplexone, ihre herstellung und verwendung
CA000414533A CA1187250A (en)	1981-10-28	1982-10-29	Polymeric polydonor complexons and the method thereof
US06/437,619 US4407978A (en)	1981-10-28	1982-10-29	Polymeric polydonor complexons and method for preparation thereof

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS817919A CS226911B1 (en)	1981-10-28	1981-10-28	Polymere polydonor komplexons and method of their manufacture polymere polydonor

Publications (1)

Publication Number	Publication Date
CS226911B1 true CS226911B1 (en)	1984-04-16

Family

ID=5429141

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS817919A CS226911B1 (en)	1981-10-28	1981-10-28	Polymere polydonor komplexons and method of their manufacture polymere polydonor

Country Status (6)

Country	Link
US (1)	US4407978A (de)
CA (1)	CA1187250A (de)
CS (1)	CS226911B1 (de)
DD (1)	DD233034A3 (de)
DE (1)	DE3240006A1 (de)
GB (1)	GB2115422B (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0331829A1 (de) *	1988-03-10	1989-09-13	The Dow Chemical Company	Chelatbildende Harze und Herstellung davon
US4732946A (en) *	1983-12-08	1988-03-22	The Dow Chemical Company	Process for the preparation of chelation resins
DE3703922A1 (de) *	1987-02-09	1988-08-18	Sonnenschein Accumulatoren	Verfahren zum entfernen von schwermetallen aus boeden
DE4012099A1 (de) *	1990-04-14	1991-10-17	Meyer Fa Rud Otto	Verfahren zur selektiven abtrennung von zweiwertigen metallionen aus waessrigen loesungen
EP0554407A1 (de) *	1990-10-26	1993-08-11	Genta Incorporated	Nichtaromatische organische polymerreagentien für die festphasensynthese von oligomeren
DE4141889C2 (de) *	1991-12-18	1993-10-07	Fraunhofer Ges Forschung	Verfahren zur Entfernung von Schwermetallen
ES2140469T3 (es) *	1992-10-14	2000-03-01	Nycomed Imaging As	Composiciones y metodos terapeuticos y de diagnostico por obtencion de imagenes.
US5817292A (en) *	1992-10-14	1998-10-06	Nycomed Imaging As	MR imaging compositions and methods
WO1994009056A1 (en) *	1992-10-14	1994-04-28	Sterling Winthrop Inc.	Chelating polymers
GB2292943A (en) *	1994-08-09	1996-03-13	Univ Surrey	Metal ion ligating materials
DE19507803C2 (de) *	1995-03-06	2003-05-08	Gsf Forschungszentrum Umwelt	Verfahren zur Reduzierung der Schwermetallgehalte von schwermetallhaltigen Verbrennungs- und Pyrolyserückständen
KR100327576B1 (ko) *	1999-06-26	2002-03-14	박종섭	193ｎｍＡｒＦ광을 이용한 초미세 패턴 형성 공정에서 반사방지막으로 사용할 수 있는 유기 반사방지 중합체 및 그의 제조방법
ES2524786T5 (es) *	2007-08-06	2019-06-19	Max Planck Gesellschaft	Uso de quelantes inmovilizados para purificación de proteínas recombinantes por cromatografía de iones metálicos inmovilizados y método de purificación de proteínas recombinantes

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3957362A (en) *	1972-10-02	1976-05-18	Corneal Sciences, Inc.	Hydrogels and articles made therefrom
CH621561A5 (en) *	1974-01-14	1981-02-13	Ceskoslovenska Akademie Ved	Process for producing a bromocyan-activated, hydrophilic, polymeric carrier for biologically active compounds in dried form
US4281233A (en) *	1977-05-03	1981-07-28	Ceskoslovenska Akademie Ved	Hydrophilic macroporous three dimensional copolymers of hydroxyalkyl acrylates or methacrylates with crosslinking agents and the method of their manufacturing

1981
- 1981-10-28 CS CS817919A patent/CS226911B1/cs unknown
1982
- 1982-10-19 DD DD82244155A patent/DD233034A3/de not_active IP Right Cessation
- 1982-10-28 DE DE19823240006 patent/DE3240006A1/de not_active Withdrawn
- 1982-10-28 GB GB08230876A patent/GB2115422B/en not_active Expired
- 1982-10-29 CA CA000414533A patent/CA1187250A/en not_active Expired
- 1982-10-29 US US06/437,619 patent/US4407978A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
CA1187250A (en)	1985-05-14
DD233034A3 (de)	1986-02-19
GB2115422A (en)	1983-09-07
US4407978A (en)	1983-10-04
DE3240006A1 (de)	1983-07-07
GB2115422B (en)	1985-04-03

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