US4166804A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Polymeric color indicators and a method of their preparation
Assignee: Czech Academy of Sciences
•
Filing: 1977-10-14
•
Granted: 1979-09-04
•
Expires: 1997-10-14
Abstract
Abstract Polymeric color pH indicators are prepared which are insoluble in the measured aqueous medium and show a certain range of color change. These polymeric indicators are the product of copolymerization of a hydrophilic comonomer, selected from esters, amides and N-substituted amides of acrylic and methacrylic acid, with 0.1- 30 wt.% of a comonomer. The comonomer forms the pH-indicating color center by a subsequent coupling with a suitable diazonium salt or a passive component. Vinylic monomers comprising an aromatic system in the molecule are suitable as the functional comonomers. The indicators are prepared by radical copolymerization of the comonomers either in a suspension or in a solution, followed by the subsequent coupling with a diazonium compound, or diazotizing and coupling with a passive component, to obtain the pH-indicating sites of polymer. The product is in the form of small spherical macroporous particles suitable for pH indication in flow-through column processes, in small volumes, or on a microscope stage, or in the form of a solution applicable as a paint and indicating the pH of vessels, reactors, etc. coated therewith, or useful for application to inert carriers.
Inventors
- 👤 Miroslav Bleha
- 👤 Zdenek Plichta
- 👤 Eva Votavova
- 👤 Jaroslav Kalal
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 22:44
CPC Classifications
G; G01; G01N; G01N31/00; G01N31/22; G01N31/221
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
106 words
Polymeric color changing pH indicators insoluble in aqueous medium when used for pH measurement thereof, said indicators being prepared by free radical polymerization of at least one comonomer selected from the group consisting of acrylic esters, methacrylic esters, acrylamide, methacrylamide, N-methylacrylamide, N-methylmethacrylamide, N-ethylacrylamide, N-ethylmethacrylamide, N-hydroxypropylmethacrylamide, and N-hydroxypropylmethylacrylamide, with from 0.1 to 30 weight percent of a functional monomer selected from the group consisting of N-ethyl-N-(2-methacryloyl) aniline and N-ethyl-N-(2-methacryloylethyl)-N'-acetyl-p-phenylenediamine to form a polymer, subsequently diazo-coupling said polymer with an aromatic active agent through the available functional sites of said monomer and functionally active sites of said agent. to set a pH color indicating center in said polymer.
Claim 2
Dependent Claim
106 words
Polymeric color changing pH indicators insoluble in aqueous medium when used for pH measurement thereof, said indicators being prepared by free radical polymerization of at least one comonomer selected from the group consisting of acrylic esters, methacrylic esters, acrylamide, methacrylamide, N-methylacrylamide, N-methylmethacrylamide, N-ethylacrylamide, N-ethylmethacrylamide, N-hydroxypropylmethacrylamide, and N-hydroxypropylmethylacrylamide, with from 0.1 to 30 weight percent of a functional monomer selected from the group consisting of N-ethyl-N-(2-methacryloyl) aniline and N-ethyl-N-(2-methacryloylethyl)-N'-acetyl-p-phenylenediamine to form a polymer, subsequently diazo-coupling said polymer with an aromatic active agent through the available functional sites of said monomer and functionally active sites of said agent. to set a pH color indicating center in said polymer.
Claim 3
Dependent Claim
25 words
Polymeric color changing pH indicators according to claim 1 wherein said active agent comprises a diazotized aromatic amine and said functional monomer is N-ethyl-N-(2-methylcryloylethyl) aniline.
Claim 4
Dependent Claim
43 words
Polymeric color changing pH indicators according to claim 2 wherein said aromatic amine is selected from the group consisting of aniline and its carboxy, sulfo, hydroxy, and amino derivatives; β -naphthylamine, α-naphthylamine, and their sulfo, carboxy, and amino derivatives; aminoanthraquinone and derivatives thereof.
Claim 5
Dependent Claim
51 words
Polymeric color changing pH indicators according to claim 1 wherein said active agent is selected from the group consisting of phenol derivatives; α-and β -naphthols and their sulfo or amino and hydroxy derivatives; derivatives of 1-methyl-3-phenyl-5-pyrazolon; and amino derivatives of naphthalene; said functional monmer is n=ethyl-N-(2-methacryloylethyl)-N'-acetyl-p-phenylenediamine, and said polymer is diazotized.
Claim 6
Dependent Claim
107 words
Method for preparing polymeric color changing pH indicators insoluble in aqueous medium when used for pH measurement comprising the steps of free radical polymerizing at least one comonomer selected from the group consisting of acrylic esters, methacrylic esters, acrylamide, methacrylamide, N-methylacrylamide, N-methylmethacrylamide, N-ethylacrylamide, N-ethylemelhacrylamide, N-hydroxypropylacrylamide, and N-hydroxypropylmethacrylamide, with from 0.1 to 30 weight percent of a functional monomer selected from the group, consisting of N-ethyl-N-(2-methacryloylethyl) aniline and N-ethyl-N-(2-methacryloylethyl)-N-acetyl-phenylenediamine, to form a polymer, subsequently diazo coupling said polymer with an aromatic, active agent through the available functional sites of said monomer and functionally active sites of said agent to set a pH color indicating center in said polymer.
Claim 7
Dependent Claim
107 words
Method for preparing polymeric color changing pH indicators insoluble in aqueous medium when used for pH measurement comprising the steps of free radical polymerizing at least one comonomer selected from the group consisting of acrylic esters, methacrylic esters, acrylamide, methacrylamide, N-methylacrylamide, N-methylmethacrylamide, N-ethylacrylamide, N-ethylemelhacrylamide, N-hydroxypropylacrylamide, and N-hydroxypropylmethacrylamide, with from 0.1 to 30 weight percent of a functional monomer selected from the group, consisting of N-ethyl-N-(2-methacryloylethyl) aniline and N-ethyl-N-(2-methacryloylethyl)-N-acetyl-phenylenediamine, to form a polymer, subsequently diazo coupling said polymer with an aromatic, active agent through the available functional sites of said monomer and functionally active sites of said agent to set a pH color indicating center in said polymer.
Claim 8
Dependent Claim
17 words
Method according to claim 5, wherein from 0.5 to 20 weight percent of the monomer is employed.
Claim 9
Dependent Claim
20 words
Method according to claim 5, wherein said active agent comprises a diazotized aromatic amine and said moner is N-ethyl-N-(2-methacryloylethyl) aniline.
Claim 10
Dependent Claim
40 words
Method according to claim 7, wherein said aromatic amine is selected from the group consisting of aniline and its carboxy, sulfo, hydroxy and amino derivatives, β -naphthylamine, α -naphthylamine, and their sulfo-carboxy and amino derivatives, and aminoanthraquinone and derivatives thereof.
Claim 11
Dependent Claim
48 words
Method according to claim 5 wherein said active agent is selected from the group consisting of phenol derivatives; α- and β -naphthols and their sulfo and amino and hydroxy derivatives; derivatives of 1-methyl-3-phenyl-5-pyrazalone, and amino derivatives of naphthalene; said functional monomer is N-ethyl-N-(2-methacryloylethyl)-N'-acetyl-p-phenylenediamine, and said polymer is diazotized.
References Cited (Backward Citations)
US2732382A
Cited
US2929829A
Cited
US3544484A
Cited
US4029598A
Cited
US3925267A
Cited
US3904373A
Cited
DE2436257A1
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1982-09-03 | 1983-03-05 | 1983-09-04 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1986-09-03 | 1987-03-05 | 1987-09-04 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1990-09-03 | 1991-03-05 | 1991-09-04 | $7700.00 | Window Closed / Lapsed |