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US4380587A Expired / Lapsed US ⏱️ 0.0 years remaining

Film badge for determining carbonyl compounds

Assignee: Arthur D Little Inc
•
Filing: 1981-08-20
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Granted: 1983-04-19
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Expires: 2001-08-20
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Abstract

Abstract Method for the determination of fluidic-contained aldehydes. The method comprises bringing into contact said aldehyde and a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for the aldehydes thereby forming nucleating crystals; treating said nucleating crystals with a metastable supersaturated solution in which said nucleating crystals can grow; growing said nucleating crystals to form an optically measurable film of crystals; and optically measuring said film of crystals to determine the concentration of fluidic-contained aldehydes.

Inventors

  • 👤 Martin Koocher

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 08:23
CPC Classifications
G; G01; G01N; G01N25/00; G01N25/14; G01N31/00; G01N31/22; G01N31/223; G01N31/224; Y; Y10; Y10S; Y10S436/00; Y10S436/902; Y10T; Y10T436/00; Y10T436/20; Y10T436/200833

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 85 words
A method for determining fluidic-contained aldehyde comprising a. contacting a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for the aldehyde with the fluidic-contained aldehyde to form nucleating sites; b. treating said nucleating sites with a metastable supersaturated solution in which said nucleating sites can grow; c. growing said nucleating sites to form an optically measurable film of crystals; and d. optically measuring said film of crystals to determine the concentration of fluidic-contained aldehyde.
Claim 2
Independent Claim 85 words
A method for determining fluidic-contained aldehyde comprising a. contacting a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for the aldehyde with the fluidic-contained aldehyde to form nucleating sites; b. treating said nucleating sites with a metastable supersaturated solution in which said nucleating sites can grow; c. growing said nucleating sites to form an optically measurable film of crystals; and d. optically measuring said film of crystals to determine the concentration of fluidic-contained aldehyde.
Claim 3
Dependent Claim 15 words
The method according to claim 1 wherein said chemically inert substrate is a polymeric film.
Claim 4
Dependent Claim 69 words
The method according to claim 2 wherein said derivatizing agent for said fluidic-contained aldehyde is adipic dihydrazide; benzoylhydrazine; isonicotinic acid hydrazide; nicotinic acid hydrazide; oxalyl dihydrazide; oxamic hydrazide; salicylhydrazide; 2,4-dinitrophenylhydrazine; semicarbazide; dimethone or dimedone; p-nitrophenylhydrazine; phenylhydrazine; thiosemicarbazide; bromobenzohydrazine (o,m,p); 2,4-dinitromethylphenylhydrazine; p-carboxphenylhydrazine; nitrobenzenesulfonhydrazine; p-nitrobenzohydrazine; diphenylhydrazine; 2-naphthylhydrazine; p-chlorobenzohydrazine; m-chlorobenzohydrazine; nitroguanylhydrazine; α-(α,4-nitrophenyl)-α-methylhydrazine; xenylsemicarbazide; tolylsemicarbazide (o,m,p); phenylsemicarbazide; 1-naphthylsemicarbazide; 2-naththylsemicarbazide; 3,5-dinitrophenylsemicarbazide; dibromomethone; benzothiazole; benzothiazoline; aminomorpholines; hydrazinobenzoic acid; 5-(1-phenylmethyl)semioxazide 1,3-cyclohexadione; 1,2-bis(p-methoxybenzylamino)ethane or p-hydroxybenzoic acid anhydride.
Claim 5
Dependent Claim 17 words
The method according to claim 3 wherein said sites are 0.01 μm to 1.0 μm in size.
Claim 6
Dependent Claim 75 words
The method according to claim 1 wherein said supersaturated/metastable solution is an aqueous solution of the fluidic-contained aldehyde reaction product of adipic dihydrazide; benzoylhydrazine; isonicotinic acid hydrazide; nicotinic acid hydrazide; oxalyl dihydrazide; oxamic hydrazide; salicylhydrazide; 2,4-dinitrophenylhydrazine; semicarbazide; dimethone or dimedone; p-nitrophenylhydrazine; phenylhydrazine; thiosemicarbazide; bromobenzohydrazine (o,m,p); 2,4-dinitromethylphenylhydrazine; p-carboxyphenylhydrazine; nitrobenzenesulfonhydrazine; b-nitrobenzohydrazine; diphenylhydrazine; 2-naphthylhydrazine; p-chlorobenzohydrazine; m-chlorobenzohydrazine; nitroguanylhydrazine; α-(α,4-nitrophenyl)-α-methylhydrazine; xenylsemicarbazide; tolylsemicarbazide (o,m,p); phenylsemicarbazide; 1-naphthylsemicarbazide; 2-napthylsemicarbazide; 3,5-dinitrophenylsemicarbazide; dibromomethone; benzothiazole; benzothiazoline; aminomorpholines; hydrazinobenzoic acid; 5-(1-phenylmethyl)semioxazide; 1,3-cyclohexadione; 1,2-bis(p-methoxybenzylamino)ethane or p-hydroxybenzoic acid hydrazide.
Claim 7
Dependent Claim 98 words
A film badge useful for determining the presence or time-average amounts of fluidic-contained aldehyde comprising a container having a chamber therein, said chamber enclosing a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for said aldehyde, the size of said particles being in the micron to submicron range, and superimposed on said chamber and said substrate a porous fluid flow attenuating layer, said porous fluid flow attenuating layer causing the flow of said fluidic-contained aldehyde to contact said substrate layer to form nucleating sites for crystal growth.
Claim 8
Dependent Claim 98 words
A film badge useful for determining the presence or time-average amounts of fluidic-contained aldehyde comprising a container having a chamber therein, said chamber enclosing a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for said aldehyde, the size of said particles being in the micron to submicron range, and superimposed on said chamber and said substrate a porous fluid flow attenuating layer, said porous fluid flow attenuating layer causing the flow of said fluidic-contained aldehyde to contact said substrate layer to form nucleating sites for crystal growth.
Claim 9
Independent Claim 91 words
A method for determining a fluidic-contained carbonyl compound comprising a. contacting a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for the carbonyl compound with the fluidic-contained carbonyl compound to form nucleating sites; b. treating said nucleating sites with a metastable supersaturated solution in which said nucleating sites can grow; c. growing said nucleating sites to form an optically measurable film of crystals; and d. optically measuring said film of crystals to determine the concentration of fluidic contained carbonyl compound.
Claim 10
Independent Claim 91 words
A method for determining a fluidic-contained carbonyl compound comprising a. contacting a chemically inert substrate having adhered to the surface thereof a substantially monodisperse system of particles of a derivatizing agent for the carbonyl compound with the fluidic-contained carbonyl compound to form nucleating sites; b. treating said nucleating sites with a metastable supersaturated solution in which said nucleating sites can grow; c. growing said nucleating sites to form an optically measurable film of crystals; and d. optically measuring said film of crystals to determine the concentration of fluidic contained carbonyl compound.
Claim 11
Dependent Claim 21 words
The method of claim 7 wherein said carbonyl compound is selected from the group consisting of ketones, ketoesters, ketoacids and isocyanates.
Claim 12
Dependent Claim 68 words
The method of claim 8 wherein the derivatizing agent for said carbonyl compound is adipic dihydrazide; benzoylhydrazide; isonicotinic acid hydrazide; nicotinic acid hydrazide; oxalyl dihydrazide; oxamic hydrazide; salicylhydrazide; 2,4-dinitrophenylhydrazine; semicarbazide; dimethone or dimedone; p-nitrophenylhydrazine; phenylhydrazine; thiosemicarbazide; bromobenzohydrazine (o.m.p.); 2,4-dinitromethylphenylhydrazine; p-carboxyphenylhydrazine; nitrobenzenesulfonhydrazine; p-nitrobenzohydrazine; diphenylhydrazine; 2-naphthylhydrazine; p-chlorobenzohydrazine; m-chlorobenzohydrazine; nitroguanylhydrazine; α-(α,4-nitrophenyl)-αmethylhydrazine; xenylsemicarbazide; tolylsemicarbazide (o.m.p.); phenylsemicarbazide; 1-naphthylsemicarbazide; 2-naphthylsemicarbazide; 3,5-dinitrophenylsemicarbazide; dibromomethone; benzothiazole; benzothiazoline; aminomorpholines; hydrazinobenzoic acid; 5-(1-phenylmethyl)semioxazide; 1,3-cyclohexadione; 1,2-bis(p-methoxybenzylamino)ethane or p-hydroxybenzoic acid hydrazide.
Claim 13
Dependent Claim 17 words
The method of claim 9 wherein said nucleating sites at 0.01 μm to 1.0 μm in size.

References Cited (Backward Citations)

US3642449A Cited
US3645696A Cited
US3950980A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-04-18 1986-10-18 1987-04-19 $2000.00 Window Closed / Lapsed
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11.5 Years (Year 12) 1994-04-18 1994-10-18 1995-04-19 $7700.00 Window Closed / Lapsed

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