US3131030A - Reagent carrier for gas detecting tubes - Google Patents

Reagent carrier for gas detecting tubes Download PDF

Info

Publication number
US3131030A
US3131030A US83723A US8372361A US3131030A US 3131030 A US3131030 A US 3131030A US 83723 A US83723 A US 83723A US 8372361 A US8372361 A US 8372361A US 3131030 A US3131030 A US 3131030A
Authority
US
United States
Prior art keywords
grains
reagent
detecting
reagent carrier
carrier
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
US83723A
Inventor
Karl F Grosskopf
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Application granted granted Critical
Publication of US3131030A publication Critical patent/US3131030A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/15—Inorganic acid or base [e.g., hcl, sulfuric acid, etc. ]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/17—Nitrogen containing
    • Y10T436/173845—Amine and quaternary ammonium

Definitions

  • Detecting tubes are devices utilized for detecting the presence of gases, suspended materials, or the like in air or other gases.
  • the air or gas to be sampled is drawn through one of these tubes by means of a suction device.
  • the detecting tube is filled with a carrier generally of granular structure upon which a reagent is precipitated in order to detect certain components of the air or gas being sampled.
  • Inorganic carrier substances are used as the reagent characters and, in particular, silica gels are used.
  • These conventional inorganic reagent carriers have the disadvantage of being porous and thus absorbing the reagent.
  • the inorganic carriers are not chemically inert with respect to the reagent and/or the components being detected in the sample air or gas.
  • the object of this invention is to produce a reagent carrier which avoids the disadvantages of the conventional reagent carriers for detecting tubes.
  • this and other objects of the invention are obtained by using as a reagent carrier plastics which are brittle at normal temperatures ranging approximately from 20 to +20 C.
  • These reagent carriers have the advantage in that they are not penetrated either by the reagent or by the component being detected, and the plastics do not react with the components of the reagent.
  • chemically defined materials are utilized as the plastic reagent carriers. Whenever possible, the plastics must not contain any softener in order to eliminate the possibility of dissolving the reagent or the component of the air or gas being detected.
  • Brittle or frangible plastics are defined in this inven tion as non-porous plastics which break up or crack under impact at normal temperatures, as from 20 to +20 C.
  • the grain size of the plastics used as the reagent carrier ranges betwen 0.2 and 2.0 mm. and preferably between 1.0 and 1.2
  • the grains of the plastic reagent carriers of this invention have a predetermined liquid holding capacity on the surface of each grain, said capacity being measured by the roughness of the surface of the grain or of the superficifl structure of the grain for any given grain size.
  • the liquid surface holding capacity for the grains of plastic reagent carrier of this invention is approximately 2 milliliters of isopropyl alcohol and preferably milliliters per 100 grams of the plastic grains, with the grain size of the individual grains being approximately from 1.0 to 1.2
  • the grains for the carrier can be composed of plastic polystyrene.
  • a polystyrene of clear glass granulation is used.
  • plastics can be used of the coumarone type resin.
  • the plastic grains of this invention for use as the reagent carrier for a detecting tube are preferably produced as follows.
  • the raw material consists of commercial coarse grains having a size of from approximately 3 to 5 mm. These coarse grains are broken up in a grinding mill or comminutor and then screened to obtain the desired fractional siZe grains.
  • the coarse grains preferably are cooled to the lowest practical temperature immediately before being ground. This cooling has the advantage of providing rough surfaces on the fine grains obamen Patented Apr. 28, 1964 "ice.
  • the plastic grains 1 are poured into a glass detecting tube 2 and are held in the tube by packing 3.
  • the ends 4- of the tube are then sealed.
  • the ends 4 are broken and the air or other gas drawn through the tube to detect the presence of any particular component in the air or gas.
  • EXAMPLE 1 Preparation of a Detecting Tube Reagent Carrier for Filling a Detecting Tube for the Purpose of Detecting Hydrogen Fluoride
  • 5 milligrams of a conventionally prepared alizarinezirconium dye lacquer was precipitated from an alcohol solution onto 100 grams of granular polystyrene having grains of a size from between 1.0 and 1.2 mm. and a liquid surface holding capacity of 5 milliliters of isopropyl alcohol, as determined on the basis of the 100 grams of the reagent carrier.
  • the 100 grams of grains were then impregnated with an excess of 5 mg. alizarine. The alcohol was then evaporated. Following this, 2 ml.
  • This prepared material was easily flowable and poured into the detecting tube 2 in the usual manner and held in place by the packing 3.
  • This packing or retaining element was made of a material inert to hydrofluoric acid and composed, for example, of Teflon (fluorinated polyethylenes) or polyethylene.
  • This detecting tube is used for the determination of HF in air. When an air test sample in the amount of 2 liters is taken, the range of measurement is bet-ween 2 micrograms and 30 micrograms HF per liter of air.
  • EXAMPLE 2 Preparation of a Detecting Tube Filler for the Detection of Acid Vapors
  • a polystyrene reagent carrier of the type described in Example 1 was used. 100 grams of the grains of polystyrene having a grain size of from 1.0 to 1.2 mm. were impregnated with a solution composed of 1.5 ml. butanol, 1.5 ml. of universal indicator, and 0.2 ml. n/ 10 NaOH. The solvent was then evaporated. Test tube 2 was then filled with this filler. The range of measurement of the detecting tube was approximately 1 microgram to 20 micrograms of acid vapor per liter of air using an air test sample of 1 liter. This measurement range was determined on the basis of detecting S0 as the acid vapor.
  • EXAMPLE 3 Preparation of a Detecting Tube Filler for the Detection of Hydrazine in Air
  • the reagent carrier was composed of polystyrene grains as set forth in Example 1. 100 grams of the grains were impregnated with 0.5 ml. of a 0.25% solution of methyl violet in ethylene glycol. Test tube 2 was filled with this prepared filler and had a measurement range of from 1 to 20 micrograms of hydrazine per liter of air when using an air test sample of 1 liter.
  • An indicator for a detecting tube comprising a gas detecting reagent coating on a carrier composed of non-porous grains of a plastic which is brittle at normal temperatures ranging from about minus 20- to plus 20 degrees centigrade.
  • An indicator as in claim 1 said grains having a size ranging from about 0.2 to 2.0 mm.
  • An indicator as in claim 2 said grains having a size ranging from about 1.0 and 1.2 mm. and having a liquid holding surface capacity of from about 2 milliliters to 5 milliliters of isopropyl alcohol per 100 grams of said grains.
  • An indicator as in claim 3 said grains comprising a plastic selected from the class consisting of colorless synthetic and natural resins.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Description

INVENTOR Karl Grosskopf aw, A'EIDTORNEYLIS Ap 1964 K; F. GROSSKOPF REAGENT CARRI ER FOR GAS DETECTING TUBES Filed Jan. 19, 1961 0 0 4a 0 A0 :40 00 04 000 cannon r afln o a a n aan nak a o a n@oo n o w J United States Patent 3,131,030 REAGENT CARRIER FOR GAS DETECTlNG TUBES Karl E. Grosskopt, llubeck, Germany, assignor to Otto Heinrich Drager, Lubeck, Germany Filed Jan 19, 1961, Ser. No. 83,723 Claims priority, application Germany Jan. 29, 1960 4 Claims. (Cl. 23-254) This invention relates to a reagent carrier for detecting tubes.
Detecting tubes are devices utilized for detecting the presence of gases, suspended materials, or the like in air or other gases. The air or gas to be sampled is drawn through one of these tubes by means of a suction device. The detecting tube is filled with a carrier generally of granular structure upon which a reagent is precipitated in order to detect certain components of the air or gas being sampled. Inorganic carrier substances are used as the reagent characters and, in particular, silica gels are used. These conventional inorganic reagent carriers have the disadvantage of being porous and thus absorbing the reagent. Furthermore, in many cases, the inorganic carriers are not chemically inert with respect to the reagent and/or the components being detected in the sample air or gas.
The object of this invention is to produce a reagent carrier which avoids the disadvantages of the conventional reagent carriers for detecting tubes.
In general, this and other objects of the invention are obtained by using as a reagent carrier plastics which are brittle at normal temperatures ranging approximately from 20 to +20 C. These reagent carriers have the advantage in that they are not penetrated either by the reagent or by the component being detected, and the plastics do not react with the components of the reagent. Above all, chemically defined materials are utilized as the plastic reagent carriers. Whenever possible, the plastics must not contain any softener in order to eliminate the possibility of dissolving the reagent or the component of the air or gas being detected.
Brittle or frangible plastics are defined in this inven tion as non-porous plastics which break up or crack under impact at normal temperatures, as from 20 to +20 C.
The grain size of the plastics used as the reagent carrier ranges betwen 0.2 and 2.0 mm. and preferably between 1.0 and 1.2
The grains of the plastic reagent carriers of this invention have a predetermined liquid holding capacity on the surface of each grain, said capacity being measured by the roughness of the surface of the grain or of the superficifl structure of the grain for any given grain size.
Preferably the liquid surface holding capacity for the grains of plastic reagent carrier of this invention is approximately 2 milliliters of isopropyl alcohol and preferably milliliters per 100 grams of the plastic grains, with the grain size of the individual grains being approximately from 1.0 to 1.2
The grains for the carrier can be composed of plastic polystyrene. Preferably a polystyrene of clear glass granulation is used.
Also, plastics can be used of the coumarone type resin.
The plastic grains of this invention for use as the reagent carrier for a detecting tube are preferably produced as follows. The raw material consists of commercial coarse grains having a size of from approximately 3 to 5 mm. These coarse grains are broken up in a grinding mill or comminutor and then screened to obtain the desired fractional siZe grains. The coarse grains preferably are cooled to the lowest practical temperature immediately before being ground. This cooling has the advantage of providing rough surfaces on the fine grains obamen Patented Apr. 28, 1964 "ice.
' tained from the coarse grains. Plastic polystyrene cooled to -10 C. and then broken to a grain size of, for example, from 0.2 to 2.0 mm. produces fine grains having a liquid surface holding capacity of about 5 milliliters of isopropyl alcohol per grams of grains.
The means by which the objects of the invention are obtained are described more fully with reference to the accompanying drawing which is a cross-sectional View through a detecting tube containing a filler of the plastic reagent carrier.
In the drawing, the plastic grains 1 are poured into a glass detecting tube 2 and are held in the tube by packing 3. The ends 4- of the tube are then sealed. When the tube is being used, the ends 4 are broken and the air or other gas drawn through the tube to detect the presence of any particular component in the air or gas.
The operation of the invention is as described in the following examples:
EXAMPLE 1 Preparation of a Detecting Tube Reagent Carrier for Filling a Detecting Tube for the Purpose of Detecting Hydrogen Fluoride 5 milligrams of a conventionally prepared alizarinezirconium dye lacquer was precipitated from an alcohol solution onto 100 grams of granular polystyrene having grains of a size from between 1.0 and 1.2 mm. and a liquid surface holding capacity of 5 milliliters of isopropyl alcohol, as determined on the basis of the 100 grams of the reagent carrier. In order to increase the sensitivity of detection, the 100 grams of grains were then impregnated with an excess of 5 mg. alizarine. The alcohol was then evaporated. Following this, 2 ml. ethylene glycol plus 0.5 ml. glacial acetic acid was added to the grains. This prepared material was easily flowable and poured into the detecting tube 2 in the usual manner and held in place by the packing 3. This packing or retaining element was made of a material inert to hydrofluoric acid and composed, for example, of Teflon (fluorinated polyethylenes) or polyethylene. This detecting tube is used for the determination of HF in air. When an air test sample in the amount of 2 liters is taken, the range of measurement is bet-ween 2 micrograms and 30 micrograms HF per liter of air.
EXAMPLE 2 Preparation of a Detecting Tube Filler for the Detection of Acid Vapors A polystyrene reagent carrier of the type described in Example 1 was used. 100 grams of the grains of polystyrene having a grain size of from 1.0 to 1.2 mm. were impregnated with a solution composed of 1.5 ml. butanol, 1.5 ml. of universal indicator, and 0.2 ml. n/ 10 NaOH. The solvent was then evaporated. Test tube 2 was then filled with this filler. The range of measurement of the detecting tube was approximately 1 microgram to 20 micrograms of acid vapor per liter of air using an air test sample of 1 liter. This measurement range was determined on the basis of detecting S0 as the acid vapor.
EXAMPLE 3 Preparation of a Detecting Tube Filler for the Detection of Hydrazine in Air The reagent carrier was composed of polystyrene grains as set forth in Example 1. 100 grams of the grains were impregnated with 0.5 ml. of a 0.25% solution of methyl violet in ethylene glycol. Test tube 2 was filled with this prepared filler and had a measurement range of from 1 to 20 micrograms of hydrazine per liter of air when using an air test sample of 1 liter.
Having now described the means by which the objects of the invention are obtained,
I claim:
1. An indicator for a detecting tube comprising a gas detecting reagent coating on a carrier composed of non-porous grains of a plastic which is brittle at normal temperatures ranging from about minus 20- to plus 20 degrees centigrade.
2. An indicator as in claim 1, said grains having a size ranging from about 0.2 to 2.0 mm.
3. An indicator as in claim 2, said grains having a size ranging from about 1.0 and 1.2 mm. and having a liquid holding surface capacity of from about 2 milliliters to 5 milliliters of isopropyl alcohol per 100 grams of said grains.
4. An indicator as in claim 3, said grains comprising a plastic selected from the class consisting of colorless synthetic and natural resins.
References Cited in the file of this patent UNITED STATES PATENTS Murray June 16, Srnidth Feb. 8, Shepherd Nov. 8, Wittlin Aug. 7, Jarvis Mar. 24,
FOREIGN PATENTS Australia Aug. 26, Great Britain Dec. 17,
OTHER REFERENCES Kenner Products Co., Color Go Round, 912 Syca- 15 more, Cincinnati 2, Ohio, August 1959.

Claims (1)

1. AN INDICATOR FOR A DETECTING TUBE COMPRISING A GAS DETECTING REAGENT COATING ON A CARRIER COMPOSED OF NON-POROUS GRAINS OF A PLASTIC WHICH IS BRITTLE AT NORMAL TEMPERATURES RANGING FROM ABOUT MINUS 20 TO PLUS 20 DEGREES CENTIGRADE.
US83723A 1960-01-29 1961-01-19 Reagent carrier for gas detecting tubes Expired - Lifetime US3131030A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE3131030X 1960-01-29

Publications (1)

Publication Number Publication Date
US3131030A true US3131030A (en) 1964-04-28

Family

ID=8087348

Family Applications (1)

Application Number Title Priority Date Filing Date
US83723A Expired - Lifetime US3131030A (en) 1960-01-29 1961-01-19 Reagent carrier for gas detecting tubes

Country Status (1)

Country Link
US (1) US3131030A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455656A (en) * 1965-07-06 1969-07-15 Mine Safety Appliances Co Detection of volatile hydrazine compounds
US3455655A (en) * 1965-06-01 1969-07-15 Mine Safety Appliances Co Detection of missile fuels in gas atmosphere
US3787184A (en) * 1970-03-23 1974-01-22 Us Army A method and composition for detecting amine compounds
US4259287A (en) * 1978-12-22 1981-03-31 Dragerwerk Aktiengesellschaft Testing tube construction for measuring sodium hydroxide and/or calcium oxide
US10278617B1 (en) 2013-03-15 2019-05-07 Invoy Holdings, Llc Method and apparatus for sensing ammonia in breath

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2286636A (en) * 1941-10-01 1942-06-16 Chaude R Wickard Insecticide
US2461089A (en) * 1944-06-22 1949-02-08 Smidth Leonard Process of forming granulated synthetic resin compositions
US2487077A (en) * 1943-12-28 1949-11-08 Us Commerce Colorimetric gas detection
US2757632A (en) * 1953-10-09 1956-08-07 Wittlin Albert Fluid flow tube
GB805853A (en) * 1955-03-07 1958-12-17 Wolfen Filmfab Veb A process for removing acidic or basic vapours from gases
US2879005A (en) * 1954-12-29 1959-03-24 Melvin Sobel Method of refining scrap plastic and apparatus therefor

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2286636A (en) * 1941-10-01 1942-06-16 Chaude R Wickard Insecticide
US2487077A (en) * 1943-12-28 1949-11-08 Us Commerce Colorimetric gas detection
US2461089A (en) * 1944-06-22 1949-02-08 Smidth Leonard Process of forming granulated synthetic resin compositions
US2757632A (en) * 1953-10-09 1956-08-07 Wittlin Albert Fluid flow tube
US2879005A (en) * 1954-12-29 1959-03-24 Melvin Sobel Method of refining scrap plastic and apparatus therefor
GB805853A (en) * 1955-03-07 1958-12-17 Wolfen Filmfab Veb A process for removing acidic or basic vapours from gases

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455655A (en) * 1965-06-01 1969-07-15 Mine Safety Appliances Co Detection of missile fuels in gas atmosphere
US3455656A (en) * 1965-07-06 1969-07-15 Mine Safety Appliances Co Detection of volatile hydrazine compounds
US3787184A (en) * 1970-03-23 1974-01-22 Us Army A method and composition for detecting amine compounds
US4259287A (en) * 1978-12-22 1981-03-31 Dragerwerk Aktiengesellschaft Testing tube construction for measuring sodium hydroxide and/or calcium oxide
US10278617B1 (en) 2013-03-15 2019-05-07 Invoy Holdings, Llc Method and apparatus for sensing ammonia in breath

Similar Documents

Publication Publication Date Title
Zhang et al. Reentrant coil-to-globule-to-coil transition of a single linear homopolymer chain in a water/methanol mixture
Scrimgeour et al. A simplified method for deuterium/hydrogen isotope ratio measurements on water samples of biological origin
US2880072A (en) Method of determining carbon dioxide in gases
JPS5819988B2 (en) Device for detecting free water in hydrocarbon fuels
CA2011100A1 (en) Centrifuged material layer measurements taken in an evacuated tube
Smith et al. A review of methods for the determination of hold-up volume in modern liquid chromatography
US3350175A (en) Colorimetric indicator device for the determination of gases
US3131030A (en) Reagent carrier for gas detecting tubes
US3574281A (en) Dilatometer cell
US3378348A (en) Indicator for the determination of sulfur dioxide and hydrogen sulfide
Doube et al. Studies of poly (vinyl chloride)/solution chlorinated polyethylene blends by inverse gas chromatography
US3312527A (en) Carbon monoxide determination
US3112998A (en) Reagent for detection of arsenic hydride or phosphorous hydride
US2963351A (en) Determination of nitrogen dioxide
US2736638A (en) Detection of sulfur dioxide
斎藤正明 et al. Improvements for Measurement of 222Rn in Water.
Gage The efficiency of absorbers in industrial hygiene air analysis
Mitchell Jr Methods for the determination of water in polymers
US2942952A (en) Determination of gaseous chlorine and bromine
US4292042A (en) Analysis of vinyl acetate
Cadenhead et al. Specific gravities of lunar materials using helium pycnometry
US3455654A (en) Detection of alcohols in gas atmospheres
US3455655A (en) Detection of missile fuels in gas atmosphere
JPS60157029A (en) Temperature load indicator
US2839368A (en) Spot testing