US3455654A - Detection of alcohols in gas atmospheres - Google Patents

Detection of alcohols in gas atmospheres Download PDF

Info

Publication number
US3455654A
US3455654A US460478A US3455654DA US3455654A US 3455654 A US3455654 A US 3455654A US 460478 A US460478 A US 460478A US 3455654D A US3455654D A US 3455654DA US 3455654 A US3455654 A US 3455654A
Authority
US
United States
Prior art keywords
alcohol
reagent
alcohols
air
color change
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
US460478A
Inventor
Paul W Mcconnaughey
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.)
MSA Safety Inc
Original Assignee
Mine Safety Appliances 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.)
Filing date
Publication date
Application filed by Mine Safety Appliances Co filed Critical Mine Safety Appliances Co
Application granted granted Critical
Publication of US3455654A publication Critical patent/US3455654A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22Investigating 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
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/20Oxygen containing
    • Y10T436/203332Hydroxyl containing
    • Y10T436/204165Ethanol

Definitions

  • United States Patent U.S. Cl. 23-232 4 Claims ABSTRACT OF THE DISCLOSURE A method of detecting alcohols in air in accordance with which the air is passed into contact with a reagent consisting essentially of a soluble hexavalent chromium compound and a pentavalent phosphoric acid supported by an inert carrier.
  • a reagent consisting essentially of a soluble hexavalent chromium compound and a pentavalent phosphoric acid supported by an inert carrier.
  • the reagent undergoes a color change which affords a qualitative determination of the presence of alcohol.
  • Quantitative determination is possible by mounting the reagent in a transparent tube and determining the length over which the color change occurs upon passing a fixed volume of air at a fixed fiow rate through the tube, the length over which the color change occurs being compared with calibrated results.
  • alcohols are used as solvents, in the manufacture of a large number of other compounds, in toilet and other preparations, and for various other purposes. Many of these alcohols are capable of causing determatitis; the vapors of others in air may be hazardous to humans, exhibiting varying toxicity ranging from relatively harmless to definitely hazardous depending on the particular alcohol and the concentration present in the air being breathed. Also some alcohols when present in air present a fire or explosion hazard.
  • a copending application Ser. No. 460,479 filed June 1, 1965, by Charles A. Plantz and David G. Hannan, and assigned to the owner of this application, discloses and claims a reagent for the detection of hydrazine, volatile alkyl hydrazines, red fuming nitric acid, etc., which comprises a composition of a hexavalent chromium compound and an acid of pentavalent phosphorus on an inert carrier which in the presence of moisture undergoes a characteristic and easily observable color change promptly upon contact with the said compounds.
  • the aforesaid reagent is especially adapted to the practice of the method of this invention.
  • the reagent is disposed within a transparent container and the atmosphere to be tested is passed through it.
  • the atmosphere to be tested is passed through it.
  • the reagent changes from its normal yellow color to green. This was unexpected because there is no chemical relationship between the foregoing nitrogen compounds and alcohols.
  • the reagent may be disposed in a glass or other transparent tube of small diameter the ends of which are sealed as described in US. Patent 2,174,349 to John B. Littlefield.
  • the reagent tube is used by breaking the seals and aspirating the atmosphere to be tested through it. Appearance of the color change indicates, of course, the presence of an alcohol.
  • Color standards for comparison with the color change may be provided in the manner known in this general testing field.
  • the hexavalent chromium compound may be supplied as chromium trioxide (CrO or .as a soluble chromate or dichromate, e.g., potassium (or other alkali metal) chromate (K CrO.,,) or dichromate (K Cr O
  • the phosphoric acid may be orthophosphoric acid (H PO or metaphosphoric acid (HPO or other acid of pentavalent hosphorus.
  • the two constituents of the reagents may be used in such proportions as to provide per ml. of silica gel about 0.022 gm. to 24 gms. of pentavalent phosphorus and about 0.0145 gm. to 2.6 gms. of hexavalent chromium.
  • the most vivid color change contrast is to be had by the use of about 0.05 gm. to 3 gms. of chromium trioxide and from about 0.15 gram to 9 gms. of metaphosphoric acid per 100 milliliters of silica gel, most suitably of 8 to 14 mesh size, with the preferred proportions being 0.53 gm. of chromium trioxide and 1.67 gms. of metaphosphoric acid.
  • the reagent may be prepared satisfactorily by addition of the reagents to about 16 milliliters of water and mixing the silica gel with the solution.
  • a relatively coarse silica gel say of about 8 to 14 mesh
  • the introduction of water causes it to break down into particles finer than are desirable for the purposes of the invention. This may be avoided by using silica gel that has been humidified by exposure to humid air.
  • the impregnated silica gel is then vacuum dried until it is free flowing, preferably to a water content of about 10 to 12 percent by weight.
  • the carrier preferably a granular adsorbent, does not enter into the color-producing reaction but serves merely as an inert physical carrier for the reagent, thus avoiding the necessity for liquid reagents with their attendant disadvantages.
  • various carriers that might be used in HCl purified silica gel which, being colorless, insures maximum intensity of the color change.
  • the invention is applicable also to the quantitative determination of a wide variety of alcohols in air, and in many cases to determination of the Threshold Limit Value (T.L.V.) of the ACGIH, i.e., the concentration to which all workers may be exposed repeatedly day after day without ad verse effect.
  • T.L.V. Threshold Limit Value
  • the occurrence of the color change may be used to show the presence of an alcohol.
  • a fixed volume of air at a fixed flow rate supplied, for example, by a pump such as that described in US. Patent 3,166,938 to Weyrauch et al.
  • the length over which the color change occurs as in the tubes referred to above
  • quantitative determination is possible by comparison with calibrated re sults.
  • a pump such as described above delivering 100 ml. of air per stroke iso-amyl alcohol was calibrated as follows.
  • the tubes were 3.011 mm. ID. with a reagent bed depth of 50 mm. i5 mm. held in place by end plugs of fiber glass tape. They were first sealed at one end, dried at 250 C. overnight, filled and the other end sealed.
  • Stain length Stain length, Stain length, Isoamyl alcohol in 5 pump stroke pump stroke air-cone. (p.p.m.) mm.) (mm.)
  • the length over which the stain is produced by a given alcohol will generally be greater as a result of passage of a larger volume of air, as indicated by the foregoing table, thus increasing the sensitivity and utility of the invention.
  • n-Amyl alcohol N.L. 25-2 000 Iso-amyl alcohol. 100 50-1, 000 Sec-amyl alcohol N .L. 25-2, 000 Tert-amyl alcohol N .L. 25-2, 000 n-Butyl alcohoL. 100 50-4, 000 Iso-butyl alcohol N.L. 50-4, 000 Sec-butyl alcohol N .L.
  • Methyl alcohol 2 1 900 Methyl amyl alcohol (methyl isobutyl carbinol) 25 25-1, 00 2-methyl cyclohexanol 100 25-8000 Iso-propyl alcohol 400 100-10, 000 Propyl alcohol N.L- 000 N.L.-No threshold limit value listed in the ACGIH Threshold Limit Values Booklet for 1964.
  • the reagents of the invention may not give fully accurate quantitative results below about. 60 F. (stain length short); below that temperature acceptable results will be had at 40 to 60 P. if the tube is warmed in the hand while testing so that no correction factor will be necessary.
  • the stain may have a light end point when first formed but after about two minutes the stain intensity increases to give a clear end point. Tests have shown that when protected from the atmosphere the reagents of this invention may be expected to have a shelf like of about two years.
  • silica gel as the reagent carrier it will be understood that other substances may be used such as alumina, glass cloth, filter paper, and the like.
  • a method of detecting an alcohol in air consisting of passing air, to be tested for the presence of alcohol, into contact with a reagent consisting essentially of a soluble hexavalent chromium compound and a pentavalent phosphoric acid supported by an inert carrier and providing from 0.0145 gram to 2.6 grams of hexavalent chromium and from 0.022 gram to 24 grams of pentavalent phosphorus per 100 ml. of silica gel, the reagent undergoing a color change in the presence of said alcohol.
  • said reagent consisting essentially of chromium trioxide and metaphosphoric acid supported by silica gel in the proportions of about 0.15 gram to 3 grams of chromium trioxide and from about 0.15 to 9 grams of metaphosphoric acid.
  • the reagent consisting of chromium trioxide and metaphosphoric acid in the proportion of 0.53 gram of the former to 1.67 gram of the latter.

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)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)

Description

United States Patent U.S. Cl. 23-232 4 Claims ABSTRACT OF THE DISCLOSURE A method of detecting alcohols in air in accordance with which the air is passed into contact with a reagent consisting essentially of a soluble hexavalent chromium compound and a pentavalent phosphoric acid supported by an inert carrier. In the presence of an alcohol the reagent undergoes a color change which affords a qualitative determination of the presence of alcohol. Quantitative determination is possible by mounting the reagent in a transparent tube and determining the length over which the color change occurs upon passing a fixed volume of air at a fixed fiow rate through the tube, the length over which the color change occurs being compared with calibrated results.
A variety of alcohols are used as solvents, in the manufacture of a large number of other compounds, in toilet and other preparations, and for various other purposes. Many of these alcohols are capable of causing determatitis; the vapors of others in air may be hazardous to humans, exhibiting varying toxicity ranging from relatively harmless to definitely hazardous depending on the particular alcohol and the concentration present in the air being breathed. Also some alcohols when present in air present a fire or explosion hazard.
It is among the objects of this invention to provide a simple, rapid and reliable method of detecting the pres ence of alcohols in air, that may be practiced by nontechnical persons, that is rapid, that is satisfactory for plant, field and laboratory use, that requires only simple, inexpensive and readily available materials and apparatus, and that is applicable to quantitative determinations.
A copending application Ser. No. 460,479, filed June 1, 1965, by Charles A. Plantz and David G. Hannan, and assigned to the owner of this application, discloses and claims a reagent for the detection of hydrazine, volatile alkyl hydrazines, red fuming nitric acid, etc., which comprises a composition of a hexavalent chromium compound and an acid of pentavalent phosphorus on an inert carrier which in the presence of moisture undergoes a characteristic and easily observable color change promptly upon contact with the said compounds.
I have discovered, and it is upon this that the present invention is predicated, that the aforesaid reagent is especially adapted to the practice of the method of this invention. In accordance with it the reagent is disposed within a transparent container and the atmosphere to be tested is passed through it. When an alcohol is present the reagent changes from its normal yellow color to green. This was unexpected because there is no chemical relationship between the foregoing nitrogen compounds and alcohols.
Satisfactory response of the reagent to the presence of alcohols is had by passing the atmosphere, as by an aspirator or a pump, to be tested through the reagent in the container. When used with gas mask canisters a satisfactory way for the protection of personnel resides in the use of canisters of the gas mask type such as are shown in Patent No. 1,537,519 to M. Yablick, as well as in various other patents. If the canister fill is not of this reagent it "ice sufiices to position a thin layer of the reagent against the canister window. In the presence of an alcohol the color change is visible through the canister window beginning at the inlet end of the canister and progressing toward the outlet end as the reagent is progressively reacted. Thus the position of the color front gives an immediate indication of the degree of exhaustion of the canister, and when the color change has occurred up toward the outlet it is evident that the discard point has been reached.
Alternatively, for spot checks the reagent may be disposed in a glass or other transparent tube of small diameter the ends of which are sealed as described in US. Patent 2,174,349 to John B. Littlefield. The reagent tube is used by breaking the seals and aspirating the atmosphere to be tested through it. Appearance of the color change indicates, of course, the presence of an alcohol.
Color standards for comparison with the color change may be provided in the manner known in this general testing field.
The hexavalent chromium compound may be supplied as chromium trioxide (CrO or .as a soluble chromate or dichromate, e.g., potassium (or other alkali metal) chromate (K CrO.,,) or dichromate (K Cr O The phosphoric acid may be orthophosphoric acid (H PO or metaphosphoric acid (HPO or other acid of pentavalent hosphorus.
The two constituents of the reagents may be used in such proportions as to provide per ml. of silica gel about 0.022 gm. to 24 gms. of pentavalent phosphorus and about 0.0145 gm. to 2.6 gms. of hexavalent chromium.
The most vivid color change contrast is to be had by the use of about 0.05 gm. to 3 gms. of chromium trioxide and from about 0.15 gram to 9 gms. of metaphosphoric acid per 100 milliliters of silica gel, most suitably of 8 to 14 mesh size, with the preferred proportions being 0.53 gm. of chromium trioxide and 1.67 gms. of metaphosphoric acid.
The reagent may be prepared satisfactorily by addition of the reagents to about 16 milliliters of water and mixing the silica gel with the solution. When a relatively coarse silica gel is used, say of about 8 to 14 mesh, the introduction of water causes it to break down into particles finer than are desirable for the purposes of the invention. This may be avoided by using silica gel that has been humidified by exposure to humid air. The impregnated silica gel is then vacuum dried until it is free flowing, preferably to a water content of about 10 to 12 percent by weight.
The carrier, preferably a granular adsorbent, does not enter into the color-producing reaction but serves merely as an inert physical carrier for the reagent, thus avoiding the necessity for liquid reagents with their attendant disadvantages. Among the various carriers that might be used in HCl purified silica gel which, being colorless, insures maximum intensity of the color change.
The invention is applicable also to the quantitative determination of a wide variety of alcohols in air, and in many cases to determination of the Threshold Limit Value (T.L.V.) of the ACGIH, i.e., the concentration to which all workers may be exposed repeatedly day after day without ad verse effect.
In the practice of the invention as described above the occurrence of the color change may be used to show the presence of an alcohol. Or, using a fixed volume of air at a fixed flow rate (supplied, for example, by a pump such as that described in US. Patent 3,166,938 to Weyrauch et al.) the length over which the color change occurs, as in the tubes referred to above, quantitative determination is possible by comparison with calibrated re sults. For example, using a pump such as described above delivering 100 ml. of air per stroke iso-amyl alcohol was calibrated as follows. The tubes were 3.011 mm. ID. with a reagent bed depth of 50 mm. i5 mm. held in place by end plugs of fiber glass tape. They were first sealed at one end, dried at 250 C. overnight, filled and the other end sealed.
Stain length, Stain length, Isoamyl alcohol in 5 pump stroke pump stroke air-cone. (p.p.m.) mm.) (mm.)
The length over which the stain is produced by a given alcohol will generally be greater as a result of passage of a larger volume of air, as indicated by the foregoing table, thus increasing the sensitivity and utility of the invention.
Other alcohols were similarly calibrated:
Calibra- T.L.V tion Compound (ppm (p.p.m.)
n-Amyl alcohol N.L. 25-2, 000 Iso-amyl alcohol. 100 50-1, 000 Sec-amyl alcohol N .L. 25-2, 000 Tert-amyl alcohol N .L. 25-2, 000 n-Butyl alcohoL. 100 50-4, 000 Iso-butyl alcohol N.L. 50-4, 000 Sec-butyl alcohol N .L. 50-4, 000 Tert-butyl alcohol 100 100-800 Cyclohexanol (hexalln) 50 25-1, 000 Ethyl alcohol 1, 000 200-10, 000 Ethylene glycol monobutyl ether (2-butoxyethanol) (butyl Cellosolve) 50 25-800 Ethylene glycol monoethyl ether (Z-ethoxyethanol) 200 50-1, 000 Furl'uryl alcohol. 50 25-500 Methyl alcohol 2 1 900 Methyl amyl alcohol (methyl isobutyl carbinol) 25 25-1, 00 2-methyl cyclohexanol 100 25-8000 Iso-propyl alcohol 400 100-10, 000 Propyl alcohol N.L- 000 N.L.-No threshold limit value listed in the ACGIH Threshold Limit Values Booklet for 1964.
The foregoing data illustrate the general applicability of the invention to alcohols, and to wide ranges of concentration in air. A few alcohols (benzyl alcohol, glycidol) produce very short stain lengths up to saturated vapor in air and therefore calibration is of little value although the occurrence of staining shows the presence of those alcohols. Diacetone alcohol is the only alcohol in air that has been found to produce only a trace of change up to 100 p.p.m. in air.
The reagents of the invention may not give fully accurate quantitative results below about. 60 F. (stain length short); below that temperature acceptable results will be had at 40 to 60 P. if the tube is warmed in the hand while testing so that no correction factor will be necessary.
Changes in water vapor content of the air (20 to RH) being tested do not interfere with the results. Likewise, such organic compounds as acetone, benzene and hexane do not interfere. And the results are acceptably independent at from 70 to F. The stain may have a light end point when first formed but after about two minutes the stain intensity increases to give a clear end point. Tests have shown that when protected from the atmosphere the reagents of this invention may be expected to have a shelf like of about two years.
Although the invention has been described with particular reference to silica gel as the reagent carrier it will be understood that other substances may be used such as alumina, glass cloth, filter paper, and the like.
According to the provisions of the patent statutes, I have explained the principle of my invention and have described what I now consider to represent its best embodiment. However, I desire to have it understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described.
I claim:
1. In a method of detecting an alcohol in air the step consisting of passing air, to be tested for the presence of alcohol, into contact with a reagent consisting essentially of a soluble hexavalent chromium compound and a pentavalent phosphoric acid supported by an inert carrier and providing from 0.0145 gram to 2.6 grams of hexavalent chromium and from 0.022 gram to 24 grams of pentavalent phosphorus per 100 ml. of silica gel, the reagent undergoing a color change in the presence of said alcohol.
2. A method according to claim 1, said reagent consisting essentially of chromium trioxide and metaphosphoric acid supported by silica gel in the proportions of about 0.15 gram to 3 grams of chromium trioxide and from about 0.15 to 9 grams of metaphosphoric acid.
3. A method according to claim 1, the reagent having a water content of about 10 to 12 percent by weight.
4. A method according to claim 2, the reagent consisting of chromium trioxide and metaphosphoric acid in the proportion of 0.53 gram of the former to 1.67 gram of the latter.
References Cited UNITED STATES PATENTS 2,939,768 6/1960 Grosskopf 23-232 3,223,488 12/1965 Luckey 23-254 OTHER REFERENCES Merck Index, seventh edn., p. 1003, 1960.
MORRIS O. WOLK, Primary Examiner R. M. REESE, Assistant Examiner US. Cl. X.R. 23254
US460478A 1965-06-01 1965-06-01 Detection of alcohols in gas atmospheres Expired - Lifetime US3455654A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US46047865A 1965-06-01 1965-06-01

Publications (1)

Publication Number Publication Date
US3455654A true US3455654A (en) 1969-07-15

Family

ID=23828866

Family Applications (1)

Application Number Title Priority Date Filing Date
US460478A Expired - Lifetime US3455654A (en) 1965-06-01 1965-06-01 Detection of alcohols in gas atmospheres

Country Status (3)

Country Link
US (1) US3455654A (en)
JP (1) JPS507471B1 (en)
GB (1) GB1151595A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951855A (en) * 1971-07-08 1976-04-20 Cand-Aire Industries, Inc. Breath alcohol test medium
US4791065A (en) * 1986-03-13 1988-12-13 Grobel Research Corporation Ethanol sensitive solid
US5403749A (en) * 1992-08-13 1995-04-04 Serguei V. Khartchenko Reagent for the determination of ethanol and method of determination of presence of ethanol in the human body
US5552324A (en) * 1992-06-05 1996-09-03 Supelco, Inc. Method and apparatus for determining the concentration of readily oxidizable organic vapors in gas samples

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2939768A (en) * 1956-12-31 1960-06-07 Drager Otto H Alcohol testing reagent
US3223488A (en) * 1962-08-06 1965-12-14 Luckey Lab Inc Device for alcohol determination

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2939768A (en) * 1956-12-31 1960-06-07 Drager Otto H Alcohol testing reagent
US3223488A (en) * 1962-08-06 1965-12-14 Luckey Lab Inc Device for alcohol determination

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951855A (en) * 1971-07-08 1976-04-20 Cand-Aire Industries, Inc. Breath alcohol test medium
US4791065A (en) * 1986-03-13 1988-12-13 Grobel Research Corporation Ethanol sensitive solid
US5552324A (en) * 1992-06-05 1996-09-03 Supelco, Inc. Method and apparatus for determining the concentration of readily oxidizable organic vapors in gas samples
US5403749A (en) * 1992-08-13 1995-04-04 Serguei V. Khartchenko Reagent for the determination of ethanol and method of determination of presence of ethanol in the human body

Also Published As

Publication number Publication date
JPS507471B1 (en) 1975-03-26
GB1151595A (en) 1969-05-07

Similar Documents

Publication Publication Date Title
Dasgupta et al. Determination of atmospheric sulfur dioxide without tetrachloromercurate (II) and the mechanism of the Schiff reaction
Siggia et al. Quantitative analysis of mixtures of primary, secondary, and tertiary aromatic amines
US3350175A (en) Colorimetric indicator device for the determination of gases
JPS5899753A (en) Composition for detecting hydride gas and method of detecting hydride gas
US2569895A (en) Detection of carbon monoxide by palladous sulfite and/or palladosulfites
Katz Analysis of inorganic gaseous pollutants
Armstrong et al. A Fluorometric Procedure for the Determination of Cerous Ion.
US3455654A (en) Detection of alcohols in gas atmospheres
US3378348A (en) Indicator for the determination of sulfur dioxide and hydrogen sulfide
Pik et al. The determination of dissolved chromium (III) and chromium (VI) and particulate chromium in waters at μg l-1 levels by thin-film x-ray fluorescence spectrometry
US3455656A (en) Detection of volatile hydrazine compounds
Brydia Determination of bisphenol A and impurities by gas chromatography of their trimethylsilyl ether derivatives
Meddle et al. A method for the determination of aromatic isocyanates in air in the presence of primary aromatic amines
US3312527A (en) Carbon monoxide determination
US4489164A (en) Colorimetric method for detecting aldehydes in air
US3455655A (en) Detection of missile fuels in gas atmosphere
Hanker et al. Fluorometric method for estimation of cyanide
Roberts et al. The determination of small amounts of cyanide in the presence of ferrocyanide by distillation under reduced pressure
US4466942A (en) Gaseous contaminant dosimeter
Martinz Jr et al. Ultraviolet determination of total phenols
US3684456A (en) Determination of alcohol
Haslam et al. The detection of “additional elements” in plastic materials by the oxygen flask combustion method
US2942952A (en) Determination of gaseous chlorine and bromine
US4256462A (en) Method and composition for determination of n-nitrosamines
COOK et al. Monitoring and analysis of personnel exposures to hydrazines at a rocket propellant plant