US3455654A - Detection of alcohols in gas atmospheres - Google Patents
Detection of alcohols in gas atmospheres Download PDFInfo
- 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
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- 150000001298 alcohols Chemical class 0.000 title description 13
- 238000001514 detection method Methods 0.000 title description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 28
- 235000019441 ethanol Nutrition 0.000 description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000000741 silica gel Substances 0.000 description 10
- 229910002027 silica gel Inorganic materials 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 6
- 229940117975 chromium trioxide Drugs 0.000 description 6
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 6
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 6
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 6
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000011007 phosphoric acid Nutrition 0.000 description 4
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 231100000627 threshold limit value Toxicity 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- -1 alkyl hydrazines Chemical class 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 231100001261 hazardous Toxicity 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QEJORCUFWWJJPP-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO.CCCCOCCO QEJORCUFWWJJPP-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- NDVWOBYBJYUSMF-UHFFFAOYSA-N 2-methylcyclohexan-1-ol Chemical compound CC1CCCCC1O NDVWOBYBJYUSMF-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
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
- Y10T436/20—Oxygen containing
- Y10T436/203332—Hydroxyl containing
- Y10T436/204165—Ethanol
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.
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- 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
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)
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)
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 |
-
1965
- 1965-06-01 US US460478A patent/US3455654A/en not_active Expired - Lifetime
-
1966
- 1966-05-26 GB GB23743/66A patent/GB1151595A/en not_active Expired
- 1966-05-27 JP JP41033647A patent/JPS507471B1/ja active Pending
Patent Citations (2)
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)
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 |
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