US3238020A - Acid-base test materials - Google Patents
Acid-base test materials Download PDFInfo
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- US3238020A US3238020A US126880A US12688061A US3238020A US 3238020 A US3238020 A US 3238020A US 126880 A US126880 A US 126880A US 12688061 A US12688061 A US 12688061A US 3238020 A US3238020 A US 3238020A
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- acid
- test
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- 239000000463 material Substances 0.000 title claims description 16
- 238000012360 testing method Methods 0.000 title description 69
- 239000002253 acid Substances 0.000 claims description 46
- 150000001875 compounds Chemical class 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 5
- 230000007935 neutral effect Effects 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 28
- 239000003921 oil Substances 0.000 description 23
- 239000002585 base Substances 0.000 description 19
- 150000007513 acids Chemical class 0.000 description 15
- 235000011187 glycerol Nutrition 0.000 description 14
- 239000000243 solution Substances 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 238000005057 refrigeration Methods 0.000 description 6
- 230000001235 sensitizing effect Effects 0.000 description 6
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 6
- 229940029284 trichlorofluoromethane Drugs 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 150000007824 aliphatic compounds Chemical class 0.000 description 4
- -1 aliphatic organic compounds Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000003507 refrigerant Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 239000011368 organic material Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000008121 dextrose Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000873 masking effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- VADKRMSMGWJZCF-UHFFFAOYSA-N 2-bromophenol Chemical compound OC1=CC=CC=C1Br VADKRMSMGWJZCF-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- BELBBZDIHDAJOR-UHFFFAOYSA-N Phenolsulfonephthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 BELBBZDIHDAJOR-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002696 acid base indicator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical class C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- CEQFOVLGLXCDCX-WUKNDPDISA-N methyl red Chemical compound C1=CC(N(C)C)=CC=C1\N=N\C1=CC=CC=C1C(O)=O CEQFOVLGLXCDCX-WUKNDPDISA-N 0.000 description 1
- PGSADBUBUOPOJS-UHFFFAOYSA-N neutral red Chemical compound Cl.C1=C(C)C(N)=CC2=NC3=CC(N(C)C)=CC=C3N=C21 PGSADBUBUOPOJS-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229960003531 phenolsulfonphthalein Drugs 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- PRZSXZWFJHEZBJ-UHFFFAOYSA-N thymol blue Chemical compound C1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C(=CC(O)=C(C(C)C)C=2)C)=C1C PRZSXZWFJHEZBJ-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 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
- G01N31/221—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 for investigating pH value
-
- 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. ]
Definitions
- Acid-base test papers such as Congo Red, Litmus, Brilliant Yellow and the like are old and well known for testing aqueous systems or systems which are soluble in water for the presence of acids or bases. However, they have little or no use when testing for the presence of acids in oils, solvents and the like which are water insoluble. This is primarily due to the fact that the oil is absorbed on the paper, masking whatever effect the presence of acid in the oil might have on the test paper. Also, some of the indicators used in the test papers are soluble in oils and are partially extracted from the paper with the result that the effect of acids or bases is more difficult to observe.
- Acids may occur in oils or other water-insoluble materials for several reasons.
- cleaning such engines or refrigeration equipment it is generally desired to remove all of the acid present because of the severe corrosion it causes. This is done by washing the equipment with solvent, oil or the refrigerant until the system is free of acid. It is immediately found however that testing for the presence of acid when oil is present, as it will be both in engines and refrigeration equipment being repaired, can be a very time consuming affair.
- an acid-base test material containing from about 5% to about 50% by weight of a hygroscopic, neutral sensitizer chosen from the strong acid salts of strong bases and polyhydroxy aliphatic organic compounds.
- the present invention consists of improved acid-base test papers or other cellulosic materials into which has been incorporated from about 5% to about 50% by Weight of a sensitizer chosen from polyhydroxy aliphatic organic compounds and the strong acid salts of strong bases.
- the polyhydroxy compounds may be relatively simple compounds such as glycerine, ethylene glycol, di, tri and other ethylene glycols, propylene glycol, more complicated structures such as some of the naturally occurring sugars, e.g. glucose, sucrose, soluble starches and the like or synthetic compounds such as sorbitol, pentaerythrit-ol, erythritol and the like.
- the strong acid salts of strong bases include the salts of the alkali metal or alkaline earth metal hydroxides. The acid portion of these compounds include hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfuric acid and nitric acid.
- Acid-base indicators which are used in test papers are organic dyes which change color with a change in the concentration of hydrogen ion. Usually these dyes contain either basic groups, eg amino groups, or acidic groups which can react with the acid or base present. Some typical examples of such dyes which are used are: Congo Red, Brilliant Yellow, Litmus, Neutral Red, Bromphenol Red, Phenol Red, Thymol Blue, Methyl Red and the like. These dyes are substantive to other cellulosic material substrates as well as to paper. Usually, however, they are also somewhat oil soluble and can be extracted from the paper with organic solvents such as oils. A large number of such types of test papers are used. Certain test papers also contain more than one indicator and these also may be used.
- the present invention is directed primarily to paper test strips, other materials can be used in place of paper. Examples are cotton cloth, felt and the like as well as inert, porous materials which are inert to acids and bases as well as organic solvents.
- the test papers of this invention are prepared by addition of one of the sensitizing agents to the indicator dye, paper combination during some stage of manufacture. Being essentially nonvolatile, the sensitizing agents do not evaporate from the test paper after manufacture. This is, of course, a prime requirement of the sensitizing agent for the whole purpose is defeated if the sensitizing agent is lost from the test paper. Glycerine is the preferred polyhydroxy compound because it is relatively cheap, does not evaporate and seems to give the best results.
- the limits of concentration of the sensitizing agents is determined, on the lower limit, by the minimum amount of material which must be present to obtain the desired results. This minimum appears to be about 5% by weight.
- the upper limit is determined by how much of the agent the test paper can hold. Paper, and the other useful substrates, are highly absorbent, but about 50% by weight appears to be a practical upper limit. There is certainly no advantage gained from using more than 50%.
- the preferred concentration is about 25-50% by weight of the total indicator mass.
- the presence of the sensitizing agents in the test papers serves two purposes. First, they prevent oils and other water-insoluble organic materials from being absorbed in the paper and/or from extracting the indicator dye from the paper. Second, the polyhydroxy compounds increase the sensitivity of the test papers to acids present in oils or other water-insoluble organic solvents. This latter point is demonstrated by the following comparison. A sample of trichlorofiuoromethane used to wash out a burned out, hermetically sealed refrigeration unit, and thus containing acids formed from the refrigerant during the burn-out, was tested with three types of Congo Red acid test paper.
- Congo Red paper which had been previously wetted with water was found to be the least sensitive to acids present in the organic material; in other words, it took the highest concentrations of acid to cause the color change. Paper which was not pretreated in any way was somewhat more sensitive, detecting somewhat lower concentrations of acid. Surprisingly, test papers containing glycerine are the most sensitive, detecting the lowest concentrations of acids in the organic material.
- Oils particularly when they have been used for a period of time, are highly colored. While solvents such as trichlorofluoromethane, which are used to wash out burned-out refrigeration units, are not colored in themselves, they usually pick up enough oil or other colored materials during the washing process to give them some color also. Thus materials such as those just mentioned may be colored and, if absorbed in the presently available test paper, would mask any color change which might occur in the dye indicator. This is particularly true when the concentration of acid is low.
- the acid-base test papers of this invention can be used for testing liquids which are water soluble or contain water but there appears to be no advantage gained under such conditions in using these papers.
- the primary advantage of these new acid-base test papers is for the acid-base testing of oils or water-insoluble liquids.
- These papers can also be used to test gases for the presence of acidic or basic materials and there is an advantage gained over ordinary wetted test papers.
- Example 1 Congo Red test paper strips were dipped in a solution of 20 volume percent glycerine, 80 volume percent anhydrous methanol, then air dried. The dried paper strips contained 35-40% by weight glycerine. The dried papers still had a slightly damp feeling.
- Treated and untreated test paper strips were torn across the narrow dimension to give a rough, torn edge.
- the torn edge of both treated and untreated test strips was dipped into the acid solutions and the adhering solution was allowed to drain and evaporate. The edges of the test strips were then examined.
- Example 2 Strips of Congo Red paper were dipped into the following liquids and hung up to drain and/or dry: glycerine, ethylene glycol, diethylene glycol, triethylene g ycol, tetraethylene glycol, propylene glycol, 19 wt. percent aqueous dextrose, .20 wt. percent aqueous sorbitol, 38 wt. percent aqueous sucrose and 6 wt. percent aqueous, soluble starch.
- the treated papers contained 25- 35% by weight of the agent in each case.
- the strips were torn and the torn edges dipped in a solution of hydrogen chloride in trichlorofluoromethane of acid number of about 0.02 mg. KOH/g. After draining and drying, they were compared with untreated strips which had been dipped in the same solution.
- test papers treated with glycerine and the glycols retained a damp feeling but the papers treated with solids such as dextrose, sorbitol, sucrose and starch did not.
- solids such as dextrose, sorbitol, sucrose and starch did not.
- the dry-feeling treated test papers were more sensitive by visual observation than the untreated test papers.
- Example 3 Strips of Congo Red test paper were dipped in a 30 wt. percent aqueous solution of CaCl '2H O and others in a 20 wt. percent aqueous solution of LiBr. The strips were then dried by hanging in air, giving papers containing about 25-35 wt. percent of additive. The strips retained a quite damp feeling and were darker red than glycerinetreated or untreated dry strips.
- Example 2 On testing as in Example 2, the treated test papers were found to be more sensitive than the untreated strips but were less sensitive than the glycerine treated strips.
- Example 4 Strips of Brilliant Yellow, red litmus, and blue litmus test papers were immersed in a 20 volume percent solution of glycerine in anhydrous methanol as in Example 1. The strips were then dried overnight. The treated strips of Brilliant Yellow and red litmus test papers proved to be more sensitive than the corresponding untreated test papers when exposed simultaneously to weak ammonia fumes.
- the blue litmus was tested by immersion in a hydrogen chloride solution in trichlorofiuoromethane with an acid number of 0.04 mg. KOH/ g.
- the treated test paper was more sensitive than the untreated paper, the former giving a strong, clear test while the latter gave a weak and doubtful color change.
- An acid indicator consisting of a porous cellulosic material substrate containing an organic dye which is capable of undergoing a color change at a pH of less than 7.0 and from about 5% to about 50% by weight of a neutral, Water soluble, saturated aliphatic polyhydroxy compound composed entirely of carbon, hydrogen and oxygen.
- An acid indicator as defined in claim 1 wherein said polyhydroxy aliphatic compound is ethylene glycol.
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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)
Description
United States Patent O 3,238,020 ACTH-BASE TEST MATERlALS Bernhardt Joseph Eisemau, .lra, Wilmington, DeL, assignor to E. L du Pont de Nemours and Company, Wilmington, DeL, a corporation of Delaware No Drawing. Filed July 26, 1961, Ser. No. 126,880 5 Claims. (Cl. 23-253) This invention relates to novel acid-base test materials. More particularly this invention relates to acid-base test materials that are adaptable for use in non-aqueous, water insoluble systems.
Acid-base test papers such as Congo Red, Litmus, Brilliant Yellow and the like are old and well known for testing aqueous systems or systems which are soluble in water for the presence of acids or bases. However, they have little or no use when testing for the presence of acids in oils, solvents and the like which are water insoluble. This is primarily due to the fact that the oil is absorbed on the paper, masking whatever effect the presence of acid in the oil might have on the test paper. Also, some of the indicators used in the test papers are soluble in oils and are partially extracted from the paper with the result that the effect of acids or bases is more difficult to observe.
Acids may occur in oils or other water-insoluble materials for several reasons. One is the oils contained as lubricants in internal combustion engines where a certain amount of acid is formed. Another is in refrigeration equipment when a motor burnout has occurred with resulting decomposition of part of the refrigerant, particularly when the refrigerant is one of the halogenated hydrocarbon types which are so widely used at present. In cleaning such engines or refrigeration equipment, it is generally desired to remove all of the acid present because of the severe corrosion it causes. This is done by washing the equipment with solvent, oil or the refrigerant until the system is free of acid. It is immediately found however that testing for the presence of acid when oil is present, as it will be both in engines and refrigeration equipment being repaired, can be a very time consuming affair. This is because oil is absorbed on ordinary test papers, which otherwise detect acid quite rapidly, giving the paper the color of the oil and masking the color change which may occur in the paper. It has been necessary therefore to resort to more laborious methods for detecting acids in the presence of oils. One such method is described by Bergstrom et al. in US. Patent 2,770,530.
It is an objective of this invention therefore to provide a series of acid-base test materials for testing for the presence of acids in non-aqueous systems. It is a further object to provide acid-base test materials for detection of acids in oils and other water-insoluble liquids. Other objects will appear hereinafter.
These and other objects are accomplished by using an acid-base test material containing from about 5% to about 50% by weight of a hygroscopic, neutral sensitizer chosen from the strong acid salts of strong bases and polyhydroxy aliphatic organic compounds.
The present invention consists of improved acid-base test papers or other cellulosic materials into which has been incorporated from about 5% to about 50% by Weight of a sensitizer chosen from polyhydroxy aliphatic organic compounds and the strong acid salts of strong bases. The polyhydroxy compounds may be relatively simple compounds such as glycerine, ethylene glycol, di, tri and other ethylene glycols, propylene glycol, more complicated structures such as some of the naturally occurring sugars, e.g. glucose, sucrose, soluble starches and the like or synthetic compounds such as sorbitol, pentaerythrit-ol, erythritol and the like. As a practical matter, there is no limitation on the number of carbon atoms in the polyhydroxy compounds. The strong acid salts of strong bases include the salts of the alkali metal or alkaline earth metal hydroxides. The acid portion of these compounds include hydrogen chloride, hydrogen bromide, hydrogen iodide, sulfuric acid and nitric acid.
Acid-base indicators which are used in test papers are organic dyes which change color with a change in the concentration of hydrogen ion. Usually these dyes contain either basic groups, eg amino groups, or acidic groups which can react with the acid or base present. Some typical examples of such dyes which are used are: Congo Red, Brilliant Yellow, Litmus, Neutral Red, Bromphenol Red, Phenol Red, Thymol Blue, Methyl Red and the like. These dyes are substantive to other cellulosic material substrates as well as to paper. Usually, however, they are also somewhat oil soluble and can be extracted from the paper with organic solvents such as oils. A large number of such types of test papers are used. Certain test papers also contain more than one indicator and these also may be used.
Although the present invention is directed primarily to paper test strips, other materials can be used in place of paper. Examples are cotton cloth, felt and the like as well as inert, porous materials which are inert to acids and bases as well as organic solvents.
The test papers of this invention are prepared by addition of one of the sensitizing agents to the indicator dye, paper combination during some stage of manufacture. Being essentially nonvolatile, the sensitizing agents do not evaporate from the test paper after manufacture. This is, of course, a prime requirement of the sensitizing agent for the whole purpose is defeated if the sensitizing agent is lost from the test paper. Glycerine is the preferred polyhydroxy compound because it is relatively cheap, does not evaporate and seems to give the best results. The limits of concentration of the sensitizing agents is determined, on the lower limit, by the minimum amount of material which must be present to obtain the desired results. This minimum appears to be about 5% by weight. The upper limit is determined by how much of the agent the test paper can hold. Paper, and the other useful substrates, are highly absorbent, but about 50% by weight appears to be a practical upper limit. There is certainly no advantage gained from using more than 50%. The preferred concentration is about 25-50% by weight of the total indicator mass.
The presence of the sensitizing agents in the test papers serves two purposes. First, they prevent oils and other water-insoluble organic materials from being absorbed in the paper and/or from extracting the indicator dye from the paper. Second, the polyhydroxy compounds increase the sensitivity of the test papers to acids present in oils or other water-insoluble organic solvents. This latter point is demonstrated by the following comparison. A sample of trichlorofiuoromethane used to wash out a burned out, hermetically sealed refrigeration unit, and thus containing acids formed from the refrigerant during the burn-out, was tested with three types of Congo Red acid test paper. Congo Red paper which had been previously wetted with water was found to be the least sensitive to acids present in the organic material; in other words, it took the highest concentrations of acid to cause the color change. Paper which was not pretreated in any way was somewhat more sensitive, detecting somewhat lower concentrations of acid. Surprisingly, test papers containing glycerine are the most sensitive, detecting the lowest concentrations of acids in the organic material.
The color change of most of these novel test papers containing one of the polyhydroxy organic compounds is most readily observed at the torn, rough edge of a piece of test paper. It has been observed that a torn edge will undergo the color change while the body of the test paper is unaffected. This is particularly true when the concentration is low. This phenomenon has a great advantage in detecting the presence of low concentrations of acid because the changed color along the torn edge stands out in sharp contrast to the unaltered color of the body of the test paper. This is the recommended method for using most of the test papers of this invention, particularly with low acid concentrations. Of course, when the concentration of acids is high, the color of the body of the test paper changes color also.
Oils, particularly when they have been used for a period of time, are highly colored. While solvents such as trichlorofluoromethane, which are used to wash out burned-out refrigeration units, are not colored in themselves, they usually pick up enough oil or other colored materials during the washing process to give them some color also. Thus materials such as those just mentioned may be colored and, if absorbed in the presently available test paper, would mask any color change which might occur in the dye indicator. This is particularly true when the concentration of acid is low.
The acid-base test papers of this invention can be used for testing liquids which are water soluble or contain water but there appears to be no advantage gained under such conditions in using these papers. The primary advantage of these new acid-base test papers is for the acid-base testing of oils or water-insoluble liquids. These papers can also be used to test gases for the presence of acidic or basic materials and there is an advantage gained over ordinary wetted test papers.
The following examples will better illustrate the practice of the present invention; however, the invention is not intended to be limited to these examples. Parts are by weight unless otherwise indicated.
Example 1 Congo Red test paper strips were dipped in a solution of 20 volume percent glycerine, 80 volume percent anhydrous methanol, then air dried. The dried paper strips contained 35-40% by weight glycerine. The dried papers still had a slightly damp feeling.
For test purposes, two sets of solutions were made up, one by dissolving anhydrous hydrogen chloride in trichlorofluoromethane and the other by dissolving anhydrous hydrogen chloride in a solution of one volume of refrigeration grade oil in two volumes of trichlorofluoromethane. Solutions of acid numbers of 0.04 and 0.02 mg. KOH/g. were prepared in each case.
Treated and untreated test paper strips were torn across the narrow dimension to give a rough, torn edge. The torn edge of both treated and untreated test strips was dipped into the acid solutions and the adhering solution was allowed to drain and evaporate. The edges of the test strips were then examined.
It was found that the torn edge of the glycerine treated test strip which was dipped into the oil-containing solution of acid number 0.04 was a strong blue color, standing out in sharp contrast to the bright red side of the paper. The blue edge of the untreated paper, although present, was much more ditficult to see. Glycerine treated paper which was dipped into the oil-containing solution of acid number 0.02 gave a clear blue edge but the blue of the edge of the untreated test paper was doubtful at best.
Tests with oil free trichlorofluoromethane of acid number 0.02 gave a blue edge on the glycerine treated paper which was clearly discernible (there was no change in the color of the body of the paper) but there was no clear indication of acidity with the untreated paper.
4 Example 2 Strips of Congo Red paper were dipped into the following liquids and hung up to drain and/or dry: glycerine, ethylene glycol, diethylene glycol, triethylene g ycol, tetraethylene glycol, propylene glycol, 19 wt. percent aqueous dextrose, .20 wt. percent aqueous sorbitol, 38 wt. percent aqueous sucrose and 6 wt. percent aqueous, soluble starch. The treated papers contained 25- 35% by weight of the agent in each case.
The strips were torn and the torn edges dipped in a solution of hydrogen chloride in trichlorofluoromethane of acid number of about 0.02 mg. KOH/g. After draining and drying, they were compared with untreated strips which had been dipped in the same solution.
All of the treated test papers showed greater sensitivity than the untreated paper, giving a readily recognizable blue color at the torn edge.
The test papers treated with glycerine and the glycols retained a damp feeling but the papers treated with solids such as dextrose, sorbitol, sucrose and starch did not. The dry-feeling treated test papers were more sensitive by visual observation than the untreated test papers.
Example 3 Strips of Congo Red test paper were dipped in a 30 wt. percent aqueous solution of CaCl '2H O and others in a 20 wt. percent aqueous solution of LiBr. The strips were then dried by hanging in air, giving papers containing about 25-35 wt. percent of additive. The strips retained a quite damp feeling and were darker red than glycerinetreated or untreated dry strips.
On testing as in Example 2, the treated test papers were found to be more sensitive than the untreated strips but were less sensitive than the glycerine treated strips.
Example 4 Strips of Brilliant Yellow, red litmus, and blue litmus test papers were immersed in a 20 volume percent solution of glycerine in anhydrous methanol as in Example 1. The strips were then dried overnight. The treated strips of Brilliant Yellow and red litmus test papers proved to be more sensitive than the corresponding untreated test papers when exposed simultaneously to weak ammonia fumes.
The blue litmus was tested by immersion in a hydrogen chloride solution in trichlorofiuoromethane with an acid number of 0.04 mg. KOH/ g. The treated test paper was more sensitive than the untreated paper, the former giving a strong, clear test while the latter gave a weak and doubtful color change.
In the case of red and blue litmus, the color change was most clearly observed on the rough edge of a torn strip of the paper. With Brilliant Yellow however, better results are obtained using the flat side of the test strip rather than an edge of the test paper. At a higher but undetermined concentration, the same results are obtained with acetic acid.
However, weak organic acids, vis. acetic, propionic, butyric and hexanoic acids, in trichlorofluoromethane (acid No. 0.2 mg. KOH/g.) give only a weak test on the flat side of glycerine treated Congo Red test paper. No clear development of color was obtained on the torn edge.
The above examples clearly demonstrate that the novel test papers prepared according to this invention are superior to untreated test papers for detecting the presence of strong acids in nonaqueous, water-insoluble systems. These acid-base test papers offer a cheap, efficient and rapid method for detecting the presence of acids in such systems which does not require more than ordinary skill, and the ability to detect color changes, on the part of the user. For these reasons, the new test papers of this invention are a valuable contribution to the art.
As many widely different embodiments of this invention may be made without departing from the spirit and scope thereof, it is to be understood that this invention is not limited to the specific embodiments thereof except as defined in the appended claims.
The embodiments of this invention in which an exclusive property or privilege is claimed are defined as follows:
1. An acid indicator consisting of a porous cellulosic material substrate containing an organic dye which is capable of undergoing a color change at a pH of less than 7.0 and from about 5% to about 50% by weight of a neutral, Water soluble, saturated aliphatic polyhydroxy compound composed entirely of carbon, hydrogen and oxygen.
2. An acid indicator as defined in claim 1 wherein said polyhydroxy aliphatic compound is glycerine.
3. An acid indicator as defined in claim 1 wherein said polyhydroxy aliphatic compound is ethylene glycol.
4. An acid indicator as defined in claim 1 wherein the amount of said polyhydroxy aliphatic compound is 25% to 50% by Weight.
5. An acid indicator as defined in claim 1 wherein said cellulosic material substrate is paper and wherein the amount of said polyhydroxy aliphatic compound is 25- 50% by Weight.
References Cited by the Examiner UNITED STATES PATENTS MORRIS O. WOLK, Primary Examiner.
ANTHONY SCIAMANNA, DELBERT E. GANTZ,
Examiners.
Claims (1)
1. AN ACID INDICATOR CONSISTING OF A PROUS CELLULOSIC MATERIAL SUBSTRATE CONTAINING AN ORGANIC DYE WHICH IS CAPABLE OF UNDERGOING A COLOR CHANGE OF A PH OS LESS THAN 7.0 AND FROM ABOUT 5% TO ABOUT 50% BY WEIGHT OF A NEUTRAL, WATER SOLUBLE, SATURATED ALIPHATIC POLYHYDROXY COMPOUND COMPOSED ENTIRELY OF CARBON, HYDROGEN AND OXYGEN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US126880A US3238020A (en) | 1961-07-26 | 1961-07-26 | Acid-base test materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US126880A US3238020A (en) | 1961-07-26 | 1961-07-26 | Acid-base test materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3238020A true US3238020A (en) | 1966-03-01 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US126880A Expired - Lifetime US3238020A (en) | 1961-07-26 | 1961-07-26 | Acid-base test materials |
Country Status (1)
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| US (1) | US3238020A (en) |
Cited By (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3370981A (en) * | 1963-09-23 | 1968-02-27 | Minnesota Mining & Mfg | Electron beam recording medium with amino-azo indicator and halogenated polymer coating |
| US3404962A (en) * | 1964-10-22 | 1968-10-08 | Honeywell Inc | Apparatus for detecting a constituent in a mixture |
| US3425867A (en) * | 1963-09-23 | 1969-02-04 | Minnesota Mining & Mfg | Electron beam recording medium with acid sensitive indicator and halogenated polymer coating |
| US3468636A (en) * | 1964-03-12 | 1969-09-23 | Leslie D Macleod | Ion exchange material and method of making same |
| US3507269A (en) * | 1965-04-26 | 1970-04-21 | Homer H Berry | Clinical diagnostic device for halitosis |
| US3528780A (en) * | 1968-04-05 | 1970-09-15 | Us Air Force | Visual ammonia detector |
| US3544276A (en) * | 1967-05-24 | 1970-12-01 | William Edward Merwitz Sr | Refrigerant sampling and testing device |
| US3653838A (en) * | 1970-02-09 | 1972-04-04 | Mobil Oil Corp | Method for determining basicity of used oils |
| FR2382896A1 (en) * | 1977-03-11 | 1978-10-06 | Minnesota Mining & Mfg | WATER VAPOR AND FORMALDEHYDE STERILIZATION INDICATOR |
| WO1982002251A1 (en) * | 1980-12-19 | 1982-07-08 | Mining & Mfg Minnesota | Method and article for determining free acid concentration in liquid |
| US4654309A (en) * | 1980-12-19 | 1987-03-31 | Minnesota Mining And Manufacturing Co. | Test method and article for estimating the concentration of free acid in liquid |
| US4728499A (en) * | 1986-08-13 | 1988-03-01 | Fehder Carl G | Carbon dioxide indicator device |
| US4822743A (en) * | 1984-12-13 | 1989-04-18 | Lockheed Corporation | Method and cloth for detecting leaks in closed bodies |
| US5749358A (en) * | 1996-10-10 | 1998-05-12 | Nellcor Puritan Bennett Incorporated | Resuscitator bag exhaust port with CO2 indicator |
| US20050227369A1 (en) * | 2004-04-13 | 2005-10-13 | The Lubrizol Corporation, A Corporation Of The State Of Ohio | Rapid analysis of functional fluids |
| WO2006112827A1 (en) * | 2005-04-14 | 2006-10-26 | The Lubrizol Corporation | Rapid analysis of functional fluids |
| US20070083094A1 (en) * | 2005-10-11 | 2007-04-12 | Colburn Joel C | Medical sensor and technique for using the same |
| US20080076993A1 (en) * | 2006-09-27 | 2008-03-27 | Nellcor Puritan Bennett Incorporated | Medical sensor and technique for using the same |
| US20080072913A1 (en) * | 2006-09-25 | 2008-03-27 | Baker Clark R | Carbon dioxide-sensing airway products and technique for using the same |
| US20080075633A1 (en) * | 2006-09-25 | 2008-03-27 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080078394A1 (en) * | 2006-09-25 | 2008-04-03 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080081003A1 (en) * | 2006-09-25 | 2008-04-03 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080083265A1 (en) * | 2006-09-25 | 2008-04-10 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080206874A1 (en) * | 2007-02-28 | 2008-08-28 | The Lubrizol Corporation | Analysis of Functional Fluids |
| US20080206879A1 (en) * | 2007-02-28 | 2008-08-28 | The Lubrizol Corporation | Analysis of Functional Fluids Using a Redox Indicator |
| US20090165801A1 (en) * | 2007-12-31 | 2009-07-02 | Nellcor Puritan Bennett Llc | Carbon dioxide detector having an acrylic based substrate |
| US20090246797A1 (en) * | 2008-03-28 | 2009-10-01 | Nellcor Puritan Bennett Llc | Medical device for the assessment of internal organ tissue and technique for using the same |
| US7811276B2 (en) | 2005-11-10 | 2010-10-12 | Nellcor Puritan Bennett Llc | Medical sensor and technique for using the same |
| US8062221B2 (en) | 2005-09-30 | 2011-11-22 | Nellcor Puritan Bennett Llc | Sensor for tissue gas detection and technique for using the same |
| US20190025268A1 (en) * | 2017-07-19 | 2019-01-24 | American Sterilizer Company | Chemical indicator for monitoring hydrogen peroxide sterilization and disinfection processes |
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Cited By (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3370981A (en) * | 1963-09-23 | 1968-02-27 | Minnesota Mining & Mfg | Electron beam recording medium with amino-azo indicator and halogenated polymer coating |
| US3425867A (en) * | 1963-09-23 | 1969-02-04 | Minnesota Mining & Mfg | Electron beam recording medium with acid sensitive indicator and halogenated polymer coating |
| US3468636A (en) * | 1964-03-12 | 1969-09-23 | Leslie D Macleod | Ion exchange material and method of making same |
| US3404962A (en) * | 1964-10-22 | 1968-10-08 | Honeywell Inc | Apparatus for detecting a constituent in a mixture |
| US3507269A (en) * | 1965-04-26 | 1970-04-21 | Homer H Berry | Clinical diagnostic device for halitosis |
| US3544276A (en) * | 1967-05-24 | 1970-12-01 | William Edward Merwitz Sr | Refrigerant sampling and testing device |
| US3528780A (en) * | 1968-04-05 | 1970-09-15 | Us Air Force | Visual ammonia detector |
| US3653838A (en) * | 1970-02-09 | 1972-04-04 | Mobil Oil Corp | Method for determining basicity of used oils |
| FR2382896A1 (en) * | 1977-03-11 | 1978-10-06 | Minnesota Mining & Mfg | WATER VAPOR AND FORMALDEHYDE STERILIZATION INDICATOR |
| US4298569A (en) * | 1977-03-11 | 1981-11-03 | Minnesota Mining And Manufacturing Company | Steam-formaldehyde sterilization indicator |
| WO1982002251A1 (en) * | 1980-12-19 | 1982-07-08 | Mining & Mfg Minnesota | Method and article for determining free acid concentration in liquid |
| EP0067171A4 (en) * | 1980-12-19 | 1983-04-18 | Minnesota Mining & Mfg | Method and article for determining free acid concentration in oils. |
| US4654309A (en) * | 1980-12-19 | 1987-03-31 | Minnesota Mining And Manufacturing Co. | Test method and article for estimating the concentration of free acid in liquid |
| US4822743A (en) * | 1984-12-13 | 1989-04-18 | Lockheed Corporation | Method and cloth for detecting leaks in closed bodies |
| US4728499A (en) * | 1986-08-13 | 1988-03-01 | Fehder Carl G | Carbon dioxide indicator device |
| US5749358A (en) * | 1996-10-10 | 1998-05-12 | Nellcor Puritan Bennett Incorporated | Resuscitator bag exhaust port with CO2 indicator |
| US20050227369A1 (en) * | 2004-04-13 | 2005-10-13 | The Lubrizol Corporation, A Corporation Of The State Of Ohio | Rapid analysis of functional fluids |
| US7754488B2 (en) | 2004-04-13 | 2010-07-13 | The Lubrizol Corporation | Rapid analysis of functional fluids |
| WO2006112827A1 (en) * | 2005-04-14 | 2006-10-26 | The Lubrizol Corporation | Rapid analysis of functional fluids |
| US8062221B2 (en) | 2005-09-30 | 2011-11-22 | Nellcor Puritan Bennett Llc | Sensor for tissue gas detection and technique for using the same |
| US20070083094A1 (en) * | 2005-10-11 | 2007-04-12 | Colburn Joel C | Medical sensor and technique for using the same |
| US7811276B2 (en) | 2005-11-10 | 2010-10-12 | Nellcor Puritan Bennett Llc | Medical sensor and technique for using the same |
| US8431088B2 (en) | 2006-09-25 | 2013-04-30 | Covidien Lp | Carbon dioxide detector having borosilicate substrate |
| US7992561B2 (en) | 2006-09-25 | 2011-08-09 | Nellcor Puritan Bennett Llc | Carbon dioxide-sensing airway products and technique for using the same |
| US20080072905A1 (en) * | 2006-09-25 | 2008-03-27 | Baker Clark R | Carbon dioxide-sensing airway products and technique for using the same |
| US20080078394A1 (en) * | 2006-09-25 | 2008-04-03 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080081003A1 (en) * | 2006-09-25 | 2008-04-03 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080083265A1 (en) * | 2006-09-25 | 2008-04-10 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080072913A1 (en) * | 2006-09-25 | 2008-03-27 | Baker Clark R | Carbon dioxide-sensing airway products and technique for using the same |
| US8454526B2 (en) | 2006-09-25 | 2013-06-04 | Covidien Lp | Carbon dioxide-sensing airway products and technique for using the same |
| US8449834B2 (en) | 2006-09-25 | 2013-05-28 | Covidien Lp | Carbon dioxide detector having borosilicate substrate |
| US8431087B2 (en) | 2006-09-25 | 2013-04-30 | Covidien Lp | Carbon dioxide detector having borosilicate substrate |
| US20080075633A1 (en) * | 2006-09-25 | 2008-03-27 | Rafael Ostrowski | Carbon dioxide detector having borosilicate substrate |
| US20080077036A1 (en) * | 2006-09-25 | 2008-03-27 | Baker Clark R | Carbon dioxide-sensing airway products and technique for using the same |
| US8420405B2 (en) | 2006-09-25 | 2013-04-16 | Covidien Lp | Carbon dioxide detector having borosilicate substrate |
| US20080077034A1 (en) * | 2006-09-25 | 2008-03-27 | Baker Clark R | Carbon dioxide-sensing airway products and technique for using the same |
| US8109272B2 (en) | 2006-09-25 | 2012-02-07 | Nellcor Puritan Bennett Llc | Carbon dioxide-sensing airway products and technique for using the same |
| US8128574B2 (en) | 2006-09-25 | 2012-03-06 | Nellcor Puritan Bennett Llc | Carbon dioxide-sensing airway products and technique for using the same |
| US20080076993A1 (en) * | 2006-09-27 | 2008-03-27 | Nellcor Puritan Bennett Incorporated | Medical sensor and technique for using the same |
| US8396524B2 (en) | 2006-09-27 | 2013-03-12 | Covidien Lp | Medical sensor and technique for using the same |
| US20080206874A1 (en) * | 2007-02-28 | 2008-08-28 | The Lubrizol Corporation | Analysis of Functional Fluids |
| US20080206879A1 (en) * | 2007-02-28 | 2008-08-28 | The Lubrizol Corporation | Analysis of Functional Fluids Using a Redox Indicator |
| US20090165801A1 (en) * | 2007-12-31 | 2009-07-02 | Nellcor Puritan Bennett Llc | Carbon dioxide detector having an acrylic based substrate |
| US20090246797A1 (en) * | 2008-03-28 | 2009-10-01 | Nellcor Puritan Bennett Llc | Medical device for the assessment of internal organ tissue and technique for using the same |
| US20190025268A1 (en) * | 2017-07-19 | 2019-01-24 | American Sterilizer Company | Chemical indicator for monitoring hydrogen peroxide sterilization and disinfection processes |
| US10823715B2 (en) * | 2017-07-19 | 2020-11-03 | American Sterilizer Company | Chemical indicator for monitoring hydrogen peroxide sterilization and disinfection processes |
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