US2870077A - Cells for electro-chemical measurements - Google Patents

Cells for electro-chemical measurements Download PDF

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US2870077A
US2870077A US374309A US37430953A US2870077A US 2870077 A US2870077 A US 2870077A US 374309 A US374309 A US 374309A US 37430953 A US37430953 A US 37430953A US 2870077 A US2870077 A US 2870077A
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cell
liquids
solution
tube
reservoir
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US374309A
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Kushner Jack
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H Z Corp
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H Z Corp
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/4166Systems measuring a particular property of an electrolyte

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  • my cell comprises a left tube and right tube 11 in butt-alinement therewith.
  • the tubes are of glass or other electrically non-conducting material and are preferably transparent.
  • Rubber tubing 12 or other suitable support is used to hold tubes 10 and 11 in alinement.
  • a thin coating of platinum or other noble metal is on the interior 13 and exterior 14 of tube 10 near and over an end 15 thereof.
  • the platinum coating which is applied in known manner, is a unitary one and electrically and otherwise continuous from 13 to 15 to 14.
  • a protective band 16 of metal such as copper, is secured around the film 14. Electrical contact with the platinum is made by means of suitable metal clips 17, which may be joined by wire 18 to one terminal 19 of an automatic recording device 20.
  • Tube 11 is joined to a calomel half-cell unit by means of a capillary tube 21 at the junction of tube 11 and a T tube 22.
  • One arm of this T tube 22 contans calomel material (mercurous chloride and mercury) and a wire 23 which is in contact with terminal 39 of recorder 20.
  • the other arm 24 is joined together, atits upper end, to a reservoir 25 for suitable solution, preferably potassium chloride 26.
  • a valve or screw clamp 27 is advantageously employed.
  • the illustrated means comprise a conventional air bulb 28 which is joined to air reservoir 29 by means of a fitting 30 having a check valve 31 to prevent the escape of air from reservoir 29 to bulb 28.
  • a screw clamp or valve 32 also is provided for closing rubber tubing 33, if desired.
  • Fitting 30 also has another opening to which one end of tubing 34 is secured. The other end of tubing 34 terminates in liquid reservoir 25, a stopper 35, through which the end of tubing 34 passes, affording air-tightness to the top of the reservoir 2'5.
  • An air gauge 36 for determining the pressure on the capillary 21 is provided in series with tubing 34.
  • a concentrated solution of the gum in water is first prepared, filtered and diluted. Potassium chloride is added at 10 C. until the solution is saturated.
  • the thickness of the noble metal film 13 is not of critical importance unless it becomes so great as to offer material resistance to the flow of 'the material being tested. Film thicknesses within the range of 0.001 to 0.05 millimeter have, however, been found to yield satisfactory results.
  • the area of the noble metal coating is likewise not critical. I have foundthat areas less than /2 square centimeter are not to be recommended, however. For a cell with an inside diameter of tubes 10, 11 of A, an area of 5 square centimeters is desirable.
  • the capillary tube advantageously should permit a flow of solution 26 at the rate of 0.05 to 2 milliliters per hour.
  • the solution 26 gives desirable results when it has a concentration of about 10 percent by Weight of gum.
  • other gums such as arabic, agar and accacia can be used.
  • solution 26 having a relative viscosity of 16 to 20, compared to water at 25 C. is desirable.
  • liquid which is to be tested is fed into tube 10 in the direction shown by the arrow 37 alongside of tube 10 and the liquid flows out of tube 11 as shown by arrow 38.
  • Sufiicient pressure is applied to the solution 26 in the capillary 21 by compressing the air bulb 28.
  • a liquidliquid interface is formed by the liquid under test and the solution 26 from reservoir 25.
  • the resulting potential can be read from the recorder 20 and, if desired, a per- 7 manent record of this potential, showing fluctuations, if any, during every moment of the test, may be obtained by suitable conventional, recording charts and instruments (not shown) all of which are encompassed by the general term recorder.
  • My novel cells may be employed to yield excellent results on a variety of flowing liquids whose electrochemical characteristics are being determined.
  • my novel cell lends itself to the determination of the concentration of chlorine, chro' mates, organic matter, sulfites, oxidation-reduction potential,-e. g. in-dye baths, and the obtaining of measurements on any material that gives a stable potential.
  • A- clean,- sharp, liquid junction which remains stable at all rates of liquid flow isobtained.
  • a further advantage of my novel cell is that any bubbles of gas which may accumulate in the T tube 22 will not interfere with the readings as they will be blown through the capillary 21 by reason of the aforesaid pressure.
  • a cell suitable for making continuous electrochemical measurements on liquids flowing therethrough which comprises, in combination, straight tubular means providing continuously substantially unobstructed flow for said liquids to'be measured, means at the end of said means providing for the introduction and discharge of liquids, a-noble metal electrode comprising a'thin coating on-a zone of the inner surface of said tubular means, means for establishing electrical contactwith said coating, a half cell having a reservoir for an electrolyte, said reservoir communicating with said tubular means through a restricted flow passage, means for establishing electrical contact with said half-cell, and means for applying a substantially constant pressure capable of maintaining substantiallyconstant flow of the electrolyte into said tubular means.
  • A- cell in accordance with claim 1, whereinsaid straight tubular means comprise two members inabutting alinement with each other and said noble metal-electrode coating is on the inner andouter surface of-on'e-e'nd of one of said members.
  • said constant pressure means comprise air under pressure

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
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Description

Jan. 20, 1959 J. .KUSHNER I 2,370,077
CELLS FOR ELECTRO-CHEMICAL MEASUREMENTS Filed Au 14. 1953 *4 208.72%? c220? Ewing if arm ya m MM QM KEN CELLS FOR ELECTRO-CHEMICAL lWEASUREMEN TS Jack Kushner, Hicksville, N. Y., assignor, by mesne assignments, to H. Z. Corporation, Ridgewood, N. J., a 1 corporation of New Jersey Application August 14, 1953, Serial No. 374,309
5 Claims. c1. 204- 195 manner in which I now prefer to practice the invention,
the following detailed description, taken in-connection with the acompanying drawing," being intended for the purpose of illustration.
Referring to the drawing, which is a side elevation, in part section, in part schematic, and in part broken away, my cell comprises a left tube and right tube 11 in butt-alinement therewith. The tubes are of glass or other electrically non-conducting material and are preferably transparent. Rubber tubing 12 or other suitable support is used to hold tubes 10 and 11 in alinement. A thin coating of platinum or other noble metal is on the interior 13 and exterior 14 of tube 10 near and over an end 15 thereof. In other words, the platinum coating, which is applied in known manner, is a unitary one and electrically and otherwise continuous from 13 to 15 to 14. A protective band 16 of metal such as copper, is secured around the film 14. Electrical contact with the platinum is made by means of suitable metal clips 17, which may be joined by wire 18 to one terminal 19 of an automatic recording device 20.
Tube 11 is joined to a calomel half-cell unit by means of a capillary tube 21 at the junction of tube 11 and a T tube 22. One arm of this T tube 22 contans calomel material (mercurous chloride and mercury) and a wire 23 which is in contact with terminal 39 of recorder 20. The other arm 24 is joined together, atits upper end, to a reservoir 25 for suitable solution, preferably potassium chloride 26. To help control the flow of the solution 26 through the capillary 21 a valve or screw clamp 27 is advantageously employed.
To prevent the contamination of the solution 26 by whatever liquid is flowing through tube 11, means for insuring a positive downward pressure on the solution 26 in the capillary 21 are provided. The illustrated means comprise a conventional air bulb 28 which is joined to air reservoir 29 by means of a fitting 30 having a check valve 31 to prevent the escape of air from reservoir 29 to bulb 28. A screw clamp or valve 32 also is provided for closing rubber tubing 33, if desired. Fitting 30 also has another opening to which one end of tubing 34 is secured. The other end of tubing 34 terminates in liquid reservoir 25, a stopper 35, through which the end of tubing 34 passes, affording air-tightness to the top of the reservoir 2'5. An air gauge 36 for determining the pressure on the capillary 21 is provided in series with tubing 34.
United S fltS Patentf ice In addition to the novel combination of parts set forth as constituting by invention, my invention also encompasses certain other advantageous features. Thus, I have found that optimum results are obtained when careful control of the viscosity of the potassium chloride solution 26 is exercised. This is an important consideration as practical reasons limit one cell to a particular size of capillary; and hence if the solution 26 is not viscous enough too much of it may flow into the capillary, with undesirable consequences. solution having too high a viscosity is not desirable for practical reasons.
Accordingly, I prefer to employ an aqueous, saturated solution of potassium chloride which contains any natural gum soluble in water to an extent suflicient to increase the viscosity so that positive pressure is required to cause the solution to pass through the capillary 21 at a desirable rate.
In preparing the solution 26 a concentrated solution of the gum in water is first prepared, filtered and diluted. Potassium chloride is added at 10 C. until the solution is saturated.
It will be understood that variations in the thickness and area of the noble metal film, in the size of the capillary tube 21, andin the composition of the electrolyte solution 26 may be made in order to obtain optimum results. Without limiting myself to the figures hereinafter given, I can state as follows:
-The thickness of the noble metal film 13 is not of critical importance unless it becomes so great as to offer material resistance to the flow of 'the material being tested. Film thicknesses within the range of 0.001 to 0.05 millimeter have, however, been found to yield satisfactory results.
The area of the noble metal coating is likewise not critical. I have foundthat areas less than /2 square centimeter are not to be recommended, however. For a cell with an inside diameter of tubes 10, 11 of A, an area of 5 square centimeters is desirable.
The capillary tube advantageously should permit a flow of solution 26 at the rate of 0.05 to 2 milliliters per hour.
The solution 26 gives desirable results when it has a concentration of about 10 percent by Weight of gum. In addition to ghatti gum, other gums such as arabic, agar and accacia can be used. In general, solution 26 having a relative viscosity of 16 to 20, compared to water at 25 C. is desirable.
In using my cell, liquid which is to be tested is fed into tube 10 in the direction shown by the arrow 37 alongside of tube 10 and the liquid flows out of tube 11 as shown by arrow 38.
Sufiicient pressure is applied to the solution 26 in the capillary 21 by compressing the air bulb 28. As the liquid in tube 11 passes the capillary opening a liquidliquid interface is formed by the liquid under test and the solution 26 from reservoir 25. The resulting potential can be read from the recorder 20 and, if desired, a per- 7 manent record of this potential, showing fluctuations, if any, during every moment of the test, may be obtained by suitable conventional, recording charts and instruments (not shown) all of which are encompassed by the general term recorder.
My novel cells may be employed to yield excellent results on a variety of flowing liquids whose electrochemical characteristics are being determined. Thus, in
the case of boiler feed water, it is important to know the concentration of dissolved oxygen therein at all times. By simply placing my novel cell in series with the boiler feed water, and substituting a polarograph for the recorder, electrical readings .re quickly and accurately ob- On the other hand, a
3 failed, and from these readings, by suitable calculations well. understood in the art,.the desired dataon dissolved oxygen concentration can be obtained. Any necessary corrective action can then be taken as indicated by the readings and/or calculations.-
Insimilar manner; my novel cell lends itself to the determination of the concentration of chlorine, chro' mates, organic matter, sulfites, oxidation-reduction potential,-e. g. in-dye baths, and the obtaining of measurements on any material that gives a stable potential.
Itwillnow be apparent to those skilled in the art that my.- novel cells have certain unique advantages. lend themselves ina technically-simple manner to utilization inconnection with liquids which can be passed therethrough'without causing any adverse effects on the apparatus and hence on the data obtained. This is a special consideration-in the treatment of liquids such as slurries, raw-sewage and-semi-liquids which normally may contain fibrous inclusions and abrasive particles. Also, a continuous, liquiddiquidjunction, between the K01 solution Mind the liquid under test is assured because of the pressure on the solution. The capillary tube 21, moreoven-is such that the KCl'will flow into tube 11 at a slowrate, thereby minimizing the amount of contamination of one liquid by the other. A- clean,- sharp, liquid junction which remains stable at all rates of liquid flow isobtained. A further advantage of my novel cell is that any bubbles of gas which may accumulate in the T tube 22 will not interfere with the readings as they will be blown through the capillary 21 by reason of the aforesaid pressure.
While Ihave described-myinvention in detailin its preferred embodiment, it will be obvious to those skilled in-the art,.after understanding my invention, that various changes and modifications may be made therein without They departing from the spirit o'r meanness I aim' time appended claims to cover all such modifications and changes.
I claim:
1. A cell suitable for making continuous electrochemical measurements on liquids flowing therethrough which comprises, in combination, straight tubular means providing continuously substantially unobstructed flow for said liquids to'be measured, means at the end of said means providing for the introduction and discharge of liquids, a-noble metal electrode comprising a'thin coating on-a zone of the inner surface of said tubular means, means for establishing electrical contactwith said coating, a half cell having a reservoir for an electrolyte, said reservoir communicating with said tubular means through a restricted flow passage, means for establishing electrical contact with said half-cell, and means for applying a substantially constant pressure capable of maintaining substantiallyconstant flow of the electrolyte into said tubular means.
2. A- cell in accordance with claim 1, whereinsaid straight tubular means comprise two members inabutting alinement with each other and said noble metal-electrode coating is on the inner andouter surface of-on'e-e'nd of one of said members.
3. A cell in accordance with claim 1, wherein means for continuously recording the voltage are alsoprovided.
4. A' cell in accordance with claim 1, wherein said constant pressure-means comprise air under pressure;
5.-A cell-in accordance with claim 2, wherein said constant pressure means comprise air under pressure;
Coleman Feb. 23, 1943'

Claims (1)

1. A CELL SUITABLE FOR MAKING CONTINUOUS ELECTROCHEMICAL MEASUREMENTS ON LIQUIDS FLOWING THERETHROUGH WHICH COMPRISES, IN COMBINATION, STRAIGHT TUBULAR MEANS PROVIDING CONTINUOUSLY SUBSTANTIALLY UNOBSTRUCTED FLOW FOR SAID LIQUIDS TO BE MEASURED, MEANS AT THE END OF SAID MEANS PROVIDING FOR THE INTRODUCTION AND DISCHARGE OF LIQUIDS, A NOBLE METAL ELECTRODE COMPRISING A THIN COATING ON A ZONE OF THE INNER SURFACE OF SAID TUBULAR MEANS, MEANS FOR ESTABLISHING ELECTRICAL CONTACT WITH SAID COATING, A HALF CELL HAVING A RESERVOIR FOR AN ELECTROLYTE, SAID RESERVOIR COMMUNICATING WITH SAID TUBULAR MEANS THROUGH A RESTRICTED FLOW PASSAGE, MEANS FOR ESTABLISHING ELECTRICAL CONTACT WITH SAID HALF-CELL AND MEANS FOR APPLYING A SUBSTANTIALLY CONSTANT PRESSURE CAPABLE OF MAINTAINING SUBSTANTIALLY CONSTANT FLOW OF THE ELECTROLYTE INTO SAID TUBULAR MEANS.
US374309A 1953-08-14 1953-08-14 Cells for electro-chemical measurements Expired - Lifetime US2870077A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3047488A (en) * 1953-12-29 1962-07-31 Gulf Research Development Co Reference electrode
US3051631A (en) * 1959-04-07 1962-08-28 Diamond Alkali Co Method and apparatus for the control of oxidation-reduction reactions
US3214354A (en) * 1961-07-24 1965-10-26 Union Carbide Corp Measurement of catalyst activity
US3216915A (en) * 1961-12-12 1965-11-09 Beckman Instruments Inc Flow cell for ion potential measurements
US3222264A (en) * 1960-04-25 1965-12-07 Nesh Florence Method of determining the chloride ion concentration in water
US3410779A (en) * 1965-04-01 1968-11-12 Honeywell Inc Measuring apparatus with pressure amplifier
FR2582102A1 (en) * 1985-05-14 1986-11-21 Commissariat Energie Atomique Cell for continuous measurement of redox potentials
US4874487A (en) * 1986-07-18 1989-10-17 Raychem Corporation Corrosion protection

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2311976A (en) * 1939-01-25 1943-02-23 Edwin D Coleman ph measurement and control device

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2311976A (en) * 1939-01-25 1943-02-23 Edwin D Coleman ph measurement and control device

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3047488A (en) * 1953-12-29 1962-07-31 Gulf Research Development Co Reference electrode
US3051631A (en) * 1959-04-07 1962-08-28 Diamond Alkali Co Method and apparatus for the control of oxidation-reduction reactions
US3222264A (en) * 1960-04-25 1965-12-07 Nesh Florence Method of determining the chloride ion concentration in water
US3214354A (en) * 1961-07-24 1965-10-26 Union Carbide Corp Measurement of catalyst activity
US3216915A (en) * 1961-12-12 1965-11-09 Beckman Instruments Inc Flow cell for ion potential measurements
US3410779A (en) * 1965-04-01 1968-11-12 Honeywell Inc Measuring apparatus with pressure amplifier
FR2582102A1 (en) * 1985-05-14 1986-11-21 Commissariat Energie Atomique Cell for continuous measurement of redox potentials
US4874487A (en) * 1986-07-18 1989-10-17 Raychem Corporation Corrosion protection

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