US2345498A - Salt-bridge tube and method of producing it - Google Patents

Salt-bridge tube and method of producing it Download PDF

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US2345498A
US2345498A US437153A US43715342A US2345498A US 2345498 A US2345498 A US 2345498A US 437153 A US437153 A US 437153A US 43715342 A US43715342 A US 43715342A US 2345498 A US2345498 A US 2345498A
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salt
bridge
tube
glass
plug
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George A Perley
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Leeds and Northrup Co
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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
    • G01N27/28Electrolytic cell components
    • G01N27/30Electrodes, e.g. test electrodes; Half-cells

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  • My invention relates to salt-bridge tubes such as employed with reference electrodes oi ion concentration cells, and more particularly relates to methods of making, iii a salt-orldge tube, a
  • minute passage comprised in or constituting the salt-bridge connection providing for difiusion oi the salt-bridge solution into another solution ex I terior to the salt-bridge tube and for electrical conduction between the two solutions.
  • Fig. 1 partly diagrammatic, illustrates a typical arrangement for recording changes in ion-concentration
  • Figs. 2 to 4 illustrate successive stages of lormation of a salt-bridge tube shown in Fig. 1;
  • Fig. 5 illustrates a, modification of the saltbridge tube of Fig. 4.
  • FIG. 6 and 7 illustrate another modification of my invention.
  • FIG. 1 as exemplary of a system with which the invention may be employed, so
  • lution S whose hydrogen-ion concentration or hydroxyl-ion concentration, generically termed pH, is to be measured, is passed through the flow channel 8, which maybe generallyof the-type disclosed inmy United States Letters Patent 2,l08,293,comprising a chamber 2 in which is disposed a suitable measuring electrode, for er;-
  • the 'difierence of potential developed by the ion-concentration cell comprising the measuring and reference electrodes may be measured by any" suitable system, such for example as disclosed in United States Letters Patent 2,108,294,
  • th movable contact member t is moved alternately to engage first one and then the other of the contacts iii, ll; each time the contact 9 is moved into engagement with contact it, the condenser it is subjected to voltage developed by the ion.- concentration cell 3, s and each time contact it engages the fixed contact it, the condenser 02 is subjected to the effective voltage of potentiometer 35, i. e., the potential difieirence existbetween slide-wire contact its and a terminal it of the slide-wire.
  • connection of condenser l2 alternately to the ion-concentration cell and to the potentiometer slide-wire effects no flow of displacement current to or from condenser it; in consequence, the potential of the grid it of tube V remains constant and there is no change in magnitude of current traversing resistance ll in circuit with the anode to of the tube V and a suitable source oi current, such as battery as.
  • a serious disadvantage of the first group preeluding their satisfactory use in industrial recording systems is that they require the bridge opening, region of contact between the bridge and test solutions, frequently to be cleaned or renewed as otherwise there are established secondary junction potentials of magnitude correspending with intolerable error.
  • junction When this type of junction is used it is desirable or necessary that the junction be flushed before each pH measurement and that fresh salt-bridge solution be supplied at the interface, contact plane of the salt-bridge and test solutions, each time a liquid junction is formed.
  • fresh salt-bridge solution be supplied at the interface, contact plane of the salt-bridge and test solutions, each time a liquid junction is formed.
  • a serious disadvantage of the second type or group of salt-bridge connections is the need for relatively large volumetric flow of the salt-bridge solution to avoid contamination of the salt-bridge solution by back diffusion thereinto of the test solution. Consequently the maintenance and cost of operation of such type junction is excessive particularly when, asin industrial applications, continuous measurements of pH are desired. 7
  • the salt-bridge connection or opening is provided by a crack or slit 8 of such extremely narrow width, for example from about .000025 centimeter to preferably not more than about .0005 centimeter, that the velocity through and from the salt-bridge connection is so high there is no possibility of contamination of the salt-bridge solution by back diffusion of the test solution; more particularly, the velocity is within the range which the liquid junction of the salt-bridge is subjected to pressure differences as high as 28" of mercury; even when the salt-bridge solution is subjected to such high differential pressure continuous recording of pH for long periods of time, weeks, is entirely, and for the first time, practical.
  • opening 25 there are deor opening 25, Fig. 2.
  • the cross sectional area of this opening may correspond, for example, with the area of a circle of about 1.5 millimeters diameter, though the hole is not necessarily circular in cross section; the thickness of the tube wall may be about 1 millimeter.
  • the glass of tube 1 is still soft and tacky a small molten or tacky globule of another glass, one having suitably different temperature coefficient of expansion, is brought into engagement with opening 25 and is drawn into it by capillary action.
  • This globule forms a block or plug 26, Fig. 3, completely filling or sealing the opening 25 and more or less fused into or bonded to the glass comprising the tube 1; when the difference in the temperature coeficients is small, the seal is preferably what is termed in the glass-blowing art as a cold seal.
  • the'seal plug 26 is of glass having higher I temperature coeflicient of expansion than the glass comprising tube 1, it shinks during cooling more rapidly than the tube wall and as a result there is produced, Fig. 4, a crack, fracture or slit 8 extending to greater or less extent about the plug.
  • the length and width of the crack may be reasonably closely determined by selection of glasses having suitably different temperature coefficients of expansion and by selection of the cross-sectional area of opening 25; in general, the smaller the difference between the coeflicients of expansion of the glasses comprising tube I and plug 26, the narrower is the slit or crack 8.
  • the other modifications the
  • ' slit is too narrow to be blocked by particles of solid matter which may be present or formed in the salt-bridge solution.
  • the following table indicates characteristics of the salt-bridge connections made in accordance with the foregoing method from various glasses therein identified.
  • the salt-bridge tube or at least the end of it immersed in the test solution must be of relatively small diameter, for example about 3.5 millimeters, the method and construction illustrated in Figs. 6 and 7 is preferred.
  • the opening 253 at one end of tube 13 is sealed by a globule of glass having a suitably different it, closing the hole in the heated tube with a plug of another glass having substantially different eoeflicient of expansion, and thereafter cooling the tube to produce, because of different rates of contraction of the glasses, a crack at or adjacent the plug.
  • the glass comprising the tube or body, 1 or 13 should be of relatively high chemical and mechanical resistance: the glass comprising plug 28 or 263 should, for long life, be of relatively high chemical resistance but, without appreciable effect upon accuracy of the measurement, may be of less chemically resistant glass.
  • the range of choice of suitable glasses is of course wider when the salt-bridge tube is to be used only in a predetermined portion of the pH range rather than throughout a range from 0. pH to 14 pH.
  • a salt-bridge tube having a wall of glass, a plug of glass fused to said wall and having a coefficient of expansion higher than that of the glass of said wall, and for a salt-bridge connection in said wall, at least one crack around said plug and of width not exceeding about .0005

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Description

March 28, 1944. e. A. PERLEY 2,345,493
SALT-BRIDGE TUBES AND METHODS OF PRODUCING THEM- Filed April 1, 1942 INVENTOR. Gconca A. PERLEY ATTORNEY.
Patented Mar. 28, 1944 UNITED s'mrss SALT-BRIDGE "some AND METHOD or raoo ioma 1r George A. Perley, Wyncote, Fa", assisnor to Leeds and Northrup Qompany, Philadelphia, Pa a corporation of Pennsylvania Application April 1, 1942, Serial No. 437,153
7! Claims. (6i. bod-195) My invention relates to salt-bridge tubes such as employed with reference electrodes oi ion concentration cells, and more particularly relates to methods of making, iii a salt-orldge tube, a
minute passage comprised in or constituting the salt-bridge connection providing for difiusion oi the salt-bridge solution into another solution ex I terior to the salt-bridge tube and for electrical conduction between the two solutions.
In accordance with my invention, while the glass constituting the salt-bridee tube is at tem perature sufiiciently high to render it taclry, small hole ther in is sealed by plug oi material, such as another glass, having diiiereht,
preferably higher, coefficient ofeapansiou so that, upon cooling of the glasses, there is pro duced a oracle or slit having the hereinafter described advantages for forming a salt-bridge connection.
My invention iurther resides in the salt-bridge tubes and methods of making them heremaiter described and claimed.
For an understanding oi my invention, reierence is made to the accompanying drawing, in which:
Fig. 1, partly diagrammatic, illustrates a typical arrangement for recording changes in ion-concentration;
Figs. 2 to 4 illustrate successive stages of lormation of a salt-bridge tube shown in Fig. 1;
Fig. 5 illustrates a, modification of the saltbridge tube of Fig. 4.
Figs. 6 and 7 illustrate another modification of my invention.
Referring to Fig. 1 as exemplary of a system with which the invention may be employed, so
lution S whose hydrogen-ion concentration or hydroxyl-ion concentration, generically termed pH, is to be measured, is passed through the flow channel 8, which maybe generallyof the-type disclosed inmy United States Letters Patent 2,l08,293,comprising a chamber 2 in which is disposed a suitable measuring electrode, for er;-
amplea glass electrode 3, and a chamber in which is disposed a suitable reference electrode 5. iBetweenthe reference electrode and solution S ell-maimed a salt-bridge'comprising a suitable salt-bridge solutions, for example potassium chloride, confinedwithin tube l having an opening orsalt-bridge connection 8, of character hereinafter more fully explained, aifording a path for electrical conduction between the reference electrode 5 and the solution S.
The 'difierence of potential developed by the ion-concentration cell comprising the measuring and reference electrodes, may be measured by any" suitable system, such for example as disclosed in United States Letters Patent 2,108,294,
or 2,285,482, or application Serial No. 457,845,
Williams filed September 10, 1942.
In the system shown in Fig. 1, which is claimed in aforesaid Williams application, th movable contact member t is moved alternately to engage first one and then the other of the contacts iii, ll; each time the contact 9 is moved into engagement with contact it, the condenser it is subjected to voltage developed by the ion.- concentration cell 3, s and each time contact it engages the fixed contact it, the condenser 02 is subjected to the effective voltage of potentiometer 35, i. e., the potential difieirence existbetween slide-wire contact its and a terminal it of the slide-wire. If these two voltages are equal, the connection of condenser l2 alternately to the ion-concentration cell and to the potentiometer slide-wire effects no flow of displacement current to or from condenser it; in consequence, the potential of the grid it of tube V remains constant and there is no change in magnitude of current traversing resistance ll in circuit with the anode to of the tube V and a suitable source oi current, such as battery as.
When, however, the fixed contacts ill and ii are not at the same potential, due for example to change in the pl-l of solution S, the movement of contact 9 from engagement with one to the other of the fixed contacts causes flow of displacement current to or from condenser l2 and accordingly the potential of the grid I6 is decreased or increased and therefore causes, because of its effect upon the anode current 'of tube V, change in magnitude of the voltage drop across the resistance I1.
Upon increase or decrese of the voltage drop across resistance ll, displacement current flows to or from the condenser 2t connected in series with galvauometer 2| across resistance ll. As more fully explained in the aforesaid Patent 2,285A82 to Wunsch, the deflections of the galvanometer are utilized to efiect a rebalancing adjustment of the movable element of the potentiometer slide-wire l5 and to position a pen or equivalent marker element which traces upon the chart or sheet 22 a curve representing the variation, with time, of the selected ion-concentration of solution S. The oscillation of contact 9 between contacts is and H may be efiected by cam 23 driven at constant speed by connection for example to a suitable shaft of the mechanism 24, preferably of the type disclosed in United States Letters Patent 1,935,732, Squibb.
In ion-concentration measuring systems in general, the path providing for electrical conduction between the salt-bridge solution and the test solution have been, either of the type com- 'prising ground glass plugs, closed stop-cocks,
A serious disadvantage of the first group preeluding their satisfactory use in industrial recording systems is that they require the bridge opening, region of contact between the bridge and test solutions, frequently to be cleaned or renewed as otherwise there are established secondary junction potentials of magnitude correspending with intolerable error. In many of the salt-bridge connections of the first type or group, there'are a multitude of paths for diffusion of thesalt-bridge solution into the test solution as well as for the reverse diffusion of the test solution in the salt-bridge solution; the mechanical resistance to flow of the salt-bridge solution may vary greatly in the different paths yet all paths may contribute in the interchange of ions between the salt-bridge and test solutions with the result there is often, and usually, ultimately established a constrained diffusion type of junction which is a source of serious variation in potential and therefore of error of measurement.
When this type of junction is used it is desirable or necessary that the junction be flushed before each pH measurement and that fresh salt-bridge solution be supplied at the interface, contact plane of the salt-bridge and test solutions, each time a liquid junction is formed. In industrial recording of pH, it is not feasible to make the frequent cleansing or renewal operations necessary to insure reasonably high accuracy of the pH measurments.
A serious disadvantage of the second type or group of salt-bridge connections, those comprising cylindrical openings of small diameter, is the need for relatively large volumetric flow of the salt-bridge solution to avoid contamination of the salt-bridge solution by back diffusion thereinto of the test solution. Consequently the maintenance and cost of operation of such type junction is excessive particularly when, asin industrial applications, continuous measurements of pH are desired. 7
Another. disadvantage of this type of saltbridge connection is that it may to varying extent be blocked by particles of solid matter, for example-precipitate from the salt-bridge solution.
In accordance with the present invention, the salt-bridge connection or opening is provided by a crack or slit 8 of such extremely narrow width, for example from about .000025 centimeter to preferably not more than about .0005 centimeter, that the velocity through and from the salt-bridge connection is so high there is no possibility of contamination of the salt-bridge solution by back diffusion of the test solution; more particularly, the velocity is within the range which the liquid junction of the salt-bridge is subjected to pressure differences as high as 28" of mercury; even when the salt-bridge solution is subjected to such high differential pressure continuous recording of pH for long periods of time, weeks, is entirely, and for the first time, practical.
Though not limited thereto, there are deor opening 25, Fig. 2. The cross sectional area of this opening may correspond, for example, with the area of a circle of about 1.5 millimeters diameter, though the hole is not necessarily circular in cross section; the thickness of the tube wall may be about 1 millimeter. While the glass of tube 1 is still soft and tacky a small molten or tacky globule of another glass, one having suitably different temperature coefficient of expansion, is brought into engagement with opening 25 and is drawn into it by capillary action. This globule forms a block or plug 26, Fig. 3, completely filling or sealing the opening 25 and more or less fused into or bonded to the glass comprising the tube 1; when the difference in the temperature coeficients is small, the seal is preferably what is termed in the glass-blowing art as a cold seal.
When the'seal plug 26 is of glass having higher I temperature coeflicient of expansion than the glass comprising tube 1, it shinks during cooling more rapidly than the tube wall and as a result there is produced, Fig. 4, a crack, fracture or slit 8 extending to greater or less extent about the plug. The length and width of the crack may be reasonably closely determined by selection of glasses having suitably different temperature coefficients of expansion and by selection of the cross-sectional area of opening 25; in general, the smaller the difference between the coeflicients of expansion of the glasses comprising tube I and plug 26, the narrower is the slit or crack 8. As in the other modifications, the
' slit is too narrow to be blocked by particles of solid matter which may be present or formed in the salt-bridge solution.
By way of example, the following table indicates characteristics of the salt-bridge connections made in accordance with the foregoing method from various glasses therein identified.
of from about 10 cm. per hour to about cm.
so low, for example .002 cubic centimeter per hour to .02 cubic centimeter per hour that the maintenance cost of salt-bridge solution for continuous recording is negligible. It is feasible to (The electrical resistance of the salt-bridge .per hour although the volumetric rate of flow is connection is measured with salt-bridge solution inside and outside of the tube; when lower resistance is desired one or more additional saltbridge connections may be made in the same tube in accordance with the methods herein de- The surfaces of the passage defined by the crack have the extreme smoothness or gloss of a glass fracture and so offer inappreciable frictional resistance to flow of the salt-bridge solution. Aside from other considerations, potassium chloride is preferred over other salt-bridge solutions in the crack type of salt-bridge connection because of its lower viscosity (10.95 millipoises at C.)
It is usually not detrimental to satisfactory performance if the crack 8 extends entirely about the plug because its almost inevitable dissymmetry locks the plug firmly in position.
When the glass comprising tube 'I-is of the higher coefficeint of expansion, upon cooling of the tube and plug, Fig. 5, one or more short cracks 8A extending away from the boundary of the plug and tube through the tube wall are formed. Th'ese cracks afford a salt-bridge connection having substantially the same desirable characteristics including constancy of junction potential, within about .003 volt over long periods of-uninterrupted use, as the modification shown in Fig. 4.
Particularly when the salt-bridge tube, or at least the end of it immersed in the test solution must be of relatively small diameter, for example about 3.5 millimeters, the method and construction illustrated in Figs. 6 and 7 is preferred.
The opening 253 at one end of tube 13 is sealed by a globule of glass having a suitably different it, closing the hole in the heated tube with a plug of another glass having substantially different eoeflicient of expansion, and thereafter cooling the tube to produce, because of different rates of contraction of the glasses, a crack at or adjacent the plug.
2. The method of forming a passage for a salt bridge connection through the wall of a salt bridge tube which comprises forming a small hole through said wall, heating the tube to temperature effecting tackiness of the glass comprising temperature coeificient of expansion. After the globule has fused or bonded to the end of the tube and while both are still at high temperature, the open end of tube 13 is blown into to shape the globule into a plug or thimble 263. As the assembly cools, a crack 83 is produced due to the different rates of contraction of the two glasses; the crack extends through the wall and to greater or less extent around the periphery of the tube at the junction of the two glasses. The salt-bridge connection afforded by crack 813 has the same desirable operating characteristics discussed above in connection with the other modifications.
In selection of the glasses for all modifications, the glass comprising the tube or body, 1 or 13, should be of relatively high chemical and mechanical resistance: the glass comprising plug 28 or 263 should, for long life, be of relatively high chemical resistance but, without appreciable effect upon accuracy of the measurement, may be of less chemically resistant glass. The range of choice of suitable glasses is of course wider when the salt-bridge tube is to be used only in a predetermined portion of the pH range rather than throughout a range from 0. pH to 14 pH.
What I claim is:
1. The method of forming a passage for a salt bridge connection through the wall of a salt bridge tube which comprises forming a small hole through said wall, heating the tube to temperature eflecting tackiness of the glass comprising it, closing the hole in the heated tube with a plug of another glasshaving higher coefiicient of expansion, and thereafter cooling the tube and plug to produce, because of different rates of contraction of the glasses, a crack around the plug.
3. The method of forming a passage for a salt bridge connection through the wall of a salt bridge tube which comprises forming a small hole through said wall, heating the tube to temperature eifecting'tacky state of the glass comprising it, closing the hole in the heated tube with a plug of another glass having lower coefficient of expansion, and thereafter cooling the tube and plug to form, because of different rates of contraction of the glasses, a crack in the tube extending away from the plug.
4. The method of forming a passage for a saltbridge connection through a salt-bridge tube of glass which comprises heating the tube to temperature effecting tackiness of the glass around an opening in the tube, closing the opening with a plug of glass having substantially diiferent coefllcient of expansion, and thereafter cooling the tube to produce, because of different rates of contraction of the glasses, a crack at or adjacent the plug.
5. The method of forming a passage for a saltbridge connection through a salt-bridge tube of glass which comprises heating an open end of the tube to temperature effecting tackiness of the glass, closing the open end of the tube with a plug with said plug and of width not exceeding about .0005 centimeter.
7. A salt-bridge tube having a wall of glass, a plug of glass fused to said wall and having a coefficient of expansion higher than that of the glass of said wall, and for a salt-bridge connection in said wall, at least one crack around said plug and of width not exceeding about .0005
centimeter.
' GEORGE A. PERLEY.
US437153A 1942-04-01 1942-04-01 Salt-bridge tube and method of producing it Expired - Lifetime US2345498A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2705220A (en) * 1951-01-23 1955-03-29 Beckman Instruments Inc Electro-chemical apparatus
US2755243A (en) * 1952-05-13 1956-07-17 Beckman Instruments Inc Electrochemical electrode structure
US2758079A (en) * 1950-03-29 1956-08-07 Leeds & Northrup Co Electrolytic determination of the concentration of a constituent in a fluid
US3122431A (en) * 1958-12-29 1964-02-25 Coulter Electronics Method of making a scanner element for particle analyzers
US3208927A (en) * 1961-10-23 1965-09-28 Beckman Instruments Inc Liquid junction
US3423304A (en) * 1964-11-17 1969-01-21 Beckman Instruments Inc Leak structure and method for producing same
US3975681A (en) * 1975-01-10 1976-08-17 Xerox Corporation Electrode for measuring thickness of dielectric layers on conductive substrates
US4906348A (en) * 1987-08-21 1990-03-06 Hitachi, Ltd. Flow-through cell provided with reference electrode

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3327204A (en) * 1963-04-15 1967-06-20 Beckman Instruments Inc Fluid sample examining apparatus

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2758079A (en) * 1950-03-29 1956-08-07 Leeds & Northrup Co Electrolytic determination of the concentration of a constituent in a fluid
US2705220A (en) * 1951-01-23 1955-03-29 Beckman Instruments Inc Electro-chemical apparatus
US2755243A (en) * 1952-05-13 1956-07-17 Beckman Instruments Inc Electrochemical electrode structure
US3122431A (en) * 1958-12-29 1964-02-25 Coulter Electronics Method of making a scanner element for particle analyzers
US3208927A (en) * 1961-10-23 1965-09-28 Beckman Instruments Inc Liquid junction
US3423304A (en) * 1964-11-17 1969-01-21 Beckman Instruments Inc Leak structure and method for producing same
US3975681A (en) * 1975-01-10 1976-08-17 Xerox Corporation Electrode for measuring thickness of dielectric layers on conductive substrates
US4906348A (en) * 1987-08-21 1990-03-06 Hitachi, Ltd. Flow-through cell provided with reference electrode

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