WO1986001601A1 - Ion-sensitive electrode and method of making the same - Google Patents
Ion-sensitive electrode and method of making the same Download PDFInfo
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- WO1986001601A1 WO1986001601A1 PCT/US1985/001682 US8501682W WO8601601A1 WO 1986001601 A1 WO1986001601 A1 WO 1986001601A1 US 8501682 W US8501682 W US 8501682W WO 8601601 A1 WO8601601 A1 WO 8601601A1
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- ion
- bulb
- tube
- membrane
- electrode
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/36—Glass electrodes
Definitions
- the invention relates to ion-sensitive electrodes and comprises a flat surface electrode formed from a portion of a bulb of ion-selective membrane material fused to the end of a tube through the use of radiation. It is particularly useful in forming low resistance electrodes from high resistivity material.
- Ton-sensitive electrodes measure the activity of ions in solution (both aqueous and non-aqueous)and are well known in the art of analytical chemistry.
- pH is a measure of the activity of hydrogen ions in solution, and is an important parameter for many chemical processes.
- Another example is the measurement of sodium ions in foods or biological fluids.
- Ion-sensitive electrodes are commonly formed from a tubular shell having one end sealed with an ion- selective membrane.
- the membrane is selectively permeable to ions of one type, while excluding others present in the sample solution, inside the tube there is a means for providing a fixed potential, either a solution of fixed composition or a solid conductor in contact with the membrane.
- the potential across the membrane, measured from the internal contact, through the sample to a second reference contact provides a measure of the sample ion activity.
- Ion-selective membranes are most commonly formed with either a bulbous or a flat shape.
- bulbous-shaped electrodes are more readily formed than flat-membrane electrodes, and are suitable for measurements of liquid samples where there is a significant quantity of liquid available for measurement.
- Flat-membrane electrodes are desirable, or even required, for measuring samples where there is a limited quantity of material available, and for measuring moist solids where the membrane must be pressed against the sample without immersion in it.
- the membranes used for ion-sensitive electrodes typically present a high input impedence to the measuring instrument, e.g., up to 1000-20000 megohms. This impedence limits the accuracy of measurements because of noise pickup in the electrode.
- the ion- selective membranes for pH-sensing electrodes are commonly formed from glass.
- high selectivity for a hydrogen ion is typically also accompanied by high resistivity, and thus the improved sensitivity otherwise obtainable from the material is masked by the increased noise pickup caused by the higher resistivity.
- This can be particularly a problem with flat surface membranes in which conventional manufacturing techniques place stringent limits on the extent to which the membrane thickness (and thus, its resistance for a material of given resistivity) may be controlled.
- Flat- embrance surface ion-sensitive electrodes are commonly constructed by a dipping process in which a tubular section of glass is immersed in a molten bath of membrane material.
- a bead of molten material typically adheres to the end of the tubular section, and is fabricated into a flat membrane on cooling.
- the molten glass must have a coefficient of expansion closely matching that of the tube. If the coefficients of expansion of the tube and the molten glass differ greatly, either the tube or the membrane material will frequently crack upon cooling, due to differing rates of contraction. Further, the seal between -the tube and the membrane glass is often irregularly formed and prone to failure.
- dipping processes are difficult to control for uniformity and repeatability of membrane thickness. Sample to sample thickness variations may lead to large variations in strength or electrical resistance.
- the pH glass may be ground to a desired thickness for the flat membrane required. Grinding is a time consuming process and results in a high percentage of defective electrode bodies due to accidental breaking of the thinned membrane material. Further the grinding process introduces micro- grooves and stresses into the membrane, impurities from the grinding material may also embed themselves into the areas that are ground and thereby distort membrane properties. Finally, there is a physical limit to the thickness to which one can grind a material, without breaking that material. The limitation is due to the impact nature of the grinding process and the brittle nature of membrane material. This limitation has prevented the use, in flat or substantially flat membranes, of low-sodiu ⁇ . interference high-resistivity glass. A need therefore exists for a new method of manufacturing electrode bodies which will allow for the development of improved electrodes utilizing improved materials and having none of the drawbacks of conventional electrodes.
- the invention comprises an ion-sensitive electrode which is formed from a bulb of ion-selective membrane material, which is transparent to radiation, and a tube of radiation-absorptive materials.
- the bulb is rested upon the tube and the interface between the tube and bulb then irradiated so as to heat the tube to a molten state to therby secure bonding between the tube and a spherical section of the bulb, in particular, in the preferred embodiment, the assembly is irradiated with infrared radiation focused on the end face or 'lip' of the tube at the surface which contacts the bulb. This melts, the tube wall to an extent sufficient to form a bond with the membrane without melting the membrane . Thereafter, the tube is slightly pressured with gas (e.g., a quick puff of air , such as is common in manual gla ⁇ sblowing techniques) while the interface is still molten to reduce bonding stresses.
- gas e.g., a quick puff of air , such as is common in manual gla
- the bulb is of a substantially larger diameter than the tube, e.g., two or more times as large.
- the tube subtends a portion of the spherical surface of the bulb which varies relatively little in height with respect to the end face of the tube.
- the bulb diameter is twice, that of the tube, the subtended portion of the membrance projects less than 14% of the tube diameter beyond the end face of the tube. The result is a membrane that is substantially flat.
- a flat-membrane, low-interference, low resistance, pH electrode is formed from a glass bulb less than .025 inches thick and having a resistivity value greater then 10 ⁇ ohm-centimeters.
- Figure 1 is an expanded cross sectional view of a portion of an electrode formed by a dipping process. It depicts the prior art.
- Figure 2 is a partial cross-section view of an ion-sensitive electrode.
- Figure 3 is a view of the electrode body prior to membrane bonding in which an infrared light source is shown schematically.
- Figure 3A is an enlarged view of a portion of Figure 3A.
- Figure 4 is an expanded cross-section of the operational end of the ion-sensitive electrode of Figures 2 and 3.
- FIG 1 a typical flat membrane electrode formed by the usual dipping process characteristic of the prior art is shown.
- the membrane material 5 which is bonded to the tube 8 during the dipping process has an irregular contour on its inner surface 6. This irregular contour cannot be corrected by grinding and as a result, varies with each electrode manufactured. This results in a membrane of variable and high resistance and thus of adverse noise pickup characteristics.
- An improved ion sensitive electrode 10 is shown in Figure 2.
- the electrode 10 has an electrode body 12 of generally tubular shape having one end thereof sealed by a substantially flat membrane 14.
- the electrode body is formed from an energy absorbent (preferably infrared- absorbent) glass tube and a bulbous membrane preform as detailed below. Use of the bulbous preform for the electrode body permits the manufacture of flat surface electrodes with high resistivity membrane materials.
- an internal filling solution 16 provides an electrically conductive path between the membrane and an electrode element 18 which measures a potential difference caused by a change in the ion concentration in the sample filling solution.
- the membrane 14 is preferably formed from a pH or other ion selective glass. Such glasses are typically a mixture of several oxides including i2 ⁇ , CS2O, La2U3, CaO, and a2 ⁇ . A variety of other similar constituents have also been used. Further, the membrane 14 is formed of a thin, substantially flat material, preferably less than 0.025 inches thick, and as thin as .005 inches. This is a far thinner membrane section than previously could be used on flat membrane ion exchange electrodes, and therefore can be formed of low-interference materials such as low-sodium interference glasses having resistivities greater than 10 ⁇ ohm-centimeters.
- an outer protective tube 20 is placed around it.
- This outer tube is preferably constructed, of resilient plastic and is attached to the membrane end of the inner tube 12 by means of a shock absorbing rubber gasket 22.
- a cap 24 and lead wires 26 are attached at the remote end of the electrode body to complete the structure.
- a preform 30 is formed in the shape of a cylindrical tube having a bulbous head 32 with a diameter substantially larger than that of the end of body 12 on which the membrane is to be formed.
- the preform 30 may advantageously be made from a low sodium-interference, high resistivity material which is transparent to infrared radiation.
- the bulb 32 is formed to a reduced wall thickness, e.g. on the order of 0.005 inches. The wall thickness of the bulb is easily controlled by varying the bulb radius (R) for a given amount of glass.
- the flatness of the bulb is controlled by selection of the ratio of bulb diameter to tube diameter.
- the tube departs from flatness by less, than fourteen per cent of the tube diameter.
- the bulb is structurally quite strong and thus is relatively stable and easy to handle.
- the slightly arched shpae is beleved to contribute to the strengh, since glass is stronger in compression than tension.
- a flat plate of similar thickness would be extremely fragile and quite difficult to handle.
- the bulb has a relatively constant wall thickness so that membrane thickness, and therefore resistance, may be closely controlled.
- the preform 30 is placed over one end of the electrode body 12, with the bulb resting directly on the edge of the tubular body 12.
- the body 12 preferably comprises an infrared absorbent glass.
- Infrared absorbent glass is commonly called "green glass”; examples include 'SRI' glass and 'STI* glass manufactured by the Nippon Electric Glass Co., Ltd., 1-1 KAKUDA-CHO, KITADU, Osaka, Japan, as well as certain glasses manufactur ⁇ by the Schoot Company, e.g. Schott No. 4840E glass.
- the next step in the manufacture of the electrode body is to focus a beam of radiation, such as from an infrare ⁇ source 15, slightly above the interface between the bulb 32 and the end 12a of body 12.
- a beam of radiation such as from an infrare ⁇ source 15
- the light passes through the infrared transparent bulb 32 with little absorption and thus little heating, and evenly heats the 'lip' of the infrared absorptive glass tube 12 at its area of contact with the membrane..
- the tube is rotated at this, time in order to keep the heating uniform.
- the radiation is then brought to a focus at the interface so as to melt the lip of the tube to thereby enable fusing of the tube to the membrane.
- the infrared energy is then removed (e.g., the source is turned off).
- the melting point of the glass of the tube is lower than that of the membranous bulb. If this were not the case, the thin bulb might soften and collapse during the fusing process.
- the main section of the membrane material which is thin and unsupported, does not need to be polished or ground.
- the electrode body 12, with the fused membrane material 14 is then ready for final assembly and the electrode element 18 can be inserted into the body and terminated at the opposite end of the housing.
- the improved ion-sensitive electrode made by the above process is capable of superior operation when compared with previous flat surface, ion-sensitive pH electrodes.
- the method of manufacture, as described above permits virtually flat membrane wall thicknesses as low as .005 inches and therefore allows the use of much higher resistivity materials for flat membranes than those available previously.
- high performance materials desirable for the reduced sodium interference effects which characterize them but hithereto contraindicated by their high resistivity which led to increased electerical noise pickup, can now advantageously be used to form pH electrodes operable over a wide pH range.
- This process of manufacture also makes advantageous use of the highly uniform wall thicknesses that can be achieved in blowing glass bulbs.
- the bulb 32 of membrane material is blown to-a uniform desired wall thickness; as a result the membrane formed on the tube 12 also possesses a uniform wall thickness. This avoids the undesirable electrode resistance variations discussed in reference to figure 1.
- the membrane is also structurally improved by the use of this process.
- the uniform joint between the tube bo ⁇ y 12 and membrane 14 is quite strong and less likely to separate than the joints formed by previous methods. Further, microscratches and stresses which are induced by conventional grinding of a membrane surface to the proper thicknesses for flat membranes are completely eliminated by this process.
- the membraneous bulb needs no further processing after its fusing to the tubular body of the electrode probe. This results in an improved membrane surface with less likelihood of electrode cracking.
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Abstract
An ion-sensitive electrode and method of making such electrode wherein an ion selective glass membrane (14) is rested on the edge of a tubular body (12), a radiation source (15) is passed through the transparent membrane (14) or bulb (32) to heat the body (12) at its area of contact with the membrane (12), the tube (12) is rotated to keep heating uniform so as to melt the lip of tube (12) to enable fusing of the tube (12) to the membrane.
Description
Ion-Sensitive Electrode and Method of making the same.
Field of the invention
The invention relates to ion-sensitive electrodes and comprises a flat surface electrode formed from a portion of a bulb of ion-selective membrane material fused to the end of a tube through the use of radiation. It is particularly useful in forming low resistance electrodes from high resistivity material.
Background of the Invention Ton-sensitive electrodes measure the activity of ions in solution (both aqueous and non-aqueous)and are well known in the art of analytical chemistry. One example of such a measurement is pH, which is a measure of the activity of hydrogen ions in solution, and is an important parameter for many chemical processes.
Another example is the measurement of sodium ions in foods or biological fluids.
Ion-sensitive electrodes are commonly formed from a tubular shell having one end sealed with an ion- selective membrane. The membrane is selectively permeable to ions of one type, while excluding others present in the sample solution, inside the tube there is a means for providing a fixed potential, either a solution of fixed composition or a solid conductor in contact with the membrane. The potential across the
membrane, measured from the internal contact, through the sample to a second reference contact provides a measure of the sample ion activity.
Ion-selective membranes are most commonly formed with either a bulbous or a flat shape. For membranes formed in the glassy state, bulbous-shaped electrodes are more readily formed than flat-membrane electrodes, and are suitable for measurements of liquid samples where there is a significant quantity of liquid available for measurement. Flat-membrane electrodes, in contrast, are desirable, or even required, for measuring samples where there is a limited quantity of material available, and for measuring moist solids where the membrane must be pressed against the sample without immersion in it. The membranes used for ion-sensitive electrodes typically present a high input impedence to the measuring instrument, e.g., up to 1000-20000 megohms. This impedence limits the accuracy of measurements because of noise pickup in the electrode. In particular, the ion- selective membranes for pH-sensing electrodes are commonly formed from glass. In common pH-sensing glasses, high selectivity for a hydrogen ion is typically also accompanied by high resistivity, and thus the improved sensitivity otherwise obtainable from the material is masked by the increased noise pickup caused by the higher resistivity. This can be particularly a
problem with flat surface membranes in which conventional manufacturing techniques place stringent limits on the extent to which the membrane thickness (and thus, its resistance for a material of given resistivity) may be controlled.
Flat- embrance surface ion-sensitive electrodes are commonly constructed by a dipping process in which a tubular section of glass is immersed in a molten bath of membrane material. A bead of molten material typically adheres to the end of the tubular section, and is fabricated into a flat membrane on cooling. The molten glass must have a coefficient of expansion closely matching that of the tube. If the coefficients of expansion of the tube and the molten glass differ greatly, either the tube or the membrane material will frequently crack upon cooling, due to differing rates of contraction. Further, the seal between -the tube and the membrane glass is often irregularly formed and prone to failure. In addition, dipping processes are difficult to control for uniformity and repeatability of membrane thickness. Sample to sample thickness variations may lead to large variations in strength or electrical resistance.
Once the dipped tube has cooled, the pH glass may be ground to a desired thickness for the flat membrane required. Grinding is a time consuming process and
results in a high percentage of defective electrode bodies due to accidental breaking of the thinned membrane material. Further the grinding process introduces micro- grooves and stresses into the membrane, impurities from the grinding material may also embed themselves into the areas that are ground and thereby distort membrane properties. Finally, there is a physical limit to the thickness to which one can grind a material, without breaking that material. The limitation is due to the impact nature of the grinding process and the brittle nature of membrane material. This limitation has prevented the use, in flat or substantially flat membranes, of low-sodiuτ. interference high-resistivity glass. A need therefore exists for a new method of manufacturing electrode bodies which will allow for the development of improved electrodes utilizing improved materials and having none of the drawbacks of conventional electrodes.
Summary of the nvention
The invention comprises an ion-sensitive electrode which is formed from a bulb of ion-selective membrane material, which is transparent to radiation, and a tube of radiation-absorptive materials. The bulb is rested upon the tube and the interface between the tube and bulb
then irradiated so as to heat the tube to a molten state to therby secure bonding between the tube and a spherical section of the bulb, in particular, in the preferred embodiment, the assembly is irradiated with infrared radiation focused on the end face or 'lip' of the tube at the surface which contacts the bulb. This melts, the tube wall to an extent sufficient to form a bond with the membrane without melting the membrane . Thereafter, the tube is slightly pressured with gas (e.g., a quick puff of air , such as is common in manual gla≤sblowing techniques) while the interface is still molten to reduce bonding stresses.
In the preferred embodiment of the invention, the bulb is of a substantially larger diameter than the tube, e.g., two or more times as large. When a segment of the inner portion of the bulb is rested on the tube, the tube subtends a portion of the spherical surface of the bulb which varies relatively little in height with respect to the end face of the tube. For example, when the bulb diameter is twice, that of the tube, the subtended portion of the membrance projects less than 14% of the tube diameter beyond the end face of the tube. The result is a membrane that is substantially flat.
An important consequence of this method of construction is that it permits the use of high- resistivity, low sodium error materials for the membrane.
e.g. materials whose selectivity for hydrogen ion as opposed to sodium ion is of the order of 1013 or more and preferably as high as 10*4 or more. This is because the glasses used for the membrane can be blown into structurally strong bulbs having cross sections thinner then those which can be found in conventionally constructed flat surface electrode membranes. Thus, while the resistivity of the material is higher, its resistance is lower due to the membrane's reduced thickness. For example, with the present techniques, a flat-membrane, low-interference, low resistance, pH electrode is formed from a glass bulb less than .025 inches thick and having a resistivity value greater then 10^ ohm-centimeters. The sensitivity of this electrode extends the useable response to values of pH = 14.
Brief Description of the Drawings
The foregoing and other features and advantages of the invention will be apparent from the following more particular description of the preferred embodiment of the invention, as illustrated in the accompanying drawings, in which like reference characters refer to the same parts throughout the different views. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the invention.
Figure 1 is an expanded cross sectional view of a portion of an electrode formed by a dipping process. It depicts the prior art.
Figure 2 is a partial cross-section view of an ion- sensitive electrode.
Figure 3 is a view of the electrode body prior to membrane bonding in which an infrared light source is shown schematically.
Figure 3A is an enlarged view of a portion of Figure 3A.
Figure 4 is an expanded cross-section of the operational end of the ion-sensitive electrode of Figures 2 and 3.
Detailed Description of the Invention
In figure 1, a typical flat membrane electrode formed by the usual dipping process characteristic of the prior art is shown. The membrane material 5 which is bonded to the tube 8 during the dipping process has an irregular contour on its inner surface 6. This irregular contour cannot be corrected by grinding and as a result, varies with each electrode manufactured. This results in a membrane of variable and high resistance and thus of adverse noise pickup characteristics. An improved ion sensitive electrode 10 is shown in Figure 2. The electrode 10 has an electrode body 12 of
generally tubular shape having one end thereof sealed by a substantially flat membrane 14. The electrode body is formed from an energy absorbent (preferably infrared- absorbent) glass tube and a bulbous membrane preform as detailed below. Use of the bulbous preform for the electrode body permits the manufacture of flat surface electrodes with high resistivity membrane materials. As is common in ion sensitive electrodes, an internal filling solution 16 provides an electrically conductive path between the membrane and an electrode element 18 which measures a potential difference caused by a change in the ion concentration in the sample filling solution.
The membrane 14 is preferably formed from a pH or other ion selective glass. Such glasses are typically a mixture of several oxides including i2θ, CS2O, La2U3, CaO, and a2θ. A variety of other similar constituents have also been used. Further, the membrane 14 is formed of a thin, substantially flat material, preferably less than 0.025 inches thick, and as thin as .005 inches. This is a far thinner membrane section than previously could be used on flat membrane ion exchange electrodes, and therefore can be formed of low-interference materials such as low-sodium interference glasses having resistivities greater than 10^ ohm-centimeters. Although such materials have high resistivities, preferably about
2.5 X 106 ohm-centimeters, the reduced membrane thickness offsets the increased resistivity, and results in a • membrane with overall moderate resistance. Accordingly, electrical noise pick up is significantly reduced and a more accurate measurement of an increased pH range is obtained. For example, flat-membrane electrodes capable of measuring pH over the range of 0 to 14 can produced by the present process.
In order to protect the glass electrode body 12 from accidental breakage during use, an outer protective tube 20 is placed around it. This outer tube is preferably constructed, of resilient plastic and is attached to the membrane end of the inner tube 12 by means of a shock absorbing rubber gasket 22. A cap 24 and lead wires 26 are attached at the remote end of the electrode body to complete the structure.
The electrode of Figure 2 is manufactured as follows: Referring to Figure 3, a preform 30 is formed in the shape of a cylindrical tube having a bulbous head 32 with a diameter substantially larger than that of the end of body 12 on which the membrane is to be formed. As mentioned above, for pH electrodes, the preform 30 may advantageously be made from a low sodium-interference, high resistivity material which is transparent to infrared radiation. Further the bulb 32 is formed to a reduced wall thickness, e.g. on the order of 0.005
inches. The wall thickness of the bulb is easily controlled by varying the bulb radius (R) for a given amount of glass.
The flatness of the bulb is controlled by selection of the ratio of bulb diameter to tube diameter. In particular, with reference to Figure 3A, the departure 'h' of the bulb membrane from perfect flatness (h=0) can readily be computed as
]/a, where r is the tube radius and a is the ratio, r/R, of tube radius to bulb radius. For a ratio of a=0.5, h=0.268r, that is,the subtended portion of the membrane sealing, the tube departs from flatness by less, than fourteen per cent of the tube diameter. For a=0-33, the departure is less than nine per cent. Despite its limited thickness, the bulb is structurally quite strong and thus is relatively stable and easy to handle. Further, the slightly arched shpae is beleved to contribute to the strengh, since glass is stronger in compression than tension. A flat plate of similar thickness would be extremely fragile and quite difficult to handle. Further, the bulb has a relatively constant wall thickness so that membrane thickness, and therefore resistance, may be closely controlled. The preform 30 is placed over one end of the electrode body 12, with the bulb resting directly on the edge of the tubular body 12. As mentioned above, the
body 12 preferably comprises an infrared absorbent glass. Infrared absorbent glass is commonly called "green glass"; examples include 'SRI' glass and 'STI* glass manufactured by the Nippon Electric Glass Co., Ltd., 1-1 KAKUDA-CHO, KITADU, Osaka, Japan, as well as certain glasses manufacturά by the Schoot Company, e.g. Schott No. 4840E glass.
The next step in the manufacture of the electrode body is to focus a beam of radiation, such as from an infrareα source 15, slightly above the interface between the bulb 32 and the end 12a of body 12. The light passes through the infrared transparent bulb 32 with little absorption and thus little heating, and evenly heats the 'lip' of the infrared absorptive glass tube 12 at its area of contact with the membrane.. The tube is rotated at this, time in order to keep the heating uniform. The radiation is then brought to a focus at the interface so as to melt the lip of the tube to thereby enable fusing of the tube to the membrane. The infrared energy is then removed (e.g., the source is turned off). It should be noted that the melting point of the glass of the tube is lower than that of the membranous bulb. If this were not the case, the thin bulb might soften and collapse during the fusing process. As the assembly begins to cool, it is useful to slightly pressurize the air space within the tubular
section 12 in order to promote formation of a uniform seal joint 34 (Figure 4) between the glass electrode body and the membrane 14. This slight pressurization of the air space also eliminates internal stresses created by the fusin process in the membrane 14 and the joint 34. As the fused assembly cools, the remainder of the membrane material tends to crack and fall away. The fused assembly then need only be polished at any ragged edges about the periphery of the membrane 14 before it is ready for use. The main section of the membrane material, which is thin and unsupported, does not need to be polished or ground. The electrode body 12, with the fused membrane material 14 is then ready for final assembly and the electrode element 18 can be inserted into the body and terminated at the opposite end of the housing.
The improved ion-sensitive electrode made by the above process is capable of superior operation when compared with previous flat surface, ion-sensitive pH electrodes. The method of manufacture, as described above, permits virtually flat membrane wall thicknesses as low as .005 inches and therefore allows the use of much higher resistivity materials for flat membranes than those available previously. Thus, high performance materials, desirable for the reduced sodium interference effects which characterize them but hithereto
contraindicated by their high resistivity which led to increased electerical noise pickup, can now advantageously be used to form pH electrodes operable over a wide pH range. This process of manufacture also makes advantageous use of the highly uniform wall thicknesses that can be achieved in blowing glass bulbs. The bulb 32 of membrane material is blown to-a uniform desired wall thickness; as a result the membrane formed on the tube 12 also possesses a uniform wall thickness. This avoids the undesirable electrode resistance variations discussed in reference to figure 1.
The membrane is also structurally improved by the use of this process. The uniform joint between the tube boαy 12 and membrane 14 is quite strong and less likely to separate than the joints formed by previous methods. Further, microscratches and stresses which are induced by conventional grinding of a membrane surface to the proper thicknesses for flat membranes are completely eliminated by this process. The membraneous bulb needs no further processing after its fusing to the tubular body of the electrode probe. This results in an improved membrane surface with less likelihood of electrode cracking.
Finally, it should be noted that the process used in the manufacture of this improved ion sensitive electrode substantially reduces the cost of manufacture. Since
hand grinding and polishing is largely eliminated, the most time consuming and delicate operation in the construction of flat surface ion sensitive electrodes has been eliminated. Further, waste caused by membrane breakage during grinding and polishing is also eliminated.
While the invention has been particularly shown and described with reference to the preferred embodiment thereof, it will be understood by those skilled in the art, that various changes in form and detail may be made therein without departing from the spirit and scope of the invention as defined by the appended claims. It is possible, for example, to utilize other electromagnetic energy sources such as ultraviolet light to fuse the material of the body to the membrane material. Further, the materials used to construct the probe need not be limited to glasses: ceramic and epoxy .materials have also been used in ion sensitive electrode devices with good results. In appropriate cases, an intermediate meltable bonding material, compatabile with both the tubular wall material and the membrane material, may be used to effectuate the desired bond in cases where the membrane material and the tubular wall material may not themselves be sufficiently directly compatible. What is claimed as new and desired to be secured by Letters Patent of the United States is:
Claims
1. A method of forming an ion-sensitive electrode comprising the steps of: a. forming a bulb of ion-selective membrane material which is transparent to radiation; b. resting said bulb of upon a. tube of radiation absorbtive material; and c. irradiating said bulb and said tube in order to form a bond therebetween.
2. An ion-sensitive electrode formed according to the methoα of claim 1.
3. The method of forming an ion-sensitive electrode claimed in claim 1 wherein said bulb and said tube are irradiated with infrared radiation.
4. An ion-sensitive electrode formed according to the method of claim 1 wherein said ion-selective membrane material comprises glass having a resistivity value greater than 105 ohm-centimeters.
5. An ion-sensitive electrode formed according to the method of claim 1 which has a flat membrane surface.
6. The method of forming an ion-sensitive electrode claimed in claim 1 wherein said bulb of ion-sensitive membrane material is less than .025 inches thick.
7. An ion-sensitive electrode comprising a tubular body bonded at one end to a flat thin membrane of high resistivity material which is selectively permeable to an ion whose concentration is to be measured.
8. An ion-sensitive electrode of low electrical resistance comprising a body of an infrared absorbent material bonded by infrared radiation to an ion-selective membrane of high resistivity and limited thickness and comprising material transparent to infrared radiation.
9. The ion selective electrode of claim 8 wherein said membrane material forms a flat ion-selective surface.
10. The ion-sensitive electrode of claim 8 wherein said ion-selective membrane is less than .025 inches thick.
11. The ion-sensitive electrode of claim 8 wherein said membrane material is of low sodium error material.
12. The ion sensitive electrode of claim 8 wherein said ion-selective membrane is formed from a portion of a bulb that is bonded to said body by infrared radiation.
13. The ion selective electrode of claim 8 wherein the membrane material rests on an upright end wall of the tube of infrared absorbent material during bonding.
14. The ion-sensitive electrode of claim 8 wherein said electrode is sensistive to hydrogen ions for measring acidity.
15. A method of manufacturing an ion sensitive electrode body, having a portion formed of an ion-selective membrane material, comprising the steps of: inserting an end of a tube of infrared absorbent material into a bulb of ion- selective membrane material so that said end of said tube contacts an inner surface of said bulb; and illuminating said bulb and said tube with infrared radiation to thereby fuse said end of said tube of infrared absorbent material to the inner surface of said bulb.
16. The method of manufacturing an electrode body of claim 15 further comprising the step of: slightly pressurizing said glass housing after fusing said tube to said bulb in order to eliminate internal stresses in said infrared absorbant glass.
17. The method of manufacturing an electrode body of claim 15 wherein said ion-selective membrane material is selectively permeable to hydrogen ions.
18. The method of manufacturing an electrode body of claim 15 wherein said ion-selective membrane material comprises a limited portion of the surface ofsaid bulb to thereby form a substantially flat surface
19. The methold of claim 19 wherein the said bulb has a radius of at least twice the radius of said tube.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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DE3590404A DE3590404C2 (en) | 1984-09-05 | 1985-09-03 | Ion-sensitive electrode |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US64759984A | 1984-09-05 | 1984-09-05 | |
US647,599 | 1984-09-05 |
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WO1986001601A1 true WO1986001601A1 (en) | 1986-03-13 |
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PCT/US1985/001682 WO1986001601A1 (en) | 1984-09-05 | 1985-09-03 | Ion-sensitive electrode and method of making the same |
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---|---|
CA (1) | CA1242764A (en) |
CH (1) | CH671466A5 (en) |
DE (2) | DE3590404C2 (en) |
GB (1) | GB2176898B (en) |
WO (1) | WO1986001601A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5208887A (en) * | 1990-01-22 | 1993-05-04 | Amp Incorporated | Method and apparatus for terminating a fiber-optic cable without adhesive |
CN109387551A (en) * | 2017-08-14 | 2019-02-26 | 恩德莱斯和豪瑟尔分析仪表两合公司 | Manufacture method, ISE half-cell, sensor and the multi-parameter sensor of ISE half-cell |
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US3282818A (en) * | 1963-03-12 | 1966-11-01 | Beckman Instruments Inc | Electrochemical liquid junction structure and method for producing same |
US3282817A (en) * | 1963-02-20 | 1966-11-01 | Corning Glass Works | Glass electrode and method of making the same |
US3523777A (en) * | 1967-06-29 | 1970-08-11 | Beckman Instruments Inc | Method of making electrochemical glass electrode assembly |
US3741884A (en) * | 1972-05-04 | 1973-06-26 | Beckman Instruments Inc | Electrochemical electrode liquid junction structure and method for producing same |
US3853731A (en) * | 1973-03-12 | 1974-12-10 | Owens Illinois Inc | Solid state junction glass electrode and method of making said electrode |
US3855095A (en) * | 1966-01-03 | 1974-12-17 | Beckman Instruments Inc | Electrochemical electrode assembly and method of making same |
US3923625A (en) * | 1971-06-30 | 1975-12-02 | Corning Glass Works | Reinforced glass electrode structure |
US4162211A (en) * | 1977-02-25 | 1979-07-24 | Beckman Instruments, Inc. | Combination electrode assembly |
US4328082A (en) * | 1980-06-26 | 1982-05-04 | Beckman Instruments, Inc. | Solid state ion-sensitive electrode and method of making said electrode |
US4485001A (en) * | 1984-02-21 | 1984-11-27 | Beckman Instruments, Inc. | Sterilizable pH electrode and method for producing the same |
-
1985
- 1985-09-03 DE DE3590404A patent/DE3590404C2/en not_active Expired - Fee Related
- 1985-09-03 DE DE19853590404 patent/DE3590404T1/de active Pending
- 1985-09-03 WO PCT/US1985/001682 patent/WO1986001601A1/en active Application Filing
- 1985-09-03 GB GB08610242A patent/GB2176898B/en not_active Expired
- 1985-09-04 CA CA000489961A patent/CA1242764A/en not_active Expired
-
1986
- 1986-09-03 CH CH189086A patent/CH671466A5/de not_active IP Right Cessation
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
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US3282817A (en) * | 1963-02-20 | 1966-11-01 | Corning Glass Works | Glass electrode and method of making the same |
US3282818A (en) * | 1963-03-12 | 1966-11-01 | Beckman Instruments Inc | Electrochemical liquid junction structure and method for producing same |
US3855095A (en) * | 1966-01-03 | 1974-12-17 | Beckman Instruments Inc | Electrochemical electrode assembly and method of making same |
US3523777A (en) * | 1967-06-29 | 1970-08-11 | Beckman Instruments Inc | Method of making electrochemical glass electrode assembly |
US3923625A (en) * | 1971-06-30 | 1975-12-02 | Corning Glass Works | Reinforced glass electrode structure |
US3741884A (en) * | 1972-05-04 | 1973-06-26 | Beckman Instruments Inc | Electrochemical electrode liquid junction structure and method for producing same |
US3853731A (en) * | 1973-03-12 | 1974-12-10 | Owens Illinois Inc | Solid state junction glass electrode and method of making said electrode |
US4162211A (en) * | 1977-02-25 | 1979-07-24 | Beckman Instruments, Inc. | Combination electrode assembly |
US4328082A (en) * | 1980-06-26 | 1982-05-04 | Beckman Instruments, Inc. | Solid state ion-sensitive electrode and method of making said electrode |
US4485001A (en) * | 1984-02-21 | 1984-11-27 | Beckman Instruments, Inc. | Sterilizable pH electrode and method for producing the same |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5208887A (en) * | 1990-01-22 | 1993-05-04 | Amp Incorporated | Method and apparatus for terminating a fiber-optic cable without adhesive |
CN109387551A (en) * | 2017-08-14 | 2019-02-26 | 恩德莱斯和豪瑟尔分析仪表两合公司 | Manufacture method, ISE half-cell, sensor and the multi-parameter sensor of ISE half-cell |
US11460429B2 (en) | 2017-08-14 | 2022-10-04 | Endress+Hauser Conducta Gmbh+Co. Kg | Method for producing an ISE half-cell, ISE half-cell, sensor, and multi-parameter sensor |
Also Published As
Publication number | Publication date |
---|---|
DE3590404C2 (en) | 1998-04-16 |
GB8610242D0 (en) | 1986-05-29 |
GB2176898A (en) | 1987-01-07 |
CH671466A5 (en) | 1989-08-31 |
CA1242764A (en) | 1988-10-04 |
GB2176898B (en) | 1988-06-08 |
DE3590404T1 (en) | 1987-01-29 |
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