The present disclosure relates to an ion-sensitive electrode, a measurement unit for an ion-sensitive electrode, for example a solid-state ion-sensitive electrode, and to a method for manufacturing the ion-sensitive electrode or the measurement unit.
In laboratories and industrial processes, ion-sensitive glass electrodes are often used for measuring ion activities, in particular pH-values. These electrodes or pH-electrodes include for example a thin ion-sensitive glass membrane, which is attached or melted to the end piece of a glass shaft of the glass electrode.
Principles of pH-measurement and related pH-electrodes are described in “A guide to pH-measurement”, March 2016, Mettler-Toledo GmbH. The pH-electrode can have a glass shaft having a thin glass membrane at one end that is sensitive to H+-ions. An outer gel layer forms on the outside of the glass membrane, when the membrane is exposed to a measurement solution. In addition, an inner gel layer forms on the inside of the glass membrane, as the electrode is filled with an internal buffer. The H+-ions either diffuse into or diffuse out of the outer gel layer, depending on the H+-ion concentration or the pH-value of the measurement solution. If the solution is alkaline the H+-ions diffuse out of the layer and a negative charge is established on the outer side of the membrane. As the internal buffer has a constant pH-value, the potential on the inner surface of the membrane remains constant during the measurement. Therefore, the potential measured by the pH-electrode is the difference between the constant inner and the variable outer charge of the ion-sensitive glass membrane. Additionally, the inner buffer contains a constant concentration of chloride that produces a constant potential to the silver/silver chloride (Ag/AgCl) electrode immersed in the same inner buffer. This electrochemical chain connects the potential of the glass membrane to the potential of the electrical wire leading out of the electrode.
The potential measured by the pH-electrode is compared to a reference potential provided by a reference electrode, such as an Ag/AgCl-electrode immersed in a reference solution, which is indirectly in contact with the measurement solution via a junction. This known reference electrode will therefore always produce the same, constant potential, irrespective of the solution to be measured.
Ion sensitive electrodes with a glass membrane exhibit excellent measurement properties. pH-electrodes for example show favourable properties in terms of slope, long-term stability, selectivity and detection limit, but also have disadvantages. Classic glass electrodes can only be used in a given orientation. In addition, glass electrodes show mechanical weaknesses, as they can break easily with the result that bits of broken glass get into the measurement solution, which must strictly be avoided, for example in processes of the food industry.
DE19714474A1 discloses an electro-chemical sensor with an ion-sensitive glass membrane, which is in direct contact with a steel-ceramic substrate. All layers are produced by thick film technology. It is stated, that in layered structures with a metal layer and a glass layer having different thermal expansion coefficients the glass layer may be damaged or even destroyed when exposed to temperature changes, which cause cracks or fissures. In order to avoid this problem, DE3727485A1 discloses the use of layers that exhibit thermal expansion coefficients a, which are identical or differ at most by a value Δα<6 10−7/K.
DE19714474A1, further discloses, that the problem of glass breaking occurs not only with solid-state electrodes but also with known glass electrodes that include a thin glass membrane melted to a glass shaft as described in “A guide to pH-measurement”, March 2016, Mettler-Toledo GmbH. In order to avoid glass breakage with this type of electrodes, it is recommended in DE2220841A1 that the adjoining materials exhibit thermal expansion coefficients α, which are identical or differ at most by a value Δα<7 10−7/K. Hence, the problem of glass breakage occurs in various embodiments of known electrodes including a thin-walled ion-sensitive glass membrane.
DE2220841A1 discloses an ion-sensitive electrode, in which an inner buffer solution creating a constant potential is replaced by metal deposited on an ion-sensitive glass membrane. An ion-sensitive electrode is referred to as solid-state ion-sensitive electrode, when its internal buffer is replaced by solid material. Such measures allow electrodes to be manufactured with significantly reduced dimensions, but known ion-sensitive electrodes with a solid internal buffer also show considerable drawbacks.
Due to the high impedance of ion-sensitive glass membranes, the electrical isolation of metal elements can be critical. Further, due to the exposure to ambient chemical reactants such as oxygen (O2), water (H2O), nitrogen (N2), carbon dioxide (CO2), etc., specific metal electrodes may be damaged or destroyed. Furthermore, chemical interactions between specific electrically conducting layers and the glass layer may occur, which may lead to damage or destruction of the glass layer. Still further, performance and properties of ion-selective solid-state electrodes compared to known ion-sensitive electrodes are still not as desired. Furthermore, limitations of the measurement range and insufficient stability with regard to pressure and temperature were experienced.
U.S. Pat. No. 4,632,732A discloses a solid-state electrode with an ion-sensitive glass membrane connected to a glass tube and a solid contact material of lithium-vanadium-oxide (LixV2O5), which forms an intercalation electrode. The solid contact material is sintered to the inner side of the glass membrane and electrically connected to a shielded electrode cable.
DE3727485A1 discloses another solid-state electrode with an ion-sensitive glass membrane connected to a glass tube and an intercalation electrode of material also used for lithium batteries. Such intercalation electrodes may exhibit intrinsic electrochemical hysteresis, which may impair the performance of the ion-sensitive electrode. Furthermore, exposure of the electrode materials to ambient chemical reactants (such as O2, H2O, N2, CO2, etc.) may further degrade performance.
Further, with regard to using a single phase or multiphase lithium layer adjoining a thin-walled ion-sensitive glass membrane, it is important to note that studies of lithium/silicon-dioxide (Li/SiO2) systems have shown that in these systems a substantial reduction of the glass matrix can occur, which significantly degrades the performance of the ion-selective electrode and drastically limits its lifespan.
DE19620568A1 discloses an ion-sensitive glass electrode including a double layer glass membrane with an inner glass layer with electronic and ionic conductivity and an ion-sensitive glass layer facing the measurement solution. The glass layers are melted together and form a thin walled spherical or cylindrical membrane, which is attached or melted to one end of a glass electrode shaft having a linear thermal expansion coefficient matching those of the glass layers, see DE2220841A1. The inner surface of the electrode body, formed by the membrane and the electrode shaft, is completely covered with a solid adherent silver layer connected to a contact wire. Inside the electrode body an elastic support body is provided, that for example, is made of silicone rubber. The elastic support body has a sealing function, which is sufficient for the materials used, but would scarcely fulfil the sealing requirements of materials that are easily reacting with ambient chemical reactants.
DE10018750C2 discloses another ion-sensitive glass electrode including a glass membrane with an outer side in contact with a measurement solution and with an inner side in firm contact with a metal contact layer, which is connected to an internal conductor.
U.S. Pat. No. 4,133,735A discloses an ion-sensitive electrode with a substrate having a planar wafer surface, on which a continuous conducting layer is formed by either thin-film vapour deposition or thick-film screening processes. A first region of the continuous conducting layer and related portions of the wafer surface are covered by a continuous membrane layer of a pH-sensitive glass. An insulated connecting lead is connected directly to a second region of the conducting layer. Alternatively, an electronic device chip with output leads is bonded to the wafer and connected with its input via the connecting lead to the second region of the conducting layer. The exposed conducting elements of the electrode, including the second region of the conducting layer, the active device chip, and all exposed portions of the leads, are covered by a protective fluid-tight seal. The seal may be formed from a flattened, non-pH-sensitive glass tube filled with a cured epoxy resin. Alternatively, the seal may be formed from heat-shrinkable tubing, e.g. composed of polyvinyl chloride, filled with an appropriate hydrophobic potting material such as beeswax. A sealing of this type, which is used in the art, does not satisfy the demands of electrode materials that are more sensitive to the exposure of ambient chemical reactants (such as O2, H2O, N2, CO2, etc.).
U.S. Pat. No. 4,280,889A discloses a solid-state ion-sensitive electrode using silver/silver chloride (Ag/AgCl) electrodes as a reference electrode and as a pH measuring electrode, which can be provided as separate units or combined in a common encapsulation. For both electrodes, a layered structure with an insulating substrate is provided, on which a first layer of chromium followed by a second layer of silver, a third layer of silver chloride and a final ion sensitive glass layer are deposited. For the pH measuring electrode, the thermal expansion coefficients of the glass layer and the adjoining layer of silver chloride are matched, so that cracks in the glass layer are avoided. For the reference electrode, the thermal expansion coefficients of the glass layer and the adjoining layer of silver chloride are not matched, so that cracks in the glass layer are randomly caused during temperature cycling of the reference electrode. These cracks provide ion conduction paths to the silver chloride layer from an aqueous solution in which the reference electrode is immersed during ion concentration measurements. U.S. Pat. No. 4,280,889A, therefore, discloses matching thermal expansion coefficients of adjoining layers of a layered structure in order to avoid cracks in the glass layer and to not matching adjoining layers of a layered structure to create cracks fulfilling a specific function.
EP0420983A1 discloses a solid phase electrode with an ion-sensitive membrane connected to a glass tube and that is provided with a solid phase contact made of an oxide compound on the side facing the glass tube.
WO/0104615A1 discloses a solid-state electrode including a metal core of a lithium alloy, which adheres firmly to the inner face of an ion-sensitive glass membrane containing lithium, and which is melted to a lower end of a glass tube made of conventional glass. The metal core is protected from ambient influences by a metal sealing plug inserted into the glass tube. However, it appears that this kind of sealing is not optimal, as ambient chemical reactants (such as O2, H2O, N2, CO2, etc.) may intrude through capillaries remaining between the inside of the glass tube and the outside of the metal core. Such capillaries may result through changes of the ambient temperature; e.g., during measurement processes.
Hence, drawbacks of known ion-sensitive electrodes as well as known solid-state ion-sensitive electrodes are that cracks and fissures can occur in the ion-sensitive glass membrane or ion-sensitive glass layer. Further drawbacks relate to the destruction of the materials used or layers when exposed to ambient chemical reactants, or the destruction of the ion-sensitive glass membrane when exposed to the adjoining metal layers. Critical is also can be the impact of mechanical forces and tensions during handling and operation of the ion-sensitive electrode, which may lead to damage of the glass membrane.
A solid-state ion-sensitive electrode is disclosed, for measuring an ion activity in a measurement solution, such as a pH value, with a layered structure, the electrode comprising: a glass layer as ion-sensitive glass membrane; and a substrate as first holding member, which directly or via at least one intermediate layer adheres to the ion-sensitive glass membrane, wherein the ion-sensitive glass membrane is held under compressive stress by the first holding member over a whole range or part of the range of a specified operating temperature of the ion-sensitive electrode.
A method for manufacturing an ion-sensitive solid-state electrode is also disclosed for measuring an ion activity in a measurement solution, such as a pH value, the method comprising: a) providing at least one holding member; b) providing an ion-sensitive glass membrane; and c) connecting the ion-sensitive glass membrane to the at least one holding member such that the ion-sensitive glass membrane is held under compressive stress over a whole range or part of the range of a specified operating temperature of the ion-sensitive electrode.
The technical solution disclosed herein, as well as other beneficial advantages of the present disclosure, will be apparent to those skilled in the art upon reading the following detailed description of exemplary embodiments of the present disclosure, with reference to the attached drawings, wherein:
The present disclosure is directed to defining an improved ion-sensitive electrode, such as a pH electrode, and an improved measurement unit for such an ion-sensitive electrode provided with an ion-sensitive glass membrane. Further, a method for manufacturing such an improved ion-sensitive electrode and improved measurement unit can be defined.
Exemplary embodiments of an improved ion-sensitive glass can be provided in a non-solid-state embodiment as well as in a solid-state embodiment, and for example, provided with an improved measurement unit.
Exemplary embodiments of an improved ion-sensitive electrode and measurement unit can have improved robustness and durability so that an increased lifespan can be realised even in a demanding process environment. In particular, for example, the ion-sensitive glass membrane can be well protected, so that cracks and fissures in the ion-sensitive glass membrane can be avoided. In further embodiments, the elements of the ion-sensitive electrode can be protected against ambient chemical and physical influences when being stored, handled or used for measurement purposes.
The exemplary method can allow assembling of the exemplary ion-sensitive electrode as solid-state embodiment or non-solid-state embodiment, is, for example, without additional effort.
The solid-state ion-sensitive electrode and measurement unit, that serves to measure an ion activity in a measurement solution, include a layered structure with a glass layer as ion-sensitive glass membrane, and a substrate as first holding member, which directly or via at least one intermediate layer adheres to the ion-sensitive glass membrane. The at least one holding member is connected to the ion-sensitive glass membrane and keeps the ion-sensitive glass membrane under compressive stress over the whole range or part of the range of the specified operating temperature of the ion-sensitive glass electrode.
The exemplary measurement unit, which is provided for a solid-state ion-sensitive glass electrode, includes a layered structure with a substrate and the ion-sensitive glass membrane in the embodiment of a glass layer, which directly or via at least one intermediate layer adheres to the substrate.
According to exemplary embodiments of the disclosure, the ion-sensitive glass membrane is connected to the at least one holding member such that the ion-sensitive glass layer is kept or held under compressive stress over the whole range or part of the range of the specified operating temperature of the ion-sensitive electrode. Hence, there is a unitary stress condition maintained in the ion-sensitive glass membrane or in ion-sensitive glass layer. Ambiguous stress conditions, which could harm the glass matrix, changing between tensile stress and compressive stress within regions of the ion-sensitive glass membrane or glass layer are avoided.
In contradiction to known techniques, the disclosure is not directed to avoiding stress in the ion-sensitive electrode. According to the disclosure, the exemplary ion-sensitive electrode in solid-state or non-solid-state embodiments is produced and/or assembled in such a way that stress, namely compressive stress, is always present in the glass membrane. In solid-state embodiments, the glass membrane is for example, present as a glass layer in a layered structure. The desired stress state is for example, a biaxial stress or more specifically an equibiaxial stress. In this state, every element of the ion-sensitive membrane is under the same pressure from all sides within a plane. Maintaining this state at least approximately, for example, over the whole range or part of the range of the specified operating temperature of the ion-sensitive electrode, has shown that cracks and fissures can be avoided. Exposing the ion-sensitive glass membrane to high changes of the operating temperature, which can significantly reduce the lifespan of known ion-sensitive electrodes, has practically no impact on the lifespan of the exemplary ion-sensitive electrodes. Hence, by exposing exemplary ion-sensitive glass membranes to stress, namely compressive stress, their integrity can be maintained over an extended lifespan.
Creating compressive stress within an ion-sensitive glass layer or glass membrane can be achieved in different ways. Compressive stress can be induced into the ion-sensitive glass membrane or glass layer, e.g. by applying distributed forces across a practically linear, for example, annular, and/or planar connection, e.g. across a practically linear connection with an annular or tubular second holding member and/or across a planar connection with a first holding member in exemplary embodiments of a substrate layer, which may exhibit the form of a disc. The ion-sensitive layer can be mounted under compressive stress or without mechanical stress at a suitable process temperature. In exemplary embodiments discussed below, compressive stress in the ion-sensitive membrane is created by the connection to a mounting element, which after connection contracts by a desired extent, thereby exerting for example, radial forces onto the ion-sensitive glass layer, which is for example, a circular element, such as a disc. In the layered structure, materials with suitable thermal expansion coefficients are for example, selected for the dominant layers, which under thermal treatment expand and after contraction put pressure on the connected ion-sensitive glass layer. Alternatively or in addition, materials with suitable thermal expansion coefficients are selected for the first and/or second or further holding member(s) and the ion-sensitive glass membrane, which under thermal treatment expand and after contraction put pressure on the connected ion-sensitive glass layer.
The materials are for example, selected such that the thermal expansion coefficient of the ion-sensitive glass layer is smaller than the thermal expansion coefficient of the substrate. The ion-sensitive glass layer and the substrate are then connected or deposited upon one another, with the electrically conducting layer and optionally at least one intermediate layer in between, at a process temperature above the maximum operating temperature of the measurement unit, which is for example, around 150° C. (e.g., plus or minus 10%). Of course, not only finished layered units can be connected in this way, but layers can also be produced or built partially or completely by any thin-film or thick film technology at the selected process temperature.
After connecting the ion-sensitive glass layer and the substrate, for example via the electrically conducting layer and the intermediate layer, if present, the process temperature is lowered and the ion-sensitive glass layer and substrate will contract accordingly. Due to the higher thermal expansion coefficient the substrate will contract stronger than the ion-sensitive glass layer and will exert corresponding forces or pressure onto the ion-sensitive glass layer. These contraction forces applied by the substrate are for example radially aligned and can point to the centre of the ion-sensitive glass layer. As the planar connection between the substrate and the ion-sensitive glass layer was established at the first process temperature, e.g. around 300° C., the ion-sensitive membrane will always exhibit a compressive stress regardless of the temperature currently present during measurement. The first process temperature is above the temperature of the measurement process, which for example does not exceed 150° C. The constantly pressurised glass layer is stabilised and will not exhibit cracks or fissures during thermal cycles or normal mechanical handling.
The connection of the second holding member and the ion-sensitive glass membrane having different thermal expansion coefficients is done analogously. Connection of a first loop-shaped or ring-shaped sealing surface of the second holding member and a first loop-shaped or ring-shaped contact surface of the ion-sensitive glass layer is done at a process temperature above the maximum operating temperature of the measurement unit.
In exemplary embodiments, process temperatures are always selected with regard to the materials used for the layered structure and/or the second holding member. The differences of the thermal expansion coefficients and the related materials can be selected according to given requirements and the conditions of use of the ion-sensitive electrode. In order to maintain compressive stress in the ion-sensitive glass layer over the whole range of the operating temperature, i.e. the ion-sensitive membrane, the material of the ion-sensitive glass layer and the material of the first and/or second holding member can be selected such that the related thermal expansion coefficients of the adjoining materials differ by a value for example, in an exemplary range from 1% -12.5%. For example, a value is selected in the range from 7.5% -11.5%. While it is desired to maintain the compressive stress in the ion-sensitive glass layer over the complete operational temperature range of the measurement processes, significant reduction of undesirable stress in the ion-sensitive glass layer is also accomplished, when the range of the operation temperature is not fully covered. In the event that peak temperatures are seldom reached, such peak temperatures may be disregarded if other requirements need to be taken into account as well.
In an exemplary embodiment, a first holding member is an annular glass member or tubular glass member having an annular end face, which is welded to the ion-sensitive glass membrane or which is bonded to the ion-sensitive glass membrane by means of bonding material.
In another exemplary embodiment a first holding member is a substrate, for example, a disc-shaped substrate, and the ion-sensitive glass membrane is a glass layer, which directly or via at least one intermediate layer adheres to the substrate, and wherein the ion-sensitive glass membrane, the at least one intermediate layer and the substrate form a layered structure. In an exemplary embodiment, this layered structure together with a related second holding member, e.g. an annular glass member, forms the measurement unit. An ion-sensitive electrode including the layered structure or the measurement unit is a solid-state ion-sensitive electrode.
A first intermediate layer of the layered structure is for example, an electrically conducting layer. In another exemplary embodiment, a first intermediate layer is an electrically conducting layer directly adjoining the substrate and a second intermediate layer is a solid-state electrolyte layer, which adjoins on one side the electrically conducting layer and on the other side the ion-sensitive glass membrane.
In an exemplary embodiment, the second holding member includes ceramic or glass. The solid-state measurement unit can therefore be integrated into any structure of any ion-sensitive electrode. Furthermore, the applied technology allows the solid-state measurement unit to be designed and configured practically with any desired dimensions. Due to the rigidity and improved encapsulation, the solid-state measurement unit can be applied in any processes, such as industrial processes with high demand.
The substrate respective the first holding member includes at least one of the following exemplary materials: metal, steel, ceramic, glass, glass ceramic, polymer compound, fibre composite material. The substrate is for example, disk shaped. Further, the substrate has a thickness for example, in the exemplary range of 0.2 mm-1.5 mm, selected according to the mechanical stability desired or required. The use of a metal or steel substrate has the further advantage, that the resulting layered structure can be comparatively thin while still being mechanical stable and durable.
The electrically conducting layer includes a metal or metal alloy, for example, an alkali metal or alkali metal alloy, such as lithium or a lithium alloy, with a reduction potential of for example at least 1.0 V. The substrate and the electrically conducting layer may be a unitary part with homogeneous material over the whole cross-section. The electrically conducting layer may also be an integral part of the substrate, wherein one side exhibits specific metallic properties and may be coated by a film of metal, for example, an alkali metal or an alloy including alkali metal.
The solid-state electrolyte layer, if present, is for example, made of a solid-state electrolyte that conducts ions released from the electrically conducting layer. In an exemplary embodiment, the electrically conducting layer includes or consists of lithium or a lithium alloy, so that the solid-state electrolyte layer would transfer lithium ions. Here, the solid-state electrolyte separates the electrically conducting layer from the ion-sensitive glass layer or glass membrane so that a reduction of the glass matrix by the material of the electrically conducting layer is avoided.
The ion-sensitive glass layer is for example made of a glass that for example, conducts ions of the electrically conducting layer. If the electrically conducting layer includes or consists of lithium or a lithium alloy then the ion-sensitive glass layer would transfer lithium ions.
Exemplary ion-sensitive sensitive electrodes may be assembled in various ways. In an exemplary embodiment of a solid-state electrode the ion-sensitive glass membrane is for example, provided with a first ring-shaped contact surface and the substrate is provided with a second ring-shaped contact surface. The annular or tubular glass member is provided with a first ring-shaped sealing surface sealingly connected to the first ring-shaped contact surface of the ion-sensitive glass membrane, and is provided with a second ring-shaped sealing surface connected to the second ring-shaped contact surface of the substrate. After connecting the respective contact surfaces and sealing surfaces, the first and second ring-shaped contact surfaces of the layered structure are sealingly connected by an annular section of the annular or tubular glass member. The first and second contact surface and the first and second sealing surface are ring-shaped or loop-shaped and form closed loops with any suitable form, for example, a circular, rectangular, oval or any other curved form.
In an exemplary embodiment, the first and second ring-shaped sealing surfaces and/or the first and second ring-shaped contact surfaces form circular closed loops and/or are arranged concentrically or offset from one another. Arranging the ring-shaped sealing surfaces and the ring-shaped contact surfaces in closed loops ensures perfect sealing.
In an exemplary embodiment, the for example, disc shaped substrate has an upper side facing a lower side of the second holding member. With its lower side the substrate faces the electrically conducting layer, if present the solid-state electrolyte layer, and the upper side of the ion-sensitive glass layer. The ion-sensitive glass layer faces with its lower side the measurement solution.
The second holding member is for example sealingly connected in two separate contact regions with the substrate, in a first region with the ion-sensitive glass layer and in a second region with the substrate. The layers of the layered structure are therefore hermetically sealed, thus inhibiting access of ambient chemical reactants such as O2, H2O, N2, CO2, etc. to the contact regions of the layers of the layered structure, particularly to the sensitive electrically conducting layer and any intermediate layer.
Hence, hermetically sealing the layered structure allows using materials that otherwise may easily be destroyed by exposure to ambient chemical reactants. Furthermore, as the electrically conducting layer and, if present, the solid-state electrolyte layer are perfectly protected, these layers can be applied with a minimum thickness for example, in the range from 10 nm to 10 μm by any deposition process, such as PVD and/or electroplating on the substrate or possibly the glass layer that are serving as a carrier for the deposited material.
In an exemplary embodiment, the first and second ring-shaped sealing surfaces and/or the first and second ring-shaped contact surfaces form circular closed loops and/or are arranged concentrically or offset from one another. Arranging the ring-shaped sealing surfaces and the ring-shaped contact surfaces in closed loops ensures perfect sealing.
The layered structure is for example, provided with a first stepped profile with the ion-sensitive glass layer having a diameter that is larger than the diameter of the substrate and for example, the adjoining electrically conducting layer, and if present the solid-state electrolyte layer. The first stepped profile of the layered structure complements a second stepped profile provided at the lower side of the second holding member. Using first and second stepped profiles that are complementing one another has multiple advantages. Arranging the connections between the second holding member and the ion-sensitive glass layer, respective the second holding member and the substrate, on different levels ensures good separation between these connections. Further, mechanical engagement between the stepped profiles increases mechanical stability. Still further, the use of stepped profiles avoids the requirement of a larger displacement of the connecting zones relative to the central axis of the measurement unit, which therefore can be manufactured with smaller dimensions.
Further, for example, with the stepped profiles, the first ring-shaped contact surface can be located on the upper side of the ion-sensitive glass layer and the second ring-shaped contact surface can be located on the upper side of the substrate. This arrangement facilitates assembly and manufacturing processes, in particular the position processes, mounting processes as well as fusing or melting processes.
The first ring-shaped sealing surface of the second holding member is for example, arranged in a first plane, and the second ring-shaped sealing surface of the second holding member is arranged in a second plane, which first and second planes are aligned in parallel to the substrate, for example, with a distance between one another that corresponds at least approximately to the thickness of the substrate plus the thickness of the electrical conducting layer and, if present, the solid-state electrolyte layer. The planar arrangement of the layers and sealing and contact surfaces further facilitates manufacturing processes.
The measurement unit, which is provided for an ion-sensitive solid-state electrode, such as a pH-electrode, that serves to measure an ion activity in a measurement solution, includes a layered solid-state structure with an ion-sensitive glass layer that is provided with a first ring-shaped contact surface and that directly or via solid-state electrolyte layer adheres to an electrically conducting layer, which adheres to a substrate that is provided with a second ring-shaped contact surface and with a second holding member, which is provided with a first ring-shaped sealing surface sealingly connected to the first ring-shaped contact surface of the ion-sensitive glass layer and which is provided with a second ring-shaped sealing surface connected to the second ring-shaped contact surface of the substrate; and wherein the first and second ring-shaped sealing surfaces of the second holding member are sealingly connected by an annular section of the second holding member.
Various processes and materials can be used for bonding the first ring-shaped sealing surface and the first ring-shaped contact surface of the ion-sensitive glass layer as well as the second ring-shaped sealing surface and the second ring-shaped contact surface of the substrate with one another.
Bonding may for example be accomplished by diffusion of the adjoining ring-shaped sealing and contact surfaces. For example, the ring-shaped sealing and contact surfaces are arranged on material that is suitable for diffusion bonding at a suitable process temperature.
A bonding connection may for example use a bonding material including glass that is arranged, melted and solidified between the adjoining ring-shaped sealing and contact surfaces. The applied glass bonding material for example, diffuses into the ring-shaped sealing and contact surfaces, thus establishing a unitary bridge or bond between the ring-shaped sealing and contact surfaces. The glass bonding material is for example, a sealing glass paste that may be dispensed or screen printed onto the ring-shaped sealing surfaces and/or the ring-shaped contact surfaces and that is then sealed to or fused with the adjoining sealing and contact surfaces by applying at least one thermal cycle with which the glass bonding material and/or the adjoining materials are heated to the sealing temperature.
A bonding connection may also include (e.g., consist of) a bonding material including a metal that is arranged, melted and solidified between the adjoining ring-shaped sealing and contact surfaces.
For example, bonding is established by creating several layers, which optionally include an adhesion layer, for example including or consisting of Ti, Cr or TiW, with a thickness in an exemplary range of 10 nm to 500 nm, that is used to establish adhesion with the corresponding ring-shaped sealing or contact surface. Optionally, a stress relief layer is provided for example including or consisting of Cu, with a thickness in an exemplary range of 100 nm to 2000 nm, which serves to absorb compressive or tensile stress occurring within the layered structure. For example, a wetting/barrier layer for example including or consisting of nickel (Ni), nickel-vanadium (NiV), nickel-phoshor (NiP), with a thickness in an exemplary range of 100 nm to 5000 nm, and/or an oxidation protection layer for example including or consisting of gold (Au), with a thickness in an exemplary range of 10 nm to 200 nm, are provided in addition. Optionally, a solder layer is plated on top, for example including or consisting of tin (Sn), tin-silver (SnAg), tin-gold (SnAu), indium (In) based alloy or any other suitable soldering alloy. Material for the soldering layer are selected that have an acceptable processing temperature, so that layers or material of the layered structure are not impaired or overheated during bonding processes.
In further exemplary embodiments, bonding material is deposited in form of preforms, such as a first annular sealing preform placed between the first ring-shaped sealing surface and the first contact surface, as well as a second annular sealing preform placed between the second ring-shaped sealing surface and the second contact surface. The preforms made of glass or metal are then melted and solidified. The preforms include or consist of a single material but may also include a plurality of materials or an alloy. Furthermore, a preform may include (e.g., consist of) a single layer or a plurality of layers, such as at least one of the following layers: an adhesion layer, a stress relief layer, a wetting/barrier layer, an oxidation protection layer, a solder layer. These layers can be selected and combined according to the specific requirements.
As mentioned, the process temperature TP applied to the layers of the layered structure can be selected to be above the maximum operating temperature TOmax of the measurement unit. For example, the process temperature TP is by a factor k higher than the maximum operating temperature TOmax of the measurement unit; which factor k=Tp/TOmax is for example, in an exemplary range of 1.1 to 2.0 or more. For tin solder the ratio would for example be in the range of 1.1 to 1.3. For a glass frit the ratio would for example be in the range of 1.4 to 1.5.
The measurement unit according to the disclosure for example, includes an electrical module, such as a rigid or flexible PCB that may be used to collect, distribute and/or process information or signals. The electric module may include a processing unit and interfaces, with which electrical devices can be controlled or signals, e.g. received from a connected sensor, can be processed. For example, the electrical module is connected to a thermal sensor. The electrical module is placed on the upper side of the substrate and is for example, connected by reflow soldering. For this purpose, the upper side of the substrate, e.g. a metal disc, is provided with a solderable layer, e.g. a Ni/Au layer.
The second holding member for example, encloses a cavity or hollow space. As described above, at the lower side, the second holding member exhibits a stepped profile arranged in a circle, to ensure that the layered structure is completely surrounded and hermetically sealed. The electrical module is for example, accessible through the cavity. Furthermore, a lead-off wire connected to the electrical module or to the layered structure, for example, the electrically conducting layer, and optionally other wires can pass through. After assembly, the hollow space is filled and sealed with a moulding compound, such as an epoxy compound, which covers the upper side of the substrate and, if present the electrical module. The moulding compound for example, laterally adjoins the sealingly connected second ring-shaped sealing surface and the second contact surface, which are fused to one another, so that a dual stage sealing results. The second holding member may be a long tube or a relatively small hollow cylindrical part, which can be mounted within a tube of an ion-sensitive electrode. In other words, in an exemplary embodiment the at least one holding member may be a main part of the ion-sensitive electrode, which needs to be closed by a cap only. In another exemplary embodiment the at least one holding member is held at the front side of the main part of the ion-sensitive electrode (see
Hence, the exemplary solution can be used for solid-state and non-solid-state ion-sensitive electrodes, which essentially include an ion-sensitive glass membrane 11 or an ion-sensitive glass layer 11. The structure and assembly processes of the exemplary solid-state ion-sensitive electrode 10 of
In the exemplary embodiment of a pH-electrode, the ion-sensitive glass layer 11 may be provided with a known pH-sensitive glass composition, such as is also used for glass membranes of known non-solid-state pH-electrodes. The ion-sensitive glass layer 11 is for example, provided in the exemplary embodiment of a glass wafer, which for example, exhibits a thickness in the range between 0.05 mm and 1 mm or higher. In an embodiment, the ion-sensitive glass layer 11 is deposited by a known thin-film technology, e.g. sputtering, onto the intermediate layer 12, the electrically conducting layer 13, or directly onto the metal substrate 14, in which the electrically conducting layer 13 may be integrated. However, as only a thin electrically conducting layer 13 is required, this electrically conducting layer 13 is for example, applied to the substrate 14 by thick-film or thin-film technology as well. The solid-state electrolyte layer 12, if present, is for example, applied by thick-film or thin-film technology to the electrically conducting layer 13 or to the substrate 14, when the electrically conducting layer 13 is an integral part of the substrate 14. The sequence of building up the layers 11, 12, 13, 14 may also be reversed. It is also possible to connect any two layers 11, 12 or 12, 13 or 13, 14 in pairs that are further connected. For example, the layers 12 and 13 may be connected to each other, before being connected to layer 11 or 14. The solid-state electrolyte layer 12 may be applied to the ion-sensitive glass membrane 11 or to the electrically conducting layer 13.
In an exemplary embodiment, the second holding member 18, which for example, exhibits a maximum electrical resistance, is made of ceramic or glass. The substrate 14 for example, includes at least one of the following materials: metal, steel, ceramic, glass, glass ceramic, polymer compound, or fibre composite material. The electrically conducting layer 13 includes a metal or metal alloy with a reduction potential of at least 1.0 V, for example, an alkali metal or a compound containing alkali metal, such as lithium or a lithium alloy. The solid-state electrolyte layer 12, if present, is made of a solid-state electrolyte that for example, conducts ions of the electrically conducting layer 13, such as lithium ions. The ion-sensitive glass layer 11 is made of a glass that for example, conducts ions of the electrically conducting layer 13, such as lithium ions. Described below are materials and processes for manufacturing the layered structure 6.
In an exemplary embodiment, the electrically conducting layer 13 includes (e.g., consists of) lithium or a lithium alloy. The solid-state electrolyte layer 12, which may be applied to this electrically conducting layer 13 or to the ion-sensitive glass layer 11, is a solid-state electrolyte layer that is conducting lithium ions. The solid-state electrolyte layer may include (e.g., consist of) or may include for example: lithiumborate, such as B2O3—Li2O, lithium borat-sulphate (LiBSO), such as B2O3—0.8Li2O—0.8Li2SO4, lithium borophosphate (LiOP), such as ½x Li2O—BPO4, generally Li2O—B2O3—P2O5, lithium-aluminate, such as Li5AlO4, lithium-borosilicate, such as Li2O—B2O3—SiO2, lithium-gallium oxide, such as Li5GaO4, lithium-germanate, such as Li(4−3x)AlxGeO4, lithium-phosphate, such as Li(1+x)Ti2SixP(3−x)O12 or Li(1+x)MxTi(2−x)(PO4)3 with M=Al, Ga, Fe, Sc, In, Lu, Y, La, lithium-phosphorus-oxynitride, such as Li3PO4−xNx, lithium-silicate-aluminate, such as LiAlSi2O6, LiAlSiO4, Li9SiAlO8, lithium-silicate, such as Li2SiO4, Li4SiO4, Li2SiO3, Li2Si2O5, lithium-silicon Phosphate, such as Li3.6Si0.6P0.4O4, lithium-silicon-phosphorus-oxynitride, such as Li4SiO4−x—Li3PO4−yNx+y, lithium-thiogermanate, Li2GeS3, Li4GeS4, Li6GeS5, lithium-titanate, such as Li2Zr(1−x)TixO3, lithium-vanadate, lithium-compounds, such as Li2S—SiS2—Li3PO4 or Li7P3S11, lithium-zinc oxides, such as Li6ZnO4, lithium-boron-oxynitride (Li—B—O—N), such as Li3.09BO2.53N0.52, sulphide, such as Li2S—GeS2, and/or thio-lithium-germanium-compound, such as Li10GeP2S12, Li3.25Ge0.25P0.75S4,
or mixtures thereof.
In an exemplary embodiment, the solid-state electrolyte layer 12 includes an alkali metal-solid-state electrolyte compound, particularly a lithium-phosphorus-oxynitride-compound (LiPON), which is applied for example by sputtering. Further, thin-film processes suitable for applying the solid-state electrolyte layer 12 are for example: pulsed laser deposition, magnetron sputtering, reactive magnetron sputtering, CVD, vapour deposition, reactive vapour deposition, procedures, and plasma assisted chemical vapour deposition, such as plasma assisted CVD or vacuum plasma spray coating. The solid-state electrolyte layer 12 for example, exhibits a layer thickness in an exemplary range from 50 nm to 5000 nm or higher. Most suitable are layer thicknesses in an exemplary range from 100 nm to 1000 nm.
Subsequently the electrically conducting layer 13, which includes an alkali metal such as metallic lithium, i.e. pure lithium, an alloy including lithium-(0) or a lithium-solid-state compound, is applied to the solid-state electrolyte layer 12. The layer thickness of the electrically conducting layer 13 is for example, in an exemplary range between 10 nm to 10 μm or higher.
As described above, the measurement principle of the exemplary ion-sensitive electrode 10 and the solid-state measurement unit 1 is based on the ionic reaction between the measurement solution 5 and the ion-sensitive glass layer 11. The ion conducting solid-state electrolyte layer 12 supports a reversible redox reaction between ionic and metallic lithium at the interface between the solid-state electrolyte layer 12 and the electrically conducting layer 13, so that a measurement signal is provided at a suitable electrical contact, which is provided at the electrically conducting layer 13. Damage to the ion-sensitive glass layer 11, which is separated from the electrically conducting layer 13 by the solid-state electrolyte layer 12, is avoided.
As materials used for the layered structure 6, such as lithium for the electrically conducting later 13, are highly reactive to ambient chemical reactants such as O2, H2O, N2, CO2, etc., the measurement unit 1 is provided with a hermetic encapsulation, which can prevent such chemical reactants from entering the measurement unit 1. At the same time, it can be important that direct electric contact as well as leakage currents are avoided. This is achieved with the encapsulation of the layered structure 6, which will be described with reference to
The holding member 18 has an annular shape with a circular wall having an outer side 186 and an inner side 187, and it has a stepped profile at the lower side 184, which is facing the layered structure 6. The annular section 189 is therefore an integral part of the circular wall of second holding member 18. Due to the stepped profile the first and second sealing surfaces 181 and 182 are laterally adjoining one another and are vertically displaced from one another. The measurement unit 1 can therefore be built in small dimensions.
Due to the hollow cylindrical shape of the second holding member 18, the first and second ring-shaped sealing surfaces 181, 182 and the thereto corresponding first and second ring-shaped contact surfaces 111, 141 of the ion-sensitive glass layer 11 and the substrate 14 form circular closed loops that are arranged concentrically to one another.
Further, the exemplary disc shaped substrate 14 has an upper side facing the lower side 184 of the second holding member 18 and a lower side facing the upper sides of the electrically conducting layer 13, the upper side if present, of the solid-state electrolyte layer 12, and the upper side of the ion-sensitive glass layer 11, which faces with its lower side the measurement solution 5. The first ring-shaped contact surface 111 is located on the upper side of the ion-sensitive glass layer 11 and the second ring-shaped contact surface 141 is located on the upper side of the substrate 14. Both ring-shaped contact surfaces 111, 141 are provided on the upper side of the layered structure 6 and can therefore easily be connected to the first and second sealing surfaces 181, 182 of the second holding member 18.
The stepped profile provided at the lower side 184 of the second holding member 18 corresponds to a stepped profile of the layered structure 6 with the for example, circular ion-sensitive glass layer 11 having a diameter d11 that is larger than the diameter d14 of the for example, circular substrate 14 (see
The first ring-shaped sealing surface 181 of the second holding member 18 is arranged in a first plane and the second ring-shaped sealing surface 182 of the second holding member 18 is arranged in a second plane, which planes are aligned in parallel to the substrate 14 with a distance between one another that corresponds to the thickness th14 of the substrate 14 plus the thickness of the solid-state electrolyte layer 12 and the electrically conducting layer 13.
In the exemplary embodiment of
As described above, connections between the layered structure 6 and the second holding member 18 can be established in other ways, e.g. by melting and diffusing material of the adjoining ring-shaped sealing and contact surfaces 181, 111; 182, 141. Glass bonding material, e.g. a glass powder or glass paste, can also be arranged, melted and solidified between the adjoining ring-shaped sealing and ring-shaped contact surfaces 181, 111; 182, 141. Bonding material can also be deposited with any deposition process, e.g. by thick film technology and/or thin-film technology. A glass bonding material, e.g. glass powder, can be used for bonding purposes. Such bonding material can be structured in several layers as described above.
Still further,
A lead-off wire 2 is connected to an electrical contact 20, which is connected to the electrically conducting layer 13 or to the electrical module 16.
It has been described above that in further exemplary embodiments the ion-sensitive glass layer 11 is held under constant compressive stress, acting inward with distributed forces, for example, over the whole range of the specified operating temperature of the solid-state measurement unit 1 or the ion-sensitive electrode 10. Steps for reaching the desired state of the ion-sensitive glass layer 11 are described below.
In an exemplary embodiment, in order to obtain an ion-sensitive electrode with a constantly pressurised ion-sensitive glass layer, the thermal expansion coefficients of the connected materials are selected as follows. The thermal expansion coefficient α11 of the ion-sensitive glass layer 11 is smaller than the thermal expansion coefficient α18 of the second holding member 18.
As symbolically shown in
In exemplary solid-state embodiments of the ion-sensitive electrodes 10, i.e. in the exemplary measurement unit 1, a pressurised ion-sensitive glass layer 11 is for example, reached by suitably selecting the thermal expansion coefficients of the layers 11, 12, 13, 14 of the layered structure 6.
As shown in
Connecting a tubular second holding member 18′ to an ion-sensitive glass membrane 11 with the described geometrical dimensions can have an advantage of perfect alignment of the related end pieces, which for example, have identical wall thicknesses. However, where only small deviations between the geometrical dimensions of the tubular holding member 18′ and the ion-sensitive glass membrane 11 are required to provide compressive stress within the ion-sensitive glass membrane 11, the inner diameters d18i and d11i can be approximately equivalent and the adaptation can be done by the welding or bonding material 181 which for example, connects the tubular holding member 18′ to the ion-sensitive glass membrane 11.
It will be appreciated by those skilled in the art that the present disclosure can be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The presently disclosed embodiments are therefore considered in all respects to be illustrative and not restricted. The scope of the disclosure is indicated by the appended claims rather than the foregoing description and all changes that come within the meaning and range and equivalence thereof are intended to be embraced therein.
100 measurement system
111 first contact surface
141 second contact surface
151 first annular sealing preform
152 second annular sealing preform
181 welding or bonding connection
182 second sealing surface
Number | Date | Country | Kind |
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18154257.2 | Jan 2018 | EP | regional |
This application claims priority as a continuation application under 35 U.S.C. § 120 to PCT/EP2019/052147, which was filed as an International Application on Jan. 29, 2019 designating the U.S., and which claims priority to European Application 18154257.2 filed in Europe on Jan. 30, 2018. The entire contents of these applications are hereby incorporated by reference in their entireties.
Number | Date | Country | |
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Parent | PCT/EP2019/052147 | Jan 2019 | US |
Child | 16942351 | US |