Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01B—BOILING; BOILING APPARATUS ; EVAPORATION; EVAPORATION APPARATUS
  • B01B1/00—Boiling; Boiling apparatus for physical or chemical purposes ; Evaporation in general
  • B01B1/005—Evaporation for physical or chemical purposes; Evaporation apparatus therefor, e.g. evaporation of liquids for gas phase reactions
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B3/00—Ohmic-resistance heating
  • H05B3/10—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor
  • H05B3/12—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
  • H05B3/14—Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
  • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
  • A24F40/40—Constructional details, e.g. connection of cartridges and battery parts
  • A24F40/44—Wicks
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
  • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
  • A24F40/40—Constructional details, e.g. connection of cartridges and battery parts
  • A24F40/46—Shape or structure of electric heating means
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B3/00—Ohmic-resistance heating
  • H05B3/40—Heating elements having the shape of rods or tubes
  • H05B3/42—Heating elements having the shape of rods or tubes non-flexible
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
  • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
  • A24F40/10—Devices using liquid inhalable precursors
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
  • A24F40/00—Electrically operated smoking devices; Component parts thereof; Manufacture thereof; Maintenance or testing thereof; Charging means specially adapted therefor
  • A24F40/40—Constructional details, e.g. connection of cartridges and battery parts
  • A24F40/46—Shape or structure of electric heating means
  • A24F40/465—Shape or structure of electric heating means specially adapted for induction heating
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B2203/00—Aspects relating to Ohmic resistive heating covered by group H05B3/00
  • H05B2203/021—Heaters specially adapted for heating liquids
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
  • H05B2203/00—Aspects relating to Ohmic resistive heating covered by group H05B3/00
  • H05B2203/022—Heaters specially adapted for heating gaseous material

Definitions

• the invention generally relates to an electrically conductive porous sintered body.
• the invention relates to an evaporator unit comprising a liquid reservoir or liquid buffer and a heating unit for storing and controlled release of evaporable substances.
• the evaporator unit can be used here in particular in electronic cigarettes, in medication administration devices, room humidifiers and/or heatable evaporators.
• the evaporators can be devices for the provision, delivery and/or distribution of substances in a gas phase, for example in the room air, in the form of gases, vapors and/or aerosols.
• fragrances or active substances in particular insect repellents, can be used as substances.
• Electronic cigarettes also referred to below as e-cigarettes, or similar devices such as electric pipes or shishas, are being used to an increasing extent as an alternative to tobacco cigarettes.
• electronic cigarettes include a mouthpiece and vaporizer unit, and an electrical power source operatively connected to the vaporizer unit.
• the evaporator unit has a liquid reservoir which is connected to a heating element.
• Certain medicaments are advantageously administered in a gaseous or vaporized form, for example as an aerosol.
• Vaporizers according to the invention can be used for the storage and dispensing of such medicaments, particularly in delivery devices for such medicaments.
• Thermally heatable evaporators are increasingly being used to provide an ambience with fragrances.
• these can be bars, hotel lobbies and/or vehicle interiors, for example the interiors of motor vehicles, in particular passenger cars.
• a liquid reservoir is also connected to a heating element in the evaporator unit used in this case.
• the liquid reservoir includes a Liquid, which is usually a carrier liquid such as propylene glycol or glycerin, in which additives such as fragrances and flavorings and/or nicotine and/or medication are dissolved and/or generally contained.
• the carrier liquid is bound to the inner surface of the liquid reservoir by adsorption processes. If necessary, a separate liquid reservoir is provided in order to supply liquid to the liquid reservoir.
• the liquid stored in the liquid reservoir is vaporized by heating a heating element, desorbed from the wetted surface of the liquid reservoir and can be inhaled by the user. Temperatures of over 200°C can be reached here.
• the liquid reservoir or liquid buffer must therefore have a high absorption capacity and a high adsorption effect, and at the same time the liquid must be released or transported quickly at high temperatures.
• liquid reservoirs or wicks can be formed by a porous or fibrous organic polymer.
• Corresponding components can be produced quite easily, but there is a risk here that the polymeric material will be heated too high and decompose, for example if the component runs dry. This not only has a disadvantageous effect on the service life of the liquid reservoir or wick and thus the evaporator unit, but there is also the risk that decomposition products of the fluid to be evaporated or even of the liquid reservoir will be released and inhaled by the user.
• evaporator units are also used whose liquid reservoirs consist of porous glass or ceramics. Due to the higher temperature stability of these liquid stores, a more compact construction of the evaporator and thus of the electronic cigarette as a whole can be implemented.
• local evaporation can be achieved by using a low pressure combined with a high temperature.
• the low pressure is achieved, for example, by the suction pressure when puffing on the cigarette during consumption, so the pressure is regulated by the consumer.
• the temperatures in the liquid reservoir required for evaporation are generated by a heating unit. Temperatures of more than 200°C are usually reached here in order to ensure rapid evaporation.
• the heating output is usually provided by an electrical heating coil operated by means of a battery or accumulator.
• the required heating power depends on the volume to be evaporated and the effectiveness of the heating.
• the heat transfer from the heating coil to the liquid should take place by non-contact radiation.
• the heating coil is attached as close as possible to the evaporation surface, but preferably without touching it.
• the liquid often overheats and decomposes.
• EP 2 764 783 A1 describes an electronic cigarette with an evaporator that has a porous liquid reservoir made of a sintered material.
• the heating element can be designed as a heating coil or as an electrically conductive coating, with the coating being deposited only on parts of the lateral surfaces of the liquid reservoir.
• the evaporation is locally limited.
• US 2011/0226236 A1 describes an inhaler in which the liquid reservoir and the heating element are cohesively connected to one another.
• Liquid reservoir and heating element form a flat composite material.
• the liquid reservoir for example made of an open-pored sintered body, acts as a wick and directs the liquid to be evaporated to the heating element.
• the heating element is applied to one of the surfaces of the liquid reservoir, for example in the form of a coating.
• the evaporation takes place in a locally limited manner on the surface, so that there is also a risk of overheating.
• evaporator units are known from the prior art, in which the evaporation takes place not only on the surface of the liquid reservoir, but over its entire volume.
• the vapor develops not only locally on the surface, but throughout the volume of the liquid reservoir.
• the vapor pressure within the liquid reservoir is largely constant and capillary transport of the liquid to the surface of the liquid reservoir is still ensured. Accordingly, the evaporation rate is no longer minimized by capillary transport.
• a prerequisite for a corresponding evaporator is an electrically conductive and porous material. If an electrical voltage is applied, the entire volume of the evaporator heats up and evaporation takes place throughout the volume.
• Corresponding evaporators are described in US 2014/0238424 A1 and US 2014/0238423 A1.
• the liquid reservoir and the heating element are combined in one component, for example in the form of a porous body made of metal or a metal mesh.
• the disadvantage here is that in the porous bodies described, the ratio of pore size to electrical resistance cannot be easily adjusted. Degradation of the coating can also occur after the application of the conductive coating as a result of subsequent sintering.
• the materials described in the prior art mentioned above are not suitable, or only suitable to a limited extent, for producing composites by means of a sintering process which have both a high, adjustable porosity and good electrical conductivity. In general, ceramics are also difficult to coat continuously due to their fine porosity and rough surface.
• the problem of low dimensional stability of the sintered body or its precursor during production can also occur.
• the glasses used have good joining properties, the relatively low softening temperatures required for this lead to poor dimensional stability of the workpiece at high temperatures.
• this can lead to deformation or shrinkage of the workpiece during the sintering process.
• this can also have a disadvantageous effect on the porosity of the sintered body.
• pore formers which are only removed from the sintered body after the sintering process has ended and thus stabilize the workpiece during sintering.
• the pore formers used are usually water-soluble salts with high temperature stability and a high melting point.
• the disadvantage of this method is that only a limited selection of pore formers is available.
• an additional process step is required to wash out the pore-forming agent.
• Another object of the invention is to provide an evaporator comprising a sintered body.
• the invention strives for good heatability and simple adjustability of the electrical resistance and porosity of the liquid reservoir.
• Another object of the invention is to provide a method for producing a corresponding electrically conductive sintered body.
• an object of the invention is to enable the use of the sintered body in an evaporator.
• the sintered body according to the invention is particularly suitable for use in an evaporator unit.
• An evaporator according to the present invention includes the electrically conductive sintered body.
• the electrically conductive sintered body is designed as a composite of at least two electrically conductive materials and at least one dielectric material.
• the sintered body has at least one first electrically conductive material and at least one second electrically conductive material, the first electrically conductive material having a lower electrical conductivity than the second electrically conductive material.
• the electrical conductivity of the first electrically conductive material is preferably less than 30 S/pm, in particular up to 10 S/pm.
• the second electrically conductive material preferably has an electrical conductivity of more than 10 S/pm, particularly preferably more than 30 S/pm.
• the conductivity values given here refer to their value at room temperature.
• the at least one first conductive material forms a framework for the sintered body. This framework serves to create a stable element that remains mechanically stable even at the sintering temperature.
• At least one of the electrically conductive materials used ie the first or the second electrically conductive material, has a resistance with a positive temperature coefficient.
• Both electrically conductive materials particularly preferably have such a positive temperature coefficient. This makes it easier to control the electrical heating of the sintered body and supports rapid heating from room temperature.
• a carrier liquid is stored in the porous evaporator by adsorptive interactions, which liquid can contain, for example, fragrances and flavorings and/or medicines, including active substances and/or nicotine dissolved in suitable liquids.
• liquid can contain, for example, fragrances and flavorings and/or medicines, including active substances and/or nicotine dissolved in suitable liquids.
• the sintered body has an open porosity in the range of 10 to 90%, preferably in the range of 50 to 75%, based on the volume of the sintered body.
• the sintered body has a large inner surface area for desorption with simultaneous high mechanical stability and enables good subsequent flow of the liquid to be evaporated or the medium to be evaporated.
• At least 90%, in particular at least 95%, of the total pore volume is preferably present as open pores.
• the open porosity can be determined using measuring methods according to DIN EN ISO 1183 and DIN 66133.
• the sintered body preferably contains only a small proportion of closed pores. As a result, the sintered body has only a small dead volume, i.e. a volume that does not contribute to the absorption and release of the liquid to be evaporated.
• the sintered body preferably has a proportion of closed pores of less than 15% or even less than 10% of the total volume of the sintered body.
• the open porosity can be determined as described above.
• the total porosity is calculated from the density of the body.
• the difference between the total porosity and the open porosity then results as the proportion of closed pores.
• the sintered body even has a proportion of closed pores of less than 5% of the total volume, which can occur as a result of the process.
• the sintered body contains one of the materials glass, ceramic, glass ceramic, plastic or a combination of these materials as the dielectric material.
• dielectric material and electrically conductive materials form the composite material of the sintered body.
• a dielectric or dielectric material is referred to in particular as an electrically weakly or non-conductive substance in which the charge carriers present are not freely movable, or at least are not freely movable at room temperature.
• the proportion of dielectric material is at least 5% by volume, with one embodiment of the invention providing a proportion of dielectric material in the composite material in the range from 5 to 70% by volume, preferably in the range from 10 to 50% by volume.
• the total proportion of electrically conductive material in the composite material is at most 95% by volume.
• the proportion of electrically conductive material in the composite material is a total of 30 to 95% by volume, preferably 50 to 90% by volume.
• the proportions listed above relate to the composite material of the sintered body, i.e. the pore volume or the proportion by volume of the pores in the sintered body is not taken into account here.
• the sintered body contains at least two different dielectric materials.
• the dielectric materials used have no appreciable electrical conductivity at room temperature.
• the electrically conductive materials are connected to each other through the dielectric material.
• the electrical conductivity of the first electrically conductive material is preferably in the range of up to ⁇ 30 S/pm, preferably in the range from 0.01 to 20 S/pm, particularly preferably in the range from 1 to 10 S/pm and the electrical conductivity of the second electrically conductive material preferably in the range of >10 S/pm, preferably >20 S/pm, most preferably >30 S/pm, in particular in the range of up to 70 S/pm.
• the proportion of the first electrically conductive material in the sintered body is greater than the proportion of the second electrically conductive material.
• the first electrically conductive material enables the sintered body to have high mechanical strength and dimensional stability. Due to the relatively low electrical conductivity of the first electrically conductive material of at most 30 S/pm, the content of the first electrically conductive material no longer has an exponential effect on the electrical conductivity of the sintered body, in contrast to materials with high electrical conductivity, but rather almost linearly out. This enables good adjustability of the electrical conductivity of the sintered body.
• sintered bodies with high contents of the first electrically conductive material can be realized without increasing the electrical conductivity of the sintered body too much.
• basic electrical conductivity with high homogeneity over the entire sintered body is also achieved, particularly in embodiments with relatively high contents of the first electrically conductive material.
• Contents of the first electrically conductive material in the composite of 30 to 90% by volume, preferably 40 to 80% by volume and particularly preferably 55 to 75% by volume have proven to be particularly advantageous.
• the content of the first electrically conductive material in the composite is 30 to 80% by volume, preferably 40 to 70% by volume and particularly preferably 50 to 65% by volume.
• a classification of the electrically conductive materials can be made in particular on the basis of their electrical conductivity.
• the materials of classes C and B can be used with preference for the formation of the metal framework, in particular because of their at least partially inexpensive commercial availability, and can be used to achieve or set a basic electrical conductivity of the sintered body.
• Class A materials can preferably be used to achieve, set or fine-tune a desired or required electrical conductivity of the sintered body.
• the materials from at least one class are preferably put together according to the rule that the electrical conductivity of the first material is lower than the electrical conductivity of the at least one second material.
• class C and/or B are combined with class A, preferably class C with class A.
• the sintered body contains a material from class C and/or class B as the first electrically conductive material and a material from class A as the second electrically conductive material. Combining class B with class C is also conceivable.
• the sintered body contains a class C material as the first electrically conductive material and a class B material as the second electrically conductive material.
• the sintered body has titanium, chromium, steel, manganese, nickel, copper, silicon or corresponding alloys, such as typical heat conductor alloys, in particular CuMnNi alloys (e.g. Konstanten®) or FeCrAI alloys (e.g. Kanthai ®) on. Mixtures or combinations of the above materials are also possible.
• stainless steel in particular stainless and/or scale-resistant or heat-resistant stainless steel, for example type 1.4828 or 1.4404, as the first electrically conductive material has proven to be particularly advantageous.
• stainless steel not only has an electrical conductivity that is advantageous for use as the first electrically conductive material but also one without chemical resistance.
• stainless steel is resistant to high temperatures and can also be used in medical areas. Another advantage lies in its relatively low production costs.
• the desired electrical conductivity of the sintered body is set based on its basic conductivity by the type of second electrically conductive material and its content in the sintered body.
• the composite has a content of second electrically conductive material in the range from 5 to 50% by volume, preferably 10 to 30% by volume and particularly preferably 15 to 25% by volume.
• aluminum, copper and precious metals in particular platinum, gold, silver, and their mixtures and/or their alloys have proven to be advantageous as the second electrically conductive material.
• Mixing at least two of the above materials is also possible.
• Precious metals offer in addition to a high electrical Conductivity also has the advantage that they are inert or at least largely inert to the components of the dielectric material even at high temperatures, ie in particular materials that have little or no tendency to react with the dielectric material and/or to form oxides or other chemical changes. Inertness is therefore also an important criterion for the selection of other electrically conductive materials and/or their alloys and/or mixtures, apart from the precious metals and/or their alloys and/or mixtures. This is particularly advantageous in embodiments in which glasses are used as the dielectric material.
• the use of silver or gold or alloys with at least one of these metals as the second electrically conductive material is particularly advantageous.
• the sintered body has stainless steel (class C) as the first electrically conductive material and silver (class A) as the second electrically conductive material.
• a development of the invention provides that all of the electrically conductive material present in the sintered body is first and second electrically conductive material.
• the electrically conductive material apart from an optional coating, is formed only by the at least one first and at least one second electrically conductive material, without a further conductive phase being present to a greater extent.
• the proportion of one or more other conductive phases or metals is less than 3% by volume.
• the material of the electrically conductive particles has a resistance with a positive temperature coefficient. This makes it easier to control the electrical heating of the sintered body and supports rapid heating from room temperature.
• the temperature coefficient of the electrical resistance is close to zero, in particular less than 0.00025 K ⁇ 1 . This is the case, for example, with some copper-nickel alloys such as Konstantan®. Constant has a temperature coefficient of -0.000074 K' 1 . Likewise, NiCrO 2 with a temperature coefficient of -+0.00011 K' 1 can be used.
• electrically conductive materials in particular metals, which have a temperature coefficient of electrical Resistance of >-0.075 1/K, but preferably >-0.0001 1/K, particularly preferably >0.0001 1/K.
• the electrically conductive material has a temperature coefficient of the electrical resistance of ⁇ 0.008 1/K.
• the content of electrically conductive particles used in each case, in particular of the second electrically conductive material, is dependent on the respective material of the electrically conductive particles, in particular on their electrical conductivity and on the shape of the particles used.
• An embodiment of the invention provides that the maximum distance between two adjacent electrically conductive particles is less than 30 ⁇ m or even less than 10 ⁇ m. Due to this small distance between the electrically conductive particles, the current can flow through electron tunnel effects. According to a development of this embodiment, the electrically conductive particles are at least partially spaced apart from one another. In this case, the electrically conductive particles are insulated from one another by the dielectric material and/or pores. An average distance between adjacent electrically conductive particles of less than 30 ⁇ m, preferably in the range of less than 10 ⁇ m, has proven particularly advantageous.
• the electrically conductive material is in particulate form, with the particles of the first and second electrically conductive material forming a homogeneous mixture.
• the electrically conductive particles are held together by the dielectric material.
• the second electrically conductive particles are homogeneously distributed in the sintered body.
• the homogeneous distribution of the second electrically conductive particles in the composite ensures that the sintered body has a homogeneous conductivity in the range from 0.1 to 10 5 S/m throughout the volume.
• the electrical conductivity of the sintered body is in the range from 10 to 10,000 S/m.
• the electrical conductivity of the sintered body according to the invention enables the corresponding vaporizer to be used in an electronic cigarette.
• the sintered body has an electrical resistance in the range from 0.05 ohms to 5 ohms, preferably 0.1 to 5 ohms.
• the evaporator is operated with a voltage in the range from 1 to 12 V and/or with a heating capacity of at least 1 to 500 watts, in particular 1 to 300 watts, preferably 1 to 150 watts. In this case, the evaporator heats up through the application of a current in its entire volume, so that the desorption of the liquid stored in the evaporator begins.
• devices according to another development can also be operated at voltages of 110V, 220V/230V or even 380V. Electrical resistances of up to 3000 ohms and outputs of up to 1000 W or more are advantageous here.
• the device is an inhaler for the medical field.
• the evaporator unit can have higher operating voltages, in particular operating voltages in the range from >12V to 110V, resistances of more than 5 ohms and/or heating outputs of more than 80W.
• the device is an inhaler for the medical field.
• the evaporator devices of this development can also be designed for evaporation in larger rooms, for example as a smoke machine.
• the entire accessible surface of the sintered body made of composite material forms the evaporation surface. Due to the electrical conductivity of the sintered body according to the invention, the current flow takes place over the entire body volume of the sintered body. Accordingly, the liquid to be vaporized is vaporized on the entire surface of the sintered body. Thus, the steam forms not only locally on the lateral surface of the sintered body but also on the inner surface of the sintered body.
• evaporators which have a local heating device, for example a heating coil or an electrically conductive coating on the outer surfaces of the evaporator body
• capillary transport from the inside of the sintered body to a local heating device is not necessary, i.e. over relatively long distances, not necessary, since with the evaporator according to the invention whose entire volume is heated.
• This has an advantageous effect on the service life of the evaporator unit.
• local overheating of the evaporator can lead to decomposition processes in the liquid to be evaporated.
• the proportion of dielectric material in the sintered body leads to good mechanical stability and strength of the sintered body.
• a sintered body in the form of a Composite ie a sintered body in which the dielectric material and electrically conductive particles are distributed homogeneously or at least largely homogeneously, offers the advantage, unlike subsequently coated sintered bodies, that properties of the sintered body, such as its pore size or the proportion of open pores in the sintered body not be adversely affected.
• the electrical conductivity of the sintered body can be influenced not only by the electrical conductivity of the electrically conductive material used and its content in the sintered body, but also by the particle size of the electrically conductive particles and by the particle shape or particle geometry.
• the use of electrically conductive particles, in particular for the second electrically conductive material, which deviate from the round particle shape, that is to say essentially spherical particles, has proven to be advantageous.
• the electrically conductive particles therefore have a flat, platelet-like shape and are also referred to as platelets.
• the composite has electrically conductive particles with a long-grained or elongated geometry. In particular, these particles have an acicular geometry.
• platelet-shaped or elongated particles can form a continuous framework of electrically conductive material within the sintered body even with relatively low filling levels, so that the corresponding sintered body has an electrical conductivity in the range according to the invention despite a relatively low filling level of the electrically conductive material. Accordingly, a required electrical conductivity of a sintered body can be achieved with elongate electrically conductive particles with a lower volume fraction than with spherical particles. Other options for reducing this volume part, also compared to elongated particles, often also associated with further reduced costs, can be achieved by platelet-shaped particles.
• the use of flat, platelet-shaped or elongated electrically conductive particles is particularly advantageous when the degree of filling of the electrically conductive material in the sintered body is relatively low.
• electrically conductive particles with the geometries described above, a network of electrically conductive material can be formed in the sintered body even with low filling levels, so that electrical conduction can be ensured and when a voltage or a Current flow through the sintered body of a suitable size, for example, a use as a heating element or in an evaporator is made possible.
• the sintered body has electrically conductive particles with a platelet-shaped or elongated geometry.
• the electrically conductive particles have a maximum thickness dmax and a maximum length lmax, where dmax ⁇ Imax applies.
• Electrically conductive particles have proven particularly advantageous for which the following applies: 2 dmax *• Imax, preferably 3 dmax ⁇ Imax, particularly preferably 7 dmax ⁇ Imax.
• the electrically conductive particles in the sintered body have an average particle size (dso) in the range from 0.1 ⁇ m to 1000 ⁇ m, preferably in the range from 1 to 200 ⁇ m, most preferably from 1 to 50 ⁇ m.
• the particle sizes, in particular the dso value, of the first and second conductive particles differ.
• the ratio of the larger to the smaller dso value is preferably at least 2:1, preferably at least 5:1. In specific embodiments, this ratio can also be chosen to be larger, for example at least 7:1 or even at least 10:1.
• both the first conductive particles and the second conductive particles can have the larger particle sizes or dso values.
• electrically conductive particles with a smaller particle size, in particular the second electrically conductive material it is advantageous if the degree of filling of the electrically conductive particles in the corresponding sintered bodies is increased in order to achieve sufficient electrical conductivity.
• the electrical conductivity is reduced by the use of very small electrically conductive particles.
• Electrically conductive particles that are too large, in particular of the first electrically conductive material can in turn greatly reduce the electrical resistance in the sintered body in local areas, so that the sintered body is inhomogeneous in terms of electrical resistance. This in turn can lead to local overheating in the sintered body and to inhomogeneous evaporation. This effect is all the more pronounced, the greater the electrical conductivity of the corresponding electrically conductive particles.
• very large electrically conductive Particles and the associated inhomogeneous structure of the sintered body have an adverse effect on its mechanical strength.
• the pores have an average pore size in the range from 1 m to 1000 m.
• the average pore size of the open pores of the sintered body is preferably in the range from 50 to 800 ⁇ m, particularly preferably in the range from 100 to 600 ⁇ m.
• Pores with appropriate sizes are advantageous because they are small enough to generate sufficiently large capillary forces and thus ensure the supply of liquid to be evaporated, especially when used as a liquid store in an evaporator, while at the same time they are large enough to allow the vapor to be released quickly to allow. It is also conceivable to advantageously provide more than one pore size or more than one pore size range, for example a bimodal pore size distribution with large pores and small pores, in a sintered body.
• the proportion of electrically conductive particles with a given or required electrical conductivity of a sintered body with low porosity can turn out to be lower than in sintered bodies with higher porosity.
• the respective use or its requirements, as described above, for example the transport of a liquid to be evaporated versus the evaporation capacity, can thus be taken into account by suitable adjustments to the material composition and porosity.
• the dielectric material in the sintered body is thermally stable to temperatures of at least 300°C or even at least 400°C.
• the dielectric material has a softening point T g which is below the melting point of the first electrically conductive material, preferably below the melting point of the first and the second electrically conductive material in the sintered body.
• the dielectric material of the sintered body comprises a glass.
• the glass content in the sintered body is at least 5% by volume. According to a further embodiment, however, only a small proportion of glass, less than 5% by volume, can be provided, for example in order to bind other particles, for example ceramic particles.
• the use of glass as the dielectric material is advantageous with regard to the processability in the production of the sintered body and the temperature stability and the mechanical strength. Glasses with no or a relatively low alkali content have proven to be particularly advantageous. Under alkali-free glasses or glasses without alkali content are understood here glasses whose Composition Alkalis are not deliberately added.
• a low alkali content in particular a low sodium content, is advantageous here from a number of points of view.
• glasses with a relatively low alkali content show low alkali diffusion even at high temperatures, so that the glass properties do not change or hardly change even when the evaporator is heating.
• the low alkali diffusion of the glasses is also advantageous when the sintered body is used as an evaporator, since no such components that may escape interact with the electrically conductive material and/or an optionally present coating of the sintered body and/or with the liquid to be evaporated. The latter is particularly relevant when using the optionally coated sintered body as an evaporator in medical inhalers.
• An alkali content of the glass of at most 15% by weight or even at most 6% by weight has proven particularly advantageous.
• the evaporator contains a glass as the dielectric material.
• a borosilicate glass in particular with the following components, has proven to be particularly advantageous:
• glasses can also be used as the dielectric material.
• bismuth glasses or zinc glasses have also proven to be suitable.
• the last-named glasses or similar glasses with other oxides are understood to mean that these include corresponding oxidic components, eg Bi 2 O 3 or ZnO, as an essential component, for example at least 50% by weight or even up to 80% by weight.
• the thermal expansion behavior of the dielectric component can also be influenced by the selection of the respective dielectric material, in particular a glass. There is a low thermal expansion of this in the application as an evaporator advantageous with regard to thermal shock resistance or thermal cycling of the sintered body. This can occur, for example, when using the composite in an electronic cigarette due to repeated, often very short, heating cycles.
• the inertness or chemical resistance of the glass is also relevant, for example with regard to possible reactions or their avoidance of glass with electrically conductive material, in particular during the production process of a sintered body by thermal Treatment, for example during the sintering process.
• the dielectric material it is advantageous for the dielectric material to be inert to the auxiliary materials used in the production process, for example to sintering aids or pore-forming agents.
• the sintered body for example as an evaporator or a component in an evaporator, high chemical resistance or low reactivity of the glass to the substances to be evaporated, for example propylene glycol, glycerol, water and/or mixtures thereof and/or additives therein, is essential.
• Glasses with a high chemical resistance are preferably used, in particular glasses with a water resistance of class 3, particularly preferably glasses with a water resistance of class 1 or 2 (measured according to ISO 719). Furthermore, glasses with a low proportion of network modifiers and/or with a high proportion of network formers have proven to be advantageous in terms of their chemical resistance.
• the glass has a proportion of network formers of at least 50% by weight, preferably a proportion of network formers of at least 70% by weight.
• Network formers are understood to mean, in particular, glass components which contribute to the formation of oxygen bridges in the glass, for example SiO2, B2O3 and Al2O3.
• crystallizable glasses or partially crystallized glasses can also be used as dielectric materials if processing below the melting temperature of the first electrically conductive material used is possible. Therefore, when using ceramics as a dielectric material with usually high melting temperatures, especially if these are above those of the metals used, sinter-promoting substances, e.g. a glass, preferably a glass described above, are added so that a liquid phase is formed of this glass, a sintered body is sintered or can be sintered by means of liquid phase sintering. According to one embodiment of the invention, the sintered body has a mixture of at least two different dielectric materials.
• the dielectric components is a glass.
• the proportion of glass is at least 5% by volume of the dielectric material.
• this embodiment can be advantageous in particular in the case of sintered bodies with a total content of dielectric material of less than 25% by volume or even less than 10% by volume.
• Alternative dielectric components can be glass ceramics, ceramics or plastics, provided processing below the melting temperature of the electrically conductive material used is possible.
• a glass ceramic within the meaning of the present disclosure is understood to mean the conversion product of a green glass, i.e. a crystallizable glass, by heating to appropriate temperatures at which ceramization takes place.
• the glass ceramic has both a glassy phase and crystallites.
• the usually high sintering temperature of the ceramics must be taken into account. Therefore, when ceramics are used as a dielectric material, especially if the sintering temperature of the ceramics is above the melting point of the metals used, sinter-promoting substances are added, so that a liquid phase of precisely this sinter-promoting substance is formed and a sintered body is sintered by means of liquid-phase sintering or .is sinterable. Glasses in particular, and in particular the glasses described above, have proven to be particularly advantageous as sinter-promoting materials.
• the sintered body has a mixture of at least two different dielectric materials.
• the dielectric portion of the sintered body is a composite comprising the dielectric materials used in each case.
• it can be a composite of glass and ceramic.
• the composite is a compound material.
• the ceramic proportion is at least 50% by volume, preferably at least 75% by volume, most preferably at least 90% by volume. based on the intended volume fraction of the dielectric material.
• One embodiment of the invention even provides that the proportion of ceramic in the total dielectric material of the sintered body is at least 80% by volume, preferably at least 90% by volume and very particularly preferably at least 95% by volume. Sintered bodies whose dielectric material is completely or at least almost completely ceramic are also possible without departing from the invention.
• the then essentially melted glass portion also makes a positive contribution to the coatability of such a sintered body with a ceramic portion of the dielectric material.
• the grain size of the glass selected is not larger than that of the ceramic component.
• Bimodal or multimodal distributions with regard to the grain size distributions of the glass and ceramic components are also possible and allow the grain sizes of all materials to be adapted to one another on a case-by-case basis.
• the addition of a volume fraction of glass or the replacement of a volume fraction of the glass ceramic by a glass can be advantageous with regard to the sinterability of the workpiece.
• a further variant provides that further materials can be added to a mixture of electrically conductive and dielectric materials in order, for example, to influence the processing or production of a sintered body.
• This can be, for example, so-called sintering aids for modifying the sintering conditions, eg setting, especially lowering the processing temperature and/or materials that allow the properties of the sintered body to be modified or these can be adjusted.
• a sinter-promoting agent for example a glass, advantageously a glass as described above, sintering occurs with the formation of a liquid phase at temperatures at which the electrically conductive material does not melt.
• the thermal conductivity can be adjusted with regard to thermal insulation versus heating capacity, heating rate or heating of surrounding components, for example in the case of an e-cigarette, or also the surface properties of the sintered body with regard to absorption, desorption and/or subsequent flow of media to be evaporated will.
• the corresponding dielectric materials should in principle have adequate chemical resistance and resistance to water and the components of liquids to be evaporated, for example propylene glycol and glycerin, but also to metals.
• temperature-stable polymers such as polyetheretherketone (PEEK), polyetherketoneketone (PEKK) or polyamides (PA) are suitable as plastics.
• the evaporator has a mechanical electrical contact, an electrical contact through an electrically conductive connector or a materially bonded electrically conductive connection.
• the electrical contact is preferably made by a soldered connection.
• a variant of the invention provides that the sintered body additionally has an electrically conductive coating.
• An electrically conductive coating that extends over the entire surface of the sintered body has proven to be particularly advantageous.
• the surfaces of the sintered body, which are formed by the pore surfaces in the interior of the sintered body, are also provided with the electrically conductive coating. This is particularly advantageous since the coated sintered body also has a homogeneous electrical conductivity.
• ITO indium tin oxide
• AZO aluminum-doped zinc oxide
• TiN titanium nitride
• the coating may also include one of the materials in combination with other layer components.
• the electrical conductivity of the evaporator can be modified without changing the composition of the sintered body as a result of the additional coating, which, depending on the coating method, can only be applied partially or in sections to a sintered body.
• the electrical conductivity of the sintered body can be adjusted or set, in particular increased and/or homogenized, by the coating. This can, for example, for the production of evaporators with special high electrical conductivities can be used by coating sintered bodies with a relatively high content of electrically conductive material. This also makes it possible to set a required electrical conductivity based on predetermined basic conductivity of sintered bodies as composites of dielectric material and electrically conductive material by applying suitable layer thicknesses of the coating.
• any fluctuations in the conductivity of the sintered body or its basic conductivity can also be easily compensated for in this way.
• a composite with a locally adapted conductivity for example through a local limitation of the conductivity, can be realized. Zones with different electrical conductivities can thus be obtained by lateral structuring of the coating on the sintered body.
• the sintered body can be divided into local heating zones and/or storage zones. The targeted setting of transport zones and transport routes can also be carried out in this way.
• the surface properties, for example the surface activity or surface energy, of the sintered body or vaporizer can also be influenced by means of a coating, for example to change or adjust the absorption, transport and release or vaporization of a liquid.
• the inertness of the sintered body can also be further improved by being passivated, so to speak, by a coating, for example to protect against corrosion, degradation or aging due to reaction with air or with liquid to be evaporated, especially during operation.
• Thermomechanical properties of the sintered body can also be adjusted, improved or adjusted, such as mechanical strength and/or thermal conductivity.
• a coating can address one or more of these properties.
• the sintered body already has electrical conductivity due to the content of the first and second electrically conductive material, only relatively small layer thicknesses are required compared to a coating of sintered bodies that do not contain any electrically conductive material.
• the amount of coating material required for the sintered body according to its basic electrical conductivity can be reduced, for example by up to 90%, in order to achieve comparable electrical conductivity
• the average layer thickness of the electrically conductive coating is preferably less than 10 ⁇ m or even less than 1 ⁇ m, down to a few nanometers or a few 10 nm.
• the necessary or possible layer thickness is essentially dependent on the type and production method of the coating.
• the coating is made with ITO or TiN.
• ITO coatings have an electrical conductivity in the range from a few 10 4 S/m to a few 10 6 S/m and a TiN coating from a few S/m to a few 10 -3 S/m. Due to the low layer thicknesses of the coating, on the one hand only a small amount of coating material is required. At the same time, the risk of smaller pores being closed by the coating and thus no longer being available as evaporation volume is significantly reduced.
• the necessary or sufficient layer thickness depends on the electrical conductivity of the layer material.
• the layer thickness to be or can be achieved also depends on the coating methods, for example by means of liquid or gas phase deposition, or galvanically. Such methods are used to apply layers, preferably densely and homogeneously, to a sintered body in order to set the required electrical conductivity and the heating behavior required during operation, for example uniformly or locally in the volume of the sintered body.
• the evaporators according to the invention are particularly suitable for use as a component in an electronic cigarette, a medical inhaler, a fragrance dispenser or a room humidifier.
• the evaporator can also be used for the indirect evaporation of liquids or solids, for example waxes or resins.
• a further development of the invention provides that air or gas flows through the sintered body and heats it.
• One possible use of this development is in medical inhalers. It can also be used as a radiant heater.
• Another aspect of the invention is the provision of a method for manufacturing an evaporator.
• the method according to the invention comprises at least the following method steps a) to e): a) providing a first electrically conductive material, a second electrically conductive material and a dielectric material in powder form, b) mixing the powder provided in step a) with a pore former, c) production of a green body from the powder mixture provided in step b) by pressing, casting or extruding, d) heating of the green body provided in step e) to a temperature Tburnout and e) sintering of the green body produced in step c) at a sintering temperature Tsinter.
• steps c) to e) can also take place in parallel or simultaneously or sequentially in a unit, e.g. an extruder or in injection molding, optionally also comprising step b).
• a unit e.g. an extruder or in injection molding, optionally also comprising step b.
• such methods can also be applied to the other dielectric materials, but they are often complex and less easy to control.
• the term sintering is also understood here as a process step leading to the solidification of such a body.
• the proportion of the total electrically conductive material in the total materials provided in step a) is a maximum of 95% by volume. According to a preferred embodiment, the proportion of electrically conductive material is in the range from 30 to 90% by volume, preferably in the range from 40 to 80% by volume. Glasses, crystallizable glasses or glass ceramics or ceramics or plastics or mixtures thereof in powder form are provided as the dielectric material in step a). According to one embodiment of the invention, the proportion of dielectric material in the materials provided in step a) is 5 to 70% by volume, preferably 10 to 50% by volume. In this case, the dielectric material preferably has a lower softening or melting point than the electrically conductive material.
• the sintered body contains glass, crystallizable or at least partially crystallized glass as the dielectric material, the Trü joining temperature of which is below the melting point Tsmp of the first electrically conductive material, preferably below the melting temperature of all electrically conductive materials in the sintered body.
• the Trüge joining temperature is understood to mean the temperature range in which the viscosity of the glass is in the range between 10 4 and 10 8 dPas.
• the joining temperature Trüge is preferably at least 10° C., preferably at least 50° C., below the melting temperature of the first electrically conductive material and/or the second electrically conductive material.
• the proportion of dielectric material is in the range from 5 to 70% by volume, preferably in the range from 10 to 60% by volume and particularly preferably in the range from 15 to 40% by volume.
• glass, glass ceramics, ceramics or mixtures thereof or plastics in powder form are provided as the dielectric material.
• step b) at least one pore-forming agent is added to the powder provided in step a), and a homogeneous mixture is produced.
• the proportion of pore-forming agent in the mixture provided in step b) is preferably 40 to 80% by volume, preferably 50 to 75% by volume.
• a green body is produced from the mixture provided in step b). This can be done, for example, by pressing or extrusion processes or by a casting process.
• a slip is produced from the mixture provided in step b) and subsequently cast.
• the pore former has a decomposition temperature T decomposition and/or an evaporation temperature T vaporization which is below the sintering temperature T sinter in step d) and/or below the joining temperature T rt of the dielectric material.
• T decomposition and/or an evaporation temperature T vaporization which is at least 10° C., preferably at least 50° C. and particularly preferably at least 100° C. below the sintering temperature T sinter and/or at least 10° C., preferably at least 50°C lower than the T joining temperature of the dielectric material.
• an organic material for example based on polysaccharides, is used as the pore former.
• the use of inorganic salts is also possible, provided their decomposition temperature and/or evaporation temperature is below the joining temperature of the dielectric glass.
• the green body is sintered.
• the sintering temperature corresponds at least to the softening point of the dielectric material, so that the dielectric material forms a coherent matrix as a result of the sintering process.
• the sintering temperature is lower than the melting temperature of the electrically conductive material, so that the particle structure of the electrically conductive material is at least largely retained.
• step e) the sintering can take place at a temperature which enables a sintered body with high mechanical strength. Since the melting point Tschmeiz of the first electrically conductive material is both above the burnout temperature Tburnout in step d) and above the joining temperature Trü of the dielectric material, the green body or the workpiece has high dimensional stability throughout the entire manufacturing process, even after the pore-forming agent has been removed.
• the melting point Tschmeiz of the first electrically conductive material is above the sintering temperature Tsinter in step e).
• the first electrically conductive material therefore has the function of a shape stabilizer during the production process and thus enables the production of dimensionally stable, porous sintered bodies.
• the burnout in step c) means that a washing process after the sintering process to remove the pore-forming agent can be dispensed with.
• the comparatively high melting point of the first electrically conductive material also ensures that the dimensional stability of the electrically conductive particles in the sintered body and thus also the electrical conductivity of the sintered body is not impaired by the sintering process.
• the melting point of the second electrically conductive material is therefore preferably also above the sintering temperature Tsinter in step e).
• the sintered bodies produced using the method according to the invention have a high mechanical stability, so that post-processing of the sintered body, for example for surface treatment or shaping, is possible.
• the sintered body is ground, drilled, polished, milled and/or turned in a step f) following step e).
• step g) of the sintered body which follows steps e) and/or f). Contacting by applying an electrically conductive paste has proven to be particularly advantageous.
• the dielectric material provided in step a) has a thermal stability to temperatures of at least 300° C. or even at least 400 °C.
• a glass is provided as the dielectric material.
• the glass provided in step a) has a transformation temperature T g in the range of more than 300°C, in particular in the range from 500 to 800°C.
• T g transformation temperature
• step d) sintering can be carried out at sintering temperatures which ensure the dimensional stability of the electrically conductive particles.
• the glass transition temperature is well above the operating temperature of the evaporator.
• An embodiment of the invention provides that in step a) a glass with an alkali content ⁇ 15% by weight or even ⁇ 6% by weight or even an alkali-free glass is provided.
• Corresponding glasses show a high mechanical strength, good chemical and thermal resistance and do not react at all or hardly at all with the electrically conductive materials even at high temperatures.
• a borosilicate glass is preferably provided as the dielectric material in step a).
• the electrically conductive particles provided in step a) have an average particle size (dso) in the range from 0.1 to 1000 ⁇ m, preferably in the range from 1 to 50 ⁇ m.
• the particles of the dielectric material provided in step a) have an average particle size (dso) in the range from 1 to 50 ⁇ m.
• the mean particle size (dso) of the dielectric material is less than 30 ⁇ m.
• Corresponding particle sizes of the dielectric material lead to sintered bodies in which the maximum distance between adjacent electrically conductive particles is less than 30 ⁇ m or even less than 10 ⁇ m. This ensures current conduction in the corresponding sintered body even with low levels of electrically conductive material.
• a particularly homogeneous mixture can also be obtained by matching the grain sizes of the powders of dielectric and electrically conductive material so that segregation or demixing of the powders or agglomeration of a powder due to widely differing grain sizes is avoided.
• a homogeneous mixture in step b) in turn has an advantageous effect on the homogeneity of the composite and thus also on the homogeneity of the electrical conductivity. Furthermore, grain sizes of the powder or of a powder that are too small should be avoided as far as possible, even if these are matched to one another in terms of grain sizes, in order to minimize unnecessary dust generation during their processing.
• the first electrically conductive materials used in step a) are materials with an electrical conductivity of at most 30 S/pm, preferably titanium, chromium, steel, manganese, silicon or corresponding alloys. Combinations of the above materials are also possible.
• the particles of the electrically conductive material provided in step a), in particular of the second electrically conductive material have a platelet-shaped geometry, preferably a platelet-shaped geometry with a maximum thickness d max and a maximum length Imax, where d max applies ⁇ Imax up.
• d max applies ⁇ Imax up.
• Corresponding geometries are particularly suitable for use in sintered bodies with a small proportion of electrically conductive materials, ie in sintered bodies in which a current flow is realized to a large extent by electron tunnel currents.
• platelet-shaped particles whose maximum length is at least twice the maximum width have proven to be advantageous.
• the ratio of the maximum thickness to the maximum length is 1:2 to 1:7.
• step h) after step e) and/or step f) an electrically conductive coating, in particular a coating, particularly preferably an oxidic ITO or AZO or nitridic, in particular TiN-containing, or metallic Coating applied to the sintered body.
• a coating particularly preferably an oxidic ITO or AZO or nitridic, in particular TiN-containing, or metallic Coating applied to the sintered body.
• the coating is applied to the surface of the sintered body by means of a sol-gel process or a CVD process. It is also conceivable, especially since the sintered body already has at least one basic conductivity, to also consider galvanically applicable or processable layer materials, for example gold, silver or copper and/or combinations thereof, for example as a layer sequence.
• FIG. 1 shows a schematic representation of a conventional evaporator
• FIG. 2 shows a schematic representation of a sintered body with electrical contacting on the lateral surfaces of the sintered body
• FIG. 3 shows a schematic representation of an embodiment of an evaporator according to the invention
• FIG. 4 shows a schematic representation of an embodiment of a sintered body according to the invention in cross section
• FIG. 5 shows an enlarged detail of the cross section shown in FIG. 4 and
• FIG. 7 shows a schematic representation of a further exemplary embodiment with an additional electrically conductive coating on the sintered body.
• a heating coil 3 is positioned in the upper portion of the sintered body 2 so that the corresponding portion 2a of the sintered body 2 is heated by heat radiation. The heating coil 3 is therefore brought very close to the lateral surfaces of the sintered body 2 and should not touch the lateral surfaces if possible. In practice, however, direct contact between the heating wire and the jacket surface is often unavoidable.
• the liquid 1 evaporates in the heating area 2a. This is represented by the arrows 5.
• FIG. The evaporation rate depends on the temperature and the ambient pressure. The higher the temperature and the lower the pressure, the faster the evaporation of the liquid in the heating area 2a.
• the liquid 1 evaporates only locally on the lateral surfaces of the heating area 2a of the sintered body, this local area must be heated with relatively high heating power in order to achieve rapid evaporation within 1 to 2 seconds. Therefore high temperatures of more than 200°C have to be applied. Height
• heating power particularly in a locally narrowly limited area, can lead to local overheating and thus possibly to decomposition of the liquid 1 to be evaporated and the material of the liquid reservoir or wick.
• a unit for example a voltage, power and/or temperature adjustment, control or regulation unit (not shown here) can be installed, which, however, is at the expense of battery life and limits the maximum amount of evaporation.
• Disadvantages of the evaporator shown in FIG. 1 and known from the prior art are the local heating method and the associated ineffective heat transport, the complex and expensive control unit and the risk of overheating and decomposition of the liquid to be evaporated and the storage/wick material.
• FIG. 2 shows an evaporator unit known from the prior art, in which the heating element 30 is arranged directly on the sintered body 20 .
• the heating element 30 is firmly connected to the sintered body 20 .
• Such a connection can be achieved in particular by the heating element 30 being in the form of a layer resistor.
• an electrically conductive coating structured like a ladder is applied to the sintered body 20 in the manner of a layer resistor.
• a coating applied directly to the sintered body 20 as a heating element 30 is advantageous, among other things, in order to achieve good thermal contact, which enables rapid heating.
• the evaporator unit shown in FIG. 2 also has only a locally limited evaporation surface, so that there is also a risk of the surface overheating here.
• FIG 3 schematically shows the structure of an evaporator with a sintered body 6 according to the invention.
• the porous sintered body 2 in FIGS. 1 and 2 it is immersed in the liquid 1 to be evaporated.
• the liquid to be evaporated is transported into the entire volume of the sintered body 6 by capillary forces (represented by the arrows 4).
• capillary forces represented by the arrows 4
• the sintered body 6 is large surface heated.
• FIG Volume area between the electrical contacts of the sintered body 6 formed A capillary transport to the lateral surfaces or heated surfaces or elements of the sintered body 6 is therefore not necessary.
• the evaporation in the volume proceeds much more efficiently than by means of a heating coil in a locally limited heating area, the evaporation can take place at much lower temperatures and with a lower heating power.
• a lower electrical power requirement is advantageous insofar as this increases the usage time per battery charge or smaller rechargeable batteries or batteries can be installed.
• the sintered body 10 has a composite material
• the composite material 11 has an electrical conductivity in the range from 0.1 to 10 5 S/m. If a voltage is applied to the sintered body 10, current flows through the entire volume of the sintered body 10 and is thus heated. A section of the sintered body 10 is shown enlarged in FIG. 5 .
• the composite material 11 contains as a main component the first electrically conductive material 13a and between or on the first electrically conductive material 13a, preferably homogeneously, electrically conductive particles of the second electrically conductive material 13b. In this case, the electrically conductive particles 13a and 13b are held together by the dielectric material 13c. In the embodiment shown in FIG. 5, the electrically conductive particles 13a and 13b have a platelet-shaped geometry.
• the sintered body 10 can be heated by a current flow. Accordingly, a heating device in the form of a power source can be provided for this purpose. In general, however, inductive heating is also possible without restriction to specific exemplary embodiments. Accordingly, in one embodiment, an inductive heating device is provided for this purpose, which is set up to generate an induction field. For inductive heating, the sintered body 10 is designed to absorb energy from the induction field and heat up as a result. In general, inductive heating is particularly easy to implement when the sintered body comprises an electrically conductive material that is ferromagnetic. For this purpose, a ferromagnetic high-grade steel is preferably provided as a first conductive material. Electrically conductive materials selected in this way also open up the possibility of carrying out the sintering process by means of inductive heating can be. Heating in the sintering process using microwaves or capacitive technology is also conceivable.
• a corresponding sintered body 6 as example 1 with an electrical conductivity of approx. 1 S/m and a porosity of approx -150pm) and 10 Vol% silver (d50 of 1-1 Opm) are obtained in step a).
• a pore-forming agent preferably an organic pore-forming agent, is added, followed by the production of a green body. This is subsequently heated by thermal treatment in a regular furnace atmosphere to a temperature which approximately corresponds to the softening point of the glass used and sintered to form the sintered body 6 .
• the sintered body has a porosity of 55% by volume.
• the composite material contains 23% by volume borosilicate glass (FIOLAX®) as the dielectric material, 60% by volume stainless steel 1.4404 as the first electrically conductive material and 17% by volume silver as the second electrically conductive material.
• the particles of the electrically conductive materials have an average grain size d50 in the range from 20 to 60 ⁇ m.
• the electrical conductivity of the sintered body is 2000 S/m.
• the electrical conductivity is determined by measuring the resistance, e.g ), arranged or attached manually, mechanically.
• the dielectric portion of the sintered body contains both glass and ceramic.
• the ceramic portion in the dielectric material is 85% by volume and the portion of glass in the dielectric material is 15% by volume. Electrical conductivities in the range from 1 to 10 S/m can also be obtained here.
• a glass-ceramic proportion can also be formed by presenting a crystallizable glass in the green body, which during sintering with the appropriate Temperature for a ceramization of this glass ceramized and then exists as a glass ceramic. Below such a temperature, a crystallizable glass remains in the glassy state.
• FIG. 6 shows an SEM photograph of a cross section through a sintered body according to the invention as a further exemplary embodiment.
• stainless steel was used as the framework-forming metal.
• the stainless steel particles are essentially round, in particular oval to spherical. Some of these round particles 23 can be seen as round, light gray elements in the SEM image. In the REM image, the glass shows a similar contrast to the stainless steel and can therefore hardly be differentiated in the image.
• the sintered particles 24 of the second electrically conductive material, here silver particles appear as very light areas. The pores can be seen in the image as black areas.
• the mean grain sizes of the first and the second conductive material can be different.
• the average grain size of the second electrically conductive material is preferably smaller than the average grain size of the first electrically conductive material (stainless steel particles in the example).
• FIG. 7 shows the structure of a coated sintered body 6 with open porosity using a schematic cross section through a further exemplary embodiment.
• the coated sintered body 1 has a porous composite material 11 made of dielectric material, first electrically conductive material and second electrically conductive material with open pores 12a, 12b. A portion of the open pores 12b forms the lateral surfaces of the sintered body with their pore surface, while another portion of the pores 12a form the interior of the sintered body. All surfaces of the sintered body have an electrically conductive coating 9a, for example in the form of an ITO coating. If a voltage is applied to the sintered body, the current flows through the entire volume of the sintered body.
• a correspondingly coated sintered body 6 as example 8 can be obtained here by first producing a sintered body with a relatively low electrical conductivity in the range from 0.1 to 100 S/m. In order to obtain the desired, higher electrical conductivity, for example in the range from 100 to 600 S/m, the sintered body is subsequently provided with an electrically conductive coating, for example a coating containing ITO or AZO. Due to the basic electrical conductivity of the sintered body, 50% less coating material is required here (compared to a sintered body without electrically conductive material). Furthermore, the coating process is also less time consuming. In this way, the process time required for the coating process can be reduced by up to 70%.

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• 2020
  • 2020-11-19 DE DE102020130560.5A patent/DE102020130560A1/de active Pending
• 2021
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