METHOD FOR INFLUENCING SOOT DEPOSITS ON SENSORS

Abstract

A method is described for controlling the soot deposition on sensors. A sensor element is provided, which includes a first electrode and a second electrode. Different measuring voltages U1 and U2 can be applied to the sensor element. During a first time period t1, the sensor element is operated at a higher voltage U1 until a triggering threshold AP of the sensor element is exceeded, while it is operated at a voltage U2, which is different from higher voltage U1, U2 being lower than voltage U1, during a second time period t2.

Description

BACKGROUND INFORMATION

Particle emission requirements for internal combustion engines, in particular compression-ignition internal combustion engines, are becoming increasingly stricter. As the introduction of further standards is being planned, the soot emissions downstream from the internal combustion engine, i.e., downstream from a diesel particle filter, must be monitored during the driving operation. In addition, prediction of the diesel particle filter load is to be provided for determining the soot input and optimizing the regeneration strategy or monitoring regeneration in order to ensure a high degree of system reliability for the diesel particle filter system.

Currently, resistive particle sensors for conductive particles are known in which two or more metallic electrodes are provided, the particles, in particular soot particles, which deposit on these sensors short-circuiting the electrodes meshing in a comb-like manner and thus modifying the impedance of the electrode structure. With increasing particle concentration on the sensor surface, a decreasing resistance, i.e., an increasing current at a constant applied voltage, is thus measurable between the electrodes. Normally a threshold value, a triggering threshold, is defined, and the time of accumulation is assumed as a measure for the deposited soot particle mass. For regenerating the sensor element after the deposition of soot thereon, the sensor element must usually be burned free with the aid of an integrated heating element. The sensor is unable to detect the amount of soot during the phase of being burned free.

German Published Patent Application No. 101 49 333 describes a sensor device for measuring the moisture of gases. A resistance measuring structure cooperating with a soot layer is provided on a substrate; furthermore, a temperature measuring device is provided. The temperature measuring device includes a resistance thermometer and means for measuring a frequency-dependent AC resistance. Furthermore, a heating device is associated with the sensor device. The particle size of the soot particles contained in the soot layer is between 20 nm and 150 mm.

PCT International Published Patent Application No. 03/006976 describes a sensor for detecting particles and a method for checking its function. The sensor is used for detecting particles in a gas flow, in particular for detecting soot particles in an exhaust gas flow. At least two measuring electrodes are situated on a substrate made of insulating material. The measuring electrodes are at least partially covered by a catching sleeve. A heating element is also associated with the sensor. The sensor's particle detecting function, in particular its soot detecting function, is monitored by assigning a capacitor to the measuring electrodes of the sensor and ascertaining the capacitance of this capacitor. When the capacitance of the capacitor differs from the setpoint value, an error message is generated. To burn off the deposited soot particles, the sensor is heated, and afterwards the resistance of the insulation between the measuring electrodes of the sensor is measured. The resistance of the insulation measured after heating the sensor is used as the correcting quantity for operating the sensor.

SUMMARY OF THE INVENTION

The approach according to the present invention makes it possible to influence the deposition rate of particles on the sensor via electronic measures, i.e., variable measures which may be taken during the operation of the sensor. Since the soot concentrations upstream and downstream from the diesel particle filter may differ considerably depending on the technology used, however, cost considerations make identical sensors desirable. The method proposed according to the present invention allows the particular sensors used to be adjusted to the area of use, i.e., whether they are situated upstream or downstream from the diesel particle filter. The method proposed according to the present invention allows the sensitivity range of the sensors to be set to the optimum concentration range, the sensor trigger time to be minimized, and the subsequent measuring time to be maximized. This is achieved by applying different voltages to the sensor. If a higher voltage is selected for operating the sensor, the soot layer builds up more rapidly than for a sensor operating with a lower voltage. In order to have the triggering threshold exceeded as fast as possible and to obtain a rapidly analyzable, i.e., measurable, signal, the sensor is operated at a first, higher voltage U₁. Subsequently the system switches over to a second voltage U₂ in order to achieve a longer measuring time. During the extended measuring time, the variation of the signal is continuously monitored, and information concerning the occurrence of soot surges may be obtained from the signal gradient. Following the method proposed according to the present invention, first the accumulation time until the triggering threshold is reached, characterized by considerable measuring uncertainties, it is implemented by operating the sensor element using a high voltage, and subsequently the sensor element is operated at a reduced voltage in order to extend the measuring time. Consequently, the measuring uncertainties occurring during the accumulation time have no significant effect.

By taking variable measures, dependent on the location of the sensor, during the operation of the sensor, the deposition rate of soot particles on the sensor and thus the sensitivity range of the sensor may be electronically adjusted for a predefined, fixed sensor design and a predefined, fixed construction regarding installation and application, and thus it may be optimally adapted to the location of the sensor in question. The same sensor may be directly electronically adjusted for different applications, for example, for high soot concentrations or for an on-board diagnosis. The sensor situated in front of the diesel particle filter system is used for detecting the soot mass deposited in the diesel particle filter.

The sensor situated upstream from the diesel particle filter system is used for enhancing the system's reliability and for ensuring operation of the diesel particle filter under optimum conditions. Since those factors depend, to a considerable extent, on the soot mass deposited in the diesel particle filter, accurate measurement of the particle concentration upstream from the diesel particle filter, in particular ascertaining a high particle concentration upstream from the diesel particle filter, is very important.

A sensor installed downstream from the diesel particle filter offers the option of performing on-board diagnosis and is also used for ensuring proper operation of the exhaust gas treatment system.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a top view onto a sensor having an electrode structure.

FIG. 2 shows a side view onto the electrode structure applied onto a substrate and covered by a soot particle layer.

FIG. 3 shows the electric field formed on the electrode structure according to FIGS. 1 and 2.

FIG. 4 shows a sensor signal which is established for a first, higher voltage U₁, which attains a triggering threshold after a time period t₁.

FIG. 5 shows a sensor signal which is established over time for a second, lower voltage U₂.

FIG. 6 shows a switchover strategy for the sensor element.

DETAILED DESCRIPTION

Sensor element 1 includes a substrate 7 used as a support, which may be made of an aluminum oxide ceramic, for example. A resistance measuring structure, having a first comb electrode 3 and a second comb electrode 4, is applied to substrate 7 used as support. The resistance measuring structure including first comb electrode 3 and second comb electrode 4 is used for measuring the electric resistance of a particle layer 5—see the illustration of FIG. 2, which covers first comb electrode 3 and second comb electrode 4 of sensor element 1. When a voltage is applied to voltage terminals 2 of sensor element 1, an inhomogeneous electric field 6 is formed between meshing comb electrodes 3, 4, see the illustration of FIG. 3, where the inhomogeneous electric field 6 is represented by field lines 9.

The particles, in particular soot particles, depositing on sensor element 1 may be considered electric dipoles in the electric field. Inhomogeneous electric field 6 exerts a resulting force on the electric dipole, i.e., in the present case on the soot particles, which are attracted to electrodes 3, 4 and thus deposit thereon as particle layer 5. If the soot particles are charged, they are subject to the effect of an additional force toward electrodes 3, 4 according to the equation {right arrow over (F)}=q·{right arrow over (E)}, and deposit on sensor element 1 (F=force; q=charge; E=intensity of electric field).

If the flow containing the particles passes by sensor element 1 illustrated in FIG. 1, an electric force is exerted on the particles contained in the flow, which is a function of the applied voltage U₁, for example, 21 V or U₂=10 V. By varying the voltage applied to sensor element 1 at voltage terminals 2, an additional, controllable variable may be imposed on the diffusion-controlled process of soot deposition to influence the mass flow of soot particles onto sensor surface 1.1 of sensor element 1.

This means that, if a higher voltage U₁=21 V is applied, the soot layer builds up more rapidly due to the stronger inhomogeneous electric field 6 than when a lower voltage U₂, for example 10 V, is applied, creating a weaker inhomogeneous electric field 6.

FIG. 2 shows the side view of the sensor element according to FIG. 1.

FIG. 2 shows that a soot particle layer 5 has built up above the comb-like meshing electrodes 3 and 4. This layer covers electrodes 3, 4, and 8. If sensor element 1 is operated at an increased voltage U₁, for example, 21 V, particle layer 5 builds up more rapidly on the top of comb-like meshed electrodes 3 and 4, and its thickness increases faster compared to operating sensor element 1 at a lower voltage U₂.

FIG. 3 schematically shows the inhomogeneous electric field formed, represented by its field lines 9 and equipotential lines 10.

Meshing first comb electrode 3 and second comb electrode 4 are connected to a voltage source, for example, to the vehicle's electric system. Depending on the voltage, either voltage U₂ of 10 V, for example, or a higher voltage U₁ of 21 V, inhomogeneous electric field 6 illustrated in FIG. 3, represented by field line 9, is formed at meshing first comb electrodes 3 and second comb electrodes 4 above the free spaces therebetween.

FIGS. 4 and 5 show the triggering of sensor element 1 in operation using a first voltage U₁ of 21 V, for example, and in operation using a second voltage U₂ of 10 V, for example. In the embodiments of FIGS. 4 and 5 no switchover between the two voltages U₁ and U₂ has occurred.

FIG. 4 shows that triggering threshold AP of approximately 1 μA is exceeded by sensor signal 10 after a time period t₁. Due to the application of increased voltage U₁ of 21 V, for example, sensor signal 10 rapidly increases and exceeds triggering threshold AP after a relatively short time period t₁. Triggering threshold AP may be set arbitrarily, also at 2 μA or 3 μA. Due to the increased voltage U₁, sensor signal 10 rapidly and steeply increases, which is shown by gradient 16 and by curve 13 of the sensor signal. After reaching measurable currents, i.e., after exceeding triggering threshold AP, direct information on the amount of soot deposited per unit time on surface 1.1 of sensor element 1 may be obtained from gradient 16 and its variation over time axis 15. The operation of sensor element 1 after triggering threshold AP has been exceeded is highly desirable, since errors and cross-influences are visible after triggering threshold AP has been exceeded. After reaching triggering threshold AP after time period t₁, the operation of sensor element 1 at increased voltage U₁ of 21 V, for example, is switched over to an operation at a lower voltage U₂ of 10 V, for example, as depicted in FIG. 6.

Time period t₁, during which sensor element 1 is operated at an increased voltage U₁, is used for rapidly reaching triggering threshold AP for sensor signal 10, since sensor element 1 delivers no data during time period t₁.

The switchover strategy between increased voltage U₁ of 21 V, for example, and lower voltage U₂ of 10 V, for example, is given by the fact that time period t₁ until triggering threshold AP is reached is shortened due to the application of a high voltage U₁ and the subsequent time period t₂, i.e., the actual measuring time, characterized by visible changes in the signal, is prolonged due to the application of low voltage U₂ such as 10 V, for example. This results in a lower particle deposition rate on surface 1.1 of sensor element 1 due to the weaker inhomogeneous electric field 6, due to which a longer time goes by until saturation is attained and sensor element 1 must therefore be regenerated.

FIG. 5 shows that, during time period t₂, i.e., the actual measuring time, sensor signal 10 has a flat signal gradient 17; therefore, it does not rise as rapidly as sensor signal 10 according to FIG. 5, when sensor element 1 is operated at a first, increased, voltage U₁ of 21 V, for example.

The operation of sensor element 1 according to FIGS. 1 and 2 at an increased voltage U₁ of 21 V, for example, during time period t₁ and, after switching over, at a voltage U₂ of 10 V during second time period t₂ was described above. In principle, any voltage generatable in the vehicle's electric system may be used, and the choice of the particular voltage level may be adapted to the particular application. The voltages are preferably between 0 V and 42 V; however, higher voltages are also conceivable. In general, higher voltages are to be preferred up to the point where triggering threshold AP is exceeded, and the voltage is to be switched over to a lower value after triggering threshold AP has been exceeded.

Soot deposition, i.e., buildup of particle layer 5, is influenced by inhomogeneous electric field 6 generating field gradients above the surface of sensor element 1. In addition to the above-described variation of voltages U₁, U₂ applied to sensor element 1, the structure of first comb electrode 3 and second comb electrode 4 may also be modified. In general, small distances between first comb electrode 3 and second comb electrode 4 result in high field gradients. In addition to the embodiment variants of the electrodes as comb electrodes 3, 4 depicted in FIGS. 1 and 2, they may also have a different design, for example, as linearly shaped electrodes or as electrodes in the shape of a network or a grid, which are contacted underneath a network electrode or grid electrode.

The selection of a suitable electrode layout and the type of electrode surface may also contribute to a local increase in the field intensity. The selection of the electrode layout and the type of electrode surface may be optimally adapted, at the time the sensor is manufactured, to the later application.

FIG. 6 shows that, after time period t₁, within which sensor element 1 may be operated at an increased voltage U₁ of approximately 21 V, the operating voltage of sensor element 1 is reduced to a lower voltage U₂ of 10 V, for example. Sensor element 1 may thus be operated in an optimum operating state, which makes a substantial extension of the measuring time possible after triggering threshold AP has been exceeded. A comparison of time periods t₁ and t₂ according to FIG. 6 shows that the triggering time may be shortened by applying a high voltage U₁ and the measuring time (time period t₂) may be extended by applying a low voltage U₂.

LIST OF REFERENCE NUMERALS

• 1 sensor element
• 1.1 sensor surface
• 2 voltage terminals
• 3 first comb electrode
• 4 second comb electrode
• 5 particle layer (soot layer)
• 6 electric field
• 7 substrate
• 8 electrodes
• 9 field line
• 10 sensor signal [μA]
• c soot concentration [mg/m³]
• AP triggering threshold
• 13 curve of sensor signal 10 at U₁=21 V
• 14 curve of sensor signal 10 at U₂=10 V
• 15 time axis
• 16 signal gradient for U₁
• 17 signal gradient for U₂
• 18 point in time of signal increase
• 19 point in time of switchover U₁ first voltage
• 20 point in time of switchover U₂ second voltage
• t₁ time period of U₁
• t₂ time period of U₂

Claims

1.-8. (canceled)

9. A method for controlling a deposition of particles on a sensor element which has a first electrode and a further electrode, comprising: applying to the sensor element a first voltage U1 and a second voltage U2 at voltage terminals;operating the sensor element at an increased voltage U1 during a first time period t1; andafter a triggering threshold AP of the sensor element has been exceeded, operating the sensor element at a lower voltage U2 that is less than the increased voltage U1.

10. The method as recited in claim 9, wherein the time period t1 until the triggering threshold AP of the sensor element is exceeded is minimized by the selection of the voltage level of the first voltage U1.

11. The method as recited in claim 9, wherein the sensor element is operated at a lower voltage U2 during the second time period t2 in order to extend the measuring time.

12. The method as recited in claim 9, wherein the voltage U1 which is applied to the voltage terminals of the sensor element is between 10 V and 42 V.

13. The method as recited in claim 9, wherein the second voltage U2 which is applied to the voltage terminals of the sensor element is between 0 V and 10 V.

14. The method as recited in claim 9, wherein the ratio between the first time period t1 and second time period t2 is determined by the voltage difference between the first measuring voltage U1 and the second measuring voltage U2.

15. The method as recited in claim 9, wherein the voltages U1, U2 are group voltages.

16. The method as recited in claim 9, wherein voltages U1, U2 are applied to an electrode structure in such a way that an inhomogeneous electric field of maximum possible intensity is formed on one surface of the sensor element.