This invention generally relates to gas sensors, and more specifically, to gas sensors for detecting one or more gases in a sample of an environment or flow stream.
There is growing interest in monitoring and controlling air quality in both indoor and outdoor environments, including carbon dioxide concentration. There are several types of gas sensors that can monitor carbon dioxide (CO2) or other gases.
The present invention is directed toward a gas sensor, and more specifically, a gas sensor for detecting carbon dioxide and other gases in a gas sample, and in some cases humidity. The gas sensor includes a sensor for sensing a desired gas and a heater for heating the sensor. During operation, a controller provides power to the heater to heat the sensor to an operating temperature, which is above ambient temperature. In some embodiments, the sensor and heater are thermally isolated from some or all of the remainder of the sensor, such as the sensor substrate. This may help reduce the amount of power that is required to heat the heater and sensor to the operating temperature. This may make it more energy efficient to heat the sensor to an operating temperature at spaced time intervals. The gas sensor of the present invention may be ideally suited for battery powered and/or wireless applications.
Methods of sensing a gas are also disclosed. One illustrative method includes the steps of providing a solid electrolyte layer including lanthanum oxide, contacting the solid electrolyte layer with a gas sample, heating the solid electrolyte layer from 100 degrees Celsius to an operating temperature with a first amount of energy, and determining a concentration of carbon dioxide in the gas sample based on first amount of energy.
Another illustrative method includes the steps of providing a solid electrolyte layer including lanthanum oxide, contacting the solid electrolyte layer with a gas sample, heating the solid electrolyte layer to about 100 degrees Celsius with a water desorbing amount of energy, heating the solid electrolyte layer from about 100 degrees Celsius to a carbon dioxide desorbing temperature with a carbon dioxide desorbing amount of energy, and then determining a humidity level in the gas sample based on the water desorbing amount of energy and determining a concentration of carbon dioxide in the gas sample based on the carbon dioxide amount of energy.
The present disclosure is directed toward a gas sensor, and more specifically, a gas sensor for detecting carbon dioxide and other gases, and in some cases, humidity, in a gas sample.
In the illustrative embodiment, the heater layer 16 is made from a resistive material that generates heat when a current is passed therethrough. To increase the heat the can be delivered to the sensor 12, as well as the uniformity of the heat, the heater layer 16 may be configured to meander back and fourth along the area of the sensor 12, as better shown in
In the illustrative embodiment, the solid electrolyte layer 22 may be made from a suitable solid electrolyte material. For example, if the gas to be detected is CO2 and/or humidity, the solid electrolyte may be lanthanum oxide, La2O3 (CAS No.: 1312-81-8) available from Sigma Aldrich Chemical Company, Milwaukee Wis. The solid electrolyte layer 22 can be a layer of La2O3 or a layer of material (such as silica, for example) doped with La2O3, as desired.
Lanthanum oxide is a useful solid electrolyte since it absorbs water and carbon dioxide at ambient temperature and desorbs water as it is heated to 100 degrees Celsius and then desorbs carbon dioxide as it is heated above 100 degrees Celsius. As such, a single heating cycle of the gas sensor can provide accurate concentration measurements of both water (e.g., humidity) and carbon dioxide in a gas sample. With the physical properties (i.e., specific absorption capacity, volume, and mass) of lanthanum oxide and the amount of heat applied to lanthanum oxide, a concentration of both water and carbon dioxide can be determined based on the change in thermal mass with differential thermal analysis. One illustrative differential thermal analysis sensor is described in U.S. Pat. No. 6,238,085, and is incorporated by reference herein. In one illustrative embodiment, the gas sensor has an ultimate carbon dioxide sensitivity of 5 ppm.
Control electronics 28 may be provided on or in the substrate 14, or elsewhere, as desired. Control electronics 28 can be coupled to the heater layer 16 via traces 30a and 32b, and the lower electrode layer 20 and the upper electrode layer 24 via traces 32a and 32b, as best shown in
Referring to
Above 100 degrees Celsius, carbon dioxide begins to desorb from the RH/CO2 sensor, causing the CO2 sensor to heat up at a slower rate than the control sensor. At time equal to TC2, the control sensor reaches a temperature of 500 degrees Celsius. At time equal to TCO2, the CO2 sensor reaches a temperature of 500 degrees Celsius. At a temperature of about 500 degrees Celsius substantially all of the carbon dioxide has desorbed from the sensor. The difference in the areas under each curve (above 100 degrees Celsius) is the amount of energy required to desorb the carbon dioxide from the sensor. Knowing the physical properties of the solid electrolyte and carbon dioxide, a total amount of carbon dioxide desorbed from the sensor can be determined. A concentration of carbon dioxide in the gas sample can then be determined based on known equilibrium constants of carbon dioxide and the solid electrolyte at ambient absorption temperatures and pressures.
In some embodiments, a control sensor may, or may not, be provided. The control sensor can be identical in construction to the gas sensor without the lanthanum oxide. The control sensor can be coupled to the controller and provide a control heating profile for the gas sensor. Thus, a differential heating profile, or differential energy amount can be determined and used to determine desorbed carbon dioxide and/or humidity from the gas sensor. When a control sensor is not provided, the desorbed carbon dioxide and/or humidity can be determined from calculated sensor characteristic data previously known or determined and may be stored in a memory within the controller.
In some embodiments, the sensor 12 may be thermally isolated from some or all of the remainder of the gas sensor 10. In the embodiment shown in
Because the amount of power required to heat the sensor 12 to the operating temperature is reduced, and/or because the sensor 12 is only heated when a reading is desired, the gas sensor 10 may be suited for battery powered and/or wireless applications. For example, the control electronics 28 may be powered by a battery 56, and/or the control electronics 28 may wirelessly transmit an output signal from the gas sensor 10 via an antenna 58.
A gas sample 110 from an environment may be provided to the gas sensor 104 through the absorber 106. The absorber may include an absorbent material that absorbs unwanted constituents or gases from the sample 110 before the sample 110 reaches the gas sensor 104. For example, the absorber may absorb one or more interference gases. In some cases, interference gases can reduce the reliability or accuracy of the measurements made by the gas sensor 104.
The gas sensor assembly 100 may further include a number of leads 108. The leads 108 may provide a mechanical and/or electrical connection between the gas sensor assembly 100 and an external board or the like, when desired.
Numerous advantages of the invention covered by this document have been set forth in the foregoing description. It will be understood, however, that this disclosure is, in many respects, only illustrative. Changes may be made in details, particularly in matters of shape, size, and arrangement of parts without exceeding the scope of the invention. The invention's scope is, of course, defined in the language in which the appended claims are expressed.
Number | Name | Date | Kind |
---|---|---|---|
4151060 | Isenberg et al. | Apr 1979 | A |
4937059 | Kolts et al. | Jun 1990 | A |
5124021 | Kaneyasu et al. | Jun 1992 | A |
5397541 | Post | Mar 1995 | A |
5434551 | Chen et al. | Jul 1995 | A |
5448905 | Stetter et al. | Sep 1995 | A |
5695624 | Garzon et al. | Dec 1997 | A |
6006582 | Bhandari et al. | Dec 1999 | A |
6144285 | Higashi | Nov 2000 | A |
6200445 | Yokota et al. | Mar 2001 | B1 |
6203805 | Collins et al. | Mar 2001 | B1 |
6238085 | Higashi et al. | May 2001 | B1 |
6254749 | Yokota et al. | Jul 2001 | B1 |
6265222 | DiMeo, Jr. et al. | Jul 2001 | B1 |
6325905 | Matsui et al. | Dec 2001 | B1 |
6368479 | Yokota et al. | Apr 2002 | B1 |
6447658 | Wu et al. | Sep 2002 | B1 |
6468407 | Clyde et al. | Oct 2002 | B2 |
6514397 | LaBarge et al. | Feb 2003 | B2 |
6555159 | Clyde et al. | Apr 2003 | B2 |
6579435 | Wang et al. | Jun 2003 | B2 |
6579436 | Wang et al. | Jun 2003 | B2 |
6585872 | Donelon et al. | Jul 2003 | B2 |
6709558 | LaBarge et al. | Mar 2004 | B2 |
6723217 | Duce et al. | Apr 2004 | B1 |
6793788 | Wang et al. | Sep 2004 | B2 |
6797138 | Detwiler et al. | Sep 2004 | B1 |
6800158 | Polikarpus et al. | Oct 2004 | B2 |
6916384 | Jain et al. | Jul 2005 | B2 |
6922639 | Kawase et al. | Jul 2005 | B2 |
20040084308 | Cole et al. | May 2004 | A1 |
20040158410 | Ono et al. | Aug 2004 | A1 |
20050019578 | Bosteels | Jan 2005 | A1 |
20050230246 | Lemaster et al. | Oct 2005 | A1 |
20050230250 | Imamura et al. | Oct 2005 | A1 |
20050241136 | Wu et al. | Nov 2005 | A1 |
Number | Date | Country | |
---|---|---|---|
20070045129 A1 | Mar 2007 | US |