Compositional state detection system and method

• US 4,808,824 A
• Filed: 09/17/1987
• Issued: 02/28/1989
• Est. Priority Date: 09/17/1987
• Status: Expired due to Fees

• Current Assignee: Abbas M. Sinnar
• Original Assignee: Abbas M. Sinnar
• Inventors: Sinnar, Abbas M.
• Primary Examiner(s): Howell, Janice A.
• Application Number:
  US07/097,691
• Time in Patent Office: 530 Days
• Field of Search: 250/339, 250/340, 244/134 E
• US Class Current: 250/339.11
• CPC Class Codes: F25B 2700/111 using an emitter and receiver, e.g. sensing by emitting light or other radiation and receiving reflection by a sensor
• CPC Class Codes: F25D 21/02 Detecting the presence of frost or condensate
• CPC Class Codes: G01B 11/0633 using one or more discrete wavelengths
• CPC Class Codes: G01N 21/3554 for determining moisture content
• CPC Class Codes: G01N 21/3577 for analysing liquids, e.g. polluted water

Abstract

An ice detection and measurement system (100) is provided to detect the formation of ice and/or water (40) on a surface (49) and measure the thickness thereof. The ice detection and measurement system (100) includes a radiation source (10) having a wide band emission (12) whose bandwidth is in the infrared portion of the electromagnetic spectrum. The wide band infrared emission (12) is directed to a wavelength selector (20) for providing a discontinuous transmission alternating between a pair of narrow band infrared signals each centered at a different predetermined discrete wavelength. The discontinuous alternating signal (22) is applied to optical system (30) where it is divided into two beams (32 and 34) for application to respective detectors (50 and 60). Reference detector (60) includes photoconductive cell (65) for conversion of beam (34) to a reference signal for each of the discrete wavelengths transmitted by beam (34). Test detector (50) includes photoconductive cell (55) for receipt of beam (34 ) after transmission through the ice and/or moisture (40) formed on the surface (49) of infrared transparent cover (51), for establishing a test signal responsive to infrared radiation absorbed at each of the two discrete wavelengths. The test and reference signals at each of the two discrete wavelengths are compared in microcomputer (70) for detecting and measuring ice accumulation, to distinguish icing, frost and water accumulation, and to monitor the progress of the icing/de-icing process.

Claims

1. A method of determining the compositional state and any transition between states of a chemical compound comprising the steps of:

(a) simultaneously applying at least two discrete energy wavelengths within the electromagnetic energy spectrum to (1) said chemical compound for providing a test signal, and, (2) at least one energy detector for providing an energy wavelength reference, each of said discrete energy wavelengths being selected from a wavelength spectrum of absorption for said chemical compound;

(b) detecting said two discrete energy wavelengths passing through or reflected from said chemical composition;

(c) establishing the amount of energy absorbed by said chemical compound at each of said discrete energy wavelengths; and

,

(d) determining (1) transitional changes between two states of said chemical compound and (2) a thickness dimension of said chemical compound for each of said two state by (1) comparing said absorbed energy at each of said discrete energy wavelengths with the absorption characteristics of said chemical compound at each of said discrete energy wavelengths for each of said two states and (2) computing said thickness dimensions from a predetermined relationship for said energy absorbed.

2. The method of determining the compositional state of a chemical compound as recited in claim 1 where the step of simultaneously applying said two discrete energy wavelengths includes the step of establishing a discontinuous signal source for each of said energy wavelengths.

3. The method of determining the compositional state of a chemical compound as recited in claim 2 where the step of establishing said discontinuous signal source includes the step of optically chopping said two discrete energy wavelengths.

4. The method of determining the compositional state of a chemical compound as recited in claim 2 where the step of simultaneously applying said two discrete energy wavelengths includes the steps of:

(a) filtering a wideband source of electromagnetic energy to obtain said two discrete energy wavelengths; and

,

(b) establishing at least two distinct optical paths for (1) impinging said chemical composition, and (2) providing said energy wavelength reference, through division of said discontinuous signal source for each of said wavelengths.

5. The method of determining the compositional state of a chemical compound as recited in claim 2 where one of said discontinuous signal sources has an approximating wavelength at 1.6 microns, and the other of said discontinuous signal sources has an approximating wavelength at 1.82 microns or 1.42 microns.

6. The method of determining the compositional state of a chemical compound as recited in claim 1 where the step of detecting said two discrete energy wavelengths applied to said chemical compound includes the step of applying said two discrete energy wavelengths to an energy detector subsequent to (1) transmission through, or, (2) reflection from said chemical compound.

7. The method of determining the compositional state of a chemical compound as recited in claim 1 where the step of detecting includes the step of applying each of said two discrete energy wavelengths to said reference energy detector in a discrete manner.

8. The method of determining the compositional state of a chemical compound as recited in claim 1 where the step of establishing the amount of energy absorbed by said chemical compound at each of said discrete energy wavelengths includes the step of comparing said test signal with said energy reference at each of said discrete energy wavelengths.

9. The method of determining the compositional state of a chemical compound as recited in claim 1 where the step of simultaneously applying said two discrete energy wavelengths is preceded by the step of selecting said two wavelengths from said wavelength spectrum of absorption for substantially maximizing a difference in absorption between said two states of said chemical compound.

10. The method of determining the compositional state of a chemical compound as recited in claim 1 where said chemical compound is water.

11. A system for comparing the energy absorption at two discrete wavelengths of electromagnetic energy for the detection of the presence of differing phases of a compound, and simultaneously measure the thickness of each of said phases on a surface, comprising:

(a) energy source means having a signal spectrum in the electromagnetic bandwidth, said signal spectrum having at least two of said discrete energy wavelengths for said comparison of said energy absorptive, said discrete energy wavelengths being selected from a wavelength spectrum of absorption for said differing phases of said compound wherein the difference in absorption between phases is substantially maximized;

(b) wavelength selection and projection means for establishing a first and second transmission of each of said two discrete energy wavelengths where said first transmission of said two discrete energy wavelengths is a reference signal and said second transmission of said two discrete energy wavelengths is a test signal;

(c) detection means for receiving said reference and test signals, said test signal being received after impingement with said surface; and

,

(d) processor means for comparing said signals received by said detection means to compute the thickness of each of said phases.

12. The energy absorption comparison system as recited in claim 11 where said energy source is a wide band source of infrared radiation having wavelengths in the approximating range of 1 to 20 microns.

13. The energy absorption comparison system as recited in claim 11 where said energy source comprises a first laser for generating a narrow band emission at one of said two discrete energy wavelengths, and a second laser for generating a narrow band emission at the other of said two discrete energy wavelengths.

14. The energy absorption comparison system as recited in claim 12 where said wavelength selection and projection means comprises:

(a) a monochromator for selecting each of said two discrete energy wavelengths;

(b) a filter assembly for removing undesired second order wavelengths;

(c) a lens assembly for collimating said two discrete energy wavelengths;

(d) an optical chopper for modulating each of said two discrete energy wavelengths to form a pulsed output; and

,

(e) a beam splitter assembly for dividing each of said two discrete energy wavelengths to form said test signals and said reference signals.

15. The energy absorption comparison system as recited in claim 11 where said detection means includes (1) at least one reference detector for establishing a reference level for each of said two discrete energy wavelengths, and (2) at least one test detector for establishing a detection signal for each of said two discrete energy wavelengths, said detection signal being responsive to absorption of said test signal at each of said two discrete energy wavelengths.

16. The energy absorption comparison system as recited in claim 15 where said processor means includes a microcomputer for comparing said detection signal at each of said two discrete energy wavelengths with the absorption characteristics for each of said phases of said compound to detect said phases and provide said measurement thereof.

17. The energy absorption comparison system as recited in claim 16 where said reference detector includes a lead sulfide photoconductive cell for conversion of said reference signal to said reference level for each of said two discrete energy wavelengths.

18. The energy absorption system as recited in claim 17 where said test detector includes (1) an infrared transparent cover for establishing said surface for the formation of said differing phases of said compound, and (2) a lead sulfide photoconductive cell for conversion of said test signal after impingement with said cover to said detection signal for each of said two discrete energy wavelengths.

19. The energy absorption comparison system as recited in claim 18 where said compound is H₂ O, and said differing phases comprise a liquid water phase and a solid ice phase.

20. The energy absorption comparison system as recited in claim 19 where said two discrete energy wavelengths comprise a first approximating wavelength at 1.6 microns and a second approximating wavelength at 1.82 microns or 1.42 microns.