Fiber optic detector and method for using same for detecting chemical species

• US 5,457,313 A
• Filed: 02/01/1994
• Issued: 10/10/1995
• Est. Priority Date: 02/01/1994
• Status: Expired due to Fees

• Current Assignee: The United States of America As Represented By The Secretary of Agriculture
• Original Assignee: United States Of America As Represented By The Department Of Energy
• Inventors: Buchanan, Bruce R., Baylor, Lewis C.
• Primary Examiner(s): Allen, Stephone B.
• Application Number:
  US08/189,823
• Time in Patent Office: 616 Days
• Field of Search: 250/226, 250/227.21, 250/227.23, 250/483.1, 250/459, 422/82.05, 422/86
• US Class Current: 250/227.21
• CPC Class Codes: G01N 21/78 producing a change of colour
• CPC Class Codes: G01N 21/8507 Probe photometers, i.e. with optical measuring part dipped into fluid sample
• CPC Class Codes: G02B 6/3624 Fibre head, e.g. fibre probe termination optical details of light guide terminations G02B6/241; reshaping of light guides G02B6/2552; optical details of coupling light into or out of fibre end G02B6/262

Abstract

An optical sensing device for uranyl and other substances, a method for making an optical sensing device and a method for chemically binding uranyl and other indicators to glass, quartz, cellulose and similar substrates. The indicator, such as arsenazo III, is immobilized on the substrate using a chemical binding process. The immobilized arsenazo III causes uranyl from a fluid sample to bind irreversibly to the substrate at its active sites, thus causing absorption of a portion of light transmitted through the substrate. Determination of the amount of light absorbed, using conventional means, yields the concentration of uranyl present in the sample fluid. The binding of uranyl on the substrate can be reversed by subsequent exposure of the substrate to a solution of 2,6-pyridinedicarboxylic acid. The chemical binding process is suitable for similarly binding other indicators, such as bromocresol green.

Claims

1. Apparatus for indicating the presence of a concentration of a substance in a sample, said apparatus for use with means for transmitting and receiving light, said apparatus comprising:

an indicator that reacts with said substance to form a reaction product with said substance; and

a substrate translucent to said light,

said indicator being chemically immobilized on said substrate so that, when said sample contacts said substrate and said indicator forms said reaction product on said substrate and said light is transmitted through said substrate by said transmitting and receiving means, said reaction product absorbs a portion of said light,

said reaction product absorbing said portion of said light in proportion to said concentration of said substance; and

means in optical communication with said substrate for determining said concentration from said light received from said substrate.

2. The apparatus as recited in claim 1, wherein said indicator is immobilized on said substrate by soaking said substrate in a solution containing said indicator for a preselected length of time.

3. The apparatus as recited in claim 1, wherein said substance is uranyl and wherein said indicator is arsenazo III.

4. The apparatus as recited in claim 1, wherein said reaction product indicates a pH for said sample and wherein said indicator is bromocresol green.

5. The apparatus as recited in claim 1, wherein said indicator is immobilized to said substrate by a method comprising the steps of:

silyating said substrate by

soaking said substrate in a silane coupling solution, and then curing said substrate;

amidizing said substrate by

soaking said substrate in a solution containing chloroform, triethylamine and 4-nitrobenzoyl chloride;

reducing said substrate by

soaking said substrate in a reducing solution, and then heating said substrate;

diazotizating said substrate by

soaking said substrate in a solution containing sodium nitrite and hydrochloric acid,

cooling said substrate, and then

rinsing said substrate with a cleaning solution; and

placing said substrate in a solution containing said indicator for a preselected length of time.

6. The apparatus as recited in claim 1, wherein said substrate is selected from the group consisting of glass lenses, glass microscope slides, glass wool, quartz lenses, quartz rods, quartz plates and cellulose matrices.

7. The apparatus as recited in claim 1, wherein said light transmitting and receiving means further comprises optical fibers, and wherein said apparatus further comprises a housing having a proximal end and a distal end, said substrate attached to said distal end.

8. A method for determining a concentration of uranyl in a sample, said method comprising the steps of:

placing a substrate having a uranyl-responsive indicator chemically immobilized thereon in said sample so that said indicator comes in contact with said sample, said indicator binding said uranyl to form a reaction product;

transmitting light through said substrate, said indicator absorbing a portion of said light in proportion to said concentration of said uranyl;

collecting light transmitted through said substrate; and

comparing said transmitted light to said collected light to determine the absorbance of said reaction product in said sample whereby said concentration can be determined.

9. The method as recited in claim 8, further comprising the step of exposing said substrate to 2,6-pyridinedicarboxylic acid whereby said uranyl is freed from said indicator.

10. The method as recited in claim 8, wherein said indicator is arsenazo III.

11. The method as recited in claim 8, wherein said substrate is a cellulose matrix and wherein said indicator is immobilized thereon by dyeing said cellulose matrix with a solution containing said indicator.

12. The method as recited in claim 8, wherein said substrate is selected from the group consisting of fiber optic lens assemblies, glass lenses, glass microscope slides, glass wool, quartz lenses, quartz rods and quartz plates.

13. The method as recited in claim 8, wherein said method is for use with a first optical fiber and a second optical fiber, and said transmitted light is transmitted by said first optical fiber and said collected light is collected by said second optical fiber, and said method further comprises the step of reflecting said light passing through said substrate to said second optical fiber.

14. The method as recited in claim 8, wherein said indicator is immobilized thereon by a method comprising the steps of:

rinsing said substrate with at least one cleaning solution;

silyating said substrate by

soaking said substrate in a silane solution for a first preselected length of time, and then

curing said substrate for a second preselected length of time;

amidizing said substrate by

soaking said substrate in a solution containing chloroform, triethylamine and 4-nitrobenzoyl chloride for a third preselected length of time,

cooling said substrate for a fourth preselected length of time, and then

rinsing said substrate with a cleaning solution;

reducing said substrate by

soaking said substrate in a reducing solution for a fifth preselected length of time;

diazotizating said substrate by

soaking said substrate in a solution containing sodium nitrite and hydrochloric acid for a sixth preselected length of time, and then

rinsing said substrate with a cleaning solution; and

soaking said substrate in a solution containing said indicator for a seventh preselected length of time.

15. A method for immobilizing an indicator to a substrate, said substrate for use in detecting the presence of a substance in a fluid sample, said method comprising the steps of:

rinsing said substrate with at least one cleaning solution;

silyating said substrate by

soaking said substrate in a silane solution for approximately 15 minutes, and then

curing said substrate for approximately 30 minutes at a temperature of approximately 110°

C.;

amidizing said substrate by

soaking said substrate in a solution containing chloroform, triethylamine and 4-nitrobenzoyl chloride for approximately 15 minutes at a temperature of approximately 50°

C.;

reducing said substrate by

soaking said substrate in a reducing solution heated at a temperature within a range of approximately 35°

-40°

C. for approximately 45 minutes;

diazotizating said substrate by

soaking said substrate in a solution containing sodium nitrite and hydrochloric acid for approximately 30 minutes at a temperature of approximately 5°

C., and then

rinsing said substrate with a cleaning solution; and

binding said indicator to said substrate by

soaking said substrate in a solution containing said indicator for approximately 30 minutes,

removing said substrate from said solution, and then

rinsing said substrate with a cleaning solution.

16. The method as recited in claim 15, wherein said indicator is arsenazo III for detecting uranyl in said sample.

17. The method as recited in claim 15, wherein said indicator is bromocresol green for indicating pH in said sample.

18. The method as recited in claim 15, wherein said substrate is selected from the group consisting of glass lenses, glass microscope slides, glass wool, quartz lenses, quartz rods and quartz plates.

19. The method as recited in claim 15, wherein said substrate is a cellulose matrix and wherein said binding step further comprises dyeing said cellulose matrix with said indicator.