IP Library › Granted Patent US 12,253,462
Granted Patent B2
US 12,253,462 · App. 18/082,629 · Granted Mar 18, 2025

Monitoring gas impurities with total sulfur detection

Inventors: Martin L. Spartz (Ellington, CT); Kelly Renee McPartland (West Hartford, CT); Anthony S. Bonanno (Ellington, CT); Adam R. Klempner (Gardner, MA)
Assignee: MLS ACQ, Inc.
G01N21/3504G01N21/3577G01N2021/3545G01N2021/3595
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,253,462
App. No.
18/082,629
Granted
Mar 18, 2025
Kind
B2
Abstract

A system and method for determining impurities in a beverage grade gas such as CO 2 or N 2 relies on FTIR gas analysis for measuring non-sulfur impurities as well as SO 2 . CO 2 % also can be determined. A multiplexer selects a sample gas from multiple gas samples. Conversion of reduced sulphur present in some impurities to SO 2 is conducted in an oxidizing furnace. Climate control and measurements of oxygen gas impurities also can be provided.

Claims (41)

1. A system for analyzing a beverage grade gas, the system comprising:

a multiplexer for selecting a gas sample from multiple gas samples;

a spectrometer including a gas cell for detecting an absorbance spectrum of gas in the gas cell;

an oxidizing furnace for converting reduced sulfur present in the gas sample to SO 2 ;

an arrangement including a device for directing the gas sample to the spectrometer or to the oxidizing furnace; and

a computer module for operating the multiplexer, the oxidizing furnace and/or the device for directing the gas to the spectrometer or to the oxidizing furnace;

wherein the computer module is configured to operate the device for directing the gas to the spectrometer to switch conditions in the gas cell between an atmospheric pressure and a pressure above atmospheric.

2. The system of claim 1 , wherein the gas cell is a multiple path type cell and/or wherein the gas cell is configured for pressures higher than atmospheric.

3. The system of claim 1 , wherein the spectrometer is provided with a FTIR detector for measuring SO 2 and non-sulfur impurities in the sample gas.

4. The system of claim 1 , further comprising conduits, valves, an oxygen analyzer, and/or controls for pressure, temperature and/or flow rates.

5. The system of claim 1 , wherein the system does not include a UV fluorescence apparatus.

6. The system of claim 1 , wherein the multiplexer is configured to receive gas feeds from multiple plant locations.

7. The system of claim 1 , wherein the computer module further comprises one or more functions for collecting, analyzing and/or reporting data from the spectrometer.

8. The system of claim 1 , wherein the computer module comprises connections to one or more of the multiplexer, the spectrometer and the oxidizing furnace and/or is configured for local area network communications.

9. The system of claim 1 , further comprising software for collecting, analyzing and/or reporting data.

10. The system of claim 1 , further comprising calibration information for pure CO 2 and/or one or more impurity for the spectrometer.

11. A method for analyzing a beverage grade gas, the method comprising:

(a) selecting a gas sample from multiple gas samples;

(b) directing a first portion of the gas sample to a gas cell;

(c) measuring impurities present in the gas cell with a spectrometer, wherein the impurities include SO 2 ;

(d) directing a second portion of the gas sample to an oxidizing furnace;

(e) converting reduced sulfur present in the second portion to SO2;

(f) directing gas exiting the oxidizing furnace to the gas cell;

(g) measuring a total SO2 in the gas cell;

(h) repeating steps (a) through (g); and

(i) switching conditions in the gas cell between an atmospheric pressure and a pressure above atmospheric.

12. The method of claim 11 , wherein step (c) is conducted at a pressure higher than atmospheric and/or wherein step (g) is conducted at atmospheric pressure.

13. The method of claim 11 , wherein total SO 2 measured in the second portion of the gas sample is compared with SO 2 measured by the spectrometer in the first portion of the gas sample to determine a TRS amount.

14. The method of claim 13 , further comprising controlling gas pressure and/or gas temperature in the gas sample cell and/or purging the sample gas cell after step (c).

15. The method of claim 11 , wherein data obtained for impurities in the first portion of the gas sample are compared with calibration data.

16. The method of claim 11 , wherein the impurities are selected from the group consisting of SO 2 , total sulfur, NH 3 , CO, NO, NO 2 , H 2 O, hydrogen cyanide (HCN), CS 2 , methanol, acetaldehyde, methane, total hydrocarbons, benzene and total aromatic hydrocarbons and the beverage grade gas is CO 2 or N 2 .

17. The method of claim 11 , wherein the gas sample is selected from multiple gas samples, obtained from different locations in a plant, by a multiplexer.

18. The method of claim 11 , further comprising measuring oxygen gas present in the sample gas.

19. The method of claim 11 , wherein a CO 2 % in the first portion of the gas sample is determined by the spectrometer and compared to calibration information.

20. The method of claim 11 , further comprising controlling at least one of steps (a) through (h) automatically.

21. The method of claim 11 , wherein the method does not include detecting SO 2 by UV fluorescence.

22. A system, comprising:

a spectrometer including a gas cell for detecting an absorbance spectrum of gas in the gas cell;

an oxidizing furnace for converting reduced sulfur present in the gas to SO 2 ;

an arrangement including a device for directing the gas to the gas spectrometer; and

a computer module configured to operate the device for directing the gas to the spectrometer to switch conditions in the gas cell between an atmospheric pressure and a pressure above atmospheric.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2022
From: SPARTZ, MARTIN L.; MCPARTLAND, KELLY RENEE; BONANNO, ANTHONY S.; KLEMPNER, ADAM R.
To: MLS ACQ, INC. D/B/A MAX ANALYTICAL TECHNOLOGIES
Reel/Frame 062178/0898 →
Continuity (2)
Provisional Application 63290416 · Dec 16, 2021
Related Publication 20230194419A1 · Jun 22, 2023
References Cited (5)
US 5544208A · Pao · 1996 [cited by examiner]
US 9606088B2 · Spartz et al. · 2017 [cited by applicant]
US 10054486B2 · Spartz et al. · 2018 [cited by applicant]
US 10408746B2 · Spartz et al. · 2019 [cited by applicant]
US 10761018B2 · Spartz et al. · 2020 [cited by applicant]