Fire suppression composition

Information

  • Patent Grant
  • 10953257
  • Patent Number
    10,953,257
  • Date Filed
    Friday, April 19, 2019
    5 years ago
  • Date Issued
    Tuesday, March 23, 2021
    3 years ago
Abstract
Disclosed herein is a fire suppression composition including CF3I, an anti-freeze compound, and an odorant compound, wherein the anti-freeze compound and the odorant compound are radical scavengers.
Description
BACKGROUND

Exemplary embodiments of the present disclosure pertain to the art of fire suppression compositions.


Halon 1301 has frequently been employed as a fire suppression agent but there is currently a desire to replace Halon 1301 with more environmentally friendly fire suppression agents or blends of agents. Some of the proposed alternatives to Halon 1301 are less stable than Halon 1301 so solutions must be found that will improve the stability of the alternative fire suppression agents and allow the alternative fire suppression agents to be stored in the fire extinguisher system for extended periods of time.


BRIEF DESCRIPTION

Disclosed is a fire suppression composition including CF3I, an anti-freeze compound, and an odorant compound, wherein the anti-freeze compound and the odorant compound are radical scavengers.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the anti-freeze compound may include methanol, ethanol, propanol, ethylene glycol, propylene glycol, glycerol or a combination thereof.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may have a freezing point less than or equal to −85° F. under storage conditions.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may include two or more carbon-carbon double bonds. The odorant compound may further include a hydroxyl group, an iodine group, or both.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may be aromatic. The odorant compound may further include a hydroxyl group, an iodine group, or both.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may be present in an amount less than or equal to 1 weight percent, based on the total weight of the fire suppression composition.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the anti-freeze compound may be present in an amount less than or equal to 2 weight percent, based on the total weight of the fire suppression composition.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the fire suppression composition may have a freezing point less than or equal to −85° F. under storage conditions.


A fire suppression composition including at least 30 wt % CF3I based on the total weight of the fire suppression composition, an anti-freeze compound, and an odorant compound, wherein the anti-freeze compound and the odorant compound are radical scavengers.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the anti-freeze compound may include methanol, ethanol, propanol, ethylene glycol, propylene glycol, glycerol or a combination thereof.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may have a freezing point less than or equal to −85° F. under storage conditions.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may include two or more carbon-carbon double bonds. The odorant compound may further include a hydroxyl group, an iodine group, or both.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may be aromatic. The odorant compound may further include a hydroxyl group, an iodine group, or both.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the odorant compound may be present in an amount less than or equal to 1 weight percent, based on the total weight of the fire suppression composition.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the anti-freeze compound may be present in an amount less than or equal to 2 weight percent, based on the total weight of the fire suppression composition.


In addition to one or more of the features described above, or as an alternative to any of the foregoing embodiments, the fire suppression composition may have a freezing point less than or equal to −85° F. under storage conditions.







DETAILED DESCRIPTION

A detailed description of one or more embodiments of the disclosed apparatus and method are presented herein by way of exemplification and not limitation with reference to the FIGURES.


CF3I and blends including CF3I are an environmentally attractive alternative to fire suppression agents like Halon 1301 because CF3I has a lower ozone depletion potential. The lower ozone depletion potential is due to the lower stability of the molecule. The lower stability (or the increased tendency to degrade) presents a challenge for long term storage of CF3I or blends containing CF3I as a fire suppression agent. CF3I forms radicals as it degrades and these radicals can initiate further degradation and undesirable by products. The lower stability has discouraged the use of CF3I and CF3I blends in applications requiring long term storage. Long term storage is define herein as greater than or equal to 5 years. In some embodiments the fire suppression composition can be stored for 5-20 years. One approach to resolving the storage problem is to include one or more radical scavenging agents in the fire suppression composition.


Additionally, CF3I has a cardiosensitization level below the concentration needed for fire suppression. Accordingly, it is desirable to include an odorant as an early warning indicator in the case of an accidental release of the fire suppression composition.


The fire suppression system stores the fire suppression composition in liquid form under pressure and releases the composition by a reduction in pressure and expansion through a valve. If water is present in the composition the water can freeze due to the drop in temperature and clog the valve. An anti-freeze compound is needed to lower the freezing point of the composition as a whole, including any water that may be present.


By employing an anti-freeze compound and an odorant that are radical scavengers the foregoing needs can be met with a minimum of components and interactions. Simplifying the number of components minimizes the risk of unforeseen interactions between the components over time in storage and simplifies the distribution of the components when released into a protected space.


The fire suppression agent includes CF3I optionally in combination with one or more of HFC-125, HCFO-1233zd(E), Novec 1230, and CO2. When used in combination with another fire suppression agent the CF3I may be present in an amount greater than or equal to 30 weight percent, or, greater than or equal to 35 weight percent, or, greater than or equal to 40 weight percent, based on the total weight of the fire suppression composition. Exemplary compositions are shown in the following table.


















CF3I
HFC-125



45 wt %
55 wt %



CF3I
Novec 1230



44 wt %
56 wt %



CF3I
HFCO-1233zdE



65 wt %
35 wt %










Exemplary anti-freeze compounds include methanol, ethanol, propanol, ethylene glycol, propylene glycol, glycerol or a combination thereof. The anti-freeze compound is employed in an amount sufficient to reduce the freezing point of the composition to less than or equal to −85° F. at under storage conditions. The anti-freeze may be present in an amount less than or equal to 2.5 wt %, more specifically 0.5 to 2.0 wt %, based on the total weight of the fire suppression composition.


The odorant is an organic compound which can function as a radical scavenger. The odorant has at least two carbon-carbon double bonds which may be conjugated. In some embodiments the odorant is aromatic. The odorant may further comprise a hydroxyl group or an iodine group. The odorant may have a melting point below the minimum operating temperature −85° F.


Exemplary odorants include 2-phenoxyethanol, citronellol, citronellal, limonene, methyl salicylate, and combinations thereof.


The odorant may be present in an amount less than or equal to 1 wt %, based on the total weight of the fire suppression composition. In some embodiments the odorant is present in an amount less than or equal to 0.75 wt %, based on the total weight of the fire suppression composition.


Operating conditions, as used herein, refer to temperatures of −65° F. to 200° F. and pressures of 1.05 to 15.7 PSIA (7.24 to 101.3 kPa A).


Storage conditions, as used herein, refer to temperatures of −85 to 205° F. and pressures of 11 to 15.7 PSIA.


The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the present disclosure. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, element components, and/or groups thereof.


While the present disclosure has been described with reference to an exemplary embodiment or embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the present disclosure. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the present disclosure without departing from the essential scope thereof. Therefore, it is intended that the present disclosure not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this present disclosure, but that the present disclosure will include all embodiments falling within the scope of the claims.

Claims
  • 1. A fire suppression composition comprising CF3I, an anti-freeze compound, and an odorant compound, wherein the anti-freeze compound and the odorant compound are radical scavengers and the anti-freeze compound is present in an amount of 0.5 to 2.5 wt %, based on the total weight of the fire suppression composition.
  • 2. The fire suppression composition of claim 1, wherein the anti-freeze compound comprises methanol, ethanol, propanol, ethylene glycol, propylene glycol, glycerol or a combination thereof.
  • 3. The fire suppression composition of claim 1, wherein the odorant compound has a freezing point less than or equal to −85° F. under storage conditions.
  • 4. The fire suppression composition of claim 1, wherein the odorant compound comprises two or more carbon-carbon double bonds.
  • 5. The fire suppression composition of claim 4, wherein the odorant compound further comprises a hydroxyl group, an iodine group or both.
  • 6. The fire suppression composition of claim 1, wherein the odorant compound is an aromatic compound.
  • 7. The fire suppression composition of claim 6, wherein the odorant compound further comprises a hydroxyl group, an iodine group or both.
  • 8. The fire suppression composition of claim 1, wherein the odorant compound is present in an amount less than 1 wt %, based on the total weight of the fire suppression composition.
  • 9. The fire suppression composition of claim 1, wherein the anti-freeze compound may be present in an amount of 0.5 to 2 wt %, based on the total weight of the fire suppression composition.
  • 10. The fire suppression composition of claim 1, wherein the fire suppression composition has a freezing point less than or equal to −85° F. under storage conditions.
  • 11. A fire suppression composition comprising at least 30 wt % CF3I based on the total weight of the fire suppression composition, an anti-freeze compound, and an odorant compound, wherein the anti-freeze compound and the odorant compound are radical scavengers and the anti-freeze compound is present in an amount of 0.5 to 2.5 wt %, based on the total weight of the fire suppression composition.
  • 12. The fire suppression composition of claim 11, wherein the anti-freeze compound comprises methanol, ethanol, propanol, ethylene glycol, propylene glycol, glycerol or a combination thereof.
  • 13. The fire suppression composition of claim 11, wherein the odorant compound has a freezing point less than or equal to −85° F. under storage conditions.
  • 14. The fire suppression composition of claim 11, wherein the odorant compound comprises two or more carbon-carbon double bonds.
  • 15. The fire suppression composition of claim 14, wherein the odorant compound further comprises a hydroxyl group, an iodine group or both.
  • 16. The fire suppression composition of claim 11, wherein the odorant compound is an aromatic compound.
  • 17. The fire suppression composition of claim 16, wherein the odorant compound further comprises a hydroxyl group, an iodine group or both.
  • 18. The fire suppression composition of claim 11, wherein the odorant compound is present in an amount less than 1 wt %, based on the total weight of the fire suppression composition.
  • 19. The fire suppression composition of claim 11, wherein the anti-freeze compound may be present in an amount of 0.5 to 2 wt %, based on the total weight of the fire suppression composition.
  • 20. The fire suppression composition of claim 11, wherein the fire suppression composition has a freezing point less than or equal to −85° F. under storage conditions.
US Referenced Citations (57)
Number Name Date Kind
2692649 McCreary Oct 1954 A
4179218 Erdmann et al. Dec 1979 A
5155357 Hemond Oct 1992 A
5281816 Jacobson et al. Jan 1994 A
5616742 Robin et al. Apr 1997 A
5695688 Nimitz et al. Dec 1997 A
5902009 Singh et al. May 1999 A
6116348 Drakin Sep 2000 A
6181426 Bender et al. Jan 2001 B1
6526764 Singh et al. Mar 2003 B1
7142105 Chen Nov 2006 B2
7178604 Meserve et al. Feb 2007 B2
7384519 Cottrell et al. Jun 2008 B2
8004684 Powell et al. Aug 2011 B2
8733463 Meier May 2014 B2
9170163 Susko Oct 2015 B2
9182331 Hariram Nov 2015 B2
9207172 Seebaluck et al. Dec 2015 B2
9233264 Graham et al. Jan 2016 B2
9298193 Susko Mar 2016 B2
9957061 Stehman et al. May 2018 B2
10130909 Low et al. Nov 2018 B2
10493399 Low et al. Dec 2019 B2
20020055175 Casal et al. May 2002 A1
20050016741 Paulkovich Jan 2005 A1
20050145820 Waldrop et al. Jul 2005 A1
20050178566 Meserve et al. Aug 2005 A1
20060232773 Barton et al. Oct 2006 A1
20060243944 Minor Nov 2006 A1
20060273223 Haaland et al. Dec 2006 A1
20080011159 Thomas et al. Jan 2008 A1
20080186489 Ahn Aug 2008 A1
20090085224 Choi et al. Apr 2009 A1
20100162738 Low et al. Jul 2010 A1
20100257881 Perti Oct 2010 A1
20140216770 Gibson et al. Aug 2014 A1
20140231660 Fabre et al. Aug 2014 A1
20140233017 Hariram Aug 2014 A1
20150041157 Mitchell et al. Feb 2015 A1
20150328489 Mondino Nov 2015 A1
20150376546 Diaz Gomez Dec 2015 A1
20160096051 Baker et al. Apr 2016 A1
20160296780 Singh et al. Oct 2016 A1
20170072235 Ferguson et al. Mar 2017 A1
20180002586 Low et al. Jan 2018 A1
20180201817 Close et al. Jul 2018 A1
20180217054 Deguchi et al. Aug 2018 A1
20180318623 Richard et al. Nov 2018 A1
20190024126 Beckham et al. Jan 2019 A1
20190055442 Singh Feb 2019 A1
20190083927 Low et al. Mar 2019 A1
20190085224 Sethi et al. Mar 2019 A1
20190161663 Sethi et al. May 2019 A1
20190168035 Conboy Jun 2019 A1
20190177589 Sethi et al. Jun 2019 A1
20200208882 Ota et al. Jul 2020 A1
20200333233 Simpson et al. Oct 2020 A1
Foreign Referenced Citations (7)
Number Date Country
108195796 Jun 2018 CN
2439209 Dec 2007 GB
60139262 Jul 1985 JP
08277389 Oct 1996 JP
2018153463 Oct 2018 JP
9743012 Nov 1997 WO
2010001430 Jan 2010 WO
Non-Patent Literature Citations (18)
Entry
Final Office Action for U.S. Appl. No. 16/388,975; Application Filing Date Apr. 19, 2019; dated Apr. 16, 2020; 16 pages.
Final Office Action for U.S. Appl. No. 16/413,100; Application Filing Date May 15, 2019; dated Apr. 16, 2020, 17 pages.
Non-Final Office Action for U.S. Appl. No. 16/388,959; Application Filing Date Apr. 19, 2019; dated May 26, 2020; 33 pages.
European Search Report for European Application No. 19212840.3; Application Filing Date: Dec. 2, 2019; dated Jul. 14, 2020, 9 pages.
European Search Report for European Application No. 19212780.1; Date of Filing: Dec. 2, 2019; dated Jun. 24, 2020; 6 pages.
Non-Final Office Action for U.S. Appl. No. 16/413,166, Application Filing Date May 15, 2019, NFOA Notification Date: Nov. 7, 2019, 11 pages.
European Search Report for European Application No. 19211917.0; Application Filing Date: Nov. 27, 2019; dated Jun. 23, 2020; 7 pages.
European Search Report for European Application No. 19212793.4; Application Filing Date: Dec. 2, 2019; dated Jun. 23, 2020, 7 pages.
European Search Report for European Application No. 19212814.8; Application Filing Date: Dec. 2, 2019; dated Jun. 23, 2020, 14 pages.
3M™ Novec™ Brand, 3M™ Novec™ 1230 Fire Protection Fluid, Technical Data, Jan. 2020, 12 pages.
Final Office Action for U.S. Appl. No. 16/413,166, Application Filing Date May 15, 2019, FOA Notification Date: Mar. 9, 2020, 14 pages.
Non-Final Office Action for U.S. Appl. No. 16/413,100; Application Filing Date May 15, 2019; Notification Date Jan. 9, 2020, 19 pages.
Non-Final Office Action for U.S. Appl. No. 16/388,975; Application Filing Date Apr. 19, 2019; Noification Date Jan. 9, 2020; 24 pages.
Non-Final Office Action for U.S. Appl. No. 16/388,967; Application Filing Date: Apr. 19, 2019; Notification Date: Aug. 4, 2020, 42 pages.
Extended European Search Report for European Application No. 19212814.8; Application Filing Date: Dec. 2, 2020; dated Sep. 29, 2020; 12 pages.
Final Office Action for U.S. Appl. No. 16/388,959; Application Filing Date: Apr. 19, 2019; dated Sep. 9, 2020; 22 pages.
Non-Final Office Action for U.S. Appl. No. 16/388,975; Application Filing Date: Apr. 19, 2019; dated Sep. 18, 2020; 31 pages.
Non-Final Office Action for U.S. Appl. No. 16/413,100; Application Filing Date: May 15, 2019; dated Sep. 17, 2020; 29 pages.
Related Publications (1)
Number Date Country
20200330809 A1 Oct 2020 US