IP Library Granted Patent US 9,062,168
Granted Patent B2
US 9,062,168 · App. 13/646,785 · Granted Jun 23, 2015

Method for filling concrete block cavities with expanding foam insulation

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 9,062,168
App. No.
13/646,785
Granted
Jun 23, 2015
Kind
B2
Abstract

The invention described herein generally pertains to the use of low boiling point, low vapor pressure blowing agents with froth polyurethane or polyisocyanurate foams to achieve superior cavity filling than when using conventional higher vapor pressure or more ozone-depleting blowing agents.

Claims (102)

1. A process for filling a cavity with a frothable polyurethane or a polyisocyanurate pour-in-place foam system, said process comprising the step of:

adding a two-component polyurethane or polyisocyanurate uncured foam to said cavity, said two-component polyurethane or polyisocyanurate curing into a cured foam, each of said two components used to make the cured foam comprising an effective amount of at least one blowing agent, including miscible blends and azeotropes thereof, said blowing agent comprising formula (I):

[CV a ] m -A-[CX b ] n —B—[CY c ] o -D-[CZ d ] p

wherein

C is a carbon atom;

V, X, Y and Z are independently selected from the group consisting of H, F and Cl;

a & d are independently selected from the integral values ranging from 0 to 3 inclusive;

b & c are independently selected from the integral values ranging from 0 to 2 inclusive;

o, p & n are equal to 1;

m is selected from the integral values ranging from 0 to 1 inclusive;

A, B and D are covalent bonds sufficient to satisfy the available bonding sites of adjacent carbon atoms, if such carbon atoms are present;

said at least one blowing agent having a boiling point between approximately 5-50° C., and an ozone depletion potential of not greater than 0.05;

a first component comprising a B-side blend which comprises at least:

a polyol blend having an average hydroxyl number of approximately 350 or greater, said polyol blend comprising;

25-45 wt % of the B-side blend of an oxypropylated aliphatic amine polyether polyol having an average functionality of 3;

5-15 wt % of the B-side blend of a sucrose glycerine propoxylated polyether polyol having an average functionality of between about 4.5-5.0;

5-15 wt % of the B-side blend of a phthalic acid aromatic polyester polyol having an average functionality of about 2.2;

2-15 wt % of the B-side blend of a halogenated phthalate diol having an average functionality of 2;

said B-side blend containing 50-75 wt % polyols comprising at least the oxypropylated aliphatic amine polyether polyol, the sucrose glycerine propoxylated polyether polyol, the phthalic acid aromatic polyester polyol and the halogenated phthalate diol;

1-5 wt % of a water-emulsifiable polysiloxane surfactant in the B-side blend;

a second component comprising at least one A-side diisocyanate;

a pressure differential between said A-side and said B-side of less than or equal to 30 psig and an A-side/B-side weight ratio approximately equal to or greater than 1.0;

said cured foam having a closed cell content of at least 90%;

the cured foam having a parallel compressive strength in excess of 25 psi;

a reaction of said B-side blend and said A-side diisocyanate delayed for at least 10 seconds after dispensing from a mixer affixed to a foam-dispensing tool.

2. The process of claim 1 wherein

said covalent bonds A, B and D are independently selected from the group consisting of single, double and triple covalent bonds.

3. The process of claim 1 wherein formula (I) is selected from the group consisting of

1,1,1,3,3-pentafluoropropane, 1,1,1,3,3-pentafluorobutane, 1,1,1,4,4,4-hexafluoro-2-butene, trans-3,3,3-trifluoro-1-chloro-propene, miscible blends and azeotropes thereof and further wherein formula (I) is a major amount of said blowing agent.

4. The process of claim 3 wherein said blowing agent has

a boiling point between approximately 10-40° C.

5. The process of claim 4 wherein a vapor pressure of said blowing agent is

approximately 5 psi (34.5 kPa) to 30 psi (206.9 kPa) at 75° F. (24° C.).

6. The process of claim 1 which further comprises the step of:

monitoring a temperature exotherm of said polymerization to determine if said cavity is being completely filled.

7. The process of claim 6 wherein said step of monitoring is by

an Infrared camera.

8. The process of claim 6 which further comprises the step of:

drilling a hole beneath an obstruction as determined by monitoring said temperature exotherm.

9. The process of claim 7 which further comprises the step of:

adding additional foam into said hole beneath said obstruction to completely fill said cavity.

10. The process of claim 1 wherein

said halogenated phthalate diol comprises at least approximately 30% bromine.

11. The process of claim 1 wherein

said foam system has a reaction profile gel and tack time which is less than approximately 90 seconds.

12. The process of claim 11 wherein

said reaction profile gel and tack time is less than approximately 60 seconds.

13. The process of claim 12 wherein

said reaction profile gel and tack time is less than approximately 45 seconds.

14. A process for filling a cavity with a frothable two-component polyurethane or a polyisocyanurate pour-in-place foam system, said frothable polyurethane or frothable polyisocyanurate curing into a cured foam, said process comprising the steps of:

adding the two-component uncured polyurethane or polyisocyanurate foam to said cavity, each of said two components used to make the cured foam comprising an effective amount of at least one blowing agent, including miscible blends and azeotropes thereof, said blowing agent comprising formula (II):

[CU e ] q -E-[CW f ] r —F—[CV a ] m -A-[CX b ] n —B—[CY c ] o -D-[CZ d ] p

wherein

C is a carbon atom;

U, W, V, X, Y and Z are independently selected from the group consisting of H, F and Cl;

d & e are independently selected from the integral values ranging from 0 to 3 inclusive;

a, b, c & f are independently selected from the integral values ranging from 0 to 2 inclusive;

o, p & n are equal to 1;

m, q & r are independently selected from the integral values ranging from 0 to 1 inclusive;

A, B, D, E and F are covalent bonds sufficient to satisfy the available bonding sites of adjacent carbon atoms, if such carbon atoms are present;

said blowing agent having a boiling point between approximately 5-50° C., and an ozone depletion potential of not greater than 0.05;

a first component comprising a B-side blend which comprises at least:

a polyol blend having an average hydroxyl number of approximately 350 or greater, said polyol blend comprising;

25-45 wt % of the B-side blend of an oxypropylated aliphatic amine polyether polyol having an average functionality of 3;

5-15 wt % of the B-side blend of a sucrose glycerine propoxylated polyether polyol having an average functionality of between about 4.5-5.0;

5-15 wt % of the B-side blend of a phthalic acid aromatic polyester polyol having an average functionality of about 2.2;

2-15 wt % of the B-side blend of a halogenated phthalate diol having an average functionality of 2;

said B-side blend containing 50-75 wt % polyols comprising at least the oxypropylated aliphatic amine polyether polyol, the sucrose glycerine propoxylated polyether polyol, the phthalic acid aromatic polyester polyol and the halogenated phthalate diol;

1-5 wt % of the B-side of a water-emulsifiable polysiloxane surfactant;

a second component comprising at least one A-side diisocyanate;

a pressure differential between said A-side and said B-side of less than or equal to 30 psig and an A-side/B-side weight ratio approximately equal to or greater than 1.0;

said cured foam having a closed cell content of at least 90%;

the cured foam having a parallel compressive strength in excess of 25 psi;

a reaction of said B-side blend and said A-side diisocyanate delayed for at least 10 seconds after dispensing from a mixer affixed to a foam-dispensing tool.

15. The process of claim 14 wherein

said covalent bonds A, B and D are independently selected from the group consisting of single, double and triple covalent bonds.

16. The process of claim 14 wherein formula (I) is selected from the group consisting of

1,1,1,3,3-pentafluoropropane, 1,1,1,3,3-pentafluorobutane, 1,1,1,4,4,4-hexafluoro-2-butene, trans-3,3,3-trifluoro-1-chloro-propene, miscible blends and azeotropes thereof and further wherein formula (I) is a major amount of said blowing agent.

17. The process of claim 16 wherein said blowing agent has

a boiling point between approximately 10-40° C.

18. The process of claim 17 wherein a vapor pressure of said blowing agent is

approximately 5 psi (34.5 kPa) to 30 psi (206.9 kPa) at 75° F. (24° C.).

19. The process of claim 14 which further comprises the step of:

monitoring a temperature exotherm of said polymerization to determine if said cavity is being completely filled.

20. The process of claim 19 wherein said step of monitoring is by

an Infrared camera.

21. The process of claim 19 which further comprises the step of:

drilling a hole beneath an obstruction as determined by monitoring said temperature exotherm.

22. The process of claim 21 which further comprises the step of:

adding additional foam into said hole beneath said obstruction to completely fill said cavity.

23. The process of claim 14 wherein

said covalent bonds A, B, D, E and F are independently selected from the group consisting of single, double and triple covalent bonds.

24. The process of claim 14 wherein formula (II) is selected from the group consisting of

1,1,1,3,3-pentafluoropropane, 1,1,1,3,3-pentafluorobutane, 1,1,1,4,4,4-hexafluoro-2-butene, 3,3,3-trifluoro-1-chloro-propene, miscible blends and azeotropes thereof and further wherein formula (II) is a major amount of said blowing agent.

25. The process of claim 14 wherein

said halogenated phthalate diol comprises at least approximately 30% bromine.

26. The process of claim 14 wherein

said foam system has a reaction profile gel and tack time which is less than approximately 90 seconds.

27. The process of claim 26 wherein

said reaction profile gel and tack time is less than approximately 60 seconds.

28. The process of claim 27 wherein

said reaction profile gel and tack time is less than approximately 45 seconds.

Assignments (16)
ASSIGNMENT OF 2ND LIEN SECURITY INTEREST (REEL 054888 / FRAME 0048) Recorded Sep 15, 2023
From: ANTARES CAPITAL LP
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 064923/0317 →
SECURITY AGREEMENT (SECOND LIEN) Recorded Jan 4, 2021
From: ICP CONSTRUCTION, INC.; GARDNER-GIBSON, INC.; GARDNER ASPHALT CORPORATION; PLI-DEK, LLC; SUN COATINGS, INC.
To: ANTARES CAPITAL, L.P., AS COLLATERAL AGENT
Reel/Frame 054888/0048 →
SECURITY AGREEMENT (FIRST LIEN) Recorded Dec 31, 2020
From: ICP CONSTRUCTION, INC.; GARDNER-GIBSON, INC.; GARDNER ASPHALT CORPORATION; PLI-DEK, LLC; SUN COATINGS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 054883/0265 →
MERGER Recorded Dec 30, 2020
From: ICP ADHESIVES AND SEALANTS, INC.
To: ICP MERGER OPCO, LLC
Reel/Frame 054775/0076 →
MERGER Recorded Dec 30, 2020
From: ICP MERGER HOLDCO, LLC; ICP MERGER OPCO, LLC
To: ICP CONSTRUCTION, INC.
Reel/Frame 054775/0198 →
RELEASE OF SECURITY INTEREST : RECORDED AT REEL/FRAME - 044037-0515; 044037-0590; 045792-0510 AND 050426-0086 Recorded Dec 30, 2020
From: GOLDMAN SACHS MIDDLE MARKET LENDING CORP.
To: ICP ADHESIVES AND SEALANTS, INC.; LENOX ACQUISITION, LLC; PLI-DEK, LLC; ICP CONSTRUCTION, INC.
Reel/Frame 054871/0203 →
RELEASE OF SECURITY INTEREST Recorded Dec 29, 2020
From: ANTARES CAPITAL LP, AS AGENT
To: ICP ADHESIVES AND SEALANTS, INC.; LENOX ACQUISITION, LLC; PLI-DEK, LLC; ICP CONSTRUCTION, INC.
Reel/Frame 054866/0395 →
SECURITY INTEREST Recorded Nov 6, 2017
From: ICP ADHESIVES AND SEALANTS, INC.
To: GOLDMAN SACHS MIDDLE MARKET LENDING CORP., AS COLLATERAL AGENT
Reel/Frame 044037/0515 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAME 038247/0001 Recorded Nov 4, 2017
From: NXT CAPITAL, LLC
To: ICP ADHESIVES AND SEALANTS, INC.
Reel/Frame 044682/0157 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAME 038365/0461 Recorded Nov 4, 2017
From: MARANON CAPITAL, L.P.
To: ICP ADHESIVES AND SEALANTS, INC. (F/K/A FOMO PRODUCTS)
Reel/Frame 044367/0168 →
SECURITY INTEREST Recorded Nov 3, 2017
From: ICP ADHESIVES AND SEALANTS, INC.
To: ANTARES CAPITAL LP, AS COLLATERAL AGENT
Reel/Frame 044026/0202 →
MERGER AND CHANGE OF NAME Recorded Sep 27, 2016
From: FOMO PRODUCTS, INC.; ICP ADHESIVES AND SEALANTS, INC.
To: ICP ADHESIVES AND SEALANTS, INC.
Reel/Frame 039868/0587 →
CHANGE OF NAME Recorded Aug 18, 2016
From: FOMO PRODUCTS, INC.
To: ICP ADHESIVES AND SEALANTS, INC.
Reel/Frame 039479/0889 →
SECURITY INTEREST Recorded Apr 25, 2016
From: FOMO PRODUCTS, INC.
To: MARANON CAPITAL, L.P., AS AGENT
Reel/Frame 038365/0461 →
SECURITY INTEREST Recorded Apr 11, 2016
From: FOMO PRODUCTS, INC.
To: NXT CAPITAL, LLC, AS AGENT
Reel/Frame 038247/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2012
From: TAYLOR, ANTHONY J.
To: FOMO PRODUCTS, INC.
Reel/Frame 029089/0056 →