IP Library Patent Application 17705786
Patent Application
App. No. 17/705,786

PHENOLIC RESIN COMPOSITIONS AS BINDERS IN REFRACTORY ARTICLES

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Patent No.
US None
App. No.
17/705,786
Abstract

A liquid phenolic resin composition for use as a binder for a refractory article, the phenolic resin composition comprising a phenol formaldehyde resin, wherein the phenolic resin composition has a reduced vaporization percentage of phenolic compounds. The phenolic resin composition is used in refractory compositions comprising at least 50 wt. % of one or more refractory aggregate(s), based on a total weight of the refractory composition. There is also disclosed a refractory article, such as a brick, formed into a shape comprising said refractory composition and heating until the phenolic resin composition is at least 20% cured and having a green strength after curing at 170° C. for 5 hours sufficient for handling the solid without falling apart. Ladles for transporting and pouring molten metals can be made with an inner liner formed by stacking at least two bricks along the bottom and sides of a ladle shaped metal outer liner, and then heating the stacked bricks to a temperature sufficient to carbonize the resin thereby forming the inner liner of the ladle.

Claims (49)

1 . A liquid phenolic resin composition for use as a binder for a refractory article, the phenolic resin composition comprising a phenol formaldehyde resin,

wherein the phenolic resin composition has a vaporization percentage of phenol of less than 4.1% as measured by the following steps:

(a) curing 5 grams of liquid resin at 170° C. for 5 hours to form a solid;

(b) cooling the solid to room temperature and then weighing 1 gram of the solid;

(c) heating the 1 gram of solid in a tube furnace from room temperature to 1000° C. at 15° C./minute, and then being held at 1000° C. under an inert atmosphere for 10 minutes to form a vaporized composition;

(d) collecting the vaporized composition that vaporizes off from the solid in step (c);

(e) quantifying the amount of phenol that vaporized from the solid in step (c); and

(f) determining the amount of the vaporized phenol as a percentage of the 1 gram of cooled solid in step (b).

2 . The phenolic resin composition according to claim 1 , wherein the phenolic resin composition meets one or more of the following properties:

e) viscosity is 50-10,000 cPs, as measured with a Brookfield RVF viscometer using a No. 1 spindle at 20 rpm, at 25° C.;

f) pH is 7 to less than 11;

g) nonvolatile content is 65-85 wt. %; and

h) free formaldehyde of less than about 0.3 wt. %.

3 . The phenolic resin composition according to claim 1 , wherein the vaporization percentage of the phenol is less than Reference Sample R-1 as measured during a step of heating the phenolic resin composition to at least 1000° C.

4 . The phenolic resin composition according to claim 1 , wherein the number average molecular weight (Mn) of the phenol formaldehyde resin is less than 3000 g/mol as measured by gel permeation chromatography (GPC), or the weight average molecular weight (Mw) of the phenol formaldehyde resin is less than 5000 g/mol, as measured by GPC, or the phenol formaldehyde resin has a polydispersity (Mw/Mn) is less than 10.

5 . A liquid phenolic resin composition for use as a binder for a refractory article, the phenolic resin composition comprising a phenol formaldehyde resin formed from one or more phenolic compound(s) (P) and one or more formaldehyde compound(s) (F), wherein the phenol formaldehyde resin is optionally formed in the presence of a reaction catalyst, said phenolic resin composition has the following feature (I) and/or (II), wherein

feature (I) the phenol formaldehyde resin has a molar ratio (MR) of F to P of greater than 1.2, and

feature (II) the phenolic resin composition further comprises one or more vapor suppressant(s).

6 . The phenolic resin composition according to claim 5 , wherein the phenolic resin composition has a vaporization percentage of (P) as measured by the following steps:

(a) curing 5 grams of liquid resin at 170° C. for 5 hours to form a solid;

(b) cooling the solid to room temperature and then weighing 1 gram of the solid;

(c) heating the 1 gram of solid in a tube furnace from room temperature to 1000° C. at 15° C./minute, and then being held at 1000° C. under an inert atmosphere for 10 minutes to form a vaporized composition;

(d) collecting the vaporized composition that vaporizes off from the solid in step (c);

(e) quantifying the amount of (P) that vaporized from the solid in step (c); and

(f) determining the amount of the vaporized (P) as a percentage of the 1 gram of cooled solid in step (b);

wherein the vaporization percentage of the one or more phenolic compounds which is less than a reference phenolic resin composition lacking both features (I) and (II).

7 . The phenolic resin composition according to claim 6 , wherein the vaporization percentage of the (P) is less than 4.1%.

8 . The phenolic resin composition according to claim 5 , wherein the phenolic resin composition meets one or more of the following properties:

a) viscosity is 50-10,000 cPs, as measured with a Brookfield RVF viscometer using a No. 1 spindle at 20 rpm, at 25° C.;

b) pH is 7 to less than 11;

c) nonvolatile content is 65-85 wt. %; and

d) free formaldehyde of less than about 0.3 wt. %.

9 . The phenolic resin composition according to claim 5 , wherein the vaporization percentage of the (P) is less than Reference Sample R-1.

10 . The phenolic resin composition according to claim 1 , wherein the phenolic resin composition further comprises one or more vapor suppressant(s) selected from magnesium-containing compound; manganese-containing compound; iron-containing compound; cobalt-containing compound; nickel-containing compound; copper-containing compound; tin-containing compound; phosphorus-containing compound; silicon-containing compound; aluminum-containing compound; zinc-containing compound; molybdenum-containing compound; boron-containing compound; zirconium-containing compound; vanadium-containing compound; chromium-containing compound, calcium-containing compound, tungsten-containing compound, titanium-containing compound, niobium-containing compound, cerium-containing compound and mixtures thereof, or wherein the one or more vapor suppressant(s) is one or more plant-based component(s).

11 . The phenolic resin composition according to claim 1 , wherein the phenolic resin composition further comprises one or more vapor suppressant(s) present in an amount of 0.01 to 20 parts by weight per 100 parts by weight of the phenolic resin composition.

12 . The phenolic resin composition according to claim 5 , wherein the phenolic resin composition further comprises one or more vapor suppressant(s) selected from magnesium-containing compound; manganese-containing compound; iron-containing compound; cobalt-containing compound; nickel-containing compound; copper-containing compound; tin-containing compound; phosphorus-containing compound; silicon-containing compound; aluminum-containing compound; zinc-containing compound; molybdenum-containing compound; boron-containing compound; zirconium-containing compound; vanadium-containing compound; chromium-containing compound, calcium-containing compound, tungsten-containing compound, titanium-containing compound, niobium-containing compound, cerium-containing compound and mixtures thereof, or wherein the one or more vapor suppressant(s) is one or more plant-based component(s).

13 . The phenolic resin composition according to claim 12 , wherein the phenolic resin composition further comprises one or more vapor suppressant(s) present in an amount of 0.01 to 20 parts by weight per 100 parts by weight of the phenolic resin composition.

14 . The phenolic resin composition according claim 1 , further comprising one or more adhesion promotor(s).

15 . The phenolic resin composition according claim 14 , wherein the one or more adhesion promotor(s) is one or more silane coupling agent(s).

16 . The phenolic resin composition according claim 5 , wherein the phenolic resin composition has the feature (I) the phenol formaldehyde resin has a molar ratio (MR) of F to P of greater than 1.2 and further comprises one or more adhesion promotor(s).

17 . The phenolic resin composition according claim 16 , wherein the one or more adhesion promotor(s) is one or more silane coupling agent(s).

18 . A refractory composition comprising the phenolic resin composition according to claim 1 and at least 50 wt. % of one or more refractory aggregate(s), based on a total weight of the refractory composition.

19 . A refractory composition comprising the phenolic resin composition according to claim 5 and at least 50 wt. % of one or more refractory aggregate(s), based on a total weight of the refractory composition.

20 . A refractory article formed into a shape comprising said refractory composition according to claim 18 and heating until the phenolic resin composition is at least 20% cured and having a green strength after curing at 170° C. for 5 hours sufficient for handling the solid without falling apart.

21 . A refractory article formed into a shape comprising said refractory composition according to claim 19 and heating until the phenolic resin composition is at least 20% cured and having a green strength after curing at 170° C. for 5 hours sufficient for handling the solid without falling apart.

22 . The refractory article according to claim 20 , wherein the article is a brick.

23 . The refractory article according to claim 21 , wherein the article is a brick.

24 . A ladle for transporting and pouring molten metals, wherein said ladle is formed with an inner liner formed by stacking at least two bricks according to claim 22 along the bottom and sides of a ladle shaped metal outer liner, and then heating the stacked bricks to a temperature sufficient to carbonize the resin thereby forming the inner liner of the ladle.

25 . A ladle for transporting and pouring molten metals, wherein said ladle is formed with an inner liner formed by stacking at least two bricks according to claim 23 along the bottom and sides of a ladle shaped metal outer liner, and then heating the stacked bricks to a temperature sufficient to carbonize the resin thereby forming the inner liner of the ladle.

Assignments (7)
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Apr 22, 2026
From: ARCLIN USA LLC; THE WILLAMETTE VALLEY COMPANY LLC; ECLECTIC PRODUCTS LLC; RG DISPERSANTS USA LLC; POLYMER SOLUTIONS GROUP; FLOW POLYMERS, LLC; ARCLIN SURFACES INC.; SASCO CHEMICAL GROUP, LLC; POLYMER SOLUTIONS GROUP FINANCE, LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 075436/0160 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Apr 22, 2026
From: ARCLIN USA LLC; THE WILLAMETTE VALLEY COMPANY LLC; ECLECTIC PRODUCTS LLC; RG DISPERSANTS USA LLC; POLYMER SOLUTIONS GROUP; FLOW POLYMERS, LLC; ARCLIN SURFACES INC.; SASCO CHEMICAL GROUP, LLC; POLYMER SOLUTIONS GROUP FINANCE, LLC
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 075436/0117 →
CHANGE OF ASSIGNEE ADDRESS Recorded Feb 19, 2024
From: ARCLIN USA LLC
To: ARCLIN USA LLC
Reel/Frame 066624/0673 →
NOTES PATENT SECURITY AGREEMENT Recorded May 25, 2023
From: HARBISONWALKER INTERNATIONAL, INC.; HARBISONWALKER INTERNATIONAL HOLDINGS, INC.; HARBISONWALKER INTERNATIONAL MINERALS, INC.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 063784/0481 →
SECURITY AGREEMENT Recorded May 25, 2023
From: HARBISONWALKER INTERNATIONAL, INC.; HARBISONWALKER INTERNATIONAL HOLDINGS, INC.; HARBISONWALKER INTERNATIONAL MINERALS, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 063783/0851 →
BNPP PATENT SECURITY AGREEMENT Recorded May 25, 2023
From: HARBISONWALKER INTERNATIONAL, INC.; HARBISONWALKER INTERNATIONAL HOLDINGS, INC.; HARBISONWALKER INTERNATIONAL MINERALS, INC.
To: BNP PARIBAS
Reel/Frame 063784/0283 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2022
From: PENDALWAR, SHEKHAR L.; WRIGHT, JAMES T.; ARTHUR, LISA M.; RIEDLINGER, DARREN A.; CELIKBAG, YUSUF; VENTZ, TOMASZ
To: HARBISONWALKER INTERNATIONAL HOLDINGS, INC.; ARCLIN USA LLC
Reel/Frame 059435/0526 →