CATALYST SYSTEM FOR CURING PHENOLIC RESOLE RESINS

Abstract

The present invention relates to a catalyst system which improves the work life of acid-catalyzed resole resins at higher ambient temperatures and provides extended shelf life. The catalyst system comprises an inorganic acid catalyst and one or more polyhydric alcohols. In particular, the present invention relates to a catalyst system wherein the inorganic acid and the alcohol do not convert to an ester when added to the resole resin.

Claims

1. A catalyst system for improving the cure time of acid-catalyzed resole resins at higher ambient temperatures which comprises an inorganic acid and one or more polyhydric alcohols.

2. The catalyst system as claimed in claim 1, wherein the inorganic acid and polyhydric alcohol do not react to form an ester when added to the resole resin.

3. The catalyst system as claimed in claim 1, wherein the inorganic acid is phosphoric acid.

4. The catalyst system as claimed in claim 1, wherein the polyhydric alcohol is glycerol and/or glycol.

5. The catalyst system as claimed in claim 1, which further comprises an amine.

6. The catalyst system as claimed in claim 5, wherein the amine is morpholine.

7. The catalyst system as claimed in claim 1, which further comprises a solvent.

8. The catalyst system as claimed in claim 7, wherein the solvent is water or an aliphatic alcohol.

9. The catalyst system as claimed in claim 1, which comprises phosphoric acid in a range of 20 to 70 wt %, glycol and/or glycerol in a range of 0 to 50 wt %, and water in a range of 0 to 35 wt %.

10. The catalyst system as claimed in claim 9, wherein the weight percentage of phosphoric acid:glycol and/or glycerol:water is in a ratio of 50:20:30.

11. A resole resin comprising the catalyst system as claimed in claim 1.

12. A method for preparation of the resole resin comprising the steps of: preparing a catalyst by mixing an inorganic acid and one or more polyhydric alcohols, mixing a resole resin with the catalyst.

13. The method as claimed in claim 12, wherein the catalyst is prepared by mixing phosphoric acid in a range of 20 to 70 wt %, glycol and/or glycerol in a range of 0 to 50 wt %, and water in a range of 0 to 35 wt %.

14. The method as claimed in claim 13, wherein the weight percentage of phosphoric acid:glycol and/or glycerol:water is in a ratio of 50:20:30.

Description

BRIEF DESCRIPTION OF FIGURES

[0024] FIG. 1: P-31 NMR of the catalyst according to the present invention comprising a phosphoric acid, ethylene glycol, and glycerol.

[0025] FIG. 2: P-31 NMR of the catalyst according to the present invention comprising a phosphoric acid, ethylene glycol, glycerol, and morpholine.

[0026] FIG. 3: P-31 NMR on a 3-month old catalyst according to the present invention to show that there is no ester formation with time. Initially it is a mixture and continues to be a mixture with no ester formation.

[0027] FIG. 4: Comparison of P-31 NMR data for prior art catalyst Phencat-382 wherein the acid and alcohol form an ester and the P-31 NMR of the catalyst of the present invention.

SUMMARY OF INVENTION

[0028] In one aspect, the present invention provides a catalyst system for improving the cure time of acid-catalyzed resole resins at higher ambient temperatures which comprises an inorganic acid and one or more polyhydric alcohols.

[0029] In another aspect, the present invention comprises the resole resin composition comprising the catalyst system and a method for its preparation.

[0030] Yet another embodiment of the present invention comprises a process for the preparation of the resole resin composition comprising the catalyst system of the present invention.

[0031] This invention is based on the objective of increasing the time period for the phenol formaldehyde resole resin to gel and then cure. Once the initiation step is slowed down, the subsequent propagation of the reaction kinetics takes place at a controlled rate. Controlling the reaction kinetics helps in providing slower release of water molecules during the cure that escape out thereby leading to lesser voids on the cured specimen.

[0032] The novel feature includes identifying certain chemical types of compounds that can prolong the gel formation, especially at high ambient temperatures. These are based on small polyhydric, dihydric/trihydric aliphatic alcohols and inorganic acid which are stable and do not react to form an ester.

DETAILED DESCRIPTION

[0033] For the purposes of the following detailed description, it is to be understood that the invention may assume various alternative variations and step sequences.

[0034] Thus, before describing the present invention in detail, it is to be understood that this invention is not limited to particularly exemplified embodiments. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments of the invention only, and is not intended to limit the scope of the invention in any manner.

[0035] The present invention is based upon the finding that specific inorganic acids when employed in conjunction with an alcohol when added to the resole as such without forming the ester result in better advantages with respect to work life when compared with the esters which are known and used in the prior art.

[0036] One embodiment of the present invention provides a catalyst system for improving the cure time of acid-catalyzable resole resins at higher ambient temperatures which comprises an inorganic acid and one or more polyhydric alcohols.

[0037] In a specific embodiment, the inorganic acid and the polyhydric alcohol are added as such to the resole, and these components retain their identity in the resole resin during the storage period without converting to the ester. The above fact is important since it results in catalysts having a better gel time and total curing time than the catalysts having preformed esters. Gel time indicates the time taken for a mixed resin system to gel or become so highly viscous that it can no longer be considered workable, and cure time refers to the time needed to reach optimum viscosity at a certain temperature. Both these factors determine the work life of the resin system.

[0038] Suitable inorganic acids which can be used for the purposes of the present invention include, but are not limited to phosphoric acid, sulfuric acid, nitric acid, hydrochloric acid partially neutralised poly acids, example sodium dihydrogen phosphate

[0039] Examples of polyhydric alcohols which may be used include polyols that can be used to produce the partial phosphate esters include the following or blends of two or more of these:

[0040] Glycerol, glycol, aliphatic di, tri and poly alcohols, pentaerithritol, its derivatives, all alicylic and cyclic mono, di, tri and poly alcohol, polyethylene glycols, inositol, partially methylated polyols like monoglyme, diglyme and other related compounds.

[0041] The ratio of the inorganic acid to the alcohol may vary from 1:1 to 1:10.

[0042] In a specific embodiment, the catalyst system comprises phosphoric acid in a range of 20 to 70 wt %, glycol and/or glycerol in a range of 0 to 50 wt/, and water in a range of 0 to 35 wt %. In a further specific embodiment, the weight percentage of phosphoric acid:glycol and/or glycerol:water is in a ratio of 50:20:30.

[0043] The invention involves an inorganic acid instead of the conventional highly reactive organic acids like para toluene, para xylene or para benzene sulfonic acids or their derivatives.

[0044] Further, in the catalyst system of the present invention, the acid and the alcohol do not react to form the ester as is the case in the prior art, but they retain their identity. The same is evident from the P-31 data provided in FIGS. 1 and 2.

[0045] Further, amines may be added to the above catalyst system. The addition of amines, besides the alcohol and glycerol, gives a more controlled reaction rate that help in lowering the exotherm generated during cure.

[0046] Suitable amines which may be used include, but are not limited to morpholine, aliphatic, aromatic, cyclic, acyclic primary, tertiary and secondary amines, their derivatives, triethylamine, triethanol amine, quaternary ammonium salts e.g. tetramethyl ammonium salt, EDTA, trimethyl aminoethanol, hydrazine, choline, phosphatidylcholine etc.

[0047] The catalyst system may also comprise one or more solvents to make a water based, or solvent based catalyst. Suitable solvents may be chosen from aliphatic alcohols or other polar solvents.

[0048] In an embodiment, phosphoric acid is the inorganic acid, and at least one of glycerine or glycol or their combination is the alcohol. Other acids like alpha olefin sulfonic acids and linear alkylbenzene sulfonic acid are also useful as a catalyst.

[0049] Another embodiment of the invention relates to a resole resin composition capable of being thermally cured and having both a long work life and a fast curing rate, and a method for its preparation.

[0050] The resole resin composition comprises a mixture of (a) a phenol-formaldehyde resole resin, and (b) a catalyst system comprising an inorganic acid and one or more polyhydric alcohols.

[0051] Suitable resoles which may be used include, but are not limited to phenol and formaldehyde, but included are reaction products of all alkyl, aryl, cylic, acylic substituted phenols, cresols and substituted cresols, resorcinol, catechol, para di hydroxy benzenes and their substituted compounds, naphthols, all substituted naphthols and other benzene ring containing aromatic, aliphatic hydroxy, di hydroxyl and poly hydroxyl compounds with formaldehyde resins

[0052] The percentage of the catalyst in the resole may range from 2 to 20%.

[0053] The catalyst of the present invention may be employed as the sole curing (hardening) agent and may constitute about 2-20 weight percent of the phenolic resin solids and more preferably about 8-12 weight percent although higher or lower proportions may be employed depending on specific applications.

[0054] A variety of other modifiers can also be added into the resole resin in order to improve toughness and other cured resin properties. These modifiers include, for example, chain terminating phenols, glycols with or without halogen substitution for additional fire retardancy, polyester polyols, polyether polyols, alkyl phenols, hydroxyl containing acrylates and the like and mixtures thereof. The proportion of such modifiers incorporated into the resole resin composition typically ranges from 5 to 35 weight percent (based on the phenol component). Other modifiers such as fire retardants and fillers can be added to complete the phenolic resole resin composition. Reactive modifiers can be added to the resole resin after it has been formulated such as di- and higher polyols, e.g., di- or polyhydric phenols, resorcinol, phloroglucinol, and the like. Finally, modifiers to achieve special effects in particular applications may be appropriate, e.g., polyvinylbutyrals or epoxies for better impact strength in composites.

[0055] Another component which may be added to the phenolic resole resin compositions of the present invention is an organic solvent. While the resin composition is predominantly aqueous, a variety of organic solvents can be used in diluting the phenolic resole resin composition to a desired solids concentration or viscosity for certain applications. Suitable organic solvents include aromatic solvents including benzene, toluene, xylene, ethylbenzene, and the like, polar solvents such as furfural, furfuryl alcohol, various Cellosolves, carbitols, ketones, and various alcohols such as ethylene glycol, benzyl alcohol and the like. Generally, such organic solvents may constitute up to 50 weight percent of the total solvent, and preferably not more than 25 weight %. For environmental reasons, water is the preferred as the sole solvent.

[0056] Yet another embodiment of the present invention comprises a process for the preparation of the resole resin composition comprising the catalyst system of the present invention by preparing a catalyst by mixing an inorganic acid and one or more polyhydric alcohols, and optionally an amine and mixing a resole resin with the catalyst.

[0057] Most of the consumers in tropical countries do not have a controlled temperature/humidity shop floors to manufacture phenolic components. In the summer months, the ambient shop floor temperature reaches over 40 C. and the existing catalysts do not give sufficient work time to make large size components. The catalysts developed in this invention gives about 3 to 4 times longer work life at high ambient temperatures that would enable customers to make large size components.

[0058] Accordingly, advantages of the present invention include a catalyst system which imparts improved shelf life to resole resin formulations. Another advantage is that the speed of cure of the shelf stable resole formulations also is hastened. A further advantage is the ability to impart improved shelf stability to standard base-catalyzed resole resin used in the industry for acid curing while maintaining cure speed. These and other advantages will be readily apparent to those skilled in the art based upon the disclosure contained herein.

[0059] The following examples are provided to better illustrate the claimed invention and are not to be interpreted in any way as limiting the scope of the invention. All specific materials, and methods described below, fall within the scope of the invention. These specific compositions, materials, and methods are not intended to limit the invention, but merely to illustrate specific embodiments falling within the scope of the invention. One skilled in the art may develop equivalent materials, and methods without the exercise of inventive capacity and without departing fmm the scope of the invention. It is the intention of the inventors that such variations are included within the scope of the invention.

EXAMPLES

All Gel Time Studies are Carried Out at 35-38 C.

Example 1

[0060] A resole resin (AHRF-2794-83) was synthesized from the following ingredients and possessed the following properties:

TABLE-US-00001 TABLE 1 Resole 1 Ingredient Amount Phosphoric acid 1500 g Ethylene glycol 900 g Glycerol 600 g

[0061] Procedure: 1500 g of phosphoric acid (85%) was added to the mixture of ethylene glycol (900 g) and glycerol (600 g). The mixture was cooled using ice water bath.

[0062] 200 g of resin (please specify the resin) was mixed with 16 g of the catalyst prepared above to give the following results:

TABLE-US-00002 Gel Time 30 min Total curing 32 min

Example 2

[0063] A resole resin (AHRF-2794-83 A) was synthesized from the following ingredients and possessed the following properties:

TABLE-US-00003 TABLE 2 Resole 1 Ingredient Amount Phosphoric acid 1500 g Ethylene glycol 900 g Glycerol 600 g Morpholine 120

[0064] 1500 g of phosphoric acid (85%) was added to the mixture of ethyelene glycol (900 g) and glycerol (600 g). The mixture was cooled using ice water bath. Then 150 g of morpholine was added and cooled.

[0065] 200 g of resin (please specify the resin) was mixed with 16 g of the catalyst prepared above to give the following results:

TABLE-US-00004 Gel Time 52 min Total curing 55 min

Example 3

[0066] A resole resin (AHRF-2794-85) was synthesized from the following ingredients and possessed the following properties:

TABLE-US-00005 TABLE 3 Resole 1 Ingredient Amount Phosphoric acid 50 g Ethylene glycol 30 g Glycerol 20 g Morpholine 1.25 g

[0067] Procedure: 50 g of phosphoric acid was added to the mixture of ethyelene glycol (30 g) and glycerol (20 g). 1.25 g of morpholine was added to it. The mixture was cooled using ice water bath.

[0068] 200 g of resin (please specify the resin) was mixed with 16 g of the catalyst prepared above to give the following results:

TABLE-US-00006 Gel Time 1 hour 6 minutes Total curing 1 hour 18 minutes

Example 4

[0069] A resole resin (AHRF-2794-92) was synthesized from the following ingredients and possessed the following properties

TABLE-US-00007 TABLE 4 Resole 1 Ingredient Amount Phosphoric acid 150 g Ethylene glycol 90 g Glycerol 60 g Morpholine 7.25 g

[0070] Procedure: 150 g of phosphoric acid was added to the mixture of ethyelene glycol (30 g) and glycerol (20 g). The mixture was cooled in ice water bath, then 7.5 g of morpholine was added slowly and cooled to room temperature.

[0071] 200 g of resin (please specify the resin) was mixed with 8 g of the catalyst prepared above to give the following results:

TABLE-US-00008 Gel Time 50 minutes Total curing 53 minutes

Example 5 (Prior Art)

[0072] Gel time and Total curing time for prior art catalyst Phencat-382:

TABLE-US-00009 Gel Time 10 min Total curing 12 min

Comparative Example

[0073] In order to evaluate its cure response shelf life, samples of the resoles of the present invention were catalyzed with different catalysts, and subjected to comparative studies as follows:

TABLE-US-00010 POT LIFE TEST VALUES TEMPERATURE OF TESTING - (35-38 C.) Resin: Cellobond: J 2027 X (Batch No. HX477) % pot life Lab note addition of resin + book S. Description of catalyst catalyst reference NO of catalyst to resin mix-minutes page 1 Conventional catalyst 8 10 minutes 2794-90 (Phencat 382) 2 Newly developed catalyst- 8 32 minutes 2794-89 1 (without additive) (AHRF-2794-83) (Batch No. 170731-3 Kg) 3 Newly developed catalyst-2 8 50 minutes 2794-92 (with additive) (AHRF-2794-92) (Batch No. 170802-3 Kg) 4 Newly developed catalyst-3 8 52 minutes 2794-95 (with additive) (AHRF-2794-83A) (Batch No. 170807-3 Kg) 5 Conventional catalyst 6 18 minutes 2794-94 (Phencat 382) 6 Newly developed catalyst- 6 50 minutes 2794-92 1 (without additive) (AHRF-2794-83) (Batch No. 170731-3 Kg) 7 Newly developed catalyst-2 6 95 minutes 2794-94 (with additive) (AHRF-2794-92) (Batch No. 170802-3 Kg)

[0074] The above Table gives the Summary of the invention.

[0075] These results demonstrate the shelf life of the catalyzed resole resin is greater with the inventive catalyst system than with an equivalent resole resin containing only the acid catalyst in twice the amount.