CONCENTRATED SOLUTION OF POLY(FURFURYL ALCOHOL) FOR SIZING ORGANIC OR MINERAL FIBRES

Abstract

An aqueous poly(furfuryl alcohol) solution contains: from 40% to 85% by weight of poly(furfuryl alcohol), from 15% to 60% by weight of water, and less than 1.5% by weight of furfuryl alcohol. The solution exhibits a pH of greater than 7.0, preferably of between 7.2 and 10.0. A process for the manufacture of a product based on mineral or organic fibers which are bonded by an organic binder can use such an aqueous poly(furfuryl alcohol) solution in the diluted form.

Claims

1. An aqueous poly(furfuryl alcohol) solution comprising: from 40% to 85% by weight of poly(furfuryl alcohol), from 15% to 60% by weight of water, and less than 1.5% by weight of furfuryl alcohol, wherein said solution exhibits a pH of greater than 7.0.

2. The aqueous solution as claimed in claim 1, wherein the poly(furfuryl alcohol) and the water together represent at least 95% by weight of the solution.

3. The aqueous solution as claimed in claim 1, wherein the solution contains from 50% to 80% by weight of poly(furfuryl alcohol).

4. The aqueous solution as claimed in claim 1, wherein the solution is devoid of formaldehyde.

5. The aqueous solution as claimed in claim 1, wherein the solution contains less than 1.0% by weight of furfuryl alcohol.

6. The aqueous solution as claimed in claim 1, wherein the solution exhibits a pH of between 7.3 and 9.5.

7. The aqueous solution as claimed in claim 1, wherein a Brookfield viscosity of the solution, determined at 20 C., after adjustment of the dry matter content to 40% by weight, by removal or addition of water, is between 5 and 1000 mPa.Math.s.

8. A process for manufacturing a product based on mineral or organic fibers which are bonded by an organic binder, said process comprising: (a) preparing a binding composition exhibiting a pH of greater than 7 by dilution with water of an aqueous poly(furfuryl alcohol) solution as claimed in claim 1, (b) applying the binding composition to mineral or organic fibers, before or after stage (b), (c) forming an assemblage of mineral or organic fibers, and (d) heating the assemblage of sized mineral or organic fibers until curing of the binding composition.

9. The process as claimed in claim 8, wherein the stage (a) of preparing the binding composition additionally comprises the addition of adjuvants.

10. The process as claimed in claim 8, wherein stage (a) does not comprise the addition of an acid to the aqueous poly(furfuryl alcohol) solution.

11. The process as claimed in claim 8, wherein stage (b) precedes stage (c).

12. The process as claimed in claim 8, wherein the assemblage of mineral or organic fibers is a woven or nonwoven textile, a mat of fibers, a board of fibers or a fiber-based molded product.

13. The process as claimed in claim 8, wherein the binding composition exhibits a dry matter content of between 2% and 20% by weight.

14. The process as claimed in claim 8, wherein the fibers are mineral fibers and the assemblage of mineral fibers exhibits, after the curing stage (d), a loss on ignition (LOI) of between 1% and 20%.

15. The process as claimed in claim 8, wherein stage (d) comprises the heating of the assemblage of fibers at a temperature of between 120 and 250 C. for a time of between 1 and 10 minutes.

16. The aqueous solution as claimed in claim 1, wherein said solution exhibits a pH of between 7.2 and 10.0.

17. The aqueous solution as claimed in claim 1, wherein the poly(furfuryl alcohol) and the water together represent at least 98% by weight of the solution.

18. The aqueous solution as claimed in claim 1, wherein the solution contains from 60% to 77% by weight of poly(furfuryl alcohol).

19. The aqueous solution as claimed in claim 1, wherein the solution contains less than 0.2% by weight of furfuryl alcohol.

20. The aqueous solution as claimed in claim 1, wherein the solution exhibits a pH of between 7.5 and 8.5.

Description

EXAMPLE 1

[0071] Three aqueous poly(furfuryl alcohol) solutions having a dry matter content of 30% are prepared by dilution of BioRez resin (TransFurans Chemicals, Belgium) and then their pH is adjusted by addition of aqueous ammonia (NH.sub.4OH) to a value of 4.9, of 7.1 and of 9.0 respectively.

[0072] A 55 mm6 mm rectangle cut from a filter of nonbonded glass microfibers (Whatman, reference 1822-150) is impregnated with approximately 300 mg of each of these solutions.

[0073] These rectangles impregnated with resin solution are introduced into a dynamic mechanical thermal analysis (DMTA) device and the temperature of the sample holder is gradually increased (4 C./minute), starting from 25 C., up to 250 C., the storage modulus (E) in 3-point bending (frequency of 1 Hz, strain of 0.1%) being continuously measured.

[0074] FIG. 1 shows the change in the storage modulus as a function of the temperature for each of the three samples (pH 4.9, pH 7.1, pH 9.0).

[0075] It may be observed that the crosslinking temperature is essentially the same for the three samples, that is to say that a sample according to the invention exhibiting a pH of 7.1 or of 9.0 crosslinks at the same temperature as a comparative sample at pH 4.9. The storage moduli of the two samples at pH 4.9 and 9.0 are also virtually identical.

[0076] On the other hand, the stability on storage at ambient temperature of these three solutions is highly dependent on the pH. At 25 C., the viscosity of the solution at pH 4.9 doubles in about 21 days, whereas that of the solution at pH 7.1 increases by only 7% during this time and that of the solution at pH 9.0 increases by less than 4% in 21 days.

EXAMPLE 2

[0077] Aqueous poly(furfuryl alcohol) solutions having a dry matter content of 20% are prepared by dilution of BioRez resin and then their pH is adjusted by addition of aqueous ammonia (NH.sub.4OH), of hexamethylenediamine (NMDA) or of polyethyleneimine (PEI, Lupasol FG) to basic pH (see table 1).

[0078] The crosslinking start temperature is determined by dynamic mechanical thermal analysis (DMTA), which makes it possible to characterize the viscoelastic behavior of a polymeric material. Two strips of paper made of glass microfibers are cut out and superimposed. Thirty milligrams of aqueous solution having a dry matter content of 20% are deposited homogeneously over the strips, which are then horizontally attached between two jaws of an RSAIII device (Texas Instruments). An oscillating component equipped with a device for measuring the stress as a function of the strain applied is positioned on the upper face of the sample. The device makes it possible to determine the modulus of elasticity E. The sample is heated to a temperature varying from 20 to 250 C. at the rate of 4 C./min. The curve of variation in the modulus of elasticity E (in MPa) as a function of the temperature (in C.) is plotted from the measurements, the general appearance of the curve being given in FIG. 1.

[0079] The DMTA curves are modelled in three straight-line segments: [0080] 1) tangent to the curve before the start of the reaction, [0081] 2) slope of the straight line during the increase in the modulus during reaction, [0082] 3) tangent to the curve after the end of the increase in the modulus.

[0083] The crosslinking start temperature (CST) is the temperature at the intersection of the first two straight lines.

[0084] The crosslinking start temperature for each of the samples prepared is shown in table 1 below.

TABLE-US-00001 TABLE 1 Crosslinking start temperature Base added pH (DMTA, in C.) None 4.6 119 NH.sub.4OH 7.1 121 NH.sub.4OH 8.8 125 HMDA 7.1 119 HMDA 9.0 122 PEI 7.1 116 PEI 9.0 112

[0085] It is observed that the crosslinking start temperatures are not significantly increased by the addition of base. The system thus retains its reactivity under hot conditions, while being stabilized at ambient temperature.

EXAMPLE 3

[0086] Aqueous poly(furfuryl alcohol) solutions having a dry matter content of 20% are prepared by dilution of BioRez resin and then their pH is adjusted by addition of aqueous ammonia (NH.sub.4OH), of hexamethylenediamine (NMDA) or of polyethyleneimine (PEI, Lupasol FG) to basic pH (see table 2).

[0087] Two series of glass fabrics are respectively impregnated with these aqueous binding compositions and then the fabrics are passed over a suction device which makes it possible to remove the surplus of solution. The impregnated glass fabrics are subsequently cured in a drying oven thermostatically controlled at 220 C. After cooking at 220 C. for 120 and 150 seconds, a sample is subjected to a determination of the tensile strength. For this, the fabrics are cut into bands (250 mm50 mm) and their ends are inserted into the jaws of a tensile testing device.

[0088] The maximum force (in newtons) measured at the moment of failure is shown in table 2.

TABLE-US-00002 TABLE 2 Cooking Maximum force at the pH time moment of failure (N) Biorez 4.6 120 s 93.6 Biorez 4.6 150 s 93.5 Biorez + NH.sub.3 7.1 120 s 92.6 Biorez + NH.sub.3 7.1 150 s 91.9 Biorez + NH.sub.3 8.8 120 s 79.6 Biorez + NH.sub.3 8.8 150 s 85.2 Biorez + HMDA 7.1 120 s 84.2 Biorez + HMDA 7.1 150 s 85.6 Biorez + HMDA 9.0 120 s 80.7 Biorez + HMDA 9.0 150 s 81.3 Biorez + PEI 7.1 120 s 101.8 Biorez + PEI 7.1 150 s 94.7 Biorez + PEI 8.8 120 s 98.4 Biorez + PEI 8.8 150 s 100.6

[0089] It is found that all of the samples prepared exhibit satisfactory tensile strengths. The stabilization of the binder compositions by addition of a base up to basic pH is thus not reflected by a deterioration in the mechanical properties of the finished products.