Method for increasing the reacitivity of lignin, and a resin composition comprising said lignin

Abstract

The present invention relates to a method for increasing the reactivity of lignin which method comprises the following steps; providing a mixture comprising lignin and an alkali solution wherein the concentration of the alkali solution of the mixture is between 5-50% by weight, storing said mixture for a period of at least 1 day whereby the reactivity of the lignin is increased. The present invention also relates to a resin composition comprising said lignin and use of said resin composition.

Claims

1. A method for increasing the reactivity of lignin which method comprises the following steps: providing a mixture consisting of lignin and an alkali solution wherein the concentration of the alkali of the mixture is between 10-50% by weight, storing said mixture for a period of at least 1 day whereby the reactivity of the lignin is increased, wherein the storage is done at room temperature that is between 20-30° C.

2. The method according to claim 1 wherein the lignin is stored for a period of 1 day 12 weeks.

3. The method according to claim 1 wherein the lignin is dissolved in the alkali solution.

4. The method according to claim 1 wherein the mixture comprises 10-80% by weight of lignin.

5. The method according to claim 1 wherein the alkali comprises at least one of sodium hydroxide, potassium hydroxide, calcium hydroxide and magnesium hydroxide.

6. The method according to claim 1 wherein the method comprises the step of separating the lignin from the mixture after storage.

7. A resin composition comprising lignin treated according to the method according to claim 1.

8. The resin composition according to claim 7 wherein the resin is a lignin-phenol-formaldehyde resin.

9. The method according to claim 1 wherein the mixture comprises 25-50% by weight of lignin.

Description

FIGURES

(1) FIG. 1: Shows the viscosity change of mixtures of lignin, phenol, formaldehyde, water and alkali catalyst during heating described in Examples A

(2) FIG. 2: Shows the viscosity change of mixtures of lignin, phenol, formaldehyde, water and alkali catalyst during heating described in Examples B.

(3) FIG. 3: Shows DSC scan of Resin from Example 7.

(4) FIG. 4: Shows DSC scan of Resin from Example 8.

EXAMPLES

Example A

(5) In Example A three different resins samples were prepared and compared. The resins were prepared as described below in Example 1, Example 2 and Example 3. Example 1 describes a resin comprising a lignin stored in alkali for 4 weeks, Example 2 describes a resin comprising a lignin stored in alkali for 8 weeks and Example 3 describes a resin comprising a lignin that has not been stored in alkali as a reference.

Example 1—Activation of Dry Lignin 4 Weeks

(6) Kraft lignin was dissolved at a concentration of 25% (w/w) in 10% NaOH solution and the mixture was stored for 4 weeks at room temperature (20-23° C.).

(7) After storage, lignin was precipitated by lowering the pH. The precipitated lignin was then separated, washed and dried as a powder. Finally, the powder was used as a partial substitute of phenol during synthesis of a phenol-formaldehyde resin. Lignin, phenol, formaldehyde, water and alkali catalyst were mixed. A phenol substitution degree by lignin of 50% was used (by weight) together with a phenol-formaldehyde ratio of 1.8 (by weight). Alkali was added as a 45% solution (by weight) at alkali-to-phenol ratio of 0.5 (by weight). Additional water was added to reach a final solid content of 47-48% (by dry weight). The mixture was then heated to 80° C. until a final viscosity of ˜500 cP was achieved. Viscosity was measured by using a Brookfield DV-II+LV viscometer which was kept at 25° C. by using a recirculation water bath. Samples were withdrawn from the reaction vessel, cooled and the viscosity was obtained.

Example 2—Activation of Dry Lignin 8 Weeks

(8) Kraft lignin was dissolved at a concentration of 25% (w/w) in 10% NaOH solution and the mixture was stored for 8 weeks at room temperature (20-23° C.).

(9) After storage, lignin was precipitated by lowering the pH. The precipitated lignin was then separated, washed and dried as a powder. Finally, the powder was used as a partial substitute of phenol during synthesis of a phenol-formaldehyde resin as described in Example 1.

Example 3—Comparative Example

(10) Kraft lignin powder from lignin that has not been subjected to alkali storage was used as a partial substitute of phenol during synthesis of a phenol-formaldehyde resin. Lignin, phenol, formaldehyde, water and alkali catalyst were mixed. A phenol substitution degree by lignin of 50% was used (by weight) together with a phenol-formaldehyde ratio of 1.8 (by weight). Alkali was added as a 45% solution (by weight) at alkali-to-phenol ratio of 0.5 (by weight). Additional water was added to reach a final solid content of 47-48% (by dry weight). The mixture was then heated to 80° C. until a final viscosity of ˜500 cP was achieved.

(11) The viscosity of the resins described in Examples 1-3 are shown in FIG. 1. The improved reactivity of resins comprising the stored lignin was observed as the viscosity increase was substantially faster compared to the resin comprising the lignin which was not subjected to storage in alkali.

Example B

(12) In Example B two different resins samples were prepared and compared. The resins were prepared as described below in Example 4 and Example 5. Example 4 describes a resin comprising a lignin stored in alkali for 1 week and Example 5 describes a resin comprising a lignin that has not been stored in alkali as a reference.

Example 4—Activation of Lignin in Alkali 1 Week

(13) Lignin-phenol-formaldehyde resin was synthesized in two steps. In the first step, lignin dispersion was prepared by mixing of 42.6 g of lignin (96% lignin), 37.4 g of water and 23 g of 45% sodium hydroxide solution for 90 minutes in a glass reactor equipped with condenser, overhead stirrer and thermometer. The lignin dispersion was stored for 1 week at room temperature.

(14) In the 2nd step, the stored lignin, 40 g of phenol and 110 g of 37% formaldehyde solution were added to the glass reactor and mixed. The pH of the solution was adjusted to 11.5 with the addition of an aqueous solution of 45% sodium hydroxide. The reaction mixture was cooked at 80° C. until the viscosity of the reaction mixture reached a certain viscosity. The viscosity was measured at 25° C. using a Brookfield DV-II+LV viscometer. After the reaction mixture reached the certain viscosity, it was cooled rapidly to room temperature using a cold water bath.

Example 5: Comparative Example Ratio

(15) Lignin-phenol-formaldehyde resin was synthesized with a degree of substitution of the phenol with lignin equal to about 50% by weight. In the first step, lignin dispersion was prepared by mixing of 42.6 g of lignin (96% lignin), 40 g of phenol, 37.4 g of water and 110 g of 37% formaldehyde solution for 90 minutes in a glass reactor equipped with condenser, overhead stirrer and thermometer. In the 2nd step, the pH of the solution was adjusted to 11.5 with the step-wise addition of an aqueous solution of 45% sodium hydroxide (42 g). The reaction mixture was cooked at 80° C. until the viscosity of the reaction mixture reached a certain viscosity. The viscosity was measured at 25° C. using a Brookfield DV-II+LV viscometer. After the reaction mixture reached the certain viscosity, it was cooled rapidly to room temperature using a cold water bath.

(16) Results from Example B are shown in FIG. 2. The improved reactivity of the resin comprising stored lignin was observed as the viscosity increase was substantially faster compared to the resin comprising the lignin which was not subjected to storage in alkali.

Example C

(17) In this example the gel time of resins comprising lignin that have been stored at different alkali charges and for different times were investigated. The gel time of the final resins in each example were investigated by mean of gel time analysis according to ISO 9396.

(18) The gel times for the resins described in Examples 5-8 were compared. Example 5 describes a resin comprising a lignin that was not stored in alkali (see preparation of the resin above), Example 6 describes a resin comprising lignin stored at a high alkali concentration for 1 week, Example 7 describes a resin comprising lignin stored at a low alkali concentration for 1 week and Example 8 describes a resin comprising lignin stored at a high alkali concentration for 1 day.

Example 6—High Alkali Storage 1 Week

(19) Lignin-phenol-formaldehyde resin, with a degree of substitution of the phenol with lignin equal to about 50% by weight, for preparing plywood panel was cooked in a 5 L glass reactor.

(20) In the first step, lignin dispersion was prepared by mixing of 463 g of lignin (95% lignin), 411 g of water and 253 g of 45% sodium hydroxide solution for 90 minutes in the glass reactor, giving a final alkali concentration of 10% w/w. After mixing for 90 minutes, the lignin dispersion was stored for 1 week at room temperature.

(21) After storage, the lignin dispersion, 444 g of phenol and 1210 g of 37% formaldehyde solution were added to the glass reactor. The temperature of the reaction mixture was increased to 60° C. and kept constant for 30 minutes. Then, the temperature was increased to 80° C. and the viscosity was measured at 25° C. using a Brookfield viscometer. The temperature of the reaction mixture was maintained at 80° C. until it reached a viscosity of 350-450 cP.

(22) At this stage, an additional amount of 187 g of 45% sodium hydroxide solution was added to the mixture giving the pH of 11.3-11.5 and the reaction temperature was lowered to 75° C. When the desired viscosity (400-450 cP) was achieved, the reaction was cooled down to room temperature (20° C.).

Example 7: Low-Alkali Storage for 1 Week

(23) Lignin-phenol-formaldehyde resin, with a degree of substitution of the phenol with lignin equal to about 50% by weight, for preparing plywood panel was cooked in a 5 L glass reactor.

(24) In the first step, lignin dispersion was prepared by mixing of 463 g of lignin (95% lignin), 411 g of water and 98 g of 45% sodium hydroxide solution for 90 minutes in the glass reactor giving a final alkali concentration of 4% w/w. After mixing for 90 minutes, the lignin dispersion was stored for one week at room temperature.

(25) After storage, the lignin dispersion, 155 g 45% alkali solution, 444 g of phenol and 1210 g of 37% formaldehyde solution were added to the glass reactor. The temperature of the reaction mixture was increased to 60° C. and kept constant for 30 minutes. Then, the temperature was increased to 80° C. and the viscosity was measured at 25° C. using a Brookfield viscometer. The temperature of the reaction mixture was maintained at 80° C. until it reached a viscosity of 350-450 cP.

(26) At this stage, an additional amount of 187 g of 45% sodium hydroxide solution was added to the mixture giving the pH of 11.3-11.5 and the reaction temperature was lowered to 75° C. When the desired viscosity (400-450 cP) was achieved, the reaction was cooled down to room temperature (20° C.).

Example 8: High Alkali Storage for 1 Day

(27) Lignin-phenol-formaldehyde resin, with a degree of substitution of the phenol with lignin equal to about 50% by weight, for preparing plywood panel was cooked in a 5 L glass reactor.

(28) In the first step, lignin dispersion was prepared by mixing of 463 g of lignin (95% lignin), 411 g of water and 253 g of 45% sodium hydroxide solution for 90 minutes in the glass reactor giving a final alkali concentration of 10% w/w. After mixing for 90 minutes, the lignin dispersion was stored for one day at room temperature.

(29) After storage, the lignin dispersion, 444 g of phenol and 1210 g of 37% formaldehyde solution were added to the glass reactor. The temperature of the reaction mixture was increased to 60° C. and kept constant for 30 minutes. Then, the temperature was increased to 80° C. and the viscosity was measured at 25° C. using a Brookfield viscometer. The temperature of the reaction mixture was maintained at 80° C. until it reached a viscosity of 350-450 cP. At this stage, and additional amount of 187 g of 45% sodium hydroxide solution was added to the mixture giving the pH of 11.3-11.5 and the reaction temperature was lowered to 75° C. When the desired viscosity (400-450 cP) was achieved, the reaction was cooled down to room temperature (20° C.).

(30) The results of the gel time for the different resins investigated in Example C are shown in Table 1.

(31) TABLE-US-00001 TABLE 1 Gel time of resin from Examples 5-8 Samples Gel time (min) Resin from Example 5 67 Resin from Example 6 27 Resin from Example 7 65 Resin from Example 8 26

(32) As can be seen in Table 1, storage of lignin in low-alkali conditions is detrimental to the reduction of gel time for the resins while the positive effects of gel time for the resins comprising lignin stored in high-alkali conditions can be seen already after 1 day of storage.

Example D

(33) In this Example a thermal analysis of the resins were investigated. Differential scanning calorimetry (DSC) for two different resins described in Example 9 and Example 10 were done.

(34) Example 9 describes a resin comprising lignin that was stored for two weeks at high alkali concentrations and Example 10 describes a resin comprising lignin that was not stored as a reference sample.

Example 9: Synthesis of Resin for Plywood Production

(35) Lignin-phenol-formaldehyde resin, with a degree of substitution of the phenol with lignin equal to about 50% by weight, for preparing plywood panel was cooked in a 5 L glass reactor.

(36) In the first step, lignin dispersion was prepared by mixing of 463 g of lignin (95% lignin), 411 g of water and 253 g of 45% sodium hydroxide solution for 90 minutes in a glass reactor equipped with condenser, overhead stirrer and thermometer. After mixing for 90 minutes, the lignin dispersion was stored for two weeks at room temperature.

(37) After storage, the lignin dispersion, 444 g of phenol and 1210 g of 37% formaldehyde solution were added to the glass reactor. The temperature of the reaction mixture was increased to 60° C. and kept constant for 30 minutes. Then, the temperature was increased to 80° C. and the viscosity was measured at 25° C. using a Hoppler viscometer. The temperature of the reaction mixture was maintained at 80° C. until it reached a viscosity of 350-450 cP. At this stage, an additional amount of 187 g of 45% sodium hydroxide solution was added to the mixture giving the pH of 11.3-11.5 and the reaction temperature was lowered to 75° C. When the desired viscosity (400-450 cP) was achieved, the reaction was cooled down to room temperature (20° C.). The resin was thereafter used for plywood manufacturing and testing.

Example 10: Synthesis of Resin for Plywood Production—Comparative Example

(38) Lignin-phenol-formaldehyde resin for preparing plywood panel was cooked in a 5 L glass reactor.

(39) Firstly, 463 g of lignin (95% lignin), 444 g of phenol, 411 g of water and 1210 g of 37% formaldehyde solution were added to the glass reactor equipped with condenser, overhead stirrer and thermometer.

(40) Secondly, 253 g of NaOH solution (45%) was added slowly to prevent excessive heat development and giving a pH of 10.2-10.5. The temperature was kept constant at 60° C. for 30 minutes and was then increased to 80° C. The viscosity was measured at 25° C. using a Hoppler viscometer. The temperature of the reaction mixture was maintained at 80° C. until it reached a viscosity of 400-450 cP.

(41) At this stage, more 187 g of sodium hydroxide solution was added to the mixture giving the pH of 11.3-11.5 and the reaction temperature was lowered to 75° C. When the desired viscosity (400-450 cP) was achieved, the reaction was cooled down to room temperature (20° C.).

(42) The final resin was investigated by DSC. The resin was used for plywood manufacturing and testing.

(43) The DSC scan of the resins described in Example 9 is shown in FIG. 3 and the DSC scan of the resin described in Example 10 is shown in FIG. 4. As can be seen in the DSC analysis, the resin in Example 9 displayed a thermogram with only one distinguishable exothermic signal (at 128° C.) while the resin from the Comparable Example 10 produced two peaks (111° C. and 140° C.). Presence of additional signals in the exothermic peak is a clear indication of a non-uniform curing behavior where interfering side-reactions are occurring.

(44) Furthermore, the gel time of the resins in Example 9 and Example 10 were investigated by mean of gel time analysis according to ISO 9396. The results can be found in Table 2.

(45) TABLE-US-00002 TABLE 2 Gel time of resin from Examples 9-10 Samples Gel time (min) Resin from Example 9 28 Resin from Example 10 57

(46) Combining the results from the DSC with the clearly observed reduction in gel time in Table 2 it is thus evident that the lignin composition used in Example 9 has been activated as the final resin displays had a significant faster rate of curing.

Example E

(47) In this example Plywood was produced with the resins described in Example 9 and Example 10 as described above.

Example 11: Plywood Production

(48) Veneers were sawn to 550×550 mm.sup.2 size and conditioned in 20° C., 65% RH prior to manufacture. Glues comprising resin from Examples 9 and 10 were formulated according to Table 3.

(49) TABLE-US-00003 TABLE 3 Composition of glue for Plywood board Component Amount [%] Resin from Example 9 and Example 10 77.5 Water 8 Olive seed flour 10.7 NaOH (35%) 3.8

(50) Target glue content was 180 g glue/m.sup.2 which was spread on one side. Hot pressing was performed at 140° C. with a pressure of 1 MPa, with repeated release of steam during the first 4 minutes. The total pressing time was 10 minutes. After hot-pressing, the boards were cooled between two aluminum plates at room temperature.

(51) Prior to evaluation all samples were conditioned according to EN636 class 3 test method. Shear strength was evaluated according to EN314 test method. Average data from 3 boards is presented in Table 4.

(52) TABLE-US-00004 TABLE 4 Plywood board shear strength Board resin Shear Strength (MPa) Average Ex. 9 1.52 Ex. 10 1.38

(53) From Table 4 it is evident that the plywood board based on the resin where the lignin composition has been subjected to storage displays similar and even somewhat improved physical characteristics as compared to the reference resin where the lignin was not subjected to storage.

(54) In view of the above detailed description of the present invention, other modifications and variations will become apparent to those skilled in the art. However, it should be apparent that such other modifications and variations may be effected without departing from the spirit and scope of the invention.