Patent Application
20070151686
The present invention relates to the use of protein hydrolysate derived from keratin-containing material in the wet-end of a papermaking process, a process for preparing a paper product, and paper pulp and paper products comprising such a protein hydrolysate additive.
In the papermaking industry a wide variety of additives is applied to improve properties of the finished paper product. Such properties include, for instance, printability, wet/dry strength, softness and wetting properties. Generally, the amounts of additives to be used need to be carefully controlled because most of these additives are expensive chemicals.
Object of the present invention is to provide a new class of cheap additives, which can attractively be used in the production of paper products.
Surprisingly, it has now been found that protein hydrolysate derived from keratin-containing material can attractively be used as a paper product additive with high retention.
Accordingly, the present invention relates to the use of a protein hydrolysate derived from keratin-containing material as an additive in the wet-end of a papermaking process.
The present invention enables the production of very high quality paper products in a very cost-effective manner. The paper products obtained in accordance with the present invention display excellent quality properties in terms of strength and volume per mass.
It will be appreciated that with the term wet-end is meant the stage of the papermaking process prior to the dry-end stage (the stage where the paper product to be made is dried).
The protein hydrolysate to be used in accordance with the present invention can be derived from a wide variety of keratin-containing materials. The keratin-containing materials can suitably be derived from mammals and/or birds. Suitable keratin-containing materials from which the protein hydrolysate can be derived include mammalian hair, animal hooves, claws, horns, and feathers. The protein hydrolysate is preferably derived from mammalian hair and/or feathers. More preferably, the protein hydrolysate is derived from mammalian hair, in particular from livestock, and more particularly from pigs and chicken feathers.
The protein hydrolysate to be used in accordance with the present invention can suitable be prepared by subjecting the keratin-containing material to an oxidation treatment in which the keratin-containing material is contacted with a solution, which comprises a bleaching agent. The solution to be used in the oxidation treatment has been made alkaline (above pH 7) or acidic (below pH 7). Preferably, the solution has been made alkaline by the addition of NaOH, KOH and/or NH4OH or acidic by the addition of one or more (organic) acid(s). A wide variety of (organic) acids can be used, including acetic acid and formic acid.
The pH value of the alkaline solution to be used in step (a) is preferably in the range of from 9-13, more preferably in the range of from 10-12. The pH value of the acidic solution is preferably in the range of from 3-7, more preferably in the range of from 4-6.
Suitable bleaching agents include organic and inorganic peroxides. Preferably, use is made of a bleaching agent selected from the group of hypohalides, perborates, percarbonates, organic peroxides, or hydrogen peroxide. More preferably, the bleaching agent comprises hydrogen peroxide. One single bleaching agent or a mixture of bleaching agents can suitably be applied in the alkaline or acidic solution. In the alkaline solution preferably inorganic peroxides are used, whereas in the acidic solution preferably organic peroxides are used. Suitably, the bleaching agent is used in an amount in the range of from 0.1% (w/w) to 40% (w/w), preferably in the range of from 0.3% (w/w) to 30% (w/w), based on total alkaline or acidic solution.
In the oxidation treatment the keratin-containing material can suitably be contacted with the alkaline or acidic solution over a period of time in the range of from 5 minutes to 16 hours, preferably in the range of from 15 minutes to 10 hours. The temperature to be applied in the oxidation treatment can suitably be in the range of from room temperature to 100° C., preferably in the range of from 30° C. to 80° C.
The keratin-containing material can be one type of keratin-containing material or it can be a mixture of different types of keratin-containing materials.
The keratin-containing material to be subjected to the oxidation treatment is preferably first subjected to a washing step in which soluble components, such as for instance blood, urine remnants and other animal components, are removed from the keratin-containing material before the keratin-containing material is subjected to the oxidation step. The protein hydrolysate obtained in the oxidation treatment and contained in the solution can subsequently be recovered by separating it from the remaining keratin-containing material. This can be established by means of known techniques. For this purpose use can, for instance, be made of a conventional filtering system. In this way a solution of the protein hydrolysate can be obtained. In order to recover the protein hydrolysate from the protein hydrolysate solution so obtained, the pH value of the solution can suitably be adjusted so as to allow the protein hydrolysate to precipitate, after which the protein hydrolysate precipitate can be recovered by methods known per se. The pH of the solution is preferably adjusted so as to be in the range of from 1 to 5, more preferably to be in the range of 2 to 4. The pH adjustment can be established by adding in a controlled manner, for instance by way of titration, an organic and/or inorganic acid to the solution. Suitable acids include hydrochloric acid, sulphuric acid, acetic and formic acid, and the like.
Suitably, the pH adjustment can be carried out over a period of time in the range of from 5 minutes to 10 hours, preferably in the range of from 20 minutes to 8 hours The temperature to be applied during the pH adjustment can suitably be in the range of from 15° C. to 100° C., preferably in the range of from 25° C. to 70° C.
Suitably, the protein hydrolysate precipitate obtained can be dissolved in a liquid medium to obtain a solution, which can be used as a paper product additive. Such a liquid medium suitably includes virgin and/or recycled cellulose fibres and/or known additives used in the wet-end of the paper process. Preferably, water or recycled water is used as the liquid medium. To the protein hydrolysate solution so obtained one or more other paper product additives can be added before the solution is used to produce a paper product. These other additives may contribute to different properties of the paper product to be obtained. The concentration of the protein hydrolysate will suitably be in the range of from 0.1% (w/w) to 50% (w/w), based on total fibre weight. Preferably, the concentration of the protein hydrolysate is in the range of from 0.3% (w/w) to 40% (w/w), based on total fibre weight.
Alternatively, the protein hydrolysate precipitate can as such be added to a solution containing one or more other additives to be used in the manufacturing of a paper product. In another suitable embodiment the protein hydrolysate precipitate is added directly to the paper pulp where after it is thoroughly mixed with other paper pulp components.
Preferably, the protein hydrolysate additive is used in the form of a solution.
The present invention also relates to a process for preparing a paper pulp comprising mixing in the wet-end a protein hydrolysate derived from keratin-containing material with virgin and/or recycled cellulose fibres, and recovering the paper pulp so obtained.
The present invention also relates to paper pulp obtainable by such a process. Suitably, such paper pulp comprises protein hydrolysate derived from keratin-containing material in an amount in the range of from of from 0.1 to 50 wt. %, based on total paper pulp. Preferably, such paper pulp comprises protein hydrolysate derived from keratin-containing material in an amount in the range of from 0.3 to 40 wt. %, based on total paper pulp.
The present invention further relates to a process for preparing a paper product comprising mixing the wet-end of a papermaking process a protein hydrolysate derived from keratin-containing material with virgin and/or recycled cellulose fibres, dewatering the mixture so obtained, pressing the dewatered material, drying the pressed material, and recovering the paper product so obtained.
Further, the present invention also relates to a paper product obtainable by such a process. Suitably, such paper product comprises protein hydrolysate derived from keratin-containing material in an amount in the range of from 0.1 to 50 wt. %, based on total paper product. Preferably, such paper product comprises protein hydrolysate derived from keratin-containing material in an amount in the range of from 0.3 to 40 wt. %, based on total paper product.
In the context of the present invention the term “paper product” is meant to include all sorts of papers, such as printing paper, tissue/hygiene, newspaper, office paper, specialties, but also materials such as cardboard, folding board, box board, undulated board, corrugated board, and 3D board and the like.
Preparation of Protein Hydrolysate.
To a mixture of 250 grams of hair was added 9 litres of water and subsequently the pH of the mixture was brought to a level suitable for bleaching. Then the temperature of the mixture was raised to 65-70° C. and 200 ml of a 30% (w/w) solution of hydrogen peroxide (pH 11) or 60 ml of a 32% (w/w) of peracetic acid (pH 5) was added. The mixture was then stirred for 16 hours after which the hydrolysate was isolated by lowering the pH of the reaction mixture to 3. Once the precipitate was formed it was collected through filtration and dried at 70° C. After drying, the obtained product may optionally be grinded into a powder.
Evaluation of the Protein Hydrolysate
The hydrolysate (0, 1, 5, 10, 15% (w/w)) was mixed with virgin cellulose fibres from Eucalyptus in such a way that for each mixture a constant weight of cellulose fibres was obtained. Also sheets were using only the virgin Eucalyptus cellulose fibres for comparison and evaluation results are depicted as 0% (w/w). The sheets were obtained by using a FRET (Formation and Retention Tester), using a vacuum of 0.5 bar. The sheets were dried at 100° C., using a Rapid Köthen drying cell. For each mixture three sheets were made.
From each mixture the paper properties were determined
Retention of the Protein Hydrolysate
Hand sheets were made on a Rapid Köthen (RK) sheet former as described above, and 360 mg of the keratine hydrolysate were added to the reservoir of the RK containing the fibre mixture (about 5 gram). Afterwards the filtrate (7 litres) was analysed according to the method of Bradfort on the protein content. It was measured that 0.722 mg/l was left in the filtrate. From this data it can be concluded that no less than 98.6% of the keratine hydrolysate was retained on the fibre.
Volume Per Mass (cm3/gram):
The volume per mass was calculated by dividing the thickness of the sheet by weight per m2. Table 1 gives the results of the different sheets
The volume per mass was reduced with increase of % protein hydrolysate. It seems that the protein hydrolysate was able to fill the pores formed by the cellulose fibre web.
Porosity:
The effect of the addition of protein hydrolysate is depicted in
Short Compression Test:
The influence of protein hydrolysate as additive in cellulose pulp on the SCT index is depicted in
Z-Directional Tensile:
The influence of protein hydrolysate on the Z-directional tensile is depicted in
Tensile Index:
This parameter is measured to evaluate the force at break and gives an indication of the length of the paper needed before it breaks.
Stretch at Break:
This parameter gives an indication of the amount of stretch of the paper sheet before it breaks. The results are depicted in
| Number | Date | Country | Kind |
|---|---|---|---|
| 04075539.9 | Feb 2004 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/NL05/00120 | 2/18/2005 | WO | 10/19/2006 |
