WO2010057946A1 - Composition contenant une hydrophobine destinée au collage de produits en papier - Google Patents

Composition contenant une hydrophobine destinée au collage de produits en papier Download PDF

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Publication number
WO2010057946A1
WO2010057946A1 PCT/EP2009/065467 EP2009065467W WO2010057946A1 WO 2010057946 A1 WO2010057946 A1 WO 2010057946A1 EP 2009065467 W EP2009065467 W EP 2009065467W WO 2010057946 A1 WO2010057946 A1 WO 2010057946A1
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Prior art keywords
hydrophobin
adhesive
seq
composition
weight
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PCT/EP2009/065467
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German (de)
English (en)
Inventor
Ulf Baus
Thorsten Montag
Thomas Subkowski
Claus Bollschweiler
Franz-Josef Landen
Original Assignee
Basf Se
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Publication date
Application filed by Basf Se filed Critical Basf Se
Priority to CA 2743236 priority Critical patent/CA2743236A1/fr
Priority to EP20090760511 priority patent/EP2358837B1/fr
Publication of WO2010057946A1 publication Critical patent/WO2010057946A1/fr
Priority to US13/109,103 priority patent/US20110281129A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J189/00—Adhesives based on proteins; Adhesives based on derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L89/00—Compositions of proteins; Compositions of derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J125/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Adhesives based on derivatives of such polymers
    • C09J125/02—Homopolymers or copolymers of hydrocarbons
    • C09J125/04—Homopolymers or copolymers of styrene
    • C09J125/08—Copolymers of styrene
    • C09J125/14—Copolymers of styrene with unsaturated esters
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/30—Multi-ply
    • D21H27/32—Multi-ply with materials applied between the sheets
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31971—Of carbohydrate
    • Y10T428/31993—Of paper

Definitions

  • the present invention relates to compositions comprising at least one hydrophobin (H) and an adhesive (K) and a corresponding method for bonding paper products, in particular for the adhesive binding of printed products.
  • Adhesive binding is understood to mean binding methods for books and other printed products, adhesives being applied to the back of the cut book block, optionally under fences, which ensure the cohesion of the sheets.
  • the perfect binding takes place without fanning the book block, so that the adhesive adheres only to the sheet edges. Nevertheless, in order to achieve a high strength of the perfect binding, the book block back is roughened before the application of the adhesive in order to achieve a larger adhesive surface and thus a higher strength of the bond. Ensuring the required strength values is not satisfactorily resolved to this day despite constant technical developments.
  • hot melt adhesives hot melt adhesives
  • reactive hot melt adhesives eg polyurethane hot melt adhesives, so-called PUR adhesives
  • waterborne adhesives for example dispersion adhesives
  • thermoplastic polymer for example, ethyl vinyl acetate copolymers
  • the disadvantage here is that a high energy input is necessary and the hot glue has a high viscosity.
  • the bonds obtained also do not have sufficient flexibility. This leads to a disadvantageous plan-impact behavior (lay flat) and to open books open by itself.
  • aqueous adhesives (sometimes referred to in the literature as cold or white glue) are used in postpress and especially in bookbinding.
  • aqueous adhesives based on natural polymers such as glutin (glutin glue) or starch (or starch derivatives) and adhesives based on synthetic polymers (such as polyvinyl alcohol) and dispersion adhesives are used.
  • glutin glutin glue
  • starch starch derivatives
  • synthetic polymers such as polyvinyl alcohol
  • dispersion adhesives are used for the Buckbackenklebeitati in bindery mainly dispersion adhesives are used.
  • the dispersion adhesives used consist predominantly of 40 to 60 percent aqueous dispersions based on synthetic, film-forming polymers, preferably polyvinyl acetate or other polyvinyl esters. They represent an important group of adhesives in the field of postpress and can be used for almost all adhesive work.
  • the advantage of the aqueous adhesives is that they have relatively low viscosities and thus penetrate better into the pores of the paper.
  • the resulting adhesive film is significantly thinner and more flexible compared to hot glueing.
  • Combinations eg two-stage processes using dispersion adhesives and hot melt adhesives are also described in the prior art (see, for example, WO 1985/04669).
  • Important for bonding with dispersion adhesives is the accessibility of the paper fiber, which is usually improved by special back processing, such as special cutting processes (see EP-A 1 063 104).
  • An object of the present invention is to increase the adhesion of an aqueous adhesive to the fiber material.
  • the resulting adhesive film should also have a high flexibility.
  • adhesive composition in the bookbindery should have good processability. These include, for example, that the adhesive composition has a low viscosity and sets quickly to ensure good processability and short process times in the manufacturing process. It has now been found that a surprisingly significant improvement in the mechanical stability and flexibility of the resulting adhesive films can be achieved by adding special proteins, the hydrophobins, to adhesives for the bonding of paper products (for example in the adhesive binding of books).
  • the adhesive composition according to the invention and the associated process according to the invention fulfill the abovementioned requirements such as high flexibility of the adhesive film, good processability and short process times.
  • Hydrophobins are small, cysteine-rich proteins of about 100 to 150 amino acids, which z. B. occur in filamentous fungi such as Schizophyllum commune. They usually have 8 cysteine units in the molecule. Hydrophobins can be isolated from natural sources, but they can also be obtained by means of genetic engineering, as disclosed, for example, in WO 2006/082251 or WO 2006/131 564. In the prior art, the use of hydrophobins has already been proposed for various applications.
  • WO 1996/41882 proposes the use of hydrophobins as emulsifiers, thickeners, surface-active substances, for hydrophilicizing hydrophobic surfaces, for improving the water resistance of hydrophilic substrates, for producing oil-in-water emulsions or for water-in-oil emulsions ,
  • EP-A 1 252 516 discloses the coating of various substrates with a hydrophobin-containing solution at a temperature of 30 to 80 0 C. Furthermore, the use of hydrophobins as demulsifying agent, for example (see WO 2006/103251), (as evaporation retarders see WO 2006 / 128877) and pollution inhibitor (see WO 2006/103215) have already been proposed.
  • Document DE-A 10 328 509 describes an aqueous adhesive for book production, to which gelatin or a fine colloidal gelatin solution has been added as a component. This is to ensure that the aqueous portion of the dispersion penetrates more easily into the paper structure.
  • composition of the invention for bonding paper products (or in particular consisting of):
  • composition of the invention may have different consistencies depending on the method of application and the adhesive used. It is possible for the composition to have a high viscosity pasty consistency, i. has a high adhesive content, or is a low-viscosity liquid with a low adhesive content.
  • the composition of the invention also comprises the adhesive film on a paper product at all stages of the bonding process (such as a ready-dried perfect binding on the spine and the perfect binding film on the spine prior to drying).
  • the composition comprises:
  • Z further additives
  • a single hydrophobin (H) two or more hydrophobins can be used together.
  • a single adhesive (K) two or more adhesives may be used together.
  • compositions comprising:
  • the composition (eg at the processing temperature) has a dynamic viscosity in the range from 500 to 2000 mPas, preferably a viscosity in the range from 500 to 1000 mPas.
  • hydrophobins are to be understood below to mean polypeptides of the general structural formula (I)
  • X is selected for each of the 20 naturally occurring amino acids (Phe, Leu, Ser, Tyr, Cys, Trp, Pro, His, GIn, Arg, Ne Met, Thr, Asn, Lys, VaI, Ala, Asp, Glu, GIy) can stand.
  • the radicals X may be the same or different.
  • the indices standing at X each represent the number of amino acids in the respective subsequence X
  • C stands for cysteine, alanine, serine, glycine, methionine or threonine, at least four of the radicals named C being cysteine
  • the indices n and m independently represent natural numbers between 0 and 500, preferably between 15 and 300.
  • the polypeptides according to the formula (I) are further characterized by the property that at room temperature after coating a glass surface, they increase the contact angle of a water droplet of at least 20 °, preferably at least 25 ° and particularly preferably 30 °, in each case compared with the contact angle of a water droplet of the same size with the uncoated glass surface.
  • the amino acids designated C 1 to C 8 are preferably cysteines. However, they can also be replaced by other amino acids of similar space filling, preferably by alanine, serine, threonine, methionine or glycine. However, at least four, preferably at least 5, more preferably at least 6 and in particular at least 7, of the positions C 1 to C 8 should consist of cysteines.
  • Cysteines can either be reduced in the proteins according to the invention or can form disulfide bridges with one another. Particularly preferred is the intramolecular formation of CC bridges, in particular those with at least one, preferably 2, more preferably 3 and most preferably 4 intramolecular disulfide bridges. In the exchange of cysteines described above by amino acids of similar space filling, it is advantageous to exchange in pairs those C positions which are capable of forming intramolecular disulfide bridges with one another.
  • cysteines, serines, alanines, glycines, methionines or threonines are also used in the positions indicated by X, the numbering of the individual C positions in the general formulas may change accordingly.
  • X, C and the indices standing at X and C have the above meaning
  • the indices n and m are numbers between 0 and 350, preferably 15 to 300
  • the proteins further by the above-mentioned Distinguish contact angle change and it is still at least 6 of the radicals named C is cysteine. Most preferably, all of the C radicals are cysteine.
  • the proteins are further characterized by the abovementioned contact angle change, and at least 6 of the C named residues are cysteine. Most preferably, all of the C radicals are cysteine.
  • radicals X n and X m may be peptide sequences, growing naturally linked to a hydrophobin. However, one or both of the residues may also be peptide sequences that are not naturally present a hydrophobin are linked. Including such radicals X N and / or X m are to be understood, in which a naturally occurring in a hydrophobin peptide sequence is extended by a non-naturally occurring in a hydrophobin peptide sequence.
  • X n and / or X m are naturally non-hydrophobin-linked peptide sequences, such sequences are generally at least 20, preferably at least 35 amino acids long. They may, for example, be sequences from 20 to 500, preferably 30 to 400 and particularly preferably 35 to 100 amino acids.
  • Such a residue, which is not naturally linked to a hydrophobin will also be referred to below as a fusion partner.
  • the proteins may consist of at least one hydrophobin part and one fusion partner part which in nature do not coexist in this form. Fusion hydrophobins from fusion partner and hydrophobin part are described, for example, in WO 2006/082251, WO 2006/082253 and WO 2006/131564.
  • the fusion partner portion can be selected from a variety of proteins. Only a single fusion partner can be linked to the hydrophobin moiety, or several fusion partners can also be linked to a hydrophobin moiety, for example at the amino terminus (X n ) and at the carboxy terminus (X m ) of the hydrophobic moiety. However, it is also possible, for example, to link two fusion partners with a position (X n or X m ) of the protein according to the invention.
  • fusion partners are proteins which occur naturally in microorganisms, in particular in Escherischia coli or Bacillus subtilis.
  • fusion partners are the sequences yaad (SEQ ID NO: 16 in WO 2006/082251), yaae (SEQ ID NO: 18 in WO 2006/082251), ubiquitin and thioredoxin.
  • fragments or derivatives of said sequences which comprise only a part, for example 70 to 99%, preferably 5 to 50%, and particularly preferably 10 to 40% of said sequences, or in which individual amino acids or nucleotides are opposite the said sequence are changed, wherein the percentages in each case refers to the number of amino acids.
  • the fusion hydrophobin has in addition to the fusion partner mentioned as one of the groups X n or X m or as a terminal
  • affinity domain affinity tag / affinity tail
  • anchor groups which can interact with certain complementary groups and can serve the easier workup and purification of the proteins.
  • affinity domains include (His) k , (Arg) k , (Asp) k , (Phe) k , or (Cys) k groups, where k is generally a natural number from 1 to 10. It may preferably be a (His) k group, where k is 4 to 6.
  • the group X n and / or m X may consist exclusively of such an affinity domain or a naturally or non-naturally linked to a hydrophobin radical X n and X m is extended by a terminal affinity domain.
  • hydrophobins used according to the invention may also be modified in their polypeptide sequence, for example by glycosylation, acetylation or else by chemical crosslinking, for example with glutaric dialdehyde.
  • a characteristic of the hydrophobins or their derivatives used according to the invention is the change of surface properties when the surfaces are coated with the proteins.
  • the change in the surface properties can be experimentally determined, for example, by measuring the contact angle of a water drop before and after coating the surface with the protein and determining the difference between the two measurements.
  • contact angle measurements is known in principle to the person skilled in the art.
  • the measurements refer to room temperature and water drops of 5 ⁇ l and the use of glass slides as substrate.
  • the exact experimental conditions for an exemplary method for measuring the contact angle are shown in the experimental part.
  • the fusion proteins used according to the invention have the property of increasing the contact angle by at least 20 °, preferably at least 25 °, particularly preferably at least 30 °, in each case compared with the contact angle of a water droplet of the same size with the uncoated glass surface.
  • hydrophobins for carrying out the present invention are the hydrophobins of the type dewA, rodA, hypA, hypB, sc3, basfi, basf2. These hydrophobins including their sequences are disclosed, for example, in WO 2006/082251. Unless stated otherwise, the sequences given below refer to the sequences disclosed in WO 2006/082,251. An overview table with the SEQ ID numbers can be found in WO 2006/082 251 on page 20.
  • Particularly suitable according to the invention are the fusion proteins yaad-Xa-dewA-his (SEQ ID NO: 20), yaad-Xa-rodA-his (SEQ ID NO: 22) or yaad-Xa-basfl-his (SEQ ID NO: 24) with the polypeptide sequences given in parentheses and the nucleic acid sequences coding therefor, in particular the sequences according to SEQ ID NO: 19, 21, 23.
  • the hydrophobin yaad-Xa-dewA-his is particularly preferably used.
  • proteins which, starting from the amino acid sequences shown in SEQ ID NO. 20, 22 or 24 shown by exchange, insertion or deletion of at least one, up to 10, preferably 5, more preferably 5% of all amino acids, and still have the biological property of the starting proteins at least 50%, are particularly preferred embodiments.
  • the biological property of the proteins is hereby understood as the change in the contact angle already described by at least 20 °.
  • Particularly suitable derivatives for carrying out the present invention are from yaad-Xa-dewA-his (SEQ ID NO: 20), yaad-Xa-rodA-his (SEQ ID NO: 22) or yaad-Xa-basfl-his (SEQ ID NO: 24) derivatives derived from truncation of the yaad fusion partner.
  • yaad-Xa-dewA-his SEQ ID NO: 20
  • yaad-Xa-rodA-his SEQ ID NO: 22
  • yaad-Xa-basfl-his SEQ ID NO: 24
  • the truncated residue should comprise at least 20, preferably at least 35, amino acids.
  • a truncated radical having 20 to 293, preferably 25 to 250, particularly preferably 35 to 150 and for example 35 to 100 amino acids can be used.
  • An example of such a protein is yaad40-Xa-dewA-his (SEQ ID NO: 26 in PCT / EP2006 / 064720), which has a 40 amino acid truncated yaad residue.
  • a cleavage site between the hydrophobin and the fusion partner or the fusion partners can be used to cleave off the fusion partner and release the pure hydrophobin in underivatized form (for example, by BrCN cleavage of methionine, factor Xa, enterokinase, thrombin, TEV cleavage Etc.).
  • hydrophobins contained in the paper product-sticking composition of the present invention can be prepared chemically by known methods of peptide synthesis such as Merrifield solid-phase synthesis.
  • Naturally occurring hydrophobins can be isolated from natural sources by suitable methods. As an example, let Wösten et. al., Eur. J. Cell. Bio. 63, 122-129 (1994) or WO 1996/41882.
  • a genetic engineering preparation for hydrophobins without fusion partner from Talaromyces thermophilus is described by US 2006/0040349.
  • the preparation of fusion proteins can preferably be carried out by genetic engineering methods in which one for the fusion partner and one for the hydrophobin part co- dating nucleic acid sequence, in particular DNA sequence, are combined so that the desired protein is produced in a host organism by gene expression of the combined nucleic acid sequence.
  • a production method for example, is disclosed by WO 2006/082251 or WO 2006/082253.
  • the fusion partners facilitate the production of hydrophobins considerably. Fusion hydrophobins are produced in genetically engineered processes with significantly better yields than hydrophobins without fusion partners.
  • the fusion hydrophobins produced by the host organisms according to the genetic engineering process can be worked up in a manner known in principle and purified by known chromatographic methods.
  • the simplified work-up and purification process disclosed in WO 2006/082253, pages 1 1/12 can be used.
  • the fermented cells are first separated from the Fermetationsbrühe, digested and the cell debris of the inclusion bodies (inclusion bodies) separately. The latter can be done advantageously by centrifuging.
  • the inclusion bodies for example by acids, bases and / or detergents can be digested in a manner known in principle in order to release the fusion hydrophobins.
  • the inclusion bodies with the fusion hydrophobins used according to the invention can generally be completely dissolved within about 1 h already using 0.1 M NaOH.
  • the solutions obtained can - if necessary after setting the desired pH - are used without further purification for carrying out this invention.
  • the fusion hydrophobins can also be isolated from the solutions as a solid. The isolation can preferably be effected by means of spray granulation or spray drying, as described in WO 2006/082253, page 12.
  • the amount of fusion hydrophobins is generally from 30 to 80% by weight with respect to the amount of all proteins.
  • the isolated products containing fusion hydrophobins can be stored as solids and dissolved for use in the respective desired media.
  • the fusion hydrophobins can be used as "pure" hydrophobins for the practice of this invention. Cleavage is advantageously carried out after isolation of the inclusion bodies and their dissolution.
  • the hydrophobin (H) used is at least one fusion hydrophobin having a polypeptide sequence selected from the group of SEQ ID NO: 20; SEQ ID NO 22; SEQ ID NO 24.
  • composition according to the invention described above contains hydrophobin in a range from 0.001 to 10% by weight (based on the total composition), preferably in the range from 0.005 to 10% by weight, particularly preferably in the range from 0.01 to 5% by weight. %, most preferably in the range of 0.01 to 1 wt .-%.
  • the composition for bonding paper products contains at least one hydrophobin (component H) in the range of 0.001 to 0.1 wt .-%.
  • the component K contained in the composition according to the invention may quite generally be understood to mean an adhesive (cf. DIN EN 923), i. a non-metallic material that can bond parts together by adhesion (adhesion) and internal strength (cohesion).
  • Adhesives can be physically setting adhesives (for example hot melt adhesives, dispersion adhesives or adhesives) or chemically setting adhesives (reactive adhesives), for example polyurethane adhesives.
  • the composition for bonding paper products contains at least one adhesive (K), which is usually used in paper and print finishing.
  • K adhesive
  • such adhesives commonly used in post-press finishing are not listed:
  • Adhesives based on natural or semi-natural polymers Adhesives based on natural or semi-natural polymers
  • Dextrin adhesives made by thermal or chemical degradation of potato, corn, wheat, cassava, tapioca and rice starch;
  • Adhesives based on synthetic polymers such as
  • Hot melt adhesives for example based on vinyl acetate (hot-melt adhesives)
  • dispersion adhesives containing homo- or copolymers of vinyl acetate, ethyl vinyl acetate, acrylates, styrene acrylate and dispersion adhesives containing polyurethane are examples of polyurethane.
  • dispersion adhesives are understood as meaning a dispersion of an organic base material (for example a polymer or copolymer of vinyl esters or acrylates) in liquid dispersion media in which the organic base material is insoluble.
  • the dispersions may optionally also contain plasticizers, resins or fillers.
  • Aqueous-based dispersion adhesives contain water as a main component of the dispersant.
  • the adhesive component (K) of the composition consists of a dispersion adhesive, especially on an aqueous basis.
  • dispersion adhesives containing homo- or copolymers of vinyl acetate, ethyl vinyl acetate, acrylates, styrene acrylate or a polyurethane.
  • the adhesive component K contains at least one of the following dispersion adhesives:
  • Emuldur ® (BASF, Ludwigshafen, Germany) (anionic polyester-polyurethane in aqueous dispersion), - adhesin ® A7362 (Henkel, Dusseldorf, Germany), (polyvinyl acetate),
  • composition of the invention may optionally contain 0-90 wt .-% of one (or more) solvent and / or dispersant (L), preferably water is used.
  • solvent and / or dispersant preferably water is used.
  • other polar, water-miscible solvents and / or dispersants such as alcohols (for example methanol, ethanol, n-propanol, n-butanol, isopropanol, cyclohexanol); Carboxylic acids (eg formic acid, acetic acid); Carboxylic acid esters (eg ethyl acetate), ketones (eg acetone) are used. It is also possible to use mixtures of different solvents and / or dispersants as component (L).
  • the solvent and / or dispersant (L) also contains non-polar solvents.
  • the definition of the solvent and / or dispersant (L) includes, for example, dispersants of a dispersion adhesive and solvents of the hydrophobin component.
  • composition of the invention may optionally contain further additives (Z) z.
  • Z additives
  • Z are, for example:
  • plasticizers a) plasticizers, b) fillers, c) preservatives, d) light stabilizers, e) defoaming agents, f) rheology improvers, for example
  • the composition according to the invention contains as "further additive" (Z) at least one wetting agent in the range from 0.0001 to 10% by weight, in particular in the range from 0.0001 to 1% by weight, preferably Range of 0.0001 to 0.1 wt .-% (each based on the total composition).
  • a wetting agent in the context of the invention is a surfactant, ie a surface-active substance, which reduces the surface tension of a liquid in which the surfactant is dissolved or the interfacial tension to a second liquid phase.
  • a wetting agent (also referred to below as wetting agent for short) under In particular, it supports the wetting of a surface by the liquid in which the wetting agent is dissolved.
  • the wetting agent may in particular be selected from the group consisting of: ethoxylated alcohols, ethoxylated acids (such as ethoxylated carboxylic acids, ethoxylated fatty acids), siloxanes, modified (eg polyether-modified) siloxanes, in particular trisiloxanes, ionic surfactants, but in particular anionic surfactants and highly dispersed silicas.
  • Particularly suitable adducts of ethoxylated alcohols are addition products of from 0 to 30 mol of ethylene oxide, in particular from 10 to 25, in particular from 12 to 20, mol of ethylene oxide and / or from 0 to 5 mol of propylene oxide to linear fatty alcohols having from 8 to 22 carbon atoms (for example stearyl alcohols, Cetyl alcohols) can be used.
  • Alkylpolyethylene glycols may preferably be selected from the group consisting of polyethylene glycol (12 to 20) stearyl ether, polyethylene glycol (12 to 20) isostearyl ether, polyethylene glycol (12 to 20) cetyl ether, polyethylene glycol (12 to 20) isocetyl ether, polyethylene glycol ( 12 to 20) oleyl ether, polyethylene glycol (12 to 20) lauryl ether, polyethylene glycol (12 to 20) isolauryl ether and polyethylene glycol (12 to 20) cetyl stearyl ether.
  • fatty acid ethoxylates (acylpolyethylene glycols), in particular adducts of 0 to 30 moles of ethylene oxide, in particular 10 to 25, in particular 12 to 25 moles of ethylene oxide, and / or 0 to 5 moles of propylene oxide with linear fatty acids having 8 to 22 C can be used as wetting agents.
  • Atoms eg stearic acid, isostearic acid, oleic acid
  • a surfactant may be used selected from the group of polyethylene glycol (20) glyceryl laurate, polyethylene glycol (6) glyceryl caprate / caprinate, polyethylene glycol (20) glyceryl oleate, polyethylene glycol (20) glyceryl isostearate and polyethylene glycol (18) glyceryl oleate / cocoate.
  • sorbitan mono- and diesters of saturated and unsaturated fatty acids having 6 to 22 carbon atoms and optionally their Ethylenoxidanla- gerungs located at 0 to 30 moles of ethylene oxide, in particular 10 to 25 mol, in particular 12 to 25 mol.
  • ethoxylated sorbitan fatty acid esters can selected from the group polyethylene glycol (20) sorbitan monolaurate (Tween®20), polyethylene glycol (20) sorbitan monostearate, polyethylene glycol (20) sorbitan monoisostearate, polyethylene glycol (20) sorbitan monopalmitate and polyethylene glycol (20) sorbitan monooleate as surfactant (wetting agent) ,
  • surfactants are ethoxylated fatty amines, fatty acid amides, fatty acid alkanolamides, fatty acid amide polyethylene glycols, polypropylene glycol ethoxylates (poloxamers, Pluronics®); Fatty acid N-methylglucamides, sucrose esters; Polyglycol ethers, alkylpolyglycosides, phosphoric acid esters (mono-, di- and tri-phosphoric acid esters ethoxylated and non-ethoxylated).
  • ionic surfactants preferably anionic surfactants, such as mono-, di- or tri-phosphoric esters, sodium stearate, sodium lauryl sulfate, sodium lauryl sarcosinate, sodium dioctyl sulfosuccinate, sodium diisooctyl sulfosuccinate (eg Emulsogen®SF8), sodium alkylnaphthalenesulfonate, fatty alcohol sulfates, alkyl ether sulfate (eg lauryl diglycol ether sulfate sodium salt ), ethoxylated alkyl ether carboxylic acid or its salts (eg, sodium laureth (11 EO) carboxylate).
  • anionic surfactants such as mono-, di- and tri-alkyl quats and their polymeric derivatives.
  • siloxanes and / or a modified siloxane are used as surfactant (wetting agent).
  • the siloxanes may in particular be oligomeric or polymeric siloxanes and / or modified siloxanes.
  • oligomeric and / or polymeric siloxanes which are modified by alkyl, vinyl or amino groups.
  • polyether-modified siloxanes such as a polyether-modified trimethoxysilane (Dynsylan®4144).
  • Particularly preferred is the use of polyether-modified trisiloxanes.
  • Preferred polyether-modified siloxanes are obtainable by reacting linear or cyclic optionally modified mono-, oligo- and / or polysiloxanes with ethylene oxide and / or propylene oxide.
  • addition products of 0 to 30 mol of ethylene oxide, in particular 10 to 25 mol, in particular 12 to 20 mol and / or 0 to 5 mol of propylene oxide to linear and / or cyclic mono-, oligo- and / or polysiloxanes can be used as polyether-modified siloxanes, preferably trisiloxanes.
  • siloxanes selected from the group heptamethyltrisiloxane, lauryltrisiloxane and stearyltrisiloxane. Furthermore, amino-, alkyl- and / or vinyl-modified siloxanes and / or oligosiloxanes (eg surfactants of the brands Dynasyllan® and Dynasyllan®Hydrosil) can be used.
  • the composition described contains, as further additive (Z), at least one surfactant (wetting agent) in the range from 0.0001 to 10% by weight, in particular in the range from 0.0001 to 1% by weight, preferably in the range from 0.0001 to 0.1% by weight, selected from the group consisting of polyether-modified trisiloxane (eg BreakTru®, Dynasyl®4144), alkyl-modified siloxanes, amino-modified siloxanes, amino- / alkyl-modified siloxanes (eg Dynasyl ®Hydrosil2627), heptamethyltrisiloxane (Silwet® L-77), polyoxyethylene (20) sorbitan monolaurate (polysorbate 20, Tween® 20), octylphenol polyethylene glycol (9-10) ether (Triton®), polyethylene glycol (12 to 20) stearyl ether, polyethylene glycol (12 to 20) lauryl ether and poly
  • the composition for bonding paper products contains (or preferably consists of) the following components:
  • compositions comprising (or preferably consisting of) the following components:
  • Polypeptide sequence selected from the group SEQ ID NO: 20; SEQ ID NO 22 or SEQ ID NO 24.
  • composition consists of at least two parts which are manufactured separately, delivered and applied to the paper product. These parts comprise at least one adhesive (component K) and one hydrophobin (component H).
  • the parts preferably comprise an aqueous dispersion adhesive (K) and an aqueous solution of at least one hydrophobin.
  • paper products are to be understood in particular as meaning graphic papers, packaging papers, tissue papers and special papers.
  • graphic papers e.g. Photo prints and digital prints.
  • Packaging papers are papers, cardboard and cardboard for packaging purposes.
  • Hygiene papers in the context of the invention are papers with high volume and high suction power, which are typically used in sanitary or kitchen applications.
  • special papers refers to papers and cardboards for special technical purposes.
  • the invention relates to graphic papers. More preferably, the invention relates to graphic papers which have already been subjected to a printing process, in particular to photographic prints and digital prints. However, it is also possible to use non-printed papers within the scope of the invention.
  • paper products also include products which have been produced by the joining of the abovementioned paper products, that is, for example, products or intermediate products of bookbinding, such as books, brochures, catalogs, writing pads, book blocks, envelopes.
  • the present invention further comprises a method for bonding a paper product, wherein the components of the above-described composition are applied to the paper product.
  • a composition containing at least one hydrophopin (H) and subsequently a composition containing the adhesive (K) is applied to the paper product (two-stage method).
  • the components of the composition described above are mixed and applied to a paper product.
  • an aqueous solution of at least one hydrophobin (H) is mixed with an aqueous dispersion adhesive (K) and optionally further additives (Z) and applied to the paper product. It can (optionally purified) hydrophobin solutions are used, as obtained in one of the described production process for Hydrophopin.
  • the composition thus obtained is applied to the printed product in a suitable standard application device.
  • the adhesive optionally containing a solvent and / or dispersant (L) and other additives ( Z) applied to the paper product to be bonded.
  • dilute hydrophobin solutions having a hydrophobin content of 0.001 to 0.1% by weight are applied.
  • solvents the above-mentioned solvents and / or dispersants can be used individually or as mixtures, but preferably water.
  • an aqueous solution containing from 0.001 to 10% by weight, preferably 0.005 to 10% by weight, particularly preferably 0.01 to 5% by weight, very particularly preferably in the range of 0, is initially applied to the paper product. 01 to 1 wt .-% of at least one hydrophobin (H) and then applied a composition containing the adhesive (K).
  • an aqueous solution containing from 0.001 to 0.1% by weight of at least one hydrophobin (component H) is applied to the paper product.
  • the paper product may be dried after applying the hydrophopin solution and before applying an adhesive component ("two-shot process").
  • the application is carried out without intermediate drying, i. "Wet on wet.”
  • a hydrophobin-containing solution is applied to the paper product and immediately afterwards applied to the wet fibers, an adhesive component, for example via a nozzle.
  • an aqueous solution containing from 0.001 to 10% by weight of at least one hydrophobin (H) and immediately thereafter without intermediate drying (“wet-on-wet") an aqueous dispersion adhesive (K) is first applied to the paper product wherein the hydrophobin is a fusion hydrophobin having a polypeptide sequence selected from the group of SEQ ID NO: 20, SEQ ID NO 22, SEQ ID NO 24, and wherein the paper product is a book block back.
  • the above-described hydrophobin solution contains as further additive (Z) at least one wetting agent in the range from 0.0001 to 10% by weight, preferably in the range from 0.001 to 10% by weight. , furthermore preferably in the range from 0.005 to 10% by weight, particularly preferably in the range from 0.01 to 5% by weight, particularly preferably in the range from 0.01 to 1% by weight.
  • the hydrophobin solution contains as further additive (Z) at least one wetting agent in the range of 0.0001 to 0.1 wt .-%.
  • the stated wt.% Data are based on the total amount of aqueous hydrophobin solution.
  • wetting agents can be used.
  • at least one surfactant (wetting agent) selected from the group consisting of polyether-modified trisiloxane (eg BreakTru®, Dynasyl®4144), alkyl-modified siloxanes, amino-modified siloxanes, amino- / alkyl-modified siloxanes (eg, Dynasyl® Hydrosil2627), heptamethyltrisiloxane (Silwet® L-77), polyoxyethylene (20) sorbitan monolaurate (polysorbate 20, Tween® 20), octylphenol polyethylene glycol (9-10) ether (Triton®), polyethyl - Glycol (12 to 20) stearyl ether, polyethylene glycol (12 to 20) lauryl ether and polyethylene glycol (12 to 20) cetyl ether.
  • surfactant wetting agent selected from the group consisting of polyether-modified trisiloxane (eg BreakTru®, Dyna
  • a hydrophobin solution described above can be used in a two-step process as described in the present application, wherein the hydrophobin solution has a surface tension in the range of 10 to 50 mN / m, in particular in the range of 20 to 40 mN / m , often in the range of 30 to 35 mN / m.
  • the surface tension of the hydrophobin solution is important for certain fields of application and can also be adjusted in a targeted manner by the type and amount of wetting agent additionally used.
  • dried hydrophobins or (optionally purified) hydrophobin solutions can be used, as obtained in one of the described production process for hydrophobin.
  • the order can in particular be carried out with the aid of a known manual or mechanical method, such as nozzle or roller application.
  • composition according to the invention preferably takes place in a binding machine for dispersion adhesives (so-called cold glues) with a nozzle application system.
  • a binding machine for dispersion adhesives so-called cold glues
  • nozzle application system Preferably, before the application process, there is a step for book block spine processing in which the fibers of the sheet edges are uncovered.
  • the invention further encompasses the use of at least one hydrophobin in a process for bonding paper products.
  • the invention also includes the use of at least one hydrophobin as an adjuvant in compositions for bonding paper products in post-press processing.
  • a preferred embodiment of the invention comprises the use of at least one hydrophobin as described above, wherein the hydrophobin is used as adjuvant in aqueous adhesives in the post-processing.
  • the use in bookbinding and in particular the binding of book blocks is particularly preferred.
  • At least one hydrophobin is used according to the invention as an auxiliary in aqueous dispersion adhesives in the print finishing, preferably in the adhesive bonding of printed products, in particular printed products of digital or photo printing.
  • fusion protein with a polypeptide sequence selected from the group of SEQ ID NO: 20; SEQ ID NO 22; SEQ ID NO 24 as an excipient in aqueous dispersions in the adhesive bonding of paper products.
  • composition according to the invention is preferably used as an adhesive system in all steps of the print finishing.
  • print finishing covers all the work steps by which the intended products with their respective shapes and properties are produced from the printed (or else unprinted) precursors.
  • methods and steps of bookbinding are to be understood which include an adhesive bond.
  • the invention further relates to paper products, such as books, brochures, writing blocks, which have been bonded with a composition according to the invention described above.
  • the invention relates to bookbinding products such as books, brochures, catalogs, calendars, writing pads or similar printed matter bound with a composition of the invention described above.
  • hydrophobin A a fusion hydrophobin with the complete fusion partner yaad
  • hydrophobin B a fusion hydrophobin with a fusion partner shortened to 40 amino acids yaad40-Xa-dewA-his
  • hydrophobin B a fusion hydrophobin with a fusion partner shortened to 40 amino acids yaad40-Xa-dewA-his
  • the hydrophobins were prepared according to the procedure described in WO 2006/082253.
  • the products were worked up according to the simplified purification process according to Example 9 of WO 2006/82253 and spray-dried according to Example 10.
  • the total protein content of the obtained, dried products was in each case about 70 to 95% by weight, the content of hydrophobins was about 40 to 90% by weight with respect to the total protein content.
  • the products were used as such for the experiments.
  • Example 2 Application Testing of Hydrophobins
  • the spray-dried fusion hydrophobins containing product were-products in water with the addition of 50 mM Na acetate pH 4 and 0.1 wt.% Polyoxye- Thylen (20) -sorbitanmonolaureat (Tween ® 20) dissolved.
  • the concentration of the product was 100 ⁇ g / mL in aqueous solution.
  • the samples are air-dried and the contact angle (in degrees) of a drop of 5 ⁇ l of water at room temperature is determined.
  • the contact angle measurement was performed on a device Dataphysics Contact Angle System OCA 15+, Software SCA 20.2.0. (November 2002). The measurement was carried out according to the manufacturer's instructions.
  • Untreated glass gave a contact angle of 15 ° to 30 ° ⁇ 5 °.
  • Coating with the fusion hydrophobin yaad-Xa-dewA-his ⁇ gave a contact angle increase of more than 30 °; a coating with the fusion hydrophobin yaad40-Xa-dewA-his also gave a contact angle increase of more than 30 °.
  • a book block (DIN A4, ie back length of 297 mm) was clamped in a book block pliers, so that the edge to be bound protrudes about 2 mm freely from the pliers (so-called notice board).
  • This book block is roughened by a milling device. This pretreatment exposes the fibers.
  • the adhesive dispersion had a viscosity (measured with Ford cup, 5 mm nozzle) of ⁇ 1000 mPas.
  • Book blocks each 2 cm thick were glued together from various types of paper (# 1 to # 5) as described in Example 3.
  • book blocks without hydrophobin pretreatment were also roughened with a thickness of 2 cm, analogously to the above-described methods, and in a binding machine of the type Ribler Junior Binder or Ribler Express Binder (manufacturer Ribbler, Stuttgart, DE) via a nozzle with the one described above Adhesive recipe glued.
  • the leaf pull-out forces (in N / cm) were determined by the so-called page-pull test.
  • the perfect binding to be tested was clamped open in the pull-test device. Then, a single sheet is released with a clamping rail under gradually increasing tensile force from the perfect binding or charged to paper tear. The higher the required tensile force in N / cm, the stronger the perfect binding.
  • the results of the page-pull test are shown in Figure 1.
  • the five results refer to different paper grades 1 to 5.
  • the dark bars represent the results with hydrophobin, the light bars represent the results without hydrophobin pretreatment. It can be seen that the strength values with hydrophobin are 20-100% higher than the comparative examples without hydrophobin.
  • the adhesive bond was flattened and viewed under the microscope. It was pulled on a blade edge, with the adhesive seam stretched. If the adhesive separates from the paper fiber, it is an adhesion failure. If, on the other hand, the adhesive does not adhere to the paste piercing fiber in the middle of the glue seam is a cohesive failure.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

L'invention concerne des compositions contenant a) 0,001–10 % en poids d'une hydrophobine (H), b) une colle (K), c) éventuellement un solvant et/ou un agent de dispersion (L) et d) éventuellement d'autres additifs (Z), ainsi qu'un procédé de collage de produits en papier, notamment de reliure adhésive de produits imprimés.
PCT/EP2009/065467 2008-11-19 2009-11-19 Composition contenant une hydrophobine destinée au collage de produits en papier WO2010057946A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CA 2743236 CA2743236A1 (fr) 2008-11-19 2009-11-19 Composition contenant une hydrophobine destinee au collage de produits en papier
EP20090760511 EP2358837B1 (fr) 2008-11-19 2009-11-19 Composition contenant une hydrophobine pour coller des produits a base de papier
US13/109,103 US20110281129A1 (en) 2008-11-19 2011-05-17 Composition comprising a hydrophobin for gluing paper products

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08169418.4 2008-11-19
EP08169418 2008-11-19

Related Child Applications (1)

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US13/109,103 Continuation-In-Part US20110281129A1 (en) 2008-11-19 2011-05-17 Composition comprising a hydrophobin for gluing paper products

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WO2010057946A1 true WO2010057946A1 (fr) 2010-05-27

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Publication number Priority date Publication date Assignee Title
WO2019162438A1 (fr) * 2018-02-22 2019-08-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Procédés et dispositifs pour fabriquer un produit présentant des éléments collés

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BRPI1010003A2 (pt) * 2009-03-09 2018-06-12 Basf Se uso de uma mistura, e, composição

Citations (1)

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Publication number Priority date Publication date Assignee Title
US20060040349A1 (en) * 2004-08-18 2006-02-23 Sweigard James A Thermophilic hydrophobin proteins and applications for surface modification

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GB0002663D0 (en) * 2000-02-04 2000-03-29 Biomade B V Method of stabalizing a hydrophobin-containing solution and a method of coating a surface with a hydrophobin
DE102005015043A1 (de) * 2005-03-31 2006-10-05 Basf Ag Verwendung von Polypeptiden als Haftvermittler
MX2007012021A (es) * 2005-03-31 2008-03-14 Basf Ag El uso de polipeptidos como promotores de adhesion.

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060040349A1 (en) * 2004-08-18 2006-02-23 Sweigard James A Thermophilic hydrophobin proteins and applications for surface modification

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019162438A1 (fr) * 2018-02-22 2019-08-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Procédés et dispositifs pour fabriquer un produit présentant des éléments collés

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CA2743236A1 (fr) 2010-05-27
EP2358837B1 (fr) 2013-05-01
EP2358837A1 (fr) 2011-08-24
US20110281129A1 (en) 2011-11-17

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