It is prior art to return paper waste from natural fibrous materials for economically expedient reuse. For this purpose, mechanical and chemical processes are often usually used together for dispersion, removing printing ink (de-inking), bleaching, cleaning (washing) and screening.

As a result of the increased input of mixed waste paper as a source of raw material in papermaking, large quantities of solid or water-soluble, sticky constituents are also carried into the paper machine circuits. They constitute a significant cause of so-called"stickies"and "white pitch"which, because of their hydrophobic properties, are often deposited on hot and moving parts and in the wires and felts of paper machines and can therefore lead to paper web breaks.

"stickies"is understood to mean sticky deposits in the form of organic complexes, which are formed from the waste paper by the agglomeration of disruptive materials which interact with one another. All sticky deposits which are introduced exclusively via the raw materials are referred to as"primary stickies". If, on the other hand, the formation of the sticky contaminants is brought about only after reaction with additives, then these deposits are referred to as"secondary stickies". The main source for sticky contaminants are adhesives from paper conversion, but also synthetic binders from paper finishing.

"white pitch"is a special case of"sticky"formation, which is associated with the use of polyvinyl acetate and styrene butadiene latices, for example from coated paper broke (Das Papier (1998) 10 A, V 36-V 41 ; Wochenblatt für Papierfabrikation (1990) 8, 310-313).

The aforementioned"stickies"and"white pitch"are to be viewed as disruptive materials in papermaking, which as far as possible have to be"neutralized"in terms of their stickiness or separated.

In order to ensure effective treatment of disruptive materials, the size distribution of the disruptive materials to be encountered is critical for the thermal, chemical and/or mechanical processes to be used.

A rough distinction is drawn between macrostickies for particle sizes above 150 urn, which can largely be removed from the stock circulation by means of the aforementioned separating processes, and microstickies made of sticky contaminants between 1 urn and 150 um.

In most cases, microstickies do not cause any problems in papermaking if they do not agglomerate. In addition, they are then below the visibility limit.

In order to prevent re-agglomeration of the microstickies to a large extent, various processes are known for the chemical modification of the stickies remaining in the stock stream and their absorption on carrier materials with a high specific surface and on the fibrous material.

Here, the following procedures have been tried and tested in practice, but lead only to partial success.

1. Dispersion with the aim of changing the charging of the stickies by means of anionic and non-ionic dispersants By this means, colloidal, charged particles are formed which counteract agglomeration and deposition. The wetting properties of the dispersant are very important in this case, since the"stickies"are generally hydrophobic.

2. Reducing the tackiness of the stickies by -Fixing the highly anionic disruptive materials by means of highly cationic fixing agents (forming so-called polyelectrolyte complexes ; the reaction product is then attracted to the anionic fibre), -Absorption on synthetic fibres, pigments with a high specific surface (e. g. talc, modified clay, mica, smectite, bentonite), often with subsequent flocculation by means of polymers to bind together separable macroflocs, -Covering (masking) with non-ionogenic hydrophilic polymers or anionic zirconium compounds, in particular of zirconium acetate and ammonium zirconium carbonate.

Known highly cationic fixing agents are polyethylene imine (PEI), polydiallyldimethyl- ammonium chloride (PDADMAC), polyvinyl amine (PVAm), polyaluminium chloride (PAC), polyacrylamide (PAAM) and so on. The range of action of fixing agents extends, depending on the type and modification of the chemicals used, from about 1 nm to 50 um particle size of the microstickies (Das Papier (1998) 10 A, V 36-V 41).

Solids with a low surface energy exhibit a hydrophobic behaviour and therefore have a high affinity with hydrophobic substances, such as stickies. These absorption agents also include, amongst others, the synthetic fibres polyester, polyamide and polypropylene.

Further adsorption agents used are primarily various types of talc with a specific surface modification and grain size distribution which, because of their hydrophobic and organophilic surface, are capable of depositing on sticky constituents and carrying them out with the paper. Adhesive particles encapsulated in this way show a lower tendency to deposition on hot machine parts. Combating sticky deposits by means of talc has some drawbacks, however. For example, the system is very sensitive to shear. In addition, talc is difficult to retain and often leads to blinding of the felts. Talc can have a detrimental effect on resin sizing and stabilizes foam.

For partial overflocking, highly concentrated flocking agents, such as aluminium sulphate, aluminate, acids and so on, are used.

Known masking agents for stickies are, amongst others, ethoxilated nonylphenols and ethoxilated dodecylphenols having at least 9 mol ethylene oxide, whose use is limited to dosage rates of 10 ppm because of an extreme tendency to foaming (Wochenblatt fur Papierfabrikation (1990) 8, 310-313).

In addition, graft copolymers of polyalkylene oxide and partially saponified vinylacetate (up to 15% saponification) with a weight ratio of 1 : 0. 2 to 1 : 10, are used as masking agents, if appropriate in combination with other papermaking aids, it being possible for the polyalkylene oxide to be polyethylene, polypropylene or polybutylene oxide (EP 0571144 Al).

Likewise, alkoxylation products, which are obtained by reacting alkylene oxides with Ciao-22 carbonic acid derivatives and/or Cl022 carbonic acids, act as masking agents (DE 195 15 273 Al).

A hydrophilic polymer based on vinyl alcohol, which contains some hydrophobic groups such as acetates, propionates, butyrates or oleates and has molecular weights from 2 000 to 125 000 or more (EP 0220001 Bl), is used under the commercial name BETZ DETACH (trademark of the BETZ company) to combat the stickiness of hydrophobic stickies by means of covering them with a hydrophilic film over a wide pH and temperature range. This partially saponified polyvinyl alcohol (PVAL) is usually metered in the thick stock area, in order to ensure an adequate reaction time of 20-30 min with the stock to be treated, given good and thorough mixing. The necessary dosage rates to combat stickies successfully depend on the type and quantity of the waste paper used.

Any influence by other aids is ruled out because of their non-ionic charge (Wochenblatt far Papierfabrikation (1990) 8, 310-313).

An excess of PVAL would have an extremely detrimental effect on the papermaking process and on effluent loading, since it is not needed to cover the sharply varying proportion of stickies, depending on the selected dispersion conditions (shear intensity, pH and temperature range, combination of aids).

The formation of foam and an increase in the disruptive materials carried by the waste water (COD and BOD content) result. An additional difficulty is the poor biodegradability of PVAL.

On the other hand, underdosing with PVAL would lead to inadequate masking of all the sticky constituents.

In relation to the pulping of separated base paper broke, the selective adsorption capability of alkali modified bentonites with respect to various water-soluble polymers, in particular with respect to PVAL, in effluent has been demonstrated (Wochenblatt fur Papierfabrikation (1996) 4, 148-152).

Accordingly, 130 mg of dissolved PVAL is bound by 1 g of bentonite (ratio about 1 : 7. 5).

Practical investigations on effluent with different disruptive material loadings and types ultimately led to the result that, in practice, for safety reasons, eight to nine times the quantity of bentonite, based on the water-soluble PVAL proportion in the effluent, is used. As a result, at least 90 % of the dissolved PVAL from the effluent could be absorped and carried out with the paper. As a result of the combined use of bentonite and cationic fixing agent, such as PAC and PEI, in the preparation of broke, the content of dissolved hydrocolloids in the effluent could be reduced still further.

This beneficial action of a combined use of alkali modified bentonite and cationic fixing agent for the absorption of PVAL dissolved in the effluent has until now been practised only in the pulping of separated base paper broke surface-sized with PVAL and CMC.

A use of the aforementioned combination in the dispersion of waste paper and coated broke, in which partially saponified polyvinyl alcohol is added as a masking agent for microstickies, appears to be ruled out, since a very wide range of disruptive material loadings and a multiplicity of sticky constituents of varied chemical composition would lead to uncontrolled interactions.

The object of the invention was, therefore, to use the positive properties of partially saponified polyvinyl alcohols as a chemical agent for masking sticky constituents (microstickies) more effectively, from a process engineering point of view, for papermaking which will be less susceptible to disruption and more environmentally friendly with respect to protecting water supplies.

Surprisingly, the expected disruptive interactions could largely be avoided by selecting the correct dosing sequence of the individual components and the correct dosing location, depending on application.

For this purpose, it was necessary first of all for partially saponified PVAL to be introduced in a certain excess at that point in the process of preparing waste paper and coated broke where either macrostickies had already been removed by known separation processes and only microstickies were predominantly still present in the stock system, or even no macrostickies could still be formed.

The point of addition for masking sticky microstickies can therefore be located in the thick stock and also in the thin stock area, depending on the selected preparation and separation technique.

What is claimed is a process for reducing sticky contaminants, in particular those with a finely divided composition (microstickies) in the preparation of stock systems containing waste paper and of coated broke, characterized in that, after mechanical preparation has been carried out and, if necessary, coarse sticky constituents (macrostickies) have been separated, the stock system has added to it at least one water-soluble organic polyol, in particular a water-soluble polyvinyl alcohol or a mixture of various water-soluble organic polyols, in particular a mixture of various water-soluble polyvinyl alcohols, and bentonite and, if appropriate, further chemical additives and fillers.

The organic polyvinyl alcohols used are water-soluble polymers with proportions of vinyl alcohol or a copolymer of vinyl alcohol and vinyl acetate, which contain hydrophobic groups and are hydrolyzed to more than 70% by weight.

The organic polyvinyl alcohols are used after the mechanical preparation in proportions from 0. 05 to 2% by weight, in particular from 0. 1 to 1. 0% by weight, based on fibrous material, in combination with bentonites with a high specific surface, preferably alkali modified bentonites, in proportions from 1 to 10% by weight, based on fibrous material.

The organic polyvinyl alcohols used have a molecular weight from 1 000 to 250 000, preferably 90 000 to 150 000.

The polyol may also be a water-soluble organic copolymer which contains repeating units of vinyl alcohol and of non-ionic hydrophilic monomers, ionic hydrophilic monomers and/or hydrophobic monomers, the water-soluble organic copolymers comprising at least 20 mol% vinyl alcohol.

Examples of hydrophobic monomers are vinyl acetate, propylene oxide, methacrylate, methylethacrylate, octadecylacrylate, n-octadecylacrylamide, styrene, allyl stearate, vinyl stearate, ethene, propene, n-butene, isobutene, pentene, dodecene, octadecene and vinyl ether higher than methyl.

Examples of non-ionic hydrophilic monomers are vinyl pyrrolidone, ethylene oxide and acrylamide.

The copolymer can have random distribution of the monomer units or various degrees of block formations and/or alternations in the polymer.

Block formation means that in the copolymer there are regions which are formed by only one of the monomers, while in the case of alternation, a monomer of one sort is always bound to a monomer of the other sort.

The polyvinyl alcohols may also be modified, for example by cationic groups.

In a preferred process, the prepared stock mixture also has added to it cationic fixing agents in proportions from 0. 05 to 1% by weight (commercially available), based on fibrous material.

In a likewise preferred process, further conventional chemical additives (such as, inter alia, dry strengthening agents, wet strengthening agents and sizing agents) and fillers (inter alia, clay, calcium carbonate and talc) are mixed in.

What is also claimed is paper which is produced by means of a secondary fibrous material mixture prepared in accordance with the process of the invention.

The process according to the invention, comprising a combination of partially saponified polyvinyl alcohol, alkali modified bentonite and cationic fixing agents, is explained by the following exemplary embodiments : Exemplary embodiment 1 By means of a high-speed laboratory stirrer (10 000 rev/min) small cut paper pieces of constant fibrous composition and with an addition of different contact adhesives of about 10% was disintegrated at a consistency of 4% for a period of 5 min until it was free of specks (microstickies below the visibility limit of about 150) mi).

The stock mixture prepared in this way then had added to it, in a different sequence, various hydrophilicization agents, in particular partially saponified polyvinyl alcohols as masking agents, pigments with a high specific surface, in particular bentonites, as adsorption agents, and various cationic fixing agents of different chemical composition. The amount added was 1% by weight (commercially available) in the case of fixing and masking agents and, respectively, 5% by weight (solids) in the case of adsorption agents, based on fibrous material.

Following each addition of one of the abovementioned products, attention is paid to adequate thorough mixing before any possible addition of a further product. Following the addition of partially saponified polyvinyl alcohols, attention is paid to an action time of 30 min in accordance with the recommendation of the chemical suppliers before a further product is added to the stock mixture.

The preparation conditions, such as pH and temperature, can be varied over a wide range.

Then, laboratory sheets are formed in accordance with the ZELLCHEMING standard method and dried, and in addition filtrates from the stock samples are taken in order to determine the chemical oxygen demand (COD).

Since to date no method of determining microstickies below 150 um in stock systems exists, recourse must be made to COD determination, although this permits only a statement about the trend towards sticky loading (Wochenblatt fur Papierfabrikation (1997) 9, 468-477).

Therefore, composite materials from the formed, moist paper sheets are additionally prepared together with aluminium foil by being compressed with one another within 30 seconds in a hot press at 20 bar pressure and 130°C and later, following cooling and intermediate storage under standard conditions (24 h at 23°C/50% relative humidity), the forces needed to separate the two layers, approximating to the FINAT method, can be determined. The higher the separation force, the higher is the residual stickiness of the microstickies. In addition, the stickiness of any residues adhering to the laboratory stirrer, and their elimination by means of a powerful water jet, are assessed.

The results of some laboratory trials are presented in Tables 1 to 6. The results were deliberately selected at a dispersion temperature of 60°C, since partially saponified polyvinyl alcohols are only effective as a masking agent above 100°F (38°C).

If, for example, the additives already mentioned are added as individual components to a fibrous stock mixture with an addition of 10% adhesive of different composition, then in general a decrease in the stickiness of the microstickies is found on the basis of the separation force measurements (Tables 1, 3 and 5). In this case, fixing agents can be just as effective as adsorption or hydrophilicization agents (masking agents).

However, as expected, talc is generally less beneficial in its effect than bentonite as an adsorption agent (Tables 1 and 3).

On the other hand, hydrophilicization agents based on partially saponified polyvinyl alcohols belong in the group of additives which bring about the lowest reduction in the COD value in the filtrate, and to some extent even increase it. In this case, the degree of saponification and further properties of the polyvinyl alcohols used, such as molecular weight, viscosity and so on, appear to play a part (Tables 1 and 5).

This points to the fact that polyvinyl alcohol is no longer deposited on the microstickies but also strays into the effluent in dissolved form.

A remedy is provided only by the combination of partially saponified polyvinyl alcohol and alkali modified bentonite (Table 2, Variant A3 + B2). A fixing agent which is additionally used can, if necessary, reduce the COD value still further (Table 2, Variant A3 + B2 + A1), but in the least favourable case, can also make the separation force and COD values worse again (Table 2, Variant A3 + B2 + B1). From this it is possible to derive the fact that, depending on the stock and adhesive system used, the optimum fixing agent in this combination of additives has to be found.

Using the combination according to the invention of polyvinyl alcohol/bentonite (Table 2, Variant A3 + B2), it is clear that the best results with respect to the reduction of the stickiness of microstickies can be achieved. If, on the other hand, the adsorption agent bentonite (B2) is replaced by talc (A2), then this combination (polyvinyl alcohol A3 + talc A2) is less effective by far if the separation force values are used as a basis (Table 2), or even disadvantageous in the case of a different adhesive addition (rubber instead of acrylate adhesive, Table 6).

Combinations of adsorption agents (talc or bentonite) with fixing agents were likewise not very effective with respect to reducing the separation force (Table 4).

Exemplary embodiment 2 A broke paper had about 5% (solids) of an acrylate contact adhesive added to it, and this stock mixture was well and thoroughly mixed under practical conditions in a technical centre pulper for a period of about 45 min at a moderate consistency of 6% and a temperature of about 60°C. The pH of the stock mixture was adjusted to about 6.

In the order specified, the following were then added to the stock mixture as additives : 1. partially saponified polyvinyl alcohol (1%) 2. alkali modified bentonite (2. 5% solids) 3. cationic fixing agent (0. 6%) in each case a mixing period of 30 min (in the case of polyvinyl alcohol) and, respectively 10 min being maintained before the addition of the next component.

The COD content of originally about 320 mg 02/1 in the filtrate was reduced to below 150 mg 02/1 by means of this combination.

Residual stickiness of the microstickies in the formed paper sheet, which could be demonstrated by dyeing with a special blue dye, could no longer be demonstrated by means of separation force measurement (initial value of the sample without additives was more than 5 N).

This therefore confirms the positive results of the combination of partially saponified polyvinyl alcohol/bentonite/cationic fixing agent from the laboratory trial (Exemplary embodiment 1).

This stock mixture, thus treated in accordance with the invention, was used to produce new paper without any disruptive deposits in the paper machine system (machine part, water circulation).

Table 1: Influence of additives on the reduction of the stickiness of stickies (microstickies)<BR> ACRYLATE ADHESIVE I DISPERSION: pH = 7 at 60°C Addition as indivisual component no additive cationic fixing agent adsorptiona gent hydrophilicizaiton angent (masking agent) A1 B1 A2 B2 A3 B3 Separation force, N 6.17 3.66 3.98 3.53 3.91 4.49 3.34 COD, mg 02/1 18569 100 116 123 162 134 Sticky residues many Removability poor Fixing agent: 1 Dicyan diamide<BR> B1 Methylol amide<BR> Adsorption agent: A2 Talc(cationic)<BR> B2 Bentonite (alkali activated)<BR> Hydrophilicization agent (masking agent): A3 partially saponified polyvinyl alcohol I (DETAC#)<BR> B3 partially saponified polyvinyl alcohol II (RATIFIX#) (Clariant trademark) Table 2:<BR> Influence of the combination of additives on the reduction of the stickiness of stickies (microstickies)<BR> ACRYLATE ADHESIVE I Dispersion: pH = 7 at 60°C Addition as combination of additives no adsorptiona gent hydrophilicization hydrophilicization agent additive + fixing agent agent + adsorption agent + adsorption agent + fixing agent A2+B1 B2+B1 A3+A2 A3+B2 A3+B2+A1 A3+B2+B1 Separation force, N 6.17 6.78 6.92 5.28 3.01 3.30 4.37 COD, mg O2/I 185 268 243 121 116 39 248 Fixing agent; A1 dicyan diamide<BR> B1 Methylol amide<BR> Adsorption agent: A2 talc (cationic)<BR> B2 Bentonite (alkali activted)<BR> Hydrophilicization agent (masking agent): A3 partially saponified polyvinyl alcohol I (DETAC#) Table 3:<BR> Influence of additives on the reduction of teh stickiness of stickies (microstickies)<BR> ACRYLATE ADHESIVE II Dispersion: pH < 3 at 60°C Addition as individual component no additive cationic fixing agent adsorption agent C1 A2 B2 Separation force, N 4.28 3.29 3.71 3.80 COD, mg O2/I 112 110 88 165 Sticky residues few Removability good Fixing agent: C1 POL YDADMAC#<BR> Adsorption agent: A2 Talc (cationic)<BR> B2 Bentonite (alkali activated) Table 4:<BR> Influence of the combinaiton of additives on the reduction of teh stickiness of stickies (microstickies)<BR> ACRYLATE ADHESIVE II Dispersion: pH < 3 at 60°C Additions as combinaiton of additives no additive adsorptiona gent As+ adsorption agent B2+ fixing agent C1 fixing agent C1 Separation force, N 4.29 4.36 4.28 COD, mg O2/I 112 82 46 Fixing agent: C1 POL YDADMAC#<BR> Adsorption agent: A2 Talc(cationic)<BR> B2 Bentonite (alkali activated) Table 5:<BR> Influence of additives on the reduction of the stickiness of stickies (microstickies)<BR> ACRYLATE ADHESIVE II Dispersion: pH < 3 at 60°C<BR> Addition as individual component no additive adsorption agent A2 hydrophilicization agent (masking agent) B3 Separation force, N 4.91 4.85 4.20 COD, mg O2/I 171 156 212 Sticky residues many Removability poor Adsorption agent: A2 Talc (cationic)<BR> hydrophilicization agent (masking agent): B3 partially saponified polyvinyl alcohol II (RATIFIX#) Table 6:<BR> Influence of the combinaiton of additives on the reduction of teh stickiness of stickies (microstickies)<BR> RUBBER ADHESIVE Dispersion: pH = 7 at 60°C Addition as combinaiton of hydrophilicization agent no additive (masking agent) A3 + adsorption agent A2 Separation force, N 4.91 5.85 COD, mgO2/I 171 214 Adsorption agent: A2 Talc (cationic)<BR> Hydrophilicization agent (masking agent): A3 partially sponified polyvinyl alcohol I (DETAC#)