EP1434829A1

EP1434829A1 - Method of gluing hydrophobic and oleophobic substrates which are intended for packaging

Info

Publication number: EP1434829A1
Application number: EP02785513A
Authority: EP
Inventors: Nicolas Sajot; Benoít POLLACCHI; Saida Sellak
Original assignee: Bostik Findley SA
Current assignee: Bostik SA
Priority date: 2001-10-02
Filing date: 2002-10-01
Publication date: 2004-07-07
Also published as: WO2003029379A8; US20050059759A1; FR2830257B1; US20080221247A1; JP2005504164A; WO2003029379A1; FR2830257A1; AU2002350812B2

Abstract

The invention relates to a method of gluing substrates which are hydrophobic and oleophobic as a result of having been treated earlier using a fluorinated compound, said substrates being intended for packaging. The inventive method consists in applying an adhesive to at least one of the substrates, said adhesive comprising: a) 5 to 50 wt. % of at least one styrenic block copolymer and, preferably, 15 to 30 %.; b) 20 to 60 wt. % of at least one tackifying resin which is compatible with the non-styrene phase and, preferably, 35 to 55 %; c) 0 to 20 wt. % of at least one tackifying resin which is compatible with the styrene phase and, preferably, 5 to 15 %; d) 5 to 25 wt. % of at least one thermofusible wax and, preferably, 10 to 17 %; e) 3 to 20 wt. % of liquid plasticisers which are normally used in thermofusible adhesives; and f) additives. In this way, said mixture presents the following characteristics: (i) a viscosity of between 400 and 3000 mPa.s at 170 DEG C and, preferably, between 700 and 1400 mPa.s; and (ii) a softening point included between 75 and 120 DEG C.

Description

METHOD OF ASSEMBLING BY ADHESIVE HYDROPHOBIC AND OLEOPHOBIC SUBSTRATES FOR THE MARKET

PACKAGE

The subject of the present invention is a method of assembling by bonding of substrates rendered oleophobic and hydrophobic using an adhesive based on styrene block copolymers. It also relates to adhesives allowing the bonding of so-called difficult substrates such as those rendered oleophobic and hydrophobic. Bonding materials from the packaging industry, especially paper and cardboard, is a well-known technique. In practice, manufacturers use a wide range of adhesives and in particular hot-melt adhesives, very often called by professionals Hot Melt or HMA, initials in English for Hot Melt Adhesives, an abbreviation which will be used subsequently to designate them. These HMAs are generally composed of the following main constituents: a polymer which gives the final adhesive its structure, a "tackifier" main adhesion agent and a plasticizer such as a wax or a mineral oil which gives the adhesive its thermal properties and rheological. In the vast majority of cases, the choice of adhesive will be based primarily on the selection of the polymer. The polymer used in HMA consists for example of ethylenic type copolymers such as ethylene vinyl acetate (EVA), amorphous poly-alphaolefins (APAO), polyolefins synthesized by metallocene catalysis, low weight polyethylenes molecular or amorphous polypropylenes. It is also proposed for the polymer block copolymers of styrene where the latter is associated with a co-monomer such as isoprene or butadiene, hydrogenated forms of these components. The choice will naturally be made on a structural property criterion but which largely takes into account the concept of raw material prices.

However, certain packaging variants pose specific adhesion problems, “difficult” packaging, which is in particular the case of packaging (cardboard for cases, kraft for bags, etc.) beforehand. treated to give them resistance to liquids (hydrophobes) and oils and fats (lipophobes). In addition, this type of packaging which must naturally present all the conventional advantages known in terms of protection of the materials to be packaged, robustness, longevity, appearance or various other functionalities can be subjected to significant variations in temperature ranging generally from - 10 °. C at + 40 ° C, or even -40 ° C at + 80 ° C. Indeed, the preparation of food products for example, as well as their conservation or the conditions in which they are stored, require that the packaging is resistant and continues to perform its function under extreme temperatures. Thus, the bonding must be effective during all of the packaging operations or the packaging life cycle.

The permanent improvement of the barrier properties to water, oils and fatty substances, of supports intended for the packaging market, due in particular to the evolution and effectiveness of mass or "size press" treatments ( on the front and back) with ever more efficient fluoropolymers, makes it sometimes difficult to effectively bond this type of support, with the usual adhesives, especially when the packaging is subjected to significant temperature variations. A recent example of this development is the use of fluorinated compounds such as fluorinated polyacrylates in the treatment of supports intended for packaging in order to give them oleophobic and hydrophobic barrier properties, namely a high level of resistance to water and a high level of resistance to oils and fatty substances. These fluorinated compounds of different types are used in the aqueous phase and are therefore water-soluble. These are either small fluorinated molecules, for example fluorinated phosphate salts or fluorinated sulphate salts or fluorinated acrylic copolymers, that is to say copolymers of which at least one monomer contains a perfluorinated unit, the other non-fluorinated monomers being acrylic or vinyl. The latter type of fluorinated compounds are fluorinated latexes, that is to say dispersions of copolymers in water in the presence of a surfactant, ie copolymers water-soluble or water-dispersible, copolymers in general of cationic type.

These fluorinated compounds are used either in the bulk of the substrate, for example paper, or in surfacing of said substrate. The adhesive must be able to respond to a whole series of sometimes contradictory constraints linked both to the conditions of use of the packaging and to the nature of the various substrates used, identical or different or composite materials, most of the time to based on paper or cardboard, but also on metal (aluminum) or plastics (polyethylene, polypropylene, polyethylene terephthalate, polystyrene ...) at least one of which is a substrate made difficult by a treatment based on fluorinated compounds such than fluorinated polyacrylates. It should also be added that the operating conditions for applying adhesives play an important role.

In order to illustrate the diversity of the constraints, it may be mentioned for the bonding of the bags the bonding of the handles where the adhesive must be deposited on the support treated with a fluorinated compound. Besides the quality of the bonding, the cohesion of the glue is important for this application. longitudinal bonding where the bead is deposited on the edge of one of the substrates to be assembled, the open time of the adhesive is the critical parameter for this step due to the machine rate. It is generally between 1 and 10 s. transverse bonding where the bead of glue is deposited on the width of one of the substrates to be assembled. The machinability is the critical parameter here for this step, the hot melt streak being able to cause machine fouling during application. sticking the bottom or closing the bag: this is mainly an application targeted by “pinch bottoms” bags. The adhesive bead (s) being (are) deposited (s) on the support (s), the setting speed as well as the machinability are here the critical parameters. Since the contents are hot, when the bag is closed, the adhesive must withstand temperatures of the order of at least 60 ° C., so as not to reopen. In the field of making cases, it should be noted for: the formation of cases where the bead of adhesive is deposited on the tab of the case or on the treated side. The adhesive must have good performance between -10 ° C to + 60 ° C, for the packaging and transport of the cases. - the case closure where the adhesive bead is deposited on the cardboard flap (s). The setting speed, its temperature resistance and its machinability are the critical parameters here.

The implementations described here are simply examples of the most commonly encountered difficulties. The adhesive must be able to be used for any assembly in which at least one of the supports has undergone a hydrophobic and oleophobic treatment.

The adhesive must therefore have very specific and sometimes contradictory characteristics, short setting time, good wetting power, very good thermal behavior of the adhesion after temperature cycles between - 10 ° C and + 60 ° C, or even between - 40 ° C and + 80 ° C as well as a low viscosity due to the fluorinated treatment.

The method according to the invention intends to solve this problem, in particular by selecting the polymer and its structure.

The subject of the invention is a method of assembling by gluing so-called difficult substrates intended for making packaging, which consists in applying to at least one of the substrates an adhesive comprising: a) 5 to 50% by weight of block copolymer obtained from styrenic monomers and from at least one other co-monomer such as ethylene, propylene, isoprene, butadiene, butylene or any other co-monomer forming a two-phase medium with the styrene phase. b) 20 to 60% by weight of at least one tackifying resin compatible with the non-styrenic phase. having a softening point measured according to standard EN 1238 of between 5 and 150 ° C, c) 0 to 20% by weight of at least one tackifying resin compatible with the styrenic phase d) 5 to 25% by weight of at least one wax, among the waxes conventionally used in hot-melt adhesives having a melting point of between 70 to 120 ° C. e) 3 to 20% by weight of liquid plasticizers conventionally used in hot-melt adhesives such as mineral oils, with paraffinic or naphthenic character, or also polybutenes or phthalates, said adhesive having a viscosity of between 400 and 3000 mPa.s to 170 ° C and a softening point, measured using the so-called ball-ring method, between 75 and 120 ° C. The adhesive of the process of the invention can optionally comprise various additives such as antioxidants ...

Component a) according to the method of the invention, (the copolymer) has a structure of the di-block, tri-block or multi-block type, linear, radial or star, the intermediate block consisting of at least one of the co- monomers listed above and may undergo a hydrogenation phase. The block copolymer or the mixture of block copolymers comprises a mass percentage of the styrene phase in the polymer of between 10 and 40% and preferably between 20 and 35%, a mass percentage of di-block structures in the variable polymer generally between from 0 and 50%, a flow index (MFl = Melt Flow Index) measured according to condition 10 of standard NFT 51-016 between 2 and 70 g / 10min.

Component a) is preferably a styrene-ethylene butylene-styrene block copolymer (denoted SEBS) or any other similar structure. It is possible to mix this constituent a) with other polymers such as ethylene copolymers, polyolefins, polymers obtained by metallocene catalysis. The content of the adhesive in constituent a) generally between 5 and 50% by mass is preferably between 15 and 30%.

Component b) is mainly chosen from the resins conventionally used in hot-melt adhesives such as: rosin or its derivatives, rosin ester, optionally hydrogenated, polyterpenes, terpene-phenolics or their derivatives, optionally hydrogenated polymers from aliphatic or aromatic cuts or mixtures of these cuts, having a softening point measured according to standard EN 1238 of between 5 and 150 ° C, preferably between 70 and 125 ° C. The majority resin will preferably be non-aromatic with a marked polar character. The content of component b) is between 20 and 60% by mass and preferably between 35 and 55%.

Component c) consists of a resin or a mixture of conventionally used resins such as polymers from aromatic cuts, or else poly-alphamethylstyrene. It is preferably chosen from resins resulting from the polymerization of alphamethylstyrene, for example having a softening point measured according to standard EN 1238 of between 80 and 160 ° C. The content of component c) is between 0 and 20% by mass and preferably between 5 and 15%.

Component d) is mainly chosen from so-called microcrystalline waxes conventionally used in hot-melt adhesives, having a melting point (ASTM D127 method) of between 70 and 100 ° C, preferably between 80 and 95 ° C. In minor amount, component d) may contain synthetic waxes such as polyolefins with short and rather linear chains, obtained by polymerization according to conventional methods (Ziegler Natta; Fischer Tropsch), the melting point of which is measured according to the standard (ASTM method). D127) is high, generally between 80 and 150 ° C and preferably between 90 and 120 ° C. The content of component d) is between 5 and 25%, and preferably between 10 and 17% by mass.

Other types of polymers may be present in a minority in the adhesive, for example ethylene-vinyl acetate (EVA) copolymers, polyolefins of various processes or types, other block copolymers of styrene. The various additives will, for example, be the antioxidants conventionally used in hot-melt adhesives or in the processing industry. thermoplastics such as hindered phenolic derivatives, phosphites or their mixtures.

The viscosity of the hot-melt adhesive of the process of the invention will be between 400 and 3000 mPa.s at 170 ° C and preferably between 700 and 1400. Its softening point measured according to the so-called ball-ring method known from l the skilled person will be between 75 and 120 ° C.

The adhesive according to the process of the invention is obtained by mixing a), b), c), d) and e) as well as any additives, by any suitable means, for example by simple mixing at a temperature between 150 and 170 ° C. The adhesive can be easily characterized by chemical analysis according to conventional deformulation and identification methods for the various fractions, in particular by infrared spectrometry, 1 H and 13 C nuclear magnetic resonance, elementary micro-analysis, gel or high permeation chromatography. -performance or by differential calorimetry (DSC or Difficult Scannning Calorimetry).

On a practical level, the adhesives of the process of the invention are applied according to the conventional methods used in the field of hot-melt adhesives, on the packaging line or, on the contrary, on the margin thereof. From a melting tank, using heated and heat-insulated pipes, by extrusion nozzles: controlled removal of one or more cords on a first support, docking of the second support with possible pressing of the adhesive joint as well realized. HMAs of low viscosities can be applied by any other possible means such as for example lip nozzle, multi-stroke nozzles, disc, impression or also by the Sift Proof process developed by the company Nordson. The temperature of the adhesive at the time of application is conventionally between 150 and 180 ° C.

This type of process is carried out according to certain specific parameters. For example, the machine open time is the time that elapses between the application of the adhesive on the first substrate and the approach of the second substrate.

The machine pressing time, meanwhile, is the time immediately after bonding during which the two bonded substrates are kept in contact with a force at least equal to the reopening force of the packaging without adhesive.

The adhesive is applied to thin substrates, that is to say a thickness generally between 0.05 and about 2 mm, these substrates being able to be part of a thicker complex structure. This substrate can often be based on paper or cardboard, such as virgin or recycled kraft, having a low density or on the contrary a compact thin substrate, optionally treated with a fluorinated compound or on the surface with acrylic or UV crosslinked varnishes, or specific coatings, possibly with uncoated areas, reserves, to allow the removal and attachment of the adhesive on the substrate.

The nature of the various substrates used is chosen from identical or different or composite materials, mostly based on paper or cardboard, metal for example aluminum or plastics such as polyethylene, polypropylene, polyethylene terephthalate, polystyrene, ...

EXAMPLES

The method of the invention is illustrated by 6 examples in which, under conditions representative of use, the performances of various HMA formulas of the prior art and of HMAs according to the invention have been compared.

To evaluate the performance of HMAs in the process according to the invention, various tests are carried out: determinations of viscosity, open time, setting time, heat resistance and temperature (- 10 ° C to + 60 ° C) .

To assess the open time, we deposit, with a setting time of 1 s, at a temperature of 170 ° C, on a standard cardboard with double fluting (covers 140 and 200 g / m ² with a cobb at 1800 respectively 135g / m ² and 145 g / m ² measured according to standard EN 20535), a bead of adhesive, at a quantity of 2 g per linear meter, then a second cardboard of the same kind is displayed on said cardboard after successive delays of 1, 2, 3, 4, 5 ... seconds and this as long as the defibration of the cardboard is less than 90% of the surface covered by the adhesive joint. The open time corresponds to the maximum duration at the end of which the adhesive secures the two cartons.

The setting time is evaluated by performing the reverse operation with an adhesive having an open time of 1 s and by carrying out the take-off operation of the two cartons after successive delays of 1, 2, 3, 4, 5 ... seconds and this until the adhesive has secured the two cartons, that is to say that more than 90% of defibration of the surface of glued cardboard is obtained. The setting time corresponds to the minimum duration at the end of which the adhesive secures the two cartons.

The holding heat is assessed by using the method SAFT (shear adhesion failure temperature): Samples were prepared in the same way as for determining the open time and setting time, on flexible substrates INTEGRAL type ^®, ALIPACK ^® or cartons treated with fluorinated compound. One day after gluing, one of the supports is suspended while on the other one hangs a mass of 250 g (for a sample width of 5 cm), thus causing a force of creep on the bead. adhesive. The whole is placed in an oven and subjected to a temperature rise from 23 ° C. at a rate of 5 ° C. per half hour. The result of the test is the temperature at which the assembly failed under the creep stress.

Temperature resistance tests are performed in the same way as for the evaluation of open time, but employees supports are flexible media type INTEGRAL ^®, ^® ALIPACK or cardboard treated with fluorine compound. After manual bonding, with a bead of adhesive of 2 g / linear meter, at 170 ° C and a pressing time of 1 s, the samples are subjected to the agreed temperature, in a ventilated oven. The operation is carried out on at least 4 samples which are taken as the average.

The supports used for our tests are FORAPERLE ^® 325 treated paper or cardboard at a concentration of approximately 3%. By measuring the oleophobia on these fibrous cellulosic supports, according to the standardized method of the TAPPI 559 test kit, values are found between 8 and 12, or even greater than 12. In addition, the typical characteristics for kraft paper are as follows:

The raw materials used in the examples are as follows

The examples including the comparative examples which follow, the results of which are grouped in the table on pages 12 and 13, will make the invention better understood.

EXAMPLES 1 A6:

Examples 1 and 2 relate to first generation adhesives of the prior art on EVA base (ex. 1) and on APAO base (ex. 2), Examples 3 and 4 are comparative examples using SEBS bases described in l prior art and examples 5 and 6 of the examples based on SEBS according to the method of the invention. In light of these examples, we see that:

It is necessary to make a judicious choice of the SEBS (s) to use. As shown in Example 4, SEBS with a low MF1 (Melt Flow Index) gives a high viscosity which is unsuitable for the process according to the invention. - The use of SEBS with adapted MFl (example 3) is however not sufficient. It is especially necessary to combine a mixture of oil and wax according to the invention, in order to obtain good adhesion at -10 ° C.

The amorphous polymers of APAO type (example 2) do not make it possible to fill the specifications in terms of setting speed. As for the EVAs (example 1), they are not versatile enough to guarantee bonding between - 10 ° C and + 60 ° C on the hydrophobic and oleophobic supports, said to be difficult, according to the process of the invention.

The combination of SEBS with adapted MFl, of hydrogenated polar resin as well as of oil and wax (example 5 and 6) according to the invention is a necessary condition to meet all of the application specifications.

The thermal resistance at + 60 ° C, with low viscosity products, can only be achieved with suitable SEBS with MFl, combined with waxes. The latter make it possible to reduce the viscosity of the rubbers, as shown in Examples 5 and 6, without penalizing the thermal resistance.

The thermal resistance at -10 ° C., combined with the characteristics described above, is achieved by determining with precision the right polymer / resin ratio (examples 5 and 6). An excess of resin tends to stiffen the adhesive, and deteriorate the resistance to cold (example 3).

a: comparative; b; according to the invention; ç: Results expressed in% defibration; RA = adhesive failure; RC. cohesive rupture of the adhesive joint

Claims

1) Method of assembling by bonding of substrates rendered hydrophobic and oleophobic by prior treatment by means of a fluorinated compound intended for the packaging market consisting in applying to one at least of the substrates a hot-melt adhesive comprising:

5 to 50% by weight of at least one styrenic block copolymer and preferably 15 to 30%,

20 to 60% by weight of at least one tackifying resin compatible with the non-styrenic phase and preferably 35 to 55%,

0 to 20% by weight of at least one tackifying resin compatible with the styrenic phase and preferably 5 to 15%,

- 5 to 25% by weight of at least one hot-melt wax, and preferably 10 to 17%, - 3 to 20% by weight of liquid plasticizers conventionally used in hot-melt adhesives, such as the adhesive resulting from this mixture present :

- a viscosity between 400 and 3000 mPa.s at 170 ° C, and preferably between 700 and 1400 mPa.s. - a softening point between 75 and 120 ° C.

2) Process according to claim 1 characterized in that the block copolymers according to the invention are obtained from styrenic monomers and from at least one other monomer such as ethylene, propylene, isoprene, butadiene, butylene or any other monomer forming a two-phase medium with the styrene phase, constituting a structure of the di-block, tri-block or multi-block, linear, radial or star type, the intermediate block consisting of at least one of the listed monomers above, said block copolymers or mixtures of block copolymers having:

a mass percentage of the styrene phase in the polymer of between 10 and 40%, and preferably between 20 and 35%,

- a mass percentage of diblock structure between 0 and 50%, - a flow index (MFl = Melt Flow Index) according to condition No. 10 of standard NFT 51-016 between 2 and 70 g / 10min.

3) Process according to claim 2 characterized in that the styrenic block copolymer is a copolymer of the Styrene / Ethylene / Butadiene / Styrene type (SEBS).

4) Method according to claim 1 characterized in that the tackifying resin or the mixture of resins compatible with the non-styrenic phase is chosen from:

- rosin or its derivatives, in particular rosin esters, optionally hydrogenated,

- polyterpenes, terpene-phenolics or their derivatives,

- optionally hydrogenated polymers from aliphatic or aromatic cuts or mixtures of these cuts, having a softening point measured according to standard EN 1238 of between 5 and 150 ° C, preferably between 75 and 120 ° C.

5) Method according to claim 4 characterized in that the tackifying resin compatible with the non-styrenic phase is non-aromatic with marked polar character.

6) Method according to claim 1 characterized in that the tackifying resin or the mixture of resins compatible with the styrenic phase is chosen from polymers derived from aromatic cuts or derived from the polymerization of alpha methyl styrene, having a softening point measured according to standard EN 1238 between 60 and 160 ° C.

7) Method according to claim 1 characterized in that the wax is chosen mainly from the so-called microcrystalline waxes having a melting point measured according to the ASTM D 127 method, between 70 and 10 ° C and preferably between 80 and 95 ° C.

8) Method according to claim 1 characterized in that the liquid plasticizer or the mixture of liquid plasticizers is chosen from mineral oils, paraffinic or naphthenic, polybutenes or phthalates.

9) Hot melt adhesive comprising of: 5 to 50% by weight of at least one styrenic block copolymer and preferably 15 to 30%,

- 20 to 60% by weight of at least one tackifying resin compatible with the non-styrenic phase and preferably 35 to 55%, - 0 to 20% by weight of at least one tackifying resin compatible with the styrenic phase and preferably 5 to 15%,

5 to 25% by weight of at least one hot-melt wax, and preferably 10 to 17%,

- 3 to 20% by weight of liquid plasticizers conventionally used in hot-melt adhesives, such as the adhesive resulting from this mixture has:

- A viscosity between 400 and 3000 mPa.s at 170 ° C, and preferably between 700 and 1400 mPa.s a softening point between 75 and 120 ° C. 10) Adhesive according to claim 9 characterized in that the block copolymers are obtained from styrenic monomers and from at least one other monomer such as ethylene, propylene, isoprene, butadiene, butylene or any other monomer forming a two-phase medium with the styrene phase, constituting a structure of the di-block, tri-block or multi-block, linear, radial or star type, the intermediate block consisting of at least one of the monomers listed above, said block copolymers or mixtures of block copolymers having:

- a mass percentage of the styrene phase in the polymer of between 10 and 40%, and preferably between 20 and 35%, - a mass percentage of diblock structure of between 0 and 50%,

- a flow index (MFl = Melt Flow Index) according to condition No. 10 of standard NFT 51 - 016 between 2 and 70 g / 10min.

1 1) An adhesive according to claim 10 characterized in that the styrenic block copolymer is a copolymer of the Styrene / Ethylene / Butadiene / Styrene type (SEBS). 12) Adhesive according to claim 9 characterized in that the tackifying resin or the mixture of resins compatible with the non-styrenic phase is chosen from:

- polyterpenes, terpene-phenolics or their derivatives,

13) Adhesive according to claim 12 characterized in that the tackifying resin compatible with the non-styrenic phase is non-aromatic with marked polar character.

14) Adhesive according to claim 9 characterized in that the tackifying resin or the mixture of resins compatible with the styrenic phase is chosen from polymers resulting from aromatic cuts or resulting from the polymerization of alpha methyl styrene, having a softening point measured according to standard EN 1238 between 60 and 160 ° C.

15) Adhesive according to claim 9 characterized in that the wax is mainly chosen from so-called microcrystalline waxes having a melting point measured according to the ASTM D 127 method, between 70 and 120 ° C and preferably between 80 and 95 ° vs.

16) Adhesive according to claim 9 characterized in that the liquid plasticizer or the mixture of liquid plasticizers is chosen from mineral oils, of paraffinic or naphthenic nature, polybutenes or phthalates.

17) Packages made of thin substrates, at least one of which has been treated to be made hydrophobic and lipophobic, assembled together by means of an adhesive of claims 9 to 16. 18) Packages according to claim 17 characterized in that they consist of identical, different or composite materials chosen from paper, cardboard, a metal such as aluminum or plastics such as polyethylene, polypropylene, polyethylene terephthalate and polystyrene.