METHOD FOR REDUCING THE WINDING LEVEL ADHESIVENESS OF AN ADHESIVE TAPE ROLL
20180009002 · 2018-01-11
Inventors
Cpc classification
B05D1/62
PERFORMING OPERATIONS; TRANSPORTING
C09J7/401
CHEMISTRY; METALLURGY
B29C63/02
PERFORMING OPERATIONS; TRANSPORTING
International classification
B05D1/00
PERFORMING OPERATIONS; TRANSPORTING
B05D5/08
PERFORMING OPERATIONS; TRANSPORTING
B29C63/02
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The invention relates to a method for reducing end face stickiness of a roll (1) of adhesive tape, by supplying a precursor (18) to a plasma stream (20), using the plasma stream (20) enriched with the precursor (18) to coat a carrier film (2) with a passivation coat (3) in a plasma process, placing a carrier film section (5) by its passivation-coated side onto an end face (4) of the roll (1) of adhesive tape, removing the carrier film section (5) and leaving at least part of the passivation coat (6) on the end face (4) and reducing its end face stickiness.
Claims
1. A method for reducing end face stickiness of a roll of adhesive tape, comprising: supplying a precursor to a plasma stream, using the plasma stream enriched with the precursor to coat a carrier film with a passivation coat in a plasma process, placing a carrier film section by its passivation-coated side onto an end face of the roll of adhesive tape, and removing the carrier film section and leaving at least part of the passivation coat on the end face and reducing its end face stickiness.
2. The method as claimed in claim 1, wherein the precursor is supplied to a plasma stream at a plasma nozzle, and the plasma stream enriched with the precursor is directed at a surface of the carrier film.
3. The method as claimed in claim 1, wherein a liquid precursor is vaporized and then supplied to a carrier gas.
4. The method as claimed in claim 1, wherein siloxanes are used as precursor.
5. The method as claimed in claim 4, wherein HMDSO is used as precursor.
6. The method as claimed in claim 1, wherein the carrier film section is pressed with a laminating roller onto the end face.
7. The method as claimed in claim 1, wherein the carrier film is provided with a passivation coat 10 nm to 600 nm thick.
8. The method as claimed in claim 1, wherein a material selected from the group consisting of PET, PVC, PC, PP, and PE is selected for the carrier film.
9. The method as claimed in claim 1, wherein an apolar polymer is selected as material of the carrier film.
10. The method as claimed in claim 1, wherein the roll of adhesive tape is removed by slitting from a wide adhesive tape roll.
11. The method as claimed in claim 10, wherein while the wide adhesive tape roll is being slit up into rolls of adhesive tape, the carrier film is being plasma-coated.
Description
[0026] The invention is described with reference to a working example in four figures, in which:
[0027]
[0028]
[0029]
[0030]
[0031] The method of the invention for reducing end face stickiness of a roll 1 of adhesive tape is based on first fabricating a carrier film 2 having a passivation coat 3 by means of a plasma jet 10 which is shown in
[0032] In accordance with
[0033] The roll end face 4 here refers to the two end-face sides of the rolled-up roll 1 of adhesive tape. The roll 1 of adhesive tape has a substrate web 7 and has the pressure-sensitive adhesive web 8 applied to one side of the substrate web 7. The substrate web 7 may be a film, a fabric or paper.
[0034] The roll 1 of adhesive tape shown in
[0035] The substantially circular end-face side of the roll 1 of adhesive tape, shown in
[0036] In other embodiments of the roll 1 of adhesive tape, the adhesive tape 9 has a very small ratio of a thickness of the substrate web 7 to a thickness of the pressure-sensitive adhesive web 8. With adhesive tapes 9 of this kind, which are referred to as thick-layer products, it is common to use viscoelastic materials for the substrate webs 7 with their own adhesive properties, and so the entire end face 4 of the roll 1 of adhesive tape is adhesive.
[0037] As a result of the tackiness of the roll end face 4, after contact with other objects, the roll 1 of adhesive tape on removal is destroyed or deformed and can no longer be deployed for use. This is a problem in particular with narrow rolls, which have only a low mechanical strength.
[0038] The tackiness of the roll end face 4 is reduced by application of a part of the passivation coat 6. For this purpose, in a first method step in accordance with
[0039] The treatment of a surface of the carrier film 2 takes place at or close to atmospheric pressure, although the pressure in the electrical discharge chamber of the plasma jet 10 or in the process gas channel may be higher. A plasma here refers to an atmospheric pressure plasma, which is an electrically activated, homogeneous, reactive gas which is not in thermal equilibrium, having a pressure close to the ambient pressure in an active region. Generally speaking, the pressure is 0.5 bar more than the ambient pressure. The electrical discharges and the ionization processes in the electrical field cause activation of the process gas, and highly excited states are generated in the gas constituents. The gas or gas mixture used is referred to as process gas 12. The precursor 18, in gas form or as an aerosol, is then supplied to the process gas 12 in the plasma nozzle 16, which is connected via a gas-conducting channel to the precursor unit 17, and it is this precursor 18 that forms the actual passivation coating 3 on the surface of the carrier film 3.
EXAMPLE 1
[0040] In this example, hexamethyldisiloxane is supplied to the process gas and is excited in the process gas, significantly increasing its reactivity at the same time. As a result, the siloxane is accommodated optimally on the surface of the carrier film 2 and attaches firmly. In this example, a plasma polymerization layer is generated using the PlasmaPlus plasma technology of Plasmatreat GmbH.
[0041] The experimental system comprises the following parameters, conditions, and technical data: [0042] Carrier film 1: siliconized BOPP [0043] Plasmajet 10: Generator FG 5001 from Plasmatreat GmbH, fixed nozzle 216028WE [0044] Precursor 18: Hexamethyldisiloxane (HMDSO); [0045] Precursor quantity: 40 g/hour [0046] Number of treatments: 1-3-fold [0047] Treatment rate: 80 rpm for rotary table with the carrier film 2, corresponding to an application rate of 5 m/min of the plasma nozzle 16 [0048] Distance of plasma nozzle 16 from carrier film 2: 15 mm [0049] PCT (Pulse Cycle Time): 100%
[0050] BOPP here stands for biaxially oriented Polypropylenes. PCT (Pulse Cycle Time) means that the plasma discharge is modulated by pulsing. The switching on and off may improve the service lives of the electrodes and influence the formation of the reactive species. In this case, operation takes place with continuous discharge.
[0051] After the plasma coating of the carrier film 2, the carrier film section 5 removed is laminated onto the end face 4 of the roll 1 of adhesive tape using a 4 kg roller and is immediately removed. On the carrier film section 5 removed, the complement of the transferred part of the passivation coat 6 is recognizable as a result of refraction of light. In the present example, for the tesa product ACXplus 7055, a significantly reduced peel adhesion on the roll end face 4 was found. The treated rolls 1 of adhesive tape no longer adhere by the end face 4 to smooth or metallic substrates, and can be picked up again without deformation.
EXAMPLE 2
[0052] A second example uses the indirect plasma process PlasmaLine® from VITO, Belgium. This plasma treatment was developed for the finishing of plastics surfaces on the basis of the corona technology under atmospheric conditions. It constitutes a DBD (dielectric barrier discharge) system. One construction of the plasma nozzle is illustrated in “Atmospheric DBD plasma processes for production of lightweight composites” (Vangeneugden et al., 2013, 21.sup.st International Symposium on Plasma Chemistry (ISPC 21), Sunday 4 Aug.-Friday 9 Aug. 2013, Cairns Convention Centre, Queensland, Australia).
[0053] Using a slotted nozzle, a linear atmospheric plasma is blown out via the process gas 12 onto the carrier film 2 to be treated, without the need for a counterelectrode 15. The introduction of reactive chemicals into the stream of process gas produces a thin, functional passivation coat 3, without altering the properties of the base material of the carrier film 2. The plasma stream 20 in the case of APTES is driven forward by its flow rate from the electrode tip 13 and after a short distance is guided onto the carrier film 2. With this process, the carrier film 2 coated was siliconized BOPP, and the parameters set were as follows: [0054] Distance of nozzle from [0055] BOPP for treatment: 3.5 mm [0056] Speed: 5 m/min [0057] Power: 2500 W [0058] Process gas stream: 900 sl/min [0059] Type of aerosol: APTES [0060] Number of treatments: 5-times
[0061] APTES is 3-aminopropyltriethoxysilane. After the plasma treatment of the carrier film 2, the carrier film section 5 is laminated with a 4 kg roller onto the end face 4 of the roll 1 of adhesive tape and is immediately removed. The complement of the transferred part of the passivation coat 6—in the present case a plasma polymerization coat—can be seen on the removed section 5 of carrier film as a result of refraction of light. With the tesa® product ACXplus 7055, a significantly reduced peel adhesion of the roll end face 4 can be observed. The treated rolls 1 of adhesive tape no longer adhere by the roll end face 4 on a smooth or metallic substrate, and could be picked up again without deformation.
[0062] One class of monomers frequently used as a precursor in plasma processes are siloxanes. They consist of a skeleton of silicon and of oxygen atoms with a plurality of hydrocarbon radicals. Depending on the monomer parameters and plasma parameters used, it is possible to deposit quartzlike passivation coats 3 with a variable hydrocarbon fraction (SiOxCyHz).
[0063] Preference is given to the deposition of pure SiOx passivation coats 3, which can be produced in the form of thin, glasslike coats.
[0064] For the deposition of passivation coats, the following polyfunctional siloxanes are suitable: HMDSO (hexamethyldisiloxane); TEOS (tetraethoxysilane); PDMS (polydimethylsiloxane). In the case of the deposition of the frequently employed HMDSO as passivation coat, in the plasma, there is typically first elimination of hydrogen and of whole methyl groups, which react in the presence of oxygen to form water, CO, and CO.sub.2. The Si-O-Si framework is usually retained as a building block for the quartzlike polymer layer as passivation coat 3.
[0065] As carrier films 2 it is possible in principle to utilize all polymeric films, including more particularly films of PET, PVC, PC, PP, or PE.
[0066] However, the anchorage to apolar polymers of a passivation coat 3 to be transferred is much less pronounced, and so the transfer of the passivation coat 3 to the roll end face 4 is easier. It has emerged as being advantageous, moreover, that siliconized carrier films 2 significantly enhance transfer and can be removed with less expenditure of force.
List of Reference Numerals
[0067] 1 roll of adhesive tape [0068] 2 carrier film [0069] 3 passivation coat [0070] 4 roll end face [0071] 5 carrier film section [0072] 6 detached part of passivation coat [0073] 7 substrate web [0074] 8 pressure-sensitive adhesive web [0075] 9 adhesive tape [0076] 10 plasma jet [0077] 11 inlet [0078] 12 process gas [0079] 13 electrode tip [0080] 14 alternating voltage [0081] 15 counterelectrode [0082] 16 plasma nozzle [0083] 17 precursor unit [0084] 18 precursor [0085] 19 precursor nozzle [0086] 20 plasma stream