EP0037370A2 - Matériau d'enregistrement au charbon sans support - Google Patents

Matériau d'enregistrement au charbon sans support Download PDF

Info

Publication number
EP0037370A2
EP0037370A2 EP81730040A EP81730040A EP0037370A2 EP 0037370 A2 EP0037370 A2 EP 0037370A2 EP 81730040 A EP81730040 A EP 81730040A EP 81730040 A EP81730040 A EP 81730040A EP 0037370 A2 EP0037370 A2 EP 0037370A2
Authority
EP
European Patent Office
Prior art keywords
layer
top layer
solution
color
synthetic resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP81730040A
Other languages
German (de)
English (en)
Other versions
EP0037370A3 (en
EP0037370B1 (fr
Inventor
Ulrich Kohle
Hans Paffhausen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pelikan International Corp Bhd
Original Assignee
Pelikan GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pelikan GmbH filed Critical Pelikan GmbH
Priority to AT81730040T priority Critical patent/ATE22042T1/de
Publication of EP0037370A2 publication Critical patent/EP0037370A2/fr
Publication of EP0037370A3 publication Critical patent/EP0037370A3/de
Application granted granted Critical
Publication of EP0037370B1 publication Critical patent/EP0037370B1/fr
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41MPRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
    • B41M5/00Duplicating or marking methods; Sheet materials for use therein
    • B41M5/10Duplicating or marking methods; Sheet materials for use therein by using carbon paper or the like

Definitions

  • the invention relates to a carrier-free carbon material with a color layer in which the color components are dispersed in a binder layer consisting of synthetic resin, and with a synthetic resin cover layer covering the color layer on the back.
  • Such carbon materials are used in writing and printing units for writing, e.g. B. as typewriters in typewriters or as so-called printing blankets (these are broadband tapes) in high-speed printers. Due to the structure of the color layer, they can be overwritten several times.
  • the invention is intended to improve a strapless carbon material with a rear cover layer applied in solution in such a way that it possesses both good conformability and good strength and can be used universally in all writing and printing units.
  • the cover layer consists of a solvent-soluble, non-reactive polyurethane resin.
  • the invention is based on the recognition that the selection of material for the top layer a key K Rite criterion for the usefulness of the strapless carbon material represents. What is surprising is with a solvent-soluble, non-reactive polyurethane resin that is applied in solution and then physically dried, a material has been found which combines good conformability (due to good values for the tensile elongation and elasticity) with good strength. In addition, there is also an excellent bond with another synthetic resin binder, e.g. B. polyvinyl chloride, polyvinyl acetate or polyamide-containing color layer, which is by no means a matter of course for different materials for the top layer and the color layer.
  • another synthetic resin binder e.g. B. polyvinyl chloride, polyvinyl acetate or polyamide-containing color layer, which is by no means a matter of course for different materials for the top layer and the color layer.
  • Solvent-soluble, non-reactive polyurethane resins which are commercially available in various types, represent a special group of substances. They are fully reacted, but have a predominantly linear structure compared to a conventional fully reacted polyurethane resin, which is three-dimensionally crosslinked and insoluble in solvents on, possibly with branched side chains, and usually also have a lower molecular weight. They can be derived from aromatic or aliphatic hydrocarbons. All types of this particular group of substances are suitable for the purposes of the invention.
  • NCO isocyanurate Triisocyanurates with free NCO groups
  • NCO isocyanurate polyisocyanates which are derived from isocyanuric acid by replacing its three H atoms with hydrocarbon radicals which in turn carry free NCO groups. They react with reactive OH groups to form a high-strength polyurethane resin that is three-dimensionally cross-linked and, in its pure state, is also very brittle.
  • this NCO isocyanurate is added to the solution containing the solvent-soluble, non-reactive polyurethane resin. It can no longer react with the polyurethane resin (since it no longer contains NCO-reactive OH groups), but it reacts e.g. B. with water from the air or the solvent to form a three-dimensional polyurethane network which penetrates the layer of the solvent-soluble, non-reactive polyurethane resin and thus additionally solidifies, without an increase in the layer thickness being necessary.
  • plasticizers the preferred plasticizers being substances from the group of phthalic acid esters. It has surprisingly been found that such a plasticizer-added y-penschmiegsamkeit affects the elasticity in the sense of a better low T, without a negative effect on the train resilience or to affect the color layer in terms of its intensity, productivity or aging stability. As a result, it is possible, with the layer thickness of the cover layer remaining the same, to adjust its conformability and its strength largely independently of one another.
  • a material was used which was composed of an 18 ⁇ m thick paint layer and a 15 ⁇ m thick cover layer.
  • the top layer solution was first applied to an auxiliary backing (film or adhesive paper) and physically dried.
  • the color layer solution was then applied to the completely dry top layer and also physically dried. Preferential; The same solvent was used for the top layer and the color layer.
  • the carbon material could be pulled off the auxiliary carrier and cut to the desired width. It was' irrelevant whether the material was pulled off and cut in one work step or whether a jumbo roll was initially wound between the material being pulled off and cut, both ways were equally feasible in terms of the strength of the tape. In no case (in contrast to the material according to DE-PS 12 13 438 discussed at the outset) was it necessary to cut the material on the auxiliary carrier so that the auxiliary carrier could be reused.
  • the formulation of the color layer was the same in all examples, as follows:
  • the binder solution was a 25% solution of polyvinyl chloride acetate copolymer in methyl ethyl ketone.
  • the PUR resin in this and in all the following examples was a soluble non-reactive aromatic linear polyurethane from Bayer AG, Leverkusen, with Han Designation "Desmolac 2100".
  • a writing tape made with this basic formulation of the top layer and suitable for many areas of use had the following properties:
  • the stretching force is equal to the force that is absorbed by the tape without changing its shape, and thus a measure of the strength, while the elongation at break is a measure of the elasticity of the tape.
  • the NCO isocyanate used in all of the following examples was the product supplied by Bayer AG, Leverkusen, under the name "Haftvermittler 2005”.
  • a writing tape produced with such a modified cover layer had the following properties:
  • the stretching force has increased compared to the basic formulation, but the elongation at break has decreased somewhat, but without assuming undesirably low values.
  • a writing tape made with this slightly more modified recipe had the following properties:
  • the stretching force has increased even further as a result of the greater modification compared to Example 2, but at the same time the elongation at break has dropped to relatively low values which are undesirably low for some areas of use.
  • Palatinol 0 is a plasticizer from the group of phthalic acid esters.
  • a writing tape made with this softened top layer had the following properties:

Landscapes

  • Laminated Bodies (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Color Printing (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
EP81730040A 1980-03-21 1981-03-21 Matériau d'enregistrement au charbon sans support Expired EP0037370B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT81730040T ATE22042T1 (de) 1980-03-21 1981-03-21 Traegerloses carbonmaterial.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3010859 1980-03-21
DE19803010859 DE3010859A1 (de) 1980-03-21 1980-03-21 Traegerloses carbonmaterial

Publications (3)

Publication Number Publication Date
EP0037370A2 true EP0037370A2 (fr) 1981-10-07
EP0037370A3 EP0037370A3 (en) 1982-01-13
EP0037370B1 EP0037370B1 (fr) 1986-09-10

Family

ID=6097874

Family Applications (1)

Application Number Title Priority Date Filing Date
EP81730040A Expired EP0037370B1 (fr) 1980-03-21 1981-03-21 Matériau d'enregistrement au charbon sans support

Country Status (4)

Country Link
EP (1) EP0037370B1 (fr)
AT (1) ATE22042T1 (fr)
DE (2) DE3010859A1 (fr)
DK (1) DK131581A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0342371A3 (fr) * 1988-05-16 1991-01-23 Pelikan Aktiengesellschaft Méthode pour la fabrication d'un ruban de colorant thermofusible pour l'impression par le transfert thermique

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1070918B (de) * 1956-03-08 1959-12-10 Fa. Günther Wagner, Hannover Kohlenpapier mit einer Kunststoffrackenschicht
GB1218031A (en) * 1967-08-04 1971-01-06 Columbia Ribbon & Carbon Self-supporting transfer elements and processes for making self-supporting transfer elements
GB1217844A (en) * 1967-11-25 1970-12-31 Columbia Ribbon & Carbon Improvements in or relating to pressure-sensitive transfer elements
FR2021920A1 (en) * 1968-10-30 1970-07-24 Kores Spa Colour printing using polymer resins for - colour transfer surfaces
GB1380786A (en) * 1972-06-23 1975-01-15 Ozalid Group Holdings Ltd Pressure-sensitive transfer elements

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0342371A3 (fr) * 1988-05-16 1991-01-23 Pelikan Aktiengesellschaft Méthode pour la fabrication d'un ruban de colorant thermofusible pour l'impression par le transfert thermique

Also Published As

Publication number Publication date
DE3175286D1 (en) 1986-10-16
EP0037370A3 (en) 1982-01-13
EP0037370B1 (fr) 1986-09-10
DK131581A (da) 1981-09-22
ATE22042T1 (de) 1986-09-15
DE3010859A1 (de) 1981-10-01

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