Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
  • B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
  • B41M5/00—Duplicating or marking methods; Sheet materials for use therein
  • B41M5/124—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components
  • B41M5/165—Duplicating or marking methods; Sheet materials for use therein using pressure to make a masked colour visible, e.g. to make a coloured support visible, to create an opaque or transparent pattern, or to form colour by uniting colour-forming components characterised by the use of microcapsules; Special solvents for incorporating the ingredients
  • B41M5/1655—Solvents

Definitions

• This invention relates to pressure-sensitive mark-recording systems.
• the most familiar form of pressure-sensitive mark-recording system is the so-called carbonless copying paper which comprises a two-sheet system in which the under surface of the top sheet has a coating of microcapsules of a solution of a colourless chromogen, while the upper surface of the lower (receiver) sheet has an absorbent coating including a sensitizing agent for the chromogen.
• a successful carbonless copying paper system needs to meet a number of criteria. For example the marks on the receiver sheet should develop rapidly to a legible intensity of colour and a legible mark should persist for as long as the sheet is required to be kept. Whether the various criteria are met depends on a number of factors including the nature of the chromogen, the solvent and the sensitizing agent, and many different materials of each category have been proposed. Chromogens'which have been proposed include phthalide derivatives, for example crystal violet lactone, and Malachite green lactone, indole-substituted pyromellitides, leucauramines, and diphenylmethane derivatives such as Michler's hydrol.
• Solvents which have been proposed include hydrocarbons, for instance petroleum fractions or synthetic.hydrocarbons such as hydrogenated terphenyls, halogenated hydrocarbons, for instance chlorinated biphenyls, and esters, for instance alkyl adipates and alkyl phthalates.
• the sensitizing agent is usually an acid clay, for example an attapulgite or bentonite clay, or an acidic organic polymer, for example a phenol-aldehyde polymer or a partially or wholly hydrolysed styrenemaleic anhydride or ethylene-maleic anhydride polymer.
• the chromogens which are probably most frequently referred to in the art are the phthalide derivatives, especially crystal violet lactone. These chromogens are usually used in solution in a hydrocarbon type solvent.
• a hydrocarbon type solvent One reason for this choice of solvent is that although the phthalide colour-formers are soluble in esters, for example, it is found that esters and certain other solvents having similar polarity to the esters, show too great a tendency to compete with the chromogen in affinity for the sensitizing agent, so that in some cases, no colour development occurs. This is especially so with certain acid clay sensitizing agents.
• chromogens that are diphenyl methane derivatives are less subject to this limitation and . can be used in conjunction with solvents such as esters, advantages of the latter over hydrocarbons being that the chromogens dissolve more readily and have higher solubilities.
• solvents such as esters
• diphenyl methane derivatives for instance Michler's hydrol
• chromogens in pressure sensitive mark-recording systems is described jn, for example, British Patent Specification 1,381,928 and U.S. Patent Specification 4,000,087.
• the present invention concerns an improvement relating to the use in pressure-sensitive mark-recording systems, of chromogens that are diphenyl methane derivatives.
• a pressure-sensitive mark-recording system of the invention comprises (a) sheet material, (b) mark-forming components supported by the sheet material and arranged in juxtaposition but in unreactive condition, the said components comprising a chromogen which is a derivative of diphenylmethanol or of diphenylmethylamine and an acid clay sensitizer for the chromogen which produces a colour from the chromogen when brought into contact with the chromogen in the presence of a liquid solvent for the chromogen comprising an aliphatic benzyl phthalate and (c) the said liquid solvent supported by the sheet material but separated from the sensitizing agent by a physical barrier which is rupturable on the application of a marking instrument to the sheet material.
• solvents for example xylene or dibutyl phthalates
• use of solvents in accordance with the present invention results in an improvement in the resistance to fading of the marks on the receiver sheet 1 during storage, particularly if storage occurs under conditions where fading is due to the action of oxygen.
• one of the phthalate carboxyl'groups is esterified by an aliphatic group and the other by a benzyl group.
• the aliphatic group can, for example, contain up to 24 carbon atoms, and may have a straight or a branched chain.
• alkyl group for example an ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, n-hexyl, isohexyl, n-octyl, 2-ethylhexyl, decyl,tetradecyl or octadecyl group.
• Preferred alkyl groups contain from 2 to 12 carbon atoms.
• the aliphatic-group may be an alkoxyalkyl or a group derived from an alkyl group by the replacement of more than one -CH 2 - group by the same number of oxygen atoms, and it may thus be, for istance, an ethoxyethyl or a 3,6,9-trioxaundecyl group.
• the aliphatic group is one derived from an alkyl ester of a hydroxy-carboxylic acid, for example a C 1-18 alkyl ester of glycolic acid, beta- hydroxypropionic acid or gamma-hydroxybutyric acid; or from a hydroxyalkyl ester of an aliphatic carboxylic acid, where the hydroxyalkyl radical and the aliphatic carboxylic acid may each contain up to 12 carbon atoms.
• Examples of such aliphatic groups are butoxycarbonylmethyl, (2-ethylhexyloxy)carbonylmethyl, 2(ethylcarbonyoxy) ethyl and 7(2,6,6,8-tetramethyl-4-oxa-3-oxononyl).
• benzyl is intended to cover both unsubstituted benzyl C 6 H 5 CH 2 - and substituted benzyl, especially alkyl-substituted benzyl.
• the nucleus of the benzyl group may contain up to three alkyl substituents, each, for example, being an alkyl group having up to four carbon atoms, for instance methyl or ethyl; or one or both methylene hydrogen atoms of the benzyl group may be replaced by a similar alkyl group.
• aliphatic benzyl phthalates useful in the present invention are butyl unsubstituted-benzyl phthalates, for instance n-butyl benzyl phthalate and isobutyl benzyl phthalate octyl unsubstituted-benzyl phthalates, for instance n-octyl benzyl phthalate and 2-ethylhexyl benzyl phthalate, and 7(2,6,6,8- tetramethyl-4-oxa-3-xononyl) unsubstituted-benzyl phthalate.
• butyl unsubstituted-benzyl phthalates for instance n-butyl benzyl phthalate and isobutyl benzyl phthalate
• octyl unsubstituted-benzyl phthalates for instance n-octyl benzyl phthalate and 2-ethylhexyl benzy
• the solvents used in the present invention can contain more than one aliphatic benzyl phthalate, for example mixtures of alkyl benzyl phthalates having a range of alkyl group sizes, for instance a C 5 -C 7 , a C 7 -C 9 or a C 8 -C 12 range.
• the solvents may optionally contain other components, for instance dialkyl phthalates such as dibutyl phthalate and dioctyl phthalates, and various hydrocarbons, for example C 6-12 alkylbenzenes, kerosene or other petroleum fractions which are useful.as diluents in certain circumstances to reduce the viscosity of the solvent.
• the solvent contains at least 50% by weight of an aliphatic benzyl phthalate or of a mixture of aliphatic benzyl phthalates.
• the proportions by weight of the aliphatic benzyl phthalate and the diluent in mixtures may, for example, range from 50:50 to 90:10, for example 60:40, 70:30, 75:25 or 80:20.
• the solvent is preferably one having a viscosity in the range 5 to 15 centi- stokes at 38°C.
• the concentration of the chromogen in a solution of the invention is generally of the same order as that in known solutions of chromogens which are diphenylmethanol or diphenylmethylamine derivatives, for example from 0.25 to 5%, more particularly from 0.4 to 4.0% by weight of the solution.
• Chromogens which are especially suitable for use in the present invention include Michler's hydrol, i.e. bis(p-dimethylaminophenyl)methanol, its ethers, for example the methyl ether of Michler's hydrol and the benzyl ether of Michler's hydrol, aromatic sulfonic and sulfinic esters of Michler's hydrol, for example the p-toluenesulfinate of Michler's hydrol, and derivatives of bis(p-dimethylaminophenyl) methylamine, for example N/5is(p-dimethylaminophenyl) methyl]morpholine.
• Michler's hydrol i.e. bis(p-dimethylaminophenyl)methanol
• its ethers for example the methyl ether of Michler's hydrol and the benzyl ether of Michler's hydrol
• the capsule wall or shell is preferably made from a synthetic polymer, for example a polyurethane resin, a urea-formaldehyde resin, a melamine-formaldehyde resin or a polyamide resin.
• a synthetic polymer for example a polyurethane resin, a urea-formaldehyde resin, a melamine-formaldehyde resin or a polyamide resin.
• the use of such resins as shell-forming material in encapsulation is described in, for example, U.S. Patent 3,016,308, British patent 939,264 and U.S. Patent 3,429,827. Shells-of this kind can be made significantly less permeable to the aliphatic benzyl phthalates used in the present invention than shells made of natural polymeric material such as gelatin.
• the acid clay used as sensitizing agent for the chromogen in the present invention can be any of those conventionally used for this purpose, including bentonite and attapulgite.
• the naturally occurring clay may be subjected to various treatments such as acid extraction or calcination before use as the sensitizing agent.
• the mark-recording system of the present invention can be prepared according to well known conventional procedures. Descriptions of methods for preparing both the dye-carrying paper and clay-coated receiving paper are to be found in the literature.
• a preferred embodiment of this invention comprises a two-sheet system wherein the acid clay is carried by one sheet and a marking fluid comprising a chromogen and solvent is carried by a second sheet
• the invention is not limited to such systems alone.
• the - only essential requirement is that the chromogen and the acid clay be maintained in a separate or unreactive condition until pressure is applied to the system and. that upon the application of pressure the chromogen and acid clay are brought into reactive contact.
• the - chromogen and acid clay present in a dry and unreactive state on a common carrier and to have the solvent alone carried on a separate sheet whereupon the application of pressure would release the solvent into the chromogen-acidic material mixture and promote localized reaction and colour development.
• Table 1 shows the results obtained using one manufacturer's clay-coated receiver sheets, the solvent in each case being a blend of the phthalate with either ALB in the proportions by weight 7:3 or with kerosene in the proportions by weight 8:2.
• Comparison of Solvent 1 with Solvents 2-5, or of Solvent 6 with Solvent 7 shows that the print intensity fades significantly more slowly when the phthalate is an aliphatic benzyl phthalate than when the phthalate is dibutyl phthalate.
• Table 2 shows the results obtained using a second manufacturer's clay-coated receiver sheets.
• Table 3 shows the results obtained using the second manufacturer's clay coated receiver sheets, the solvent being in each case a blend of the phthalate with ALB in the proportions by weight 7:3.

Landscapes

• Color Printing (AREA)
• Holo Graphy (AREA)
• Optical Recording Or Reproduction (AREA)
• Jib Cranes (AREA)
• Image Analysis (AREA)

Priority Applications (1)

Applications Claiming Priority (2)

Publications (2)

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Family Applications (1)

Country Status (7)

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Citations (5)

• 1979
  • 1979-05-10 DE DE7979300801T patent/DE2963924D1/de not_active Expired
  • 1979-05-10 EP EP79300801A patent/EP0005921B1/fr not_active Expired
  • 1979-05-10 AT AT79300801T patent/ATE1699T1/de active
  • 1979-05-24 FI FI791647A patent/FI70180C/fi not_active IP Right Cessation
  • 1979-05-28 AU AU47478/79A patent/AU528695B2/en not_active Ceased
  • 1979-05-29 JP JP6569279A patent/JPS552090A/ja active Pending
  • 1979-05-30 CA CA328,731A patent/CA1126026A/fr not_active Expired

Patent Citations (8)

Non-Patent Citations (1)

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