US3865613A - Pressure-sensitive copying systems - Google Patents

Pressure-sensitive copying systems Download PDF

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Publication number
US3865613A
US3865613A US287714A US28771472A US3865613A US 3865613 A US3865613 A US 3865613A US 287714 A US287714 A US 287714A US 28771472 A US28771472 A US 28771472A US 3865613 A US3865613 A US 3865613A
Authority
US
United States
Prior art keywords
dibenzylbenzenes
sheet
mixture
pressure
sensitive copying
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.)
Expired - Lifetime
Application number
US287714A
Other languages
English (en)
Inventor
John Edward Ross
David James Marshall
Brian Samuel Chapman
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.)
Arjo Wiggins Ltd
Original Assignee
Wiggins Teape Research and Development Ltd
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 Wiggins Teape Research and Development Ltd filed Critical Wiggins Teape Research and Development Ltd
Application granted granted Critical
Publication of US3865613A publication Critical patent/US3865613A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • B41M5/124Duplicating 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
    • B41M5/165Duplicating 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
    • B41M5/1655Solvents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S428/00Stock material or miscellaneous articles
    • Y10S428/914Transfer or decalcomania
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982Particulate matter [e.g., sphere, flake, etc.]
    • Y10T428/2984Microcapsule with fluid core [includes liposome]

Definitions

  • This invention relates to pressure-sensitive copying systems of the kind in which an initially colourless colour-former held in microcapsules is reacted, upon rupturing of the microcapsules by an applied pressure, with a co-reactant material to form distinctive coloured marks.
  • Such systems will be referred to hereinafter as systems of the kind defined above.
  • Such systems can be of the type in which the microcapsules are carried on one surface of a transfer sheet, referred to as a CB (coated back) sheet and the coreactant material is carried on one surface of a record sheet, referred to as a CF (coated front) sheet, or can be of the autogeneous type in which the microcapsules and the co-reactant material are carried on the same surface ofa single sheet.
  • CB coated back
  • CF coated front sheet
  • CB sheets carry a coating of microcapsules, which may be separate or in capsular units, i.e., clusters of capsules, each microcapsule comprising a wall of hydrophilic colloid material such as gelatin, containing a colourless, chromogenic material (colour-former) of basic reactant chemical properties which in use contacts and is coloured by a co-reactant material, such as attapulgite clay, acid treated montmorillonite clay, or particles of an oil-soluble, acidic phenolic polymeric material (generally in combination with kaolin clay), carried by a CF sheet, to provide distinctive coloured marks on the CF sheet.
  • a co-reactant material such as attapulgite clay, acid treated montmorillonite clay, or particles of an oil-soluble, acidic phenolic polymeric material (generally in combination with kaolin clay) carried by a CF sheet, to provide distinctive coloured marks on the CF sheet.
  • Such contact and colouration can be caused by rupture of microcapsule
  • microcapsules and capsular units are well known, as are various methods of coating microcapsules and capsular units on to a base sheet to provide a CB sheet and coating a coreactant material on to a base sheet to provide a CF sheet, and such methods will not therefore be described in detail herein.
  • the internal phase of a microcapsule that is the material within the microcapsule wall, comprises one or more.
  • colour-formers which are in the nature of dye substances, typically crystal violet lactone (CVL) and benzoyl leuco methylene blue (BLMB), or 3,3-bis (dialkyl indolyl) phthalides, or 3-dialkylamino- 6-alkyl- 7-alkylamino fluoranes, or 3dialkylamino-7- dialkylamino fluoranes.
  • These colour-formers are dissolved in a solvent, typically hydrogenated terphenyl or mono isopropyl bi-phenyl, and diluted with, for example, kerosene.
  • the dye substances CVL and BLMB are normally used together, since CVL is effective to provide a rapid colouration and BLMBis effective to provide a lasting colouration, on reaction with commonly used co-reactant materials such as those mentioned above.
  • the two principal tests being the calendar intensity Cl test and the smudge test.
  • Other tests which are used are windowfading, office-fading and ream decline tests. All of these tests are well-known and will not therefore be described in detail herein. It is sufficient to state that the CI test is a measure of print intensity, that is the distinctiveness of the mark produced, and the result is expressed as a percentage, the lower the percentage the better the print intensity, and that the smudge test is a measure of resistance of the CB sheet to accidental rupture of microcapsules, the result being expressed as a number less than 100, the higher the number the better the CB sheets resistance to accidental microcapsule rupture.
  • the window-fading and office-fading tests measure the print intensity after exposure to sunlight and artificial light, respectively, for various periods of time, while the ream decline test measures the initial print intensity obtained with sheets which have been stored in the ream for various periods.
  • the present invention is particularly concerned with the internal phase of the microcapsules used in pressure-sensitive copying systems of the kind defined above.
  • a sheet for use in a pressure-sensitive copying system comprises a base sheet carrying a coating of the microcapsules, each microcapsule containing an organic, initially colourless,
  • Dimethyldibenzylbenzenes approx. 35 to 40%
  • Trimethyldibenzylbenzenes approx. 10% approx. 99%
  • Lipinol T has a very low level of toxicity in various mammalian species, the lethal dose being in excess of 20 g/kg. Thus, Lipinol T presents no toxic hazard to man under normal conditions when used as the solvent in the internal phase of pressure-sensitive copying system microcapsules.
  • the preferred dibenzylbenzenes mixture has the following advantages: cheapness, better initial print intensity (CI test) for a given CB sheet coating weight when used with a CF sheet having an oil-soluble acidic phenolic polymeric material/kaolin clay coating; high colour-former solubility, thus allowing high dilution; slower fade rate with the windowfading test; less smell both during manufacture and from the manufactured CB sheet. Further the preferred mixture has no adverse effects with regard to the officefading and ream decline tests.
  • the preferred dibenzylbenzenes mixture has a viscosity between 35 and 45 c? at 20C; a density of 1.0 to 1.04 g/ml; a distillation range at 20 mm Hg of 240 to 260C and a flash point of about 180C.
  • the preferred dibenzylbenzenes mixture is a suitable solvent for many other colour-formers which are used in pressure-sensitive copying systems, and specifically for:
  • a control CB sheet was produced by coating microcapsules containing a standard internal phase comprising hydrogenated terphenyl as the solvent, kerosene as the diluent, and both CVL and BLMB as colourformers, on to a base sheet with a coating weight of approximately 65 g/m
  • the ratio of solvent to diluent was 4:] w/w.
  • composition of the Lipinol T is given by the suppliers, Huls (U.K.) Ltd as follows:
  • a sheet for use in a pressure-sensitive copying system comprising a base sheet carrying a coating of the microcapsules, each microcapsule containing an organic, initially colourless, colour-former, dissolved in a solvent which includes a mixture of dibenzylbenzenes of the general formula where R to R are selected from the group comprising hydrogen, alkyl groups containing less than 5 carbon atoms or alkaryl groups containing 7 or 8 carbon atoms.
  • Trimethyldibenzylbenzenes approx. 10% approx. 99%
  • the balance consisting of impurities of higher molecular weight.

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  • Color Printing (AREA)
US287714A 1971-09-23 1972-09-11 Pressure-sensitive copying systems Expired - Lifetime US3865613A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB4447471 1971-09-23
GB278572*[A GB1361638A (en) 1971-09-23 1972-01-20 Pressure-sensitive copying systems

Publications (1)

Publication Number Publication Date
US3865613A true US3865613A (en) 1975-02-11

Family

ID=26237725

Family Applications (1)

Application Number Title Priority Date Filing Date
US287714A Expired - Lifetime US3865613A (en) 1971-09-23 1972-09-11 Pressure-sensitive copying systems

Country Status (15)

Country Link
US (1) US3865613A (enrdf_load_stackoverflow)
JP (1) JPS4841816A (enrdf_load_stackoverflow)
AR (1) AR194275A1 (enrdf_load_stackoverflow)
AT (1) AT322577B (enrdf_load_stackoverflow)
BE (1) BE789190A (enrdf_load_stackoverflow)
BR (1) BR7206566D0 (enrdf_load_stackoverflow)
CA (1) CA966306A (enrdf_load_stackoverflow)
CH (1) CH560110A5 (enrdf_load_stackoverflow)
DE (1) DE2245785A1 (enrdf_load_stackoverflow)
DK (1) DK130340B (enrdf_load_stackoverflow)
FI (1) FI57071C (enrdf_load_stackoverflow)
FR (1) FR2154207A5 (enrdf_load_stackoverflow)
GB (1) GB1361638A (enrdf_load_stackoverflow)
IT (1) IT980999B (enrdf_load_stackoverflow)
NL (1) NL167121C (enrdf_load_stackoverflow)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4957815A (en) * 1987-07-16 1990-09-18 Societe Atochem Polyarylalkane oligomer compositions containing xylene units, process for their manufacture, and products containing the same

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5949132B2 (ja) * 1976-02-04 1984-11-30 三菱電機株式会社 電解加工装置
US4130299A (en) * 1977-09-12 1978-12-19 Monsanto Company Low-odor dye solvents for pressure-sensitive copying systems
JPS55169372U (enrdf_load_stackoverflow) * 1979-05-23 1980-12-05
JPS6141593A (ja) * 1984-08-06 1986-02-27 Nippon Petrochem Co Ltd 感圧紙染料用溶剤

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3016308A (en) * 1957-08-06 1962-01-09 Moore Business Forms Inc Recording paper coated with microscopic capsules of coloring material, capsules and method of making
US3627581A (en) * 1970-10-19 1971-12-14 Ncr Co Pressure-sensitive record material

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3016308A (en) * 1957-08-06 1962-01-09 Moore Business Forms Inc Recording paper coated with microscopic capsules of coloring material, capsules and method of making
US3627581A (en) * 1970-10-19 1971-12-14 Ncr Co Pressure-sensitive record material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4957815A (en) * 1987-07-16 1990-09-18 Societe Atochem Polyarylalkane oligomer compositions containing xylene units, process for their manufacture, and products containing the same

Also Published As

Publication number Publication date
DE2245785A1 (de) 1973-03-29
JPS4841816A (enrdf_load_stackoverflow) 1973-06-19
NL7212663A (nl) 1973-03-27
BR7206566D0 (pt) 1973-09-27
AR194275A1 (es) 1973-06-29
GB1361638A (en) 1974-07-30
FI57071C (fi) 1980-06-10
DK130340C (enrdf_load_stackoverflow) 1975-07-07
NL167121C (nl) 1981-11-16
FR2154207A5 (fr) 1973-05-04
NL167121B (nl) 1981-06-16
IT980999B (it) 1974-10-10
DK130340B (da) 1975-02-10
AT322577B (de) 1975-05-26
BE789190A (fr) 1973-03-22
CH560110A5 (fr) 1975-03-27
CA966306A (en) 1975-04-22
FI57071B (fi) 1980-02-29

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