GB1416990A - Transfer sheet material - Google Patents
Transfer sheet materialInfo
- Publication number
- GB1416990A GB1416990A GB5921471A GB5921471A GB1416990A GB 1416990 A GB1416990 A GB 1416990A GB 5921471 A GB5921471 A GB 5921471A GB 5921471 A GB5921471 A GB 5921471A GB 1416990 A GB1416990 A GB 1416990A
- Authority
- GB
- United Kingdom
- Prior art keywords
- optionally substituted
- colour
- colour former
- developer
- benzyl
- 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
Links
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
- B41M5/132—Chemical colour-forming components; Additives or binders therefor
- B41M5/136—Organic colour formers, e.g. leuco dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Color Printing (AREA)
Abstract
1416990 Transfer sheet WIGGINS TEAPE LTD 20 Feb 1973 [21 Dec 1971] 59214/71 Heading D2B A transfer sheet material comprises a base sheet having on one surface a coating containing one or more colour formers each having the formula where A and B are optionally substituted 1, 4-arylene residues, X 1 is hydroxy, alkoxy or optionally substituted amino radical, and X 2 is hydrogen, hydroxy or optionally substituted amino radical. A and B are preferably 1, 4- phenylene residues, and the substituents in A, B may be alkyl, amino, dialkylamino, hydroxy, alkoxy, carboxy and sulpho. The substituents in A, B may also bridge A and B to produce a compound of formula: where Z represents a direct link, oxygen, sulphur or -NR-, where R is hydrogen or an optionally substituted alkyl, aryl or aralkyl radical e.g. 2-methyl benzyl, benzyl or methyl. X 1 and X 2 may have the formula -NR 1 R 2 where R 1 and R 2 are hydrogen or an optionally substituted alkyl, aralkyl oraryl radical. Examples of R 1 and R 2 are methyl, ethyl, propyl, butyl, #-hydroxyethyl, #-chloroethyl, 4-methoxy-benzyl, 2 methylbenzyl, benzyl, 2-methylphenyl, 4 - methylphenyl, 3 - chlorophenyl, naphth-2-yl, and phenyl. The colour former may be in the form of a salt with HCI, HBr, HNO 3 or H 2 SO 4 or with a Group IA metal, a Group IIA metal, optionally substituted ammonium, optionally substituted hydrazine, optionally substituted hydroxylamine, optionally substituted cyanidine, or a heterocyclic base. The colour formers are leuco compounds of dyes of the indamine, azine, oxazine, thiazine and carbazole series and may be prepared by reduction of such dyes. Example 1 describes the preparation of leuco gallocyanine from gallocyanine and Table 1 lists other dyes which may be reduced to produce a colour former for use in the present invention. Tables 2 and 3 list examples of colour formers for use in spirit duplicating and pressure sensitive copying systems respectively. The base sheet may be of paper, polypropylene or polyethylene terephthalate. The colour former may be evenly distributed throughout the coating, or may be present in solution in microcapsules in the coating. The colour former may be used with an acid clay developer. In a pressure sensitive copying system, the coated surface of the transfer sheet is placed in contact with a surface of a copy sheet carrying the developer. If a plurality of copies are required intermediate copy sheets are interposed between the two sheets, each intermediate copy sheet having on on side a colour former as above, and on the other the developer. In a hectographic copying system, the colour former may be mixed with castor oil, 10 ethyl cellulose and toluene to form the coating material, and the developer may be attapulgite or montmorillonite clay.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5921471A GB1416990A (en) | 1971-12-21 | 1971-12-21 | Transfer sheet material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5921471A GB1416990A (en) | 1971-12-21 | 1971-12-21 | Transfer sheet material |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1416990A true GB1416990A (en) | 1975-12-10 |
Family
ID=10483305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5921471A Expired GB1416990A (en) | 1971-12-21 | 1971-12-21 | Transfer sheet material |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1416990A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0339869A2 (en) * | 1988-04-26 | 1989-11-02 | Minnesota Mining And Manufacturing Company | Novel phenazine dyes |
US5428161A (en) * | 1984-10-01 | 1995-06-27 | Minnesota Mining And Manufacturing Company | Phenazine dyes |
-
1971
- 1971-12-21 GB GB5921471A patent/GB1416990A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5428161A (en) * | 1984-10-01 | 1995-06-27 | Minnesota Mining And Manufacturing Company | Phenazine dyes |
EP0339869A2 (en) * | 1988-04-26 | 1989-11-02 | Minnesota Mining And Manufacturing Company | Novel phenazine dyes |
EP0339869A3 (en) * | 1988-04-26 | 1991-11-13 | Minnesota Mining And Manufacturing Company | Novel phenazine dyes |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |