EP0716634A1 - Pressure-sensitive record materials - Google Patents
Pressure-sensitive record materialsInfo
- Publication number
- EP0716634A1 EP0716634A1 EP94925547A EP94925547A EP0716634A1 EP 0716634 A1 EP0716634 A1 EP 0716634A1 EP 94925547 A EP94925547 A EP 94925547A EP 94925547 A EP94925547 A EP 94925547A EP 0716634 A1 EP0716634 A1 EP 0716634A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- colour
- formers
- fluoran
- solvent
- vegetable
- 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
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
- B41M5/165—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 record materials of the kind comprising a base sheet, typically of paper, coated with a rupturable material confining droplets of a solution of colour-forming substances, which when released by rupture of the material undergo a colour-forming reaction to produce an image either on the base sheet itself or on a further, receptor sheet in face-to-face contact with the coated face of the base sheet.
- the invention is applicable to so-called "carbon-less" copy papers which rely on two coatings formed respectively on the contiguous faces of superimposed sheets of paper, namely a coating containing the colour-forming substance in the micro-capsules, on the back of the uppermost sheet (usually known as a CB coating) and a coating of a receptor layer on the front of the lowermost sheet (usually known as a CF coating).
- Colour-forming chemicals are typically dissolved in an oily solvent and encapsulated by well known techniques, and when such capsules are ruptured by mechanical pressure, as by impact of a type bar of a typewriter, the chemicals are released and react to form a visible mark on the CF coating of the adjacent sheet.
- the droplets may be dispersed throughout a continuous phase coating of the rupturable material.
- paper for use in such copying systems is of three types, distinguished by their coatings, namely CB sheets having a CB coating on the underside to form the top sheet of the set, CF sheets having a CF coating on the upper side to form the bottom sheet of a set, and optionally CFB sheets having a CF coating on the upper side and a CB coating on the underside to form one or more intermediate sheets of a set where required.
- Such coatings are normally applied by a continuous process to cover the entire area of the appropriate face of the sheet.
- colour-formers e.g. various chromogenic materials
- organic solvents often aromatic solvents
- US patent 4859650 also proposes the use of plant, animal or paraffin oils as solvents, and also admits that these are relatively poor solvents for conventional colour-formers, but proposes to overcome this difficulty by the use of a special type of triphenylmethane leuco-dye which is more soluble in such oils, preferably together with the addition of up to 20% of a conventional synthetic solvent.
- the use of such special leuco-dyes may be more costly than more conventional colour-formers and since the addition of synthetic solvents is required in practice to achieve an acceptable result, the full environmental advantages of natural solvents are muted.
- the present invention arises from a discovery that natural vegetable and animal oils can successfully be employed, without necessarily employing any conventional synthetic solvent, for a group of colour- formers in conventional micro-capsules, and more particularly that sufficiently concentrated solutions of this group of colour-formers in such vegetable or animal oils can be achieved to provide good imaging, and good shelf-life characteristics.
- compositions for use as the internal phase of a coating of rupturable material for application to a base sheet to form pressure-sensitive record material, the composition comprising one or more colour-formers of which at least 90% are monoamino and/or diamino fluoran derivatives, dissolved in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils.
- a pressure-sensitive record material of the kind comprising a base sheet coated with one or more colour-formers characterised in that at least 90% of said colour formers are monoamino and/or diamino fluoran derivatives, and said colour- formers are dissolved in a solvent comprising 80% to 100% of an animal or vegetable oil, dissolution of said colour-formers being carried out at a temperature above 100°C, and typically at up to 135°C.
- oils which may be used include rape seed oil, cotton seed oil, olive oil, corn oil, wheat oil, soy oil, castor oil, thistle oil, ground nut oil, sunflower oil, grape seed oil, coconut oil, sesame oil, whale oil, sperm oil, fish oil cod-liver oil or any mixtures of one or more of these.
- the colour-forming substances which may be employed in accordance with the invention include chromogenic materials such as particularly, but not exclusively,
- One or more such chromogenic materials can be totally dissolved in a solvent consisting of up to 100% vegetable and/or animal oils to provide an internal phase for use in pressure-sensitive copying systems. It will however be understood that the solution may contain other additives to modify the characteristics or performance of the copying systems.
- a pressure-sensitive record material comprising a base sheet coated with a rupturable material confining droplets of an internal phase comprising a solution made in accordance with the above-specified method.
- micro-capsules containing a solution of colour-formers in an organic solvent by coacervation characterised in that at least 90% of said colour- formers comprise monoamino and/or diamino fluoran derivatives, dissolved at a temperature in excess of 100°C in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils to form an internal phase solution which is subsequently subject to coacervation at a temperature below 70°C.
- the micro-capsules in accordance with the invention and used for the pressure-sensitive copying paper are prepared by conventional methods and as such do not require an in depth description.
- micro-capsules can be prepared by the coacervation of gelatine and one or more other polymers such as carboxymethyl cellulose, gum arabic etc., in conventional manner.
- micro-capsules produced may be blended with other additives including a binder, such as starch or polyvinyl alcohol or a mixture of both, and undissolved buffer or "stilt" material such as calibrated wheat starch or finely ground cellulose floe (or a mixture of both) to prevent premature rupture of the coating composition during processing and subsequent handling.
- a binder such as starch or polyvinyl alcohol or a mixture of both
- undissolved buffer or "stilt" material such as calibrated wheat starch or finely ground cellulose floe (or a mixture of both) to prevent premature rupture of the coating composition during processing and subsequent handling.
- the above coating composition may be applied to a range of paper substrates (40 gsm-150gsm) by use of standard coating techniques designed to apply a closely monitored wet film weight e.g. air knife, offset gravure, metering roll.
- Et ethyl (CH 3 -CH,-)
- Bu-t tert-butyl ((CH 3 ) 2 -CH-CH r )
- Ph phenyl (C,,H Stamm-)
- the three selected chromogenic materials used in this example (A,B,C) were mixed in the proportions indicated in Table I such that an intense black print is subsequently obtained in use.
- the mixture of chromogenic materials was dispersed into deodorised refined rape seed oil and the temperature raised to 115°C.
- the internal phase solution was emulsified in a mixture of gelatine and carboxymethyl cellulose (CMC) at 55 ⁇ 5°C to a mean capsule size of approximately 5 micron as measured using a Coulter Counter, (iii) Coacervation Process
- the emulsion (ii above) was diluted by the addition of soft water and the pH adjusted by the addition of 20% Sodium Hydroxide to a pH value 9.0 -9.5.
- Dilute acetic acid was added to reduce the pH of the gelatine below the isoelectric point resulting in a change in charge of the gelatine and, on further acidification, the formation of liquid coacervates results from the phase separation and inter-relation with the negatively charged C.M.C. in conventional manner.
- liquid coacervates are attracted to the nucleus or core material (i.e. the internal phase solution produced at (i) above) and coalesce to form a liquid wall.
- the dispersion was cooled at 8°C - 10°C in order to gel the liquid walls of the coacervates.
- the cross linked dispersion was returned to ambient temperature and allowed to homogenise and condition (e.g. age) for a predetermined period (1-3 hours).
- the resultant capsule dispersion was blended with a suitable binder (e.g. starch or starch/P.V.A. mixture) and a suitable "stilt buffer” (e.g. cellulose floe or calibrated wheat starch) to produce a mixture suitable for coating onto a sheet material by conventional means.
- a suitable binder e.g. starch or starch/P.V.A. mixture
- a suitable "stilt buffer” e.g. cellulose floe or calibrated wheat starch
- the four selected chromogenic materials ( A,B,C,D) were mixed in the proportions indicated in Table I such that an intense black print is subsequently obtained in use.
- these four chromogenic materials were initially dispersed in a solvent comprising deodorised refined rape-seed oil at a concentration of 6.9% at ambient temperature and the temperature was increased to 115°C and then decreased.
- the colour-formers used are all fluoran derivatives and the solvents are 100% animal or vegetable oil
- additional non-fluoran colour-formers may be included at up to 10% of the colour-former formulation, and that other non-animal or vegetable oil solvents may be included in the solvent at up to 20% of the solvent if required, although the use of 100% fluoran colour-formers and 100% animal or vegetable oils as solvents is entirely satisfactory.
Landscapes
- Color Printing (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
An internal phase solution for a coating of rupturable material for application to a base sheet to form a pressure-sensitive record material comprises one or more colour-formers of which at least 90 % are monoamino and/or diamino fluoran derivatives dissolved in a solvent comprising 80 % to 100 % of one or more vegetable and/or animal oils. Preferably the colour-formers comprise only monoamino and/or diamino fluoran derivatives and the solvent comprises only one or more vegetable and/or animal oils. Dissolution of the colour-formers in the solvent may take place at a temperature in the range 100 DEG C to 135 DEG C and micro-capsules containing such a colour-former solution may be formed by conventional coacervation processes below 70 DEG C.
Description
Title:- "Pressure-sensitive record materials" Description of invention
This invention relates to pressure-sensitive record materials of the kind comprising a base sheet, typically of paper, coated with a rupturable material confining droplets of a solution of colour-forming substances, which when released by rupture of the material undergo a colour-forming reaction to produce an image either on the base sheet itself or on a further, receptor sheet in face-to-face contact with the coated face of the base sheet.
In particular, but without limitation, the invention is applicable to so- called "carbon-less" copy papers which rely on two coatings formed respectively on the contiguous faces of superimposed sheets of paper, namely a coating containing the colour-forming substance in the micro-capsules, on the back of the uppermost sheet (usually known as a CB coating) and a coating of a receptor layer on the front of the lowermost sheet (usually known as a CF coating). Colour-forming chemicals are typically dissolved in an oily solvent and encapsulated by well known techniques, and when such capsules are ruptured by mechanical pressure, as by impact of a type bar of a typewriter, the chemicals are released and react to form a visible mark on the CF coating of the adjacent sheet.
Alternatively, the droplets may be dispersed throughout a continuous phase coating of the rupturable material.
Conveniently, paper for use in such copying systems is of three types, distinguished by their coatings, namely CB sheets having a CB coating on the underside to form the top sheet of the set, CF sheets having a CF coating on the upper side to form the bottom sheet of a set, and optionally CFB sheets having a CF coating on the upper side and a CB coating on the underside to form one or more intermediate sheets of a set where required. Such coatings are normally applied by a continuous process to cover the entire area of the appropriate face of the sheet.
Conventionally colour-formers, e.g. various chromogenic materials, have normally been dissolved in a range of organic solvents, often aromatic solvents, which afford adequate solubility for such colour-formers and enable a good image to be produced.
Other proposals have been made with regard to the use of alternative solvents, which have environmental advantages, for the colour-formers, but so far no wholly acceptable alternative solvent has been found.
Whilst the use of animal or vegetable oils as solvents for colour- formers is suggested in the patent literature, it is generally acknowledged that they do give rise to solubility problems. For example, British Patent 1429578 includes various vegetable oils in a list of suitable solvents for conventional colour-formers and admits that some of the listed solvents have low solubility for the colour- formers, but they can be used because the invention requires different concentrations of colour-former solution at different positions within the coating, so that the relatively poor solvents can be used for the more dilute colour-former solutions required by that invention.
US patent 4859650 also proposes the use of plant, animal or paraffin oils as solvents, and also admits that these are relatively poor solvents for conventional colour-formers, but proposes to overcome this difficulty by the use of a special type of triphenylmethane leuco-dye which is more soluble in such oils, preferably together with the addition of up to 20% of a conventional synthetic solvent. The use of such special leuco-dyes may be more costly than more conventional colour-formers and since the addition of synthetic solvents is required in practice to achieve an acceptable result, the full environmental advantages of natural solvents are muted.
Indeed many different systems of colour-formers and solvents have been proposed, including some which employ, at least in part, animal or vegetable oils as solvents. European Patent specification 0520639 Al published 30th December 1992 contains a lucid summary of such proposals which are directed to various improvements in the performance of the copy paper in various respects,
but generally where the use of animal or vegetable oils as solvents is proposed either it is found necessary to use a synthetic oil as a co-solvent, or systems using animal or vegetable oils as solvents have been evaluated only as control examples to verify the superior performance of other solvent/colour-former systems, for example as in European Patent specification 0520639 itself.
Against this background, the present invention arises from a discovery that natural vegetable and animal oils can successfully be employed, without necessarily employing any conventional synthetic solvent, for a group of colour- formers in conventional micro-capsules, and more particularly that sufficiently concentrated solutions of this group of colour-formers in such vegetable or animal oils can be achieved to provide good imaging, and good shelf-life characteristics.
In accordance with one aspect of the present invention we provide a composition, for use as the internal phase of a coating of rupturable material for application to a base sheet to form pressure-sensitive record material, the composition comprising one or more colour-formers of which at least 90% are monoamino and/or diamino fluoran derivatives, dissolved in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils.
It has been found that whilst such oils do not afford sufficiently good solubility for most colour-formers in current use, they can be used for colour- formers based on amino fluorans.
However, to achieve the required solubility it may be necessary to perform the step of dissolving such colour-formers at a temperature above that normally employed, for example in the range 100°C to 135°C and in accordance with another aspect of the invention we provide a method of manufacturing a pressure-sensitive record material of the kind comprising a base sheet coated with one or more colour-formers characterised in that at least 90% of said colour formers are monoamino and/or diamino fluoran derivatives, and said colour- formers are dissolved in a solvent comprising 80% to 100% of an animal or vegetable oil, dissolution of said colour-formers being carried out at a temperature above 100°C, and typically at up to 135°C.
Once such a solution has been formed at such an elevated temperature, it can subsequently be cooled and processed in generally conventional manner to form the required rupturable coating to provide a product which has a good shelf life and good image forming properties in a manner which could not be achieved by dissolving other colour-forming substances, such as triphenylmethane leuco-dye stuffs, in the same solvents at the-temperatures, generally below 100°C, normally employed.
In this way, we have found it possible to use a solvent which is up to 100% animal and/or vegetable oil.
The oils which may be used include rape seed oil, cotton seed oil, olive oil, corn oil, wheat oil, soy oil, castor oil, thistle oil, ground nut oil, sunflower oil, grape seed oil, coconut oil, sesame oil, whale oil, sperm oil, fish oil cod-liver oil or any mixtures of one or more of these.
The colour-forming substances which may be employed in accordance with the invention include chromogenic materials such as particularly, but not exclusively,
2'-(octylamino)-6'-(diethylamino) fluoran,
2'-anilo-3'-methyl-6'(diethylamino) fluoran,
6'(diethylamino)-2'-(l,l-dimethylethyl) fluoran,
6 '-(dibutylamino)-3 '-methyl-2 '-(phenylamino)-spirofisobenzofuran-
1 (3H),9 '-[9H]xanthen]-3-one, which are fluoran derivatives, as distinct from triphenalmethane leuco-dye stuffs.
One or more such chromogenic materials can be totally dissolved in a solvent consisting of up to 100% vegetable and/or animal oils to provide an internal phase for use in pressure-sensitive copying systems. It will however be understood that the solution may contain other additives to modify the characteristics or performance of the copying systems.
According to a further aspect of the invention we provide a pressure- sensitive record material comprising a base sheet coated with a rupturable
material confining droplets of an internal phase comprising a solution made in accordance with the above-specified method.
In accordance with a still further aspect of the invention we provide a method of forming micro-capsules containing a solution of colour-formers in an organic solvent by coacervation, characterised in that at least 90% of said colour- formers comprise monoamino and/or diamino fluoran derivatives, dissolved at a temperature in excess of 100°C in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils to form an internal phase solution which is subsequently subject to coacervation at a temperature below 70°C.
Apart from the preparation and composition of the internal phase or core material, the micro-capsules in accordance with the invention and used for the pressure-sensitive copying paper are prepared by conventional methods and as such do not require an in depth description.
Using as internal phase the solution of chromogenic materials dissolved in animal and/or vegetable oil, micro-capsules can be prepared by the coacervation of gelatine and one or more other polymers such as carboxymethyl cellulose, gum arabic etc., in conventional manner.
The micro-capsules produced may be blended with other additives including a binder, such as starch or polyvinyl alcohol or a mixture of both, and undissolved buffer or "stilt" material such as calibrated wheat starch or finely ground cellulose floe (or a mixture of both) to prevent premature rupture of the coating composition during processing and subsequent handling.
The above coating composition may be applied to a range of paper substrates (40 gsm-150gsm) by use of standard coating techniques designed to apply a closely monitored wet film weight e.g. air knife, offset gravure, metering roll.
In order to effect total dissolution of the chromogenic materials at the required concentration it is necessary to raise the temperature of the animal and/or vegetable oils to temperatures well above those required for conventional
internal phase solvents such as alkylated naphthalene, chlorinated paraffins and hydrogenated terphenyls.
Experiment has shown that in order to affect total dissolution of the chromogenic materials it is necessary to raise the temperature of the oil to 100°C- 135°C as compared with the temperatures required for conventional internal phase solvents which are generally below 100°C.
The invention is illustrated by the following non-limiting specific examples. All formulations are expressed by weight unless otherwise stated, and the specific colour formers employed in these examples are as follows:-
A) 2'-(Octylamino)-6'-(diethylamino)fluoran:
B) 2'-Anilino-3'-methyl-6'(diethylamino)fluoran:
(B)
C) 6'-(diethylamino)-2'-(l,l-dimethylethyl)-spiro[isobenzofuran-l(3H),9'- [9H]xanthen]-3-one,
Et
D) 6 '-(dibutylamino)-3 '-methyl-2 '-(phenvlamino)- Spiro[isobenzofuran- l(3H),9 '-[9H]xanthen]-3-one,
where - Me = methyl (CH,-)
Et = ethyl (CH3-CH,-) Bu-t = tert-butyl ((CH3)2-CH-CHr) Ph = phenyl (C,,H„-)
The above-identified colour-formers were used in the following combinations as set out in Table 1.
COLOUR FORMER
A
B
C
D
100 100
EXAMPLE 1 : (i) Preparation of internal Phase Solution
The three selected chromogenic materials used in this example (A,B,C) were mixed in the proportions indicated in Table I such that an intense black print is subsequently obtained in use.
The mixture of chromogenic materials was dispersed into deodorised refined rape seed oil and the temperature raised to 115°C.
In order to ensure total dissolution the temperature was held for 30 minutes. The concentration of the chromogenic materials dispersed in rape seed oil was 6.9%.
The dissolution characteristics of the solvent system during the temperature rise and fall were determined by turbidimetrv with the following results:-
showing that substantially complete solution was attained and maintained.
The above solution was then allowed to cool at 60°C and maintained at this temperature, (ii) Preparation of Emulsion
The internal phase solution was emulsified in a mixture of gelatine and carboxymethyl cellulose (CMC) at 55 ± 5°C to a mean capsule size of approximately 5 micron as measured using a Coulter Counter, (iii) Coacervation Process
The emulsion (ii above) was diluted by the addition of soft water and the pH adjusted by the addition of 20% Sodium Hydroxide to a pH value 9.0 -9.5.
Dilute acetic acid was added to reduce the pH of the gelatine below the isoelectric point resulting in a change in charge of the gelatine and, on further acidification, the formation of liquid coacervates results from the phase separation and inter-relation with the negatively charged C.M.C. in conventional manner.
On further acidification the liquid coacervates are attracted to the nucleus or core material (i.e. the internal phase solution produced at (i) above) and coalesce to form a liquid wall.
When further acidification resulted in the desired degree of clustering acidification was stopped, (iv) Cooling
The dispersion was cooled at 8°C - 10°C in order to gel the liquid walls of the coacervates.
At 8°C - 10°C the liquid walls were cross linked by the addition of an aldehyde (e.g. formaldehyde) and followed by an increase in pH by the further addition of 20% sodium hydroxide to pH 9.0. (v) Agein /Finishing
The cross linked dispersion was returned to ambient temperature and allowed to homogenise and condition (e.g. age) for a predetermined period (1-3 hours).
After ageing the resultant capsule dispersion was blended with a suitable binder (e.g. starch or starch/P.V.A. mixture) and a suitable "stilt buffer"
(e.g. cellulose floe or calibrated wheat starch) to produce a mixture suitable for coating onto a sheet material by conventional means.
The pressure-sensitive record material thus produced has been found to have a good shelf life and to provide intense colour-forming. EXAMPLE 2:
The four selected chromogenic materials ( A,B,C,D) were mixed in the proportions indicated in Table I such that an intense black print is subsequently obtained in use. In this example these four chromogenic materials were initially dispersed in a solvent comprising deodorised refined rape-seed oil at a concentration of 6.9% at ambient temperature and the temperature was increased to 115°C and then decreased.
The subsequent preparation of the emulsion the co-acervation process, cooling and ageing/finishing proceeded as in Example 1.
Laboratory scale encapsulations have also been made and tested with similar good results, utilising other vegetable oils such as sunflower oil and animal oils such as cod liver oil and beef dripping, and various mixtures of such oils.
Whilst in the above-described Examples the colour-formers used are all fluoran derivatives and the solvents are 100% animal or vegetable oil, it is to be understood that additional non-fluoran colour-formers may be included at up to 10% of the colour-former formulation, and that other non-animal or vegetable oil solvents may be included in the solvent at up to 20% of the solvent if required, although the use of 100% fluoran colour-formers and 100% animal or vegetable oils as solvents is entirely satisfactory.
Claims
1. A composition, for use as the internal phase of a coating of rupturable material for application to base sheet to form a pressure-sensitive record material, the composition comprising one ore more colour-formers of which at least 90% are monoamino and/or diamino fluoran derivatives, dissolved in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils.
2. A composition according to Claim 1 wherein the solvent comprises 100% of one or more vegetable and/or animal oils.
3. A composition according to Claim 1 or Claim 2 wherein the colour- formers comprise one or more of the following amino fluorans,
2'-(octylamino)-6'-(diethylamino) fluoran,
2'-anilo-3'-methyl-6'(diethylamino) fluoran,
6'(diethylamino)-2'-(l,l-dimethylethyl) fluoran,
6 '-(dibutylamino)-3 '-methyl-2 '-(phenylamino)-spiro[isobenzofuran- l(3H),9'-[9H]xanthen]-3-one.
4. A method of manufacturing a pressure-sensitive record material of the kind comprising an base sheet coated with a rupturable material confining droplets of a solution of one or more colour-formers characterised in that at least 90% of said colour-formers are monoamino and/or diamino fluoran derivatives, and said colour-formers are dissolved in a solvent comprising 80% to 100% of an animal or vegetable oil, dissolution of said colour-formers being carried at a temperature above 100°C.
5. A method according to Claim 4 wherein dissolution of said colour- formers is carried out at a temperature of up to 135°C.
6. A method according to Claim 4 or Claim 5 wherein the solvent comprises 100% of one or more vegetable and/or animal oils.
7. A method according to Claim 6 wherein the colour-formers comprise one or more of the following amino fluorans,
2'-(octylamino)-6'-(diethylamino) fluoran,
2'-anilo-3'-methyl-6'(diethylamino) fluoran,
6'(diethylamino)-2'-(l,l-dimethylethyl) fluoran,
6 '-(dibutylamino)-3 '-methyl-2 '-(phenylamino)-spiro[isobenzofuran- l(3H),9'-[9H]xanthen]-3-one.
8. A pressure-sensitive record material comprising a base sheet coated with a rupturable material confining droplets of an internal phase comprising one or more colour-formers of which at least 90% are monoamino and/or diamino fluoran derivatives, dissolved in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils.
9. A material according to Claim 8 wherein said solvent comprises 100% of one or more vegetable and/or animal oils.
10. A material according to Claim 8 or Claim 9 wherein the colour- formers comprise one or more of the following amino fluorans,
2'-(octylamino)-6'-(diethylamino) fluoran,
2'-anilo-3'-methyl-6'(diethylamino) fluoran,
6'(diethylamino)-2'-(l,l-dimethylethyl) fluoran,
6 '-(dibutylamino)-3 '-methyl-2 '-(phenylamino)-spirofisobenzofuran- l(3H),9'-[9H]xanthen]-3-one.
11. A method of forming micro-capsules containing a solution of colour- formers in an organic solvent by coacervation, characterised in that at least 90% of said colour-formers comprise monoamino and/or diamino fluoran derivatives, dissolved at a temperature in excess of 100°C in a solvent comprising 80% to 100% of one or more vegetable and/or animal oils to form an internal phase solution which is subsequently subject to coacervation at a temperature below 70°C.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB939318371A GB9318371D0 (en) | 1993-09-04 | 1993-09-04 | Pressure-sensitive record materials |
| GB9318371 | 1993-09-04 | ||
| PCT/GB1994/001921 WO1995007187A1 (en) | 1993-09-04 | 1994-09-05 | Pressure-sensitive record materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0716634A1 true EP0716634A1 (en) | 1996-06-19 |
| EP0716634B1 EP0716634B1 (en) | 1998-05-06 |
Family
ID=10741516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP94925547A Revoked EP0716634B1 (en) | 1993-09-04 | 1994-09-05 | Pressure-sensitive record materials |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0716634B1 (en) |
| JP (1) | JPH09502135A (en) |
| AT (1) | ATE165771T1 (en) |
| CA (1) | CA2170740C (en) |
| DE (1) | DE69410102T2 (en) |
| GB (1) | GB9318371D0 (en) |
| WO (1) | WO1995007187A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9414637D0 (en) * | 1994-07-20 | 1994-09-07 | Wiggins Teape Group The Limite | Presure-sensitive copying material |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4913456A (en) * | 1972-06-06 | 1974-02-05 | ||
| JPS5030088B2 (en) * | 1973-04-16 | 1975-09-29 | ||
| JPS58189030A (en) * | 1982-04-28 | 1983-11-04 | Kanzaki Paper Mfg Co Ltd | Preparation of microcapsule |
| JPH0741738B2 (en) * | 1989-03-27 | 1995-05-10 | 日本製紙株式会社 | Coloring material |
| GB9113086D0 (en) * | 1991-06-18 | 1991-08-07 | Wiggins Teape Group Ltd | Solvent compositions for use in pressure-sensitive copying paper |
| ES2125306T5 (en) * | 1992-06-04 | 2006-04-01 | Arjo Wiggins Limited | PIEZOSENSIBLE RECORD MATERIAL. |
-
1993
- 1993-09-04 GB GB939318371A patent/GB9318371D0/en active Pending
-
1994
- 1994-09-05 JP JP7508519A patent/JPH09502135A/en active Pending
- 1994-09-05 WO PCT/GB1994/001921 patent/WO1995007187A1/en not_active Application Discontinuation
- 1994-09-05 CA CA002170740A patent/CA2170740C/en not_active Expired - Fee Related
- 1994-09-05 EP EP94925547A patent/EP0716634B1/en not_active Revoked
- 1994-09-05 DE DE69410102T patent/DE69410102T2/en not_active Expired - Fee Related
- 1994-09-05 AT AT94925547T patent/ATE165771T1/en not_active IP Right Cessation
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9507187A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2170740C (en) | 2003-02-25 |
| DE69410102T2 (en) | 1998-09-03 |
| EP0716634B1 (en) | 1998-05-06 |
| GB9318371D0 (en) | 1993-10-20 |
| WO1995007187A1 (en) | 1995-03-16 |
| ATE165771T1 (en) | 1998-05-15 |
| CA2170740A1 (en) | 1995-03-16 |
| JPH09502135A (en) | 1997-03-04 |
| DE69410102D1 (en) | 1998-06-10 |
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