US3035935A

US3035935A - Hectographic coloring paper having a transfer coat containing lower alkyl mercapto triphenyl carbinol

Info

Publication number: US3035935A
Application number: US856027A
Authority: US
Inventors: Harbort Ludwig
Original assignee: Individual
Current assignee: Individual
Priority date: 1958-12-01
Filing date: 1959-11-30
Publication date: 1962-05-22
Anticipated expiration: 1979-05-22
Also published as: DE1054095B

Description

May 22, 1962 L. HARBORT HECTOGRAPHIC COLORING PAPER HAV LOWER ALKYL MEIRCAPTO TRIPHENYL CARBINOL Filed NOV. 35, 1959 PAPER INC A TRANSFER COAT CONTAINING WAX COAT CONTAINING A LOWER ALKYL. MERCAPTO TRIPHENYL CARBINOL LUDWIG HARBORT INVENTOR United States Patent 3,035,935 HECTOGRAPHIC COLORING PAPER HAVING A TRANSFER COAT CONTAINING LOWER ALKYL MERCAPTO TRIPHENYL CARBINOL Ludwig Harbort, Hannover, Germany, assignor to Gunther Wagner, Hannover, Germany Filed Nov. 30, 1959, Ser. No. 856,027 Claims priority, application Germany Dec. 1, 1958 9 Claims. (Cl. 117-362.)

The present invention relates to a hectographic coloring paper for producing hectographic copies according to the alcohol transfer process.

The drawing illustrates the invention and shows the broad concept of the invention as covered by the claims in a lower alkyl mercaptotriphenyl carbinol.

It is well-known that when using hectographing papers containing the usual basic dyes it is often almost unavoidable that the hectographic copies, as well as the hands and even the clothing of the persons working with such papers will be soiled by particles flaking oflE the colored coating.

There have been numerous proposals of means for avoiding this disadvantage. Thus, for example, it has been proposed to use in place of basic dyes the components of azo dyes which are only weakly colored and to develop the pigmentation on the copy paper by means of an alkaline substance which is contained in the copying fluid.

In actual practice, however, this method has the disadvantage that only completely wood-free, alkali-resistant papers can be used for the copy paper, and that the inex pensive types of wood-pulp paper which are used primarily in the conventional transfer processes must be avoided since they become decolorized by the alkaline copying fluid.

A further disadvantage of the transfer papers prepared with diazo compounds and components of difierent dyes consists in the fact that they are to a certain extent sensitive to light and must therefore be stored under cover, which is often considered a very great inconvenience.

Even the proposed application of carbinols or carbinolic ethers of triphenyl methane dyes cannot be regarded as a completely satisfactory and practical solution of the problem since the alkaline substances which are added to the coating material for stabilizing the same and for protecting it fiom undesirable influences of acids are subject to the influence of the carbon dioxide in the air and are neutralized a relatively short time. The consequence of this is that the carbon dioxide of the air is no longer kept away and will react with the carbinols or the carbinolic ethers. This means that these papers can be stored only for a very limited period and therefore do not comply with the requirements of actual practice.

For the same reason, these papers are also soon affected by the influences of other acids, for example, when the papers are touched by the hands which always carry traces of organic acids due to secretions of the skin. It is therefore unavoidable when handling these papers that the hands will be soiled.

It has now been found according to the present invention that the mentioned difliculties may be avoided if triphenyl carbinols or triphenyl carbinolic ethers are used which contain methyl mercapto groups. Examples of these materials are, for instance, the following compounds: (I) 4,4-di-(rnethyl mercapto)-triphenyl carbinol and (II) 4,4',4-tri- (methyl mercapto)-triphenyl carbinol 3,035,935 Patented May 22, 1962 I OH SCs t SOH.

The production of alkyl-mercapto-triphenyl-carbinol and triphenylcarbinoles is described in an article by K. Brand and O. Stallmann in Journal fiir praktische Chemie (107), 1924, pages 358 to 382.

These compounds are likewise colorless substances just like the corresponding carbinol bases of the known triphenyl methane dyes with dimethyl amino groups, but they differ from the latter very characteristically by their reaction to acids. While the carbinols of the triphenyl methane dyes with dimethyl amino groups such as, for example, the crystal violet carbinol, are extremely sensitive to acids and are converted into the respective dyes already by traces of the weakest inorganic and organic acids, the methyl mercapto triphenyl carbinols are entirely indilferent to weak inorganic or organic acids. Only very strong organic and inorganic acids such as, for example, trichloroacetic acid or hydrochloric acid will be able to convert these carbinols and the ethers thereof into the corresponding, intensively colored dye salts. Therefore, when handling hectographic coloring papers which contain carbinol bases or carbinol ethers with methyl mercapto groups in place of carbinol bases or carbinolic ethers of the usual triphenyl methane, there is no possibility of soiled hands, regardless of whether these papers are fresh or have already been stored for a considerable length of time. Furthermore, the hectographic coloring papers which are produced with methyl mercapto triphenyl carbinol bases have an unlimited stability in storage since the new compounds are stable and will not go into reaction with the carbon dioxide of the air. A further advantage "of these papers is that the dyes produced from the methyl mercapto triphenyl carbinols by a reaction with acids are more intensive and productive than the known triphenyl methane dyes with dimethyl amino groups, which is due to the stronger bathochrome effect of the methyl mercapto group in comparison to the dimethyl amino group. It is therefore possible to attain the desired color intensity of the copies already with considerably less amounts of substance than with triphenyl carbinol bases containing dimethy-l amino groups.

In accordance with the extremely low quantity of mercapto compound which is transferred at every printing operation upon the alcohol-moistened sheet of copy paper, there is also only a very small quantity of strong acid required for coating the same in order to start the color reaction. Thus, there is absolutely no danger in handling or working with the duplicating paper.

It has further been found according to the invention that triphenyl carbinols which contain methyl mercapto as well as dimethyl amino groups within the same molecule may be used with considerable advantage for coating hectographic coloring papers since it is easily possible by gradually replacing the methyl mercapto groups with amino groups to graduate the sensitivity to acids at any desired degree, which is of a great advantage for the particular purpose of the hectographic paper.

Example I A mixture of 20 parts of 4-methyl mercapto-triphenyl carbinol and 50 parts of wait is finely ground up, melted, and applied in the usual manner upon a suitable paper base. The resulting paper produces violet copies.

Example II A mixture of 50 parts of 4,4'-di(methyl mercapto)- triphenyl carbinol and 50 parts of wax is treated in the same manner as stated in Example I for; coating the paper base. The resulting paper produces blue copies.

Example 111 claim is:

1. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing as a compound for producing a color reaction a lower alkyl mercapto triphenyl carbinol.

2. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing as a compound for producing a color reaction a lower alkyl amino lower alkyl mercapto triphenyl carbinol.

3. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing a methyl mercapto triphcnyl carbinol and wax.

4. A transfer coloring paper for the alcohol trans fer process in an acid medium having a coating containing 4-methyl mercapto triphenyl carbinol and Wax.

5. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing about 20 parts of 4-methyl mercapto triphenyl carbinol and about parts of wax.

6. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing 4.4'-dimethyl mercapto triphenyl carbinol and wax.

7. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing about 50 parts of 4,4-dimethyl mercapto triphenyl carbinol and about 50 parts of wax.

8. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing 4-dimethyl amino 4,4"-di-methyl mercapto triphenyl carbinol and wax.

9. A transfer coloring paper for the alcohol transfer process in an acid medium having a coating containing about 20 parts of 4-di-methyl amino 4',4-di-rnethy1 merpacto triphenyl carbinol and about 50 pants of wax.

References Cited in the file of this patent UNITED STATES PATENTS 2,748,024 Klimkowski et a1 May 29, 1956 2,755,200 Balon et a1. July 17, 1956 2,755,201 Webber et al July 17, 1956 2,755,202 Balon et al July 17, 1956 2,927,041 Davis Mar. 1, 1960 FOREIGN PATENTS 3,149 Great Britain A. Mar. 10, 1885

Claims

1. A TRANSFER COLORING PAPER FOR THE ALCOHOL TRANSFER PROCESS IN AN ACID MEDIUM HAVING A COATING CONTAINING AS A COMPOUND FOR PRODUCING A COLORR REACTION A LOWER ALKYL MERCAPTO TRIPHENYL CARBINOL.