Abstract: Provided is an acceptor sheet useful for receiving marking material in imagewise fashion by means of mass transfer printing. The acceptor sheet comprises a substrate which has a microrough surface, wherein the coating is comprised of polymer particles which have not coalesced to form a uniform, continuous film. Such acceptor sheets exhibit superior mass transfer printing properties, and in particular superior wax thermal transfer printing properties, as compared to acceptor sheets having smooth coatings comprised of film-forming polymers.

Abstract: An ink jet transparency is provided which exhibits a unique ability to maintain the edge acuity of ink patterns or blocks on the transparency. The ink jet transparency comprises a substantially transparent resinous support, e.g., a polyester film, and a substantially clear coating thereon which includes a specific fluorosurfactant. The presence of the fluorosurfactant of the present invention in the clear coating prevents trailing of the ink-jet ink. As a result, patterns and ink blocks do not trail into one another on the transparency, but maintain their defined shape and size.

Abstract: An ink jet transparency is provided which exhibits improved wetting properties, thereby resulting in an even surface distribution of ink on the transparency. The ink jet transparency comprises a substantially transparent resinous support, e.g., a polyester film, and a substantially clear coating thereon which includes a non-volatile organic acid. Glycolic acid, citric acid, malonic acid, tartaric acid, maleic acid, fumaric acid, malic acid and succinic acid are among the preferred non-volatile organic acids employable in the present invention. The presence of the organic acid results in greatly improved wetting of ink jet ink in solid block areas, preventing the ink from coalescing onto itself. Undesired voids and pin holes in those areas where the ink has been applied are therefore avoided.

Abstract: A coated ink jet printing substrate where said coating utilizes an insolubilized hydrophilic polymer.

Abstract: Substituted 2,2'-dihydroxydiphenyl sulfide, sulfoxide, and sulfone compounds, and their use as azo coupling components in light-sensitive diazo compositions. The novel compounds couple with rapidly developing diazonium compounds to provide lemon-yellow dyes, and can be used in combination with blue and violet couplers to provide a green-black diazo image in higher density areas with a neutral black in lower density areas.

Abstract: Novel diazonium salts which possess excellent photo speed, good thermal stability, exceptional resistance to discoloration in the D.sub.min areas, rapid development, and allow a wide range of azo dye colors are provided. The diazonium salts are of the following formula: ##STR1## wherein R.sub.1 is tertiary butyl or tertiary amyl; Y is hydrogen, alkyl, hydroxyalkyl, cyanoalkyl, cycloalkyl, aralkyl, alkoxy, aryloxy, aralkoxy, aralkylthio, arylthio, alkylthio, halogen, allyl, allyloxy, allylthio, cyanoalkoxy, hydroxyalkoxy, methoxyalkoxy, trifluoroalkyl, alkylacetylamino, morpholino, or dialkyl carbonamido;R.sub.2 and R.sub.3 are the same or different, and are alkyl, aralkyl, allyl, cyanoalkyl, hydroxyalkyl, hydrogen, acyl, cycloalkyl, beta-chloroalkyl, branched alkyl, or a structure wherein R.sub.2 and R.sub.3 may be linked together to form a heterocyclic structure; andX is an anion.

Abstract: Negative-working diazography formulation is comprised of (i) at least one hexafluorophosphate diazonium salt adapted to photolytically cleave into an acid catalyst, (ii) at least one acid labile enolic, preferably arylenolic blocked-coupler adapted to be converted in the presence of acid to an active azo-coupling component, and (iii) an effective amount of an additive, such as p-toluenesulfonyl benzamide, capable of controlling the pH of films prepared from said formulation when subjected to a clearing step as defined herein.

Abstract: Negative-working diazography material is comprised of (i) at least one hexafluorophosphate diazonium salt adapted to photolytically cleave into an acid catalyst, (ii) at least one acid labile enolic, preferably arylenolic blocked-coupler adapted to be converted in the presence of acid to an active azo-coupling component, and (iii) an effective amount of at least one additive such as benzotriazole, urea, thiourea and derivatives thereof. The additives are believed to react with the acid released during imaging to the extent that migration thereof into the areas which have not been exposed to light is reduced or eliminated. The reduction in the migration of the liberated acid improves the D-min and line acuity of the image obtained from the formulation and the presence of the additive provides a means for decreasing the photo speed of the formulation.

Abstract: Light-sensitive diazo compositions which comprise a resorcinol substituted in the 2-position with an alkyl group and in the 4-position with an aralkyl group as the yellow azo coupling component, and diazotype materials prepared therefrom.