摘要:
Photographic elements, diffusion transfer assemblages and processes are described which employ a novel nondiffusible compound having a releasable pyridylazopyrazole or pyrimidylazopyrazole dye moiety. The compound contains in the ortho position of the azopyrazole moiety a metal chelating group, a salt thereof or a hydrolyzable precursor thereof, and a ballasted carrier moiety which is capable of releasing the diffusible azo dye under alkaline conditions. The dye is transferred imagewise to an image-receiving layer where it is contacted with metal ions to form a metal-complexed azo dye transfer image of excellent stability.
摘要:
Photographic elements, diffusion transfer assemblages and processes are described which employ a novel nondiffusible compound having a releasable pyridylazopyrazole or pyrimidylazopyrazole dye moiety. The compound contains in the ortho position of the azopyrazole moiety a metal chelating group, a salt thereof or a hydrolyzable precursor thereof, and a ballasted carrier moiety which is capable of releasing the diffusible azo dye under alkaline conditions. The dye is transferred imagewise to an image-receiving layer where it is contacted with metal ions to form a metal-complexed azo dye transfer image of excellent stability.
摘要:
Aqueous thiocarbonate solutions are stabilized by the addition of base, sulfide and/or polysulfide, and the stability and safety of the more concentrated solutions containing 1 weight percent or more equivalent CS.sub.2 as a thiocarbonate are achieved as reflected by significant reduction of CS.sub.2 partial pressure in such solutions.
摘要:
Biuret is removed from biuret-containing aqueous urea solutions in a multi-cycle process which involves sequential (A) removal of biuret by contact with an anion exchanger and (B) regeneration of the anion exchanger, in which method, in one or more cycles, the anion exchanger regenerant comprises an aqueous solution of a strong base which has been employed to regenerate the anion exchanger in a previous cycle. This procedure allows for recycling, and thus reuse, of the strong base regenerant which results in significant economy. Methods are also provided in which (A) one or both of the aqueous urea solution and regenerant have a relatively low calcium equivalent content, (B) a substantially non-alkaline regenerant is employed either as the only regenerant in one or more cycles or as a partial regenerant before regeneration with the strong base regenerant, (C) the carbonate content of one or more of the aqueous process streams is controlled and/or reduced, and/or (D) the concentration of biuret in the recycled strong base regenerant is periodically reduced. All of these factors contribute to process economy, anion exchanger life, and more efficient, less frequent regeneration.
摘要:
Methods are provided for recovering biuret from aqueous urea solutions and for producing relatively concentrated biuret-containing extracts which involve contacting a biuret-containing aqueous urea solution with the hydroxide ion form of an anion exchanger to retain at least a portion of the biuret on the exchanger, contacting the resulting biuret-containing ion exchanger with an aqueous extractant under conditions sufficient to form a biuret-containing extract, and contacting the resulting biuret-containing extract with the same or other biuret-containing anion exchanger in the same or subsequent cycles under conditions sufficient to increase the biuret concentration of the extract. The biuret-containing urea feed solution may also contain higher molecular weight urea condensation products, and the biuret can be selectively separated from such condensation products by the disclosed methods. Extracts containing about 1 weight percent biuret or more can be obtained from which biuret can be crystallized at temperatures above 0.degree. C., and purified biuret of as much as 99.9 percent plus purity can be obtained from solutions containing higher molecular weight urea condensation products such as triuret, melamine, ammelide, and/or others. An integrated process also is provided which involves heating urea at a temperature sufficient to form biuret (in the presence or absence of higher molecular weight urea condensation products) and recovering biuret from an aqueous solution of the resulting pyrolyzed urea as described.
摘要:
Oligomeric thiocarbonates such as hexathiodicarbonate salts and thioesters are used as pesticides and preservatives. Certain oligomeric thiocarbonate salts, notably quaternary ammonium hexathiodicarbonates, are prepared. The compounds are stabilized with added base and/or sulfide.
摘要:
Aqueous thiocarbonate solutions are stabilized by the addition of base, sulfide and/or polysulfide, and the stability and safety of the more concentrated solutions containing 1 weight percent or more equivalent CS.sub.2 as a thiocarbonate are achieved as reflected by significant reduction of CS.sub.2 partial pressure in such solutions. The stabilized thiocarbonate solutions are employed to control pests in soil.
摘要:
Aqueous thiocarbonate solutions are stabilized by the addition of base, sulfide and/or polysulfide, and the stability and safety of the more concentrated solutions containing 1 weight percent or more equivalent CS.sub.2 as a thiocarbonate are achieved as reflected by significant reduction of CS.sub.2 partial pressure in such solutions.
摘要:
Aqueous thiocarbonate solutions are stabilized by the addition of base, sulfide and/or polysulfide, and the stability and safety of the more concentrated solutions containing 1 weight percent or more equivalent CS.sub.2 as a thiocarbonate are achieved as reflected by significant reduction of CS.sub.2 partial pressure in such solutions. Also, deposit formation in irrigation systems delivering such thiocarbonates, such as drip emitters and sprinkler heads, is reduced or eliminated with minor amounts of sodium hexametaphosphate.
摘要:
Aqueous thiocarbonate solutions are stabilized by the addition of base, sulfide and/or polysulfide, and the stability and safety of the more concentrated solutions containing 1 weight percent or more equivalent CS.sub.2 as a thiocarbonate are achieved as reflected by significant reduction of CS.sub.2 partial pressure in such solutions.