A salt-forming compound represented by the following general formula (3): ##STR00001##
where X.sup.1 and X.sup.2 each independently represent an aromatic ring group optionally containing a substituent; Y represents a divalent hydrocarbon group that the carbon atom directly bound to X.sup.1 or X.sup.2 does not have a π bond; Z.sup.+ represents an organic cation group; e represents an integer of from 1 to 4; and when e is 2 or more, a plurality of Ys and a plurality of Z.sup.+ s may be each the same or different; A.sup.c- represents a heteropolyoxometalate anion which is a c-valent anion and which has an oxidation-reduction potential larger than −0.3 V relative to the silver/silver chloride electrode; f and c are each an integer of 2 or more; g is an integer of 1 or more; and the salt-forming compound is a normal salt that f×e=c×g.

Methods of isolating phenols from phenol-containing media. The methods include combining a phospholipid-containing composition with the phenol-containing medium to generate a combined medium, incubating the combined medium to precipitate phenols in the combined medium and thereby form a phenol precipitate phase and a phenol-depleted phase, and separating the phenol precipitate phase and the phenol-depleted phase. The methods can further include extracting phenols from the separated phenol precipitate phase. The extracting can include mixing the separated phenol precipitate phase with an extraction solvent to solubilize in the extraction solvent at least a portion of the phenols originally present in the phenol precipitate phase.

The present disclosure provides a continuous process for the synthesis coupled compounds of diazonium salts including azo dyes involving in-situ generation of diazonium salts. It further discloses a set up to carry out the process for the synthesis of coupled compounds of diazonium salts.

A color material dispersion liquid including a color material, which is a salt-forming compound of an organic dye with a heteropolyoxometalate, a dispersant and a solvent, wherein the organic dye is at least one organic dye selected from the group consisting of a porphyrin dye, a tetraazaporphyrin dye, a phthalocyanine dye and a squarylium dye, and wherein the heteropolyoxometalate is a heteropolyoxometalate which has an oxidation-reduction potential larger than −0.3 V relative to the silver/silver chloride electrode.

The present invention relates to a method for preparing lycopene crystals with high purity and low harm. The method comprises the following steps: (1) mixing lycopene oleoresin with a mixed solvent consisting of an alkane and a lower alcohol, and heating and stirring the resultant for dissolution to form a homogenous solution; (2) cooling the homogenous solution for crystallization, filtering the resultant to obtain a filter cake; and (3) washing the filter cake successively using a lower alcohol and an alkane, and drying the resultant to obtain lycopene crystals. According to the method provided by the present invention, lycopene crystals can be obtained using a mixed solvent by means of one step crystallization, and the crystal content is further improved and harmful substances in the crystals are reduced by means of a two-step crystal washing process to obtain lycopene crystals with high purity and low harm. The method is fast and convenient, lycopene crystals with high purity, low harm, and sanitary safety can be produced, and the method is suitable for industrial production.

A salt-forming compound represented by the following general formula (3):

##STR00001##

where X.sup.1 and X.sup.2 each independently represent an aromatic ring group optionally containing a substituent; Y represents a divalent hydrocarbon group that the carbon atom directly bound to X.sup.1 or X.sup.2 does not have a π bond; Z.sup.+ represents an organic cation group; e represents an integer of from 1 to 4; and when e is 2 or more, a plurality of Ys and a plurality of Z.sup.+ s may be each the same or different; A.sup.c− represents a heteropolyoxometalate anion which is a c-valent anion and which has an oxidation-reduction potential larger than −0.3 V relative to the silver/silver chloride electrode; f and c are each an integer of 2 or more; g is an integer of 1 or more; and the salt-forming compound is a normal salt that f×e=c×g.

The present invention relates to a new crystal form of the compound of formula and a process for its preparation. The compound may be used in compositions for inks, paints and plastics, especially in a wide variety of printing systems and is particularly well-suited for security applications.

##STR00001##

The present invention refers to a process for purifying leucoindigo salt solutions, for removal of aromatic amines, particularly aniline and N-methylaniline, comprising: adding to a purification vessel a leucoindigo salt solution containing aromatic amines, said solution in the form of a stationary mass; bubbling with a controlled flow rate an inert gas in the purification vessel, by means of a device submerged at the surface of the stationary mass; injecting with a controlled flow rate a gas purification current into the vessel, by means of a device submerged at the stationary mass; and recovering the purified solution from the vessel. It also refers to the use of inert gas in a process for purifying leucoindigo salt solutions, acting as a gas anti-foaming agent, to reduce foam and chances of product stripping during processing.

A reactive disperse yellow dye is suitable for supercritical CO.sub.2 anhydrous dyeing. The reactive disperse yellow dye in has a parent of azo structure, and has monochlorometriazinyl groups thereon. The reactive disperse yellow dye can be used for supercritical CO.sub.2 anhydrous dyeing of cellulose fiber, protein fiber, chemical fiber and the blended fabrics thereof, and has good dyeing effect particularly for cotton-polyester blended products.

An object of the present invention is to provide a method for removing geniposide or genipin or both from a material containing geniposide or genipin or both.

The present invention is a method for removing geniposide or genipin or both from a material containing geniposide or genipin or both,

the method comprising treating the material containing geniposide or genipin or both using an activated carbon having

(a) a methylene blue adsorption ability of 50 ml/g or more; and

(b) an iodine adsorption ability of 750 mg/g or more, thereby removing geniposide or genipin or both.