Provided is a compound capable of accelerating the enzymatic reaction catalyzed by peroxidase. The present invention provides a peroxidase reaction accelerating agent comprising a compound represented by formula (I) and a method for measuring hydrogen peroxide using the same.

There are provided a paste-like composition for pressure measurement, including a microcapsule that encompasses an electron-donating dye precursor and an electron-accepting compound that causes the electron-donating dye precursor to develop a color, and a pressure measurement method using the paste-like composition for pressure measurement.

A method of detecting an amine-based additive in wellbore servicing fluid (WSF) comprising contacting an aliquot of WSF with an amine detector reagent and aqueous medium to form a detection solution; wherein the amine detector reagent comprises an amine detector compound, and a polar organic solvent (POS) with flash point >105° C.; wherein the WSF comprises the amine-based additive; and wherein the detection solution is characterized by at least one absorption peak wavelength in 380-760 nm; detecting an absorption intensity for detection solution at a wavelength within ±20% of the at least one absorption peak wavelength; comparing the absorption intensity of detection solution at the wavelength within ±20% of the at least one absorption peak wavelength with a target absorption intensity of amine-based additive to determine the amount of amine-based additive in WSF; and comparing the amount of amine-based additive in WSF with a target amount of amine-based additive.

An object of the present invention is to provide a gardenia blue pigment that can stably maintain the color tone even after heating under acidic conditions, and a method for producing the gardenia blue pigment. A gardenia blue pigment that can stably maintain the color tone even after heating under acidic conditions is obtained by carrying out the following first and second steps: the first step of reacting walnut peptide, bitter melon peptide, and/or soy peptide with genipin in a solvent without the supply of a gas containing oxygen; and the second step of treating the reaction solution obtained in the first step with the supply of a gas containing oxygen.

A dye ink composition includes: a compound A represented by the general formula (I-1) as defined herein; a compound B represented by the general formula (I-2) as defined herein; at least one of a compound C-I represented by the general formula (I-3-1) as defined herein or a compound C-II represented by the general formula (I-3-2) as defined herein; a compound D represented by the general formula (I-4) as defined herein; and water.

A liquid electrophotographic ink composition is described. The liquid electrophotographic ink composition comprises a ceramic pigment, a polymer resin, a glass frit, and a liquid carrier. Also described is a heat transferable printed image, a process for printing a heat transferable image and a process for heat transfer printing using the liquid electrophotographic ink composition.

A dyeing method includes immersing a fiber into a dye for dyeing the fiber, in which the dye includes indigo and indirubin, and the indigo and the indirubin have a weight ratio of 20:1 to 80:1. The indigo in the dye has a concentration of 0.1% o.w.f. to 5% o.w.f. The dyed fiber may simultaneously have high luminance, high color saturation, high strength of colorization, and sufficient colorfastness.

Solution comprising about 1 to about 25 wt % of a dye that loses its colour during radical cure and about 75 to about 99 wt % of a solvent mixture, said solvent mixture comprising cyclopentanone and dimethylsulphoxide in a weight ratio of about 60:40 to about 95:5.

A dye printing treatment liquid composition is used to be adhered to a cloth and includes a polyester resin and water, the polyester resin includes a structural unit derived from an aromatic compound and a structural unit derived from a non-aromatic compound, the aromatic compound includes a phthalic acid, the non-aromatic compound includes a (poly)alkylene glycol, a content of a structural unit derived from the phthalic acid with respect to 100 percent by mole of the polyester resin is 15 to 85 percent by mole, and a content of a structural unit derived from the (poly)alkylene glycol with respect to 100 percent by mole of the polyester resin is 15 to 85 percent by mole.

Fluorescence titration of methylene blue, rhodamine B and rhodamine 6G (R6G) by silver nanoparticle (AgNP) all resulted in an initial steep quenching curve followed with a sharp turn and a much flatter quenching curve. At the turn, there are about 200,000 dye molecules per a single AgNP, signifying self-assembly of approximately 36 layers of dye molecules on the surface of the AgNP to form a micelle-like structure. These fluorescence-quenching curves fit to a mathematical model with an exponential term due to molecular self-assembly on a AgNP surface, or “self-assembly shielding effect”, and a Stern-Volmer term (nanoparticle surface enhanced quenching). Such a “super-quenching” by AgNP can only be attributed to “pre-concentration” of the dye molecules on the nanoparticle surface that yields the formation of micelle-like self-assembly, resulting in great fluorescence quenching. Overall, the fluorescence quenching titration reveals three different types of interactions of dye molecules on AgNP surface: 1) self-assembly (methylene blue, rhodamine B and R6G), 2) absorption/tight interaction (tryptamine and fluorescein), and 3) loose interaction (eosin Y). We attribute the formation of micelle-like self-assembly of these three dye molecules on AgNP to their positive charge, possession of nitrogen atoms, and with relatively large and flat aromatic moieties.