Abstract: A photopolymerization sensitizer may not cause problems of dusting or coloring of a cured product due to bleeding of additives such as the photopolymerization sensitizer on the surface, e.g., by blooming at the time of photo-curing or during storage of the cured product, and which provides a practically sufficient photo-curing rate. A 9,10-bis(alkoxycarbonylalkyleneoxy)anthracene compound having ester groups, of formula (I): wherein A is a C1-20 alkylene group, optionally branched by an alkyl group, R is a C1-20 alkyl group, optionally branched by the alkyl group, the C1-20 alkyl group optionally being a cycloalkyl group or a cycloalkylalkyl group, and X and Y are independently a hydrogen, a C1-8 alkyl group, or a halogen.

Abstract: A conventional polymerization inhibitor is for example an agent to scavenge radicals generated during storage of a radical polymerizable compound and used to stably handle the radical polymerizable compound, but is unnecessary when the radical polymerizable compound is to be subjected to radical polymerization reaction, and is preferably removed at the time of the radical polymerization reaction. The object of the present invention is to obviate inconvenience of removing the polymerization inhibitor at the time of radical polymerization. The radical polymerization control agent contained in a radical polymerizable composition of the present invention functions as a radical polymerization inhibitor for example stored in a dark place, but loses its radical polymerization inhibiting effect when polymerization is initiated while being irradiated with light at a certain specific wavelength at the time of polymerization.

Abstract: To provide a photopolymerization sensitizer which will not cause problems of dusting or coloring of a cured product by bleeding of additives such as the photopolymerization sensitizer on the surface e.g. by blooming at the time of photo-curing or during storage of the cured product, and which imparts a practically sufficient photo-curing rate. An oligomer of a 9,10-bis(substituted oxy)anthracene compound having repeating units represented by the following formula (1): wherein n represents a repetition number and is from 2 to 50, each of X and Y which may be the same or different, is a hydrogen atom, a C1-8 alkyl group or a halogen atom, and A is a bivalent substituent.

Abstract: The purpose of the present invention is to provide a photopolymerizable composition which can act as a photopolymerization sensitizer that is active against light having a wavelength falling within a wavelength range of from 300 to 500 nm, and which has such a property that coloring of a cured product produced by polymerizing a photopolymerizable composition containing the photopolymerization sensitizer is less. A photopolymerization sensitizer composition characterized by comprising a photopolymerization sensitizer containing an alkoxyanthracene compound represented by the formula (1) and a singlet oxygen quencher; and a photopolymerizable composition containing the photopolymerization sensitizer composition: in the formula (1), n represents an integer of 1 or 2; R represents a C1-12 alkyl group; and X represents a hydrogen atom or a C1-8 alkyl group.

Abstract: A radical polymerization method may use a compound having a polycyclic aromatic skeleton and an endoperoxide compound having a polycyclic aromatic skeleton. An endoperoxide compound may have a polycyclic aromatic skeleton of formula (1), and a compound may have a polycyclic aromatic skeleton, which is a raw material of the endoperoxide compound: wherein R is a C1-10 alkyl group, an alkoxymethyl group having a C1-5 alkoxy group, a C6-10 aryl group, an alkylcarbonyl group having a C1-10 alkyl group, an arylcarbonyl group having a C6-20 aryl group, an alkyloxycarbonyl group having a C1-10 alkyl group, an aryloxycarbonyl group having a C6-10 aryl group, an alkyloxycarbonylmethyl group having a C1-12 alkyl group or an aryloxycarbonylmethyl group having a C6-12 aryl group.

Abstract: A photopolymerization sensitizer may not cause problems of dusting or coloring of a cured product due to bleeding of additives such as the photopolymerization sensitizer on the surface, e.g., by blooming at the time of photo-curing or during storage of the cured product, and which provides a practically sufficient photo-curing rate. A 9,10-bis(alkoxycarbonylalkyleneoxy)anthracene compound having ester groups, of formula (I): wherein A is a C1-20 alkylene group, optionally branched by an alkyl group, R is a C1-20 alkyl group, optionally branched by the alkyl group, the C1-20 alkyl group optionally being a cycloalkyl group or a cycloalkylalkyl group, and X and Y are independently a hydrogen, a C1-8 alkyl group, or a halogen.

Abstract: To provide a photopolymerizable composition which can be quickly cured by light of from 300 nm to 450 nm, and a cured product of which is less colored. A photopolymerization sensitizer composition containing a compound represented by the following formula (1) and a compound, of which the maximum value of an absorption coefficient in a wavelength region ranging from at least 400 nm to at most 500 nm is higher than the maximum value of an absorption coefficient in a wavelength region ranging from at least 400 nm to at most 500 nm of said compound; and a photopolymerizable composition containing the photopolymerization sensitizer composition.

Abstract: A conventional polymerization inhibitor is for example an agent to scavenge radicals generated during storage of a radical polymerizable compound and used to stably handle the radical polymerizable compound, but is unnecessary when the radical polymerizable compound is to be subjected to radical polymerization reaction, and is preferably removed at the time of the radical polymerization reaction. The object of the present invention is to obviate inconvenience of removing the polymerization inhibitor at the time of radical polymerization. The radical polymerization control agent contained in a radical polymerizable composition of the present invention functions as a radical polymerization inhibitor for example stored in a dark place, but loses its radical polymerization inhibiting effect when polymerization is initiated while being irradiated with light at a certain specific wavelength at the time of polymerization.

Abstract: [OBJECT] The purpose of the present invention is to provide a photopolymerizable composition which can act as a photopolymerization sensitizer that is active against light having a wavelength falling within a wavelength range of from 300 to 500 nm, and which has such a property that coloring of a cured product produced by polymerizing a photopolymerizable composition containing the photopolymerization sensitizer is less. [SOLUTION TO PROBLEM] A photopolymerization sensitizer composition characterized by comprising a photopolymerization sensitizer containing an alkoxyanthracene compound represented by the formula (1) and a singlet oxygen quencher; and a photopolymerizable composition containing the photopolymerization sensitizer composition: in the formula (1), n represents an integer of 1 or 2; R represents a C1-12 alkyl group; and X represents a hydrogen atom or a C1-8 alkyl group.

Abstract: To provide a photopolymerization sensitizer which will not cause problems of dusting or coloring of a cured product by bleeding of additives such as the photopolymerization sensitizer on the surface e.g. by blooming at the time of photo-curing or during storage of the cured product, and which imparts a practically sufficient photo-curing rate. An oligomer of a 9,10-bis(substituted oxy)anthracene compound having repeating units represented by the following formula (1): wherein n represents a repetition number and is from 2 to 50, each of X and Y which may be the same or different, is a hydrogen atom, a C1-8 alkyl group or a halogen atom, and A is a bivalent substituent.

Abstract: To provide a photopolymerizable composition which can be quickly cured by light of from 300 nm to 500 nm, and a cured product of which is less colored. A photopolymerizable composition comprising a compound having an anthracene skeleton represented by the following formula (1), a compound having a benzophenone skeleton and a radical polymerizable compound: wherein each of R1 and R2 which may be the same or different, is a C1-20 alkyl group, a C6-20 aryl group, an alkylcarbonyl group having a C1-20 alkyl group, an arylcarbonyl group having a C6-20 aryl group, an alkyloxycarbonyl group having a C1-20 alkyl group, or an aryloxycarbonyl group having a C6-20 aryl group, and each of X and Y which may be the same or different, is a hydrogen atom or a C1-8 alkyl group.

Abstract: To provide a photopolymerizable composition which can be quickly cured by light of from 300 nm to 450 nm, and a cured product of which is less colored. A photopolymerization sensitizer composition containing a compound represented by the following formula (1) and a compound, of which the maximum value of an absorption coefficient in a wavelength region ranging from at least 400 nm to at most 500 nm is higher than the maximum value of an absorption coefficient in a wavelength region ranging from at least 400 nm to at most 500 nm of said compound; and a photopolymerizable composition containing the photopolymerization sensitizer composition.

Abstract: To provide a photopolymerizable composition which can be quickly cured by light of from 300 nm to 500 nm, and a cured product of which is less colored. A photopolymerizable composition comprising a compound having an anthracene skeleton represented by the following formula (1), a compound having a benzophenone skeleton and a radical polymerizable compound: wherein each of R1 and R2 which may be the same or different, is a C1-20 alkyl group, a C6-20 aryl group, an alkylcarbonyl group having a C1-20 alkyl group, an arylcarbonyl group having a C6-20 aryl group, an alkyloxycarbonyl group having a C1-20 alkyl group, or an aryloxycarbonyl group having a C6-20 aryl group, and each of X and Y which may be the same or different, is a hydrogen atom or a C1-8 alkyl group.

Abstract: An industrially advantageous process is presented whereby a high purity anthracene diether can be produced in good yield. An aqueous medium containing an alkali salt of 9,10-anthracenediol is added to an organic solvent containing an etherifying agent in the presence or absence of a quaternary ammonium compound or a quaternary phosphonium compound, to carry out the etherifying reaction to produce the anthracene diether.

Abstract: A lignocellulose material is cooked by means of an alkaline cooking liquor containing polysulfides in the presence of a quinone-hydroquinone compound, of which the oxidation-reduction potential in the form present during the cooking, which potential is a value calculated as a standard oxidation-reduction potential (Ea) with a hydrogen ion activity of 1, is within a range of from 0.12 to 0.25V to the standard hydrogen electrode potential. It is thereby possible to cook the lignocellulose material with a low Kappa number and in good yield and at the same time, to reduce the amount of the chemical solution used and to reduce the load on a recovery boiler.

Abstract: A gypsum-based building material comprising gypsum as the main material and an anthraquinone compound incorporated.

Abstract: A gypsum-based building material comprising gypsum as the main material and an anthraquinone compound incorporated.

Abstract: In a process for producing kraft pulp, the process is made closed, the yield of pulp is improved and environmental problems are minimized. An alkaline solution containing Na2S which flows in a process of producing kraft pulp, is electrolyzed by an electrolytic oxidation method; a liquid which is formed at an anode side and contains a polysulfide type sulfur in an amount of 6 g/l or more, is added, as it is or after being causticized, to the process before a chip has the maximum temperature, and a NaOH solution formed at a cathode side, is added to at least one step of the process after the chip has the maximum temperature till a final bleaching stage; and at least chemicals in the step wherein NaOH is added, among chemicals discharged in all steps from a cooking step till the final bleaching stage, are recovered and reused.

Abstract: The present invention has an object to obtain a cooking liquor containing polysulfide-sulfur at a high concentration by minimizing by-production of thiosulfate ions. The present invention is a method for producing polysulfides, which comprises introducing a solution containing sulfide ions into an anode compartment of an electrolytic cell comprising the anode compartment provided with a porous anode, a cathode compartment provided with a cathode, and a diaphragm partitioning the anode compartment and the cathode compartment, for electrolytic oxidation to obtain polysulfide ions, characterized in that the porous anode is disposed so that a space is provided at least partly between the porous anode and the diaphragm, and the apparent volume of the porous anode is from 60% to 99% based on the volume of the anode compartment.

Abstract: A lignocellulose material is cooked by means of an alkaline cooking liquor containing polysulfides in the presence of a quinone-hydroquinone compound, of which the oxidation-reduction potential in the form present during the cooking, which potential is a value calculated as a standard oxidation-reduction potential (Ea) with a hydrogen ion activity of 1, is within a range of from 0.12 to 0.25V to the standard hydrogen electrode potential. It is thereby possible to cook the lignocellulose material with a low Kappa number and in good yield and at the same time, to reduce the amount of the chemical solution used and to reduce the load on a recovery boiler.