Abstract: The present invention provides a photopolymerization initiator capable of exhibiting excellent sensitivity to photopolymerization and ensuring a sufficient pot life under ambient light, and a dental photocurable composition comprising the photopolymerization initiator. More specifically, the present invention provides a photopolymerization initiator (c) used in a dental photocurable composition, comprising: (c-1) a photosensitizer, (c-2) a polymerization accelerator, and (c-3) an aryliodonium salt represented by the formula (1): [Chemical Formula 1] [(R1)2I]+[(R2)bPF6-b]???(1) wherein, R1 represents an organic group bonded to I, R2 represents an alkyl group in which a part of hydrogen atoms is substituted with a flourine atom, and b represents the number thereof which is an integer of from 1 to 5, and a dental photocurable composition comprising the photopolymerization initiator.

Abstract: [Problem] To provide a dental photocurable composition having sufficient mechanical property and being excellent in color tone selectivity because of having a small color difference between before curing and after curing. [Solution] To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator, (D) photopolymerization accelerator and (E) filler, wherein, the dental photocurable composition comprises (B-1) ?-diketone compound as the (B) photosensitizer, and the dental photocurable composition comprises, with respect to 100 parts by mass of the (A) polymerizable monomer, 0.15 parts by mass or less of the (B-1) ?-diketone compound, 0.5 parts by mass or more of the (C) photoacid generator, and 100 parts by mass or more of the (E) filler.

Abstract: To provide a dental photocurable composition which can exhibit excellent mechanical characteristics even after returning from a low temperature to room temperature. To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator and (D) photopolymerization accelerator and the (C) photoacid generator may include only (C-1) iodonium salt-based compound of an anion having log S of ?4 or less.

Abstract: [Problem] To provide a photocurable composition having a high curing depth. [Solution] To provide a photocurable composition of the present disclosure comprises (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator, and (D) photopolymerization accelerator, wherein, the photocurable composition comprises (D-1) amine compound represented by formula (1) as the (D) photopolymerization accelerator. (In the formula (1), R1 is a substituent represented by formula (2), and R2 and R3 are substituents represented by formula (2) or substituents selected from —OH group, —O— group, —S— group, —NH—C(O)—NH— group, —C(O)—O— group, —OC(O)— group, —OC(O)—NH— group, —NH—C(O)—O— group, halogen, an organic group which may have an alkoxysilyl group, an aromatic ring which may have a substituent and an alicyclic heterocycle which may have a substituent.

Abstract: A method for manufacturing a glass substrate having a strain point of 680° C. or higher, the method includes: a step of melting a glass raw material; and a step of forming a molten glass, in which the forming step includes a step of cooling the molten glass such that a cooling time in a temperature range from an annealing point of the glass substrate to 500° C. is 35 seconds or more, and in a case where a cooling profile indicating a temperature change with respect to the cooling time is linearly approximated by a least-squares method in the temperature range from the annealing point of the glass substrate to 500° C., a coefficient of determination R2 in the least-squares method is 0.7 or more.

Abstract: [Problem] To provide a dental photocurable composition which has sufficient mechanical property and whose rheological property is not deactivated even after long-term storage. [Solution] The dental photocurable composition of the present disclosure comprises (A) polymerizable monomer, (B) photosensitizer, (D) photopolymerization accelerator and (E) filler, wherein, the dental photocurable composition comprises (D1) aliphatic tertiary amine compound represented by formula (1) as the (D) photopolymerization accelerator, and the dental photocurable composition comprises (E1) hydrophobized silica fine particle having an average diameter of primary particle of 1 to 40 nm as the (E) filler.

Abstract: [Problem] To provide a dental curable composition having good mechanical property and good storage stability before and after curing. Solution The dental curable composition of the present disclosure comprises (A) polymerizable monomer, (BC) polymerization initiator, (D) polymerization accelerator and (E) filler, wherein, the (BC) polymerization initiator comprises (B) photopolymerization initiator and/or (C) chemical polymerization initiator, the (B) photopolymerization initiator comprises (B1) photosensitizer and (B2) photoacid generator, the (C) chemical polymerization initiator comprises (C1) organic peroxide, the (E) filler comprises (E1) surface-treated basic filler, and the (E1) surface-treated basic filler is treated with (F1) surface treatment agent represented by the formula (1) and/or condensate thereof.

Abstract: [Problem] To provide a dental adhesive composition having excellent storage stability and adhesive strength. [Solution] To provide a dental adhesive composition, comprising (A) polymerizable monomer, (D) photopolymerization accelerator, and (F) volatile organic solvent, wherein, the dental adhesive composition comprises (A-1) polymerizable monomer having an acidic group as the (A) polymerizable monomer, and the dental adhesive composition comprises (D-1) aliphatic tertiary amine compound represented by formula (1) as the (D) photopolymerization accelerator.

Abstract: [Problem] To provide a photocurable composition having a high curing depth. [Solution] To provide a photocurable composition of the present disclosure comprises (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator, and (D) photopolymerization accelerator, wherein, the photocurable composition comprises (D-1) amine compound represented by formula (1) as the (D) photopolymerization accelerator. (In the formula (1), R1 is a substituent represented by formula (2), and R2 and R3 are substituents represented by formula (2) or substituents selected from —OH group, —O— group, —S— group, —NH—C(O)—NH— group, —C(O)—O— group, —OC(O)— group, —OC(O)—NH— group, —NH—C(O)—O— group, halogen, an organic group which may have an alkoxysilyl group, an aromatic ring which may have a substituent and an alicyclic heterocycle which may have a substituent.

Abstract: To provide a dental photocurable composition which can exhibit excellent mechanical characteristics even after returning from a low temperature to room temperature. To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator and (D) photopolymerization accelerator and the (C) photoacid generator may include only (C-1) iodonium salt-based compound of an anion having log S of ?4 or less.

Abstract: [Problem] To provide a dental photocurable composition having sufficient mechanical property and being excellent in color tone selectivity because of having a small color difference between before curing and after curing. [Solution] To provide a dental photocurable composition, comprising (A) polymerizable monomer, (B) photosensitizer, (C) photoacid generator, (D) photopolymerization accelerator and (E) filler, wherein, the dental photocurable composition comprises (B-1) ?-diketone compound as the (B) photosensitizer, and the dental photocurable composition comprises, with respect to 100 parts by mass of the (A) polymerizable monomer, 0.15 parts by mass or less of the (B-1) ?-diketone compound, 0.5 parts by mass or more of the (C) photoacid generator, and 100 parts by mass or more of the (E) filler.

Abstract: The present invention provides a photopolymerization initiator capable of exhibiting excellent sensitivity to photopolymerization and ensuring a sufficient pot life under ambient light, and a dental photocurable composition comprising the photopolymerization initiator. More specifically, the present invention provides a photopolymerization initiator (c) used in a dental photocurable composition, comprising: (c-1) a photosensitizer, (c-2) a polymerization accelerator, and (c-3) an aryliodonium salt represented by the formula (1): [Chemical Formula 1] [(R1)2I]+[(R2)bPF6-b]???(1) wherein, R1 represents an organic group bonded to I, R2 represents an alkyl group in which a part of hydrogen atoms is substituted with a fluorine atom, and b represents the number thereof which is an integer of from 1 to 5, and a dental photocurable composition comprising the photopolymerization initiator.

Abstract: To provide a one paste type dental adhesive composition which has mechanical characteristics and aesthetic property required in the restoration material, is superior in durable adhesive strength to the tooth substance, and is hard to be affected by the polymerization shrinkage stress and exhibits excellent durable adhesive strength even if the composition of the present invention is collectively filled and cured. To provide a dental adhesive composition comprising: (a) an acidic group-non-containing polymerizable monomer, (b) an acidic group-containing polymerizable monomer, (c) a filler, (d) a photo polymerization initiator, and (e) a chain transfer agent, wherein the chain transfer agent (e) contains ?-alkylstyrene compound.

Abstract: To provide an organic-inorganic composite filler containing; a polymerizable monomer (a) having at least one functional group selected from the group consisting of —OH group, —NH— group, and —NH2 group, a polymerizable monomer (b) having no functional group selected from the group consisting of —OH group, —NH— group, and —NH2 group, a polymerization initiator (c), an inorganic filler (d), and a silane compound (e) which generates —OH group by hydrolysis.

Abstract: A target object information acquisition apparatus includes a driving support ECU configured to select, when two or more sensor target objects detected by one of radar sensors among the grouped sensor target objects are present, the sensor target object having a shortest distance with respect to an own vehicle among the two or more sensor target objects detected as a width calculation sensor target object. The driving support ECU is configured to calculate a width of the fusion target object using the lateral position with respect to the own vehicle of the selected width calculation sensor target object.

Abstract: To provide a one paste type dental adhesive composition which has mechanical characteristics and aesthetic property required in the restoration material, is superior in durable adhesive strength to the tooth substance, and is hard to be affected by the polymerization shrinkage stress and exhibits excellent durable adhesive strength even if the composition of the present invention is collectively filled and cured. To provide a dental adhesive composition comprising: (a) an acidic group-non-containing polymerizable monomer, (b) an acidic group-containing polymerizable monomer, (c) a filler, (d) a photo polymerization initiator, and (e) a chain transfer agent, wherein the chain transfer agent (e) contains ?-alkylstyrene compound.

Abstract: In a driving assist apparatus for assisting a lane change from an own lane to a target lane, when a post-smoothing probability obtained by smoothing a time course change in “a lane presence possibility which increases with the possibility that a target is another vehicle traveling in the target lane (target lane other vehicle)” is greater than a threshold value, that target can be extracted as the target lane other vehicle. The post-smoothing probability requires some length of time to coincide with the lane presence possibility. Therefore, if after completion of a lane change, another lane change is immediately started in the same direction, there arises a possibility that the target lane other vehicle cannot be extracted properly. Therefore, in the case where after completion of a lane change, another lane change is started in the same direction, the lane change is not started until a re-change prohibition time elapses.

Abstract: When lane change assist control for assisting a lane change from an own lane (original lane) to an adjacent target lane is performed, the determination as to whether or not another vehicle is in the target lane may be made based on the own lane width, the own vehicle's deviation from the lateral center of the own lane (own lane deviation), and the lateral position of the another vehicle. When the vehicle enters the target lane, own lane switching in which the own lane deviation changes by the lane width occurs and makes it impossible to properly perform the above determination. In view of this, after occurrence of own lane switching, the above determination is made based on a value obtained by adding the own lane width to the another vehicle lateral position or a value obtained by subtracting the own lane width from the another vehicle lateral position.

Abstract: A lane changing support apparatus includes a plurality of radar sensors and a driving support ECU. The driving support ECU determines whether or not a target object is highly likely to have entered a blind spot area of the radar sensors based on fusion target object information, when starting an extrapolation process of the fusion target object. When the driving support ECU determines that the fusion target object is highly likely to have entered the blind spot, the driving support ECU prohibits the lane changing support control to a lane in the side of this blind spot area.

Abstract: In a driving assist apparatus for assisting a lane change from an own lane to a target lane, when a post-smoothing probability obtained by smoothing a time course change in “a lane presence possibility which increases with the possibility that a target is another vehicle traveling in the target lane (target lane other vehicle)” is greater than a threshold value, that target can be extracted as the target lane other vehicle. The post-smoothing probability requires some length of time to coincide with the lane presence possibility. Therefore, if after completion of a lane change, another lane change is immediately started in the same direction, there arises a possibility that the target lane other vehicle cannot be extracted properly. Therefore, in the case where after completion of a lane change, another lane change is started in the same direction, the lane change is not started until a re-change prohibition time elapses.