Abstract: Shown is a compound represented by formula (1). For example, R1 is alkyl having 1 to 15 carbons; MES is a mesogen group having at least one ring; Sp1 is a single bond or alkylene having 1 to 10 carbons; M1 is methyl; and R2, M2 and M3 are hydrogen.

Abstract: Compound (1) is provided. R1-MES-Sp1-P1??(1) In compound (1), R1 is alkyl having 1 to 15 carbons; MES is a mesogen group having an at least one ring; Sp1 is a single bond or alkylene having 1 to 10 carbons, and in the alkylene, at least one hydrogen is replaced by group (1a); P1 is group (1e) or (1f); wherein, M1, M2, M3 and M4 are hydrogen; Sp2 and Sp3 are a single bond or alkylene having 1 to 10 carbons; R2 is alkyl having 1 to 15 carbons; R3 is group (1g), (1h) or (1i); wherein, Sp4 and Sp5 are a single bond or alkylene having 1 to 10 carbons; S1 is >CH—, and S2 is >C<; and X is —OH.

Abstract: Provided is a polar compound having high chemical stability, high capability of aligning liquid crystal molecules, high solubility in a liquid crystal composition, and a large voltage holding ratio when used in a liquid crystal display device. The compound is represented by formula (1): in which, for example, R1 is alkyl having 1 to 15 carbons; MES is a mesogen group having at least one ring; Sp1 is a single bond or alkylene having 1 to 10 carbons; M1 and M2 are hydrogen; and R2 is a group represented by formulas (1a) to (1c): in which, Sp2 and Sp3 are a single bond or alkylene having 1 to 10 carbons; S1 is >CH—; S2 is >C<; and X1 is —OH.

Abstract: Shown is a compound represented by formula (1). For example, R1 is alkyl having 1 to 15 carbons; MES is a mesogen group having at least one ring; Sp1 is a single bond or alkylene having 1 to 10 carbons; M1 is methyl; and R2, M2 and M3 are hydrogen.

Abstract: A compound represented by formula (1). For example, R1, R2 and R3 are alkyl having 1 to 15 carbons; ring A1 and ring A3 are cyclohexyl or phenyl, ring A2 is 1,4-cyclohexylene or 1,4-phenylene; Z1 and Z2 are a single bond or alkylene having 1 to 10 carbons; a is 0, 1, 2, 3 or 4; c, d and e are 0, 1, 2, 3 or 4; and P1 to P3 are a polymerizable group represented by formula (P-1); wherein M1 and M2 are hydrogen or alkyl having 1 to 5 carbons; and R4 is a polar group represented by formulas (1a) to (1c); wherein Sp5 and Sp6 are a single bond or alkylene having 1 to 10 carbons; S1 is >CH—, and S2 is >C<; and X1 is —OH.

Abstract: Provided is a polar compound that has high chemical stability and high capability of aligning liquid crystal molecules, and has a large voltage holding ratio when used in a liquid crystal display device. The compound represented by formula (1) is applied. For example, R1 is alkyl having 1 to 15 carbons; rings A1 to A5 are 1,4-cyclohexylene or 1,4-phenylene; Z1 and Z5 are a single bond or alkylene having 1 to 10 carbons; a and b are 0 to 4, and a sum of a and b is 4 or less; d is 1 to 4; c and e are 0 to 4; P1 to P3 are a polymerizable group represented by formulas (P-1) to (P-5): in which M1 to M3 are hydrogen or alkyl having 1 to 5 carbons; and R2 is a group represented by formulas (1a) to (1c): in which Sp1 to Sp5 are a single bond or alkylene having 1 to 10 carbons; S1 is >CH—; S2 is >C<; and X1 is —OH.

Abstract: Provided is a polar compound having high chemical stability, high capability of aligning liquid crystal molecules, high solubility in a liquid crystal composition, and a large voltage holding ratio when used in a liquid crystal display device. The compound is represented by formula (1): in which, for example, R1 is alkyl having 1 to 15 carbons; MES is a mesogen group having at least one ring; Sp1 is a single bond or alkylene having 1 to 10 carbons; M1 and M2 are hydrogen; and R2 is a group represented by formulas (1a) to (1c): in which, Sp2 and Spa are a single bond or alkylene having 1 to 10 carbons; S1 is >CH—; S2 is >C<; and X1 is —OH.

Abstract: A polar compound has a high chemical stability, high ability to align liquid crystal molecules and high solubility in a liquid crystal composition, and causes no decrease of liquid crystallinity of the liquid crystal composition, a liquid crystal composition contains the compound, and a liquid crystal display device includes the composition. The compound is represented by formula (1), the composition contains the compound, and the liquid crystal display device uses the composition. In formula (1), R1 is alkyl having 3 to 15 carbons, alkenyl having 4 to 15 carbons or the like; a is an integer from 2 to 12; and R2 is a group represented by formula (1a), formula (1b) or formula (1c). In the formulas, S1 and S2 are independently a single bond, alkylene having 1 to 10 carbons; S3 is >CH— or >N—; S4 is >C< or >Si<; and X1 is —OH, —NH2 or the like.

Abstract: Shown is a liquid crystal compound satisfying at least one of physical properties such as high stability to heat, light and so forth, a high clearing point, a low minimum temperature of a liquid crystal phase, small viscosity, suitable optical anisotropy, large negative dielectric anisotropy, a suitable elastic constant and excellent compatibility with other liquid crystal compounds. The compound is represented by formula (1). In the formula, for example, R1 and R2 are alkyl having 1 to 15 carbons, and ring A1, ring A2 and ring A3 are 1,4-cyclohexylene or 1,4-cyclohexenylene, Z1, Z2 and Z3 are a single bond or —(CH2)2—, a, b and c are 0 or 1, and a sum of a, b, and c is 0, 1 or 2.

Abstract: Subject It is to provide a polymerizable compound having a high polymerization reactivity, a high conversion yield and a high solubility in a liquid crystal composition, a polymerizable composition including the compound, a liquid crystal composite prepared from the composition and a liquid crystal display device containing this composite. Means for Solving the Subject A compound represented by formula (1). In this formula, for example, P1 and P2 are —SCO—CH?CH2; Sp1 and Sp2 are a single bond; ring A1, ring A2, ring A3 and ring A4 are 1,4-phenylene; Z1, Z2 and Z3 are a single bond; and a is 1, and b and c is 0.

Abstract: A polar compound has a high chemical stability, high ability to align liquid crystal molecules and high solubility in a liquid crystal composition, and causes no decrease of liquid crystallinity of the liquid crystal composition, a liquid crystal composition contains the compound, and a liquid crystal display device includes the composition. The compound is represented by formula (1), the composition contains the compound, and the liquid crystal display device uses the composition. In formula (1), R1 is alkyl having 3 to 15 carbons, alkenyl having 4 to 15 carbons or the like; a is an integer from 2 to 12; and R2 is a group represented by formula (1a), formula (1b) or formula (1c). In the formulas, S1 and S2 are independently a single bond, alkylene having 1 to 10 carbons; S3 is >CH— or >N—; S4 is >C< or >Si<; and X1 is —OH, —NH2 or the like.

Abstract: An object is to provide a liquid crystal compound satisfying at least one of physical properties such as a high stability to heat and light, a high clearing point, a low minimum temperature of a liquid crystal phase, a small viscosity, a suitable optical anisotropy, a large dielectric anisotropy, a suitable elastic constant and an excellent compatibility with other liquid crystal compounds, a liquid crystal composition containing the compound, and a liquid crystal display device including the composition. A solution is a compound represented by formula (1). In formula 1, R1 is alkyl having 1 to 10 carbons, for example; ring A1 and ring A2 are independently 1,4-cyclohexylene or 1,4-phenylene; Z1 and Z2 are independently a single bond or —CF2O—; L1 and L2 are halogen; and a is 1 or 2.

Abstract: An object is to provide a liquid crystal compound satisfying at least one of physical properties such as a high stability to heat and light, a high clearing point, a low minimum temperature of a liquid crystal phase, a small viscosity, a suitable optical anisotropy, a large dielectric anisotropy, a suitable elastic constant and an excellent compatibility with other liquid crystal compounds, a liquid crystal composition containing the compound, and a liquid crystal display device including the composition. A solution is a compound represented by formula (1). In formula 1, R1 is alkyl having 1 to 10 carbons, for example; ring A1 and ring A2 are independently 1,4-cyclohexylene or 1,4-phenylene; Z1 and Z2 are independently a single bond or —CF2O—; L1 and L2 are halogen; and a is 1 or 2.

Abstract: Subject It is to provide a polymerizable compound having a high polymerization reactivity, a high conversion yield and a high solubility in a liquid crystal composition, a polymerizable composition including the compound, a liquid crystal composite prepared from the composition and a liquid crystal display device containing this composite. Means for Solving the Subject A compound represented by formula (1). In this formula, for example, P1 and P2 are —SCO—CH?CH2; Sp1 and Sp2 are a single bond; ring A1, ring A2, ring A3 and ring A4 are 1,4-phenylene; Z1, Z2 and Z3 are a single bond; and a is 1, and b and c is 0.

Abstract: Based on a fuel supplying amount in accordance with an engine operating condition, a discharge amount of a predetermined fuel component contained in exhaust gas to be discharge per unit time is estimated, and integrated by an accumulation amount of the fuel component accumulated in an exhaust purification element. Furthermore, according to an exhaust gas temperature that flows into the element, an amount of the fuel component to be removed from the element per unit time is estimated, and the amount is subtracted from the accumulation amount. When the accumulation amount is equal to or greater than a predetermined value, a determination is made that a timing to forcefully remove the fuel component accumulated in the element has arrived. Then, an alarming lamp is lightened, and a forceful removing processing is performed by raising a temperature of the exhaust gas above a temperature at which the fuel component is removed.

Abstract: In order to maintain a high NOx purification rate of a NOx reduction catalytic converter even in the case in which an NOx emission amount from an engine changes suddenly, in an exhaust emission purifying apparatus for an engine that reduces and purifies NOx in exhaust gas using ammonia generated from an injection-supplied urea aqueous solution, after engine starting, when an exhaust temperature exceeds a predetermined temperature T (step S1), an amount of urea aqueous solution corresponding to an actual engine operating state is injection-supplied (steps S3 to S5). On the other hand, at a change of the transmission speed ratio based on a driver's shift operation, an engine operating state after the change of the transmission speed ratio is predicted (steps S2, S6), and an amount of urea aqueous solution corresponding to the predicted engine operating state is injection-supplied before the change of the transmission speed ratio is completed (steps S7, S8).

Abstract: In an exhaust filter, a urea hydrolysis catalyst is supported on a first portion of an inner wall of a cell passage on the inlet side, and a first NOx reducing catalyst is supported on a second portion of the inner wall of the inlet-side passage downstream of the first portion. A second NOx reducing catalyst is supported on a third portion of an inner wall of a cell passage on the outlet side where the third portion overlaps with the first portion in a direction of intersection with the exhaust flow into the exhaust filter or is downstream of the first portion. An oxidation catalyst is supported on a fourth portion of the inner wall of the outlet-side passage downstream of the third portion where the fourth portion overlaps with the second portion in the direction of intersection or is downstream of the second portion.

Abstract: In an exhaust gas purification apparatus for an engine includes a bubble generation device, the bubble generation device for mixing nano-sized to micro-sized bubbles into a liquid reducing agent or a precursor thereof injection-supplied from an injection nozzle is disposed in a reducing agent supply system running from a reducing agent tank to the injection nozzle. When the liquid reducing agent or the precursor thereof is injection-supplied from the injection nozzle, the liquid reducing agent or the precursor thereof is divided by bubbles, and the bubbles are radically inflated and burst by a pressure change and a temperature change at the time of injection-supplying, so that microparticulation of the liquid reducing agent or the precursor thereof is facilitated.

Abstract: Based on a fuel supplying amount in accordance with an engine operating condition, a discharge amount of a predetermined fuel component contained in exhaust gas to be discharge per unit time is estimated, and integrated by an accumulation amount of the fuel component accumulated in an exhaust purification element. Furthermore, according to an exhaust gas temperature that flows into the element, an amount of the fuel component to be removed from the element per unit time is estimated, and the amount is subtracted from the accumulation amount. When the accumulation amount is equal to or greater than a predetermined value, a determination is made that a timing to forcefully remove the fuel component accumulated in the element has arrived. Then, an alarming lamp is lightened, and a forceful removing processing is performed by raising a temperature of the exhaust gas above a temperature at which the fuel component is removed.

Abstract: The exhaust purification apparatus including a control unit which estimates: a deposition amount of urea crystal in an exhaust system per unit time based on a dosing flow rate of a urea aqueous solution injected to the exhaust upstream side of a SCR converter and an exhaust gas temperature; and an accumulation amount of the urea crystal by sequentially integrating the deposition amount. The control unit further estimates: an amount of the urea crystal to be removed from the exhaust system per unit time according to the exhaust gas temperature; and an accumulation amount of the remaining urea crystal by sequentially subtracting the estimated amount, from the accumulation amount. When the accumulation amount is equal to or greater than a predetermined amount, it is determined that a timing to forcefully remove the accumulated urea crystal has arrived. Then, an alarm is activated and a forceful removing processing is performed by raising the exhaust gas temperature.