An object of the present invention is to provide a chemical liquid purification method which makes it possible to obtain a chemical liquid having excellent defect inhibition performance. Another object of the present invention is to provide a chemical liquid. The chemical liquid purification method according to an embodiment of the present invention is a chemical liquid purification method including obtaining a chemical liquid by purifying a substance to be purified containing an organic solvent, in which a content of the stabilizer in the substance to be purified with respect to the total mass of the substance to be purified is equal to or greater than 0.1 mass ppm and less than 100 mass ppm.

The current invention relates to long α-ω di-functional linear molecules as building blocks closing the gap between small molecules and polymers, or in a polycondensated form, in the production of oligomers and/or polymers, surfactants, lubricants, coatings, colloidal stabilizing surface chains/molecules.

A process can be used for recovering 1-methoxy-2-propanol and 2-methoxy-1-propanol from an aqueous effluent stream by liquid-liquid-extraction, followed by extractive distillation, distillation of methoxypropanols from the extraction solvent, and distillative separation of the methoxypropanol isomers. Recovered extraction solvent is recycled to the extraction and extractive distillation. Heat transfer from recovered extraction solvent to the extract fed to the extractive distillation reduces energy demand of the process. A facility for this process contains a countercurrent extraction column, an extractive distillation column, a solvent recovery distillation column, an isomer separation distillation column, and a heat exchanger for transferring heat from recovered extraction solvent to the extract fed to the extractive distillation.

A process can be used for recovering 1-methoxy-2-propanol and 2-methoxy-1-propanol from an aqueous effluent stream by liquid-liquid-extraction, followed by extractive distillation, distillation of methoxypropanols from the extraction solvent, and distillative separation of the methoxypropanol isomers. Recovered extraction solvent is recycled to the extraction and extractive distillation. Heat transfer from recovered extraction solvent to the extract fed to the extractive distillation reduces energy demand of the process. A facility for this process contains a countercurrent extraction column, an extractive distillation column, a solvent recovery distillation column, an isomer separation distillation column, and a heat exchanger for transferring heat from recovered extraction solvent to the extract fed to the extractive distillation.

There is provided a fluorine-containing ether compound represented by the following formula. R.sup.1—R.sup.2—CH.sub.2—R.sup.3—CH.sub.2—OCH.sub.2CH(OH)CH.sub.2O—CH.sub.2—R.sup.3—CH.sub.2—R.sup.4—R.sup.5 (in the formula, R.sup.3 represents a perfluoropolyether chain; R.sup.2 and R.sup.4 represent a divalent linking group having a polar group and may be the same or different from each other; R.sup.1 and R.sup.5 represent a terminal group bonded to an oxygen atom of R.sup.2 or R.sup.4 and may be the same or different from each other; and at least one of R.sup.1 and R.sup.5 is an organic group having 1 to 8 carbon atoms and at least one of hydrogens included in the organic group is substituted by a cyano group).

A higher secondary alcohol alkoxylate precursor is obtained by reacting a long-chain olefin with a (poly)alkylene glycol. The precursor has a content of (poly)alkylene glycol of 0.2% by mass or lower with respect to the total mass of the higher secondary alcohol alkoxylate; a higher secondary alcohol alkoxylate adduct which is an alkylene oxide adduct of the higher secondary alcohol alkoxylate precursor; and a higher secondary alkyl ether sulfate ester salt which is a sulfated product of the higher secondary alcohol alkoxylate precursor or the higher secondary alcohol alkoxylate adduct.

A higher secondary alcohol alkoxylate precursor is obtained by reacting a long-chain olefin with a (poly)alkylene glycol. The precursor has a content of (poly)alkylene glycol of 0.2% by mass or lower with respect to the total mass of the higher secondary alcohol alkoxylate; a higher secondary alcohol alkoxylate adduct which is an alkylene oxide adduct of the higher secondary alcohol alkoxylate precursor; and a higher secondary alkyl ether sulfate ester salt which is a sulfated product of the higher secondary alcohol alkoxylate precursor or the higher secondary alcohol alkoxylate adduct.

A higher secondary alcohol alkoxylate precursor is obtained by reacting a long-chain olefin with a (poly)alkylene glycol. The precursor has a content of (poly)alkylene glycol of 0.2% by mass or lower with respect to the total mass of the higher secondary alcohol alkoxylate; a higher secondary alcohol alkoxylate adduct which is an alkylene oxide adduct of the higher secondary alcohol alkoxylate precursor; and a higher secondary alkyl ether sulfate ester salt which is a sulfated product of the higher secondary alcohol alkoxylate precursor or the higher secondary alcohol alkoxylate adduct.

A fluorine-containing ether compound represented by a formula (1) shown below.

R.sup.1—(O(CH.sub.2).sub.a).sub.b-[A]-[B]—O—CH.sub.2—R.sup.2—CH.sub.2—R.sup.3  (1)

(In the formula (1), R.sup.1 is an alkyl group which may have a substituent, or an organic group having at least one double bond or triple bond. Further, a represents an integer of 2 to 4, and b is 0 or 1. [A] is represented by a formula (2): —(OCH.sub.2CH(OH)CH.sub.2).sub.c— (wherein c is 1 or 2). [B] is represented by a formula (3): —(O(CH.sub.2).sub.eCH(OH)CH.sub.2).sub.d— (wherein d is 0 or 1, and e represents an integer of 2 to 4). However, the sum of c in the formula (2) and d in the formula (3) is 2. R.sup.2 is a perfluoropolyether chain. R.sup.3 is represented by a formula (4): —(OCH.sub.2CH(OH)CH.sub.2).sub.2—O—CH.sub.2(CH.sub.2).sub.fOH (wherein f represents an integer of 2 to 5).

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. ##STR00001## In formula (1), R.sup.1 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 R.sup.2 is a group represented by formula (1a), formula (1b) or formula (1c). ##STR00002## In the formulas, S.sup.1 and S.sup.2 are independently a single bond, alkylene having 1 to 10 carbons; S.sup.3 is >CH— or >N—; S.sup.4 is >C< or >Si<; and X.sup.1 is —OH, —NH.sub.2 or the like.