Provided is a polymer having a sharp melting peak and allowing easy adjustment of the melting peak temperature. Specifically provided is a polymer having two or more kinds of constitutional units containing an alkyl group having 14 or more and 30 or less carbon atoms, wherein the proportions of the number of the two or more kinds of constitutional units containing an alkyl group having 14 or more and 30 or less carbon atoms are each 20% or more, with respect to 100% of the total number of all constitutional units containing an alkyl group having 14 or more and 30 or less carbon atoms. An enthalpy of fusion of the polymer observed within a temperature range of 10° C. or higher and lower than 60° C. in differential scanning calorimetry is 30 J/g or more.

A thermoplastic elastomer composition includes: at least one elastomer component selected from the group consisting of elastomeric polymers each of which has a side chain containing a hydrogen-bond cross-linkable moiety having a carbonyl-containing group and/or a nitrogen-containing heterocycle and has a glass-transition point of 25° C. or below, and elastomeric polymers each of which contains a hydrogen-bond cross-linkable moiety and a covalent-bond cross-linking moiety in a side chain and has a glass-transition point of 25° C. or below; a clay, a content ratio of which is 20 parts by mass or less relative to 100 parts by mass of the elastomer component; and an α-olefin-based resin having no chemical-bond cross-linking moiety.

There is provided a method for producing a carboxyl group-containing polymer composition that is excellent in all of the following: dispersibility in water or the like immediately after the preparation, storage stability, and the transparency of a neutral viscous solution thereof. A method for producing a carboxyl group-containing polymer composition, the carboxyl group-containing polymer composition comprising a carboxyl group-containing polymer (A) that is a copolymer of monomers comprising an α,β-unsaturated carboxylic acid (a-1) and a compound (a-2) having at least two ethylenically unsaturated groups per molecule; and a nonionic surfactant (B), the method comprising the step of copolymerizing the monomers, wherein in the step, the nonionic surfactant (B) is added into the system when the polymerization degree of the α,β-unsaturated carboxylic acid (a-1) has reached 70 to 100%.

Provided is a binder composition for a non-aqueous secondary battery electrode that can form a slurry composition for a non-aqueous secondary battery electrode having excellent dispersibility and a non-aqueous secondary battery having excellent cycle characteristics. The binder composition for a non-aqueous secondary battery electrode contains: a polymer that includes a monomer unit including a functional group that is bondable with a cationic group and a (meth)acrylic acid ester monomer unit, and that has a weight-average molecular weight of 250,000 or less; and an organic compound that includes at least two cationic groups.

Provided is a binder composition for a non-aqueous secondary battery electrode that can form a slurry composition for a non-aqueous secondary battery electrode having excellent dispersibility and a non-aqueous secondary battery having excellent cycle characteristics. The binder composition for a non-aqueous secondary battery electrode contains: a polymer that includes a monomer unit including a functional group that is bondable with a cationic group and a (meth)acrylic acid ester monomer unit, and that has a weight-average molecular weight of 250,000 or less; and an organic compound that includes at least two cationic groups.

Provided is a binder composition for a non-aqueous secondary battery electrode that can form a slurry composition for a non-aqueous secondary battery electrode having excellent viscosity stability and a non-aqueous secondary battery having excellent cycle characteristics. The binder composition for a non-aqueous secondary battery electrode contains: a polymer that includes a monomer unit including a functional group that is bondable with a cationic group and a (meth)acrylic acid ester monomer unit; and an organic compound that includes at least two cationic groups. The binder composition for a non-aqueous secondary battery electrode has a viscosity change rate of 400% or less when left at rest at a temperature of 60 C. for 30 days.

Provided is a binder composition for a non-aqueous secondary battery electrode that can form a slurry composition for a non-aqueous secondary battery electrode having excellent viscosity stability and a non-aqueous secondary battery having excellent cycle characteristics. The binder composition for a non-aqueous secondary battery electrode contains: a polymer that includes a monomer unit including a functional group that is bondable with a cationic group and a (meth)acrylic acid ester monomer unit; and an organic compound that includes at least two cationic groups. The binder composition for a non-aqueous secondary battery electrode has a viscosity change rate of 400% or less when left at rest at a temperature of 60 C. for 30 days.

A liquid composition that is an aqueous liquid composition that emits light when irradiated with ultraviolet light contains a resin particle, the resin particle containing a unit that has a polar group and containing a complex composed of a sulfur-bridged calixarene and a lanthanoid ion, the polar group being at least one selected from the group consisting of an ester group, a carboxy group, a hydroxy group, an ether group, an amino group, an amide group and a cyano group.

A charge-transfer salt formed from a material comprising a repeat unit of formula (I) and an n-dopant: wherein BG is a backbone group of the repeat unit; R.sup.1 is a ionic substituent comprising at least one cationic or anionic group; n is at least 1; R.sup.2 is a non-ionic substituent; and m is 0 or a positive integer; the material further comprising a counterion balancing the charge of the cationic or anionic group.

##STR00001##

A compound of formula (I): (Core)n-(X)m wherein Core is a core group; n is 0 and m is 1, or n is 1 and m is at least 1; and X is a group of formula (II): wherein: R.sup.1, R.sup.3 and R.sup.5 are each independently H or a substituent; R.sup.2 and R.sup.4 are each a substituent; one of R.sup.1-R.sup.5 is a direct bond or divalent linking group linking the group of formula (II) to Core in the case where n is 1; x and y are 0, 1, 2, 3 or 4; and the compound of formula (I) is substituted with at least one ionic substituent. The compound may be used as an n-dopant to dope an organic semiconductor.

##STR00001##