An amphoteric betaine-type polycarboxylic acid water reducer and a preparation method therefor are provided in the present invention. An unsaturated betaine-type monomer A and an acrylic acid-type polyethylene glycol monomer B are placed in a reaction container, stirred until uniform and then an acrylic acid-type monomer C is added, the stirring is continued and water is added to make adjustments so as to make the total mass of the monomers account for 10%-20% of the total mass of the aqueous solution; and under the protection of an inert gas, the temperature is raised to 60° C.-100° C., an aqueous initiator solution is added, maintaining the temperature and reacting for 4-6 h, and after the reaction is completed, the solution is cooled to room temperature, and the pH value thereof is adjusted to 5-7 to prepare the amphoteric betaine-type polycarboxylic acid water reducer.

A reverse-phase suspension polymerization process for the manufacture of polymer beads comprising forming aqueous monomer beads comprising an aqueous solution of water-soluble ethylenically unsaturated monomer or monomer blend and polymerizing the monomer or monomer blend to form polymer beads while suspended in a non-aqueous liquid, and recovering polymer beads, in which the process comprises, providing in a vessel (1) a volume (2) of non-aqueous liquid wherein the volume of non-aqueous liquid extends between at least one polymer bead discharge point (3) and at least one monomer feed point (4), feeding the aqueous monomer or monomer blend through orifices (5) into, or onto, the non-aqueous liquid to form aqueous monomer beads, allowing the aqueous monomer beads to flow towards the polymer bead discharge point subjecting the aqueous monomer beads to polymerization conditions to initiate polymerization to form polymerizing beads, wherein the polymerizing beads have formed polymer beads when they reach the polymer bead discharge point, removing a suspension of the polymer beads in non-aqueous liquid from the vessel at the polymer bead discharge point and recovering water soluble or water swellable polymer beads from the suspension. The invention also relates to the apparatus suitable for carrying out a reverse-phase suspension polymerization and polymer beads obtainable by the process or employing the apparatus.

A curable composition contains a betaine monomer having a predetermined structure and a polyfunctional (meth)acrylamide compound having a predetermined structure.

A polymer compound having a weight average molecular weight in the range of 1,000 to 500,000, and contains one or more repeating units represented by formula (1) and one or more repeating units represented by formula (2): ##STR00001## R.sup.1 represents a hydrogen atom or a methyl group; Rf.sub.1 represents a linear or branched alkyl group having 1 to 4 carbon atoms or a phenyl group, and has at least one fluorine atom or a trifluoromethyl group in Rf.sub.1; Z.sub.1 represents a single bond, an arylene group having 6 to 12 carbon atoms or —C(═O)—O—R.sup.2—; R.sup.2 represents a linear, branched or cyclic alkylene group having 1 to 12 carbon atoms, an arylene group having 6 to 10 carbon atoms or an alkenylene group having 2 to 10 carbon atoms, and may have an ether group, a carbonyl group or an ester group in R.sup.2; and “a” is 0<a≤1.0, and ##STR00002## “b” is 0<b<1.0.

A polymer compound having a weight average molecular weight in the range of 1,000 to 500,000, and contains one or more repeating units represented by formula (1) and one or more repeating units represented by formula (2): ##STR00001## R.sup.1 represents a hydrogen atom or a methyl group; Rf.sub.1 represents a linear or branched alkyl group having 1 to 4 carbon atoms or a phenyl group, and has at least one fluorine atom or a trifluoromethyl group in Rf.sub.1; Z.sub.1 represents a single bond, an arylene group having 6 to 12 carbon atoms or —C(═O)—O—R.sup.2—; R.sup.2 represents a linear, branched or cyclic alkylene group having 1 to 12 carbon atoms, an arylene group having 6 to 10 carbon atoms or an alkenylene group having 2 to 10 carbon atoms, and may have an ether group, a carbonyl group or an ester group in R.sup.2; and “a” is 0<a≤1.0, and ##STR00002## “b” is 0<b<1.0.

The present invention relates to superabsorbent polymer having an improved absorption speed through micropores formed inside, and a method for preparing the same.

Terpolymers and use thereof are provided comprising one or more nonionic monomers, one or more anionic monomers and one or more cationic monomers, These terpolymers and compositions containing may be used as flocculants, for example, for treating tailings, such as oil sands tailings, to facilitate solid-liquid separation, for example, in order to efficiently recycle water and/or to reduce the volume of tailings which may be transferred to a tailings pond and/or to a dedicated disposal area.

Terpolymers and use thereof are provided comprising one or more nonionic monomers, one or more anionic monomers and one or more cationic monomers, These terpolymers and compositions containing may be used as flocculants, for example, for treating tailings, such as oil sands tailings, to facilitate solid-liquid separation, for example, in order to efficiently recycle water and/or to reduce the volume of tailings which may be transferred to a tailings pond and/or to a dedicated disposal area.

Zwitterionic copolymers, coating compositions (e.g., aqueous coating compositions and articles containing such copolymers, and methods of coating such coating compositions; wherein the copolymer includes: (a) first monomeric units derived from monomers of Formula (I) CH.sub.2═CR.sup.1—(CO)—X—R.sup.2—[-Q-R.sup.3—].sub.n—Y (I) or salts thereof, wherein: R.sup.1 is hydrogen or methyl; X is oxy or —NH—; R.sup.2 is an alkylene optionally including catenary oxygen; R.sup.3 is an alkylene; Q is —(CO)O—, —NR.sup.4—(CO)—NR.sup.4—, or —(CO)—NR.sup.4—; R.sup.4 is hydrogen or alkyl; n is equal to 0 or 1; and Y is phosphonic acid, phosphonate, phosphoric acid, or phosphate; and (b) second monomeric units derived from monomers of Formula (II) CH.sub.2═CR.sup.1—(CO)—X—R.sup.2—[-Q-R.sup.3—].sub.n—[NR.sup.5R.sup.6]+—R.sup.7—Z— (II) wherein: R.sup.1 is hydrogen or methyl; X is oxy or —NH—; R.sup.2 is alkylene optionally including catenary oxygen; R.sup.3 is alkylene; Q is —(CO)O—, —NR.sup.4—(CO)—NR.sup.4—, or —(CO)—NR4-; R.sup.4 is hydrogen or alkyl; n is equal to 0 or 1; R.sup.5 and R.sup.6 are each independently an alkyl, aryl, or a combination thereof, or R.sup.5 and R.sup.6 both combine with the nitrogen to which they are both attached to form a heterocyclic ring having 3 to 7 ring members; R.sup.7 is alkylene; and Z″ is carboxylate or sulfonate.

CH.sub.2═CR.sup.1—(CO)—X—R.sup.2—[-Q-R.sup.3-].sub.n—Y  (I)

CH.sub.2═CR.sup.1—(CO)—X—R.sup.2—[-Q-R.sup.3—].sub.n—[NR.sup.5R.sup.6].sup.+—R.sup.7—Z.sup.−  (II)

An ink jet method includes an ejecting step of ejecting a radiation-curable ink jet composition from an ink jet head and an irradiating step of irradiating the ejected radiation-curable ink jet composition with an ultraviolet ray at an irradiation intensity of 3 to 10 W/cm.sup.2 by using a light emitting diode. The radiation-curable ink jet composition contains monofunctional monomers including a nitrogen-containing monofunctional monomer. The amount of the nitrogen-containing monofunctional monomer relative to the total amount of the radiation-curable ink jet composition is 5 to 40 mass %.