Abstract: The present disclosure provides an antibacterial hydrophilic compound. The antibacterial hydrophilic compound may react, induced by light through a hydrogen abstraction group in the structural formula thereof, with a C—H group and thus bind to a surface of a material having the C—H group (for example, chemical fibers such as polyester, chinlon, and the like; plastics, rubbers, and other similar materials), which can impart a durable antibacterial activity and hydrophilicity to the material. The antibacterial hydrophilic compound has a relatively strong binding force to the surface of the material without damaging the mechanical properties of the raw material. The present disclosure also provides a modified material that is modified by the antibacterial hydrophilic compound.

Abstract: The present disclosure provides an antibacterial hydrophilic compound. The antibacterial hydrophilic compound may react, induced by light through a hydrogen abstraction group in the structural formula thereof, with a C—H group and thus bind to a surface of a material having the C—H group (for example, chemical fibers such as polyester, chinlon, and the like; plastics, rubbers, and other similar materials), which can impart a durable antibacterial activity and hydrophilicity to the material. The antibacterial hydrophilic compound has a relatively strong binding force to the surface of the material without damaging the mechanical properties of the raw material. The present disclosure also provides a modified material that is modified by the antibacterial hydrophilic compound.

Abstract: A textile having a surface that is coated with a compound of formula I or formula II.

Abstract: The present disclosure provides an antibacterial hydrophilic compound. The antibacterial hydrophilic compound may react, induced by light through a hydrogen abstraction group in the structural formula thereof, with a C—H group and thus bind to a surface of a material having the C—H group (for example, chemical fibers such as polyester, chinlon, and the like; plastics, rubbers, and other similar materials), which can impart a durable antibacterial activity and hydrophilicity to the material. The antibacterial hydrophilic compound has a relatively strong binding force to the surface of the material without damaging the mechanical properties of the raw material. The present disclosure also provides a modified material that is modified by the antibacterial hydrophilic compound.

Abstract: A method for preparing an amphoteric shape-memory polyurethane and an amphoteric shape-memory polyurethane prepared by the method, the method including: 1) polymerizing monomer A and monomer B to synthesize a polyurethane; and 2) contacting monomer D and the polyurethane to conduct a ring-opening reaction on a nitrogen group of the polyurethane, to yield an amphoteric shape-memory polyurethane. The monomer A is a N-alkyl dialkanolamine having a formula I. The monomer B is a polyisocyanate, and the monomer D is an alkyl sulfonate.

Abstract: The present disclosure relates to the field of shape memory materials, it discloses a betaine-based shape memory polymer and the preparation method thereof. The polymer is formed through free radical polymerization of an unsaturated betaine monomer, an acrylic monomer, and an ethylene glycol divinyl ether monomer with the addition of an initiator. The betaine-based shape memory polymer has thermosensitive shape memory property and wet sensitive shape memory property, and it has good biocompatibility and an excellent shape memory property, antibacterial property. It is of great potential for use in engineering, construction, daily life and medical service.

Abstract: A textile having a surface that is coated with a compound of formula I or formula II.

Abstract: 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.

Abstract: A method for preparing an amphoteric shape-memory polyurethane and an amphoteric shape-memory polyurethane prepared by the method, the method including:1) polymerizing monomer A and monomer B to synthesize a polyurethane; and 2) contacting monomer D and the polyurethane to conduct a ring-opening reaction on a nitrogen group of the polyurethane, to yield an amphoteric shape-memory polyurethane. The monomer A is a N-alkyl dialkanolamine having a formula I. The monomer B is a polyisocyanate, and the monomer D is an alkyl sulfonate.

Abstract: The present disclosure relates to the field of shape memory materials, it discloses a betaine-based shape memory polymer and the preparation method thereof. The polymer is formed through free radical polymerization of an unsaturated betaine monomer, an acrylic monomer, and an ethylene glycol divinyl ether monomer with the addition of an initiator. The betaine-based shape memory polymer has thermosensitive shape memory property and wet sensitive shape memory property, and it has good biocompatibility and an excellent shape memory property, antibacterial property. It is of great potential for use in engineering, construction, daily life and medical service.

Abstract: 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.

Abstract: The present invention relates to the field of organic synthesis, and provides an organosilicon betaine type antimicrobial compound having a general formula I and preparation thereof: the antimicrobial compound provided by the present invention has a reactive functional group—siloxane, which can be subjected to chemical bonding with many material interfaces, thereby endowing a material or article surface treated with the antimicrobial compound I persistent antimicrobial activity. Also, the preparation of the compound has a simple process and easily controlled conditions, and is easy to be industrialized, which facilitates its wide applications.

Abstract: The present invention relates to the field of organic synthesis, and provides an organosilicon betaine type antimicrobial compound having a general formula I and preparation thereof: the antimicrobial compound provided by the present invention has a reactive functional group—siloxane, which can be subjected to chemical bonding with many material interfaces, thereby endowing a material or article surface treated with the antimicrobial compound I persistent antimicrobial activity. Also, the preparation of the compound has a simple process and easily controlled conditions, and is easy to be industrialized, which facilitates its wide applications.