Biodegradable elastic hydrogels for bioprinting
US-2024132650-A1 · Apr 25, 2024 · US
US2017145138A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017145138-A1 |
| Application number | US-201515300076-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 10, 2015 |
| Priority date | Apr 11, 2014 |
| Publication date | May 25, 2017 |
| Grant date | — |
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The invention provides new water soluble polymers for the use in industrial processes, where large quantities of water is handled, such as sludge dewatering and papermaking. These new polymers are water soluble cross-linked block copolymers, wherein the block copolymers are cross-linked together using a cross-linking agent. Each of the block copolymers contain two different blocks, and these blocks are formed from different monomers. The blocks are linked together with a molecular spacer derived from a bifunctional initiator used during the polymerization of the blocks. The monomers used in polymerizing the blocks are different with each other and they are selected from a group consisting of N-vinylformamide, acrylic acid, acrylamide and water-soluble derivatives thereof.
Opening claim text (preview).
1 . A water soluble cross-linked block copolymer comprising block copolymers cross-linked together using a cross-linking agent, and wherein i. each of the block copolymers contain a first block and a second block, and the first and the second block are formed from different monomer compositions, ii. the first and second blocks are linked together with a molecular spacer derived from a bifunctional initiator used during the polymerization of said blocks, and iii. the monomer compositions used in forming the first and second blocks contain one or more monomers selected from a group comprising water-soluble non-ionic, cationic or anionic (meth)acrylic monomers, cationic non-acrylic monomers, itaconic acid, and N-vinylformamide, and derivatives thereof. 2 . The water soluble cross-linked block copolymer according to claim 1 , wherein the one or more monomers are selected from a group comprising (meth) acrylamide, N-methylolacrylamide, N-methylolmethacrylamide, (meth)acrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate, stearyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, glycidyl methacrylate, 2-acrylamide-2-methylpropanesulfonic acid (AMPS), dimethylaminoethylacrylate, diethylaminoethyl acrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, N,N-dimethylaminopropylacrylamide, N,N-dimethylaminopropylmethacrylamide, 2-N-morpholinoethyl methacrylate, 2-diisopropylaminoethyl methacrylate, 1-(2-methacryloyloxyethyl) imidazole, 2-(tert-butylamino)ethyl methacrylate, N,N-dimethylaminoethyl acrylamide, N-[2-(dimethylamino)-1,1-dimethylethyl] acrylamide, N-vinylformamide, and their methyl chloride or methyl sulfate quaternaries or mixtures thereof; or methacrylamidopropyltrimethylammonium chloride (MAPTAC), dimethylaminoethylacrylate methyl chloride (Q9), itaconic acid and diallyldimethylammonium chloride (DADMAC). 3 . The water soluble cross-linked block copolymer according to claim 1 , wherein both the first and the second block are formed of homopolymers. 4 . The water soluble cross-linked block copolymer according to claim 1 , wherein the first block is a random copolymer and the second block is homopolymer or random copolymer. 5 . The water soluble cross-linked block copolymer according to claim 1 , wherein the first or second block is an NVF-based block comprising a homopolymer, which is formed from N-vinylformamide (NVF) monomer. 6 . The water soluble cross-linked block copolymer according to claim 5 , wherein the formamide groups of the NVF-based block are at least partially hydrolyzed to amino groups. 7 . The water soluble cross-linked block copolymer according to claim 1 , wherein it is polymerized by using a bifunctional initiator having the formula (I) wherein R is H, or C 1-5 -alkyl, and n is from 1 to 10. 8 . The water soluble cross-linked block copolymer according to claim 1 , wherein the cross-linking agent is a radical polymerizable cross-linking agent. 9 . The water soluble cross-linked block copolymer according to claim 1 , wherein the cross-linking agent is selected from a group comprising N,N′-methylenebisacrylamide (MBA),1,4-bis(acryloyl)piperazine, N,N′-(1-methyl-1,2-ethanediyl)bis(2-propenamide), N,N′-propylidenebis(2-propenamide), N,N′-butylidenebis(2-propenamide), N,N′-1,12-dodecanediylbis(2-propenamide), N,N′-1,9-nonanediylbis(2-propenamide), N,N′-1,5-pentanediylbis(2-propenamide), N,N′-1,4-butanediylbis(2-propenamide), N,N′-1,6-hexanediylbis(2-propenamide), N,N′-ethylidenebis(2-propenamide), N,N′-1,3-propanediylbis(2-propenamide), N,N′-1,2-ethanediylbis(2-propenamide), N,N′-1,4-cyclohexanediylbis(2-propenamide), N,N′-1,8-octanediylbis(2-propenamide), N,N′-bisacryloylyimidazoline, ethyleneglycoldimethacrylate, 1,4-diacroyl piperazine, pentaerythritoltriacrylate, trimethylpropanetrimethylacrylate, and pentaerythritoltetraacrylate. 10 . A method for preparing a water soluble cross-linked block copolymer, wherein at least two different monomers are polymerized via a two-step copolymerization the method comprising the following steps: i. the first block of the block copolymer is polymerized using a bifunctional initiator, ii. the second block of the block copolymer is then polymerized using the same initiator, iii. the first or second blocks are cross-linked using a crosslinking agent either during the polymerization of said blocks, or as a separate crosslinking step after the steps i) and ii) are performed, wherein the monomers used in polymerizing the first and second blocks are different with each other and they are selected from a group comprising water-soluble non-ionic, cationic or anionic (meth)acrylic monomers, cationic non-acrylic monomers, itaconic acid, and N-vinylformamide, and derivatives thereof. 11 . A method according to claim 10 , wherein the monomers are selected from a group comprising (meth)acrylamide, N-methylolacrylamide, N-methylolmethacrylamide, (meth)acrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, lauryl methacrylate, stearyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, glycidyl methacrylate, 2-acrylamide-2-methylpropanesulfonic acid (AMPS), dimethylaminoethyl acrylate, diethylaminoethyl acrylate, dimethylaminoethyl methacrylate, diethylaminoethyl methacrylate, N,N-dimethylaminopropylacrylamide, N,N-dimethylaminopropylmethacrylamide, 2-N-morpholinoethyl methacrylate, 2-diisopropylaminoethyl methacrylate, 1-(2-methacryloyloxyethyl) imidazole, 2-(tert-butylamino)ethyl methacrylate, N,N-dimethylaminoethyl acrylamide, N-[2-(dimethylamino)-1,1-dimethylethyl] acrylamide, N-vinylformamide, and their methyl chloride or methyl sulfate quaternaries or mixtures thereof; or methacrylamidopropyltrimethylammonium chloride (MAPTAC), dimethylaminoethylacrylate methyl chloride (Q9), itaconic acid and diallyldimethylammonium chloride (DADMAC). 12 . A method according to claim 10 , wherein the polymerization of the first block two different monomers are used and thus a random copolymer is formed. 13 . A method according to claim 10 , wherein the polymerization of the second block two different monomers are used and thus a random copolymer is formed. 14 . A method according to claim 10 , wherein the cross-linking agent is N,N′-methylenebisacrylamide (MBA). 15 . A paper making process or a sludge dewatering or water purification process, comprising adding the water soluble cross-linked block copolymer according to claim 1 to pulp or water, respectively. 16 . The process according to claim 15 , wherein the cross-linked block copolymer is used in paper making process as a fixative, a drainage agent, a retention agent, a dry strength agent, a coating agent, a surface sizing agent, or as an emulsifiers for sizing. 17 . The method according to claim 16 , wherein the dosing amounts of cross-linked block copolymer/pulp are between 50 g/1000 kg to 2 000 g/1000 kg, preferably between 100 g/1000 kg to 1000 g/1000 kg, more preferably between 100 g/1000 kg to 500 g/1000 kg. 18 . The method according to claim 15 , wherein the cross-linked block copolymer is used in slu
Reinforcing agents · CPC title
with addition of chemical agents · CPC title
Retention agents or drainage improvers · CPC title
obtained by reactions only involving unsaturated carbon-to-carbon bonds · CPC title
using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent · CPC title
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