Kroger et al., 2023 - Google Patents
Efficient isolation method for highly charged phosphorylated cellulose nanocrystalsKroger et al., 2023
View HTML- Document ID
- 15056641460613701272
- Author
- Kroger M
- Badara O
- Paakkonen T
- Schlapp-Hackl I
- Hietala S
- Kontturi E
- Publication year
- Publication venue
- Biomacromolecules
External Links
Snippet
Phosphorylation of cellulose nanocrystals (CNCs) has remained a marginal activity despite the undisputed application potential in flame-retardant materials, sustainable high-capacity ion-exchange materials, or substrates for biomineralization among others. This is largely …
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
- C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
- C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/05—Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/02—Oxy-cellulose; Hydrocellulose; Cellulosehydrate, e.g. microcrystalline cellulose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0003—General processes for their isolation or fractionation, e.g. purification or extraction from biomass
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B31/00—Preparation of derivatives of starch
- C08B31/08—Ethers
- C08B31/12—Ethers having alkyl or cycloalkyl radicals substituted by heteroatoms, e.g. hydroxyalkyl or carboxyalkyl starch
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Liu et al. | Highly efficient and sustainable preparation of carboxylic and thermostable cellulose nanocrystals via FeCl3-catalyzed innocuous citric acid hydrolysis | |
Rana et al. | Cellulose nanocrystals: Pretreatments, preparation strategies, and surface functionalization | |
Kroger et al. | Efficient isolation method for highly charged phosphorylated cellulose nanocrystals | |
Fiss et al. | Mechanochemical phosphorylation of polymers and synthesis of flame-retardant cellulose nanocrystals | |
Thomas et al. | Nanocellulose, a versatile green platform: from biosources to materials and their applications | |
Vanderfleet et al. | Insight into thermal stability of cellulose nanocrystals from new hydrolysis methods with acid blends | |
Kokol et al. | Characterisation and properties of homo-and heterogenously phosphorylated nanocellulose | |
Božič et al. | Enzymatic phosphorylation of cellulose nanofibers to new highly-ions adsorbing, flame-retardant and hydroxyapatite-growth induced natural nanoparticles | |
Rol et al. | Cellulose phosphorylation comparison and analysis of phosphorate position on cellulose fibers | |
Zhang et al. | Nickel metal–organic framework derived hierarchically mesoporous nickel phosphate toward smoke suppression and mechanical enhancement of intumescent flame retardant wood fiber/poly (lactic acid) composites | |
Ghanadpour et al. | Phosphorylated cellulose nanofibrils: a renewable nanomaterial for the preparation of intrinsically flame-retardant materials | |
Salama et al. | Recent trends in elaboration, processing, and derivatization of cellulosic materials using ionic liquids | |
Xu et al. | Complete valorization of bamboo biomass into multifunctional nanomaterials by reactive deep eutectic solvent pretreatment: Towards a waste-free biorefinery | |
Granström | Cellulose derivatives: synthesis, properties and applications | |
Zahra et al. | Close packing of cellulose and chitosan in regenerated cellulose fibers improves carbon yield and structural properties of respective carbon fibers | |
Patoary et al. | Phosphorylation of nanocellulose: State of the art and prospects | |
CN109487546B (en) | Efficient and environment-friendly preparation method of cationic nano-fibrillated cellulose | |
Messa et al. | Phosphorylated cellulose nanofibrils from sugarcane bagasse with pH tunable gelation | |
JP2018529013A (en) | Method for dewatering water-soluble polymers | |
Khakalo et al. | Production of high-solid-content fire-retardant phosphorylated cellulose microfibrils | |
Xu et al. | Preparation and properties of cellulose-based films regenerated from waste corrugated cardboards using [Amim] Cl/CaCl2 | |
Hou et al. | A systematic study for the structures and properties of phosphorylated pulp fibers prepared under various conditions | |
Chen et al. | Heat soaking pretreatment for greener production of phosphorylated cellulose nanofibrils with higher charge density | |
Hopson et al. | A new approach for the use of cellulose-rich solids from biorefinery in the formulation of gel-like materials | |
Sun et al. | High lignin-containing nanocelluloses prepared via TEMPO-mediated oxidation and polyethylenimine functionalization for antioxidant and antibacterial applications |