Abstract: Described herein are binding proteins that specifically bind to human CD33, and in particular to bispecific binding proteins that specifically bind to human CD33 and human CD3. Also described herein are bispecific tandem diabodies that bind to CD33 and CD33, and their uses for immunotherapy of CD33+ cancers, diseases and conditions such as acute myeloid leukemia (AML).

Abstract: The present invention relates to nanofibrillar cellulose. Furthermore, the invention relates to a method for the manufacture of nanofibrillar cellulose, and to a nanofibrillar cellulose obtainable by said method. The invention also relates to uses of the nanofibrillar cellulose.

Abstract: A method of reducing the amount propylene chlorohydrin produced in a reaction to make a hydroxypropylated/crosslinked starch comprising removing residual propylene oxide from alkaline slurry. The residual propylene oxide is removed by the dewatering the alkaline slurry or by washing the starch in slurry at a pH of around 10. The starch is then neutralized in an acid solution and recovered from the second slurry and may or may not be washed, depending on whether the slurry while at pH around 10 to make a hydroxypropylated/crosslinked starch having less than 1 ppm propylene chlorohydrin.

Abstract: The invention concerns a process for the manufacture of an acylated polymer composition comprising amylose and/or amylopectin, comprising a pre-treatment step in the presence of an acid, and optionally one additive selected from the group of a hydroxycarboxylic acid and a salt in combination with a polycarboxylic acid. After pre-treatment, the polymer is acylated and, preferably, subjected to a post-treatment step with an acid. The products obtained are useful as additives in varnishes, lacquers, coatings, thickeners, adhesives or binders, and preferably inks.

Abstract: Provided herein are organic solvent-based processes for the removal of rubber from non-Hevea plants such as guayule shrubs. By the use of the processes, solid purified rubber can be obtained that contains 0.05-0.5 weight % dirt, 0.2-1.5 weight % ash, and 0.1-4 weight % resin (when it has been dried so as to contain 0.8 weight % volatile matter).

Abstract: A process for polymerizing ethylene to obtain an ethylene-based polymer in a plant, wherein the plant includes a reactor in fluid communication with a recycle connection, wherein the process includes a polymerization phase, a partial shutdown phase, and the steps of reducing the pressure in the reactor for entering into the partial shutdown phase from the polymerization phase; and increasing the pressure in the reactor for exiting from the partial shutdown phase and re-entering the polymerization phase.

Abstract: The invention relates to an aqueous coagulatable polymer dispersion comprising at least one polymer which is dispersed in an aqueous phase, thermoplastic micro-spheres which contain a propellant, and at least one additional component which is selected from the group consisting of polyols, polyamines, and thermoplastic polymers. The invention further relates to a coagulate which can be obtained by the thermal and/or mechanical and/or ultrasonically-initiated coagulation of the aqueous polymer dispersion according to the invention, to an adhesive comprising or consisting of the coagulate, to a substrate which is completely or partly coated with said coagulate, to a method for producing such a coated substrate, and to coated substrates which can be obtained using said method. The coagulate can be used as an adhesive or as a binder in 3D-printing methods.

Abstract: An object of the invention is to provide an EVOH which has improved melt moldability and is excellent in terms of gas barrier property and secondary formability. The present invention relates to an ethylene-vinyl alcohol copolymer that, when examined by liquid chromatography, gives an ethylene content distribution curve which has at least two peaks and in which the ethylene content (a) of a component that shows a highest peak (A), the ethylene content (b) of a component that shows a second highest peak (B), and the proportion (v) and distribution of component(s) (V) having ethylene contents (w) corresponding to specific regions (W) are within specific ranges.

Abstract: Embodiments in accordance with the present invention encompass compositions encompassing a procatalyst and a thermal or photoactivator along with one or more monomers which undergo vinyl addition polymerization when said composition is heated to a temperature from 50° C. to 100° C. to form a substantially transparent film. The monomers employed therein have a range of refractive index from 1.4 to 1.6 and thus these compositions can be tailored to form transparent films of varied refractive indices. Accordingly, compositions of this invention are useful in various opto-electronic applications, including as coatings, encapsulants, fillers, leveling agents, among others.

Abstract: Propylene is polymerised in the presence of a polymerisation catalyst comprising a solid catalyst component, an organoaluminium compound and an external electron donor, the process comprising the steps of (i) contacting propylene and hydrogen with the polymerisation catalyst in polymerisation conditions in a polymerisation reactor to produce a polymer of propylene; (ii) recovering the polymer of propylene from the polymerisation reactor; wherein the polymer of propylene has MFR of from more than 100 to 10000 g/10 min.

Abstract: This invention relates to the use of quinolinyldiamido transition metal complexes and catalyst systems with an activator and a metal hydrocarbenyl chain transfer agent, such as an aluminum vinyl-transfer agent (AVTA), to produce branched propylene-ethylene-diene terpolymers.

Abstract: The invention relates to an efficient polymerization process and its use to produce novel copolymers with a specific microstructure. In particular, the invention relates to butyl rubbers with novel microstructure, preferably those obtainable by copolymerization of monomer mixtures comprising isobutylene and isoprene. In a further aspect the invention relates to halogenated copolymers obtainable from such novel copolymers by halogenation.

Abstract: Monomodal copolymers of ethylene and molding compositions comprising such copolymers, wherein the copolymers have a density determined according to DIN EN ISO 1183-1, variant A in the range from 0.938 to 0.944 g/cm3, a melt index MFR21 determined according to ISO 1133 at 190° C. under a load of 21.6 kg in the range from 12 to 17 g/10 min, a weight average molar mass Mw in the range from 140 000 g/mol to 330 000 g/mol, a polydispersity Mw/Mn in the range from 9 to 17, and a content of comonomer side chains per 1000 carbon atoms Cx equal to or above a value defined via equation (I) Cx=128.7?134.62×d?, wherein d? is the numerical value of the density of the copolymer in g/cm3, the use of the copolymers for producing injection-molded articles, as well as injection-molded articles comprising the copolymers, and process for the preparation of such monomodal copolymers.

Abstract: The present invention relates generally to a polyvinyl alcohol composition having higher amorphous polyvinyl alcohol polymer content and various end uses thereof.

Abstract: Adhesive compositions that are optically transparent include a (meth)acrylate-based copolymer having a refractive index of at least 1.48, and particles of a thermoplastic polymer. At least some of the particles have an average particle size that is larger than the wavelength of visible light. The adhesive compositions are prepared by hot melt processing packaged adhesive compositions.

Abstract: The present disclosure provides a method for efficiently producing an ?-alkylstyrene ?-chloroacrylate copolymer having a high monomer conversion rate. According to the present disclosure, the method for producing a copolymer containing 30 mol % to 70 mol % of an ?-alkylstyrene unit and 30 mol % to 70 mol % of an ?-chloroacrylate unit includes a step of performing solution polymerization of a monomer composition containing ?-alkylstyrene and ?-chloroacrylate, and uses ketone as a polymerization solvent for the solution polymerization.

Abstract: The material according to the invention is an acrylic copolymer, which is crosslinked, viscoelastic, flexible and deformable at room temperature and hydrophobic, of at least 50 wt % of acrylic or methacrylic monomers and cinnamic alcohol. The mixture of monomers preferably includes: —at least one arylalkoxy-acrylate or one arylalkoxy-methacrylate; at least one hydroxylated acrylate and one hydroxylated methacrylate; at least one ethoxylated diol diacrylate and one ethoxylated diol dimethacrylate; and cinnamic alcohol. Said material is obtained in a single step of radical polymerization and is presented in the form of a three-dimensional macromolecular network including a cinnamic alcohol unit. Said material is used for manufacturing intraocular lenses (1).

Abstract: A polystyrene-g-(polyisobutylene-b-polystyrene) is taught. The polystyrene-g-(polyisobutylene-b-polystyrene) is synthesized by first providing a polystyrene backbone. Once the polystyrene backbone is provided, the polystyrene backbone is acetylated to provide acetyl groups on the polystyrene backbone. Next, the acetyl groups are converted to —C(CH3)2OH groups. Finally, the living polymerization of isobutylene is initiated, which is then followed by the living block polymerization of styrene. A polymer network of polystyrene-g-(polyisobutylene-b-polystyrene)s is also provided.

Abstract: The present invention relates to a vinyl chloride-based copolymer which has good processability and thus is capable of providing molded articles having good appearance characteristics, for example, transparency, a method for preparing the same, a thermoplastic resin composition containing the same, and a thermoplastic resin molded article produced from the thermoplastic resin composition. The vinyl chloride-based copolymer includes N-vinyllactam-based polymer compound derived units and unsaturated fatty acid ester derived units at an appropriate ratio, and may have improved structure stability and good processability due to the N-vinyllactam-based polymer compound derived units and improved plasticity and processability due to the internal plasticizer action of the unsaturated fatty acid ester derived units. Therefore, the vinyl chloride-based copolymer according to the present invention may be easily applied in industries that need thereof.

Abstract: The present invention relates to the preparation and use of copolymers composed of N-(2-hydroxypropyl) methacrylamide (HPMAA) and carboxybetaine methacrylamide (CBMAA). The invention further describes polymer brushes having structure I S—R-polymer??(I) wherein S is a substrate; R is a residue of a polymerization initiator or a RAFT agent bound to the substrate; and “polymer” is the copolymer of N-(2-hydroxypropyl) methacrylamide and carboxybetaine methacrylamide Furthermore, production of these polymer brushes, containing random or block copolymers grafted to or from a substrate is described. The copolymer brushes are suitable for protecting substrates from deposition and/or adhesion of biological substances, and/or against thrombus formation. The brushes functionalized by covalent attachment of bioactive substances to CBMAA monomer units are particularly suitable for specific interaction with target biological substances which is not affected by nonspecific deposition of non-target compounds.

Abstract: A method of producing a methacrylate block copolymer includes operations of (a) preparing a polymer solution comprising a methacrylate polymer block by polymerizing a methacrylate monomer using a polymerization initiator and a reversible addition-fragmentation chain transfer (RAFT) agent in the presence of water or an organic solvent; (b) preparing a polymer solution comprising an acrylate polymer block-containing methacrylate diblock copolymer by adding an acrylate monomer and a styrene monomer to the polymer solution prepared in operation (a); (c) preparing a polymer solution comprising a methacrylate polymer block-containing methacrylate triblock copolymer by adding a methacrylate monomer to the polymer solution prepared in operation (b); and (d) collecting a polymer prepared after operations (b) and (c) and removing the RAFT agent present at a terminal of the polymer by using an amine-based organic material.

Abstract: A star block copolymer and a thermoplastic elastomer including plurality of the star block copolymers and a method of making both is taught. The star block copolymers of the present invention include a core component having an ?-methylstyrene oligomer wherein arms emanate from the core component and the arms are poly(isobutylene-block-styrene) diblock copolymers.

Abstract: Embodiments of the present disclosure are directed to polyurethane prepolymers, more particularly, to polyurethane formulations including a polyurethane prepolymer that can form polyurethanes. As an example, a polyurethane formulation can include a polyurethane prepolymer and a polyol composition including polyols, water, and a catalyst, where the polyurethane prepolymer is a reaction product of a monol and an excess amount of a polyisocyanate.

Abstract: The photoelastic polyurethane resin has a Young's modulus at 25° C. of 2 to 5 MPa, a photoelastic constant at 25° C. of 1000×10?12 Pa?1 to 100000×10?12 Pa?1, and a glass transition temperature of ?60° C. to ?21° C.

Abstract: A reaction system for forming a viscoelastic polyurethane foam includes an isocyanate component that has at least one isocyanate and an isocyanate-reactive component that is a mixture formed by adding at least a polyol component, an additive component, and a preformed aqueous polymer dispersion. The mixture includes, based on the total weight of the mixture, from 50.0 wt % to 99.8 wt % of a polyol component including at least one polyether polyol, from 0.1 wt % to 50.0 wt % of an additive component including at least one catalyst, and from 0.1 wt % to 6.0 wt % of a preformed aqueous polymer dispersion. The preformed aqueous polymer dispersion has a solids content from 10 wt % to 80 wt %, based on the total weight of the preformed aqueous polymer dispersion, and is one of an aqueous acid polymer dispersion or an aqueous acid modified polyolefin polymer dispersion in which the polyolefin is derived from at least one C2 to C20 alpha-olefin.

Abstract: An aluminum-chelate-based latent curing agent is capable of showing excellent solvent resistance and excellent storage stability at room temperature without impairing low temperature rapid curability of resin composition, when preparing one-pack type thermosetting epoxy resin composition by blending aluminum-chelate-based latent curing agent holding aluminum-chelating agent on porous resin particles obtained by subjecting polyfunctional isocyanate compound to interfacial polymerization into alicyclic epoxy resin showing extremely high cationic polymerizability. Aluminum-chelate-based latent curing agent for curing thermosetting epoxy resin is configured such that aluminum-chelating agent is held on porous resin obtained by subjecting polyfunctional isocyanate compound to interfacial polymerization, and that surface activity inhibition treatment is performed by epoxy-alkoxy-silane coupling agent.

Abstract: Embodiments in accordance with the present invention relate generally to polycarbonate polymers having repeat units derived from adamantane epoxide monomers and methods of using such polymers and compositions containing them. The compositions thus formed are useful in a variety of optoelectronic device fabrications.

Abstract: A lipid derivative in which a hydrophilic polymer is bound through a cyclic benzylidene acetal linker, and which can accurately control a hydrolysis rate in the weakly acidic environment of a living body to detach the hydrophilic polymer from a lipid membrane structure. The lipid derivative is represented by formula (1): wherein, R1 and R6 are each independently a hydrogen atom or a hydrocarbon group; R2, R3, R4 and R5 are each independently an electron-withdrawing or electron-donating substituent or a hydrogen atom; R7 is a hydrocarbon group having from 8 to 24 carbon atoms, an acyl group having from 8 to 24 carbon atoms, a cholesterol derivative, a glycerolipid, a phospholipid or a sphingolipid; P is a hydrophilic polymer; s is 1 or 2, t is 0 or 1, and s+t is 1 or 2; and Z1 and Z2 are each independently a selected divalent spacer.

Abstract: A (A) polyamic acid solution which can be (i) used to form a film that does not peel off even in a case where the film has a large thickness, and (ii) stably stored at a room temperature, and (B) a laminate that can be suitably used for production of a flexible device. An alkoxysilane-modified polyamic acid solution that can be obtained by reacting (a) an alkoxysilane compound containing the amino group and (b) a polyamic acid solution, and has a molar ratio of 0.980 or more and 0.9995 or less, which molar ratio is obtained by dividing a total number of moles of an aromatic tetracarboxylic dianhydride by a total number of moles of an aromatic diamine.

Abstract: A polymer is provided. The polymer includes a first repeating unit represented by Formula (I) and a second repeating unit represented by Formula (II): wherein Y1 and Y2 are independently —H, —CH3, or —CH2CH3; n is an integer ranging from 1 to 25; and the molar ratio of the first repeating unit to the second repeating unit is from 5:95 to 15:45. A resin composition including the aforementioned polymer is also provided.

Abstract: The present invention provides an amic acid ester oligomer having a structure of Formula (1) or (1?): wherein G, P, R, Rx, D, E and m are as defined in the specification. The present invention also provides a polyimide precursor composition comprising the amic acid ester oligomer, as well as a polyimide prepared from the composition.

Abstract: A method of preparing an organosiloxane comprises cohydrolyzing a mixture comprising a first silane compound having the general formula R2SiX2 and a second silane compound having the general formula R3SiR1 in the presence of an aqueous acid, wherein each R is independently selected from H and a hydrocarbyl group, each X is an independently selected halogen atom, and R1 is X or OSiR3. The organosiloxane is prepared in a reaction product. Optionally, the method comprises isolating the organosiloxane from the reaction product. The organosiloxane has the general formula R3SiO(R2SiO)nH, wherein n is an integer from 1 to 200.

Abstract: An organic group-modified organosilicon resin having the average compositional formula (1), which is solid or liquid at 25° C., is suited for use in cosmetics. The resin is able to form an emulsion having a pleasant feel on use, a high internal water phase, and stability over time. In formula (1), a, b, c, d, e, and f are numbers: 0?a?400, 0<b?200, 0?c?400, 0?d?320, 0?e?320, 0<f?1,000, and 0.5?(a+b+c)/f?1.5.

Abstract: The invention relates to polyurethane organopolysiloxanes and their applications, in particular for the finishing of textile fabrics and textile fibres.

Abstract: A method of producing a transparent polymer aerogel can include dissolving gel precursors consisting of radical polymerizable monomers and crosslinkers, radical initiators, and a chain transfer agent (CTA) in a reaction solvent, placing the gel precursors into a substrate, polymerizing the gel on the substrate, optionally removing the wet gel from the mold, optionally performing at least one solvent exchange on the gel, and drying the solvent-exchanged gel.

Abstract: The present invention relates to a method for a super absorbent polymer. The method for preparing a super absorbent polymer according to the present invention makes it possible to provide a super absorbent polymer in which characteristics such as a centrifuge retention capacity and an absorption rate are improved in a balanced manner.

Abstract: A method of manufacturing a polymer coated cellulose nanocrystal composite material begins with an aqueous cellulose nanocrystal (CNC) suspension mixture. The aqueous CNC suspension mixture is dried to remove the liquid solvent from the aqueous CNC suspension mixture to form a dry CNC powder. Diethylenetriamine (DETA) is combined with melted Maleated-anhydride Polypropylene (MAPP) to form a DETA-functionalized MAPP (MA) mixture. The MA mixture is cooled and pelletized to form MA pellets. The MA pellets, the dry CNC powder, and a neat polypropylene (PP) are combined to form a CNC-PP mixture. The CNC-PP mixture is compounded by melting, subsequently cooled and pelletized to form CNC-PP pellets.

Abstract: Disclosed are a method of preparing a resin powder and an integrated reactor for the same. When a coagulation process is performed using an acidic coagulant in the integrated coagulator for latex coagulation and aging according to the present invention, a remaining acidic coagulant is also removed from a reactor through neutralization, and thus, a resin powder having enhanced moist-heat resistance and thermal stability may be prepared.

Abstract: Disclosed are a lithium salt/polyacrylonitrile/thermosetting resin composite material and a preparation method therefor. 100 parts of polyacrylonitrile and 550-1100 parts of N,N-dimethyl formamide by mass are stirred at a temperature of 25° C.-80° C., and a uniform and transparent polyacrylonitrile solution is obtained; further, 8-36 parts of a lithium salt is added; and the mixture is stirred until a uniform and transparent lithium salt/polyacrylonitrile solution is obtained. A heat-curable resin is added to the lithium salt/polyacrylonitrile solution, and is uniformly mixed. The obtained composite solution is made into a film, and a lithium salt/polyacrylonitrile/thermosetting resin composite material is then obtained after curing and post-treatment.

Abstract: A polyolefin-based thermoplastic elastomer and a crosslinked body of the same which can undergo a silane-crosslinking process excellent in productivity and have a rubber property required as a substitute material for EPDM is disclosed herein and can use a silane-crosslinkable ethylene-propylene copolymer characterized in that an organic peroxide (B) and a silane coupling agent (C) are compounded with an ethylene-propylene copolymer resin (A) which comprises 5 to 25% by mass of an ethylene component and 75 to 95% by mass of a propylene component, and whose MFR measured at 230° C. and with a load of 2.16 kg applied is 20.0 g/10 min or less. and further a compounded amount of the organic peroxide is 0.1 to 0.6 pts. mass based on 100 pts. mass of the ethylene-propylene copolymer resin (A) and a one-minute half-life temperature of the organic peroxide is 175.2° C. or less.

Abstract: The production of a protein free synthetic polyisoprene which has both low levels of chemical impurities and good physical properties has yet to be realized. It has now been envisioned that the use of neodymium catalyzed polyisoprene will offer the combined advantages of both a clean, as well as, high cis-1,4 polymer. Synthesis of polyisoprene rubber using a neodymium based catalyst system is described. Characterization of the material shows the absence of an ultra high molecular weight fraction and the presence of very high cis-1,4-microstructure. Gum stock and black filled compound studies comparing neodymium polyisoprene with natural rubber, titanium polyisoprene, and lithium polyisoprene have been performed. Results indicate that polyisoprene rubber synthesized using a neodymium catalyst system (Nd—PI) has similar stress-strain and tear properties as synthetic titanium polyisoprene.

Abstract: A process for making microwave-irradiated nanocomposites comprising graphene nanoplatelets dispersed in a polymer matrix, showing improved structural and electrical properties, is provided. The nanocomposites may be made using a solution casting technique, and may have a bilayer structure comprising a graphene-enriched layer in contact with a polymer-enriched layer. The nanocomposite may be used as a shielding material on electrical devices to decrease electromagnetic interference.

Abstract: A method and system to produce treated Cellulose Filaments (CF) and CF products are provided. Feedstock comprising CF in a water solution are mixed with a debonder to produce a mixed stream. The mixed stream is filtered yielding separate filtered and filtrate streams. The filtrate stream comprises at least a portion of the debonder. The filtered stream is dried to produce treated CF. The debonder is one of an alcohol, glycol ether, ester-containing quaternary ammonium salt, amido amine quaternary ammonium salt, disubstituted amide or a mixture thereof. The filtrate stream may be recycled. The mixed stream may be washed before filtering to remove debonder. A thermoplastic polymer-treated Cellulose filament composite material is formable by associating the treated CF with a thermopolymer such as polyolefin, polyurethane (PU), polypropylene (PP), polyester (PE), polylactic acid (PLA), polyhydroxyalkanoates (PHA), polyamide (PA), and ethylene vinyl acetate (EVA) or a mixture.

Abstract: The disclosure relates to thermosetting reinforced resin compositions and methods of forming boards, sheets and/or films using of porous particulates impregnated with embedded live monomer and/or oligomer and/or polymer configured to partially leach out a functional terminal end of the live monomer and/or oligomer and/or polymer and react with a cross-linking agent and photoinitiated polymer radicals to form a reinforced board, sheet and/or film of hybrid interpenetrating networks.

Abstract: A method, i.e., trapping of structural coloration (TOSC), for fabricating solid 3D network-structured photonic crystals featuring tunable visible structural colorations includes the steps: a PS-PVP copolymer is dissolved in a chloride-containing solvent and is cast as an initial film, the copolymer self-assembles into 3D periodic network-structured morphology; the copolymer in the initial film is swollen in a polar solvent to form a solvated film; the solvated film is dried to form a solid photonic crystal. During evaporation of the polar solvent, the PVP blocks of the copolymer become glassy and form a thin glassy layer on the surface of the solvated film such that the 3D network structures of the copolymer in solvated state can be preserved into the solid photonic crystal revealing the similar periodicity and dimension to that in solvated state, which is very distinct from the film having 1D lamellar structure.

Abstract: Disclosed is a flexible composite prepreg material. The prepreg material includes a fiber bundle of fiber tows having a predetermined cross-sectional shape, wherein exterior surface fibers of said fiber bundle have a thin, irregular sheath of matrix resin on and around said exterior surface fibers of said fiber bundle, wherein substantial number interior fibers filaments remain uncoated by the matrix resin, with discreet areas of through the thickness resin bridges made of the matrix resin.

Abstract: The invention relates to storage-stable one-component (1K) polyurethane prepregs and to shaped bodies produced therefrom.

Abstract: A three-dimensionally printed article comprises a build material and a support material, the support material comprising a hydroxypropyl methylcellulose having a DS of at least 1.0 and an MS of at least 0.6, wherein DS is the degree of substitution of methoxyl groups and MS is the molar substitution of hydroxypropoxyl groups. The support material can be removed from the build material by contacting the support material with water.

Abstract: A heat energy storage system may have a shape-stabilized composite prepared using an easy impregnation method involving a porous Ca2+-doped MgCO3 matrix and PEG as the functional phase. The heat storage capability, microstructures, and interactions with the PEG/CaMgCO3 composite can be characterized by DSC, SEM imaging, FT-IR spectroscopy, and TGA. Likely because of the synergistic phase change effect of CaMgCO3 and PEG, the PEG/CaMgCO3 composites can have high thermal enthalpies, and their enthalpy efficiencies are substantially higher than those of traditional shape stabilized PCMs. The functional material PEG can permeate porous CaMgCO3 matrices under capillary action. Liquid PEG can be stabilized within the porous matrix, and/or the CaMgCO3 matrix can improve the thermal stability of the PEG. The high heat energy storage properties and good thermal stability of such organic-inorganic composites offers utility in a range of applications, including thermal energy storage.

Abstract: An aerogel comprising an open-cell structured polymer matrix that includes a polyamic amide polymer is described.