1845 results about "Melt viscosity" patented technology

Low viscosity ternary mixtures of benzoxazine, epoxy and phenolic resins have been developed. The blends render homogeneous and void free cured specimen with a wide range of properties. Melt viscosity values as low as 0.3 Pa.s at 100° C. can be achieved. The phenolic resin acts as a cure accelerator to the system, besides its typical function as a hardener of epoxy resin. Glass transition temperatures Tg as high as 170° C. can also be obtained.

Disclosed are polyester shrink films comprising a voiding agent dispersed within a continuous polyester phase. The voiding agent comprises at least one first polymer and at least one second polymer, in which the polymer components have selected physical properties such as glass transition temperature, melting point, tensile modulus, surface tension, and melt viscosity. The resulting shrink films have high opacity, a low coefficient of friction, lower density, low shrink force, and good printability. The films are useful for sleeve label and other shrink film applications, and their lower density allows them to be readily separated from soft drink bottles, food containers and the like during recycling operations. Also disclosed is a process for separating a void-containing polyester from a mixture of polymers.

A toner is provided that contains a particulate toner material (mother toner) having an average circularity of from 0.93 to 0.99, and including a modified polyester resin and a colorant; and an external additive in an amount of from 0.3 to 5.0 parts by weight per 100 parts by weight of the mother toner, wherein the toner has a melting viscosity of from 70 to 140 Pa·s at 160° C., a weight-average particle diameter of from 3 to 7 μm, a ratio thereof to a number-average particle diameter of from 1.91 to 1.25, wherein particles satisfy at least one of (I) and (II): (I) particles having a diameter of 4 μm or less in an amount less than 10% by number; or (II) particles having a diameter of 8 μm or more in an amount less than 2% by volume, along with a one or two component developer containing the toner, a cartridge containing the toner, an image forming method using the toner and an image forming apparatus using the toner.

Polymers that have extremely high melt viscosities are very difficult to extrude and stretch making it difficult to synthesize fibers of such polymers via conventional methods. A process is provided for producing a polymer fiber which involves blowing a mixture of a polymer and a gas through a nozzle such that polymer micro- and/or nano-fibers are produced. The polymer fibers are characterized in that they have a diameter less than the diameter of the outlet aperture of the nozzle.

A resin composition exhibiting excellent antistaticity and static charge dissipating performance and having extremely small variations of antistatic properties (saturated static voltage and half-life period of static voltage) on the surface of a molded article and a transportation jig for electronic field made of the above resin composition are provided by using a resin composition produced by compounding (A) 100 parts by weight of a thermoplastic resin with (B) 1 to 30 parts by weight of a carbon fiber having a diameter of 1 nm to 1 mum, a length of 1 mum to 3 mm and a volume resistivity of smaller than 1 OMEGAcm and (C) 5 to 200 parts by weight of an antistatic polymer having a surface resistivity of 108 to 1011OMEGA (measured under impressed voltage of 500V), a melting point of 100° C. or above, an apparent melt viscosity of 10 to 1,000 Pa.s at apparent shear rate of 1,000 sec-1 at 260° C. and an apparent melt viscosity ratio of the antistatic polymer to the thermoplastic resin of 0.01 to 1.3 under the above condition.

The invention provides a stretch blow molded container formed from a thermoplastic resin material which comprises polyglycolic acid having (a) a repeating unit represented by the following formula (1): (b) a melt viscosity, eta * [as measured at a temperature of (the melting point, Tm of the polymer+20 DEG C.) and a shear rate of 100/sec] of 500-100,000 Pa.s; (c) a melting point, Tm of at least 180 DEG C.; (d) a melt enthalpy, DELTA Hm of at least 20 J/g; and (e) a density of at least 1.50 g/cm3 as measured in an unoriented, crystallized form, wherein the stretch blow molded container has tensile strength (in a circumferential direction) of at least 100 MPa and a carbon dioxide permeability (as measured at a temperature of 23 DEG C. and 80% relative humidity; in terms of the thickness of 50 mu m) of 300 cc/m2.day.atm or smaller at the body sidewall thereof, and a production process thereof.

Disclosed are multicomponent fibers derived from a blend of a sulfopolyester with a water non-dispersible polymer wherein the as-spun denier is less than about 6 and wherein the water dispersible sulfopolyester exhibits a melt viscosity of less than 12,000 poise measured at 240° C. at a strain rate of 1 rad/sec, wherein the sulfopolyester comprising less than about 25 mole % of residues of at least one sulfomonomer, based on the total moles of diacid or diol residues, and wherein said poly(ethylene) terephthalate has an inherent viscosity of less than 0.55 dL/g. The multicomponent fiber is capable of being drawn at a relatively high fiber speed, particularly at least about 2000 m/min, and may be used to produce microdenier fibers. Fibrous articles may be produced from the multicomponent fibers and microdenier fibers. Also disclosed is a process for multicomponent fibers, nonwoven fabrics, and microdenier webs.

The invention relates to a foamed fluoropolymer, preferably a polyvinylidene fluoride (PVDF) structure, such as from Kynar® resins. The foamed structure is continuous self-supporting, sized, and has a dense skin. The foamed structure is manufactured in a process using foaming agents and nucleating agents. The structure is sized into a specific shape during the manufacturing process—requiring a good melt viscosity of the PVDF foam. In one process, a master batch containing the nucleating agent is used. The foamed article could be a sheet, film, profile, tube, pipe, article, rod foam-core structure, or other self-supporting shape. Foamed tubes, pipes, rods, sheets and conduit are especially useful. The foamed structure of the invention provides added value by being lighter weight, more flexible, and more impact resistant than a comparable non-foamed PVDF structure. It also has increased hysteresis, increased insulation properties, reduced dielectric constant, and increased compressibility.

A production method of a water-absorbent resin includes the steps of: obtaining a hydrogel by supplying monomer liquid to a reaction device so that the monomer liquid is polymerized; and detaching the hydrogel from the reaction device, wherein the reaction device's surface in contact with the monomer liquid at a position where polymerization occurs is made of a fluororesin having a melt viscosity of less than 1×10⁸ poise at 380° C. On this account, it is possible to obtain a water-absorbent resin having less amounts of an extractable content with high productivity and it is possible to carry out continuous production for an extended period of time.

Disclosed are novel compositions for the preparation of void-containing articles comprising a polymer matrix and a voiding agent The voiding agent comprises at least one first polymer and at least one second polymer, which are selected on the basis of physical properties such as glass transition temperature, tensile modulus, melting point, surface tension, and melt viscosity. Shaped articles such as sheet, film, bottles, tubes, labels, and sleeves may prepared from these compositions. Also disclosed are polyester shrink films prepared using a voiding agent comprising a novel blend of cellulosic and olefinic polymers. The resulting shrink films have better opacity, lower density, reduced shrink force, and improved printability as compared with most standard voiding agents. The films are useful for sleeve label and other shrink film applications and their lower density allows them to be readily separated from soft drink bottles, food containers and the like during recycling operations.

The invention relates compositions containing at least one silane-grafted polyolefin, and in particular, to compositions containing at least one silane-grafted ethylene/α-olefin polymer, which has a melt viscosity less than 50,000 cP, and adhesives containing the same. In one embodiment, the at least one silane-grafted ethylene/α-olefin polymer is formed from an ethylene/α-olefin polymer that has a molecular weight distribution from 1 to 3.5. The invention also relates to the preparation of the silane-grafted polymers, by reacting, for example, an ethylene/α-olefin polymer with at least one silane compound and at least one initiator.

The invention discloses an inorganic powder highly filled polyvinyl alcohol composite material, which consists of the following components in parts by weight: 10-60 parts of polyvinyl alcohol, 30-80 parts of inorganic powder, 5-30 parts of plasticizing agent and 5-15 parts of flow modifying agent. Further, the composite material has the tensile strength of 17.0-75.0 MPa and the breaking elongation of 70-450%, and the melt viscosity is 1.0*10<2> to 5.0*10<3> Pa s at 180 DEG C when the shearing rate is 10<2>-10<3> s<-1>. The invention further discloses a preparation method of the inorganic powder highly filled polyvinyl alcohol composite material. By using the inorganic powder highly filled polyvinyl alcohol composite material and the preparation method, not only can inorganic powder highly filled polyvinyl alcohol be realized, the cost of the composite material be greatly reduced, but also the flowability of the composite material can be guaranteed; the favorable thermoplastic processing of the composite material is realized; the obtained composite material is excellent in combination property; products such as a fiber, a sheet and a thin film can be prepared through a routine thermoplastic processing method; and the inorganic powder highly filled polyvinyl alcohol composite material is used for the fields of writing paper, printing paper, instrument and meter packaging films, wallpaper, heat-insulating gaskets, toys and the like. The preparation method provided by the invention is simple in process and short in flow and industrial production is easy to realize.

Polyimide copolymers were obtained containing 1,3-bis(3-aminophenoxy)benzene (APB) and other diamines and dianhydrides and terminating with the appropriate amount of reactive endcapper. The reactive endcappers studied include but should not be limited to 4-phenylethynyl phthalic anhydride (PEPA), 3-aminophenoxy-4'-phenylethynylbenzophenone (3-APEB), maleic anhydride (MA) and nadic anhydride (5-norbornene-2,3-dicarboxylic anhydride, NA). Homopolymers containing only other diamines and dianhydrides which are not processable under conditions described previously can be made processable by incorporating various amounts of APB, depending on the chemical structures of the diamines and dianhydrides used. By simply changing the ratio of APB to the other diamine in the polyimide backbone, a material with a unique combination of solubility, Tg, Tm, melt viscosity, toughness and elevated temperature mechanical properties can be prepared. The copolymers that result from using APB to enhance processability have a unique combination of properties that include low pressure processing (200 psi and below), long term melt stability (several hours at 300 DEG C. for the phenylethynyl terminated polymers), high toughness, improved solvent resistance, improved adhesive properties, and improved composite mechanical properties. These copolyimides are eminently suitable as adhesives, composite matrices, moldings, films and coatings.