Abstract: Provided is a packaged hydrogen-generating agent, the hydrogen-generating reaction of which is highly stable and repeatable, and which preferably is resistant to influence from changes in the environmental temperature. Also provided are a method for manufacturing said package, and a hydrogen generation method. The packaged hydrogen-generating agent is provided with: a hydrogen-generating agent (1); a covering material (2) which encloses the hydrogen-generating agent (1) and allows deformation; and a water-absorbing body (3), part of which is in contact with the hydrogen-generating agent (1). The covering material (2) preferably covers at least the area around the contact part (3a) where the water-absorbing body (3) and the hydrogen-generating agent (1) are in contact, so as to create a firm attachment at the contact part (3a).

Abstract: The present invention provides a novel oxygen absorbent composition being capable of realizing an oxygen absorbent not responding to a metal detector, being suppressed in the increase of the odor intensity after the absorption of oxygen and having an excellent oxygen absorption performance over a wide range of humidity conditions from low humidity to high humidity, and provides an oxygen absorbent package using the oxygen absorbent composition.

Abstract: A process for replacing the stabilization of (meth)acrylic monomers, wherein phenothiazine is removed from phenothiazine-containing (meth)acrylic monomers by adsorption on activated carbon, and then a moderately active polymerization inhibitor is optionally added.

Abstract: Systems, devices, methods, and compositions are described for providing an x-ray shielding system including a flexible layer including a support structure having a plurality of interconnected interstitial spaces that provide a circulation network for an x-ray shielding fluid composition.

Abstract: A mannich-base inhibitor for decalcification, a preparation method and application thereof are provided. The inhibitor comprises 10-80% mannich-base component calculated in the total weight percent of the inhibitor, while the rest is at least one compound selected from imidazoline inhibitor with molecular weight between 110 and 750, and alkynyloxy amine inhibitor. The mannich-base inhibitor component is prepared through mannich reaction with 1 mol organic polyamine containing three or more primary amine bases and/or secondary amine bases, 3-7 mol ketones, and 3-7 mol aldehydes. The inhibitor which can be effectively compounded and cooperated with oil demulsifying agent and oil decalcifying agent, have the advantages of stable property, strong absorbability, high film strength and film density with its inhibition rate exceeding 90%.

Abstract: Compositions comprising an alkyl 3-hydroxybutyrate and one or more additional components are provided. The compositions of the present invention may include at least one alkyl 3-hydroxybutyrate having at least 3 and not more than 5 carbon atoms, along with one or more additional components including, for example, alkyl butyrates, alkyl acetates, alkyl alcohols, and dimers and/or trimers of the alkyl 3-hydroxybutyrate. Such compositions may be products of, for example, the hydrogenation of an acetoacetate-containing composition.

Abstract: This invention is to a biomass composition of 5 and 6 carbon sugars, lignin, and cellulose which has been steam exploded and the composition has a very high enzyme accessibility at 24 hours for hydrolysis.

Abstract: The present invention relates to a particulate superabsorbent polymer composition comprising a polymer comprising a neutralized aluminum salt solution applied to the surface of a particulate superabsorbent polymer; wherein an aqueous solution of the neutralized aluminum salt has a pH value from about 5.5 to about 8 and the particulate superabsorbent polymer composition has a mean particle size distribution of from 300 to 400 ?m, an original Free Swell Gel Bed Permeability (FSGBP) of about 20×10?8 cm2 to about 200×10?8 cm2; and subsequent to subjecting the particulate superabsorbent polymer composition to the Processing Test, the particulate superabsorbent polymer composition has a permeability stability index of from about 0.60 to about 0.99 and having particles having a particle diameter of larger than 600 ?m in an amount of less than about 15 wt % of the particulate superabsorbent polymer composition and as specified by standard sieve classification.

Abstract: A negative electrode active material for an electric device includes an alloy containing silicon in a range from 27% by mass to 100% by mass exclusive, aluminum in a range from 0% by mass to 73% by mass exclusive, niobium in a range from 0% by mass to 58% by mass exclusive, and inevitable impurities as a residue. The negative electrode active material can be obtained with a multi DC magnetron sputtering apparatus by use of, for example, silicon, aluminum and niobium as targets. An electric device using the negative electrode active material can achieve a high cycle property while keeping a high discharge property.

Abstract: The present invention provides a radical composition capable of suppressing elution of electrode components in an electrolyte solution when used in an electrode for a secondary battery, and a battery using the radical composition. The present invention relates to a radical composition including a pyrroline nitroxide polymer and polyethylene glycols.

Abstract: The invention concerns a capture mass for capturing heavy metals in a liquid or gaseous effluent, comprising a porous solid support, copper sulphide and at least one second metal sulphide the metal of which is selected from the group constituted by chromium, manganese, iron, cobalt and nickel, and in which the ratio of the percentage by weight of the metal or metals other than copper to the percentage by weight of copper is in the range 0.01 to 2. The invention also concerns a process for preparing said capture mass and a process for capturing heavy metals in a gaseous or liquid effluent, in which said effluent is brought into contact with said capture mass.

Abstract: A fabrication method of thermoelectric materials using core-shell structured nano-particles and thermoelectric materials fabricated by the same are provided. The method includes preparing core-shell structured nano-particles having thermoelectric elements coated on the surface thereof (step 1); adding and mixing the prepared core-shell structured nano-particles of step 1, bismuth (Bi) salts, tellurium (Te) salts and a surfactant in a solvent (step 2); adding and dispersing a reducing agent in the mixture of step (step 3); and heating the mixture of step 3 in which reducing agent is added and dispersed (step 4). According to the present invention, thermoelectric materials, nano-phase is homogeneously dispersed inside of thermoelectric grain boundary, can be fabricated and if the fabricated materials are used after sintering and bulking, the thermoelectric materials are maintained in a state that the nano-particles remain in dispersed phase even after sintering.

Abstract: A negative electrode active material for an electric device includes an alloy containing, in terms of mass ratio, 35%?Si?78%, 7%?Sn?30%, 0%<Ti?37% and/or 35%?Si?52%, 30%?Sn?51%, 0%<Ti?35%, and inevitable impurities as a residue. The negative electrode active material can be obtained with a multi DC magnetron sputtering apparatus by use of, for example, silicon, tin and titanium as targets. An electric device employing the negative electrode active material can keep a high discharge capacity and ensure a high cycle property.

Abstract: A production process for lithium-silicate-based compound according to the present invention is characterized in that: a lithium-silicate compound being expressed by Li2SiO3 is reacted with a transition-metal-element-containing substance including at least one member being selected from the group consisting of iron and manganese at 550° C. or less within a molten salt including at least one member being selected from the group consisting of alkali-metal nitrates as well as alkali-metal hydroxides in an atmosphere in the presence of a mixed gas including carbon dioxide and a reducing gas. In accordance with the present invention, it is possible to produce lithium-silicate-based materials, which are useful as a positive-electrode active material for lithium-ion secondary battery, and the like, at low temperatures by means of relatively easy means.

Abstract: A cobalt oxide is disclosed and is represented by a chemical formula of Co1-yMyO2, wherein 0?y?0.9, and M is selected from the group consisting of alkali metal elements, alkaline-earth metal elements, Group-13 elements, Group-14 elements, transition metal elements, and rare-earth elements. A composite of cobalt oxide includes a cobalt oxide and an aluminum phosphate layer coated on a surface of the cobalt oxide.

Abstract: There is provided a producing method of metal fine particles or metal oxide fine particles for producing metal fine particles or metal oxide fine particles by atomizing raw materials by performing processes including an oxidizing process and a reducing process to the raw materials composed of metal or a metal compound.

Abstract: The present invention relates to a particulate superabsorbent polymer composition having improved stability comprising a polymer comprising from about 0.01 wt % to about 5 wt % of a neutralized aluminum salt solution applied to the surface of a particulate superabsorbent polymer; wherein an aqueous solution of the neutralized aluminum salt has a pH value from about 5.5 to about 8 and the particulate superabsorbent polymer composition has an original Free Swell Gel Bed Permeability (FSGBP) of about 20×10?8 cm2 to about 200×10?8 cm2 and a compressibility of from about 1.30 mm2/N to about 4 mm2/N prior to subjecting the particulate superabsorbent polymer composition to a Processing Test; and subsequent to subjecting the particulate superabsorbent polymer composition to the Processing Test, the particulate superabsorbent polymer composition has a permeability stability index of from about 0.60 to about 0.99.

Abstract: The present disclosure relates to a floating type adsorbent for removal of phosphate that can effectively remove phosphate from aqueous phase through reaction between an amine function attached on the surface of a sponge and phosphate. This adsorbent can be regenerated by desorbing the adsorbed phosphate, a method for fabricating same and a method for regeneration the floating type adsorbent for removal of phosphate. The floating type adsorbent for removal of phosphate according to the present disclosure is fabricated by immersing a sponge in a mixture solution of an amine precursor and anhydrous toluene to form an amine function on the surface of the sponge. The amine precursor may be 3-aminopropyltriethoxysilane (APTES) and the APTES and the anhydrous toluene may be mixed at a volume ratio of 0.5-1:1.

Abstract: The use of a composition that includes a metal salt and an oil soluble amine formaldehyde reaction product scavenges H2S that is present in aqueous fluids (e.g. produced water liquid streams), natural gas and in oil and mixtures thereof (e.g. mixed production streams that contain all three phases) better than either component when used alone. The resulting scavenger combination significantly increases the reaction rate and the overall scavenging efficiency, i.e. capacity over each component when used alone, in the same total amount. Non-limiting examples of the metal salt include zinc or iron carboxylates, and a non-limiting example of an oil soluble amine formaldehyde reaction product is the reaction product of dibutylamine with formaldehyde.

Abstract: Positive electrode active substance particles including a compound having at least a crystal system belonging to a space group of R?3m and a crystal system belonging to a space group of C2/m, and boron. The compound is a composite oxide comprising at least Li, Mn, and Co and/or Ni; a relative intensity ratio [(a)/(b)] of a maximum diffraction peak intensity (a) observed at 2?=20.8±1° in a powder X-ray diffraction pattern of the positive electrode active substance as measured using a Cu-Ku ray to a maximum diffraction peak intensity (b) observed at 2?=18.6±1° in the powder X-ray diffraction pattern, is 0.02 to 0.5; a content of Mn in the positive electrode active substance particles such that a molar ratio of Mn/(Ni+Co+Mn) is not less than 0.55; and the positive electrode active substance particles include boron in an amount of 0.001 to 3% by weight.