Abstract: Embodiments of the present disclosure relate to articles, coated articles and methods of coating such articles with a rare earth metal containing oxide coating. The coating can contain at least a first metal (e.g., a rare earth metal, tantalum, zirconium, etc.) and a second metal that have been co-deposited onto a surface of the article. The coating can include a homogenous mixture of the first metal and the second metal and does not contain mechanical segregation between layers in the coating.

Abstract: Provided according to embodiments of the invention are varistor ceramic formulations that include zinc oxide (ZnO). In particular, varistor ceramic formulations of the invention may include dopants including an alkali metal compound, an alkaline earth compound, an oxide of boron, an oxide of aluminum, or a combination thereof. Varistor ceramic formulations may also include other metal oxides. Also provided according to embodiments of the invention are varistor ceramic materials formed by sintering a varistor ceramic formulation according to an embodiment of the invention. Further provided are varistors formed from such ceramic materials and methods of making such materials.

Abstract: The present invention is a method for manufacturing a high-performance composite active material of zinc oxide powder, which is a method for manufacturing a high-performance composite active zinc oxide material powder as an aid for an operation of shaping and vulcanization of rubber/plastic materials, generally carried out by mixing an alkali solution and a calcium compound, in combination with addition of a zinc salt to directly carry out a chemical reaction therewith through mixture so as to obtain a precipitation solution of a predetermined pH value, following a process of filtering to remove water to form an intermediate powder material, which is subjected to drying to form zinc oxide long crystal material exhibiting nanometer scale high performance composite activity, helping achieve a purpose of diversification of application of zinc oxide power in industry.

Abstract: A catalyst comprising: a titanium oxide having an anatase-type crystal structure, and having the vertices and the ridge lines, wherein in a single titanium oxide particle, a vertex density per unit surface area is 8.0×10?4 nm?2 or more, and a ridge line density per unit surface area is 5.0×10?2 nm or more, or a ridge line density per unit volume is 8.0×10?3 nm?2 or more. A complex comprising: a material having a porous structure; and said catalyst. A membrane electrode assembly comprising: an anode; cathode; and an electrolyte membrane, wherein the cathode carries said catalyst on at least a surface of the cathode.

Abstract: A lithium secondary cell having an operating voltage ?4.35 sV, comprising a cathode comprising a doped L1CoO2 active material, an anode comprising graphite, and an electrolyte comprising a carbonate-based solvent, a lithium salt and both a succinonitrile (SN) and a lithium bis(oxalato)borate (LiBOB) additive wherein during the discharge at 45° C. from a state of charge (SOC) of 100% at 4.5V to a SOC of 0 at 3V at a C/10 rate the difference of the SOC at 4.42V and 4.35V is at least 7% but less than 14%, and wherein the active material is doped by at least 0.5 mole % of either one or more of Mn, Mg and Ti.

Abstract: The nanocomposite system for hydrogen storage is a composite of MgH2 powder with ZrNi5 powder and a combination of Nb2O5, TiC and VC. Preferably, the MgH2 is in nanocrystalline form and the ZrNi5 is significantly in a Friauf-Laves phase. The nanocomposite system is formed by combining the MgH2 powder with the ZrNi5, Nb2O5, TiC and VC, preferably in amounts of 4 wt. % ZrNi5+1 wt. % Nb2O5+0.5 wt. % TiC+0.5 wt. % VC, to form a mixture, and then performing reactive ball milling on the mixture. Preferably, the reactive ball milling is performed for a period of 50 hours.

Abstract: An emissions treatment apparatus includes a first mechanism arranged to receive an exhaust gas, wherein the first mechanism is supplied with a first substance arranged to react with a first exhaust compound to process the exhaust gas, the first substance being chemically derived from an electrolyte source. The emissions treatment apparatus further comprises a second mechanism arranged to receive the exhaust gas after its reaction with the first exhaust compound; wherein the second mechanism receives a second substance arranged to react with a second exhaust compound to further process the exhaust gas, the second substance being chemically derived from an electrolyte source.

Abstract: The present invention relates to a process for the continuous preparation of core-shell nanoparticles, comprising a core of a core material, preferably of a semiconductor material, and a shell of a shell material, preferably of a semiconductor material, wherein selected starting materials for the shell material are mixed with a dispersion of nanoparticles of the core material and are passed continuously through a reaction zone of a tubular reactor, and other starting materials for the shell material are fed to the reaction zone of the tubular reactor at two or more locations, preferably via a tubular membrane, and the starting materials for the shell material react in the reaction zone to form a shell around the nanoparticles of the core material. The invention also relates to the tubular reactor with the membrane and its use for the continuous synthesis of core-shell nanoparticles.

Abstract: The present invention provides a device including a titania nanotube membrane having a plurality of titania nanotubes on a titanium substrate where the titania nanotubes are open at both ends and capable of allowing diffusion of liquids or solids from one side of the membrane to the other through the titania nanotubes. Methods of making the titania nanotube membrane are also provided.

Abstract: The present invention relates to an n-heterocyclic carbene (NHC) type palladium catalyst and its preparation method as well as applications. Its preparation process is as below: select glyoxal as the raw material to synthesize glyoxaldiimine in the presence of Lewis acid or Bronsted acid, and then react with paraformaldehyde to get the NHC type ligand. Use palladium(II) to react with the compound containing carbon-nitrogen double bonds to get palladium(II) cyclic dimer; make the palladium cyclic dimer and the NHC type ligand coordinated to get the NHC type palladium catalyst. The palladium catalyst with a brand new structure according to the present invention, boasts high activity and multi-purpose.

Abstract: A method for preparing a composition including synthetic mineral particles, in which: a hydrogel that is a precursor of the synthetic mineral particles is prepared, and the hydrogel is subjected to a hydrothermal treatment, characterized in that at least one step of the hydrothermal treatment is carried out with the addition of at least one carboxylate salt to the treatment medium, the carboxylate salt having the formula R—COOM?, where M? denotes a metal selected from the group consisting of Na and K, and R is selected from H and the alkyl groups that include fewer than 10 carbon atoms.

Abstract: Methods for synthesizing metal nanoparticles and the nanoparticles so produced are provided. The methods include addition of surfactant to a novel reagent complex between zero-valent metal and a hydride. The nanoparticles produced by the method include oxide-free, zero-valent tin nanoparticles useful in fabricating a battery electrode.

Abstract: An automatic method or the classification of the Degrees of Maturation (DM) for fired iron ore pellets, independent of human intervention, based on the digital acquisition of microscopy images of polished cross sections, and their processing, analysis and classification by a suitable software procedure.

Abstract: Electrodes employing as active material magnesium nanoparticles synthesized by a novel route are provided. The nanoparticle synthesis is facile and reproducible, and provides magnesium nanoparticles of very small dimension and high purity for a wide range of metals. The electrodes utilizing these nanoparticles thus may have superior capability. Magnesium ion electrochemical cells employing said electrodes are also provided.

Abstract: This invention relates to whitlockite and a method for manufacturing the same. The method includes adding, to water, a calcium ion supplying material and a cation supplying material containing a cation (X) other than the calcium ion to prepare a cation aqueous solution, adding a phosphoric acid supplying material to the cation aqueous solution, and aging the cation aqueous solution including the phosphoric acid supplying material. As a result, whitlockite having high purity and high crystallinity can be mass produced using a simple process.

Abstract: Disclosed herein is a treated ore solid comprising a reduced amount of a contaminant, for example arsenic, compared to the ore solid prior to treatment. Also disclosed are temperature and pressure modifications, parameters, and methods for treating an ore solid by pressure oxidation leaching of enargite concentrates. The disclosed methods and processes may be applied to copper sulfide orebodies and concentrates containing arsenic. In some cases, the disclosed methods and systems extract, remove, or reduce contaminants, for example arsenic, from an ore containing solution at moderately increased temperature, pressure, and oxygen concentration, and in the presence of an acid.

Abstract: Disclosed are a transition metal precursor for preparation of a lithium composite transition metal oxide, the transition metal precursor including a composite transition metal compound represented by Formula 1 below and a hydrocarbon compound, and a method of preparing the same: MnaMb(OH1?x)2??(1) wherein M is at least two selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr, and second period transition metals; 0.4?a?1; 0?b?0.6; a+b?1; and 0<x<0.5. The transition metal precursor includes a particular composite transition metal compound and a hydrocarbon compound, and thus, when a lithium composite transition metal oxide is prepared using the same, carbon may be present in lithium transition metal oxide particles and/or on surfaces thereof, whereby a secondary battery including the lithium composite transition metal oxide exhibits excellent rate characteristics and long lifespan.

Abstract: The method described herein allows for melt stabilization and vapor-phase synthesis of a cesium germanium halide utilizing germanium dihalides formed in situ. This disclosure allows for the melting of cesium germanium halides without decomposition, which allows for growing crystals of these materials from the melt. This disclosure allows for a direct synthesis of these materials without the use of water or the introduction of other possible contaminants.

Abstract: A method of preparing hydrotalcite for a PVC stabilizer, which comprises: forming crystals of hydrotalcite represented by a formula of M(II)XM(III)Y(OH)N(Am—)Z. nH2O, wherein M(II) is a divalent metal selected from Mg2+, Ni2+ and Zn2+; M(III) is a trivalent metal selected from Al3+, Fe3+, Cr3+ and Co3+; and Am— is an anion selected from CO32-, OH—, NO3-, SO42- and halides; and depositing zinc (Zn) onto the hydrotalcite by using any one method of electrode-position, chloride ion deposition, and plasma deposition to provide zinc-deposited hydrotalcite.

Abstract: The present invention addresses the problem of providing producing processes for garnet precursor microparticles (a precursor for microparticles of garnet structure) and microparticles of garnet structure. One of the processing processes comprises mixing ions of at least two elements with a basic substances that contain the at least two elements. The thin-film fluid is formed between at least two processing surfaces which are approachably and separably arranged facing each other with at least one of the processing surfaces rotating relative to the other. In the processing process, the precipitated microparticles are garnet precursor microparticles, and the molar ratio between the at least two elements in the garnet precursor microparticles is regulated by controlling the pH of the thin-film fluid after the mixing. Microparticles of garnet structure can be obtained by subjecting the garnet precursor microparticles to heat treatment.

Abstract: This invention pertains to method for imparting a durable antimicrobial activity to substrates, particularly textiles. An acetate-free metal and peroxide antimicrobial treatment formulation is prepared from a metal derivative, hydrogen peroxide and a source of hydroxide ion. The substrate is treated with the composition and dried to afford the treated substrate with antimicrobial activity. Zinc salts, ions, or complexes are preferred.

Abstract: Disclosed is a transition metal precursor used for preparation of lithium composite transition metal oxide, the transition metal precursor comprising a composite transition metal compound represented by the following Formula 1: M(OH1?x)2?yAy/n??(1) wherein M comprises two or more selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr and second period transition metals; A comprises one or more anions except OH1?x; 0?x?0.5; 0.01?y?0.5; and n is an oxidation number of A. The transition metal precursor according to the present invention contains a specific anion. A lithium composite transition metal oxide prepared using the transition metal precursor comprises the anion homogeneously present on the surface and inside thereof, and a secondary battery based on the lithium composite transition metal oxide thus exerts superior power and lifespan characteristics, and high charge and discharge efficiency.

Abstract: A method for producing a coated material having an oxidizable metal-containing coating, including the step of applying to a base material (11) an oxidizable metal-containing coating fluid containing a particulate oxidizable metal, a carbon component, a thickener, and water using a coating apparatus (1) and a coating fluid preparation step in which a thickener solution prepared by dissolving the thickener in water, the particulate oxidizable metal, and the carbon component or an aqueous dispersion of the carbon component are put and mixed in a preparation tank (3) to prepare the oxidizable metal-containing coating fluid. In the coating fluid preparation step, the particulate oxidizable metal is added to the thickener solution.

Abstract: Systems, compositions, and methods for removing a substance or substances from a material, such as a gas or liquid material, are described. The compositions can comprise composite removal particles. In some embodiments, the composite removal particles can be comprised of support particles made from an inexpensive carrier material, and a reactive particle borne on the support particle. The reactive particle reacts with the substance or substances in the material. The reacted composite removal particles can then be removed from the material, which reduces the amount of the substance or substances present in the material. The composite removal particles are useful for removing pollutants, such as mercury, from exhaust gases, such as flue gas from a power plant combustion unit, and from other materials such as natural gas, liquefied natural gas, fuels, hydrocarbons, petrochemicals, and refinery streams.

Abstract: A method for providing a porous metal implant. A mixture of a biocompatible metal, a spacing agent, and a binder is provided. The mixture is formed into a shaped the spacing agent is removed to form a plurality of pores in the implant. A shaped porous metal implant is also provided.

Abstract: The disclosure provides an oxygen carrier comprised of a plurality of metal oxide particles in contact with a plurality of MgO promoter particles. The MgO promoter particles increase the reaction rate and oxygen utilization of the metal oxide when contacting with a gaseous hydrocarbon at a temperature greater than about 725° C. The promoted oxide solid is generally comprised of less than about 25 wt. % MgO, and may be prepared by physical mixing, incipient wetness impregnation, or other methods known in the art. The oxygen carrier exhibits a crystalline structure of the metal oxide and a crystalline structure of MgO under XRD crystallography, and retains these crystalline structures over subsequent redox cycles. In an embodiment, the metal oxide is Fe2O3, and the gaseous hydrocarbon is comprised of methane.

Abstract: In one embodiment of the present disclosure an electrocatalyst support for a fuel cell is provided which includes a doped titania metal oxide. The dopant includes a valve metal. The doped titania metal oxide has a BET surface area of greater than 20 m2/g.

Abstract: This invention relates to treated geothermal brine compositions containing reduced concentrations of iron, silica, and manganese compared to the untreated brines. Exemplary compositions contain a concentration of manganese less than 10 mg/kg, a concentration of silica ranging from less than 10 mg/kg, and a concentration of iron less than 10 mg/kg, and the treated geothermal brine is derived from a Salton Sea geothermal reservoir.

Abstract: This invention relates to treated geothermal brine compositions containing reduced concentrations of iron, silica, and zinc compared to the untreated brines. Exemplary compositions contain concentration of zinc ranges from 0 to 300 mg/kg, concentration of silica ranges from 0 to 30 mg/kg, concentration of iron ranges from 0 to 300 mg/kg. Exemplary compositions also contain reduced concentrations of elements like lithium, manganese, arsenic, barium, and lead. Exemplary compositions include Salton Sea brines containing a concentration of zinc less than 10 mg/kg, a concentration of silica ranging from less than 10 mg/kg, and a concentration of iron less than 10 mg/kg.

Abstract: Provided are a method of producing mixed powder comprising noble metal powder and oxide powder, wherein powder of ammonium chloride salt of noble metal and oxide powder are mixed, the mixed powder is subsequently roasted, and ammonium chloride is desorbed by the roasting process in order to obtain mixed powder comprising noble metal powder and oxide powder, and mixed powder comprising noble metal powder and oxide powder, wherein chlorine is less than 1000 ppm, nitrogen is less than 1000 ppm, 90% or more of the grain size of the noble metal powder is 20 ?m or less, and 90% or more of the grain size of the oxide powder is 12 ?m or less. Redundant processes in the production of noble metal powder are eliminated, and processes are omitted so that the inclusion of chlorine contained in the royal water and nitrogen responsible for hydrazine reduction reaction is eliminated as much as possible.

Abstract: This invention relates to treated geothermal brine compositions containing reduced concentrations of silica, iron, and potassium compared to the untreated brines. Exemplary compositions of the treated brine contain a concentration of silica ranging from about 0 mg/kg to about 15 mg/kg, a concentration of iron ranging from about 0 mg/kg to about 10 mg/kg, and a concentration of potassium ranging from about 300 mg/kg to about 8500 mg/kg. Other exemplary compositions of the treated brines also contain reduced concentrations of elements like rubidium, cesium, and lithium.

Abstract: A composition comprising a polyhydroxyoxoaluminum cation detectable at 76 ppm by 27Al NMR that is present in a relative abundance on a 27Al NMR spectrograph that is greater than any other polyhydroxyoxoaluminum cation detectable by 27Al NMR. Also, disclosed are methods of making the composition.

Abstract: A method for preparing a suspension of LDH particles comprises the steps of preparing LDH precipitates by coprecipitation to form a mixture of LDH precipitates and solution; separating the LDH precipitates from the solution; washing the LDH precipitates to remove residual ions; mixing the LDH precipitates with water; and subjecting the mixture of LDH particles and water from step (d) to a hydrothermal treatment step by heating to a temperature of from greater than 80° C. to 150° C. for a period of about 1 hour to about 144 hours to form a well dispersed suspension of LDH particles in water.

Abstract: The present invention provides a supported reactant for in situ remediation of soil and/or groundwater contaminated with a halogenated hydrocarbon consisting essentially of an adsorbent impregnated with elemental iron, wherein the adsorbent is capable of adsorbing the halogenated hydrocarbon. In one embodiment, the adsorbent is activated carbon.

Abstract: A method for completely reducing an inorganic halide to obtain a non-halogen inorganic substance and/or hydride thereof and preferably anhydrous hydrogen halide fluid using inorganic halide substances, such as sulfur hexafluoride, nitrogen trifluoride, tungsten hexafluoride, uranium hexafluoride and others by reduction with a reducing agent at a proper temperature. The reducing agents may be molecular hydrogen, inorganic hydrides and inorganic metallic elements; molecular hydrogen is preferable, but in certain instances the inorganic hydrides are used, as well as inorganic metallic elements such as calcium and magnesium.

Abstract: This invention relates to whitlockite and a method for manufacturing the same. The method includes adding, to water, a calcium ion supplying material and a cation supplying material containing a cation (X) other than the calcium ion to prepare a cation aqueous solution, adding a phosphoric acid supplying material to the cation aqueous solution, and aging the cation aqueous solution including the phosphoric acid supplying material. As a result, whitlockite having high purity and high crystallinity can be mass produced using a simple process.

Abstract: An electrochemically reacting composition which can be utilized as a source of heat as well as hydrogen, comprising the active materials aluminum, magnesium and iron, a filler material such as a silica sand, a hydrogen scavenger such as potassium permanganate, additives such as sodium silicate and an electrolyte such as sodium chloride.

Abstract: Provided in one embodiment is a method for producing a composition, comprising: heating a first material comprising an amorphous alloy to a first temperature; and contacting the first material with a second material comprising at least one fiber to form a composition comprising the first material and the second material; wherein the first temperature is higher than or equal to a glass transition temperature (Tg) of the amorphous alloy.

Abstract: In an industrial purple nano-needle tungsten oxide preparation method, ammonium paratungstate 5(NH4)2O.12WO3.5H2O, tungstic acid mWO3.nH2O (m?1, n?1), or tungsten oxide WOx (2?x?3) is used as a raw material for preparing the purple nano-needle tungsten oxide in an inclined rotating furnace pipe. At an inlet of the furnace pipe, the raw material is pushed from a feed inlet of a feeding device into the heated furnace pipe. The inclined furnace pipe is rotated to gradually move the raw material from a low temperature area to a high temperature area. The raw material at the high temperature area inside the furnace pipe is reduced by H2 to form the nano-needle purple tungsten oxide. The inclined furnace pipe is rotated to move the WO2.72 towards a discharging end, and the purple tungsten oxide WO2.72 is discharged from a discharge outlet of a discharging device and cooled to room temperature by the discharging device.

Abstract: A composite metal precursor including a composite metal hydroxide represented by Formula 1 below, wherein an amount of magnesium (Mg) in the composite metal hydroxide is less than or equal to 0.005 wt %, an electrode active material formed from the same, a positive electrode including the same, and a lithium secondary battery employing the same: (A1-x-yBxCy)(OH)2 ??[Formula 1] wherein in Formula 1, x, y, A, B, and C are as described in the detailed description.

Abstract: To obtain a non-aqueous electrolyte secondary battery having high capacity, high output and good cyclability, nickel manganese composite hydroxide particles are a precursor for a cathode active material having lithium nickel manganese composite oxide with a hollow structure and a small and uniform particle size. An aqueous solution for nucleation includes a metallic compounds that contains nickel and a metallic compound that contains manganese, but does not include a complex ion formation agent that forms complex ions with nickel, manganese and cobalt. After nucleation is performed, an aqueous solution for particle growth is controlled so that the temperature of the solution is 60° C. or greater, and so that the pH value that is measured at a standard solution temperature of 25° C. is 9.5 to 11.5, and is less than the pH value in the nucleation step.

Abstract: The object of the invention is to provide a bioactive agent in which the bioactive effectiveness of ferric iron salt and/or ferric ferrous iron salt contained therein is stabilized, making long term preservation possible, so that the bioactive agent can be useful as an original solution for medical use, as a soil conditioner, or the like. An iron-magnesium mixture solution is provided in the invention, wherein the iron-magnesium mixture solution is produced by mixing an aqueous solution containing a ferric iron salt and/or a ferric ferrous iron salt in a concentration of not less than 0.5 mol/L as iron in the ferric iron salt and/or the ferric ferrous iron salt, and an aqueous solution containing a magnesium salt in a concentration of not less than 0.2 mol/L as magnesium in the magnesium salt.

Abstract: A voltage nonlinear resistor is made of a sintered body that mainly includes zinc oxide grains, spinel grains including zinc and antimony as main ingredients, and a bismuth oxide phase, in which the bismuth oxide phase includes at least one of alkali metals selected from the group of potassium and sodium at a ratio in the range of 0.036 at % or higher and 0.176 at % or lower. The voltage nonlinear resistor has good voltage nonlinearity and loading service life characteristics, and can be used for a lightning arrester.

Abstract: A multiphase hydrogen storage material comprises a lithium compound and a lithium conductor. The hydrogen storage material is capable of undergoing hydrogenation and dehydrogenation cycles during which the rate of lithium transport is enhanced by the presence of the lithium conductor. A solid state hydrogen storage device and a process of storing and supplying hydrogen are also disclosed.

Abstract: A hydrogen storage material includes: a first storage material body (1) which stores hydrogen; and a second storage material body (2) which stores hydrogen, and coats a surface of the first storage material body (1). A hydrogen equilibrium pressure (HP) of the second storage material body (2) is lower than that of the first storage material body (1) at the hydrogen generation temperature of the first storage material body (1).

Abstract: The present invention provides a positive electrode active material for lithium ion batteries, which realizes a lithium ion battery that is, while satisfying fundamental characteristics of a battery (capacity, efficiency, load characteristics), low in the resistance and excellent in the lifetime characteristics. In the positive electrode active material for lithium ion batteries, the variation in the composition of transition metal that is a main component inside of particles of or between particles of the positive electrode active material, which is defined as a ratio of the absolute value of the difference between a composition ratio inside of the particles of or in a small area between the particles of the transition metal and a composition ratio in a bulk state to the composition ratio in a bulk state of the transition metal, is 5% or less.

Abstract: A refractory composition and processes for manufacture are provided where the compositions possess improved refractory alkali resistance and superior handling properties. Compositions and processes for their manufacture may include a plurality of ceramic particles and a binder sintered to the particles wherein the binder includes crystalline aluminum orthophosphate distributed as the result of an in situ reaction of aluminum metaphosphate with alumina. Kits provided according to the invention provide materials for use in manufacture of a composition where the kit includes aluminum metaphosphate and a nonfacile additive.

Abstract: A method of removing mercury and/or sulfur from a fluid stream comprising contacting the fluid stream with a sorbent comprising a core and a porous shell formed to include a plurality of pores extending therethrough and communicating with the core. The core comprises a copper compound selected from the group consisting of a basic copper oxysalt, a copper oxide, and a copper sulfide.

Abstract: The present invention generally relates to materials and methods for catalytic reactions, including transition metal-catalyzed cross-coupling reactions. The materials may be stable metal complexes that do not require special handling or processing conditions. In some cases, materials of the invention advantageously may be synthesized in one synthetic step without the need for isolation of intermediate compounds. Also, materials of the invention may be synthesized from inexpensive and readily available starting materials, under relatively mild reaction conditions that do not require the exclusion of air, water, and the like. In some embodiments, the material is a N-heterocyclic carbene metallacycle complex. Such materials and methods may be useful in the production of fine chemicals, advanced materials and specialty polymers.

Abstract: A decomposer for an organohalogen compound, containing iron particles comprising iron and iron oxide, wherein the iron particles have a metallic iron content of 15% or more by mass, wherein the metallic iron content is a content of metallic iron in the outermost surface layer of the iron particles to which the ion beam etching has been applied twice under the following etching conditions: degree of vacuum in a chamber: 2.0×10?2 Pa accelerating voltage of an ion gun: 10 kV emission current: 10 mA etching time: 14 seconds. The decomposer need not contain copper and has the ability to satisfactorily decompose an organohalogen compound. A method for producing the decomposer is also provided.