Abstract: A lead-acid battery is disclosed. The lead-acid battery has a container with a cover and includes one or more compartments. One or more cell elements are provided in the one or more compartments. The one or more cell elements comprise a positive electrode, the positive electrode having a positive substrate and a positive electrochemically active material on the positive substrate; a negative electrode, the negative electrode having a negative substrate and a negative active mass on the negative substrate, wherein the negative active mass comprises a leady oxide, a synthetic organic expander, a very fine particle barium sulfate, and plurality of conductive carbons; and an absorbent glass mat separator between the positive plate and the negative plate. Electrolyte is provided within the container. One or more terminal posts extend from the container or the cover and are electrically coupled to the one or more cell elements.

Abstract: The disclosure relates to the manufacturing of a lead-acid battery that includes a composite that includes lead oxide and a nanomaterial. A method of preparing the composite is disclosed. In one embodiment, an in-situ sol-gel reaction of a solution occurs in the presence of lead oxide to produce a composite that includes the lead oxide and a nanomaterial (e.g., a nano-oxide). The solution may include a precursor that includes metal alkoxide or silicate. The composite may include the lead oxide and the nanomaterial dispersed or distributed among particles of the lead oxide. A lead-acid battery may be manufactured using the composite. Various properties of a lead-acid battery may be improved by using the composite as part of the active material including a longer life expectancy, increased specific energy and increased power-to-weight ratio.

Abstract: The disclosure relates to the manufacturing of a lead-acid battery that includes a composite that includes lead oxide and a nanomaterial. A method of preparing the composite is disclosed. In one embodiment, an in-situ sol-gel reaction of a solution occurs in the presence of lead oxide to produce a composite that includes the lead oxide and a nanomaterial (e.g., a nano-oxide). The solution may include a precursor that includes metal alkoxide or silicate. The composite may include the lead oxide and the nanomaterial dispersed or distributed among particles of the lead oxide. A lead-acid battery may be manufactured using the composite. Various properties of a lead-acid battery may be improved by using the composite as part of the active material including a longer life expectancy, increased specific energy and increased power-to-weight ratio.

Abstract: In an embodiment, an apparatus includes a battery shaped to be situated within a housing. The battery has a shape that substantially conforms to a shape of a cavity that is defined at least in part by a non-cylindrical curved portion of the housing. The battery includes a contoured conductive mesh formed by shaping a substantially planar conductive mesh to include at least one curved conductive mesh portion. Other embodiments are described and claimed.

Abstract: An auxiliary electrode for a lithium-ion battery includes a lithium source material. The auxiliary electrode is configured to selectively couple to a negative electrode of a lithium-ion battery to provide lithium for formation of a solid-electrolyte-inter-phase layer on a negative electrode.

Abstract: Methods and apparatus for detecting abnormality of a battery pack are disclosed. The battery pack includes multiple battery cells coupled in series via at least one connecting wire. A first voltage drop between a positive electrode and a negative electrode of the battery pack is detected. A first set of voltage drops between a positive electrode and a negative electrode of each battery cell in the battery pack is also detected. A total voltage drop across the at least one connecting wire in the battery pack is calculated based on an absolute difference between the first voltage drop and a sum of the first set of voltage drops. Whether the battery pack is abnormal is determined by assessing the total voltage drop across the at least one connecting wire with respect to a predetermined threshold.

Abstract: A mounting structure for an in-vehicle power battery may be provided. The mounting structure may comprise an upper cover (3), a suspension tray (1) and a bracket device (2) for supporting at least a part of a peripheral bottom portion of the suspension tray (1). The suspension tray (1) may be hermetically connected with the upper cover (3), forming a sealed space for receiving the power battery. The bracket device (2) may be detachably fixed to a bottom surface of the body floor. Further, a vehicle (100) comprising the mounting structure described above may also be provided.

Abstract: An energy storage device comprising at least one negative electrode, wherein each negative electrode is individually selected from (i) an electrode comprising negative battery electrode material; (ii) an electrode comprising capacitor electrode material; (iii) a mixed electrode comprising either—a mixture of battery and capacitor electrode material or—a region of battery electrode material and a region of capacitor electrode material, or—a combination thereof, and wherein the energy storage device either comprises at least one electrode of type (iii), or comprises at least one electrode of each of types (i) and (ii),—at least one positive electrode, wherein the positive electrode comprises positive battery electrode material and a charging ability-increasing additive, such as one or a mixture of: (a) carbon nanomaterial, vapor grown carbon fiber, fullerene, or a mixture thereof, and (b) tin dioxide conductive materials.

Abstract: An antimony based anode material for a rechargeable battery comprises nanoparticles of composition SbMxOy where M is a further element selected from the group consisting of Sn, Ni, Cu, In, Al, Ge, Pb, Bi, Fe, Co, Ga, with 0?x<2 and 0?y?2.5+2x. The nanoparticles form a substantially monodisperse ensemble with an average size not exceeding a value of 30 nm and by a size deviation not exceeding 15%. A method for preparing the antimony based anode material is carried out in situ in a non-aqueous solvent and starts by reacting an antimony salt and an organometallic amide reactant and oleylamine.

Abstract: A lead-acid battery of the present invention includes electrode plate units, each including a positive electrode plate, a negative electrode plate, and a separator. The positive electrode plate is a positive electrode grid filled with paste including powder of lead oxide as a main component. The negative electrode plate is a negative electrode grid filled with paste including powder of lead oxide as a main component, and including carbon black. The positive electrode plate faces the negative electrode plate. The separator is provided between the positive electrode plate and the negative electrode plate. The positive electrode grid includes gates, each being generally diamond-shaped, and being more than or equal to 50 mm2 and less than or equal to 100 mm2 in area. The carbon black has a DBP oil absorption of more than or equal to 140 ml/100 g and less than or equal to 340 ml/100 g.

Abstract: The present invention provides a process for producing a graphene-enhanced anode active material for use in a lithium battery. The process comprises (a) providing a continuous film of a graphene material into a deposition zone; (b) introducing vapor or atoms of a precursor anode active material into the deposition zone, allowing the vapor or atoms to deposit onto a surface of the graphene material film to form a sheet of an anode active material-coated graphene material; and (c) mechanically breaking this sheet into multiple pieces of anode active material-coated graphene; wherein the graphene material is in an amount of from 0.1% to 99.5% by weight and the anode active material is in an amount of at least 0.5% by weight, all based on the total weight of the graphene material and the anode active material combined.

Abstract: The present invention provides an anode electrode of a lithium-ion battery, comprising an anode active material-coated graphene sheet, wherein the graphene sheet has two opposed parallel surfaces and at least 50% area of one of the surfaces is coated with an anode active material and wherein the graphene material is in an amount of from 0.1% to 99.5% by weight and the anode active material is in an amount of at least 0.5% by weight (preferably at least 60%), all based on the total weight of the graphene material and the anode active material combined.

Abstract: This invention provides a nanocomposite-based lithium battery electrode comprising: (a) A porous aggregate of electrically conductive nano-filaments that are substantially interconnected, intersected, physically contacted, or chemically bonded to form a three-dimensional network of electron-conducting paths, wherein the nano-filaments have a diameter or thickness less than 1 ?m (preferably less than 500 nm); and (b) Sub-micron or nanometer-scale electro-active particles that are bonded to a surface of the nano-filaments with a conductive binder material, wherein the particles comprise an electro-active material capable of absorbing and desorbing lithium ions and wherein the electro-active material content is no less than 25% by weight based on the total weight of the particles, the binder material, and the filaments. Preferably, these electro-active particles are coated with a thin carbon layer. This electrode can be an anode or a cathode.

Abstract: The invention relates to Chevrel-phase materials and methods of preparing these materials utilizing a precursor approach. The Chevrel-phase materials are useful in assembling electrodes, e.g., cathodes, for use in electrochemical cells, such as rechargeable batteries. The Chevrel-phase materials have a general formula of Mo6Z8 and the precursors have a general formula of MxMo6Z8. The cathode containing the Chevrel-phase material in accordance with the invention can be combined with a magnesium-containing anode and an electrolyte.

Abstract: Disclosed is an electrode for secondary batteries including an electrode mixture including an electrode active material, binder and conductive material coated on a current collector wherein a conductive material is coated to a thickness of 1 to 80 ?m on the current collector and the electrode mixture is coated on a coating layer of the conductive material so as to improve electrical conductivity.

Abstract: Disclosed are a method of manufacturing an electrode for secondary batteries that includes surface-treating a current collector so as to have a morphology wherein a surface roughness Ra of 0.001 ?m to 10 ?m is formed over the entire surface thereof to enhance adhesion between an electrode active material and the current collector and an electrode for secondary batteries that is manufactured using the method.

Abstract: A composite particle is provided. The particle comprises a first particle component and a second particle component in which: (a) the first particle component comprises a body portion and a surface portion, the surface portion comprising one or more structural features and one or more voids, whereby the surface portion and body portion define together a structured particle; and (b) the second component comprises a removable filler; characterised in that (i) one or both of the body portion and the surface portion comprise an active material; and (ii) the filler is contained within one or more voids comprised within the surface portion of the first component.

Abstract: An additive for producing positive active compositions for lead accumulators based on finely divided 4-basic lead sulphate having an average particle size of less than about 3 ?m and also finely divided silica, where the additive additionally contains red lead (2PbO.PbO2), is described. The finely divided silica prevents, in particular, agglomeration of the particles of the 4-basic lead sulphate, while the red lead leads to an optimized distribution of all constituents of the additive in the battery paste. The use of red lead also gives a cost advantage. Despite the replacement of part of the 4-basic lead sulphate by red lead, the properties achieved in the later use in battery operation are no worse. Thus, the batteries display, for example, improved charging behavior and a higher high-current discharging stability.

Abstract: The lead-acid battery of the present invention includes electrode plate units, each including a positive electrode plate, negative electrode plate, and a separator. The positive electrode plate is a positive electrode grid filled with paste of lead suboxide powder. The negative electrode plate is a negative electrode grid filled with paste of lead suboxide powder and carbon black. The positive electrode plate faces the negative electrode plate. The separator is provided between the positive electrode plate and the negative electrode plate. The amount of DBP oil absorption of the carbon black is more than or equal to 140 ml/100 g and less than or equal to 340 ml/100 g. The negative electrode plates are joined together by a strap of a lead alloy substantially without antimony.

Abstract: The present disclosure relates to an anode active material comprising a composite of a core-shell structure, a lithium secondary battery comprising the same, and a method of manufacturing the anode active material. According to an aspect of the present disclosure, there is provided an anode active material of a core-shell structure comprising a core including alloyed (quasi)metal oxide-Li (MOx—Liy) and a shell including a carbon material coated on a surface of the core. According to another aspect of the present disclosure, there is provided a method of manufacturing the anode active material of the core-shell structure. According to an aspect of the present disclosure, an anode active material with high capacity, excellent cycle characteristics and volume expansion control capacity, and high initial efficiency is provided.

Abstract: This invention relates to a negative electrode material for lithium-ion batteries comprising silicon and having a chemically treated or coated surface influencing the zeta potential of the surface. The active material consists of particles or particles and wires comprising a core (11) comprising silicon, wherein the particles have a positive zeta potential in an interval between pH 3.5 and 9.5, and preferably between pH 4 and 9.5. The core is either chemically treated with an amino-functional metal oxide, or the core is at least partly covered with OySiHx groups, with 1<x<3, 1<y<3, and x>y, or is covered by adsorbed inorganic nanoparticles or cationic multivalent metal ions or oxides.

Abstract: An anode, a lithium battery including the anode, and a method of manufacturing the anode. The anode includes: an anode active material including a metal alloyable with lithium; and a metal-carbon composite conducting agent having a density of 3.0 grams per cubic centimeter or greater.

Abstract: An electrochemical storage device comprises a plurality of layer electrodes, wherein each layer electrode includes a first charged sector and a second charged sector, wherein the second charged sector is charged oppositely compared to the first charged sector, and wherein the plurality of layer electrodes are assembled with respect to each other such that the first charged sector of a first plate of the plurality of layer electrodes is laid below the second charged sector of a second plate of the plurality of layer electrodes located immediately above the first plate, wherein the charges of the first charged sectors of the first and second plates have a first sign and the charges of the second charged sectors of the first and second plates have a second sign that is opposite the first sign; a separator sector located, and enabling ionic charge exchange between the first charged sector of the first plate and the second charged sector of the second plate.

Abstract: The present disclosure provides an embodiment of an integrated structure that includes a first electrode of a first conductive material embedded in a first semiconductor substrate; a second electrode of a second conductive material embedded in a second semiconductor substrate; and a electrolyte disposed between the first and second electrodes. The first and second semiconductor substrates are bonded together through bonding pads such that the first and second electrodes are enclosed between the first and second semiconductor substrates. The second conductive material is different from the first conductive material.

Abstract: There is disclosed a lead storage battery comprising a group of plates housed in a battery jar, and an electrolyte injected therein to impregnate the group of plates with the electrolyte, thus performing formation treatment, the lead storage battery being adapted to be used in a partial state of charge where the state of charge is confined within the range of more than 70% to less than 100%, wherein the group of plates are formed of a stack constituted by a large number of negative substrates comprising grid substrates filled with a negative active material, by a large number of positive substrates comprising grid substrates filled with a positive active material, and by a porous separator interposed between the negative electrodes and positive electrodes, and the electrolyte contains at least one kind of ion selected from the group consisting of aluminum ions, selenium ions and titanium ions.

Abstract: An Advanced Graphite, with a lower degree of ordered carbon domains and a surface area greater than ten times that of typical battery grade graphites, is used in negative active material (NAM) of valve-regulated lead-acid (VRLA) type Spiral wound 6V/25 Ah lead-acid batteries. A significant and unexpected cycle life was achieved for the Advanced Graphite mix where the battery was able to cycle beyond 145,000 cycles above the failure voltage of 9V in a non-stop, power-assist cycle-life test. Batteries with Advanced Graphite also showed increased charge acceptance power and discharge power compared to control groups.

Abstract: Provided is a composite including lead oxide particles (PbO2) and functionalized carbon nanotubes (CNTs).

Abstract: Provided are a composite and a method of preparing an anode slurry including the same. More particularly, the present invention provides a composite including a (semi) metal oxide, a conductive material on a surface of the (semi) metal oxide, and a binder, and a method of preparing an anode slurry including preparing a composite by dispersing a conductive material in an aqueous binder and then mixing with a (semi) metal oxide, and mixing the composite with a carbon material and a non-aqueous binder.

Abstract: Provided are a composite for an anode active material and a method of preparing the same. More particularly, the present invention provides a composite for an anode active material including a (semi) metal oxide and an amorphous carbon layer on a surface of the (semi) metal oxide, wherein the amorphous carbon layer comprises a conductive agent, and a method of preparing the composite.

Abstract: Provided are a porous composite expressed by Chemical Formula 1 and having a porosity of 5% to 90%, and a method of preparing the same: MOx??<Chemical Formula 1> where M and x are the same as described in the specification. According to the present invention, since a molar ratio (x) of oxygen to a molar ratio of (semi) metal in the porous composite is controlled, an initial efficiency of a secondary battery may be increased. Also, since the porous composite satisfies the above porosity, a thickness change rate of an electrode generated during charge and discharge of the secondary battery may be decreased and lifetime characteristics may be improved.

Abstract: Positive active material pastes for flooded deep discharge lead-acid batteries, methods of making the same and lead-acid batteries including the same are provided. The positive active material paste includes lead oxide, a sulfate additive, and an aqueous acid. The positive active material paste contains from about 0.1 to about 1.0 wt % of the sulfate additive. Batteries using such positive active material pastes exhibit greatly improved performance over batteries with conventional positive active material pastes.

Abstract: A composite cathode active material, a method of preparing the composite cathode active material, and a cathode and a lithium battery each including the composite cathode active material. The composite cathode active material includes a core including a lithium intercalatable oxide which enables intercalation and deintercalation of lithium; and a coating layer disposed on at least a portion of the core, wherein the conductive layer includes a lithium metal oxide which is an inactive lithium ion conductor, and wherein the lithium metal oxide contains a metal which has an atomic weight of 27 Daltons or more and is selected an element of Groups 3 to 14 of the Periodic Table of the Elements.

Abstract: A cathode composite material includes a cathode active material and a coating layer coated on a surface of the cathode active material. The cathode active material includes a layered type lithium transition metal oxide. A material of the coating layer is a lithium metal oxide having a crystal structure belonging to C2/c space group of the monoclinic crystal system. The present disclosure also relates to a lithium ion battery including the cathode composite material.

Abstract: Embodiments of the invention provide batteries, electrodes, and methods of making the same. According to one embodiment, a battery may include a positive plate having a grid pasted with a lead oxide material, a negative plate having a grid pasted with a lead based material, a separator separating the positive plate and the negative plate, and an electrolyte. A nonwoven glass mat may be in contact with a surface of either or both the positive plate or the negative plate to reinforce the plate. The nonwoven glass mat may include a plurality of first coarse fibers having fiber diameters between about 6 ?m and 11 ?m and a plurality of second coarse fibers having fiber diameters between about 10 ?m and 20 ?m.

Abstract: Provided is an anode active material including lithium metal oxide particles having an internal porosity ranging from 3% to 8% and an average particle diameter (D50) ranging from 5 ?m to 12 ?m. According to the present invention, since the high-density lithium metal oxide particles are included, the adhesion to an anode may be significantly improved even by using the same or smaller amount of a binder that is required during the preparation of an anode slurry, and high rate characteristics of a secondary battery may be improved by decreasing the average particle diameter of the lithium metal oxide particles.

Abstract: An electrode plate for a battery comprising a plurality of electrodes in a grid where the grid defines a plurality of spaces. A paste disposed in the spaces has a top surface and a bottom surface. The paste is narrowed in the space, defining a distance between the top surface of the paste and the bottom surface of the paste that is less than the thickness of the plate over the electrodes. A retention layer of porous fabric is impressed on the top and/or bottom surface of the paste. Electrolyte disposed in electric communication with the electrodes.

Abstract: Disclosed is an anode active material comprising a lithium metal oxide represented by the following Formula 1, wherein the anode active material is surface-coated with a silane compound and a silicon content of the silane compound is 0.01 to 5% by weight, based on the total amount of the anode active material: LiaM?bO4?cAc??(1) wherein M? is at least one element selected from the group consisting of Ti, Sn, Cu, Pb, Sb, Zn, Fe, In, Al and Zr; a and b are determined according to an oxidation number of M? within ranges of 0.1?a?4 and 0.2?b?4; c is determined according to an oxidation number within a range of 0?c<0.2; and A is at least one monovalent or bivalent anion. Disclosed is also a secondary battery comprising the same.

Abstract: A carbon black having a combination of properties with values in ranges selected to promote high conductivity, high hydrophobicity, and reduced outgassing in lead acid batteries while maintaining high charge acceptance and cycleability. The carbon black has a Brunauer-Emmett-Teller (BET) surface area ranging from 100 m2/g to 1100 m2/g combined with one or more properties, e.g., a surface energy (SE) of 10 mJ/m2 or less, and/or a Raman microcrystalline planar size (La) of at least 22 ?, e.g., ranging from 22 ? to 50 ?. In some cases, the carbon black has a statistical thickness surface area (STSA) of at least 100 m2/g, e.g., ranging from 100 m2/g to 600 m2/g.

Abstract: Provided is an electrochemical device comprising multi-stacked unit cells of full cells or bicells and a separation film disposed therebetween, whereby the separation film and separators are alternately stacked between electrode layers with an opposite polarity. Herein, as the separation film is formed of a material having a higher thermal shrinkage rate than that of the separator, the thermal stability of the device can be secured by stable induction of shutdown via thermal behavior of the separation film, without causing short-circuiting due to thermal shrinkage of the separator even when a temperature of a battery suddenly rises by internal or external factors.

Abstract: A secondary battery includes: a fiber negative electrode having a surface on which a negative electrode active material coating is formed, the coating containing a compound of AaMbXcZd; a fiber positive electrode including a positive electrode active material coating containing nickel hydroxide; an aqueous electrolyte solution; and a separator. The negative electrode coating has an uncoated surface. A is selected from the group consisting of Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr, and Ba; M is selected from the group consisting of Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Nb, Mo, Ru, Pd, Ag, Ta, W, Pr, Sm, Eu, and Pb; X is selected from the group consisting of B, Al, Si, P, S, Ga, and Ge; Z is selected from the group consisting of O, S, N, F, Cl, Br, and I; and 0?a?6, 1?b?5, 0?c?4, 0<d?12, and 0?a/b?4.

Abstract: A negative active material, a method for preparing the negative active material and a lithium ion battery comprising the same are provided. The negative active material may comprise: a core, an intermediate layer consisting of a first material and an outmost layer consisting of a second material, which is coated on a surface of the intermediate layer. The first material may be at least one selected from the group consisting of the elements that form alloys with lithium, and the second material may be at least one selected from the group consisting of transition metal oxides, transition metal nitrides and transition metal sulfides.

Abstract: A positive electrode for a lithium-ion secondary battery includes a positive-electrode mixture layer, which includes a positive-electrode active material containing lithium composite oxide, a conductive material, and a binder, and a current collector. The positive-electrode mixture layer contains a compound including sulfur and/or phosphorous, a first polymer serving as a main binder, and a second polymer different from the first polymer.

Abstract: An anode protector of a lithium-ion battery and a method for fabricating the same are provided. A passivation protector (110) is formed on a surface of an anode (102) in advance by film deposition, such as atomic layer deposition (ALD). The passivation protector (110) is composed of a metal oxide having three dimensional structures, such as columnar structures. Accordingly, the present invention is provided with effective protection of the anode electrode structure and maintenance of battery cycle life under high-temperature operation.

Abstract: Positive active material pastes for flooded deep discharge lead-acid batteries, methods of making the same and lead-acid batteries including the same are provided. The positive active material paste includes lead oxide, a sulfate additive, and an aqueous acid. The positive active material paste contains from about 0.1 to about 1.0 wt % of the sulfate additive. Batteries using such positive active material pastes exhibit greatly improved performance over batteries with conventional positive active material pastes.

Abstract: Lithium-ion battery comprising: (a) a positive electrode comprising an amorphous chalcogenide which comprises lithium ions or which can conduct lithium ions; (b) a negative electrode; (c) a separator between the positive electrode and the negative electrode, wherein the separator comprises a non-woven material composed of fibres, preferably polymer fibres; (d) a non-aqueous electrolyte.

Abstract: An electrode active material includes a core capable of intercalating and deintercalating lithium; and a surface treatment layer disposed on at least a portion of a surface of the core, wherein the surface treatment layer includes a lithium-free oxide having a spinel structure, and an intensity of an X-ray diffraction peak corresponding to impurity phase of the lithium-free oxide, when measured using Cu—K? radiation, is at a noise level of an X-ray diffraction spectrum or less.

Abstract: Positive active material pastes for flooded deep discharge lead-acid batteries, methods of making the same and lead-acid batteries including the same are provided. The positive active material paste includes lead oxide, a sulfate additive, and an aqueous acid. The positive active material paste contains from about 0.1 to about 1.0 wt % of the sulfate additive. Batteries using such positive active material pastes exhibit greatly improved performance over batteries with conventional positive active material pastes.

Abstract: Provided are an anode active material for a lithium secondary battery, a method for preparing same, and a lithium secondary battery including same. An anode active material for a lithium secondary battery according to the present invention includes: active particles by means of which lithium ions may be absorbed/released; and a coating layer coated on the surface of the active particles, wherein the coating layer includes a first material which is a hollow nanofiber and a second material which is a carbon precursor or LTO.

Abstract: A lithium ion secondary battery is provided with a positive electrode, a negative electrode containing an active material, and an electrolytic solution, wherein the active material includes a core portion capable of occluding and releasing lithium ions, an amorphous or low-crystalline coating portion disposed on at least a part of the surface of the core portion, and a fibrous carbon portion disposed on at least a part of the surface of the coating portion, and the coating portion contains Si and O as constituent elements, while the atomic ratio y (O/Si) of O relative to Si satisfies 0.5?y?1.8.

Abstract: A lead-acid battery comprising: at least one lead-based negative electrode; at least one lead dioxide-based positive electrode; at least one capacitor electrode; and electrolyte in contact with the electrodes; wherein a battery part is formed by the lead based negative electrode and the lead dioxide-based positive electrode; and an asymmetric capacitor part is formed by the capacitor electrode and one electrode selected from the lead based negative electrode and the lead-dioxide based positive electrode; and wherein all negative electrodes are connected to a negative busbar, and all positive electrodes are connected to a positive busbar. The capacitor electrode may be a capacitor negative electrode comprising carbon and an additive mixture selected from oxides, hydroxides or sulfates of lead, zinc, cadmium, silver and bismuth, or a capacitor negative electrode comprising carbon, red lead, antimony in oxide, hydroxide or sulfate form, and optionally other additives.