Lg Chem, Ltd

Lg Energy Solution, Ltd.

Sk on Co., Ltd.

Samsung Electronics Co., Ltd.

Korea Advanced Institute of Science and Technology

Sk Innovation Co., Ltd.

Lg Chern, Ltd.

Min Suk Kang

Wang Mo Jung

Sang Beom Lee

Sang Wook Lee

So Ra Baek

Eun Sol Lho

Sun Sik Shin

Chi Ho Jo

Ji Hoon Ryu

Joon Ho Shin

Chi Hyun Jang

Wen Xiu Wang

Dong Hun Lee

Min Gu Kang

Hye Lim Jeon

Kwang Ho Lee

Sung Ho Lee

Dong Won Lee

Soo Ho Kim

Jong Hyung Kwun

Chan Ho Min

Young Hyun Jeon

Ji Yae Do

Min Cheol Beak

Hyu Dae Kim

Sang Min Park

Byung Chun Park

Tae Soo Kwon

Dong Ho Cho

Chul Han Park

Ji Young Park

Tak Ki Yu

Yong Hyun Cho

Ju Kyung Shin

Sang Han Lee

In Yong Jeong

Woo Geun Ahn

Ji Hyang Son

Yoon Ji Lee

Bang Chul Jung

Jae Young Choi

Wan Uk Choi

A cathode for a lithium secondary battery includes a cathode current collector, and a cathode active material layer including a first cathode active material layer and a second cathode active material layer sequentially stacked on the cathode current collector. The first cathode active material layer includes a first cathode active material particle having a secondary particle structure, and the second cathode active material layer includes a second cathode active material particle having a single particle shape. An adhesive force of the first cathode active material layer to a surface of the cathode current collector is greater than an adhesive force of the second cathode active material layer to a surface of the first cathode active material layer.

Cathode for lithium secondary battery and lithium secondary battery including the same

A cathode active material for a lithium secondary battery according to an embodiment of the present disclosures a plurality of composite particles, each of which comprises a lithium metal phosphate particle, and a carbon coating formed on at least a portion of a surface of the lithium metal phosphate particle. A standard deviation of thickness values of the carbon coating measured by an X-ray photoelectron spectroscopy (XPS) for five different composite particles of the plurality of composite particles is 15 nm or less.

Cathode active material for lithium secondary battery and lithium secondary battery including the same

A positive electrode active material for a secondary battery includes a lithium composite transition metal oxide including nickel (Ni), cobalt (Co), and manganese (Mn), and a glassy coating layer formed on surfaces of particles of the lithium composite transition metal oxide, wherein, in the lithium composite transition metal oxide, an amount of the nickel (Ni) in a total amount of transition metals is 60 mol % or more, and an amount of the manganese (Mn) is greater than an amount of the cobalt (Co), and the glassy coating layer includes a glassy compound represented by Formula 1.LiMO  [Formula 1]

Positive electrode active material for secondary battery, method of preparing the same, and lithium secondary battery including the positive electrode active material

In one arrangement, the present disclosure relates to a positive electrode active material including a nickel-cobalt-manganese-based lithium transition metal oxide which contains nickel in an amount of 60 mol % or more based on a total number of moles of metals excluding lithium, wherein the nickel-cobalt-manganese-based lithium transition metal oxide is doped with doping element M(where the doping element Mis a metallic element including Al) and doping element M(where the doping element Mis at least one metallic element selected from the group consisting of Mg, La, Ti, Zn, B, W, Ni, Co, Fe, Cr, V, Ru, Cu, Cd, Ag, Y, Sc, Ga, In, As, Sb, Pt, Au, and Si), where the doping element Mcan be in an amount of 100 ppm to 10,000 ppm, and the doping element Mand the doping element Mare included in a weight ratio of 50:50 to 99:1.

Positive electrode active material, and positive electrode and lithium secondary battery which include the positive electrode active material

Cathode active materials for lithium secondary batteries and lithium secondary batteries including the cathode active materials are disclosed. In some implementations, a cathode active material for a lithium secondary battery includes a lithium metal phosphate particle having a crystallite size in a range from 150 nm to 450 nm in a direction of a crystallographic plane (020) as measured by an X-ray diffraction (XRD) analysis. In some implementations, a lithium secondary battery includes a cathode including a cathode active material layer that includes a cathode active material for a lithium secondary battery, and an anode facing the cathode. In some implementations, an electrode crystallite size ratio defined by Equation 4 is in a range from 0.5 to 0.9.

Provided is a method of decomposing phenol-based by-product, and more particularly, a method of decomposing phenol-based by-product including: introducing a phenol-based by-product stream, a first stream of a side discharge stream from a decomposition device, and a process water stream to a mixing device and mixing the streams; introducing a discharge stream from the mixing device to a layer separation device to phase-separate the discharge stream into an oil phase and an aqueous phase; passing an oil stream discharged from the layer separation device through any one or more of a first heat exchanger and a second heat exchanger and introducing the oil stream to the decomposition device to carry out decomposition; and supplying the first stream of the side discharge stream from the decomposition device to the mixing device, forming a mixed stream of a second stream of the side discharge stream with a lower discharge stream and discharging the mixed stream, and recovering effective components from an upper discharge stream.

Method for decomposing phenol-based by-product

A method of washing an ion exchange resin, including washing an ion exchange resin with deionized water (DI water) one or more times to prepare a washed ion exchange resin; and storing the washed ion exchange resin in dionized water. A method for producing bisphenol A using the method of washing an ion exchange resin. The resulting bisphenol A has improved purity, thermal stability, color, and the like.

Method for washing ion exchange resin and method for preparing bisphenol A

The present invention provided a positive electrode active material for a lithium secondary battery including lithium cobalt oxide particles. The lithium cobalt oxide particles include lithium deficient lithium cobalt oxide having Li/Co molar ratio of less than 1, belongs to an Fd-3m space group, and having a cubic crystal structure, in surface of the particle and in a region corresponding to a distance from 0% to less than 100% from the surface of the particle relative to a distance (r) from the surface to the center of the particle. In the positive electrode active material for a lithium secondary battery according to the present invention, the intercalation and deintercalation of lithium at the surface of a particle may be easy, and the output property and rate characteristic may be improved when applied to a battery. Accordingly, good life property and the minimization of gas generation amount may be attained even with large sized positive electrode active material.

Positive electrode active material for lithium secondary battery, method of preparing the same and lithium secondary battery including the same

The present disclosure relates to a positive electrode active material for a secondary battery, the positive electrode active material being a lithium composite transition metal oxide particle including nickel (Ni) and cobalt (Co) and including at least one of manganese (Mn) and aluminum (Al), wherein the lithium composite transition metal oxide particle includes 60 mol % or greater of the nickel (Ni) in all metals excluding lithium, a doping element is doped on the lithium composite transition metal oxide particle, and the particle intensity of the lithium composite transition metal oxide particle is 210 MPa to 290 MPa.

Positive electrode active material for secondary battery, preparation method thereof, and positive electrode for secondary battery including same

A lithium secondary battery according to an embodiment of the present invention includes an electrode assembly including a separation layer, and a plurality of cathodes and a plurality of anodes separated by the separation layer and repeatedly stacked, and a gas adsorption layer coated on a single surface of an outermost anode among the plurality of anodes.

Lithium secondary battery

Provided is a method of decomposing phenolic by-products, and more particularly, a method of decomposing phenolic by-products including: supplying a phenolic by-product stream to a decomposition device to perform thermal decomposition; separating an upper discharge stream including effective components and a lower discharge stream including materials having a high boiling point in the decomposition device; supplying the lower discharge stream from the decomposition device, a side discharge stream from the decomposition device, and a process water stream to a mixing device and mixing these streams; and supplying a discharge stream from the mixing device to a layer separation device to separate the discharge stream from the mixing device into an oil phase and an aqueous phase.

Method of decomposing phenolic by-products

A cathode active material for a lithium secondary battery according to an embodiment of the present invention includes a lithium composite oxide particle that contains lithium and transition metals including an excess amount of nickel. The lithium composite oxide particle satisfies a predetermined XRD peak area relation. A lithium secondary battery using the cathode active material and providing improved stability and durability is provided.

The present disclosure provides a method for decomposing a phenolic by-product, the method including: a step S10 of injecting and mixing a bisphenol A by-product produced in a bisphenol A production process, a mixed by-product stream of phenol by-products produced in a phenol production process, a decomposition apparatus side discharge stream, and a process water stream in a mixing apparatus; a step S20 of injecting a mixing apparatus discharge stream discharged from the mixing apparatus into a phase separation apparatus and phase-separating the mixing apparatus discharge stream into an oil-phase stream and a liquid-phase stream; a step S30 of feeding the oil-phase stream, which is phase-separated in the step S20 and discharged from the phase separation apparatus, to a decomposition apparatus to decompose the oil-phase stream; and a step S40 of circulating the decomposition apparatus side discharge stream obtained by the decomposition in the step S30 to the mixing apparatus in the step S10.

Method for decomposing phenolic by-product

The present disclosure relates to a method of decomposing a phenolic by-product, including: a step of feeding and thermally cracking a phenolic by-product stream to and in a decomposition apparatus, recovering an active ingredient from a top discharge stream, and discharging a high-boiling substance through a bottom discharge stream; a step of pressurizing each of a side discharge stream of the decomposition apparatus and a bottom discharge stream of the decomposition apparatus; a step of mixing the pressurized side discharge stream of the decomposition apparatus and the pressurized bottom discharge stream of the decomposition apparatus with each other to form a mixed stream; and a step of passing a part of the mixed stream through a reboiler, circulating the part of the mixed stream to the decomposition apparatus, and discharging a residual mixed stream.

Method of decomposing phenolic by-product

Growing community of inventors

Daejeon, South Korea

Min Suk Kang