IP Library Granted Patent US 9,359,219
Granted Patent B1
US 9,359,219 · App. 14/880,010 · Granted Jun 7, 2016

Surface-modified cyanide-based transition metal compounds

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Quick Facts
Patent No.
US 9,359,219
App. No.
14/880,010
Granted
Jun 7, 2016
Kind
B1
Abstract

A system, method, and articles of manufacture for a surface-modified transition metal cyanide coordination compound (TMCCC) composition, an improved electrode including the composition, and a manufacturing method for the composition. The composition, compound, device, and uses thereof according to A x Mn (y-k) M j k [Mn m (CN) (6-p-q) (NC) p (Che) r q ] z . (Che) r w (Vac) (1-z) .nH 2 O (wherein Vac is a Mn(CN) (6-p-q) (NC) p (Che) r q vacancy); wherein Che is an acid chelating agent; wherein: A=Na, K, Li; and M=Mg, Al, Ca, Sc, Ti, V, Cr, Fe, Co, Ni, Cu, Zn, Ga, Pd, Ag, Cd, In, Sn, Pb; and wherein 0<j≦4; 0≦k≦0.1; 0≦(p+q)<6; 0<x≦4; 0≦y≦1; 0<z≦1; 0<w≦0.2; 0<n≦6; −3≦r≦3; and wherein: x+2(y−k)+jk+(m+(r+1)q−6)z+wr=0.

Claims (16)

1. A method for manufacturing an environment-stabilized transition metal cyanide coordination compound (TMCCC) material, comprising:

a) producing a particulated TMCCC material; and thereafter

b) combining the particulated TMCCC material with a solution including a material containing an acid group to produce a stabilized TMCCC material;

wherein said stabilized TMCCC material includes:

at least one composition represented by Formula I:

A x Mn (y-k) M j k [Mn m (CN) (6-p-q) (NC) p (Che) r q ] z .(Che) r w (Vac) (1-z) .n H 2 O  (Formula I)

wherein, in Formula I, each A is an independently selected alkali metal Li, Na, or K; and each dopant M may optionally be at least one independently selected alkaline earth metal Mg or Ca, post-transition metal Al, Ga, In, Sn, or Pb, or transition metal Sc, Ti, V, Cr, Fe, Co, Ni, Cu, Zn, Pd, Ag, or Cd having an average valence j; and Che represents an acid chelating agent which includes ligand binding atoms that form one or more covalent linkages with Mn or with Mn and M; and

wherein 0<j≦4, 0≦k≦0.1, 0≦(p+q)≦6, 0<x≦4, 0<y≦1, 0<z≦1, 0<w≦0.2; −3≦r≦3; and 0≦n≦6;

wherein x+2(y−k)+jk+(m+(r+1)q−6)z+wr=0; and

wherein Formula I includes one or more Mn(CN) (6-p-q) (NC) p (Che) r q complexes each including an Mn atom, and wherein p is an average number of NC groups found in said one or more Mn(CN) (6-p-q) (NC) p (Che) r q complexes; and

wherein q is an average number of Che groups found in said one or more Mn(CN) (6-p-q) (NC) p (Che) r q complexes; and

wherein m is an average valence of said Mn atoms found in said one or more Mn(CN) (6-p-q) (NC) p (Che) r q complexes;

wherein (Vac) identifies a Mn(CN) (6-p-q) (NC) p (Che) r q vacancy

wherein CN identifies a cyano group; and

wherein NC identifies an isocyano group.

2. The method of claim 1 wherein said solution comprises one or more components selected from the group consisting of formic acid, acetic acid, gluconic acid, malic acid, citric acid, homo citric acid, succinic acid, lactic acid, malonic acid, aspartic acid, 3,4-dihydroxybenzoic acid, 2,3-dihydroxybenzoic acid, tartaric acid, salicylic acid, glutamic acid, oxalic acid, 2,3-Di mercapto-1-propane sulfonic acid, meso-2,3-di mercapto succinic acid, glycine, alanine, imino di acetic acid, EDTA (ethylene diamine tetra-acetic acid), EGTA ethylene glycol-bis(2-amino ethyl ether)-N,N,N′,N′-tetra acetic acid), EDDS (ethylene di amine-N,N′-di succinic acid), NTA (nitrilo-tri-acetic acid), DTPA (diethyl triamine penta-acetic acid), PDTA (1,3-propylene diamine penta-acetic acid), MGDA (methyl glycine diacetic acid), β-ADA (β-alanine diacetic acid), HEIDA (N-(2-hydroxyethyl)imino diacetic acid), DHEG (N,N-bis(2-hydroxyethyl)glycine), HEDTA (hydroxy ethyl-ethylene diamine tri-acetic acid), quadrol (N,N,N′,N′-tetrakis-2-hydroxyisopropyl-ethylendiamine), DTPMP (diethylene triaminopenta (methylene phosphonic acid)), EDTMP (ethylene diaminotetra(methylene phosphonic acid)), HDTMP (hexamethylene diaminotetra (methylene phosphonic acid)), ATMP (aminotrimethylene phosphonic acid), HEDP (hydroxyethane dimethylene phosphonic acid), PBTC (2-butane phosphate 1,2,4-tricarboxylic acid), phosphoric acid, pyrophosphoric acid, and combinations thereof.

Assignments (9)
SECURITY INTEREST Recorded Sep 10, 2025
From: NATRON (ASSIGNMENT FOR THE BENEFIT OF CREDITORS), LLC
To: MERCURIA INVESTMENTS US, INC.
Reel/Frame 072829/0132 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2025
From: NATRON ENERGY, INC.
To: NATRON (ASSIGNMENT FOR THE BENEFIT OF CREDITORS), LLC
Reel/Frame 072836/0466 →
SECURITY INTEREST Recorded Jun 3, 2025
From: NATRON INTERMEDIATE, INC.; NATRON HOLDINGS, INC.; NATRON ENERGY, INC.
To: MERCURIA INVESTMENTS US, INC.
Reel/Frame 071480/0329 →
RELEASE OF SECURITY INTEREST Recorded Apr 1, 2025
From: MERCURIA INVESTMENTS US, INC.
To: NATRON ENERGY, INC.
Reel/Frame 070705/0013 →
RELEASE OF SECURITY INTEREST Recorded Nov 26, 2024
From: NANODIMENSION III, L.P.; NANODIMENSION IV, L.P.; ND CAPITAL OPPORTUNITY FUND I, L.P.; THE EIGER TRUST
To: NATRON ENERGY, INC.
Reel/Frame 069450/0867 →
SECURITY INTEREST Recorded Aug 21, 2024
From: NATRON ENERGY, INC.
To: MERCURIA INVESTMENTS US, INC.
Reel/Frame 068748/0393 →
SECURITY INTEREST Recorded Aug 8, 2024
From: NATRON ENERGY, INC.
To: NANODIMENSION III, L.P.; NANODIMENSION IV, L.P.; ND CAPITAL OPPORTUNITY FUND I, L.P.; THE EIGER TRUST
Reel/Frame 068520/0081 →
CHANGE OF NAME Recorded Jun 30, 2017
From: ALVEO ENERGY, INC.
To: NATRON ENERGY, INC.
Reel/Frame 043071/0965 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2015
From: MOTALLEBI, SHAHROKH, DR.; WESSELLS, COLIN DEANE, DR..; VALENCIA, CHRISTIAN, MR.
To: ALVEO ENERGY, INC.
Reel/Frame 036768/0845 →