Nickel recovery from precipitate of NCA lithium-ion battery leach liquor by using disodium ethylene diamine tetraacetate

The nickel cobalt aluminium oxides (NCA) type Li-ion battery is a type of battery currently used in electric vehicles. The UGM battery team has recycled this type of battery to obtain high purity lithium metal. Aside from lithium, the NCA battery contains high-value metals, nickel is one of them. This experiment aims to test the ease of nickel to chelate with disodium ethylene diamine tetraacetate (EDTA). The experiment was carried out by means of a triple neck flask for 4 hours. The samples were taken at certain minutes and then fitted using a pseudo homogeneous first-order reaction equation. The chelate formed was further processed through multilevel precipitation or electrodialysis to separate nickel. Based on the experiment, nickel formed chelates optimally at 60°C using 0.086 M EDTA with the reaction constant for nickel being 1.4819 min−1. The Arrhenius constant and activation energy for nickel were 3.48×1011min−1 and 76,907 J/mole, respectively.

pH-responsive polymer-based biomacromolecule nanosponges as biodegradable carriers for DOX delivery

Cellulose is the most abundant renewable biomaterial on earth and beta-cyclodextrin (BCD) is among the most commonly used biocompatible drug encapsulation agents. Combining these bio-organic materials is a very powerful approach to greatly enhance the bioavailability of many drugs. These systems also allow for optimal selective drug release profiles, high biocompatibility, as well as “green nanomedicine” approaches that are eco-friendly in their synthesis and have minimal ecological toxicity. herein, we designed a new type of green and biopolymer-based nanosponge drug carriers which is polymerized by crosslinking beta-cyclodextrin ethylene diamine (βCD-EDA) with bifunctional hairy nanocellulose (BHNC). BHNC contains, besides aldehyde groups, carboxyl groups which can react with amino groups in βCD-EDA. Firstly, the crosslinker βCD-EDA was obtained through a simple nucleophilic substitution reaction between beta-cyclodextrin carbonyl imidazole (βCD-CI) and ethylene diamine (EDA). Secondly, BHNC was functionalized with the crosslinker βCD-EDA through a facile nucleophilic substitution crosslinking reaction of the BHNC activated carboxyl groups by the amines of βCD-EDA. We refer to the polymerized highly crosslinked BHNC-βCD-EDA network as BBE. Various ratios of βCD-EDA and BHNC were polymerized with the help of DMTMM as an activator, which resulted in different morphological shapes of BBE, and thus in different release profiles and pH-responsiveness. Unlike other polymer-based βCDs and nanosponges, these new types of crosslinked polymer were prepared in a green and safe solvent (water) and with very short reaction times and at low temperatures. Finally, the BBE polymers were tested as biocompatible nanocarriers for controllable doxorubicin (DOX) delivery. These hyper crosslinked polymers show a high capacity for loading DOX with extended drug release. Furthermore, breast cancer cell cultures show lower cell viability when DOX was loaded in various BBEs than control samples or DOX alone, indicating that our DOX-BBE drug delivery systems are better anticancer agents than DOX alone.

Synthesis and structure determination of racemic (Δ/Λ)-tris(ethylenediamine)cobalt(III) trichloride hemi(hexaaquasodium chloride)

The synthesis and crystal structure of the title racemic compound, [Co(C2H8N2)3]Cl3.{[Na(H2O)6]Cl}0.5, are reported. The trivalent cobalt atom, which resides on a crystallographic threefold axis, is chelated by a single ethylene diamine (en) ligand and yields the tris-chelate [Co(en)3]3+ cation with distorted octahedral geometry after the application of crystal symmetry. The sodium cation (site symmetry \overline{3}), has a single water molecule bound to it in the asymmetric unit and yields a distorted, octahedrally coordinated hydrated [Na(H2O)6]+ cation after the application of symmetry. One of the chloride ions lies on a general position and the other has \overline{3} site symmetry. An extensive array of C—H...O, N—H...Cl and O—H...Cl hydrogen bonds exists between the ethylene diamine ligands, the water molecules of hydration, and the anions present, thereby furnishing solid-state stability.

Molecular rearrangement of pyrazino[2,3-c]quinolin-5(6H)-ones during their reaction with isocyanic acid

A new tetrahydropyrazino[2,3-c]quinolin-5(6H)-ones were prepared from 3-chloroquinoline-2,4(1H,3H)-diones and ethylene diamine. In their reaction with HNCO, an unprecedented molecular rearrangement produced new types of hydantoin derivatives. All prepared compounds are characterized using their 1H, 13C, and 15N NMR spectra and the results of the X-ray analysis are also presented. A proposed mechanism of rearrangement is discussed in this essay.

Implementation of Metallic Film Electrodes for Catalytic Adsorptive Stripping Voltammetric Determination of Germanium(IV)

In the present work, it has been shown that bismuth film electrodes deposited on screen-printed carbon supports could be successfully used to provide well-shaped, sensitive and reproducible catalytic adsorptive stripping signals of Ge(IV) in the presence of catechol and V(IV)-HEDTA (HEDTA-N-hydroxyethyl-ethylene diamine-triacetic acid) complex.