ChemInform Abstract: IRON(III) COMPLEXES WITH ETHYLENEDIAMINETETRAACETIC ACID OR NITRILOTRIACETIC ACID AND PHENOL

1976 ◽  
Vol 7 (15) ◽  
pp. no-no
Author(s):  
S. KOCH ◽  
G. ACKERMANN
2006 ◽  
Vol 39 (4) ◽  
pp. 544-549 ◽  
Author(s):  
Dong-Mei Sun ◽  
Qing-Sheng Wu ◽  
Ya-Ping Ding

A biomimetic supported liquid membrane (SLM) system was employed to control the morphology of strontium carbonate. Some interesting morphologies, including rods, shuttles and spheres, can be readily generated by using citric acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid as cooperative modifiers in the mineralization process, under the conditions of pH 10, 0.01% of crystal modifier and ambient temperature. Seeking the cooperative balance of the SLM, the modifier agent and its concentration is the key factor in this system. In addition, this method was successfully applied to the morphology control of other alkaline earth metal carbonates, indicating its general applicability in materials preparation.


2019 ◽  
Vol 322 (3) ◽  
pp. 1915-1929
Author(s):  
James A. O’Hanlon ◽  
Robert D. Chapman ◽  
Frank Taylor ◽  
Melissa A. Denecke

Abstract The aminopolycarboxylic acids (APCAs), ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA) and nitrilotriacetic acid (NTA), are used as decontamination agents throughout the nuclear industry; therefore, APCAs are often found in radioactive waste. Limits of acceptance on APCAs are imposed on wastes consigned to the Low Level Waste Repository (LLWR) because, when present in the waste, the ligands have the potential to mobilise otherwise surface-bound or solid radionuclides, making them available for transport to groundwater and ultimately to the bio-sphere. A selective and sensitive methodology to detect and quantify these ligands in a range of complex matrices is advantageous in supporting waste acceptance processes. A reversed-phase high-performance liquid chromatography (HPLC) procedure has been applied for quantification of EDTA, DTPA and NTA in their Fe(III)-complex form. Method validation results show linearity (r2 > 0.999), precision (intra/inter-day %RSD ≤ 10%), accuracy (recovery = 100 ± 3%), sensitivity (minimum limits of detection = 0.31, 0.38 and 4.3 μM for EDTA, DTPA and NTA, respectively) and selectivity (simultaneous determination of the three APCA complexes achieved with baseline resolution) for Fe(III)-APCAs in aqueous solution. Chromatographic peak overlap is observed for samples containing Fe(III)- and Co(III)-EDTA; two deconvolution methods (2D least-squares fitting vs. PARAFAC) were applied to resolve the peaks and the performances compared. The optimised HPLC method was applied to trench leachate samples from the LLWR site. EDTA was detected with 0.4 μM < concentrations < 1 μM in samples from four of the six sampling locations tested. The levels are not considered sufficient to increase the risk of radionuclide mobilisation. The technique is considered to be robust and will be considered further in informing limits of acceptance on APCAs.


2015 ◽  
Vol 12 (1) ◽  
pp. 33 ◽  
Author(s):  
Richard F. Carbonaro ◽  
Alan T. Stone

Environmental context Oxidation of CrIII (trivalent chromium) to CrVI (hexavalent chromium) is of environmental concern because CrVI is a known mutagen and carcinogen. Our results show that hydrous manganese oxide (HMO) is capable of oxidising soluble CrIII complexed with iminodiacetic acid and nitrilotriacetic acid to CrVI at appreciable rates. CrVI production from soluble CrIII organic complexes is therefore expected to occur in natural and engineered systems that contain HMO. Abstract MnIII,IV (hydr)oxides are believed to be the principal oxidants of CrIII in the subsurface. In nearly all previous work on this subject, the CrIII reactant was prepared from inorganic salts (e.g. nitrate, chloride, sulfate). In our present work, CrIII complexes with the synthetic chelating agents iminodiacetic acid (IDA) and nitrilotriacetic acid (NTA) were reacted with hydrous manganese oxide (HMO) over a wide pH range to examine rates of reaction and product distribution. Capillary electrophoresis was used to quantify changes in reactant (CrIII–IDA and CrIII–NTA) and product (CrVI, free IDA and free NTA) concentrations as a function of time. In addition, a small number of experiments were performed using solutions prepared from CrIII alum (KCr(SO4)2·12H2O(s)) as the CrIII reactant. CrIII–IDA and CrIII–NTA were oxidised to CrVI, but rates were considerably lower than those obtained using inorganic CrIII. Within the timescales of our experiments, complete conversion of CrIII–NTA occurred at pH >7, but not under moderately acidic conditions, even when there was a large stoichiometric excess of HMO. MnCl2 addition experiments indicated that the observed reaction inhibition was attributable to MnII generation during the reaction. Our previous work has shown that citric acid, IDA, NTA and ethylenediaminetetraacetic acid solubilise CrIII from amorphous Cr(OH)3(s) at appreciable rates. The results of this study show that HMO is capable of oxidising the resulting soluble CrIII complexes, providing a viable mechanism for CrIII oxidation to CrVI over a wide pH range.


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