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Oxalic acid

About: Oxalic acid is a research topic. Over the lifetime, 11584 publications have been published within this topic receiving 173263 citations. The topic is also known as: ethanedioic acid & H2ox.


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Journal ArticleDOI
TL;DR: In this paper, an effective decomposition of antibiotic sulfadiazine (SD) in a Fe0-catalyzed sonochemical Fenton like system (Sono-FL) was demonstrated.
Abstract: Effective decomposition of antibiotic sulfadiazine (SD) in a Fe0-catalyzed sonochemical Fenton like system (Sono-FL) was demonstrated. By using the response surface methodology (RSM), an optimized experimental condition of pH 7.00, 0.94 mM Fe0, 1.90 mM persulfate (PS) and 20 W ultrasound (US) power was concluded, which could reach the predicted SD degradation efficiency of 90%. Afterwards, effects of wastewater matrix (five inorganic anions and two chelating agents) on the SD degradation were investigated in the system, respectively. It was found that the SD degradation could be inhibited by SO42−, NO3−, HCO3−/CO32− and H2PO4− to different extents. Cl− would lead to an enhancement with a low dosage (5 mM), but an inhibition with a high dosage (100 mM). Unexpectedly, chlorinated organic intermediates were also found as SD decomposed. Appropriate dosages of oxalic acid (OxA) or EDTA could benefit the SD degradation in the Sono-FL system, while excessive chelating agents would play as competitive pollutants. It was summarized that inorganic anions would mainly react with SO4 − and/or OH to form sub-radicals of less oxidative potential. OxA and EDTA would not only participate in complexing dissolution of Fe0 but also provide additional oxidants such as H2O2 and [FeIVO]2+, through the electron transfer reactions caused by the iron-ligands species.

222 citations

Journal ArticleDOI
TL;DR: In this article, it is demonstrated that hydrogen peroxide, electrogenerated at a reticulated vitreous carbon cathode by the reduction of oxygen in the presence of Fe(II) is a powerful oxidant for organic compounds.

221 citations

Journal ArticleDOI
TL;DR: In this article, the relative effectiveness of PO 4 at 0.1 and 0.5 M and pH values of 3 and 6.7 was investigated, and the extent to which PO 4 added to 0. 1 M PO 4 prevented readsorption of As(V) or Se(IV) to goethite during the dissolution of an amorphous Fe oxide was also assessed.
Abstract: Phosphate and OH- are often used for the extraction of As and Se from soils, either as single extractants or as part of a sequential extraction scheme. However, the recovery of As and Se species and the integrity of the resulting solution speciation merit investigation. In this study the relative effectiveness of PO 4 at 0.1 and 0.5 M and pH values of 3 and 6.7 and 0.1 M OH to extract As(III), As(V), dimethylarsinic acid (DMA), monomethylarsonic acid (MMA), p-arsanilic acid (p-ASA), roxarsone (ROX), Se(IV) and Se(VI) sorbed to goethite and an amorphous Fe oxide were compared, and the speciation in the resulting extract was determined. The extent to which 0.1 M PO 4 added to 0.25 M NH 2 OH.HCl or 0.175 M Na oxalate/ 0.1 M oxalic acid prevents readsorption of As(V) or Se(IV) to goethite during the dissolution of an amorphous Fe oxide was also assessed. Hydroxide was the most effective extractant for desorption of all species except As(III) from both oxide surfaces. Arsenite was extracted most efficiently by 0.5 M PO 4 at low pH; however, amorphous Fe oxide exhibited a strong affinity for As(III) with a maximum of 18% of As(III) extracted by 0.5 M PO 4 at pH 2.8. Partial oxidation of As(III) to As(V) occurred in all extractions where an Fe oxide solid phase was present, but only in the hydroxide extract in the absence of a Fe solid phase. Addition of 0.1 M PO 4 to extractants used for the dissolution of the amorphous Fe oxide prevented the readsorption of As(V) and Se(IV) to goethite.

216 citations

Journal ArticleDOI
TL;DR: A strain lacking both glucose oxidase (goxC) and OAH (prtF) produced citric acid from sugar substrates in a regular synthetic medium at pH 5 and under these conditions production was completely insensitive to Mn2+.
Abstract: The external pH appeared to be the main factor governing oxalic acid production by Aspergillus niger. A glucose-oxidase-negative mutant produced substantial amounts of oxalic acid as long as the pH of the culture was 3 or higher. When pH was decreased below 2, no oxalic acid was formed. The activity of oxaloacetate acetylhydrolase (OAH), the enzyme believed to be responsible for oxalate formation in A. niger, correlated with oxalate production. OAH was purified from A. niger and characterized. OAH cleaves oxaloacetate to oxalate and acetate, but A. niger never accumulated any acetate in the culture broth. Since an A. niger acuA mutant, which lacks acetyl-CoA synthase, did produce some acetate, wild-type A. niger is apparently able to catabolize acetate sufficiently fast to prevent its production. An A. niger mutant, prtF28, previously isolated in a screen for strains deficient in extracellular protease expression, was shown here to be oxalate non-producing. The prtF28 mutant lacked OAH, implying that OAH is the only enzyme involved in oxalate production in A. niger. In a traditional citric acid fermentation low pH and absence of Mn2+ are prerequisites. Remarkably, a strain lacking both glucose oxidase (goxC) and OAH (prtF) produced citric acid from sugar substrates in a regular synthetic medium at pH 5 and under these conditions production was completely insensitive to Mn2+.

214 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023292
2022561
2021266
2020352
2019482
2018455