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Query: UMLS:C0205700 (ash)
 15,125 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The adsorption of Congo red from solution was carried out using calcium-rich fly ash with different contact times, concentrations, temperatures, and pHs. While the amount of dye adsorbed per unit weight of fly ash increases with increasing concentration and temperature, it decreases slightly with increasing pH. The adsorption was between 93 and 98% under the conditions studied. Kinetic studies showed that the adsorption process obeyed the pseudo-second-order kinetic model. It was also determined that the adsorption isotherm followed Freundlich and Dubinin-Radushkevich models. From thermodynamic studies, it was seen that the adsorption was spontaneous and endothermic. Desorption studies suggested that desorption was 29.18% in the presence of 0.1 N HCl and was 47.21% in the presence of CH(3)COOH (50% v/v). This indicated that most of the dye was held by fly ash via chemisorption as well as ion exchange. Furthermore, FTIR study also shows that a chemisorption process occurs between CR and fly ash, probably indicating dye/fly ash complexing.
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PMID:Adsorption of Congo red from aqueous solution onto calcium-rich fly ash. 1514 8

The effect of coexisting metals in a sample on the determination of lead and cadmium in plastics used for food contact materials was investigated. In the official method specified in the Japanese Food Sanitation Law, contents of lead and cadmium are determined by a dry incineration method using sulfuric acid. It was assumed that sometimes, coexisting metals in a sample may form insoluble sulfate and that lead sulfate might be adsorbed into the insoluble sulfate. Therefore, hydrochloric acid was added to the ash, to turn formed insoluble sulfate into soluble compounds (HCl addition method). We found that recoveries of cadmium were not affected in the presence of other metals except when calcium exceeded 20 mg/g in both methods. Recoveries of lead decreased in the presence of barium exceeding 0.1 mg/g or calcium exceeding 10 mg/g in the official method. However, improvement of recoveries was achieved with the HCl addition method and by reducing the sample amount to one-tenth (0.1 g) of that specified in the official method.
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PMID:[Effect of coexisting metals on determination of lead and cadmium in the plastic materials test of the Japanese Food Sanitation Law]. 1516 58

The limitations facing land filling and recycling and the planned ban on sea disposal of sludge leads to the expectation that the role of sludge incineration will increase in the future. The expected increase in sludge incineration will also increase scrutiny of the main drawbackto sewage sludge incineration--the formation of hazardous air pollutants (HAPs). Despite the extensive body of knowledge available on sewage sludge combustion, very few studies have been conducted on the formation of HAPs during sludge combustion. In this work, the interactions between sewage sludge pyrolysis products and sludge ash were investigated using a dual chamber flow reactor system and a horizontal laboratory scale reactor. The results of this study shows that sludge ash can catalyze oxidation and chlorination of organics. In the absence of HCl in the gas stream, sludge ash acts as an oxidizing catalyst, but in the presence of HCl, sludge ash acts as a chlorination catalyst producing high yields of organochloride compounds.
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PMID:Form1ation and destruction of chlorinated pollutants during sewage sludge incineration. 1521 73

The present study deals with the production of citric acid from a ram horn peptone (RHP) by Aspergillus niger NRRL 330. A medium from RHP and a control medium (CM) were compared for citric acid production using A. niger in a batch culture. For this purpose, first, RHP was produced. Ram horns were hydrolyzed by treatment with acids (6 N H(2)SO(4), 6 N HCl) and neutralizing solutions. The amounts of protein, nitrogen, ash, some minerals, total sugars, total lipids and amino acids of the RHP were determined. RHP was compared with peptones with a bacto-tryptone from casein and other peptones. The results from RHP were similar to those of standard peptones. The optimal concentration of RHP for the production of citric acid was found to be 4% (w/w). A medium prepared from 4% RHP was termed ram horn peptone medium (RHPM). In comparison with CM, the content of citric acid in RHPM broth (84 g/l) over 6 days was 35% higher than that in CM broth (62 g/l). These results show that citric acid can be produced efficiently by A. niger from ram horn.
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PMID:Ram horn peptone as a source of citric acid production by Aspergillus niger, with a process. 1524 90

Pathways of pentachlorophenol dechlorination have been investigated on municipal waste incineration fly ash at 200 degrees C under nitrogen atmosphere. Thermodynamic calculations have been carried out for these dechlorination conditions using the method of total Gibbs energy minimization for the whole system consisting of gaseous components, i.e., chlorinated phenols, phenol, hydrogen chloride and the Cu3Cl3 trimer and of solid Cu2O and CuCl2 components. The effects of water, temperature and of the amounts of the reaction components on the thermodynamic equilibrium have been discussed and the experimental results compared with the calculated thermodynamic data.
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PMID:Dechlorination ability of municipal waste incineration fly ash for polychlorinated phenols. 1526 59

Several batch studies that were made up of the acid extraction and the solvent extraction were performed to recover phosphorus from the waste-activated sludge (WAS) incinerator ash. In the acid extraction, the extraction efficiency of phosphorus relied on the acid type, liquid(acid)-to-solid (L(acid)S) ratio, and acid concentration. Phosphorus in the WAS incinerator ash was completely extracted by 1 M HCl at the L(acid)S ratio of 6.4:1. Subsequently, the solvent extraction was conducted to separate and concentrate phosphorus further from the acid extract. The efficiency of solvent extraction was affected mainly by the solvent type, liquid (solvent)-to-liquid (the acid extract) (L(solv)L(acid ext)) ratio, and hydrogen ion concentration. Under the appropriate condition, 76% of phosphorus in the acid extract was extracted to 1-butanol phase, which corresponded to 80.1% as the mass fraction of phosphorus to total elements. Prior to the solvent extraction, the addition of bis (2-ethylhexyl) phosphoric acid (D2EHPA), which was available for removing aluminum from the acid extract, led to an additional increase in the term of the mass fraction of phosphorus to total elements. Overall results indicated that phosphorus in the WAS incinerator ash could be efficiently recovered and be a potential renewable resource.
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PMID:Study on the recovery of phosphorus from waste-activated sludge incinerator ash. 1575 73

The contents of transition metal ions iron, copper, zinc, and manganese were simultaneously determined in pig feed using an ion chromatographic technique (IC) preceded by dry ashing. Employing ion exchange, the ions were separated on an IonPac CS5A column used in combination with a pyridine-2,6-dicarboxylic acid based eluent. The separation was followed by spectrophotometric detection after postcolumn reaction with 4-(2-pyridylazo)resorcinol. Dry ashing parameters were varied to assess their role in potential analyte loss. Quantitative recoveries (>95%) were obtained for all analytes with a dry ashing method that included a moderate temperature-time regime and ash leaching support in the form of sonication and heat treatment. The use of HCl as leaching acid and the presence of alkaline earths in the matrix solution did not interfere with the chromatographic separation.
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PMID:Evaluation of dry ashing in conjunction with ion chromatographic determination of transition metal ions in pig feed samples. 1576 6

In this paper, 0.1 mol x L(-1) HCl, 6 mol x L(-1) HCl, pH 7.0 1 mol x L(-1) NH4Ac was oscillated and 6 mol x L-' HCI was boilled to extract and determine K, Na, Ca, Zn, Fe, Mn, Mg and Cu. Comparing with classical method that popularly used HNO3-HCl04 to degest and ash samples,the results indicated that for macroelement K,Na and Mg several extraction methods are similar to classical method,the recovery was 90%-115%,for microelement Zn, Mn and Fe could be extracted using pH7.0 1 mol x L(-1) NH4Ac, 0.1 mol x L(-1) HCI, 6 mol x L(1) HCI oscillating,the recovery was 100%-115%. Cu could be analysed using 6 mol x L(-1) HCI boiling. But the results of Ca were not better because of the enhancement effect. The results with ash sample were lower because many elements were lost when ash temperature was up to 450 degrees C. These methods of exatraction pretreatment are simple and rapid. The recovery and precision are satisfactory.
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PMID:[Study on pretreatment for the determination of several nutrition element in eggs with AAS]. 1581 76

Five experiments were conducted to determine Lys and P bioavailabilities of distillers dried grains with solubles (DDGS), which was derived from corn fermentation in a modern nonbeverage ethanol plant. In experiment 1, we used the precision-fed cecectomized rooster assay and estimated the true digestibility of Lys in DDGS to be 75%. In experiments 2, 3, 4, and 5 the relative bioavailabilities of Lys and P were assessed using slope-ratio chick growth experiments. In experiments 2 and 3, Lys-deficient basal diets containing 0.40 or 0.60% digestible Lys respectively, were formulated. A linear growth response (P < 0.05) was observed from the addition of 0.10 and 0.20% L-Lys from L-Lys x HCl and 10 and 20% DDGS to the basal diets. Body weight gain was regressed on Lys intake from L-Lys x HCl and DDGS, and the ratio of the slopes indicated the relative bioavailable Lys in DDGS. The values as a percentage of total Lys (0.83) in DDGS yielded availability estimates of 80% for experiment 2 and 100% for experiment 3. In experiments 4 and 5, a P-deficient basal diet containing 0.12% nonphytate P was formulated. A linear growth and tibia bone ash (%) response (P < 0.05) were observed from the addition of 0.05 and 0.10% P from K2HPO4 and 2 levels of DDGS (5 and 10% for experiment 4 and 7 and 14% for experiment 5). Tibia bone ash (%) was regressed on P intake from K2HPO4 and DDGS, and the ratio of slopes indicated the relative bioavailability of P in DDGS. The values as a percentage of total P (0.74%) in DDGS yielded availability estimates of 68% for experiment 4 and 54% for experiment 5.
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PMID:The bioavailability of lysine and phosphorus in distillers dried grains with solubles. 1584 14

Leaching of ash and dried sewage sludge were investigated and compared with the leaching results of sludge residue from supercritical water oxidation (SCWO). This article focuses on how the composition of ash and sludge residues influences the extraction of phosphate and heavy metals and if different treatment temperatures of the sludge effect the leachability. Results showed that acid leaching gave a higher release of phosphate than alkaline leaching for all ash and sludge residue samples. Also, alkaline leaching dissolved phosphate with a lower metal contamination than acid leaching. Furthermore, it was found that iron had a low release at both alkaline and acid leaching from ash and from SCWO residue. The difference in composition of ash and sludge residue samples had no significant influence on release of phosphate at high concentrations of acid. Phosphate release from ash, dried sludge at 300 degrees C and SCWO residue showed similar results at 1M acid leaching. However, it seems to be easier to release phosphate from the SCWO residue than from the ash at low acid concentrations. SCWO residue showed higher release than the other ashes at 0.5M HCl. Results for alkaline leaching showed higher release from ash at 1M NaOH than from SCWO residue or from dried sludge at 300 degrees C. The leaching of phosphate from dried sludge seems to be temperature dependent, as the dried sludge treated at higher temperature showed less release of phosphate. It was found that the pre-treatment of the ash may be important for better release of phosphate.
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PMID:Phosphorus release from ash, dried sludge and sludge residue from supercritical water oxidation by acid or base. 1596 83


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