scholarly journals Phosphorus extracted by ion exchange resins and mehlich-1 from oxisols (latosols) treated with different phosphorus rates and sources for varied soil-source contact periods

2013 ◽  
Vol 37 (3) ◽  
pp. 667-677 ◽  
Author(s):  
Irio Fernando de Freitas ◽  
Roberto Ferreira Novais ◽  
Ecila Mercês de Albuquerque Villani ◽  
Sarah Vieira Novais
Keyword(s):  
Sandy Loam ◽  
Extraction Methods ◽  
Available P ◽  
Molar Ratio ◽  
P Availability ◽  
Triple Superphosphate ◽  
Experimental Conditions ◽  
Reactive Phosphate ◽  
Exchange Resins ◽  
P Sources

Despite the large number of studies addressing the quantification of phosphorus (P) availability by different extraction methods, many questions remain unanswered. The aim of this paper was to compare the effectiveness of the extractors Mehlich-1, Anionic Resin (AR) and Mixed Resin (MR), to determine the availability of P under different experimental conditions. The laboratory study was arranged in randomized blocks in a [(3 x 3 x 2) + 3] x 4 factorial design, with four replications, testing the response of three soils with different texture: a very clayey Red Latosol (LV), a sandy clay loam Red Yellow Latosol (LVA), and a sandy loam Yellow Latosol (LA), to three sources (triple superphosphate, reactive phosphate rock from Gafsa-Tunisia; and natural phosphate from Araxá-Minas Gerais) at two P rates (75 and 150 mg dm-3), plus three control treatments (each soil without P application) after four contact periods (15, 30, 60, and 120 days) of the P sources with soil. The soil acidity of LV and LVA was adjusted by raising base saturation to 60 % with the application of CaCO3 and MgCO3 at a 4:1 molar ratio (LA required no correction). These samples were maintained at field moisture capacity for 30 days. After the contact periods, the samples were collected to quantify the available P concentrations by the three extractants. In general, all three indicated that the available P-content in soils was reduced after longer contact periods with the P sources. Of the three sources, this reduction was most pronounced for triple superphosphate, intermediate for reactive phosphate, while Araxá phosphate was least sensitive to the effect of time. It was observed that AR extracted lower P levels from all three soils when the sources were phosphate rocks, while MR extracted values close to Mehlich-1 in LV (clay) and LVA (medium texture) for reactive phosphate. For Araxá phosphate, much higher P values were determined by Mehlich-1 than by the resins, because of the acidity of the extractor. For triple superphosphate, both resins extracted higher P levels than Mehlich-1, due to the consumption of this extractor, particularly when used for LV and LVA.

scholarly journals Phosphorus availability in oxidic soils treated with lime and silicate applications

2014 ◽  
Vol 38 (4) ◽  
pp. 1215-1222 ◽  
Author(s):  
Aline da Silva Sandim ◽  
Leonardo Theodoro Büll ◽  
Ariane Reis Furim ◽  
Géssica da Silva Lima ◽  
Jader Luis Nantes Garcia
Keyword(s):  
Soil Acidity ◽  
Extraction Methods ◽  
Steelmaking Slag ◽  
P Availability ◽  
Triple Superphosphate ◽  
Soil P ◽  
P Content ◽  
Corn Plants ◽  
Furnace Slag ◽  
P Desorption

Based on the assumption that silicate application can raise soil P availability for crops, the aim of this research was to compare the effect of silicate application on soil P desorption with that of liming, in evaluations based on two extractors and plant growth. The experiment was carried out in randomized blocks with four replications, in a 3 × 3 × 5 factorial design, in which three soil types, three P rates, and four soil acidity correctives were evaluated in 180 experimental plots. Trials were performed in a greenhouse using corn plants in 20-dm³ pots. Three P rates (0, 50 and 150 mg dm-3) were applied in the form of powder triple superphosphate and the soil was incubated for 90 days. After this period, soil samples were collected for routine chemical analysis and P content determination by the extraction methods resin, Mehlich-1 and remaining P. Based on the results, acidity correctives were applied at rates calculated for base saturation increased to 70 %, with subsequent incubation for 60 more days, when P content was determined again. The acidity correctives consisted of: dolomitic lime, steelmaking slag, ladle furnace slag, and wollastonite. Therefore, our results showed that slags raised the soil P content more than lime, suggesting a positive correlation between P and Si in soil. Silicon did not affect the extractor choice since both Mehlich-1 and resin had the same behavior regarding extracted P when silicon was applied to the soil. For all evaluated plant parameters, there was significant interaction between P rates and correctives; highest values were obtained with silicate.

scholarly journals Growth and yield of sugarcane as a function of phosphorus doses and forms of application

2016 ◽  
Vol 20 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Abel W. de Albuquerque ◽  
Leopoldo de A. Sá ◽  
William A. R. Rodrigues ◽  
Adriano B. Moura ◽  
Manoel dos S. Oliveira Filho
Keyword(s):  
Experimental Design ◽  
Phosphate Rock ◽  
Stem Diameter ◽  
Growth And Yield ◽  
Sugar Mill ◽  
Triple Superphosphate ◽  
Reactive Phosphate ◽  
Reactive Phosphate Rock ◽  
Industrial Yield ◽  
P Sources

ABSTRACT This study aimed to evaluate sugarcane growth and its agricultural and industrial yield influenced by phosphorus (P) sources and forms of application. The experiment was carried out at the Paisa Sugar Mill, in Penedo-AL, Brazil, from February 2012 to February 2013. The adopted experimental design was a randomized block in a factorial arrangement, with four replicates. The treatments consisted of five doses of triple superphosphate applied in the planting furrow (0, 50, 100, 150 and 200 kg ha-1 of P2O5), and three doses of Bayóvar reactive phosphate rock (0, 100 and 200 kg ha-1 of P2O5) applied in the total area. Phosphorus applied in the planting furrow improved sugarcane quality through the reduction of fiber and increases in purity, corrected pol, total recoverable sugar, ton of pol per hectare (TPH) and ton of sugarcane per hectare (TSH). The Bayóvar reactive phosphate rock promoted increases in stem diameter at 120 days after planting (DAP), TPH and TSH. For the interaction triple superphosphate applied in the planting furrow x Bayóvar reactive phosphate rock applied in the total area, there were significant differences in the number of tillers at 30 DAP, stem diameter at 120 DAP and TSH.

scholarly journals Grafting of (3-Chloropropyl)-Trimethoxy Silane on Halloysite Nanotubes Surface

2021 ◽  
Vol 11 (12) ◽  
pp. 5534
Author(s):  
Asmaa M. Abu El-Soad ◽  
Giuseppe Lazzara ◽  
Alexander V. Pestov ◽  
Daria P. Tambasova ◽  
Denis O. Antonov ◽  
...  
Keyword(s):  
Active Site ◽  
Chemical Engineering ◽  
Coupling Reaction ◽  
Ammonium Hydroxide ◽  
Halloysite Nanotubes ◽  
Chemical Activity ◽  
Molar Ratio ◽  
New Materials ◽  
Experimental Conditions ◽  
Trimethoxy Silane

Modified halloysite nanotubes (HNTs-Cl) were synthesized by a coupling reaction with (3-chloropropyl) trimethoxysilane (CPTMS). The incorporation of chloro-silane onto HNTs surface creates HNTs-Cl, which has great chemical activity and is considered a good candidate as an active site that reacts with other active molecules in order to create new materials with great applications in chemical engineering and nanotechnology. The value of this work lies in the fact that improving the degree of grafting of chloro-silane onto the HNT’s surface has been accomplished by incorporation of HNTs with CPTMS under different experimental conditions. Many parameters, such as the dispersing media, the molar ratio of HNTs/CPTMS/H2O, refluxing time, and the type of catalyst were studied. The greatest degree of grafting was accomplished by using toluene as a medium for the grafting process, with a molar ratio of HNTs/CPTMS/H2O of 1:1:3, and a refluxing time of 4 h. The addition of 7.169 mmol of triethylamine (Et3N) and 25.97 mmol of ammonium hydroxide (NH4OH) led to an increase in the degree of grafting of CPTMS onto the HNT’s surface.

scholarly journals Photocatalytic Treatment of Wastewater Containing Simultaneous Organic and Inorganic Pollution: Competition and Operating Parameters Effects

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 855
Author(s):  
Ahmed Amine Azzaz ◽  
Salah Jellali ◽  
Nasser Ben Harharah Hamed ◽  
Atef El Jery ◽  
Lotfi Khezami ◽  
...  
Keyword(s):  
Ultra Violet ◽  
Degradation Process ◽  
Molar Ratio ◽  
Experimental Conditions ◽  
Retention Capacity ◽  
Isotherm Study ◽  
Related Data ◽  
Ph Values ◽  
Pseudo Second Order ◽  
Maximum Retention

In the present study, methylene blue (MB) removal from aqueous solutions via the photocatalytic process using TiO2 as a catalyst in the presence of external ultra-violet light (UV) was investigated. The results of adsorption in the absence of UV radiation showed that adsorption reached an equilibrium state at 60 min. The experimental kinetic data were found to be well fitted by the pseudo-second-order model. Furthermore, the isotherm study suggested that dye uptake by TiO2 is a chemisorption process with a maximum retention capacity of 34.0 mg/g. The photodegradation of MB was then assessed under various experimental conditions. The related data showed that dye mineralization decreased when dye concentrations were increased and was favored at high pH values and low salt concentrations. The simultaneous presence of organic and inorganic pollution (Zinc) was also evaluated. The effect of the molar ratio Zn2+/MB+ in the solution at different pH values and NaCl concentrations was also monitored. The corresponding experimental results showed that at low values of Zn2+ in the solution (30 mg/L), the kinetic of the MB removal became faster until reaching an optimum at Zn2+/MB+ concentrations of 60/60 mg/L; it then slowed down for higher concentrations. The solutions’ carbon contents were measured during the degradation process and showed total mineralization after about 5 h for the optimal Zn2+/MB+ condition.

scholarly journals Reaktive E=C(p–p)π Systeme, XXXIV Addition von Alkoholen oder primären Aminen an Phosphaalkene F3CP=C(F)OR. Neue Trifluormethylphosphane und -phosphaalkene/Reactive E = C( p – p ) π-Systems, XXXIV Addition of Alcohols or Primary Amines to Phosphaalkenes F3CP= C(F)OR . Novel Trifluoromethylphosphanes and Phosphaalkenes

1993 ◽  
Vol 48 (1) ◽  
pp. 58-67 ◽  
Author(s):  
Joseph Grobe ◽  
Duc Le Van ◽  
Gudrun Lange
Keyword(s):  
High Resolution Mass Spectrometry ◽  
Molar Ratio ◽  
Primary Amines ◽  
The Novel ◽  
Experimental Conditions ◽  
Pull System ◽  
Fragment Ions ◽  
New Compounds ◽  
C Nmr

The course of the reactions o f fluorophosphaalkenes F3CP = C (F)OR [R = Me (1), Et (2)] with methanol or ethanol strongly depends on the experimental conditions. Thus at 70 °C a mixture of the 2-phosphapropionic acid ester F3CP (H )CO2R [R = Me (3), Et (4)] and trifluoromethylphosphane H2PCF3 is formed [molar ratio: 3 or 4 /H2 CF3 ≈1/1]. If the precursors F3CP (H )CO2R [R = Me (3), Et) are used as starting materials, the reaction with ROH under the same conditions affords 3 and 4, respectively, (90 to 95% yield) with only traces of H2PCF 3. In the presence o f iPr2NH these precursors react with R′OH to give the novel trifluoromethylphosphaalkenes F3CP = C (OR )OR [R /R′: Me/Me (6); E t/E t (7); Me/Et (8)]. With Et2NH , 3 undergoes an addition/elimination process yielding the interesting push/pull system Et2N(F)C = P-CO2Me (5). 1 and 2 react with primary amines R′NH2 (R′= tBu, Me) with stereoselective formation of the fairly labile phosphaalkenes F3CP = C(OR)NHR′ [R /R′: Me/tBu (9), Et/tBu(10), Me/Me (11)] with trans-positions for CF3 and NHR′.The new compounds 3 -11 were characterized by spectroscopic investigations (1H , 19F, 31P, 13C NMR ; IR, MS) and determination of M+ or typical fragment ions [M+ -OR ] by high resolution mass spectrometry.

Ash from the thermal gasification of pig manure—effects on ryegrass yield, element uptake, and soil properties

Soil Research ◽  
2012 ◽  
Vol 50 (5) ◽  
pp. 406 ◽  
Author(s):  
Ksawery Kuligowski ◽  
Robert John Gilkes ◽  
Tjalfe Gorm Poulsen ◽  
Baiq Emielda Yusiharni
Keyword(s):  
Soil Ph ◽  
Pig Manure ◽  
P Availability ◽  
Higher Plant ◽  
Regulatory Limits ◽  
P Content ◽  
Relative Agronomic Effectiveness ◽  
Elemental Uptake ◽  
Plant Yields ◽  
P Sources

Effects of thermally gasified pig manure ash (GA) and lime-free gasified ash (LF-GA) on properties of an acidic soil (pH 4.5) and the growth and elemental uptake of ryegrass (Lolium rigidum Gaudin) were investigated. The GA was an effective liming agent (2% addition raised soil pH from 4.5 to 7.9); both GA and LF-GA increased soil electrical conductivity and bicarbonate-extractable phosphorus (P). Soil fertilised with LF-GA supported slightly higher plant dry matter (DM) yield than GA (1.5–1.7 v. 1.2–1.5 g DM/kg soil) for the first harvest, due to greater initial P availability at pH <5 than at pH >6. However, plant yields for the subsequent two harvests were similar, as soil acidity dissolved lime in untreated ash (GA) over time. Maximum yields for ash-treated soil and soil treated with mono-calcium phosphate (MCP) were similar. Relative agronomic effectiveness of P sources for three harvests, based on plant P content compared with values for MCP, were 6, 11, and 12% for GA and 19, 10, and 33% for LF-GA. Internal efficiency of P utilisation was similar for all three P sources for each harvest, indicating that differences in yield were mostly a consequence of differences in P supply. Heavy metal concentrations in plants fertilised with ash were minor and within regulatory limits. In general, application of ash did not systematically affect the concentrations of elements (Al, B, Cd, Mg, Mn, Fe, Pb, S, Se) in plants.

The agronomic effectiveness of reactive phosphate rocks 1. Effect of the pasture environment

1997 ◽  
Vol 37 (8) ◽  
pp. 921 ◽  
Author(s):  
P. W. G Sale ◽  
R. J. Gilkes ◽  
M. D. A. Bolland ◽  
P. G. Simpson ◽  
D. C. Lewis ◽  
...  
Keyword(s):  
North Carolina ◽  
Phosphate Rock ◽  
Surface Soil ◽  
Annual Rainfall ◽  
Triple Superphosphate ◽  
Agronomic Effectiveness ◽  
P Sorption ◽  
Reactive Phosphate ◽  
Reactive Phosphate Rock ◽  
Very High

Summary. The agronomic effectiveness of directly applied North Carolina reactive phosphate rock was determined for 4 years from annual dry matter responses at 26 permanent pasture sites across Australia as part of the National Reactive Phosphate Rock Project. Fertiliser comparisons were based on the substitution value of North Carolina reactive phosphate rock for triple superphosphate (the SV50). The SV50 was calculated from fitted response curves for both fertilisers at the 50% of maximum yield response level of triple superphosphate. The reactive phosphate rock was judged to be as effective as triple superphosphate in the 1st year (and every year thereafter) at 4 sites (SV50 >0.9), and was as effective by the 4th year at 5 sites. At another 9 sites the reactive phosphate rock was only moderately effective with SV50 values between 0.5 and 0.8 in the 4th year, and at the final 8 sites it performed poorly with the 4th year SV50 being less than 0.5. Pasture environments where the reactive phosphate rock was effective in the 1st year were: (i) those on sandy, humic or peaty podsols with an annual rainfall in excess of 850 mm; (ii) those on soils that experienced prolonged winter inundation and lateral surface flow; and (iii) tropical grass pastures in very high rainfall areas (>2300 mm) on the wet tropical coast on North Queensland. The highly reactive North Carolina phosphate rock became effective by the 4th year at sites in southern Australia where annual rainfall exceeded 700 mm, and where the surface soil was acidic [pH (CaCl2) <5.0] and not excessively sandy (sand fraction in the A1 horizon <67%) but had some phosphorus (P) sorption capacity. Sites that were unsuitable for reactive phosphate rock use in the medium term (up to 4 years at least) were on very high P-sorbing krasnozem soils or high P-sorbing lateritic or red earth soils supporting subterranean-clover-dominant pasture, or on lower rainfall (< 600 mm) pastures growing on soils with a sandy A1 horizon (sand component >84%). No single environmental feature adequately predicted reactive phosphate rock performance although the surface pH of the soil was most closely correlated with the year-4 SV50 (r = 0.67). Multiple linear regression analysis found that available soil P (0–10 cm) and the P sorption class of the surface soil (0–2 cm), together with annual rainfall and a measure of the surface soil"s ability to retain moisture, could explain about two-thirds of the variance in the year-4 SV50 . The results from this Project indicate that there are a number of specific pasture environments in the higher rainfall regions of Australia where North Carolina reactive phosphate rock can be considered as an effective substitute P fertiliser for improved pasture.

scholarly journals Field evaluation of water or citrate soluble phosphorus in modified phosphate rocks for soybean

2001 ◽  
Vol 58 (1) ◽  
pp. 165-170 ◽  
Author(s):  
Luís Ignácio Prochnow ◽  
José Francisco da Cunha ◽  
Ariel Francisco Candiotti Ventimiglia
Keyword(s):  
Field Evaluation ◽  
Water Soluble ◽  
Ammonium Citrate ◽  
Low Grade ◽  
Triple Superphosphate ◽  
Single Superphosphate ◽  
Standard Source ◽  
Extractable P ◽  
P Fertilizers ◽  
P Sources

Ten P fertilizers were collected (commercial fertilizers) or synthesized (experimental sources) in order to obtain single superphosphates varying in water and citrate solubility. A standard source of P was also produced by crystallization of the water-soluble fraction of a triple superphosphate. Eleven P sources were band applied to a medium textured Xanthic Hapludox, in Bahia, Brazil (low content of resin-extractable P) at a rate of 80 kg ha-1 of NAC + H2O (neutral ammonium citrate plus water) soluble P2O5, with soybean as the crop which was grown to maturity. A check plot (control) was included in the study. Three of the P sources [single superphosphate produced from Araxa phosphate rock (PR), low-grade single superphosphate produced from Lagamar PR and the standard source of P] were also applied at rates to provide 40 and 120 kg ha-1 of NAC + H2O soluble P2O5. Yield of soybean was evaluated by analysis of variance with mean comparison performed utilizing LSD lines, considering the P sources applied at a rate of 80 kg ha-1 of P2O5 + control. Regression procedures were used to study the relation between yield of soybean and rates of P2O5. The fertilizers tested performed equally well as a source of P for soybean. The level of water-soluble P did not influence fertilizer performance.

Treatability of textile dye-bath effluents by advanced oxidation: preparation for reuse

1999 ◽  
Vol 40 (1) ◽  
pp. 183-190 ◽  
Author(s):  
N. H. Ince ◽  
G. Tezcanlı
Keyword(s):  
Organic Carbon ◽  
Total Organic Carbon ◽  
Azo Dye ◽  
Uv Light ◽  
Advanced Oxidation ◽  
Membrane System ◽  
Molar Ratio ◽  
Textile Dye ◽  
Experimental Conditions ◽  
Solids Content

Treatability of textile dye-bath effluents by advanced oxidation with Fenton and Fenton-like reagents (FeII/H2O2 and FeIII/H2O2), in the presence and absence of UV light was investigated, using a reactive azo-dye (Procion Red HE7B), and typical dye bath constituents. Under the experimental conditions employed, it was found that with 20 min UV irradiation, complete color removal and 79% total organic carbon degradation is possible, when the system is operated at pH=3, and with a H2O2/Fe(II) molar ratio of 20:1. The increased dissolved solids content of the treated solution implies the necessity of an appropriate membrane system to make the effluent reusable in the dye/wash processes.

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