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Ultisol
CHEMOSPHERE · 2023 · IF 8.8

Effects of soil pH and organic carbon content on in vitro Cr bioaccessibility in Ultisol, Alfisol, and Inceptisol

Yang-xiao-xiao Shi,Jia-qi Cui,Feng Zhang,Ke-wei Li,Jun Jiang,Ren-kou Xu

Hexavalent chromium (Cr(VI)) is a toxic heavy metal and its mobility and bioaccessibility in soils are influenced by soil properties. In this study, the soil pH and organic carbon contents of Ultisol , Alfisol , and Inceptisol were adjusted before they were polluted with 230 mg kg −1 Cr(VI). Alkaline digestion, sequential extraction, and an in vitro experiment were conducted to study the valence state, species, and bioaccessibility of Cr in the soils. The results showed that a high soil pH was not favorable for reduction of Cr(VI); therefore the Cr(VI) and exchangeable Cr contents were positively related to soil pH. Soil organic carbon promoted the reduction of Cr(VI). Almost all Cr(VI) was reduced to Cr(III) when the soil organic carbon content reached 10 g kg −1 . Chromium bioaccessibility in simulated gastric and intestinal phase solutions was influenced by Cr(VI) and Cr(III) adsorption/desorption, dissolution/precipitation, and redox reactions. Chromium bioaccessibility differences between the gastric and intestinal phases were associated with the Cr(VI)/Cr(III) ratio. Acidic conditions and a high organic carbon content promoted the conversion of Cr(VI) to Cr(III). When soil pH was increased from 4.01 to 5.85, Cr(VI) in Alfisol without the addition of humic acid increased from 96.38 to 174.78 mg kg −1 , the exchangeable Cr proportion increased from 9.7% to 22.6%, and Cr bioaccessibility increased from 41.29% to 49.14% in the gastric phase and from 41.32% to 48.24% in the intestinal phase. When the organic carbon content increased from 3.95 to 9.28 g kg −1 in Alfisol, Cr(VI) content decreased from 167.66 to 20.52 mg kg −1 , which led to a decrease in Cr bioaccessibility from 49.15% to 13.8% in the gastric phase and from 45.85% to 7.67% in the intestinal phase. Therefore, acidic conditions and increasing soil organic carbon levels can reduce the health risk posed by Cr in soils.

CAS / MDL: 1415-93-6
研究领域: 环境科学 · 土壤学
✓ 已验证 产品关联 DOI PubMed 高影响因子
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ENVIRONMENTAL GEOCHEMISTRY AND HEALTH · 2024 ·Vol. 46 ·期 8 ·1-12 · IF 3.2

Differential immobilization of cadmium and changes in soil surface charge in acidic Ultisol by chitosan and citric acid: effect of their functional groups

Xu Ren-kou,Nkoh Jackson Nkoh

Soil organic matter plays an important role in cadmium adsorption and immobilization. Since different organic matter components affect cadmium adsorption processes differently, selecting the right organic substrate and knowing how to apply it could improve cadmium remediation. This study compares the effects of two contrasting organic molecules; chitosan and citric acid, on cadmium adsorption and speciation in acidic Ultisol. The adsorption of chitosan to Ultisol significantly increased the soil positive charge while adsorption of citric acid increased the soil negative charge. At pH 5.0, the maximum amount of cadmium adsorbed in excess chitosan was 341% greater than that in excess citric acid. About 73–89% and 60–62% of adsorbed cadmium were bound to Fe/Mn oxides and organic matter/sulfide at pH 4.0 while this fraction was 77–100% and 57–58% for citric acid and chitosan at pH 5.0, respectively. This decrease in the complexing ability of chitosan was related to the destabilizing effect of high pH on chitosan’s structure. Also, the sequence through which chitosan, citric acid, and cadmium were added into the adsorption system influenced the adsorption profile and this was different along a pH gradient. Specifically, adding chitosan and cadmium together increased adsorption compared to when chitosan was pre-adsorbed within pH 3.0–6.5. However, for citric acid, the addition sequence had no significant effect on cadmium adsorption between pH 3.0–4.0 compared to pH 6.5 and 7.5, with excess citric acid generally inhibiting adsorption. Given that the action of citric acid is short-lived in soil, chitosan could be a good soil amendment material for immobilizing cadmium.

CAS / MDL: 9012-76-4
研究领域: 环境科学 · 土壤学
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Crop & Pasture Science · 2023 ·Vol. 74 ·期 12 ·1318-1333 · IF 1.9

Role of carbon and nitrogen mineralisation of chitosan and crop straws in ameliorating acidity of acidic Ultisols

Jackson Nkoh Nkoh,Peng Guan,Ren-yong Shi,Ru-hai Wang,Jiu-yu Li,Ren-kou Xu

Context Carbon (C) and nitrogen (N) transformation processes in soils play an important role in the fluctuation of soil pH. Incorporation of chitosan and crop straws, byproducts from fishery and agriculture, into acidic soils can increase soil pH through decarboxylation, decomposition, N immobilisation and ammonification.Aims The study was designed to evaluate the transformation of organic N and C from chitosan and/or crop straws and their effects on soil physicochemical properties.Methods Chitosan, rice straw and maize straw were incubated with two acidic Ultisols from Langxi (Soil 1) and Yingtan (Soil 2) differing in initial pH. Six treatments were prepared in triplicate: control (no amendment), 4% chitosan, 4% rice straw, 4% maize straw, 2% chitosan+2% rice straw, and 2% chitosan+2% maize straw. Soil pH, N transformation and CO2 evolution were estimated at different time intervals.Key results After 40days of incubation, control soil pH decreased by 0.35 and 0.32 units for Soils 1 and 2, respectively. Rice straw, maize straw, chitosan, rice straw–chitosan and maize straw–chitosan significantly increased soil pH by 0.51, 0.17, 2.27, 1.78 and 2.02 units for Soil 1, and 0.71, 0.16, 0.67, 0.49 and 0.68 units for Soil 2 (P<0.01). The respective treatments decreased exchangeable acidity by 62%, 51%, 95%, 95% and 95% for Soil 1 and 75%, 69%, 88%, 88% and 87% for Soil 2. In treatments containing chitosan, the pH increase resulted from ammonification of organic N and mineralisation of organic C, with the effect higher in Soil 1 than Soil 2.Conclusions Amending acidic soils with chitosan and crop residues can effectively increase soil pH and slow soil acidification rate.Implications This study provides useful information for amelioration of acidic soils.

CAS / MDL: 9012-76-4
研究领域: 土壤学 · 环境科学
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CHEMOSPHERE · 2022 · IF 8.943

The mechanism for enhancing phosphate immobilization on colloids of oxisol, ultisol, hematite, and gibbsite by chitosan

Jackson Nkoh Nkoh,Ke-wei Li,Yang-xiao-xiao Shi,Jiu-yu Li,Ren-kou Xu

Phosphorus (P) availability in highly weathered soils is significantly influenced by the contents of iron (Fe)/aluminum (Al) oxides, clay minerals, and organic matter. With the increasing interest in biofertilizers (e.g. chitosan), it is important to understand how they affect P adsorption profiles on colloids of weathered soils rich in Fe/Al oxides. Thus, the effect of chitosan on the adsorption of P to colloids of hematite, gibbsite , Oxisol , and Ultisol was studied through electrokinetic measurements, spectroscopic analysis , and adsorption edge/isotherm profiles. The presence of chitosan significantly improved the surface positive charge and the decreasing trend of surface positive charge was slower for chitosan-treated colloids compared to the control with increasing pH. At pH 5.0, all the colloids were positively charged, with the oxides containing more positve charges than the soil colloids. At this pH value, the surface coverage capacity of P was 99.1, 61.6, 50.5, and 37.5 mmol kg⁻ 1 for Oxisol, Ultisol, hematite, and gibbsite, respectively. This suggests that clay minerals in soil colloids were vital in enhancing P adsorption. In the presence of chitosan, the surface coverage capacity of P was increased by 111%, 173%, 647%, and 488% for Oxisol, Ultisol, gibbsite, and hematite, respectively. Drawing inferences from spectroscopic analysis, citric acid desorption profile, and zeta potential analysis, we suggest that chitosan (CH) enhanced P adsorption by promoting the formation of (i) citric acid “undisplaceable” inner-sphere P complexes such as [Colloid-OP- O -CH] and [Colloid-OP- N -CH] , (ii) citric acid “displaceable” outer-sphere P complexes such as {[Colloid- O -CH]-OP} and {[Colloid- N -CH]-OP} , and (iii) water “leachable or soluble” P complexes such as {[Colloid-CH] + PO 4 ³⁻} and {[Colloid-OP]⁻CH + } . Thus, applying chitosan as a biofertilizer (source of N) along with P in highly weathered soils could improve P availability while reducing P leaching .

CAS / MDL: 21645-51-2 9012-76-4
研究领域: 土壤学 · 环境科学
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CHEMOSPHERE · 2023 · IF 8.8

Effect of carbon and nitrogen mineralization of chitosan and its composites with hematite/gibbsite on soil acidification of an Ultisol induced by urea

Jackson Nkoh Nkoh,Peng Guan,Jiu-yu Li,Ren-kou Xu

Chitosan is a biodegradable polymer with a vast range of applications. Along with its metal composites, chitosan has been applied in the remediation of polluted soils as well as a biofertilizer . However, little attention has been given to the degradation of chitosan composites in soil and how they affect soil respiration rate and other physicochemical parameters. In this study, the degradation of chitosan and its composites with gibbsite and hematite in an acidic Ultisol and the effect on urea (200 mg N kg −1 ) transformation were investigated in a 70-d incubation experiment. The results showed that the change trends of soil pH, N forms, and CO 2 emissions were similar for chitosan and its composites when applied at rates <5 g C kg −1 . At a rate of 5 g C kg −1 , the C and N mineralization trends suggested that the chitosan-gibbsite composite was more stable in soil and this stability was owed to the formation of a new chemical bond (CH–N–Al-Gibb) as observed in the Fourier-transform infrared spectrum at 1644 cm −1 . The mineralization of the added materials significantly increased soil pH and decreased soil exchangeable acidity ( P  < 0.01). This played an important role in decreasing the amount of H + produced during urea transformation in the soil. The soil's initial pH was an important factor influencing C and N mineralization trends. For instance, increasing the initial soil pH significantly increased the nitrification rate and chitosan decomposition trend ( P  < 0.01) and thus, the contribution of chitosan and its composites to increase soil pH and inhibit soil acidification during urea transformation was significantly decreased ( P  < 0.01). These findings suggest that to achieve long-term effects of chitosan in soils, applying it as a chitosan-gibbsite complex is a better option.

CAS / MDL: 9012-76-4 11097-59-9
研究领域: 土壤科学 · 环境科学
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