有机酸对铝氧化物吸附磷的影响

以存在不同配位阴离子 (硫酸根、磷酸根、草酸根、柠檬酸根 )时合成的铝氧化物为对象 ,用平衡吸附法研究了草酸、柠檬酸等的浓度和 pH对铝氧化物吸附磷的影响 ,并讨论有机酸影响磷吸附的机制。结果表明 :六种合成铝氧化物的最大吸磷量 (Xm)介于 0.189～ 0.838mmol/g ,以Al(OH)x的吸磷量最高 ,铝 柠檬酸复合物 (Al-CA)的吸磷量最低 ;有机酸浓度升高时 ,铝氧化物的吸磷量降低 ,且柠檬酸的影响程度高于草酸 ;先加 pH为 2的草酸或酒石酸 ,Al(OH)x对磷的次级吸附量最低 ,而有机酸pH为 3时 ,Al(OH)x对磷的次级吸附量达最高 ,有机酸溶液 pH由 4增至 9,铝氧化物吸磷量变化不大或逐渐降低。有机酸与磷混合加入同单加磷相比 ,pH 3时差异较小 ,pH 4～ 6时差异最显著 ,pH 7～ 8时又减小 ;有机酸降低铝氧化物吸磷量的机理包括酸性溶解和络合竞争两方面 ,在 pH 2时以前者为主 ,pH 3～ 9时以后者为主 ,且铝氧化物表面的吸附点位对供试配位阴离子都是亲合的     

铝同晶替代对铁(氢)氧化物表面活性的影响研究进展

铝同晶替代现象在铁(氢)氧化物中普遍存在，可改变铁(氢)氧化物的结构、表面特性和反应活性，影响土壤中元素的行为、形态和归趋。运用文献计量法分析了铝同晶替代铁(氢)氧化物的国内外研究现状，分别综述了铝同晶替代对铁(氢)氧化物晶体结构、表面电荷和界面过程的影响，从静电作用、比表面积、位点组成与密度、Fe/Al位点亲和性以及空位缺陷等方面阐明了铝同晶替代对铁(氢)氧化物表面活性和吸附行为的影响机制。在此基础上，提出了未来研究应着眼于构建铝替代量–结构–反应活性定量关系、深入探究铝同晶替代铁(氢)氧化物不同晶面上的界面机制，以及将研究对象与体系过渡到实际土壤等。     

氧化还原条件下有机物料对酸性土壤pH、铁形态和铜吸附解吸的影响

研究了添加有机物料对水稻土、红壤和砖红壤在干湿交替一次以后土壤pH、铁的形态和对铜吸附解吸行为的影响。结果表明,添加有机物料使得土壤pH升高,且随着有机物料加入量的增加而升高。与对照相比,添加有机物料可使水稻土、红壤和砖红壤的pH分别上升1.55、0.8和1.33个pH单位。红壤和砖红壤中无定形氧化铁含量增加,而水稻土中变化不大。在铜的平衡浓度为0.2 mmol/L时,添加有机物料培养可使水稻土、红壤和砖红壤铜的吸附量分别增加6.7、10.3和3.6 mmol/kg。     

外源有机质存在下钙铝交互作用对茶园土壤铝的吸附能力与活性的影响

通过实验室模拟,研究不同含量外源有机质存在下（5%、10%和15%）,钙铝交互作用（钙/铝摩尔浓度比为1∶2、1∶1和2∶1）对茶园土壤铝的吸附能力和活性的影响。结果表明,钙铝交互作用显著增加了茶园土壤对铝的吸附量,外源有机质对钙铝交互作用下茶园土壤铝的吸附作用影响不明显;钙铝交互作用使茶园土壤水溶态铝含量增加,交换态铝含量下降,且随钙/铝比的增大交换态铝含量下降越显著;但外源有机质使钙铝交互作用下茶园土壤的水溶态铝含量下降,同时交换态铝含量显著增加。总的看,外源有机质使钙铝交互作用下茶园土壤活性铝含量增加,且随外源有机质含量的增加,活性铝含量增加的越显著。     

三种铁氧化物的磷吸附解吸特性以及与磷吸附饱和度的关系

采用三种人工合成铁氧化物(针铁矿、赤铁矿和水铁矿)比较了结晶态和无定形铁氧化物对磷的吸附—解吸特性以及与磷吸附饱和度的关系。结果表明,三种铁氧化物的磷吸附特性均可用Langumir方程来描述,相关系数均大于0.9,达到极显著水平。从磷最大吸附量(Qm)、吸附反应常数(K)和最大缓冲容量(MBC)三项吸附参数综合考虑,水铁矿(无定形)对磷的吸附无论在容量还是强度方面均比结晶态铁氧化物针铁矿和赤铁矿大得多。水铁矿吸附的磷比针铁矿和赤铁矿所吸附的磷更难解吸;水铁矿的大量活性表面并没有表现出增加磷释放的作用。磷吸附饱和度有望作为评价土壤或铁氧化物磷吸附—解吸的强度和容量因子的一个综合指标。     

中国南亚热带乡土针阔树种人工林土壤不同形态铁铝氧化物对有机碳含量的影响

[目的] 探究南亚热带地区乡土针阔树种人工林土壤不同形态铁铝氧化物对土壤有机碳含量的作用特征,为深入理解该地区乡土树种人工林土壤有机碳积累机理提供科学依据。[方法] 以位于广西壮族自治区凭祥市的中国林业科学研究院林业试验中心的马尾松(Pinus massoniana)纯林、格木(Erythrophleum fordii)纯林和马尾松—格木混交林3个乡土针阔树种人工林为研究对象,应用电感耦合等离子体发射光谱仪以及重铬酸钾法分别测定各林分不同土层(0—20,20—40,40—60 cm)土壤铁铝氧化物含量和有机碳含量,采用方差分析法检验各观测指标在不同林分不同土层间的差异性,利用Pearson相关分析法探讨土壤不同形态铁铝氧化物与有机碳之间的关系。[结果] 马尾松—格木混交林土壤有机碳含量显著高于马尾松林和格木林,且3个林分土壤有机碳含量均随土层深度增加而减少;3个人工林土壤中各形态铁铝氧化物含量总体表现为：游离态氧化铁(Fe_d)＞游离态氧化铝(Al_d)＞无定形氧化铁(Fe₀)＞无定形氧化铝(Al_o)＞络合态氧化铁(Fe_p)＞络合态氧化铝(Al_p);土壤Fe_d与土壤有机碳含量显著负相关(p＜0.05),而土壤Fe_o,Fe_p和Al_p与土壤有机碳含量呈显著正相关关系(p＜0.05)。[结论] 南亚热带乡土针阔树种人工林土壤Fe_d含量高,因而增强了土壤有机碳的矿化能力,Fe_o,Fe_p和Al_p含量虽少,但有助于提升土壤有机碳的固持与稳定。     

成土年代系列土壤的铝硅氧化物变化特征

对海南岛北部玄武岩上发育的不同成土年龄系列土壤研究表明，随土壤年龄的增加，土壤中ＡｌＮａ和Ａｌｄｗｙｎdir辏? ｆｑｕｇdir     

添加无定形铝氧化物对雷竹林土壤有机质矿化的影响

土壤中无定形铝氧化物对有机质的存在有很大的影响,由于雷竹特殊的经营方式导致土壤中有机质快速积累,为了解无定形铝氧化物对土壤中快速积累的有机质分解产生的影响,本文通过往不同种植年限的雷竹林土壤中增加不同量的无定形铝氧化物(0、2、10、20、40 g/kg)以及室内密闭培养法测定CO2的释放量来反映有机质的分解状况,以便了解无定形铝氧化物对快速增加的雷竹林土壤有机质分解的影响,了解集约经营下的雷竹林土壤有机质的变化趋势及稳定性.结果表明,无定形铝氧化物的加入可显著抑制土壤有机质的分解,当无定形铝氧化物的加入量为40 g/kg时,对0年(水稻)、1年、5年、15年雷竹林土壤有机质分解的抑制率分别为56.97%、60.75%、58.87%、44.25%;0年(水稻)土壤加入无定形铝氧化物0、2、10、20、40 g/kg,对有机质分解的抑制效率分别为7.49%、38.04%、50.79%、56.98%.无定形铝氧化物对有机质分解的抑制效率随其加入量的增加而提高,但随土壤有机质含量的增加而下降.     

低分子量有机酸对高岭石中铝释放的影响

选择了几种土壤中可能存在的低分子量脂肪羧酸 ,研究了它们对高岭石中铝释放的影响。结果表明 ,有机酸可以通过络合作用促进高岭石中铝的释放。几种有机酸对体系中可溶性铝影响的大小顺序为 :草酸 >柠檬酸 >丙二酸 >苹果酸 >乳酸。草酸、柠檬酸和乳酸对可溶性铝释放的促进作用随体系pH的升高而减小 ,其中草酸体系中可溶性铝随pH的变化幅度最大。在苹果酸体系中 ,可溶性铝随pH的升高而稍有增加。体系中的可溶性铝随有机酸浓度的增加而增加 ,而交换性铝随柠檬酸浓度的增加而减少 ,先随苹果酸浓度增加而增加 ,然后又逐渐减少。与对照相比 ,柠檬酸和草酸使交换性铝的量减小 ,苹果酸和乳酸在低pH下使交换性铝明显增加 ,而苹果酸在较高pH下使交换性铝减少。有机酸影响释放出的铝在固液相间的分配比 ,苹果酸在低pH下使体系中释放出的大部分铝以交换性形态存在 ,而在较高pH下 ,大部分铝以可溶形态存在。在草酸体系中 ,释放出铝的大部分都以可溶形态存在。不同有机酸的不同表现与体系中铝的溶解平衡、铝的吸附 -解吸平衡、有机酸的吸附 -解吸平衡、有机酸的离解平衡和铝与有机酸的络合 -离解平衡有关。     

铁氧化物-胡敏酸复合物对磷的吸附吸附

本试验通过设置不同磷酸根浓度、 pH和不同电解质及电解质强度梯度,研究磷酸根在针铁矿-胡敏酸（HA）复合物和赤铁矿-胡敏酸（HA）复合物表面的吸附特性。X射线衍射（XRD）、 扫描电镜（SEM）和红外光谱（FTIR）图谱显示: 铁氧化物包覆胡敏酸后其内部结构特性保持不变; 氧化铁与胡敏酸通过氢键形成粒径大、 表面光滑的铁氧化物-HA复合微粒,且复合物比表面减小; 形成的氧化铁-胡敏酸复合物对磷的吸附能力增强,且针铁矿复合物的吸附能力大于赤铁矿复合物,均为多层吸附过程; pH增高抑制铁氧化物复合物对磷的吸附,同时电解质浓度增加促进复合体对磷的吸附,且反应后体系pH随之降低。     

Meta-analysis of experimental warming on soil invertase and urease activities

Soil enzymes are regulate terrestrial carbon (C) and nitrogen (N) cycles, and how the activity of these enzymes are affected by soil warming duration is unclear. In the study, the effect of experimental soil warming duration (<2 years and >2 years) on invertase and urease activities were examined by meta-analysis. Soil warming increased invertase activity by 22% (<2 years) and 16% (>2 years), respectively, while they increased urease by 29% and 9%. Meta-analysis of soil warming experiments found that warming by less than 1.5°C increased invertase by 22%, while warming it by more than 1.5°C increased invertase by 29%; the corresponding increases in urease were 16% and 8%. These effects of experiment warming differed among ecosystem types, with warming-induced increases being greatest in forest ecosystem. The results of this meta-analysis suggest that invertase and urease become less responsive to warming over longer periods and invertase with greater warming-responsiveness than urease activity.     

有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响

Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found.     

The use of reflectometric test kits for estimating nitrification and soil invertase activity in the field

The objective of this study was to test the applicability of different reflectometric test kits for the determination of potential nitrification and the activity of invertase in soil directly in the field. For the investigation of nitrification in the field, the incubation time was reduced because a linear correlation between incubation time and nitrification rates was found. Likewise, a linear correlation between invertase activity and the incubation temperature was observed which allowed for the calculation of temperature‐dependent factors. Activity measurements in the field at lower temperatures in comparison to the standard procedure were corrected by these factors. Ten different soils were investigated for potential nitrification and invertase activity with standard methods in comparison to field tests with reflectometric detection of the reaction products. The results showed that the reflectometric test kits are suitable for the estimation of potential nitrification and invertase activity directly in the field.     

Phosphate adsorption on uncoated and humic acid-coated iron oxides

Purpose

The phosphate adsorption on natural adsorbents is of particular importance in regulating the transport and bioavailability of phosphates in environmental system. In soils, oxides are often associated with organic matter and form mineral-organic complexes. The aim of the present paper was to investigate the mechanisms of phosphate adsorption on these complexes.

Materials and methods

Phosphate adsorption on uncoated and humic acid (HA)-coated iron oxide complexes was investigated at different ionic strengths and pH by isotherm experiments and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy.

Results and discussion

Results showed that HA-coated iron oxide complexes caused a decrease in the specific surface area (SSA) and the isoelectric point (IEP) of oxides. Phosphate adsorption on iron oxides was insensitive to changes of ionic strength, while it increased on the complexes with increasing ionic strength. The presence of HA decreased the maximum adsorption and the affinity of phosphate on the complexes. The zeta potential of phosphate-bound iron oxides linearly reduced with the increment of phosphate surface coverage, while the zeta potential of complexes with adsorbed phosphate kept at the same level. ATR-FTIR analysis suggested the formation of phosphate-metal complexation. The presence of HA promotes the formation of the monodentate phosphate complexes at pH 4.5 and significantly influenced phosphate species at pH 8.5.

Conclusions

The amount of phosphate adsorbed was reduced, and the phosphate speciation was also influenced when phosphate was adsorbed on HA-coated iron oxide complexes compared with phosphate adsorption on pure goethite and hematite.

     

Influence of iron oxides on cobalt adsorption by soils

Eleven soils from Denmark and Tanzania were extracted with ammonium acetate (controls), EDTA, and dithionite-EDTA (DE) to fractionate iron (and manganese) oxides. The amounts of cobalt adsorbed and acidity desorbed by the extracted soils as well as by two synthetic iron oxides were determined, using 0.85 mM cobalt in 0.2 m NaNO₃.
No significant correlations were found between cobalt adsorption and the contents of extractable manganese or organic matter, presumably because of their low contents. The major part of the cobalt adsorption (by DE-extracted samples) was due to the clay fraction and was associated with the release of approximately one proton per adsorbed Co. The remaining cobalt adsorption was attributed to the iron oxides. This portion of adsorbed cobalt was well described by considering soil iron oxides composed of only two fractions, an EDTA-extractable fraction of high reactivity and a less reactive fraction corresponding to the difference between DE-extractable iron and EDTA-extractable iron. Approximately 1.7 protons were released per Co adsorbed by these iron oxide fractions and by the synthetic iron oxides.
The amounts of cobalt adsorbed by the soil iron oxides were well predicted from the contents and specific surfaces of the two iron oxide fractions together with the specific cobalt adsorption of synthetic iron oxides.     

The influence of iron oxides on phosphate adsorption by soil

Soils from Denmark and Tanzania were extracted with ammonium acetate (controls), EDTA to dissolve amorphous iron oxides, and dithionite-EDTA (DE) to dissolve crystalline iron oxides. The phosphate adsorption capacities of the extracted soils were taken as the maximum quantity of phosphate adsorbed computed from the Langmuir equation. The decreases in the phosphate adsorption capacity following EDTA extraction and DE extraction were attributed to the removal of iron oxides. Close correlations (P<0.001) were found (i) between EDTA-extractable iron (amorphous iron oxides) and the decrease in phosphate adsorption capacity following EDTA extraction, and (ii) between the difference between DE-extractable iron and EDTA-extractable iron (crystalline iron oxides) and the further decrease in phosphate adsorption capacity following DE extraction. The phosphate adsorption capacity, estimated to be approximately 2.5 μmol P m^?2, was in good agreement with the capacity of various synthetic iron oxides. The calculated phosphate adsorption capacity of soil iron oxides, obtained from the contents and specific surfaces of amorphous and crystalline iron oxides together with the phosphate adsorption capacity per m² for synthetic iron oxides, compared favourably with the measured phosphate adsorption capacity.     

长期施肥对黑土酶活性和微生物呼吸的影响

以农业部哈尔滨黑土生态环境重点野外科学观测试验站28年长期定位试验为平台,研究了长期施用不同肥料对黑土酶活性及微生物呼吸强度的影响。结果表明,长期不同施肥处理后黑土过氧化氢酶、转化酶和脲酶的活性均产生较大的差异,有机无机肥料配合施用处理的土壤中脲酶和转化酶活性显著地高于单施化肥、有机肥和不施肥处理,施肥对土壤过氧化氢酶具有一定的抑制作用。相同施肥条件下0~20 cm土层土壤过氧化氢酶、转化酶和脲酶的活性均高于20~40 cm土层酶活性。此外,施肥对土壤真菌、细菌的呼吸都有一定的抑制作用。