除草剂草甘膦在几种土壤和矿物上的吸附研究

通过批平衡实验考察了草甘膦在几种性质不同土壤和矿物上的吸附行为。研究发现土壤对草甘膦有较强的吸附能力，草甘膦在土壤上吸附量的大小与土壤理化性质密切相关。草甘膦在土壤和矿物上的吸附符合Freundlich吸附方程，其在土壤上的吸附常数K与土壤粘粒含量呈正相关，并随土壤氧化铁和氧化铝含量增加而增加，而与土壤的pH呈显著负相关。草甘膦在高岭石上的吸附量要比在蒙脱石上大，而草甘膦在金属离子饱和的蒙脱石和高岭石上的吸附研究结果表明，草甘膦在钠、钙、铁离子饱和的矿物上的吸附能力依次为Fe-蒙脱石〉Ca-蒙脱石〉Na-蒙脱石和Fe-高岭石〉Ca-高岭石〉Na-高岭石。     

EFFECT OF pH ON THE REACTION OF SODIUM FLUORIDE WITH HYDROUS OXIDES OF SILICON, ALUMINIUM, AND IRON, AND WITH POORLY ORDERED ALUMINOSILICATES

The release of hydroxyl ions from silica and ferric oxide gels on treatment with sodium fluoride solution is very small above pH values of 7.6 and 9 respectively. Hydroxyl release from alumina gel and poorly ordered aluminosilicates is appreciable at pH 9 and varies little with pH, but that from crystalline forms of alumina decreases with decrease of pH. For poorly ordered aluminosilicates, the ratio (OH′ released at pH 8.0): (OH′ released at pH 6.8) is directly proportional to the mole fraction Al/(Al+Si). The measurement of hydroxyl release at differing pH values may enable determination of hydrous alumina separately from the total poorly ordered inorganic gel material; moreover, the amount of hydroxyl released at high pH values is related to phosphate sorption capacity.     

SIMULATION OF THE WATER BALANCE OF SOIL COLUMNS AND FALLOW SOILS

A model is described that predicts the evaporation of water from, and the distribution of water in, a soil column evaporating into a constant environment. It is based on a numerical solution of the flow equation and requires only the initial water distribution in the column, the equilibrium (air-dry) water content at the soil surface and the relationship between volumetric water content and diffusivity. The model predictions show good agreement with a published analytical solution and with experimental results. Modifications to the model that allow for rewetting of the sod by rainfall, and changes in atmospheric conditions above the soil, enable predictions to be made of the water balance of a fallow field. In general, good agreement was obtained with the measured distribution of water deficits in the soil profile, although the predicted water content of the surface 2.5 cm of soil showed systematic differences from the measured values. The reasons for this are discussed.     

THE COVARIANCE OF PHOSPHATE SORPTION WITH OTHER SOIL PROPERTIES IN SOME BRITISH AND TROPICAL SOILS

Phosphate sorption capacity estimated by Piper's (1942) ‘anion exchange capacity’ and Bache and Williams's (1971) phosphate sorption index were correlated with soil pH, clay, organic matter, ‘free iron oxides’ and ‘extractable aluminium’ (McLean et al., 1958) for topsoil and subsoil samples from twenty tropical and twenty British acidic soil profiles. These two groups of soils did not differ significantly in phosphate sorption. Extractable aluminium and free iron oxide were well correlated with phosphate sorption, free iron oxide being superior to aluminium in freely drained British soils but not in poorly drained ones. Organic matter content correlated well with phosphate sorption for the poorly drained British soils, and for the tropical soils when sorption capacitywas measured using a high phosphate concentration.     

DETECTION OF CLAY IN SOIL SOLUTION WITH METHYLENE-BLUE PAPER AND THE ASSESSMENT OF CLAY MOBILITY IN SOILS

The adsorption of methylene blue and the accompanying colour change appears to be a fairly specific and sensitive reaction for colloidal soil clay, especially when used with chromatography paper as a supporting medium. Thus minute amounts of clay in migrating soil solutions can be detected, and stability and electro-phoretic mobility of very dilute suspensions evaluated.     

几种常见矿物与硼作用的红外光谱特性研究

对几种常见矿物及其与硼反应的红外光谱比较发现 ,硼在供试矿物上解吸的图谱更接近硼在矿物上吸附的图谱 ,而与无硼矿物图谱相差较大 ,故硼在几种常见矿物上都表现出不同程度的滞后性。针铁矿吸附硼后 ,在 1 40 0～ 1 44 0cm- 1 和 1 0 0 0～ 1 2 0 0cm- 1 范围处谱峰有不同程度的增强 ;水锰矿、三羟铝石和Ca 蒙脱石吸附硼后 ,此处谱峰却减弱 ,而在30 0 0～ 360 0cm- 1 处的谱峰 ,也随硼的吸附而明显减弱 ;Ca 蒙脱、三羟铝石吸附硼后 ,其图谱在 1 40 0～ 1 44 0cm- 1 和 1 62 0～ 1 670cm- 1 处的谱峰变化相似 ;水锰矿吸附硼的图谱在 1 0 0 0cm- 1 和 1 40 0～ 1 44 0cm- 1 处与三羟铝石吸附硼的图谱也有相似之处。     

海南岛土壤粘粒矿物特征与土壤系统分类

研究了海南岛不同母质土壤的粘粒矿物特征:都含有较多的高岭石,其中玄武岩发育土壤粘粒中高岭石最多,但其结晶最差。片岩和紫色砂岩发育土壤含相当多的水云母,粘粒部分水云母含量高达40％～45％,石灰岩发育土壤水云母含量亦较高,达20％～37％,此类水云母属二八面体型的水化白云母。玄武岩和花岗岩发育的“湿润”土壤粘粒中针铁矿与赤铁矿的含量之比为（3～4）:1,而花岗岩发育的“常湿”土壤粘粒中只有针铁矿,不见赤铁矿存在,证明土壤中氧化铁矿物的类型是土壤湿润状况的反应,在中国土壤系统分类中可以用来区分“湿润”和“常湿”土壤的一个指标。     

土壤和氧化铁对氟化物的吸附和解吸

本文研究了两种土壤(砖红壤和黄棕壤)和两种合成氧化铁(无定形氧化铁和针铁矿)对氟化钠溶液的吸附和解吸现象,讨论了氟离子吸附的吸附等温线特征.根据实验资料和吸附等温线的拟合情况,我们认为,砖红壤和无定形氧化铁用Langmuir公式来描述,黄棕壤和针铁矿用Freundlich公式来描述更为适宜.氟离子的解吸量均低于吸附量.研究结果表明,由于水洗和醇洗,一部分以静电引力所吸附的氟离子被洗去,造成氟离子解吸量偏低.     

中国土壤中粘粒矿物的分布规律

土壤粘粒部分的组成和性质在土壤发生学及土壤肥力特性的研究中都占很重要的位置。过去认为土壤粘粒中的无机物都是非晶形的,自从伦琴射线衍射应用到土壤学研究中后,大家都公认土壤粘粒部分含有晶形结构的矿物。     

THE USE OF CATHODOLUMINESCENCE IN THE IDENTIFICATION OF SOIL MINERALS

An apparatus, based on an optical microscope system, has been constructed for the subjective observation of cathodoluminescence, and the value of the technique has been determined for the examination of minerals and soils. The use of cathodoluminescence for the specific identification of minerals was found to be limited by the observation of different luminescent colours from the same minerals, and the same luminescent colour from different minerals. However, a sufficient variety of luminescent colours is believed to exist to allow the method to be used in conjunction with others for the identification of mineral grains. An examination of the trace element levels in a small group of mineral separates was found to be uninformative in trying to explain the variations in luminescent colours found.     

降解菌HD接种和非接种根围土壤中丁草胺的降解动力学研究

测定了小麦、棉花、水稻和玉米根围土壤和非根围土壤中丁草胺的降解特征和降解菌变化动态。结果表明,种植作物丰富了土壤微生物,根围土壤丰富的微生物对丁草胺的降解具有显著的促进作用。根围土壤中丁草胺的降解是非根围土壤的1.63～2.34倍,相应的半衰期缩短为非根围土壤的 42.2％～72.8％。根围土壤接种处理后这种促进作用得到进一步加强,其降解速率是非根围土壤的1.68～2.83倍,半衰期为非根围土壤的34.4％～59.4％。试验结果表明,作物根围是丁草胺残留快速降解的微环境,作物根围接种处理可以强化丁草胺残留的微生物降解。     

水稻土的物理机械性质与机械化耕作的关系

土壤机械化耕作措施应当密切考虑土壤物理机械性质,这些性厦是随着土壤合水量而变化,从而影响耕作的难易。因此,从探求土壤适耕性出发,开展土壤物理机械性厦的研究是十分必要的。     

红黄壤的轻矿物和重矿物

本文研究了玄武岩发育的红壤,花岗岩发育的红壤和山地黄壤中的轻、重矿物。轻矿物的主要成份是石英和长石,石英/长石的比率是玄武岩发育的红壤>花岗岩发育的红壤>花岗岩发育的山地黄壤。重矿物的主要成份是各种含铁矿物及铁氧化物裹着的石英粒,此外还有少量的角闪石、锆石、云母和电气石等。锆石与土壤的风化强度变化有密切关系,作为土壤风化演变过程的指示矿物是很合适的。     

衡山土壤的粘粒矿物

衡山的土壤,随着海拔高度的增加,依次分布着成土过程由强到弱的红壤、山地黄壤和山地草甸土.这个规律在粘粒矿物的组成上得到较好的反映.从山脚到山顶高岭石渐减,而三水铝石渐增.埃洛石则普遍存在,但以B,C层为多.风化程度较低的次要矿物如水云母、水黑云母、14(Å)过渡矿物和绿泥石等也是衡山的上部较多.从粘粒矿物组成的特点判断,衡山上部不存在山地黄棕壤,而只有山地黄壤和山地草甸土.衡山上部土壤的三水铝石含量很高,以致粘粒的硅铝率甚小.三水铝石可能是斜长石的直接风化产物.由这种方式产生的富铝化现象,在发生学上有别于热带土壤的富铝化作用.     

THE WEATHERING OF CHLORITIC MINERALS IN SOME SCOTTISH SOILS

The mineralogy of 14 chloritic soils of various drainage classes developed on different parent materials from the Loch Awe area of Argyllshire, Caithness, and the Southern Uplands reveals only minor variations'in clay mineralogy with profile depth, the frequent presence of primary minerals indicating that all the soils are immature, and that weathering is at an early stage. Iron-rich chlorite generally persists throughout the profiles, varying little in amount or chemical composition between horizons; where identifiable, the polytype is II b. Oxidation of iron modifies the thermal characteristics of the chlorite in all the freely-drained soils but usually only in the surface horizons of gleys. Irrespective of soil type or drainage class, in most profiles chlorite weathers only slightly, probably by vermiculitization around the edges of flakes.     

THE EQUILIBRIA OF K:Al EXCHANGE IN CLAY MINERALS AND ACID SOILS1

Conventional K: Al exchange isotherms for montmorillonite showed that Al³⁺ was strongly preferred to K⁺ in o-oin solutions. The exchange coefficient, K', calculated using the isotopically exchangeable K, was greater than unity and did not vary with the Al-saturation or with the initial pH of the AlCl₃ solutions. Isotherms for vermiculite, illite, and soils in o·oin solutions also showed Al³⁺-preference but unlike those for montmorillonite were not asymptotic to q_Al/q_o= 1, q_Al being the amount of adsorbed Al and q_o the total adsorbed (Al + K), indicating that some of the isotopically exchangeable K could not easily be exchanged by Al³⁺ ions; this difficultly exchangeable K (DEK) was estimated for each exchanger. K' values for vermiculite, illite, and soils were less than unity and did not vary with Al-saturation or initial pH if the isotopically exchangeable K was corrected for DEK. This showed that K⁺ was adsorbed more strongly than Al³⁺. Strengths of K⁺ adsorption referred to Al³⁺ as the counter-cation were in order: soils > vermiculite, illite > montmorillonite.