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1.
王洁  李传勋  郭霄  卢萌盟 《岩土力学》2022,43(10):2828-2840
软土固结过程中展现出明显的非线性压缩和渗透特性,同时竖井的淤堵效应常导致井阻在固结过程中随深度和时间不断演化,但目前能考虑井阻随时空演化的竖井地基非线性固结解析解还很鲜见。通过引入孔隙比与有效应力及孔隙比与渗透系数间的半对数模型描述了土体的非线性固结特性,建立了能同时考虑井阻随时空变化和涂抹影响的竖井地基非线性固结模型,并采用分离变量法获得了固结模型的解析解。将特定参数下固结解的计算结果与实测数据、已有的竖井地基固结解答进行了对比分析以验证其可靠性。最后,对竖井地基的非线性固结性状开展了大量计算分析。结果表明:竖井渗透系数随深度线性衰减越明显则地基固结速率越慢;外荷载一定时,随着软土压缩指数cc与渗透率指数ck之比的增大,竖井地基固结速度减慢;在cc /ck值不变的情况下,外荷载增加,地基固结速率加快。在涂抹区的3种径向渗透系数变化模式中,抛物线变化模式下的地基固结速度最快,线性变化模式下的地基固结速度次之,恒定模式下的地基固结速度最慢,且这种性状并不因为考虑井阻变化或土体非线性固结特性而发生改变。  相似文献   

2.
许波  雷国辉  郑强  刘加才 《岩土力学》2014,35(6):1607-1616
为评估涂抹区土体压缩和渗透系数变化对含竖向排水体地基固结的影响,采用等体积应变假设,考虑涂抹区土体的压缩变形及其水平向渗透系数沿径向分别呈线性和抛物线分布,并考虑井阻作用以及地基附加球应力沿深度任意分布,推导了随时间线性堆载预压条件下固结微分方程的显式解析解答,分析了涂抹区半径、水平向渗透系数的分布模式、以及体积压缩系数对地基整体平均固结度的影响。结果表明,涂抹区土体采用均匀折减的水平向渗透系数明显低估了地基的固结速率,而当涂抹区半径较大时,不考虑涂抹区土体的压缩变形将会高估地基的固结速率。在含竖向排水体地基固结问题的分析中,这些影响不可忽视。  相似文献   

3.
根据浙江沿海地区滩涂围垦中的淤泥基础海堤工程设计经验,认为软土工程中竖井地基固结计算需考虑井阻随时间的影响,基于竖井渗透系数随时间指数衰减关系假定,利用竖井地基径向固结理论和等应变假设,并考虑多级线性加载及循环荷载等复杂荷载作用,重新推导了考虑井阻非线性影响下竖井地基固结解析解,通过与TANG X W等(2000)、Zhu G等(2004)恒定井阻地基固结理论的对比,验证了本文理论的正确性。根据本文理论,通过对比分析,认为线性加载时间越长,竖井地基前期固结速率越慢,与骤加恒载工况差异越显著。在循环荷载作用下,地基固结速率一般介于荷载最大值和荷载最小值的恒载情况之间;且固结度随外荷载的波动而相应地滞后性震荡,竖井渗透系数衰减越快,其震荡越明显,最终趋向于稳定震荡。  相似文献   

4.
《岩土力学》2017,(9):2574-2582
基于径向固结理论和等应变假设,考虑真空预压过程中真空泵故障、漏气等不利影响以及排水体井阻时空非线性影响,推导了以排水体中超静孔隙水压uw为函数的3阶拟线性偏微分方程,并将膜下真空度随时间的变化曲线作为边界条件,考虑吹填土的自重固结影响,分别给出了真空预压地基考虑漏气影响且排水体渗透系数随深度线性衰减及时间指数衰减时的固结解析解。最后通过与现有多个固结解的对比分析,认为它们一般为新解的特例,并通过算例计算比较分析,认为井阻随时间影响参数A_2对固结度的影响比随深度影响参数A_1更敏感。当参数A_2足够大时,则认为排水体很快就淤堵以至于不具备排水能力,参数A1则可等效反映真空度随深度的衰减影响,且真空预压过程中漏气对地基固结度具有直接影响,漏气越严重则固结排水越慢,需延长真空预压时间,以保证真空预压效果。  相似文献   

5.
基于Barron砂井地基等应变固结理论及Gibson一维大变形固结理论,同时考虑了砂井的井阻效应、径向渗透系数的变化及竖向渗流等因素,推导建立了更具普遍性的砂井地基大变形固结方程,并采用有限差分法对该方程进行了求解。通过将所求的差分解答与已有的固结模型及小变形解析解进行比较,对差分解答的正确性进行了验证。基于差分解答,对砂井地基的大变形固结性状展开分析。分析表明:砂井的井阻效应会降低砂井地基的固结速率,但当砂井的渗透系数增大到一定程度时,砂井的井阻效应可忽略;径向渗透系数的变化模式会对砂井地基的固结速率产生较大影响,相比于线性变化模式,抛物线变化模式下的固结速率较快;竖向渗流加快了砂井地基的固结速率,当井径比较小时,应考虑竖向渗流对砂井地基固结速率的影响;压缩指数与渗透指数的比值越大,砂井地基的固结速率越慢。  相似文献   

6.
在软基处理工程中,经常出现竖井打设变密而地基固结效率降低的现象。鉴于此,建立了重叠涂抹区内土体水平向渗透系数的分布函数,给出了涂抹区重叠时竖井地基超静孔压和平均固结度的解析解。通过分析不同工况下竖井地基固结度随竖井间距的变化情况,探究了竖井间距减小而地基固结效率不增反减的成因。最后,探讨了涂抹作用和井阻作用对竖井最小临界间距的影响。结果表明:相邻竖井涂抹区重叠是竖井地基中出现竖井最小临界间距的根本原因。涂抹作用越大,则竖井最小临界间距越大;具体表现为当地基扰动程度增大时或涂抹区半径增大时,竖井最小临界间距随之增大。井阻作用越大,则竖井最小临界间距越小;具体表现为当竖井渗透系数减小时、竖井长度增大时或竖井半径减小时,竖井最小临界间距随之减小。  相似文献   

7.
李红坡  梅国雄  肖涛  陈征 《岩土力学》2020,41(5):1560-1566
在软基处理工程中,经常出现竖井打设变密而地基固结效率降低的现象。鉴于此,建立了重叠涂抹区内土体水平向渗透系数的分布函数,给出了涂抹区重叠时竖井地基超静孔压和平均固结度的解析解。通过分析不同工况下竖井地基固结度随竖井间距的变化情况,探究了竖井间距减小而地基固结效率不增反减的成因。最后,探讨了涂抹作用和井阻作用对竖井最小临界间距的影响。结果表明:相邻竖井涂抹区重叠是竖井地基中出现竖井最小临界间距的根本原因。涂抹作用越大,则竖井最小临界间距越大;具体表现为当地基扰动程度增大时或涂抹区半径增大时,竖井最小临界间距随之增大。井阻作用越大,则竖井最小临界间距越小;具体表现为当竖井渗透系数减小时、竖井长度增大时或竖井半径减小时,竖井最小临界间距随之减小。  相似文献   

8.
史蓝天  李传勋  杨洋 《岩土力学》2023,44(1):183-192
竖井排水固结法中井阻随时空演变(即由淤堵和弯折所引起的竖井排水能力下降)的现象已引起广泛关注,且变井阻对竖井地基固结速率的影响不容忽略。但目前能同时考虑变荷载及井阻随时间和空间变化的固结解析解还鲜有报道。考虑井阻随时空演变过程,引入实际中广泛采用的单级或多级加载模式,建立了竖井地基固结模型,并应用分离变量法获得固结模型的解析解答。通过与已有的解析解、有限差分解及工程实测值进行对比分析,充分验证了该模型的正确性。通过大量的计算,分析变井阻参数对竖井地基固结性状的影响。结果表明:竖井地基固结速率随竖井最终排水能力的增大而加快,随深度井阻参数及时间井阻参数的增大而减缓,且时间井阻参数的影响更为显著。  相似文献   

9.
叶观宝  张晴雯  张振 《岩土力学》2016,37(12):3356-3364
真空联合堆载预压与混凝土芯砂石桩复合地基相结合是处理深厚软土地基的一种新方法。该方法既能利用预制混凝土芯桩提高地基承载力,又能利用砂石外壳缩短排水路径、传递真空负压,加快固结。根据真空联合堆载预压下混凝土芯砂石桩复合地基的固结特点,将堆载预压和真空预压的固结效应分开考虑,然后再进行叠加,推导出了真空联合堆载预压下混凝土芯砂石桩复合地基的平均固结度解析解,并利用三维数值模拟对平均固结度解析解进行了验证。通过对解析解的参数分析,探讨了置换率、涂抹区大小及渗透系数、混凝土芯砂石桩长径比和芯桩率对混凝土芯砂石桩复合地基固结特性的影响。结果表明,混凝土芯砂石桩复合地基的固结速率随着置换率和芯桩率的增大而增大,随涂抹区和砂石外壳直径之比、未扰动区和涂抹区渗透系数之比、长径比的增大而减小。  相似文献   

10.
以往的非饱和土竖井地基研究中未同时考虑竖井的井阻和涂抹作用,大部分按理想竖井进行研究,然而井阻和涂抹作用是影响非饱和土竖井地基固结的重要因素。针对这种情况,本文基于Fredlund非饱和土一维固结理论及等应变假设,引入变量将超孔隙压力耦合控制方程组转化为等价的线性偏微分方程组,考虑涂抹和井阻条件,并采用分离变量法和待定系数法,推导出了瞬时荷载下同时考虑井阻和涂抹作用的非饱和土竖井地基等应变固结解析解。将所得解析解进行退化,与既有的饱和土竖井地基等应变固结解析解对比,验证了本文解析解的正确性,并应用典型算例分析了井阻和涂抹作用对竖井地基固结的影响。结果表明,井阻因子G、井径比N、涂抹系数α及涂抹半径与竖井半径比S这四者任何一个值减小,非饱和土竖井地基的固结速度都将变快;井阻因子G小于0.1时,建议实际工程中不考虑井阻作用的影响;当涂抹半径与竖井半径比S大于5时,涂抹作用对竖井地基固结的影响与S=5时无明显差异。实际工程中建议提高非饱和土竖井地基的透水能力并减少施工扰动,以降低井阻和涂抹作用对非饱和土竖井地基固结影响。  相似文献   

11.
In order to avoid the pollution of trace metals in marine environment, it is necessary to establish the data and understand the mechanisms influencing the distribution of trace metals in marine environment. The concentration of heavy metals (Fe, Mn, Cr, Cu, Ni, Pb, Zn, Co and Cd) were studied in sediments of Ennore shelf, to understand the metal contamination due to heavily industrialized area of Ennore, south-east coast of India. Concentration of metals shows significant variability and range from 1.7 to 3.7% for Fe, 284–460 μg g−1 for Mn, 148.6–243.2 μg g−1 for Cr, 385–657 μg g−1 for Cu, 19.8–53.4 μg g−1 for Ni, 5.8–11.8 μg g−1 for Co, 24.9–40 μg g−1 for Pb, 71.3–201 μg g−1 for Zn and 4.6–7.5 μg g−1 for Cd. For various metals the contamination factor (CF) and geoaccumulation index (I geo) has been calculated to assess the degree of pollution in sediments. The geoaccumulation index shows that Cd, Cr and Cu moderately to extremely pollute the sediments. This study shows that the major sources of metal contamination in the Ennore shelf are land-based anthropogenic ones, such as discharge of industrial wastewater, municipal sewage and run-off through the Ennore estuary. The intermetallic relationship revealed the identical behavior of metals during its transport in the marine environment.  相似文献   

12.
Isothermal thermogravimetric experiments have been carried out to determine the reaction kinetics of the dehydration processes in fuller's earth, a natural Ca-montmorillonite. Dehydration in swelling clays is a complex reaction, and analysis of the thermogravimetric data using empirical rate equations and time-transformation analysis reveals that the nature of the rate controlling mechanism is dependent upon both the temperature regime of the sample as well as the extent of reaction. For fuller's earth, we find that the dehydration kinetics are dominated by a nucleation and growth mechanism at low temperatures and fractions transformed (stage I), but above 90 °C the last stages of the reaction are diffusion controlled (stage II). The activation energy for dehydration during stage I is around 35 kJ · mol−1, whereas the removal of water during stage II requires an activation energy of around 50 kJ · mol−1. These two stages of dehydration are associated with primary collapse of the interlayer (stage I) and movement of water that is hydrated to cations within the interlayer (stage II). Received: 28 August 1998 / Revised, accepted: 27 January 1999  相似文献   

13.
Although, the Eastern Desert of Egypt forms about 22% of the surface area of the country, the area is undeveloped due to the limited availability of water. The morphologic units of the Eastern Desert consist of a number of drainage basins covering about 147,820 km2 (66.5% of the total surface area of the Eastern Desert). The basins drain the occasional rainwater, either towards the Nile Valley or to the Red Sea, causing flood hazards. The availability of water from the hydrologic systems of these basins could be improved by constructing runoff controlling systems in these areas (e.g. dykes and partially effective dams), which could save and make use of a considerable amount of water. The groundwater resources in the Eastern Desert can be divided into four main water-bearing units: the fractured crystalline Pre-Cambrian aquifer, the Nubian sandstone aquifer, the fractured limestone and sandstone aquifer and the Quaternary aquifer. The most productive aquifer is the Nubian sandstone while the fractured limestone and sandstone (Miocene) are only productive along the eastern part of the desert. The Quaternary aquifer occurs along the major dry washes (wadis) and is considered of limited potential as it is recharged mainly from the occasional rainfall. Detailed assessment of these aquifers should be carried out locally for further development of the area.
Resumen Aunque el Desierto Oriental de Egipto constituye alrededor del 22% de la superficie del país, esta área no se encuentra desarrollada por causa de la escasez de agua. Las unidades morfológicas del Desierto Oriental consisten de un número de cuencas de drenaje que cubren alrededor de 147,820 km2 (66.5% del área superficial total del Desierto Oriental). Estas cuencas drenan las aguas lluvias ocasionales, bien hacia el Valle del Nilo o hacia el Mar Rojo, causando amenazas de inundación. La disponibilidad de agua a partir de los sistemas hidrológicos de estas cuencas, puede ser mejorada al construir sistemas de control de escorrentía allí (Ej. Diques y presas de efectividad parcial), las cuales podrían almacenar y permitir el uso de una cantidad considerable de agua. Los recursos de agua subterránea en el Desierto Oriental, pueden dividirse en cuatro unidades principales portadoras de agua: El acuífero fracturado cristalino Pre – Cámbrico, el acuífero de la Arenisca de Nubia, el acuífero de arenisca y caliza fracturadas y el acuífero Cuaternario. El acuífero más productivo es la arenisca de Nubia, mientras que la arenisca y caliza fracturadas (Mioceno), son productivas únicamente a lo largo de la parte oriental del desierto. El acuífero Cuaternario se encuentra a lo largo de las corrientes intermitentes mayores (Wadis) y se le considera de potencial limitado por ser recargado principalmente a partir de lluvia ocasional. Una evaluación detallada de estos acuíferos debe llevarse a cabo localmente, para el desarrollo adicional de esta área.

Résumé Bien que le Désert Est occupe 22% de la surface de lEgypte, la région est sousdeveloppée à cause de la ressource en eau limitée. Les unités morphologiques consistent en des bassins drainant qui couvrent une surface de 147,820 km2 ,représentant 66.6% de la surface du Désert Est. Les bassins drainent les plues intermittentes vers la vallée du Nil ou vers la Mer Rouge en provocant des inondations. On peut augmenter la ressource en eau dans cette région en réalisant des systèmes de contrôle de ruissellements (des digues...) qui peuvent sauver et utiliser un volume considérable deau. La ressource en eau souterraine du Désert Est est cantonnée dans quatre grandes structures: l› aquifère fracturé cristallin Précambrien, l› aquifère gréseux Nubien, l› aquifère calcaire et gréseux et l› aquifère quaternaire. Le plus productif est l› aquifère gréseux Nubien tendis que les calcaire et les grèses dage miocène sont productives seulement dans la partie est du désert. L› aquifère quaternaire se trouve au long des oueds sèches et on considéré quil a un potentiel limité, étant rechargé seulement par les plues intermittentes. Pour le futur développement de la région il est nécessaire une évaluation détaillée, à léchelle locale de ces aquifères.
  相似文献   

14.
The lithostratigraphy, depositional environment and age of the Marwar Supergroup have been reviewed in the light of report of δ13C depletion recorded in the carbonates of the Bilara Group (middle part of Marwar Supergroup) and discovery of trilobite-like trace fossils from the ·Red bedsŽ of Nagaur Group (upper part of Marwar Supergroup). The δ13C depletion observed in Bilara carbonates is not a result of glaciation rather due to rapid burial and poor water circulation in the low energy water of the protected basin. Secondly, the trace fossils are, in fact, traces of notostracan crustaceans found in shallow fluvial and shallow lacustrine environment. The present paper also records a spiral, burrowing trace-fossil, possibly Gyrolithes, from a cross-bedded sandstone of the Jodhpur Group.  相似文献   

15.
A pressure-volume-temperature data set has been obtained for lawsonite [CaAl2Si2O7(OH)2.H2O], using synchrotron X-ray diffraction and an externally heated diamond anvil cell. Unit-cell volumes were measured to 9.4 GPa and 767 K by angle dispersive X-ray diffraction using imaging plates. Phase changes were not observed within this pressure-temperature range, and lawsonite compressed almost isotropically at constant temperature. The P-V-T data have been analyzed using a Birch- Murnaghan equation of state and a linear equation of state expressed as β=–1/V0 (∂V/∂P) T . At room temperature, the derived equation of state parameters are: K 0=124.1 (18) GPa K'0 set to 4) and β–1=142.0(24) GPa, respectively. Our results are intermediate between previously reported measurements. The high-temperature data show that the incompressibility of lawsonite decreases with increasing temperature to ∼500 K and then increases above. Hence, the second order temperature derivative of the bulk modulus is taken into account in the equation of state; a fit of the volume data yields K 0=123.9(18) GPa, (∂K/∂T)P=–0.111(3) GPa K–1, (∂2 K/∂T 2)P=0.28(6) 10–3 GPa K–2, α0=3.1(2) 10–5 K–1, assuming K'0=4. Received: 2 June 1998 / Revised, accepted: 12 Ocotber 1998  相似文献   

16.
In situ X-ray diffraction measurements of Fe- and Al-bearing MgSiO3-rich perovskite (FeAl-Pv), which was synthesized from a natural orthopyroxene, were performed at pressures of 19–32 GPa and temperatures of 300–1,500 K using a combination of a Kawai-type apparatus with eight sintered-diamond anvils and synchrotron radiation. Two runs were performed using a high-pressure cell with two sample chambers, and both MgSiO3 perovskite (Mg-Pv) and FeAl-Pv were synthesized simultaneously in the same cell. Thus we were able to measure specific volumes (V/V 0) of Mg-Pv and FeAl-Pv at the same P−T conditions. At all the measurement conditions, values of the specific volume of FeAl-Pv are consistent with those of Mg-Pv within 2 Standard Deviation, strongly suggesting that effect of incorporation of iron and aluminum on the thermoelastic properties of magnesium silicate perovskite is undetectable in this composition, pressure, and temperature range. Two additional runs were performed using a high-pressure cell that has one sample chamber and unit-cell volumes of FeAl-Pv were measured at pressures and temperatures up to 32 GPa and 1,500 K, respectively. All the unit-cell volume data of FeAl-Pv perovskite were fitted to the high temperature Birch–Murnaghan equation of state and a complete set of thermoelastic parameters of this perovskite was determined with an assumption of K′ 300,0 = 4. The determined parameters are K 300,0 = 243(3) GPa, (∂K T,0/∂T) P = −0.030(8) GPa/K, a 0 = 2.78(18) × 10−5 K−1, and b 0 = 0.88(28) × 10−8 K−2, where a 0 and b 0 are the coefficients of the following expression describing the zero-pressure thermal expansion: α T,0 = a 0 + b 0 T. The equation-of-state parameters of FeAl-Pv are in good agreement with those of MgSiO3 perovskite at the conditions corresponding to the uppermost part of the lower mantle.  相似文献   

17.
 Ca-chloride waters are defined as those in which Q=rCa/r(SO4+HCO3)>1, rNa/rCl<0.80, rMg/rCa<0.5 and wCl/wBr<286 (r=meq l–1 and w=mg l–1). Throughout the last 50 years, different models for the formation of such waters have been suggested. These models include: (1) filtration through semipermeable membranes under conditions of highly compacted argillaceous sediments, (2) deaquation of seawater by evaporation and/or by freezing followed by dolomitization, (3) hydrolysis of plagioclase and biotites in igneous metamorphic rock masses, (4) radiolytic modification of residual metamorphic fluids, and (5) dissolution of chalks followed by ion exchange on smectites. The better understanding of processes and of natural environments leading to the evolution and natural occurrence of such brines, is imperative for the prospection and further sustained exploitation of such waters. Received: 11 October 1996 · Accepted: 24 February 1997  相似文献   

18.
激光焦平面变化对LA-ICPMS锆石U-Pb定年准确度的影响   总被引:3,自引:0,他引:3  
元素分馏是影响LA-ICPMS锆石U-Pb定年准确度的重要因素之一,通常利用标样进行校正。激光聚焦位置变化会引起剥蚀坑形貌及U-Pb分馏的改变,标样和样品聚焦条件不一致将导致标样难以准确校正样品,并最终影响定年结果的准确性,但影响的程度、机制及可容忍范围目前尚不清楚。为此,文章以91500为标样、GJ-1为样品,详细研究了聚焦偏离30μm范围内剥蚀标样与样品锆石的剥蚀坑形貌变化以及由此导致的U-Pb定年误差。实验表明,在距离锆石表面30μm范围内,标样和样品焦平面同步变化时,二者U-Pb分馏形式及程度基本一致,激光焦平面偏离所引起的样品年龄与TIMS推荐值的偏差小于1%;当二者聚焦不同步时,标样与样品的U-Pb分馏差别显著,年龄偏差最大可超过3%。激光聚焦不同步导致的标样与样品剥蚀坑纵横比差异是引起年龄误差的根本原因,激光焦平面偏离锆石表面超过15μm,剥蚀坑坑口明显变大,纵横比减小,U-Pb分馏形式及程度发生改变。通过预剥蚀锆石,观察剥蚀坑轮廓,使激光焦平面在距离锆石样品表面15μm范围内,可确保标样与样品剥蚀坑形貌及U-Pb分馏状态一致,提高LA-ICPMS定年的准确度。  相似文献   

19.
On the south-eastern edge of Russia, the chemical composition of rainwater is controlled by sea salts, terrestrial material, as well as volcanic (Kuril islands volcanic area) and anthropogenic emissions, mostly in the southern part of the area. The predominant major ions of the Primorye, Sakhalin and the Kuril Islands rainwaters were respectively HCO3–SO42−, Ca–Na, and of Cl–Na. Concentration of trace elements changes within 1–2 orders of magnitude but some difference in the distribution of the elements between continental and island rainwater is found. The concentration of the chemical elements in the particulate fraction varies from < 10% to 90% of the total concentration (dissolved + particulate) with the following distribution: Tl, Na, Ca, Sr, Zn, Cd (< 10%)–Be, Th, Bi, Rb, U, K, Sc (10–20%)–Cu, Mn, Mg, Mo, Se, Ba, Ni, As, Ag, Cs, Co, Y, Ga, V (20–50%)–Sb, Pb, Ge, Cr, Fe, Al (50–90%).The concentration of elements of the particulate fraction of the rainwater usually is significantly different from concentrations in the crust, including both higher and lower concentrations. The terrestrial contribution to dissolved elements was evaluated and follows the decreasing order: Fe > K, Mg, Ca > Ba, Sr > Na (65–1%). Close order was found for total (dissolved and solid) concentrations. Sea salt contribution to dissolved element concentration in the rainwater decrease in the following order: Cl, Mg > K, SO4 > Ca > HCO3, Ba, Fe (78–0.1%). Calculation of anthropogenic and volcanic inputs for two ions (Cl and SO42−) shows that anthropogenic inputs for the Vladivostok and Yuzno-Sakhalinsk cities can be evaluated as 15–20% of Cl and up to 80–90% of SO42−. Volcanic components in the Kuril Islands, where anthropogenic inputs are absent, can reach up to 76% of SO42− and 36% of Cl.  相似文献   

20.
We investigate the performance of sample preparation of gold ores using vibratory (bowl, ring and puck type) mills in common use in mineral analytical laboratories. The main criteria for effective grinding are using reduced grinding charge masses ≤ ca. 50% of nominal bowl capacity and using a grinding aid to prevent caking. We show that gold particles of millimetre scale can be comminuted to ≤ 100 µm by grinding in silica flour, bauxite, synthetic carborundum, or mixtures of silica and these materials using times of up to 5 min and that 95% < 50 µm is achievable with extended grinding. This suggests that modified grinding techniques can be used to make sample masses ≤ 5 g viable for routine determination of gold in geological samples. We also demonstrate homogenisation of a gold‐bearing copper sulfide mineral flotation concentrate alone and in mixtures with silica by extended grinding at reduced charge masses. To support this work, we develop a convenient new benchmark of gold ore sample preparation performance ‘G’, an apparent maximum gold particle size interpolated from replicate analytical variance in order to overcome the limitations of laborious sieve fraction analysis of gold particle size. We show useful agreement between G and sieve fraction analysis of gold particle size in samples and test the viability of G experimentally and by analysis of literature data.  相似文献   

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