CA2995159A1 - Leaching system which enhances monitoring of species in a fluid - Google Patents
Leaching system which enhances monitoring of species in a fluid Download PDFInfo
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- CA2995159A1 CA2995159A1 CA2995159A CA2995159A CA2995159A1 CA 2995159 A1 CA2995159 A1 CA 2995159A1 CA 2995159 A CA2995159 A CA 2995159A CA 2995159 A CA2995159 A CA 2995159A CA 2995159 A1 CA2995159 A1 CA 2995159A1
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/84—Systems specially adapted for particular applications
- G01N21/85—Investigating moving fluids or granular solids
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/251—Colorimeters; Construction thereof
- G01N21/253—Colorimeters; Construction thereof for batch operation, i.e. multisample apparatus
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/47—Scattering, i.e. diffuse reflection
- G01N21/49—Scattering, i.e. diffuse reflection within a body or fluid
- G01N21/53—Scattering, i.e. diffuse reflection within a body or fluid within a flowing fluid, e.g. smoke
- G01N21/534—Scattering, i.e. diffuse reflection within a body or fluid within a flowing fluid, e.g. smoke by measuring transmission alone, i.e. determining opacity
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/84—Systems specially adapted for particular applications
- G01N2021/8411—Application to online plant, process monitoring
- G01N2021/8416—Application to online plant, process monitoring and process controlling, not otherwise provided for
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2201/00—Features of devices classified in G01N21/00
- G01N2201/08—Optical fibres; light guides
- G01N2201/0826—Fibre array at source, distributing
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2201/00—Features of devices classified in G01N21/00
- G01N2201/08—Optical fibres; light guides
- G01N2201/0833—Fibre array at detector, resolving
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
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- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Abstract
Description
FLUID
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present document is based on and claims priority to U.S.
Provisional Application Serial No.: 62/035205, filed August 8, 2014, which is incorporated herein by reference in its entirety.
BACKGROUND
System monitoring during leaching operations may involve sampling and laboratory analysis of leach solutions by atomic absorption (AA) spectrometry or inductively coupled plasma (ICP) techniques, both of which may involve rigorous sample collection, preservation, processing, and laboratory technician activities in an analytical facility.
Although such facilities may be located in a central laboratory of a mine, some mines do not have in-house analytical capabilities. In this situation, the samples are instead shipped to commercial labs in different cities and/or countries. However, such sampling and off-line analysis may be limited in that real-time adjustments to the processing system may not be possible, e.g. adjustments resulting from delay between sample collection and processing.
In addition, data collection frequency and detection of time dependent fluctuations may be limited when discrete samples are collected from the process stream (e.g., as compared to a continuous measurement system). These shortcomings have given rise to various in-line systems, such as the Ion Selective Electrodes (ISE) system that has been utilized for copper analysis. However, the ISE systems and/or others have limitations when operating at high solution concentrations and/or in complex solution matrices.
As result, ISE and/or other conventional detectors may be primarily utilized to determine copper at low concentrations (e.g., less than about 10 ppm or 10 mg/L) in relatively fresh water.
Such measurements may also not be well suited to poor quality (e.g., high amounts of suspended solids) and/or complex industrial process waters, such as mine leaching circuits.
SUMMARY
copper, in a fluid flow stream. Additionally, the data obtained via the flow cell may be provided to a data processing system which may be used to automatically determine information, such as constituent concentration, within the flow stream. In many applications, the in-situ fiber optic transmission system and flow cell may be used in combination with the data processing system to provide real-time information on the flow stream.
BRIEF DESCRIPTION OF THE DRAWINGS
DETAILED DESCRIPTION
across the top of the leaching lift. With many conventional systems, such information often is lost.
The light may be transmitted into a small volume flow through a sampler that may continuously induce flow across the light path. In some applications, the flow of fluid may be induced by a vacuum pump and/or other motive force at the surface.
Additionally, the flow of fluid may be induced via osmotic gradients established by desiccants (such as silica gel, anhydrite, and/or other salts) or via continuous capillary flow to a sink at a constant potential due to a lower pressure head than at the location of a flow cell, e.g. sensor, used to detect the constituent.
However, spectrophotometric techniques may be utilized for detecting a variety of metals or other dissolved constituents in an aqueous or non-aqueous solution generated by a hydrometallurgical process. Furthermore, pH and other bulk properties of the solution may be detected via suitable detection systems with the addition of indicator components.
In a specific embodiment, an in-situ system as described in greater detail below may be used for monitoring of copper concentration in solution by ultraviolet-visible light (UV-Vis) infrared absorption spectroscopy. Real-time sensing of copper (or other constituents) in leaching operations may be utilized according to various applications.
Examples of such applications include the first application of leach solution to an ore material in a vat leaching system, in a pad leaching system, in a heap and dump leaching system, and/or in other suitable systems. An example is a mining system employing a heap/dump leaching operation for recovery of copper.
leach solution 28, within the flow cell 46. The beam of collated light 52 is at a known initial intensity and generated by a light emitter 54 which may be part of the detection system 48.
Dissolved elemental species in solution have specific absorption frequencies as a result of scattering interactions with light. The relative absorption can be related to the concentration of the dissolved element through the Beer-Lambert law, set forth below as Equation (1):
A = -104-4) = E = L
(1) where A is the measured absorbance, /0 is the intensity of the incident light at a given wavelength, Is is the transmitted intensity, c the concentration of the absorbing species, and L the path length through the sample. For each species and wavelength, c is a constant known as the molar absorbtivity or extinction coefficient, which is a molecular property in a given solvent at a particular temperature and pressure having units of 1 / M
= cm or AU / M = cm. The absorbance A and the extinction coefficient c may be defined in terms of the natural logarithm instead of the base 10 logarithm.
In some applications, however, the Beer-Lambert law may not hold as a universal relationship for the concentration and absorption of all substances so other appropriate laws relationships may be utilized. For example, UVNis spectroscopy may be utilized in the quantitative determination of solutions of transition metal ions, such as copper and iron, and highly conjugated organic compounds. As described above, this same technology may be utilized for a solution containing a dissolved species that absorbs light of selected frequencies. Examples of other mineral commodities that may be processed by hydrometallurgical techniques that may benefit from real-time, spatially-distributed concentration analysis according to one or more aspects of the present disclosure may include, gold, silver, manganese, chromium, cobalt, uranium, and/or one or more associated byproducts. Selected hydrometallurgical process systems described herein may be used to accommodate such applications.
pressure gradient may be induced across the flow cell 46 to cause pore fluid within the heap 24 to flow into the cell 46. The light that passes through the flow cell 46 may be absorbed, and the intensity attenuation may be measured by the detector/spectrometer 50 attached to the outlet portion of fiber optic cable 38.
OPTICS, INC. However, other types of detectors 50 may be used in certain applications.
The monitoring system 30 also may comprise various types of light sources, such as those in the UV-VIS wavelength range. Additionally, monitoring system 30 may comprise one or more sheathed fiber optic lines 38 or other suitable light transmission lines 38 which enable incident transmitted light distribution to flow through one or more cells 46 and/or for relay of transmitted light back to the one or more detectors, e.g spectrophotometer 50.
The flow cell 46 also may comprise various leach solution containing elements 62, as illustrated in Figure 4. Examples of elements 62 comprise various sample cell cuvettes, flow-through cells, capillary media, tubes, and/or other elements selected according to the parameters of the specific application. Additional examples of elements 62 include one or more micro-sized flow-through cells and flow cells having one or more acid and/or chemical-resistant windows (e.g. windows comprising sapphire) and/or light-transmissive capillary media. As described in greater detail below, the flow cells 46 also may instructed as or with sensors.
Depending on the application, the microlysimeters may comprise fluid catchments and/or containers and/or filter candles, such as filter candles formed of porous ceramic material or other suitable materials. The selected materials effectively exclude sediments and/or suspended solid matter in the analyzed fluid. The flow induction mechanism 64 also may comprise a suction pump or may utilize a moisture ore osmotic potential differential induced by silica gel, an anhydrite or salt block, and/or a moisture wick to atmosphere.
non-limiting example of a calibration matrix for concentration ranges applicable to solution mining of copper ores is set forth below in table provided in Figure 5.
families of microcontrollers, one or more embedded soft/hard processors in one or more field-programmable gate arrays (FPGAs) or other suitable devices. In some applications, other processors from other families also may be appropriate.
a volatile (e.g., random access) memory 74 and/or a non-volatile (e.g., read-only) memory 76, via a bus 78. The volatile memory 74 may comprise static random access memory (SRAM), synchronous dynamic random access memory (SDRAM), dynamic random access memory (DRAM), RAMBUS dynamic random access memory (RDRAM), and/or other types of random access memory devices. Similarly, the non-volatile memory 76 may comprise flash memory and/or other desired types of suitable memory devices. One or more memory controllers (not shown) may control access to the main memory and/or 76.
through a filter media to, for example, exclude suspended solids interferences; and into a light path. The light path is provided by fiber optic system 36 and the light path may be conducted by a fiber optic and/or other cable 38 for determination of absorbance spectra.
The flow of fluid through or along the flow cell(s) 46 may be induced utilizing an active or passive mechanism 64, thus providing a method for altering gradients, e.g.
a method that may utilize capillary rise into the light path of a sensor. Other active and/or passive mechanisms 64 may be configured for inducing the flow via pressure induced gradients, moisture induced gradients, temperature induced gradients, and/or osmotic induced gradients. The embodiments described herein may be used to promote flow from a pore space of the media into a flow cell and a siffl( such that the concentration of the species in the pore solution can be tracked over specified intervals of time by adjustment of the residence time in the flow cell(s) 46.
concentrations for copper) between sensors 90. An output may be displayed to an operator via output device 84. Examples of such an output include: a data array/table of copper and/or one or more other concentrations; a single and/or multiple sensor time series concentration of copper and/or one or more other concentrations; a two-dimensional and/or other cross-sectional display along a sensor string array or linking multiple arrays at sensor intercepts that show copper and/or other constituent gradients as contours, grey scale, other color schemes, and/or cloud diagrams, among other formats; a three-dimensional isocon display showing the copper and/or other constituent concentration gradients superimposed on a leach solution plume distribution; and/or other suitable types of rendered and/or processed data displays utilizing geodata visualization techniques and/or graphics, e.g. PETREL and SURFER visualization software available from Schlumberger Corporation.
However, some applications may utilize other media exhibiting total internal reflection along one or more axes of symmetry, e.g. ULEXITE.
diffusion and/or metered flow from a reservoir attached to the flow cell;
chemical gradient flow from an exchange cartridge attached to the flow cell; and other suitable techniques for releasing the indicator agent to the flow cell 46 containing the target solution. In some applications, the detection system 48 may be used to detect one or more dissolved chemical species in solution that have been chromatically separated from interfering species by flow through an ion exchange column.
copper and/or non-metal concentrations in situ. The light energy may be ultraviolet light, visible light, and/or infrared light. Additionally, the methodology to be used within a heap leach operation, within other solution mining units, in other associated conveyance systems, and/or in systems in which fluid analysis is performed at the source. By way of example, the constituents/species detected may be copper, precious metals, e.g. gold or silver, base metals, e.g. iron, zinc, cobalt, uranium, pH, bacteria, color, and/or other aqueous or non-aqueous species that produce an absorbance spectra when illuminated with light energy.
The processing system may utilize a calibration methodology according to selected characteristics and chemometric techniques to render a quantifiable copper and/or other constituent concentration. The concentration may be displayed in real time on a computer screen or other display output for operator interpretation.
For example, concentrations of copper may be determined between the cells 46/sensors 90.
hollow glass spheres. In such applications, the copper and/or other metal bearing solution may flow by capillary action along the pore spaces and interstices of the flow cell along the surfaces of the hollow glass spheres. The light is thus limited to passage through the surface film of solution that is held by surface tension along the glass or other surface of the sphere. Light energy may be absorbed by dissolved copper and/or other constituent species in the capillary fluid film held by surface tension between the spheres.
Light entering the spheres may pass through and exit the other surface of the sphere where it may intercept another film of leach solution that enters the cell.
The light may exit the cell 46 and be transmitted to a signal processing unit of detection system 48 and/or data processing control system 44 by one or more fiber optic cables or other suitable cables 38. By calibration against one or more reference solutions, the signal and/or data processing system may be utilized to compensate for the integral effects of multiple absorption paths through each capillary layer. A compensation for the path light reduction by the hollow sphere is thus possible. The degree of saturation may be determined by advanced signal processing utilizing, for example, a known concentration and/or independent water content measurement and/or calibration against known solution application rates and average degrees of saturation within the ore media. This calibration may be utilized to estimate the average path length of light passing through the capillary flow cell.
Additionally, the detection systems may utilize spectrophotometers 50 or other types of detectors for detecting the presence of the desired species, e.g. copper. Similarly, many types of data processing control systems 44 may be utilized with various software modules to enable the desired analysis of data collected via the flow cells 46.
Claims (20)
establishing a flow of leach solution in a leaching system;
locating a flow cell in situ within the leaching system at a source where the leach solution is being applied so the flow cell receives samples of leach solution from the flow of leach solution in the leaching system;
transmitting light energy through the flow cell and through the leach solution in the flow cell;
using spectroscopy to evaluate the light energy passing through the leach solution in the flow cell; and processing data resulting from the spectroscopy to determine concentration of a species in the leach solution.
a leach system having a plurality of flow cells disposed in a pattern throughout a region through which leach propagates, the plurality of flow cells being incorporated into a monitoring system which directs light through the plurality of flow cells and through leach solution within the flow cells, the monitoring system further comprising a detector to detect a desired constituent within the leach solution in real time.
locating a grid of cells throughout a system of porous material through which a fluid flows;
coupling the grid of cells with a fiber optic system;
transmitting light energy via the fiber optic system through the fluid which moves into the cells of the grid of cells; and monitoring the fluid in situ and in real time for characteristic changes in the fluid to determine a concentration of a specific constituent in the fluid.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462035205P | 2014-08-08 | 2014-08-08 | |
| US62/035,205 | 2014-08-08 | ||
| PCT/US2015/043914 WO2016022746A1 (en) | 2014-08-08 | 2015-08-06 | Leaching system which enhances monitoring of species in a fluid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2995159A1 true CA2995159A1 (en) | 2016-02-11 |
| CA2995159C CA2995159C (en) | 2020-07-28 |
Family
ID=55264537
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2995159A Active CA2995159C (en) | 2014-08-08 | 2015-08-06 | Leaching system which enhances monitoring of species in a fluid |
Country Status (2)
| Country | Link |
|---|---|
| CA (1) | CA2995159C (en) |
| WO (1) | WO2016022746A1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3814283B1 (en) * | 2018-06-29 | 2023-05-31 | Hach Company | Suspended solids measurement of wastewater |
| JP7591031B2 (en) * | 2019-08-26 | 2024-11-27 | パーティクル・メージャーリング・システムズ・インコーポレーテッド | Triggered sampling system and method - Patents.com |
| CN116822391B (en) * | 2022-12-15 | 2024-05-07 | 长江大学 | Theoretical method of nonlinear seepage of bulk fluid in heavy oil reservoirs |
| PE20252359A1 (en) * | 2022-12-22 | 2025-10-06 | Ingenieria E Informatica Sg Tis Spa | AUTONOMOUS SYSTEM FOR MONITORING VARIABLES IN LEACHING HEAPS |
| AU2024333224A1 (en) * | 2023-09-02 | 2026-04-09 | Fluid Photonics Corporation | Adaptive hydrometallurgical process control system and methods of using the same |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6542231B1 (en) * | 2000-08-22 | 2003-04-01 | Thermo Finnegan Llc | Fiber-coupled liquid sample analyzer with liquid flow cell |
| WO2004027099A1 (en) * | 2002-09-17 | 2004-04-01 | Frank Kenneth Crundwell | Heap leach process |
| FI119132B (en) * | 2005-06-15 | 2008-07-31 | Mine On Line Service Oy | Method and apparatus for treatment of ore |
| EP2486399A2 (en) * | 2009-10-08 | 2012-08-15 | GE Healthcare UK Limited | Multi-stream high-pressure liquid chromatography module |
| BR112013013608B1 (en) * | 2010-12-02 | 2020-10-13 | Wsp Global Inc. | method for monitoring the progress of leaching operations |
-
2015
- 2015-08-06 CA CA2995159A patent/CA2995159C/en active Active
- 2015-08-06 WO PCT/US2015/043914 patent/WO2016022746A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CA2995159C (en) | 2020-07-28 |
| WO2016022746A1 (en) | 2016-02-11 |
| WO2016022746A9 (en) | 2016-05-19 |
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