Department Surface Waters - Research and Management

A new portable CE instrument is presented. The instrument features the concurrent separation of anions and cations in parallel channels. Each channel has a separate buffer container to allow independent optimization of separation conditions. The microfluidics circuit is based on off-the-shelf parts, and can be easily replicated; only four valves are present in the design. The system employs a miniature automated syringe pump, which can apply both positive and negative pressures (-100 to 800 kPa). The application of negative pressure allows a semi-automatic mode of operation for introducing volume-limited samples. The separations are performed in a thermostatted compartment for improved reproducibility in field conditions. The instrument has a compact design, with all components, save for batteries and power supplies, arranged in a briefcase with dimensions of 52 × 34 × 18 cm and a weight of less than 15 kg. The system runs automatically and is controlled by a purpose-made graphical user interface on a connected computer. For demonstration, the system was successfully employed for the concurrent separation and analysis of inorganic cations and anions in sediment porewater samples from Lake Baldegg in Switzerland and of metal ions in a sample from the tailing pond of an abandoned mine in Argentina.

A novel micro-injector for capillary electrophoresis for the handling of samples with volumes down to as little as 300 nL was designed and built in our laboratory for analyses in which the available volume is a limitation. The sample is placed into a small cavity located directly in front of the separation capillary, and the injection is then carried out automatically by controlled pressurization of the chamber with compressed air. The system also allows automated flushing of the injection chamber as well as of the capillary. In a trial with a capillary electrophoresis system with contactless conductivity detector, employing a capillary of 25 μm diameter, the results showed good stability of migration times and peak areas. To illustrate the technique, the fast separation of five inorganic cations (Na⁺, K⁺, NH₄⁺, Ca²⁺, and Mg²⁺) was set up. This could be achieved in less than 3 min, with good limits of detection (10 μM) and linear ranges (between about 10 and 1000 μM). The system was demonstrated for the determination of the inorganic cations in porewater samples of a lake sediment core.

Distinct layers of iron(III) and manganese(IV) (Fe/Mn) oxides are found buried within the reducing part of the sediments in Lake Baikal and cause considerable complexity and steep vertical gradients with respect to the redox sequence. For the on-site investigation of the responsible biogeochemical processes, we applied filter tube samplers for the extraction of sediment porewater combined with a portable capillary electrophoresis instrument for the analyses of inorganic cations and anions. On the basis of the new results, the sequence of diagenetic processes leading to the formation, transformation, and dissolution of the Fe/Mn layers was investigated. With two exemplary cores we demonstrate that the dissolution of particulate Fe and Mn is coupled to the anaerobic oxidation of CH₄ (AOM) either via the reduction of sulphate (SO₄²⁻) and the subsequent generation of Fe(II) by S(−II) oxidation, or directly coupled to Fe reduction. Dissolved Fe(II) diffuses upwards to reduce particulate Mn(IV) thus forming a sharp mineral boundary. An alternative dissolution pathway is indicated by the occurrence of anaerobic nitrification of NH₄⁺ observed at locations with Mn(IV). Furthermore, the reasons and consequences of the non-steady-state sediment pattern and the resulting redox discontinuities are discussed and a suggestion for the burial of active Fe/Mn layers is presented.

Careful extraction and analysis of porewater from sediment cores are critical for the investigation of small-scale biogeochemical processes. Firstly, small sample volumes and high spatial resolution are required. Secondly, several chemical species in the anaerobic porewater are sensitive to oxidation when brought in contact with ambient air. Here we present the combination of a special sampling technique and an analytical method for the porewater extraction of a varved sediment core from Lake Baldegg in central Switzerland, using MicroRhizon samplers and a portable capillary electrophoresis (CE) instrument. MicroRhizon filter tubes of 1 mm diameter and 20 mm length are suitable for fast retrieval of particle-free porewater samples directly from the sediment core. Since the time-span between sampling and analysis is less than 20 seconds, oxygen-sensitive Fe(II) can be analyzed in one go together with Na⁺, K⁺, Ca²⁺, Mg²⁺, NH₄⁺, and Mn(II) without splitting, acidification or dilution of the sample. The major inorganic cations and anions of the sediment porewater can be determined in less than 15 minutes. Detection limits are in the sub-micromolar concentration range. The capillary electrophoresis instrument used in this study requires sample volumes of only 20 μL. These remarkable small sample volumes allow the minimization of disturbance of the sediment cores and a high spatial resolution of the sediment profile, even in sediments with low water content. The equipment is inexpensive, easy to handle, fully portable and therefore suitable for environmental on-site applications.

A capillary electrophoresis (CE) instrument with capacitively coupled contactless conductivity detection (C⁴D) based on a sequential injection analysis (SIA) manifold was refined. Hydrodynamic injection was implemented to avoid a sampling bias by using a split-injection device based on a needle valve for precise adjustment. For safety and reliability, the integrity of the high voltage compartment at the detection end was fully maintained by implementing flushing of the high voltage interface through the capillary. With this set-up, extended fully automated monitoring applications are possible. The system was successfully tested in the field for the determination of the concentration levels of major inorganic cations and anions in a creek over a period of 5 days.

Drainage water diverted from a farm pasture, which was heavily loaded with manure, was monitored during a rain event. Concurrent anion and cation determinations at intervals of 10 min could be achieved with a new capillary electrophoresis system employing dual injection at opposite ends of the separation capillary. The flow injection approach enabled automation of the sampling process. Interruption of the separation voltage was not necessary. Contactless conductivity detection with an electrolyte solution optimized for the purpose allowed the facile simultaneous detection of the inorganic ions Cl^-, NO₃^-2, SO₄^2-, HPO₄^2-, NO^2-, NH₄⁺, K⁺, Ca²⁺, Na⁺ and Mg²⁺ and the acquisition of temporal concentration profiles of these species. The detection limits achieved were between 20 and 200 mg l^-1 for all ions and the repeatability of peak areas and peak heights was better than 1%. The quantitative results were verified by analysing individual samples later in the laboratory with photometry and ion chromatography and the average deviations were found to be between 4 and 12%. This contribution presents a further step in the development of capillary electrophoresis towards a fully automated, low maintenance field method.