Effects of freeze-thaw cycling on the engineering properties of vegetation concrete.

Vegetation concrete has been widely applied for the ecological restoration of bare steep slopes in short-term frozen and non-frozen soil regions in China. However, field experiments conducted in seasonally frozen soil regions have revealed decreases in the bulk density, nutrient content and vegetation coverage. This study aimed to clarify the evolution process and mechanism of the engineering properties of vegetation concrete under atmospheric freeze-thaw (F-T) test conditions. The physical, mechanical, and nutrient properties of vegetation concrete were investigated using six F-T cycles (0, 1, 2, 5, 10 and 20) and two initial soil water contents (18 and 22%). The results revealed decreases in the acoustic wave velocity and cohesive forces and an increase in the permeability coefficient of the vegetation concrete owing to F-T action. X-ray diffraction tests indicated that the decreased cohesive force was closely related to the overall decrease in the content of gelling hydration products in the vegetation concrete. Additionally, the contents of NH4+-N, PO43-P and K+ in the vegetation concrete increased, whereas that of NO3--N decreased. The loss rates of these soluble nutrients increased, indicating that the nutrient retention capacity of the vegetation concrete had decreased. Specifically, the decreased nutrient retention capacity was mainly related to the disintegration and fragmentation of larger aggregates due to F-T action. This study provides theoretical support for future research on improving the anti-freezing capability of ecological slope protection substrates in seasonally frozen soil regions.

High-Precision In Situ Total Alkalinity Analyzer Capable of Month-Long Observations in Seawaters.

Total alkalinity (TA) is an essential variable for the study of physical and biogeochemical processes in coastal and oceanic systems, and TA data obtained at high spatiotemporal resolutions are highly desired. The performance of the current in situ TA analyzers/sensors, including precision, accuracy, and deployment duration, cannot fully meet most research requirements. Here, we report on a novel high-precision in situ analyzer for surface seawater TA (ISA-TA), based on an automated single-point titration with spectrophotometric pH detection, and capable of long-term field observations. The titration was carried out in a circulating loop, where the titrant (a mixture of HCl and bromocresol green) and seawater sample were mixed in a constant volume ratio. The effect of ambient temperature on the TA measurement was corrected with an empirical formula. The weight, height, diameter, and power consumption of ISA-TA were 8.6 kg (in air), 33 cm, 20 cm, and 7.3 W, respectively. A single measurement required ∼7 min of running time, ∼32 mL of seawater, and ∼0.6 mL of titrant. ISA-TA was able to operate continuously in the field for up to 30 days, and its accuracies in the laboratory and field were 0.5 ± 1.7 µmol kg-1 (n = 13) and 10.3 ± 2.8 µmol kg-1 (n = 29) with precisions of 0.6-0.8 µmol kg-1 (n = 51) and 0.2-0.7 µmol kg-1 (n = 8), respectively. This study provides the research community with a new tool to obtain seawater TA data of high temporal resolution.

Automated spectrophotometric analyzer for rapid single-point titration of seawater total alkalinity.

An automated analyzer was developed to achieve fast, precise, and accurate measurements of seawater total alkalinity (AT) based on single-point titration and spectrophotometric pH detection. The single-point titration was carried out in a circulating loop, which allowed the titrant (hydrochloric acid and bromocresol green solution) and a seawater sample to mix at a constant volume ratio. The dissolved CO2 in the sample-titrant mixture was efficiently removed by an inline CO2 remover, which consists of a gas-permeable tubing (Teflon AF2400) submerged in a sodium hydroxide (NaOH) solution. The pH of the mixture was then measured with a custom-made spectrophotometric detection system. The analyzer was calibrated against multiple certified reference materials (CRMs) with different AT values. The analyzer features a sample throughput time of 6.5 min with high precision (±0.33-0.36 µmol kg(-1); n = 48) and accuracy (-0.33 ± 0.99 µmol kg(-1); n = 10). Intercomparison to a traditional open-cell AT titrator showed overall good agreement of 0.88 ± 2.03 µmol kg(-1) (n = 22). The analyzer achieved excellent stability without recalibration over 11 days, during which time 320 measurements were made with a total running time of over 40 h. Because of its small size, low power consumption requirements, and its ability to be automated, the new analyzer can be adapted for underway and in situ measurements.

A high precision, fast response, and low power consumption in situ optical fiber chemical pCO2 sensor.

A sensor system suitable for monitoring changes in partial pressure of carbon dioxide (pCO(2)) in surface seawater or in the atmosphere has been developed. Surface seawater samples are pumped into a PVC tube enclosing an inner Teflon AF tube, which served as a long pathlength gas-permeable liquid-core waveguide for spectrophotometry. The Teflon cell contains a pH-sensitive indicator-buffer solution consisting of bromothymol blue (BTB) and sodium carbonate. Carbon dioxide in the sample diffuses into the indicator-buffer solution to reach equilibrium, resulting in pH changes, which are detected by changes in the absorbance of BTB at wavelengths of 620 and 434 nm. The pCO(2) in the sample is then derived from the pH change. The sensor has a response time of 2 min at the 95% equilibrium value and a measurement precision of 0.26-0.37% in the range 200-800 microatm pCO(2). This chemical sensor takes advantage of a combination of long pathlength, multiple wavelength detection, indicator solution renewal, and in situ automatic control technology, and has the feature of low power consumption (the average being approximately 4 W with a peak of approximately 8 W).