This work concerns with the liquid injection in arc plasma spraying for the development of finely structured ceramics coatings. Nanostructured coatings can be now achieved with nanopowders dispersed in a liquid (SPS: Suspension Plasma Spraying) or with a salt dissolved into a liquid (SPPS: Solution Precursor Plasma Spraying) injected into the plasma jet. Controlling electric arc instabilities confined in non-transferred arc plasma torch is therefore a key issue to get reproducible coating properties. Adjustment of parameters with a mono-cathode arc plasma allows a new resonance mode called "Mosquito". A pulsed arc plasma producing a periodic regular voltage signal with modulation of enthalpy is obtained. The basic idea is to synchronize the injection system with the arc to introduce the liquid material in each plasma oscillation in the same conditions, in order to control the plasma treatment of the material in-fly. A custom-developed pulsed arc plasma torch is used with a drop-on-demand dispenser triggered by the arc voltage. A delay is added to adjust the droplets emission time and their penetration into the plasma gusts. Indeed, the treatment of droplets is also shown to be dependent on this injection delay. A TiO₂ suspension and an aqueous solution of aluminium nitrate were optimized to get ejectable inks forming individual droplets. The feasibility of the process was demonstrated for SPS and SPPS techniques. Coatings from the suspension and the solution were achieved. First synchronized sprayings show a good penetration of the droplets into the plasma. Coatings show a fine structure of cauliflowers shapes. The synchronization of the ejection allows a control of morphology and a better deposition efficiency. Further investigations will find the optimal operating parameters to show the full potential of this original liquid injection technique.

This paper presents an experimental approach to the study of the compressive strength, isothermal calorimetry and life cycle assessment (LCA) of alkali-activated pastes based on soda–lime–silica glass, established to investigate the effect of the nature and proportion of the activator. Four different activators are compared: Portland cement, sodium silicate, sodium carbonate (at four percentages by weight: 5, 10, 15 and 25 wt% relative to glass) and sodium hydroxide (3.5 wt%). Portland cement and sodium carbonate were added in dry form (powder), while sodium hydroxide (pellets) and silicate were used in solution. At room temperature, glass exhibited slow reaction kinetics, with mechanical performance increasing significantly beyond 28 days of curing. The nature of the activator had a direct impact on the mechanical performance of the activated glass. Cement-activated pastes and those containing 25 wt% of sodium carbonate developed strength at an early age (0–7 days). The other activators showed lower strength development before 28 days of reaction. While a higher activator content improved short-term performance, it also increased the environmental impact, primarily due to the activator. The LCA, conducted on 11 indicators, revealed that the environmental impact was largely driven by the type and amount of activator used. A performance impact indicator (PII) related to global warming was introduced to compare pastes with different performance values. At an early age (0–28 days), the PII was lower when the activator level was high but decreased over time as the strength improved. In terms of long-term performance (360 days), hydroxide and sodium carbonate (10 wt%) achieved compressive strengths of 91 and 74 MPa, respectively. These systems offered a balance between high performance and a reduced environmental impact, making them of interest for sustainable applications.