Scanning magnetic microscopy is a new tool that has recently been used to map magnetic fields with good spatial resolution and field sensitivity. This technology has great advantages over other instruments; for example, its operation does not require cryogenic technology, which reduces its operational cost and complexity. Here, we describe the construction of a customizing scanning magnetic microscope based on commercial Hall-effect sensors at room temperature that achieves a spatial resolution of 200 µm. Two scanning stages on the x- and y-axes of precision, consisting of two coupled actuators, control the position of the sample, and this microscope can operate inside or outside a magnetic shield. We obtained magnetic field sensitivities better than 521 nTrms/√Hz between 1 and 10 Hz, which correspond to a magnetic momentum sensitivity of 9.20 × 10–10 Am2. In order to demonstrate the capability of the microscopy, polished thin sections of geological samples, samples containing microparticles and magnetic nanoparticles were measured. For the geological samples, a theoretical model was adapted from the magnetic maps obtained by the equipment. Vector field maps are valuable tools for the magnetic interpretation of samples with a high spatial variability of magnetization. These maps can provide comprehensive information regarding the spatial distribution of magnetic carriers. In addition, this model may be useful for characterizing isolated areas over samples or investigating the spatial magnetization distribution of bulk samples at the micro and millimeter scales. As an auxiliary technique, a magnetic sweep map was created using Raman spectroscopy; this map allowed the verification of different minerals in the samples. This equipment can be useful for many applications that require samples that need to be mapped without a magnetic field at room temperature, including rock magnetism, the nondestructive testing of steel materials and the testing of biological samples. The equipment can not only be used in cutting-edge research but also serve as a teaching tool to introduce undergraduate, master's and Ph.D. students to the measurement methods and processing techniques used in scanning magnetic microscopy.

The synthesis of metal nanoparticles (NPs) using microfluidic reactors has become a major method for limiting reagent consumption and achieve a precise control of the morphological properties. Failure in realizing the reproducibility of the results is mostly associated with the accumulation of metallic nanostructures on the walls of the microfluidic devices, periodically removed by acid treatment. In this study, we show that ns-pulsed laser ablation (PLA) in water can be a safe, effective, and green method for the regeneration of clogged microfluidic reactors. The effect of the laser-pulse fluence on the removal of metallic nanostructures was studied for the first time on silver (Ag) thin films with a thickness of 50 nm deposited over SiO2 substrates, using 3-mercaptopropyl trimethoxysilane as a chemical adhesion layer. As point of novelty, the experimental results show that at low fluence (F < 0.1 J/cm2), ablation is principally caused by delamination of the thin film associated with the thermoelastic force while thermal processes inducing phase conversion of the metal dominate at higher fluence. Low-fluence regimes are better suited for the single-pulse removal of the nanomaterial, whereas in high F regimes, we observed melting and recondensation of the metal on the SiO2 surface so that multiple pulse interactions were necessary for complete ablation of the thin film. For the delamination and the phase transformation processes, the threshold fluences were 3.7 × 10−2 and 7.0 × 10−2 J/cm2, respectively. The experimental setup in the thermoelastic PLA regime was applied to unclog glass microfluidic devices used for synthesizing citrate-stabilized AgNPs. Using this simple and easily achievable laser-scanning experimental configuration, we demonstrated that PLA in water is a reliable and efficient technique, with results comparable to acidic treatment in terms of efficiency and time necessary for the complete removal of the Ag nanomaterial.