Starch-based pH-sensing films with bacterial nanocellulose (BNC) and red cabbage anthocyanins (RCA) as active components were investigated in this research. Their structural, physical, surface and colorimetric properties were analyzed, mainly as a function of BNC concentration. The aim of the research was to relate the changes in the intermolecular interactions between the components of the films (starch, anthocyanins and BNC) to the physical, surface and colorimetric properties that are important for the primary intended application of the produced films as pH indicators in smart packaging. The results showed that maize starch (MS) was more suitable as a matrix for the stabilization of anthocyanins compared to potato starch (PS). PS-based films showed a lower value of water contact angle than MS-based films, indicating stronger hydrophilicity. The swelling behavior results indicate that the concentrations of BNC in MS-based films (cca 10%) and the concentration of about 50% BNC in PS-based films are required if satisfactory properties of the indicator in terms of stability in a wet environment are to be achieved. The surface free energy results of PS-based films with BNC were between 62 and 68 mJ/m² and with BNC and RCA between 64 and 68 mJ/m²; for MS-based films, the value was about 65 mJ/m² for all samples with BNC and about 68 mJ/m² for all samples with BNC and RCA. The visual color changes after immersion in different buffer solutions (pH 2.0–10.5) showed a gradual transition from red/pink to purple, blue and green for the observed samples. Films immersed in different buffers showed lower values of 2 to 10 lightness points (CIE L*) for PS-based films and 10 to 30 lightness points for MS-based films after the addition of BNC. The results of this research can make an important contribution to defining the influence of intermolecular interactions and structural changes on the physical, surface and colorimetric properties of bio-based pH indicators used in smart packaging applications.

Using disposable screen-printed electrodes is a convenient way of monitoring environmental pollution, production process control etc. Usually, commercially available screen-printed electrodes are used, but more and more studies are being carried out in the field of printing electrodes on thinner, low-cost and versatile substrates, including paper. In the present research, the comparison of screen-printed electrodes printed on different paper-based materials is presented. Two unique and innovative invasive plant-based papers made from (1) Japanese knotweed, (2) Canadian and Giant goldenrod and (3) commercially available cardboard were used as a printing material for the electrodes. The selected paper substrates were characterized, and screen-printed electrodes were printed. The influence of substrates’ properties and pre- or post-treatment of the screen-printed electrodes on the electrochemical behaviour is thoroughly analyzed. The results indicate that the printing substrate (roughness) had the most significant influence on the cyclic voltammetry response. Comparing pre- and post-treatment of screen-printed electrodes, it was shown that grinding influenced the electrochemical activity significantly, while corona discharge does not have as significant influence. Besides, it was shown that the invasive plant-based papers are viable alternatives to commercially available papers and can be used as low-cost and eco-friendly alternatives for disposable screen-printed electrodes.

Sustainability demands circular and material solutions with an emphasis on using local resources. Using alternative fibers from invasive plants and agro-residue promotes local production in smaller paper mills, which have additional benefits for the environment (protecting the local species, reducing agro-industrial waste). In electrophotography printing, toner adhesion is a vital quality parameter showing the prints' resistance against different mechanical stress, leading to toner particle detachment. This study tested six different papers made from invasive plants Japanese Knotweed, Black Locust, Canadian Goldenrod, agro-industrial residues Miscanthus, and Tomato stems and waste jute bags. The papers were printed with electrophotography, and three different toner adhesion methods were used to evaluate the toner adhesion. Paper properties like roughness, surface energy and surface resistivity were tested. The results indicate that uncoated agro-industrial residue and invasive plant papers with low surface roughness, low surface energy and high surface resistivity result in low toner adhesion. The cellulose content of the papers acquired with FTIR analysis did not influence the adhesion. Papers with surface energy over 35 mJ/m(2) and surface resistivity below 5E + 10(12) ohm values resulted in excellent paper toner adhesion (high IGT printability tester and tape pull test). High grammage and long fibers also improved the adhesion.

Simple, low-cost methods for sensing volatile organic compounds that leave no trace and do not have a detrimental effect on the environment are able to protect communities from the impacts of contaminants in water supplies. This paper reports the development of a portable, autonomous, Internet of Things (IoT) electrochemical sensor for detecting formaldehyde in tap water. The sensor is assembled from electronics, i.e., a custom-designed sensor platform and developed HCHO detection system based on Ni(OH)₂–Ni nanowires (NWs) and synthetic-paper-based, screen-printed electrodes (pSPEs). The sensor platform, consisting of the IoT technology, a Wi-Fi communication system, and a miniaturized potentiostat can be easily connected to the Ni(OH)₂–Ni NWs and pSPEs via a three-terminal electrode. The custom-made sensor, which has a detection capability of 0.8 µM/24 ppb, was tested for an amperometric determination of the HCHO in deionized (DI) and tap-water-based alkaline electrolytes. This promising concept of an electrochemical IoT sensor that is easy to operate, rapid, and affordable (it is considerably cheaper than any lab-grade potentiostat) could lead to the straightforward detection of HCHO in tap water.