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Due to the higher potential for enhancing nutrient use efficiency, nanofertilizer (NF) is crucial in sustainable crop production. Thus, foliar-applied mixed nanofertilizer (MNFf) and commercial fertilizer (CF) into the soil (CFs) were claimed together ([MNFf + CFs]) and comparative nutrient use efficiency (NUE), productivity, and nutritional properties of tomato fruits were investigated. The mixed nanofertilizer (MNF) was prepared in our laboratory and characterized using scanning electron microscopy, X-ray diffraction, and Fourier transform infrared. To avoid the interference of other factors, all the treatments were divided into three groups: (i) blank treatment (no fertilizer), (ii) CF treatment, and (iii) combined [MNFf + CFs] treatment. The vegetative growth and qualitative and quantitative attributes of tomatoes were recorded, and the NUE, total production, and benefit–cost ratio (BCR) were also calculated. In addition, comparative nutritional properties for all treatments were analyzed. The plant’s height, stem diameter, root length, photosynthetic pigments, leaf minerals, and qualitative traits of tomato fruits were significantly (p < 0.05) increased by [MNFf + CFs] treatment compared to CFs. The protein, fiber, Fe, Zn, and K contents were significantly (p < 0.05) increased by 23.80, 38.10, 44.23, 60.01, and 2.39%, respectively, with the [MNFf + CFs] treatment as compared to CFs, while the ash and protein contents were both lower than the untreated tomato. Moreover, [MNFf + CFs] treatment has significantly (p < 0.05) increased the antioxidant properties. The NUE, total production, and BCR were also increased by 26.08, 26.04, and 25.38%, respectively, with the same treatment. Thus, [MNFf + CFs] treatment could be a potential alternative for reducing the excess use of CF.

A novel polyazo dye (SDMAPD3BS) was synthesized and its application as a universal acid–base indicator was investigated. This molecule can be used as a universal indicator for all types of acid–base reactions.

In this work, we have proposed a new formulation of a hybrid nanofertilizer (HNF) for slow and sustainable release of nutrients into soil and water. Urea-modified hydroxyapatite was synthesized, which is a rich source of nitrogen, calcium, and phosphate. Nanoparticles such as copper, iron, and zinc were incorporated into urea-modified hydroxyapatite to increase the efficiency of the proposed fertilizer. Different techniques including powder X-ray powder diffraction, Fourier-transform infrared spectroscopy, and scanning electron microscopy were used to get insight into the properties, morphology, and structure of the as-prepared fertilizer. The developed HNF was used in a field experiment on the ladies’ finger (Abelmoschus esculentus) plant. The slow release of HNF was observed during leaching studies and confirmed the availability of Ca2+, PO43–, NO2–, NO3–, Cu2+, Fe2+, and Zn2+. Furthermore, the presence of Cu2+, Fe2+, and Zn2+ nutrients in ladies’ finger was confirmed by the inductively coupled plasma-optical emission spectrometry (ICP-OES) experiment. A considerable increase in the physicochemical properties such as swelling ratio and water absorption and retention capacities of the proposed fertilizer was observed, which makes the fertilizer more attractive and beneficial compared with the commercial fertilizer. The composition of the proposed HNF was functionally valuable for slow and sustainable release of plant nutrients. The dose of prepared HNF applied was 50 mg/week, whereas the commercial fertilizer was applied at a dose of 5 g/week to A. esculentus. The obtained results showed a significant increase of Cu2+, Fe2+, and Zn2+ nutrient uptake in A. esculentus as a result of slow release from HNF.

In this work, a robust and reliable electrochemical sensor was developed for sensitive detection of non-electroactive melamine (MEL) using a modified glassy carbon electrode with ascorbic acid (AA) as the active recognition element. To increase the current signal of AA, the working electrode was successively modified with l-arginine (l-Arg) and reduced graphene oxide-copper nanoflower composite. The voltammetry measurements denoted that the hydrogen bonding was formed between AA and MEL. Using the optimum conditions, the proposed enhanced sensor can detect MEL concentrations ranging from 10 × 10-9 to 9.0 × 10-8 M with a detection limit of 5.0 × 10-9 M that is proportional to the decrease of AA in the anodic peak current. Finally, the proposed sensor was successfully applied for the determination of MEL in commercial infant milk samples and good recovery values were obtained.

The application of porous polymeric monolith (PPM) columns as an effective tool for bacterial cell lysis within microfluidic chips is demonstrated. By taking advantage of the large surface area and controllable pore size inherent to PPMs, we developed a double mechanism cell lysis technique. The bacterial cell wall is mechanically sheared by flowing through the porous medium of the PPM column, but it is also damaged and disintegrated by physical contact with the antibacterial polymeric biocide covering the porous surface. This leads to leakage of the intracellular contents. The stable and non-leaching antibacterial column introduced in this work alleviates the need for chemical or enzymatic lysins and their potential release of polymerase chain reaction (PCR) inhibitors. The PPM columns were obtained by the photoinitiated free radical copolymerization of n-butyl methacrylate (BuMA) and N-(tert-butyloxycarbonyl)aminoethyl methacrylate (Boc-AEMA) in the presence of a cross-linker and porogenic solvents. The porous network was synthesized directly inside a microfluidic channel fabricated in a cross-linked poly(methyl methacrylate) (X-PMMA) substrate by laser micromachining. After removing the Boc protecting group with phosphoric acid, an amphiphilic and cationic network structure reminiscent of synthetic mimics of antimicrobial peptides (SMAMPs) was obtained. The antibacterial activity of the PPM columns was tested against Bacillus subtilis (B. subtilis) and Escherichia coli (E. coli) cells. Cell lysis was evidenced by DNA release, which was then amplified by PCR and confirmed by gel electrophoresis, to verify that the antibacterial monolithic columns did not strongly interfere with the PCR process.