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The Malpighian Tubules (MTs) are the main excretory organs in most insects. They play a key role in the production of primary urine and osmoregulation, selectively reabsorbing water, ions, and solutes. Besides these functions conserved in most insects, MTs can serve some specialized tasks at different stages of some species’ development. The specialized functions include the synthesis of mucopolysaccharides and proteins for the building of foam nests, mucofibrils for the construction of dwelling tubes, adhesive secretions to help the locomotion, and brochosomes for protection as well as the usage of inorganic salts to harden the puparia, eggs chorion, and pupal cells’ closing lids. MTs are also the organs responsible for the astonishing bioluminescence of some Diptera glowworms and can go through some drastic histological changes to produce a silk-like fiber utilized to spin cocoons. The specialized functions are associated with modifications of cells within the entire tubules, in specific segments, or, more rarely, modified secretory cells scattered along the MTs. In this review, we attempted to summarize the observations and experiments made over more than a century concerning the non-excretive functions of insects’ MTs, underlying the need for new investigations supported by the current, advanced technologies available to validate outdated theories and clarify some dubious aspects.

Inorganic salt pretreatment of lignocellulosic biomass has proven to be an efficient way to increase the efficiency of enzymatic saccharification. However, it is not clear that this improvement is the result of modification of the lignocellulosic substrate after pretreatment, or removal of inhibitor, or enhancement of cellulase or a combination of these events. Therefore, this study aimed to analyze the effects of inorganic salts on kinetics of cellulase enzymes (celluclast 1.5L and accellerase 1500). Two substrates rich in cellulose content [carboxymethylcellulose (CMC), avicel (AV)] and lignocellulose substrate [sugarcane bagasse (SB)] were considered. The enzymatic saccharification was carried with and without the addition of inorganic salts (NaCl and KCl) at 0.5 M and 1.0 M concentration. The kinetic parameters, Km and Vm, were determined to mechanically understand the pattern of inhibition and enhancement of inorganic salts on enzymatic saccharification. The kinetics parameters of celluclast 1.5L and accellerase 1500 for hydrolysis of CMC and AV with NaCl showed uncompetitive inhibition. Whereas, influences of KCl on both cellulase were differentiated to function in inhibition or enhancement modes when challenged with different substrates. On the other hand, enzymatic hydrolysis efficiencies of SB using both cellulases were enhanced under addition of NaCl and KCl, by increasing Vm of celluclast 1.5L from 0.303 to 0.635 mg/mL min (0.5 M KCl) and accellerase 1500 from 0.383 to 0.719 mg/mL min (1.0 M NaCl). The details of kinetic analysis in this work revealed the mechanism of inorganic salts on cellulase kinetics to be involved in substrate modification and removal of inhibitor.Graphic abstract

The effects of pH, inorganic ion concentration, and dephosphorylation by hydrolysis on the transparency and viscosity of phosphorylated cellulose nanofibers (P-CNF) with different phosphate group contents and degrees of fibrillation were studied in order to boost its use as a rheology modifier. From the neutralization titration curve of P-CNF dispersions, acidity values of pKa1 = 3.1 and pKa2 = 8.3 were determined. These values were almost constant regardless of the amount of phosphate groups. The P-CNF dispersion maintained high transparency and viscosity in the pH range of 3–11 owing to a wide range of acidity values and the buffer capacity of the phosphate group. The viscosity of P-CNF dispersions was influenced by the amount of phosphate groups and the degree of fibrillation, which also affected the viscosity behavior of the dispersion when inorganic salts were added. The long-term storage stability of phosphate groups introduced on P-CNF was also examined by accelerated (heating) test. The hydrolysis reaction of P-CNFs took several days to reduce the phosphorous content to one-tenth of the initial content at 80 °C. Kinetic analysis showed that dephosphorylation proceeded as a first order reaction, as found for other phosphorylated esters. As dephosphorylation proceeded, the transparency and viscosity of the P-CNF dispersion decreased because P-CNFs tended to aggregate through hydrogen bonding, which also seemed to suppress dephosphorylation. Furthermore, the activation energy of deesterification obtained was 130.0 kJ/mol. The decrease in the ratio of phosphate groups was highest when the degree of anion neutralization of the phosphate groups was 50%.

The microalgae industry shows a promising future in the production of high-value products such as pigments, phycoerythrin, polyunsaturated fatty acids, and polysaccharides. It was found that polysaccharides have high biomedical value (such as antiviral, antibacterial, antitumor, antioxidative) and industrial application prospects (such as antioxidants). This study aimed to improve the polysaccharides accumulation of Porphyridium purpureum CoE1, which was effectuated by inorganic salt starvation strategy whilst supplying rich carbon dioxide. At a culturing temperature of 25 °C, the highest polysaccharide content (2.89 g/L) was achieved in 50% artificial seawater on the 12th day. This accounted for approximately 37.29% of the dry biomass, signifying a 25.3% increase in polysaccharide production compared to the culture in 100% artificial seawater. Subsequently, separation, purification and characterization of polysaccharides produced were conducted. Furthermore, the assessment of CO2 fixation capacity during the cultivation of P. purpureum CoE1 was conducted in a 10 L photobioreactor. This indicated that the strain exhibited an excellent CO2 fixation capacity of 1.66 g CO2/g biomass/d. This study proposed an efficient and feasible approach that not only increasing the yield of polysaccharides by P. purpureum CoE1, but also fixing CO2 with a high rate, which showed great potential in the microalgae industry and Bio-Energy with Carbon Capture and Storage.

This work screened out the optimal conditions for pretreatment of natural lignocellulose with inorganic salts and provided a simple, easy-to-operate, low-cost, clean and efficient pretreatment method for the efficient degradation of natural lignocellulose by strains. The results showed that the optimal pretreatment inorganic salt was FeCl2 with a concentration of 11%, pretreatment at 60 °C for 48 h, and the solid–liquid ratio was 1:11 (g/mL). According to the characterization results, after pretreatment of FeCl2 solution, the smooth and dense structure of natural lignocellulose surface became rough and irregular, and surface fiber bundles showed spalling and fracture. Subsequently, the enzymes produced by solid-state fermentation of Aspergillus fumigatus were easier to enter the interior, which increased the contact area between materials and enzymes, and increased the amount of enzymatic loads, thereby improving the biodegradation effect.

Carbon dots (CDs) have been widely adopted as optical materials because of their excellent luminescent properties. However, most of the reported synthetic methods are conducted in solvents, especially hydrothermal/solvothermal reactions, leading to intractable problems such as toxic and flammable solvents, complex and inseparable by-products, and dangerously high pressures and temperatures. Solid-phase synthesis of CDs in air is an effective solution to overcome the above issues, but solid reactions always result in uncontrolled growth and agglomeration of nanoparticles. In this study, some inorganic salts are selected as catalysts for synthesizing CDs in solid states and air, which also play as dispersants to hinder CDs aggregation. In the meantime, some aromatic derivatives containing hydroxyl and amino groups are chosen as carbon sources, ground with the optimized catalyst, and then heated together in air. The production yields are affected by the reaction time and reactant ratio, while the graphitization degrees of the CDs are determined by the reaction temperature. The I G / I D value of their Raman spectra increases from 0.59 to 0.85, and the particle size decreases from 2.5 to 1.4 nm when the synthesis temperature is increased from 200 to 280 °C. The as-prepared CDs show emission peaks ranging from 366 to 606 nm, with the photoluminescence (PL) quantum yield up to 53%. Their emission color variation mainly results from different carbon sources, which can be ascribed to the differences in the element composition, functional groups, and graphitic nitrogen content of these CDs. By dispersing CDs of different concentrations into polyvinyl alcohol (PVA) and combining them with blue LEDs, cold, standard, and warm white light emitting devices (WLEDs) are prepared, with a color rendering index (CRI) up to 84. Since the as-prepared CDs have antioxidant ability at high temperature, the as-prepared WLEDs have long lifespans, remaining the effective white luminescence after 72 h continuous work.

The preparation of coal water slurry (CWS) using wastewater, which contains inorganic and organic components, is one method of wastewater utilization. In this study, the effect of inorganic salts on the viscosity of CWS was examined. The results show that monovalent salts (NaCl, KCl) decreased the viscosity of CWS. The viscosity of CWS was not affected by bivalent salts (CaCl 2 , MgCl 2 ). However, CWS combined with trivalent salt (AlCl 3 ) sharply increased the viscosity. The zeta potential of CWS with inorganic salts increased which can enhance the electric repulsion and beneficial to reduce the viscosity. The content of free water in CWS with trivalent salt decreased, and the freedom of the free water in CWS with trivalent salt decreased which were all bad to the viscosity and the adsorption of the dispersant on the particles. Compared with the surface polarity of the particles without inorganic salts, the surface polarity of the particles with divalent salts was similar to those without inorganic salts. Under the comprehensive influence, divalent salt has little effect on the viscosity of CWS.

Polyaniline (PANI), due to the various and controllable shapes, the environmental stability, the excellent physical and chemical property, has gained significant attention. PANI with abundant morphologies were successfully prepared through adjusting and controlling the state of the initial micelle-like in the micelle-like system composed by aniline and organic acids with relatively weak intermolecular interaction. Although the influence of the inorganic salts on their morphology, including the surface and the diameter, was investigated, the influence of salt on the nucleation of PANI was still unclear. Therefore, PANI nanofibers were fabricated through the addition of inorganic salt such as NaCl, MgSO 4 and AlCl 3 into the micelle-like composed of aniline and D-camphor-10-sulfonic acid. The influence of types and concentration of inorganic salts, doped acids and temperature on PANI was studied by Transmission Electron Microscope (TEM), UV-vis and Fourier Transform Infrared Spectroscopy (FTIR) spectroscopy. In addition, in situ UV-vis and 1 H Nuclear Magnetic Resonance technology (NMR) were applied to observe the process of aniline polymerization, and it was indicated the polymerization rate of aniline changed after the addition of inorganic salt NaCl into the initial solution.

Inorganic salts were used for the pretreatment of oil palm empty fruit bunches (OPEFB) to enhance the delignification and saccharification yield of OPEFB. The sequential pretreatment of OPEFB using sodium phosphate dodecahydrate (Na3PO4.12H2O) and zinc chloride (ZnCl2) proved to be an effective approach. OPEFB was delignified by 58.8%, producing a maximum total reducing sugar (TRS) yield of 0.97 g/g under optimum pretreatment conditions of 15% Na3PO4.12H2O, 60 min (30 min/stage) pretreatment time, 10% solid to liquid ratio, and pretreatment temperature of 121 °C. In addition, structural and morphological analysis of the pretreated OPEFB using field emission scanning electron microscope (FESEM), Fourier transform infrared (FTIR) spectroscopy, and X- ray diffraction (X-RD) revealed major structural changes, such as the generation of porous structure, which allows for better enzyme accessibility. Moreover, recycle experiments showed encouraging findings, as the spent pretreatment liquid with pH adjustment can be recycled efficiently for at least 5 times without a substantial decrease in its effectiveness.

In order to study the effect of inorganic salt additives on the surface tension of a sodium dodecylbenzene sulfonate (SDBS) solution, the surface tension of the mixed system of six common inorganic salt additives, NaCl, CaCl2, AlCl3, Na2SO4, Na2CO3, and NaHCO3, and SDBS was measured, and the effects of the inorganic salt types, surfactant concentrations and inorganic salt concentrations on the surface tension of the SDBS solution were studied. On this basis, three inorganic salts, NaCl, CaCl2 and Na2SO4, were selected, and their effects on the critical micelle concentration (CMC) of the SDBS solution were studied. The experimental results showed that different inorganic salts had different effects on the surface tension of the SDBS solution. The order of effect of the six inorganic salts on the surface tension of the SDBS solution was CaCl2 > NaCl > Na2SO4 > NaHCO3 > Na2CO3 > AlCl3; when the mass fraction of the SDBS solution is high, the influence of the inorganic salts on the surface tension of the SDBS solution is relatively small; with an increase in the concentration of the preferred inorganic salt additives, the surface tension of the SDBS solution decreases first, then tends to be stable, and then increases; a reduction in the critical micelle concentration by the three selected inorganic salt additives shows the trend of 0.7% NaCl > 0.5% CaCl2 > 0.5% Na2SO4.