Facile green synthesis route for new ecofriendly photo catalyst for degradation acid red 8 dye and nitrogen recovery.

This study novelty is that new photo catalyst prepared from sustainability low cost precursors. Dark red color hydrogel composites have been easily prepared from gelatin biopolymer using a simple sol-gel method. Gelatin doped by cobalt chloride, and silver nanoparticles (SNPs) in the presence of traces amount of sodium dodecyl sulfate surfactant and calcium chloride. Water-insoluble Gelatin composites are thermally stable photocatalysts for the degradation of toxic anionic acid red 8 dye. Promising photodynamic activity confirmed by fluorescence emission at λmax 650 nm. Optical absorption in Vis. light enhanced photo catalytic activity. Silver nanoparticles enhanced crystallinity, and improved optical properties and porosity. Dopants by CoCl2 and silver nanoparticles increased band gap of gelatin composites from (1.82 to 1.95) indicating interfacial charge separation. Low band gaps improved photo catalytic activity. Optical band gaps (Eg) lower than 2.0 eV indicates high catalytic activity in the photo degradation acid red 8 dye using Vis. light, wavelength 650 nm. Percent removal efficiency (%Re) of the dye at 500 ppm initial concentration, pH 1, contact time 30 min., and 0.20 g L-1 dose photo catalyst reached 95%. pH not affects removal efficiency. So, gelatin composites removed AR8 dye by photodegradation mechanism rather than adsorption due to photodynamic activity. Kinetics of photodegradation followed pseudo first order kinetic with rate constant k1 5.13 × 10-2 min.-1 Good electrical conductivity and magnetic properties (effective magnetic moment (µeff 4.11 B.M) improved dye degradation into simple inorganic species. Nutrients NH4+, and NO3- degradation products recovered by using alumina silicate clay via a cation exchange mechanism.

Tenability on schiff base Hydrazone derivatives and Frontier molecular orbital.

Context hydrazine compounds based on 1,3,5-triazine were synthesised and their molecular structures were characterised by elemental analysis, Electronic, IR and 1H NMR spectra. The spectral behaviour of the newly prepared compounds in organic solvents of different polarities was extensively studied and correlated to the molecular structure. In this study, 1,3,5-Triazine derivatives (L1, L6, L7, L8) have been subjected to theoretical studies using the Semi-empirical PM3 quantum chemical method. The physical-chemical properties of some Hydrazone derivatives are determined theoretically. The molecular geometry, the Highest Occupied Molecular Orbital (HOMO) - Lowest Unoccupied Molecular Orbital (LUMO) energy gap, molecular hardness (η), ionisation energy (IE), Electron affinity and total energy were analysed, and applications as biological effects were done.

A Comparative Analysis of Pervaporation and Membrane Distillation Techniques for Desalination Utilising the Sweeping Air Methodology with Novel and Economical Pervaporation Membranes.

This study used the sweeping air approach to conduct a comparative analysis of pervaporation (PV) and membrane distillation (MD) in the context of desalinating saline/hypersaline water. An experimental setup of the sweeping air arrangement was designed and built at a laboratory size to conduct the research. The desalination process using PV used innovatively designed cellulose acetate (CA) membranes specifically adapted for this purpose. Conversely, in the studies involving MD, hydrophobic polytetrafluoroethylene (PTFE) membranes were utilised. CA membranes were fabricated in our laboratory using the phase inversion approach. The physicochemical characteristics of the membranes were assessed using many methodologies, including FTIR spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), contact angle measurement, and water uptake analysis. This facilitated a more comprehensive comprehension of the impact of the alkaline treatment on these features. The variables that were examined included the kind of membrane, the pore size of the PTFE membrane, the composition of the casting solution of CA, the concentration of the feed solution, the temperature of the feed, and the temperature of the condenser cooling water. The morphologies of the membranes were examined using SEM. The study's findings indicated that the use of MD resulted in a greater flow and a remarkable percentage of salt rejection (% SR). Furthermore, it was observed that the flux was positively correlated with the feed temperature, while it exhibited an inverse relationship with the cooling water temperature. Moreover, it was observed that the impact of the pore size of the PTFE membrane on the desalination process was found to be minimal. The most optimal outcomes obtained were 13.35 kg/m2 h with a percentage salt rejection (% SR) of 99.86, and 17.96 kg/m2 h with a % SR of 99.83 at a temperature of 70 °C, while using MD and PV technologies, respectively. Furthermore, both methods demonstrated the capability to desalinate very salty solutions with a salinity level of up to 160 g/L, thereby yielding potable water in a single step.

A Comparison of Capacitive Deionization and Membrane Capacitive Deionization Using Novel Fabricated Ion Exchange Membranes.

Another technique for desalination, known as membrane capacitive deionization (MCDI), has been investigated as an alternative. This approach has the potential to lower the voltage that is required, in addition to improving the ability to renew the electrodes. In this study, the desalination effectiveness of capacitive deionization (CDI) was compared to that of MCDI, employing newly produced cellulose acetate ion exchange membranes (IEMs), which were utilized for the very first time in MCDI. As expected, the salt adsorption and charge efficiency of MCDI were shown to be higher than those of CDI. Despite this, the unique electrosorption behavior of the former reveals that ion transport via the IEMs is a crucial rate-controlling step in the desalination process. We monitored the concentration of salt in the CDI and MCDI effluent streams, but we also evaluated the pH of the effluent stream in each of these systems and investigated the factors that may have caused these shifts. The significant change in pH that takes place during one adsorption and desorption cycle in CDI (pH range: 2.3-11.6) may cause problems in feed water that already contains components that are prone to scaling. In the case of MCDI, the fall in pH was only slightly more noticeable. Based on these findings, it appears that CDI and MCDI are promising new desalination techniques that has the potential to be more ecologically friendly and efficient than conventional methods of desalination. MCDI has some advantages over CDI in its higher salt removal efficiency, faster regeneration, and longer lifetime, but it is also more expensive and complex. The best choice for a particular application will depend on the specific requirements.

Prospects of Polymeric Nanocomposite Membranes for Water Purification and Scalability and their Health and Environmental Impacts: A Review.

Water shortage is a major worldwide issue. Filtration using genuine polymeric membranes demonstrates excellent pollutant separation capabilities; however, polymeric membranes have restricted uses. Nanocomposite membranes, which are produced by integrating nanofillers into polymeric membrane matrices, may increase filtration. Carbon-based nanoparticles and metal/metal oxide nanoparticles have received the greatest attention. We evaluate the antifouling and permeability performance of nanocomposite membranes and their physical and chemical characteristics and compare nanocomposite membranes to bare membranes. Because of the antibacterial characteristics of nanoparticles and the decreased roughness of the membrane, nanocomposite membranes often have greater antifouling properties. They also have better permeability because of the increased porosity and narrower pore size distribution caused by nanofillers. The concentration of nanofillers affects membrane performance, and the appropriate concentration is determined by both the nanoparticles' characteristics and the membrane's composition. Higher nanofiller concentrations than the recommended value result in deficient performance owing to nanoparticle aggregation. Despite substantial studies into nanocomposite membrane manufacturing, most past efforts have been restricted to the laboratory scale, and the long-term membrane durability after nanofiller leakage has not been thoroughly examined.

An Investigation into a Miniature Saltless Solar Pond.

A simple, miniature saltless Solar Pond (SP) was designed and constructed in the present work. It consisted of a Plexiglas container with a square cross-section, within which cruciform baffles were suspended in the upper half of the pond, and copper coil tubing was fitted in the middle of the lower zone to function as a heat exchanger without disturbing the pond's inertia. Different variables' effect on the water's temperature rise at various vertical locations within the pond were investigated. These variables included the presence of the cruciform baffles, the inclination of a mirror fixed to the top rim of the pond, a glass transparent cover (GC), and the presence or absence of a gel thickening material to increase the water viscosity inside the SP, the climatic conditions, and the presence of glass wool (GW) in the lower section of the SP. For an experiment, an estimated energy balance was performed, and the thermal storage efficiency was calculated. The best obtained thermal storage efficiency was 32.58% in the presence of the cruciform baffles, a 45° inclination of a mirror fixed to the top rim of the SP, at an ambient temperature of 30 °C on a calm, sunny day with a wind speed of 7 km/h.

Macro-Reticular Ion Exchange Resins for Recovery of Direct Dyes from Spent Dyeing and Soaping Liquors.

Dyes are a major class of organic pollutants that are well-known for their harmful impact on aquatic life and humans. Several new strategies for removing colours from industrial and residential effluents have recently emerged, with adsorption being the best option. The current study looked at the recovery of direct dyes from aqueous streams for reuse using macro-reticular ion exchange resins (IERs). The investigation includes dyeing single jersey cotton grey textiles with direct dyes from the Isma dye Company in Kafr El Dawar, Egypt. After centrifuging and separating the supernatant liquid, solutions from thirteen different dyes, produced at an average concentration between the wasted and soaping liquor concentrations, were calculated spectrophotometrically from the first dyeing trials. Kinetic data were well fitted with pseudo-second-order rate kinetics. The amounts of dye retained by the anion exchangers increased with a rise in temperature in the case of Strong Base Resin (SBR) and vice versa for Weak Base Resin (WBR). Batch adsorption experiments with SBR and WBR were conducted for each dye, and both Freundlich and Langmuir isotherms were constructed. It was found that adsorption obeyed both isotherms, that monolayer adsorption took place, and that the dye molecular weight, structure, and solubility, as well as the type of anionic resin used, had varying effects on the extent of absorption. The monolayer sorption capacities Q0 determined from the Langmuir isotherm model for the strongly and weakly basic anion exchangers were found to be 537.6 and 692 mg/g for Direct Yellow RL, respectively. As a result, Yellow RL exhibited the greatest adsorption on both SBR and WBR. Orange GRLL, Blue 3B, and Congo Red, on the other hand, were the poorest colours absorbed by the IERs, whereas Blue RL demonstrated good adsorption by SBR and accelerated adsorption by WBR. Most of the dyes may be recovered and reused in this manner.

Removal of copper metal by cementation using a rotating iron cylinder.

The rate of the copper(II)/iron cementation reaction in the presence of surfactant (SAS) was determined by measuring the rate of cementation of copper on a rotating Fe cylinder from a CuSO(4) solution in the absence and the presence of SAS using an atomic absorption spectrophotometer. The rate of cementation reaction is decreased by an increasing concentration of SAS, temperature and number of rotation. It is found that the order of the rate of decrease of the cementation reaction in the presence of SAS is as follows, Triton X-100 < SDS < SOS. The rate of the cementation reaction was also found to decrease with the addition of small amounts of alcohol. In the presence of alcohol, the amount of decrease ranged from 11.47 to 47.8% depending on the type and as well as the concentration of alcohol used. The effect of mixed surfactant (SAS) on cementation reaction was given. Thermodynamic parameters Delta H(*), Delta S(*), and Delta G(*) were calculated.

Reduction of Cr(VI) in presence of some amino compounds.

The rate of reduction of Cr(VI) to Cr(III) in 0.05 M K2Cr2O7 has been studied and was found to be first order. The rate of reaction was measured in the absence of amino compounds and in the presence of o-nitroaniline, p-nitroaniline, m-toulidine, p-chloroaniline, and o-bromoaniline at four different temperatures. The rate of reaction was found to decrease with the addition of amines. Thermodynamic parameters DeltaG*, DeltaH*, and DeltaS* were calculated from the study.

Effect of sodium dodecyl sulfate on the rate of hydrogen evolution at a cathode.

The effect of H(2) evolution on the mass-transfer coefficient of cathode reduction of potassium ferricyanide at a mercury cathode was studied with the aim of (i) comparing the mass transfer behavior at a Hg cathode with that at solid electrodes under gas-evolving conditions and (ii) testing the effect of anionic surface-active agent on the mass transfer behavior of an H(2)-evolving Hg cathode. It is found that the mass transfer coefficient at the Hg cathode was much higher than the value at a solid cathode. The mass transfer coefficient at H(2)-evolving Hg was found to decrease in the presence of sodium dodecyl sulfate (SDS) surfactant by an amount ranging from 58.8 to 76%, depending on the H(2) discharge rate and the SDS concentrations.

Cementation reactions in the presence of nitrogen compounds.

The effect of aniline derivatives on the rate of cementation of copper from dilute copper sulfate solution on iron rods was investigated. The variables studied were concentration of CuSO(4), temperature, organic additives, and their concentrations. It was found that the cementation reaction was first-order in the presence and in the absence of additives. Nitrogen compounds were found to decrease the rate of cementation by 10 to 80% depending on the type of inhibitor as well as its concentration.The adsorption isotherm, the effect of temperature, and the percentage inhibition show that the order of inhibition is p-chloroaniline>o-chloroaniline>m-chloroaniline and p-chloroaniline>p-aminobenzoic acid>p-aminoacetophenone. The thermodynamic parameters DeltaS( not equal ), DeltaG( not equal ), DeltaH( not equal ) were given.

Kinetics and thermodynamics studies of copper exchange on Na-montmorillonite clay mineral.

The kinetics of Cu ion exchange on Na-montmorillonite clay has been investigated at 20, 30, and 40 degrees C in water, methanol, and ethanol. The reaction is endothermic in nature. Solvent effects on the reaction rate have been discussed. The thermodynamic activation parameters were calculated and discussed in terms of solvation effects. A multiple reaction rate order equation was used to describe the adsorption process. Lower rates and higher activation energies (Ea) were observed in aqueous solution than in either of the alcohols. The Ea values ranged from 20.88 kJmol(-1) in water to 9.20 kJmol(-1) in ethanol, while at 20 degrees C the rate constant (k) varied from 0.111 ppm(-1)s(-1) in water to 0.205 ppm(-1)s(-1) in ethanol. The main factor influencing the rate of the adsorption process is the mobility of the adsorbed Cu cations, which is apparently larger in alcohols than in water, due to the difference in the molar activation energy of the solvent. The determined isokinetic temperature indicates that the reaction is enthalpy-controlled, where the interaction between solvent and clay surface plays an important role. A reaction mechanism that describes the solvent effect on the rate of Cu ion exchange is proposed.