Collated/Represented/Studied 1. Analysing flux filtration system is composed of For a given set of operating decline in dead- an air-pressurized feed tank conditions (feed concentration, end filtration connected to a 50-mL filtration transmembrane pressure), the cell (Millipore). Filtration permeate versus volume data are experiments are conducted at collected from a series of five different pressures and different runs. Plot of cumulative permeate concentrations of suspension. volume V vs. time t— The permeate is collected in a comparison between beaker and the cumulative experimental and calculated permeate mass is measured via curves for four experiments an electronic balance (C=10−2 gL−1 and P = 0.3 bar). connected to a computer for on- [ 0.2μm; 0.8μm; 5μm; 8μm] line data acquisition. 2. Membrane The unstirred batch The conductivity, total dissolved filtration of experiments are conducted in a solids (TDS), and pH of all leather plant 150mL filtration cell made of samples are measured at room effluent: Flux stainless steel. The operating temperature. Total solids (TS) of decline pressures are 414, 552 and 828 all the samples are measured. mechanism kPa for NF experiments Flux data taken for 200 DA and 400 Da membranes and compared with the model predicted values .During NF, complete pore blocking prevailed up to about 150 s; standard pore blocking controlled the flux decline thereafter up to about 1650 s and beyond that, the flux decline was controlled by the cake formation mechanism. 3. Ultrasound The tests were performed in a The volumetric flux of permeate assisted extraction tangential filtration system (Jv) was calculated by Equation and nanofiltration using flat sheet membranes-270 (1), and the average permeate of phenolic Da. the system pressure was flux (Js) was obtained from the compounds from maintained at 20 bar and straight line inclination described artichoke solid temperature was 25 C. The by the function (in paper). The wastes initial feed volume was 900 mL flux decrease (Df) was and the concentration process calculated. were carried out to a volume reduction factor of 2.5. Surface membranes characterization- 1. Atomic force microscopy (AFM) 2. Infrared fourier transformed spectroscopy. The attenuated total reflectance (ATR) was used to investigate the functional groups and molecular structures on the membranes surfaces, before and after the filtration process The permeate fluxes shown in this work, that ranged from 8.42 to 25.27 L/m2h. during the nanofiltration of 50% EtOH extract, the reducing volume factor was reached around three hours of process (Fig. 4), whereas for the concentration process with 75% EtOH extract, the time required to reach the same factor was more than twice. After the concentration processes, a significant increase in surface roughness in relation to virgin membranes was observed, due to feed solute deposition on membranes surface. This result was another indicator of the cake formation during concentration. 4. Membrane The different fluxes were At preset time intervals, permeate performance and monitored over time after a was collected and further application of period of stabilization analyzed. Gallic acid and tannic ultrafiltration at a feed flow rate of 4.5 ± 0.25 acid concentration was assessed. and nanofiltration L h1 and 35oC. Membrane membrane separation operations to ethanol/water selectivity was evaluated in were carried out in concentration extract of total recirculation mode. The mode, at 35 C and a fixed TMP - Eucalyptus bark feed solution was circulated for 14 bar for NF membrane about 1 h until the steady state. Afterwards, 5. Separation of a A cross-flow NF device was SEM imaging of membrane done high-value used. Both self-made and before and after the process. Flux pharmaceutical commercial membranes were data was studied. compound from tested. A feed container (3 L) waste ethanol by supplies the liquid feed solution nanofiltration to the membrane cell by a plunger pump which has a capacity of 420 L/h and a maximal working pressure of 14 bar. SEM imaging of membrane done before and after the process. 6. Separation and Membrane filtration The retention (R) of selected purification of experiments were performed by membranes towards specific phenolic using a lab crossflow compounds was determined. The compounds from membrane filtration unit. All permeate flux (Jp) was pomegranate juice experiments were performed at determined. The fouling index by ultrafiltration a TMP of 10 bar and an (FI) was calculated. Permeate and nanofiltration operating temperature of 25 ± 1 and retentate samples coming o membranes C. from different experiments were immediately frozen and kept at 18 C until analysed. Samples were analysed for total phenols, total soluble solids (TSS), anthocyanins, sugars and total antioxidant activity (TAA). the mass balance of the process at WRF 5 for total anthocyanins, polyphenols and sugars, is reported.