scholarly journals Oriented membranes processes for facilitated extraction and recovery of some industrial dyes across polymer inclusion membranes containing Chitin as new extractive agent

Author(s):  
Y Chaouqi ◽  
M El Bouchti ◽  
R Ouchn ◽  
Z Habibi ◽  
O Cherkaoui ◽  
...  
1969 ◽  
Vol 42 (1) ◽  
pp. 221-234 ◽  
Author(s):  
Charles R. Hackenbrock ◽  
Arnold I. Caplan

The energized uptake of low levels of Ca2+ in the presence and absence of phosphate by isolated rat liver mitochondria, and the perturbation effected by this activity on ultrastructural and metabolic parameters of mitochondria have been investigated. In the presence of phosphate, low levels of Ca2+ are taken up by mitochondria and result in various degrees of ultrastructural expansion of the inner mitochondrial compartment. This indicates that low levels of Ca2+ in the presence of phosphate, are accumulated in an osmotically active form into the water phase of the inner compartment. The first clearly observable quantitative increase in the volume of the inner compartment occurs after the accumulation of 100 nmoles Ca2+/mg protein. An accumulation of 150–200 nmoles Ca2+/mg protein, which is equivalent to the osmolar concentration of endogenous K+, is required to effect a doubling of the volume of the inner compartment. This degree of osmotic perturbation occurs as mitochondria transform from a condensed to an orthodox conformation. The osmotically induced orthodox conformation differs from the mechanochemically induced orthodox conformation previously described, in that its development is concomitant with a marked decrease in acceptor control and oxidative phosphorylation efficiency and it fails to transform to a condensed conformation in response to addition of ADP. In the absence of added phosphate, a maximum of 190 nmoles Ca2+/mg protein was found to be taken up by mitochondria (state 6). Ca2+ is apparently bound under state 6 conditions since the uptake does not effect an ultrastructural expansion of the inner compartment. Phosphate added after state 6 Ca2+ binding, however, results in an immediate ultrastructural expansion of the inner compartment. The addition of phosphate to mitochondria in the absence of exogenous Ca2- fails to effect an osmotic ultrastructural transformation. Under state 6 conditions, the binding of between 40 and 190 nmoles Ca2+/mg protein results in the formation of dense matrix inclusions which appear to be composed of tightly packed, concentrically oriented membranes. Under conditions in which the bound Ca2+ is subsequently released, there is a concomitant loss in the density of these matrix inclusions, leaving behind morphologically distinct membrane whorls in the mitochondrial matrix.


2010 ◽  
Author(s):  
◽  
Peterson Thokozani Ngema

Globally there is renewed interest in the production of alternate fuels in the form of bioethanol and biodiesel. This is mainly due to the realization that crude oil stocks are limited hence the swing towards more renewable sources of energy. Bioethanol and biodiesel have received increasing attention as excellent alternative fuels and have virtually limitless potential for growth. One of the key processing challenges in the manufacturing of biofuels is the production of high purity products. As bioethanol is the part of biofuels, the main challenge facing bioethanol production is the separation of high purity ethanol. The separation of ethanol from water is difficult because of the existence of an azeotrope in the mixture. However, the separation of the ethanol/water azeotropic system could be achieved by the addition of a suitable solvent, which influences the activity coefficient, relative volatility, flux and the separation factor or by physical separation based on molecular size. In this study, two methods of high purity ethanol separation are investigated: extractive distillation and pervaporation. The objective of this project was to optimize and compare the performance of pervaporation and extraction distillation in order to produce high purity ethanol. The scopes of the investigation include:  Study of effect of various parameters (i) operating pressure, (ii) operating temperature, and (iii) feed composition on the separation of ethanol-water system using pervaporation.  Study the effect of using salt as a separating agent and the operating pressure in the extractive distillation process. The pervaporation unit using a composite flat sheet membrane (hydrophilic membrane) produced a high purity ethanol, and also achieved an increase in water flux with increasing pressure and feed temperature. The pervaporation unit facilitated separation beyond the ethanol – water system azeotropic point. It is concluded that varying the feed temperature and the operating pressure, the performance of the pervaporation membrane can be optimised. v The extractive distillation study using salt as an extractive agent was performed using the low pressure vapour-liquid equilibrium (LPVLE) still, which was developed by (Raal and Mühlbauer, 1998) and later modified by (Joseph et al. 2001). The VLE study indicated an increase in relative volatility with increase in salt concentration and increase in pressure operating pressure. Salt concentration at 0.2 g/ml and 0.3 g/ml showed complete elimination of the azeotrope in ethanol-water system. The experimental VLE data were regressed using the combined method and Gibbs excess energy models, particular Wilson and NRTL. Both models have shown the best fit for the ethanol/water system with average absolute deviation (AAD) below 0.005. The VLE data were subjected to consistency test and according to the Point test, were of high consistency with average absolute deviations between experimental and calculated vapour composition below 0.005. Both extractive distillation using salt as an extractive agent and pervaporation are potential technologies that could be utilized for the production of high purity ethanol in boiethanol-production.


2018 ◽  
Vol 2 (2) ◽  
pp. 75 ◽  
Author(s):  
Agung Ari Wibowo ◽  
Cucuk Evi Lusiani ◽  
Rizqy Romadhona Ginting ◽  
Dhoni Hartanto

Pemisahan n-propil asetat dari campuran terner n-propil asetat/n-propanol/air merupakan salah satu proses yang tidak dapat dilakukan dengan distilasi sederhana. Adanya azeotrop terner minimum dari campuran tersebut menyebabkan n-propil asetat hanya dapat dipisahkan dari campuran n-propanol dan air salah satunya dengan metode distilasi ekstraktif. Distilasi ekstraktif merupakan proses vaporisasi parsial dengan menambahkan suatu agen pemisah non-volatil yang disebut sebagai sovent atau agen ekstraktif. Solvent yang digunakan dalam simulasi proses ini adalah campuran DMSO (Dimetil Sulfoksida) dan Gliserol dengan komposisi 50 % massa dengan perbandingan 1:2 untuk massa umpan kolom : solvent. Feed yang digunakan adalah n-propanol (10 kmol/jam) dan asam asetat (13 kmol/jam) masing-masing pada suhu 25°C dan tekanan 101,3 kPa. Hasil n-propil asetat terbaik diperoleh saat solvent diumpankan pada stage 5 dengan fraksi mol n-propil asetat pada distilat 0,9975 disertai dengan minimumnya energi reboiler yang digunakan pada konfigurasi kolom ini.n-Propyl acetate separation of the n-propyl acetate /n-propanol/water mixture composition can't be done by simple distillation. The existence of minimum ternary azeotrope on the mixture causes n-propyl acetate can be separated only by extractive distillation method. Extractive distillation is a partial vaporization process in the presence of a non-volatile separating agent called as solvent or extractive agent. Solvent used in the simulation process is DMSO (Dimethyl Sulfoxide)-Glycerol mixture (50% mass) with a ratio of 1: 2 for column feed : solvent. n-Propanol (10 kmol/hour) and acetic acid (13 kmol/hour) are fed into reactor (before extractive distillation process) at 25°C and 101.3 kPa, respectively. The best results of n-propyl acetate were obtained when the solvent was fed to stage 5 in which mole fraction of n-propyl acetate in distillate 0.9975 accompanied by the minimum reboiler energy used in this column configuration.


2021 ◽  
Vol 63 (4) ◽  
pp. 462-469
Author(s):  
M. V. Mamchich ◽  
N. D. Goletsky ◽  
L. I. Tkachenko ◽  
A. N. Viznyi ◽  
A. A. Naumov ◽  
...  
Keyword(s):  

2002 ◽  
Vol 83 (6) ◽  
pp. 3336-3350 ◽  
Author(s):  
Stephan L. Grage ◽  
Junfeng Wang ◽  
Timothy A. Cross ◽  
Anne S. Ulrich

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