Influence of Cross-Linking and Process Parameters on the Separation Performance of Poly(dimethylsiloxane) Nanofiltration Membranes

2005 ◽  
Vol 44 (9) ◽  
pp. 3238-3248 ◽  
Author(s):  
John P. Robinson ◽  
E. Steve Tarleton ◽  
Katrin Ebert ◽  
Chris R. Millington ◽  
Arian Nijmeijer
2015 ◽  
Vol 476 ◽  
pp. 50-58 ◽  
Author(s):  
Yan Lv ◽  
Hao-Cheng Yang ◽  
Hong-Qing Liang ◽  
Ling-Shu Wan ◽  
Zhi-Kang Xu

Author(s):  
Xiaoguang Zhang ◽  
Xuexing Chen ◽  
Qingchun Chen ◽  
Zhaolong Deng ◽  
Yan Liu ◽  
...  

A series of nanofiltration membranes were prepared by interfacial polymerization of piperazine and terephthaloyl chloride on the surface of polyacrylonitrile (PAN) ultrafiltration membranes. ZnO nanoparticles were incorporated in the active separation layer to modify the performances of the membranes. The preparation conditions as the monomer concentration, dosage of nano-ZnO particles and the reaction time on removal of a simulated radioactive nuclide Co (II) were investigated. Fourier transform infrared in attenuated total reflection mode verified the formation of polyamide on the PAN ultrafiltration membrane. The scanning electron microscope images showed that the nano-ZnO particles can homogeneously fixed on the membrane surface. The retention of Co (II) increased with increasing the dosage of nano-ZnO in the range of 0∼0.03 g. Further adding more nano-ZnO, the rejection rate of Co (II) first decreased and then increased. The concentration of piperazine and terephthaloyl chloride showed similar effect on removal of Co (II) ion. 5 minutes polymerization time was sufficient to form an active separation layer on the substrate membrane which changed the separation mechanism from ultrafiltration to nanofiltration. The separation performance of NF3 prepared by the following conditions was optimum: 0.03g nano-ZnO, 0.6 wt% piperazine, 0.5 wt% terephthaloyl chloride, and the reaction time was 15 min. The rejection rates of 1000 mg/L Na2SO4 and Co2+ in CoCl2 solution were 90% and 75% respectively. The Co (II) removal rate can be increased to nearly 90% by using ethylenediaminetetraacetic acid disodium salt. Increasing the operation pressure or the feeding concentration of Co (II) can also improve the performances of the membranes in this experiment.


2021 ◽  
Vol 9 ◽  
Author(s):  
Hong Ju ◽  
Jinzhuo Duan ◽  
Haitong Lu ◽  
Weihui Xu

As a new type of membrane material, graphene oxide (GO) can easily form sub-nanometer interlayer channels, which can effectively screen salt ions. The composite membrane and structure with a high water flux and good ion rejection rate were compared by the cross-linking of GO with three different diamine monomers: ethylenediamine (EDA), urea (UR), and p-phenylenediamine (PPD). X-ray photoelectron spectroscopy (XPS) results showed that unmodified GO mainly comprises π-π interactions and hydrogen bonds, but after crosslinking with diamine, both GO and mixed cellulose (MCE) membranes are chemically bonded to the diamine. The GO-UR/MCE membrane achieved a water flux similar to the original GO membrane, while the water flux of GO-PPD/MCE and GO-EDA/MCE dropped. X-ray diffraction results demonstrated that the covalent bond between GO and diamine can effectively inhibit the extension of d-spacing during the transition between dry and wet states. The separation performance of the GO-UR/MCE membrane was the best. GO-PPD/MCE had the largest contact angle and the worst hydrophilicity, but its water flux was still greater than GO-EDA/MCE. This result indicated that the introduction of different functional groups during the diamine monomer cross-linking of GO caused some changes in the performance structure of the membrane.


Polymer ◽  
2019 ◽  
Vol 180 ◽  
pp. 121666 ◽  
Author(s):  
Victor A. Kusuma ◽  
Christina Chen ◽  
James S. Baker ◽  
Megan K. Macala ◽  
David Hopkinson

Desalination ◽  
2006 ◽  
Vol 191 (1-3) ◽  
pp. 254-261 ◽  
Author(s):  
Ying Kong ◽  
Deqing Shi ◽  
Hongwei Yu ◽  
Yunfang Wang ◽  
Jinrong Yang ◽  
...  

2006 ◽  
Vol 280 (1-2) ◽  
pp. 734-743 ◽  
Author(s):  
Da-Xin Wang ◽  
Xiao-Lin Wang ◽  
Yasuhiro Tomi ◽  
Masaaki Ando ◽  
Takuji Shintani

COSMOS ◽  
2013 ◽  
Vol 09 (01) ◽  
pp. 37-46 ◽  
Author(s):  
S. M. P. KALAISELVI ◽  
T. L. TAN ◽  
R. S. RAWAT ◽  
P. LEE ◽  
S. P. HEUSSLER ◽  
...  

The usage of chemically-amplified, negative tone SU-8 photoresist is numerous, spanning industrial, scientific and medical fields. Hence, in this study, some preliminary studies were conducted to understand the dosage and heat treatment requirements of the SU-8 photoresist essential for pattern generation using X-ray lithography. In this work, using Synchrotron as the X-ray source, SU-8 photoresist was characterized for X-ray lithography in terms of its process parameters such as X-ray exposure dose, post exposure bake (PEB) time and temperature for various photoresist thicknesses which is considered worthwhile in view of applications of SU-8 for the fabrication of very high aspect ratio micro structures. The process parameters were varied and the resultant cross linking of the molecular chains of the photoresist was accurately monitored using a Fourier Transform Infra-Red (FTIR) spectrometer and the results are discussed. The infrared absorption peak at 914 cm-1 in the spectrum of the SU-8 photoresist was found to be a useful indicator for the completion of cross linking in the SU-8 photoresist. Results show that the cross linking of the SU-8 photoresist is at a higher rate from 0 J/cm3 to 30 J/cm3 after which the peak almost saturates regardless of the PEB time. It is a good evidence for the validation of dosage requirement of SU-8 photoresist for effective completion of cross linking, which in turn is a requirement for efficient fabrication of micro and nano structures. An analogous behavior was also observed between the extent of cross linking and the PEB time and temperature. The rate of cross linking declines after a certain period of PEB time regardless of PEB temperature. The obtained results also show a definite relation between variation of the absorbance area of the peak at 914 cm-1 and the X-ray exposure dose.


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