کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9684634 | 1456206 | 2005 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Fundamental studies of a new hybrid (inorganic-organic) positively charged membrane. II. Membrane preparation via alcoholysis reaction and amination processes of silicone and titanate coupling agents
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
تصفیه و جداسازی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
A series of novel inorganic-organic hybrid positively charged membranes were prepared by coupling of 3-glycidoxypropyltrimethoxysilane (GPTMS) and mixed GPTMS/Ti(O-n-C4H9)4 in n-butyl alcohol (BuOH) solution at various temperatures and then followed quaternary amination with trimethyl amine (TMA). The synthesized membranes were characterized by IEC, streaming potential, pure water flux, FT-IR, TGA measurements as well as SEM observations. It was exhibited that anion exchange capacities (IECs) of the membranes decreased with increasing curing temperature within a range of (1.4-3.1) Ã 10â2 mequiv. cmâ2 coated for one time and (3.5-4.6) Ã 10â2 mequiv. cmâ2 coated for two times. The positive charge of the membranes was approved by these IEC values as well as FT-IR spectrum of step products and streaming potential values. The thermal stability was tested by TGA analysis and showed that the membranes doped with titanium could undergo a curing temperature up to 300 °C. Pure water flux showed that they decreased with increasing curing temperature, the composition of precursor and dip-coating times, respectively. SEM observations indicated that the membranes became thicker and denser with increasing content of titanium, but excessive Ti-content would decrease the stability of SiOTi bonds in the membranes.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Membrane Science - Volume 264, Issues 1â2, 1 November 2005, Pages 87-96
Journal: Journal of Membrane Science - Volume 264, Issues 1â2, 1 November 2005, Pages 87-96
نویسندگان
Junsheng Liu, Tongwen Xu, Ming Gong, Yanxun Fu,