Organo-Silica Membrane Prepared from TEOS-TEVS Modified with Organic-Acid Catalyst for Brackish Water Desalination

The sol gel process is one of the processes used in the manufacture of thin films on membranes because it can control the pore size in the resulting silica matrix. In addition, another way to build membrane size can be done by adding catalysts and precursors to be used. In this study, using a combination of tetraethyl ortho silicate (TEOS) and triethoxy vinyl silane (TEVS) precursors and citric acid as a catalyst to produce a silica matrix with mesoporous size so that it is suitable for application in the desalination process. The organo silica membrane was calcined at 350 ° C for 1 hour using the RTP calcination technique under vacuum, thus preventing the decomposition of carbon in the silica matrix. The membrane was dipcoated 4 times to obtain 4 layers. The FTIR (Fourier-transform Infrared Spectroscopy) test was carried out to see the functional groups on xerogel, namely silanol, siloxane and carbon. In addition, the performance of this membrane is carried out by desalination through pervaporation using 0.3% NaCl feed water with variations in feed air temperature, namely 25 ℃, 40 ℃ and 60 ℃. The resulting flux of air value increased with increasing feed water temperature, namely 6.1; 11.2; and 12.1 kg.m-2h-1 while the resulting salt rejection was 99.72; 99.64 and 99.23%. So that the organo silica membrane is suitable when applied to the desalination process through pervaporation.

Study the impact of A nanomixture of carbon black and clay on the mechanical properties of A series of irradiated natural rubber/ butyl rubber blend

A series of natural rubber/ butyl rubber NR/IIR blend loaded with N660 carbon black CB and triethoxy vinyl silane treated clay nano particles (TCNP) were prepared using gamma irradiation in the presence of polyfunctional monomer, trimethylolpropane triacrylate (TMPTA). The effect of incorporating different content of N660 carbon black and 5 part per hundred of rubber (phr) of treated clay on the mechanical properties of the prepared nano composites have been investigated. The additions of TCNP into CB/ rubber composites markedly increase their tensile strength due to the increase of the cross-link density. These results indicated that the TCNP may be enclosed or trapped in the occluded structure of CB. The effect of CB and TCNP content on the tensile strength (σ), elongation at break (εb %) and modulus of elasticity (E, MPa) of natural rubber/ butyl rubber NR/IIR blend have been investigated. The incorporation of 5 phr of TCNP into 30 phr carbon black loaded NR/ IIR composites results in the increased tensile strength value by about 60%. Finally, theoretical models were used to interpret the experimental results.

Deconvolution of TEOS/TEVS Xerogel by Single or Dual Organic Catalyst Addition

Currently, xerogel has been applied as a filtration material, especially in membrane desalination. However, the xerogel matrix structure for desalination have to be designed properly in order to allow rejection of salt and obtain good hydro-stability, thus, silica precursor in the form of TEOS (tetraethyl orthosilicate)/TEVS (triethoxy vinyl silane) and organic acid catalyst are suitable material for fabrication. The aim of this study is therefore to fabricate and perform deconvolution of TEOS/TEVS xerogel by adding single or dual catalyst, using FTIR (Fourier-transform Infrared Spectroscopy) and Fityk software. The xerogel was fabricated by dried silica sol and calcined using RTP technique (rapid thermal processing) at 450 °C. Prior to this fabrication, the silica sol was synthesized by sol gel method, using a mixture of silica precursor TEOS/TEVS, ethanol solvent, and varied addition of single catalyst (citric acid) as well as dual catalyst (citric acid + ammonia) for 2 hours, at 50 °C. Subsequently, the xerogel was characterized by FTIR and the deconvolution was obtained through Gaussian approach, with Fityk software. All TEOS/TEVS xerogel samples indicated existence of silanol (Si-OH), siloxane (Si-O-Si) and silica-carbon (Si-C) functional groups. The xerogel deconvolution of TEOS/TEVS using single catalyst exhibit a peak area ratio of Si-OH/Si-O-Si, and this is similar to the dual catalyst counterpart of 0.24 (unit area) and 1.86 (unit area), for Si-C area ratio. This shows the addition of single catalyst was enough to produce deconvolution in TEOS/TEVS xerogel, dominated by siloxane functional group and carbon bonds with the ability to enhance membrane material hydro-stability’s fabrication.

Short-Chained Platinum Complex Catalyzed Hydrosilylation under Thermomorphic Conditions: Heterogeneous Phase Separation at Ice Temperature

Homogeneous catalysts PtCl2[5,5′-bis-(n-ClCF2(CF2)3CH2OCH2)-2,2′-bpy] (2A) and PtCl2[5,5′-bis-(n-HCF2(CF2)3CH2OCH2)-2,2′-bpy] (2B), which contained short fluorous chains, were synthesized and used in catalysis of hydrosilylation of alkynes. In these reactions the thermomorphic mode was effectively used to recover these catalysts from the reaction mixture up to eight cycles by taking advantage of heterogeneous phase separation at ice temperature. This kind of catalysis had previously been observed in fluorous catalysts of platinum containing about 50% F-content, but in this work the percentage of F-content is decreased to only about 30%, by which we termed them as “very light fluorous”. Our new type of catalyst with limited number of F-content is considered as the important discovery in the fluorous technology field as the reduced number of fluorine atoms will help to be able to comply the EPA 8-carbon rule. The metal leaching after the reaction has been examined by ICP-MS, and the testing results show the leaching of residual metal to be minimal. Additionally, comparing these results to our previous work, fluorous chain assisted selectivity has been observed when different fluorous chain lengths of the catalysts are used. It has been found that there exists fluorous chain assisted better selectivity towards β-(E) form in the Pt-catalyzed hydrosilylation of non-symmetric terminal alkyne when the Pt catalyst contains short fluorous chain (i.e., 4 Cs). Phenyl acetylenes showed the opposite regioselectivity due to pi-pi interaction while using the same catalyst via Markovnikov’s addition to form terminal vinyl silane, which is then a major product for Pt-catalyzed hydrosilylation of terminal aryl acetylene with triethylsilane. Finally, the kinetic studies indicate that the insertion of alkyne into the Pt-H bond is the rate-determining step.

Impact of a nanomixture of carbon black and clay on the mechanical properties of a series of irradiated natural rubber/butyl rubber blend

A series of natural rubber/butyl rubber NR/IIR blend loaded with N660 carbon black (CB) and triethoxy vinyl silane treated clay nanoparticles (TCNPs) were prepared using gamma irradiation in the presence of a polyfunctional monomer, trimethylolpropane triacrylate (TMPTA). The effect of incorporating different contents of N660 CB and five parts per hundred of rubber (phr) of treated clay on the mechanical properties of the prepared nanocomposites has been investigated. The addition of TCNP to CB/rubber composites markedly increase their tensile strength due to the increase of the cross-link density. These results indicated that the TCNP may be enclosed or trapped in the occluded structure of CB. The effect of CB and the TCNP content on the tensile strength (σ), elongation at break (ε b, %), and modulus of elasticity (E, MPa) of natural rubber/butyl rubber NR/IIR blend have been investigated. The incorporation of 5 phr of TCNP into 30 phr CB-loaded NR/IIR composites results in the increased tensile strength value by about 60%. Finally, theoretical models were used to interpret the experimental results.

FTIR STUDIES OF THE TEOS/TEVS XEROGEL STRUCTURE USING RAPID THERMAL PROCESSING METHOD

The tetraethyl orthocycate (TEOS) is mainly used as a silica precursor. Silanol content of silica material is the main cause of low hydrostability which led to resulting in poor performance, especially in water treatment. The stronger bond strength formed by incorporating a carbon structure from triethoxy vinyl silane (TEVS). The xerogel fabrication resulted in the composition of TEOS: TEVS: EtOH: HNO3: H2O: NH3 to be 0.9: 0.1: 38: 0.00078: 5: 0.0003. . The purpose is to study the structure of organosilica xerogel calcined at 350oC, 450oC and 600oC in the Fourier-transform infrared (FTIR) using rapid thermal processing. The deconvolution of FTIR spectra calculated using the Fityk software. The result of the best xerogel peak shows at calcination of 450°C with peak area siloxane of 15.39, silanol of 3.32 and silica carbon of 3.85.

Trifluoromethanesulfonamide vs. Non-Fluorinated Sulfonamides in Oxidative Sulfamidation of the C=C Bond: An In Silico Study

A theoretical analysis of the reaction of oxidative sulfamidation of several alkenes was performed in order to explain the various experimental observations and different reactivity of triflamide and non-fluorinated sulfonamides. Transformations occurring in the system alkene–sulfonamide in the presence of oxidative system (ButOCl + NaI) were analyzed at the MP2/DGDZVP//B3LYP/DGDZVP level of theory using the IEF-PCM method for taking into account the solvent acetonitrile (MeCN) effect. As the model substrates, styrene, trimethyl(vinyl)silane, dimethyl(divinyl)silane and diphenyl(divinyl)silane were chosen and mesylamide, triflamide, tosylamide and p-nosylamide were taken as the reagents. ButOI generated from ButOCl and NaI reacts with sulfonamides to give N-iodinated sulfonamides RSO2NHI and RSO2NI2 as active intermediates, the iodinating activity of the latter being notably higher. The analysis allowed to answer such challenging questions as different reactivity of nonfluorinated sulfonamides leading to aziridination and of triflamide resulting in the formation the main products of bis-triflamidation, or different regioselectivity of halogenation of styrene and trimethyl(vinyl)silane caused by a linear intermediate iodonium cation in the former case and a cyclic one in the latter.