3-aminopropyl Trimethoxysilane Research Articles

One-pot synthesis of quinazolinone heterocyclic compounds using functionalized SBA-15 with natural material ellagic acid as a novel nanocatalyst

The nanoporous compound SBA-15 was functionalized using (3-aminopropyl)trimethoxysilane (APTES). Then the obtained product was modified with ellagic acid (ELA), a bioactive polyphenolic compound. The structure of the prepared nanoporous composition SBA-15@ELA was extensively characterized and confirmed by various techniques, such as Fourier-transform infrared (FT-IR) spectroscopy, Energy dispersive X-ray (EDX) elemental analysis, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), X-ray diffraction (XRD), transmission electron microscopy (TEM) and N2 adsorption–desorption isotherms (BET). The novel, recoverable, heterogenous SBA-15@ELA nanoporous compound was used to investigate its catalytic effect in the synthesis of 4-oxo-quinazoline derivatives (19 examples) with high yields (78–96%), as an important class of nitrogen-containing heterocyclic compounds. The use of an inexpensive mesoporous catalyst with a high surface area, along with easy recovery by simple filtration are among the advantages of this catalysis research work. The catalyst has been used in at least 6 consecutive runs without a significant loss of its activity.

Construction of 2D/2D NH2-TiO2/ReS2 molecular-connected heterojunction to achieve selective carrier transport for photocatalytic hydrogen production

The 2D/2D heterojunction photocatalyst demonstrates a broad range of applications owing to its large interface contact area. At present, most of the current 2D/2D structures are constructed by self-assembly, which mainly forms a relatively weak van der Waals force at the interface. This poses a challenge to achieving effective carrier separation. Here, we proposed an innovative strategy of molecular-connected heterojunctions to address this challenge. The strategy uses (3-aminopropyl) trimethoxysilane (APTMS) to modify the surface of TiO2 and construct NH2-TiO2/ReS2 heterojunction, which not only alters the material’s Zeta potential but also uses molecular chains connecting TiO2 and ReS2. Simultaneously, the design of molecular-connected heterojunction changes the work function of TiO2, leading to the transformation of the TiO2/ReS2 heterojunction from type-Ⅰ to S-scheme, thereby achieving a selective carrier separation. The constructed NH2-TiO2/ReS2 photocatalytic heterojunction composite has a hydrogen production rate of 451.3 μmol g-1 h−1, which is over 11 and 3 times than TiO2 and TiO2/ReS2, respectively, and exhibits excellent long-term photocatalytic stability. This study presents a novel approach for achieving strong interface bonding and introduces an innovative approach for constructing 2D/2D photocatalytic heterojunctions.

Green-AgNPs modified membrane for monitoring mercury ions in cosmetic sample using pre-concentration assisted voltammetry technique

The carcinogenic and teratogenic properties of mercury have driven the necessity for the development of highly sensitive methods capable of detecting even trace amounts of the element. In response to this need, an analysis technique has been established for mercury ions, employing preconcentration methods utilizing filter paper modified by silver nanoparticles (AgNPs) and 3-Amino propyl trimethoxy silane (APTMS). This method allows for the detection of mercury ions through the voltammetry technique, ensuring accurate and reliable results. Upon conducting analyses using this method, it was found that the tested cosmetic samples were free from Hg2+ ions, indicating the absence of mercury contamination in the cosmetics under investigation. The correlation coefficient derived from the graph of the analysis results stands at an impressive value of 0.9976, affirming the strong relationship between the measured concentrations and the actual mercury content. Additionally, the method demonstrates excellent sensitivity, as evidenced by the low limit of detection (LOD) value of 0.0483 mM and the limit of quantification (LOQ) value of 0.1611 mM.

Amine-containing yolk-shell structured magnetic organosilica nanocomposite as a highly efficient catalyst for the Knoevenagel reaction.

The yolk-shell structured silica nanocomposites have been considered by many researchers due to their specific physical and chemical properties. These materials have been widely used in adsorption and catalysis processes. Especially, the void space of yolk-shell nanostructures can provide a unique environment for storage, compartmentation, and confinement in host-guest interactions. In this paper, for the first time, the preparation, characterization, and catalytic application of a novel amine-containing magnetic methylene-based periodic mesoporous organosilica with yolk-shell structure (YS-MPMO/pr-NH2) are developed. The magnetic periodic mesoporous organosilica nanocomposite was synthesized through surfactant-directed co-condensation of bis(triethoxysilyl)methane (BTEM) and tetraethoxysilane around Fe3O4 nanoparticles. After Soxhlet extraction, the surface of YS-MPMO nanocomposite was modified with 3-aminopropyl trimethoxysilane to deliver YS-MPMO-pr-NH2 nanocatalyst. This catalyst was characterized by using EDX, FT-IR, VSM, TGA, XRD, nitrogen-sorption, and SEM analyses. The catalytic activity of YS-MPMO/pr-NH2 was studied in the Knoevenagel reaction giving the corresponding products in a high yield and selectivity. The YS-MPMO/pr-NH2 nanocatalyst was recovered and reused at least four times without a significant decrease in efficiency and activity. A leaching test was performed to study the nature of the catalyst during reaction conditions Also, the catalytic performance of our designed nanocomposite was compared with some of the previous catalysts used in the Knoevenagel reaction.

Optimization of the mass ratio of siloxane crosslinkers for poly(2,6-dimethyl-1,4-phenylene oxide) anion exchange membranes to improve acid enrichment by electrodialysis

Proton blocking anion exchange membranes (AEMs), which are employed in electrodialysis technology, show promise in acid recovery from industrial waste. A series of poly(2,6-dimethyl-1,4-phenylene oxide) (PPO) membranes were prepared using (3-aminopropyl)trimethoxysilane (APTMS) and weakly functionalized bases including N-butylimidazole (N-BuIm). Were networked to create AEMs with low leak rates. It was discovered that the appropriate concentration of siloxane crosslinker raised the membrane matrix's density and lowered the AEM matrix's hydrophilicity. Thermogravimetric measurements and water absorption have confirmed this, and the membranes in this series even swell up to 8.61 %. The maximum H+ concentration concentrated by the cross-linked AEM (BPPO/5Si) during the ED with a current density of 10 mA∙cm−2 was 2.35 M, which was higher than the concentration concentrated by the uncross-linked AEM (BPPO/OSi), which was 1.90 M (beginning concentration: 1.00 M). The current efficiency was 44.8 % and the energy consumption was only 1.81 kW ∙h∙kg−1. A balance between proton blocking and SO42− ions transport was achieved by the optimized AEM, which exhibited increased hydrophobicity and smaller ion clusters. The improved AEM was found to have fewer ionic clusters and greater hydrophobicity. For cross-linked AEMs, a trade-off between SO42− ions transport and proton blocking was thus accomplished. This work is thought to offer direction for developing sophisticated proton blocking AEMs.

Preparation and thermostability of a Si/P/N synergistic flame retardant containing triazine ring structure for cotton fabrics

A new synergistic flame retardant named Bisiminopropyl trimethoxysilane-1,3,5-triazine-O-bicyclic pentaerythritol phosphate (BTPODE) was synthesized, which is a type of Si/P/N flame retardant. This was accomplished by grafting aminopropyl trimethoxysilane and bicyclic pentaerythritol phosphate onto a triazine ring structure, serving as an intermediate. The structure of BTPODE was determined using nuclear magnetic resonance (1H NMR, 13C NMR, and 31P NMR) and Fourier transform infrared spectroscopy (FT-IR). SEM was used to detect the surface morphology of cotton fabrics, which suggested that BTPODE had been resoundingly stick to cotton fabrics. The flame retardant properties of cotton fabrics were evaluated by measuring the limiting oxygen index (LOI) and conducting vertical flammability experiments. Cotton fabrics with a weight gain of 20.73 % achieved an LOI value of 32.5 %. Thermogravimetric (TG) experiments demonstrated the samples' good thermostability. Furthermore, under nitrogen conditions, the char residue of cotton fabric with a weight gain of 20.73 % was 36.85 %. The cone calorimetry test (CONE) showed a significant reduction in the TSP value, indicating a certain level of smoke suppression performance. Finally, based on the obtained experimental results, the fire-retardant mechanism principle of the flame retardant was deduced.

SiO2–modified APTMS nanocoatings encapsulating FeNi: Amplifying microwave absorption and corrosion resistance

Corrosion is a major challenge for the reliable operation of ferromagnetic absorbers (FMAs) in extreme environments. Herein, we employed a one–pot method to construct SiO2–modified (3–Aminopropyl)trimethoxysilane (APTMS) nanocoatings on the FeNi surface, using tetraethyl orthosilicate and APTMS as precursors. The resulting APTMS/SiO2 nanocoating (thickness: 12.0–29.3 nm) contained numerous –NH2 and –OH functional groups, contributing to the generation of dipole polarizations. The nanocoating also improved the interfacial polarization and the impedance matching of FeNi@APTMS/SiO2, enhancing its microwave absorption (MA) properties. At 2.00 mm, FeNi@APTMS/SiO2 exhibited a maximum effective absorption bandwidth of 9.23 GHz, outperforming FeNi's 8.01 GHz. Moreover, the radar cross–section value of FeNi@APTMS/SiO2 reached as high as 27.84 dB·m2. Moreover, the nanocoating acted as a barrier to isolate the FeNi from the corrosive medium and prevent the formation of corrosive microcells with NaCl solutions, increasing the corrosion resistance of FeNi. The corrosion rate of FeNi@APTMS/SiO2 was measured at 4.71 × 10–11 m/s, which was 5.81 times lower than that of FeNi. This research highlights the advantages of APTMS/SiO2 for MA and corrosion protection, offering valuable insights into the development of corrosion–resistant FMAs.

Fabrication of Functional Coating Layer for Emerging Transparent Electrodes using Antimony Tin Oxide Nano-colloid

This study fabricated a functional coating layer for transparent electrodes using antimony tin oxide nanopowder. The wet grinding method was employed to create a stable dispersion solution of antimony tin oxide nanopowder with aminopropyl tri-methoxysilane and acetyl acetone as primary dispersing agents. Various concentrations of these dispersing agents were used to determine optimal conditions, followed by a gel reaction to form a stable solution. The primary objective was to provide a viable alternative to indium-based transparent electrodes, specifically indium tin oxide, by incorporating antimony oxide. This approach not only addresses limitations associated with indium, but also enhances mechanical properties. The methodology involves the utilization of antimony tin oxide nanopowder and various solvents including ethanol and aforementioned dispersing agents to create a stable antimony tin oxide sol through wet grinding. Effects of dispersant concentration and milling time on the secondary particle size of the antimony tin oxide sol were thoroughly evaluated. Furthermore, this study examined sheet resistance of resulting coating layers by conducting a comparative analysis between antimony tin oxide and indium tin oxide under similar conditions. Findings of this study meticulously detailed in subsequent sections of the manuscript provide valuable insights into optimizing the entire process, encompassing synthesis, coating, heat treatment, and the production of high-quality transparent conductive coatings. These techniques and outcomes can significantly contribute to the development of more sustainable and cost-effective alternatives to traditional indium-based transparent electrodes.

Modification of Hydroxysodalite Nanoparticles by (3-aminopropyl)trimethoxysilane and Isatoic Anhydride as a Novel Composite for Efficient Sorption of Cu(II) Ions from Aqueous Media

Modification of Hydroxysodalite Nanoparticles by (3-aminopropyl)trimethoxysilane and Isatoic Anhydride as a Novel Composite for Efficient Sorption of Cu(II) Ions from Aqueous Media

Fluorescent and visual sensing of sodium dodecylbenzene sulfonate with an aminosilane self-condensation promoting and electrostatic attraction effect-based ratiometric probe

BackgroundIncreasing attention has been paid to sodium dodecylbenzene sulfonate (SDBS) detection because it could cause damage to human body and environmental water. For example, SDBS must not be detected on tableware surface according to national standard of China (GB 14934-2016). However, there is no report heretofore addressing SDBS sensing on surfaces. More importantly, the interferents often affect the sensing performance of analytical approaches. Hence, there is an urgent need to establish a method with good anti-interference ability for SDBS detection both on tableware surfaces and in water. ResultsInspired by a finding that SDBS could cause the generation of white turbidity in (3-aminopropyl)trimethoxysilane (APTMS, an aminosilane) aqueous solution, APTMS modified Mn doped ZnS quantum dots (QDs) and fluorescent (FL) whitening agent (FWA) were constructed as a ratiometric probe for FL and visual sensing of SDBS. The modified QDs aggregated and settled in presence of SDBS, which was likely to be connected to the stimulatory effect of SDBS on the APTMS self-condensation and the electrostatic attraction. The FL emission from the QDs at 605 nm then decreased dramatically, whereas that at 425 nm was virtually constant owing to FWA. SDBS sensing could be achieved by calculating the ratio change of their FL intensities. The detection limits of FL and visual methods were found to be 0.011 and 10 μg/L, respectively, making it one of the most sensitive approaches in literature. Finally, it was successfully utilized for SDBS detection on tableware surfaces and in water. SignificanceHerein, the specific interaction between SDBS and APTMS was reported and the reaction mechanisms were explored for the first time. The proposed probe based on the effect described above provided a promising potential for SDBS analysis owing to high sensitivity, selectivity, anti-interference ability, and stability (in 20 days).

Kinetic Suppression of Photoinduced Halide Migration in Wide Bandgap Perovskites via Surface Passivation.

In this work, we study the kinetics of photoinduced halide migration in FA0.8Cs0.2Pb(I0.8Br0.2)3 wide (∼1.69 eV) bandgap perovskites and show that halide migration slows down following surface passivation with (3-aminopropyl) trimethoxysilane (APTMS). We use scanning Kelvin probe microscopy (SKPM) to probe the contact potential difference (CPD) shift under illumination and the kinetics of surface potential relaxation in the dark. Our results show that APTMS-passivated perovskites exhibit a smaller CPD shift under illumination and a slower surface potential relaxation in the dark. We compare the evolution of the photoluminescence spectra of APTMS-passivated and unpassivated perovskites under illumination. We find that APTMS-passivated perovskites exhibit more than 5 times slower photoluminescence red-shift, consistent with the slower surface potential relaxation as observed by SKPM. These observations provide evidence for kinetic suppression of photoinduced halide migration in APTMS-passivated samples, likely due to reduced halide vacancy densities, opening avenues to more efficient and stable devices.

Enhancing blue phosphorescence in matrix-free carbon dots through covalent crosslinking

Room temperature phosphorescence (RTP) of carbon dots (CDs) has received extensive attention due to its excellent performance and promising application. Here, a novel kind of matrix-free CDs with blue phosphorescence emission was synthesized by a simple one-step hydrothermal method of heating (3-Aminopropyl) trimethoxysilane (APTMS) and phosphoric acid in aqueous solution. The obtained CDs show a phosphorescence lifetime of 315.73 ms, and the absolute photoluminescence quantum yield (PLQY) and the phosphorescence quantum yield (PQY) can reach up to 37.8 % and 12.4 %, respectively. From the experimental results, we speculate that the generation of RTP is attributed to the restriction effect of the covalent crosslinking structure of SiOSi, SiOC, or SiC bonds formed on the CDs surface. In addition, phosphoric acid as a crosslinking agent and heteroatom dopant can promote the formation of cross-linked structures and facilitate the intersystem crossing (ISC) process, thus enhancing room temperature phosphorescence. Finally, the CDs were successfully used in information encryption and anti-counterfeiting.

Facile Fabrication of Transparent Hydrophobic Spectral Converting Thin Film of Cyclic Silica-Silane Structure

There is a growing demand for advanced coatings with remarkable physical properties such as high transparency, water resistance, spectrum conversion, and dust repellence, which can be used in a variety of applications. In this study, we built thin films using silicon quantum dots and a silane-based material composite, resulting in a unique mix of hydrophobicity, self-cleaning and the ability to convert ultraviolet (UV) to visible spectrum. The use of silicon quantum dots in the film results in spectrum conversion from UV to visible wavelengths, taking advantage of their broad UV absorption and concurrent visible light emission. Concurrently, a silica-silane based layer of tetraethyl orthosilicate, N, N dimethyl amino propyl trimethoxy silane, and 3-chloro-propyl trimethoxy silane is integrated, imparting not only water resistance but also dust resistance. The challenging synthesis chemistry exemplifies the several stages required to create a spectral-converting hydrophobic layer. Given its inherent transparency, coupled with UV-to-visible spectrum conversion capabilities, this novel layered structure have a potential in outer coating of solar photovoltaic systems and various outdoor glass applications.

Chemical vapour deposition in narrow capillaries: Electro-osmotic flow control in capillary electrophoresis

BackgroundIn capillary electrophoresis (CE), the inner surface of fused-silica capillaries is commonly covalently modified with liquid silanes to control electroosmotic flow (EOF). This liquid phase deposition (LPD) approach is challenging for long and narrow-diameter capillaries (≥1 m, ≤25 μm ID) inhibiting commercial production. Here, we use chemical vapour deposition (CVD) to covalently modify capillaries with different silanes. Using a home-built CVD device, capillaries were modified with neutral (3-glycidyloxypropyl) trimethoxysilane (GPTMS), the weak base (3-aminopropyl) trimethoxysilane (APTMS), the weak acid 3-mercaptopropyltrimethoxysilane (MPTMS) and the neutral hydrophobic trichloro(1H,1H,2H,2H-perfluorooctyl) silane (PFOCTS). Gas-phase modification of GPTMS with acid and ammonia allowed further modification of the surface prior to molecular layer deposition (MLD) of poly(p-phenylene terephthalamide) (PPTA) using the self-limiting sequential reaction between terephthalaldehyde (TA) and p-phenylenediamine (PD) vapours. ResultsCapillaries coated with GPTMS by CVD showed a greater reduction in EOF at all pH values than the conventional LPD. APTMS showed a reduction of the EOF at pH 9, with EOF reversal observed below pH 6. MPTMS provided a slightly lower EOF than an unmodified capillary at high pH, and a slightly higher EOF at lower pH. PFOCTS provided the most consistent EOF as a function of pH. The deposition of successive layers of PPTA resulted in increased surface coverage of the polymer and a greater reduction in EOF at pH higher than 5. The stability of a 10 μm ID GPTMS coated capillary was tested at pH 8.8 in a 200 mM CHES/Tris BGE for the separation of inorganic anions. Over 1.5 months of continuous operation (≈4130 runs), the reproducibility of the apparent mobilities for chloride, nitrite, nitrate and sulfate were 2.43%, 2.56%, 2.63% and 3.05%, respectively. The intra-day and inter-day column-to-column reproducibility and batch-to-batch reproducibility for all the coated capillaries ranged between 0.34% and 3.95%. SignificanceThe study demonstrates the superior performance of CVD coating for suppressing the EOF compared to LPD allowing the easy modification of long lengths of narrow capillary. The variation in silane, and the ability of MLD to modify and control the surface chemistry, provides a simple and facile method for surface modification. The stability of these coatings will allow long-term capillary electrophoresis monitoring of water chemistry, such as for monitoring fertiliser run-off in natural waters.

Platinum nanoparticle-decorated reduced graphene oxide nanosheets: A recyclable and highly efficient catalyst towards the reduction of para-nitrophenol and methylene blue

The present study focuses on the design and development of Pt nanoparticle (PtNPs) decorated reduced graphene oxide (RGO) nanohybrid as an efficient heterogeneous catalyst towards the reduction of p-nitrophenol (p-NP) and methylene blue (MB). The citrate reduction of chloroplatinic acid in the presence of amino-propyl trimethoxy silane (APTMS) modified graphene oxide (GO) produced RGO/PtNPs nanohybrid comprised of uniform and high-density distribution of smaller-sized PtNPs. The APTMS provide efficient nucleation points via their amino groups and thereby play a vital role in regulating the size as well as the distribution of the anchored PtNPs in the present approach. The morphological and structural characterization of RGO/PtNPs nanohybrid was done by using X-ray powder diffraction, scanning and transmission electron microscopy, Fourier transform infrared and Raman spectroscopic techniques. The homogeneous and high-density dispersion of smaller-sized PtNPs endows superior catalytic activity to RGO/PtNPs nanohybrid. The nanohybrid exhibited outstanding catalytic performance enabling rapid reduction of both p-NP and MB at ambient conditions. The estimated rate constants for p-NP and MB reduction were 15.9 × 10−3, and 187 × 10−3 s−1 respectively, which outperform the rate constants of several previously reported metal-based GO/RGO nanocatalysts. The recycling tests showed that the nanohybrid maintained good catalytic stability even after the fifth recycle run. The RGO/PtNPs nanohybrid can be exploited for sustainable and efficient catalytic reduction of other environmental pollutants also. Further, the strategy followed in the present study to achieve homogenous and high-density distribution of Pt nanoparticles could be adopted for the anchoring of other metal/metal oxide/semiconductor nanoparticles.

Graphene interleaved SiOx/C spheres Via molecular polymerization as high-stability lithium-ion battery anodes

SiOx/carbon composite materials are a promising candidate for lithium-ion battery anodes because of their high capacity. However, their widespread application is hindered by poor electrical conductivity, and stability due to the volume expansion during cycling. Herein, electrodes comprised of spherical carbon-coated silicon oxide particles, interleaved between electrochemically exfoliated graphene, were prepared via molecular polymerization followed by physical mixing. The spherical silicon oxide was obtained by the carbonization of the reaction product between dialdehyde and (3-aminopropyl) trimethoxysilane. The interleaved graphene flakes both provided electrically conductive pathways between particles and formed a porous supporting structure between the silicon oxide particles and the graphene flakes, enabling a buffering for the volume expansion. A range of SiOx/C-G anodes are obtained by adjusting the content of graphene. The assembled batteries with an optimal graphene ratio (SiOx/C: G = 2:1 (w/w)) exhibit superior Li-ion storage behavior, including high cycle stability, with capacity retention of 88.6 % and high coulombic efficiency of 99 % after 250 cycles under 0.1 A·g−1. Promisingly, it was verified that with the support from the outer robust graphene layer and the porous support structure, the volume expansion of silicon oxide particles during lithiation/delithiation processes was suppressed, leading to a more stable solid electrolyte interface (SEI) layer.

Dual-silane coupling agents co-grafted on black particles for fast response and high contrast ratio electrophoretic display

As the Internet of Things (IoT) significantly improves people's lifestyles, flexible and low-power displays will become essential to real-time human-computer interaction. Electrophoretic display (EPD) has many advantages, such as low power consumption, flexibility, and high sunlight visibility, which is necessary for IoT terminal display. However, preparing electrophoretic particles with high charge and spatial resistance is difficult. Herein, dual-silane coupling agents, (3-Aminopropyl) trimethoxysilane (APS) and vinyltrimethoxysilane (VTS), were co-grafted on the black particles to optimize the electrophoretic particles' dispersity and charge. To evaluate the charge content and dispersity of particles, we measured the particles with zeta potential, dynamic light scattering, and long-term standing treatment. Fe3O4-APS0.5VTS0.5-PLMA, selected as the black particles for EPD, had an average particle size and zeta potential of 300 nm and 25 mV, respectively. Besides, the concentration of the black and white particle would significantly affect the EPD's performance. When optimizing the white and black particle concentration to 4:1, the contrast ratio of EPD was up to 13.2. In addition, the EPD has a response time of 200 ms and exhibits an invertible black and white state under ±15 V. Finally, to improve the stability of electrophoretic particles, the particles were encapsulated in microcups and driven to the black and white state under 30 V. This work demonstrated that dual-silane coupling agent particles have the potential to achieve the fast response and high contrast ratio EPD.

Removal of Hexamethyldisiloxane via a Novel Hydrophobic (3-Aminopropyl)Trimethoxysilane-Modified Activated Porous Carbon.

Volatile methyl siloxanes (VMS) must be removed because the formation of silica in the combustion process seriously affects the resource utilization of biogas. Herein, a series of APTMS ((3-aminopropyl)trimethoxysilane)-modified activated porous carbon (APC) adsorbents (named APTMS@APC) were prepared for VMS efficient removal. The as-prepared adsorbents were characterized using SEM, FTIR, Raman, X-ray diffraction analyses, and N2 adsorption/desorption. The results showed that the surface modification with APTMS enhanced the hydrophobicity of APC with the water contact angle increasing from 74.3° (hydrophilic) to 127.1° (hydrophobic), and meanwhile improved its texture properties with the SBET increasing from 981 to 1274 m2 g-1. The maximum breakthrough adsorption capacity of APTMS@APC for hexamethyldisiloxane (L2, model pollutant) was 360.1 mg g-1. Effects of an inlet L2 concentration (31.04-83.82 mg L-1) and a bed temperature (0-50 °C) on the removal of L2 were investigated. Meanwhile, after five adsorption-desorption cycles, the APTMS@APC demonstrated a superior cycling performance. This indicated that the hydrophobic APTMS@APC has a great significance to remove VMS.

Amine-grafted H-MFI zeolite precursors as acidic-basic catalysts for deacetalization-Knoevenagel condensation

Amorphous and semi-crystalline precursors of zeolites have a large number of silanols that can be used to anchor organic functionalities, like silane-based amines, resulting in formation of basic sites. This work describes the use of amorphous and semi-crystalline precursors of H-MFI zeolite reacting with aminopropyltrimethoxysilane (APTMS) to produce bifunctional acidic-basic catalysts for the deacetalization-Knoevenagel condensation. The effect of precursors crystallinity on the catalytic performance is explained by the formation of Brønsted acidic sites, which catalyze the deacetalization step, and on the propylamine anchoring capacity, controlled by the amount of external silanols present in the aluminosilicate. It is shown that the aluminosilicates with lower crystallinity provide a higher yield of the end product ethyl trans-α-cyanocinnamate due to the greater number of grafted propylamine groups. These results provide new insights into the preparation of acidic-basic catalysts for converting bulky molecules.

Amine-functionalized reduced graphene oxide-supported silver nanoparticles for superior catalytic reduction of organic pollutants.

In this work, a simple and environmentally friendly approach has been followed to synthesize amine-functionalized reduced graphene oxide (RGO)-supported silver nanoparticle (AgNPs) having superior catalytic efficiency towards the reduction of organic pollutants. RGO/AgNPs nanohybrid was synthesized by a one-pot hydrothermal reduction of silver nitrate in the presence of amino-propyl trimethoxy silane (APTMS)-functionalized graphene oxide (GO) nanosheets. The structural and morphological characterization of as-synthesized RGO/AgNPs nanohybrid was done by using XRD, SEM, TEM, FT-IR, and Raman spectroscopy techniques. APTMS plays an important role in controlling the size of anchored AgNPs on the nanohybrid in the present study. The -NH2 groups on the surface of APTMS-modified GO function as effective and well-organized nucleation centers facilitating uniform growth of discrete and smaller-sized spherical AgNPs on the surface of RGO nanosheets. In the absence of APTMS, the nanohybrid comprised of bigger-sized AgNPs with few hundred of nanometers in dimension. The catalytic efficiency of RGO/AgNPs nanohybrid was evaluated for the reduction of two model organic pollutants: 4-nitrophenol (4-NP) and methylene blue (MB). Due to the synergistic effects of RGO, APTMS, and Ag components, RGO/AgNPs nanohybrid developed in the present study exhibited superior catalytic activity towards the reduction of 4-NP and MB in comparison with previously reported graphene/graphene oxide/reduced graphene oxide-supported AgNPs catalysts. The catalytic reduction of 4-NP and MB followed pseudo-unimolecular kinetics and the rate constants were found to be 18.83 × 10-3 s-1 and 131.5 ×10-3 s-1 respectively for 4-NP and MB. Furthermore, RGO/AgNPs nanohybrid showed admirable recyclability with negligible loss in its activity until five recycle runs. The superior catalytic activity, favorable kinetic parameters, and sustained catalytic efficiency after recycling make RGO/AgNPs nanohybrid a promising catalyst for the reduction of organic pollutants in environmental remediation.