Salt intake knowledge, attitude and behaviour in a rural population of Bangladesh

Abstract not available Bangabandhu Sheikh Mujib Medical University Journal 2023;16(2): 124-12

Kenaf cellulose-based poly(amidoxime) ligand for adsorption of rare earth ions

A well-known adsorbent, poly(amidoxime) ligand, was prepared from polyacrylonitrile (PAN) grafted kenaf cellulose, and subsequent characterization was performed by Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FESEM) and inductively coupled plasma mass spectrometry (ICP-MS). The adsorption capacities of the prepared ligand for rare earth metals are found to be excellent, with adsorptions of La 3+ , Ce 3+ , Pr 3+ , Gd 3+ and Nd 3+ experimentally determined to be 262, 255, 244, 241 and 233 mg·g −1 , respectively, at pH 6. The experimental values of the adsorption of rare earth metals are well matched with the pseudo-second-order rate equation. The reusability of the adsorbent is examined for seven cycles of sorption/desorption, demonstrating that the proposed adsorbent could be reused for over seven cycles without any significant loss in the original removal capability of the ligand

Applications of bio-resource based sustainable heterogeneous Pd-Nanocatalyst for Cross-Coupling and Michael addition reactions

The development of efficient and cost-effective catalysts from renewable sources is crucial for sustainable chemistry. Herein, we developed a bio-heterogeneous Pd-nanocatalyst (PdNc@PA) by incorporating palladium nanoparticles into biodegradable kenaf-cellulose modified with poly(amidoxime) ligands. The catalyst has demonstrated remarkable stability and exceptional catalytic performance in a range of cross-coupling including Mizoroki-Heck, Suzuki-Miyaura, and Tamejiro-Hiyama reactions of inactivated aryl chlorides resulting in high yields of the desired coupling products. Additionally, PdNc@PA was also found to be effective in Michael addition reactions producing N, S, O-alkylated products in high yields. Furthermore, the PdNc@PA catalyst demonstrated robustness and recoverability allowing it to be reused across successive cycles without significant loss of catalytic activity. The incorporation of renewable resources in catalyst development offers an environmentally conscious alternative to traditional synthetic approaches. This research highlights the potential of utilizing biodegradable materials as catalyst supports, which could significantly diminish environmental impact and waste production. Moreover, this study demonstrates the versatility of PdNc@PA as a proficient and reusable catalyst for a diverse array of organic reactions. These discoveries provide an encouraging pathway towards the development of sustainable and economically viable catalysts suitable for industrial applications

Bio-waste corn–cob cellulose supported poly (amidoxime) palladium nanoparticles for Suzuki-Miyaura cross-coupling reactions

Waste corn-cob cellulose supported poly(amidoxime) palladium nanoparticles (PdNs@PA) were prepared by the surface modification of waste corn-cob cellulose through graft co-polymerization and subsequent amidoximation. The supported nanoperticles showed high catalytic activity (45-400 mol ppm) towards Suzuki-Miyaura cross-coupling of aryl bromides/chlorides with organoboronic acids to give the corresponding biaryl products up to 99 % yield with high turnover number (TON) 19777 and turnover frequency (TOF) 4944 h−1. The PdNs@PA was easily recovered from the reaction mixture and reused several times without significant loss of its catalytic activity

Synthesis of poly(hydroxamic acid) ligand from polymer grafted corn-cob cellulose for transition metals extraction

Poly(hydroxamic acid) ligand was synthesized using ester functionalities of cellulose-graft-poly(methyl acrylate) copolymer, and products are characterized by Fourier transform infrared spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, and X-ray photoelectron spectroscopy analysis. The poly(hydroxamic acid) ligand was utilized for the sensing and removal of transition metal ions form aqueous solutions. The solution pH is found a key factor for the optical detection of metal ions, and the reflectance spectra of the [Cu-ligand]n+ complex were observed to be the highest absorbance 99.5% at pH?6. With the increase of Cu2+ ion concentration, the reflectance spectra were increased, and a broad peak at 705?nm indicated that the charge transfer (p-p transition) complex was formed. The adsorption capacity with copper was found to be superior, 320?mg?g-1, and adsorption capacities for other transition metal ions were also found to be good such as Fe3+, Mn2+, Co3+, Cr3+, Ni2+, and Zn2+ were 255, 260, 300, 280, 233, and 223?mg?g-1, respectively, at pH?6. The experimental data show that all metal ions fitted well with the pseudo-second-order rate equation. The sorption results of the transition metal ions onto ligand were well fitted with Langmuir isotherm model (R2?>?0.98), which implies the homogenous and monolayer character of poly(hydroxamic acid) ligand surface. Eleven cycles sorption/desorption process were applied to verify the reusability of this adsorbent. The investigation of sorption and extraction efficiency in each cycle indicated that this new type of adsorbent can be recycled in many cycles with no significant loss in its original detection and removal capability

Highly active kenaf bio-cellulose based poly (hydroxamic acid) copper catalyst for Aza-Michael addition and click reactions

Bio-heterogeneous kenaf cellulose supported poly(hydroxamic acid) Cu(II) complex and corresponding copper nanoparticles (CuN@PHA) were synthesized and characterized. Cellulose supported poly(hydroxamic acid) copper nanoparticles was successfully applied to the Aza-Michael addition reaction of amines with α,β-unsaturated carbonyl/cyano compounds and poly(hydroxamic acid) Cu(II) complex was applied to the Click reactions of organic azides with alkynes in presence of sodium ascorbate as highly active catalysts under mild reaction conditions. The copper nanoparticles (50 mol ppm) selectively boosted Aza-Michael addition reaction to give the corresponding alkylated products in up to 96 % yield, whereas poly(hydroxamic acid) Cu(II) complex (0.25 mol%) efficiently promoted Click reaction to give the corresponding 1,2,3-triazoles in up to 94 % yields. Excellent reusability of the supported copper catalysts were found with no significant loss of catalytic activity for several cycles having high turnover number (TON) 18000 and turnover frequency (TOF) 3000 h−1 in the Aza-Michael addition reaction

Poly(amidoxime) ligand derived from waste palm fiber for the removal of heavy metals from electroplating wastewater

A waste material known as palm oil empty fruit bunch (EFB) is used as a source of cellulose for the development of polymeric materials for the removal of metal ions from industrial wastewater. A poly(acrylonitrile)-grafted palm cellulose copolymer was synthesized by a conventional free radical initiating process followed by synthesis of a poly(amidoxime) ligand by oximation reaction. The resulting products were characterized by FT-IR, FE-SEM, EDX, TGA, DSC, and XPS. The poly(amidoxime) ligand was used to coordinate with and extract a series of transition metal ions from water samples. The binding capacity (qe) of the ligand with the metal ions such as copper, iron, cobalt, nickel, and lead were 260, 210, 168, 172, and 272 mg g−1 , respectively at pH 6. The adsorption process followed the pseudo-first-order kinetic model (R2 > 0.99) and as well as the Freundlich isotherm model (R2 > 0.99) indicating the occurrence of a multi-layer adsorption process in the amidoxime ligand adsorbent. Results from reusability studies show that the ligand can be recycled for at least 10 cycles without any significant losses to its initial adsorption capacity. The synthesized polymeric ligand was shown to absorb heavy metals from electroplating wastewater with up to 95% efficiency

Silica-coated magnetic palladium nanocatalyst for Suzuki-Miyaura cross-coupling

A silica-coated magnetically separable Schiff-base palladium nanocatalyst was developed. Amorphous silica was used to encapsulate the magnetic Fe3O4 and an organic amine functionality was added to the silica surface. The amino group was treated with 1, 10- phenanthroline-2,9-dicarboxaldehyde to produce a Schiff-base, which was then treated with palladium to produce the silica coated magnetic Schiff-base palladium nanocatalyst. The palladium nanocatalyst was fully characterized using several spectroscopic techniques. The HR-SEM image of silica coated Fe3O4 revealed a globular shape with a diameter of 145 nm, along with this the average palladium nanoparticle size was 3.5 ± 0.6 nm. The successful functionalization and the appearances of the palladium species as a magnetic catalyst was confirmed by FT-IR and XRD analysis. The palladium nanocatalyst was successfully applied for the construction of CAC bonds via Suzuki- Miyaura reaction. With a variety of organoboronic acids, the catalyst displayed great performance for electron-poor and electron-rich aryl halides, resulting in excellent yields of the corresponding cross-coupling products. The magnetic catalyst was retrieved from the reaction vial using an external strong magnet, and it was reused seven times without a significant drop in the production of the corresponding biaryl product