A handheld-type total integrated capillary electrophoresis system for SARS-CoV-2 diagnostics: Power, fluorescence detection, and data analysis by smartphone.

A micro-capillary electrophoresis (μCE) system is one of the widely adopted techniques in the molecular diagnostics and DNA sequencing due to the benefits of high resolution, rapid analysis, and low reagent consumption, but due to the requirements of bulky high-power suppliers and an expensive laser-induced fluorescence detector module, the conventional set-up of μCE system is not adequate for point-of-care (POC) molecular diagnostics. In this study, we constructed a miniaturized and integrated μCE system which can be manipulated by a smartphone. The smartphone not only powers two boost converters and an excited laser, but also controls the relay for the power switch.

Immobilization of Ni Complex on Amine-Grafted SiO₂ for Ethylene Polymerization.

The results on the In-Situ synthesis of Ni complex on amine-grafted SiO2 and its ethylene polymerization were explained. SiO2/2NS/(DME)NiBr2 and SiO2/3NS/(DME)NiBr2(Ni(II) bromide ethylene glycol dimethyl ether) catalysts were active for ethylene polymerization. The highest activity was shown at the polymerization temperature of 25 °C, and SiO2/2NS/(DME)NiBr2 exhibited higher activity than SiO2/3NS/(DME)NiBr2.

Epoxide-functionalization of polyethyleneimine for synthesis of stable carbon dioxide adsorbent in temperature swing adsorption.

Amine-containing adsorbents have been extensively investigated for post-combustion carbon dioxide capture due to their ability to chemisorb low-concentration carbon dioxide from a wet flue gas. However, earlier studies have focused primarily on the carbon dioxide uptake of adsorbents, and have not demonstrated effective adsorbent regeneration and long-term stability under such conditions. Here, we report the versatile and scalable synthesis of a functionalized-polyethyleneimine (PEI)/silica adsorbent which simultaneously exhibits a large working capacity (2.

L-Lactide Ring-Opening Polymerization with Tris(acetylacetonate)Titanium(IV) for Renewable Material.

A new Ti-type of catalyst for L-lactide polymerization was synthesized by reaction of titanium(IV) isopropoxide (TTIP) with acetylacetone (AA). Moreover, PLA was prepared by the bulk ring-opening polymerization using synthesized Ti catalyst. Polymerization behaviors were examined depending on monomer/catalyst molar ratio, polymerization temperature and time.

Construction of late transition metal complex on amine-functionalized SiO2 and SBA-15 for L-lactide polymerization.

We report the in-situ synthesis of a late transition metal catalyst on amine-functionalized SBA-15 and amorphous silica and their ring opening polymerizations of L-lactide. Funtionalizations of SBA-15 and amorphous silica with N-[3-(trimethoxysilyl)propyl]-ethylenediamine (2NS) were carried out to in-situ synthesize late transition metal catalysts on the surface of nanoporous materials. FT-IR spectra indicates that the 1,2-dimethoxyethane ligand did not participate in the reaction when (DME)NiBr2 was immobilized on the amine-functionalized silica.

Preparation of single-site catalyst inside the functionalized nanopore of silica and its ethylene polymerization.

Amorphous silica have been functionalized with organo-silane, and (n-BuCp)2ZrCI2 and methylaluminoxane (MAO) were subsequently immobilized on the functionalized silica for the further evaluation as a catalyst of ethylene polymerization. Four organo-silanes such as 3-aminopropyltrimethoxysilane (1NS), N-[(3-trimethoxysilyl)propyl]ethylenediamine (2NS), N1-[3-(trimethoxysilyl)propyl]diethylenetriamine (3NS), and 4-(triethoxysilyl)butyronitrile (1NCy), were employed for this study. The Zr content and polymerization activity of the supported catalysts were strongly dependent on the kind and structure of organo-silane.

A selective functionalized mesoporous silica-supported Rh catalyst for effective 1-octene hydroformylation.

Through different functionalization methods, three kinds of Rh-immobilized mesoporous silicas have successfully been prepared to investigate catalytic behavior, including yield and the linear/branched ratio of aldehyde (L/B) in 1-octene hydroformylation. A conventional post grafting method and two kinds of selective bifunctionalized methods for modification of the mesoporous silica have been applied for this purpose. A relatively high L/B (> 2.

Synthesis, X-ray structures, and controlled ring opening polymerization behavior of L-lactide using titanium complexes chelated by tetradentate diamine-diethanolate ligand.

The synthesis and characterization of LTi(O-i-Pr)(2) (1) and LTiCl(2) (2) complexes containing a new [ONNO]-type tetradentate diamine-diethanolate ligand such as (HOCMe(2)CH(2)NMeCH(2)CH(2)NMeCH(2)CMe(2)OH) (LH(2)) was achieved. Single-crystal X-ray analyses revealed that monomeric complexes 1 and 2 had pseudo-C(2) and pseudo-C(1) symmetric distorted octahedral geometry, respectively. Interestingly, complex 1 has fac-fac geometry for tetradentate L around a Ti centre in both solid and solution, whereas complex 2 has different geometry in solid (mer-fac, C(1)) and solution (fac-fac, C(2)).

Catalytic pyrolysis of oilsand bitumen over nanoporous catalysts.

The catalytic cracking of oilsand bitumen was performed over nanoporous materials at atmospheric conditions. The yield of gas increased with application of nanoporous catalysts, with the catalytic conversion to gas highest for Meso-MFI. The cracking activity seemed to correlate with pore size rather than weak acidity or surface area.

Synthesis of functionalized mesoporous material with various organo-silanes.

Two kinds of ordered mesoporous silicas, SBA-15 and MSU-H, have been synthesized and functionalized by direct and post synthesis method to widen their various application possibilities. In this study, phenyltrimethoxysilane (PTMS), methacryloxy-methyltrimethoxysilane (MAMTMS), 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (ECETMS), and N(beta-aminoethyl)-gamma-aminopropylmethyldimethoxysilane (AEAPMDMS) were used as a silane precursor for the functionalization. The post synthesis was more effective method to sustain ordered pore structure than the direct synthesis method under our experimental conditions.

Influence of nanopores of MCM-41 and SBA-15 confining (n-BuCp)2ZrCl2 on copolymerization of ethylene-alpha-olefin.

The effect of nanopore in mesoporous materials confining (n-BuCp),ZrCl2 and methylaluminoxane (MAO) on ethylene-1-hexene and ethylene-1-octene copolymerization was investigated on the basis of the copolymerization results, and the analysis of the supported catalyst and the copolymers. SBA-15 and MCM-41 together with amorphous silica were employed as supports, which are capable of confining (n-BuCp)2ZrCl2 and MAO in the nanopore. The copolymerization activities of MCM-41-supported (n-BuCp)2ZrCl2 were higher than those of SBA-15 and SiO2 although that its Zr content was quite lower than those of SBA-15 and SiO2.

The preparation and low-k application of asymmetric functionalized cyclodextrin templated nanoporous silsesquioxane films.

Several kinds of Asymmetric Functionalized Cyclodextrin (AFCD), as a porogen, have been introduced for the first time to investigate their potential in the field of low-k applications. The novel AFCD templated films were compared in terms of their pore forming efficiency and the pore structure, such as pore size and pore size distribution. Of the AFCDs, btCD and tbsCD showed fairly good pore forming efficiencies.

Catalytic decomposition of 1,2-dichlorobenzene using Pt-loaded nanoporous zeolite MFI catalyst.

Nanoporous zeolite MFI was prepared by using HClO4 as a promoter. A significant proportion of the synthesized zeolite MFI nanoparticles exhibited nanoporous characteristics. Although the synthesis of the zeolite MFI was completed within 6 h, the crystallinity of all the zeolite MFI was shown to be high.