7 results about "Enhanced selectivity" patented technology

Disclosed herein is a method for converting ethanol to 1,3-butadiene, wherein the method utilizes H2 produced during a first step of the method for subsequent conversions involved in the method. In particular aspects, H2 produced from converting ethanol to acetaldehyde is used to promote the conversion of the acetaldehyde to 1,3-butadiene. The H2 promotes enhanced catalyst stability, as well as enhanced selectivity and yields of the 1,3-butadiene product. In particular aspects, the method comprises two steps to produce the 1,3-butadiene from the ethanol and H2 produced from a first step facilitates enhanced selectivities and yields for the second step.

The present disclosure relates to a gas sensing method with enhanced selectivity. Specifically, the present disclosure relates to a gas sensing method for more accurately distinguishing various types of gases through a process of analyzing a correlation of two or more kinetic or static parameters from a temperature-dependent resistance change of a gas sensor according to two or more temperature conditions by changing the temperature of a captured external gas via a temperature control device.

Provided are proteins that bind rare earth metals. The proteins may have enhanced REE / REE selectivity. The proteins may have four EF hand motifs each having 11, 12, or 13 amino acids residues. Each EF hand motif is separated by 12 or 13 amino acid residues, where each amino acid residue is any canonical amino acid residue and at least one amino acid residue is a hydrophobic amino acid residue. When the EF hand motif has 12 amino acid residues, the motif may have the following sequence: X1-X2-X3-X4-X5-X6-X7-X8-X9-X10-X11-E. Also provided are devices and kits comprising a protein of the present disclosure. Also provided are methods of using the proteins and devices.

The application discloses a kind of twin ZSM-5 molecular sieve and synthesis method thereof, belong to inorganic chemistry technical field.The twin ZSM-5 molecular sieve is covered by the (010) crystal surface of one coffin-shaped ZSM-5 to the (100) crystal surface of another coffin-shaped ZSM-5, so that the molecular sieve surface has higher straight channel exposure ratio.Preparation process includes: (i) water, sodium hydroxide, aluminum source, template agent, silicon source are mixed and stirred to obtain synthesis gel A;(ii) three kinds of molecular sieves MCM-35, MOR, MCM-22 are added to alkaline environment according to the ratio of 1:2:4, and alkaline heat treatment is carried out to obtain mixture B containing "mfi, mor, mel" three kinds of structural units;(iii) A, B are mixed according to the water content of 1:1, and ZSM-5 molecular sieve product is obtained by hydrothermal crystallization.For the "primary aromatic hydrocarbon mixture" obtained after benzene, toluene, p-xylene are separated from the aromatic hydrocarbon mixture obtained by petroleum and non-petroleum route, twin ZSM-5 molecular sieve shows enhanced selectivity to o-xylene and m-xylene due to higher "straight channel exposure ratio" on the surface.

The use of selective deposition of silicon nitride can eliminate conventional patterning steps by allowing silicon nitride to be deposited only in selected and desired areas. Using a silicon iodide precursor alternately with a thermal nitrogen source in an ALD or pulsed CVD mode, silicon nitride can be deposited preferentially on a surface such as silicon nitride, silicon dioxide, germanium oxide, SiCO, SiOF, silicon carbide, silicon oxynitride, and low k substrates, while exhibiting very little deposition on exposed surfaces such as titanium nitride, tantalum nitride, aluminum nitride, hafnium oxide, zirconium oxide, aluminum oxide, titanium oxide, tantalum oxide, niobium oxide, lanthanum oxide, yttrium oxide, magnesium oxide, calcium oxide, and strontium oxide.

This application relates to site-specific conjugation of antibody lysine residues using solid phase immobilized microbial transglutaminase MTG and MTG in solution. Site-specific modification of proteins using microbial transglutaminase (MTG) is a powerful and versatile strategy for controlled modification of proteins under physiological conditions. We present evidence that solid phase microbead immobilization can be used to site-specifically and efficiently link different functional molecules important for further downstream applications to therapeutically relevant proteins, including scFV, Fab fragments and antibodies. We demonstrate that MTG remains firmly immobilized and there is no detectable column bleed and the enzyme activity is maintained during continuous operation, which allows for convenient recycling of the enzyme, thus outperforming solution phase MTG conjugation. Furthermore, it is shown that immobilized MTG exhibits an enhanced selectivity for certain residues in the presence of several reactive residues, all of which are targeted if conjugation is performed in solution. Site-specific lysine conjugation of antibodies using immobilized and solution MTG with a highly efficient glutamine-containing peptide is also reported. In addition, the generation of bis-site-specific conjugated IgGl with site-specific conjugation of both glutamine and lysine residues of an IgGl antibody using immobilized and solution MTG is reported. Site-specific glutamine conjugation with small peptides containing lysine residues and functional moieties is also described.

This provides a catalyst system and corresponding method for a single-stage conversion of syngas into fuel boiling range products, which is effective for naphtha production (C5-C9) or distillate production (C6-C9). 10 -C 20 It exhibits enhanced selectivity. This enhanced selectivity for naphtha production or distillate production is related to the increased selectivity for higher boiling range components (C...). 21+ The reduced selectivity is provided together with the )