Synthesis of multifunctional additives for solid propellants:Structure,properties and mechanism

To simplify the composite propellant formulation and address the current issue of the single-functionality present in existing additives,the multi-cyano,amine-based polybutadiene(AEHTPB-CN)was prepared based on AEHTPB by adopting appropriate synthesis strategies.By replacing 10% of HTPB binder in the propellant formulation,it can effectively enhance the interfacial bond strength between the propellant binder matrix and solid fillers(AP(ammonium perchlorate)and RDX(cyclotrimethylene-trinitramine)),the mechanical properties of the HTPB/AP/RDX/Al propellant were superior to blank control propellant with an improvement of 35.4% in tensile strength,62.0% enhancement in elongation at break,and reduce the propellant burn rate by 10.7% with any energy loss.The function mechanism of AEHTPB-CN was systematically elucidated through experiments and computer simulation techniques.The results show that the tertiary amine group in AEHTPB-CN can react with AP to form ammonium ionic bonds,and the hydroxyl and cyano groups can form hydrogen bonding interactions with AP,which enables AEHTPB-CN to be firmly adsorbed on the AP surface through chemical and physical interactions.For RDX,the interfacial bonding effect of AEHTPB-CN is attributed to their ability to form C-H···N≡C weak hydrogen bonding interaction between the cyano group and RDX methylene group.

Modification of MgO·Al_2O_3 spinel inclusions in Al-killed steel by Ca-treatment

The modification of MgO·Al2O3 spinel inclusions in Al-killed steel by Ca-treatment has been studied by industrial trials and thermodynamic calculations.In the industrial trials,samples were taken systematically during the refining process in which the molten steel was treated by calcium,and the characters of the inclusions were analyzed using scanning electron microscopy （SEM） and energy dispersive spectra （EDS）.The effects of Ca-treatment were evaluated by tracking the compositions of the inclusions.The results show that the modification of MgO·Al2O3 spinel inclusions by Ca-treatment is effective and the transformation sequence of the inclusions during the refining is Al2O3 →MgO·Al2O3 →liquid complex inclusions.The modification of spinel inclusions by Ca-treatment was calculated by FactSage 6.0 utilizing its free-energy minimization routines.The results of thermodynamic calculations indicate that spinel inclusions are easier to be modified than Al2O3 inclusions and the spinel inclusions in 30CrMo steel would transform to liquid complex inclusions when the content of dissolved Ca in the molten steel exceeds 1×10-6.Also,the results show that adding more calcium into the molten steel would lower the contents of Al2O3 and MgO and increase the CaO content of the inclusions,while the change in SiO2 content is little.

CHEMICAL MODIFICATION OF THE SURFACE OF CALCIUM ALGINATE GEL BEADS

The chemical modification of the surface of calcium alginate gel beads (CAGB) via grafting copolymerization with vinyl acetate (VAc) was studied. The optimum reaction conditions with activation and graft copolymerization two steps were explored. First, 5 grams CAGB with 2.5 mm initial diameter was initiated with 0.0493 mol/L K2S2O8 at 51 °C for 30 min in 15 mL 1 % PVA/H2O. Then 4.34 moi/L VAc was added dropwise and the reaction was allowed to proce at 48 °C for 3 h. The grafting efficiency could come up to 30%. It was found the stability of modified CAGB in the air and in electrolyte solutions was greatly improved.

Chemical Modification and Fluorescence Spectrum of Tryptophan Residues in Pullulanase

Tryptophan（Trp） residues in a pullulanase were modified by N-bromosuccinimide（NBS）. The results of the Spande method indicate that there are 18 Trp residues in the pullulanase and nine of them are located on the surface af the enzyme. Three of these Trp residues are nonessential residues which show the fastest reaction rate according to the Zou＇s plot. Two of the seven relative faster reacting residues are essential for the activity of the enzyme. The other eight are the slowest in the reaction rate or non-reactive residues for the reaction. The fluorescence and circular dichroism（CD） spectra of the pullulanase have been changed after the reaction with NBS. Potassium iodide（KI） and acrylamide also have remarkable influences on the fluorescence spectra of the pullulanase.

Chemically Modified Ordered Mesoporous Carbon/Polyaniline Composites for Electrochemical Capacitors

Chemically modified ordered mesoporous carbon CMK-3 materials were prepared by means of an easy wet-oxidative method in 2 mol/L nitric acid aqueous solution. A large amount of oxygen-containing functional groups were introduced onto the CMK-3 surface. Modified CMK-3（m-CMK-3） and aniline monomer were polymerized via an in situ chemical oxidative polymerization method. Morphological characterizations of m-CMK-3/PANI （polyaniline） composites were carried out via field emission scanning electron microscopy（SEM）. Their electrochemical properties were investigated with cyclic voltammetry, galvanostatic charge-discharge, and electrochemical impedance spectroscopy. The m-CMK-3/PANI composites have excellent properties in capacitance, and the highest specific capacitance（SC） value was up to 489 F/g, suggesting their potential application in the electrode material for electrochemical capacitors.

Structural Characterization and Chemical Modification of a Glucan from Spores of Ganoderma lucidum

A linear alpha -D-(1-->3)-glucan, named PSG, was obtained from the spores of Ganoderma lucidum. The synthesis of positively and negatively charged polyelectrolytes from PSG was developed. Amine groups and carboxymethyl groups were introduced through nucleophilic substitution with 3-chloropropylamine or chloroacetic acid, respectively, Reaction conditions were varied to obtain insight into the influence of variables on the degree of substitution.

Dyeing of Polyester and Nylon with Semi-synthetic Azo Dye by Chemical Modification of Natural Source Areca Nut

Various azo compounds(Modified dyes)have been synthesised by chemical modification of areca nut extract(epicate-chin),a plant-based Polyphenolic compound to get semi-synthetic dyes.Three different primary amines namely p-nitro aniline,p-anisidine and aniline,were diazotized to form their corresponding diazonium salts which were further coupled with an areca nut extract.Preliminary characterization of the areca nut extract and the resultant azo compounds(Modified dyes)was carried out in terms of melting point,solubility tests,thin layer chromatography,UV-Visible and FTIR spectroscopy.These modified dyes were further applied on polyester and nylon fabrics and%dye exhaustion was evaluated.Dyed fabrics were further tested for their fastness properties such as wash fastness,rubbing fastness,light fastness and sublimation fastness.The results of the fastness tests indicate that,all the three modified dyes have good dyeability for polyester and nylon fabrics.The dyed fabrics were also tested for ultraviolet protection factor which showed very good ultraviolet protection.

Surface Chemical Modification of Cellulose Nanocrystals and Its Application in Biomaterials

Cellulose nanocrystals(CNCs) have been widely applied in biomaterials and show great biocompatibility and mechanical strength. In this review, the chemical reactions applied in CNC surface modification and their application in CNC based biomaterials are introduced. Furthermore, the conjugation of different functional molecules and nanostructures to the surface of CNCs are discussed, with focus on the binding modes, reaction conditions, and reaction mechanisms. With this introduction, we hope to provide a clear view of the strategies for surface modification of CNCs and their application in biomaterials, thus providing an overall picture of promising CNC-based biomaterials and their production.

Chemical Modifications of Layered Double Hydroxides in the Supercapacitor

Layered double hydroxides are one class or kind of 2 D layered materials that are considered promising for use in the supercapacitor.Although there have been many studies on the structure,composition,properties,and electrode fabrication of layered double hydroxides,none summarize the effects of various modification methods on the structure and performance of layered double hydroxides in the supercapacitor.In a bid to fill this gap,in this review,we summarize the progress of modification methods such as exfoliation,intercalation,vacancy,doping,phase transformation,and composition regulation of layered double hydroxides in the field of the supercapacitor and put forward some opinions regarding the progress of research on the methods used in modifying the layered double hydroxides.

Initial Activation of Hydrogen-Storage Alloy Electrode by Chemical Modification

The hydrogen storage alloy electrode of Mm(NiCoMnAl) 5 was activated by etching the alloy in a hot concentrated KOH solution. The electrochemical measurement demonstrates that the modified alloy electrode can reach its stable capacity at the first charge/discharge cycle and also shows low overpotential, indicating full activation of the etched alloy material. It was found from ICP, SEM and EDAX analyses that the activation process leads to surface modification by reconstructing of a new electroactive surface.

Modification of Cellulose by Hydrophobic Long-chain Molecules: Advances and Prospects

Cellulose,a natural polymer material with abundant natural sources,is non-toxic,renewable,and biodegradable,making it one of the most promising green materials.Its inherent hydrophilicity dramatically limits the development and application of cellulose products.Hydrophobic modification can significantly change cellulose properties and endow it with additional functions depending on the types of modifying molecules.Controlled modification of cellulose by long-chain hydrophobic molecules is challenging.Significant advances took advantage of new reaction systems and copolymerization.This paper reviews recent innovations in long-chain cellulose hydrophobic modification.A brief value-adding assessment provides a reference for green changes of cellulose to make it fit for future applications.

The Construct of A Neutral Medium Applicable Electrochemiluminescent Sensor Based on the Chemical Modification of Cysteine and Luminol

In the phosphate buffer solution of pH＞7,the cysteine sensitized the electrochemiluminescence (ECL) of luminol.It could be modified on the surface of platinum electrode and furthermore adsorbing the luminol on its exterior to construct an ECL sensor.The ECL intensity of this sensor was strong enough and very stable.There wasn't obvious decrease of ECL intensity for thirty times of using in 48 hours with the relative standard deviation (RSD) of 0.98%.It could be used to determine some quenching effective molecules such as superoxide dismutase (SOD) with negative response upon the concentration range from 4.8 IU/ml to 57.6 IU/ml.

Rapid Selection of Phage Se-scFv with GPX Activity via Combination of Phage Display Antibody Library with Chemical Modification

Glutathione peroxidase（GPX） plays an important role in scavenging reactive oxygen species. A series of catalytic antibodies with GPX activity have been generated by the authors of＇ this study. To obtain humanized catalytic antibodies, the phage-displayed human antibody library was used to select novel antibodies by repetitive screening, Phage antibodies, scFv-B8 and scFv-H6 with the GSH-binding site, were obtained from the library by enzyme-linked immu- nosorbent assay（ELISA） analysis with 4 rounds of scelection against their respective haptens, S-2,4-dinitriphenyl t-butyl ester（GStI-s-DNP-Bu） and S-2,4-dinit,-iphenyl t-hexyl ester（GSH-s-I）NP-He）. Nevertheless, several studies need to be condueted to determine whether scFv-B8 and seFv-tI6 possess GPX activity. 1＇o enhance the speed of the selection, selenocysteine（Sec, the catalytic group of GPX） was incorporated directly into the phages, scFv-B8 and seFv-H6, by chemical mutation to form the phages Se-scFv-B8 and Se-scFv-H6. The GPX activities were found to be 3012 units/μmol and 2102 units/μmol, respectively. To improve the GPX activity of the phage Se-scFv-B8, DNA shuffling was used to construct a secondary library and another positive phage antibody scFv-B9 was screened out by another panning against GSH-s-DNP-Bu. When Sec was incorporated via chemical mutation into the phage antibody scFv-B9, its GPX activity reached 3560 units/μmol, which is 1.17-fold higher than the phage antibody Se-scFv-B8 and almost approached the order of magnitude of native GPX. The rapid selection is the prerequisite for generating humanized Se-seFv with GPX activity.

Chemical modification of silicene

Silicene is a two-dimensional(2D) material, which is composed of a single layer of silicon atoms with sp2–sp3mixed hybridization. The sp2–sp3mixed hybridization renders silicene excellent reactive ability, facilitating the chemical modification of silicene. It has been demonstrated that chemical modification effectively enables the tuning of the properties of silicene. We now review all kinds of chemical modification methods for silicene, including hydrogenation, halogenation,organic surface modification, oxidation, doping and formation of 2D hybrids. The effects of these chemical modification methods on the geometrical, electronic, optical, and magnetic properties of silicene are discussed. The potential applications of chemically modified silicene in a variety of fields such as electronics, optoelectronics, and magnetoelectronics are introduced. We finally envision future work on the chemical modification of silicene for further advancing the development of silicene.

Chemical Modification of Amino Acid Residues in Human Plasminogen

The chemical modification of human plasminogen(HPg) was studied with 1-ethyl-3-(3- dimethyl aminopropyl) carbodiimide(EDC), N -acetylimidazole(NAI), 1,2-cyclohexanedione(CHD), chloramine T(Ch-T) and N -bromosuccinimide(NBS) as modifying reagents at its carboxyl group, tyrosine, arginine, methionine and tryptophan residues, respectively. The results indicate that tyrosine and arginine residues are not essential for HPg activity, while carboxyl groups, methionine and tryptophan residues are important for the activity of HPg. The Keech and Farrant′s kinetic analysis reveals that one tryptophan residue, one methionine residue and two carboxyl groups are essential for HPg activity.

A Novel β-1,4-N, 6-O-Diacetylmuramidase from Streptomyces griseus and its Chemical Modification

A novel lysozyme named β-1, 4-N, 6-O-diacetylmuramidase R2 was purified and characterized from Streptomyces griseus. The molecular weight of the enzyme was determined by MALDI-TOF-MS as 23.5 kDa. The N-terminal amino acid sequence was DTSGVQGIDVSHWQG. Chemical modification of β-1, 4-N, 6-O-diacetylmuramidase R2 indicated that sulfhydryl group and carbamidine of arginine residues are not essential for the activity of the enzyme, but lysine residues and imidazole of histidine residues are essential for the activity. The number of essential tryptophan and carboxyl groups was found that only one tryptophan residue and three carboxyl groups in the active site.

UV Spectral Analysis of the Chemical Modification and Photolysis of Acetylacetone Modified Alumina Aqueous Solution

Acetylacetone was firstly introduced into the aqueous media with the presence of aluminum sec-butoxide and pep-tizator. It was confirmed that the UV (ultraviolet) absorption band of acetylacetone underwent 14 nm of red-shift due to the formation of the six-membered ring of the complex between alumina and acetylacetone in the aqueous solution. It was also found that the chemical modification can be dissociated by the UV irradiation with a wavelength shorter than 286 nm as a result of the excitation of π-π* transition in the complex.

Improving the fatigue endurance of lead zirconate titanate thin films through PbO interfacial modification

The effects of the modification of electrode/ceramic interfaces through a chemical solution deposition-derived PbO buffer layer on the fatigue endurance of lead zirconate titanate（PZT） thin films were investigated.The grain size and the surface roughness of the PZT films increased through PbO interfacial modification.Moreover,the PZT films with PbO interfacial modification had a better crystallographic structure and no evident secondary phases were observed.While the remanent polarization and dielectric constant were reduced,the fatigue endurance was improved.Based on the results,the mechanism for the fatigue endurance improvement was discussed.

Site-directed Chemical Modification of Recombinant Human aFGF Mutant with Polyethylene Glycol

A new product PEGylated rhaFGF was obtained by site-directed chemical modification.When compared with unmodified rhaFGF, PEGylated rhaFGF showed comparable bioactivity and superior stability at 37℃ in mouse serum and the stronger resistant potency to trypsin. This was accompanied by a substantial decreasing tmmunogenicity.Site-specific PEGylation of rhaFGF may increase its therapeutic potency in humans.

Chemical Modification of Tryptophan Residues in Superoxide Dismutase from Camellia Pollen and Its Fluorescence Spectrum

The amino acid composition of the superoxide dismutase（SOD） from camellia pollen was measured and the tryptophan（Trp） residues were modified by using N-bromosuccinimide（NBS）. The results show that there are 21 Trp residues in an SOD molecule and seven of which are located on the surface of the enzyme. By researching the fluorescence spectra of the native SOD and the modified SOD, we have found that the emission wavelength of Trp is at 335 nm and the fluorescence intensity will decrease when the enzyme is modified. The results also show that potassium iodide（KI） can significantly quench the fluorescence of the native SOD, but it has a less pronounced effect on the modified enzyme. Glycerin as a surface activation reagent can stabilize the fluorescence of the modified enzyme.