Preparation of partially end-capped amino-terminated hyperbranched polymer and dyeing properties enhancement to polyurethane membrane

2017 ◽  
Vol 88 (20) ◽  
pp. 2319-2328
Author(s):  
Longfang Ren ◽  
Jin Geng ◽  
Na Wang ◽  
Zidong Guo
Keyword(s):  
Water Solubility ◽  
Raw Materials ◽  
Mass Ratio ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Hydrogen Bond Interaction ◽  
Dyeing Properties ◽  
X Ray ◽  
Blend Membranes ◽  
Polyurethane Membrane

In this study, a series of products with different water solubility, which were named as partial end-capped amino-terminated hyperbranched polymers (HBPs) 1–6, were obtained by changing the mass ratio of raw materials. The structure was characterized by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). The polyurethane was respectively mixed with partial end-capped amino-terminated HBPs to prepare different blend membranes by the drying method. The results showed that the water solubility of partial end-capped amino-terminated HBPs had obvious effects on the dyeing properties of blend membranes. When the mass ratio of amino-terminated HBP and single-blocked isophorone diisocyanate was 3:2, the performance of prepared partial end-capped amino-terminated HBP 4 was the best. The structures of blend membranes were characterized by FTIR spectroscopy, X-ray diffraction and scanning electron microscopy (SEM). When the mass fraction of partial end-capped amino-terminated HBP 4 was 2%, dye uptake improved from 12% to 85%. The dry-rub fastness and wet-rub fastness reached 4.5 and 3, respectively. The K/S values indicated that the surface chroma also deepened. The results indicated that partial end-capped amino-terminated HBP and polyurethane had hydrogen-bond interaction and certain phase separation.

Preparation, Characterization and Hemostatic Properties of Chitosan Caffeates

2019 ◽  
Vol 814 ◽  
pp. 365-371
Author(s):  
Si Tong Lu ◽  
Dong Ying Zhang ◽  
Zhang Hu ◽  
Si Dong Li ◽  
Pu Wang Li
Keyword(s):  
Caffeic Acid ◽  
Freeze Drying ◽  
Water Solubility ◽  
Crystal Form ◽  
Positive Control ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Yunnan Baiyao ◽  
Better Than

In this paper, chitosan and caffeic acid were used as starting materials to prepare chitosan caffeates by reflux-heating and freeze-drying. The structures of chitosan caffeates were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and potentiometric titration. At the same time, the physical properties of chitosan caffeates were tested and the hemostatic properties were evaluated. The results showed that four chitosan caffeates with different mass ratios of chitosan and caffeic acid (1:1, 1:2, 1:4, 1:6) had been successfully prepared, which enhanced the water solubility. FTIR analysis demonstrated that caffeic acid had been successfully grafted onto chitosan chains. XRD showed that the crystal form of chitosan changed to some extent and the chain had some regularity in some directions, but its crystallinity reduced. Chitosan caffeates, particularly mass ratio of 1:1, showed excellent hemostatic properties and even better than chitosan and the positive control (Yunnan Baiyao), which were expected to be developed as an effective biomaterial for hemostasis.

Preparation of A14SiC4 by Solid-State Reaction

2011 ◽  
Vol 399-401 ◽  
pp. 817-821
Author(s):  
Xiao Hong Liu ◽  
Hui Wang ◽  
Ling Ke Zeng ◽  
Cheng Ji Deng
Keyword(s):  
Carbon Black ◽  
Raw Materials ◽  
Heating Temperature ◽  
Argon Atmosphere ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Higher Temperature ◽  
Flake Structure ◽  
Scanning Electron

In this paper, A14SiC4 was synthesized by using flint, aluminum and carbon black as raw materials，and they mass ratio was 28:50:22. The samples were fired at 1500°C、1600°C and 1700°C in an argon atmosphere. The phase compositions were determined by X-ray diffraction (XRD), the microstructures were examined by scanning electron microscope (SEM) and the elemental and quantitative compositions were determined by the energy dispersive X-ray spectroscopy (EDX). The results showed that the flint reacted with the carbon black, and produced Al2O3 and SiC firstly; meanwhile Al4C3 as intermediate product formed by the reaction between Al and C. Then a certain Al4C3 reacted with SiC, and produced A14SiC4; most Al4C3 reacted with the Al2O3, and produced Al4O4C at higher temperature. Subsequently, the Al4O4C and the SiC reacted with carbon black, and produced A14SiC4. The formed quantity of A14SiC4 increased as the heating temperature was raised, and crystal structure was the flake structure of 1-2μm thickness and about 10μm length. The formation mechanism of A14SiC4 was also discussed.

scholarly journals Nano-CL-20/HMX Cocrystal Explosive for Significantly Reduced Mechanical Sensitivity

2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Chongwei An ◽  
Hequn Li ◽  
Baoyun Ye ◽  
Jingyu Wang
Keyword(s):  
Spray Drying ◽  
Raw Materials ◽  
Drop Height ◽  
Drying Method ◽  
X Ray Diffraction ◽  
Mechanical Sensitivity ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Friction Sensitivity ◽  
Scanning Electron

Spray drying method was used to prepare cocrystals of hexanitrohexaazaisowurtzitane (CL-20) and cyclotetramethylene tetranitramine (HMX). Raw materials and cocrystals were characterized using scanning electron microscopy, X-ray diffraction, differential scanning calorimetry, Raman spectroscopy, and Fourier transform infrared spectroscopy. Impact and friction sensitivity of cocrystals were tested and analyzed. Results show that, after preparation by spray drying method, microparticles were spherical in shape and 0.5–5 µm in size. Particles formed aggregates of numerous tiny plate-like cocrystals, whereas CL-20/HMX cocrystals had thicknesses of below 100 nm. Cocrystals were formed by C–H⋯O bonding between –NO2 (CL-20) and –CH2– (HMX). Nanococrystal explosives exhibited drop height of 47.3 cm, and friction demonstrated explosion probability of 64%. Compared with raw HMX, cocrystals displayed significantly reduced mechanical sensitivity.

Synthesis of Ba2B5O9Cl Whiskers via Flux Method

2012 ◽  
Vol 535-537 ◽  
pp. 2567-2570
Author(s):  
Dong Hai Zhu ◽  
Xue Ying Nai ◽  
Qian Qian Song ◽  
Shan Yun ◽  
Yong Xing Zhang ◽  
...  
Keyword(s):  
Sintering Temperature ◽  
Raw Materials ◽  
Mass Ratio ◽  
Optimum Conditions ◽  
X Ray Diffraction ◽  
Flux Method ◽  
High Quality ◽  
X Ray ◽  
Scanning Electron Microcopy ◽  
Scanning Electron

Ba2B5O9Cl whiskers with uniform morphology were synthesized by a simple flux method, using BaCl2•2H2O, H3BO3 as the starting materials, and KCl as the flux. The products were characterized by X-ray diffraction (XRD) and scanning electron microcopy (SEM), and the optimum conditions for preparing high quality Ba2B5O9Cl whiskers were studied. Results show that a sintering temperature around 700 °C, an Ba/B mole ratio of 1:3 and a raw materials to flux mass ratio of 1:2 lead to uniform orthorhombic Ba2B5O9Cl whiskers with a diameter of 0.4-1.0 µm and a length of 10-25 µm.

Effect of SiC on Microstructures and Properties of Clay Foam Ceramics

2010 ◽  
Vol 105-106 ◽  
pp. 620-622
Author(s):  
Jian Guang Bai ◽  
Guang Liang Liu ◽  
Jian Feng Yang
Keyword(s):  
Compressive Strength ◽  
Bulk Density ◽  
Moisture Absorption ◽  
Raw Materials ◽  
Sintering Behavior ◽  
Powder Size ◽  
Mass Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Foam Ceramic

A foam ceramic was prepared using clay, SiC, Fe2O3, feldspar and other raw materials as main starting material in a furnace at 1140~1170oC for 15~25min. Effects of silicon carbide’s content and powder size on the bulk density, moisture absorption rate and compressive strength were studied, and the fracture surface morphology was observed and analyzed using Scanning Electron Microscope (SEM) and X-ray diffraction analysis (XRD). The results show that SiC powder reacted with Fe2O3, Fe3O4, CO2, iron, SiO2 and form foam. The sintering behavior and properties of the foam ceramics are influenced by the content and particle size of SiC, when the content of SiC is as high as 8%, and the mass ratio of grain size is 1:1, the foam ceramics with the rate of moisture absorption is 0.05%, the bulk density is 0.32g/cm3, and compressive strength is than 2.2MPa.

scholarly journals Waste and Solar Energy: An Eco-Friendly Way for Glass Melting

2021 ◽  
Vol 5 (2) ◽  
pp. 16
Author(s):  
Isabel Padilla ◽  
Maximina Romero ◽  
José I. Robla ◽  
Aurora López-Delgado
Keyword(s):  
Solar Energy ◽  
Environmental Sustainability ◽  
Raw Materials ◽  
Glass Melting ◽  
Glass Network ◽  
X Ray Diffraction ◽  
X Ray ◽  
Concentrated Solar Energy ◽  
Calcium Source ◽  
The Aluminum Industry

In this work, concentrated solar energy (CSE) was applied to an energy-intensive process such as the vitrification of waste with the aim of manufacturing glasses. Different types of waste were used as raw materials: a hazardous waste from the aluminum industry as aluminum source; two residues from the food industry (eggshell and mussel shell) and dolomite ore as calcium source; quartz sand was also employed as glass network former. The use of CSE allowed obtaining glasses in the SiO2-Al2O3-CaO system at exposure time as short as 15 min. The raw materials, their mixtures, and the resulting glasses were characterized by means of X-ray fluorescence, X-ray diffraction, and differential thermal analysis. The feasibility of combining a renewable energy, as solar energy and different waste for the manufacture of glasses, would highly contribute to circular economy and environmental sustainability.

A 2-D Zn(II) coordination polymer based on 4,5-imidazoledicarboxylate and bis(benzimidazole) ligands: synthesis, crystal structure and fluorescence properties

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Xinzhao Xia ◽  
Lixian Xia ◽  
Geng Zhang ◽  
Yuxuan Jiang ◽  
Fugang Sun ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Coordination Polymer ◽  
Zigzag Chain ◽  
Supramolecular Framework ◽  
X Ray Diffraction ◽  
Hydrothermal Conditions ◽  
Hydrogen Bond Interaction ◽  
X Ray ◽  
New Type ◽  
Solid State Fluorescence

Abstract In this work, a new type of zinc(II) coordination polymer {[Zn(HIDC)(BBM)0.5]·H2O} n (Zn-CP) was synthesized using 4,5-imidazoledicarboxylic acid (H3IDC) and 2,2-(1,4-butanediyl)bis-1,3-benzimidazole (BBM) under hydrothermal conditions. Its structure has been characterized by infrared spectroscopy, elemental analysis and single crystal X-ray diffraction analysis. The Zn(II) ion is linked by the HIDC2− ligand to form a zigzag chain by chelating and bridging, and then linked by BBM to form a layered network structure. Adjacent layers are further connected by hydrogen bond interaction to form a 3-D supramolecular framework. The solid-state fluorescence performance of Zn-CP shows that compared with free H3IDC ligand, its fluorescence intensity is significantly enhanced.

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

Facile Solid State Method Route Synthesis and Enhance Visible Light Activities of BiVO4 by Doping Co

2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu
Keyword(s):  
Solid State ◽  
Visible Light ◽  
Catalytic Effect ◽  
Catalytic Properties ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
Solid State Method ◽  
Illumination Time ◽  
X Ray ◽  
State Method

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.

The Roman Ceramics of Salobrena (Granada-Spain) and their Raw Materials

1992 ◽  
Vol 267 ◽  
Author(s):  
Ana M De Andres ◽  
Isabel MuÑOZ
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Raw Materials ◽  
Third Century ◽  
Western Coast ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Third ◽  
Good Number ◽  
Scanning Electron

ABSTRACTNineteen roman ceramic sherds found near Salobreña (Granada, Spain), in the western coast of the Mediterranean Sea, as well as different ceramic clays from the surroundingsare studied. Both clays and ceramic sherds are characterizad by X-ray diffraction and spectrometry, differential thermal analysis, and scanning electron and optical microscopies. A good number of the ceramic pieces, among which some “Terrae Sigillatae”, have a composition similar to that of the local clays and, thus, have been probably manufactured at Salobreña. Only a few of them have a foreign origin. For most of them, the firing temperature was about 800-850 °C, although some have been produced at 900-1000 °C, and some others at 1000-1100 °C. It is concluded that Salobreña appearsto have been an important settlement just in the third century of the Christian era.

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