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 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A zinc-aluminum layered double hydroxide (ZnAl-LDH)/alumina bilayer film has been fabricated on an aluminum substrate by a one-step hydrothermal crystallization method. The LDH film was uniform and compact. XRD patterns and SEM images showed that the LDH film was highly oriented with the c-axis of the crystallites parallel to the substrate surface. The alumina layer existing between the LDH film and the substrate was formed prior to the LDH during the crystallization process. Polarization measurements showed that the bilayer film exhibited a low corrosion current density value of 10(-8) A/cm(2), which means that the LDH/alumina bilayer film can effectively protect aluminum from corrosion. Electrochemical impedance spectroscopy (EIS) showed that the impedance of the bilayer was 16 MOmega, meaning that the film served as a passive layer with a high charge transfer resistance. The adhesion between the film and the substrate was very strong which enhances its potential for practical application.
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PMID:One-step hydrothermal crystallization of a layered double hydroxide/alumina bilayer film on aluminum and its corrosion resistance properties. 1944 23

The synergistic effect of steam explosion pretreatment and sodium hydroxide post-treatment of Lespedeza stalks (Lespedeza crytobotrya) has been investigated in this study. In this case, Lespedeza stalks were firstly exploded at a fixed steam pressure (22.5 kg/m(2)) for 2-10 min. Then the steam-exploded Lespedeza stalks was extracted with 1 M NaOH at 50 degrees C for 3 h with a shrub to water ratio of 1:20 (g/ml), which yielded 57.3%, 53.1%, 55.4%, 52.8%, 53.2%, and 56.4% (% dry weight) cellulose rich fractions, comparing to 68.0% from non-steam-exploded material. The content of glucose in cellulose rich residues increased with increment of the steaming time and reached to 94.10% at the most severity. The similar increasing trend occurred during the dissolution of hemicelluloses. It is evident that at shorter steam explosion time, autohydrolysis mainly occurred on the hemicelluloses and the amorphous area of cellulose. The crystalline region of cellulose was depolymerized under a prolonged incubation time. The characteristics of the cellulose rich fractions in terms of FT-IR and CP/MAS (13)C NMR spectroscopy and thermal analysis were discussed, and the surface structure was also investigated by SEM.
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PMID:Influence of steaming explosion time on the physic-chemical properties of cellulose from Lespedeza stalks (Lespedeza crytobotrya). 1950 52

The composition of hydrolyzed Al species is essential for the understanding of coagulation with Al-based coagulants. Surface characteristics of flocs formed by coagulation with two distinct polyaluminum chloride (PACl) coagulants were identified. One commercial coagulant (PACl-C) with voluminous monomeric Al and colloidal Al(OH)(3) and a custom-made PACl (PACl-Al(13)) containing high Al(13) content were applied to destabilize kaolin particles. The flocs formed by PACl-C and PACl-Al(13) at neutral and alkaline pH ranges, respectively, were observed by FE-SEM and HR-TEM. In addition, the Al composition of these flocs was characterized by XPS and HR-XRD, and the imaging of Al(OH)(3) precipitates and Al(13) aggregates were conducted by SEM as well as tapping mode AFM in liquid system. The observations of flocs indicate that the morphology of Al(OH)(3)-rich flocs are fluffy and porous around the edge of flocs, while the Al(13)-aggregate flocs have a glossy contour and irregular structure. Both Al(OH)(3)-rich and Al(13)-aggregate flocs do not possess well-formed crystalline structure except for the Al(13)-like crystal exists in the Al(13)-aggregate flocs. Among Al(OH)(3) precipitates, colloidal Al(OH)(3) is micro-scale in size, while amorphous Al(OH)(3) is nano-scale. During the formation of Al(13) aggregates, some coiled and clustered Al(13) aggregates with smoother surface were observed. The XPS study on floc surface showed that tetrahedral (Al(IV)) /octahedral (Al(VI)) Al ratio on the surfaces of PACl-C and PACl-Al(13) flocs is 1:1.6 and 1:9.9, respectively. Of the in situ formed Al(13), almost half of Al-hydroxide precipitates on the surface of Al(OH)(3)-rich flocs possess the Al(IV) center. It also found that the irregularly aggregated Al(13) with a similar Al(13) crystalline structure subsists on the surface of Al(13)-aggregate flocs.
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PMID:The origin of Al(OH)(3)-rich and Al(13)-aggregate flocs composition in PACl coagulation. 1959 64

Through Hydroxyl (-OH) reacting with isocyanate group (-NCO), 13 Wt% nano-hydroxyapatite (n-HA)/polyurethane (PU) composite guided bone regeneration membrane was synthesized by use of solvent evaporation method. Its surface character was analyzed by XRD, IR, TG, contact angle, water absorption, elongation and combustion test and SEM. The results indicate that nano-HA/PU has good homogeneity,the interface between the inorganic mineral and organic polymer is optimized to create proper combination; that n-HA crystals are similar to the apatite crystals in natural bone, HA/PU composite membrane has good hydrophilicity mechanical behavior; and that many pores are observed on the membrane which help cells' metabolism. So the HA/PU composite membrane, thus prepared, has the potential for use in guided bone regeneration and tissue engineering.
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PMID:[Preparation and characterization of nano-hydroxyapatite/polyurethane composite bio-film]. 1963 70

In order to comprehensive utilization of iron ore tailings, this experimental research was to investigate the possibility of using the residues after iron recovery from iron ore tailings as raw materials for the preparation of cementitious material, abbreviated as TSC, including analyses of its mechanical properties, physical properties and hydration products. The TSC1 was prepared by blending 30% the residues, 34% blast-furnace slag, 30% clinker and 6% gypsum. Meanwhile, the raw iron ore tailings (before iron recovery) with the same proportion of TSC1 were selected to compare the cementitious activity of raw tailings and the residues after magnetizing roasting, denoted by TSC0. The hydration products of them were mostly ettringite, calcium hydroxide and C-S-H gel, characterized by XRD, IR and SEM. It was found that ettringite and C-S-H gel were principally responsible for the strength development of TSC mortars with curing time. The results showed that the kaolinite of the tailings was decomposed completely after magnetizing roasting, which promoted the cementitious property of TSC1. Moreover, the mechanical properties of TSC1 are well comparable with those of 42.5 ordinary Portland cement according to Chinese GB175-2007 standard.
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PMID:Innovative methodology for comprehensive utilization of iron ore tailings: part 2: The residues after iron recovery from iron ore tailings to prepare cementitious material. 1978 71

To improve the corrosion resistance and biological performance of commercially pure titanium (cp-Ti) substrates, potassium hydroxide was employed to modify the surfaces of titanium substrates, followed by biomimetic deposition of apatite on the substrates in a simulated body fluid. The morphologies of native and treated titanium substrates were characterized by field emission scanning electron microscopy (FE-SEM). Treatment with potassium hydroxide led to the formation of intermediate layers of potassium titanate on the surfaces of titanium substrates, while apatite was subsequently deposited onto the intermediate layer. The formation of potassium titanate and apatite was confirmed by thin-film X-ray diffraction and FE-SEM equipped with energy dispersive spectroscopy, respectively. Electrochemical impedance spectroscopy showed that the formed potassium titanate layer improved the corrosion-resistance properties of titanium substrates. The influence of modified titanium substrates on the biological behavior of mesenchymal stem cells (MSCs), including osteogenic differentiation, was investigated in vitro. Compared with cp-Ti substrates, MSCs cultured onto alkali- and heat-treated titanium substrates and apatite-deposited titanium substrates displayed significantly higher (P<0.05 or P<0.01) proliferation and differentiation levels of alkaline phosphatase and osteocalcin in 7 and 14day cultures, respectively. More importantly, our results suggest that the modified titanium substrates have great potential for inducing MSCs to differentiate into osteoblasts. The approach presented here may be exploited to fabricate titanium-based implants.
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PMID:Surface engineering of titanium with potassium hydroxide and its effects on the growth behavior of mesenchymal stem cells. 1996 80

In this paper, we demonstrated a facile hydrothermal route leading to the generation of a new cobalt hydroxide, Co(OH)(3), nanobelt. This new product of Co(OH)(3) nanobelts was well characterized and identified by SEM, TEM, XRD, EDX, XPS, EXAFS, Raman, TGA and SQUID. Additionally, through systematic investigations on morphological evolution, it was found that the size and shape of Co(OH)(3) nanobelts were adjustable in large scale, e.g. from 50 to 1.5 microm in length and 5 microm to 20 nm in width, by means of fine experimental parameter control. Furthermore, the unique pseudo-single-crystalline Co(3)O(4) nanobelts were produced from Co(OH)(3) precursors via heating treatment. This is the first synthesis of Co(OH)(3) with tunable shapes and sizes, which may find important applications as gas sensors, catalysts, and electrode materials, owing to the specific large surface-to-volume ratio and other unique properties endowed by typical 1D nanobelts.
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PMID:Co(OH)3 nanobelts: synthesis, characterization and shape-preserved transformation to pseudo-single-crystalline Co3O4 nanobelts. 2000 1

Magnesium alloys have a low specific density and a high strength to weight ratio. This makes them sought after light weight construction materials for automotive and aerospace applications. These materials have also recently become of interest for biomedical applications. Unfortunately, the use of magnesium alloys in many applications has been limited due to its high susceptibility to corrosion. One way to improve the corrosion resistance of magnesium alloys is through the deposition of protective coatings. Many of the current pretreatments/coatings available use toxic chemicals such as chromates and hydrofluoric acid. One possible environmentally friendly alternative is organosilane coatings which have been shown to offer significant corrosion protection to both aluminum alloys and steels. Organosilanes are ambifunctional molecules that are capable of covalent bonding to metal hydroxide surfaces. In order for covalent bonding to occur, the organosilane must undergo hydrolysis in the coating bath followed by a condensation reaction with the surface. There are a number of factors that influence the rates of these reactions such as pH and concentration of reactants. These factors can also influence competing reactions in solution such as oligomerization. The rates of hydrolysis and condensation of 3-mercaptopropyltrimethoxy silane in methanol have been analyzed with (1)H NMR and ATR-FTIR. The results indicate that organosilane oligomers begin to form in solution before the molecules are fully hydrolyzed. The organosilane films deposited on magnesium alloy AZ91 at a variety of concentrations and pre-hydrolysis times were characterized with a combination of ATR-FTIR, ellipsometry and SEM/EDS. The results show that both organosilane film thickness and uniformity are affected by the chemistry occurring in the coating bath prior to deposition.
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PMID:Influence of coating bath chemistry on the deposition of 3-mercaptopropyl trimethoxysilane films deposited on magnesium alloy. 2006 43

The catalytic activity of modified carbon powder (Vulcan XC-72R) for oxygen reduction reaction (ORR) in an air-breathing cathode of a microbial fuel cell (MFC) has been investigated. Chemical modification was carried out by using various chemicals, namely 5% nitric acid, 0.2N phosphoric acid, 0.2N potassium hydroxide and 10% hydrogen peroxide. Electrochemical study was performed for ORR of these modified carbon materials in the buffer solution pH range of 6-7.5 in the anodic compartment. Although, these treatments influenced the surface properties of the carbon material, as evident from the SEM-EDX analysis, treatment with H(2)PO(4), KOH, and H(2)O(2) did not show significant activity during the electrochemical test. The HNO(3) treated Vulcan demonstrated significant ORR activity and when used in the single-chamber MFC cathode, current densities (1115mA/m(2), at 5.6mV) greater than those for a Pt-supported un-treated carbon cathode were achieved. However, the power density for the latter was higher. Such chemically modified carbon material can be a cheaper alternative for expensive platinum catalyst used in MFC cathode construction.
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PMID:Effect of chemically modified Vulcan XC-72R on the performance of air-breathing cathode in a single-chamber microbial fuel cell. 2017 Oct 90

Three different pretreatment methods for switchgrass were studied. Aqueous sodium hydroxide (0.5-10% w/v, 90 degrees C, 1h), dilute H(2)SO(4) (0.5-6.0% v/v, 121 degrees C, 1h) and hot water (100 degrees C, 1h) were employed in this study to determine how each method affected the digestibility of switchgrass during enzymatic hydrolysis. Switchgrass pre-treated with 0.5% w/v sodium hydroxide generally produced glucose in higher concentrations than sulfuric acid and hot water pre-treated samples. SEM studies on the pre-treated samples revealed a great deal of pore formation in the NaOH pre-treated samples and little or no physical changes on the acid and hot water pre-treated samples. Lignin analysis carried out on the pre-treated samples showed a considerable decrease in lignin content in the NaOH pre-treated samples and only a slight decrease in lignin content for the other pretreatment methods studied.
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PMID:Comparison of different pretreatment methods based on residual lignin effect on the enzymatic hydrolysis of switchgrass. 2021 64


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