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Monohydrate
Kinds of Monohydrate Terms modified by Monohydrate Selected AbstractsChemInform Abstract: Exploration of Chiral Induction on Epoxides in Lipase-Catalyzed Epoxidation of Alkenes Using (2R,3S,4R,5S)-(-)-2,3:4,6-Di-O-isopropylidiene-2-keto-L-gulonic Acid Monohydrate.CHEMINFORM, Issue 46 2009Kuladip Sarma Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Synthesis and Structure of the Ammonium Sesquicarbonate Monohydrate (NH4)4 [H2(CO3)3]×H2O.CHEMINFORM, Issue 37 2003Guenter Margraf Abstract For Abstract see ChemInform Abstract in Full Text. [source] Pseudo-Isomerism by Different Jahn,Teller Ordering: Crystal Structures of the Hemihydrate and the Monohydrate of (pyH)[MnF(H2PO4)(HPO4)].CHEMINFORM, Issue 40 2002Ronald Stief Abstract For Abstract see ChemInform Abstract in Full Text. [source] ChemInform Abstract: (-)-Gibberic Acid (I): Hydrogen-Bonding Pattern of the Monohydrate of a Non-racemic Tetracyclic ,-Keto Acid Derivative of Gibberellin A3.CHEMINFORM, Issue 47 2001Hugh W. Thompson Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] ChemInform Abstract: Amarisolide Monohydrate, a 2-(,-Glucosyl)neoclerodane (I)CHEMINFORM, Issue 47 2001Ruben A. Toscano Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] ChemInform Abstract: Crystal Structure, Infrared and Raman Spectra of Copper Trihydrogenperiodate Monohydrate, CuH3IO6×H2O.CHEMINFORM, Issue 19 2001M. Botova Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Thermochemical Properties and Decomposition Kinetics of Ammonium Magnesium Phosphate MonohydrateCHINESE JOURNAL OF CHEMISTRY, Issue 1 2007Jian Wu Abstract Ammonium magnesium phosphate monohydrate NH4MgPO4·H2O was prepared via solid state reaction at room temperature and characterized by XRD, FT-IR and SEM. Thermochemical study was performed by an isoperibol solution calorimeter, non-isothermal measurement was used in a multivariate non-linear regression analysis to determine the kinetic reaction parameters. The results show that the molar enthalpy of reaction above is (28.795±0.182) kJ/mol (298.15 K), and the standard molar enthalpy of formation of the title complex is (,2185.43±13.80) kJ/mol (298.15 K). Kinetics analysis shows that the second decomposition of NH4MgPO4·H2O acts as a double-step reaction:an nth-order reaction (Fn) with n=4.28, E1=147.35 kJ/mol, A1=3.63×1013 s,1 is followed by a second-order reaction (F2) with E2=212.71 kJ/mol, A2=1.82×1018 s,1. [source] A study of primary nucleation of calcium oxalate monohydrate: II.CRYSTAL RESEARCH AND TECHNOLOGY, Issue 7 2004Effect of urinary species Abstract Kidney stones consist of various organic and inorganic compounds. Calcium oxalate monohydrate (COM) is the main inorganic constituent of kidney stones. However, the mechanisms for the formation of calcium oxalate kidney stones are not well understood. In this regard, there are several hypotheses including nucleation, crystal growth and/or aggregation of formed COM crystals. The effect of some urinary species such as oxalate, calcium, citrate, and protein on nucleation and crystallization characteristics of COM is determined by measuring the weight of formed crystals and their size distributions under different chemical conditions, which simulate the urinary environment. Statistical experimental designs are used to determine the interaction effects among various factors. The data clearly show that oxalate and calcium promote nucleation and crystallization of COM. This is attributed to formation of a thermodynamically stable calcium oxalate monohydrate resulting from supersaturation. Citrate, however, inhibits nucleation and further crystal growth. These results are explained on the basis of the high affinity of citrate to combine with calcium to form soluble calcium citrate complexes. Thus, citrate competes with oxalate ion for binding to calcium cations. These conditions decrease the amount of free calcium ions available to form calcium oxalate crystals. In case of protein (mucin), however, the results suggest that no significant effect could be measured of mucin on nucleation and crystal growth. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Ca for Er substitution in tetragonal ErPO4 · H2O crystallised from phosphoric acid solutionCRYSTAL RESEARCH AND TECHNOLOGY, Issue 2 2004R. Kijkowska Abstract Erbium phosphate monohydrate with limited Ca for Er substitution, obtained through crystallisation from boiling phosphoric acid solution has been characterised by X-ray diffraction, Ir-spectroscopy and thermal analysis (TGA-DTA) methods. The difference in the electric charge between di-valent calcium and tri-valent erbium in the solid crystallised was compensated by simultaneous substitution of HPO42- for PO43- . Ca incorporation in erbium phosphate made expansion of tetragonal ErPO4 · H2O unit cell. After ignition at 900 °C the tetragonal crystal modification was maintained but the unit cell parameters of all the investigated phosphates, whether Ca-substituted or Ca-free, contracted to the same level. The unique contraction of the unit cell was resulted from recrystallisation of Ca-substituted into Ca-free erbium phosphate, while Ca was transferred into Ca(PO3)2 formed as a separate phase. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Electrode Modified with Cobalt Cyclohexylbutyrate for the Determination of Low Molecular Weight Thiol Group Bearing Compounds Using Catalytic Stripping VoltammetryELECTROANALYSIS, Issue 3 2010Petr Jakubec Abstract Glassy carbon electrode, modified with cobalt(II) cyclohexylbutyrate monohydrate immobilized in polystyrene matrix is usable for determination of thiol group bearing compounds both in oxidized and reduced forms using catalytic stripping voltammetry. The measurements are carried out in acetate buffer (pH,4.3) containing Tween 40. After the accumulation step at ,850,mV vs. Ag/AgCl a peak at ,170,mV is observed on linear sweep voltammogram, the height of which is proportional to the concentration of added thiol. Addition of carbon nanotubes into polystyrene film enhances the sensitivity of the modified electrode. The detection limit is 1×10,6,mol dm,3 for all studied thiols. The electrode can be regenerated by exposing it to the potential between 300,600,mV. [source] Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover studyEUROPEAN JOURNAL OF NEUROLOGY, Issue 4 2005C. Kornblum The purpose of our randomized, double-blind, placebo-controlled crossover study in 15 patients with chronic progressive external ophthalmoplegia (CPEO) or Kearns,Sayre syndrome (KSS) because of single large-scale mitochondrial (mt) DNA deletions was to determine whether oral creatine (Cr) monohydrate can improve skeletal muscle energy metabolism in vivo. Each treatment phase with Cr in a dosage of 150 mg/kg body weight/day or placebo lasted 6 weeks. The effect of Cr was estimated by phosphorus-31 magnetic resonance spectroscopy (31P-MRS), clinical and laboratory tests. 31P-MRS analysis prior to treatment showed clear evidence of severe mitochondrial dysfunction. However, there were no relevant changes in 31P-MRS parameters under Cr. In particular, phosphocreatine (PCr)/ATP at rest did not increase, and there was no facilitation of post-exercise PCr recovery. Clinical scores and laboratory tests did not alter significantly under Cr, which was tolerated without major side-effects in all patients. Cr supplementation did not improve skeletal muscle oxidative phosphorylation in our series of patients. However, one explanation for our negative findings may be the short study duration or the limited number of patients included. [source] Surprises in a ,Simple' System: 2,4-Diaminobenzenesulfonic AcidHELVETICA CHIMICA ACTA, Issue 9 2003Janice The search for the polymorphic forms of 2,4-diaminobenzenesulfonic acid (DBSA), known to exist since 1880, has revealed a surprisingly rich solid-state system for such a simple molecule. A monohydrate, a dimoiric hydrate, an anhydrate and two polymorphic forms of the hydrochloride of this material have thus far been prepared. Their characterization by microscopic and thermal methods, FT-IR spectroscopy, and single-crystal structure determination are described. [source] Syntheses, spectral property, and antimicrobial activities of 6-,-amino dibenzo [d,f][1,3,2]dioxaphosphepin 6-oxidesHETEROATOM CHEMISTRY, Issue 1 2007M. Kasthuraiah Diethyl ,-aminophosphonates (4) were prepared in excellent yield from three-component reaction of aldehydes (1), amines (2), and triethylphosphite (3) under solvent-free conditions in the presence of ceric ammonium nitrate (CAN) and were reacted with 2,2,-dihydroxybiphenyl (5) using p -toluene sulfonic acid monohydrate (PTSA) as a catalyst to obtain 6-,-aminodibenzo[d f][1,3,2]dioxaphosphepin 6-oxides (6) in good yield. It is a first report on the cyclizations of 4 with 5. An antimicrobial activity of numbers of 6 is evaluated. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:2,8, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20244 [source] Desorption kinetics of model polar stratospheric cloud films measured using Fourier Transform Infrared Spectroscopy and Temperature-Programmed DesorptionINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 5 2001Birgit G. Koehler This study combines Fourier transform infrared (FTIR) spectroscopy and temperature-programmed desorption to examine the evaporation kinetics of thin films of crystalline nitric acid hydrates, solid amorphous H2O/HNO3 mixtures, H2O,ice, ice coated with HCl, and solid HNO3. IR spectroscopy measured the thickness of each film as it evaporated, either at constant temperature or during a linear temperature ramp (temperature-programmed infrared, TPIR). Simultaneously, a mass spectrometer measured the rate of evaporation directly by monitoring the evolution of the molecules into the gas phase (temperature-programmed desorption, TPD). Both TPIR and TPD data provide a measurement of the desorption rate and yield the activation energy and preexponential factor for desorption. TPD measurements have the advantage of producing many data points but are subject to interference from experimental difficulties such as uneven heating from the edge of a sample and sample-support as well as pumping-speed limitations. TPIR experiments give clean but fewer data points. Evaporation occurred between 170 and 215 K for the various films. Ice evaporates with an activation energy of 12.9 ± 1 kcal/mol and a preexponential factor of 1 × 1032±1.5 molec/cm2 s, in good agreement with the literature. The beta form of nitric acid trihydrate, ,,NAT, has an Edes of 15.6 ± 2 kcal/mol with log A = 34.3 ± 2.3; the alpha form of nitric acid trihydrate, ,,NAT, is around 17.7 ± 3 kcal/mol with log A = 37.2 ± 4. For nitric acid dihydrate, NAD, Edes is 17.3 ± 2 kcal/mol with log A = 35.9 ± 2.6; for nitric acid monohydrate, NAM, Edes is 13 ± 3 kcal/mol with log A = 31.4 ± 3. The ,,NAT converts to ,,NAT during evaporation, and the amorphous solid H2O/HNO3 mixtures crystallize during evaporation. The barrier to evaporation for pure nitric acid is 14.6 ± 3 kcal/mol with log A = 34.4 ± 3. © 2001 John Wiley & Sons, Inc. Int J Chem Kinet 33: 295,309, 2001 [source] One-Pot Suzuki/Heck Sequence for the Synthesis of (E)-Stilbenes Featuring a Recyclable Silica-Supported Palladium Catalyst via a Multi-Component Reaction in 1,3-PropanediolADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 11-12 2010Lionel Joucla Abstract The synthesis of (E)-stilbenes was performed following a one-pot Suzuki/Heck sequence through the use of potassium vinyltrifluoroborate. The combination of heterogeneous palladium/silica (Pd/SiO2) catalyst with potassium phosphate monohydrate (K3PO4,H2O) as base resulted in useful to good isolated yields regardless of the ortho- , meta- or para- substitution of the aryl halides employed. In a sustainable approach, we found that bio-sourced 1,3-propanediol could advantageously replace N -methylpyrrolidone (NMP) as similar yields were obtained. Moreover, the reactivity gap between aryl iodides and bromides resulting from the use of 1,3-propanediol allowed an efficient multi-component approach toward the synthesis of (E)-stilbenes. Furthermore, this heterogeneous catalyst was found to be extremely robust despite the use of aerobic conditions and was successfully re-used over several cycles. [source] Role of uric acid in different types of calcium oxalate renal calculiINTERNATIONAL JOURNAL OF UROLOGY, Issue 3 2006FÉLIX GRASES Aim:, The presence of uric acid in the beginning zone of different types of ,pure' calcium oxalate renal calculi was evaluated with the aim of establishing the degree of participation of uric acid crystals in the formation of such calculi. Methods:, The core or fragment of different types of ,pure' calcium oxalate renal calculi was detached, pulverized and uric acid extracted. Uric acid was determined using a high-performance liquid chromatography/mass spectrometry method. Results:, In calcium oxalate monohydrate (COM) papillary calculi with a core constituted by COM crystals and organic matter, 0.030 ± 0.007% uric acid was found in the core. In COM papillary calculi with a core constituted by hydroxyapatite, 0.031 ± 0.008% uric acid was found in the core. In COM unattached calculi (formed in renal cavities) with the core mainly formed by COM crystals and organic matter, 0.24 ± 0.09% uric acid was found in the core. In COM unattached calculi with the core formed by uric acid identifiable by scanning electron microscopy (SEM) coupled to X-ray microanalysis, 20.8 ± 7.8% uric acid was found in the core. In calcium oxalate dihydrate (COD) unattached calculi containing little amounts of organic matter, 0.012 ± 0.004% uric acid was found. In COD unattached calculi containing little amounts of organic matter and hydroxyapatite, 0.0030 ± 0.0004% of uric acid was found. Conclusions:, From these results it can be deduced that uric acid can play an important role as inducer (heterogeneous nucleant) of COM unattached calculi with the core formed by uric acid identifiable by SEM coupled to X-ray microanalysis (these calculi constitute the 1.2% of all calculi) and in COM unattached calculi with the core mainly formed by COM crystals and organic matter (these calculi constitute the 10.8% of all calculi). [source] Urolithiasis in Okinawa, Japan: A relatively high prevalence of uric acid stonesINTERNATIONAL JOURNAL OF UROLOGY, Issue 8 2003RAYHAN ZUBAIR HOSSAIN Abstract Aim:, The aim of the present study was to investigate the composition of urinary tract stones in patients from Okinawa, the most southern island group of Japan. Methods:, The study was conducted by 12 hospitals in Okinawa. A total of 1816 urinary tract calculi were obtained from 1816 patients (1323 males; 493 females). The patients had a mean age of 53 ± 15.3 years (mean ± SD). The calculi were examined to determine their chemical composition. Stone samples were analyzed by computed infrared spectrophotometer. Results:, Pure stones comprised 58.4% of the total, with calcium oxalate stones accounting for 40% (21% monohydrate [whewellite]; 6.6% dihydrate [weddellite]; and 12.4% combined monohydrate and dihydrate stones), uric acid/urate stones for 9.6%, calcium phosphate stones for 5.1%, and struvite stones for 3.7%. The other 41.6% of the stones consisted of calcium oxalate mixed with other components. The male-to-female ratio was 2.7 : 1. Conclusion:, In our series, calcium oxalate stones accounted for 81.6% of the urinary tract calculi, while uric acid/urate stones accounted for 15.8%. Uric acid stones, predominantly the anhydrous and/or dihydrate forms, showed a relatively high prevalence. Calcium oxalate stones, predominantly in the form of whewellite, showed a high prevalence among pure calculi; while the predominant combinations among mixed calculi were weddellite + calcium phosphate and whewellite + uric acid/urate. [source] Nanoparticles of CdCl2 with closed cage structuresISRAEL JOURNAL OF CHEMISTRY, Issue 1 2001Reshef Tenne Nanoparticles of various layered compounds having a closed cage or nanotubular structure, designated also inorganic fullerene-like (IF) materials, have been reported in the past. In this work IF -CdCl2 nanoparticles were synthesized by two methods. In one technique, a high temperature evaporation and subsequent condensation of dried cadmium chloride powder was used. In the other method, electron beam irradiation of the source powder led to its recrystallization into closed nanoparticles with a nonhollow core. The two methods are shown to produce nanoparticles of different topologies. While mostly spherical nested structures are obtained from the high temperature process, polyhedra with hexagonal or elongated rectangular characters are obtained by the electron beam induced process. The analysis also shows that, while the source (dried) powder is orthorhombic cadmium chloride monohydrate, the crystallized IF cage consists of the anhydrous 3R polytype which is not stable as bulk material in ambient atmosphere. Consistent with previous observations, this study shows that the seamless structure of the IF materials can stabilize phases, which are otherwise unstable in ambient conditions. [source] The crystal structure of perdeuterated methanol hemiammoniate (CD3OD·0.5ND3) determined from neutron powder diffraction data at 4.2 and 180,KJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2 2010A. D. Fortes The crystal structure of perdeuterated methanol hemiammoniate, CD3OD·0.5ND3, has been solved from neutron powder diffraction data collected at 4.2 and 180,K. The structure is orthorhombic, space group Pn21a (Z = 4), with unit-cell dimensions a = 12.70615,(16), b = 8.84589,(9), c = 4.73876,(4),Å, V = 532.623,(8),Å3 [,calc = 1149.57,(2),kg,m,3] at 4.2,K, and a = 12.90413,(16), b = 8.96975,(8), c = 4.79198,(4),Å, V = 554.656,(7),Å3 [,calc = 1103.90,(1),kg,m,3] at 180,K. The crystal structure was determined by ab initio methods from the powder data; atomic coordinates and isotropic displacement parameters were subsequently refined by the Rietveld method to Rp, 2% at both temperatures. The crystal structure comprises a three-dimensionally hydrogen-bonded network in which the ND3 molecules are tetrahedrally coordinated by the hydroxy moieties of the methanol molecule. This connectivity leads to the formation of zigzag chains of ammonia,hydroxy groups extending along the c axis, formed via N,D···O hydrogen bonds; these chains are cross-linked along the a axis through the hydroxy moiety of the second methanol molecule via N,D···O and O,D···O hydrogen bonds. This `bridging' hydroxy group in turn donates an O,D···N hydrogen bond to ammonia in adjacent chains stacked along the b axis. The methyl deuterons in methanol hemiammoniate, unlike those in methanol monoammoniate, do not participate in hydrogen bonding and reveal evidence of orientational disorder at 180,K. The relative volume change on warming from 4.2 to 180,K, ,V/V, is + 4.14%, which is comparable to, but more nearly isotropic (as determined from the relative change in axial lengths, e.g.,a/a) than, that observed in deuterated methanol monohydrate, and very similar to what is observed in methanol monoammoniate. [source] Examination of whewellite kidney stones by scanning electron microscopy and powder neutron diffraction techniquesJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 1 2009Michel Daudon Kidney stones made of whewellite, i.e. calcium oxalate monohydrate, exhibit various morphological aspects. The crystalline structure of whewellite at the atomic scale was revisited through a single-crystal neutron study at room temperature using a four-circle automated diffractometer. The possible relationships between the various morphological types of whewellite stones and their structural characteristics were examined at the mesoscopic scale by the use of scanning electron microscopy and at the nanometric scale by powder neutron diffraction. All types of whewellite stones displayed a similar structure at the nanometric scale. However, significant differences were found at the mesoscopic scale. In particular, the crystallites in kidney stones resulting from a genetic hyperoxaluria exhibited a peculiar structure. There was a close relationship between stone morphology and crystallite organization at the mesoscopic level and the effectiveness of extracorporeal shockwave lithotripsy. [source] Comparison of poly(o -anisidine) and poly(o -anisidine- co -aniline) copolymer synthesized by chemical oxidative methodJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010J. Longun Abstract In this study, poly(o -anisidine) [POA], poly(o -anisidine- co -aniline) [POA- co -A], and polyaniline [PANi] were chemically synthesized using a single polymerization process with aniline and o -anisidine as the respective monomers. During the polymerization process, p -toluene sulfonic acid monohydrate was used as a dopant while ammonium persulfate was used as an oxidant. N -methyl-pyrolidone (NMP) was used as a solvent. We observed that the ATR spectra of POA- co -A showed features similar to those of PANi and POA as well as additional ones. POA- co -A also achieved broader and more extended UV,vis absorption than POA but less than PANi. The chemical and electronic structure of the product of polymerization was studied using Attenuated Total Reflectance spectroscopy (ATR) and UV,visible spectroscopy (UV,vis). The transition temperature of the homopolymers and copolymers was studied using differential scanning calorimetry and the viscosity average molecular weight was studied by using dilute solution viscometry. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Studies on synthesis and characterization of a novel acrylic aromatic amide oligomer of aminolysed endproducts generated from pet waste with hydrazine monohydrate and its photocuring with acrylate monomersJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2010R. K. Soni Abstract A novel acrylic aromatic amide oligomer was synthesized by using depolymerized end product of PET waste with hydrazine monohydrate. The end product of aminolysed PET waste was synthesized under ambient conditions and was used in the preparation of novel acrylic oligomer with the reaction of acryloyl chloride prepared from acrylic acid. The acrylic oligomer was characterized by spectroscopic techniques, such as FTIR, 1H-NMR, UV, Mass spectrometry, and by other analytical techniques such as, Iodine value, TGA, and DSC. The proposed structure of the oligomer is supported by its spectral analysis and the same is inferred from other techniques. The acrylic oligomer mixed with other acrylate monomers such as methylmethacrylate, ethylhexylacrylate, acrylic acid, and photoinitiator, can be cured by UV radiation and can thus be used as an adhesion promoter on metal/glass surface. This article presents the possibility of using a difunctional aromatic amide oligomer with excellent hydrogen bonding capacity as an alternative to urethane acrylates in radiation curable formulations. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Preparation and properties of the single-walled carbon nanotube/cellulose nanocomposites using N -methylmorpholine- N -oxide monohydrateJOURNAL OF APPLIED POLYMER SCIENCE, Issue 6 2010Dong-Hun Kim Abstract Single-walled carbon nanotube (SWNT)/cellulose nanocomposite films were prepared using N -methylmorpholine- N -oxide (NMMO) monohydrate as a dispersing agent for the acid-treated SWNTs (A-SWNTs) as well as a cellulose solvent. The A-SWNTs were dispersed in both NMMO monohydrate and the nanocomposite film (as confirmed by scanning electron microscopy) because of the strong hydrogen bonds of the A-SWNTs with NMMO and cellulose. The mechanical properties, thermal properties, and electric conductivity of the nanocomposite films were improved by adding a small amount of the A-SWNTs to the cellulose. For example, by adding 1 wt % of the A-SWNTs to the cellulose, tensile strain at break point, Young's modulus, and toughness increased , 5.4, , 2.2, and , 6 times, respectively, the degradation temperature increased to 9°C as compared with those of the pure cellulose film, and the electric conductivities at , (the wt % of A-SWNTs in the composite) = 1 and 9 were 4.97 × 10,4 and 3.74 × 10,2 S/cm, respectively. Thus, the A-SWNT/cellulose nanocomposites are a promising material and can be used for many applications, such as toughened Lyocell fibers, transparent electrodes, and soforth. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source] Effects of incorporating nanosized calcium phosphate particles on properties of whisker-reinforced dental composites,,JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2007Hockin H. K. Xu Abstract Clinical data indicate that secondary caries and restoration fracture are the most common problems facing tooth restorations. Our ultimate goal was to develop mechanically-strong and caries-inhibiting dental composites. The specific goal of this pilot study was to understand the relationships between composite properties and the ratio of reinforcement filler/releasing filler. Nanoparticles of monocalcium phosphate monohydrate (MCPM) were synthesized and incorporated into a dental resin for the first time. Silicon carbide whiskers were fused with silica nanoparticles and mixed with the MCPM particles at MCPM/whisker mass ratios of 1:0, 2:1, 1:1, 1:2, and 0:1. The composites were immersed for 1,56 days to measure Ca and PO4 release. When the MCPM/whisker ratio was changed from 0:1 to 1:2, the composite flexural strength (mean ± SD; n = 5) decreased from 174 ± 26 MPa to 138 ± 9 MPa (p < 0.05). A commercial nonreleasing composite had a strength of 112 ± 14 MPa. When the MCPM/whisker ratio was changed from 1:2 to 1:1, the Ca concentration at 56 days increased from 0.77 ± 0.04 mmol/L to 1.74 ± 0.06 mmol/L (p < 0.05). The corresponding PO4 concentration increased from 3.88 ± 0.21 mmol/L to 9.95 ± 0.69 mmol/L (p < 0.05). Relationships were established between the amount of release and the MCPM volume fraction vMCPM in the resin: [Ca]= 42.9 v, and [PO4] = 48.7 v. In summary, the method of combining nanosized releasing fillers with reinforcing fillers yielded Ca- and PO4 -releasing composites with mechanical properties matching or exceeding a commercial stress-bearing, nonreleasing composite. This method may be applicable to the use of other Ca,PO4 fillers in developing composites with high stress-bearing and caries-preventing capabilities, a combination not yet available in any dental materials. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source] Physical Properties of Co-crystalline Sugar and HoneyJOURNAL OF FOOD SCIENCE, Issue 9 2005A.P.E. Maulny ABSTRACT: Clear and partially granulated honeys, were co-crystallized with sucrose in 3 proportions, 90:10, 85:15, 80:20, respectively. The products obtained by centrifugal filtration from both honeys were found by high-performance liquid chromatography to contain between 1% and 2% of honey. The moisture content of the products increased with the amount of honey added, whereas their powder flowability decreased. Differential scanning calorimetry showed a decrease in the overall crystallinity of the solidified products with an increase in the amount of honey added. Neither crystalline fructose nor glucose was detected by powder X-ray diffraction in any of the co-crystalline products. Glucose monohydrate crystallized on storage in some co-crystalline materials prepared from granulated honey. [source] Crystallization Kinetics and X-ray Diffraction of Crystals Formed in Amorphous Lactose, Trehalose, and Lactose/Trehalose MixturesJOURNAL OF FOOD SCIENCE, Issue 5 2005Song Miao ABSTRACT: Effects of storage time and relative humidity on crystallization kinetics and crystal forms produced from freeze-dried amorphous lactose, trehalose, and a lactose/trehalose mixture were compared. Samples were exposed to 4 different relative water vapor pressure (RVP) (44.1%, 54.5%, 65.6%, 76.1%) environments at room temperature. Crystallization was observed from time-dependent loss of sorbed water and increasing intensities of peaks in X-ray diffraction patterns. The rate of crystallization increased with increasing storage humidity. Lactose crystallized as ,-lactose monohydrate, ,-anhydrous, and anhydrous forms of ,- and ,-lactose in molar ratios of 5:3 and 4:1 in lactose and lactose/trehalose systems. Trehalose seemed to crystallize as a mixture of trehalose dihydrate and anhydrate in trehalose and lactose/trehalose systems. The crystal forms in a mixture of lactose and trehalose did not seem to be affected by the component sugars, but crystallization of the component sugars was delayed. Time-dependent crystallization of lactose and trehalose in the lactose-trehalose mixture could be modeled using the Avrami equation. The results indicated that crystallization data are important in modeling of crystallization phenomena and predicting stability of lactose and trehalose-containing food and pharmaceutical materials. Keywords: crystallization, lactose, trehalose, crystal form, X-ray diffraction [source] A review of nutrition in Duchenne muscular dystrophyJOURNAL OF HUMAN NUTRITION & DIETETICS, Issue 5 2009Z. E. Davidson Abstract Duchenne muscular dystrophy (DMD) is a recessive X linked genetic disorder characterised by progressive muscle weakness and reduced muscle tone. Affecting only boys, it limits life expectancy to approximately 20 years. A literature review was conducted using MEDLINE and the Cochrane Library, employing the term ,Duchenne muscular dystrophy'. A total of 1491 articles in English were recovered. These papers were searched thematically under the headings: body composition (n = 10), energy expenditure (n = 10), nutrition (n = 6), corticosteroid therapy (n = 55) and gene therapy (n = 199). Key dietetic practice points were identified relevant to nutritional management. Papers supporting these key themes were assigned a level of evidence and grade of recommendation. There is limited high-quality evidence to guide the nutritional management of boys with DMD. Currently, the majority of evidence is based on expert opinion and clinical expertise. Delayed growth, short stature, muscle wasting and increased fat mass are characteristics of DMD and impact on nutritional status and energy requirements. The early introduction of steroids has altered the natural history of the disease, but can exacerbate weight gain in a population already susceptible to obesity. Prior to commencing steroids, anticipatory guidance for weight management should be provided. Malnutrition is a feature of end stage disease requiring a multidisciplinary approach, such as texture modification and supplemental feeding. Micronutrient requirements are yet to be determined but, as a result of corticosteroid treatment, vitamin D and calcium should be supplemented. Some evidence exists supporting supplementation with creatine monohydrate to improve muscle strength. More research is needed to provide a higher quality of evidence for dietitians working within this area. [source] Synthesis and biodistribution in mice of a new 99mTc nitrido complex for brain imagingJOURNAL OF LABELLED COMPOUNDS AND RADIOPHARMACEUTICALS, Issue 10 2004Junbo Zhang Abstract The bis(N -cyclopentyl dithiocarbamato) nitrido technetium-99m complex 99mTcN(CPEDTC)2 was synthesized by the reduction of 99mTcO into [99mTc,N]2+ with stannous chloride in the presence of succinic dihydrazide and propylenediamine tetraacetic acid, followed by the addition of sodium N -cyclopentyl dithiocarbamate monohydrate. The radiochemical purity (RCP) of the product was over 90% as measured by thin layer chromatography(TLC) and high performance liquid chromatography(HPLC). In vitro studies showed that the complex possessed good stability under physiological conditions. Its partition coefficient studies indicated it was a good lipophilic complex. The electrophoresis results showed the complex was neutral. The biodistribution results in mice indicated that 99mTcN(CPEDTC)2 was significantly retained into the brain. The brain uptake(ID%/g) was 3.58, 5.26, 3.73 and 2.72 and the brain/blood ratios were 0.79, 1.69, 1.59 and 1.58 at 5, 30, 60 and 90 min post-injection, respectively. These results suggested potential usefulness of the complex as a new brain perfusion imaging agent. Copyright © 2004 John Wiley & Sons, Ltd. [source] Growth and aggregation of vaterite in seeded-batch experimentsAICHE JOURNAL, Issue 11 2004Jens-P. Abstract Seeded-batch crystallization experiments allowing study of the growth and aggregation of the Vaterite modification of calcium carbonate are reported. Results are reported for initial relative supersaturation (, = S , 1) values in the range 1.66 to 6.70, stirrer speeds in the range 400 and 1200 rpm, and at temperatures of 25 and 40°C. It is found that in all cases the linear rate of growth of the particles is size independent and depends on relative supersaturation squared. The aggregation process is apparently size independent with a rate constant that is directly proportional to the instantaneous growth rate and decreases with increasing stirrer speed. The behavior of the aggregation rate constant is very well described by the model recently proposed by Liew et al., in which the efficiency of the aggregation process is predicted to depend only on the dimensionless strength of the particles and the nature of the flow field. It is concluded that Vaterite forms aggregates with crystalline bridges having an effective strength of approximately 25% of that of calcite or calcium oxalate monohydrate. The fitted parameter L,*/M50 takes on a value of 0.18 ± 0.02. The kinetics and associated model are capable of describing the evolving particle size distributions very well. Finally, a hypothesis is advanced to describe the aggregation of small inorganic crystals in supersaturated solutions. © 2004 American Institute of Chemical Engineers AIChE J, 50: 2772,2782, 2004 [source] Water sorption induced transformations in crystalline solid surfaces: characterization by atomic force microscopyJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 9 2010Dabing Chen Abstract The effect of water sorption on the mobility of molecules on the surface of a crystalline anhydrous solid was investigated to understand the mechanism of its transformation to the corresponding hydrate. Theophylline was chosen as the model compound. The transition water activity for anhydrate to hydrate transformation, RHT, and the deliquescence RH, RH0, was determined to be 62% and 99%, respectively (25°C). Atomic force microscopy (AFM) was used to study the surface changes of theophylline above and below the transition water activity. Contact-mode AFM showed that the jump-to-contact distance increased appreciably above RHT, suggesting formation of solution on the surface. At RHT,<,RH,<,RH0, using dynamic (AC/"tapping" mode) AFM, the movements of surface steps were visualized. These results from AFM indicated that, below RH0, the formation of a thin solution film significantly increased surface mobility. Furthermore, when the anhydrate crystal surface was seeded with the hydrate, the propagation of a new hydrate phase was observed by polarized light microscopy. In conclusion, atomic force microscopy provided direct evidence that the phase transformation of anhydrous theophylline to theophylline monohydrate in the solid-state is mediated by a surface solution as a result of water adsorption. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:4032,4041, 2010 [source] | |||||||||||||||||||||||||||||||||||||