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71.
A hydrogen ion-selective poly(vinyl chloride) (PVC) membrane electrode was developed using p-tert-butylcalix[4]arene-oxacrown-4 as ionophore. Apart from the ionophore, plasticisers and lipophilic anions were blended, in various proportions, with PVC in tetrahydrofurane and mixtures so prepared were poured onto glass surfaces to form the membrane. 2-Nitrophenylpentylether has proved to be the best alternative as plasticiser and the lipophilic anions tried have turned out to have an adverse effect on the pH response. The electrode of the optimum characteristics had a composition of 2% p-tert-butylcalix[4]arene-oxacrown-4, 68.3% o-NPPE and 29.7% PVC. The electrode showed an apparent Nernstian response in the pH range 2-11 with a slope of 54.2±0.4 mV pH−1 at 20±1 °C. It has a rapid potential-response to changes of pH, high ion selectivity towards lithium, sodium and potassium, and other characteristics comparable to those reported for the conventional pH glass membrane electrode. It appears to be a suitable potentiometric indicator electrode specifically for hydrofluoric acid solutions. 相似文献
72.
Determination of glyoxal and methylglyoxal in the serum of diabetic patients by MEKC using stilbenediamine as derivatizing reagent 总被引:1,自引:0,他引:1
An analytical method has been developed for the separation of glyoxal (Go), methylglyoxal (MGo), and dimethylglyoxal (DMGo) by MEKC using stilbenediamine (SD) as derivatizing reagent, separation time 6.5 min, SDS as micellar medium at pH 8, and sodium tetraborate (0.1 M) as buffer. Uncoated fused-silica capillary, effective length 50 cm x 75 microm id; applied voltage 20 kV and photodiode array detection, were used. Calibration was linear within 0.02-150 microg/mL with detection limits 3.5-5.8 ng/mL. Go and MGo, observed for diabetic and healthy volunteers, were within 0.098-0.193 microg/mL Go and 0.106-0.245 microg/mL MGo with RSD 1.6-3.5 and 1.7-3.4%, respectively, in diabetics against 0.016-0.046 microg/mL Go and 0.021-0.066 microg/mL MGo with RSDs 1.5-3.5 and 1.4-3.6%, respectively, in healthy volunteers. Go and MGo in diabetics were also measured by standard addition and DMGo as an internal standard. Additives do not contribute significantly to Go and MGo matrix. 相似文献
73.
The present article describes the solvatochromic effect including solvent system selection, time study and a detailed complexation
study along with exploration of extraction properties of 5,11,17,23-tetrakis[(diethylamino)methyl]-25,26,27,28-tetrahydroxycalix[4]arene
(4) that bears nitrogen atom as a donor group available for chelating metal ions. Complexation properties of 4 toward selected transition metal ions have been investigated by UV-visible and fluorescence spectroscopies. The% efficiency
of 4 toward selected transition metal ions was found in order Cu2+> Ni2+> Hg2+> Zn2+> Co2+> Cd2+> Pb2+. It has been noticed that 4 is not only proved to be an efficient Cu2+ selective chromoionophore but also possesses an effective extraction property for transferring Cu2+ ions from an aqueous to dichloromethane layer. The FT-IR spectroscopic method has also been applied for further confirmation
of the complexation phenomenon of 4 with Cu2+ ion and found adequate. 相似文献
74.
Fakhar N. Memon Shahabuddin Memon 《Journal of inclusion phenomena and macrocyclic chemistry》2013,77(1-4):413-420
Biomolecules that exist in two enantiomeric forms are generally characterized by their physiological action, e.g. l-alanine is a physiological active form of an essential amino acid. The recognition/separation of one of the enantiomers is an important task as they are used as food supplement or pharmacological products where essentially pure enantiomeric forms are required. Therefore, the quantitation of undesirable enantiomers in drug raw material is the challenging task for pharmacists and chemists. Present study demonstrates the differential recognition of l-alanine amino acid by 5,11,17,26-tetrakis-[(N,N-dimethylamino)methyl]-25,26,27,28-tetrahydroxy-calix[4]arene (3). Another characteristic feature of this study is the use of methyl orange as a UV–visible spectrophotometric probe for the determination of stability constant of host–guest inclusion complexes by adopting competitive inclusion method and 1:1 complexation ratio was confirmed by Benesi-Hildebrand equation. Thermodynamics of the recognition have been evaluated that provided the significant distinction for both isomers, i.e. d and l-alanine and it has been deduced that compound 3 may be employed in chromatographic columns for their separation. Thus, the study provides a broad spectrum of its applications in varying fields of analytical and pharmaceutical science. 相似文献
75.
The article describes the syntheses and extraction properties of two p‐tert‐butylcalix[6]arene nitrile derivatives (3 and 4). The trinitrile derivative 3 has been synthesized from 5,11,17,23,29,35‐hexa‐tert‐butyl‐37,38,39,40,41,42‐hexahydroxy‐calix[6]arene 1. The compound 1 was directly converted to its hexanitrile derivative (4). In these syntheses, it was considered to explore the role of nitrile sites in the extraction of various metal cations and HCr2O7 ?/Cr2O7 2? anions. The liquid‐liquid extraction properties of 3 and 4 towards selected alkali/transition metal cations and HCr2O7 ?/Cr2O7 2? anions are reported. It has been observed that receptor 3 does not extract alkali/transition metal cations effectively, but shows affinity towards HCr2O7 ?/Cr2O7 2? anions at low pH. The compound 4 is an effective form for transferring Ni2+ selectively, while it shows poor transferring ability for HCr2O7 ?/Cr2O7 2? anions from an aqueous into a dichloromethane layer. It was observed that the cavity size of the calix[n]arenes and the cooperativity of the functionalities play important roles in two phase extraction systems. 相似文献
76.
The article describes the synthesis and characterisation of the Cr(III)-rutin complex along with an estimate of its antioxidant activity. The complex was characterised using elemental analysis, UV-VIS, IR, conductance data, thermal, and gravimetric analyses. In the UV-VIS study, a bathochromic shift of approximately 98 nm indicates the formation of a rutin complex by more than one chelating site. The FT-IR spectra clearly show the formation of the Cr—O bond between rutin and Cr(III) at 494 cm?1, while the thermal study shows the presence of eight coordinated water molecules in the complex. The gravimetric analysis quantitatively proves the presence of four chloride ions. From these data, the formula of the Cr(III)-rutin complex was deduced as [Cr2(C27H28O16)(H2O)8]Cl4. Moreover, the antioxidant study of the complex was evaluated by using 2,2′-diphenyl-1-picrylhydrazyl (DPPH) free-radical, ferric-reducing, and phosphomolybdenum assays, which show that the complex has a higher antioxidant activity than rutin. 相似文献
77.
Jamil R. Memon Saima Q. Memon M.I. Bhanger M.Y. Khuhawar Geoffrey C. Allen G. Zuhra Memon A.G. Pathan 《European Polymer Journal》2008,44(5):1501-1511
The removal of Cd(II) using polystyrene foam chemically modified with 2,2′-bipyridine has been investigated. The modified polystyrene foam has been characterized by FT-IR spectroscopy, thermogravimetry, elemental analysis and scanning electron microscopy. The solid was employed as a Cd(II) adsorption from aqueous solutions at room temperature. The effects of several variables (pH, shaking speed, agitation time, metal concentration and presence of other ions in the medium) have been studied using batch technique. Flame atomic absorption spectrometry was used to determine the Cd(II) ion concentration in the filtrate after the adsorption process. Maximum sorption 90% was achieved at pH 7 after 30 min of shaking time. Sorbed metal ions have been desorbed with 5 ml of 2 M HNO3 with the detection limit of 16.7 ng ml−1. The Langmuir, Freundlich and D–R isotherm equation were used to describe partitioning behavior of the system at room temperature. Kinetic and thermodynamic behavior of modified polystyrene foam for Cd(II) ion removal was also studied. Br−, PO43−, Pb2+, Ni2+ and Cr(VI) suppress the sorption to some extent. The possible sorption mechanism of Cd(II) ions onto modified sorbent is also discussed. Method was utilized to remove Cd(II) ions from aqueous media. 相似文献
78.
New potential humic acid stationary phase toward drug components: Development of a chemometric‐assisted RP‐HPLC method for the determination of paracetamol and caffeine in tablet formulations
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Mustafa Topkafa Hamide Filiz Ayyildiz Fakhar N. Memon Huseyin Kara 《Journal of separation science》2016,39(13):2451-2458
A new humic acid based stationary phase has been used, for the first time, to achieve the separation and quantification of paracetamol and caffeine in pharmaceutical preparations under reversed‐phase high‐performance liquid chromatography conditions. Central composite design was applied as a powerful tool to optimize the most dominant parameters that influence the resolution of reversed‐phase high‐performance liquid chromatography, that is, mobile phase composition (acetonitrile percentage in water), flow rate, and column temperature. The optimum conditions were obtained as 21.69%, 1.5 mL/min, and 15°C, respectively, with the aid of a second‐order quadratic model and desirability function. Under the optimum conditions, the peaks could be baseline separated within 10 min. For the developed reversed‐phase high‐performance liquid chromatography method, the linearity was investigated in the concentration ranges of 2–160 mg/mL (R2 = 0.999) for paracetamol and 2–9.9 mg/mL (R2 = 0.991) for caffeine. Mean recoveries for paracetamol and caffeine were 95.90 and 95.68%, respectively. The limits of detection and quantification were 4.1 × 10‐4 and 1.3 × 10‐3 mg/mL for paracetamol and 1.6 × 10‐4 and 5.0 × 10‐4 mg/mL for caffeine. The results showed that the new humic acid based stationary phase is very suitable for the separation of paracetamol and caffeine in pharmaceutical preparations and, thus it can be used effectively in the pharmaceutical industry. 相似文献
79.
Memon JR Memon SQ Bhanger MI Memon GZ El-Turki A Allen GC 《Colloids and surfaces. B, Biointerfaces》2008,66(2):260-265
This study describes the use of banana peel, a commonly produced fruit waste, for the removal of Cd(II) from environmental and industrial wastewater. The banana peel was characterized by FT-IR and scanning electron microscopy (SEM) coupled with energy dispersive X-ray (EDX) analysis. The parameters pH, contact time, initial metal ion concentration and temperature were investigated and found to be rapid ( approximately 97% within 10min). The Langmuir adsorption isotherm was used to describe partitioning behavior for the system at room temperature. The value of Q(L) was found to be (35.52mgg(-1)) higher than the previously reported materials. The binding of metal ions was found to be pH-dependent with the optimal sorption occurring at pH 8. The retained species were eluted with 5mL of 5x10(-3)M HNO(3) with the detection limit of 1.7x10(-3)mgL(-1). Kinetics of sorption followed the pseudo-first-order rate equation with the rate constant k, equal to 0.13+/-0.01min(-1). Thermodynamic parameters such as Gibbs free energy at 303K (-7.41+/-0.13kJmol(-1)) and enthalpy (40.56+/-2.34kJmol(-1)) indicated the spontaneous and endothermic nature of the sorption process. The developed method was utilized for the removal of Cd(II) ions from environmental and industrial wastewater samples using flame atomic absorption spectrophotometer (FAAS). 相似文献
80.
Syed Ahmad Tirmizi Feroza Hamid Wattoo Muhammad Hamid Sarwar Wattoo Saadia Sarwar Allah Nawaz Memon Allah Bux Ghangro 《Arabian Journal of Chemistry》2012,5(3):309-314
Cimetidine, a histamine H2-receptor, has a structure which enables it to act as a chelating agent. The formation of nickel(II) complex with cimetidine has been studied spectrophotometrically at an absorption maximum of 622 nm at different temperatures. The data show that nickel(II) and cimetidine combine in the molar ratio of 1:2. The stability constants of the complex were calculated to be 1.40–2.4 × 108 by continuous variation method and 1.24–2.4 × 108 by mole ratio method at 25 and 40 °C, respectively. The immediately formed complex shows stability with respect to time and temperature. 相似文献