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21.
Rheological properties of poly (ethylene‐acrylic acid) (PEA) and low density poly ethylene (LDPE) blends having varied amounts of LDPE from 0 to 100% have been evaluated at different temperatures (115, 120, and 130°C) and shear rates (61.33–613.30 s?1) using a Monsanto processability tester. A reduction in the melt viscosity of the PEA/LDPE blends was noticed with increasing the shear rate. The observed positive deviation in the experimental melt viscosities of the blends is an indication of the synergy present in the blends during melt processing. The activation energy (Ea) of flow calculated using Arrhenius relation for PEA, LDPE, and their respective blends lies in the range 29.98–40.56 kJ mol?1. The experimental activation energy of flow of the blends was higher than that obtained from the additivity rule. Highest activation energy was noticed for the blends containing 60–80% by weight of LDPE in PEA/LDPE blends, which is an indication for the miscibility of the blends at these ratios. The physicomechanical properties such as density, tensile behavior, tear strength, and hardness (Shore A) of PEA, LDPE, and their blends have been evaluated as a function of varying amounts of LDPE. The obtained physicomechanical properties of the PEA/LDPE blends lie in between that of pure polymers. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
22.
The effect of heat flux levels on burning behavior and heat transmission properties of hybrid fabrics and composites has been investigated using cone calorimeter and heat transmission techniques. The hybrid fabric structures woven out of E‐glass (warp) and polyether ether ketone (PEEK) (weft) and E‐glass (warp) and polyester (weft) have been studied at high heat flux levels keeping in view the flame retardant requirements of structural composites. The performance of the glass–PEEK fabric even at high heat flux levels of 75 kW/m2 was comparable with the performance of glass–polyester fabric evaluated at 50 kW/m2. The results further demonstrate that glass–PEEK hybrid fabrics exhibit low peak heat release rate, low heat release rate, low heat of combustion, suggesting an excellent combination of materials and fall under the low‐risk category and are comparable with the performance of carbon fiber‐epoxy‐based systems. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   
23.
A series of interpenetrating polymer networks (IPNs) of castor oil based polyurethane/polyacrylonitrile (PU/PAN: 80/20, 60/40, 50/50, 40/60 and 20/80) were synthesized by condensation reaction of castor oil with methylene diisocyanate and acrylonitrile, employing benzoyl peroxide (BPO) and ethylene glycol dimethylacrylate (EGDM) as initiator and crosslinkers respectively. The physical, chemical, optical and some of the mechanical properties of PU/PAN were studied. Phase stabilization in IPNs was investigated by wide angle X-ray (WAXS) profile analysis. Variation of crystal size distribution was studied in these polymer networks. Paper presented at the 5th IUMRS ICA98, October 1998, Bangalore  相似文献   
24.
A series of styrene–butadiene rubber (SBR) composites have been prepared with different weight ratios of polyacetylene based conducting carbon black (CCB) (0–90 phr). The SBR–CCB systems are characterized for dimensional stability which is enhanced by increasing the CCB loading because of enhancement in polymer-filler interaction. The electrical properties such as dielectric constant (εr), dissipation factor (tan δ) and dielectric loss (ε″) of the composites have been studied. The influence of different loading of CCB (0–90 phr), frequency of ac (100 Hz–30 MHz) and temperature (25–75 °C) on the electrical properties was studied. An increase in dielectric constant and tan δ of the SBR composites was observed with increase in CCB content and ac frequency. This is due to enhancement of filler–filler interaction and the increase in continuity of conducting phase. The surface morphology has been studied using scanning electron microscopy (SEM).  相似文献   
25.
The present study envisages the preparation of microspheres containing indomethacin (IM) as model drug and bees wax as carrier, and to compare the in vitro release and pharmacokinetics of prepared IM formulation with commercially available oral formulation Microcid®SR. The microsphere formulations were prepared by meltable emulsified dispersion and cooling induced solidification. Surface morphology of microspheres has been evaluated using scanning electron microscopy (SEM). The SEM images revealed the spherical shape of microspheres and more than 98.0% of the isolated microspheres were in the size range 115–855 μm. Differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) spectroscopy studies indicated that the drug after encapsulation with bees wax was stable and compatible. A single dose randomized complete cross over study of IM (75 mg) microspheres was carried out on 8 healthy Albino sheeps. Plasma IM concentrations and other pharmacokinetic parameters obtained were statistically analyzed. The T max, C max, AUCO-24 and T 1/2 values of Microcid®SR and optimized formulation were 3.0 h, 2038 ± 51.31 ng/ml, 9528 ± 129.65 ng/ml h?1, and 2.59 ± 0.02 h?1; and 3.2 h, 1940 ± 22.61 ng/ml, 8751 ± 41.32 ng/ml h?1, and 2.68 ± 0.02 h?1, respectively. Beeswax microspheres showed controlled release and it can be concluded that both the prepared formulation and Microcid®SR are bioequivalent.  相似文献   
26.
The parent repeating sequence of elastin, poly(GVGVP) has been synthesized by solution phase method and characterized by 13C and 1H‐NMR spectroscopy. The poly(GVGVP) and poly(vinyl pyrrolidone) (PVP) interactions have been examined in solution phase by the viscometric method at 24 °C. The interaction parameters such as α, β, µ, and Δ[η]m indicated the miscible nature of poly(GVGVP)/PVP blends. Immiscibility occurred when the quantity of poly(GVGVP) is lesser than 60%. In the solid phase, Fourier transform infrared spectroscopic scrutiny of the thin films of poly(GVGVP)/PVP blends indicated the presence of strong intermolecular interaction such as hydrogen bonds linking the blend components. This result was further supported by glass transition temperature (Tg), scanning electron microscopic, and X‐ray diffraction studies. The blending of poly(GVGVP) with PVP may provide an opportunity to produce new materials for potential biomedical applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46699.  相似文献   
27.
Castor oil based chain extended polyurethanes (PUs) have been prepared using citric acid and maleic acid as chain extenders. Molecular transport of n‐alkanes into prepared carboxylic acid chain extended PUs has been studied at different temperatures, viz., 25, 40, and 60°C using a gravimetric sorption method. The sorption (S), the diffusion (D), and the permeation (P) coefficients for n‐alkane penetrants have been calculated. Transport data are affected by the nature of the interacting solvent molecules, molar volume, solubility parameters, temperature, and the structural variation of the chain extended PUs. The temperature dependence of the transport coefficient has been used to estimate the kinetic parameters for the processes of diffusion (ED) and permeation (EP) from the Arrhenius plots. The van't Hoff relation was used to obtain enthalpy (ΔH) and entropy (ΔS) of sorption process. POLYM. ENG. SCI., 47:2057–2064, 2007. © 2007 Society of Plastics Engineers  相似文献   
28.
A series of polyvinyl alcohol (PVA)/starch films were cast by the solvent method. Mechanical, optical, wide‐angle X‐ray scattering (WAXS), and biodegradation studies of starch‐filled PVA films were carried out. With the addition of starch there was an increase in haze and diffusion of light, whereas there was only slight change associated with tensile behavior and burst strength of the PVA film. Microstructural parameters, such as crystal size (〈N〉) and lattice distortion (g, in %) were estimated using one‐dimensional Hosemann's paracrystalline model along with WAXS data. These parameters quantify the changes in the PVA/starch systems, which resulted in the observed physical properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 12: 630–635, 2004  相似文献   
29.
Composites were fabricated by impregnating the jute nonwoven fabric in acrylonitrile–butadiene (NBR) latex. The effect of different pickup ratio (dry, wt/wt) of NBR latex to jute nonwoven fabric, viz., 0.5 : 1, 1 : 1.5, 1.5 : 1, 2 : 1, and 2.5 : 1 on the water absorption behavior of the composites were evaluated. Water absorption studies were carried out at different temperatures, viz. 30, 50, and 70°C, based on immersion weight gain method. From the sorption result, the diffusion (D) and permeation (P) coefficients of water penetrant have been calculated. Significant increase in the diffusion and permeation coefficients was observed with increase in the temperature of sorption experiments. Drastic reductions in diffusion and permeation coefficients were noticed with increase in the pickup ratio of NBR on to jute nonwoven fabric. Attempts were made to estimate the empirical parameters like n, which suggests the mode of transport, and K is a constant that depends on the structural characteristics of the composite in addition to its interaction with water. The temperature dependence of the transport coefficients has been used to estimate the activation energy parameter for diffusion (ED) and permeation processes (Ep) from Arrhenius plots. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2045–2050, 2006  相似文献   
30.
Linear low‐density polyethylene (LLDPE) with different fillers such as silica, mica, and soy protein isolate were compounded using a single screw extruder and blown into films by a Konark blow‐film machine. The filled LLDPE films were characterized for physicomechanical and optical properties. Barrier properties such as water vapor transmission rate and oxygen transmission rate of the filled LLDPE films were also reported. Microcrystalline parameters such as crystal size (〈N〉) and lattice distortion (g in %) of the filled LLDPE films were estimated from the wide‐angle X‐ray scattering method using Hosemann's paracrystalline model. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2938–2944, 2003  相似文献   
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