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91.
N,N,N‐trimethylchitosan (TMC) was prepared by reacting purified chitosan with iodomethane, in the presence of sodium hydroxide, water and sodium iodide, at room temperature. The reaction medium was N‐methyl‐2‐pyrrolidone. Different samples of TMC were obtained by adding to the reaction medium a fixed volume (5.5 mL) of aqueous NaOH solutions at different concentrations (15, 20, 30 and 40 wt.‐%) and carrying out the reactions for 9 or 24 h. The features observed in the 1H and 13C NMR spectra of these chitosan derivatives, in respect of the chemical shift, number and relative intensity of the signals, depended strongly on the excess of NaOH and H3CI added to the reaction medium, but when the lowest excess was employed, the characteristics of the derivative were not affected by the reaction time to the same extent. The average degree of quaternization of these N‐methylated derivatives of chitosan ranged from 10.5% to 44.8%, according to the reaction conditions. Increasing the excess of NaOH, in reactions carried out for 9 h, resulted in TMC samples with progressively higher content of trimethylated sites however, the reaction yields were correspondingly lower and O‐alkylation was favored in these cases.

1H NMR spectrum of sample [AX]24h dissolved in D2O (Cp = 10 g/L).  相似文献   

92.
An investigation of heparinase immobilization   总被引:1,自引:0,他引:1  
A systematic investigation of the parameters that affect the efficiency of immobilizing heparinase onto cyanogen bromide activated crosslinked 8% agarose beads was conducted. Two experimental measures, the “fraction bound” and the “fraction retained,” were used to monitor the coupling efficiency. The fraction bound is the portion of the total initial enzyme that is bound to the agarose gel. The fraction retained is the fraction of bound enzyme that is active. The product of the two measures indicates the coupling efficiency. The activity of the immobilized heparinase was measured under conditions free of both internal and external mass transfer limitations, and thus, the fraction retained represents the true immobilized enzyme activity. Increasing the degree of activation of the beads results in an increase in the fraction bound, the fraction retained, and consequently, the coupling efficiency. As the ratio of enzyme solution to gel volume increases from 1.5 to 2.2, the fraction bound remains constant but the fraction retained decreases (heparinase concentration; 0.15 mg/mL and degree of activation; 9.5 μmol of cyanate esters/g of gel). At volume ratios greater than 2.2, both the fraction bound and the fraction retained decline continuously. Changing the heparinase concentration in the coupling solution changes the coupling efficiency in a manner similar to that of the volume ratio change. When heparin is added during the coupling process, the fraction bound declines as the heparin concentration increases, whereas the fraction retained increases up to a heparin concentration of 12 mg/mL and decreases thereafter. When arginine, lysine, and glycine are used to block the unreacted cyanate ester groups after the coupling process, the immobilized heparinase shows different pH optima of 6.5, 6.9, and 7.2, respectively. Based upon these findings, a protocol to optimize heparinase immobilization is developed.  相似文献   
93.
CTMAB胶束体系中反离子缔合度的测定   总被引:2,自引:0,他引:2  
对十六烷基三甲基淡化按(CTMAB)水胶束体系,不同方法测得其反离子缔合度产值不同【‘-\且很高于由股团电化学理论所得q值0.67问.本文以离子选择性电极法测定CTMAB水胶束体系中反离子缩合度(仁0.65),并研究了外加盐和乙醇的影响·1实验部分1.工试剂和仪器十六烷基三甲基漠化技(CP)在无水乙醇中重结晶两次,纯化物经帕环法测其表面张力在CMC附近无最低声、·淡化钾(AR),水为。次蒸馏水,PXJIC型离子计,302型PB,电极(响应范围为PB,=1.6~3.3,响应时间为5分钟)222型甘汞电极·1.2实验方法在CMCV/de的稀…  相似文献   
94.
无机盐对正负表面活性剂混合体系性质的影响   总被引:4,自引:0,他引:4  
用滴体积法测定了四种离子强度下(μ=0.02, 0.05, 0.1, 0.2 mol·kg~(-1), 支持电解质为NaBr)C_(12)H_(25)SO_4Na/C_6H_(13)(NC_5H_5)Br混合体系在五种比例(10:1, 3:1, 1:1, 1:3, 1:10)时的临界胶团活度cma(25 ℃). 提出了无机盐对正负表面活性剂混合体系临界胶团活度的影响程度的计算式.  相似文献   
95.
The concept of entanglement provides the basis of our current understanding of the flow behavior of polymer melts, Current techniques developed to investigate the degree of interpenetration of polymer chains only provide indirectly the information of the degree of entanglement in a relatively large scale (several to tens of nanometer). In this article, we report ^1H-NMR spectroscopy with dipolar filters under fast magic angle spinning for probing chain interpenetration of polymer glasses at the molecular level.  相似文献   
96.
Low molecular, water‐soluble chitosan (LMWSC) with a free amine group was prepared by the novel salts‐removal method described in this study. A weight‐average molecular weight and degree of deacetylation (DDA) of LMWSC were determined by viscometry and Kina titration, resulting in 18,579 Da and 93% DDA, respectively. In the Fourier transform infrared spectroscopic, 1H NMR, and 13C NMR spectra the absorption band by the carboxyl group derived from lactic acid and the impurities formed in the enzymatic process disappeared or were significantly lower than that of the control chitosan. Also, from the 1H NMR and 13C NMR spectra the empirical value for the area ratio of the proton and carbon corresponds nearly to its theoretical values. The matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrum identified the difference in the two adjacent peaks as 161. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3796–3803, 2002  相似文献   
97.
Protein hydrolysates have the potential to be natural and safer sources of bioactive peptides. In this study, two proteases were used to hydrolyze Chinese sturgeon (Acipenser sinensis) protein, and the hydrolysates were then purified to yield antioxidant peptides. The degree of hydrolysis of 23.56 % and 18.14 % was obtained using papain and alcalase 2.4L, respectivly, and hydrolysates had 96.80 % and 87.24 % total amino acid content, respectivly. The papain hydrolysate (PH) and alcalase 2.4L hydrolysate (AH) showed good antioxidant activity against DPPH? (IC50 of 3.64 and 3.15 mg/mL) and ABTS?+ (IC50 of 1.92 and 1.58 mg/mL), respectively. The low-molecular-weight (<1000 Da) fraction of both hydrolysates demonstrated the highest antiradical activity (IC50 of 2.59 and 2.31 mg/mL, DPPH) and (IC50 of 1.54 and 1.36 mg/mL, ABTS), respectively. Nine peptides were separated from both hydrolysates using reverse phase high performance liquid chromatography (RP-HPLC). The IC50 for ABTS?+ scavenging activity of peptide P5 with valine, glycine and asparagine (MW of 282.13 Da) from PH, and peptide P3 with histidine, glycine and alanine (MW of 302.74 Da) from AH was 0.89 and 0.72 mg/mL, respectively. The fractions and purified peptides obtained from Chinese sturgeon hydrolysates could be utilized as natural antioxidant substitutes in pharmaceuticals and food products.  相似文献   
98.
A series of PB-g-SAN impact modifiers with different ratio of PB to SAN ranging from 20.6/79.4 to 91.9/8.1 were synthesized by seeded emulsion polymerization. ABS blends were prepared by blending these PB-g-SAN impact modifiers and SAN resin. The rubber concentration of these ABS blends was kept at a constant value of 15 wt%. The influences of different impact modifier on the mechanical behavior and morphology of ABS blends have been investigated. The dynamic mechanical analysis on ABS blends shows that Tg of the rubbery phase shifts to a lower temperature, (tan δ)max of the rubbery phase increases and then decreases with the increase of PB concentration in PB-g-SAN impact modifier. A uniform dispersion of rubber particles in the matrix can be observed when PB/SAN ratio in PB-g-SAN impact modifier is in the range from 20.6/79.4 to 71.7/28.3. When it exceeds 71.7/28.3, an agglomeration of rubber particles occurs. The mechanical tests indicate that the ABS blend, in which PB/SAN ratio in the impact modifier is 71.7/28.3, has the maximum impact strength and yield strength.  相似文献   
99.
提高熔炼过程纯净度的原理及工艺   总被引:1,自引:0,他引:1  
航空发动机部件生产的主要因素是改进质量和降低成本。熔炼和铸造相关的铝合金时,冶金工艺首先遇到的难题是对纯净度的严格要求。文章通过分析去除铝熔体中夹杂的方法和几种主要原理及工艺,从而对高纯净度铝熔体进行了探索。  相似文献   
100.
口腔全瓷修复体的临床效果评价   总被引:2,自引:0,他引:2  
评价IPS Empress2全瓷修复体的临床效果。为35例患者制作了46件IPS Empress2全瓷冠,戴用期6~24个月,评价修复体的边缘完整性、解剖形态和颜色等临床指标,茵斑指数和牙龈指数与对照组采用Wilcoxon秩和检验进行比较。除2例修复体发生折裂外,修复成功率为95.65%,修复体的牙龈健康状况与对照组无统计学差异。显示全瓷修复体有令人满意的近期疗效。  相似文献   
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