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1.
研究了用弱碱性阴离子交换树脂从硫酸浸出液中吸附铀,NaOH预处理负载树脂,碳酸钠和碳酸氢钠解析负载树脂的酸性吸附-碱性淋洗工艺。研究结果表明:该工艺能有效吸附溶液中的铀酰离子,选择性高;NaOH预处理工艺在中和树脂中氢离子的同时,能有效去除硫酸根离子,并降低钼、硅、铁等杂项元素含量;通过控制碳酸钠和碳酸氢钠溶液的流速,可成功将树脂上的铀淋洗到溶液中,实现铀的净化提取。  相似文献   
2.
针对高铅Zn焙砂在浸出工艺中的行为,以Pb含量为7.20%的Zn焙砂为原料,开展了两段酸浸工艺的实验研究,将Zn焙砂中的Zn进行浸出,而Pb在渣中进行富集。实验探究了中性浸出、酸性浸出过程中温度、酸浓度、液固比、时间等不同因素对锌的浸出率和铅富集效率的影响。实验结果表明,在中性浸出过程中,Zn浸出率为90.73%,Pb在中浸渣中的富集含量为29.68%;中浸渣经酸浸处理,Zn浸出率可以达到98.60%,Pb在酸浸渣中的富集含量为36.54%。  相似文献   
3.
对纯棉织物采用柠檬酸(CA)/丁烷四羧酸(BTCA)/木糖醇免烫整理剂进行免烫整理,探讨柠檬酸质量浓度、丁烷四羧酸质量浓度、木糖醇质量浓度、焙烘时间和焙烘温度对免烫效果的影响,并测试免烫后织物的折皱回复角、白度和强力。结果表明:免烫后织物的折皱回复角与丁烷四羧酸或柠檬酸单独作用于棉织物相当,断裂强力优于两者单独作用。优化免烫整理工艺为:柠檬酸质量浓度60 g/L、丁烷四羧酸质量浓度40 g/L、木糖醇质量浓度17.5 g/L、焙烘温度170℃、焙烘时间3 min。整理后织物的折皱回复角可达267°,白度为54.5,断裂强力为248 N。  相似文献   
4.
研究硬脂酰辅酶A去饱和酶1(stearoyl-coenzyme A desaturase 1,SCD1)基因表达对草原安格斯牛血液脂肪酸组成的影响,采集38 头平均体质量(698±34) kg、48 月龄草原安格斯牛血液样品,测定其脂肪酸组成与含量,采用实时荧光定量聚合酶链式反应测定SCD1基因表达量,一代测序技术检测SCD1基因在C878T位点的突变对实验牛血液脂肪酸组成的影响,分析SCD1基因表达与脂肪酸组成间的相关性。结果表明:血液样品中共测得36 种主要脂肪酸,饱和脂肪酸(saturated fatty acids,SFA)以棕榈酸(C16:0)和硬脂酸(C18:0)为主,含量分别达22.53%和26.95%,单不饱和脂肪酸(monounsaturated fatty acids,MUFA)中油酸(C18:1 n-9c)含量最高(15.09%);由SCD1基因表达与脂肪酸组成的显著性分析结果可知,SCD1基因表达对肉豆蔻酸(C14:0)、肉豆蔻油酸(C14:1)、C16:0、棕榈油酸(C16:1)、C18:0、C18:1 n-9c、亚油酸(C18:2 n-6c)、MUFA和MUFA/SFA以及C14指数、C18指数、脂肪酸总不饱和指数和伸长指数均影响显著;相关性分析结果显示,SCD1基因表达量与C16:0、C16:1、C18:0、C18:1 n-9c和MUFA含量均呈正相关;SCD1基因在878位点处出现了C/T突变,有CC、TT和CT 3 种基因型,不同基因型与脂肪酸组成之间均无显著相关性。综上所述,草原安格斯牛血液中的SCD1基因表达对其脂肪酸组成具有调控作用,可作为遗传标记参考基因。  相似文献   
5.
黄河  黄婷  王媚  赵金松 《酿酒科技》2022,(1):97-103
白酒塑化剂安全问题受到全社会密切关注,是白酒质量控制的重点之一,也是白酒行业需要共同应对的难题。现重点回顾白酒中邻苯二甲酸酯塑化剂研究成果,分别对塑化剂的危害、白酒中塑化剂的检测技术、来源及管控现状等方面进行阐述,并对白酒中塑化剂研究方向提出展望,旨在为白酒行业进一步研究塑化剂安全问题提供参考。  相似文献   
6.
7.
《Journal of dairy science》2022,105(4):3588-3600
Fatty acid accumulation in hepatocytes induced by high concentrations of fatty acids due to lipolysis and the associated oxidative damage they cause occur most frequently after calving. Because of their role in esterification of fatty acids, diacylglycerol acyltransferase isoforms (DGAT1 and DGAT2) could play a role in the susceptibility of dairy cows to develop fatty liver. To gain mechanistic insights, we performed in vivo and in vitro analyses using liver biopsies or isolated primary hepatocytes. The in vivo study (n = 5 cows/group) involved healthy cows [average liver triacylglycerol (TAG) = 0.78%; 0.58 to 0.93%, ratio of triglyceride weight to wet liver weight] or cows diagnosed with fatty liver (average TAG = 7.60%; 5.31 to 10.54%). In vitro, hepatocytes isolated from 3 healthy female calves (1 d old, 44 to 53 kg) were challenged with (fatty acids) or without (control) a 1.2 mM mixture of fatty acids in an attempt to induce metabolic stress. Furthermore, hepatocytes were treated with DGAT1 inhibitor or DGAT2 inhibitor for 2 h followed by a challenge with (DGAT1 inhibitor + fatty acids or DGAT2 inhibitor + fatty acids) or without (DGAT1 inhibitor or DGAT2 inhibitor) the 1.2 mM mixture of fatty acids for 12 h. Data analysis of liver biopsies was compared using a 2-tailed unpaired Student's t-test. Data from calf hepatocyte treatment comparisons were assessed by one-way ANOVA, and multiplicity for each experiment was adjusted by the Holm's procedure. Data indicated that both fatty liver and in vitro challenge with fatty acids were associated with greater mRNA and protein abundance of SREBF1, FASN, DGAT1, and DGAT2. In contrast, mRNA and protein abundance of CPT1A and very low-density lipoprotein synthesis-related proteins MTTP and APOB were markedly lower. However, compared with fatty acid challenge alone, DGAT1 inhibitor + fatty acids led to greater mRNA and protein abundance of CPT1A and APOB, and greater mRNA abundance of SREBF1 and MTTP. Furthermore, this treatment led to lower mRNA abundance of FASN and DGAT2 and TAG concentrations. Compared with fatty acid challenge alone, DGAT2 inhibitor + fatty acids led to greater mRNA and protein abundance of CPT1A, MTTP, and APOB, and lower mRNA and protein abundance of SREBF1 and FASN. In addition, compared with control and fatty acids, there was greater protein abundance of GRP78 and PERK in both DGAT1 and DGAT2 inhibitor with or without fatty acids. Furthermore, compared with control and fatty acids, reactive oxygen species concentrations in the DGAT1 inhibitor with or without fatty acid group was greater. Overall, data suggested that DGAT1 is particularly relevant in the context of hepatocyte TAG synthesis from exogenous fatty acids. Disruption of both DGAT1 and DGAT2 altered lipid homeostasis, channeling fatty acids toward oxidation and generation of reactive oxygen species. Both DGAT isoforms play a role in promoting fatty acid storage into TAG and lipid droplets to protect hepatocytes from oxidative damage.  相似文献   
8.
《Journal of dairy science》2022,105(8):7097-7110
Biotin (B8), folate (B9), and vitamin B12 (B12) are involved in several metabolic reactions related to energy metabolism. We hypothesized that a low supply of one of these vitamins during the transition period would impair metabolic status. This study was undertaken to assess the interaction between B8 supplement and a supplementation of B9 and B12 regarding body weight (BW) change, dry matter intake, energy balance, and fatty acid (FA) compositions of colostrum and milk fat from d ?21 to 21 relative to calving. Thirty-two multiparous Holstein cows housed in tie stalls were randomly assigned, according to their previous 305-d milk yield, to 8 incomplete blocks in 4 treatments: (1) a 2-mL weekly i.m. injection of saline (0.9% NaCl; B8?/B9B12?); (2) 20 mg/d of dietary B8 (unprotected from ruminal degradation) and 2-mL weekly i.m. injection of 0.9% NaCl (B8+/B9B12?); (3) 2.6 g/d of dietary B9 (unprotected) and 2-mL weekly i.m. injection of 10 mg of B12 (B8?/B9B12+); (4) 20 mg/d of dietary B8, 2.6 g/d of dietary B9, and 2-mL weekly i.m. injection of 10 mg of B12 (B8+/B9B12+) in a 2 × 2 factorial arrangement. Colostrum was sampled at first milking. and milk samples were collected weekly on 2 consecutive milkings and analyzed for FA composition. Body condition score and BW were recorded every week throughout the trial. Within the first 21 d of lactation, B8?/B9B12+ cows had an increased milk yield by 13.5% [45.5 (standard error, SE: 1.8) kg/d] compared with B8?/B9B12? cows [40.1 (SE: 1.9)], whereas B8 supplement had no effect. Even though body condition score was not affected by treatment, B8?/B9B12+ cows had greater BW loss by 24 kg, suggesting higher mobilization of body reserves. Accordingly, milk de novo FA decreased and preformed FA concentration increased in B8?/B9B12+ cows compared with B8?/B9B12? cows. In addition, cows in the B8+/B9B12? group had decreased milk de novo FA and increased preformed FA concentration compared with B8?/B9B12? cows. Treatment had no effect on colostrum preformed FA concentration. Supplemental B8 decreased concentrations of ruminal biohydrogenation intermediates and odd- and branched-chain FA in colostrum and milk fat. Moreover, postpartum dry matter intake for B8+ cows tended to be lower by 1.6 kg/d. These results could indicate ruminal perturbation caused by the B8 supplement, which was not protected from rumen degradation. Under the conditions of the current study, in contrast to B8+/B9B12? cows, B8?/B9B12+ cows produced more milk without increasing dry matter intake, although these cows had greater body fat mobilization in early lactation as suggested by the FA profile and BW loss.  相似文献   
9.
针对废旧纺织品循环利用中聚酯纤维、棉纤维混纺纱线结构紧密缠绕,难以分离而无法加工的问题,采用环境友好的草酸体系选择性水解混纺织物中的棉纤维,从而释放聚酯纤维实现有效分离,并对草酸体系分离工艺进一步优化。研究表明:与无机酸相比,在相同反应条件下,草酸可达到与盐酸相当的分离效果且所得聚酯纤维形态更完整,棉纤维水解程度更低,水解产物分布更窄;在草酸浓度为0.07 mol/L、反应温度为130℃、反应时间为3 h的条件下,聚酯/棉混纺织物的分离效果最优;其中棉纤维水解为纤维素材料,得率为91.46%,另有小部分水解为葡萄糖或低聚糖;聚酯纤维回收率高达99.28%,且保留了原有聚酯纤维的性能,可直接生产加工;该反应体系可循环利用多次,实现了废旧聚酯/棉混纺织物的高效综合利用。  相似文献   
10.
以青海的黑枸杞为主要原料,以植物乳杆菌(Lactobacillus plantarum)为发酵菌种,制备黑枸杞乳酸菌饮料,并采用单因素试验和响应面试验优化其发酵工艺条件。结果表明,最佳发酵工艺条件为固液比1∶25(g∶mL),植物乳杆菌接种量2.0%,发酵时间6 h,装液量40%。在此最佳条件下,黑枸杞乳酸菌饮料感官评分为9.3分,总糖含量为0.17 mg/mL,总酸含量为1.69 g/L,花青素含量为52.75 mg/L、总黄酮含量为0.07 mg/mL、总酚含量为0.99 mg/mL。  相似文献   
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