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511.
改进GC/FID法连续观测大气中CO浓度   总被引:1,自引:0,他引:1  
改进装配有氢火焰离子化检测器(即FID)的气相色谱仪(GC),可连续监测大气中痕量气体CO浓度.本系统采用单阀双柱反吹进样技术,优选前置柱能更有效地剔除杂质,提高了分析柱效率,保持色谱基线平稳,提高分辨率和定量分析的准确率.优化后的气路设计与色谱柱的改进,使GC/FID对CO的最低检出限达到10×10-9、精密度误差小于2%,准确度在±2%之内.将气相色谱与动态气体稀释仪耦合使系统能够自动进行工作曲线校准,系统自动采样、分析和标定,无需人员职守.对北京大气CO连续观测结果表明,北京大气CO浓度变化受气象要素与排放源双重控制.  相似文献   
512.
以水解法制备的锐钛矿型TiO2为载体,制备了CuO/TiO2型光催化剂.以亚甲基蓝为对象,在可见光照射下研究了H2O3加入量、pH值和催化剂投加量对脱色效果的影响,同时与改性前的TiO2催化剂进行了脱色效果的对比.结果表明亚甲基蓝在碱性条件下能较好脱色,H2O2用量和CuO/TiO2催化剂投加量分别为每1 000 mL反应液各加入10 mL和0.1 g时脱色最好;另外,TiO2催化剂也在碱性条件下能较好脱色,H2O2用量和催化剂投加量分别为每1 000 mL反应液各加入12.5 mL和0.1 g时脱色最好.最优条件下对比实验表明,CuO/TiO2型催化剂在可见光照射下具有很高的催化活性,亚甲基蓝2 h脱色率达到88%,远好于改性前的TiO2和Degussa P25催化剂.  相似文献   
513.
Nitrate (NO(3)(-)) is a commonly found contaminant in groundwater and surface water. It has created a major water quality problem worldwide. The laboratory batch experiments were conducted to investigate the feasibility of HCl-treated zero-valent iron (Fe(0)) combined with different adsorbents as hybrid systems for simultaneous removal of nitrate (NO(3)(-)) and ammonium (NH(4)(+)) ions from aqueous solution. The maximum NO(3)(-) removal in combined Fe(0)-granular activated carbon (GAC), Fe(0)-filtralite and Fe(0)-sepiolite systems was 86, 96 and 99%, respectively, at 45 °C for 24 h reaction time. The NO(3)(-) removal rate increased with the increase in initial NO(3)(-) concentration. The NO(3)(-) removal efficiency by hybrid systems was in the order of sepiolite > filtralite > GAC. The NH(4)(+) produced during the denitrification process by Fe(0) was successfully removed by the adsorbents, with the removal efficiency in the order of GAC > sepiolite > filtralite. Results of the present study suggest that the use of a hybrid system could be a promising technology for achieving simultaneous removal of NO(3)(-) and NH(4)(+) ions from aqueous solution.  相似文献   
514.
Distinguishing and quantifying anthropogenic trace metals and phosphorus accumulated in sediment is important for the protection of our aquatic ecosystems. Here, anthropogenic proportion and potential sources of trace metals and phosphorus in surface sediments of Chaohu Lake were evaluated based on the exhaustive geochemical data. The analysis shows that concentrations of major and trace metals, and phosphorus, displayed significant spatial diversity and almost all elements were over the pre-industrial background value, which should be related to the variations of sediment composition partially. Therefore, conservative element normalization was introduced and calculated enrichment factors (EFs) of the elements were referenced highlighting the human contamination. EFs of the major and trace metals, except Zn, Pb, and Cu, were all nearly 1.0, indicating the detrital origin. The EFs of Zn, Pb, Cu and phosphorus were 1.0–10.4, 1.0–3.8, 1.0–4.9, and 1.0–7.6, respectively, showing moderate to significant contamination. Higher EFs of Zn, Pb and Cu occurred in the mouth areas of Nanfei River and Zhegao River, and they decreased to the lake center in the northwest and northeast lake areas, respectively. We deduced that anthropogenic Zn, Pb, and Cu were mainly from urban and industrial point sources and the non-point sources of atmospheric deposition contributed little to their contamination. The EFs of phosphorus showed similar spatial degradation with that of Zn, Pb, and Cu. Moreover, higher EFs (>1) of phosphorus also occurred in other areas adjacent to the river mouths besides Nanfei River and Zhegao River. This indicated that the non-point agricultural source may also be responsible for the contamination of phosphorus in Chaohu Lake in addition to the urban sewage sources. Anthropogenic phosphorus was mainly concentrated in the speciation of NaOH-P, which had higher potential biological effects than the detrital proportion. Concentrations of Zn, Pb and Cu surpassed the threshold effect concentrations (TEC) of consensus-based sediment quality guidelines of freshwater ecosystems, especially in the contaminated northwest area of Chaohu Lake. This highlighted the contributions of anthropogenic contamination to the elevated potential biological effects of trace metals. Though there had been no obvious human contamination of Cr and Ni in Chaohu Lake, concentrations were all over the TECs, which may be due to higher background levels in the parent materials of soils and bedrocks in Chaohu Lake catchment.  相似文献   
515.
Lake eutrophication is harmful and difficult to predict due to its complex evolution. As an alternative to existing mechanistic models, a Markov chain model was developed to predict the development of lake eutrophication based on an 11-year dataset in 41 lakes of the Yangtze River Basin. This model was validated using a real-time update strategy and was demonstrated to be reliable. Based on the dataset, the lake eutrophication dynamics from 2000 to 2010 were analyzed. Lakes with different trophic states from 2011 to 2050 and their responses to different water management practices were simulated based on the developed model. The simulation results show that lake eutrophication would worsen from 2011 to 2040; however, eutrophication could be significantly alleviated by changing 100 km2 of hypereutrophic lakes into eutrophic lakes per year from 2010 to 2020. The nutrient conditions in most of the lakes in the Yangtze River Basin show that phosphorus control would be more efficient than nitrogen control in eutrophication management practices. This case study demonstrates the utility of Markov chain models in using prior information to predict the long-term evolution of lake eutrophication at large spatial scales. The Markov chain technique can be easily adapted to predict evolutionary processes in other disciplines.  相似文献   
516.
采用溶液培养的方法探讨根表铁膜形成对水稻吸收积累和转运稀土元素Ce的影响。结果表明,Ce污染胁迫可抑制水稻根表铁膜的形成,根表铁膜吸附的Ce量随着溶液中Ce浓度的提高而增加。根表铁膜形成可降低水稻根系但提高水稻茎叶对Ce的吸收积累。当溶液中Ce浓度为0.1、0.5和1.0 mmol·L~(-1)时,铁膜诱导组水稻根系Ce含量分别比非诱导组水稻根系Ce含量降低38.60%、45.94%和32.75%,诱导组水稻茎叶Ce含量分别比非诱导组水稻茎叶Ce含量提高42.37%、28.87%和22.62%。根表铁膜形成可影响Ce在水稻植株中的富集和转运能力。非诱导组水稻根系富集Ce的能力远大于茎叶。诱导组水稻根系对Ce的富集能力最强,其次是根表铁膜,最后是水稻茎叶。诱导组水稻根系Ce转运系数显著大于非诱导组的根系,说明根表铁膜形成可促进水稻根部Ce向茎叶中转运。可见,根表铁膜对水稻吸收转运稀土元素的影响机理比较复杂。  相似文献   
517.
将太原东山新沟垃圾填埋场矿化垃圾筛分为900~300μm、300~150μm、150~105μm、105~90μm和90~0μm共5个不同粒径范围,制备浸出液。在分析不同粒径矿化垃圾浸出液的理化指标基础上,研究了矿化垃圾浸出液对大麦和斑马鱼胚胎生长发育的影响。结果显示,矿化垃圾浸出液p H值随粒径的减小而减小,电导率、CODCr、全盐量和总氮则随粒径的减小而增大。矿化垃圾浸出液对大麦的萌发、根长和芽长均表现出抑制作用,且抑制作用随粒径的减小而显著增加,90~0μm抑制作用最强,具体表现为染毒1 d、2 d和3 d后,大麦种子处理组萌发率为对照组的39.74%、56.38%和59.81%;染毒3 d、5 d和7 d后,根长分别为对照组的57.08%、48.33%和41.66%;芽长分别为对照组的66.60%、64.79%和61.65%。斑马鱼胚胎暴露于不同粒径的矿化垃圾浸出液中,胚胎生长发育的毒害作用与粒径大小呈现明显负相关关系,即在最小粒径90~0μm处理后,卵凝结、血循环异常、孵化率、心包水肿及脊柱畸形影响作用达到最大,这5个指标值分别为40.28%、50.00%、51.39%、31.94%和29.17%。以上研究表明,矿化垃圾浸出液对大麦和斑马鱼胚胎生长发育的毒性效应与矿化垃圾粒径分布显著相关,小粒径矿化垃圾(90~0μm)的生态毒性效应最大。  相似文献   
518.
从生物陶粒反应器中筛选出6株异养硝化细菌,将异养硝化细菌扩大培养后,建立SBR反应器并进行了氨氮去除的试验研究。在SBR反应器进入稳定运行阶段时,可以观察到系统对于氨氮的去除率稳定在82.96%左右,表现出较好的氨氮去除效果;出水亚硝酸盐含量一直维持在较低的水平,其最大值不超过3.84mg·L-1;COD的平均去除率为54.72%,基本实现了同一反应器中的有机物和氨氮的共同去除。异养硝化SBR反应器温度为29℃时,反应器对氨氮和总氮的去除能力最大为82.28%和47.27%;在pH值为8.0时,氨氮去除率最高达到80.15%。C/N〈4.5时,随着C/N比的增加,氨氮和总氮的去除率快速增加;在C/N为6时,氨氮去除率最高达到87.62%。  相似文献   
519.
施肥及秸秆还田处理下玉米季温室气体的排放   总被引:14,自引:0,他引:14  
以华北地区冬小麦-夏玉米轮作农田为研究对象,在玉米整个生长季,运用静态箱法针对正常施肥及正常施肥结合秸秆还田处理进行了为期3年N2O排放通量的连续观测,并开展了1季CO2和CH4交换通量的研究.在玉米整个生长过程中施肥阶段N2O的排放量占到了总排放量的83%—96%,表明现有化肥的使用明显导致了农田N2O排放增加.与控制地相比,施肥和耕种可导致玉米田CO2排放明显增加,且正常施肥及秸秆还田样地CO2排放主要集中在苗期至吐丝期.控制地、正常施肥样地及施肥结合秸秆还田样地CH4的累积排放量均为负值,说明旱地土壤是CH4的一个汇.秸秆还田在一定程度上增加了玉米季N2O和CO2的排放量,但对CH4的吸收有所抑制.正常施肥样地和秸秆还田样地全球净增温潜势分别为-1392.8 kg C.hm-2和-179.2 kg C.hm-2,表明华北农田在现有耕作方式下是大气温室气体的一种重要汇.  相似文献   
520.
陈艳  罗继  袁斌  刘绿叶  张艳海 《环境化学》2012,31(5):748-751
采用在线柱浓缩-超快速液相色谱联用技术测定水体中痕量百草枯和敌草快.水样无需样品前处理,过滤后即可进样.采用固相萃取小柱富集待测物,以色谱梯度泵完成样品的净化后,利用阀切换技术将待测物反冲至分析柱进行分离,以二极管阵列检测器定量.方法在1.0—20.0μg.L-1范围内线性良好,百草枯和敌草快的线性相关系数分别为0.9997和0.9989.百草枯和敌草快的检出限(S/N=3)分别为0.10、0.12μg.L-1,加标回收率在96.0%—98.0%之间.用所建立的方法测定了水中痕量的百草枯与敌草快的含量,结果令人满意.  相似文献   
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