国产bbaaaaa片,成年美女黄网站色视频免费,成年黄大片,а天堂中文最新一区二区三区,成人精品视频一区二区三区尤物

您現(xiàn)在的位置: 首頁> 研究主題> 超聲輻射

超聲輻射

超聲輻射的相關(guān)文獻(xiàn)在1990年到2021年內(nèi)共計(jì)237篇,主要集中在化學(xué)、化學(xué)工業(yè)、一般工業(yè)技術(shù) 等領(lǐng)域,其中期刊論文189篇、會議論文20篇、專利文獻(xiàn)169508篇;相關(guān)期刊111種,包括中國超聲醫(yī)學(xué)雜志、工業(yè)催化、化工進(jìn)展等; 相關(guān)會議19種,包括2013年中國工程熱物理學(xué)會多相流學(xué)術(shù)年會、2011中國西部聲學(xué)學(xué)術(shù)交流會、“佶龍杯”2010年江蘇印染學(xué)會年會等;超聲輻射的相關(guān)文獻(xiàn)由592位作者貢獻(xiàn),包括徐國財(cái)、李記太、王艷麗等。

超聲輻射—發(fā)文量

期刊論文>

論文:189 占比:0.11%

會議論文>

論文:20 占比:0.01%

專利文獻(xiàn)>

論文:169508 占比:99.88%

總計(jì):169717篇

超聲輻射—發(fā)文趨勢圖

超聲輻射

-研究學(xué)者

  • 徐國財(cái)
  • 李記太
  • 王艷麗
  • 譚德新
  • 陳志剛
  • 李同雙
  • 邊延江
  • 劉卉閔
  • 崔朋雷
  • 張冬暖
  • 期刊論文
  • 會議論文
  • 專利文獻(xiàn)

搜索

排序:

年份

    • 任益達(dá)
    • 摘要: 室溫超聲輻射下,通過采用乙酰乙酸甲酯、鹽酸羥胺和苯甲醛為反應(yīng)原料的三組分鍋反應(yīng),并以純水和1:1乙醇為溶劑的兩個(gè)反應(yīng)體系進(jìn)行對比,合成了一系列3-甲基-4-芳亞甲基-異噁唑-5(4H)-酮衍生物.通過分析不同溶劑對于此反應(yīng)的影響可以得出,以水為溶劑的反應(yīng)體系相較于1:1乙醇反應(yīng)體系反應(yīng)更困難.
    • 龍相州; 茍小龍
    • 摘要: 為了揭示超聲對液體燃料燃燒的影響機(jī)制,采用高速攝影儀、紋影儀和激光誘導(dǎo)熒光(PLIF)等測試手段對超聲場中液滴燃燒過程的相關(guān)參數(shù)進(jìn)行了測量.并結(jié)合有限元模擬軟件COMSOL MULTIPHYSICS,分析了正庚烷液滴在超聲作用下的自由基分布以及蒸發(fā)燃燒特性.結(jié)果表明,超聲對火焰形狀、燃燒速率以及自由基分布有著顯著的影響,其中超聲聲輻射力促進(jìn)流動(dòng)與蒸發(fā)是影響液滴燃燒的重要因素之一,超聲通過改變蒸氣的聚集形態(tài)進(jìn)而影響火焰.進(jìn)一步研究發(fā)現(xiàn),超聲對液滴燃燒特性的影響與聲場的分布直接相關(guān),且波節(jié)與波腹對液滴燃燒的促進(jìn)與抑制效果明顯不同.本研究在一定程度上揭示了超聲波影響液體燃料燃燒的機(jī)制,證實(shí)了超聲波在穩(wěn)燃以及燃燒調(diào)控方面的可行性.
    • ZENG Yu-cai; LIU Xiao-ling; YANG Su-zhen; GUO Li-man
    • 摘要: 在超聲輻射下,無溶劑K2CO3催化芳醛與氰基乙酸酯發(fā)生Knoevenagel反應(yīng)合成4種2-氰基肉桂酸酯和6種4H-色烯衍生物.實(shí)驗(yàn)結(jié)果表明:當(dāng)苯甲醛與氰基乙酸甲酯用量各為10 mmol,無水碳酸鉀用量為1 mmol,超聲功率為150 W,室溫下反應(yīng)30 min以94.6%高產(chǎn)率得到2-氰基肉桂酸甲酯;推電子基的4-取代苯甲醛與氰基乙酸酯的縮合產(chǎn)率明顯下降.當(dāng)水楊醛用量為10 mmol,氰基乙酸乙酯用量為22.5 mmol,無水碳酸鉀用量為0.1 mmol,超聲功率為250 W,30°C下反應(yīng)20 min以91%產(chǎn)率得到4H-色烯衍生物;推電子基的5-取代水楊醛則不能反應(yīng).產(chǎn)物結(jié)構(gòu)通過熔點(diǎn)測定、IR和1H NMR進(jìn)行表征.
    • 高旭; 楊杰; 王佳楠; 鄧仰平; 蔣小強(qiáng); 王世范
    • 摘要: 以芳香醛、乙二胺、丙酮和乙醛為起始原料,在超聲波促進(jìn)下采用一鍋煮法,合成了8個(gè)咪唑烷衍生物(c1~c8,其中c3~c8為新化合物),其結(jié)構(gòu)經(jīng)1H NMR,IR,MS(ESI)和XRD表征.與傳統(tǒng)"三步加熱"反應(yīng)相比,微波一鍋法將反應(yīng)時(shí)間從2~3 h縮短至0.5 h,總收率從50%提高至80%以上.
    • 謝曉蓉; 佘一玄; 吳會蕓; 秦志平; 高旭; 王世范
    • 摘要: 以乙酰乙酸乙酯為起始原料,在金屬鈉和碘催化下制得二乙酰琥珀酸二乙酯;在超聲波促進(jìn)下,氨基酸與二乙?;晁岫阴グl(fā)生縮合反應(yīng),合成了7個(gè)新型的N-羧基吡咯衍生物,產(chǎn)率70% ~84%,其結(jié)構(gòu)經(jīng)1 H NMR,IR和MS(ESI)表征.
    • 范超; 馬養(yǎng)民; 劉存弟; 程佩; 賈斌
    • 摘要: 在超聲輻射和哌啶催化反應(yīng)條件下,1,3-二氫吲哚-2-酮(1)與芳香醛2a~ 2m發(fā)生Knoevenagel縮合反應(yīng),合成了一系列3-芳亞甲基吲哚-2-酮衍生物3a ~3m.該方法具有產(chǎn)率高、反應(yīng)時(shí)間短、后處理簡單和環(huán)境友好等優(yōu)點(diǎn),產(chǎn)物通過1H NMR、13C NMR和HRMS手段進(jìn)行結(jié)構(gòu)表征,并通過核磁2D NOESY確定了所有化合物幾何構(gòu)型.初步抑菌活性測試結(jié)果表明,化合物3d對革蘭氏陽性菌具有較好的抑制作用,最小抑菌濃度(MIC)為15.6μg/mL,化合物3f、3g、3h和3k對油菜菌核病菌表現(xiàn)出良好的抑制活性,MIC為62.5 μg/mL,與陽性對照多菌靈相當(dāng).此外,對此類化合物的構(gòu)效關(guān)系進(jìn)行了討論.%A series of 3-arylidene-indolin-2-one derivatives were conveniently synthesized by the Knoevenagel condensation of aromatic aldehydes 2a ~ 2m with 2-dihydroindol-2-one under ultrasonic.This protocol has the advantages of higher yield,simple experimental procedures,shorter reaction time,environmentally benign procedure.The structures of all products were determined by 1H NMR,13C NMR and HRMS spectra,with the configurations confirmed by 2D NOESY analysis.The preliminary biological activities assays indicated that compound 3d possessed significant activities against Gram-positive bacteria with the minimum inhibitory concentration (MIC) of 15.6μg/mL.Compounds 3f,3g,3h and 3k showed significant inhibitory activities against Sclerotinia sclerotiorum with MIC of 62.5μg/mL,which were comparable with the positive control carbendazim.In addition,the structure-activity relationship was also discussed.
    • 安康; 梅舉; 姚麗萍; 張震; 白景峰; 湯敏
    • 摘要: 目的·評估超聲形成的聲學(xué)力能否減少心臟手術(shù)后進(jìn)入腦血管的微栓.方法·實(shí)驗(yàn)用小型豬7頭,3頭豬用于注射氣體微栓,3頭豬用于注射固體微栓,另1頭豬用于檢測超聲能量對于組織有無損傷.常規(guī)麻醉后游離并暴露右頸總動(dòng)脈、左心耳、升主動(dòng)脈和近端無名動(dòng)脈.于左心耳插入一根冷灌針頭,用于注射氣體微栓或固體微栓.將制作好的水囊超聲探頭置于升主動(dòng)脈與無名動(dòng)脈分叉處.另一超聲探頭置于右頸總動(dòng)脈用于檢測微拴.分別于關(guān)閉和開啟超聲能量后注射微栓混懸液10 mL(氣體或固體),各重復(fù)3次,觀察超聲屏蔽前后通過右頸總動(dòng)脈的微栓變化.對造影動(dòng)態(tài)圖像進(jìn)行時(shí)間-強(qiáng)度曲線分析.另取1頭豬,將水囊超聲探頭置于升主動(dòng)脈與無名動(dòng)脈分叉處,用同等強(qiáng)度的超聲能量輻射5 min,之后分別于超聲照射部位及非照射部位取少量主動(dòng)脈、氣管、食管組織,行蘇木精-伊紅染色(H-E染色).結(jié)果·超聲結(jié)果表明,在超聲能量輻射后注射微栓,右頸總動(dòng)脈內(nèi)關(guān)注區(qū)的超聲均值強(qiáng)度較未經(jīng)超聲能量輻射注射微栓時(shí)顯著下降.其中氣體微栓的超聲均值強(qiáng)度由未經(jīng)輻射的128.8±32.7降至輻射后的56.4±21.1(P=0.000);固體微栓的超聲均值強(qiáng)度由未經(jīng)輻射的109.8±19.9降至輻射后的75.4±21.9(P=0.000).超聲輻射部位與非超聲輻射部位的主動(dòng)脈、氣管、食管的組織結(jié)構(gòu)無明顯差異.結(jié)論·采用超聲輻射能夠有效屏蔽術(shù)中產(chǎn)生的微栓,減少隨血流進(jìn)入腦血管的微栓數(shù)目,可能有助于降低心臟外科手術(shù)后神經(jīng)系統(tǒng)并發(fā)癥的發(fā)生.%Objective·To evaluate if ultrasound acoustic force can reduce cerebrovascular micro-emboli after cardiac surgery. Methods·Seven pigs were used during the experiment, three for air emboli injection, three for solid emboli injection, and one for safety study. After anesthesia, right carotid artery, left atrial appendage, ascending aorta, and proximal innominate artery were exposed surgically. An intravenous catheter was inserted into left atrial appendage for injecting air or solid micro-emboli. The ultrasound transducer was placed at the bifurcation of the aorta and the innominate artery, with the sonic beacon toward the descending aorta. Micro-emboli through the right carotid artery were monitored by ultrasound transducer. Micro-emboli mixture (10 mL, air emboli or solid emboli) was injected with or without ultrasonic activation, each repeating three times. Micro-emboli through right carotid artery were measured under each condition. Ultrasonic time-intensity curves were performed and analyzed. For safety test, ultrasound with the same energy on a pig for 5 minutes was applied. The tissue samples were obtained for pathological evaluation from sonicated and non-sonicated areas of the aorta, trachea and the esophagus. Results·Ultrasonic time-intensity curve showed that the mean ultrasonic intensity of the right common carotid artery significantly decreased after ultrasonic activation. The intensity of air emboli reduced from 128.8±32.7 to 56.4±21.1 (P=0.000), while the intensity of solid emboli reduced from 109.8±19.9 to 75.4±21.9 (P=0.000). H-E staining of the surrounding tissues showed no differences between sonicated and non-sonicated areas of the aorta, trachea and the esophagus. Conclusion·Ultrasonic acoustic force can decrease the number of micro-emboli that enter the brain. Thus, it may lower the risk of postoperative neurological complications after cardiac surgery.
    • 趙煒; 李偉鋼; 劉浩淼; 劉開帥; 敖磊; 方君基; 關(guān)尹雙
    • 摘要: 分別考察了酸處理、堿處理、氧化處理和超聲輻射處理對從麥稈中脫除木質(zhì)素的影響.酸處理能降低半纖維素含量;堿處理能夠減少木質(zhì)素含量;氧化處理能減少木質(zhì)素及半纖維素含量;超聲處理較好的分散麥稈并使之與溶劑充分接觸,進(jìn)而促進(jìn)木質(zhì)素的脫除.通過正交實(shí)驗(yàn)得到從麥稈中脫除木質(zhì)素的優(yōu)化條件為:堿性H2 O2的乙醇混合溶液中NaOH濃度為1mol/L、H2 O2體積分?jǐn)?shù)為1.5%、雙氧水與乙醇體積比1:1,麥稈超聲預(yù)處理5min,麥稈用量為2.5g,固液比1:20;麥稈和混合溶液超聲處理5min,然后在80°C下處理3h.在此條件下,木質(zhì)素脫除率可達(dá)到88%.%The effects of acid treatment,base treatment,oxidation treatment and ultrasonic irradiation on the removal of lignin from wheat stalk powder (WSP ) were investigated. Hemicellulose content is decreased by acid treatment and lignin content is decreased by base treatment. Hemicellulose and lignin are decreased by oxidation treatment. Ultrasonic treatment can effectively disperse WSP and make it full contact with the solvent,thereby promoting the removal of lignin. The treatment process of WSP was optimized by orthogonal experiment in order to remove lignin from WSP. The optimum conditions of treatment are that the concentrations of NaOH and H2 O2 in alkaline and H2 O2 mixed solution are 1mol/L and 1.5%H2 O2 ,the ratio of alkaline H2 O2 to ethanol is 1:1,and that 5g of WSP is pretreated under ultrasonic irradiation for about 5min,mixed with a mixing solution of about 20times,and then treated under ultrasonic irradiation for 5min,and then treated at a temperature of 80°C for 3h. Under these conditions,the removal rate of lignin from WSP reaches 88%.
    • 林偉; 鄭永祥; 黃志斌; 史達(dá)清
    • 摘要: A rapid and efficient ultrasound-assisted method for the synthesis of 2-thioxo-2H-thiopyran and 2-amino6-thioxodihydropyridine derivatives by the reaction of 2-(1-phenylethylidene)malononitrile and carbon disulfide or isothiocyanatobenzene catalyzed by NaOH has been developed.This protocol has the advantages of simple operation,short reaction times,high yields,and environmental friendliness.The structures of all the products were characterized by 1H NMR,13C NMR,IR and MS techniques.The reported method is the efficient approach for the synthesis of 2-thioxo-2H-thiopyran and 2-amino-6-thi-oxodihydropyridine derivatives.%探索了一種超聲輻射下氫氧化鈉催化的芳亞乙基丙二腈與二硫化碳或異硫氰酸酯的反應(yīng),方便、快速地合成了2-硫代羰基-2H-噻喃和2-氨基-6-硫代羰基二氫吡啶衍生物.本方法具有操作簡單、反應(yīng)時(shí)間短、產(chǎn)率高、環(huán)境友好等優(yōu)點(diǎn).產(chǎn)物的結(jié)構(gòu)經(jīng)過核磁共振氫譜和碳譜、紅外及質(zhì)譜進(jìn)行確定.本報(bào)道的方法為合成2-硫代羰基-2H-噻喃和2-氨基-6-硫代羰基二氫吡啶衍生物提供了一條有效途徑.
    • 甘穎; 葉翠情; 邢宏龍; 高圣濤; 徐國財(cái)
    • 摘要: 在不加任何還原劑的條件下,采用超聲輻射引發(fā)溶液聚合制備納米鐵/聚(甲基丙烯酸甲酯-苯乙烯)[P (MMA-St)]復(fù)合材料。用XRD、TEM、XPS、FT-IR和TG等分析方法表征結(jié)構(gòu)、熱穩(wěn)定性以及納米鐵與基體 P (MMA-St)之間的相互作用。結(jié)果表明,納米鐵粒子具有體心立方晶系結(jié)構(gòu),粒徑在20~40 nm,且與基體中羰基碳原子和氧原子存在相互作用;納米鐵/P(MMA-St)復(fù)合材料熱穩(wěn)定性好,氮?dú)鈿夥障略?60°C開始分解,在850°C的高溫下僅損失32%。%Nano-iron/poly(methyl methacrylate-styrene)[P(MMA-St)]composites were synthesized by solution polymerization ultrasonically without addition of reducer.The morphology,microstructure,thermal stability and the interaction between nano-iron and P(MMA-St)matrix of the composites were characterized by means of techniques including X-ray diffractometer (XRD),transmission electron microscopy (TEM),X-ray photoelec-tron spectroscopy (XPS),Fourier transform infrared spectroscopy (FTIR)and thermal-gravimetry analyzer (TGA)et al.The results showed that the size of nano-iron particles was about 20-40 nm with possessed cubic face-centered structure,and there existed an interaction between nanoiron particles and CO from P(MMA-St) matrix;the nano-iron/P (MMA-St ) composites was highly thermally stable;the decomposition of it was 660 °C,and about 32% loss weight was measured at 850 °C under nitrogen atomosphere.
  • 查看更多

客服郵箱:kefu@zhangqiaokeyan.com

京公網(wǎng)安備:11010802029741號 ICP備案號:京ICP備15016152號-6 六維聯(lián)合信息科技 (北京) 有限公司?版權(quán)所有
  • 客服微信

  • 服務(wù)號