膠合物鏡 的英文怎麼說

中文拼音 [jiāojìng]
膠合物鏡 英文
cemented lens
  • : Ⅰ名詞1 (某些具有黏性的物質) glue; gum 2 (橡膠) rubber 3 (姓氏) a surname Ⅱ動詞(用膠粘) st...
  • : 合量詞(容量單位) ge, a unit of dry measure for grain (=1 decilitre)
  • : 名詞1 (東西) thing; matter; object 2 (指自己以外的人或與己相對的環境) other people; the outsi...
  • : Ⅰ名詞1 (鏡子) looking glass; mirror 2 (幫助視力或做光學實驗的器具) lens; glass 3 (姓氏) a s...
  1. We can see from the photos of the sem that the diameters of the powers of this tree land of materials obtained by the system of trion x - 100 / caprylic alcohol / cyclohexane / water are about 20 nm. by means of uv - vis, atomic absorption spectrometry and so on, nanoparticles of this three kind of anode materials are synthesized

    利用trionx - 100 /正辛醇/環己烷/水反束體系制備出三種質的粉體,掃描電子顯微照片顯示粒子的粒徑在20nm左右,分佈均勻;此外還利用uv - vis 、原子吸收光譜等測試手段,都表明成出了三種正極材料的納米粒子。
  2. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如下:皮下包埋卜周者,無細胞真皮基質漸與周圍組織粘附,顏色由蒼白轉紅;皮下包埋3周者,無細胞真皮基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ) 。光下術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在原纖維上,少量血管內皮細胞浸入基質;術后34周,無細胞真皮基質內較多的血管形成,故可認為無細胞真皮基質免疫原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真皮替代。第四部分無細胞真皮基質與自體斷層皮片復移棺的研究, sd大鼠10隻,在其背部卜方造成全厚皮膚缺損的創面
  3. When fillings is other materials ( unprocessed montmorillonite, powder coal ash, co - composite of powder coal ash and organo - montmorillonite, co - composite ofcarbonizing calcium and organo - montmorillonite ) in the binder and content of organo - montmorillonite in the binder is five percent decided by tensile - shear experiment, tensile - shear strength of binder is up to tiptop ; at the same time, this paper carries out abrasion experiment, and, by comparison, concludes abrasion property of coating is optimum when content of organo - montmorillonite in the binder coating is five percent, and observes abrasion sample under set

    粘劑中填料為其它質(未處理蒙脫土、粉煤灰、粉煤灰和有機化蒙脫土共復、碳化鈣和有機化蒙脫土共復)時,通過拉伸剪切試驗確定粘劑中有機化蒙脫土含量為5時,粘劑的拉伸剪切強度最高;同時進行了沖蝕磨損試驗,通過比較得出,當粘劑塗層中有機化蒙脫土含量達到5時,塗層的耐沖蝕磨損性能最佳,並對沖蝕磨損試樣在掃描電子顯微( set )上進行觀察。
  4. The composition of sample was identified by means of x - ray diffractometer ( xrd ). magnetic properties were measured by vibrating sample magnetometer ( vsm ). the combustion behavior and crystallization process of the gel were studied by means of differential thermal analysis - thermogravimetric analysis ( dta - tg )

    利用x射線衍射儀( xrd )確定樣品相,振動樣品磁強計( vsm )進行磁性測量,綜熱分析儀研究凝的燃燒和析晶過程,掃描電子顯微( sem )和透射電子顯微( tem )觀察粉末的形貌與粒度。
  5. The results of the uni - factor experiments and perpendicular experiments show their best mechanic synthesizing craft as followed : nvp ( 10 % wt ), kh570 ( 20 % wt ), hema ( 70 % wt ), initiator ( 0. 2 % wt ), crosslinker ( 20 % wt ), reacting 20 hours under 80 c. the factors which influenced organic silicon modified pvp hydrogel soft contact lens material ' s swelling capabilities were researched, which included temperature, monomer content, ion concentration etc. the experiments showed the equation swelling content ewc improved with the increase of nw, droped with the increase of kh570 and ion concentration, improved then droped with the raise of temperature, and hydrogels got the least ewc at 45 c. experiment carried on todiscuss water dehydration mechanism of organic silicon modified pvp hydrogel soft contact lens materials, which showed dehydration process could be divided into evaporating stage and diffusing stage

    正交實驗結果表明, nvp ? hema ? kh570共聚的機械性能最佳時,其成工藝條件為: nvp用量10 (質量百分含量,下同) , kh570用量20 , hema用量70 ,引發劑aibn用量0 . 2 ,交聯劑nmba用量0 . 2 ,反應溫度為80 ,反應時間16h 。討論了單體配比、溶脹溫度、離子濃度等因素對有機硅改性pvp水凝軟接觸透材料溶脹性能的影響。實驗得出:水凝材料的平衡溶脹度ewc隨單體nvp含量的增加而增大, ewc隨kh570用量的增加而減小,隨離子濃度的增大而略微降低,隨溶脹溫度的升高先稍微下降後有所提高, 45時平衡含水量最低。
  6. The wave - deviation methods are concerned, basing on the relations between the wave - deviation and spherical aberration, wave - color - deviation and color deviation. after the equation of optical system, initial structure resolved, the glass catalog having been allocated in the computer, the original solution can be worked out for the doublet and air - spaced doublet, triplet and air - spaced triplet rapidly and precisely. after a little modification by the computer, the satisfied results will be obtained

    論文由波像差與球差的關系,波色差與色差的關系推導出了波差法求解光學系統初始結構的方程式,再配以玻璃庫程序,可以較快、較準確地求解出雙、雙分離、三、三分離的初始解,然後再進計算機稍加校正,就可以得到滿意的結果。
  7. With the reference of many relevant materials, the author prepared a fined molybdenum disulfide powder with a average size of 800nm by ball milling, and a nano - copper with average size of 30nm in micromulsion solution method, and synthesized surface - modified titanium dioxide nanoparticles with average size of 40nm in organic media via sol - gel method. the tribological performances of three particles were studied by universal test as well, with the result of fined molybdenum disulfide powder with good reducing wear and antiwear performance at low load, nano - copper with good reducing wear and antiwear performance at high load, surface - modified titanium dioxide nanoparticles maintaining stable reducing wear and antiwear performance from low load to high load due to its characteristics of organic and inorganic nanocomposite. the results indicate that the nanocomposite is the most perspective oil additive. the reducing wear and antiwear mechanism of nano oil additive was studied with in - situ tribochemical principle. nano additives possess broadly developing prospect with its above - mentioned performance

    在參閱了大量文獻的基礎上,分別採用了球磨法、微乳液法、溶?凝法制備了超細二硫化鉬、納米銅粒子、表面修飾納米二氧化鈦,經原子力顯微測試,獲得的超細二硫化鉬的粒度平均在800nm以內,納米銅粒子平均粒度約為30nm ,表面修飾納米二氧化鈦平均粒度約為40nm ,在萬能摩擦磨損試驗機上測試了三種粒子的摩擦學特性,結果表明:在理的添加濃度范圍內,超細二硫化鉬在低載時具有優良的減摩抗磨性能,納米銅在高載時具有比較好的減摩抗磨性能,表面修飾二氧化鈦粒子因具有有機與無機復的特性,從低載到高載都保持穩定的減摩抗磨性能。
  8. The infrared spectroscopy, transmission electron microscopy, light scattering and x - ray photoelectron spectroscopy are used to characterize the polymer structure and the morphology of the latex particles. the results demonstrate that composite latex with core / shell morphology is indeed successfully prepared

    利用紅外光譜、透射電、激光粒度儀、表面能譜分析等手段對聚的化學結構及乳粒粒子形態進行了表徵。
  9. In this article, bioaerosol mass spectrometry, an instrument for real - time detection of bioaerosols using simultaneous measurement of particle aerodynamic size and intrinsic fluorescence, real - time qpcr, and fcm / fl were discussed

    性氣質譜偵測儀(指即時偵測生性氣及微粒氣動直徑之儀器) 、即時定量酵素聚反應技術、螢光染色配螢光顯微將于本文中討論之。
  10. Although, challenging work remains to determine the interfering substances ( e. g. particulates ) of different environments, distinguish the specific species with specific probe, and overcome the high detection limit of fcm ( 10 ( 4 ) - 10 ( 8 ) cells ml ( - 1 ) ), literature reports suggested that fcm / fl has a great potential for real - time monitoring of bioaerosols

    雖然不同環境其介質之量測、建立特定菌種之特定引子及克服螢光顯微之高偵測極限,均有其挑戰性,本文建議使用螢光染色配螢光顯微對生性氣即時偵測有極大潛力。
  11. Amino acid molecules imprinted polymeric composite microspheres with magnetic susceptibility ( ms - smips ) were prepared by suspension polymerization ( sp ) and inverse emulsion - suspension polymerization ( iesp ), respectively. protein molecules imprinted soft - wet gel composite microspheres with magnetic susceptibility ( ms - pigms ) were prepared by inverse suspension polymerization ( isp ) and seeded inverse suspension polymerization ( sisp ), respectively. the resulting ms - smips and ms - pigms were characterized by scanning electron microscope ( sem ), thermogravimetric analyzer ( tg ), vibrating sample magnetometer ( vsm ), infrared spectrum ( ftir ), high performance liquid chromatography ( hplc ), and so on

    分別採用懸浮聚法和反相乳液?懸浮聚法制備了氨基酸分子印跡聚磁性復微球( ms - smips ) ;分別採用反相懸浮聚法和種子反相懸浮聚法制備了蛋白質分子印跡磁性軟濕凝微球( ms - pigms ) ;用掃描電子顯微、熱重分析儀、振動樣品磁強計、紅外光譜、高效液相色譜等對所制備的ms - smips和ms - pigms進行了表徵。
  12. The synthesis process of single - wall carbon nanotubes ( swnts ) by catalytically chemical vapor deposition ( ccvd ) was investigated and the product was characterized with transmission electron microscopy ( tem ), electron diffraction ( ed ), electron dispersive spectra ( eds ) and raman scattering spectra etc. pyrolysis of methane over solid catalysts prepared with impregnation, ion - adsorption precipitation, and sol - gel technique can all lead to the growth of swnts

    本文研究了單壁納米碳管的化學氣相沉積法( cvd )制備工藝,並運用透射電子顯微( tem ) 、 x - ray能譜( eds )與喇曼( raman )光譜等分析手段,對產及催化劑進行了表徵。採用浸漬法、吸附沉澱法與溶法等制備了催化劑,併成了單壁納米碳管。
  13. The resulting polymers were characterized by " h - nmr, ir, dsc, pom, gel permention chromatography ( gpc ). the relations between structures and properties were studied systemtically. the influences of the lateral rod content on the polymers " solubility and the stability of liquid crystalline states and chemical structures were discussed in detail

    經過凝色譜( gpc ) 、偏光顯微( pom ) 、差示掃描量熱( dsc ) 、 ~ 1h - nmr和ir對聚的化學結構和液晶性進行了表徵,系統研究了聚結構和性質之間的關系。
  14. The tio2, cds and cds - tio2 films on the common glass substrate were prepared, respectively, using ti ( oc4h9 ) 4, cd ( cooch3 ) 2 and scn2h4 as raw materials by sol - gel method. the influences of manifold preparing parameters ( such as the concentration of sol, the amount of the peg. the number of coatings, the heat - treated temperature and time ) on the structure and performance were studied

    本文採用溶-凝技術,以鈦酸丁酯、乙酸鎘和硫脲為原料,以普通玻璃片為載體,制備了納米tio _ 2薄膜、 cds薄膜和cds - tio _ 2復半導體薄膜,研究了制備過程中多種制備參數(如溶的濃度,聚乙二醇( peg )的加入量,鍍膜層數,熱處理溫度及時間)對薄膜結構和性能的影響,採用x -射線衍射( xrd ) 、掃描電( sem ) 、能譜分析( edxa ) 、紫外-可見吸收光譜( uv - vis )等測試手段對各薄膜進行了結構和性表徵。
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