酸化處理 的英文怎麼說

中文拼音 [suānhuàchǔ]
酸化處理 英文
acidizing
  • : 酸構詞成分。
  • : 處名詞1 (地方) place 2 (方面; 某一點) part; point 3 (機關或機關里一個部門) department; offi...
  • : Ⅰ名詞1 (物質組織的條紋) texture; grain (in wood skin etc ) 2 (道理;事理) reason; logic; tru...
  • 酸化 : acidate; acidulate; acidize; acidification酸化泵 acidizing pump; 酸化過程 acidization; 酸化劑 aci...
  1. Aerospace ; tempering of acrylic plastics ; directives for manufacture

    航空航天.丙烯酯塑料的軟.製造規程
  2. According to the research of physiological and biochemical indicators or index, components of soluble proteins, substrate protein of phosphorylation and the activity of protein kinase in low - temperature stress in the leaves of brassica oleracea l., we tried to find the law of the physiological and biochemical response of brassica oleracea l. leaf to low temperature. at the same time, discussion on the signal transduction can also provide further evidences for revealing the mechanism of low - temperature stress. the results are showed as follows : malondialdehyde ( mda ), superoxide dismutase ( sod ), ascorbate peroxidase ( asp ) and peroxidase ( pod ) activities were changed greatly after 0 ~ 30min ' s treating with low temperature

    本文以甘藍葉片為材料,通過對低溫5脅迫下甘藍生指標、可溶性蛋白組分以及磷底物蛋白、蛋白激酶活性的研究,以期找出甘藍葉片對低溫脅迫的生響應規律,為甘藍露地越冬栽培防範寒害提供論指導,同時對低溫脅迫下甘藍逆境信號傳導進行了探討,從而為徹底弄清低溫脅迫機提供進一步的證據,研究的主要結果如下:丙二醛含量( mda ) 、超氧物歧酶( sod ) 、抗壞血過氧物酶( asp )和過氧物酶( pod )活性在低溫0 30min發生顯著變,低溫3min后,甘藍葉片內mda含量基本沒有變5min時出現第一個峰值,達到對照的104 . 10 , 10min出現低谷,僅為對照的86 . 27 ,隨后再次上升, 30min時超過第一峰值,為對照的113 . 93 。
  3. The acidtreated packing causes release of co2 from inorganic carbonates.

    酸化處理過的填料會使co2從無機碳中釋放出來。
  4. Please keep in mind that the titanium products should be cleaned by soft fabric or a litter french chalk, not by acid and alkaline detergent. for the plastic and non - stainless steel products, should not be used in the moist floor or cleaned by the water directly. and the brass products have done by oxygenation, so that you only want to clean by soft frabic

    鈦金製品,切勿用、堿性清潔劑擦洗,只需用軟布或少許滑石粉擦之即光亮如新,非不銹鋼、塑料類產品不能使用在潮溫地面或直接用水沖洗;銅製品已做氧,切勿使用擦銅劑,只需用軟布擦之即可。
  5. The residue discharged during the operation process of the plant is pollution - free clean liquid, which has solved the difficult problem of waste acid and waste liquid generated from original purification equipments

    裝置運行過程中排出的殘液為無污染的潔凈液體,解決了困擾原凈裝置的廢液廢難題。
  6. 5. the specific surface area of precipitation type of sepiolite ( short fibrous structure ) increased only from 65. 61 m2 / g to 98. 57 m2 / g. this means that this type was not the suitable catalyzer carrier candidate

    5 .沉積型(短纖維結構)海泡石經過一熱活后其比表面積僅由65 . 61擴/ g上升98 . 57擴/ g ,因此不宜作催劑載體。
  7. 2. by activation - treating sepiolite with acid modifying, the channel between crystals, the porosity and the structure changed distinctly, and the specific surface area increased to 295. 39 m2 / g from 236. 26 m2 / g

    對海泡石進行的改性活使海泡石晶間管道、孔隙度和結構產生明顯變,海泡石比表面積由236 . 36m ~ 2 g上升到295 . 39m ~ 2 g 。
  8. Methods : to treat teeth with fluoride treatments before or after etching

    方法:在蝕前後分別用氟泡沫對牙釉質進行氟
  9. Aerospace process - anodic treatment of aluminium alloys - chromic acid process 20 v dc undyed coating

    航空航天工藝.鋁合金陽極.鉻20 v直流未染色鍍層
  10. Aerospace process - anodic treatment of aluminium alloys - chromic acid process 40 v dc undyed coating

    航空航天工藝.鋁合金的陽極.鉻40 v直流未染色鍍層
  11. The results of the experiments indicates that concentration of aminosilane influences the fluorescence background of glass slide, and some factors affect immobile ratio of oligonucleotide probe, such as aminosilane treatment time, aldehyde treatment time, uv crosslinking energy, washing temperature and time

    研究表明,氨基試劑濃度對玻片熒光背景有影響,氨基試劑時間、醛基時間、紫外交聯能量和洗滌溫度和時間等工藝因素影響寡核苷探針的固定率。
  12. The key stage of fabricating gene chip is pretreatment of glass surface including the processes of nh3h2o treatment, aminosilane treatment and aldehyde treatment. the pretreatment can grow active group that can bind probe effectively on the surface of glass slide. as a result, the actively treated glass slide can suit for fabricating in - situ synthesis high density gene chips

    基因晶元制備技術的關鍵步驟是玻片表面預,即對玻片表面進行羥基、氨基和醛基,使表面生長的活性基團能有效固定寡核苷探針,以滿足原位合成高密度基因晶元對玻片的要求。
  13. Corrosion protection - chromating of aluminium - principles and methods of test

    防腐.鋁的鉻.規則和試驗方法
  14. Washers, flat, large diameter, in aluminium alloy, anodized or chromated

    經陽極或鉻的鋁合金大直徑扁平墊圈
  15. Aerospace series. washers, flat, in aluminium alloy, anodized or chromated

    航空航天系列.陽極氧或鉻鹽鈍的鋁合金平墊圈
  16. Aluminum products with shing uniform surface was prepared by electrochemical graining process, including alkaline cleaning, 1 % naoh etching, electrochemical roughing in hcl, naoh treating and anodizing in 5 % h2so4 etc

    摘要研究了鋁材無掛灰電學砂工藝。以鹽作為電解液的主成分,控制合適的電流密度和電解時間等工藝參數,通過6步,得到砂均勻、粗糙度適中及光亮的砂面。
  17. In the experiment of catalyst preparation, the catalytic activity of mno2 / c which was prepared with mn ( no3 ) 2 solution and active carbon by the means of thermal decomposition reached the highest among three kinds of catalysts, and the performance of mno2 / c was enhanced by acidification. moreover, the results showed that the catalytic activity of mno2 was also affected by different mode of catalyst and active carbon dispersed

    劑的制備實驗表明,採用硝錳溶液和活性炭共同熱分解得到的mno _ 2 / c ,具有最高的催活性,對催劑進行酸化處理能提高催劑的活性,而且催劑和活性炭的分散方式不同對其性能的影響較大。
  18. Firstly, the major ampullate glands were got from araneus ventricousus. total rna and mrna of ampullate glands were isolated and purified. double strands cdnas were synthesized in the assistance of amv - rt and e. coli dna polymerase i etc. by reverse transcription and replacement synthesis

    首先剝離大腹園蛛主壺腹腺,提取總rna和分離純mrna ,反轉錄合成cdna ,凝膠層析除去小於400bp片段,並在雙鏈cdna兩端引入ecor的銜接頭,對其進行磷酸化處理
  19. Although samples were in a hot reflux for a long time at 85 in the experiment, and 5 ? molecular sieve of the adsorbed sample was acidized by hydrofluoric acid, the analytical method was tested to have little influence on carbon isotopic composition of the saturated hydrocarbons before and after complexation

    盡管實驗過程中樣品經過85長時間加熱迴流及吸附樣品的5 ?分子篩用氫氟酸化處理,但實驗結果經儀器檢測,證明該方法對正構烷烴碳同位素值影響因素不大。
  20. At the same time, puc18 vectors were digested by ecor i enzyme and their 5 ; ends were treated by ciap

    同時以ecor酶切消puc18質粒dna , ciap對載體5端去磷酸化處理
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