precursor concentration 中文意思是什麼

precursor concentration 解釋
前驅濃度
  • precursor : n. 1. 前輩，前驅，先鋒；前任。2. 預兆；先兆。3. 預報器。4. 【原子能】前驅波；初級粒子。
  • concentration : n. 1. 集中。2. 【化學】提濃，蒸濃，濃縮；濃度；稠密度；【礦物】汰選，選礦，富化。3. 集中注意，專心。
  1. Zno nano - particles was made from precursor zn ( ac ) 2. 2h2o through the method of sol - gel. the parameters for achieving the optimum technological conditions in making zno nano - particles were obtained by carefully observing the precursor concentration, amount of solvent and precipitants, the temperature on each stages and the behavior of reactors

    在制備過程中，研究了主鹽濃度、溶劑用量、沉澱劑用量、反應各階段的工藝溫度，以及反應器等因素對實驗結果的影響，得出了制備zno納米微粒的最佳工藝參數。
  2. A series of preparation conditions and parameters were systematically studied. it is concerned that the effects of prepared method of precursor, material synthesize method, fired atmosphere, fired temperature, fired time, flux kind and content, rare earth concentration and kind and matrix on the microstructure and optical storage properties of the samples. at the same time, the optical storage mechanism was discussed in certain extent

    系統地研究了一系列的工藝條件及參數，討論了前驅物制備方法、材料合成方法、灼燒氣氛、灼燒溫度、灼燒時間、助熔劑種類及含量、稀土摻雜濃度及種類、基質成分對樣品微觀結構及光存儲性能的影響，同時對樣品的光存儲機理作了一定程度的探討。
  3. Results show that when the ratio of the ion concentration is 1. 707, ph of the reaction is 10. 0, reaction temperature is 45 and the aging time is ih, the ultra fine mn - zn ferrite precursor particle can be obtained

    得到粒度最小的參量值如下：離子濃度比為1 . 707 ，溶液ph值為10 . 0 ，水浴溫度為45 ，陳化時間為1h 。
  4. In order to obtain the mn - zn ferrite precursor particle which has itra - fme property, the optimum technological condition was obtained through the orthogonal experiments in this paper. in the co - precipitation procession of preparation the leading factors that affect the size of the particle are ratio of the ion concentration ( a ), ph of the reaction ( b ), temperature of reaction ( c ), and aging time ( d )

    本文通過拉丁正交試驗，以粒徑尺寸為考察目標，將離子濃度比（ a ） ，反應ph值（ b ） ，水浴溫度（ c ）和陳化時間（ d ）作為四參量，利用每一參量為變量進行試驗確定各參量值，從而確定製備超細錳鋅鐵氧體前驅體粉末的條件。
  5. Results showed that the factors include : solvent and concentration of limn204 precursor solution, spin - coating speed, heating speed, sintering temperature and time etc. in the end, techniques of sintering under vacuum conditions were studied

    主要有以下幾方面:溶液中離子總濃度以及分散劑濃度對成膜質量的影響;旋轉塗覆時轉速、熱處理的升溫速度、燒結溫度、燒結時間對薄膜晶型結構及性能的影響。
  6. The optimum conditions of preparation were as fellows : the concentration of zinc sulfate solution of 1. 8 - 2. omol / l, the concentration of ammonium bicarbonate solution of 1. 4 ~ 1. 6mol / l, the time of ultrasonic radiation of 25 ~ 30min. iv. preparation of active zinc oxide by means of microwave radiation to calcine precursor of basic zinc carbonate firstly, and a mechanism on preparation of ultra - fine active zinc oxide by means of microwave radiation has been investigated emphatically as well as the effects on quality of ultra - fine active zinc oxide have been analyzed and discussed in detail, the time of microwave radiation was 7 ~ 16 min ; comparing microwave radiation calcining with conventional calcining, the calcining time of microwave radiation was one thirty to one twenty, the calcining time shortened hugely, energy consumption saved hugely, the quality of product improved

    首次引入超聲波輻射制備超細活性氧化鋅前驅體堿式碳酸鋅新技術，研究了超聲波輻射制備前驅體堿式碳酸鋅的機理，並分析和討論了影響前驅體質量的各種因素，確定了最佳的前驅體制備條件為：硫酸鋅濃度為1 . 8 2 . 0mol / l ，碳酸氫銨的濃度為1 . 4 1 . 6mol / l ，超聲波輻射25 30min ； 4 、首次採用微波加熱煅燒前驅體堿式碳酸鋅制備超細活性氧化鋅的新技術，研究了微波輻射加熱煅燒前驅體制備超細活性氧化鋅的機理，並分析和討論了影響活性氧化鋅質量的各種因素，確定了最佳的超細活性氧化鋅制備條件為：微波加熱煅燒時間為7 16min ，與傳統煅燒方法相比，煅燒時間僅為傳統的1 30 1 20 ，大大縮短煅燒時間，節省能耗，提高了煅燒產品的質量； 5 、完成了從鋅浮渣中制備超細活性氧化鋅的小試試驗和擴大試驗。
  7. The synthesis of poly ( - hydroxybutyrate - co - - hydroxyvalerate ) by the strain g - iiiy from different precusor was studied. it was found that the strain g - iiiy could accumulate phbv with sucrose as carbon source and propionic acid or valeric acid as precursor. in 2l self - controlled fermentor, the dry cell weight, phbv concentration and phbv content reached 35. 8g ? l - 1, 22. 6g ? l - 1 and 38. 4 % respectively in the case of fermentation for 42 hours and the propionic acid as precursor

    研究了添加不同前體物， g - y菌株生產聚-羥基丁酸和聚-羥基戊酸共聚物（ phbv ）的發酵條件，結果表明，此菌株能以丙酸或戊酸為前體，在蔗糖為碳源的條件下合成phbv共聚物；在2l發酵罐中，以丙酸為前體，發酵16小時開始流加丙酸，根據發酵液ph值變化控制丙酸流加量，發酵42小時，細胞干重、 phbv產量和含量分別達到35 . 8g / l ， 22 . 6g / l ， 63 . 13 。
  8. The effects of precursor concentration on the characterization of ntc thermistor nanopowders

    納米粉體及其熱敏電阻特性的影響
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