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data buffer相关的网络例句

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与 data buffer 相关的网络例句 [注:此内容来源于网络,仅供参考]

This paper analyzes each case of hoisting overwind ,gives proper fix situation of the overwind buffer in overwind height and computing methods of the cushioning force for the buffer.

对提升容器过卷的各种情况进行了分析,提出了在过卷高度内,过卷缓冲装置的合理安装位置及缓冲力的确定方法。

On the basis of the analytical results of infrared spectrometry,paper chromatography,tyrosine color development reaction and the assay of anti-acid buffer capability,we confirm that chlorine dioxide in stabilized solution with sodium percarbonate as stabilizer exists in the form of chlorition (ClO2-) and exists in NaHCO3-Na2CO3 buffer system. When the stabilizer is sodium perborate,chlorine dioxide may be retained in the solution comprised of H3BO3-Na2B4O7 as a labile complex.

通过对几种样品的红外光谱分析、纸色谱分析、酪氨酸显色反应及抗酸缓冲能力的测定,证实在以过碳酸钠为稳定剂的稳定液中,ClO2以亚氯酸根离子(ClO2-)形式存在,并处在一个由NaHCO3-Na2CO3组成的缓冲体系中;在以过硼酸钠为稳定剂的稳定液中,ClO2可能是以活性配位化合物的形式存在,并处在由H3BO3-Na2B4O7组成的缓冲体系中。

Membrane affinity quantified by IAM and liposome/buffer systems was a more efficient predicator of α values than hydrophobicity from n-octanol/buffer system.

初次提出了一个特征参数—结合常数、α—来描述药物在细胞内的蓄积程度。

Membrane affinity quantified by IAM and liposome/buffer systems was a more efficient predicator of α values than hydrophobicity from n-octanol/buffer system. Consequently, not only hydrophobic force but also attractive polar extra-interactions involved in the binding to IAM and liposomal membranes but not in an n-octanol phase, ascribed to the binding process within AM. The binding to ordered lipid membrane in the larger part determined drugs'binding to AM intracellular compositions, and the ordered phospholipid plasma membrane was a potential site for drugs'binding in AM.

脂质体/水系统和磷脂膜色谱所测定的膜亲和性比正辛醇/水系统的疏水性更好的预测巨噬细胞内药物的α值,因此包含在磷脂膜色谱中但并不体现在正辛醇/水系统中药物与磷脂膜之间的额外吸引性极性作用力对药物在细胞内结合有着重要贡献;药物与有序磷脂膜的结合在很大程度上决定着药物与巨噬细胞内成分的结合,有序磷脂分子膜可能是巨噬细胞内部潜在的结合部位。

Because a class of software like Word to generate a buffer before the print files, and then transmitted to the printer, the image of a larger size, higher resolution requires a large buffer capacity, and the author of the past to help design advertising art, it Print a map generated encountered close to the situation of temporary files 300MB.

因为像Word一类软件打印之前要生成缓冲文件,再传输到打印机上,图片尺寸较大、分辨率较高时,需要的缓冲区容量也很大,笔者以前帮助广告美工出设计图时,就遇到打印一张图生成将近300MB临时文件的情况。

In the test, HSPS is tested by making use of venerability of .printer remote buffer overflow, Unicode, and .ida remote buffer overflow.

在实验中,利用。printer远程缓冲区溢出漏洞,Unicode漏洞,。ida远程缓冲区溢出漏洞对HSPS进行了测试。

Thereafter, some research work about the effect of additive percentage of pH value buffer solution and oxygen concentration in flue gas on this system of flue gas desulfurization with pyrolusite pulp in a single JBR was carried out, and it was illustrated that the optimized additive percentage of pH value buffer was 30% and 10% when oxygen concentration in flue gas is 21% and 7% respectively.

针对这一问题,通过实验在JBR反应器中考察了pH值缓冲剂添加比例和烟气氧含量对软锰矿浆烟气脱硫体系的影响,确定烟气氧含量为21%时pH值缓冲剂的最佳添加比例为30%,烟气氧含量为7%时pH缓冲剂的最佳添加比例为10%。

Most of the operating parts of the rifle were coated in Kal-Guard, a quarter-inch hole was drilled through the stock and buffer tube for drainage, and an O-ring was added to the end of the buffer assembly.

该枪的大部分部件被Kal-Guard覆盖,枪托和缓冲器管上有一个1/4英寸的孔用来排水,以及缓冲器组件末端的一个O形环。

Screen buffer size determines the amount of text which the console screen can hold, so you always see the vertical scroll bar because the buffer height is bigger than the window height.

屏幕缓冲区的大小决定了文本控制台屏幕可容纳量,所以你总是看到垂直滚动条,因为缓冲区高度大于窗口的高度大。

The factors relevant to the running buffer and their effects on separation were investigated. The buffer solution composed of 30 mmol/L sodium borate and 2.4 mmol/L β-CD was found to be the most suitable electrolyte for separation. The second order dissociation constant range of honokiol was estimated. The content range of honokiol in Cortex Magnoliae Officinalis and was 3.42-5.98 mg/g, while the mean content of honokiol in its preparation 0.021 mg/mL.

优化了厚朴提取物的分离条件,考察了缓冲溶液浓度、pH 值、β-CD的添加浓度对分离的影响,确定了最佳的分离缓冲溶液组成为30 mmol/L 硼砂和2.4 mmol/L β-CD,pH 值为9.48;推测出和厚朴酚的二级离解常数pKa2 的范围为9.94-10.83;在优化的分离条件下,测定了厚朴药材和藿香正气口服液中和厚朴酚的含量分别为3.42-5.98 mg/g、0.021 mg/mL,和厚朴酚的线性范围是0.020-0.405 mg/mL,其线性相关系数R=0.998(n=5),加样回收率为98.4-103.5%,RSD 为3.2-5.7%(n=3)。

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