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  • 002048

    第22楼2010/04/09

    是的,上面只要求在一条直线上!

    chemistryren(chemistryren) 发表:没办法,现在计量认证时有个误区,总认为标准曲线就应该是一次直线,上回我写了个二次拟合曲线上去还被退回重写.

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  • 002048

    第23楼2010/04/09

    是的,上面只要求在一条直线上!

    chemistryren(chemistryren) 发表:没办法,现在计量认证时有个误区,总认为标准曲线就应该是一次直线,上回我写了个二次拟合曲线上去还被退回重写.

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  • megastar

    第24楼2010/04/10

    你们在计算的时候,空白(0,0)点带入计算了吗?
    我的看法是不带入计算,因为工作曲线在检测限以下,工作曲线并不是直线,发生了弯曲,因此不能把空白(0,0)带入计算。

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  • chemistryren

    第25楼2010/04/11

    0点必须带入计算的。

    megastar(megastar) 发表:你们在计算的时候,空白(0,0)点带入计算了吗?
    我的看法是不带入计算,因为工作曲线在检测限以下,工作曲线并不是直线,发生了弯曲,因此不能把空白(0,0)带入计算。

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  • yubo726

    第26楼2010/04/14

    Nonlinear Through Zero
    If you expect the concentrations of your samples to be outside the linear range of the calibration curve , select this option. This option covers the widest concentration range. This calibration curve is forced to go through the point defined by the calibration blank which is set at zero absorbance and zero concentration. The equation for Nonlinear zero intercept is:
    C=K0*(K1*A+K3*A*A)/(K2*A-1)
    In this expression, C is the concentration, A is the observed absorbance or emission, K1, K2, and K3 are coefficients determined during the calibration procedure, and K0 is the reslope coefficient that is set equal to 1.0 during the initial calibration. When the number of calibration standards used exceeds the number of coefficients, the method of least squares is used to determine the coefficients.
    The blank is always analyzed first, and the reading obtained is automatically subtracted from the readings from all subsequent calibration standards.
    Linear, Calculated Intercept
    If you expect the concentrations of your samples to be within the linear range of the calibration curve, select this option. This is often the case at low absorbance values and low concentration values. The calibration blank is treated as another calibration standard by the system and the intercept with the absorbance axis is calculated rather than fixed at zero concentration.
    The equation for linear calculated intercept is:A=K1+K2*C
    Linear Through Zero
    If you expect the concentrations of your samples to be within the linear range of the calibration, select this option. This is often the case at low absorbance values and low concentration values. This calibration curve is forced to go through the point defined by the calibration blank which is set at zero absorbance and zero concentration. The equation used for zero intercept linear calibration is: C=K0(-K1*A)
    In this expression, C is the concentration and A is the absorbance or emission, K1 is a proportionality coefficient, and K0 is the reslope coefficient, which is set to 1.0 for the initial calibration.
    A calibration curve defined using this equation is forced to go through the point 0, 0, zero absorbance and zero concentration, defined by the blank. When two or more calibration standards are used, the method of least squares is used to determine K1 .
    The blank is always analyzed first, and the reading obtained is automatically subtracted from the readings from all subsequent calibration standards.

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  • 飞叶

    第27楼2010/04/16

    线性好结果却不一定准确

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  • 汉之广矣

    第28楼2013/05/03

    PE工程师给我们设置的是 线性,截距
    感觉在线性很好的时候(3个9及以上)都还行——这个时候截距是0.000几

    如果线性不好,相关系数3个9以下——这是截距比较大,正负0.1甚至更大
    这个时候是不是就要用其他的呢?

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  • 冰山

    第29楼2013/05/03

    应助达人

    哪位英语好的兄弟把这段给大家翻翻

    yubo726(yubo726) 发表:Nonlinear Through Zero
    If you expect the concentrations of your samples to be outside the linear range of the calibration curve , select this option. This option covers the widest concentration range. This calibration curve is forced to go through the point defined by the calibration blank which is set at zero absorbance and zero concentration. The equation for Nonlinear zero intercept is:
    C=K0*(K1*A+K3*A*A)/(K2*A-1)
    In this expression, C is the concentration, A is the observed absorbance or emission, K1, K2, and K3 are coefficients determined during the calibration procedure, and K0 is the reslope coefficient that is set equal to 1.0 during the initial calibration. When the number of calibration standards used exceeds the number of coefficients, the method of least squares is used to determine the coefficients.
    The blank is always analyzed first, and the reading obtained is automatically subtracted from the readings from all subsequent calibration standards.
    Linear, Calculated Intercept
    If you expect the concentrations of your samples to be within the linear range of the calibration curve, select this option. This is often the case at low absorbance values and low concentration values. The calibration blank is treated as another calibration standard by the system and the intercept with the absorbance axis is calculated rather than fixed at zero concentration.
    The equation for linear calculated intercept is:A=K1+K2*C
    Linear Through Zero
    If you expect the concentrations of your samples to be within the linear range of the calibration, select this option. This is often the case at low absorbance values and low concentration values. This calibration curve is forced to go through the point defined by the calibration blank which is set at zero absorbance and zero concentration. The equation used for zero intercept linear calibration is: C=K0(-K1*A)
    In this expression, C is the concentration and A is the absorbance or emission, K1 is a proportionality coefficient, and K0 is the reslope coefficient, which is set to 1.0 for the initial calibration.
    A calibration curve defined using this equation is forced to go through the point 0, 0, zero absorbance and zero concentration, defined by the blank. When two or more calibration standards are used, the method of least squares is used to determine K1 .
    The blank is always analyzed first, and the reading obtained is automatically subtracted from the readings from all subsequent calibration standards.

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  • jorhanm

    第30楼2013/05/04

    这个问题太棒了,强烈要求大神来解决下这个问题

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  • kahn12345

    第31楼2015/03/11

    是不是这样理解,当样品浓度较高时,原吸的线性范围没那么宽,较高吸光度处线性拟合并不理想

    majachrist(majachrist) 发表:我们用的也是PE的原吸,上次特意问过PE的维护工程师,他说如果配制的曲线浓度相对较高,吸光度也比较高,选非线性曲线好一些,如果曲线浓度偏小,可以选线性。不过,他们一般建议一概选非线性不过原点~~~~
    个人试了几次,感觉一般非线性不过原点对高低浓度都还可以满足曲线线性要求,所以就没纠结这个问题了。

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