（1）利用电磁阀切换频率加倍的功能，chromaster引进了一种新型的低压梯度系统——高频模式（High Frequent Mode）。HFM与日立独有的 “高速反馈实时控制”系统相配合，大大抑制液体脉冲，提高了梯度精度和保留时间的重现性。 （2）依靠配置的高精度注射器驱动单元，实现卓越的进样精度。 日立极大地降低了自动进样器流路内引起残留的死体积，并采用清洗外壁的泵，实现了极低的样品残留。
（3）紫外/紫外可见检测器 双波长高灵敏度检测，特别针对药物有关物质检查。双波长检测功能可在更短的数据采集间隔条件下实现，每个波长数据采集间隔可设定为800ms，甚至400ms，可以得到更好、更尖锐的峰形。
二极管阵列检测器 宽波长范围（190～900nm）和高光谱分辨率（配1024bit二极管）的chromaster二极管阵列检测器致力于打造世界上最高水平的高分辨率分析。 更低噪音 二极管阵列检测器噪音值和紫外检测器相当，支持高灵敏度分析。
方案详情
HITACHITechnical ReportInspire the NextAS/LC-052 High-Performance Liquid Chromatograph Analysis of Bisphenol A and Diphenyl Carbonate inPolycarbonate Container by HPLC Polycarbonate (PC) is a transparent noncombustible thermoplastic and has excellent heat-resistance，acid-resistance， and impact-resistance properties. As a result， it is used indishes and containers for microwave heating. The main raw materials for PC are bisphenolA (BPA)， and diphenyl carbonate (DPC)， and phenol (PH) and p-tert-butylphenol (BtPH) areused as polymerization modifiers. In the Food Sanitation Act， to prevent the health hazardscaused by the elution of chemical substances from these raw materials to food and drink，the standards for the materials and eluates are specified. This time， based on the FoodSanitation Act“Standards and Criteria for Food and Food Additives， etc.，” the material testand elution test for PC containers were performed. High-Performance LiquidChromatographChromaster@ Material Test (Analysis of Standard Solution) √The standard stock solutions are prepared by weighing 10 mg each of BPA， PH， BtPH，and DPC， and adding methanolto make the volume to 100 mL (100 ug/mL each). The standard solutions are prepared by transferring 1， 2， 3， 4， and 5 mL of the standard stock solution to separate 20mL volumetric flasks and adding purified water to make the volume to 20 mL (5，10， 15， 20， and 25 pg/mL). Figure 1 Chromatogram of Standard Solution (5 pg/mL) Figure 2 Calibration Curve Table 1 Analytical Conditions Column LaChromⅡC18 (5 pm)4.6 mm l.D. X250 mm Mobile phase (A) H20 (B) CH，CN (v/v) 30% B (0 min)→100%B (35-45 min) →30% B (45.1-60 min) Flow rate 1.0 mL/min Columntemperature 40°C Detectionwavelength UV 217 nm (DAD) Injection vol. 20 pL Table 2 Reproducibility (n=6) for StandardSolution (5 pg/mL) Component PH BPA BtPH DPC Retention time (min) Mean 7.917 13.859 17.714 21.662 %RSD 0.051 0.023 0.018 0.014 Area Mean 342788 329071 256259 140201 %RSD 0.121 0.442 0.434| 0.280 √The calibration curves of BPA， PH， BtPH， and DPC (5， 10， 15，20， 25 pg/mL) showed a correlationcoefficient (R) of 0.9993 or higher， indicating a good linearity (Figure 2). Table 2 shows the reproducibility (n=6) for 5 pg/mL. A good reproducibility result was obtained foreach component. Material Test (Analysis of Sample Solution) √The standard for the material test of PC containers specified in the Food Sanitation Acts is not more than500 pg/g for the total of BPA， PH， and BtPH and not more than 500 pg/g for DPC. √Unused PC containers were used as the samples. The samples were prepared in accordance with theprocedure described under the material test of the Food Sanitation Act (Figure 3) so as to extract thesample solutions. Sample solution concentration (ug/mL)X 20 (mL) Content in material (ug/g)= Sample weight (g) Figure 3 Preparation Method for Material Test Figure 4 Chromatogram of Sample Solution Table 3 Quantitative Analysis Results Sample solution Standard addition sample solution(Addition concentration： 10 pg/mL) Sample solutionconcentration(ug/mL) Content(ug/g) Sample solutionconcentration(ug/mL) Content(ug/g) Recoveryrate(%) Sample(1.151 g) PHBPABtPH n.d.0.1670.285 n.d.2.9024.952 9.95810.52110.638 173.032182.820184.840 99.6103.5103.5 DPC n.d. n.d. 10.375 180.275 103.8 √The result obtained from the material test for PC containers showed that BPA (incl. PH and BtPH) was less thanthe specified standard and DPC was not detected (Figure 4， Table 3). When the recovery rates were determined by adding BPA， PH， BtPH and DPC at the concentration of 10 pg/mLeach， the rates were found to be 99.6-03.8%， indicating good results (Figure 4， Table 3). Elution Test (Analysis of Standard Solution) The standard solutions are prepared by transferring 2 mL each of the material test standard solutions (5， 10，15， 20and 25 pg/mL) to separate 20 mL volumetric flasks and making the volume to 20 mL by adding purified water (0.5， 1，1.5， 2， 2.5 pg/mL). The target component for the elution test is BPA (incl. PH and BtPH). DPC is shown as a reference data. Figure 5 Chromatogram of Standard Solution(0.5 pg/mL) Figure 6 Absorption Spectrum of Standard Solution(0.5 ug/mL) Table 4 Reproducibility (n=6) for Standard Solution(0.5 ug/mL) Component PH BPA BtPH DPC Retention time ((min) Mean 7.952 13.886 17.736 21.682 %RSD 0.026 0.015 0.009 0.009 Area Mean 183755 161721 126865 62220 %RSD 0.342 0.421 0.379 0.255 Figure 7 Calibration Curve Table 5 Analytical Conditions Column LaChrom lI C18 (5 pm) 4.6 mm l.D. X250 mm Mobile phase (A)H，0 ((B) CH，CN (v/v) 30% B (0 min)→100% B (35-45 min) →30%B(45.1-60 min) Flow rate 1.0 mL/min Column temperature 40°C Detection wavelength UV 217 nm (DAD) Injection vol. 100 pL (200 pL sample loop was used) √Figure 6 shows the absorption spectrum of the standard solution (0.5 ug/mL). By using a diode allaydetector， the absorption spectrum of each component can be confirmed. The calibration curves for those components (0.5， 1， 1.5， 2， 2.5 pg/mL) showed correlation coefficients(R2) of 0.9996 or higher， indicating a good linearity (Figure 7) Elution Test (Analysis of Sample Solution) The standard for the elution test of PC containers specified in the Food Sanitation Acts is not more than 2.5 pg/g for the total of BPA， PH，and BtPH. The elution test was performed with reference to“lmplements or containers/packages that contact with food fats and oils or fat-rich foods." UnusedPC containers were used as the samples. For the sample preparation， the procedures of the solvent switch from heptane to acetonitrile andconcentration1) were added to the procedure conforming to the elution test described in the Food Sanitation Act (Figure 8). 1)2010 Method of Analysis in Health Science， Pharmaceutical Society of Japan， p. 622 Figure 8 Preparation Method for Elution Test Table 6 Quantitative Analysis Results Sample solution Standard addition sample solution(Addition concentration： 0.5 pg/mL) Sample solutionconcentration(pg/mL) Sample solution concentration (ug/mL) Recovery rate (%) Sample PHBPABtPH n.d.n.d.n.d. 0.4770.500 0.484 95.5100.096.8 DPC n.d. 0.505 101.0 Figure 9 Chromatogram of Sample Solution The result of the elution test for the PC containers indicated that BPH (incl. PH and BtPH) was not detected(Figure 9， Table 6). When the recovery rates were determined by adding BPA， PH， and BtPH at the concentration of 0.5 pg/mL each，good results were obtained with the rates of 95.5-100% (Figure 9， Table 6). Chromaster 5160 Pump， 5260 Autosampler， 5310 Column Oven， 5430 Diode Array Detector (DAD) NOTE： These data are an example of measurement； the individual values cannot be guaranteed. @Hitachi High-Tech Science Corporation Page.
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