The FT-IR difference spectroscopy and the Raman spectroscopy were used to ide ntify the polyborate ions in saturated aqueous solutions during dissolution and transformation of 2MgO·2B2O3·MgCl2·14H2O in ...The FT-IR difference spectroscopy and the Raman spectroscopy were used to ide ntify the polyborate ions in saturated aqueous solutions during dissolution and transformation of 2MgO·2B2O3·MgCl2·14H2O in different HCl solutions at 30℃. The assignments of the recorded IR-Spectroscopic frequencies and Raman shift of the borate aqueous solution are given. The existing forms of polyborate anions in saturated aqueous solution and their interaction have been discussed. The rel ationships between the existing forms of polyborate anions and the crystallizing solid phases have been gained.展开更多
[Objective] The aim was to indentify diseased leaves of broad bean by vibra- tional spectroscopy. [Method] In this paper, broad bean rust, fusarium rhizome rot, broad bean zonate spot, yellow leaf curl virus and norma...[Objective] The aim was to indentify diseased leaves of broad bean by vibra- tional spectroscopy. [Method] In this paper, broad bean rust, fusarium rhizome rot, broad bean zonate spot, yellow leaf curl virus and normal leaves were studied using Fourier transform infrared spectroscopy combined with chemometrics. [Result] The spectra of the samples were similar, only with minor differences in absorption inten- sity of several peaks. Second derivative analyses show that the significant difference of all samples was in the range of 1 200-700 cm2. The data in the range of 1 200- 700 cm＇ were selected to evaluate correlation coefficients, hierarchical cluster analy- sis （HCA） and principal component analysis （PCA）. Results showed that the correla- tion coefficients are larger than 0.928 not only between the healthy leaves, but also between the same diseased leaves. The values between healthy and diseased leaves, and among diseased leaves, are all declined. HCA and PCA yielded about 73.3% and 82.2% accuracy, respectively. [Conclusion] This study demonstrated that FTIR techniques might be used to detect crop diseases.展开更多
The C-H stretch vibrational spectra of the trisiloxane superspreading surfactant Silwet L-77 （（CH3）3Si- O-Si（CH3）（C3H6）（OCH2CH2）7-8OCH3）-O-Si（CH3）3） at the air/water interface are measured with the surfac...The C-H stretch vibrational spectra of the trisiloxane superspreading surfactant Silwet L-77 （（CH3）3Si- O-Si（CH3）（C3H6）（OCH2CH2）7-8OCH3）-O-Si（CH3）3） at the air/water interface are measured with the surface Sum Frequency Generation Vibrational Spectroscopy （SFG-VS）. The spectra are dominated with the features from the -Si-CH3 groups around 2905 cm^-1 （symmetric stretch or SS mode） and 2957 ^-1 （mostly the asymmetric stretch or AS mode）, and with the weak but apparent contribution from the -O-CH2- groups around 2880 ^-1 （symmetric stretch or SS mode）. Comparison of the polarization dependent SFG spectra below and above the critical aggregate or micelle concentration （CAC） indicates that the molecular orientation of the C-H related molecular groups remained unchanged at different surface densities of the Silwet L-77 surfactant. The SFG-VS adsorption isotherm suggested that there was no sign of Silwet L-77 bilayer structure formation at the air/water interface. The Gibbs adsorption free energy of the Silwet surfactant to the air/water interface is -42.2±0.8kcal/mol, indicating the unusually strong adsorption ability of the Silwet L-77 superspreading surfactant.展开更多
Sixty-five new vibronic levels of the Na2 4^3∑g^＋ state have been observed in the 33900-35200 cm^-1 energy region above the potential minimum of the ground state by pulsed perturbation facilitated optical-optical do...Sixty-five new vibronic levels of the Na2 4^3∑g^＋ state have been observed in the 33900-35200 cm^-1 energy region above the potential minimum of the ground state by pulsed perturbation facilitated optical-optical double resonance （PFOODR） fluorescence excitation spectroscopy. These new data fill the gap between the low-v levels mainly observed by continuous wave （CW） PFOODR spectroscopy and the high-v levels above the 3s＋3d limit observed by pulsed PFOODR with predissociation detection, Molecular constants are fitted below potential shelf around the 3s＋3d atomic limit with previously published data （mainly observed by CW PFOODR） and these new data. RKR potential curve has been calculated with the new constants. The constants are： Te= 32127.090 cm^-1,ωe=121.4099（0.20720） cm^-1, Be = 0.116287（0.0002300） cm^-1, Re=3.551 A, An error of the RKR potential curve of J. Chem. Phys. 108, 7707 （1998） is corrected.展开更多
文摘The FT-IR difference spectroscopy and the Raman spectroscopy were used to ide ntify the polyborate ions in saturated aqueous solutions during dissolution and transformation of 2MgO·2B2O3·MgCl2·14H2O in different HCl solutions at 30℃. The assignments of the recorded IR-Spectroscopic frequencies and Raman shift of the borate aqueous solution are given. The existing forms of polyborate anions in saturated aqueous solution and their interaction have been discussed. The rel ationships between the existing forms of polyborate anions and the crystallizing solid phases have been gained.
基金Supported by National Natural Science Foundation of China(30960179)Natural Science Foundation of Yunnan Province(2007A048M)~~
文摘[Objective] The aim was to indentify diseased leaves of broad bean by vibra- tional spectroscopy. [Method] In this paper, broad bean rust, fusarium rhizome rot, broad bean zonate spot, yellow leaf curl virus and normal leaves were studied using Fourier transform infrared spectroscopy combined with chemometrics. [Result] The spectra of the samples were similar, only with minor differences in absorption inten- sity of several peaks. Second derivative analyses show that the significant difference of all samples was in the range of 1 200-700 cm2. The data in the range of 1 200- 700 cm＇ were selected to evaluate correlation coefficients, hierarchical cluster analy- sis （HCA） and principal component analysis （PCA）. Results showed that the correla- tion coefficients are larger than 0.928 not only between the healthy leaves, but also between the same diseased leaves. The values between healthy and diseased leaves, and among diseased leaves, are all declined. HCA and PCA yielded about 73.3% and 82.2% accuracy, respectively. [Conclusion] This study demonstrated that FTIR techniques might be used to detect crop diseases.
文摘The C-H stretch vibrational spectra of the trisiloxane superspreading surfactant Silwet L-77 （（CH3）3Si- O-Si（CH3）（C3H6）（OCH2CH2）7-8OCH3）-O-Si（CH3）3） at the air/water interface are measured with the surface Sum Frequency Generation Vibrational Spectroscopy （SFG-VS）. The spectra are dominated with the features from the -Si-CH3 groups around 2905 cm^-1 （symmetric stretch or SS mode） and 2957 ^-1 （mostly the asymmetric stretch or AS mode）, and with the weak but apparent contribution from the -O-CH2- groups around 2880 ^-1 （symmetric stretch or SS mode）. Comparison of the polarization dependent SFG spectra below and above the critical aggregate or micelle concentration （CAC） indicates that the molecular orientation of the C-H related molecular groups remained unchanged at different surface densities of the Silwet L-77 surfactant. The SFG-VS adsorption isotherm suggested that there was no sign of Silwet L-77 bilayer structure formation at the air/water interface. The Gibbs adsorption free energy of the Silwet surfactant to the air/water interface is -42.2±0.8kcal/mol, indicating the unusually strong adsorption ability of the Silwet L-77 superspreading surfactant.
基金This work was supported by the National Natural Science Foundation of China（NSFC No. 20473042, N0. 20173029 and 10174042）, NKBRSF, and SRFDP of China and by RFBR（grant 05-03-39012） of Russia.
文摘Sixty-five new vibronic levels of the Na2 4^3∑g^＋ state have been observed in the 33900-35200 cm^-1 energy region above the potential minimum of the ground state by pulsed perturbation facilitated optical-optical double resonance （PFOODR） fluorescence excitation spectroscopy. These new data fill the gap between the low-v levels mainly observed by continuous wave （CW） PFOODR spectroscopy and the high-v levels above the 3s＋3d limit observed by pulsed PFOODR with predissociation detection, Molecular constants are fitted below potential shelf around the 3s＋3d atomic limit with previously published data （mainly observed by CW PFOODR） and these new data. RKR potential curve has been calculated with the new constants. The constants are： Te= 32127.090 cm^-1,ωe=121.4099（0.20720） cm^-1, Be = 0.116287（0.0002300） cm^-1, Re=3.551 A, An error of the RKR potential curve of J. Chem. Phys. 108, 7707 （1998） is corrected.
