Nicolet iS10 FT-IR Spectrometer
Nicolet iS10 FT-IR Spectrometer
Nicolet iS10 FT-IR Spectrometer
Nicolet iS10 FT-IR Spectrometer
Nicolet iS10 FT-IR Spectrometer
Nicolet iS10 FT-IR Spectrometer
Thermo Scientific™

Nicolet iS10 FT-IR Spectrometer

The Nicolet iS10 FTIR Spectrometer has been discontinued. Please see its replacement, the Nicolet iS20 FTIR Spectrometer.
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카탈로그 번호용도(애플리케이션)스펙트럼 범위
IQLAADGAAGFAHDMAPC바이오디젤 혼합 분석; 보석 분석; 고분자 및 플라스틱; QA/QC; 제약; 법의학7800-350 cm-1 최적화, 중적외선 KBr 빔스플리터
11000-375 cm-1 XT KBr 확장 범위 중적외선 광학부
카탈로그 번호 IQLAADGAAGFAHDMAPC
제품 가격(KRW)
-
견적 요청하기
용도(애플리케이션):
바이오디젤 혼합 분석; 보석 분석; 고분자 및 플라스틱; QA/QC; 제약; 법의학
스펙트럼 범위:
7800-350 cm-1 최적화, 중적외선 KBr 빔스플리터
11000-375 cm-1 XT KBr 확장 범위 중적외선 광학부

The Nicolet iS10 FTIR Spectrometer has been updated with the Thermo Scientific Nicolet iS20 FTIR Spectrometer.

The Nicolet iS20 FTIR Spectrometer resets the standard and pushes the limits of innovation to the next level. With its redesigned optical engine and modern industrial design, the Nicolet iS20 Spectrometer creates the perfect combination of the instrument platform FTIR users loved with the improvements they need.

The Nicolet iS10 FTIR Spectrometer has updated to the Nicolet iS20 FTIR Spectrometer.

사양
빔 스플리터KBr/Ge 중적외선 최적화(스탠더드); XT-KBr/Ge 확장 범위 중적외선(선택 옵션)
구성 요소중적외선 Ever-Glo 및 텅스텐/할로겐(둘 다 시료 컴파트먼트에서 사용자가 직접 교체 가능)
깊이(미터법)550mm
검출기 유형빠른 회수 deuterated triglycine sulfate (DTGS) (스탠더드); 액체 질소 냉각식 mercury cadmium telluride (MCT) (선택 옵션)
용도(애플리케이션)바이오디젤 혼합 분석; 보석 분석; 고분자 및 플라스틱; QA/QC; 제약; 법의학
용도(장비)SMART Accessory, TGA-IR, Continuum Microscope, 광음향, 대부분의 표준 부속품
높이(미터법)250 mm
습도주변 습기 차단을 위해 긴밀하게 밀봉됨
인터페이스PC USB 2.0
레이저HeNe
제품 유형Nicolet iS10 FT-IR Spectrometer
소스 유형중적외선 Ever-Glo 및 텅스텐/할로겐(둘 다 시료 컴파트먼트에서 사용자가 직접 교체 가능)
스펙트럼 범위7800-350 cm-1 최적화, 중적외선 KBr 빔스플리터
11000-375 cm-1 XT KBr 확장 범위 중적외선 광학부
스펙트럼 분해능0.4보다 큰 파수(wavenumber)
중량(영국식 단위)72.8 lb.
중량(미터법)33 kg
폭(영국식 단위)22.4 in.
폭(미터법)570 mm
성능 검증고객의 ISO/GLP 요건 만족을 위한 ASTM E1421,
Unit SizeEach

자주 묻는 질문(FAQ)

What is Raman spectroscopy?

In Raman spectroscopy, an unknown sample of material is illuminated with monochromatic (single wavelength or single frequency) laser light, which can be absorbed, transmitted, reflected, or scattered by the sample. Light scattered from the sample is due to either elastic collisions of the light with the sample's molecules (Rayleigh scatter) or inelastic collisions (Raman scatter). Whereas Rayleigh scattered light has the same frequency (wavelength) of the incident laser light, Raman scattered light returns from the sample at different frequencies corresponding to the vibrational frequencies of the bonds of the molecules in the sample.

If you wish to learn more about Raman spectroscopy, visit our online Raman Spectroscopy Academy (https://www.thermofisher.com/us/en/home/industrial/spectroscopy-elemental-isotope-analysis/spectroscopy-elemental-isotope-analysis-learning-center/molecular-spectroscopy-information/raman-technology.html), where you will find basic Raman tutorials, advanced Raman webinars on sample applications, and a helpful instrument guide.

Using the Beer-Lambert law in FTIR ATR for quantitative analysis of a time-sensitive, migrating substance (e.g., erucamide) in a polymer is difficult. How can this be overcome?

The Beer-Lambert law is based on stable samples and reproducible conditions. In ATR, you have two concerns. First, the sample must make contact with the crystal in a consistent manner. If the material is rough or crystalline, you must ensure reproducibility. Grinding the material to a fine powder may be necessary. Second, ATR is a surface technique, examining the sample to a depth of around 1-4 microns. If the additive or target molecule is migrating further away, you will lose the signal. In this case, transmission, which illuminates the entire sample and entire thickness, may be a viable option (depending upon thickness). In some cases, the application of pressure can change the signal due to changes in the crystallinity or orientation of polymer strands in the sample. Any deeper insights would require an understanding of the specific sample involved.

What types of sampling cells and detectors are used for protein analysis using Fourier Transform Infrared Spectroscopy (FTIR)?

One key experimental step in protein analysis is the removal of the water bands (most proteins are in buffers). This requires highly controlled path-length transmission cells or ATR. Most historical work was done in 6-10 micron path length transmission cells using BaF2 or similar windows. The analytical region is roughly between 1400 and 1750cm-1 where these windows are transmissive. Recently, ATR devices using silicon, germanium, or diamond windows have become more prevalent. Reactions or binding of proteins to the crystal can occur with ZnSe devices (due to surface charges); sometimes this is desired but often it is not. Most of the literature is based on transmission cells. Protein analysis requires skill and consistency, so training is essential for most laboratories.

What is the advantage of DRIFTS compared to ATR technique in Fourier Transform Infrared Spectroscopy (FTIR)? What is the difference?

DRIFTS is used in both mid-IR and near-IR. In the mid-IR, DRIFTS requires the sample be blended with diluents like KBr, with 3-10% sample. This is typically undesirable as the sample is now mixed. However, DRIFTS is heavily used in catalysis research where powdered material is exposed to high temperature, elevated pressures, and mixtures of reactant gases. Several accessory suppliers make devices specific for this. In the near-IR, DRIFTS is used without dilution through direct measurement - many hand-held probes exist allowing analysis through a container wall (like plastic bags) meaning the sample can be analyzed without touching or contaminating it.

ATR involves making contact with the sample by forcing it into contact with a crystal. ATR generally does not require dilution and works well with solids like credit cards or car bumpers which would be tough in DRIFTS. ATR has, for the most part, displaced DRIFTS in the mid-IR except in special cases, while DRIFTS remains a method of choice in the near-IR world.

What are some subtleties and scenarios in inorganic applications for Fourier Transform Infrared Spectroscopy (FTIR)?

Fourier Transform Infrared Spectroscopy (FTIR) responds to a change in dipole moment, regardless of whether it is organic or inorganic. Metal oxides, carbonates, and carbonyls are good examples. The basic equation states that the wavenumber is proportional to the square root of the spring constant (bond strength) and one over the square root of the reduced mass. Simply put, as mass of the atoms involved in the bond goes up, the wavenumber goes down. Many inorganics have peaks below 400cm-1, such as ferrocene, acetylferrocene and cadmium oxide. This necessitates the use of “far-IR” optics. Many forensics users have found far-IR useful in identifying paint chips, due to their inorganic content. There are several ATR accessories that now permit far-IR ATR (mostly monolithic diamond devices). The Thermo Scientific Nicolet iS50 FTIR Spectrometer was designed to make far-IR performance trivial with a built-in ATR as well. Ultimately, if you have further interest in this area, you need to speak with an FTIR sales person to understand the capabilities and limitations.