• Title/Summary/Keyword: BOC(1,1)

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Galileo BOC(1,1) Signal Tracking using GPS/Galileo Software Receiver

  • Lim, Deok-Won;Park, Chan-Sik;Lee, Sang-Jeong
    • Proceedings of the Korean Institute of Navigation and Port Research Conference
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    • v.2
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    • pp.285-289
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    • 2006
  • In this paper, a design and implementation of GPS/Galileo software receiver is given. As a GPS receiver, it is able to perform every function of receiver such as acquisition, code and carrier tracking, navigation bit extraction, navigation data decoding, pseudorange calculations, and position calculations. A method to acquire and track the Galileo BOC(1,1) signal is also required because the correlation of BOC(1,1) signal has multiple peaks different from that of GPS signal. Therefore, a method to detect the main-peak in correlation function of BOC signal is required to avoid false acquisition. In this paper, very-early, very late correlation is implemented to track the correct main peak. The performance of implemented GPS/Galileo software receiver with BOC(1,1) signal tracking feature is evaluated with GPS/Galileo IF signal generator.

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A Novel Side-Peak Cancellation Method for BOC Signal Synchronization (BOC 신호 동기화를 위한 새로운 주변 첨두 제거 기법)

  • Kim, Sang-Hun;Yoon, Tae-Ung;Lee, Young-Yoon;Han, Tae-Hee;Yoon, Seok-Ho
    • The Journal of Korean Institute of Communications and Information Sciences
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    • v.34 no.1C
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    • pp.131-137
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    • 2009
  • Binary offset carrier (BOC) signal synchronization is one of the most important steps to recover the transmitted information in global navigation satellite systems (GNSS) including Galileo and global positioning system (GPS). Generally, BOC signal synchronization is based on the correlation between the received and locally generated BOC signals. Thus, the multiple side-peaks in BOC autocorrelation are one of the main error sources in synchronizing BOC signals. Recently, a novel correlation function with reduced side-peaks was proposed for BOC signal synchronization by Julien [8]; however, Julien's correlation function not only still has the side-peaks, but also is only applicable to sine phased BOC(n, n), where n is the ratio of the pseudo random noise (PRN) code rate to 1.023 MHz. In this paper, we propose a new correlation function for BOC signal synchronization, which does not have any side-peaks and is applicable to general types of BOC signals, sine/cosine phased BOC(kn, n), where k is the ratio of a PRN chip duration to the period of a square wave sub-carrier used in BOC modulation. In addition, an efficient correlator structure is presented for generating the proposed correlation function.

Development of Galileo E5 Signal Receiving Software for AltBoc Signal Modulation (AltBOC 변조 특성을 활용한 Galileo E5 신호 수신 소프트웨어 개발)

  • Jeon, Sang-Hoon;So, Hyoung-Min;Lee, Taik-Jin;Kim, Ghang-Ho;Jeon, Seung-Il;Kim, Chong-Won;Kee, Chang-Don;Lee, Sang-Uk;Kim, Jae-Hoon
    • Journal of the Korean Society for Aeronautical & Space Sciences
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    • v.37 no.9
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    • pp.855-862
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    • 2009
  • This paper contains the signal receiving algorithm for Galileo E5 AltBOC signal and the development of Galileo E5 signal receiving software. The software runs the process from signal acquisition to extracting measurement data to get navigation solution. It uses logged IF data file as an input. In signal acquisition stage, 1ms and delayed 1ms data are used for reducing correlation ross from secondary code and navigation bit conversion. Signal tracking stage is made of two stages which are coarse tracking and fine tracking. It is for taking advantage of AltBOC characteristic and resolving ambiguity problem due to BOC modulation. The functions of software are verified by signal processing using logged IF data from commercial GNSS simulator.

HEXFEM 코드의 연소계산 검증

  • 이현철;김창효
    • Proceedings of the Korean Nuclear Society Conference
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    • 1996.05a
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    • pp.15-20
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    • 1996
  • 이 논문에서는 육방형 노심 해석용으로 제작된 코드인 HEXFEM의 연소계산 결과의 정확성을 VVER-1000 연소계산 벤치마크 문제를 통하여 검증하였으며 집합체내 연소도 구배효과에 따른 오차를 분석하였다. 집합체내 연소도 구배효과를 고려했을 때 집합체내 균일한 연소도를 가정했을 때보다 오차가 현저히 감소하였으며 Cubic Option의 결과는 제어봉이 삽입된 1주기초(BOC1 ARI), 1주기초(BOC1), 1주기말(EOC1), 2주기초(BOC2)에 대해 집합체별 상대출력 오차가 최대 0,4%로 매우 정확한 결과를 얻었고 Quadratic Option외 결과도 최대 2.0%로 비교적 정확한 결과를 얻었다.

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Part-Per-Trillion Level Determination of Alkylphenols, Chlorophenols and Bisphenol A using GC/MS-SIM in Tap Water Samples (GC/MS-SIM 방법에 의한 수돗물 중 알킬페놀, 플로로페놀과 비스페놀 A의 ppt 정량)

  • Kim, Hyub
    • Environmental Analysis Health and Toxicology
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    • v.18 no.3
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    • pp.199-208
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    • 2003
  • A new technique was proposed for the determination of alkylphenols, chlorophenols and bisphenol A in tap water samples. The sample preparation consists of a solid phase extraction (SPE) of alkylphenols, chlorophenols and bisphenol A from a water sample with XAD-4 and subsequent conversion to isobutyloxycarbonyl (isoBOC) derivatives or tert-butyldimethylsilyl (TBDMS) derivatives for sensitive analysis with the CC/MS SIM mode. The recoveries were 86.6 ∼ 105.2% (isoBOC derivatization) and 97.6∼484.5% (TBDMS derivatization), respectively. The limit of quantitation of alkylphenols, chlorophenols and bisphenol h for SIM were 0.001∼0.050 $\mu\textrm{g}$/1 (isoBOC derivatization) and 0.003∼0.050 $\mu\textrm{g}$/1 (TBDMS derivatization). The SIM responses were linear with the correlation coefficient varying 0.9755∼0.9981 (isoBOC derivatization), and 0.9908∼0.9996 (TBDMS derivatization). When these methods were applied to tap water samples, the range of concentrations were 22.8∼31.3 ng/1 in 2,4-dichlorophenol, 28.6∼70.3 ng/1 in pentachlorophenol, 15.2∼17.4 ng/1 in t-butylphenol, 10.8∼13.2 ng/1 in t-octylphenol and 17.6∼36.3 ng/l in bisphenol A, respectively.

Low Computational FFT-based Fine Acquisition Technique for BOC Signals

  • Kim, Jeong-Hoon;Kim, Binhee;Kong, Seung-Hyun
    • Journal of Positioning, Navigation, and Timing
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    • v.11 no.1
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    • pp.11-21
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    • 2022
  • Fast Fourier transform (FFT)-based parallel acquisition techniques with reduced computational complexity have been widely used for the acquisition of binary phase shift keying (BPSK) global positioning system (GPS) signals. In this paper, we propose a low computational FFT-based fine acquisition technique, for binary offset carrier (BOC) modulated BPSK signals, that depending on the subcarrier-to-code chip rate ratio (SCR) selectively utilizes the computationally efficient frequency-domain realization of the BPSK-like technique and two-dimensional compressed correlator (BOC-TDCC) technique in the first stage in order to achieve a fast coarse acquisition and accomplishes a fine acquisition in the second stage. It is analyzed and demonstrated that the proposed technique requires much smaller mean fine acquisition computation (MFAC) than the conventional FFT-based BOC acquisition techniques. The proposed technique is one of the first techniques that achieves a fast FFT-based fine acquisition of BOC signals with a slight loss of detection probability. Therefore, the proposed technique is beneficial for the receivers to make a quick position fix when there are plenty of strong (i.e., line-of-sight) GNSS satellites to be searched.

Comparison of isoButoxycarbonyl derivatives, tert.-butyldimethylsilyl derivatives, with US EPA Method in the sensitivity of Alkylphenols, Chlorophenols, and Bisphenol A Potential field-screening applications of GC/MS-SIM (기체 크로마토그래피/질량분석기를 이용한 field-screening 적용을 위한 알킬페놀류, 클로로페놀류 및 비스페놀 A의 isoBOC 유도체, TBDMS 유도체와 US EPA 방법의 비교)

  • Kim, Hyub;Hong, Jong-Ki;Kim, Yong-Hwa;Kim, Kyoung-Rae
    • Analytical Science and Technology
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    • v.15 no.3
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    • pp.196-213
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    • 2002
  • The alkylphenols, chlorophenols and bisphenol A were determined by gas chromatography/mass spectrometry-selected ion monitoring mode followed by three work-up methods for comparison; EPA method, isoBOC derivatization method and TBDMS derivatization method. Eleven phenols in water samples were extracted with dichloromethane. Also, solid-phase extraction (SPE) with XAD-4 and subsequent conversion to isobutoxycarbonyl derivatives or tert.-butyldimethylsilyl derivatives for sensitive analysis with the selected ion-monitoring (SIM) mode. The recoveries were 85.1~109.9% (EPA method) and 90.3~126.6% (isoBOC derivatization and TBDMS derivatization), respectively. The method detection limit of bisphenol A for SIM were 0.732 ${\mu}g/{\ell}$ (EPA method), 0.002 ${\mu}g/{\ell}$ (isoBOC derivatization) and 0.021 ${\mu}g/{\ell}$ (TBDMS derivatization). The SIM responses were linear with the correlation coefficient varying 0.9755~0.9981 (isoBOC derivatization), and 0.9908~0.9996 (TBDMS derivatization). When these methods were applied to treated wastewater sample from a polyethylene plant, the concentrations of 11 phenols were below the method detection limit.

Time-Division-Multiplexing Tertiary Offset Carrier Modulation for GNSS

  • Cho, Sangjae;Kim, Taeseon;Kong, Seung-Hyun
    • Journal of Positioning, Navigation, and Timing
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    • v.11 no.3
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    • pp.147-156
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    • 2022
  • In this paper, we propose Time-Division-Multiplexing Tertiary Offset Carrier (TDMTOC), a novel GNSS modulation based on Tertiary Offset Carrier (TOC) modulation. The TDMTOC modulation multiplexes two three-level signals (i.e., -1, 0, and 1) while crossing over time, and is a type of TOC modulation designed specifically for signal multiplexing. The proposed modulation generates TDMTOC subcarriers of two different phases by simply combining two Binary Offset Carrier (BOC) subcarriers by addition or subtraction. TDMTOC has better correlation and spectral properties than conventional BPSK, BOC, and MBOC modulation techniques, and has good power and spectral efficiency since it can multiplex signals without power loss similar to time division multiplexing. To prove this, we introduce the multiplexing process of TDMTOC, and compare TDMTOC with Binary Phase Shift Keying (BPSK), BOC, Composite BOC (CBOC), and Time Multiplexed BOC (TMBOC) that are currently serviced in GNSS by simulations of various aspects. Through the simulation results, we prove that TDMTOC has better correlation property than modulations currently used in GNSS, less intersystem interference due to its wide spectrum property, and robustness in multipath and noise channel environments.

Sensitive Determination of Alkylphenols, Chlorophenols, and Bisphenol A using GC/MS-SIM in Paper Materials (기체 크로마토그래피/질량분석기를 이용한 종이류 중 알킬페놀류, 클로로페놀류 및 비스페놀 A 정량)

  • Kim, Hyub;Kim, Jin-Ho
    • Environmental Analysis Health and Toxicology
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    • v.18 no.1
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    • pp.45-55
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    • 2003
  • The alkylphenols, chlorophenols and bisphenol A were determined by gas chromatography/mass spectrom-etry-selected ion monitoring (GC/MS-SIM) mode followed by two work-up methods for comparison; isoBOC derivatization method and TBDMS derivatization method. Eleven phenols in paper samples were extracted with acetonitrile. Also, solid -phase extraction (SPE) with XAD -4 and subsequent conversion to isobutoxycarbonyl derivatives or tert.-butyldimethylsilyl derivatives for sensitive analysis with the selected ion-monitoring (SIM) mode. The SIM responses were linear with the correlation coefficient varying 0.9717 ∼ 0.9995 (isoBOC derivatization), and 0.9842 ∼ 0.9980 (TBDMS derivatization). The recoveries were 82.4 ∼ 108.8%) by area ratio of phenanthrene -d$\_$10/ vs bisphenol A-d$\^$l6/. (isoBOC derivatization and TBDMS derivatization) The range of concentrations was respectively, 0.95 ∼ 1.44 ng/g in 2,4-dichlorophenol, 1.01 ∼ 1.17 ng/g in t-butylphenol,2.17 ∼ 5.84 ng/g in pentachlorophenol, 12.68 ∼ 14.88 ng/g in nonylphenol and 30.84 ∼ 153.72 ng/g in bisphenol A.

Synthesis of ($\pm$)-Methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-amines

  • Jang, Jin-Hee;Sin, Kwan-Seog;Park, Hae-Il
    • Archives of Pharmacal Research
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    • v.24 no.6
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    • pp.503-507
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    • 2001
  • trans-Metanicotine, a subtype (${\alpha}_4{\beta}_2$)-selective ligand for neuronal nicotinic acetylcholine receptor, is under clinical phase for Alzheimer's disease. An efficient synthetic route for ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-am ices, derivatives of tracts-metanicotine, was explored. Allylation reaction of aryl aldimines with allylmagnesium bromide in THF gave ($\pm$)-methyl-(1-aryl-but-3-enyl)-amines. Protection of the amines with the Boc group and following Heck reaction of the N-Boc amines with 3-bromopyridine gave ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-carbamic acid tert-butyl esters. Deprotection of the N-Boc group in aqueous 1 N-HCI solution gave the titled amines in good yields. Thus, trans-metanicotine analogues modified at the ${\alpha}-position$ of the methylamino group with amyl groups were obtained in 5 steps.

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