• Journal of Mechanical Science and Technology
• /
• 제20권10호
• /
• pp.1541-1547
• /
• 2006

An efficient procedure to obtain the optimal stacking sequence and the minimum weight of stiffened laminated composite curved panels under several loading conditions and stiffener layouts has been developed based on the finite element method and the genetic algorithm that is powerful for the problem with integer variables. Often, designing composite laminates ends up with a stacking sequence optimization that may be formulated as an integer programming problem. This procedure is applied for a problem to find the stacking sequence having a maximum critical buckling load factor and the minimum weight. The object function in this case is the weight of a stiffened laminated composite shell. Three different types of stiffener layouts with different loading conditions are investigated to see how these parameters influence on the stacking sequence optimization of the panel and the stiffeners. It is noticed from the results that the optimal stacking sequence and lay-up angles vary depending on the types. of loading and stiffener spacing.

• 한국전산구조공학회:학술대회논문집
• /
• 한국전산구조공학회 2005년도 춘계 학술발표회 논문집
• /
• pp.601-606
• /
• 2005

Welding deformations are affected by various factors. This research investigates effects of welding sequence and self-weight on welding deformation. According to the results by equivalence load method, magnitude of welding deformation with self-weight is about twice one without self-weight on parallel weld path component. But welding deformation with the components used in this research are not affected by welding sequence

• 한국컴퓨터정보학회논문지
• /
• 제21권3호
• /
• pp.57-64
• /
• 2016

This paper deals with the PCB assembly time minimization problem that the PAP (pick-and-placement) machine pickup the K-weighted group of N-components, loading, and place into the PCB placement location. This problem considers the rotational turret velocity according to component weight group and moving velocity of distance in two component placement locations in PCB. This paper suggest heavy-weight component group first pick-and-place strategy that the feeder sequence fit to the placement location Hamiltonean cycle sequence. This algorithm applies the quadratic assignment problem (QAP) that considers feeder sequence and location sequence, and the linear assignment problem (LAP) that considers only feeder sequence. The proposed algorithm shorten the assembly time than iATMA for QAP, and same result as iATMA that shorten the assembly time than ATMA.

• Kyungpook Mathematical Journal
• /
• 제45권3호
• /
• pp.413-421
• /
• 2005

In this paper, we have a further discussion about quadratically hyponormal weighted shifts with weight sequence ${\alpha}:1,1,{\sqrt{a}},\left({\sqrt{b}},{\sqrt{c}},{\sqrt{d}}\right)^{\wedge}$ on the basis of sufficient conditions for positively quadratically hyponormal weighted shifts. We set examples of quadratically hyponormal weighted shifts with weight sequence of the above form, and also establish a general method for setting examples.

• 한국미생물·생명공학회지
• /
• 제25권1호
• /
• pp.23-29
• /
• 1997

The nucleotide sequence of the estI gene encoding acetylxylan esterase I of Bacillus stearothermophilus was determined and analyzed. The estI gene was found to consist of a 810 base pair open reading frame coding for a polypeptide of 270 amino acids with a deduced molecular weight of 30 kDa. This was in well agreement with the molecular weight (29 kDa) estimated by SDS-PAGE of the purified esterase. The coding sequence was preceded by a putative ribo some binding site 10 bp upsteam of the ATG codon. Further 53 bp upstream, the transcription initiation signals were identified. The putative $_{-}$10 sequence (TCCAAT) and $_{-}$35 seqence (TTGAAT) corresponded closely to the respective consensus sequences for the Bacillus subtiis major RNA polymerase. The G+C content of the coding region of the estI was 51% whereas that of the third position of codone was 60.2%. The N-terminal amino acid sequence of the EstI deduced from the nucleotide sequence perfectly matched the corresponding region of the purified esterase described previously. Comparison with the amino acid sequence of other esterases and lipases reported so far allowed us to identify a sequence, GLSMG at positions 123 to 127 of the EstI which was reported to be the highly conserved active site sequence for those enzymes. The nucleotide sequence of the estI revealed 55.7% homology to that of the xylC coding for the acetylxylan esterase of Caldocellum saccharolyticum.

• 약학회지
• /
• 제33권6호
• /
• pp.339-344
• /
• 1989

The alkaline protease produced by Sarcodon aspratus(Berk) S. Ito. was purified from its fruit bodies. The enzyme was purified by using ammonium sulfate fractionation, tris-acryl CM-cellulose column chromtography and chromatofocusing. The protease migrated as one major band with a molecular weight of about 29,000 dalton on sodium dodecylsulfate-polyacrylamide gel electrophoresis. The amino acid sequence of the N-terminal residues(21) of the enzyme was determined by automated sequence analysis. The sequence was Val-Thr-Thr-Lys-Gln-Thr-Asn-Ala-Pro-Trp-Gly-Leu-Gly-Asn-Ile-Ser-Thr-Thr-Asn-Lys-Leu. Comparison of this sequence with the N-terminal sequence of the p-roteinase K from Tritirachium album showed high similarity, i. e. 57.8% identical residues. The protease displayed a relatively high stability in sodium dodecyl sulfate.

• Journal of Communications and Networks
• /
• 제4권3호
• /
• pp.170-175
• /
• 2002

An optical fiber code-division multiple-access (CDMA) network is proposed in which encoding is based on the use of concatenated sequences of relatively large weight. The first short component sequence in the concatenated sequence permits realistic electronic encoding of each data bit. The chips of this sequence are then all-optically encoded at substantially higher rate. In spite of the relatively large weight of the sequence the all-optical encoder is practical by virtue of the shortness of the component sequences. The use of Gold and Lempel sequences as component sequences for generating the concatenated sequences is studied and the bit-error rate (BER) performance of the proposed system is presented as a function of the received optical power with the number of simultaneous users as parameter.

• 한국통신학회논문지
• /
• 제27권2A호
• /
• pp.116-123
• /
• 2002

자켓 행렬(Jacket matrix)은 왈쉬 하다마드(Walsh Hadamard) 행렬 구조를 바탕으로 확장한 행렬이다. 왈쉬 하다마드 행렬이 +1, -1을 기본 원소로 하고 있는 반면 자켓 행렬은 $\pm$1과 $\pm$$\omega$($\pm$j, $\pm$$_2$$^{n}$ )를 각각 원소로 가질 수 있다. 이 행렬은 중앙 부근에 무게(weight)를 갖는데, 하다마드 행렬 크기의 1/4 크기로 부호 부분과 무게 부분으로 구성된다. 본 논문에서는 기존에 행렬 중앙에 강제적으로 무게를 할당하여 자켓 행렬을 구성하였으나, 어떠한 크기의 행렬도 크기와 무게만 정해주면 생성해낼 수 있는 이진 인덱스를 이용한 간단한 비트열 형태의 일반식이 제시된다. 무게는 행과 열의 이진 인덱스의 최상위 두 비트를 Exclusive-OR 연산한 결과가 1인 원소에 부여된다. 또한 분산연산(Distributed Arithmetic:DA) 알고리즘을 이용한 고속자켓변환(Fast Jacket Transform)의 VLSI 구조를 제시한다. 자켓 행렬은 cyclic한 특성을 가지고 있어서 암호화, 정보 이론 및 WCDMA의 복소수 확산 QPSK 변조부에 응용될 수 있다.

• 한국전산구조공학회논문집
• /
• 제36권5호
• /
• pp.331-338
• /
• 2023

현대의 방탄 장갑은 우수한 관통 저항성을 갖추어야할 뿐만 아니라 군인과 군용차량의 기동성이 확보되어야 하기 때문에 경량화가 중요한 개발 요소가 되었다. 이종 적층 평판 구조의 방탄 장갑의 방탄 성능은 동일 중량 대비 구성 재료의 배열에 따라 달라진다. 본 논문에서는 케블라, 초고분자량 폴리에틸렌 그리고 에바 폼으로 구성된 방탄 장갑의 적층 배열에 따른 방탄 성능을 분석한다. 구성 재료의 두께가 5mm와 6.5mm인 두 가지 경우에서 6가지 적층 배열에 대하여 7.62 × 51mm NATO 탄환의 M80 탄을 856m/s의 속도로 충돌시키는 피탄 해석을 수행하였다. 방탄 성능을 평가하기 위해 이종 적층 평판을 관통한 발사체의 잔류 속도와 잔류 에너지를 측정하였다. 시뮬레이션 결과를 통해 케블라, 초고분자량 폴리에틸렌, 에바 폼의 배열 순서를 갖는 적층 구조가 동일 중량에 대해 가장 우수한 방탄 성능을 가짐을 확인하였다.

• Archives of Pharmacal Research
• /
• 제23권2호
• /
• pp.187-195
• /
• 2000

Nucleotide sequence extending 2,3-dihydroxybiphenyl 1,2-dioxygenase gene (pcbC) and 2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoate hydrolase gene (pcbD) of Pseudomonas sp. DJ-12 was previously analyzed and the two genes were present in the order of pcbD-pcbC preceded by a promoter from Pseudomonas sp. DJ-12. In this study, a 3.8-kb nucleotide sequence located downstream of the pcbC gene was analyzed to have three open reading frames (ORFs) that are designated as orf1, pcbE and orf2 genes. All of the ORFs were preceded by each ribosome-binding sequence of 5-GGAXA-3 (X=G or A). However, no promoter-like sequence and transcription terminator sequence were found in the analyzed region, downstream of pcbC gene. Therefore, the gene cluster appeared to be present in the order of pcbD-pcbC-orf1-pcbE-orf2 as an operon, which is unique organization characterized so far in biphenyl- and PCB-degrading bacteria. The orf1 gene was composed of 1,224 base pairs which can encode a polypeptide of molecular weight 44,950 containing 405 amino acid residues. A deduced amino acid sequence of the orf1 gene product exhibited 21-33％ identity with those of indole dioxygenase and phenol hydroxylase components. The pcbE gene was composed of 783 base pairs encoding 2-hydroxypenta-2,4-dienoate hydratase involved in the 4-chlorobiphenyl catabolism. The orf2 gene was composed of 1,017 base pairs encoding a polypeptide of molecular weight 37,378 containing 338 amino acid residues. A deduced amino acid sequence of the orf2 gene product exhibited 31％ identity with that of a nitrilotriacetate monooxygenase component.