• Tribology and Lubricants
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• 제7권1호
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• pp.40-45
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• 1991

Wear performances for dibutyl 3,5-di-t-butyl 4-hydroxy benzyl phosphonate (DBP) were invesitigated using the four ball test machine under sliding and also rolling contact conditions, and compared with ZDDP. DBP showed excellent antiwear performace compared with ZDDP under severe sliding contact. Also, DBP achieved a longer fatigue life than ZDDP under rolling contact conditions. The surface of the worn balls was observed using an optical microscope, and the wear derbis generated was measured using the Particle Quantifier (PQ).

• 대한화학회지
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• 제19권5호
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• pp.367-374
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• 1975

N-X-glycylphenylalanine methyl ester(X-trifluoroacetyl or acetyl)의 글리신잔기를 광 알킬화 반응에 의해 aspartic acid 의 유도체로 전환하였다. 이 반응은 diacetyl/di-t-butyl peroxide(DBP)를 광 개시제로, acetic anhydride를 알킬화제로 하여 350nm 파장의 램프를 사용하므로써 일어난다. DBP와 acetic anhydride에 의한 열반응의 경우에도 같은 알킬화 반응을 관찰하였다. 이 열알킬화 반응은 자유라디칼 반응을 거쳐 일어나기 때문에 이와 비교하여 광 알킬화 반응도 자유라디칼 메카니즘에 의해 일어난 것으로 추측된다.

• Journal of information and communication convergence engineering
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• 제9권6호
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• pp.775-779
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• 2011

As the technology of multimedia sensor networks is desired in large numbers of applications nowadays, real-time service becomes one of the most important research challenges. Even though lots of related works have been conducted to meet this requirement in several ways, the specific traffic model for real-time has not been taken yet. Thus, it causes lack of adaptability of those approaches in real deployment. To solve this problem, in this paper, we model the application via (m,k)-firm streams which have weakly hard real-time property. And then, a novel forwarding scheme based on modified DBP (Distance-Based Priority) is proposed by considering local-DBP and stream DBP together. Local-DBP can contribute to identify the detailed causes of unsatisfied quality, that is, network congestion or wireless link failure. Simulation results reveal that (m,k)-firm is a good traffic model for multimedia sensor networks and the proposed scheme can contribute to guarantee real-time requirement well.

• 한국전기화학회:학술대회논문집
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• 한국전기화학회 1999년도 제3회 총회 및 추계학술발표회
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• pp.62-62
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• 1999

• 공업화학
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• 제20권4호
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• pp.459-463
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• 2009

본 논문에서는 poly(vinyl acetate-co-ethylene) (VAE) 에멀젼에 가소제로 많이 사용되는 di-butyl phthalate (DBP)를 혼합하여 가소제 함량에 따른 물성 변화를 고찰하였다. 시차주사열량계(Differential Scanning Calorimeter) 측정으로부터 건조한 필름의 유리전이온도($T_g$)를 측정한 결과,가소제 함량의 증가에 따라, $T_g$는 감소하는 경향을 나타내었고 반면에 에멀젼의 점도는 가소제 함량의 증가와 더불어 증가하였다. 이러한 결과는 건조한 필름상태에서 가소제는 고분자사슬의 상호작용을 방해하여 $T_g$를 감소시키며 에멀젼 상에서는 가소제가 에멀젼 입자 내로 침투하여 swelling시킴으로써 입자크기가 증가하고 점도를 상승키는 것으로 나타났다. 기계적 물성은 가소제의 함량이 증가할수록 저하되었으나 내수성은 증가되는 결과를 얻었다.

• 멤브레인
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• 제26권6호
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• pp.449-457
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• 2016

본 연구에서는 수처리 분리막의 적용을 위하여 기계적 물성과 내화학성이 우수한 poly(vinylidene fluoride)(PVDF)의 특성평가를 진행하였다. 열유도상분리법을 통한 분리막을 제조하기 위하여 사용된 희석제는 dibutyl-phthalate(DBP)를 사용하였으며, 고분자와 희석제의 비율에 따른 결정화 온도, 녹는점, 흐림점, SEM 이미지 등을 관찰하였다. 고분자의 함량이 높아질수록 결정화 온도 및 녹는점은 높아졌으며 반대로 흐림점 온도는 낮아짐을 확인하였다. 최종적으로 상평형도 작도를 통하여 고분자함량 62 wt%, 제막 온도 $125^{\circ}C$ 이상에서 안정적인 분리막이 제조 가능함을 확인할 수 있었다.

• Journal of Pharmaceutical Investigation
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• 제17권3호
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• pp.111-126
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• 1987

Methyl methacrylate-butyl methacrylate copolymer (MMBM)-dibutyl phthalate (DBP) films were investigated as a potential topical drug delivery system for the controlled release of nitrofurazone. The kinetic analysis of release data indicated that drug release followed a diffusion-controlled granular matrix model, where the quantity released per unit area is proportional to the square root of time. DBP of several hydrophobic plasticizers selected was found to give the highest release of nitrofurazone. However, hydrophilic plasticizers such as propylene glycol and polyethylene glycol 400 had no controlled release properties and acceptable film formation. The effects of changes in film composition, drug concentration, film thickness, pH of release medium, and temperature on the in vitro release of nitrofurazone were analyzed both theoretically and experimentally. The release rate constant (k') was found to be proportional to DBP content, pH, and the temperature of release medium, but independent of film thickness, and drug concentration in a range of 0.1-0.4% by weight. The linear relationship was found to exist between the log k' and DBP content. The release of nitrofurazone from MMBM-DBP (8:2) films was found to be an energy-linked process. Two energy terms were calculated ; the activation energy for matrix diffusion was 13.45 kcal/mole, and the heat of drug crystal solvation was 27.26-29.34 kcal/mole. Observation of scanning electron micrographs and microscopic photographs showed that the incorporation of DBP in films increased markedly the particle size of nitrofurazone dispersed in the film matrix, comparing with the fine dispersion of nitrofurazone in pure MMBM film alone.

• Journal of Microbiology and Biotechnology
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• 제20권10호
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• pp.1440-1445
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• 2010

Rhodococcus sp. JDC-11, capable of utilizing di-n-butyl phthalate (DBP) as the sole source of carbon and energy, was isolated from sewage sludge and confirmed mainly based on 16S rRNA gene sequence analysis. The optimum pH, temperature, and agitation rate for DBP degradation by Rhodococcus sp. JDC-11 were 8.0, $30^{\circ}C$, and 175 rpm, respectively. In addition, low concentrations of glucose were found to inhibit the degradation of DBP, whereas high concentrations of glucose increased its degradation. Meanwhile, a substrate utilization test showed that JDC-11 was also able to utilize other phthalates. The major metabolites of DBP degradation were identified as monobutyl phthalate and phthalic acid by gas chromatography-mass spectrometry, allowing speculation on the tentative metabolic pathway of DBP degradation by Rhodococcus sp. JDC-11. Using a set of new degenerate primers, a partial sequence of the 3,4-phthalate dioxygenase gene was obtained from JDC-11. Moreover, a sequence analysis revealed that the phthalate dioxygenase gene of JDC-11 was highly homologous to the large subunit of the phthalate dioxygenase from Rhodococcus coprophilus strain G9.

• 한국산학기술학회논문지
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• 제12권7호
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• pp.3072-3081
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• 2011

본 연구는 일부 종합검진 수검자들을 대상으로 BMI와 혈압, 혈액학적 및 혈액생화학적 지표와의 관련성을 검토하고자 2007년 1월부터 2009년 12월까지의 기간에 한국건강관리협회 대전지부 건강검진센터에서 종합건강검진을 받았던 20세 이상의 지역주민 3,731명(남자 2,312명, 여자 1,419명)을 분석대상으로 하였다. 연구 결과 남녀 모두 BMI가 증가할수록 SBP, DBP, TG, TC, LDL-C, AST, GGT, ALP의 평균치는 유의하게 증가하였으며, HDL-C는 유의하게 감소하였다. BMI는 SBP, DBP, TG, TC, LDL-C 및 GGT와 유의한 양의 상관관계가 인정되었고, HDL-C와는 유의한 음의 상관관계가 인정되었다. 순서형 다변량 로지스틱 회귀분석 결과 BMI가 증가함에 따라 SBP, DBP, TG, ALT, GGT의 비정상치에 대한 위험비가 유의하게 증가하였다.

• Journal of Microbiology and Biotechnology
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• 제17권10호
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• pp.1670-1674
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• 2007

Duffy binding protein (DBP) plays a critical role in Plasmodium vivax invasion of human red blood cells. We previously reported a single-chain antibody fragment (scFv) that was specific to P. vivax DBP (PvDBP). However, the stabilization and the half-life of scFvs have not been studied. Here, we investigated the effect of PEGylated scFvs on their biological activity and stability in vitro. SDS-PAGE analysis showed that three clones (SFDBII-12, -58, and -92) were formed as monomers (about 70 kDa) with PEGylation. Clone SFDBII-58 gave the highest yield of PEGylated scFv. Binding analysis using BIAcore between DBP and scFv showed that both SFDBII-12 and -58 were decreased approximately by two folds at the level of binding affinity to DBP after PEGylation. However, the SFDBII-92 clone still showed a relatively high level of binding affinity ($K_D=1.02{\times}10^{-7}\;M$). Binding inhibition assay showed that PEGylated scFv was still able to competitively bind the PvDBP and playa critical role in inhibiting the interactions between PvDBP protein expressed on the surface of Cos-7 cells and Duffy receptor on the surface of erythrocytes. When both scFvs and their PEGylated counterparts were exposed to trypsin, scFv was completely degraded only after 24 h, whereas 35% of PEGylated scFvs remained intact, maintaining their stability against the proteolytic attack of trypsin until 72 h. Taken together, these results suggest that the PEGylated scFvs retain their stability against proteolytic enzymes in vivo, with no significant loss in their binding affinity to target antigen, DBP.