• Restorative Dentistry and Endodontics
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• 제49권1호
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• pp.2.1-2.12
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• 2024

Objectives: This study aimed to determine the effects of 1-rooted mandibular second molar (MnSM) teeth on root canal anatomy complexities of the mandibular central incisor (MnCI), mandibular lateral incisor (MnLI), mandibular canine (MnCn), mandibular first premolar (MnFP), mandibular second premolar (MnSP), and mandibular first molar (MnFM) teeth. Materials and Methods: Cone-beam computed tomography images of 600 patients with full lower dentition were examined. Individuals with 1-rooted MnSMs were determined, and the complexity of root canal anatomy of other teeth was compared with individuals without 1-rooted MnSMs (Group-1; subjects with at least one 1-rooted MnSM, Group-2; subjects with more than a single root in both MnSMs). A second canal in MnCIs, MnLIs, MnCns, MnFPs, and MnSPs indicated a complicated root canal. The presence of a third root in MnFMs was recorded as complicated. Results: The prevalence of 1-rooted MnSMs was 12.2%, with the C-shaped root type being the most prevalent (9%). There were fewer complicated root canals in MnCIs (p = 0.02), MnLIs (p < 0.001), and MnFPs (p < 0.001) in Group 1. The other teeth showed no difference between the groups (p > 0.05). According to logistic regression analysis, 1-rooted right MnSMs had a negative effect on having complex canal systems of MnLIs and MnFPs. Left MnSMs were explanatory variables on left MnLIs and both MnFPs. Conclusions: In individuals with single-rooted MnSMs, a less complicated root canal system was observed in all teeth except the MnFMs.

• 한국재료학회지
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• 제6권1호
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• pp.90-98
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• 1996

Mn((Cu0.66AI0.34)1-x(Bi0.3Sb0.7)x) 및 Mn((Fe0.66AI0.34)1-x(Bi0.3Sb0.7)x) 합금계의 상의 변화와 자기적 특성을 조사하였다. Mn((Cu, SI)(Bi, Sb)) 합금계는 Bi상, MnSb상, MnBi상, k-상, Heuser상, Mn2Sb 및 $\beta$-Mn상의 혼합상으로 이루어졌으며 x가 증가함에 따라 Bi상과 Mn2Sb상이 증가하고 K-상, Heusler상 및 $\beta$-Mn상이 줄어들거나 사라졌다. 자기적 성질은 자성을 띄는 MnSb상, MnBi상, Mn2Sb상, k-상 및 Hseusler상과 비자성인 Bi상과 $\beta$-Mn상의 상대적 분율에 의해 결정됨을 알 수 있었고, 150K-200K 부근에서 그 이하로 온도가 감소함에 따라 자화값이 급격히 감소하는 현상이 나타났다. Mn((Fe, AI)(Bi, Sb))합금계는 Bi상, MnSb상, MnBi상, MnBi상,$\beta$-Mn상, k-상 및 Mn2Sb상의 혼합상으로 나타났으며, 자기적 성질은 조사한 전 조성에서 강자성을 띄고 있음을 알 수 있었다.

• 한국자기학회지
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• 제13권5호
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• pp.187-192
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• 2003

IrMn에 Mn을 첨가시킨 N $i_{80}$F $e_{20}$/[I $r_{22}$M $n_{78}$-Mn] $Co_{75}$F $e_{25}$ 다층박막을 상온에서 이온빔 증착(ion beam deposition: IBD)법으로 제작하여 그 자기적 및 열적 특성을 연구하였다. Mn이 첨가된 NiFe/[IrMn-Mn]/CoFe다층박막은 Mn이 첨가되지 않은 순수 합금 IrMn 박막 위의 CoFe 고정층 보다 큰 교환결합력( $H_{ex}$)과 방해온도(blocking temperature: $T_{b}$)을 가지고 있었다. Mn이 첨가되지 않는 I $r_{22}$M $n_{78}$ 와 CoFe 사이의 $H_{ex}$는 상온에서 거의 없었으나, 25$0^{\circ}C$ 열처리 후 100 Oe로 나타났다. IrMn 내에서 76.8-78.1 vol% Mn일 때, $H_{ex}$와 $T_{b}$는 크게 향상되었고, Mn이 0.6 vol%씩 증가함에 따라 크게 줄어들었다. NiFe/[IrMn-Mn]/CoFe 다층박막 구조에서 [(111)CoFe, NiFe]/(111)IrM $n_3$인 x-선 회절 피크비 평균값은 75.5, 77.5, 79.3 vol% Mn일 때 각각 1.4, 0.8, 0.6였다. 특히, 열처리 전 77.5과 78.7 vol% Mn일 때, $H_{ex}$는 각각 259와 150 Oe였다. 77.5 vol% Mn인 경우, $H_{ex}$가 열처리 온도 35$0^{\circ}C$까지 475 Oe였으며, 450 $^{\circ}C$에서는 200 Oe로 크게 감소하였다. 따라서 합금형 반강자성체 IrMn에서 높은 $H_{ex}$와 $T_{b}$을 얻을 수 있는 최적의 Mn 함유량의 존재를 확인하였다.다.다. 확인하였다.다.하였다.다.

• 한국자기공명학회논문지
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• 제6권1호
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• pp.20-37
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• 2002

MnAPSO-34 and Mn-impregnated SAPO-34(Mn-SAPO-34) sample were prepared with various manganese contents and studied by electron spin resonance(ESR) and electron spin echo modulation(ESEM). Electron spin echo modulation analysis of 0.07mo1 ％ Mn(relative to p) in MnAPSO-34 with adsorbed D$_{2}$O shows two deuteriums at 0.26 nm and two at 0.36 nm from Mn. This suggests that two waters hydrate an MnO$_{4}$ configuration with a D-O bond orientation for the waters as expect for a negatively charged site at low manganese content (0.1 mol％), the ESR spectra of MnAPSO-34 and MnH-SAPO-34 exhibit the same parameters(g 2.01 and A 89 G), but the spectra obtained from MnAPSO-34 samples are better resolved. The decomposition temperature of as-synthesized MnAPSO-34 were in the range of 200-600 $^{\circ}C$ of the morpholine which is 12 $^{\circ}C$ higher than that in as-synthesized MnH-SAPO-34. Infrared spectra showed that the position of a band at 3450 $cm^{-1}$ / shifted about 15 $cm^{-1}$ / toward higher energy in MnAPSO-34 versus MnH-SAPO-34. The modulation depth of the two-pulse ESE of MnAPSO-34 with adsorbed D$_{2}$O is deeper than that of MnH-SAPO-34 with adsorbed D$_{2}$O. Three-pulse ESEM of MnAPSO-34 and MnH-SAPO-34 with adsorbed deuterium oxide shows that the local environments of manganese in the hydrated samples are different, suggesting that Mn(II) is framework substituted in MnAPSO-34 since it obviously occupies an extraframework position in MnH-SAPO-34.

• Environmental Engineering Research
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• 제15권4호
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• pp.183-190
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• 2010

Biogenic Mn oxides are expected to have great potential in the control of water pollution due to their high catalytic activity, although information on biological Mn oxidation is not currently sufficient. In this study, the growth of a Mn oxidizing microorganism, Pseudomonas putida MnB1, was examined, with the Mn oxides formed by this strain characterized. The growth of P. putida MnB1 was not significantly influenced by Mn(II), but showed a slightly decreased growth rate in the presence of Pb(II) and EE2, indicating their insignificant adsorption onto the cell surface. Mn oxides were formed by P. putida MnB1, but the liquid growth medium and resulting biogenic solids were poorly crystalline, nano-sized particles. Biogenic Mn oxidation by P. putida MnB1 followed Michaelis-Menten kinetics, with stoichiometric amounts of Mn oxides formed, which corresponded with the initial Mn(II) concentration. However, the formation of Mn oxides was inhibited at high initial Mn(II) concentration, suggesting mass transfer obstruction of Mn(II) due to the accumulation of Mn oxides on the extracellular layer. Mn oxidation by P. putida MnB1 was very sensitive to pH and temperature, showing sharp decreases in the Mn oxidation rates outside of the optimum ranges, i.e. pH 7.43-8.22 and around 20-$26^{\circ}C$.

• 한국자기공명학회:학술대회논문집
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• 한국자기공명학회 2002년도 International Symposium on Magnetic Resonance
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• pp.80-80
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• 2002

MnPSO-34 and Mn-impregnated SAPO-34 (Mn-SAPO-34) sample were prepared with various manganese contents and studied by electron spin resonance (ESR) and electron spin-echo modulation (ESEM). Electron spin-echo modulation analysis of 0.07mol ％ Mn(relative to p) in MnAPSO-34 with adsorbed D$_2$O shows two deuteriums at 0.25 nm and two at 0.36 nm from Mn. This suggests that two waters hydrate an MnO4 configuration with a D-O bond orientation for the waters as expect for a negatively charged site at low manganese content (0.07 mol％), the ESR spectra of MnAPSO-34 and MnH-SAPO-34 exhibit the same parameters (g 2.02 and A 87 G), but the spectra obtained from MnAPSO-34 samples are better resolved. TGA of as-synthesized MnAPSO-34 shows that the decomposition temperature in the range 200-$600^{\circ}C$ of the morpholine is 12$^{\circ}C$ higher than that in as-synthesized MnH-SAPO-34. Infrared spectra shows that the position of a band at about 15 cm-1 toward higher energy in MnAPSO-34 versus MnH-SAPO-34. The modulation depth of the two-pulse ESE of MnAPSO-34 with absorbed D$_2$O is deeper than that of MnH-SAPO-34 with absorbed D$_2$O. Three-pulse ESEM of MnAPSO-34 and MnH-SAPO-34 with absorbed deuterium oxide shows that the local environments of manganese in the hydrated samples are different, suggesting that Mn(II) is framework substituted in MnAPSO-34 since it obviously occupies an extra-framework position in MnH-SAPO-34

• 한국전기전자재료학회논문지
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• 제11권3호
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• pp.242-247
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• 1998

In this study, we have synthesized $ZnGa_2O_4$:Mn,X powder doped with Mn, MnO, $MnF_2$ and $MnCl_2$, low voltage green emitting phosphor, in vacuum atmosphere. From PL spectra, the intensity of the emission peak, the brightness with coactivator show that $ZnGa_2O_4$:Mn,Cl > $ZnGa_2O_4$:Mn,F > $ZnGa_2O_4$:Mn,O > $ZnGa_2O_4$:Mn. These improvement of the brightness are caused by the increase of the concentration of $Mn^{2+}$ ion. In case of $ZnGa_2O_4$:Mn,Cl and ZnGa$_2$O$_4$:Mn,F, the brightness is enhanced much more, which is owed to the decrease of defect of host material. For $ZnGa_2O_4$:Mn,Cl phosphor fabricated with optimized condition, the decay time becomes short from 30 ms of the $ZnGa_2O_4$:Mn and $ZnGa_2O_4$:Mn,O to 6 ms and the brightness of CL at 1 kV, 1 mA is 60 cd/$m^2$.

• 자원환경지질
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• 제42권5호
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• pp.479-486
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• 2009

자연환경에서 망간은 +2, +3, +4가의 다양한 산화수로 존재하며 환경적으로 중요한 여러 원소들과 활발한 산화/환원반응을 함으로써 원소의 지화학적 순환에 중요한 역할을 하고 있다. 특히 망간은 다양한 산화물로 존재하며 각각 특징적인 망간의 산화상태를 나타내고 있다. 망간산화물의 지화학적 특성, 즉 망간산화물의 용해도, 흡착력, 산화/환원 능력은 산화물을 구성하는 망간의 산화수에 의해 크게 좌우되는 것으로 알려져 있다. 따라서 망간의 산화수를 결정하는 인자를 밝히는 것이 산화/환원에 민감한 여러 오염원소의 지화학적 거동을 예측하는 데 매우 중요하다. X-선 광전자 분광법(X-ray photoelectron spectroscopy, XPS)은 고체상으로 존재하는 다양한 원소의 산화상태를 밝히는데 매우 유용한 도구이다. 본 연구에서 MnO, $Mn_2O_3$, $MnO_2$에 대한 망간의 산화수를 결정하기 위해 XPS $Mn2p_{3/2}$와 Mn3s 결합에너지 스펙트럼을 측정하여 기존에 보고 된 값들과 비교하였다. 망간산화물에 대한 $Mn2p_{3/2}$ 결합에너지는 MnO, 640.9 eV; $Mn_2O_3$, 641.5 eV; $MnO_2$, 641.8 eV로서, 망간의 산화수가 증가할수록 $Mn2p_{3/2}$ 의 결합에너지가 증가하는 것으로 나타났다. 시료준비 방법 중 하나인 Ar 에칭의 경우 시료 표면의 전자구조를 변화시킬 수 있는 가능성이 확인되었다.

• The Korean Journal of Ecology
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• 제25권5호
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• pp.349-352
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• 2002

Mn 처리에 대한 소나무 묘목의 생장 및 영양상태의 반응을 수경재배법에 의하여 조사하였다. Mn 처리 농도별(0, 30, 60ppm) 배양액의 pH를 4.0으로 조절한 후, 소나무(Pinus densiflora) 2년생 묘목을 배양액에 이식하여 90일 동안 온실에서 생육시켰다. 소나무 묘목의 건물생장은 Mn 처리에 의하여 감소하였으며, 상대생장율(RGR)과 순동화율(NAR) 감소에 대한 Mn의 영향이 인정되었다. 이러한 결과는 배양액의 Mn 농도 증가에 의해 잎의 건물생산효율이 저하되었다는 것을 시사하였다. 식물체내 원소함량에 대한 Mn의 영향을 조사한 결과, 소나무 묘목의 줄기와 뿌리내 Ca 및 Mg 함량은 Mn 60ppm 처리구에서 가장 낮았으며, Mn 농도는 뿌리에 비하여 잎에서 3배 가량 높은 함량을 나타내었다. 또한 무처리구에 비해 Mn 처리구에서 순광합성 속도의 감소가 나타났다. 이상의 결과는 뿌리의 양분 흡수저해 및 뿌리에서 잎으로 이행된 Mn의 과잉축적에 의한 광합성 저해를 반영하는 것으로써, 결과적으로 소나무 묘목의 건물생장량 감소가 이들 결과의 복합적인 영향에 의해 초래되었음을 시사한다.

• 한국환경농학회지
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• 제29권1호
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• pp.77-85
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• 2010

Reactive oxygen species (ROS) are very harmful to living organisms due to the potential oxidation of membrane lipids, DNA, proteins, and carbohydrates. transformed E.coli strain QC 871, superoxide dismutase (SOD) double-mutant, with three sequence variant MnSOD1, MnSOD2, and MnSOD3 manganese superoxide dismutase (MnSOD) gene isolated from wheat. Although all QC 871 transformants grown at $37^{\circ}C$ expressed mRNA of MnSOD variants, only MnSOD2 transformant had functional SOD activity. MnSOD3 expressed active protein when grown at $22^{\circ}C$, however, MnSOD1 did not express functional protein at any growing and induction conditions. The sequence comparison of the wheat MnSOD variants revealed that the only amino acid difference between the sequence MnSOD2 and sequences MnSOD1 and 3 is phenylalanine/serine at position 58 amino acid. We made MnSOD2S58F gene, which was made by altering the phenylalaine to serine at position 58 in MnSOD2. The expressed MnSOD2S58F protein had functional SOD activity, even at higher levels than the original MnSOD2 at all observed temperatures. These data suggest that amino acid variation can result in highly active forms of MnSOD and the MnSOD2S58F gene can be an ideal target used for transforming crops to increase tolerance to environmental stresses.