• 접착 및 계면
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• 제20권3호
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• pp.110-115
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• 2019

그래핀으로 박리시키기 위한 한 가지 방법으로 산화그래핀이 많은 관심이 집중되고 있다. 산화그래핀의 산화그룹은 다양한 기능기와 수소결합을 시킬 수 있어 여러 응용분야에 이를 적용시키기 위한 연구가 활발히 진행되고 있다. 하지만 산화그래핀 자체만으로는 실질적으로 응용에 요구되어지는 기계적 물성을 만족시킬 수 없다. 따라서 본 연구에서는 홍합 단백질을 생체모사한 폴리도파민을 이용하여 산화그래핀과 결합시키고 액체-기체 계면에서 대면적의 복합체막을 형성 시켰다. 또한 폴리도파민-산화그래핀 복합체 박막의 모폴로지 구조도 제어하여 나노 링클 구조를 가지는 복합체 막을 얻었다. 기계적으로 우수하며 정교한 나노 구조를 형성할 수 있어 차세대 해수담수화 멤브레인 또는 탄소 복합재료에 이용될 수 있을 것으로 기대될 수 있다.

• 접착 및 계면
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• 제22권4호
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• pp.128-135
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• 2021

본 연구에서는 acid group을 포함하는 acid 폴리올을 합성하였고, acid 폴리올을 함량별로 도입하여 신규 폴리우레탄 접착제를 개발하였다. Acid 폴리올 도입하였을 때 acid content가 0.1~0.3 wt%일 때 기계적 물성이 최댓값을 나타냈으며, 0.5 wt% 이상의 함량에서는 기계적 물성 및 접착 강도가 감소하는 것을 확인하였다. Acid group으로는 carboxylic acid와 sulfuric acid를 도입하여 특성을 비교하였으며, carboxylic acid가 sulfuric acid보다 강한 수소 결합력을 보이며 기계적 물성을 향상시켰다. 또한, ZnO와 CaCO₃를 도입하여 입자의 크기와 물성의 상관관계를 확인하였다. ZnO와 CaCO₃를 도입한 경우 acid group과 이온결합이 형성되어 기계적 물성이 증가하는 것을 확인하였다.

• 한국응용과학기술학회지
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• 제35권4호
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• pp.1031-1037
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• 2018

수용성 비이온고분자인 Polyvinylalcohol (PVA), Polyvinylpyrrolidone (PVP), Hydroxypropyl cellusoe (HPC)와 iodine과의 착물 형성에 대한 계면활성제의 영향을 알아보기 위해 Sodiumdodecylsulfate을 포함하는 수용액에서 이들 사이의 반응을 수행하였다. PVP와 HPC에서 tri-iodide band의 적색 이동에 의하여 착물이 만들어졌다는 것을 알게되었고, PVA-iodine 착물에서는 500 nm 부근에서 고유의 특색있는 띠를 나타내었다. SDS 계면활성제의 존재는 PVA-iodine 착물의 파괴를 가져왔고, 고유의 푸른색도 사라지게 만들었다. 그러나 SDS 단량체는 PVP, HPC와 iodine의 착물 형성을 도와주는 경향을 나타내었다. 고분자 용액에서 겔이 만들어지는 것을 방해하는 n-propanol은 고분자-iodine 착물이 형성되는 것을 도와주었다. SDS가 있을 때와 없을 경우의 영향을 알아보기 위해 순수한 HPC와 HPC-iodine 착물을 만들고 이들의 성질을 조사하였다.

• Molecules and Cells
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• 제42권6호
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• pp.460-469
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• 2019

Bacterial ${\alpha}-type$ carbonic anhydrase (${\alpha}-CA$) is a zinc metalloenzyme that catalyzes the reversible and extremely rapid interconversion of carbon dioxide to bicarbonate. In this study, we report the first crystal structure of a hyperthermostable ${\alpha}-CA$ from Persephonella marina EX-H1 (pmCA) in the absence and presence of competitive inhibitor, acetazolamide. The structure reveals a compactly folded pmCA homodimer in which each monomer consists of a 10-stranded ${\beta}-sheet$ in the center. The catalytic zinc ion is coordinated by three highly conserved histidine residues with an exchangeable fourth ligand (a water molecule, a bicarbonate anion, or the sulfonamide group of acetazolamide). Together with an intramolecular disulfide bond, extensive interfacial networks of hydrogen bonds, ionic and hydrophobic interactions stabilize the dimeric structure and are likely responsible for the high thermal stability. We also identified novel binding sites for calcium ions at the crystallographic interface, which serve as molecular glue linking negatively charged and otherwise repulsive surfaces. Furthermore, this large negatively charged patch appears to further increase the thermostability at alkaline pH range via favorable charge-charge interactions between pmCA and solvent molecules. These findings may assist development of novel ${\alpha}-CAs$ with improved thermal and/or alkaline stability for applications such as $CO_2$ capture and sequestration.

• Bulletin of the Korean Chemical Society
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• 제14권2호
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• pp.200-206
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• 1993

Structures of two polymorphs of ${\alpha},{\alpha}$-trehalose octaacetate monohydrate, $C_{28}H_{38}O_{19}\;{\cdot}\;H_2O$, have been studied by X-ray diffraction method. ${\alpha},{\alpha}$-trehalose (${\alpha}$-D-glucopyranosyl ${\alpha}$-D-glucopyranoside) is a nonreducing disaccharide. The polymorph I belongs to the monoclinic $P2_1$, and has unit cell parameters of a=10.725(l), b=15.110(4), c=11.199(5) ${\AA}$, ${\beta}=108.16(2)^{\circ}$ and Z=2. The polymorph II is orthorhombic $P2_12_12_1$, with a=13.684(4), b=15.802(4), c=17.990(9) ${\AA}$ and Z=4. The final R and R$_w$ values for monoclinic polymorph I are 0.043 and 0.048 and for orthorhombic polymorph II are 0.116 and 0.118, respectively. Those R values of polymorph II are high because the large thermal motions of acetyl groups and the poor quality of the crystal. The molecular conformations in the two polymorphs are similar. Both D-glucopyranosyl rings have chair $^4C_1$ conformations and atoms of glycosidic chain ${\alpha}(1{\rightarrow}1)$ linkage are coplanar. The primary acetate groups of the pyranose residues assume both gauche-trans conformations. The molecules of two polymorphs have pseudo-C$_2$ symmetry at glycosidic O(1) atom. The bond lengths and angles are normal compared with those in other acetylated sugar compounds. The molecules in the monoclinic crystal are held by the hydrogen bonds with the water molecules and by van der Waals forces.

• Bulletin of the Korean Chemical Society
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• 제6권4호
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• pp.202-206
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• 1985

The crystal structure of The crystal structure of $Ag^+$-Exchanged Zeolite A, $Ag_{4.6}Na_{7.4}-A$, dehydrated, treated with $H_2$, and evacuated, all at $350^{\circ}C$, has been determined by single crystal x-ray diffraction methods in the cubic space group Pm3m at $24(1)^{\circ}C;$ a = $12.208(2)\AA.$ The structure was refined to the final error indices R1 = 0.088 and R2 (weighted) = 0.069 using 194 independent reflections for which II_0$ > $3{\sigma}(I_0)$. On threefold axes near the centers of 6-oxygen rings, $7.4 Na^+$ ions and $0.6 Ag^+$ ions are found. Two non-equivalent 8-ring $Ag^+$ ions are found off the 8-ring planes, each containing about $0.6 Ag^+$ ions. Three non-equivalent Ag atom positions are found in the large cavity, each containing about 0.6 Ag atoms. This crystallographic analysis may be interpreted to indicate that $0.6 (Ag_6)^{3+}$ clusters are present in each large cavity. This cluster may be viewed as a nearly linear trisilver molecule $(Ag_3)^0$ (bond lengths, 2.92 and 2.94 $\AA;$ angle, $153^{\circ})$ stabilized by the coordination of each atom to a Ag^+$ ion at 3.30, 3.33, and 3.43 $\AA$, respectively. In addition, one of the silver atoms approaches all of the 0(1) oxygens of a 4-ring at $2.76\AA.$ Altogether $7.4 Na^+$ ions, $1.8 Ag^+$ ions, and 1.8 Ag atoms are located per unit cell. The remaining $1.0 Ag^+$ ion has been reduced and has migrated out of the zeolite framework to form silver crystallites on the surface of the zeolite single crystal.

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.148-155
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• 2018

To get a better understanding of the effect of physicochemical properties and microstructure on $SO_2$ absorption behavior of DESs with different molar ratios of EmimCl and EG (from 2:1 to 1:2), densities (${\rho}$), viscosities (${\eta}$), speeds of sound (u), refractive indices ($n_D$), and thermal decomposition temperatures ($T_d$) of EmimCl-EG DESs were measured and used to obtain the other derived properties, such as thermal expansion coefficient (${\alpha}_p$) and activation energy for viscous flow ($E_{\eta}$). Moreover, FT-IR spectra and in situ variable-temperature NMR spectroscopy were employed to study the microstructures of DESs. Based on physicochemical and spectroscopic properties, the influence of the concentrations of EmimCl on the interactions in DESs was explored to be associated with their $SO_2$ absorption behavior. The results show that the interactions between $Emim^+$ and $Cl^-$ of EmimCl is gradually weakening with increasing the concentration of EG in DESs by forming of hydrogen bond interaction of $O-H{\cdots}Cl^-$, resulting in a decrease of ${\rho}$, ${\eta}$, u, $n_D$, and $T_d$ of DESs, and hindering the charge-transfer interaction of $SO_2$ with $Cl^-$ and deceasing $SO_2$ capture capacity. Moreover, the $SO_2$ absorption capacity of DESs is proportional to their ${\rho}$ and $E_{\eta}$, respectively.

• 대한금속재료학회지
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• 제46권1호
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• pp.6-12
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• 2008

Peptides with specific sequences against $LaPO_4$ and $TiO_2$ nanoparticles were discovered through peptide phage display technique as an application to biomolecular recognition of inorganic materials. Sequencing results showed that a motif consisting of serine and proline was commonly expressed in specific sequences. It was postulated that serine directly bound to nanoparticles using its terminal hydroxyl (OH) group. In this sense, oxygen atom seemed to work as a ligand to metal ions and hydrogen atom as a H-bond donor, was thought to bind to the oxygen atoms or the hydroxyl groups on particle surface. Also, it was expected that proline assists serine to make an ideal van der Waals contact between serine and nanoparticles, which optimizes the binding of peptide onto surface.

• Journal of the Korean Wood Science and Technology
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• 제50권3호
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• pp.149-158
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• 2022

To realize the infinite possibilities of materials derived from wood, it is necessary to overcome the weak moisture stability of wood. Thus, the development of an eco-friendly hydrophobic coating agent is essential, and of these, woody biomass-based materials are strongly attractive as coatings. In this study, eco-friendly hydrophobic wood coatings were prepared using carnauba wax purified from palm leaves and sprouts, and kraft lignin. The physicochemical properties of the carnauba wax/lignin blends according to the ratio of carnauba wax and lignin were observed by morphology and functional group change. In addition, the coating performance of carnauba wax/lignin blend coatings was confirmed by measuring the contact angle change. It was found that the addition of lignin could accelerate the atomization of wax particles, and that micro-roughness can be realized when applied to the actual wood surface, to ensure that the coating effect over time lasts longer. In addition, it was confirmed that the addition of lignin increases the hydrogen-bond-based interaction with the wood of the coating, thereby providing better coating stability and increasing the durability of the coating solvent under friction. The carnauba wax/lignin paint developed in this way is eco-friendly because all components are made of wood-based raw materials and have an excellent affinity with wood surfaces. Therefore, it is expected to be applicable to the coating process of wood-plastic composites and timber composites.

• 공업화학
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• 제3권4호
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• pp.595-604
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• 1992

음이온기를 갖는 카보네이트형 폴리우레탄을 NCO-말단 프레폴리머법으로 제조하여 이를 제막하고 에탄올수용액분리 성능을 검토하였다. 우레탄수지의 물성을 향상시키기 위해 카보네이트형 폴리올(PTMCG)을 사용하였고, 친수성 향상에는 사슬연장제로 ${\alpha}^{\prime},{\alpha}^{{\prime}{\prime}}$-dimethylpropionic acid를 이용하였으며, trimethylamine으로 우레탄 사슬내의 카르복실기를 이온화시켰다. 우레탄 사슬내의 음이온기 형성을 확인하기 위해 모델반응을 실시하여 IR 분광분석을 행하였으며, 합성한 우레탄수지의 IR 스펙트럼과 비교하였다. 사슬연장제와 폴리올의 반응몰비율이 3:1에서 5:1인 범위에서는 hard segment의 농도, 수소결합 등이 우레탄수지의 물성을 기여하고 있음을 알 수 있었다. DSC에 의한 열분석결과 카르복실기를 함유한 카보네이트형 폴리우레탄수지(PU)는 $Tg-25^{\circ}C$ 및 Tm $45^{\circ}C$의 값을 갖는 것으로 나타났으며, 이를 이온화하여 사슬내에 음이온성기를 갖게한 카보네이트형 폴리우레탄수지(APU)의 경우 PU 수지보다 $8{\sim}10^{\circ}C$ 정도씩 낮은 온도 영역으로 전이되는 경향을 나타내었다. PU 및 APU 수지를 용매로 N, N-dimethylformamide(DMF), 가교제로 hexamethylene diisocyanate(HMDI)를 사용하여 캐스팅법으로 투과증발막을 제조하였다. 팽윤도 측정결과 혼합물중 에탄올농도에 따라 증가하는 경향을 나타내었고, 가교를 통하여 막의 팽윤도를 조절하였으며, 이를 투과증발에 응용한 결과 선택도 2.3~9.8, 투과유량 $27{\sim}79.5g/m^2hr$를 갖는 것으로 나타났다. 또한 폴리올의 분자량을 2,000에서 1,000으로 줄임으로 분리성능을 향상시킬 수 있었다.