• 한국건축시공학회:학술대회논문집
• /
• 한국건축시공학회 2020년도 봄 학술논문 발표대회
• /
• pp.181-182
• /
• 2020

In this study, oxidized graphene nanoplatelet(GO) was prepared by oxidizing graphene nanoplatelet(GNP) with nitric acid in order to solve the problem of dispersion of GNP, one of nano materials. GNP/Epoxy and GO/Epoxy were prepared by mixing GNP, GO with 0.1, 0.3, 0.5 and 1.0 wt.% in epoxy and the mechanical properties, bond performance were evaluated. As a result, GNP/Epoxy and GO/Epoxy showed higher tensile strength than Neat Epoxy at the 0.1, 0.3 wt.%. Especially, when 0.1 wt.% of GO was incorporated into epoxy resin, it showed highest tensile strength. It was confirmed that acid treatment of GNP was effective in improving the mechanical properties of epoxy paint. However, graphene material was found that it was not effective in improving the bond strength of the epoxy paint.

• Journal of the Korean Wood Science and Technology
• /
• 제34권6호
• /
• pp.29-35
• /
• 2006

본 연구는 단판 함수율을 0%, 3%, 5%, 8%, 15%, 30%로, 지방산: 글리세롤: MDI의 당량비율을 1:1:2, 1:1:3, 1:1:4, 1:1:5, 1:1:6 으로 달리하여 상태 (비내수)접착력을 조사하였다. 함수율 0%, 3%, 5%, 8%, 15%에서는 지방산 : 글리세롤 : MDI 당량비 1:1:2 일때, KS F 3101(보통합판) 기준 접착력 $7.0kgf/cm^2$를 상회하였으며, 함수율이 커질수록 접착력이 점차 감소하여 각각 $13.7kgf/cm^2$, $1.6kgf/cm^2$, $11.2kgf/cm^2$, $9.8kgf/cm^2$, $7.4kgf/cm^2$ 순으로 나타났다. 함수율 30% 에서는 지방산 : 글리세롤 : MDI 당량비 1:1:6 일 때, 강도 $8.1kgf/cm^2$로 KS 규격 접착력을 만족하였다. KS 규격 접착력을 만족시키기 위해서는 단판의 함수율이 증가할수록 MDI 비율을 높여야 한다.

• Elastomers and Composites
• /
• 제48권4호
• /
• pp.256-262
• /
• 2013

Sulfuric acid group을 도입하여 열가소성 폴리우레탄을 제조하였으며, sulfuric acid의 함량을 변경하여 acid 함량에 따른 특성 변화를 연구하였다. 그리고 carboxylic acid를 도입한 폴리우레탄을 제조하여 비교 분석했다. 연구 결과 acid group을 도입함으로써 인장강도, 마모 등 기계적 물성 및 그립 특성이 증가하는 것을 확인할 수 있었으며, Acid 함량별로 물성을 측정한 결과, 일정한 함량까지 기계적 물성은 증가하며 일정 함량 이상에서는 기계적 물성이 감소하는 것을 확인할 수 있었다. Wet slip의 경우 또한 acid group 도입에 의해 친수성이 증가함으로 acid 함량이 증가할수록 wet slip은 증가 하는 것을 확인할 수 있었다. Carboxylic acid를 도입한 폴리우레탄과 비교 결과, 수소결합력이 약해 기계적 물성은 낮게 나타났으나 rebounding 특성은 더 높게 나타나는 것을 확인할 수 있었다.

• 한국응용과학기술학회지
• /
• 제37권1호
• /
• pp.49-55
• /
• 2020

In this study, isophorone diisocyanate (IPDI) and dimethylolbutanoic acid (DMBA) were used on the basis of poly caprolactone diol (3M, 3.5M, 4M, 4.5M) for the synthesis of water-based polyurethanes for coating on skin layers of leather. Tensile strength, elongation, and adhesive strength of the prepared samples were measured. As a result of measuring the tensile strength, the tensile strength was found to be 4.09 kgf / ㎟ when 3 moles were applied, and 1.071 kgf / ㎟ when 4.5 moles were applied. Elongation was 366 % when 3 moles of PCL were applied, and 709 % at 4.5 moles. Adhesive strength was 2.887 kgf / cm when 3 moles of PCL was applied and 0.998 kgf / cm when 4.5 moles were applied.

• Elastomers and Composites
• /
• 제31권2호
• /
• pp.104-110
• /
• 1996

The polyurethane was synthesized by the reaction of polycaprolactone diol(Mw 2000), 4,4'-diphenylmethane diisocyanate and 1,4-butanediol as the chain extender. Also, the modified polyurethane polymers based on liquid polybutadiene as a part of soft segment and dimethylolpropionic acid as a chain extender, giving polyurethane with various polarity, were synthesized. The thermal, mechanical, adhesion properties and water contact angles of the polyurethanes were examined. From the result of the water contact angle, the polarity of the acid modified PU containing 6% acid content was unchanged but mechanical and adhesion properties were improved. The water contact angles on polybutadiene modified PU films were increased with increasing polybutadiene content. The mechanical properties of the polybutadiene modified PU were higher than that of acid modified PU. However, the mechanical properties were reduced as polybutadiene content increased. The result is presumably due to phase separation between hard segment and soft segment. The peel strength of the polyurethane introduced with 5wt% polybutadiene was improved about 150% than that of unmodified PU. The same as the mechanical properties, the more polybutadiene was introduced, the lower peel strength was obtained.

• 한국응용과학기술학회지
• /
• 제25권3호
• /
• pp.341-346
• /
• 2008

Cellulose nanofibers from microfibril cellulose (MFC) was prepared by hydrobromic acid (HBr) treatment at different concentrations. Polyvinyl alcohol (PVA) composite films at various loading level of nanofibers were manufactured by a film casting method. The analysis of degree of polymerization (DP), crystallinity ($X_c$) and molecular weight ($M_w$) of cellulose after acid treatment was conducted. The mechanical and thermal properties of the cellulose nanofibers reinforced PVA films were characterized using tensile tests and thermogravimetric analysis (TGA). The DP and $M_w$ of MFC by HBr hydrolysis considerably decreased, but $X_c$ showed no significant change. After acid hydrolysis, the diameter of cellulose nanofibers was in the range of 100 to 200 nm. The thermal stability of the films was steadily improved with the increase of nanofiber loading. There was a significant increase in the tensile strength of PVA composite films with the increase in MFC loading. Finally, 5 wt.% nanofiber loading exhibited the highest tensile strength and thermal stability of PVA composite films.

• 한국염색가공학회지
• /
• 제19권4호
• /
• pp.10-17
• /
• 2007

Chitosan(CS) and cellulose acetate(CA) composite films were prepared using formic acid as a cosolvent by casting, solvent evaporating and neutralization method. This study examines if the blending method, which uses formic acid as a cosolvent is efficient in improving the mechanical properties of CS film, especially wet strength and elongation. Formic acid is an effective cosolvent for the blend of CS and CA. Under wet condition, tensile strength and elongation of the composite films were obviously higher than those of the films made from pure CS. FTIR, DSC, and X-ray diffraction showed that the composite films exhibit a high level of compatibility and that strong interaction between the CS and CA was caused by intermolecular hydrogen bonding. The affinity series of composite film to transition metal ions are Cu(II) > Cd(II) > Cr(III). The adsorption of Cu((II) ion was shown to be highly pH sensitive.

• 접착 및 계면
• /
• 제12권2호
• /
• pp.67-72
• /
• 2011

Acrylic pressure-sensitive adhesives are used in many different parts in the world. But acrylic acid in PSAs may occur unexpected results such as corroding adherends or producing by-products when applied within electronic devices. This study employed acrylic PSAs based on 2-ethylhexyl acrylate (2-EHA), 2-hydroxyethyl acrylate (2-HEA) and butyl acrylate (BA) with different coating thickness. There are two types of curing agents. One is methylaziridine derivative (MAZ) and the other is aluminum acetylacetonate (AlACA). This study examined the adhesion performance and curing behaviors using peel strength, probe tack and gel fraction. Also, the viscoelastic properties of acrylic PSAs were investigated from Advanced rheometric expansion system (ARES).

• Carbon letters
• /
• 제9권1호
• /
• pp.8-16
• /
• 2008

Oxidized activated carbons were prepared by reacting steam-activated carbon developed from pecan shells with nitric acid of varying strength (15, 30, 45 and 60%). The textural properties and the chemistry of the surface of the non-oxidized and of the oxidized carbons were determined from nitrogen adsorption and base neutralization capacities. The uptake of Pb(II) and Cd(II) from aqueous solution by these carbons was determined by kinetic and equilibrium experiments as well as by the column method. Treatment with nitric acid brought about drastic decrease in surface area and remarkable increase in the pore size of the carbon with these changes depending on the strength of nitric acid. Nitric acid increased the surface acidity by developing new surface oxygen functional groups of acidic nature. $HNO_3$-oxidized carbons exhibited high adsorption capacities for Pb(II) and Cd(II). The adsorption of these ions increased with the decrease of the surface pH of the carbon and with the increase of the solution pH from 2.5 to 6 and 7. The amount adsorbed from lead and cadmium was also related to the amount of surface acidity, the pH of the point of zero charge and on some metal ion parameters. Cadmium and lead uptake by the investigated carbons followed pseudo-second order model and the equilibrium sorption data fitted Langmuir adsorption model.

• Advances in concrete construction
• /
• 제10권3호
• /
• pp.221-236
• /
• 2020

To reduce the CO₂ emissions associated with the manufacture of portland cement (PC), an efficient alternative like an alkali-activated binder (AAB) is the requirement of the industry. To promote the use of AAB in construction activities, a practically implementable mix proportion is required. Owing to the several raw ingredients of AAB concrete and their associated uncertainties, partial replacement of PC by AAB may be adopted instead of complete replacement as per industrial requirements. Hence, the present study aims to determine an optimal proportion for partial replacement of PC with AAB and recommend a technique for it based on site conditions. Three modes of partial replacement are followed: combining all the dry ingredients for AAB and PC followed by the addition of the requisite liquids (PAM); combining the PC and the AAB concrete in two horizontal layers (PAH); and two vertical layers (PAV). 28-day old specimens are exposed to 10% v/v solutions of HCl, H₂SO₄, and HNO₃ to evaluate changes in mechanical, physical, and microstructural characteristics through compressive strength, corrosion depth, and microscopy. Based on deterioration in strength and integrity, PAH or PAV can be adopted in absence of acid attack, whereas PAM is recommended in presence of acid attack.