• 폴리머
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• 제25권2호
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• pp.226-232
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• 2001

The properties of poly(ethylene terephthalate) (PET)/maleic anhydride-grafted polypropylene (MAgPP)/poly(styrene-co-maleic anhydride)(PScMA) ternary blend were investigated. The ternary blend was immiscible based on the glass transition temperatures measured by dynamic mechanical analyzer (DMA). The degradation of MAgPP during melt mixing for 30 min at 280$^{\circ}C$ did not affect the properties of the ternary blend. The interaction among the components was confirmed from the rheological properties, which was increased with the PSCMA contents. In terms of the mechanical properties, it was observed to satisfy the mixture rule for a multiple system.

• 한국안전학회지
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• 제29권4호
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• pp.85-90
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• 2014

For the safe handling of acetic anhydride, this study was investigated the explosion limits of acetic anhydride in the reference data. And the lower flash points, upper flash points, and AITs(auto-ignition temperatures) by ignition delay time were experimented. The lower and upper explosion limits of acetic anhydride by the investigation of the literatures recommended 2.9 Vol% and 10.3 Vol.%, respectively. The lower flash point of acetic anhydride by using Setaflash closed-cup tester was experimented $49^{\circ}C$. The lower flash point acetic anhydride by using Tag and Cleveland open cup tester were experimented $55^{\circ}C$and $62^{\circ}C$, respectively. Also, this study measured relationship between the AITs and the ignition delay times by using ASTM E659 tester for acetic anhydride. The experimental AIT of acetic anhydride was $350^{\circ}C$.

• 한국가스학회지
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• 제20권3호
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• pp.66-72
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• 2016

화학산업에서 다양하게 사용되고 있는 propionic anhydride의 안전한 취급을 위해서 인화점과 최소자연발화온도를 측정하였다. Propionic anhydride의 폭발하한계는 실험에서 얻어진 하부인화점을 이용하여 계산하였다. Propionic anhydride의 인화점 측정에서 Setaflash 밀폐식은 $40^{\circ}C$, Pensky-Martens 밀폐식은 $44^{\circ}C$ 그리고 Tag 개방식은 $49^{\circ}C$, Cleveland 개방식에서는 $47^{\circ}C$로 측정되었다. ASTM E659 장치에 의한 최소자연발화온도는 $335^{\circ}C$로 측정되었다. 측정된 하부인화점 $40^{\circ}C$에 의한 폭발하한계는 1.30 Vol.%로 계산되었다. 폭발한계는 측정된 인화점이나 문헌에 제시된 인화점을 이용하여 예측 가능함을 알 수 있었다.

• Elastomers and Composites
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• 제41권1호
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• pp.10-18
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• 2006

Maleic anhydride로 처리된 저분자량 폴리부타디엔 (액상 PB)이 실리카로 보강된 SBR 배합물의 특성에 미치는 영향을 연구하였다. 실리카 분산은 액상 PB의 첨가에 의해 향상되었다. Maleic anhydride가 포함된 액상 PB가 maleic anhydride가 포함되지 않은 액상 PB보다 실리카 분산성 향상에 더 효과적임을 알 수 있었다. SBR 배합물의 점도는 액상 PB가 첨가됨에 따라 감소하였다. 가교밀도는 액상 PB의 함량이 증가함에 따라 감소하였고 가황 속도는 느려졌다. 실험 결과를 고려하면, 5 phr 이하의 소량으로 액상 PB를 첨가함으로써 실리카로 보강된 SBR 배합물의 특성을 향상시킬 수 있을 것으로 사료된다.

• Fibers and Polymers
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• 제4권4호
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• pp.182-187
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• 2003

Low molecular weight copolymers of maleic anhydride and vinyl acetate were prepared to develop formaldehyde free cross-linking agents. Since lower molecular weight is favorable for efficient penetration of the finishing agent into the cotton fibers in the padding process, the concentration of the initiator, chain transfer agent and the monomer ratios were varied to obtain copolymers of low molecular weights. The prepared polymers were characterized by GPC, $^1{H-NMR}$, FTIR, DSC and TGA. Copolymers of molecular weights of 2 000 to 10 000 were obtained and it was found that the most efficient method of controlling the molecular weight was by varying the monomer ratios. Poly(maleic anhydride-co-vinyl acetate) did not dissolve in water, but the maleic anhydride residue hydrolyzed within a few minutes to form poly(maleic acid-co-vinyl acetate) and dissolved in water. However, the maleic acid units undergo dehydration to form anhydride groups on heating above ${160}^{\circ}C$ to some extent even in the absence of catalysts. The possibility of using the copolymers as durable press finishing agent for cotton fabric was investigated. Lower molecular weight poly(maleic anhydride-co-vinyl acetate) copolymers were more efficient in introducing crease resistance, which appears to be due to the more efficient penetration of the cross-linking agent into cotton fabrics. The wrinkle recovery angles of cotton fabrics treated with poly(maleic anhydride-co-vinyl acetate) copolymers were slightly lower than those treated with DMDHEU and were higher when higher curing temperatures or higher concentrations of copolymer were used, and when catalyst, $NaH_2$$PO_2$, was added. The strength retention of the poly(maleic anhydride-co-vinyl acetate) treated cotton fabrics was excellent.

• BMB Reports
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• 제37권6호
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• pp.642-647
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• 2004

The lysine residues of Bacillus licheniformis $\alpha$-amylase (BLA) were chemically modified using citraconic anhydride or succinic anhydride. Modification caused fundamental changes in the enzymes specificity, as indicated by a dramatic increase in maltosidase and a reduction in amylase activity. These changes in substrate specificity were found to coincide with a change in the cleavage pattern of the substrates and with a conversion of the native endo- form of the enzyme to a modified exo- form. Progressive increases in the productions of $\rho$-nitrophenol or glucose, when para nitrophenyl-maltoheptaoside or soluble starch, respectively, was used as substrate, were observed upon modification. The described changes were affected by the size of incorporated modified reagent: citraconic anhydride was more effective than succinic anhydride. Reasons for the observed changes are discussed and reasons for the effectivenesses of chemical modifications for tailoring enzyme specificities are suggested.

• 공업화학
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• 제3권1호
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• pp.179-187
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• 1992

Poly(styrene-co-maleic anhydride), SMA를 DMF 용매에 약 10%(w/w) 용액으로 한 다음 aniline, p-toluidine 및 p-chloroaniline 등으로 maleic anhydride 반복 단위를 imide화 하였다. 이미드화에 있어서 환화 탈수제(cyclodehydration agents)를 사용하였으며 최적 반응조건은 다음과 같았다. (a) 반응온도 : $80^{\circ}C$ (b) 환화 탈수제의 몰비 : SMA내 anhydride/acetic anhydride/sodium acetate/triethyl amino = 1.0/2.0/0.2/1.1. 생성된 imide-modified SMA (SMI) 시료들은 이미드화도가 증가됨에 따라 $T_g$가 증가하였으나 그 변화 정도는 크지 않았다. SMI의 $T_g$는 이미드화에 사용된 아민의 종류에 따라 aniline < p-toluidine < p-chloroaniline의 순으로 $T_g$가 증가하였다.

• Elastomers and Composites
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• 제50권2호
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• pp.103-109
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• 2015

In this study, epoxy/anhydride mixing ratio for the highly silica filled compounds with chromium (III) octoate catalyst was investigated at a low curing temperature ($71^{\circ}C$ for 40 hr) by evaluating the compressive strength with the weight ratio ranges from 0.3/1.0 to 1.0/1.0 of epoxy part (Part A)/anhydride part (Part B). In case of epoxy/anhydride compounds used surface unmodified silica by coupling agent, these compounds need excess anhydride unlike the weight ratio in the conventional epoxy/anhydride compounds. In curing behavior, the epoxy/anhydride compounds containing chromium (III) octoate showed high conversions at $71^{\circ}C$ for 40 hr, even if a dipropylene glycol (DPG) was not used as a polymerization initiator. Also, DPG leads to a poor epoxy network structure. In conclusion, the appropriate weight ratio of Part A/Part B of highly silica filled epoxy/anhydride compounds with chromium (III) octoate catalyst is 0.5/1.0 and the maximum amounts of silica is 1470 phr of epoxy resin.

• Bulletin of the Korean Chemical Society
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• 제33권5호
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• pp.1643-1646
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• 2012

Three Ni-based catalysts with different clay as support were prepared and tested in the hydrogenation of maleic anhydride, among which Ni/clay1 showed best activity and selectivity. Over Ni/clay1 catalyst prepared by impregnation method, 97.14% conversion of maleic anhydride and 99.55% selectivity to succinic anhydride were obtained at $180^{\circ}C$ under a pressure of 1 MPa. Catalytic activity was greatly influenced by the temperature and weighted hourly space velocity. Catalyst deactivation studies showed that this catalyst have a long life time, the yield of MA still higher than 90% even after a reaction time of 60 h. X-ray diffraction (XRD) and $H_2$ temperature programmed reduction (TPR) were use to investigate the properties of the catalyst. XRD and TPR studies showed that Ni was present as $Ni^{2+}$ on the support, which indicated that there was no elemental nickel ($Ni^0$) and $Ni_2O_3$ in the unreduced samples. The formation of Ni was strong impact on catalytic activity.

• 약학회지
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• 제18권2호
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• pp.157-160
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• 1974

1,8-Naphthalic anhydride reacts with aromatic momocarbo-xylic acids having ${\alpha}$-hydrogen atomes such as p-nitrophenylacetic acid, p-methoxylhenylacetic acid, ${\alpha}$-naphthylacetic acid and diphenylacetic acid in the presence of freshly fused sodium acetate as a catalyst to give 1,8-(${\alpha}$-nitrophenylmalonyl)-naphthalin, 1,8-diphenylmalonyl-naphthalin, respectively. The results of these experiments show that 1,8-naphthalic anhydride yields the beta diketone type condensation products.