• 제목/요약/키워드: Formic Acid

검색결과 512건 처리시간 0.023초

In vivo Methane Production from Formic and Acetic Acids in the Gastrointestinal Tract of White Roman Geese

  • Chen, Yieng-How;Wang, Shu-Yin;Hsu, Jenn-Chung
    • Asian-Australasian Journal of Animal Sciences
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    • 제22권7호
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    • pp.1043-1047
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    • 2009
  • Three experiments were conducted to determine the conversion rate of formic and acetic acids into methane in the gastrointestinal tracts of geese. In experiment I, two sets of two 4-month-old male White Roman geese were allocated to one of two treatment groups. Each set of geese was inoculated either with formic acid or with phosphate buffer solution (PBS). After the acid or the PBS was inoculated into the esophagi of the geese, two birds from each treatment were placed in a respiratory chamber as a measurement unit for 4 h in order to determine methane production rate. In experiment II and III, 6- and 7-wk-old male White Roman goslings were used, respectively. Birds were allocated to receive either formic acid or PBS solution injected into the ceca in experiment II. Acetic acid or PBS solution injected into the cecum were used for experiment III. After either the acids or the PBS solution were injected into the cecum, two birds from each treatment were placed in a respiratory chamber as a measurement unit for 3 h; each treatment was repeated 3 times. The results indicated that formic acid inoculated into the oesophagi of geese was quickly converted into methane. Compared with the PBS-injected group, methane production increased by 5.02 times in the formic acid injected group (4.32 vs. 0.86 mg/kg BW/d; p<0.05). Acetic acid injected into the ceca did not increase methane production; conversely, it tended to decrease methane production. The present study suggests that formic acid may be converted to methane in the ceca, and that acetic acid may not be a precursor of methane in the ceca of geese.

4,5-Diphenyl-Imidazolone의 合成 及 螢光效果에 關한 硏究 (Synthesis of 4,5-Diphenyl Imidazolone and Studies on its Fluorescent Effect)

  • 전풍진;김형숙
    • 대한화학회지
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    • 제4권1호
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    • pp.70-77
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    • 1957
  • 4,5-Diphenyl Imidazolone is synthesized from Benzoin, Urea, and Acetic acid catalyser. Nowadays, it is being used as an optical bleaching agent for wool and nylon textiles. Up to now, only one process of synthesis has been known. In order to find out the best conditions governing the yield were examined under various catalysers and conditions. In this experiment, the summary of results were as follows. a. On Acetic acid catalyser. The maximum yield conditions were mol ratio (Benzoin: Urea: Acetic acid) 1 : 2 : 14, Acetic acid concentration 99.9%. Reaction temperature 115$^{\circ}$. Under reaction time of 2 hours, above yield was 96.4%. b. On Mineral acid Catalyser. In using of Sulfonic acid, the color of solution was changed dark purlish black. With other mineral acid catalysers, in spite of increasing of temperature, it was proved that Benzoin floats on the solution, so that this reaction could not be continue. c. On Phosphoric acid catalyser. It was made clear that it can not be used for this reaction. d. On Sodium hydroxide catalyser. As one of Alkali catalyser, Sodium hydroxide was examined but this was unsuitable substance for this reaction. e. On Formic acid catalysers. The maximum yield conditions were mol ratio (Benzoin: Urea: Formic acid) 1: 2: 30. Formic acid concentration 85.%. Reaction temperature 150∼110$^{\circ}$. Under reaction time of 90 minutes, the best yield was 87%. Hereby, it was proved that organic acids such as Acetic acid and Formic acid can be used. When using Acetic acid, the yield was better than Formic acid, but it takes longer reaction time than Formic acid. About the fluorescent effect, the temperature of dye-bath must not be over 904,5-Diphenyl Imidazolone is synthesized from Benzoin, Urea, and Acetic acid catalyser. Nowadays, it is being used as an optical bleaching agent for wool and nylon textiles. Up to now, only one process of synthesis has been known. In order to find out the best conditions governing the yield were examined under various catalysers and conditions. In this experiment, the summary of results were as follows. a. On Acetic acid catalyser. The maximum yield conditions were mol ratio (Benzoin: Urea: Acetic acid) 1 : 2 : 14, Acetic acid concentration 99.9%. Reaction temperature 115$^{\circ}$. Under reaction time of 2 hours, above yield was 96.4%. b. On Mineral acid Catalyser. In using of Sulfonic acid, the color of solution was changed dark purlish black. With other mineral acid catalysers, in spite of increasing of temperature, it was proved that Benzoin floats on the solution, so that this reaction could not be continue. c. On Phosphoric acid catalyser. It was made clear that it can not be used for this reaction. d. On Sodium hydroxide catalyser. As one of Alkali catalyser, Sodium hydroxide was examined but this was unsuitable substance for this reaction. e. On Formic acid catalysers. The maximum yield conditions were mol ratio (Benzoin: Urea: Formic acid) 1: 2: 30. Formic acid concentration 85.%. Reaction temperature 150∼110$^{\circ}$. Under reaction time of 90 minutes, the best yield was 87%. Hereby, it was proved that organic acids such as Acetic acid and Formic acid can be used. When using Acetic acid, the yield was better than Formic acid, but it takes longer reaction time than Formic acid. About the fluorescent effect, the temperature of dye-bath must not be over 90$^{\circ}$. and the ratio of 4,5-Diphenyl Imidazolone and water should be from 1:50000. to 1:10000. It proved that the best effect on textiles, and the best condition were dye-temperature near 704,5-Diphenyl Imidazolone is synthesized from Benzoin, Urea, and Acetic acid catalyser. Nowadays, it is being used as an optical bleaching agent for wool and nylon textiles. Up to now, only one process of synthesis has been known. In order to find out the best conditions governing the yield were examined under various catalysers and conditions. In this experiment, the summary of results were as follows. a. On Acetic acid catalyser. The maximum yield conditions were mol ratio (Benzoin: Urea: Acetic acid) 1 : 2 : 14, Acetic acid concentration 99.9%. Reaction temperature 115$^{\circ}C$. . Under reaction time of 2 hours, above yield was 96.4%. b. On Mineral acid Catalyser. In using of Sulfonic acid, the color of solution was changed dark purlish black. With other mineral acid catalysers, in spite of increasing of temperature, it was proved that Benzoin floats on the solution, so that this reaction could not be continue. c. On Phosphoric acid catalyser. It was made clear that it can not be used for this reaction. d. On Sodium hydroxide catalyser. As one of Alkali catalyser, Sodium hydroxide was examined but this was unsuitable substance for this reaction. e. On Formic acid catalysers. The maximum yield conditions were mol ratio (Benzoin: Urea: Formic acid) 1: 2: 30. Formic acid concentration 85%. Reaction temperature 150∼110$^{\circ}C$. Under reaction time of 90 minutes, the best yield was 87%. Hereby, it was proved that organic acids such as Acetic acid and Formic acid can be used. When using Acetic acid, the yield was better than Formic acid, but it takes longer reaction time than Formic acid. About the fluorescent effect, the temperature of dye-bath must not be over 90$^{\circ}C$. and the ratio of 4,5-Diphenyl Imidazolone and water should be from 1:50000. to 1:10000. It proved that the best effect on textiles, and the best condition were dye-temperature near 70$^{\circ}C$. and dye-time 15 minutes. . and dye-time 15 minutes. . and the ratio of 4,5-Diphenyl Imidazolone and water should be from 1:50000. to 1:10000. It proved that the best effect on textiles, and the best condition were dye-temperature near 70$^{\circ}C$. and dye-time 15 minutes.

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재래식과 개량식 발효식품의 유기산 분포 (Distribution of Organic Acids in Traditional and Modified Fermented Foods)

  • 오금순;강길진;홍영표;안영순;이향미
    • 한국식품영양과학회지
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    • 제32권8호
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    • pp.1177-1185
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    • 2003
  • 전통발효식품(간장 및 된장, 고추장, 감식초 등)중에 재래식과 개량식 제품의 맛과 향에 기인하는 유기산의 분포정도를 확인하고자 하였고, 아울러 식품공전에 보존료로 고시되어 있는 propionic acid가 발효과정 중에 생성됨에 따라 그 분포정도를 알고자 하였다 재래식 간장에서는 citric acid, formic acid, oxalic acid, propionic acid가, 개량식에서는 acetic acid와 lactic acid가 상대적으로 많이 검출되었으며, propionic acid는 검출되지 않았다. 재래식 및 개량식 된장 모두 유사한 분포양상을 보였으며, 재래식에서는 개량식 보다 citric acid와 succinic acid를 제외하고 약간 높은 함량을 보였다. 고추장의 경우 재래식이 개량식보다 citric acid, formic acid, acetic acid, lactic acid가 다소 높은 함량을 보였고, 그 외 다른 유기산들은 비슷한 양상을 보였다. 그러나 재래식에서는 Propionic acid가 검출된 반면 개량식에서는 전혀 검출되지 않았다. 일반 양조식초에서는 acetic acid가 주요 유기산이었고 미량의 formic acid가 검출되었으며, 감식초의 경우 acetic acid, lactic acid, propionic acid가 검 출되었다. 감식초중 flavonoid계 인 tannic acid 함량은 다소 제품별로 차이는 있었으나 그 범위는 366.9 ∼ 909.8 mg%를 보였다. 결론적으로 재래식 발효식품과 개량식 발효식품의 유기산 분포는 그 함량이 서로 달랐으며, 특히 보존료로 사용되고 있는 propionic acid는 된장을 제외한 재래식 발효식품에서 생성되었고, 개량식 발효식품에서는 생성되지 않았다. 또한 식초의 경우 감식초에서만 검출되었다.

비가연성 성분을 포함한 이성분계 액상 용액의 인화점 결정 (Flash Point Determination of Binary Liquid Solution Containing Nonflammable Component)

  • 하동명;이성진
    • 한국가스학회지
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    • 제23권3호
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    • pp.40-45
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    • 2019
  • 인화점은 가연성 액체 혼합물의 화재와 폭발의 위험성을 특징짓는 중요한 인화성 지표이다. 본 연구에서는 Seta flash 장치에 의해 water+formic acid 계와 water+acrylic acid 계의 인화점을 측정하였다. 측정한 인화점을 라울의 법칙과 경험식을 이용한 인화점 예측값과 비교하였다. 라울의 법칙을 이용한 예측 결과의 절대평균오차는 water+formic acid 계의 경우 $10.7^{\circ}C$ 였고, water+acrylic acid 계의 경우 $4.8^{\circ}C$ 이었다. 경험식을 이용한 예측 결과의 절대평균오차는 water+formic acid 계의 경우 $1.0^{\circ}C$ 였고, water+acrylic acid 계의 경우 $0.5^{\circ}C$ 이었다. 결과적으로 라울의 법칙에 의한 예측값에 비해 경험식에 의한 예측값이 측정값을 보다 잘 모사하였다.

산성 수용액 조건에서 포도당과 자일로스 반응 산물의 1H-NMR 분광분석을 이용한 정량 분석 (Quantitative Analysis of Reaction Products from Glucose and Xylose in Acidic Aqueous Medium by 1H-NMR Spectroscopic Method)

  • 신수정
    • Journal of the Korean Wood Science and Technology
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    • 제41권4호
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    • pp.287-292
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    • 2013
  • 진한 산 가수분해 반응 중 2차 가수분해 조건에서 포도당과 자일로스의 반응을 수소 핵자기 공명 분광분석을 통하여 정량적으로 분석하였다. 정량분석은 아노머성 수소, 퓨란과 개미산의 특징적인 피크를 이용하여 실시하였다. 진한 산 가수분해의 2차 가수분해 조건에서 포도당의 일부가 5-hydroxymethylfufural (5-HMF) 중간 구조를 거쳐 levulinic acid와 개미산으로 분해되었음을 확인하였다. 자일로스는 furfural 중간 구조를 거쳐 개미산으로 분해가 되었으며, 포도당은 자일로스보다 2차 가수분해 조건에서 산에 의한 퓨란계 화합물의 전이가 느리게 전환되어 단당의 안정성이 높았다. 퓨란계 화합물로 전환된 이후, 산에 민감한 5-HMF는 쉽게 formic acid와 levulinic acid로 전환되었지만, furfural은 formic acid로의 분해 반응이 더디게 진행되어 furfural의 농도가 5-HMF보다 상대적으로 높게 나타났다.

용제처리에 의한 합성섬유의 구조와 물성에 관한 연구(V) -Formic Acid 처리에 의한 Nylon 6 Filament 직물의 수축거동 및 성질변화- (Study on the Structure and the Physical Properties of Synthetic Fibers Treated with Organic Solvents (V) -The Shrinkage Behavior and Property Change of Woven Fabric Composed of Nylon 6 Filaments by Formic Acid Treatment-)

  • Lee, Yang-Hun;Park, Suk-Chul
    • 한국염색가공학회지
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    • 제1권1호
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    • pp.54-62
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    • 1989
  • The woven fabric composed of nylon 6 filaments was treated with aqueous solutions (20, 30, 40, 50, 60%) of formic acid at 3$0^{\circ}C$ for 10 minutes under unrestrained condition, and the shrinkage behavior and some kinds of properties were examined. The shrinkages of the constituent yarns and fabric were increased with formic acid concentration, but they were lower than that of the original filaments because of fabric-structural factors. And the shrinkage of the warp was lower than that of the weft because of the residual stress from weaving process. By the restraint forces such as fabric-structural factors and residual stress, the constituent filaments were damaged partially at 60% of formic acid concentration and the degree of damage on the warp was greater than on the weft. And though the fabric count were increased overall, the spacing between the warps was decreased prior to the weft and eliminated nearly at 60% of formic acid concentration. The thickness, tensile strength, elongation, and handle value of fabric were increased overall with formic acid concentration excepting that the tensile strength for both the warp and weft directions and the elongation for the warp direction were decreased instead by the damage of yarns. But the crease recovery was decreased except the case of the weft direction at 60% of formic acid concentration.

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다양한 유기산제들의 급여가 이유자돈의 성장과 영양소 소화율에 미치는 효과 (Comparison of the Efficacy of Different Organic Acids on Growth Performance and Nutrient Digestibility in Weaned Pigs)

  • 주지환;;최재용;최순천;조원탁;채병조
    • Journal of Animal Science and Technology
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    • 제51권1호
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    • pp.15-24
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    • 2009
  • 본 연구는 다양한 유기산제들의 급여가 이유자돈의 성장과 영양소 소화율에 미치는 영향을 비교하기 위하여 2번의 사양실험을 수행하였다. 실험 1과 실험 2에서는 각각 이유자돈 180두 (4처리, 3반복, 15두/반복)를 공시하였다. 실험 1은 기초사료에 formic acid, ammonium-formate, lactic acid 그리고 acid mixture를 각각 0.5%씩 첨가하여 총 5주간 사양실험을 실시하였으며, 실험 2는 formic acid, ammonium-formate, lactic acid 그리고 acid mixture를 각각 0.3%씩 첨가하여 총 6주간 사양실험을 실시하였다. Acid mixture는 formic acid와 lactic acid가 50:50의 비율로 혼합된 제제를 사용하였다. 외관상 회장아미노산 소화율을 측정하기 위하여 각 처리별 3두, 총 12두를 공시하여 T-cannula를 회장 말단부에 부착시킨 후 적응기간을 거쳐 회장내용물을 채취하였다. 사양성적은 유기산 종류에 따른 개선 효과는 없는 것으로 나타났으나 (실험 1), acid mixture 급여구에서 증체량이 lactic acid 급여구보다 높은 것으로 나타났다 (실험 2). 외관상 회장 아미노산 소화율은 lactic acid 급여구보다 acid mixture 급여구에서 개선되는 것으로 나타났다 (실험 1과 2). 실험 1과 2의 결과를 종합하였을 때 acid mixture (formic acid + lactic acid) 급여는 이유자돈의 사양성적과 외관상 회장 아미노산 소화율을 개선시키는 것으로 판단된다.

포름산 및 황산 촉매를 이용한 자일로스로부터 푸르푸랄 생산 (Furfural Production From Xylose by Using Formic Acid and Sulfuric Acid)

  • 이승민;김준석
    • Korean Chemical Engineering Research
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    • 제61권4호
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    • pp.561-569
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    • 2023
  • 푸르푸랄(furfural)은 리그노셀룰로오스 바이오매스(lignocellulose biomass)의 헤미셀룰로오스(hemicellulose) 성분 중 하나인 자일로스(xylose)로부터 생산되는 플랫폼 화학물질이다. 푸르푸랄은 페놀류 화합물이나 바이오 연료 등의 중요한 원료로 사용될 수 있다. 본 연구에서는 푸르푸랄 생산공정에서 일반적으로 사용되는 산 촉매인 황산(sulfuric acid)과 친환경적 촉매인 포름산(formic acid) 두 가지 촉매를 이용하여 회분식 반응 시스템(batch system)에서 자일로스로부터 푸르푸랄을 생산하기 위한 조건을 비교 및 최적화하였다. 자일로스의 초기 농도(10 g/L~100 g/L), 반응 온도(140~200 ℃), 황산 촉매(1~3 wt%), 포름산 촉매(5~10 wt%), 반응 시간에 따라 자일로스로부터 푸르푸랄 수율에 미치는 영향을 조사하였다. 촉매 종류에 따른 최적 조건은 다음과 같았다. 황산 촉매의 경우, 3 wt%의 촉매농도, 50 g/L의 초기 자일로스 농도, 180 ℃의 온도 10분의 반응시간에서 최대 58.97%의 푸르푸랄 수율을 얻었다. 포름산 촉매의 겨우, 5 wt%의 촉매농도, 50 g/L의 초기 자일로스 농도, 180 ℃의 온도, 150분 반응 시간에서 65.32%의 푸르푸랄 수율을 확보하였다.

개미산-과산화수소 펄핑에 의하여 생산된 백합나무 펄프의 화학적 및 역학적 특성 분석 (Chemical and Mechanical Properties of Yellow Poplar Pulp Produced by Formic Acid- Hydrogen Peroxide Pulping)

  • 심재훈;김정호;박종문;신수정
    • 펄프종이기술
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    • 제45권1호
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    • pp.6-12
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    • 2013
  • TFormic acid-hydrogen peroxide (or performic acid) pulping process needs milder reaction condition than other chemical pulping process. Two-step formic acid-hydrogen peroxide pulping process can produce the chemical pulp with similar pulp yield and lignin content compared with soda-anthraquinone process. Formic acid-hydrogen peroxide pulp can be produced less xylan content than other alkaline pulps, which favor for dissolving pulp production. Formic acid-hydrogen peroxide pulp showed better response beating than soda-anthraquinone(AQ) pulps with reaching target freeness with less beating. Also, formic acid-hydrogen peroxide pulp had better tensile index at similar freeness level compared with soda-AQ pulps.

부숙과정중(腐熟過程中) 낙엽류(落葉類) 가수분해물(加水分解物)의 유기산함량(有機酸含量) 변화(變化) (Changes of Some Organic Acids in the Hydrolysates of Decomposing Litters of Wild Grasses and Tree Leaves)

  • 김정제;최강순;신영오
    • 한국토양비료학회지
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    • 제25권4호
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    • pp.407-410
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    • 1992
  • 산야초(山野草), 활엽수(闊葉樹)와 침엽수낙엽(針葉樹落葉)을 실험실조건하(實驗室條件下)에서 90일간(日間) 부숙(腐熟)시키면서 경시적(經時的)으로 시료(試料)를 채취(採取)하여 산가수분해(酸加水分解)시킨후 6개(個)의 저분자량(低分子量)의 유기산(有機酸)을 분석(分析)한 결과(結果)는 다음과 같다. 1. Formic, acetic, succinic, malic, tartaric와 citric acid가 검출(檢出)되었으며 이중(中) malic acid는 전시료중(全試料中)에서 극(極)히 미량(微量)으로 함유(含有)되어 있었다. 2. 산야초(山野草)의 경우 저분자량(低分子量) 유기산(有機酸)의 농도(濃度)는 부숙기간(腐熟期間)이 경과(經過)함에 따라 감소(減少)했으며 formic acid와 acetic acid등(等) monocarboxylic acid는 dicarboxylic acid와 tricarboxylic acid에 비(比)해 훨씬 높은 농도(濃度)를 보였고 formic acid와 acetic acid는 상호보충(相互補充) 관계(關係)가 있었다. Citric acid는 부숙기간(腐熟期間)이 경과(經過)함에 따라 농도(濃度)가 증가(增加)하였다. 3. 활엽수낙엽(闊葉樹落葉)의 경우 부숙기간(腐熟期間)이 경과(經過)함에 따라 monocarboxylic acid농도(濃度)가 상대적(相對的)으로 높았다. Formic acid와 acetic acid사이는 상호보충(相互補充) 관계(關係)가 있음이 구명(究明)되었다. 4. 침엽수낙엽(針葉樹落葉)의 경우 부숙기간(腐熟期間)이 경과(經過)함에 따라 유기함유량(有機含有量)의 변화(變化)가 별(別)로 나타나지 않았다. 산야초(山野草)와 활엽수낙엽(闊葉樹落葉)과는 대조적(對照的)으로 dicarboxylic acid인 succinic acid농도(濃度)가 가장 높았다.

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