• Corrosion Science and Technology
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• 제10권5호
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• pp.180-188
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• 2011

In the present study, denting corrosion experiments were performed as a function of crevice gap size (50, 100 and 200 ${\mu}m$) in a solution containing 3,500 ppm NaCl + 0.2 M $CuCl_2$ (pH = 3 adjusted by HCl). The effects of chloride ion concentrations (3, 3,500 and 35,000 ppm as NaCl) were also outlined with two different crevice gap sizes (100, 200 ${\mu}m$). In addition, the effect of NiB on the denting corrosion was also investigated in a solution of 35,000 ppm NaCl + 0.2 M $CuCl_2$ (pH = 3 adjusted by HCl). The results showed that denting rate increased with the increasing crevice gap size at an initial stage and became nearly constant afterwards. As the concentration of chloride ion increased, the denting rate also increased. However, the addition of a NiB powder of 4 g/L in to the acid-chloride solution was observed to suppress the denting rate significantly.

• Corrosion Science and Technology
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• 제22권3호
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• pp.137-152
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• 2023

Polarization behavior and corrosion inhibition of copper in acidic chloride solutions containing benzotriazole were studied. Pourbaix diagrams constructed for copper in NaCl solutions with different BTAH concentrations were used to understand the polarization behavior. Open circuit potential (OCP) depended not only on chloride concentration, but also on whether a CuBTA layer was formed on the copper surface. Only when the (pH, OCP) was located well in the CuBTA region of the Pourbaix diagram, a stable corrosion inhibiting CuBTA layer was formed, which was confirmed by X-ray Photoelectron Spectroscopy (XPS) and a long-term corrosion test. The OCP for the CuBTA layer decreased logarithmically with increasing [Cl^-] activity in the solution. A minimum BTAH concentration required to form a CuBTA layer for a given NaCl concentration and pH were determined from the Pourbaix diagram. It was found that 320 ppm BTAH solution could be used to form a corrosion-inhibiting CuBTA layer inside the corrosion pit in the sprinkler copper tube, successfully reducing water leakage rate of copper tubes. These experimental results could be used to estimate water chemistry inside a corrosion pit.

• Asian-Australasian Journal of Animal Sciences
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• 제31권8호
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• pp.1073-1077
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• 2018

Nitrite plays a major role in inhibiting the growth of foodborne pathogens, including Clostridium botulinum (C. botulinum) that causes botulism, a life-threatening disease. Nitrite serves as a color-fixing agent in processed meat products. However, N-nitroso compounds can be produced from nitrite, which are considered as carcinogens. Thus, consumers desire processed meat products that contain lower concentrations (below conventional concentrations of products) of nitrite or no nitrite at all, although the portion of nitrite intake by processed meat consumption in total nitrite intake is very low. However, lower nitrite levels might expose consumers to risk of botulism poisoning due to C. botulinum or illness caused by other foodborne pathogens. Hence, lower nitrite concentrations in combination with other factors such as low pH, high sodium chloride level, and others have been recommended to decrease the risk of food poisoning. In addition, natural compounds that can inhibit bacterial growth and function as color-fixing agents have been developed to replace nitrite in processed meat products. However, their antibotulinal effects have not been fully clarified. Therefore, to have processed meat products with lower nitrite concentrations, low pH, high sodium chloride concentration, and others should also be applied together. Before using natural compounds as replacement of nitrite, their antibotulinal activities should be examined.

• Journal of Preventive Medicine and Public Health
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• 제23권1호
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• pp.1-10
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• 1990

셀레늄이 수은, 카드뮴 및 크롬의 세포독성에 미치는 영향을 파악하고자 이들 중금속을 $0.3{mu}M$에서 $10{mu}M$까지 6개 농도로 각각 희석하여 $1.2{mu}M$의 셀레늄과 함께 혈액 배양에 첨가하고, 48시간 경과후 fluorescence-plus-Giemsa 염색에 의해 2차분열 중기의 염색체에서 자매염색분체교환(SCE)현상을 관찰하여, 셀레늄을 첨가하지 않았을 때의 결과와 비교하였다. 셀레늄을 다른 중금속들의 경우와 동일한 농도로 단독 첨가한 경우 SCE빈도는 $5.9{\pm}2.64$회에서 $12.3{\pm}3.99$회의 범위로 변하였고, 수은은 $6.5{\pm}2.70$회에서 $15.7{\pm}2.75$회, 카드뮴은 $6.7{\pm}2.65$회에서 $11.2{\pm}4.13$회, 크롬은 $7.0{\pm}2.58$회에서 $14.9{\pm}6.43$회의 범위로 농도증가에 비례하여 SCE빈도가 상승하였으며, 이때 세포분열지수는 공히 농도증가에 반비례하여 고농도군에서는 현저히 낮았다. 중금속들과 $1.2{mu}M$의 셀레늄을 동시에 첨가시킨 조건에서는 수은의 경우, 셀레늄과 수은의 몰(mol)농도비가 1:1, 1:2, 1:4의 조건에서, 카드뮴의 경우 1:2 및 1:4의 조건에서 SCE빈도의 현저한 감소를 나타냈으나 크롬의 경우는 셀레늄의 첨가와 무관하였으며, 세포분열지수는 전반적으로 셀레늄의 첨가에 별다른 영향을 받지 않았다.

• 한국수산과학회지
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• 제11권2호
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• pp.103-109
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• 1978

1. 1974년 3월에서 1975년 3월사이 매월 대조일과 소조일에 낙동강 물금 부산시 상수도 구취수장 원수의 염화이온, 칼슘, 마그네슘의 량을 매시간 측정하였다. 2. 1974년 3월에서 1975년 1월사이의 염화이온 농도는 5.12-39.4 ppm에 평균값이 11.9pm, 총 경도는 27.8-70.8 ppm에 평균값이 49.5ppm였고, 1975년 2월 9일에서 3월 7일까지의 조차가 큰 기간에는 염화이온농도 10.8-876 ppm에 평균값이 89.8 ppm, 총경도는 48.0-407 ppm에 평균값이 89.9 ppm였다. 3. 계절적으로는 동계에 농도가 높고 조차가 큰 2월과 5월초 사이가 가장 높다. 염화이온농도 150 ppm를 넘은 날이 모두 2월에 들어있다. 4. 총경도 역시 염화이온농도와 비슷한 변동을 한다. 수도법의 허용한계인 300ppm를 넘는날이 2월 9일에서 3월 7일 사이에 약 4 일 정도 나타난다. 5. 수위는 하천수량과 조위로써 정해지는 까닭에 수위만으로는 염화이온 농도를 알 수가 어렵지만 염화이온농도와 수위의 시간적 변동관계는 수위가 높을 때 농도가 높으며, 2월 및 3월에서 더욱 그러하다. 6. 조위와 수위와는 약간의 시차를 두고 거의 같은 모양의 변동을 하며 최고조위에서 최고수위까지 대조일에는 약 2시간 30분, 소조일에는 약 3시간의 차가 나타난다. 끝으로 수위와 조위자료를 제공해 주신 부산시수도사업소와 부산수로국에 감사드립니다.

• 한국대기환경학회지
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• 제15권5호
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• pp.567-574
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• 1999

Volatile organic Compounds(VOC) were measured at an industrial site in Ulsan in 1997 and 1998. Twenty-four hour integrated ambient air samples were collected in 6 L SUMMA canisters during the periods of June 3 to 8, 1997 and June 12 to 17, 1998. The daily mean concentrations of the total $C_2-C_9$ VOC in 1998 were about one third of those in 1997. This decrease of VOC levels may be attributable to the measures to control the emissions of VOC and the decrease of the plant operation. The decrease in the concentrations of oxygenated hydrocarbons and alkenes, especially, contributed to the decrease of the total VOC concentrations in 1998. Lowever concentrations of alkenes compared to aromatics in 1998 were due to the decrease of ethylene and propylene. In the present study, methanol (12.0 ppb) was the most abundant species, followed by acetone (10.1 ppb), propane (6.0 ppb), and vinyl chloride (5.9 ppb). The total concentrations of hazardous air pollutants (HAPs) in 1998 were reduced compared to those in 1997. However, this decrease is due to the drastic decrease of the concentration of methanol. Except methanol, the concentrations of HAPs have not varied much. It is suspected that the VOC control strategy for the Ulsan industrial area has been successful for reducing the total VOC levels but might not be effective in reducing the concentrations of HAPs.

• Journal of Preventive Medicine and Public Health
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• 제29권3호
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• pp.495-505
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• 1996

수은이 세포성 면역반응에 미치는 효과와 그 기전을 밝히기 위해 cytokine-EMT-6 cell-NO 모형에 대조군에는 수은을 첨가하지 않았고 나머지 실험군에는 $0.05-0.8{\mu}M$의 mercury chloride를 처리하였다. 그리고 배양시간별, 수은농도별로 세포생존율, 세포성 면역의 지표인 NO를 nitrite로 간접정량하고 대사과정에 필수 에너지요소인 nitrite를 측정한 결과는 아래와 같이 요약된다. 1. EMT-6세포의 세포생존율은 대조군과 36시간째 $0.8{\mu}M(89.50%)$을 제외한 모든 수은첨가군에서 모두 90%이상의 값을 나타내었으며, 배양시간 및 첨가한 수은농도별 군간 차이는 없었고 모든 수은첨가군과에서 대조군에 비해 큰 차이가 없었다. 2. 수은에 노출된 EMT-6 세포의 nitrite 생성량 및 ATP생성량은 배양시간의 경과에 따라 전반적으로 증가하였으며 시간경과에 따른 nitrite 생성량과 ATP 생성량은 첨가한 수은농도의 변화에 따라 각 군간에 현저한 차이를 보였다. 그리고 시간경과의 영향을 보정한 상태에서도 첨가한 수은농도의 변화에 따라 각 군간 차이는 모두 현저하게 나타났다. 한편, Nitrite 생성량과 ATP 생성량은 둘 다 수은첨가군 모두에서 대조군의 값에 비해 현저하게 낮았고, 첨가된 수은농도와 nitrite 생성량 및 ATP 생성량 사이에는 높은 음의 상관관계가 있어 수은농도의 증가에 따라 용량-반응의 관계(dose-dependent)로 감소하는 경향을 보였다. 이상의 결과, 배양조건에 수은의 첨가로 인하여 nitrite 생성량과 ATP 생성량이 동시에 감소하는 바, 수은에 의한 세포성 면역의 저하는 면역세포의 NO 생성량의 감소에 의한 것으로 사료되며, 이는 수은이 세포내 에너지생산에 관련된 대사과정을 억제시키므로 나타나는 결과라고 판단된다.

• 한국산업보건학회지
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• 제17권2호
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• pp.81-88
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• 2007

The aim of this study was to investigate whether the exposure to vinyl chloride monomer(VCM) induces lipid peroxidation in workers by evaluating the concentration of malondialdehyde(MDA) in the urine in order to assess worker's oxidative stress due to exposure of vinyl chloride monomer. The subjects investigated in the study were divided into the experimental group; 18 workers exposed to VCM, and the control group; 19 workers unexposed to VCM. A gas chromatography/pulsed flame photometric detector(GC/PFPD) was utilized to analyze thiodiglycolic acid(TDGA), which was methylated with trimethylsilyldiazomethane (2.0M in diethyl ether) in urine and the urinary MDA, the product of lipid peroxidation, was determined by high-performance liquid chromatography/ultraviolet-visible detector after derivatized with 2,4-dinitrophenylhydrazine(DNPH). The concentrations of urinary TDGA in controls and VCM exposure workers were 0.13(2.01)mg/g Cr. GM(GSD) and 0.35(1.96)mg/gCr. GM(GSD), respectively. The concentrations of urinary MDA were $0.12(2.21){\mu}mol/gCr$. GM(GSD) in controls and $1.35(1.79){\mu}mol/gCr$. GM(GSD) in VCM exposure workers. As a result of simple regressions analysis between urinary concentration of TDGA and MDA in VCM exposure workers, it was found that the $R^2$ value was 0.261 (p=0.03) and the drinking and smoking did not affect their level. In conclusion, the workers exposed to VCM have a potentially to suffered by oxidative stress due to VCM exposure and the urinary MDA can be applicable to the marker of effect to assess the level of worker's VCM exposure.

• 한국학교ㆍ지역보건교육학회지
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• 제22권4호
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• pp.49-60
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• 2021

Objectives: Laboratories have various latent physical, chemical, biological, and ergonomical factors according to the diversification and fusion of research and development activities. This study aims to investigate the chemical exposure concentrations of college laboratories and evaluate their health risks, and use them as basic data to promote the health of college students. Methods: The sampling and analysis of harmful chemicals in the air in laboratories were performed using Method 1500 of the U.S. National Institute for Occupational Safety and Health (NIOSH)의 Method 1500. The harmful chemicals in the laboratories were divided into carcinogenic and non-carcinogenic chemicals. Risk assessment was performed using the cancer risk (CR) for carcinogenic chemicals and using the hazard index (HI) for non-carcinogenic chemicals. Results: The harmful chemicals in college laboratories consisted of acetone, diethyl ether, methylene chloride, n-hexane, ethyl acetate, chloroform, tetrahydrofuran, toluene, and xylenes. They showed the highest concentrations in laboratories A (acetone 0.001~2.34ppm), B (chloroform 0.95~6.35ppm), C (diethyl ether 0.08~8.68ppm), and D (acetone 0.07~14.96ppm). The risk assessment result for non-carcinogenic chemicals showed that the HI of methylene chloride was 2.052 for men and 2.333 for women, the HI of N-hexane was 4.442 for men and 5.05 for women. Thus, the HI values were higher than 1. The risk of carcinogenic chemicals is determined by an excess cancer risk (ECR) value of 1.0×10^-5, which means that one in 100,000 people has a cancer risk. The ECRs of chloroform exceeded 1.0×10^-5 for both men and women, indicating the possibility of cancer risk. Conclusion: College laboratories showed the possibility of non-carcinogenic health risks for methylene chloride, n-hexane, tetrahydrofuran (THF), toluene, and xylenes, and carcinogenic health risks for chloroform, methylene chloride. However, this study used the maximum values of measurements to determine the worst case, and assumed that the subjects were exposed to the corresponding concentrations continuously for 8 hours per day for 300 days per year. In consideration of the nature of laboratory environment in which people are intermittently exposed, rather than continuously, to the chemicals, the results of this study has an element of overestimation.

• Archives of Pharmacal Research
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• 제26권2호
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• pp.162-167
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• 2003

Liquid suppository systems composed of poloxamers and bioadhesive polymers were easy to administer to the anus and mucoadhesive to the rectal tissues without leakage after the dose. However, a liquid suppository containing diclofenac sodium could not be developed using bioadhesive polymers. since the drug was precipitated in this preparation. To develop a liquid suppository system using sodium chloride instead of bioadhesive polymers, the physicochemical properties such as gelation temperature, gel strength and bioadhesive force of various formulations composed of diclofenac sodium, poloxamers and sodium chloride were investigated. Furthermore, the pharmacokinetic study of diclofenac sodium delivered by the liquid suppository was performed. Diclofenac sodium significantly increased the gelation temperature and weakened the gel strength and bioadhesive force, while sodium chloride did the opposite. The liquid suppositories with less than 1.0％ of sodium chloride, in which the drug was not precipitated, were inserted into the rectum without difficulty and leakage. Furthermore, liquid suppository gave significantly higher initial plasma concentrations and faster Tmax of diclofenac sodium than did solid suppository, indicating that drug from liquid suppository could be absorbed faster than that from solid one in rats. Our results suggested that a thermosensitive liquid suppository system with sodium chloride and poloxamers was a more physically stable, convenient and effective rectal dosage form for diclofenac sodium.