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1.
Materials (Basel) ; 9(8)2016 Aug 04.
Article in English | MEDLINE | ID: mdl-28773776

ABSTRACT

This study focused on the development of a crack repair stick as a new repair method along with self-healing materials that can be used to easily repair the cracks in a concrete structure at the construction site. In developing this new repair technique, the self-healing efficiency of various cementitious materials was considered. Likewise, a crack repair stick was developed to apply to concrete structures with 0.3 mm or lower crack widths. The crack repair stick was made with different materials, such as cement, an expansive material (C12A7), a swelling material, and calcium carbonate, to endow it with a self-healing property. To verify the performance of the crack repair stick for concrete structures, two types of procedures (field experiment and field absorption test) were carried out. As a result of such procedures, it was concluded that the developed crack repair stick could be used on concrete structures to reduce repair expenses and for the improved workability, usability, and serviceability of such structures. On the other hand, to evaluate the self-healing performance of the crack repair stick, various tests were conducted, such as the relative dynamic modulus of elasticity test, the water tightness test, the water permeability test, observation via a microscope, and scanning electron microscope (SEM) analysis. From the results, it is found that water leakage can be prevented and that the durability of a concrete structure can be improved through self-healing. Also, it was verified that the cracks were perfectly closed after 28 days due to application of the crack repair stick. These results indicate the usability of the crack repair stick for concrete structures, and its self-healing efficiency.

2.
Materials (Basel) ; 7(1): 508-526, 2014 Jan 20.
Article in English | MEDLINE | ID: mdl-28788471

ABSTRACT

The crack self-healing behavior of high-performance steel-fiber reinforced cement composites (HPSFRCs) was investigated. High-strength deformed steel fibers were employed in a high strength mortar with very fine silica sand to decreasing the crack width by generating higher interfacial bond strength. The width of micro-cracks, strongly affected by the type of fiber and sand, clearly produced the effects on the self-healing behavior. The use of fine silica sand in HPSFRCs with high strength deformed steel fibers successfully led to rapid healing owing to very fine cracks with width less than 20 µm. The use of very fine silica sand instead of normal sand produced 17%-19% higher tensile strength and 51%-58% smaller width of micro-cracks.

3.
Toxicology ; 196(1-2): 77-86, 2004 Mar 01.
Article in English | MEDLINE | ID: mdl-15036758

ABSTRACT

2-Bromopropane (2-BP), a halogenated propane analogue, is a substitute for chlorofluorocarbones. The present study was carried out to investigate the potential adverse effects of 2-BP on pregnant dams and embryo-fetal development after maternal exposure on gestational days (GD) 6 through 19 in Sprague-Dawley rats. The test chemical was administered subcutaneously to pregnant rats at dose levels of 0, 250, 500, and 1000 mg/kg per day. All dams were subjected to caesarean section on GD 20 and their fetuses were examined for external, visceral and skeletal abnormalities. In the 1000 mg/kg group, maternal toxicity included an increase in the incidence of abnormal clinical signs, a suppression in the body weight and body weight gain, and a decrease in the food intake. Developmental toxicity included an increase in the fetal deaths, a decrease in the litter size, and a reduction in the fetal body weight. In addition, an increase in the incidence of fetal external, visceral, and skeletal abnormalities was seen. In the 500 mg/kg group, minimal developmental toxicity including decreased fetal body weight and increased fetal ossification delay was observed. There were no adverse effects on either pregnant dams or embryo-fetal development in the 250 mg/kg group. These findings suggest that a 14-day subcutaneous dose of 2-BP is embryotoxic and teratogenic at a maternally toxic dose (i.e., 1000 mg/kg per day) and is minimally embryotoxic at a nonmaternally toxic dose (i.e., 500 mg/kg per day) in Sprague-Dawley rats. In the present experimental conditions, the no-observed-adverse-effect level (NOAEL) of 2-BP is considered to be 500 mg/kg per day for dams and 250 mg/kg per day for embryo-fetal development.


Subject(s)
Embryonic and Fetal Development/drug effects , Environmental Pollutants/toxicity , Hydrocarbons, Brominated/toxicity , Mutagens/toxicity , Abnormalities, Drug-Induced/pathology , Animals , Body Weight/drug effects , Cesarean Section , Dose-Response Relationship, Drug , Eating/drug effects , Female , Growth/drug effects , Male , Pregnancy , Rats , Rats, Sprague-Dawley , Reproduction/drug effects , Skin Absorption
4.
Teratog Carcinog Mutagen ; Suppl 1: 123-36, 2003.
Article in English | MEDLINE | ID: mdl-12616603

ABSTRACT

We have recently reported that the fluoroquinolone antibacterial DW-116 induces a significant developmental toxicity in rat. The present study was conducted to better understand the teratogenic effects of DW-116 at several developmental toxic doses in rats. DW-116 was orally administered to pregnant rats from gestational day (GD) 6 through 16 at dose levels of 0, 320, 400, and 500 mg/kg/day. All dams were subjected to caesarean section on GD 20 and their fetuses were examined for external, visceral, and skeletal abnormalities. At above 400 mg/kg, severe decreases in maternal body weight gain, food consumption, litter size, fetal weight and placental weight, and severe increases in resorption rate and fetal morphological alterations were observed. At 320 mg/kg, mild decreases in maternal body weight gain, food consumption, fetal weight and placental weight, and mild increases in fetal variations and retardations were observed. These results suggest that DW-116 is embryotoxic at above 320 mg/kg/day and is embryolethal and teratogenic at above 400 mg/kg in pregnant rats and that DW-116 is a selective developmental toxicant in rat conceptuses.


Subject(s)
Anti-Infective Agents/toxicity , Embryonic and Fetal Development/drug effects , Fluoroquinolones , Piperazines/toxicity , Quinolones/toxicity , Abnormalities, Drug-Induced/genetics , Administration, Oral , Animals , Anti-Infective Agents/administration & dosage , Anti-Infective Agents/chemistry , Dose-Response Relationship, Drug , Embryonic and Fetal Development/genetics , Female , Fetal Weight/drug effects , Fetal Weight/genetics , Fetus/chemistry , Fetus/drug effects , Fetus/metabolism , Gestational Age , Maternal-Fetal Exchange/drug effects , Maternal-Fetal Exchange/genetics , Molecular Structure , Organ Size/drug effects , Organ Size/genetics , Piperazines/administration & dosage , Piperazines/chemistry , Placenta/drug effects , Pregnancy , Quinolones/administration & dosage , Quinolones/chemistry , Rats , Rats, Sprague-Dawley
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