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1 95th percentile, 30.0 mug/L) for brominated trihalomethanes.
2 with estimates of average lifetime level of trihalomethanes.
3 d carbon media was important for controlling trihalomethanes.
4 D risk, with the highest risk for brominated trihalomethanes.
5 black ashes had lower reactivity in forming trihalomethanes (55%-of-control) and haloacetic acids (6
6 ees C resulted in decreased reactivities for trihalomethane and chloral hydrate formation and diverge
7 ug/L; 95th percentile, 57.8 mug/L) for total trihalomethanes and 2.7 mug/L (IQR, 0.7-11.3 mug/L; 95th
8 of 4 trihalomethanes, including 3 brominated trihalomethanes and chloroform, were calculated using an
9 re-response association was observed between trihalomethanes and CKD risk, with the highest risk for
10 e second and third trimesters for both total trihalomethanes and five haloacetic acids when comparing
12 would be comparable to that associated with trihalomethanes and haloacetic acids at levels of regula
13 beyond the potential to form lower regulated trihalomethanes and haloacetic acids compared to chlorin
14 r-source drinking water treatment plant, the trihalomethanes and haloacetic acids each increased by u
15 Birth weight, ethnicity, and exposure to trihalomethanes and haloacetic acids in drinking water d
20 on nuclei achieved recoveries of 50-100% for trihalomethanes and haloacetonitriles and approximately
21 in commercial PAA solutions, resulted in no trihalomethanes and only low haloacetic acid concentrati
24 seawater to assess its potential to produce trihalomethanes and to determine the byproducts generate
26 of this protocol for dihaloacetonitriles and trihalomethanes and validate a novel Alternative Method
27 The water system was monitored weekly for trihalomethanes and, system-wide, it maintained geograph
28 used in caulking), disinfection byproducts (trihalomethanes), and contaminants present in source wat
34 ls (a) direct electrochemical reduction of a trihalomethane at a silver cathode to form halide ions i
35 HRs for CKD risk associated with brominated trihalomethanes at the highest 2 exposure categories (75
36 ternal exposure to drinking water brominated trihalomethanes (BTHM) in relation to MN frequency in ma
38 y of California female teachers, exposure to trihalomethane concentrations less than 80 mug/L (US cur
39 tor organic byproducts (haloacetic acids and trihalomethanes) during electrolysis dramatically exceed
41 that high levels (> or = 70 microg/liter) of trihalomethanes experienced during the second trimester
43 y loss was not associated with high personal trihalomethane exposure (> or =75 micro g/liter and > or
45 acetic acids, and haloacetonitriles, whereas trihalomethane formation decreases during chlorine photo
48 f the soils heated to 350 degrees C, whereas trihalomethane, haloacetic acid and chloropicrin yields
49 reased risk of pregnancy loss in relation to trihalomethane, haloacetic acid, or total organic halide
51 idant exposures, concentrations of regulated trihalomethanes, haloacetic acids, bromate, and chlorite
52 ribute to the formation targeted DBPs (i.e., trihalomethanes, haloacetic acids, haloacetonitriles, ch
53 limits were in the range of 0.3-10 ng/g for trihalomethanes, haloacetic acids, nitrogenous DBPs, and
54 ased chlorine reactivities and formations of trihalomethanes, haloacetonitriles, chloral hydrate, and
57 greater than those from chlorine, including trihalomethanes, haloaldehydes, haloketones, haloacetoni
58 plication of vacuum to measure six iodinated-trihalomethanes (I-THMs) in drinking water and urine.
60 addition revealed that the formation of iodo-trihalomethanes (I-THMs), especially iodoform, was great
61 fection byproducts (DBPs), such as iodinated trihalomethanes (I-THMs), which pose significant health
63 fic and pregnancy average exposures to total trihalomethane in drinking water on term low birth weigh
64 e importance of controlling the formation of trihalomethanes in water throughout treatment and distri
65 byproduct (DBP) concentrations, principally trihalomethanes, in drinking water with the expectation
66 dence time-weighted mean concentrations of 4 trihalomethanes, including 3 brominated trihalomethanes
67 ios (HRs) and 95% CIs for CKD by exposure to trihalomethane levels (US maximum contaminant level of 8
70 P concentration and ingested amount and, for trihalomethanes only, bathing/showering and integrated e
71 reactions of laser-ablated uranium atoms and trihalomethanes or carbon tetrafluoride in excess argon.
72 examined whether exposure to the four total trihalomethanes or the five haloacetic acids (two major
73 Ps (N-DBPs) (r = 0.97) and the least with Br-trihalomethanes (r = 0.29) and Br-N-DBPs (r = 0.04).
75 sachusetts with complete quarterly 1999-2004 trihalomethane (THM) and haloacetic acid (HAA) data.
76 s have used various measures to characterize trihalomethane (THM) exposures, but the relationship of
77 oad estimates and median flow conditions, on trihalomethane (THM) formation and associated risk were
80 logical studies linking drinking water total trihalomethanes (THM) with pregnancy disorders or bladde
82 pically are adopting regulations focusing on trihalomethanes (THM4) as an indicator of overall DBP ex
83 increases in the mass of the four regulated trihalomethanes (THM4) concentrations (due to increased
84 focused on the possible presence of up to 10 trihalomethanes (THMs) and 13 haloacetic acids (HAAs) in
85 toward formation of brominated and iodinated trihalomethanes (THMs) and brominated haloacetonitriles
87 carbonaceous disinfection byproducts (DBPs) (trihalomethanes (THMs) and haloacetic acids (HAAs)), and
88 DMA), total N-nitrosamines (TONO), regulated trihalomethanes (THMs) and haloacetic acids (HAAs), 1,1-
91 abolomic profile associated with exposure to trihalomethanes (THMs) and nitrate in drinking water and
92 e tap, and to evaluate if routinely measured trihalomethanes (THMs) are an appropriate proxy measure
96 loped and evaluated for the determination of trihalomethanes (THMs) at the submicromolar concentratio
98 gen exchange) on the yield and speciation of trihalomethanes (THMs) formed during water chlorination.
101 xposure was assessed by estimating levels of trihalomethanes (THMs) in tap water during pregnancy and
102 port, and fate of chloroform and three other trihalomethanes (THMs) in untreated groundwater were rev
103 ons exist between conditionally carcinogenic trihalomethanes (THMs) levels, water temperature (r = 0.
104 ancer and total, chlorinated, and brominated trihalomethanes (THMs) through various exposure routes.
105 active halogens and their potential to form trihalomethanes (THMs) when combined with synthetic sewa
106 ulated iodinated haloacetic acids (HAAs) and trihalomethanes (THMs), haloacetaldehydes, haloketones,
107 reated wastewaters met regulatory levels for trihalomethanes (THMs), haloacetic acids (HAAs), and bro
108 hanisms for eight classes of DBPs, including trihalomethanes (THMs), haloacetic acids (HAAs), haloket
110 to disinfection byproducts (DBPs), including trihalomethanes (THMs), which have been associated with
112 od samples were quantified for biomarkers of trihalomethanes (THMs): chloroform (TCM), bromodichlorom
113 enated disinfection byproducts (DBPs) (e.g., trihalomethanes, THMs and haloacetic acids, HAAs) during
114 atment combinations were capable of removing trihalomethanes to some degree and trichloramine and dic
115 loyed our methodology to determine the total trihalomethane (TTHM) content in a prepared water sample
116 estimated average nitrate (NO3-N) and total trihalomethane (TTHM) levels and the number of years exc
117 ormation potentials of haloacetonitriles and trihalomethanes under free chlorination and free bromina
119 Precision and detection limits for selected trihalomethanes were comparable to those of EPA method 5
121 nd a-bromocinnamaldehyde) and citrate (i.e., trihalomethanes) were generated via a pathway involving
122 oacetic acids (HAAs) was higher than that of trihalomethanes where dichloroacetic acid was dominant i
123 increased CKD risk, particularly brominated trihalomethanes, which are not separately regulated in c