Algicide-Fungicide and Algicide-Bactericide Method
A technology of algicide and algicide, applied in the direction of fungicide, herbicide, algicide, biocide, etc., can solve the problems of evaluation, recording, unsatisfactory, etc., and achieve low risk and corrosion resistance low effect
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Embodiment 1
[0064] In Example 1, 6.8 g of 2-pyrrolidone [reagent, manufactured by Kanto Chemical Co., Ltd.] was added to 100 g of chloroform [reagent, manufactured by Kanto Chemical Co., Ltd.], and trichloroisocyanuric acid [ Reagent, manufactured by Tokyo Chemical Industry Co., Ltd.] 9.3 g. After stirring the resulting white slurry for 6 hours, suction filtration was performed. The filtrate was concentrated with a rotary evaporator, and then cooled with ice to obtain 9.4 g of white crystals of N-chloro-2-pyrrolidone (yield 98.4%, physical properties shown below).
[0065] 1 H-NMR (CDCl 3 ,δ):
[0066] 2.28(m, 4H), 4.21(t, 2H)
[0067] IR (KBr, cm -1 ):
[0068] 2968, 1708, 1385, 1254, 1135, 820.
[0069] 4.6 g of acetic acid and 86.0 g of water were added to 9.4 g of the white crystals of N-chloro-2-pyrrolidone to prepare 100 g of an aqueous N-chloro-2-pyrrolidone solution with an available chlorine concentration of 5.5%. In addition, according to the DPD-ammonium sulfate iron (I...
Embodiment 2
[0070] In Example 2, 7.6 g of 2-piperidone [reagent, manufactured by Kanto Chemical Co., Ltd.] and 42.8 g of water were mixed, 4.6 g of acetic acid [reagent, manufactured by Kanto Chemical Co., Ltd.] was added, and the concentration of available chlorine was added to the obtained aqueous solution. It was 45.0 g of a 12% sodium hypochlorite solution [available chlorine concentration 12%, manufactured by Soya Sangyo Co., Ltd.], and prepared as 100 g of an N-chloro-2-piperidone aqueous solution having an available chlorine concentration of 5.4%. According to the DPD-ammonium iron (II) titration method, the chlorine form of the aqueous solution is the combined form.
Embodiment 3
[0071] In Example 3, 7.9 g of ε-caprolactam [reagent, manufactured by Kanto Chemical Co., Ltd.] was added to 100 g of chloroform, and 8.1 g of trichloroisocyanuric acid was added over a period of 90 minutes under ice-cooling. After stirring the produced white slurry for 6 hours, suction filtration was performed, and the filtrate was concentrated by a rotary evaporator to obtain 10.1 g of a slightly yellow transparent oil of N-chloro-ε-caprolactam (yield 97.9%, physical properties shown below).
[0072] 1 H-NMR (CDCl 3 ,δ):
[0073] 1.78(br.s, 6H), 2.45(d, 2H), 3.21(t, 2H)
[0074] IR (NaCl, cm -1):
[0075] 2933, 2858, 1672, 1452, 1191, 980.
[0076] To 10.1 g of this N-chloro-ε-caprolactam light yellow transparent oil, 10.0 g of γ-butyrolactone [reagent, manufactured by Kanto Chemical Co., Ltd.], 4.1 g of acetic acid, and 75.8 g of water were added to prepare an effective chlorine concentration of 4.7 100 g of an aqueous solution of % N-chloro-ε-caprolactam. According ...
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