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第551---600篇

551.

132:253192

Preparation of chlorine dioxide disinfectant and apparatus for

generating same.

Xu, Fei; Zhao, Liqun (Sijia Environmental Egineering Co., Ltd., Beijing,

Peop. Rep. China). Faming Zhuanli Shenqing Gongkai Shuomingshu

CN 1212839 A 7 Apr 1999, 6 pp. (Chinese). (People's Republic of

China). CODEN: CNXXEV. CLASS: ICM: A01N059-00. ICS:

C01B011-02. APPLICATION: CN 1998-101677 30 Apr 1998.

DOCUMENT TYPE: Patent CA Section: 49 (Industrial Inorganic

Chemicals) Section cross-reference(s): 61, 63

The chlorine dioxide disinfectant is prepd. by making a 540 g/L NaClO3

soln. to react with a 31% HCl soln. in neg.-pressure two-stage reactor

having 1st and 2nd-stage reaction chambers at 40* and 70*, resp., to

obtain ClO2 and Cl2, and then aerating heated air. The vol. ratio of the

NaClO3 soln. to the HCl soln. is 1:1. The app. includes charging

device, tandem two-stage reactor, heating tank, inlet duct, collection

chamber and its heating tank, water jet injector, safety device, etc.

 

 

552.

132:247439

Soil microbicidal compositions containing chlorite salts and minerals

and soil sterilization.

Ogawa, Katsutoshi (Chisso Corp., Japan). Jpn. Kokai Tokkyo Koho

JP 2000095624 A2 4 Apr 2000, 12 pp. (Japanese). (Japan).

CODEN: JKXXAF. CLASS: ICM: A01N059-08. ICS: A01N025-00;

A01N025-08; A01N025-12; C09K017-02; C09K101-00.

APPLICATION: JP 1998-268003 22 Sep 1998. DOCUMENT TYPE:

Patent CA Section: 5 (Agrochemical Bioregulators)

The compns. contain (A) alkali metal chlorites and/or alk. earth metal

chlorites as solid microbicide components and (B) solid diluents contg.

nonhygroscopic inorg. salts free of reducing compds. and/or purified,

dried, and neutral or alk. minerals contg. *0.001% metals and *0.1%

metal oxides. Soil is sterilized by uniform application of the compns.

The soil is preferably covered with poly(vinyl chloride) or polyolefin

mulch film to prevent diffusion of ClO2 to the air. The compns. also

inhibit germination of weed seeds in soils. A pot contg. alluvial soil, to

which a mixt. of 200 g Silbrite (80% NaClO2 powder) and 8 g K2SO4

was added, was covered with a PVC sheet at 24-26* for 7 days, and

then exposed to sunlight at 28-32* for 5 days. No living nematodes,

fungi, bacteria, and Actinomycetes were detected in the soil. Addn. of

Fe3O2 to the soil shortened the time to show complete microbicidal

effect.

 

 

553.

132:241714

Mouthwashes, sprays or pastes for halitosis.

Ge, Xiaoming (Peop. Rep. China ). Faming Zhuanli Shenqing Gongkai

Shuomingshu CN 1195518 A 14 Oct 1998,4 pp. (Chinese). (People's

Republic of China). CODEN: CNXXEV. CLASS: ICM: A61K007-20.

APPLICATION: CN 1997-103902 10 Apr 1997. DOCUMENT TYPE:

Patent CA Section: 62 (Essential Oils and Cosmetics)

Mouthwashes, sprays or pastes for halitosis comprise * 0.2% H2O2 or

ClO2 soln.

 

 

554.

132:241586

Detection and reduction of biofilms in industrial cooling waters.

Beardwood, Edward S.; Therrien, Jerry K. (Drew Industrial Division,

Ashland Canada Inc., Ajax, ON, Can.). Off. Proc. - Int. Water Conf.,

60th, 552-573 (English) 1999 Engineers' Society of Western

Pennsylvania. CODEN: OIWCEQ. ISSN: 0739-4977. DOCUMENT

TYPE: Journal CA Section: 61 (Water)

The detection and control of planktonic microorganisms has been well

understood and practiced over the years. However, the fouling and

corrosion assocd. with sessile bacterial development of biofilms

continues to be an area of concern. A portable online corrosion and

fouling monitor was utilized to provide early detection of biofilm

formation and subsequent detection of biofouling redn. A no. of key

points and factors influencing the detection and performance of foulant

redn. are discussed.

 

 

555.

132:241584

Cooling towers & secondary waste water makeup: four years'

operating experience.

DeBenedetto, Robert; Freedman, Arthur J.; Boschetti, Drew; Hays,

George F. (Public Service Electric and Gas Company, Ridgefield, NJ,

USA). Off. Proc. - Int. Water Conf., 60th, 331-343 (English) 1999

Engineers' Society of Western Pennsylvania. CODEN: OIWCEQ.

ISSN: 0739-4977. DOCUMENT TYPE: Journal CA Section: 61

(Water) Section cross-reference(s): 60

This report describes 4 yr of operating experience in a 650-MW

combined cycle power station incorporating film fill cooling towers

using secondary sewage effluent as makeup water. Biofouling is

controlled with chlorine dioxide. A water treatment task force was

formed and procedures were developed to resolve emerging chem.

and mech. issues.

 

 

556.

132:238543

ECF bleaching system for hard wood pulp.

Sato, Takashi; Dairaku, Toshio (Ahlstrom Sumiju K. K., Japan).

Sumitomo Jukikai Giho, 47(140), 47-50 (Japanese) 1999 Sumitomo

Jukikai Kogyo K.K. CODEN: SJGHA8. ISSN: 0387-1304.

DOCUMENT TYPE: Journal CA Section: 43 (Cellulose, Lignin, Paper,

and Other Wood Products)

Formerly, wood pulps have been bleached by elementary chlorine at

the first bleaching stage due to mainly its low cost and its high

bleachability. Since the problem of discharge of the Dioxin became hot

in the world, the ECF (Elementary Chlorine Free) bleaching methods

have been developed. And nowadays, many mills in Europe and USA

have introduced ECF method in their facilities. In addn., as the Cluste

Rule proposed by Environmental Protection Agency of USA has

become effective last year, people forecast that all new facilities would

be constructed with ECF method. Ahlstrom Sumijyu KK delivered ECF

facilities to Niigata mill of Hokuetsu Paper mills, Ltd. based on the

technol. of Ahlstrom machinery who is one of our parent companies.

And this plant is the first ECF bleaching system for hard wood pulp in

Japan and it has successfully started up in Mar. 1998. This report will

clarify the advantages of ECF method using ClO2-Oxygen-added

extn.-ClO2-neutralization-ClO2 sequence, with actual data.

 

 

557.

132:238513

Use of chlorine dioxide for the bleaching of pulp: a re-evaluation of

ecological risks based on scientific progress since 1993.

Bright, D. A.; Hodson, P. V.; Lehitinen, K. -J.; McKague, B.; Rodgers,

J.; Solomon, K. (Queen's Univ., Kingston, ON, Can.). Pulp Pap. Can.,

101(1), 53-55 (English) 2000 Southam Inc. CODEN: PPCAAA. ISSN:

0316-4004. DOCUMENT TYPE: Journal; General Review CA Section:

43 (Cellulose, Lignin, Paper, and Other Wood Products)

A review with 11 refs. on studies published since 1993 to assess the

ecol. risks assocd. with final effluents from pulp mills using 100% ClO2

in pulp bleaching processes is presented. All available data indicate

that chlorinated compds. in effluents from pulp mills that employ 100%

ClO2 bleaching are of very limited persistence and not strongly

bio-accumulative. Chlorinated compd. concns. in final effluent

(following secondary treatment) comprise a negligible risk to aquatic

organisms in comparison with the known toxicol. thresholds.

 

 

558.

132:236253

Sterilization of onions and garlic by using oxidizing agents under

pressure.

Bautista, James M.; Houry, Omar; Mirko, Dave A.; Schabel, Gary N. (

Dionex Corporation, USA). U.S. US 6045846 A 4 Apr 2000, 4 pp.

(English). (United States of America). CODEN: USXXAM. CLASS:

ICM: A23B007-157. ICS: A23L003-358. NCL: 426335000.

APPLICATION: US 1998-216084 18 Dec 1998. DOCUMENT TYPE:

Patent CA Section: 17 (Food and Feed Chemistry)

A method for sterilizing fresh produce (e.g., onions) comprises

contacting the produce with an aq. soln. of an oxidizing agent (e.g.,

hydrogen peroxide) under a pressure of at least 25 psi for sufficient

time to significantly reduce the microbiol. count. Thus, a 10% hydrogen

peroxide soln. is used at 200 psi for 60 s to sterilize onions.

 

 

559.

132:229060

Electron scattering in chlorine dioxide.

Field, D.; Jones, N. C.; Gingell, J. M.; Mason, N. J.; Lunt, S. L.; Ziesel,

J-P. (ISA, University of Arhus, Ny Munkegade DK-8000, Den.). J. Phys.

B: At., Mol. Opt. Phys., 33(5), 1039-1046 (English) 2000 Institute of

Physics Publishing. CODEN: JPAPEH. ISSN: 0953-4075.

DOCUMENT TYPE: Journal CA Section: 73 (Optical, Electron, and

Mass Spectroscopy and Other Related Properties)

Cross sections are reported for total integral and backward scattering

of electrons from chlorine dioxide (OClO) for energies in the range

20-500 meV. The measurements were made in transmission expts.

using a synchrotron radiation photoionization app. with an energy

resoln. in the incident electron beam of ~1.0 meV (FWHM). Integral

and backward scattering cross sections are reported. The present

integral cross-section values are a correction to those reported in an

earlier publication which are too low due to the presence of an impurity

in the original OClO samples. The abs. accuracy of the integral cross

sections is limited by exptl. difficulties with respect to strong rotationally

inelastic forward scattering due to the dipolar nature of the target mols.

Backward scattering data provide good evidence that dissociative

attachment occurs through p-wave attachment. Comparison is made

with predictions of the 1st Born pure dipole approxn. for both total and

backward scattering with excellent agreement >100 meV with integral

scattering data, but showing a significant underestimate for backward

scattering cross sections. Behavior at energies <100 meV represents

competition between inelastic scattering and attachment and is not well

understood.

 

 

560.

132:229035

A pump-probe photoionization mass spectrometer utilizing tunable

extreme ultraviolet laser-produced-plasma radiation.

Flesch, R.; Schurmann, M. C.; Hunnekuhl, M.; Meiss, H.; Plenge, J.;

Ruhl, E. (Fachbereich Physik, Universitat Osnabruck, Osnabruck

D-49069, Germany). Rev. Sci. Instrum., 71(3), 1319-1324 (English)

2000 American Institute of Physics. CODEN: RSINAK. ISSN:

0034-6748. DOCUMENT TYPE: Journal CA Section: 73 (Optical,

Electron, and Mass Spectroscopy and Other Related Properties)

Section cross-reference(s): 74

An exptl. device is reported that uses time-correlated nanosecond light

pulses in combination with photoionization mass spectrometry. A

primary light pulse is generated by a tunable dye laser in the UV

regime, which photolyzes neutral gas targets under collision free

conditions. Subsequently, a time-correlated extreme UV-light pulse

comes from a laser-produced plasma that is monochromatized in the

10-25 eV regime. The photolysis products are ionized by 1-photon

absorption, so that the cations are finally detected by time-of-flight

mass spectrometry. The performance of this exptl. approach was

characterized by studying the primary photolysis products of Cl dioxide.

Finally, possible applications of this approach are briefly discussed.

 

 

561.

132:227172

Use of xanthan gum for gelling chlorine dioxide.

Alliger, Howard (USA ). U.S. US 6039934 A 21 Mar 2000,8 pp.

(English). (United States of America). CODEN: USXXAM. CLASS:

ICM: A61K007-20. ICS: A61K033-20. NCL: 424053000.

APPLICATION: US 1998-128898 4 Aug 1998. DOCUMENT TYPE:

Patent CA Section: 62 (Essential Oils and Cosmetics)

The invention described relates to gelled chlorine dioxide compns.

comprising water, an acid, a water-sol. chlorite salt and a gelling agent

in two parts A and B, wherein the gelling agent is xanthan gum or a

mixt. of xanthan gum and an acid stable gelling agents. Compns.

according to the invention are storage stable for at least 6 mo,

preferably at least about year. A skin protectant compn. contained

Keltrol 2, sodium chlorite 2, sodium hydroxide 0.36, and water q.s.

100% in part A, and Keltrol 2, glycerin 40, phosphoric acid 1.3,

Nacconol 90G, 0.2, glutaraldehyde 0.03, and fragrance 0.02, and

Water q.s. 100% in part B. The gel may be used immediately upon

mixing parts A and B.

 

 

562.

132:227052

Evaluation of chlorine dioxide as a microbiological water purifier.

Ijaz, M. Khalid; Suchmann, Donna B.; Pugh, John C.; Graczyk,

Thaddeus K.; Sattar, Syed A. (MicroBio Test, Inc., Sterling, VA 20164,

USA). Chem. Times Trends, 23(1), 38-43 (English) 2000 Chemical

Specialties Manufacturers Association, Inc. CODEN: CTTRDY. ISSN:

0149-2381. DOCUMENT TYPE: Journal CA Section: 61 (Water)

Section cross-reference(s): 10

Generally, chem. disinfection is the most convenient, reliable means to

prevent transmission of infectious agents through drinking water;

however, disinfectants such as Cl2 may generate toxic byproducts and

have difficulty inactivating encysted pathogenic protozoa. In view of the

need for safer, more effective Cl2 substitutes, the ability of ClO2 to

inactivate prototypical water-borne bacteria, viruses, and protozoa

using USEPA guidelines for testing water purifiers, was studied. Test

bacteria (Klebsiella terrigena, ATCC 33257; Salmonella choleraesuis,

ATCC 10708; Escherichia coli, ATCC 11229; Legionella pneumophila,

ATCC 33153), viruses (Poliovirus type 1, ATCC VR-59; Rotavirus

SA-11, ATCC VR-899), and protozoa (Cryptosporidium parvum

oocysts from US Department of Agriculture, Beltsville, Maryland, and

Giardia muris cysts from Oregon Health Sciences University) were

suspended in USEPA water. Bacteria and virus viability was detd.

using std. in-vitro assays; neonatal mice were used to assay cyst and

oocyst viability. CLO2 exposure at a final concn. of 2 ppm in water for

10 min at pH 7, 9, and 4, and at 1*, 20*, and 5*, was effective in

producing a >6-log redn. in the titer of all bacterial strains tested.

Similar treatments of rotavirus and poliovirus produced a >4-log redn.

in titer at pH 7 and 9. Protozoa were tested only in water at pH 7, which

was exposed to either 3 or 4 ppm ClO2 for 30-min; treatment at both

CLO2 concns. totally abolished infectivity of the 2 protozoa by >3-log.

ClO2 was highly effective in inactivating representatives of bacteria,

viruses, and protozoa known to spread through exposure to polluted

waters. In addn. to its relatively fast, broad-spectrum germicidal

activity, ClO2 is less prone to generating toxic disinfection byproducts

and, like Cl2, can maintain a disinfectant residual in treated water. In

view of this, further work is needed to examine its use in municipal

water treatment and for disinfection of hospital, veterinary settings, and

food industry water.

 

 

563.

132:223988

Increase of chlorine dioxide yield.

Zheng, Zhining (Nanning Phoenix Pulp and Paper Co., Ltd., Nanning

530031, Peop. Rep. China). Zhongguo Zaozhi, 18(4), 16-19 (Chinese)

1999 Zhongguo Zaozhi Xuehui. CODEN: ZHZADC. ISSN:

0254-508X. DOCUMENT TYPE: Journal CA Section: 43 (Cellulose,

Lignin, Paper, and Other Wood Products) Section cross-reference(s):

45

The prodn. methods of ClO2 were introduced based on practice.

Prodn. of ClO2 from methanol and NaClO3 by R8 method was

described. Effects affecting the yield of ClO2 were discussed, which

were reaction efficiency and loss in the prodn. Measures for improving

the yield of ClO2 were introduced.

 

 

564.

132:223949

Deodorization of sulfur-containing solvents by oxidation.

Isganitis, Louis V.; Smith, Thomas W. (Xerox Corp., USA). U.S. US

6042640 A 28 Mar 2000, 11 pp. (English). (United States of America).

CODEN: USXXAM. CLASS: ICM: C09D011-02. ICS: C02F001-72;

C02F001-76. NCL: 106031020. APPLICATION: US 1998-106379 29

Jun 1998. DOCUMENT TYPE: Patent CA Section: 42 (Coatings, Inks,

and Related Products)

Disclosed is a process which comprises contacting a sulfur-contg.

solvent (e.g., sulfolane) with an oxidizing agent (e.g., chlorine dioxide),

the sulfur-contg. solvent contg. odor-causing impurities, thereby

reducing odor. Another embodiment of the present invention is

directed to a process for prepg. an ink compn. which comprises: (a)

contacting a sulfur-contg. solvent with an oxidizing agent, the

sulfur-contg. solvent contg. odor-causing impurities, thereby reducing

odor; and (b) admixing the sulfur-contg. solvent with water and a

colorant, thereby forming an ink compn.

 

 

565.

132:212707

Cyclodextrin-containing compositions containing preservatives.

Beck, Gary J.; Kerslake, Edward D. S.; Olejnik, Orest (Allergan Sales,

Inc., USA). PCT Int. Appl. WO 2000012137 A1 9 Mar 2000, 36 pp.

DESIGNATED STATES: W: AU, CA, JP; RW: AT, BE, CH, CY, DE,

DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE. (English). (World

Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM:

A61K047-40. APPLICATION: WO 1999-US20060 1 Sep 1999.

PRIORITY: US 1998-98854 2 Sep 1998. DOCUMENT TYPE: Patent

CA Section: 63 (Pharmaceuticals)

Compns. including a liq. medium, a cyclodextrin component and a

preservative component which has a reduced tendency to being

complexed with the cyclodextrin component. In one embodiment, the

preservative component is a chlorite component. Active (drugs)

components are included in the compns. Thus, NaCl 0.622, KCl 0.14,

CaCl2.2H2O 0.02, MgCl2.6H2O 0..06, CM-cellulose sodium salt 0.5,

boric acid 0.2, sodium borate decahydrate 0.14, brimodine tartrate 0.2,

b-cyclodextrin sulfobutyl ether 1 and water to 100%, stabilized ClO2 50

ppm. The presence of a cyclodextrin component does not have any

detrimental effect on the preservative efficacy of stabilized chlorine

dioxide. The stabilized chlorine dioxide remains free and effective as a

preservative rather than being complexed by thecyclodextrin

component. The compn. is ophthalmically acceptable.

 

 

566.

132:209562

Fluid treatment elements, methods for treating fluids and for cleaning

the treatment elements.

Haq, Tanweer U.; Miller, John D.; Geibel, Stephen A.; Acquaviva,

James (Pall Corporation, USA). PCT Int. Appl. WO 2000013767 A1

16 Mar 2000, 180 pp. DESIGNATED STATES: W: AE, AL, AM, AT,

AU, AZ, BA, BB, BG, BR, BY, CA, CH, CN, CR, CU, CZ, DE, DK, DM,

EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG,

KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MD, MG, MK, MN, MW, MX,

NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, UA,

UG, US, UZ, VN, YU, ZA, ZW, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM;

RW: AT, BE, BF, BJ, CF, CG, CH, CI, CM, CY, DE, DK, ES, FI, FR,

GA, GB, GR, IE, IT, LU, MC, ML, MR, NE, NL, PT, SE, SN, TD, TG.

(English). (World Intellectual Property Organization). CODEN: PIXXD2.

CLASS: ICM: B01D046-24. ICS: B01D053-22; B01D063-06;

B01D046-52. APPLICATION: WO 1999-US20509 9 Sep 1999.

PRIORITY: US 1998-99663 9 Sep 1998. DOCUMENT TYPE: Patent

CA Section: 47 (Apparatus and Plant Equipment) Section

cross-reference(s): 9, 16, 38, 60, 61, 76

A fluid treatment element, esp. a filter element, is described which can

be operation in dead end or crossflow filtration. The treatment element

includes a multilayer composite formed into axially extending pleats,

where adjoining pleats are in a laid-over state and pressed against

each other over a substantial portion of their height. The treatment

element is compact, with a large surface area. The element can be

made from a fluoropolymer for diffusively transferring material (gases)

from one fluid stream to another fluid stream, e.g., for transferring O3

into water. The treatment element is cleaned by backwashing or

crossflow cleaning.

 

 

567.

132:202391

Colorimetry with amaranth or Evans Blue azo dyes for determination of

residual chlorine dioxide in water.

Mantisi, Frederick; Gautier, Jean-Pierre (Elf Atochem S.A., Fr.). Eur.

Pat. Appl. EP 985929 A1 15 Mar 2000, 9 pp. DESIGNATED

STATES: R: AT, BE, CH, DE, DK, ES, FR, GB, GR, IT, LI, LU, NL, SE,

MC, PT, IE, SI, LT, LV, FI, RO. (French). (European Patent

Organization). CODEN: EPXXDW. CLASS: ICM: G01N031-22. ICS:

G01N033-18. APPLICATION: EP 1999-401774 15 Jul 1999.

PRIORITY: FR 1998-11272 9 Sep 1998. DOCUMENT TYPE: Patent

CA Section: 79 (Inorganic Analytical Chemistry) Section

cross-reference(s): 41, 61

A colorimetric method for the detn. of residual ClO2 (as water purifn.

agent) in com. water supplies (esp. potable waters), consists of prepn.

of an anal. soln. contg. an azo dye, with a color intensity modified by the

presence of ClO2, in addn. to a borate buffer and one or more masking

agents. The azo dye is amaranth or Evans Blue, which is present in 1 *

10-6 and 1* 10-3 M, preferably 2 * 10-5 and 8 * 10-4 M. The borate

buffer is present in concn. of 5 * 10-3 and 0.1 M. The pH is then

adjusted to 9.2 prior to colorimetric anal., at 521 nm for amaranth and

606 nm for Evans Blue.

 

 

568.

132:198430

Treating paper mill wastewater by chemical method.

Yu, Yongli; Su, Yongbo (Department of Chemistry, Northeast University,

Shenyang 110006, Peop. Rep. China). Gongye Shuichuli, 20(1), 39-40

(Chinese) 2000 Gongye Shuichuli Zazhishe. CODEN: GOSHFA.

ISSN: 1005-829X. DOCUMENT TYPE: Journal CA Section: 60

(Waste Treatment and Disposal) Section cross-reference(s): 43

A coagulation-ClO2 oxidn.-sand filtration-activated carbon adsorption

process for treating paper mill wastewater is presented. The optimum

coagulation agent was polyacrylamide and an org. compd. contg. Fe

and Mg, whose mol. was FenMgx(SO4)y-R. About 97% of COD was

removed.

 

 

569.

132:198294

Method of flue gas desulfurization using bauxite.

Fan, Maohong; Zhuang, Yahui (Ecological Environment Research

Centre, Chinese Academy of Sciences, Peop. Rep. China). Faming

Zhuanli Shenqing Gongkai Shuomingshu CN 1202388 A 23 Dec 1998,

8 pp. (Chinese). (People's Republic of China). CODEN: CNXXEV.

CLASS: ICM: B01D053-50. ICS: B01D053-79. APPLICATION: CN

1997-112147 16 Jun 1997. DOCUMENT TYPE: Patent CA Section:

59 (Air Pollution and Industrial Hygiene)

SOx is removed from coal burning flue gas, and converted to a water

purifying agent Al2(SO4)3, by using bauxite as absorbent and H2O2,

ClO2, or Na(K)ClO3 as oxidant, in the presence of NaHCO3. When

NaClO3 is used, the mol. ratios are controlled at at a 0.62 <(Al2O3/SO2)

<0.78, 0.55 <(NaClO3/SO2) <0.75, and 0-.05 <(NaHCO3/SO2) <0.08

and the reaction temp. is controlled at 35-100*.

 

 

570.

132:195997

Pulping method.

Li, Xuemin (Peop. Rep. China ). Faming Zhuanli Shenqing Gongkai

Shuomingshu CN 1193062 A 16 Sep 1998,5 pp. (Chinese). (People's

Republic of China). CODEN: CNXXEV. CLASS: ICM: D21C009-10.

APPLICATION: CN 1998-104755 14 Feb 1998. DOCUMENT TYPE:

Patent CA Section: 43 (Cellulose, Lignin, Paper, and Other Wood

Products)

A method is characterized by bleaching in a closed container at 0.5-7

kg/cm2 for 2-4 h using strong oxidants selected from NaClO, Ca(ClO)2,

ClO2, H2O2, and NaClO3 at effective Cl concn. 2-4%.

 

 

571.

132:195769

Application of chlorine dioxide to bleaching chemical cotton.

Jiang, Jiakuan (Hui-Min Practical Chemical Industrial Inst., Xi'an

710302, Peop. Rep. China). Xiandai Huagong, 19(7), 18-20 (Chinese)

1999 Zhongguo Huagong Xinxi Zhongxin. CODEN: HTKUDJ. ISSN:

0253-4320. DOCUMENT TYPE: Journal CA Section: 40 (Textiles and

Fibers)

The application of ClO2 in bleaching of cotton was discussed. The

bleaching condition was optimized, and the factors affecting the

bleaching effect were discussed. The chem. cotton with viscosity

>1000 MPa.s and whiteness >87% was obtained.

 

 

572.

132:193499

Chlorine dioxide-containing liquid compositions as disinfectants or

deodorizers.

Iwamoto, Tsutomu; Nakajima, Tsutomu (D.M.C. Network K. K., Japan).

Jpn. Kokai Tokkyo Koho JP 2000063217 A2 29 Feb 2000, 8 pp.

(Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM: A01N059-08.

ICS: A01N025-04; A01N025-06; A61L002-18; A61L002-20;

A61L009-01; C01B011-02. APPLICATION: JP 1999-149666 28 May

1999. PRIORITY: JP 1998-163420 11 Jun 1998. DOCUMENT TYPE:

Patent CA Section: 17 (Food and Feed Chemistry) Section

cross-reference(s): 5, 63

The invention relates to a liq. compn. contg. dissolved chlorine dioxide

gas, chloric acid and/or its salt, chlorous acid salt, and a pH-adjusting

agent, providing long-lasting disinfection or deodorization effects,

suitable for use for fruits, vegetables, cutting boards, etc., in a form of

liq., gel, foam, or aerosol. A chlorine dioxide-contg. liq. was prepd.

from a chlorine dioxide gas-dissolved soln. (2500 ppm) 250, 5 %

sodium chlorite soln. 749, 5 % sodium chlorate soln. 1 mL, and citric

acid 3 g. The liq. 50 g was combined with sodium alkylsulfonate

surfactant 225, liq. paraffin 15, and liq. propane gas 10 g to obtain a

deodorizing foam.

 

 

573.

132:193442

Chlorine dioxide treatment of seafoods to reduce bacterial loads.

Kim, J. M.; Huang, T.-S.; Marshall, M. R.; Wei, C.-I. (Food and

Environmental Toxicology Laboratory, Food Science and Human

Nutrition Dept., Univ. of Florida, Gainesville, FL 32611-0720, USA). J.

Food Sci., 64(6), 1089-1093 (English) 1999 Institute of Food

Technologists. CODEN: JFDSAZ. ISSN: 0022-1147. DOCUMENT

TYPE: Journal CA Section: 17 (Food and Feed Chemistry)

Various seafoods were treated with fresh chlorine dioxide (ClO2) solns.

(20, 40, 100, and 200 ppm total available ClO2) in 3.5% brine for 5 min,

and bacterial loads and sensory quality were evaluated after 0, 3, and 7

days storage on ice. The ClO2 treated groups at each time period had

lower bacterial counts than non-treated and brine-treated groups. The

differences in bacterial counts were significant, esp. for groups treated

with 100 and 200 ppm ClO2. Treated ClO2 solns. contained very low or

no bacterial loads. Treated red grouper and salmon with 100 or 200

ppm ClO2 developed skin discoloration (lighter color) and a chocolate

color in the gills.

 

 

574.

132:187525

The formation of ClOO following the photoexcitation of aqueous OClO

studied by two-color, time-resolved resonance Raman spectroscopy.

Thomsen, Carsten L.; Philpott, Matthew P.; Hayes, Sophia C.; Reid,

Philip J. (Box 351700, Department of Chemistry, University of

Washington, Seattle, WA 98195, USA). J. Chem. Phys., 112(2),

505-508 (English) 2000 American Institute of Physics. CODEN:

JCPSA6. ISSN: 0021-9606. DOCUMENT TYPE: Journal CA Section:

74 (Radiation Chemistry, Photochemistry, and Photographic and Other

Reprographic Processes)

The photochem. of chlorine dioxide (OClO) is investigated by two-color

time-resolved resonance Raman spectroscopy. Pump and probe

wavelengths of 390 and 260 nm, resp., are used to monitor

photoproduct formation following aq. OClO photoexcitation. Depletion

and subsequent recovery of the OClO scattering intensities is obsd.

consistent with subpicosecond reformation of OClO via geminate

recombination of the primary photoproducts. Intensity is obsd. at 1442

cm-1 consistent with ClOO formation that appears and decays with time

consts. of 27.9*4.5 ps and 398*50 ps, resp. The results presented

here represent the first direct evidence for ClOO formation following the

photoexcitation of aq. OClO.

 

 

575.

132:186685

New reprocessing system based on the precipitation method under

mild aqueous conditions.

Asanuma, Noriko; Tomiyasu, Hiroshi (Japan). Bull. Res. Lab. Nucl.

React. (Tokyo Inst. Technol.), 23, 84-85 (English) 1999 Tokyo Institute

of Technology, Research Laboratory for Nuclear Reactors. CODEN:

BRLTD9. ISSN: 0387-6144. DOCUMENT TYPE: Journal CA Section:

71 (Nuclear Technology)

A new reprocessing system for spent nuclear fuel using the formation of

carbonato complexes of actinide (VI) and (IV) ions has been studied.

This system is aimed at achieving extreme safety and overcoming

environmental problems.

 

 

576.

132:170736

Determination of chlorine dioxide, chlorite and chlorate by indigo

carmine methods in natural waters: study of interferences.

Elleouet, C.; Quentel, F.; Madec, C. L. (Laboratoire de Chimie

Analytique, UMR 6521, Universite de Bretagne Occidentale, Brest

29285, Fr.). Rev. Sci. Eau, 12(3), 561-575 (French) 1999 Lavoisier

Abonnements. CODEN: RSEAEX. ISSN: 0992-7158. DOCUMENT

TYPE: Journal CA Section: 61 (Water) Section cross-reference(s): 79

Over the last decade, chlorine dioxide has been increasingly used for

disinfecting drinking water in many countries. A guarantee for the

protection of the consumer is the presence of a sufficient residual

concn. of the bactericidal reagent in drinking water. Thus it is important

to det. exactly and accurately the levels of chlorine dioxide at the tap.

During water treatment and subsequent distribution, chlorine dioxide

can undergo a variety of redn. and disproportionation reactions

producing primarily chloride but also chlorite and chlorate, which have

been shown to cause hemolytic anemia. Reliable anal. methods are

needed to identify and det. levels of chlorine dioxide, chlorite and

chlorate in drinking water. A procedure based on the use of indigo

carmine for the detn. of each species in natural waters is suggested in

this paper. In phosphate buffer (pH 6.8), two moles of chlorine dioxide

oxidize one mole of indigo carmine. The concn. of the bactericidal

reagent can be detd. by measuring the difference in absorbance of the

dye at 610 nm before and after reaction with chlorine dioxide. This

method is selective as chlorite and chlorate do not react with indigo

carmine in phosphate buffer at pH 6.8. Although the

spectrophotometric method can be successfully used at levels of

chlorine dioxide down to 30 mg/L, the detn. of lower levels in tap water

requires a more sensitive method such as an electrochem. stripping

procedure. This anal. is based on the measurement of the decrease in

the indigo carmine signal after addn. of chlorine dioxide. The detection

limit is around 1 mg/L. At pH = 2, one mole of indigo carmine reduces

one mole of chlorite. Thus the chlorite concn. can be detd. by

measuring the indigo carmine absorbance at pH = 2. At pH = 0, indigo

carmine reacts with both chlorite and chlorate. A measurement at pH =

0 allows chlorate concns. to be detd. since the decrease in absorbance

due to the presence of chlorite can be calcd. The stability of indigo

carmine absorbance has been studied. An indigo carmine soln. prepd.

in phosphate buffer is stable over several days if kept in light-proof

bottles. It is not surprising that the presence of chlorite and chlorate

does not lead to a change in absorbance as they do not react with the

dye at pH = 6.8. A slight decrease in absorbance of an indigo carmine

soln. contg. chlorine dioxide is obsd. after about twenty hours. This

means that the chlorine dioxide concn. has to be detd. in the first hours,

which follow the addn. of the dye to the sample in order to avoid errors.

Interferences can arise from other residual oxidants, which may also be

used in water treatment, or from substances present in the sample,

which may react with indigo carmine, chlorite and chlorate.

Accordingly, we have considered the influence of humic substances,

ozone and hypochlorite. The absorbance of indigo carmine at pH = 2

and at pH = 0 does not change in presence of natural org. matter (1

mg/L). Chlorite and chlorate react with humic substances but the

kinetics are much slower than those of the reactions with indigo

carmine. Errors arising from humic substances in chlorite and chlorate

measurements are thus very weak. Ozone may interfere in analyses,

as it reacts with indigo carmine. However its existence in the

distribution network is unlikely as it also reacts with chlorine dioxide,

which is in excess, and chlorite to give chlorate. Hypochlorite causes

errors in chlorine dioxide, chlorite and chlorate detns. as a result of a

reaction with indigo carmine. In the case of chlorine dioxide detns.,

errors can be eliminated by adding ammonia to the sample before

indigo carmine. Once the validity of the procedures had been proven in

synthetic media, the methods were applied to a natural water, that of

the water distribution network of the city of Brest, France. The results

have been compared with those of other anal. techniques.

 

 

577.

132:168294

Preparation and application of high-performance chlorine dioxide

disinfectant.

Lai, Zini (Zhujiang Aquatic Product Institute, Chinese Academy of

Aquatic Product, Canton 510380, Peop. Rep. China). Guangzhou

Huagong, 27(4), 52-53 (Chinese) 1999 Guangzhou Huagong Bianjibu.

CODEN: GUHUEZ. ISSN: 1001-9677. DOCUMENT TYPE: Journal;

General Review CA Section: 49 (Industrial Inorganic Chemicals)

Section cross-reference(s): 10

A review with no refs. on ClO2 disinfectant, including the prepn. and

application of ClO2.

 

 

578.

132:167843

Chemical characteristics of lignins extracted from softwood TMP after

ozone and chlorine dioxide treatment.

Robert, D. R.; Szadeczki, M.; Lachenal, D. (CERMAV/CNRS Domaine

Universitaire, Grenoble 38041, Fr.). ACS Symp. Ser., 742(Lignin:

Historical, Biological, and Materials Perspectives, 2000), 520-531

(English) 2000 American Chemical Society. CODEN: ACSMC8.

ISSN: 0097-6156. DOCUMENT TYPE: Journal CA Section: 43

(Cellulose, Lignin, Paper, and Other Wood Products)

The role of ozonization in improving the phys. properties of softwood

thermomech. pulp (TMP) was investigated. Lignin (I) fractions were

extd. from pulp before and after ozonization and characterized by IR,

13C-NMR and GPC. Results showed the influence of the extn. method

on the I structure, with enzymic hydrolysis of the pulp giving a I fraction

richer in etherified units but more contaminated with polysaccharides

than acidolysis. The no. of carboxyl groups formed in I was also

studied, since this parameter can be correlated with pulp mech.

properties. ClO2 treatment of TMP, as compared to ozonization,

resulted in an increase of COOR(H) groups and the formation of

muconic structures clearly identified on NMR spectra.

 

 

579.

132:167838

Generation of chlorinated phenolic compounds in the bleaching

sequences DEoD (chlorine dioxide, oxidative extraction reinforced with

oxygen, and chlorine dioxide) and AZEopD (acid treatment, ozone,

oxidative extraction reinforced with oxygen and peroxide, and chlorine

dioxide).

Furtado, Jaoa L. F.; Zini, Claudia A.; Caramaoe, Elina B.; Peralba,

Maria do Carmo R. (Instituto de Quimica, Universidade Federal do Rio

Grande Do Sul, Porto Alegre 91501-9700, Brazil). Papel, 60(12),

56-61 (Portuguese) 1999 Associacao Brasileira Tecnica de Celulose

e Papel. CODEN: PAPLA3. ISSN: 0031-1057. DOCUMENT TYPE:

Journal CA Section: 43 (Cellulose, Lignin, Paper, and Other Wood

Products) Section cross-reference(s): 80

The formation of chlorinated phenolic compds. (CPCs) was monitored

in bleaching sequences DEoD (chlorine dioxide, oxidative extn.

reinforced with oxygen and chlorine dioxide) and AZEopD (acid

treatment, ozone, oxidative extn. reinforced with oxygen and peroxide

and chlorine dioxide). A kraft delignified cellulose pulp, produced from

a mixt. of 85% of Eucalyptus saligna and Acacia mearnsii. was

bleached and the filtrate was subjected to in situ acetylation to sep.

CPCs for quantification. The CPCs were detd. by gas chromatog. with

electron capture detector and gas chromatog. coupled with mass

spectrometry. Two CPCs were detected in the total filtrate (mixt. of

filtrates from each stage) from the sequence DEoD and four compds.

in the individual stage filtrates. In the sequence AZEopD, no CPC was

detected in D stage and in the mixt. from first stages filtrates (A, Z and

Eop). The CPCs vol. was below the limits established by the USEPA

in both sequences, low when compared to conventional bleaching

technologies, thus the sequences consider are environmentally

favorable alternatives.

 

 

580.

132:167812

Reactivity of lignin and problems of its oxidative destruction with peroxy

reagents.

Demin, Valerii A.; Shereshovets, Valeri V.; Monakov, Jurii B. (Institute

of Chemistry of Komi Scientific Centre, Ural Branch of the Russian

Academy of Sciences, Syktyvkar 167000, Russia). Russ. Chem. Rev.,

68(11), 937-956 (English) 1999 Turpion Ltd. CODEN: RCRVAB.

ISSN: 0036-021X. DOCUMENT TYPE: Journal; General Review CA

Section: 43 (Cellulose, Lignin, Paper, and Other Wood Products)

A review with 157 refs. on the reactivity of lignin (I) and problems of its

oxidative destruction with peroxy reagents is presented. Published

data on the reactivity and oxidn. of I and its model compds. with ClO2,

H2O2, and O3, as well as on oxidative destruction of sulfate pulp I with

various reagents during bleaching, are systematized and generalized.

Concepts of I activation towards its selective oxidn. and kinetic features

of sulfate pulp oxidative delignification are considered. Topics

discussed include: (1) I structure; (2) oxidn. of model compds.; (3)

combined action of oxidants on sulfate pulp I; (4) I activation towards

oxidative action of O and H2O2; (5) ozonolysis of sulfate pulps; (6) a

schematic approach to the selective destruction of residual I with

peroxy reagents; and (7) kinetic methods for assessment of residual I

reactivity.

 

 

581.

132:165424

Method and apparatus for preserving fruits and vegetables by using

antimicrobial agents and additional oxygen in gas streams.

Talley, Charles B. (Charvid Limited Liability Co., USA). U.S. US

6033704 A 7 Mar 2000, 9 pp. (English). (United States of America).

CODEN: USXXAM. CLASS: ICM: A23B007-144. ICS:

A23B007-152. NCL: 426320000. APPLICATION: US 1998-134655

14 Aug 1998. DOCUMENT TYPE: Patent CA Section: 17 (Food and

Feed Chemistry) Section cross-reference(s): 5

Fruits and vegetables are stored and(or) preserved by introducing an

antimicrobial agent and(or) addnl. mol. oxygen into an oxygen-contg.

gas stream that is circulated through a bed of the stored products. The

antimicrobial agent can be introduced by devices such as an atomizer

or a humidifier. Thus, chlorine dioxide is introduced by means of a

fogger into the gas stream circulating through a bed of potatoes in a

storage shed to control soft rot and other diseases.

 

 

582.

132:165386

Food preservatives containing chlorine dioxide and their application

method.

Iwamoto, Haruo; Iwamoto, Tsutomu (D.M.C. Network K. K., Japan).

Jpn. Kokai Tokkyo Koho JP 2000050851 A2 22 Feb 2000, 4 pp.

(Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM:

A23L003-3445. ICS: A23B004-16; A23B007-152. APPLICATION:

JP 1998-221513 5 Aug 1998. DOCUMENT TYPE: Patent CA

Section: 17 (Food and Feed Chemistry)

Food preservatives, useful for meat, fish, vegetables, etc. contain

dissolved ClO2-contg. aq. solns., alkali and/or alk. earth metal chlorites,

and pH adjustors. Strawberry was preserved with a gel comprising

LiClO2, ClO2, NaClO3, citric acid, and Aqualic CA (highly

water-absorbing polymer).

 

 

583.

132:162150

Exhaled nitric oxide among pulpmill workers reporting gassing

incidents involving ozone and chlorine dioxide.

Olin, A-C.; Ljungkvist, G.; Bake, B.; Hagberg, S.; Henriksson, L.; Toren,

K. (Sections of Occupational and Environmental Medicine,

Sahlgrenska University Hospital, Goeteborg, Swed.). Eur. Respir. J.,

14(4), 828-831 (English) 1999 Munksgaard International Publishers

Ltd. CODEN: ERJOEI. ISSN: 0903-1936. DOCUMENT TYPE:

Journal CA Section: 4 (Toxicology)

The aim of the study was to investigate whether measurement of nitric

oxide in exhaled air could be used for assessing the effects of irritants

on the respiratory system, in this case recurrent ozone gassing in an

occupational setting. The study population comprised bleachery

workers (n=56) from a Swedish pulpmill carrying out ozone-based pulp

bleaching since 1992 and controls (n=39). Both groups were

investigated by measuring NO in exhaled air, methacholine challenge

test, and answers to a questionnaire concerning the history of

respiratory symptoms and accidental exposure to ozone peaks. There

was no significant difference in NO output between exposed subjects

and controls (median 67.2 vs. 55.0 nL譵in-1, p=0.64). However, among

bleachery workers reporting ozone gassings, the median NO output

was 90.0 nL譵in-1 compared to 58.8 nL譵in-1 among those not

reporting such incidents (p=0.019). There was no relation between

exhaled NO and the prevalence of respiratory symptoms or bronchial

hyperresponsiveness. In a multiple regression model, only reported

ozone gassings were assocd. (p=0.016) with NO output. The results

indicate an assocn. between previous response to ozone gassing and

nitric oxide output. The increased nitric oxide output among the

bleachery workers reporting peak ozone exposure may indicate that

chronic airway inflammation is present. Further studies are needed to

evaluate the extent to which nitric oxide can be used for biol. monitoring

of respiratory health effects, and to relate it to other markers of airway

inflammation.

 

 

584.

132:157132

Ab initio study of the reorganization barrier for bent triatomic species.

Zhang, D.; Liang, F.; Feng, D.; Liu, C. (Institution of Theoretical

Chemistry, Shandong University, Jinan, Shandong, Peop. Rep. China).

Chem. Phys. Lett., 317(3,4,5), 430-436 (English) 2000 Elsevier

Science B.V. CODEN: CHPLBC. ISSN: 0009-2614. DOCUMENT

TYPE: Journal CA Section: 65 (General Physical Chemistry) Section

cross-reference(s): 67

Four scale models were used to compute the values of DEi* of several

bent triat. species with two identical bond lengths of 0/1-type

(NO2/NO2-, SO2/SO2-, ClO2/ClO2-, O3/O3-). The values of DEo* were

obtained using the Marcus dielec. continuum model and the gas-phase

mol. vol. The energies, structural parameters and potential consts. for

the triat. redox couples were detd. by ab initio MO calcn. at

MP2(FULL)/6-311+G (2D) level; DEi* are reported for all models

studied. The theor. results are compared with each other and with

literature data.

 

 

585.

132:156899

Compositions and methods for disinfecting contact lenses containing a

chlorite and a polyanionic compound.

Park, John Y.; Peng, Lin; Cafaro, Daniel P.; Dziabo, Anthony J. (

Allergan, USA). U.S. US 6024954 A 15 Feb 2000, 10 pp.,

Cont.-in-part of U.S. 5,648,074. (English). (United States of America).

CODEN: USXXAM. CLASS: ICM: A61K038-54. NCL: 424094200.

APPLICATION: US 1996-692867 2 Aug 1996. PRIORITY: US

1994-353782 12 Dec 1994. DOCUMENT TYPE: Patent CA Section:

63 (Pharmaceuticals)

Compns. for disinfecting contact lenses include a liq. medium contg. a

chlorite component, preferably a water sol. chlorite component, in a

contact lens disinfecting amt., and a polyanionic component, preferably

a water sol. polyanionic component, in an amt. effective to do at least

one of the following: inhibit formation of protein deposit material on a

contact lens immersed in the compn.; reduce the toxicity of the compn.

to the human eye, and reduce the damage to a contact lens caused by

immersing the contact lens in the compn. The compn. has a viscosity

of less than 50 cps at 25* C., an osmolality of at least about 200

mOsmol/kg, and preferably a pH in the range of about 6 to about 9. A

soln. was prepd. comprising sodium CM-cellulose 0.2, sodium chlorite

0.0625, sodium chloride 0.75, hydrochloric acid or sodium hydroxide

q.s. pH = 7.4, boric acid 0.15, and water q.s. 100%. The formulation

can be used as effective, non-irritating, non-toxic, safe and efficacious

single bottle contact lens disinfection systems which provide long

lasting and enhanced soothing and lubrication during contact lens wear.

 

 

586.

132:156881

Ostomy pouch or pouch for incontinence with deodorizing function and

its manufacture.

Gent, John A.; Steer, Graham Emery (Bristol-Myers Squibb Co., USA).

Jpn. Kokai Tokkyo Koho JP 2000042020 A2 15 Feb 2000, 7 pp.

(Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM:

A61F005-441. ICS: A61F005-445; A61L009-01. APPLICATION: JP

1999-193582 7 Jul 1999. PRIORITY: GB 1998-14723 7 Jul 1998.

DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Section

cross-reference(s): 38, 40

The pouch is manufd. by directly or indirectly fixing a support, which

comprises or has malodor counteractants, to a plastic material forming

a pouch wall. Alternatively the pouch is that comprising or contg. H2O2

generators. The support may comprise tissue paper, plastic films,

nonwoven fabrics, and/or adsorbent pads. The malodor counteractants

may be oxidant generators, H2O2 generators such as Na perborate,

ClO2 generators, etc., and addnl. contain bactericides and/or perfumes.

A sheet with a thermally-insulating surface was coated on the

non-thermally-insulating surface with a double-stick pressure-sensitive

adhesive. Particles of Na perborate were sprinkled on the adhesive

layer and compressed to remove excess particles. The sheet was cut

into 100 mm * 50 mm in size, laminated with a plastic film, and then

fabricated into an ostomy pouch. A pouch was packed with feces, kept

at body temp. for 30 min, and then opened to generate less malodor

than a control pouch with no deodorant.

 

 

587.

132:153516

Bleaching of cellulose pulp with a plurality of bleaching agents in a

single stage.

Tibbling, Ture Petter Magnus; Agarwal, Arvind Kumar (Asia Pulp &

Paper Co. Ltd., Singapore). PCT Int. Appl. WO 2000008251 A1 17

Feb 2000, 35 pp. DESIGNATED STATES: W: AL, AM, AT, AU, AZ,

BA, BB, BG, BR, BY, CA, CH, CN, CU, CZ, DE, DK, EE, ES, FI, GB,

GE, GH, GM, HR, HU, ID, IL, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR,

LS, LT, LU, LV, MD, MG, MK, MN, MW, MX, NO, NZ, PL, PT, RO, RU,

SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, UA, UG, UZ, VN, YU, ZW, AM,

AZ, BY, KG, KZ, MD, RU, TJ, TM; RW: AT, BE, BF, BJ, CF, CG, CH,

CI, CM, CY, DE, DK, ES, FI, FR, GA, GB, GR, IE, IT, LU, MC, ML, MR,

NE, NL, PT, SE, SN, TD, TG. (English). (World Intellectual Property

Organization). CODEN: PIXXD2. CLASS: ICM: D21C009-153. ICS:

D21C009-14; D21C009-16. APPLICATION: WO 1998-IB1318 31 Jul

1998. DOCUMENT TYPE: Patent CA Section: 43 (Cellulose, Lignin,

Paper, and Other Wood Products) Section cross-reference(s): 59

Cellulosic material for the prodn. of chem. pulp is fed continuously

through a bleaching line and bleached with ozone and *1 bleaching

agents consisting of chlorine dioxide, chlorine, acidic hydrogen

peroxide, peracetic acid, persulfuric acid, and org. peroxides, in a

single stage which does not contain an intermediate washing or extn.

stage and, preferably, the redox potential of the pulp immediately after

the addn. of each bleaching agent is brought down to a level of 0-~20%

of the original value of the redox potential prior to the addn. of the

subsequent bleaching agent. The use of ozone provides a significant

improvement in pulp quality, 10-20% decrease in beating energy

requirements, ~15% improvement in tear strength, a savings of ~$20

(US) per ton of pulp, reduces the impact of bleaching on the

environment, and allows for inexpensive retrofitting of existing

equipment. Thus, a (DZD)(EO)D(ED) sequence for bleaching

oxygen-delignified mill pulp using sulfuric acid, ozone, and chlorine

gave ISO brightness 89.9%, ISO Rev. brightness 88.4, viscosity 641

dm3/kg, total ClO2 46 kg/ADMT, compared with 89.3, 87.8, 705, and

47, resp., using active chlorine alone.

 

 

588.

132:153464

Short ECF sequences involving chlorine dioxide to bleach bagasse

pulp to 90% ISO.

Rajesh, K. S.; Tamilarasy, T. S.; Mohan Rao, N. R. (Tamilnadu

Newsprint and Papers Ltd., Kagithapuram 639 136, India). IPPTA,

11(2), 27-33 (English) 1999 Indian Pulp and Paper Technical

Association. CODEN: IPPTDO. ISSN: 0379-5462. DOCUMENT

TYPE: Journal CA Section: 43 (Cellulose, Lignin, Paper, and Other

Wood Products)

The use of short elemental Cl-free (ECF) sequences with ClO2 to

achieve 90% ISO brightness for bagasse kraft pulp is discussed.

Introduction of oxidative extns. is a preferred necessary step to achieve

<2.0 extd. pulp kappa no. ClO2 substitution to the 50% level is most

effective, although it cannot be termed as an ECF sequence,. E(OP)

extn. is not necessary for bagasse pulp as E(P) or E(O) serve the same

purpose; E(P) is preferable because of its simplicity in operation. E(O)

is most effective in COD decreasing, whereas E(P) is most effective in

color removal, when compared to color and COD of a conventional

sequence. The short 3-stage D-EP-D sequence is quite promising.

The strength properties, esp. tear factor, are improved, although

brightness levels are higher.

 

 

589.

132:150930

Ice with bactericide and preservatives for storing fresh fish.

Tomita, Mamoru; Kato, Ryo; Suzuki, Kiyoshi; Doi, Toyohiko; Nakamura,

Teiichi (Morinaga Milk Industry Co., Ltd., Japan). PCT Int. Appl. WO

2000008956 A1 24 Feb 2000, 25 pp. DESIGNATED STATES: W:

JP, US; RW: AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU,

MC, NL, PT, SE. (Japanese). (World Intellectual Property

Organization). CODEN: PIXXD2. CLASS: ICM: A23L003-375. ICS:

A23L003-3463; A23L003-3472; A23L003-3526; A23L003-358.

APPLICATION: WO 1999-JP2912 31 May 1999. PRIORITY: JP

1998-241049 12 Aug 1998; JP 1999-2820 8 Jan 1999. DOCUMENT

TYPE: Patent CA Section: 17 (Food and Feed Chemistry)

Ice for storing fresh fish, even after melting, to safely store fresh fish and

shellfish over a long period of time by bactericidal hypochlorous acid at

5-30 ppm contained therein in addn. to the preserving effect of a chilled

state. The ice is, not sealed in a container, contains hydrogen

peroxide, an edible colorant and a cryo-nucleation accelerator together

with * one substance selected from the group consisting of chlorine

dioxide, propionic acids, 4-hydroxybenzoic acids, polylysine, chitin,

chitosan, sorbic acids, hinokitiol, lysozyme and lactoferrins.

 

 

590.

132:150915

Manufacture of high-purity chlorine dioxide for food preservatives.

Du, Xiaoming; Pan, Cenxuan; Li, Fasheng (Luxianfeng Environmental

Protection Science and Technology Co., Ltd., Beijing, Peop. Rep.

China). Faming Zhuanli Shenqing Gongkai Shuomingshu CN 1195642

A 14 Oct 1998, 4 pp. (Chinese). (People's Republic of China).

CODEN: CNXXEV. CLASS: ICM: C01B011-02. ICS: A23L003-358.

APPLICATION: CN 1997-103875 4 Apr 1997. DOCUMENT TYPE:

Patent CA Section: 17 (Food and Feed Chemistry)

The process comprises reacting NaClO3, oxalic acid and H2SO4 to

obtain ClO2 gas; purifying the ClO2 gas with 5-15% urea soln.; and

absorbing the gas with stabilizing agent to obtain the high-purity ClO2

soln. The stabilizing agent comprises Na2CO3 1, H2O2 0.2-0.9, sodium

dodecyl benzene sulfonate 0.002-0.01 and oxinate 0.0002-0.001 parts.

 

 

591.

132:150903

Manufacture of solid stabilized chlorine dioxide for disinfectant and

fresh food preservative and deodorant.

Pan, Cenxuan; Du, Xiaoming; Li, Fasheng (Luxianfeng Environmental

Protection Science & Technology Co., Ltd., Beijing, Peop. Rep. China).

Faming Zhuanli Shenqing Gongkai Shuomingshu CN 1195641 A 14

Oct 1998, 3 pp. (Chinese). (People's Republic of China). CODEN:

CNXXEV. CLASS: ICM: C01B011-02. ICS: A01N025-18;

C09K015-02. APPLICATION: CN 1997-103874 4 Apr 1997.

DOCUMENT TYPE: Patent CA Section: 17 (Food and Feed

Chemistry)

Solid stabilized chlorine dioxide is manufd. by mixing 0.2-1.5 parts

0.2-8% ClO2 soln. and 1 part mixt. contg. different recipes. The mixt.

comprises porous mol. sieve 1, deliquescent agent 0-0.1,

control-releasing agent (kaolin or acid clay) 0-0.5 and binder (flour)

0-0.1 parts. The porous mol. sieve is selected from polyacrylic resin,

synthetic resin, actived carbon, calcium silicate and/or diatomite.

 

 

592.

132:142220

Bonding in mixed halogen and hydrogen peroxides.

Bridgeman, Adam J.; Rothery, Joanne (University Chemical

Laboratories, Cambridge CB2 1EW, UK). J. Chem. Soc., Dalton

Trans., (22), 4077-4082 (English) 1999 Royal Society of Chemistry.

CODEN: JCDTBI. ISSN: 0300-9246. DOCUMENT TYPE: Journal CA

Section: 65 (General Physical Chemistry) Section cross-reference(s):

67, 73

The geometries and vibrational frequencies of the hydrogen and

halogen peroxides XOOX' and the XOO and XO fragments (X, X' = H,

F, Cl, Br or I) were studied using non-local d. functional theory. The

X-O, X'-O and O-O bond energies were calcd. and likely dissocn. paths

for these atmospherically important or potentially important mols.

suggested. The sulfur analogs were also examd. A unified model for

these chem. diverse species is presented based on the interaction

between O2 and X鬃譞 fragments. The correlation between their

electronic structures is outlined. The antibonding nature of the

interaction between the halogen lone pairs and the p electrons of the

O2 fragments causes lengthening and weakening of the

halogen-oxygen bonds. The electronegativity of X and X' dets. the

extent and direction of the electron transfer between the O2 and X鬃譞

fragments. The O-O bond order is thus sensitive to the nature of the

substituents and the multiple bond character decreases steadily as the

electronegativity of X and X' decreases. The O-O bond strengths,

though, are also affected by steric interactions between the halogen

'lone pairs'. The O-O bonds in the HO-OX' species are thus much

stronger than the bond orders and lengths suggest.

 

 

593.

132:141645

Water purification using biodegradable polymers, oxidants, and

amidosulfonic acids.

Kleinstueck, Roland; Groth, Torsten; Joentgen, Winfried (Bayer A.-G.,

Germany). Ger. Offen. DE 19837068 A1 24 Feb 2000, 8 pp.

(German). (Germany). CODEN: GWXXBX. CLASS: ICM:

C02F005-12. APPLICATION: DE 1998-19837068 17 Aug 1998.

DOCUMENT TYPE: Patent CA Section: 61 (Water)

Waters, esp. cooling waters, are treated with biodegradable polymers

having repeating succinyl units (e.g., polyasparaginic acid), oxidants

(e.g., hydrogen peroxide, chlorine, bromine, chlorine dioxide,

hypochlorite, ozone, or their reaction products with water), and

amidosulfonic acids.

 

 

594.

132:141305

A comparison among different wastewater disinfection systems:

experimental results.

Collivignarelli, C.; Bertanza, G.; Pedrazzani, R. (Department of Civil

Engineering, Faculty of Engineering, University of Brescia, Brescia

I-25123, Italy). Environ. Technol., 21(1), 1-16 (English) 2000 Selper

Ltd., Publications Division. CODEN: ENVTEV. ISSN: 0959-3330.

DOCUMENT TYPE: Journal CA Section: 60 (Waste Treatment and

Disposal)

In this work, the efficiency and the applicability of some disinfection

systems for biol. treated wastewater were studied. The following

disinfection processes were considered: peracetic acid (PAA),

chlorine dioxide, ozone, UV light. These treatments were chosen as an

alternative to chlorination. Their applicability was investigated

considering both the removal efficiency of microorganisms and the

qual. changes in the treated effluent (e.g. presence of disinfectant

residues, disinfection byproducts, etc.). The different processes were

tested by means of pilot scale plants working in parallel; in fact they

were fed with the same wastewater (secondary effluent of a municipal

wastewater treatment plant). Finally, an economical anal. was carried

out.

 

 

595.

132:139421

Manufacture of stable chlorine dioxide.

Ding, Zhangxun; Ding, Wenjie (Peop. Rep. China ). Faming Zhuanli

Shenqing Gongkai Shuomingshu CN 1185417 A 24 Jun 1998,6 pp.

(Chinese). (People's Republic of China). CODEN: CNXXEV. CLASS:

ICM: C01B011-02. APPLICATION: CN 1996-118919 18 Dec 1996.

DOCUMENT TYPE: Patent CA Section: 49 (Industrial Inorganic

Chemicals)

The chlorine dioxide is manufd. by mixing chlorine dioxide-generating

reactants with extractant selected from aliph. or arom. hydrocarbons

and solvent gasoline in a reactor under stirring, directly absorbing the

chlorine dioxide with the extractant, sepg. from other reaction product,

adding sodium carbonate and hydrogen peroxide to the soln., sepg. to

obtain high-concn. and stable product. The reactants are selected from

sodium chlorite, HCl, H2SO4, NaCl, and chlorous acid. The chlorine

dioxide is used as disinfectant.

 

 

596.

132:138977

Hexenuronic acid in kraft pulps from radiata pine.

Allison, Robert W.; Timonen, Olli; McGrouther, Kim G.; Suckling, Ian D.

(PAPRO NZ, Forest Research, Rotorua, N. Z.). Appita J., 52(6),

448-453 (English) 1999 Appita. CODEN: APJOES. ISSN:

1038-6807. DOCUMENT TYPE: Journal CA Section: 43 (Cellulose,

Lignin, Paper, and Other Wood Products)

A wide range of kraft pulps from radiata pine was assessed for

hexenuronic acid (I) content using the acid hydrolysis/UV method

developed by Vuorinen. I contents were variable and depended on

whether pulping was performed in the lab. or mill, used continuous or

batch systems, or followed conventional or modified procedures. High

alkali concn. during pulping was probably the main factor leading to low

I levels in the final pulp. For each 10 mmol/kg of I in radiata pine kraft

pulp, kappa no. was increased by about 0.9 units. Removal of this

kappa no. contribution from I by hydrolytic pretreatment resulted in

proportional savings in subsequent ClO2 bleach chem. It was also

shown that bleaching with ClO2 was very effective at destroying I

groups, esp. at active Cl multiples of >0.20. A modification to the

Vuorinen UV method was developed to measure the low levels of I in

ClO2-bleached pulps. Overall, the content and response of I in radiata

pine pulps were similar to those reported for kraft pulps from Northern

Hemisphere softwoods.

 

 

597.

132:133616

Plant-activating agents manufactured by electrolyzing tea leaves, their

products, etc.

Suzuki, Masayoshi (Hokuetsu Giken Kogyo K. K., Japan). Jpn. Kokai

Tokkyo Koho JP 2000044420 A2 15 Feb 2000, 4 pp. (Japanese).

(Japan). CODEN: JKXXAF. CLASS: ICM: A01N065-00. ICS:

A01G007-00; C02F001-46. APPLICATION: JP 1998-251747 3 Aug

1998. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical

Bioregulators) Section cross-reference(s): 11, 19

Plant-activating agents are manufd. by adding salts to eluates or solns.

of tea leaves, tea products, garlic products, wasabi products, or *1

selected from tannins, caffeine, catechin, or chlorophylls, and

electrolyzing the mixts. Alternatively, the agents are manufd. by adding

Cl, HClO, its salts, ClO2, HClO2, its salts, HClO3, its salts, HClO4, its

salts, O3, and/or H2O2 to the eluates or solns., the products, or the

compds. NaCl was dissolved in oolong tea and the mixt. was

electrolyzed at 5 V and 3 A to give a plant-activating liq. The liq.

significantly promoted growth of daikon radish, tomato, and cabbage

after germination on a fertilizer-free sponge.

 

 

598.

132:131200

Preparation of chlorine dioxide.

Wen, Herui; Yu, Jianping (Department of Chemistry and Chemical

Engineering, Gannan Teachers College, Ganzhou 341000, Peop. Rep.

China). Xiandai Huagong, 19(11), 27-29 (Chinese) 1999 Zhongguo

Huagong Xinxi Zhongxin. CODEN: HTKUDJ. ISSN: 0253-4320.

DOCUMENT TYPE: Journal CA Section: 78 (Inorganic Chemicals and

Reactions)

A method for prepg. ClO2 from KClO3 and hydrazine sulfate was

studied. The effect of H2SO4 concn. and reaction temp. on the yield

and purity of ClO2 was discussed. The yield reached 90% with a purity

of 91%.

 

 

599.

132:127686

Study on nonadsorption-type stable solid chlorine dioxide disinfectants.

Bao, Lifeng; Pan, Xihe; Huan, Pengcheng; Lu, Zhaorong; Zhu, Renyi (

Shanghai Wenhua Disinfection Institute, Shanghai 200070, Peop. Rep.

China). Zhongguo Xiaoduxue Zazhi, 16(2), 79-83 (Chinese) 1999

Zhongguo Xiaoduxue Zazhi Bianjibu. CODEN: ZXZAFO. ISSN:

1001-7658. DOCUMENT TYPE: Journal CA Section: 63

(Pharmaceuticals) Section cross-reference(s): 17

The acidic soln. of nonadsorption-type stable solid chlorine dioxide

disinfectant (tablet or powder) shows obvious characteristic absorption

peak of chlorine dioxide on IR and UV spectrograms. The killing rates

of Escherichia coli and Staphylococcus aureus exposed to its soln.

contg. chlorine dioxide 10 mg/L for 5 min, and Bacillus subtilis var.

niger spores to its soln. contg. chlorine dioxide 250 mg/L for 10 min

were all 100% in suspension test. Its soln. contg. chlorine dioxide 100

mg/L with a 10 min contact time could destroy HBsAg antigenicity. The

chlorine dioxide content decreased by * 8.45% after storing under

air-tight condition at 56* for 2 wk. Its aq. soln. contg. chlorine dioxide

500 mg/L had slight corrosive effect on stainless steel, carbon steel

and copper and moderate corrosive effect on aluminum. Toxicity test

indicated that it belonged to actually nontoxic substances.

 

 

600.

132:122643

Chlorine dioxide as a novel oxidant for organometallic compounds.

Kuchin, A. V.; Dvornikova, I. A.; Nalimova, I. Yu. (Institute of Chemistry,

Komi Research Center, Ural Branch of the Russian Academy of

Sciences, Syktyvkar 167610, Russia). Russ. Chem. Bull., 48(10),

2001-2002 (English) 1999 Consultants Bureau. CODEN: RCBUEY.

ISSN: 1066-5285. DOCUMENT TYPE: Journal CA Section: 29

(Organometallic and Organometalloidal Compounds)

The use of ClO2 for the oxidn. of lithium tetraoctylaluminate obtained

from 1-octene and LiAlH4 gives 90% octanol. The oxidn. of Grignard

reagents with alkyl or allyl radicals occurs similarly.