The orthophosphate content of bicarbonate soil extracts

Soil Research ◽  
2001 ◽  
Vol 39 (2) ◽  
pp. 415 ◽  
Author(s):  
Joanne L. Coventry ◽  
David J. Halliwell ◽  
David M. Nash
Keyword(s):  
Molecular Weight ◽  
Plant Uptake ◽  
High Performance ◽  
Average Amount ◽  
Soil Extracts ◽  
Specific Identification ◽  
Soil P ◽  
Olsen P ◽  
Soil Solutions ◽  
Future Work

The Olsen P and Colwell P bicarbonate extraction procedures are empirically derived tests that provide an estimate of the soil P that is available for plant uptake. This paper examines each procedure using high performance liquid chromatography with flow injection analysis detection (HPLC-FIA) to specifically measure orthophosphate in bicarbonate extracts. Extract solutions from 3 soils of contrasting plant-available soil P contents were analysed for orthophosphate, total filtered (<15—45 µm) P (TFP), and either Olsen P or Colwell P. The amounts of P extracted by the Olsen procedure were not statistically different from orthophosphate (HPLC-FIA) (P > 0.05), suggesting the Olsen P test was a good measure of orthophosphate, the most immediately plant-available form of P. However, the average amount of P extracted by the Colwell procedure was 14% higher (P < 0.01) than the corresponding average orthophosphate concentration, presumably due to the presence of labile organic/condensed P, colloidal associated orthophosphate, or high molecular weight reactive P. These results suggest that there is a pool of non-orthophosphate P present in the molybdate reactive Colwell P extract that is potentially plant available. Future work should focus on specific identification of P compounds extracted from soils and soil solutions to examine their role as a source of P to plants.

A high-performance oil-free backing pump for electron microscopes

1978 ◽  
Vol 36 (1) ◽  
pp. 110-111
Author(s):  
G.K.W. Balkau ◽  
E. Bez ◽  
J.L. Farrant
Keyword(s):  
Molecular Weight ◽  
Electron Microscope ◽  
Hot Spots ◽  
High Performance ◽  
Carbonaceous Material ◽  
Contamination Rate ◽  
Low Molecular Weight ◽  
Principal Source ◽  
Rotary Pumps ◽  
Electron Microscopes

The earliest account of the contamination of electron microscope specimens by the deposition of carbonaceous material during electron irradiation was published in 1947 by Watson who was then working in Canada. It was soon established that this carbonaceous material is formed from organic vapours, and it is now recognized that the principal source is the oil-sealed rotary pumps which provide the backing vacuum. It has been shown that the organic vapours consist of low molecular weight fragments of oil molecules which have been degraded at hot spots produced by friction between the vanes and the surfaces on which they slide. As satisfactory oil-free pumps are unavailable, it is standard electron microscope practice to reduce the partial pressure of organic vapours in the microscope in the vicinity of the specimen by using liquid-nitrogen cooled anti-contamination devices. Traps of this type are sufficient to reduce the contamination rate to about 0.1 Å per min, which is tolerable for many investigations.

Calibration of methods for soil and diagnostic plant analysis in the Hungarian National Fertilization Long-term Trials. I. Comparison of soil P tests for agronomic purposes in the soils of long-term experiments

2011 ◽  
Vol 60 (2) ◽  
pp. 343-358
Author(s):  
Péter Csathó ◽  
Marianna Magyar ◽  
Erzsébet Osztoics ◽  
Katalin Debreczeni ◽  
Katalin Sárdi
Keyword(s):  
Plant Analysis ◽  
Soil P ◽  
Olsen P ◽  
Long Term Experiments ◽  
Soil P Tests

A szabadföldi trágyázási (tartam)kísérletek eredményeit talaj-, illetve diagnosztikai célú növényvizsgálatok segítségével tudjuk kiterjeszteni, általánosítani – figyelembe véve természetesen a kiterjesztés korlátait is. Célszerűnek láttuk ezen túl a talaj könnyen oldható tápelem-, közöttük P-tartalmát is meghatározni a hazánkban hivatalosan elfogadott AL- (ammónium-laktátos) módszer mellett az Európai Unióban és Észak-Amerikában alkalmazott P-tesztekkel is (CaCl2-, H2O-, Olsen-, Bray1-, LE-, Mehlich3- stb.) a hazai OMTK kísérletek talajmintáiban. A kísérleti helyek talajtulajdonságaiban megnyilvánuló jelentős különbségek lehetőséget adnak rá, hogy a talaj P-teszteket – és a növényi P-felvételt – jellegzetes hazai talajokon, sokszor szélsőséges talajparaméterek mellett vizsgáljuk. Az egyes P-szintek között a 28 év átlagában mintegy évi 50 kg P2O5·ha-1volt a különbség. A P0-szinten mért P-tartalmak jól jelezték az egyes kísérleti helyek talajának eltérő P-ellátottságát, illetve, közvetve, fizikai féleségében, pH és mészállapotában meglévő különbségeket. A P2-szinten – a hazai talajokra, P-igényes növényekre a hazai szabadföldi P-trágyázási tartamkísérleti adatbázisban talált összefüggésekre alapozott – új AL-P határértékek szerint csupán a bicsérdi csernozjom barna erdőtalajon nem javult a P-ellátottság legalább a „jó” szintig. Vizsgálataink megerősítették az AL-módszer függőségét a CaCO3-tartalomtól: a Mehlich3 módszerrel való összefüggésben a karbonátmentes és a karbonátos talajok csoportja erőteljesen elkülönült egymástól. Az AL-P korrekció elvégzése, azaz az AL-P értékeknek egy standard talajtulajdonság-sorra való konvertálása (KA: 36; pH(KCl): 6,8; CaCO3: 0,1%) látványosan csökkentette az AL-módszernek a talaj CaCO3-tartalmától való függőségét. Az AL-P és Olsen-P, valamint a korrigált AL-P és Olsen-P tartalmak összehasonlításában ugynakkor ugyanez az összefüggés nem volt állapítható, ami arra utal, hogy az Olsen módszer bizonyos fokig szintén pH- és mészállapot függő. Kísérleti eredményeink megerősítették a Sarkadi-féle AL-P korrekciós modell helytálló voltát. Fenti megállapításunkat ugyanakkor a növényi P-tartalmakkal való összefüggéseknek is igazolniuk kell. Szükséges tehát a talajvizsgálati eredményeknek a diagnosztikai célú növényvizsgálatokkal, valamint a terméseredményekkel való összevetése. A tartamkísérletek talajai lehetőséget nyújtanak a környezetvédelmi célú P-vizsgálatok értékelésére, a talaj P-feltöltöttsége környezeti kockázatának becslésére. Ezekkel a kérdésekkel a cikksorozat további részeiben kívánunk foglalkozni.

Preparation and Characterization of the High Molecular Weight [3H]Hyaluronic Acid

1992 ◽  
Vol 57 (10) ◽  
pp. 2151-2156 ◽  
Author(s):  
Peter Chabreček ◽  
Ladislav Šoltés ◽  
Hynek Hradec ◽  
Jiří Filip ◽  
Eduard Orviský
Keyword(s):  
Molecular Weight ◽  
Hyaluronic Acid ◽  
High Molecular Weight ◽  
Methyl Bromide ◽  
High Performance ◽  
Hydrogen Atoms ◽  
Isolation And Characterization ◽  
Labelling Procedure ◽  
Enzymatic Depolymerization

Two methods for the preparation of high molecular weight [3H]hyaluronic acid were investigated. In the first one, hydrogen atoms in the molecule were replaced by tritium. This isotopic substitution was performed in aqueous solution using Pd/CaCO3 as the catalyst. In the second method, the high molecular weight hyaluronic acid was alkylated with [3H]methyl bromide in liquid ammonia at a temperature of -33.5 °C. High-performance gel permeation chromatographic separation method was used for the isolation and characterization of the high molecular weight [3H]hyaluronic acid. Molecular weight parameters for the labelled biopolymers were Mw = 128 kDa, Mw/Mn = 1.88 (first method) and Mw = 268 kDa, Mw/Mn = 1.55 (second method). The high molecular weight [3H]hyaluronic acid having Mw = 268 kDa was degraded further by specific hyaluronidase. Products of the enzymatic depolymerization were observed to be identical for both, labelled and cold biopolymer. This finding indicates that the described labelling procedure using [3H]methyl bromide does not induce any major structural rearrangements in the molecule.

scholarly journals Evaluation of external contamination on the vial surfaces of some hazardous drugs that commonly used in Chinese hospitals and comparison between environmental contamination generated during robotic compounding by IV: Dispensing robot vs. manual compounding in biological safety cabinet

2021 ◽  
pp. 107815522110235
Author(s):  
Hao ML ◽  
Wang T ◽  
Zhu JQ ◽  
Song YJ ◽  
Gong TJ ◽  
...  
Keyword(s):  
Environmental Contamination ◽  
High Performance ◽  
Surface Contamination ◽  
Comparison Analysis ◽  
Sample Analysis ◽  
Average Amount ◽  
External Contamination ◽  
Biological Safety ◽  
Double Mass ◽  
Hazardous Drugs

Objectives The aims of the study were to evaluate the external contamination of hazardous drug vials used in Chinese hospitals and to compare environmental contamination generated by a robotic intelligent dispensing system (WEINAS) and a manual compounding procedure using a biological safety cabinet (BSC). Methods Cyclophosphamide, fluorouracil, and gemcitabine were selected as the representative hazardous drugs to monitor surface contamination of vials. In the comparative analysis of environmental contamination from manual and robotic compounding, wipe samples were taken from infusion bags, gloves, and the different locations of the BSC and the WEINAS robotic system. In this study, high-performance liquid chromatography coupled with double mass spectrometer (HPLC-MS/MS) was employed for sample analysis. Results (1) External contamination was measured on vials of all three hazardous drugs. The contamination detected on fluorouracil vials was the highest with an average amount up to 904.33 ng/vial, followed by cyclophosphamide (43.51 ng/vial), and gemcitabine (unprotected vials of 5.92 ng/vial, protected vials of 0.66 ng/vial); (2) overall, the environmental contamination induced by WEINAS robotic compounding was significantly reduced compared to that by manual compounding inside the BSC. Particularly, compared with manual compounding, the surface contamination on the infusion bags during robotic compounding was nearly nine times lower for cyclophosphamide (10.62 ng/cm2 vs 90.43 ng/cm2), two times lower for fluorouracil (3.47 vs 7.52 ng/cm2), and more than 23 times lower for gemcitabine (2.61 ng/cm2 vs 62.28 ng/cm2). Conclusions The external contamination occurred extensively on some hazardous drug vials that commonly used in Chinese hospitals. Comparison analysis for both compounding procedures revealed that robotic compounding can remarkably reduce environmental contamination.

scholarly journals Composition of low-molecular-weight glutenin subunits in common wheat (Triticum aestivum L.) and their effects on the rheological properties of dough

2021 ◽  
Vol 16 (1) ◽  
pp. 641-652
Author(s):  
Sławomir Franaszek ◽  
Bolesław Salmanowicz
Keyword(s):  
Molecular Weight ◽  
Rheological Properties ◽  
Common Wheat ◽  
High Performance ◽  
Triticum Aestivum L ◽  
Quality Parameters ◽  
Low Molecular Weight ◽  
Wheat Varieties ◽  
Breeding Lines ◽  
Capillary Zone

Abstract The main purpose of this research was the identification and characterization of low-molecular-weight glutenin subunit (LMW-GS) composition in common wheat and the determination of the effect of these proteins on the rheological properties of dough. The use of capillary zone electrophoresis and reverse-phase high-performance liquid chromatography has made it possible to identify four alleles in the Glu-A3 and Glu-D3 loci and seven alleles in the Glu-B3 locus, encoding LMW-GSs in 70 varieties and breeding lines of wheat tested. To determine the technological quality of dough, analyses were performed at the microscale using a TA.XT Plus Texture Analyzer. Wheat varieties containing the Glu-3 loci scheme (Glu-A3b, Glu-A3f at the Glu-A3 locus; Glu-B3a, Glu-B3b, Glu-B3d, Glu-B3h at the Glu-B3 locus; Glu-D3a, Glu-D3c at the Glu-D3 locus) determined the most beneficial quality parameters.

scholarly journals Investigating Lignin-Derived Monomers and Oligomers in Low-Molecular-Weight Fractions Separated from Depolymerized Black Liquor Retentate by Membrane Filtration

Molecules ◽  
2021 ◽  
Vol 26 (10) ◽  
pp. 2887
Author(s):  
Kena Li ◽  
Jens Prothmann ◽  
Margareta Sandahl ◽  
Sara Blomberg ◽  
Charlotta Turner ◽  
...  
Keyword(s):  
Molecular Weight ◽  
High Performance ◽  
Membrane Filtration ◽  
Black Liquor ◽  
Complex Mixture ◽  
Value Added ◽  
Kraft Pulping ◽  
Classification Model ◽  
Low Molecular Weight ◽  
Chemical Complexity

Base-catalyzed depolymerization of black liquor retentate (BLR) from the kraft pulping process, followed by ultrafiltration, has been suggested as a means of obtaining low-molecular-weight (LMW) compounds. The chemical complexity of BLR, which consists of a mixture of softwood and hardwood lignin that has undergone several kinds of treatment, leads to a complex mixture of LMW compounds, making the separation of components for the formation of value-added chemicals more difficult. Identifying the phenolic compounds in the LMW fractions obtained under different depolymerization conditions is essential for the upgrading process. In this study, a state-of-the-art nontargeted analysis method using ultra-high-performance supercritical fluid chromatography coupled to high-resolution multiple-stage tandem mass spectrometry (UHPSFC/HRMSn) combined with a Kendrick mass defect-based classification model was applied to analyze the monomers and oligomers in the LMW fractions separated from BLR samples depolymerized at 170–210 °C. The most common phenolic compound types were dimers, followed by monomers. A second round of depolymerization yielded low amounts of monomers and dimers, while a high number of trimers were formed, thought to be the result of repolymerization.

scholarly journals Effects of Molecular Weight of Functionalized Liquid Butadiene Rubber as a Processing Aid on the Properties of SSBR/Silica Compounds

Polymers ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 850
Author(s):  
Donghyuk Kim ◽  
Byungkyu Ahn ◽  
Kihyun Kim ◽  
JongYeop Lee ◽  
Il Jin Kim ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Anionic Polymerization ◽  
High Performance ◽  
Crosslink Density ◽  
Functional Group ◽  
Vital Role ◽  
Butadiene Rubber ◽  
Molecular Weights ◽  
Mooney Viscosity ◽  
Silica Dispersion

Liquid butadiene rubber (LqBR) which used as a processing aid play a vital role in the manufacturing of high-performance tire tread compounds. However, the studies on the effect of molecular weight, microstructure, and functionalization of LqBR on the properties of compounds are still insufficient. In this study, non-functionalized and center-functionalized liquid butadiene rubbers (N-LqBR and C-LqBR modified with ethoxysilyl group, respectively) were synthesized with low vinyl content and different molecular weights using anionic polymerization. In addition, LqBR was added to the silica-filled SSBR compounds as an alternative to treated distillate aromatic extract (TDAE) oil, and the effect of molecular weight and functionalization on the properties of the silica-filled SSBR compound was examined. C-LqBR showed a low Payne effect and Mooney viscosity because of improved silica dispersion due to the ethoxysilyl functional group. Furthermore, C-LqBR showed an increased crosslink density, improved mechanical properties, and reduced organic matter extraction compared to the N-LqBR compound. LqBR reduced the glass transition temperature (Tg) of the compound significantly, thereby improving snow traction and abrasion resistance compared to TDAE oil. Furthermore, the energy loss characteristics revealed that the hysteresis loss attributable to the free chain ends of LqBR was dominant.

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