scholarly journals Studies on the Relationship between Physico-chemical Properties and Crystalline Forms of Tulobuterol Hydrochloride. III. Hygroscopic Properties of Polymorphs of Tulobuterol Hydrochloride

1983 ◽  
Vol 103 (3) ◽  
pp. 336-341
Author(s):  
MASARU SAITO ◽  
MASAHIRO YAMAZAKI ◽  
KUGAKO MATSUMURA ◽  
HIDEO KATO ◽  
YASUO ITO ◽  
...  
Author(s):  
Debasmrity Mukherjee ◽  
Ashis Kumar Paul

The coast of Henry's island, extending from Saptamukhi River in the east to Bakkhali River in the West. In the hot and humid climate of the Sundarban, a negligible input of fresh water through tidal creeks, high evaporation rate at the surface area are the probable reasons behind the evolution of Hypersaline patches of Henry's and Patibunia Island. The dense salt patches develop in the abandoned portion of the surface then sinks and move out of the tidal estuaries as subterranean flow or a bottom current to make the environment more saline. Development of Saltpan is one of the major hindrances for the growth of mangroves and hampers the ecological balance of Sundarban. Present paper attempts to highlight- I) To study and identification of Geomorphological settings of both island. ii) Analysis of Physico-chemical properties of hyper saline soil. iii) Identification of hyper-saline patches and their impact on mangrove degradation. Application of remote sensing technique and GIS analysis help to find out the relationship between mangrove degradation and salinity within the islands area in the last few decades. Development of hyper saline patches and changing environmental parameters are how much responsible for the mangrove degeneration process are major issues of this paper. The Forest Department has attempted to restore the growth of mangrove and improve fragile ecosystem but without understanding the geomorphology and environmental condition, it is not possible to implement proper managemental strategies for wetland restoration process.


2018 ◽  
Vol 20 (21) ◽  
pp. 14525-14536 ◽  
Author(s):  
Daniel Lundberg ◽  
Dorota Warmińska ◽  
Anna Fuchs ◽  
Ingmar Persson

The relationship between the structural and volumetric properties of ions in solvents with different physico-chemical properties has been studied for 19 cations and six anions in six solvents.


2021 ◽  
Author(s):  
shuang han ◽  
Juan Hong ◽  
Qingwei Luo ◽  
Hanbing Xu ◽  
Haobo Tan ◽  
...  

<p>Hygroscopic properties of 23 organic compounds with different physico-chemical properties including carboxylic acids, amino acids, sugars and sugar alcohols were measured using a Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA). We converted our experimental GF data of organics at 90% RH to κ to facilitate the comparison and we find that organic compounds with different molecular functionality present quite different hygroscopicity. Compounds with extra functional groups usually show higher hygroscopicity compared to their parental molecular compounds. Moreover, some compounds share the same molecular structure or functionality but vary differently in hygroscopicity. In general, the hygroscopicity of organics increase with functional groups in the following order: (-CH3/-NH2) < (-OH) < (-COOH/C=C/C=O). For highly soluble organics, the hygroscopicity decreases with molecular weight; while for slightly soluble organics which are not fully dissolved in aerosol droplets, their hygroscopicity can be divided into two categories. One is non-hygroscopic compounds, which may not fully deliquesce in the aerosol droplets. The other is moderate hygroscopic compounds, of which the hygroscopicity is mainly limited by their water solubility. Moreover, the hygroscopicity of organic compounds generally increased linearly with O:C ratios, although some of them have the same O:C ratio of but with different hygroscopicity. The experimental determined hygroscopicity are also compared with model predictions using the Extended Aerosol Inorganics Model (E-AIM) and the UManSysProp at 10-90% RH. Both models poorly represent the hygroscopic behavior of some organics, which may due to that the phase transition and intermolecular interactions are not considered in the simulations.</p>


ASAIO Journal ◽  
1997 ◽  
Vol 43 (2) ◽  
pp. 2
Author(s):  
K. Uchida ◽  
C. Nojiri ◽  
M. Waki ◽  
D. Mizumoto ◽  
T. Kido ◽  
...  

2014 ◽  
Vol 61 (2) ◽  
pp. 49-54
Author(s):  
M. Stankovičová ◽  
Ž. Bezáková ◽  
P. Mokrý ◽  
P. Salát ◽  
M. Kočík ◽  
...  

Abstract The aim of this paper is the study of physico-chemical properties of the chosen compounds, derivatives of 2-hydroxy-3-[2-(4-methoxyphenyl) ethylamino]propyl-4-[(alkoxycarbonyl)amino]benzoates and 2-hydroxy-3-[2-(2-methoxyphenyl)ethylamino]propyl-4-[(alkoxycarbonyl) amino]benzoates with potential ultra-short beta-adrenolytic activity. The studied compounds are different in the position of the substituent on the benzene ring in the side chain as well as in the aromatic ring in position 4 with alkyl- (methylto butyl-) carbamate. The physico-chemical characteristics, for example, lipophilicity, surface activity, adsorbability, acidobasic properties etc., are very important for the explanation of the relationship between structure and biological activity of the drug. These parameters serve as the base of quantitative structure-activity study. The goal of this work is to establish the spectral characteristics of studied compounds in UV-area, pKa values, the parameters of lipophilicity (the values of Rf and RM from thin layer chromatography, retention time t´R and capacity factor k´ from liquid chromatography and experimental partition coefficients log P´ values), surface tension, critical micelle concentrations, the adsorbability of compounds expressed by percent of adsorbed compound on active charcoal β% as well as by Freundlich adsorption isotherms. The obtained values are correlated with the parameters characterising the size of molecule, for example, the number of carbon atoms on carbamate functional group.


2020 ◽  
Vol 45 (3) ◽  
pp. 12-27
Author(s):  
Wiesława Ferenc ◽  
Dariusz Osypiuk ◽  
Jan Sarzyński ◽  
Halina Głuchowska

The complexes of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) with ligand (H2L=C13H12N2O5) formed by condensation reaction of isatin and glutamic acid were synthesized. Their physico-chemical properties were characterized using elemental analysis, XRF, XRD, FTIR, TG–DSC and TG–FTIR methods and magnetic measurements (Gouy’s and SQUID-VSM methods). The complexes were obtained in crystalline forms (monoclinic or triclinic) with the formulae: M(LH)2·nH2O for Mn(II), Ni(II) and Zn(II) and ML·nH2O for Co(II) and Cu(II), where LH=C13H11N2O5–, L-=C13H10N2O52–, n = 1 for Mn(II), Cu(II) and Zn(II), n = 2 for Co(II) and n = 3 for Ni(II). In air at 293–1173 K they decompose in three steps forming finally the oxides of the appropriate metals. The gaseous decomposition products were identified as: H2O, CO2, CO, hydrocarbons and N2O. The magnetic moment values for complexes (except Zn(II) complex) show their paramagnetic properties with the ferro- and antiferromagnetic interactions between central ions. The compounds of Mn(II) and Co(II) are high spin complexes with weak ligand field. In Co(II) and Cu(II) complexes two carboxylate groups take part in the metal ion coordination while in those of Mn(II), Ni(II) and Zn(II) only one carboxylate anion coordinates to central ion.


2006 ◽  
Vol 77 (1) ◽  
pp. 37-43
Author(s):  
Naoto NAKANISHI ◽  
Shinichi KAWAKAMI ◽  
Tomoya YAMADA ◽  
Yasuhiro AOKI

2021 ◽  
Vol 22 (13) ◽  
pp. 6758
Author(s):  
B. Velasco-Rodriguez ◽  
T. Diaz-Vidal ◽  
L. C. Rosales-Rivera ◽  
C. A. García-González ◽  
C. Alvarez-Lorenzo ◽  
...  

Hyaluronic acid (HA) and gelatin (Gel) are major components of the extracellular matrix of different tissues, and thus are largely appealing for the construction of hybrid hydrogels to combine the favorable characteristics of each biopolymer, such as the gel adhesiveness of Gel and the better mechanical strength of HA, respectively. However, despite previous studies conducted so far, the relationship between composition and scaffold structure and physico-chemical properties has not been completely and systematically established. In this work, pure and hybrid hydrogels of methacroyl-modified HA (HAMA) and Gel (GelMA) were prepared by UV photopolymerization and an extensive characterization was done to elucidate such correlations. Methacrylation degrees of ca. 40% and 11% for GelMA and HAMA, respectively, were obtained, which allows to improve the hydrogels’ mechanical properties. Hybrid GelMA/HAMA hydrogels were stiffer, with elastic modulus up to ca. 30 kPa, and porous (up to 91%) compared with pure GelMA ones at similar GelMA concentrations thanks to the interaction between HAMA and GelMA chains in the polymeric matrix. The progressive presence of HAMA gave rise to scaffolds with more disorganized, stiffer, and less porous structures owing to the net increase of mass in the hydrogel compositions. HAMA also made hybrid hydrogels more swellable and resistant to collagenase biodegradation. Hence, the suitable choice of polymeric composition allows to regulate the hydrogels´ physical properties to look for the most optimal characteristics required for the intended tissue engineering application.


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