A model for collagen hydration

1971 ◽  
Vol 178 (1053) ◽  
pp. 465-476 ◽  

A detailed proton nuclear magnetic resonance study has been made of the influence of temperature and water content upon the nature of water adsorbed on collagen fibres. A refinement of a previously reported analysis of time-averaged tensor properties of the water molecule with respect to the fibre axis supports the previous conclusion that the water molecules form hydrogen-bonded chains around the collagen molecules. The experimental evidence strongly indicates that there is an inner hydration layer consisting of about 24 % water per weight of dry collagen, which is highly ordered, surrounded by a disordered outer layer of water at high-water contents. Exchange of water molecules between the inner and outer hydration layers takes place at a rapid rate. Dynamic aspects of the hydration structure are discussed, and it is suggested that the inner hydration layer imparts an appreciable degree of kinetic stability to the native conformation of the collagen molecule.

Soil Research ◽  
2012 ◽  
Vol 50 (1) ◽  
pp. 44 ◽  
Author(s):  
M. A. Mojid ◽  
H. Cho

This study explored the effects of water content and temperature on the mobility of exchangeable cations (termed the surface ionic mobility and hereafter ionic mobility) in the hydration layers of bentonite clay. The ionic mobility directly governs the surface conductivity of the clay. The investigation was done by measuring the bulk electrical conductivity (EC) of four sand–bentonite mixtures of different proportions for a wide range of water contents under constant temperature, and three bentonite samples at different water contents over 5–90°C. The ionic mobility was determined from the surface conductivity at the mean ionic strength of the hydration layers. The ionic mobility in the sand–bentonite samples increased with an increase in hydration layer thickness. For a given thickness of the hydration layer, the greater the bentonite content of a sample, the smaller was the ionic mobility. The ionic mobility in the bentonite samples at different water contents also increased, at reduced rates, with a rise in temperature. Consequently, the surface conductivity of the samples increased non-uniformly, at two different rates, with an increase in temperature. The increasing rate of this conductivity depended on temperature; over the low temperature range which depended on the water content, the rate was 0.013 dS/m.K, and over higher temperature range, the rate decreased to 0.008 dS/m.K. The commonly used temperature correction factor, 0.019 dS/m.K, for EC therefore did not hold true for the bentonite samples.


2021 ◽  
Vol 9 (7) ◽  
pp. 1896-1907
Author(s):  
Shota Yamada ◽  
Takaki Kobashi ◽  
Motohiro Tagaya

Phosphorus-containing mesoporous silica films were synthesized by the introduction of phosphoric acid. The hydration layers on the films had the asymmetric stretching vibration of water molecules to provide the specific fibronectin adsorption.


Author(s):  
Jens Konnerup-Madsen

NOTE: This article was published in a former series of GEUS Bulletin. Please use the original series name when citing this article, for example: Konnerup-Madsen, J. (2001). A review of the composition and evolution of hydrocarbon gases during solidification of the Ilímaussaq alkaline complex, South Greenland. Geology of Greenland Survey Bulletin, 190, 159-166. https://doi.org/10.34194/ggub.v190.5187 _______________ Fluid inclusions in minerals from agpaitic nepheline syenites and hydrothermal veins in the Ilímaussaq complex and in similar agpaitic complexes on the Kola Peninsula, Russia, are dominated by hydrocarbon gases (predominantly methane) and hydrogen. Such volatile compositions differ considerably from those of most other igneous rocks and their formation and entrapment in minerals reflects low oxygen fugacities and a wide range of crystallisation temperatures extending to a low-temperature solidus. Their composition reflects initial low carbon contents and high water contents of the magma resulting in the exsolution of a waterrich CO2–H2O dominated vapour phase. Fractionation of chlorides into the vapour phase results in high salinities and the subsequent development of a heterogeneous vapour phase with a highly saline aqueous-rich fraction and a methane-dominated fraction, with preferential entrapment of the latter, possibly due to different wetting characteristics. The light stable isotope compositions support an abiogenic origin for the hydrocarbons in agpaitic nepheline syenite complexes.


Author(s):  
Kai Xing ◽  
Qihai Shu ◽  
David R Lentz

Abstract There are more than 90 porphyry (or skarn) Mo deposits in northeastern China with Jurassic or Cretaceous ages. These are thought to have formed mainly in a continental arc setting related to the subduction of the Paleo-Pacific oceanic plate in the Jurassic and subsequent slab rollback in the early Cretaceous. The Jurassic Daheishan porphyry Mo deposit is one of the largest Mo deposits in NE China, which contains 1.09 Mt Mo with an average Mo grade of 0.07%. To better understand the factors that could have controlled Mo mineralization at Daheishan, and potentially in other similar porphyry Mo deposits in NE China, the geochemical and isotopic compositions of the ore-related granite porphyry and biotite granodiorite, and the magmatic accessory minerals apatite, titanite and zircon from the Daheishan intrusions, were investigated so as to evaluate the potential roles that magma oxidation states, water contents, sulfur and metal concentrations could have played in the formation of the deposit. Magmatic apatite and titanite from the causative intrusions show similar εNd(t) values from -1.1 to 1.4, corresponding to TDM2 ages ranging from 1040 to 840 Ma, which could be accounted for by a mixing model through the interaction of mantle-derived basaltic melts with the Precambrian lower crust. The Ce and Eu anomalies of the magmatic accessory minerals have been used as proxies for magma redox state, and the results suggest that the ore-forming magmas are highly oxidized, with an estimated ΔFMQ range of + 1.8 to + 4.1 (+2.7 in average). This is also consistent with the high whole-rock Fe2O3/FeO ratios (1.3–26.4). The Daheishan intrusions display negligible Eu anomalies (Eu/Eu* = 0.7–1.1) and have relatively high Sr/Y ratios (40–94) with adakitic signatures; they also have relatively high Sr/Y ratios in apatite and titanite. These suggest that the fractionation of amphibole rather than plagioclase is dominant during the crystallization of the ore-related magmas, which further indicates a high magmatic water content (e.g., >5 wt%). The magmatic sulfur concentrations were calculated using available partitioning models for apatite from granitoids, and the results (9–125 ppm) are indistinguishable from other mineralized, subeconomic and barren intrusions. Furthermore, Monte Carlo modelling has been conducted to simulate the magmatic processes associated with the formation of the Daheishan Mo deposit, and the result reveals that a magma volume of ∼280 km3 with ∼10 ppm Mo was required to form the Mo ores containing 1.09 Mt Mo in Daheishan. The present study suggests that a relatively large volume of parental magmas with high oxygen fugacities and high water contents is essential for the generation of a giant porphyry Mo deposit like Daheishan, whereas a specific magma composition (e.g., with unusually high Mo and/or S concentrations), might be less critical.


1997 ◽  
Vol 52 (6) ◽  
pp. 749-756
Author(s):  
Zofia Plesnar ◽  
Stanisław Malanowski ◽  
Zenon Lotowski ◽  
Jacek W. Morzycki ◽  
Jadwiga Frelek ◽  
...  

Abstract The cryoscopic measurements show that title compounds are strongly associated in CHCl3 solutions. The association of the 20 R epimer is distinctly less pronounced than that of the 20 S epipmer. Self-association of the 20 S epimer leads to the formation of very large com­plexes. The 20 R epimer forms associates via water molecules. The dissimilarity may be ex­plained in terms of different accessibility of the lactam carbonyl groups in the two epimers for the association. It is proposed that the association process is controlled by the configura­tion at the carbon atom C(20) and conformation around the C(20)-C(22) bond. Populations of side chain conformations of both epimers were determined by means of proton nuclear magnetic resonance. It was found for the 20 R epimer that the t and the -g rotamers are almost equally populated, and the rotamer +g is excluded. For the 20 S epimer the +g rotamer predominates over the t one, and the -g rotamer is excluded. The NMR data are fully consistent with the results of the molecular modelling studies.


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