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Nanoparticles have unique facile surface chemistry and optical properties [29].
Possible structure of AgGSH-metal ion-Cys complex forms.
Takani, Metal–amino acid chemistry.
Yamauchi, Amino acid- and protein-metal chemistry as an approach to biological functions.
Chemistry 422 (2008) 236–239

The materials possessing similar structure were also termed as “shechtmanit”.
There are temperatures of especially intensive structure changes for each melt.
Tsepelev: Equilibrium and nonequilibrium states of metal melts, Fundamental studies of the physical chemistry of metallic melts, Academia Books, 2002, pp. 214-228
Herzer, Grain structure and magnetism of nanocrystalline ferromagnets, IEEE Trans.
Anusionwu, Theoretical investigation of viscosity of some liquid metal and alloys, Physical and Chemistry of Liquids. 49 (2011) 247-258

Formation of non-stoichiometric compounds occluding counter-ions of the reactant salts in their structure has been revealed.
After annealing the morphology of the yttrium oxide particles changes: pseudo-spongy structure is formed (Fig. 4).
[13] Effect of oxygen content and charge on the structure, stability and Optoelectronic properties of yttrium oxide Clusters Natarajan Sathiyamoorthy Venkataramanan, Journal of Physical and Chemistry of Solids, 2015
Jacobson, Synthesis and Structures of Yttrium – Transition Metal Sulfates YM(OH)3(SO4), M=Ni, Cu, J.
Solid State Chemistry, 147 (1999) 641-646

However, the process of gas hydrate formation and its kinetics are not studied properly; they belong mostly to supramolecular chemistry.
The process is widely used in crystal chemistry.
System magnetization results in specific water structuring.
Pauling on the availability of clathrate structures in water; the structures play basic role in gas hydrate formation.
Industrial and engineering chemistry, 26, 1183-1187

Treatment by alkaline and HCl of 1.0 mol/L and 2.0 mol/L could increase purity while treatment of 3.0 mol/L hydrochloric acid could dissolve some element of ATP so much as form SiO2 and destroy fiber structure to clips.
Introduction Attapulgite (ATP) is a hydrated magnesium silicate mineral and with a structure consisting of ribbons of layers and specific surface area.
Fig. 1(e) shows that 3mol/L hydrochloric acid activation destroyed fiber structure of ATP and some chips appear, and as well, its bend structure as shown in Fig. 1(f).
The average bulk crystal structure of ATP can be readily revealed by X-ray diffraction [5].
Tech Vol. 431 (2006), p. 256 [6] Hong Yue. in: Advanced Inorganic Chemistry , Machinery Industry Press, China (2002) First Author: ZHA#G Zhihong Faculty of chemistry and chemical engineering, Jiangsu Polytechnic University, Changzhou 213164, China TEL: 13813560912 FAX: 0519-83290205 Email: zzhfine@163.com

Poly acrylic acid superabsorbent hydrogel for hygiene materials Hongwei Cui1,a, Shimiao Wen1,b, Tingting Zhuang1,c, Fuchen Bai1,d, Li Yu1,e 1Polymer composites engineering laboratory, Changchun institute of applied chemistry Chinese academy of sciences, Changchun, Jilin, 130062, China ahwcui@ciac.ac.cn, bwen@ciac.ac.cn, cjoy@ciac.ac.cn, dfcbai@ciac.ac.cn, liyu@ciac.ac.cn Keywords: Surface crosslink, Acrylic acid, Neutralization, absorptivity.
Scanning electron microscopy (SEM) was used to observe the surface of the PAA powder, and prove that surface crosslink promote form a kind of honeycomb structure.
But the tendency of absorptivity at 2068Pa does not obey Flory-Huggins swelling theory, because the closslinked PAA hydrogel is three-dimensional network structure, like Fig.3(b), with the dosage of MBA increasing, the network become dense, and the structure become strength and full elastic, therefore, the influence of pressure is more and more weak, the absorptivity under pressure is more close to absorptivity without pressure, then the curves are getting higher.
Chains cross-link together looks like honeycomb structure, which’s structure is only swelling, but not moving, so as to hold the solution.
Polym Compos, 32: 277–289. doi: 10.1002/pc.21046 [7]P.J.Flory，The principles of polymer Chemistry[M]，Cornell University Press，Ithaca，New York，1954.

Pyridine has an important catalytic role in Gif chemistry and under free-radical conditions it is a non-inert solvent.
It is obvious that the functionalization of the polymer support did not influence the pore structure and textural properties.
Authors thank Boyko Tsyntsarski (Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences) for the IR spectra.
Structure 205 (1999), p. 511
[9] Ullmann's Encyclopedia of Industrial Chemistry (VerlagChemie, Weinheim, 1975), p. 680

A relatively recent and cutting-edge technique in materials chemistry is the immediate production of NaBH4 nanoparticles from sodium methoxide (NaOCH3) for hydrogen storage uses.
The negative electrode has a central core and outer shell structure.
Because of their layered structure, the core-shell type cathode’s outer and central layers have distinct compositions and properties.
Sustainable Chemistry One World. 3, 1000022 (2024)
Piskin, Microwave assisted green chemistry approach of sodium metaborate dihydrate (NaBO2.2H2O) synthesis and use as raw material for sodium borohydride (NaBH4) thermochemical production.

At some point, due to the presence of a large number of repeating units, the macrocycle can open and form a linear structure with branched groups included (Figure 1).
These changes in properties are due to the ongoing process of structuring the PPS.
Apparently, under these HT conditions, destruction processes prevail over structuring processes.
Hawkins, Chemistry of the Cure of Poly(p-phenylene Sulfide), Macromolecules. 9 (1976) 189-194
Busev, Analytical Chemistry of Sulfur, Nauka, Moscow, 1975.

Intrinsic graphene is defined as a one-atomic-thick planar film of sp2-hybridized carbon atoms which are densely packed in a hexagonal crystal lattice structure.
Unfortunately, the as-grown HFLG suffers from a structural defect corresponding to a lattice distortion of carbon structure deposited on the HFLG surface.
Their results showed that graphite crystallite structures and carbon dimers (C2) were observed during the deposition process.
The lateral size of graphene spans an order of magnitude from approximately 1 nm (with two hexagonal structures) to more than 20 µm.
The surface chemistry of graphene also contributes to its biological response.